PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Yamaguchi, Takashi
Kishi, Kazuhito
Hiramatsu, Masami
Kosuge, Katsuhiro
Musha, Akihiro
Umemura, Masanari
Ishikawa, Yoshihiro
Abrégé
A cancer treatment apparatus for applying a magnetic field to a living body is disclosed. The cancer treatment apparatus includes a magnetic field generator configured to generate a magnetic field; a power supply unit configured to supply a drive current to the magnetic field generator; and a controller configured to control the drive current supplied from the power supply unit, based on information on a cross section of a portion of a living body to which the magnetic field generated by the magnetic field generator is applied.
A61N 2/02 - Magnétothérapie utilisant des champs magnétiques produits par des bobines, y compris par des boucles à spire unique ou par des électro-aimants
2.
NUCLEIC ACID CONSTRUCT CAPABLE OF MEASURING HOMOLOGOUS RECOMBINATION ACTIVITY AND UTILIZATION THEREOF
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
Disclosed are a means which enables simple and rapid detection of the presence or absence, and of the degree, of HR activity in an individual, and a means which is useful for detection and treatment of homologous recombination-restored cancer for which no treatment means is available at present. The nucleic acid construct of the present invention is a nucleic acid construct comprising a set of a first nucleic acid molecule and a second nucleic acid molecule, the first nucleic acid molecule comprising: a promoter region; and a mutant gene sequence operably linked downstream thereof, the mutant gene sequence being constituted by a gene sequence encoding a protein and a cleavage site arranged inside thereof; the second nucleic acid molecule comprising a complementation region capable of replacing, by homologous recombination, a partial region comprising the cleavage site in the mutant gene sequence, the complementation region being constituted by a first homologous region and a second homologous region. The construct is useful as a measurement reagent or kit for homologous recombination activity, a diagnostic agent for homologous recombination-deficient cancer, a therapeutic agent for homologous recombination-restored cancer, or the like.
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
C12N 15/90 - Introduction stable d'ADN étranger dans le chromosome
C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer
3.
TESTING METHOD FOR NONALCOHOLIC FATTY LIVER DISEASE (NAFLD) USING AMINO ACID
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
EA PHARMA CO., LTD. (Japon)
Inventeur(s)
Nakajima, Atsushi
Kessoku, Takaomi
Iwaki, Michihiro
Shiraishi, Seiji
Ikenoue, Yuka
Abrégé
[Problem] To provide a simpler testing method for a NAFLD or an assisting method for the diagnosis of a NAFLD, which is excellent in sensitivity and specificity. [Solution] Provided is a testing method for a nonalcoholic fatty liver disease (NAFLD), the method including a step for detecting or quantifying L-methionine in a biological sample derived from a subject.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
4.
TESTING METHOD FOR NONALCOHOLIC FATTY LIVER DISEASE (NAFLD) USING AMINO ACID
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
EA PHARMA CO., LTD. (Japon)
Inventeur(s)
Nakajima, Atsushi
Kessoku, Takaomi
Iwaki, Michihiro
Shiraishi, Seiji
Ikenoue, Yuka
Abrégé
[Problem] To provide a simpler testing method for a NAFLD or an assisting method for the diagnosis of a NAFLD, which is excellent in sensitivity and specificity. [Solution] Provided is a testing method for a nonalcoholic fatty liver disease (NAFLD), the method including a step for detecting or quantifying D-histidine in a biological sample derived from a subject.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
5.
FORMATION OF THREE-DIMENSIONAL ORGAN FROM PLURIPOTENT STEM CELLS, METHOD FOR GENERATING CELL CONDENSATE FOR SELF-ORGANIZATION
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Takebe, Takanori
Taniguchi, Hideki
Yoshikawa, Hiroshi
Abrégé
The present disclosure relates to construction of three-dimensional organs from pluripotent stem cells. The present disclosure also relates to a method of forming a cell condensate for self-organization.
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
A61L 27/36 - Matériaux pour prothèses ou pour revêtement de prothèses contenant des constituants de constitution indéterminée ou leurs produits réactionnels
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
NARA SEIKO INC. (Japon)
Inventeur(s)
Nakayama, Meijin
Oridate, Nobuhiko
Nakagawa, Hiroo
Nishiura, Sunao
Kitamura, Hitomi
Abrégé
Provided is a forceps device (1) configured to easily change a state of a ratchet mechanism (19). The forceps device (1) includes an opening/closing drive unit (6) that opens an opening/closing portion (4) when positioned at an open position (O) and closes the opening/closing portion (4) when positioned at a closed position (C), and a ratchet mechanism (19) transitions between a restriction state in which the opening/closing drive unit (6) is restricted to move in the open position (O) direction and a restriction release state in which the move is not restricted. The ratchet mechanism (19) includes an operation portion (27) that projects rearward from a main body (3) of the forceps device (1) and is operated to cause the transition of the state of the ratchet mechanism (19).
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Kishi, Kazuhito
Yamaguchi, Takashi
Hasegawa, Motokazu
Umemura, Masanari
Ishikawa, Yoshihiro
Abrégé
An alternating magnetic field having a frequency, at which a sufficient antitumor effect can be obtained, is enabled to be applied to a living body for a previously prescribed period of time while restricting an amount of heat generation from the living body. A cancer treatment apparatus includes a magnetic field generator configured to generate an alternating magnetic field to be applied to a living body, and a magnetic field controller configured to increase an intensity of the alternating magnetic field generated by the magnetic field generator stepwise until a first period of time elapses since application of the alternating magnetic field to the living body, and to set the intensity of the alternating magnetic field to a previously set maximum value from elapse of the first period of time until a timing to end the application of the alternating magnetic field.
A61N 2/02 - Magnétothérapie utilisant des champs magnétiques produits par des bobines, y compris par des boucles à spire unique ou par des électro-aimants
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Kishi, Kazuhito
Yamaguchi, Takashi
Hasegawa, Motokazu
Umemura, Masanari
Ishikawa, Yoshihiro
Abrégé
An alternating magnetic field having a frequency, at which a sufficient antitumor effect can be obtained, is enabled to be applied to a living body while restricting an amount of heat generation. A cancer treatment apparatus includes a magnetic field generator including a coil configured to generate an alternating magnetic field to be applied to a living body, and a cooler configured to cool a magnetic field application part of the living body in which a temperature rises in response to application of the alternating magnetic field.
A61N 2/02 - Magnétothérapie utilisant des champs magnétiques produits par des bobines, y compris par des boucles à spire unique ou par des électro-aimants
9.
Formation of Three-Dimensional Organ from Pluripotent Stem Cells
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Okada, Kozo
Ishihara, Keiichiro
Kobayashi, Yusuke
Abrégé
This heart failure estimation device acquires an image or video obtained by imaging the face of a patient. The heart failure estimation device extracts one or more feature parameters from the image or video. On the basis of the one or more feature parameters, the heart failure estimation device estimates the degree of heart failure of the patient.
A61B 10/00 - Instruments pour le prélèvement d'échantillons corporels à des fins de diagnostic Autres procédés ou instruments pour le diagnostic, p. ex. pour le diagnostic de vaccination ou la détermination du sexe ou de la période d'ovulationInstruments pour gratter la gorge
A61B 3/113 - Appareils pour l'examen optique des yeuxAppareils pour l'examen clinique des yeux du type à mesure objective, c.-à-d. instruments pour l'examen des yeux indépendamment des perceptions ou des réactions du patient pour déterminer ou enregistrer le mouvement de l'œil
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
A61B 5/107 - Mesure de dimensions corporelles, p. ex. la taille du corps entier ou de parties de celui-ci
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
The nucleic acid construct according to the present invention has such a structure that a protein can be expressed by the occurrence of at least two times of a recombinant reaction by single-strand annealing (SSA), is useful for the diagnosis and treatment of mismatch repair (MMR) deficient cancer, is applicable to the searching of a factor capable of regulating a reaction of MMR or SSA, an inhibitor or an activator for the reaction of MMR or SSA, and is also applicable to the prediction of whether of not a gene mutation identified in a cancer patient is a mutation that deteriorates an MMR activity. A conventional SSA construct that has been developed in the past by the present inventors has such a structure that a protein is expressed by the occurrence of one time of a SSA reaction. According to the construct of the present invention, the difference in the protein expression amount (activity) between the case where an MMR deficient is present and the case where an MMR deficient is absent occurs more greatly compared with that in the conventional SSA construct. Therefore, the construct of the present invention is expected to act on an MMR deficient cell more specifically and provide, for example, a treatment means having fewer adverse side effects.
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteursVecteurs Utilisation d'hôtes pour ceux-ciRégulation de l'expression
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C12Q 1/04 - Détermination de la présence ou du type de micro-organismeEmploi de milieux sélectifs pour tester des antibiotiques ou des bactéricidesCompositions à cet effet contenant un indicateur chimique
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
13.
CULTURE DEVICE, METHOD FOR MONITORING CULTURE SUBJECT, AND CULTURE CHIP
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kimura Hiroshi
Shirai Hiroki
Nakamura Hiroko
Ikawa Masahito
Fujiwara Kamoshita Maki
Ogawa Takehiko
Yamauchi Ishikawa Yu
Nagata Shino
Abrégé
This culture device comprises a container body that houses a culture liquid, and a culture chip that forms a culture chamber inside the container body, wherein: the container body has a light-permeable and gas-permeable bottom wall; and the culture chip has a frame that is in contact with the top surface of the bottom wall, and a membrane member that is permeable to a liquid or a liquid-containing material and is fixed to the top surface of the frame to form the culture chamber together with the bottom wall and the frame.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
MATRI SURGE CO., LTD. (Japon)
Inventeur(s)
Yagi Hiroshi
Tsuchida Tomonori
Nagata Shogo
Nishi Kotaro
Taniguchi Hideki
Kuse Yoshiki
Okamoto Satoshi
Ohtomo Mana
Abrégé
A production method for an artificial organ according to the present invention involves performing a decellularization treatment on a mammalian organ or a portion thereof to obtain a decellularized organ or a portion thereof and performing a cellularization treatment that grafts cells onto the decellularized organ or portion thereof to obtain an organ onto which the cells have been grafted. The cellularization treatment involves injecting an organoid that includes cells of the relevant organ or cells that can differentiate into cells of the relevant organ into the decellularized organ or portion thereof and infusing the blood vessels of the decellularized organ or portion thereof with cells of the relevant organ or cells that can differentiate into cells of the relevale organ. An artificial organ according to the present invention is obtained by means of the production method for an artificial organ.
Public University Corporation Yokohama City University (Japon)
Takeda Pharmaceutical Company Limited (Japon)
Inventeur(s)
Takebe, Takanori
Saiki, Norikazu
Abrégé
The present invention provides drug toxicity evaluation platforms (such as an evaluation method and a kit therefor) that enable detailed analysis of the possibility and the like of developing drug-induced damage (such as DILI) to the liver and other organs. The method for evaluating drug toxicity of the present invention includes: a step of adding a drug to a co-culture system of an organoid and blood cells; and a step of evaluating the toxicity of the drug to the organoid.
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
C12N 5/078 - Cellules du sang ou du système immunitaire
16.
IMIDAZOPYRIDINE DERIVATIVES WITH BICYCLIC STRUCTURE
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
DAIICHI SANKYO COMPANY, LIMITED (Japon)
Inventeur(s)
Namiki Hideki
Takeda Yasuyuki
Yoshikawa Kenji
Akiu Mayuko
Kawamoto Yoshito
Motoyama Keisuke
Yoshioka Shun
Minakawa Kosuke
Kadoshima Kumiko
Yoshihama Yohei
Tsunematsu Hiroki
Ono Shigeo
Yamashita Akio
Abrégé
The present invention addresses the problem of providing a novel compound having an SMG1 inhibitory activity and an anticancer effect, or a pharmaceutically acceptable salt thereof etc. A compound represented by formula (1) or a pharmaceutically acceptable salt thereof. (Here, in formula (1), R1, R2, R3, R4, X, Y, and Z are each as defined in the specification.)
C07D 471/22 - Composés hétérocycliques contenant des atomes d'azote comme uniques hétéro-atomes du système condensé, au moins un cycle étant un cycle à six chaînons avec un atome d'azote, non prévus dans les groupes dans lesquels le système condensé contient au moins quatre hétérocycles
A61K 31/395 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines
A61K 31/4375 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques le système hétérocyclique contenant un cycle à six chaînons ayant l'azote comme hétéro-atome du cycle, p. ex. quinolizines, naphtyridines, berbérine, vincamine
A61K 31/444 - Pyridines non condenséesLeurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p. ex. amrinone
A61K 31/4545 - Pipéridines non condensées, p. ex. pipérocaïne contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p. ex. pipampérone, anabasine
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
A61K 31/506 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime non condensées et contenant d'autres hétérocycles
A61K 31/519 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime condensées en ortho ou en péri avec des hétérocycles
A61K 31/5365 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec au moins un azote et au moins un oxygène comme hétéro-atomes d'un cycle, p. ex. 1,2-oxazines condensées en ortho ou en péri avec des systèmes hétérocycliques
A61K 31/5377 - 1,4-Oxazines, p. ex. morpholine non condensées et contenant d'autres hétérocycles, p. ex. timolol
A61K 31/5386 - 1,4-Oxazines, p. ex. morpholine condensées en spiro ou formant une partie de systèmes cycliques pontés
A61K 31/5395 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec au moins un azote et au moins un oxygène comme hétéro-atomes d'un cycle, p. ex. 1,2-oxazines ayant plusieurs atomes d'azote dans le même cycle, p. ex. oxadiazines
A61K 31/55 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à sept chaînons, p. ex. azélastine, pentylènetétrazole
A61K 31/551 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à sept chaînons, p. ex. azélastine, pentylènetétrazole ayant deux atomes d'azote comme hétéro-atomes d'un cycle, p. ex. clozapine, dilazèpe
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
A61K 45/00 - Préparations médicinales contenant des ingrédients actifs non prévus dans les groupes
A61P 35/02 - Agents anticancéreux spécifiques pour le traitement de la leucémie
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C07D 498/22 - Composés hétérocycliques contenant dans le système condensé au moins un hétérocycle comportant des atomes d'azote et d'oxygène comme uniques hétéro-atomes du cycle dans lesquels le système condensé contient au moins quatre hétérocycles
C07D 513/22 - Composés hétérocycliques contenant dans le système condensé au moins un hétérocycle comportant des atomes d'azote et de soufre comme uniques hétéro-atomes du cycle, non prévus dans les groupes , ou dans lesquels le système condensé contient au moins quatre hétérocycles
C07D 519/00 - Composés hétérocycliques contenant plusieurs systèmes de plusieurs hétérocycles déterminants condensés entre eux ou condensés avec un système carbocyclique commun non prévus dans les groupes ou
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Ejiri, Yoko
Ayano, Satoru
Fukuhara, Naoto
Taniguchi, Hideki
Takebe, Takanori
Abrégé
Provided is a culture chamber capable of preparing spheroids with a uniform size with high efficiency and having a micro-space structure which is designed to facilitate replacement of a medium and harvesting of cells. The culture chamber includes a plurality of recesses (10) each formed of a bottom portion (11) and an opening portion (12). The bottom portion (11) has one of a hemispherical shape and a truncated cone shape and the opening portion (12) is defined by a wall that surrounds an area from a boundary between the opening portion (12) and the bottom portion (11) to an end of each of the recesses (10), the wall having a taper angle in a range from 1 degree to 20 degrees. An equivalent diameter of the boundary is in a range from 50 μm to 2 mm and a depth from a bottom of the bottom portion (11) to the end of each of the recesses is in a range from 0.6 or more times to 3 or less times the equivalent diameter, and the wall defining the opening portion (12) forms a surface continuous to the bottom portion (11) and an inclination of the continuous surface changes at the boundary.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Miyagi, Etsuko
Murase, Mariko
Hayama, Tomonari
Ryo, Akihide
Horiuchi, Yayoi
Kobori, Hiroki
Ohtake, Norihisa
Abrégé
An object of the present invention is to provide a biomarker that enables selection of an embryo having a high rate of implantation and pregnancy, that is, an embryo having high fertility, from embryos obtained through embryo culture after in vitro fertilization in infertility treatment, and a criterion therefor. Provided is a criterion that enables identification of an ovum suitable for implantation and pregnancy based on measurement of the concentration of soluble CD163 which is present in follicular fluid collected at the same time as an ovum in ovum pick up in infertility treatment, or which is present in serum immediately before the ovum pick up.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C07K 16/28 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant d'animaux ou d'humains contre des récepteurs, des antigènes de surface cellulaire ou des déterminants de surface cellulaire
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Inamori, Masakazu
Hino, Motohiro
Amimoto, Naoki
Tatsumi, Rie
Ikeda, Kazuhiro
Taniguchi, Hideki
Okamoto, Satoshi
Abrégé
The present invention provides a method for mass producing cell aggregates such as artificial organoids through an approach that differs entirely from previous methods. Specifically, provided is a method for producing cell aggregates that includes a step in which a mixture of mesenchymal stem cells, vascular endothelial cells, and organ cells are filled into microfibers, and the mixture is suspension cultured to form cell aggregates.
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
A61K 35/28 - Moelle osseuseCellules souches hématopoïétiquesCellules souches mésenchymateuses de toutes origines, p. ex. cellules souches dérivées de tissu adipeux
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Omiya, Yasuhiro
Takano, Takeshi
Endo, Koji
Okada, Kozo
Kobayashi, Yusuke
Abrégé
This information processing device acquires speech data that is time series data of the speech spoken by a user. The information processing device computes state information that represents a cardiac condition of a user, and outputs the computed condition information on the basis of the speech data.
A61B 10/00 - Instruments pour le prélèvement d'échantillons corporels à des fins de diagnostic Autres procédés ou instruments pour le diagnostic, p. ex. pour le diagnostic de vaccination ou la détermination du sexe ou de la période d'ovulationInstruments pour gratter la gorge
Public University Corporation Yokohama City University (Japon)
Eiken Kagaku Kabushiki Kaisha (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Yasui, Ryota
Abrégé
The present invention provides a marker gene capable of detecting the undifferentiated cells that remain or become included in a differentiated cell population. Undifferentiated cells present in a differentiated cell population are detected by using at least one gene selected from the group consisting of LINC00678 and PRDM14 as an undifferentiation marker. A method of detecting undifferentiated cells; a method of using the gene as an undifferentiation marker; and a kit for detecting undifferentiated cells. A method of selecting an undifferentiated cell clone is also provided.
C12Q 1/6888 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour la détection ou l’identification d’organismes
22.
POWER SUPPLY APPARATUS AND MAGNETIC FIELD GENERATION SYSTEM
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kishi, Kazuhito
Takai, Masami
Hasegawa, Motokazu
Akaishi, Masataka
Umemura, Masanari
Ishikawa, Yoshihiro
Akimoto, Taisuke
Abrégé
A power supply apparatus includes a power supply configured to apply an alternating current to a magnetic field generation apparatus; and a controller configured to control the alternating current applied by the power supply. The controller controls the power supply to apply the alternating current having a waveform pattern including a plurality of current waveforms having different frequency spectrums from each other.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Yamaguchi, Takashi
Kishi, Kazuhito
Hasegawa, Motokazu
Umemura, Masanari
Ishikawa, Yoshihiro
Nagasako, Akane
Abrégé
[Object] To provide a cancer treatment device that monitors a magnetic field applied to an affected area or monitors a temperature of the affected area or around the affected area. [Means of Achieving the Object] A cancer treatment system includes a magnetic field generator configured to generate an alternating current magnetic field to be applied to a cancer affected area, a magnetic field measurer configured to measure a magnitude of the magnetic field generated by the magnetic field generator, wherein the cancer affected area is inserted into the magnetic field generated by the magnetic field generator to treat cancers.
A61N 2/04 - Magnétothérapie utilisant des champs magnétiques produits par des bobines, y compris par des boucles à spire unique ou par des électro-aimants utilisant des champs variables, p. ex. des champs basse fréquence ou des champs pulsés
24.
SARS-CoV-2 DETECTION KIT AND SARS-CoV-2 DETECTION METHOD
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Ujihara, Dai
Katada, Junichi
Ryo, Akihide
Abrégé
An object of the present invention is to provide a SARS-CoV-2 detection kit and a SARS-CoV-2 detection method which make it possible to simply detect SARS-CoV-2 with higher sensitivity. According to the present invention, there is provided a SARS-CoV-2 detection kit which is for specifically detecting a nucleocapsid protein contained in a biological specimen and contains at least one antibody that specifically reacts with a SARS-CoV-2 nucleocapsid protein (NP), the SARS-CoV-2 detection kit including a first container that houses a silver-containing compound, and a second container that houses a reducing agent capable of reducing silver ions, in which the antibody includes at least one antibody that belongs to a subclass IgG2b.
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
G01N 33/553 - Support métallique ou recouvert d'un métal
25.
EVALUATION METHOD, CALCULATION METHOD, EVALUATION DEVICE, CALCULATION DEVICE, EVALUATION PROGRAM, CALCULATION PROGRAM, RECORDING MEDIUM, EVALUATION SYSTEM AND TERMINAL DEVICE FOR RELATIVE PHARMACOLOGICAL ACTION OF COMBINATION OF IMMUNE CHECKPOINT INHIBITOR WITH ANTICANCER DRUG AS CONCOMITANT DRUG COMPARED TO PHARMACOLOGICAL ACTION OF IMMUNE CHECKPOINT INHIBITOR ALONE
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Azuma, Koichi
Murotani, Kenta
Sasada, Tetsuro
Tagami, Tomoyuki
Hagiwara, Asami
Imaizumi, Akira
Karakawa, Sachise
Kawasaki, Mika
Miyagi, Yohei
Tamura, Tomohiko
Saito, Haruhiro
Nakahara, Yoshiro
Wei, Feifei
Kasajima, Rika
Xiang, Huihui
Ban, Tatsuma
Abrégé
The present invention addresses the problem of providing an evaluation method, etc., capable of providing reliable information that can be used as a reference for understanding an individual difference in the expression of the relative pharmacological action of a combination of an immune checkpoint inhibitor with an anticancer drug, which is a concomitant agent, compared to the pharmacological action of the immune checkpoint inhibitor alone. The present embodiment evaluates the relative pharmacological action of a combination of an immune checkpoint inhibitor with an anticancer drug, which is a concomitant agent, in a subject to be evaluated, compared to the pharmacological action of the immune checkpoint inhibitor alone, by using the concentration of at least one metabolite selected from among Glu, Arg, Orn, Cit, His, Val, Phe, Tyr, Met, Pro, Asn, Leu, Lys, Thr, Ile, Gln, Ala, Ser, a-ABA, Trp, Gly, AnthA, hKyn, hTrp, Kyn, KynA, NP, QA and XA in the blood of the subject to be evaluated.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
26.
ANTI-SARS-CoV-2 ANTIBODY AGAINST SARS-CoV-2 ANTIGEN IN BODY FLUID, INCLUDING MUTANT; METHOD FOR DETECTING SARS-CoV-2 USING ANTIBODY; AND KIT CONTAINING ANTIBODY
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
KANTO KAGAKU KABUSHIKI KAISHA (Japon)
Inventeur(s)
Ryo, Akihide
Mihana, Yusaku
Yamaoka, Yutaro
Abrégé
The present invention addresses the problem of providing a highly sensitive and highly specific means for detecting a protein constituting a nucleocapsid derived from SARS-CoV-2. The above problem has been solved by, for example, an antibody binding to a protein constituting the nucleocapsid derived from SARS-CoV-2 or a fragment thereof, or a combination thereof; a method for detecting, from a sample, a protein constituting the nucleocapsid derived from SARS-CoV-2 using said antibody or a fragment thereof, or a combination thereof; and a kit for detecting a protein constituting the nucleocapsid derived from SARS-CoV-2, the kit containing said antibody or a fragment thereof, or a combination thereof.
C07K 16/10 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant de virus de virus à ARN
G01N 33/531 - Production de matériaux de tests immunochimiques
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
C12N 15/50 - Coronaviridae, p. ex. virus de la bronchite infectieuse, virus de la gastro-entérite transmissible
27.
Sensitive Detection Method for Undifferentiated Marker Genes
Public University Corporation Yokohama City University (Japon)
Eiken Kagaku Kabushiki Kaisha (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Yasui, Ryota
Matsui, Atsuka
Abrégé
The present invention provides a sensitive and simple detection method, and a kit therefor, which detects residual undifferentiated human pluripotent stem cells in an intermediate product and/or a final product of a regenerative medical products, using an isothermal nucleic acid amplification method, and specifically, a LAMP method. A method for detecting presence or absence of undifferentiated cells in a non-undifferentiated cell population, wherein RNA derived from an undifferentiation marker gene exhibiting a significant difference in expression level between the undifferentiated cells and the non-undifferentiated cells in a sample containing a nucleic acid derived from the cell population of interest is detected by the isothermal nucleic acid amplification method. The kit for detecting presence or absence of undifferentiated cells in a non-undifferentiated cell population comprises a reagent with which RNA derived from an undifferentiation marker gene exhibiting a significant difference in expression level between the undifferentiated cells and the non-undifferentiated cells is detected by the isothermal nucleic acid amplification method.
C12Q 1/6881 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour le typage de tissu ou de cellule, p. ex. sondes d’antigène leucocytaire humain [HLA]
28.
ANTIBODY AGAINST SARS-COV-2, METHOD FOR DETECTING SARS-COV-2 USING ANTIBODY AND KIT CONTAINING ANTIBODY
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
KANTO KAGAKU KABUSHIKI KAISHA (Japon)
Inventeur(s)
Ryo, Akihide
Yamaoka, Yutaro
Kikuchi, Sayaka
Abrégé
The present invention addresses the problem of providing a means for detecting a constituting protein of nucleocapsid derived from SARS-CoV-2. This problem has been solved by providing an antibody binding to a constituting protein of nucleocapsid derived from SARS-CoV-2 or a fragment of the antibody, a method for detecting a constituting protein of the SARS-CoV-2-derived nucleocapsid with the use of the antibody or a fragment thereof, a kit for detecting a constituting protein of the SARS-CoV-2-derived nucleocapsid, said kit containing the antibody or a fragment thereof, etc.
C07K 16/10 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant de virus de virus à ARN
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
29.
METHOD AND REAGENT FOR DETECTING PANCREATIC CANCERS
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Shibata, Wataru
Terauchi, Yasuo
Endo, Itaru
Shimizu, Yasuhiro
Ohtake, Norihisa
Myoba, Shohei
Abrégé
An object of the invention is to provide a method for detecting pancreatic cancer and a reagent that can be used for the method. The method is a method for detecting pancreatic cancer, characterized by comprising measuring the amount of TFPI2 in a body fluid collected from a subject. In addition, an antibody that specifically recognizes the TFPI2 processing polypeptide and intact TFPI2 is included in the reagent for detecting pancreatic cancer.
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
PUBLIC UNIVERSITY CORPORATION NAGOYA CITY UNIVERSITY (Japon)
PHARMA FOODS INTERNATIONAL CO., LTD. (Japon)
Inventeur(s)
Sato, Mamoru
Yamada, Michiyuki
Kanazawa, Satoshi
Toyoura, Masayoshi
Shoya, Yuji
Saito, Kenji
Yamazaki, Chihiro
Abrégé
Provided are anti-PAD4 antibodies having excellent properties and an excellent method for treatment of RA. Used are anti-PAD4 antibodies that specifically bind to an epitope containing positions 345, 347, and 348 of PAD4. These anti-PAD4 antibodies may inhibit the citrullination activity of PAD4. In addition, these anti-PAD4 antibodies may have a KD (M) of 9.0×10−9 or less. Optionally, the anti-PAD4 antibody and a TNFα inhibitor are used in combination.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
NARA SEIKO INC. (Japon)
Inventeur(s)
Nakayama Meijin
Oridate Nobuhiko
Nakagawa Hiroo
Nishiura Sunao
Kitamura Hitomi
Abrégé
Provided is a forceps device (1) that enables easy switching between states of a ratchet mechanism (19). The forceps device (1) comprises: an opening/closing drive part (6) that opens an opening/closing part (4) when positioned in an open position (O) and closes the opening/closing part (4) when positioned in a closed position (C); and a ratchet mechanism (19) that transitions between a restricted state in which movement of the opening/closing drive part (6) toward the open position (O) is restricted and an unrestricted state in which movement is not restricted. The ratchet mechanism (19) comprises an operation part (27) that protrudes rearward from a main body (3) of the forceps device (1) and is operated so as to transition the states of the ratchet mechanism (19).
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
Disclosed are a means which enables simple and rapid detection of the presence or absence, and of the degree, of homologous recombination activity in an individual, and a means which is useful for detection and treatment of homologous recombination-restored cancer for which no treatment means is available at present. The nucleic acid construct of the present invention comprises: (1) a promoter region; (2) a mutant gene sequence containing a cleavage site in a gene sequence encoding a protein; and (3) a base sequence composed of a first homologous region and a second homologous region, the base sequence being capable of replacing, by homologous recombination, a partial region in the mutant gene sequence of (2), the partial region containing the cleavage site. The nucleic acid construct of the present invention can be used as a measurement reagent or kit for homologous recombination activity, a diagnostic agent for homologous recombination-deficient cancer, a therapeutic agent for homologous recombination-restored cancer, or the like.
C12N 15/90 - Introduction stable d'ADN étranger dans le chromosome
C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
33.
CELL EVALUATION METHOD, CELL EVALUATION SYSTEM AND PROGRAM
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
NIKON CORPORATION (Japon)
Inventeur(s)
Taniguchi, Hideki
Takebe, Takanori
Ishikawa, Momotaro
Yamashita, Masafumi
Kiyota, Yasujiro
Abrégé
A cell evaluation method includes acquiring a first evaluation index and a first index calculated using the first evaluation index with respect to comparative target cells in a culture process including a cell differentiation-inducing process in which cell differentiation is induced, calculating a second index on the basis of the first evaluation index with respect to evaluation target cells different from the comparative target cells, and evaluating differentiation of the evaluation target cells by comparing the first index with the second index.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
Disclosed is means which enables simple and rapid detection of the presence or absence of mismatch repair activity, and which is useful for diagnosis and treatment of mismatch repair-deficient cancers. In an integrated-type nucleic acid construct provided by the present invention, [promoter region], [5′-side region+first homologous region], and [second homologous region+3′-side region] are placed in the same nucleic acid molecule. In a divided-type nucleic acid construct, [promoter region], [5′-side region+first homologous region], and [second homologous region+3′-side region] are placed in two different nucleic acid molecules. The nucleic acid construct of the present invention can be used as a therapeutic agent for mismatch repair-deficient cancer, as a diagnostic agent for mismatch repair-deficient cancer, or as a companion diagnostic agent for predicting an effect of an anticancer drug for mismatch repair-deficient cancer, containing the nucleic acid construct.
C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer
C12Q 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
C12N 15/85 - Vecteurs ou systèmes d'expression spécialement adaptés aux hôtes eucaryotes pour cellules animales
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
C07K 14/005 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant de virus
35.
METHOD AND REAGENT FOR DETECTING MALIGNANT OVARIAN TUMORS
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Miyagi, Etsuko
Arakawa, Noriaki
Ohtake, Ayase-Shi
Myoba, Shohei
Abrégé
An object of the present invention is to provide a method for detecting malignant ovarian tumor as distinguished from benign ovarian tumor, and a reagent that can be used for the method. Provided are a method for detecting malignant ovarian tumor (excluding high-grade serous carcinoma) as distinguished from benign ovarian tumor, characterized by measuring the amount of TFPI2 in a sample from a patient, and a reagent for detecting malignant ovarian tumor (excluding high-grade serous carcinoma) as distinguished from benign ovarian tumor contains an antibody that specifically recognizes TFPI2 processing polypeptide and intact TFPI2.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Murata, Soichiro
Ooba, Takayoshi
Abrégé
Developed is a method for creating cartilage tissue to solve the following problems. 1. Cartilage differentiation is not hindered by forming. 2. The cartilage can be formed into an intended shape without using a scaffold. A method for producing artificial cartilage tissue comprises: forming a spheroid containing cartilage precursor cells into a desired shape while seeding the spheroid onto a support; culturing the spheroid while supplying a culture medium from the front side and the rear side of the surface onto which the spheroid has been seeded, and fusing the spheroids with each other; and maturing the fused spheroid into cartilage tissue in vitro.
C12N 5/077 - Cellules mésenchymateuses, p. ex. cellules osseuses, cellules de cartilage, cellules stromales médulaires, cellules adipeuses ou cellules musculaires
A61L 27/36 - Matériaux pour prothèses ou pour revêtement de prothèses contenant des constituants de constitution indéterminée ou leurs produits réactionnels
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
Disclosed are a means that enables simple, rapid detection of the existence and degree of HR activity in an individual and a means useful in the detection and treatment of homologous recombination repair cancers. The nucleic acid construct of the present invention includes a set of a first nucleic acid molecule and a second nucleic acid molecule. The first nucleic acid molecule includes a promoter region and, operably linked downstream thereof, a mutant gene sequence having a cleavage site in the interior of a gene sequence that encodes a protein, and the second nucleic acid molecule includes a complementary region constituting a first homologous region and a second homologous region capable of substituting by homologous recombination the partial region including the cleavage site in the mutant gene sequence. The construct is useful as a reagent or kit for measuring homologous recombination activity, as a diagnostic agent for homologous recombination deletion cancers, as a therapeutic agent for homologous recombination repair cancers, etc.
C12N 15/11 - Fragments d'ADN ou d'ARNLeurs formes modifiées
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteursVecteurs Utilisation d'hôtes pour ceux-ciRégulation de l'expression
C12Q 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Taniguchi, Hideki
Nie, Yunzhong
Zheng, Yunwen
Abrégé
The disclosure provides a method for producing hepatocytes or hepatic progenitor cells; a method for suppressing hepatocyte aging using a drug causing histone hyperacetylation; a hepatocyte anti-aging agent; a method for increasing hepatocyte plasticity; and a drug for increasing hepatocyte plasticity.
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Ishikawa, Yoshihiro
Umemura, Masanari
Akimoto, Taisuke
Abrégé
A cancer treatment apparatus including a magnetic field generator that generates a magnetic field of 100 kHz to 300 kHz to be applied to affected tissues.
A61N 2/02 - Magnétothérapie utilisant des champs magnétiques produits par des bobines, y compris par des boucles à spire unique ou par des électro-aimants
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kakui, Hiroyuki
Shimizu, Kentaro K.
Yamazaki, Misako
Abrégé
The present invention relates to a method for distinguishing a first nucleic acid sequence from a second nucleic acid sequence by electrophoresis. The first nucleic acid comprises a first common sequence tract, a variable sequence tract and a second common sequence tract and the second nucleic acid comprises a first common sequence tract, optionally an variable sequence tract and a second common sequence tract. The first and the second nucleic acid sequence is contacted with a probe sequence that is reverse complementary to the first and second common sequence tract under conditions allowing the hybridization of the probe sequence to the first and second nucleic acid sequence, thereby forming a first probe hybrid and a second probe hybrid. Subsequently, the first and second probe hybrids are submitted to electrophoresis to detect the electrophoretic mobility of the first and second probe hybrid.
Public University Corporation Yokohama City University (Japon)
Takeda Pharmaceutical Company Limited (Japon)
Inventeur(s)
Takebe, Takanori
Saiki, Norikazu
Nio, Yasunori
Kawakami, Eri
Abrégé
A method for screening for a therapeutic drug for a disease involving excessive activation of a complement, using a s cytotoxicity marker associated with the complement as an index, including (1a) a step of adding a complement to a cell produced from a stem cell to cause the cell to form a cytotoxicity marker associated with the complement, and (2a) a step of adding a therapeutic drug candidate, and selecting a substance that decreases the amount of the cytotoxicity marker is provided by the present invention.
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
42.
BIOMARKER FOR DETERMINING FERTILITY, AND DETERMINING METHOD USING SAME
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Miyagi, Etsuko
Murase, Mariko
Hayama, Tomonari
Ryo, Akihide
Horiuchi, Yayoi
Kobori, Hiroki
Ohtake, Norihisa
Abrégé
The purpose of the present invention is to provide: a biomarker by which embryos having a high implantation/pregnancy probability, i.e., having high fertility can be selected from among embryos obtained by in vitro fertilization and then embryo culturing in infertility treatment; and a determination criterion thereof. The present invention provides a criterion with which an egg suitable for implantation/pregnancy can be determined, by measuring the concentration of soluble CD163 present in a follicular fluid to be collected simultaneously with the egg at the time of egg collection in infertility treatment or in a serum immediately before the egg collection.
C07K 14/705 - RécepteursAntigènes de surface cellulaireDéterminants de surface cellulaire
C07K 16/28 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant d'animaux ou d'humains contre des récepteurs, des antigènes de surface cellulaire ou des déterminants de surface cellulaire
C12N 15/12 - Gènes codant pour des protéines animales
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
43.
BIOMARKER FOR DETERMINING FERTILITY, AND DETERMINING METHOD USING SAME
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Miyagi, Etsuko
Murase, Mariko
Hayama, Tomonari
Ryo, Akihide
Horiuchi, Yayoi
Kobori, Hiroki
Ohtake, Norihisa
Abrégé
The purpose of the present invention is to provide: a biomarker by which embryos having a high implantation/pregnancy probability, i.e., having high fertility can be selected from among embryos obtained by in vitro fertilization and then embryo culturing in infertility treatment; and a determination criterion thereof. The present invention provides a criterion with which an egg suitable for implantation/pregnancy can be determined, by measuring the concentration of soluble CD163 present in a follicular fluid to be collected simultaneously with the egg at the time of egg collection in infertility treatment or in a serum immediately before the egg collection.
C07K 16/28 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant d'animaux ou d'humains contre des récepteurs, des antigènes de surface cellulaire ou des déterminants de surface cellulaire
C12N 15/12 - Gènes codant pour des protéines animales
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C07K 14/705 - RécepteursAntigènes de surface cellulaireDéterminants de surface cellulaire
44.
PRODUCTION METHOD FOR NON-HUMAN MODEL ANIMAL WITH MENTAL DISORDER OR NEUROLOGICAL DISORDER, SAID NON-HUMAN MODEL ANIMAL, AND METHOD FOR SCREENING FOR PROPHYLACTIC OR THERAPEUTIC AGENT FOR SAID MENTAL DISORDER OR NEUROLOGICAL DISORDER
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Takahashi Takuya
Miyazaki Tomoyuki
Jitsuki Susumu
Ota Wataru
Abrégé
Provided are: a method for producing a non-human model animal with a mental disorder or neurological disorder that is attributed to an increase or decrease in the expression of an AMPA receptor gene or an increase or decrease in the expression or function of an AMPA receptor in a predetermined region in the brain; a non-human model animal with the mental disorder or neurological disorder; and a screening method for discovering a prophylactic or therapeutic agent for the mental disorder or neurological disorder, using the non-human model animal. This method is for producing a non-human model animal with a mental disorder or neurological disorder that is attributed to an increase or decrease in the expression of an AMPA receptor gene or an increase or decrease in the expression or function of an AMPA receptor in a predetermined region in the brain. The method comprises: a step for decreasing or increasing at least one selected from the group consisting of the expression of the AMPA receptor gene or the AMPA receptor, and the function of the AMPA receptor, in the predetermined region of the non-human animal, compared to a wild type, or a step for inhibiting or activating a nervous pathway connecting the predetermined region with another region.
Public University Corporation Yokohama City University (Japon)
Takeda Pharmaceutical Company Limited (Japon)
Inventeur(s)
Takebe, Takanori
Saiki, Norikazu
Abrégé
The present invention provides means for producing an organoid close to an organ in a living body and capable of secretion of a plasma protein and immune response. A matrix composition of the present invention provided as such means includes: (1) a first matrix containing one or more cells selected from the group consisting of vascular cells, nerve cells, and blood cells; and (2) a second matrix containing to cells constituting an organ and/or an organoid, in which the first matrix envelops the second matrix, and the first matrix has at least one opening.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Murata, Soichiro
Abrégé
Provided is a coating-fixing agent for transplanting a cell or a tissue onto the surface of an organ, intestinal membrane, peritoneal membrane, etc. Provided are: a formulation for coating and fixing a graft, the formulation comprising alginate; a formulation kit for coating and fixing a graft, comprising a formulation containing alginate and a divalent or higher valent metal salt in combination; and a method for transplanting a graft, comprising: transplanting the graft to a transplant site of a human or a non-human animal, and coating the graft with alginate.
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Takebe, Takanori
Taniguchi, Hideki
Takahashi, Yoshinobu
Abrégé
The present invention provides a method of constituting a tissue construct in vitro using a tissue without depending on scaffold materials.
A method of integrating a biological tissue with a vascular system in vitro, comprising coculturing a biological tissue with vascular cells and mesenchymal cells. A biological tissue which has been integrated with a vascular system by the above-described method. A method of preparing a tissue or an organ, comprising transplanting the biological tissue described above into a non-human animal and differentiating the biological tissue into a tissue or an organ in which vascular networks have been constructed. A method of regeneration or function recovery of a tissue or an organ, comprising transplanting the biological tissue described above into a human or a non-human animal and differentiating the biological tissue into a tissue or an organ in which vascular networks have been constructed. A method of preparing a non-human chimeric animal, comprising transplanting the biological tissue described above into a non-human animal and differentiating the biological tissue into a tissue or organ in which vascular networks have been constructed. A method of evaluating a drug, comprising using at least one member selected from the group consisting of the biological tissue described above, the tissue or organ prepared by the method described above, and the non-human chimeric animal prepared by the method described above. A composition for regenerative medicine, comprising a biological tissue which has been integrated with a vascular system by the method described above.
A01K 67/027 - Nouvelles races ou races modifiées de vertébrés
C12N 5/00 - Cellules non différenciées humaines, animales ou végétales, p. ex. lignées cellulairesTissusLeur culture ou conservationMilieux de culture à cet effet
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
C07D 499/21 - Composés hétérocycliques contenant des systèmes cycliques thia-4 aza-1 bicyclo [3.2.0] heptane, c.-à-d. des composés contenant un système cyclique de formule p. ex. pénicillines, pénèmesCes systèmes cycliques étant ultérieurement condensés, p. ex. condensés en position 2,3 avec des hétérocycles contenant de l'oxygène, de l'azote ou du soufre avec un atome d'azote lié directement en position 6 et un atome de carbone comportant trois liaisons à des hétéro-atomes, avec au plus une liaison à un halogène, p. ex. un radical ester ou nitrile, lié directement en position 2
A61K 35/28 - Moelle osseuseCellules souches hématopoïétiquesCellules souches mésenchymateuses de toutes origines, p. ex. cellules souches dérivées de tissu adipeux
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Ujihara Dai
Katada Junichi
Ryo Akihide
Abrégé
The present invention addresses the problem of providing a SARS-CoV-2 detection kit and a SARS-CoV-2 detection method that enable the detection of SARS-CoV-2 in a simple manner and with higher sensitivity. The present invention provides a SARS-CoV-2 detection kit for specifically detecting a nucleocapsid protein (NP) contained in a biological sample, the SARS-CoV-2 detection kit comprising at least one antibody that specifically reacts with a SARS-CoV-2 nucleocapsid protein (NP), wherein the antibody includes at least one antibody of which the subclass is IgG2b, and the kit includes a first container that receives a silver-containing compound, and a second container that receives a reducing agent that can reduce silver ions.
C07K 16/10 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant de virus de virus à ARN
C12N 7/00 - Virus, p. ex. bactériophagesCompositions les contenantLeur préparation ou purification
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
Public University Corporation Yokohama City University (Japon)
Takeda Pharmaceutical Company Limited (Japon)
Inventeur(s)
Takebe, Takanori
Nio, Yasunori
Abrégé
The present invention provides a means for suppressing formation and/or proliferation of undesired cells derived from stem cells in a cell population containing cells differentiated from stem cells. The nutrition composition according to the present invention is a nutrition composition for suppressing formation and/or proliferation of undesired cells derived from stem cells in a cell population containing cells differentiated from stem cells, the nutrition composition containing at least one essential amino acid selected from the group consisting of isoleucine, leucine, methionine, lysine, phenylalanine, tryptophan, threonine and histidine except valine, and optionally containing a non-essential amino acid(s).
C12N 5/00 - Cellules non différenciées humaines, animales ou végétales, p. ex. lignées cellulairesTissusLeur culture ou conservationMilieux de culture à cet effet
A61K 31/198 - Alpha-amino-acides, p. ex. alanine ou acide édétique [EDTA]
A61K 31/4172 - Acides imidazole-alkanecarboxyliques, p. ex. histidine
A61K 31/405 - Acides indole-alkanecarboxyliquesLeurs dérivés, p. ex. tryptophane, indométhacine
A23L 33/00 - Modification de la qualité nutritive des alimentsProduits diététiquesLeur préparation ou leur traitement
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOKYO UNIVERSITY OF THE ARTS (Japon)
Inventeur(s)
Kanayama, Motohiro
Takebe, Takanori
Nishii, Syozo
Kuwabara, Toshiyuki
Uehira, Teruyo
Usuha, Ryoya
Kiriyama, Takashi
Abrégé
A game device (10) is provided with: an input unit (11A) that receives input of a physical amount which reflects at least one of a respiratory function, a deglutition function, and a vocalization function by a user who plays a game and which has a parameter with a state thereof made variable; and an adjustment unit (11B) for adjusting the parameter to be more advantageous in the development of the game as the degree in which, the state of the physical amount inputted by the input unit (11A) becomes effective as training for at least one of the respiratory function, the deglutition function, and the vocalization function of the user, become higher.
A63F 13/215 - Dispositions d'entrée pour les dispositifs de jeu vidéo caractérisées par leurs capteurs, leurs finalités ou leurs types comprenant des moyens de détection des signaux acoustiques, p. ex. utilisant un microphone
A63F 13/53 - Commande des signaux de sortie en fonction de la progression du jeu incluant des informations visuelles supplémentaires fournies à la scène de jeu, p. ex. en surimpression pour simuler un affichage tête haute [HUD] ou pour afficher une visée laser dans un jeu de tir
A63F 13/69 - Création ou modification du contenu du jeu avant ou pendant l’exécution du programme de jeu, p. ex. au moyen d’outils spécialement adaptés au développement du jeu ou d’un éditeur de niveau intégré au jeu en permettant l'utilisation ou la mise à jour d'éléments spécifiques du jeu, p. ex. déblocage d’options, d’éléments, de niveaux ou de versions cachés
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Goshima, Yoshio
Nomoto, Munetaka
Abrégé
Provided is a schizophrenia biomarker. A schizophrenia examination method including measuring the expression level of non-phosphorylated collapsin response mediator protein 2 (CRMP2) and/or phosphorylated CRMP2 in a sample derived from a subject.
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
52.
COMPOSITION FOR TREATING BLOOD COAGULATION AND/OR COMPLEMENT DISORDERS
Public University Corporation Yokohama City University (Japon)
Takeda Pharmaceutical Company Limited (Japon)
Inventeur(s)
Takebe, Takanori
Saiki, Norikazu
Kawakami, Eri
Abrégé
The present invention provides a composition suitable as a composition for treating blood coagulation and/or complement disorders (raw materials for producing therapeutic agents for these diseases) and a method for effectively producing the composition. A method for producing a composition for treating blood coagulation and/or complement disorders according to the present invention includes the following steps of: (1) embedding an organoid formed from vascular endothelial cells or vascular endothelial cells and hepatocytes, in an extracellular matrix; (2) culturing the extracellular matrix; and (3) collecting a culture supernatant from the culture obtained in the step (2).
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
MINARIS MEDICAL CO., LTD. (Japon)
Inventeur(s)
Hara Yu
Kaneko Takeshi
Murohashi Kota
Yabe Aya
Abrégé
Provided is a means for rapidly analyzing whether an interstitial pneumonia patient, who exhibits a respiratory distress symptom and is suspected to suffer from an acute exacerbation, suffers from an acute exacerbation or suffers from an acute respiratory exacerbation caused by a pathosis that is not an acute exacerbation. Provided is a method comprising: a step for obtaining the measured value of the concentration of heme oxygenase-1 in a blood specimen collected from an interstitial pneumonia patient exhibiting a respiratory distress symptom; and a step for determining, on the basis of the measured value, whether the symptom of the patient is caused by an acute exacerbation or caused by a pathosis that is not an acute exacerbation. Moreover, provided are: a kit for performing said method; and a patient sorting method and a treatment policy determination method which are based on said method.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C12Q 1/26 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir une oxydoréductase
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
54.
FOOD COMPOSITION, PHARMACEUTICAL COMPOSITION, QUASI DRUG COMPOSITION, COSMETIC COMPOSITION AND SUNDRY ARTICLE FOR PREVENTING OR TREATING COVID-19
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOKIWA PHYTOCHEMICAL CO., LTD. (Japon)
Inventeur(s)
Ryo Akihide
Miyakawa Kei
Morita Takeshi
Kuniyoshi Tomoko
Yang Jinwei
Abrégé
The purpose of the present invention is to provide a food composition, a pharmaceutical composition, a quasi drug composition, a cosmetic composition and a sundry article, each being for preventing or treating COVID-19. A food composition, a pharmaceutical composition, a quasi drug composition, a cosmetic composition and a sundry article, each being for preventing or treating COVID-19 and comprising at least one member selected from among a cat's claw extract, a ginger extract, pteropodine and a pharmaceutically acceptable salt thereof, isopteropodine and a pharmaceutically acceptable salt thereof, 6-gingerol and a pharmaceutically acceptable ether thereof and 6-shogaol and a pharmaceutically acceptable ether thereof.
A23L 33/105 - Extraits de plantes, leurs doublons artificiels ou leurs dérivés
A61K 8/35 - Cétones, p. ex. quinones, benzophénone
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61K 31/438 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle le cycle étant condensé en spiro avec des systèmes carbocycliques ou hétérocycliques
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Murata, Soichiro
Abrégé
The present invention provides a prophylactic and/or therapeutic agent for diseases accompanied by fibrosis. A pharmaceutical composition for preventing and/or treating a disease accompanied by fibrosis in an organ and/or a tissue, which comprises a cell mixture and/or a cell condensate comprising mesenchymal cells and vascular cells (and hepatocytes, optionally). An agent capable of inhibiting organ and/or tissue fibrosis, which comprises both mesenchymal cells and vascular cells or a cell condensate thereof. By transplanting into a subject a cell mixture and/or a cell condensate comprising mesenchymal cells and vascular cells (and optionally, hepatocytes), expression levels of fibrolysis enzymes (fibrolytic factors) such as MMP1 or MMP13 are elevated, which eventually enables inhibition of fibrosis in an organ and/or a tissue, as well as prevention and/or treatment of a disease accompanied by fibrosis in an organ and/or a tissue.
A61K 35/28 - Moelle osseuseCellules souches hématopoïétiquesCellules souches mésenchymateuses de toutes origines, p. ex. cellules souches dérivées de tissu adipeux
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
56.
Composition for improving or preventing nonalcoholic fatty liver
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
KYOTO PREFECTURAL PUBLIC UNIVERSITY CORPORATION (Japon)
SAGA UNIVERSITY (Japon)
Inventeur(s)
Kessoku, Takaomi
Nakajima, Atsushi
Sumida, Yoshio
Eguchi, Yuichiro
Saito, Susumu
Sauchi, Yusuke
Abrégé
An object of the present invention is to provide a composition for preventing or improving fat deposition on the liver in spite of the alcohol intake history of a level that a liver disease is not caused. The inventors found that glutathione has an effect of preventing or improving fat deposition on the liver, which is not caused by alcohol, and completed the present invention. Among nonalcoholic fat diseases, the present invention is particularly effective in an early stage of the treatment or in a case where treatment for another disease is not performed.
A61P 1/18 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles pancréatiques, p. ex. enzymes pancréatiques
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
NATIONAL UNIVERSITY CORPORATION YOKOHAMA NATIONAL UNIVERSITY (Japon)
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Ota, Hiroki
Isoda, Yutaka
Inamori, Go
Ito, Shuichi
Uozumi, Azusa
Abrégé
A bilirubin concentration measurement system including: a sensor device attachable to a subject; and a terminal device capable of wirelessly communicating with the sensor device. The sensor device includes: a light emitting diode that emits blue light; a light emitting diode that emits green light; a light detection diode that detects reflected light that is the blue light having been incident on skin of the subject and reflected, and detects reflected light that is the green light having been incident on the skin of the subject and reflected; and a communication unit that wirelessly transmits information about intensities of the reflected light detected by the photodiode. The terminal device includes: a communication unit that receives the information about the intensities of the reflected light transmitted from the sensor device; and a computing unit that calculates a bilirubin concentration using the information about the intensities of the reflected light.
A61B 5/145 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
58.
ANTIBODY AGAINST SARS-COV-2, METHOD FOR DETECTING SARS-COV-2 USING ANTIBODY AND KIT CONTAINING ANTIBODY
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
KANTO KAGAKU KABUSHIKI KAISHA (Japon)
Inventeur(s)
Ryo, Akihide
Yamaoka, Yutaro
Kikuchi, Sayaka
Abrégé
The present invention addresses the problem of providing a means for detecting a constituting protein of nucleocapsid derived from SARS-CoV-2. This problem has been solved by providing an antibody binding to a constituting protein of nucleocapsid derived from SARS-CoV-2 or a fragment of the antibody, a method for detecting a constituting protein of the SARS-CoV-2-derived nucleocapsid with the use of the antibody or a fragment thereof, a kit for detecting a constituting protein of the SARS-CoV-2-derived nucleocapsid, said kit containing the antibody or a fragment thereof, etc.
C12N 15/50 - Coronaviridae, p. ex. virus de la bronchite infectieuse, virus de la gastro-entérite transmissible
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
59.
METHOD AND REAGENT FOR DETECTING PANCREATIC CANCERS
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Shibata, Wataru
Terauchi, Yasuo
Endo, Itaru
Shimizu, Yasuhiro
Ohtake, Norihisa
Myoba, Shohei
Abrégé
The present invention addresses the problem of providing a method for detecting pancreatic cancers and a reagent usable in the method. The method for detecting pancreatic cancers is characterized by measuring the amount of TFPI2 in body fluid sampled from a subject. Furthermore, an antibody that specifically recognizes TFPI2 processing polypeptide and intact TFPI2 is included in the reagent for detecting pancreatic cancers.
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
C12N 15/12 - Gènes codant pour des protéines animales
G01N 27/62 - Recherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques en recherchant l'ionisation des gaz, p. ex. des aérosolsRecherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques en recherchant les décharges électriques, p. ex. l'émission cathodique
60.
SARS-CoV-2-DERIVED NUCLEOCAPSID FRAGMENT, AND METHOD AND KIT FOR DETECTING ANTI-SARS-CoV-2-ANTIBODY USING SAME
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
KANTO KAGAKU KABUSHIKI KAISHA (Japon)
Inventeur(s)
Ryo, Akihide
Yamaoka, Yutaro
Aizawa, Daisuke
Abrégé
The present invention addresses the problem of providing a means for accurately, easily and quickly detecting an anti-SARS-CoV-2-antibody. A solution to this problem is achieved by providing a SARS-CoV-2-derived nucleocapsid fragment, a method and a kit for detecting an anti-SARS-CoV-2-antibody from human-derived blood, plasma and/or serum with the use of the fragment, etc.
C07K 14/165 - Coronaviridae, p. ex. virus de la bronchite infectieuse aviaire
C07K 16/10 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant de virus de virus à ARN
C12M 1/34 - Mesure ou test par des moyens de mesure ou de détection des conditions du milieu, p. ex. par des compteurs de colonies
C12N 15/50 - Coronaviridae, p. ex. virus de la bronchite infectieuse, virus de la gastro-entérite transmissible
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/533 - Production de composés immunochimiques marqués avec un marqueur fluorescent
G01N 33/535 - Production de composés immunochimiques marqués avec un marqueur enzymatique
G01N 33/543 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
61.
ESTABLISHMENT OF MOUSE MODEL USING HUMAN PANCREATIC CANCER ORGANOID
NATIONAL UNIVERSITY CORPORATION KOCHI UNIVERSITY (Japon)
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniuchi, Keisuke
Taniguchi, Hideki
Abrégé
The purpose of the present invention is to provide a mouse model for pancreatic cancer similar to human pancreatic cancer. Specifically, the present invention pertains to a human pancreatic cancer mouse model which carries a pancreatic cancer organoid containing a human pancreatic cancer cell line S2-130.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Miyagi, Etsuko
Arakawa, Noriaki
Ohtake, Norihisa
Myoba, Shohei
Abrégé
The present invention addresses the problem of providing a method for detecting malignant ovarian tumors distinctly from benign ovarian tumors and a reagent that can be used in the method. This method for detecting malignant ovarian tumors (excluding high-grade serous carcinoma) distinctly from benign ovarian tumors is characterized in that the amount of TFPI2 in a sample originating from a patient is measured. In addition, an antibody that specifically recognizes TFPI2 processing polypeptide and intact TPFI2 is included in a reagent for detecting malignant ovarian tumors (excluding high-grade serous carcinoma) distinctly from benign ovarian tumors.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Miyagi, Etsuko
Arakawa, Noriaki
Ohtake, Norihisa
Myoba, Shohei
Abrégé
The present invention addresses the problem of providing a method for detecting malignant ovarian tumors distinctly from benign ovarian tumors and a reagent that can be used in the method. This method for detecting malignant ovarian tumors (excluding high-grade serous carcinoma) distinctly from benign ovarian tumors is characterized in that the amount of TFPI2 in a sample originating from a patient is measured. In addition, an antibody that specifically recognizes TFPI2 processing polypeptide and intact TPFI2 is included in a reagent for detecting malignant ovarian tumors (excluding high-grade serous carcinoma) distinctly from benign ovarian tumors.
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Abrégé
The present invention provides a marker gene capable of detecting the undifferentiated cells that remain or become included in a differentiated cell population. Undifferentiated cells present in a differentiated cell population are detected by using at least one gene selected from the group consisting of ESRG, VSNL1, THY1, SFRP2, SPP1, USP44 and CNMD as an undifferentiation marker. A method of detecting undifferentiated cells; a method of using the gene as an undifferentiation marker; and a kit for detecting undifferentiated cells. A method of selecting an undifferentiated cell clone is also provided.
C12Q 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
C12Q 1/6876 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
65.
NUCLEIC ACID CONSTRUCT THAT CAN MEASURE HOMOLOGOUS RECOMBINATION ACTIVITY, AND METHOD FOR USING SAME
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
Disclosed are a means that enables the rapid and convenient detection of the presence/absence and extent of homologous recombination activity in an individual, and a means that is not a current treatment means and is useful for the detection and treatment of homologous recombination repair cancers. A nucleic acid construct according to the present invention comprises (1) a promoter region, (2) a mutant gene sequence that has a cleavage site in the interior of a protein-encoding gene sequence, and (3) a base sequence that is a partial region in the mutant gene sequence of (2), is capable of replacing, by homologous recombination, a partial region that contains the cleavage site, and is constituted of a first homologous region and a second homologous region. This nucleic acid construct can be used, for example, as a reagent or kit for measuring homologous recombination activity, as a diagnostic agent for homologous recombination deletion cancers, and as a therapeutic agent for homologous recombination repair cancers.
C12N 15/90 - Introduction stable d'ADN étranger dans le chromosome
A61K 31/7088 - Composés ayant au moins trois nucléosides ou nucléotides
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer
C12Q 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
66.
NUCLEIC ACID CONSTRUCT, AND THERAPEUTIC OR DIAGNOSTIC AGENT FOR MISMATCH REPAIR DEFICIENT CANCERS COMPRISING NUCLEIC ACID CONSTRUCT
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Adachi, Noritaka
Abrégé
Disclosed is a means that enables simple and quick detection of the presence or absence of a mismatch repair activity and that is useful in diagnosing or treating mismatch repair deficient cancers. In an integrated type nucleic acid construct provided by the present invention, [promoter region], [5' terminal region + first homologous region] and [second homologous region + 3' terminal region] are disposed on a single nucleic acid molecule. In a split type nucleic acid construct, [promoter region] and [5' terminal region + first homologous region] are disposed on a nucleic acid molecule and [second homologous region + 3' terminal region] are disposed on another nucleic acid molecule that is different from the former nucleic acid molecule. The nucleic acid construct of the present invention can be used as a therapeutic agent for mismatch repair deficient cancers, a diagnostic agent for mismatch repair deficient cancers, a companion diagnostic agent for predicting the effect of an anticancer agent on mismatch repair deficient cancers, etc., each agent comprising the nucleic acid construct.
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteursVecteurs Utilisation d'hôtes pour ceux-ciRégulation de l'expression
A61K 38/02 - Peptides à nombre indéterminé d'amino-acidesLeurs dérivés
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
A61P 35/02 - Agents anticancéreux spécifiques pour le traitement de la leucémie
C12Q 1/6886 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour les maladies provoquées par des altérations du matériel génétique pour le cancer
67.
Method for detecting castration-resistant prostate cancer and detection reagent
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATION (Japon)
Inventeur(s)
Arakawa, Noriaki
Hirano, Hisashi
Uemura, Hiroji
Ito, Yusuke
Myoba, Shohei
Ohtake, Norihisa
Abrégé
The present invention aims to provide a method for simply and highly accurately detecting castration-resistant prostate cancer (CRPC), and a reagent that can be used for this method. By measuring the level of GDF15 propeptide present in a sample as a novel detection marker for CRPC, acquisition of castration resistance in a prostate cancer patient during or after endocrine therapy is detected. An antibody that specifically recognizes GDF15 propeptide is included in the CRPC detection reagent.
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C07K 14/475 - Facteurs de croissanceRégulateurs de croissance
C07K 16/22 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant d'animaux ou d'humains contre des facteurs de croissance
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
UNIVERSITAT ZURICH (Suisse)
HUMANOME LAB., INC. (Japon)
Inventeur(s)
Shimizu K Kentaro
Jian Qiang Sun
Tameshige Toshiaki
Sese Jun
Yamasaki Eri
Abrégé
Provided is a maturation prediction system improved in terms of ease of use, versatility, and prediction accuracy. This maturation prediction system for plants is characterized in that the system generates a first model for which weather information is input and a predicted intermediate state of a plant of interest is output and a second model for which information about the intermediate state is input and a prediction of maturation of the plant of interest is output, and in that weather information for a predicted maturation time is input to the first model and the predicted intermediate state of the plant of interest at the predicted maturation time output from the first model is input to the second model, thereby outputting a prediction of maturation of the plant of interest at the predicted maturation time.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kawasaki Nana
Ohta Yuki
Abrégé
The present invention addresses the problem of providing a biomarker that makes it possible to diagnose colon cancer. The present invention relates to a biomarker that is for assisting in the diagnosis of colon cancer and that contains a sugar chain selected from among the following substances (1)-(4): (1) at least one sugar chain that is present in alpha 1-antitrypsin and represented by formula 1 or 2; (2) a sugar chain that is present in leucine-rich alpha-2 glycoprotein and represented by formula 1; (3) at least one sugar chain that is present in alpha 1-antichymotrypsin and represented by formula 1 or 2; and (4) a sugar chain that is present in complement component 9 and represented by formula 1.
C07K 14/47 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains provenant de vertébrés provenant de mammifères
C12N 15/12 - Gènes codant pour des protéines animales
C12N 15/15 - Inhibiteurs de protéases, p. ex. antithrombine, antitrypsine, hirudine
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des micro-organismes viables
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
70.
Agent for preventing or treating fat-associated diseases and/or inflammation
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
EIKEN KAGAKU KABUSHIKI KAISHA (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Yasui, Ryota
Abrégé
Provided is a marker gene capable of detecting the persistence/admixture of undifferentiated cells in a differentiated cell population. Undifferentiated cells present in a differentiated cell population are detected by using at least one gene selected from the group consisting of LINC00678 and PRDM14 as an undifferentiation marker. Also provided are a method for detecting undifferentiated cells, a method of use as an undifferentiation marker, and an undifferentiated cell detection kit, and a method for selecting an undifferentiated cell line.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
EIKEN KAGAKU KABUSHIKI KAISHA (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Yasui, Ryota
Matsui, Atsuka
Abrégé
Provided is a sensitive and simple detection method, and a kit therefor, which detects undifferentiated human pluripotent stem cells which are mixed into an intermediate product of a regenerative medicine product and/or a final product thereof by using a nucleic acid isothermal amplification method, and specifically, the LAMP method. A method for detecting whether or not undifferentiated cells are present in a non-undifferentiated cell population, wherein RNA derived from an undifferentiated marker gene for which there is a significant difference in expression between an undifferentiated cell and a non-undifferentiated cell is detected using a nucleic acid isothermal amplification method in a specimen containing a nucleic acid derived from the cell population to be tested. A kit for testing whether or not undifferentiated cells are mixed in with a non-undifferentiated cell population, said kit containing a reagent capable of detecting RNA derived from an undifferentiated marker gene for which there is a significant difference in expression between an undifferentiated cell and a non-undifferentiated cell by using a nucleic acid isothermal amplification method.
C12Q 1/6881 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour le typage de tissu ou de cellule, p. ex. sondes d’antigène leucocytaire humain [HLA]
73.
CELL EVALUATION METHOD, CELL EVALUATION SYSTEM AND PROGRAM
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
NIKON CORPORATION (Japon)
Inventeur(s)
Taniguchi Hideki
Takebe Takanori
Ishikawa Momotaro
Yamashita Masafumi
Kiyota Yasujiro
Abrégé
This cell evaluation method comprises: in a culture stage involving the induction of cell differentiation during a process for inducing the cell differentiation, acquiring a first evaluation index relative to cells to be compared and a first index calculated with the use of the first evaluation index; calculating a second index relative to cells to be evaluated, said cells to be evaluated being different from the cells to be compared, on the basis of the first evaluation index; and then comparing the first index with the second index to thereby evaluate the differentiation of the cells to be evaluated.
C12M 1/00 - Appareillage pour l'enzymologie ou la microbiologie
C12M 1/34 - Mesure ou test par des moyens de mesure ou de détection des conditions du milieu, p. ex. par des compteurs de colonies
C12Q 1/04 - Détermination de la présence ou du type de micro-organismeEmploi de milieux sélectifs pour tester des antibiotiques ou des bactéricidesCompositions à cet effet contenant un indicateur chimique
G01N 21/17 - Systèmes dans lesquels la lumière incidente est modifiée suivant les propriétés du matériau examiné
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TAKEDA PHARMACEUTICAL COMPANY LIMITED (Japon)
Inventeur(s)
Takebe Takanori
Saiki Norikazu
Abrégé
The present invention provides a drug toxicity evaluation platform (evaluation method and kit therefor, etc.) that makes it possible to perform a detailed analysis of the likelihood that a drug will cause injury (DILI, etc.) to the liver or another organ. This method for evaluating drug toxicity includes a step for adding a drug to a co-culture of an organoid and blood cells, and a step for evaluating the toxicity of said drug to said organoid.
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
C12N 5/078 - Cellules du sang ou du système immunitaire
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des micro-organismes viables
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Nie, Yunzhong
Zheng, Yunwen
Abrégé
Provided are: a method for inducing hepatic progenitor cells which can overcome drawbacks in the prior art; and hepatic progenitor cells. Hepatocyte plasticity and senescence are controlled. A method for producing hepatocytes that includes dividing endodermal cells into hepatocytes in the presence of a member of the FGF family, HGF, and a member of IL6 family, and dexamethazone. Hepatocytes produced using the aforementioned method that can survive for 90 or more days while maintaining functionality as hepatocytes. A method for producing hepatic progenitor cells that includes culturing hepatocytes in the presence of a member of the FGF family. Alpha-fetoprotein (AFP)–negative hepatic progenitor cells produced using the aforementioned method that have proliferative ability and the ability to differentiate bidirectionally into hepatocytes and bile duct epithelial cells. A method for producing hepatocytes that includes inducing differentiation of the hepatic progenitor cells into hepatocytes. A method for producing bile duct cells that includes inducing differentiation of the hepatic progenitor cells into bile duct cells. A method for suppressing hepatocyte senescence using a drug which causes histone hyperacetylation. A hepatocyte senescence inhibitor that includes a drug that causes histone hyperacetylation as an active ingredient. A method for increasing hepatocyte plasticity using a drug that causes histone hyperacetylation. A drug that increases hepatocyte plasticity and includes a drug that causes histone hyperacetylation as an active ingredient. A method for producing a chimeric animal that includes transplanting into a non-human animal at least one cell selected from the group consisting of the hepatocytes, the hepatic progenitor cells, and the cells induced through differentiation from the hepatic progenitor cells. A composition for transplantation that includes at least one cell selected from the group consisting of the hepatocytes, the hepatic progenitor cells, and the cells induced by differentiation from the hepatic progenitor cells. A culture medium kit for inducing differentiation that includes: an agent containing FGF10, retinoic acid, and forskolin for use in a culture medium to be used to induce differentiation of the hepatic progenitor cells into bile duct cells; and a written explanation of the use of the agent in the culture medium to be used to induce differentiation. A medium containing FGF10, retinoic acid, and forskolin for inducing differentiation of the hepatic progenitor cells into bile duct cells. A liver regeneration promoter that includes a drug that causes histone hyperacetylation as an active ingredient.
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
A61K 31/573 - Composés contenant des systèmes cycliques du cyclopenta[a]hydrophénanthrèneLeurs dérivés, p. ex. stéroïdes substitués en position 17 bêta par une chaîne à deux atomes de carbone, p. ex. prégnane ou progestérone substitués en position 21, p. ex. cortisone, dexaméthasone, prednisone ou aldostérone
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TOSOH CORPORATIO (Japon)
Inventeur(s)
Arakawa, Noriaki
Hirano, Hisashi
Nakaigawa, Noboru
Yao, Masahiro
Ohtake, Norihisa
Abrégé
An object of the present invention is to provide a method for detecting renal cancer, and a reagent that can be used for the method. Provided is a method for detecting renal cancer, which includes measuring the amount of TFPI2 in a sample derived from a patient. An antibody that specifically recognizes NT-TFPI2 and intact TFPI2 is included in a detection reagent for renal cancer.
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kakui, Hiroyuki
Shimizu, Kentaro, K.
Yamazaki, Misako
Abrégé
The present invention relates to a method for distinguishing a first nucleic acid sequence from a second nucleic acid sequence by electrophoresis. The first nucleic acid comprises a first common sequence tract, a variable sequence tract and a second common sequence tract and the second nucleic acid comprises a first common sequence tract, optionally an variable sequence tract and a second common sequence tract. The first and the second nucleic acid sequence is contacted with a probe sequence that is reverse complementary to the first and second common sequence tract under conditions allowing the hybridization of the probe sequence to the first and second nucleic acid sequence, thereby forming a first probe hybrid and a second probe hybrid. Subsequently, the first and second probe hybrids are submitted to electrophoresis to detect the electrophoretic mobility of the first and second probe hybrid.
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Taniguchi, Hideki
Tadokoro, Tomomi
Abrégé
The present invention provides a method of fusing cell masses. A method of fusing cell masses, comprising seeding cell masses on a plane capable of cell adhesion and culturing the cell masses as a culture medium is fed from both the obverse and reverse sides of the cell mass-seeded plane.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Ohta, Yuki
Kawasaki, Nana
Takakura, Daisuke
Abrégé
Disclosed is a novel means for accurate qualitative and quantitative analyses for each N-glycosylation site. The method of analyzing N-linked sugar chain(s) of glycoprotein according to the present invention comprises: treating a part of a glycopeptide-containing sample to be analyzed with endo-β-N-acetylglucosaminidases to cleave off sugar chains while leaving one GlcNAc of the chitobiose core on the Asn at the N-glycosylation site; subjecting the obtained sugar chain-cleaved sample to preliminary liquid chromatography/mass spectrometry; predicting the retention time of the glycopeptide of interest and the mass-to-charge ratio (m/z) of the precursor ion in main analysis based on the results of the preliminary liquid chromatography/mass spectrometry; and carrying out the main analysis. By this method, the binding sites and structures of N-linked sugar chains in a glycoprotein can be analyzed. By using the sugar chain-cleaved sample as an internal standard in the main analysis, quantitative analysis of sugar chains at each glycosylation site also becomes possible.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C07K 16/00 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux
C12Q 1/44 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir une hydrolase une estérase
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Taniguchi, Hideki
Takebe, Takanori
Sekine, Keisuke
Abrégé
The present invention solves the following problems [1] to [3] found in conventional methods of preparing a three dimensional structure (organ primordium) by coculturing functional cells with umbilical cord-derived vascular endothelial cells and bone marrow-derived mesenchymal cells: [1] the quality of resultant organ primordia varies greatly depending on donors; [2] the growth capacities of cell sources are limited; and [3] it is difficult to secure immunocompatibility because cells are derived from different sources. An organ bud prepared from vascular cells, mesenchymal cells and tissue or organ cells, wherein each of the vascular cell, the mesenchymal cell and the tissue or organ cell has been induced from pluripotent stem cells. A method of preparing an organ bud, comprising culturing vascular cells, mesenchymal cells and tissue or organ cells in vitro, wherein each of the vascular cell, the mesenchymal cell and the tissue or organ cell has been induced from pluripotent stem cells.
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
A61L 27/36 - Matériaux pour prothèses ou pour revêtement de prothèses contenant des constituants de constitution indéterminée ou leurs produits réactionnels
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Japan Aerospace Exploration Agency (Japon)
Inventeur(s)
Taniguchi, Hideki
Tadokoro, Tomomi
Sakashita, Tetsuya
Matsumoto, Satoshi
Adachi, Satoshi
Higashibata, Akira
Abrégé
A method for aggregating cell masses includes performing a cell mass aggregating step of rotating a rotating body containing a specific gravity adjustment solution and cell masses to aggregate the cell masses, the specific gravity adjustment solution having biocompatibility, the cell masses having a lower specific gravity than the specific gravity adjustment solution.
C12N 5/00 - Cellules non différenciées humaines, animales ou végétales, p. ex. lignées cellulairesTissusLeur culture ou conservationMilieux de culture à cet effet
C12M 1/00 - Appareillage pour l'enzymologie ou la microbiologie
C12M 1/12 - Appareillage pour l'enzymologie ou la microbiologie avec des moyens de stérilisation, filtration ou dialyse
C12M 1/36 - Appareillage pour l'enzymologie ou la microbiologie comportant une commande sensible au temps ou aux conditions du milieu, p. ex. fermenteurs commandés automatiquement
C12M 3/00 - Appareillage pour la culture de tissus, de cellules humaines, animales ou végétales, ou de virus
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Takaki, Shunsuke
Abrégé
Provided is an illness aggravation estimation system that estimates aggravation of an illness in a patient with high precision. The illness aggravation estimation system acquires sickbed image data in which images of an imaging area including the sickbed of a patient are captured chronologically, analyzes the movements of the patient or of a body part of the patient captured in the acquired sickbed image data, uses the analyzed movements as a basis to perform scoring of at least one of a consciousness state and oxygen administration which are items included in indices for an early warning score, and estimates aggravation of an illness in the patient.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/11 - Mesure du mouvement du corps entier ou de parties de celui-ci, p. ex. tremblement de la tête ou des mains ou mobilité d'un membre
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TAKEDA PHARMACEUTICAL COMPANY LIMITED (Japon)
Inventeur(s)
Takebe, Takanori
Saiki, Norikazu
Nio, Yasunori
Kawakami, Eri
Abrégé
The present invention provides a method for screening a therapeutic agent of a disease, in which over-activation of a complement is engaged, by taking, as an indicator, a cytotoxic marker associated with the complement, wherein the method includes: (1a) a process for adding the complement to a cell manufactured from a stem cell, and forming the cytotoxic marker associated with the complement; and (2a) a process for adding a therapeutic agent candidate material to select a material which lowers the amount of the cytotoxic marker.
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des micro-organismes viables
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TAKEDA PHARMACEUTICAL COMPANY LIMITED (Japon)
Inventeur(s)
Takebe Takanori
Saiki Norikazu
Abrégé
The present invention provides a means for producing an organoid capable of secretion of plasma proteins, immune response, etc., in a manner close to that of an organ in a living body. As such a means, this matrix composition includes: (1) a first matrix that includes one or more cells selected from the group comprising vascular cells, nerve cells, and blood cells; (2) a second matrix that includes cells constituting an organ, and/or an organoid, and here, the first matrix encapsulates the second matrix, and the first matrix has at least one opening.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Murata, Soichiro
Abrégé
Provided is a coating-securing agent for transplanting cells or a tissue onto the surface of an organ, a mesentery, a peritoneum, etc. Provided are: a formulation which is for coating-securing an implant, and contains alginate; a formulation kit for coating-securing an implant, in which an alginate-containing formulation and a di- or higher-polyvalent metallic salt are combined; and a method for transplanting an implant, the method comprising a step for transplanting an implant onto a transplantation site of a human or a non-human animal and coating the implant with alginate.
A61L 31/12 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent
A61L 31/14 - Matériaux caractérisés par leur fonction ou leurs propriétés physiques
A61L 31/16 - Matériaux biologiquement actifs, p. ex. substances thérapeutiques
C12N 11/04 - Enzymes ou cellules microbiennes immobilisées sur ou dans un support organique piégées à l’intérieur du support, p. ex. dans un gel ou dans des fibres creuses
C12N 11/10 - Enzymes ou cellules microbiennes immobilisées sur ou dans un support organique le support étant un hydrate de carbone
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
KYOTO PREFECTURAL PUBLIC UNIVERSITY CORPORATION (Japon)
SAGA UNIVERSITY (Japon)
Inventeur(s)
Kessoku, Takaomi
Nakajima, Atsushi
Sumida, Yoshio
Eguchi, Yuichiro
Saito, Susumu
Sauchi, Yusuke
Abrégé
An object of the present invention is to provide a composition for preventing or improving fat deposition on the liver in spite of the alcohol intake history of a level that a liver disease is not caused. The inventors found that glutathione has an effect of preventing or improving fat deposition on the liver, which is not caused by alcohol, and completed the present invention. Among nonalcoholic fat diseases, the present invention is particularly effective in an early stage of the treatment or in a case where treatment for another disease is not performed.
A61P 1/16 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles de la vésicule biliaire ou du foie, p. ex. protecteurs hépatiques, cholagogues, cholélitholytiques
87.
COMPOSITION FOR TREATING BLOOD COAGULATION AND/OR COMPLEMENT DISORDERS
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TAKEDA PHARMACEUTICAL COMPANY LIMITED (Japon)
Inventeur(s)
Takebe Takanori
Saiki Norikazu
Kawakami Eri
Abrégé
The present invention provides a composition suitable for treating blood coagulation and/or complement disorders (a raw material for producing a therapeutic agent for such disorders) and an effective production method therefor. This method for producing a composition for treating blood coagulation and/or complement disorders comprises the following steps: (1) a step in which an organoid prepared from vascular endothelial cells or from vascular endothelial cells and liver cells is embedded in an extracellular matrix; (2) a step in which the extracellular matrix is cultivated; and (3) a step in which a culture supernatant is recovered from the culture cultivated in step (2).
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61K 38/36 - Facteurs de coagulation sanguine ou de fibrinolyse
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Tadokoro, Tomomi
Taniguchi, Hideki
Abrégé
The present invention provides a system for artificially inducing and regulating “tissue interactions” among multiple tissues. A construct for transplantation into a living body, which comprises a structure and a cell mass linked to each other, the structure being an object having a three-dimensional structure and capable of mimicking or resembling a structure and/or a function of the living body.
A61L 27/50 - Matériaux caractérisés par leur fonction ou leurs propriétés physiques
A61L 27/40 - Matériaux composites, c.-à-d. en couches ou contenant un matériau dispersé dans une matrice constituée d'un matériau analogue ou différent
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
C12N 5/071 - Cellules ou tissus de vertébrés, p. ex. cellules humaines ou tissus humains
A01K 67/027 - Nouvelles races ou races modifiées de vertébrés
89.
METHOD FOR EVALUATING DIFFERENTIATION RESISTANCE OF UNDIFFERENTIATED CELLS
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Abrégé
Provided is a method for predicting, in the stage of undifferentiated cells, the possibility of contamination with undifferentiated cells after the differentiation of the cells. The differentiation resistance of undifferentiated cells is evaluated by measuring (i) and/or (ii). (i) Expression level and/or promoter activity of at least one gene selected from the group consisting of ZNF354C, C12orf56, ZNF578, DPP6 and MIR886. (ii) Methylation state of the promoter of at least one gene selected from the group consisting of ZNF354C, C12orf56, ZNF578, DPP6 and MIR886.
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
C12Q 1/6876 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes
C12Q 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
90.
PROPHYLACTIC AND/OR THERAPEUTIC AGENT FOR DISEASES ACCOMPANIED BY FIBROSIS
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Murata, Soichiro
Abrégé
Provided is a prophylactic and/or therapeutic agent for diseases accompanied by fibrosis. The present invention provides: a medicinal composition for preventing and/or treating diseases accompanied by organ and/or tissue fibrosis, the composition comprising a cell mixture and/or a cell aggregate that includes mesenchymal cells and endothelial cells (hepatocytes may be further included); and an inhibitor for inhibiting organ and/or tissue fibrosis, the inhibitor comprising both mesenchymal cells and endothelial cells or a cell aggregate thereof. A cell mixture and/or a cell aggregate that includes mesenchymal cells and endothelial cells (hepatocytes may be further included) is transplanted to a subject, so that an expression of fibrinolysins such as MMP1 and MMP13 (fibrinolytic system factors) increases and can inhibit organ and/or tissue fibrosis, thereby preventing and/or treating diseases accompanied by organ and/or tissue fibrosis.
NATIONAL UNIVERSITY CORPORATION YOKOHAMA NATIONAL UNIVERSITY (Japon)
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Ota Hiroki
Isoda Yutaka
Inamori Go
Ito Shuichi
Uozumi Azusa
Abrégé
A bilirubin concentration measurement system (1) according to the present invention is provided with a sensor device (10) attachable to a test body, and a terminal device (20) capable of wirelessly communicating with the sensor device (10). The sensor device (10) is provided with: a light emitting element (12) which emits blue light; a light emitting element (13) which emits green light; an optical detection element (14) which detects reflected light due to the blue light incident on, and reflected by, a skin of the test body, and reflected light due to the green light incident on, and reflected by, the skin of the test body; and a communication unit (16) which wirelessly transmits information pertaining to the intensity of the reflected light detected by the optical detection element (14). The terminal device (20) is provided with a communication unit (21) which receives the information pertaining to the intensity of the reflected light transmitted from the sensor device (10), and a computing unit (22) which calculates a bilirubin concentration using the information pertaining to the intensity of the reflected light.
G01N 21/27 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes en utilisant la détection photo-électrique
A61B 5/1455 - Mesure des caractéristiques du sang in vivo, p. ex. de la concentration des gaz dans le sang ou de la valeur du pH du sang en utilisant des capteurs optiques, p. ex. des oxymètres à photométrie spectrale
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
TAKEDA PHARMACEUTICAL COMPANY LIMITED (Japon)
Inventeur(s)
Takebe Takanori
Nio Yasunori
Abrégé
The present invention provides a means for inhibiting formation and/or growth of non-objective cells derived from stem cells in a cell population including cells differentiated from the stem cells. A nutrition composition according to the present invention contains one or more essential amino acids selected from the group consisting of isoleucine, leucine, methionine, lysine, phenylalanine, tryptophan, threonine, and histidine, but excluding valine, optionally contains a nonessential amino acid, and inhibits formation and/or growth of non-objective cells derived from stem cells in a cell population including cells differentiated from the stem cells.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Yumura, Yasushi
Abrégé
Provided is a reproductive medicine support system which supports persons who are involved and work in reproductive medicine. Image analysis processing performed by an analysis means includes: determination processing for determining sperm imaged in video data; and analysis processing for analyzing the sperm determined in the determination processing. On a working screen, displayed are first additional displays (displays G11–G13) based on the analysis processing pertaining to sperm displayed in a display region on a main screen G1 among the sperm determined by the determination processing; and second additional displays (displays G22-G25) based on the analysis processing pertaining to all the sperm determined by the determination processing or sperm displayed in a display region of a sub-screen G2 among the sperm determined by the determination processing.
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kawasaki Nana
Ohta Yuki
Ichikawa Yasushi
Terauchi Yasuo
Shibata Wataru
Abrégé
The present invention addresses the problem of providing a pancreatic cancer determination marker having a high accuracy (correctness and precision). The present invention pertains to a pancreatic cancer determination marker, a pancreatic cancer determination method, a method for acquiring data for determining a pancreatic cancer, a pancreatic cancer determination kit, and the like.
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
G01N 33/66 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir les sucres du sang, p. ex. le galactose
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Sekine, Keisuke
Abrégé
Provided is a marker gene capable of detecting the persistence/admixture of undifferentiated cells in a differentiated cell population. Undifferentiated cells present in a differentiated cell population are detected by using at least one gene selected from the group consisting of ESRG, VSNL1, THY1, SFRP2, SPP1, USP44, and CNMD as an undifferentiation marker. A method for detecting undifferentiated cells, a method of use as an undifferentiation marker, and an undifferentiated cell detection kit. Also provided is a method for selecting an undifferentiated cell line.
C12Q 1/04 - Détermination de la présence ou du type de micro-organismeEmploi de milieux sélectifs pour tester des antibiotiques ou des bactéricidesCompositions à cet effet contenant un indicateur chimique
C12Q 1/6834 - Couplage enzymatique ou biochimique d’acides nucléiques à une phase solide
C12Q 1/6837 - Couplage enzymatique ou biochimique d’acides nucléiques à une phase solide utilisant des réseaux de sondes ou des puces à sondes
C12Q 1/6881 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour le typage de tissu ou de cellule, p. ex. sondes d’antigène leucocytaire humain [HLA]
C12Q 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/53 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Kishi, Kazuhito
Takai, Masami
Hasegawa, Motokazu
Akaishi, Masataka
Umemura, Masanari
Ishikawa, Yoshihiro
Akimoto, Taisuke
Abrégé
A power supply apparatus includes a power supply configured to apply an alternating current to a magnetic field generation apparatus; and a controller configured to control the alternating current applied by the power supply. The controller controls the power supply to apply the alternating current having a waveform pattern including a plurality of current waveforms having different frequency spectrums from each other.
Public University Corporation Yokohama City University (Japon)
Inventeur(s)
Ishikawa, Yoshihiro
Umemura, Masanari
Akimoto, Taisuke
Abrégé
A cancer treatment apparatus including a magnetic field generator that generates a magnetic field of 100 kHz to 300 kHz to be applied to affected tissues.
A61N 2/02 - Magnétothérapie utilisant des champs magnétiques produits par des bobines, y compris par des boucles à spire unique ou par des électro-aimants
98.
DRUG EVALUATION METHOD USING RECONSTRUCTED CANCER TISSUE
The purpose of the invention is to provide a method for identifying molecules involved in refractory cancers. Furthermore, the purpose of the invention is to provide a method for identifying drugs effective against refractory cancers. Additionally, the purpose of the invention is to provide a drug effective against recurrent cancers. Provided is a method for screening for molecules involved in refractory cancers, wherein the expression level of an EMT-associated molecule at pre- and post-administration of an anticancer agent is measured in stromal cells and/or cancer cells in tissue that reconstructs the cancer microenvironment, and an EMT-associated molecule presenting a higher expression level at post-administration of the anticancer agent than at pre-administration is scored as being involved in refractory cancers. Also provided is a method for screening for drugs effective against refractory cancers, wherein the expression level of an EMT-associated molecule at pre- and post-administration of an anticancer agent is measured in stromal cells and/or cancer cells in tissue that reconstructs the cancer microenvironment, and an EMT-associated molecule presenting a higher expression level at post-administration of the anticancer agent than at pre-administration is scored as being involved in refractory cancers, while a substance that can inhibit the function of this EMT-associated molecule is scored as a drug effective against refractory cancers. Further provided is a drug for treating and/or preventing tumor recurrence as a combination of an anticancer agent with an inhibitor targeted to the NOTCH3 signal.
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des micro-organismes viables
A61K 31/55 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à sept chaînons, p. ex. azélastine, pentylènetétrazole
A61K 31/7068 - Composés ayant des radicaux saccharide et des hétérocycles ayant l'azote comme hétéro-atome d'un cycle, p. ex. nucléosides, nucléotides contenant des cycles à six chaînons avec l'azote comme hétéro-atome d'un cycle contenant des pyrimidines condensées ou non-condensées ayant des groupes oxo liés directement au cycle pyrimidine, p. ex. cytidine, acide cytidylique
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
C12Q 1/6837 - Couplage enzymatique ou biochimique d’acides nucléiques à une phase solide utilisant des réseaux de sondes ou des puces à sondes
C12Q 1/6874 - Méthodes de séquençage faisant intervenir des réseaux d’acides nucléiques, p. ex. séquençage par hybridation [SBH]
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
99.
CANCER EVALUATION METHOD USING EPITHELIAL-MESENCHYMAL-TRANSITION-RELATED MOLECULE
Provided is a technique for accurately evaluating the prognosis of a cancer. This method comprises: measuring the expression level of an EMT-related molecule in cancer cells and stromal cells in a cancer tissue from a patient or a tissue reconstructing the cancer microenvironment including cancer cells from the patient; and predicting the prognosis of the patient on the basis of this level.
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des micro-organismes viables
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
A61K 31/7068 - Composés ayant des radicaux saccharide et des hétérocycles ayant l'azote comme hétéro-atome d'un cycle, p. ex. nucléosides, nucléotides contenant des cycles à six chaînons avec l'azote comme hétéro-atome d'un cycle contenant des pyrimidines condensées ou non-condensées ayant des groupes oxo liés directement au cycle pyrimidine, p. ex. cytidine, acide cytidylique
A61P 1/18 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles pancréatiques, p. ex. enzymes pancréatiques
PUBLIC UNIVERSITY CORPORATION YOKOHAMA CITY UNIVERSITY (Japon)
Inventeur(s)
Taniguchi, Hideki
Tadokoro, Tomomi
Abrégé
Provided is a method for fusing cell masses. The cell mass fusion method comprises: disseminating cell masses on a surface to which cells can adhere; and culturing the cell masses while supplying a culture medium from the front side and the rear side of the surface on which the cell masses have been disseminated.