The present disclosure provides an apparatus and a method for manufacturing a composite. In one aspect, the present disclosure provides a method for manufacturing a formulation comprising a first component and a second component. This method includes: a step for preparing a series of flow paths in which a first flow path through which a first fluid flows at a first flow velocity and a second flow path through which a second fluid flows at a second flow velocity are combined at a merging portion to form a third flow path through which a third fluid flows at a third flow velocity; a step in which the first component is injected into the first flow path at a first time; and a step in which the second component is injected into the second flow path at a second time. The first time and the second time are set so that the first component and the second component reach the merging portion at a timing when the components are mixed.
B01F 25/43 - Tubes de mélange, p.ex. dans lesquels la matière est déplacée dans une direction radiale ou partiellement inversée
B01F 33/301 - Micromixeurs utilisant des moyens spécifiques pour disposer les écoulements à mélanger, p.ex. des géométries ou des dispositions de canaux
B01F 35/92 - Systèmes de chauffage ou de refroidissement pour chauffer l'extérieur du récipient, p. ex. vestes chauffantes ou brûleurs
B01F 35/213 - Mesure des propriétés des mélanges, p.ex. de la température, de la densité ou de la couleur
B01F 35/221 - Commande ou régulation des paramètres de fonctionnement, p.ex. du niveau de matière dans le mélangeur, de la température ou de la pression
B01J 2/10 - Procédés ou dispositifs pour la granulation de substances, en général; Traitement de matériaux particulaires leur permettant de s'écouler librement, en général, p.ex. en les rendant hydrophobes dans des tambours ou cuves fixes, prévus avec des dispositifs de malaxage ou de mélangeage
C12N 15/88 - Introduction de matériel génétique étranger utilisant des procédés non prévus ailleurs, p.ex. co-transformation utilisant la micro-encapsulation, p.ex. utilisant des vésicules liposomiques
B01F 101/22 - Mélange d'ingrédients pour compositions pharmaceutiques ou médicales
The present invention addresses the problem of providing: a protein that acts as a scintillator; and a method for designing a protein that acts as a scintillator. According to the present invention, a use of a β-barrel-type fluorescent protein as a scintillator is provided, wherein the β-barrel-type fluorescent protein has a fluorescence peak at 500 nm or less. According to the present invention, a method for designing a protein that acts as a scintillator is also provided, the method comprising (A) a step for identifying a specific amino acid residue in an amino acid sequence for a β-barrel-type fluorescent protein being mutated and (B) a step for constructing, on the basis of the amino acid sequence for the protein being mutated, an amino acid sequence having a structure such that the amino acid residue identified in the step (A) is substituted by another specific amino acid residue.
The present disclosure provides an apparatus and a method for taking out a particular fraction from a flow path. More particularly, in one aspect, the present disclosure provides a method for taking out a particular fraction from a flow path. The method includes: a step for flowing a component through the flow path; a step for taking out a fraction from the collection part on the flow path by means of a dispenser provided with a valve; and a step for distributing the fraction to the receiving part. In one embodiment, the collection part is positioned in a middle portion of the flow path (a portion that is neither an inflow port nor an outflow port of the flow path).
G01N 35/10 - Dispositifs pour transférer les échantillons vers, dans ou à partir de l'appareil d'analyse, p.ex. dispositifs d'aspiration, dispositifs d'injection
A61K 31/7088 - Composés ayant au moins trois nucléosides ou nucléotides
B01F 23/45 - Mélange, p.ex. dispersion ou émulsion, selon les phases à mélanger Émulsion en utilisant le mélange à écoulement
B01F 25/43 - Tubes de mélange, p.ex. dans lesquels la matière est déplacée dans une direction radiale ou partiellement inversée
B01F 33/301 - Micromixeurs utilisant des moyens spécifiques pour disposer les écoulements à mélanger, p.ex. des géométries ou des dispositions de canaux
B01F 35/213 - Mesure des propriétés des mélanges, p.ex. de la température, de la densité ou de la couleur
B01F 35/221 - Commande ou régulation des paramètres de fonctionnement, p.ex. du niveau de matière dans le mélangeur, de la température ou de la pression
B01J 2/10 - Procédés ou dispositifs pour la granulation de substances, en général; Traitement de matériaux particulaires leur permettant de s'écouler librement, en général, p.ex. en les rendant hydrophobes dans des tambours ou cuves fixes, prévus avec des dispositifs de malaxage ou de mélangeage
B01J 4/00 - Dispositifs d'alimentation; Dispositifs de commande d'alimentation ou d'évacuation
B01J 13/02 - Fabrication de microcapsules ou de microbilles
B01F 101/04 - Mélange d'ingrédients biocides, pesticides ou herbicides utilisés dans l'agriculture ou l'horticulture, p.ex. pour la pulvérisation
OSAKA RESEARCH INSTITUTE OF INDUSTRIAL SCIENCE AND TECHNOLOGY (Japon)
Inventeur(s)
Kitano, Katsuhisa
Ikawa, Satoshi
Abrégé
This sterilization device (1) comprises: a first container (12) that accommodates an object (A01); a first decompression unit (14) that decompresses the first container; and a supply unit (15) that supplies a pernitric acid gas to the object placed under a decompressed condition provided by the first decompression unit. The sterilization device can sterilize deep portions of the object.
A61L 2/20 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contact; Accessoires à cet effet utilisant des substances chimiques des substances gazeuses, p.ex. des vapeurs
5.
WAVELENGTH CONVERSION ELEMENT, OPTICAL CIRCUIT USING SAME, AND LIGHT SOURCE DEVICE
Provided is a wavelength conversion element in which high-quality crystal part can be utilized by a simple configuration. This wavelength conversion element comprises a substrate having a main surface, and an optical waveguide disposed on the main surface of the substrate, a core of the optical waveguide including a polar member having a second-order nonlinear optical constant and a first non-polar member disposed adjacent to the polar member in a direction parallel to the main surface of the substrate, and one or both side surfaces of the polar member and the first non-polar member being in contact with each other in a cross section orthogonal to the optical axis of the optical waveguide.
Provided is a biomarker useful for the diagnosis of cancer and the development of new drugs. Further provided are a cancer examination method, a treatment agent, and a reagent for studies of cancer, in each of which the biomarker is used. A useful biomarker is provided by identifying a protein that is expressed on the surface of the membrane of an extracellular vesicle (EV) in a cancer-specific manner. The cancer examination method includes detecting a protein (biomarker) that is expressed, in a cancer-specific manner, on the surface of the membrane of an EV contained in a collected body fluid specimen to detect a cancer-specific EV. An antibody against a protein expressed on the surface of the membrane of an EV in a cancer-specific manner can be used in a cancer examination method, a cancer treatment agent, and a reagent for studies of cancer.
C07K 16/00 - Immunoglobulines, p.ex. anticorps monoclonaux ou polyclonaux
G01N 33/543 - Tests immunologiques; Tests faisant intervenir la formation de liaisons biospécifiques; Matériaux à cet effet avec un support insoluble pour l'immobilisation de composés immunochimiques
7.
NOVEL METHOD FOR DETECTING ABNORMAL CELL HAVING GENE MUTATION
Provided is a method for detecting an abnormal cell having a gene mutation, the method comprising: a step for amplifying a region corresponding to a region comprising a nucleotide sequence lying between a nucleotide located at position-1,316 and a nucleotide located at position-1,663 in SEQ ID NO:1 and/or a region corresponding to a region comprising a nucleotide sequence lying between a nucleotide located at position-1,931 and a nucleotide located at position-2,642 in SEQ ID NO: 1 to produce an amplification product, wherein SEQ ID NO:1 is included in genomic DNA derived from a peripheral blood mononuclear cell of the patient; and a step for determining the nucleotide sequence for the amplification product and detecting a nucleotide mutation. In the method, the presence of the lesion is indicated when the nucleotide mutation is detected, and the amplification is performed by a PCR using a primer having no additional sequence.
C12Q 1/6883 - 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
C12Q 1/686 - Réaction en chaine par polymérase [PCR]
The purpose is to provide a novel luminescence-related gene (nucleic acid, vector for expression) capable of imparting stronger luminescence than by known luminescence-related genes to an organism (in particular, a plant). Provided is a nucleic acid containing at least one base sequence selected from: a base sequence encoding a protein containing an amino acid sequence represented by SEQ ID NO: 1 or an amino acid sequence having 90% or more sequence identity with a sequence represented by SEQ ID NO: 1; a base sequence encoding a protein containing an amino acid sequence represented by SEQ ID NO: 2 or 3 or an amino acid sequence having 90% or more sequence identity with a sequence represented by SEQ ID NO: 2 or 3; a base sequence encoding a protein containing an amino acid sequence represented by SEQ ID NO: 4 or 5 or an amino acid sequence having 90% or more sequence identity with a sequence represented by SEQ ID NO: 4 or 5; and a base sequence encoding a protein containing an amino acid sequence represented by SEQ ID NO: 6 or an amino acid sequence having 90% or more sequence identity with a sequence represented by SEQ ID NO: 6.
A01H 1/00 - Procédés de modification des génotypes
A01H 5/00 - Angiospermes, c. à d. plantes à fleurs, caractérisées par leurs parties végétales; Angiospermes caractérisées autrement que par leur taxonomie botanique
A01H 6/82 - Solanaceae, p.ex. poivron, tabac, pomme de terre, tomate ou aubergine
C12N 1/15 - Champignons; Leurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 1/19 - Levures; Leurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 1/21 - Bactéries; Leurs milieux de culture modifiés par l'introduction de matériel génétique étranger
C12N 15/63 - Introduction de matériel génétique étranger utilisant des vecteurs; Vecteurs; Utilisation d'hôtes pour ceux-ci; Régulation de l'expression
C12N 15/82 - Vecteurs ou systèmes d'expression spécialement adaptés aux hôtes eucaryotes pour cellules végétales
9.
RESIN FILM, METAL-CLAD LAMINATE, PRINTED WIRING BOARD, AND METHOD FOR PRODUCING RESIN FILM
One purpose of the present invention is to provide a resin film and a metal-clad laminate, each of which enables the production of a printed wiring board that has excellent dimensional stability, while being reduced in transmission loss. Another purpose of the present invention is to provide a method for producing a resin film that enables the production of a printed wiring board that has excellent dimensional stability, while being reduced in transmission loss. The present invention relates to a resin film 7 which comprises a polyimide film 70 and a PTFE film 71 that is directly superposed on the polyimide film 70. With respect to the resin film 7, the peeling strength at the time when the PTFE film 71 is peeled is 0.5 N/mm or more.
B32B 27/08 - Produits stratifiés composés essentiellement de résine synthétique comme seul composant ou composant principal d'une couche adjacente à une autre couche d'une substance spécifique d'une résine synthétique d'une sorte différente
B29C 65/02 - Assemblage d'éléments préformés; Appareils à cet effet par chauffage, avec ou sans pressage
B32B 15/08 - Produits stratifiés composés essentiellement de métal comprenant un métal comme seul composant ou comme composant principal d'une couche adjacente à une autre couche d'une substance spécifique de résine synthétique
B32B 27/30 - Produits stratifiés composés essentiellement de résine synthétique comprenant une résine acrylique
B32B 27/34 - Produits stratifiés composés essentiellement de résine synthétique comprenant des polyamides
C08J 7/00 - Traitement chimique ou revêtement d'objets façonnés faits de substances macromoléculaires
H05K 1/03 - Emploi de matériaux pour réaliser le substrat
A welding inspection method includes a step S102 of removing an impurity at a surface of a weld with a surface treatment apparatus, a step S110 of irradiating the surface of the weld from which the impurity has been removed with transmission laser light, a step S120 of detecting reflected ultrasound reflected by a lower surface of a base material, and a step S150 of determining whether or not there is an internal defect in the weld based on a result of detection of reflected ultrasound.
G01N 21/17 - Systèmes dans lesquels la lumière incidente est modifiée suivant les propriétés du matériau examiné
B23K 31/12 - Procédés relevant de la présente sous-classe, spécialement adaptés à des objets ou des buts particuliers, mais non couverts par un seul des groupes principaux relatifs à la recherche des propriétés, p.ex. de soudabilité, des matériaux
A permanent magnet-type rotary electric machine comprises: a stator including: a stator core having a plurality of stator teeth formed circumferentially; stator coils arranged in the respective bottoms of a plurality of stator slots formed between the stator teeth and wound on the stator teeth in a concentrated winding manner; and stator magnets arranged near the respective openings of the plurality of stator slots, a first rotor having a plurality of pole pieces and disposed coaxially with the stator to face the stator magnets; and a second rotor having a plurality of permanent magnets and disposed coaxially with the first rotor to face the first rotor, wherein the circumferential width of stator teeth positioned between the adjacent two of the stator magnets is narrower than the circumferential width of the stator slots.
An additive manufacturing apparatus includes: a chamber; a gas supply device that supplies an ambient gas into the chamber; an irradiation device that irradiates a molding region with an energy beam in order to mold a three dimensional molding object, the molding region being provided with a powder bed fusion on which a powder is spread in the chamber; and a controller that performs control related to additive manufacturing of the molding object, wherein the controller is configured to increase a pressure of the ambient gas in the chamber to be higher than an atmospheric pressure when the molding object is molded.
B22F 10/322 - Commande ou régulation des opérations de l’atmosphère, p.ex. de la composition ou de la pression dans une chambre de fabrication d’un écoulement de gaz, p.ex. du débit ou de la direction
B22F 10/28 - Fusion sur lit de poudre, p.ex. fusion sélective par laser [FSL] ou fusion par faisceau d’électrons [EBM]
This boron compound is represented by formula (1). In formula (1), X1and X2are each independently selected from among electron-withdrawing groups, Y1and Y2are each independently selected from among hydrogen and electron-donating groups, with hydrogen not being selected for both simultaneously, R1 is selected from among C1-24 organic groups, the C1-24 organic group may have a substituent, and n is selected from among the integers from 0 to 2.
C07D 215/06 - Composés hétérocycliques contenant les systèmes cycliques de la quinoléine ou de la quinoléine hydrogénée ne comportant pas de liaison entre l'atome d'azote du cycle et un chaînon non cyclique ou ne comportant que des atomes d'hydrogène ou de carbone liés directement à l'atome d'azote du cycle avec uniquement des atomes d'hydrogène ou des radicaux ne contenant que des atomes d'hydrogène et de carbone, liés directement aux atomes de carbone du cycle comportant uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés à l'atome d'azote du cycle
In a method for creating isotope distribution data, samples for analysis having different concentrations of metabolites are prepared as samples containing metabolites of cells cultured in a medium containing a substrate labeled with a stable isotope, mass spectrometry is performed on each under the same analysis condition, mass spectrum data is analyzed for each to identify the type of the metabolites, and there are determined the number of metabolites included in a metabolite group made of unlabeled metabolites and/or isotopic isomers, and the signal intensities of mass peaks corresponding to all isotope isomers included in the metabolite group. The number of metabolites corresponding to all types of metabolites and the signal intensity are compared among the samples to select a sample for analysis for obtaining the isotope distribution, and data on the isotope distribution of the metabolite is integrated to create the isotope distribution data of the metabolite.
G01N 33/58 - Analyse chimique de matériau biologique, p.ex. de sang ou d'urine; Test par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligands; Test immunologique faisant intervenir des substances marquées
15.
METHOD FOR SEPARATING COMPONENTS USING SUPERCRITICAL FLUID CHROMATOGRAPH
A method for separating components using a supercritical fluid chromatograph, including: injecting a sample into a mobile phase containing a supercritical fluid and a modifier to introduce the sample into a column; and separating components in the sample during passing through the column; wherein the sample contains an oligonucleotide as a target component; the supercritical fluid contains carbon dioxide; and the modifier contains a solution containing at least one selected from the group consisting of ammonium, an alkylamine, and an amino alcohol, and an acid.
C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN
B01D 15/40 - Adsorption sélective, p.ex. chromatographie caractérisée par le mécanisme de séparation utilisant un fluide supercritique comme phase mobile ou comme éluant
Provided is a technique for examining an autoimmune disease. This method for examining an autoimmune disease involves (1) a step for examining the presence or absence of endogenous human herpesvirus 6B in genomic DNA of a biological sample sampled from a subject.
A solid state welding apparatus comprises a pair of compression bars, a pair of electrodes disposed around the pair of compression bars, respectively, and a controller. The controller passes a first current through the pair of electrodes while controlling the pair of compression bars to cause a first load to act on each of first and second workpieces to bring the workpieces into contact with each other, and subsequently passes a second current larger than the first current through the pair of electrodes while controlling the pair of compression bars to cause a second load to act on each of first and second workpieces.
B23K 11/30 - Caractéristiques relatives aux électrodes
B23K 11/24 - Circuits d'alimentation ou de commande appropriés
18.
WALL THICKNESS ESTIMATION METHOD, RECORDING MEDIUM, TRAINING METHOD, MODEL CONSTRUCTION METHOD, WALL THICKNESS ESTIMATION DEVICE, AND WALL THICKNESS ESTIMATION SYSTEM
A wall thickness estimation method includes: obtaining behavioral information that is based on a video in which an organ wall or a blood vessel wall is captured using four-dimensional angiography, the behavioral information being numerical information about changes over time in a position of each of a plurality of predetermined points in the organ wall or the blood vessel wall; generating estimation information using a model trained to take as an input an image indicating a physical parameter based on the behavioral information obtained in the obtaining and output an index indicating a thickness at each of the plurality of predetermined points in the organ wall or the blood vessel wall, the estimation information being information visualizing the thickness; and outputting the estimation information generated in the generating.
A resistance spot joining method includes: a protrusion forming step of forming a protrusion on at least one of a first workpiece and a second workpiece by pressing the first and second workpieces with a first load by a pressing shaft and a pressing member; a load reducing step of reducing an area of contact between the first and second workpieces by reducing a pressing force from the pressing shaft and the pressing member such that a second load is applied to the first and second workpieces; a current applying step of applying a current to the first and second workpieces; and a joining step of joining contact interfaces of the first and second workpiece to each other by pressing the first and second workpieces with a third load.
A solid state welding apparatus comprises a pair of compression bars, a pair of electrodes disposed around the pair of compression bars, respectively, and a controller. The controller controls the pair of compression bars to cause a first load to act on each of the first and second workpieces, subsequently controls the pair of compression bars to subject compressive force to load removal to cause a second load smaller than the first load to act on the first and second workpieces, and subsequently passes a current through the pair of electrodes to remove an impurity on a metal surface.
A structured illumination microscope according to the present embodiment comprises: an excitation light source for generating excitation light; an activation light source that generates activation light to activate a fluorescent substance; an objective lens that focuses the excitation light onto a sample S; a structured illumination optical system that illuminates the sample using the excitation light as a structured illumination pattern; an activation optical system that irradiates the sample with activation 2 through the objective lens; and an imaging optical system that detects fluorescence generated at the sample via the objective lens to capture a fluorescent image of the sample.
This soldering device comprises: a solder joint part-forming device that has a soldering iron and forms a solder joint part in a soldering target area; an imaging device that images the solder joint part formed in the target area from a prescribed direction; an illumination device that illuminates the solder joint part formed in the target area from the prescribed direction; and a control device. The control device: causes the imaging device to perform imaging in a state in which the illumination device is providing illumination, thereby obtaining a first image of the solder joint part; causes the imaging device to perform imaging in a state where the illumination device has stopped illuminating, thereby obtaining a second image of the solder joint part; creates a brightness difference image which indicates a difference in brightness between the first image and the second image; and makes a determination about an excess failure and/or a shortage failure of the solder joint part, on the basis of the brightness difference image.
Provided are an information processing method, a computer program, an information processing system, and an information terminal device that achieve safe and effective circulation of medical data. An information processing method according to the present invention involves a computer executing processing that receives a purchase condition for a set of non-fungible tokens (NFTs) issued for access to the medical data of patients, outputs retrieval results for a set of NFTs that match the received purchase condition and a sales condition for the retrieved set of NFTs, receives a purchase request that designates a set of NFTs to be purchased from the retrieval results, transfers the set of NFTs to a purchaser in response to the purchase request, and gives compensation that corresponds to the transfer of the set of NFTs to the registrant registered to each of the NFTs included in the set.
Y1-YX1-x1-xN, and on which the Group III nitride semiconductor layer, the active layer, and the electron blocking layer are mounted, wherein X is greater than 0 and less than or equal to 1. In the active layer, the Al composition G is equal to or greater than Y but less than (Y+0.04), and the compositional difference between the maximum Al composition of the electron blocking layer and the Al composition of the active layer is 0.18 or more.
H01L 33/32 - Matériaux de la région électroluminescente contenant uniquement des éléments du groupe III et du groupe V de la classification périodique contenant de l'azote
H01L 21/20 - Dépôt de matériaux semi-conducteurs sur un substrat, p.ex. croissance épitaxiale
25.
BISPECIFIC ANTIBODY THAT RECOGNIZES CCR8 AS ANTIGEN
Disclosed is a bispecific antibody that recognizes CCR8 as an antigen. It was found that the bispecific antibody has cytotoxic activity against CCR8-expressing cells.
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 15/63 - Introduction de matériel génétique étranger utilisant des vecteurs; Vecteurs; Utilisation d'hôtes pour ceux-ci; Régulation de l'expression
26.
COATING COMPOSITION, METHOD FOR PRODUCING COATED ARTICLE, COATED ARTICLE, AND SILSESQUIOXANE DERIVATIVE
Provided are: a coating composition which has enhanced coatability and solubility in solvents and contains POSS with alkyl groups introduced; a method for producing a coated article using the coating composition; and a produced coated article. The present invention relates to a coating composition containing a silsesquioxane derivative which has a silsesquioxane skeleton having a polyhedral structure and in which a plurality of alkyl groups having different numbers of carbon atoms are bonded to silicon atoms. The coating composition can be applied to a substrate to produce a coated article. This produced coated article has a substrate and a coating, formed on the surface of the substrate, that contains a silsesquioxane derivative which has a silsesquioxane skeleton having a polyhedral structure and in which a plurality of alkyl groups having different numbers of carbon atoms are bonded to silicon atoms.
Provided are a graphene biosensor having high resistance to foreign substances while maintaining ultra-high sensitivity characteristics of graphene, and a method for using the graphene biosensor. Provided is a graphene biosensor 1 for detecting a measurement object gas 200 included in a liquid sample 100, wherein the graphene biosensor comprises: a substrate 10; a graphene layer 30 provided on the substrate 10, comprising at least one layer of graphene, and having a graphene layer principal surface 32 on the liquid sample 100 side; a drain electrode 21 electrically connected to the graphene layer 30; a source electrode 22 electrically connected to the graphene layer 30; and a gas-permeable layer 40 that comprises a gas-permeable material that transmits the measurement object gas 200, covers the graphene layer principal surface 32, and has a permeable layer principal surface 42 on the liquid sample 100 side.
G01N 27/00 - Recherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques
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
C12M 1/42 - Appareils pour le traitement de micro-organismes ou d'enzymes au moyen d'énergie électrique ou ondulatoire, p.ex. magnétisme, ondes sonores
28.
METHOD FOR DETECTING QUANTITY OF FIRST STRUCTURE AND QUANTITY OF SECOND STRUCTURE
[Problem] To provide a method for detecting the quantity of a first structure and the quantity of a second structure, the method comprising a step for detecting the quantity of a bonded first label and the quantity of a bonded second label together. [Solution] Provided is a method for detecting the quantity of a first structure and the quantity of a second structure, the method comprising: a step for bonding a first label to a first structure; a step for releasing a second structure from the first structure; a step for boding a second label to the second structure; and a step for detecting the quantity of the bonded first label and the quantity of the bonded second label together, wherein the second structure is included in the first structure, and the first label and the second label can be detected together, but are different.
G01N 33/53 - Tests immunologiques; Tests faisant intervenir la formation de liaisons biospécifiques; Matériaux à cet effet
C07K 16/08 - Immunoglobulines, p.ex. anticorps monoclonaux ou polyclonaux contre du matériel provenant de virus
C12Q 1/70 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir des virus ou des bactériophages
G01N 33/569 - Tests immunologiques; Tests faisant intervenir la formation de liaisons biospécifiques; Matériaux à cet effet pour micro-organismes, p.ex. protozoaires, bactéries, virus
29.
FUNCTIONAL DEVICE, GUIDING CATHETER, BIOLOGICAL INTERFACE SYSTEM, AND METHOD FOR INDWELLING FUNCTIONAL DEVICE
Provided is a functional device that enables at least one among measuring the activity of tissue of a living body with high resolution and applying fine stimulation to tissue of a living body, while being minimally invasive. This functional device 1 is indwelled inside a blood vessel of a living body and performs at least one among measurement of the activity of tissue outside the blood vessel and stimulation to the tissue. The functional device 1 comprises: a sheet-like flexible substrate 3; at least one functional part formed on the substrate 3; and a wiring 12 formed on the substrate 3 and connected to the functional part, wherein at least one among at least a portion of the surface of the substrate 3 and at least a portion of the surface of the functional part is covered with an antithrombotic material.
A61B 5/37 - Modalités, c. à d. méthodes diagnostiques spécifiques Électroencéphalographie [EEG] Électroencéphalographie intracrânienne [EEG IC], p.ex. électrocorticographie [ECoG]
A61B 5/293 - Détection, mesure ou enregistrement de signaux bioélectriques ou biomagnétiques du corps ou de parties de celui-ci Électrodes bioélectriques à cet effet spécialement adaptées à des utilisations particulières pour l’électroencéphalographie [EEG] invasives
30.
DEVICE AND METHOD FOR PREDICTING ABILITY TO IMPLANT IN UTERUS AND ESTIMATING DELIVERY TIMING
The present invention provides a device and a method for predicting the ability to implant in the uterus of a mother, and a device and a method for estimating delivery timing. This device for predicting the ability to implant in the uterus of a subject comprises: an electrode that is inserted up to a position which is either in the uterine cavity or intravaginal cavity of the subject; a measurement means for measuring the bioelectrical impedance at the position; and a prediction means for predicting the ability to implant, using the measured bioelectrical impedance value as an index. A device for estimating the delivery timing of the subject according to the present invention comprises: an electrode that is brought into contact with the mucosal epithelium at a position in the uterine cavity or intravaginal cavity of the subject; a measuring means of measuring the bioelectric impedance generated between the electrode and the mucosal epithelium; and an estimation means of estimating the delivery timing of the subject using the measured value of the bioelectric impedance as an index.
A61B 10/00 - Autres méthodes ou instruments pour le diagnostic, p.ex. pour le diagnostic de vaccination; Détermination du sexe; Détermination de la période d'ovulation; Instruments pour gratter la gorge
A61B 5/0538 - Mesure de l'impédance ou de la conductivité électrique d'une partie du corps invasive, p.ex. en utilisant un cathéter
31.
PHARMACEUTICAL COMPOSITION FOR TREATING NEUROPATHIC PAIN
Disclosed is a pharmaceutical composition for treating and/or preventing central neuropathic pain, the pharmaceutical composition containing at least one component selected from the group consisting of a JAK/STAT inhibitor, a CCL2 inhibitor, and an MMP2 inhibitor. Also disclosed is a pharmaceutical composition for treating and/or preventing neuropathic pain, the pharmaceutical composition containing at least one component selected from the group consisting of a JAK/STAT inhibitor, a CCL2 inhibitor, and an MMP2 inhibitor and being to be administered at intervals of 6 days or more.
The present invention provides a single-round infectious rotavirus characterized by having a mutation in at least one viral protein of the rotavirus, which is selected from the group consisting of VP1, VP2, VP3, VP4, VP6, VP7, NSP2, NSP3, and NSP4. The single-round infectious rotavirus according to the present invention can be used in a rotavirus vaccine, a rotavirus neutralization test method, and the like.
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir des micro-organismes viables
C12Q 1/66 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir une luciférase
C12Q 1/70 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir des virus ou des bactériophages
33.
METHOD FOR PRODUCING HIGH-PURITY VASCULAR ENDOTHELIAL CELL POPULATION FROM BIOLOGICAL TISSUE OR ORGAN
Provided is a method for producing a high-purity vascular endothelial cell population from a biological tissue or an organ, the method including: using a culture vessel having a structure in which a culture medium in a first culture vessel and a culture medium in a second culture vessel can be in contact with each other via a porous membrane having pores for cell permeation; coating the culture surface of the first culture vessel with an extracellular matrix including a vascular endothelial cell migration factor; filling the first and second culture vessels with the culture medium; initiating the culture of the biological tissue or the organ in the second culture vessel; and recovering the cells that have passed through the porous membrane and have moved into the first culture vessel. Also provided is a medicine containing the vascular endothelial cell population produced by said method as an active ingredient.
A61L 27/36 - Matériaux pour prothèses ou pour revêtement de prothèses contenant des constituants de constitution indéterminée ou leurs produits réactionnels
A61P 9/10 - Médicaments pour le traitement des troubles du système cardiovasculaire des maladies ischémiques ou athéroscléreuses, p.ex. médicaments antiangineux, vasodilatateurs coronariens, médicaments pour le traitement de l'infarctus du myocarde, de la rétinopathie, de l'insuffisance cérébro-vasculaire, de l'artériosclérose rénal
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C12M 1/00 - Appareillage pour l'enzymologie ou la microbiologie
C12M 3/00 - Appareillage pour la culture de tissus, de cellules humaines, animales ou végétales, ou de virus
A control system (100) controls an operation target (2). The control system (100) comprises a detection unit (3), a first determination unit (43), a second determination unit (44), and a weight determination unit (45). The detection unit (3) detects a detection target related to autonomous control of the operation target (2). The first determination unit (43) determines the next action of the operation target (2) by voluntary control, on the basis of brain waves of an operator (P) who operates the operation target (2). The second determination unit (44) determines the next action of the operation target (2) by the autonomous control, on the basis of the detection result from the detection unit (3). The weight determination unit (45) determines, on the basis of the detection result from the detection unit (3), a first weight for the next action of the operation target (2) by the voluntary control, and a second weight for the next action of the operation target (2) by the autonomous control. The weight determination unit (45) changes the first weight and the second weight in accordance with the detection result from the detection unit (3).
NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM (Japon)
OSAKA UNIVERSITY (Japon)
NICHIA CORPORATION (Japon)
Inventeur(s)
Torimoto, Tsukasa
Kameyama, Tatsuya
Kuwabata, Susumu
Uematsu, Taro
Kubo, Tomoya
Ikagawa, Yohei
Oyamatsu, Daisuke
Abrégé
Provided is an efficient method for producing semiconductor nanoparticles that exhibit band edge emission. The method comprises performing a first heat treatment of a first mixture, which contains a Cu salt, a Ag salt, a salt containing at least one of In or Ga, a gallium halide, and an organic solvent, to obtain first semiconductor nanoparticles. At least one of the Cu salt, the Ag salt, or the salt containing at least one of In or Ga in the first mixture contains a compound having a bond formed of a metal and sulfur.
H01L 33/50 - DISPOSITIFS À SEMI-CONDUCTEURS NON COUVERTS PAR LA CLASSE - Détails caractérisés par les éléments du boîtier des corps semi-conducteurs Éléments de conversion de la longueur d'onde
C01G 15/00 - Composés du gallium, de l'indium ou du thallium
C09K 11/62 - Substances luminescentes, p.ex. électroluminescentes, chimiluminescentes contenant des substances inorganiques luminescentes contenant du gallium, de l'indium ou du thalium
NATIONAL UNIVERSITY CORPORATION UNIVERSITY OF TOYAMA (Japon)
Inventeur(s)
Kudo Takashi
Akamine Shoshin
Kurosawa Nobuyuki
Isobe Masaharu
Abrégé
The present invention pertains to: an anti-APLP1 monoclonal antibody of which the epitope is the amino acid sequence from no. 232 to no. 238 in SEQ ID NO. 1; and an anti-APLP1 monoclonal antibody in which CDR1, CDR2, and CDR3 in a light chain respectively have the amino acid sequences described in SEQ ID NO. 5, 7, and 9, and CDR1, CDR2, and CDR3 in a heavy chain respectively have the amino acid sequences described in SEQ ID NO. 12, 14, and 16. The present invention also pertains to: a method for recovering extracellular vesicles derived from brain neurons by using the anti-APLP1 monoclonal antibody of the present invention; methods for detecting a neuropsychiatric disease biomarker and for recovering neuron-derived components, the methods each comprising recovering extracellular vesicles by said method; and a test reagent and a test kit which are for use in recovering extracellular vesicles and which include the anti-APLP1 monoclonal antibody of the present invention. The present invention provides: an anti-APLP1 monoclonal antibody having a higher specificity with respect to NDE; a method for recovering extracellular vesicles by using said antibody; a method for detecting a neuropsychiatric disease biomarker using the recovered extracellular vesicles; a test drug; and a test kit.
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
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir des micro-organismes viables
G01N 33/68 - Analyse chimique de matériau biologique, p.ex. de sang ou d'urine; Test par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligands; Test immunologique faisant intervenir des protéines, peptides ou amino-acides
This adeno-associated virus (AAV) vector particle contains a capsid, wherein: the capsid includes capsid proteins VP1, VP2, and VP3; the VP3 is (A) a polypeptide consisting of the amino acid sequence set forth in one among SEQ ID NOs: 1-6 and 25-29 or (B) a polypeptide which consists of an amino acid sequence that includes deletion, substitution, addition, or a combination thereof in the amino acid sequence of the (A) polypeptide and shares a sequence identity of at least 80% with an amino acid sequence corresponding to the 18th-533rd positions of the amino acid sequence set forth in SEQ ID NO: 1 and from which the capsid can be formed; and the ratio ([VP1+VP2]/[VP3]) of the number of the VP1 and the VP2 to the number of the VP3 in the capsid is at least 0.3.
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiques; Thérapie génique
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir des micro-organismes viables
38.
WATER TREATMENT METHOD, SUBSTANCE RECOVERY METHOD, RESOURCE RECOVERY METHOD, AND RESOURCE RECOVERY PLANT
A water treatment method for recovering a specific substance dissolved in water being treated, wherein a working electrode W configured from an organic redox substance provided with selective adsorption capacity with respect to a specific substance is immersed in water being treated, the specific substance is electrochemically adsorbed to the working electrode W, the working electrode to which the specific substance is adsorbed is immersed in a recovery solution, and the specific substance is electrochemically discharged from the working electrode W, whereby a useful specific substance such as ammonia contained in wastewater can be safely and efficiently recovered.
A support apparatus includes an irradiation device for emitting a particle beam, a detection device for detecting a particle beam irradiation region, and a control unit for acquiring the irradiation region. The control unit specifies an attention region within the irradiation region in a treatment plan for a patient, and specifies the irradiation position for pre-irradiation within the attention region. The control unit instructs the irradiation device to carry out pre-irradiation with irradiation energy in the treatment plan at the irradiation position, and acquires the irradiation region detected by the detection device. The control unit further adjusts irradiation conditions in the treatment plan according to the irradiation region in the pre-irradiation and instructs the irradiation device to carry out post-irradiation under the adjusted irradiation conditions.
Provided is a polymer that has an aliphatic polyester resin skeleton and has excellent performance in strength while being biodegradable. The polymer has a cyclodextrin skeleton as a side chain of the polymer, and has a fatty acid polyester resin structure in at least one section.
According to one embodiment, an alignment processing device includes a light source, a polarizing beam splitter, a first optical system, a second optical system, a first retardation film, a second retardation film, a moving mechanism configured to move a processing substrate in which a thin film is formed, and a controller. Interfering light is formed in an exposure area by first circularly polarized light and second circularly polarized light. The controller performs control so as to repeat a process of exposing part of an area of the thin film by the interfering light and a process of moving the processing substrate.
This confocal imaging device comprises: a light source that generates illumination light; a multi-pinhole plate that is disposed at a position conjugate to the sample and has a plurality of pinholes; a drive mechanism that drives the multi-pinhole plate; an objective lens that condenses the illumination light from the multi-pinhole plate onto the sample and into which signal light from the sample is incident; an imaging lens that is disposed between the objective lens and the multi-pinhole plate and forms an image of the signal light from the sample on the multi-pinhole plate; a beam splitter that causes the signal light that has passed through the pinholes to branch from the illumination light; a telecentric lens into which the signal light is incident; and an imaging device that detects the signal light from the telecentric lens and images the sample.
A chuck apparatus is configured to hold a wafer during planarization of the wafer with the aid of anodizing. The chuck apparatus includes a chuck cover, a suction portion, and an energizing portion. The suction portion includes a suction surface that suctions the wafer. The energizing portion is provided in the suction portion so as to come into contact and energize the wafer suctioned by the suction portion. The chuck cover covers the suction portion and the energizing portion in an insulating manner while exposing the suction surface.
H01L 21/683 - Appareils spécialement adaptés pour la manipulation des dispositifs à semi-conducteurs ou des dispositifs électriques à l'état solide pendant leur fabrication ou leur traitement; Appareils spécialement adaptés pour la manipulation des plaquettes pendant la fabrication ou le traitement des dispositifs à semi-conducteurs ou des dispositifs électriques à l'état solide ou de leurs composants pour le maintien ou la préhension
44.
Disease Treatment Drug Based on Mesenchymal-Stem-Cell Mobilization
The present inventors identified many nuclear proteins contained in the extract of skin tissue by mass spectrometry, randomly selected multiple partial amino acid sequences of the nuclear proteins, chemically synthesized peptides consisting of the partial amino acid sequences, and examined their activity of mobilizing mesenchymal stem cells. As a result, it was found that these multiple peptides show the activity of mobilizing mesenchymal stem cells into peripheral blood, even though their amino acid sequences are completely different from each other. The inventors also found that fragment peptides of the nuclear proteins have therapeutic effects on diseases characterized by inflammation and abnormalities of the immune system (e.g., inflammatory bowel disease and psoriasis). Based on these findings, a new regenerative medicine technology that can overcome the problems of cell transplantation therapy is provided.
C07K 14/47 - Peptides ayant plus de 20 amino-acides; Gastrines; Somatostatines; Mélanotropines; Leurs dérivés provenant d'humains provenant de vertébrés provenant de mammifères
A61K 38/00 - Préparations médicinales contenant des peptides
A61P 1/00 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif
A medicine recommendation apparatus (2000) acquires disease information (20), gene mutation information (30), and current medication information (40). The disease information (20) is information regarding a disease that a subject suffers from. The gene mutation information (30) is information regarding a gene mutation of the subject. The current medication information (40) is information regarding a medicine that the subject is using. The medicine recommendation apparatus (2000) generates candidate medicine information (10) by using the disease information (20), the gene mutation information (30), and the current medication information (40). The candidate medicine information (10) is information regarding a candidate for a medicine use of which can be recommended to the subject or which can be prescribed to the subject.
G16H 20/10 - TIC spécialement adaptées aux thérapies ou aux plans d’amélioration de la santé, p.ex. pour manier les prescriptions, orienter la thérapie ou surveiller l’observance par les patients concernant des médicaments ou des médications, p.ex. pour s’assurer de l’administration correcte aux patients
G16H 70/40 - TIC spécialement adaptées au maniement ou au traitement de références médicales concernant des médicaments, p.ex. leurs effets secondaires ou leur usage prévu
Provided is an active ingredient of a pharmaceutical composition for treating myeloma. Specifically, provided is an antibody whose epitope is present in the region of the amino acid residue positions 20 to 109 of human integrin β7.
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
A61K 35/17 - Lymphocytes; Lymphocytes B; Lymphocytes T; Cellules tueuses naturelles; Lymphocytes activés par un interféron ou une cytokine
A61K 39/00 - Préparations médicinales contenant des antigènes ou des anticorps
C07K 16/30 - 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 provenant de cellules de tumeurs
A composition comprising skeletal myoblasts for treating liver dysfunction or improving liver function, in which the liver dysfunction can be hepatitis, liver fibrosis, liver cirrhosis, liver cancer, or liver failure. The composition can be used for promoting the proliferation of liver cells, regeneration of the liver tissue and/or angiogenesis, and providing a method for treating liver dysfunction, including a step of treating applying the composition to a site exhibiting liver dysfunction.
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
C12N 5/077 - Cellules mésenchymateuses, p.ex. cellules osseuses, cellules de cartilage, cellules stromales médulaires, cellules adipeuses ou cellules musculaires
This method for joining metal materials includes: a preparation step for superposing in a predetermined direction a first material to be joined including a first metal and a second material to be joined including a second metal; a heating step for heating a joint interface between the first material and the second material, and/or a first portion located in the vicinity of the joint interface in the first material, and/or a second portion located in the vicinity of the joint interface in the second material; and a joining step for applying toward the joint interface a pressure along a predetermined direction for joining together the first material and the second material. In the heating step, a current running along a direction intersecting the predetermined direction is passed through the joint interface, and/or the first portion, and/or the second portion.
The present invention relates to a cell structure production method comprising a step in which a plurality of cells including at least epithelial cells and vascular endothelial cells are cultured in a culture medium containing one or more growth factors that contribute to angiogenesis.
C12N 5/071 - Cellules ou tissus de vertébrés, p.ex. cellules humaines ou tissus humains
C12N 5/00 - Cellules non différenciées humaines, animales ou végétales, p.ex. lignées cellulaires; Tissus; Leur culture ou conservation; Milieux de culture à cet effet
C12N 5/077 - Cellules mésenchymateuses, p.ex. cellules osseuses, cellules de cartilage, cellules stromales médulaires, cellules adipeuses ou cellules musculaires
The present invention provides a compound which is capable of selectively delivering a cell to a disease site such as a bone or a tooth. The compound comprises a hydrophilic polymer or a derivative thereof, a bile acid or a derivative thereof, and a hydroxyapatite-directed substance which has a photolytic protective group. Also provided is a cell which has adsorbed the compound.
A61K 41/00 - Préparations médicinales obtenues par traitement de substances par énergie ondulatoire ou par rayonnement corpusculaire
A61K 47/54 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p.ex. les supports ou les additifs inertes; Agents de ciblage ou de modification chimiquement liés à l’ingrédient actif l’ingrédient non actif étant chimiquement lié à l’ingrédient actif, p.ex. conjugués polymère-médicament l’ingrédient non actif étant un agent de modification l’agent de modification étant un composé organique
A61K 47/60 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p.ex. les supports ou les additifs inertes; Agents de ciblage ou de modification chimiquement liés à l’ingrédient actif l’ingrédient non actif étant chimiquement lié à l’ingrédient actif, p.ex. conjugués polymère-médicament l’ingrédient non actif étant un agent de modification l’agent de modification étant un composé organique macromoléculaire, p.ex. une molécule oligomérique, polymérique ou dendrimérique obtenu par des réactions autres que celles faisant intervenir uniquement des liaisons non saturées carbone-carbone, p.ex. polyurées ou polyuréthanes le composé organique macromoléculaire étant un oligomère, un polymère ou un dendrimère de polyoxyalkylène, p.ex. PEG, PPG, PEO ou polyglycérol
A61L 27/18 - Matériaux macromoléculaires obtenus par des réactions autres que celles faisant intervenir uniquement des liaisons non saturées carbone-carbone
A61P 1/02 - Préparations stomatologiques, p.ex. médicaments pour le traitement des caries, des aphtes, des périodontites
A61P 17/02 - Médicaments pour le traitement des troubles dermatologiques pour traiter les blessures, les ulcères, les brûlures, les cicatrices, les cheloïdes, ou similaires
A61P 19/10 - Médicaments pour le traitement des troubles du squelette des maladies osseuses, p.ex. rachitisme, maladie de Paget de l'ostéoporose
C07J 9/00 - Stéroïdes normaux contenant du carbone, de l'hydrogène, un halogène ou de l'oxygène, substitués en position 17bèta par une chaîne de plus de deux atomes de carbone, p.ex. cholane, cholestane, coprostane
[Problem] The present invention addresses the problem of providing an agent for preventing and/or treating amyotrophic lateral sclerosis. [Solution] This agent for preventing and/or treating amyotrophic lateral sclerosis contains at least one compound selected from the group consisting of paclitaxel, docetaxel, carfilzomib, olaparib, and nicotinamide.
A61K 31/337 - Composés hétérocycliques ayant l'oxygène comme seul hétéro-atome d'un cycle, p.ex. fungichromine ayant des cycles à quatre chaînons, p.ex. taxol
A61K 31/455 - Acide nicotinique, c. à d. niacine; Ses dérivés, p.ex. esters, amides
A61K 31/502 - Pyridazines; Pyridazines hydrogénées condensées en ortho ou en péri avec des systèmes carbocycliques, p.ex. cinnoline, phtalazine
The purpose of the present invention is to provide a novel technique for manufacturing a bonded structure by direct bonding. A bonded structure in which a structure 1 and a structure 2 are bonded with a metal plating film interposed therebetween is provided.
H01L 21/60 - Fixation des fils de connexion ou d'autres pièces conductrices, devant servir à conduire le courant vers le ou hors du dispositif pendant son fonctionnement
H01L 21/52 - Montage des corps semi-conducteurs dans les conteneurs
The present application discloses a glycolipid derivative (I) represented by formula (I) (wherein each symbol is as described in the description) or a salt thereof as one of the embodiments of the invention, the glycolipid derivative (I) or a salt thereof being useful as a novel ligand for a macrophage-inducible C-type lectin receptor.
C07H 15/203 - Carbocycles monocycliques autres que des cycles cyclohexane; Systèmes carbocycliques bicycliques
A61K 31/7034 - Composés ayant des radicaux saccharide liés à des composés non-saccharide par des liaisons glycosidiques liés à un composé carbocyclique, p.ex. phloridzine
A61K 39/39 - Préparations médicinales contenant des antigènes ou des anticorps caractérisées par les additifs immunostimulants, p.ex. par les adjuvants chimiques
C07C 209/46 - Préparation de composés contenant des groupes amino liés à un squelette carboné par réduction d'acides carboxyliques ou de leurs esters en présence d'ammoniac ou d'amines ou par réduction de nitriles, d'amides d'acides carboxyliques, d'imines ou d'imino-éthers par réduction d'acides carboxyliques ou de leurs esters en présence d'ammoniac ou d'amines
C07C 211/07 - Monoamines contenant un, deux ou trois groupes alkyle, chacun ayant le même nombre d'atomes de carbone supérieur à trois
C07C 211/35 - Composés contenant des groupes amino liés à un squelette carboné ayant des groupes amino liés à des atomes de carbone de cycles autres que des cycles aromatiques à six chaînons d'un squelette carboné saturé contenant uniquement des cycles non condensés
C07D 211/14 - Composés hétérocycliques contenant des cycles pyridiques hydrogénés, non condensés avec d'autres cycles avec uniquement des atomes d'hydrogène et de carbone liés directement à l'atome d'azote du cycle ne comportant pas de liaison double entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle avec des radicaux ne contenant que des atomes de carbone et d'hydrogène liés aux atomes de carbone du cycle avec des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés à l'atome d'azote du cycle
C07D 211/46 - Atomes d'oxygène liés en position 4 comportant un atome d'hydrogène comme second substituant en position 4
C07D 211/62 - Atomes de carbone comportant trois liaisons à des hétéro-atomes, avec au plus une liaison à un halogène, p.ex. radicaux ester ou nitrile liés en position 4
C07D 265/30 - Oxazines-1, 4; Oxazines-1, 4 hydrogénées non condensées avec d'autres cycles
C07D 273/01 - Composés hétérocycliques contenant des cycles comportant des atomes d'azote et d'oxygène comme uniques hétéro-atomes du cycle, non prévus par les groupes comportant un atome d'azote
C07D 295/03 - Composés hétérocycliques contenant des cycles polyméthylène imine d'au moins cinq chaînons, des cycles aza-3 bicyclo [3.2.2] nonane, piperazine, morpholine ou thiomorpholine, ne comportant que des atomes d'hydrogène liés directement aux atomes de car contenant uniquement des atomes d'hydrogène et de carbone en plus des hétéro-éléments du cycle ne contenant qu'un hétérocycle avec les atomes d'azote du cycle liés directement à des atomes de carbone acycliques
C07D 295/13 - Composés hétérocycliques contenant des cycles polyméthylène imine d'au moins cinq chaînons, des cycles aza-3 bicyclo [3.2.2] nonane, piperazine, morpholine ou thiomorpholine, ne comportant que des atomes d'hydrogène liés directement aux atomes de car avec des radicaux hydrocarbonés substitués liés aux atomes d'azote du cycle substitués par des atomes d'azote liés par des liaisons simples ou doubles avec les atomes d'azote du cycle et les atomes d'azote substituants liés à la même chaîne carbonée, qui n'est pas interrompue par des cycles carbocycliques à une chaîne acyclique saturée
C07D 295/067 - Composés hétérocycliques contenant des cycles polyméthylène imine d'au moins cinq chaînons, des cycles aza-3 bicyclo [3.2.2] nonane, piperazine, morpholine ou thiomorpholine, ne comportant que des atomes d'hydrogène liés directement aux atomes de car avec des radicaux hydrocarbonés substitués liés aux atomes d'azote du cycle substitués par des atomes d'halogènes ou des radicaux nitro avec les atomes d'azote du cycle et les substituants liés à la même chaîne carbonée, qui n'est pas interrompue par des carbocycles
C07D 295/088 - Composés hétérocycliques contenant des cycles polyméthylène imine d'au moins cinq chaînons, des cycles aza-3 bicyclo [3.2.2] nonane, piperazine, morpholine ou thiomorpholine, ne comportant que des atomes d'hydrogène liés directement aux atomes de car avec des radicaux hydrocarbonés substitués liés aux atomes d'azote du cycle substitués par des atomes d'oxygène ou de soufre liés par des liaisons simples avec les atomes d'azote du cycle et les atomes d'oxygène ou de soufre liés à la même chaîne carbonée, qui n'est pas interrompue par des carbocycles à une chaîne acyclique saturée
Provided is a low-temperature-sintering bonding material that is easy to prepare and that, when used for sintering bonding, enables sintering at low temperatures and can provide highly reliable bonded structures. A low-temperature-sintering bonding material according to an embodiment contains silver particles and silicon particles, and more than 50% of the surface of the silicon particles is composed of silicon atoms. A low-temperature-sintering bonding material according to another embodiment contains silver particles and silicon particles, wherein sintering brings about the formation of an interface at the atomic level between the silver constituting the silver particles and the silicon constituting the silicon particles.
Provided are: a method for friction-joining galvanized steel sheets in which admixture of zinc into a joined part is effectively suppressed, and with which it is possible to obtain a joined part that is coated with a galvanized layer; and a joined structure obtained through the aforementioned joining method. A friction-joining method characterized by having a first step for bringing one member into contact with another member to form a joining interface, a second step for repeatedly causing the one member and the other member to slide on the same trajectory in a state in which pressure is applied substantially perpendicularly to the joining interface and eliminating burrs from the joining interface, and a third step for stopping the sliding and forming a joined surface, the friction-joining method also being characterized in that the one member and/or the other member is configured as a galvanized steel sheet, and in that admixture of a galvanized component into the joined surface is suppressed due to the elimination of the burrs.
B23K 20/12 - Soudage non électrique par percussion ou par une autre forme de pression, avec ou sans chauffage, p.ex. revêtement ou placage la chaleur étant produite par friction; Soudage par friction
Provided are a method for producing a protein material without using an organic solvent, the method involving ejecting a solution containing a protein material raw material into a water-based medium and drying the ejected protein material raw material, and a protein material produced by the method.
Provided is a linear friction welding method wherein, at the timing at which a newly formed surface of a first welding member 11A and a newly formed surface of a second welding member 11B make contact due to burr 12 discharge, a second pressure P2 that is greater than a first pressure P1 is applied to a welding interface such that base material parts of the first welding member 11A and the second welding member 11B which are continuous with a weld part 13 plastically deform so as to spread toward the welding interface M.
B23K 20/12 - Soudage non électrique par percussion ou par une autre forme de pression, avec ou sans chauffage, p.ex. revêtement ou placage la chaleur étant produite par friction; Soudage par friction
59.
METHOD FOR INTRODUCING NUCLEIC ACID AND/OR PROTEIN INTO CELLS
NATIONAL UNIVERSITY CORPORATION CHIBA UNIVERSITY (Japon)
Inventeur(s)
Ikawa, Masahito
Emori, Chihiro
Akita, Hidetaka
Tanaka, Hiroki
Abrégé
Disclosed, inter alia, is: a method for introducing a nucleic acid and/or protein into cells, the method comprising a step for bringing cells into contact in vitro with a lipid nanoparticle in which a nucleic acid and/or protein is internally sealed, the cells being at a stage from fertilized egg to blastula; and a method for producing cells into which a nucleic acid and/or a protein has been introduced and that are at a stage from fertilized egg to blastula, the method comprising a step for bringing cells into contact in vitro with a lipid nanoparticle in which a nucleic acid and/or protein is internally sealed, the cells being at a stage from fertilized egg to blastula.
C12N 15/88 - Introduction de matériel génétique étranger utilisant des procédés non prévus ailleurs, p.ex. co-transformation utilisant la micro-encapsulation, p.ex. utilisant des vésicules liposomiques
C12N 5/10 - Cellules modifiées par l'introduction de matériel génétique étranger, p.ex. cellules transformées par des virus
C12N 5/073 - Cellules ou tissus embryonnaires; Cellules fœtales ou tissus fœtaux
Provided is a metal sheet having excellent handleability, suppressed void formation during bonding, and excellent bondability. A metal sheet 1 according to an embodiment of the present invention has, on at least one surface (surface 31a and/or 32a), a region in which grains having an area of 40,000 nm2 or less constitute at least 50% of the surface area. In addition, the metal sheet 1 according to another embodiment of the present invention has an internal porosity of 70% or less, and has, on at least one surface (surface 31a and/or 32a), a region having a porosity of 20% or less in the vicinity of the surface and having sinterability.
B22F 5/00 - Fabrication de pièces ou d'objets à partir de poudres métalliques caractérisée par la forme particulière du produit à réaliser
B22F 7/08 - Fabrication de couches composites, de pièces ou d'objets à base de poudres métalliques, par frittage avec ou sans compactage de pièces ou objets composés de parties différentes, p.ex. pour former des outils à embouts rapportés avec une ou plusieurs parties non faites à partir de poudre
H01B 5/02 - Barres, barreaux, fils ou rubans simples; Barres omnibus
61.
DIAGNOSTIC MARKER FOR HEPATIC CANCER DEVELOPMENT IN CHRONIC HEPATIC DISEASE
The method of the present invention for evaluating the risk of developing liver cancer in a subject includes (1) a step of measuring a GDF15 level of a subject and (2) a step of relating the GDF15 level to the risk of developing liver cancer. When the GDF15 level measured in step (1) is not less than a cutoff value set in advance, the GDF15 level becomes an indicator that the subject has a high risk of developing liver cancer, and when the GDF15 level is less than the cutoff value, it becomes an indicator that the risk of developing liver cancer is low. The present invention also provides a kit for measuring GDF15 levels in a subject for use in the method of the present invention, and a diagnostic agent for evaluating the risk of developing liver cancer in a subject, which contains an anti-GDF15-specific antibody.
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 33/574 - Tests immunologiques; Tests faisant intervenir la formation de liaisons biospécifiques; Matériaux à cet effet pour le cancer
62.
CARBON MATERIAL, CATALYST, DISPERSION , ELECTRODE, BATTERY, AND ELECTROLYSIS DEVICE
B01J 35/60 - caractérisés par leurs propriétés de surface ou leur porosité
C25B 11/031 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par la configuration ou la forme perforées ou foraminées Électrodes poreuses
C25B 11/075 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé d’un seul élément catalytique ou composé catalytique
H01M 4/96 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes inertes ayant une activité catalytique, p.ex. pour piles à combustible Électrodes à base de carbone
H01M 8/10 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication Éléments à combustible avec électrolytes solides
H01M 12/06 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments hybrides; Leur fabrication composés d'un demi-élément du type élément à combustible et d'un demi-élément du type élément primaire avec une électrode métallique et une électrode à gaz
63.
CARBON MATERIAL, PRODUCTION METHOD FOR CARBON MATERIAL, CATALYST, DISPERSION LIQUID, ELECTRODE, BATTERY, AND ELECTROLYSIS DEVICE
C25B 11/052 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support Électrodes comportant un substrat et un ou plusieurs revêtements électro-catalytiques
C25B 11/054 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support Électrodes comportant des électro-catalyseurs sur un support
C25B 11/095 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé de plusieurs éléments catalytiques ou composés catalytiques au moins un des composés est de type organique
H01M 4/86 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes inertes ayant une activité catalytique, p.ex. pour piles à combustible
H01M 4/90 - Emploi de matériau catalytique spécifié
H01M 8/10 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication Éléments à combustible avec électrolytes solides
H01M 8/12 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication Éléments à combustible avec électrolytes solides fonctionnant à haute température, p.ex. avec un électrolyte en ZrO2 stabilisé
64.
COMPOSITE MATERIAL, METHOD FOR MANUFACTURING COMPOSITE MATERIAL, CATALYST, DISPERSION, ELECTRODE, AND ELECTROLYSIS DEVICE
C01B 15/029 - Préparation à partir de l'hydrogène et de l'oxygène
C25B 11/031 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par la configuration ou la forme perforées ou foraminées Électrodes poreuses
C25B 11/052 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support Électrodes comportant un substrat et un ou plusieurs revêtements électro-catalytiques
C25B 11/054 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support Électrodes comportant des électro-catalyseurs sur un support
The present invention provides: a rare-earth-doped semiconductor device which has further improved EQE %, while having excellent emission intensity; and a method for producing the rare-earth-doped semiconductor device. A rare-earth-doped semiconductor device in which an active layer that is obtained by adding a rare earth element to a base material that is composed of GaN, InN, AlN or an alloy compound semiconductor of any two or more of these compounds is arranged between an n-type layer and a p-type layer, wherein a p-type doped layer in which a p-type dopant is added together with a rare earth element is formed in the p-type layer side of the active layer. A method for producing a rare-earth-doped semiconductor device, wherein: formation of an n-type layer, formation of an active layer and formation of a p-type layer are performed by a series of formation steps under the temperature conditions of 900° C. to 1200° C. with use of an organic metal vapor deposition method without being taken out of a reaction vessel; and when the active layer is formed, a p-type doped layer is formed in the p-type layer side of the active layer by adding a p-type dopant together with a rare earth element.
H01L 33/32 - Matériaux de la région électroluminescente contenant uniquement des éléments du groupe III et du groupe V de la classification périodique contenant de l'azote
H01L 33/00 - DISPOSITIFS À SEMI-CONDUCTEURS NON COUVERTS PAR LA CLASSE - Détails
H01S 5/30 - Structure ou forme de la région active; Matériaux pour la région active
H01S 5/323 - Structure ou forme de la région active; Matériaux pour la région active comprenant des jonctions PN, p.ex. hétérostructures ou doubles hétérostructures dans des composés AIIIBV, p.ex. laser AlGaAs
National Center for Child Health and Development (Japon)
Inventeur(s)
Shimatani, Kenichiro
Sato, Hiromu
Sasai, Masao
Sawa, Yoshiki
Saito, Atsuhiro
Miyagawa, Shigeru
Abrégé
An object of the present invention is to provide a pericyte-like cell having high angiogenic potential with a higher cell proliferation ability than a primary pericyte available in the past and high VEGF expression, and a method for producing the same. Provided are a method for producing a VEGF-highly expressing pericyte-like cell, the method including selecting a CD56(−) pericyte-like cell from a population including a pericyte-like cell obtained by inducing differentiation of a pluripotent stem cell; and a VEGF-highly expressing pericyte-like cell produced by the production method.
Provided are a method and a reaction vessel for efficiently performing a chemical reaction. The method comprises: charging a mixed solution containing a polar solute and a non-polar solute into a reaction vessel; separating the mixed solution into a first solution layer mainly containing the polar solute and a second solution layer mainly containing the non-polar solute in the reaction vessel; and emitting light outside the reaction vessel toward the interface between the first solution layer and the second solution layer mainly through one of the first solution layer and the second solution layer that has a lower light absorption rate, to cause a chemical reaction of the polar solute with the non-polar solute. The reaction vessel, into which a mixed solution containing a polar solute and a non-polar solute is to be charged, is provided with a light guide unit that is disposed so as to cause light outside the reaction vessel to enter the reaction vessel and be emitted toward the interface between a first solution layer mainly containing the polar solute and a second solution layer mainly containing the non-polar solute, mainly through one of the first solution layer and the second solution layer that has a lower light absorption rate.
B01J 19/12 - Procédés utilisant l'application directe de l'énergie ondulatoire ou électrique, ou un rayonnement particulaire; Appareils à cet usage utilisant des radiations électromagnétiques
68.
PARTIAL PEPTIDE OF SARS-COV-2 SPIKE PROTEIN FOR INDUCING FOLLICULAR HELPER T CELLS
The purpose of the present invention is to provide a composition for inducing follicular helper T cells reactive with SARS-CoV-2. Provided is a partial peptide of a spike protein of SARS-CoV-2, the partial peptide containing an amino acid sequence selected from the group consisting of (1) to (17) below and having a total length of 15 amino acids or less: (1) FKIYSKHTPIN (SEQ ID NO: 1); (2) FQFCNDPFLGVYYHK (SEQ ID NO: 2); (3) KRFDNPVLPFN (SEQ ID NO: 3); (4) LLQYGSFCTQL (SEQ ID NO: 4); (5) PPAYTNSFTRGVYYP (SEQ ID NO: 5); (6) CSNLLLQYGSFCTQL (SEQ ID NO: 6); (7) SKRSFIEDLLFNKVT (SEQ ID NO: 7); (8) TGVLTESNKKFLPFQ (SEQ ID NO: 8); (9) TNGTKRFDNPVLPFN (SEQ ID NO: 9); (10) NQFNSAIGKIQ (SEQ ID NO: 10); (11) NFTISVTTEIL (SEQ ID NO: 11); (12) STEIYQAGSTPCNGV (SEQ ID NO: 12); (13) KVFRSSVLHST (SEQ ID NO: 13); (14) EIRASANLAAT (SEQ ID NO: 14); (15) NFTISVTTEILPVSM (SEQ ID NO: 15); (16) FIKQYGDCLGDIAAR (SEQ ID NO: 16); and (17) FIEDLLFNKVTLADA (SEQ ID NO: 17).
Disclosed is a carbon material which contains a fired product of a mixture that contains a first compound and a second compound, wherein: the first compound is a phthalocyanine compound that has bromine as a substituent; and the second compound contains at least one metal element that is selected from the group consisting of Fe, Co, Ni, Cu, Al and Zn.
C25B 11/031 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par la configuration ou la forme perforées ou foraminées Électrodes poreuses
C25B 11/053 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support Électrodes comportant un substrat et un ou plusieurs revêtements électro-catalytiques caractérisées par des revêtements électro-catalytiques multicouches
C25B 11/054 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support Électrodes comportant des électro-catalyseurs sur un support
C25B 11/095 - PROCÉDÉS ÉLECTROLYTIQUES OU ÉLECTROPHORÉTIQUES POUR LA PRODUCTION DE COMPOSÉS ORGANIQUES OU MINÉRAUX, OU DE NON-MÉTAUX; APPAREILLAGES À CET EFFET Électrodes; Leur fabrication non prévue ailleurs caractérisées par le matériau Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé de plusieurs éléments catalytiques ou composés catalytiques au moins un des composés est de type organique
H01M 4/86 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Électrodes Électrodes inertes ayant une activité catalytique, p.ex. pour piles à combustible
H01M 4/90 - Emploi de matériau catalytique spécifié
H01M 8/10 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication Éléments à combustible avec électrolytes solides
H01M 8/12 - PROCÉDÉS OU MOYENS POUR LA CONVERSION DIRECTE DE L'ÉNERGIE CHIMIQUE EN ÉNERGIE ÉLECTRIQUE, p.ex. BATTERIES Éléments à combustible; Leur fabrication Éléments à combustible avec électrolytes solides fonctionnant à haute température, p.ex. avec un électrolyte en ZrO2 stabilisé
70.
BOROHYDRIDE-CONTAINING COMPOSITION, HYDROGEN GENERATION SYSTEM AND FUEL CELL SYSTEM
Provided are a hydrogen boride-containing composition, a hydrogen generation system, and a fuel cell system that achieve further performance improvement of a hydrogen supply source with a hydrogen boride-containing sheet. The hydrogen boride-containing composition contains a hydrogen boride-containing sheet having a two-dimensional network consisting of (BH)n(n≥4, where n is an integer) and an electron donor. At least a portion of the electron donor is supported on the hydrogen boride-containing sheet, electrons of the electron donor are supplied to the hydrogen boride-containing sheet by external stimulus, and hydrogen is generated from the hydrogen boride-containing sheet into which the electrons are injected.
H01M 8/0606 - Combinaison d’éléments à combustible avec des moyens de production de réactifs ou pour le traitement de résidus avec des moyens de production des réactifs gazeux
C01B 3/04 - Production d'hydrogène ou de mélanges gazeux contenant de l'hydrogène par décomposition de composés inorganiques, p.ex. de l'ammoniac
C01B 6/00 - Hydrures de métaux; Monoborane ou diborane; Leurs complexes d'addition
71.
SEMICONDUCTOR NANOPARTICLES, METHOD OF PRODUCING THE SEMICONDUCTOR NANOPARTICLES, AND LIGHT-EMITTING DEVICE
NATIONAL UNIVERSITY CORPORATION TOKAI NATIONAL HIGHER EDUCATION AND RESEARCH SYSTEM (Japon)
OSAKA UNIVERSITY (Japon)
NICHIA CORPORATION (Japon)
Inventeur(s)
Torimoto, Tsukasa
Kameyama, Tatsuya
Kishi, Marino
Miyamae, Chie
Kuwabata, Susumu
Uematsu, Taro
Oyamatsu, Daisuke
Niki, Kenta
Abrégé
Semiconductor nanoparticles including Ag, In, Ga, and S are provided. In the semiconductor nanoparticles, a ratio of a number of Ga atoms to a total number of In and Ga atoms is 0.95 or less. The semiconductor nanoparticles emit light having an emission peak with a wavelength in a range of from 500 nm to less than 590 nm, and a half bandwidth of 70 nm or less, and have an average particle diameter of 10 nm or less.
H01L 33/50 - DISPOSITIFS À SEMI-CONDUCTEURS NON COUVERTS PAR LA CLASSE - Détails caractérisés par les éléments du boîtier des corps semi-conducteurs Éléments de conversion de la longueur d'onde
C09K 11/62 - Substances luminescentes, p.ex. électroluminescentes, chimiluminescentes contenant des substances inorganiques luminescentes contenant du gallium, de l'indium ou du thalium
H01L 33/00 - DISPOSITIFS À SEMI-CONDUCTEURS NON COUVERTS PAR LA CLASSE - Détails
H01L 33/06 - DISPOSITIFS À SEMI-CONDUCTEURS NON COUVERTS PAR LA CLASSE - Détails caractérisés par les corps semi-conducteurs ayant une structure à effet quantique ou un superréseau, p.ex. jonction tunnel au sein de la région électroluminescente, p.ex. structure de confinement quantique ou barrière tunnel
This bioelectric potential measurement device is provided with: an electrode sheet that acquires a biological signal; a device having a contact part that connects to the electrode sheet; and a connection member that sandwiches the electrode sheet between the connection member and the device and thereby connects the electrode sheet to the contact part. The connection member has a fitting part that fits to the device, and the electrode sheet has a shape corresponding to the fitting part.
A61B 5/25 - Détection, mesure ou enregistrement de signaux bioélectriques ou biomagnétiques du corps ou de parties de celui-ci Électrodes bioélectriques à cet effet
73.
METHOD FOR SEPARATING SOLID-PHASE JOINED BODY, METHOD FOR MANUFACTURING RECYCLED METAL MATERIAL INCLUDING SAME, AND STRUCTURE
Provided is a method for separating a solid-phase joined body having: a first joined material that is unsuitable for fusion welding; a second joined material; and a joining portion that joins the first joined material and the second joined material. The method comprises a step for heating at least one of the first joined material and the joining portion so that at least one of the first joined material and the joining portion exhibits embrittlement and/or weld cracking.
B23K 20/12 - Soudage non électrique par percussion ou par une autre forme de pression, avec ou sans chauffage, p.ex. revêtement ou placage la chaleur étant produite par friction; Soudage par friction
B23K 20/20 - Procédés particuliers permettant une séparation ultérieure, p.ex. entre les métaux de haute qualité et les déchets
B23K 26/356 - Travail par rayon laser, p.ex. soudage, découpage ou perçage pour le traitement de surface par traitement par choc
74.
METHOD FOR PRODUCING JOINED MEMBER AND JOINING DEVICE
Provided is a method for producing a joined member, the method making it possible to achieve dissimilar material joining by a process different from conventional ones. This method for producing a joined member comprises: a roughening step in which the surface of a first metal member (1), which is formed of a metal, is roughened so as to have a nanoscale relief shape by plasma processing without using a mask; and a joining step in which a second metal member (2) or a resin member (3) is joined to the roughened surface of the first metal member.
Provided is a culture method for maintaining lymphoid-biased hematopoietic stem cells (Ly-HSCs), the method including a step for culturing hematopoietic stem cells (HSCs) in a medium containing CXCL12 and/or an agonist thereof, SCF and/or an agonist thereof, TPO and/or an agonist thereof, and a vinyl polymer.
C12N 1/00 - Micro-organismes, p.ex. protozoaires; Compositions les contenant; Procédés de culture ou de conservation de micro-organismes, ou de compositions les contenant; Procédés de préparation ou d'isolement d'une composition contenant un micro-organisme; Leurs milieux de culture
76.
WEARABLE DEVICE AND HEART FAILURE DETECTION SYSTEM
[Problem] To provide an inexpensive means that makes it possible to monitor the state of the heart of a subject such as a patient with less invasiveness than before without substantially compromising reliability in acquiring heart sound. [Solution] In a wearable device 2 that is worn on a wrist of a subject for use, a sound collection unit, which has a rubber 623, for acquiring the heart sound of the subject is disposed on an upper surface 201, and a user interface unit 65 that is used by the subject is disposed on a side surface 204 along the longitudinal direction of the arm of the subject when the wearable device 2 is worn on the wrist of the subject.
A61B 5/02 - Mesure du pouls, du rythme cardiaque, de la pression sanguine ou du débit sanguin; Détermination combinée du pouls, du rythme cardiaque, de la pression sanguine; Evaluation d'un état cardio-vasculaire non prévue ailleurs, p.ex. utilisant la combinaison de techniques prévues dans le présent groupe et des techniques d'électrocardiographie; Sondes cardiaques pour mesurer la pression sanguine
A61B 5/00 - Mesure servant à établir un diagnostic ; Identification des individus
A61B 5/01 - Mesure de la température de parties du corps
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 10/00 - Autres méthodes ou instruments pour le diagnostic, p.ex. pour le diagnostic de vaccination; Détermination du sexe; Détermination de la période d'ovulation; Instruments pour gratter la gorge
77.
METHOD FOR PRODUCING CELL HAVING DNA DELETION SPECIFIC TO COL7A GENE ON ONE OF HOMOLOGOUS CHROMOSOMES
It was found that DNA greater than 100 bp can be deleted in one of homologous chromosomes by generating a plurality of nicks in a DNA region in the vicinity of a specific site in the homologous chromosomes. As an example of medical applications, it was found that destruction specific to Col7a gene having a heterozygous mutation causing dystrophic epidermolysis bullosa can be caused.
This dental composition contains a glass powder composite, the glass powder composite including a first glass powder and a second glass powder having solubility different from that of the first glass powder by pH, both the first glass powder and the second glass powder having ion sustained release properties.
The present invention predicts a condition from which a characteristic value of a target material can be obtained. A method according to one embodiment of the present invention comprises: acquiring a characteristic value of a material; inversely analyzing a model for predicting the characteristic value of the material from a feature amount of the material, and thereby predicting the feature amount of the material from the acquired characteristic value of the material; generating phase data analysis results on the basis of the predicted feature amount of the material; and indicating, on an image of a material different from the material, a pixel corresponding to a portion designated in the phase data analysis results.
G01N 3/20 - Recherche des propriétés mécaniques des matériaux solides par application d'une contrainte mécanique en appliquant des efforts permanents de flexion
80.
SILICONE-BASED POLYMER COMPOUND AND SILICONE-BASED POLYMER MATERIAL
Provided are a novel silicone-based polymer compound with excellent mechanical properties and a silicone-based polymer material containing the silicone-based polymer compound. The silicone-based polymer compound of the present invention is a silicone-based polymer compound (H) having a polysiloxane backbone as the main chain, wherein the polysiloxane backbone has at least one host group in a side chain, and the host group is a monovalent group formed by removing one hydrogen atom or one hydroxy group from a cyclodextrin or a cyclodextrin derivative.
NATIONAL UNIVERSITY CORPORATION KANAZAWA UNIVERSITY (Japon)
Inventeur(s)
Kurisu Chimura, Misato
Sakata, Yasushi
Ohtani, Tomohito
Nakajima, Kenichi
Abrégé
The present invention accurately infers the presence or absence of a disease. An information processing device (1A) comprises: an image acquisition unit (11) that acquires an image that has captured therein a target site of a subject to which a radiopharmaceutical has been administered; a variation index calculation unit (51) that calculates, on the basis of the image, a variation index (23) indicating the degree of variation in radiation dose at the target site, the radiation dose being emitted from the radiopharmaceutical accumulated in the target site of the subject; and an inference unit (12) that infers a disease at the target site of the subject on the basis of the calculated variation index (23).
Provided is a three-dimensional mammary gland model comprising a three-dimensional tissue containing cells and fragmented extracellular matrix components, wherein the cells include mature fat cells and mammary gland epithelial cells.
Provided are: a polymer material which is tough but can be easily decomposed; a method for producing the same; and a method for decomposing the polymer material. This polymer material comprises: a polymer composition containing a polymer compound H; and a photoacid generator. The polymer compound H has at least one host group in the molecule. The host group is obtained by removing one hydrogen atom or hydroxyl group from cyclodextrin or a cyclodextrin derivative, and is covalently bonded to the polymer compound H via a hemiaminal bond.
C08L 101/06 - Compositions contenant des composés macromoléculaires non spécifiés caractérisées par la présence de groupes déterminés contenant des atomes d'oxygène
B32B 27/30 - Produits stratifiés composés essentiellement de résine synthétique comprenant une résine acrylique
C08J 11/10 - Récupération ou traitement des résidus des polymères par coupure des chaînes moléculaires des polymères ou rupture des liaisons de réticulation par voie chimique, p.ex. dévulcanisation
C09J 11/06 - Additifs non macromoléculaires organiques
The present disclosure provides inducible regulatory T cells having high functionality and a stable immunosuppressive function. The present disclosure provides inducible regulatory human T cells having at least one characteristic selected from the group consisting of FoxP3+, CTLA4+, NT5E+, ITGAE (CD103)+, AREG+, CD172g+, and CD26+, and a cell population containing the same. The present disclosure also provides a composition containing such cells, a pharmaceutical composition containing such cells, methods of using the composition and pharmaceutical composition, etc.
C12N 5/0783 - Cellules T; Cellules NK; Progéniteurs de cellules T ou NK
A61K 35/17 - Lymphocytes; Lymphocytes B; Lymphocytes T; Cellules tueuses naturelles; Lymphocytes activés par un interféron ou une cytokine
A61P 1/04 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des ulcères, des gastrites ou des œsophagites par reflux, p.ex. antiacides, antisécrétoires, protecteurs de la muqueuse
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 1/18 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des troubles pancréatiques, p.ex. enzymes pancréatiques
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p.ex. antidiabétiques
A61P 19/02 - Médicaments pour le traitement des troubles du squelette des troubles articulaires, p.ex. arthrites, arthroses
A61P 19/08 - Médicaments pour le traitement des troubles du squelette des maladies osseuses, p.ex. rachitisme, maladie de Paget
A61P 21/04 - Médicaments pour le traitement des troubles du système musculaire ou neuromusculaire de la myasthénie
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p.ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
The present invention provides a biomarker for predicting prognosis in a sepsis patient, the biomarker comprising IL-1β and TNF-α. The index for predicting the prognosis in a sepsis patient is the blood concentration ratio of IL-1β with respect to TNF-α.
G01N 33/68 - Analyse chimique de matériau biologique, p.ex. de sang ou d'urine; Test par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligands; Test immunologique faisant intervenir des protéines, peptides ou amino-acides
The present invention provides an organoid characterized by comprising a layered structure of a sheet-like retinal pigment epithelial cell layer and a layer containing visual cells. The present invention also provides a method for producing an organoid, the method comprising: (1) a step for inducing differentiation of retinal progenitor cells from pluripotent stem cells; and (2) a step for carrying out adherent culture of the obtained retinal progenitor cells using a medium containing at least either a serum-free supplement or serum.
A61K 35/36 - Substances provenant de mammifères; Compositions comprenant des tissus ou des cellules non spécifiés; Compositions comprenant des cellules souches non embryonnaires; Cellules génétiquement modifiées Épiderme; Cellules épithéliales; Kératinocytes; Cellules de Langerhans; Cellules ectodermiques
C12Q 1/02 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismes; Compositions à cet effet; Procédés pour préparer ces compositions faisant intervenir des micro-organismes viables
G01N 33/50 - Analyse chimique de matériau biologique, p.ex. de sang ou d'urine; Test par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligands; Test immunologique
87.
METHOD FOR SEPARATING OR CONCENTRATING ND PARTICLES HAVING GROUP-14 COLOR CENTER
The present invention provides a method for separating or concentrating nanodiamond (ND) particles having a group-14 color center that comprises: irradiating a dispersion liquid containing mixed particles of ND particles having a color center (a group-14 color center) of any one group 14 element selected from the group consisting of Si, Ge, Sn, and Pb and ND particles not having the group-14 color center with laser light having an energy equal to or greater than the resonant absorptive energy of the group-14 color center; and selectively moving the ND particles having the group-14 color center by means of light pressure generated by resonant absorption of the laser light.
Provided are: a solid-state joining method with which it is possible to control the discharge direction of burrs and to realize sufficient joining strength; a solid-state joined joint and a solid-state joined structure that are obtained through the solid-state joining method; and a solid-state joining device that can be suitably used in the solid-state joining method. A solid-state joining method characterized by having a first step for bringing end parts of one material being joined and another material being joined into butting contact with one another and forming a joining interface, a second step for increasing the temperature in the vicinity of the joining interface by using an external heating means, and a third step for plastically deforming the joining interface to thereby discharge burrs and form a solid-state joined interface, the plate thickness of the end part of the one material being joined and/or the other material being joined is reduced, and the solid-state joining method having a gradient such that the plate thickness decreases on a side where discharge of the burrs is suppressed.
B23K 20/12 - Soudage non électrique par percussion ou par une autre forme de pression, avec ou sans chauffage, p.ex. revêtement ou placage la chaleur étant produite par friction; Soudage par friction
An object of the present invention is to provide a pericyte-like cell having high angiogenic potential with a higher cell proliferation ability than a primary pericyte available in the past and high VEGF expression, and a method for producing the same. Provided are a method for producing a VEGF-highly expressing pericyte-like cell, the method including selecting a CD56(−) pericyte-like cell from a population including a pericyte-like cell obtained by inducing differentiation of a pluripotent stem cell; and a VEGF-highly expressing pericyte-like cell produced by the production method.
The present invention provides a pharmaceutical composition for treating arthrosis, the pharmaceutical composition comprising a composition containing extracellular vesicles derived from a culture supernatant of mesenchymal stem cells. The pharmaceutical composition is characterized in that a culture medium for the mesenchymal stem cells satisfies the following requirements (1) and (2): (1) the culture medium is a chemically defined medium that does not contain a component derived from an animal of a different species from a subject to be treated; and (2) the number of microparticles each having a particle diameter of 1 to 1000 nm is less than 1×109 particles/mL before use.
Provided is a technique to carry out mass spectrometry of a wide variety of subject compounds to be analyzed, each of which is extracted in a supercritical fluid. A mass spectrometer (1) includes: a supercritical fluid introduction section (3) for introducing and releasing, to vacuum, a supercritical fluid in which a subject compound for mass spectrometry is contained (extracted); an ionization section (4) that ionizes the subject compound which is extracted in the supercritical fluid, the ionization being carried out in the vacuum by a molecular reaction involving proton transfer; and a mass measurement section (5) that measures a mass of the subject compound which has been ionized.
G01N 27/62 - Recherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques en recherchant les décharges électriques, p.ex. l'émission cathodique
H01J 49/04 - Dispositions pour introduire ou extraire les échantillons devant être analysés, p.ex. fermetures étanches au vide; Dispositions pour le réglage externe des composants électronoptiques ou ionoptiques
H01J 49/14 - Sources d'ions; Canons à ions utilisant un bombardement de particules, p.ex. chambres d'ionisation
H01J 49/26 - Spectromètres de masse ou tubes séparateurs de masse
92.
BIOLOGICAL-SIGNAL-PROCESSING SYSTEM, SIGNAL-PROCESSING DEVICE, COMPUTER PROGRAM, AND METHOD FOR GENERATING BIOLOGICAL SIGNAL
NATIONAL UNIVERSITY CORPORATION KOBE UNIVERSITY (Japon)
OSAKA UNIVERSITY (Japon)
Inventeur(s)
Izumi Shintaro
Araki Teppei
Murase Sho
Abrégé
The present invention makes it possible, even when the electrode arrangement is different from a predetermined electrode arrangement, to obtain a necessary multi-channel biological signal. A biological-signal-processing system according to the present disclosure is provided with: m electrodes that are attached to a living body in a first arrangement; and a signal-processing device that executes a process of inputting a p-channel first biological signal acquired from the m electrodes into a generation model and outputting a q-channel second biological signal from the generation model. The q-channel second biological signal is a signal corresponding to a signal obtained from n (n is an integer of 3 or more) electrodes attached to the living body in a second arrangement. The second arrangement is an electrode arrangement different from the first arrangement in terms of at least one of the number of electrodes and the attachment positions. The generation model is configured to output a q-channel second biological signal when a p-channel first biological signal is input.
The present invention addresses the problem of providing a method for identifying an optical isomer of a low-molecular-weight compound, the method making it possible to analyze whether the optical isomer is in a D-form or an L-form for each measured low-molecular-weight compound. This method for identification comprises: a low-molecular-weight compound electrophoresis step which is performed using a device including measurement electrodes for measuring a tunnel current at the time when a low-molecular-weight compound passes therethrough, and in which a voltage is applied so as to straddle the measurement electrodes of the device, thereby allowing the low-molecular-weight compound contained in a sample solution to pass through the measurement electrodes by electrophoresis; a measurement step in which a tunnel current at the time when the low-molecular-weight compound passes through a gap between the measurement electrodes is measured; and an analysis step in which it is determined, from the measured tunnel current, whether an optical isomer is in a D-form or an L-form for every measured low-molecular-weight compound.
Follicular helper T cells specific to SARS-COV-2 virus are provided. The present disclosure is based on the finding of public TfhTCR specific to spike (S) protein common to various patients, and has identified for the first time a public TCR specific to the SARS-COV-2 virus and its MHC and antigenic epitopes to promote efficient immune responses, particularly those of B cells that produce neutralizing antibodies. For example, the present disclosure provides a composition containing an epitope specific to SARS-COV-2 virus for inducing a follicular T cell.
C07K 14/005 - Peptides ayant plus de 20 amino-acides; Gastrines; Somatostatines; Mélanotropines; Leurs dérivés provenant de virus
A61K 38/00 - Préparations médicinales contenant des peptides
A61K 39/00 - Préparations médicinales contenant des antigènes ou des anticorps
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
95.
PHARMACEUTICAL COMPOSITION FOR PREVENTING AND/OR TREATING KIDNEY INJURY, AND AUTOPHAGY ACTIVATOR
An object of this invention is to provide a pharmaceutical composition for preventing and/or treating acute kidney injury, and an autophagy activator. The invention relates to, for example, a pharmaceutical composition for preventing and/or treating acute kidney injury, comprising a compound represented by formula (1), a salt thereof, or a prodrug thereof:
An object of this invention is to provide a pharmaceutical composition for preventing and/or treating acute kidney injury, and an autophagy activator. The invention relates to, for example, a pharmaceutical composition for preventing and/or treating acute kidney injury, comprising a compound represented by formula (1), a salt thereof, or a prodrug thereof:
wherein
A is an optionally substituted benzene ring;
B is an optionally substituted aryl or an optionally substituted heteroaryl;
X is an oxygen atom or a sulfur atom; Y is a nitrogen atom or a carbon atom;
of is a single or double bond when Y is a carbon atom, or
of is a single bond when Y is a nitrogen atom;
each R1 independently represents lower alkyl, or
two R1s may be bound to each other to form a spiro ring or a crosslinked structure, or
two R1s may be bound to each other to form a saturated fused heterocycle together with nitrogen and carbon atoms constituting a ring containing Y;
p is 0, 1, or 2; or
(R1)p is oxo.
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p.ex. rifampine, thiothixène
A61K 31/4439 - Pyridines non condensées; Leurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un cycle à cinq chaînons avec l'azote comme hétéro-atome du cycle, p.ex. oméprazole
A61K 31/454 - Pipéridines non condensées, p.ex. pipérocaïne contenant d'autres systèmes hétérocycliques contenant un cycle à cinq chaînons avec l'azote comme hétéro-atome du cycle, p.ex. pimozide, dompéridone
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 31/4995 - Pyrazines ou pipérazines formant une partie de systèmes cycliques pontés
96.
DRUG FOR PREVENTING AND/OR TREATING DISEASE OR CONDITION RELATED TO REDUCED CEREBRAL BLOOD FLOW
The present invention provides a drug for preventing and/or treating a disease or condition related to reduced cerebral blood flow, the drug being characterized by containing mammalian vascular endothelial cells positive for the cell surface marker CD157 and being used such that the vascular endothelial cells are delivered intracerebrally. The present invention also provides a drug for cerebral revascularization, the drug characterized by containing mammalian vascular endothelial cells positive for cell surface marker CD157 and being used such that the vascular endothelial cells are delivered intracerebrally.
A61P 25/28 - Médicaments pour le traitement des troubles du système nerveux des troubles dégénératifs du système nerveux central, p.ex. agents nootropes, activateurs de la cognition, médicaments pour traiter la maladie d'Alzheimer ou d'autres formes de démence
C12N 5/071 - Cellules ou tissus de vertébrés, p.ex. cellules humaines ou tissus humains
An analysis device includes an analysis unit configured to receive scattered light, transmitted light, fluorescence, or electromagnetic waves from an observed object located in a light irradiation region light-irradiated from a light source and analyze the observed object on the basis of a signal extracted on the basis of a time axis of an electrical signal output from a light-receiving unit configured to convert the received light or electromagnetic waves into the electrical signal.
G06V 10/82 - Dispositions pour la reconnaissance ou la compréhension d’images ou de vidéos utilisant la reconnaissance de formes ou l’apprentissage automatique utilisant les réseaux neuronaux
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
G01N 15/10 - Recherche de particules individuelles
G01N 15/14 - Recherche par des moyens électro-optiques
G01N 15/1404 - Manipulation du flux, p.ex. focalisation hydrodynamique
G01N 21/01 - Dispositions ou appareils pour faciliter la recherche optique
G01N 21/27 - Couleur; Propriétés 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
G06F 18/21 - Conception ou mise en place de systèmes ou de techniques; Extraction de caractéristiques dans l'espace des caractéristiques; Séparation aveugle de sources
G06F 18/28 - Détermination de motifs de référence représentatifs, p.ex. en faisant la moyenne ou en déformant; Génération de dictionnaires
G06V 10/772 - Détermination de motifs de référence représentatifs, p.ex. motifs de valeurs moyennes ou déformants; Génération de dictionnaires
G06V 10/778 - Apprentissage de profils actif, p.ex. apprentissage en ligne des caractéristiques d’images ou de vidéos
The present inventors have discovered that a peptide derived from HMGB1 can be used as a therapeutic and/or preventive agent for fatty liver, nonalcoholic steatohepatitis, and various symptoms accompanied by the fatty liver. On the basis of this discovery, the present application provides a use of the peptide derived from HMGB1 which is different from conventional uses.
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
Provided is a new vaccine against mammal arenavirus infections. This vaccine contains lipid nanoparticles each including mRNA encoding a nucleoprotein (NP) or a glycoprotein precursor (GPC) of arenavirus.
A61K 31/7105 - Acides ribonucléiques naturels, c. à d. contenant uniquement des riboses liés à l'adénine, la guanine, la cytosine ou l'uracile et ayant des liaisons 3'-5' phosphodiester
A61K 31/7115 - Acides nucléiques ou oligonucléotides ayant des bases modifiées, c. à d. autres que l'adénine, la guanine, la cytosine, l'uracile ou la thymine
The present invention provides: a useful production method for a fluoroalkyl aromatic compound; and a compound obtained by the production method. Said production method is for a compound represented by formula (4), and comprises a step C for reacting a compound represented by formula (1) and a compound represented by formula (3), in the presence of a reducing agent, a copper compound, and a ligand. (1): RF-X1(3): Ar-X2(4): Ar-RF(In the formulae, RFrepresents a fluoroalkyl group optionally having at least one substituent, X1represents Cl, Br, or I, X2 represents Cl, Br, or I, and Ar represents an aryl group optionally having at least one substituent or a heteroaryl group optionally having at least one substituent.)
C07C 17/266 - Préparation d'hydrocarbures halogénés par des réactions comportant un accroissement du nombre des atomes de carbone dans le squelette par des réactions de condensation d'hydrocarbures et d'hydrocarbures halogénés
C07C 19/10 - Composés acycliques saturés contenant des atomes d'halogène contenant du fluor et du chlore
C07C 21/18 - Composés acycliques non saturés contenant des atomes d'halogène contenant des liaisons doubles carbone-carbone contenant du fluor