In one aspect, the present disclosure provides a microRNA-33 (miR-33) inhibitor comprising a peptide nucleic acid covalently bound to a pH low insertion peptide. In another aspect, the present disclosure provides a method of treating pulmonary fibrosis in a subject, the method comprising administering to the subject a therapeutically effective amount of the miR-33 inhibitor. In some embodiments, the pulmonary fibrosis is idiopathic pulmonary fibrosis.
C12N 15/11 - Fragments d'ADN ou d'ARNLeurs formes modifiées
A61K 31/713 - Acides nucléiques ou oligonucléotides à structure en double-hélice
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 rénale
C12N 15/113 - Acides nucléiques non codants modulant l'expression des gènes, p. ex. oligonucléotides anti-sens
2.
LOW-DIMENSIONAL METAL-HALIDE PEROVSKITES FOR INFRARED, TETRAHERTZ, AND MILLIMETER-WAVE LIGHT DETECTION
Described herein is a construct including an FGF21 polypeptide, which includes residues 186-198 and residues 200-209 of FGF21. The FGF21 polypeptide includes one or more mutations that confers FGF21 polypeptide stronger affinity with β-Klotho as compared with a corresponding wild-type FGF21 polypeptide. Also described herein is a composition including the construct, as well as methods of modulating the FGF21/FGFR/β-Klotho signaling pathway or the FGF19/FGFR/β-Klotho signaling pathway and methods of treating, ameliorating and/or preventing diseases or disorders associated with mis-regulation (such as up- or down-regulation) of the signaling pathways.
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
C07K 14/50 - Facteur de croissance des fibroblastes [FGF]
C07K 14/71 - RécepteursAntigènes de surface cellulaireDéterminants de surface cellulaire pour des facteurs de croissanceRécepteursAntigènes de surface cellulaireDéterminants de surface cellulaire pour des régulateurs de croissance
C07K 16/40 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre des enzymes
G01N 33/74 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des hormones
4.
Polymeric Composites Having Oriented Nanopores and Methods of Making the Same
The present invention relates to the development and fabrication of thin-film polymer composite materials containing vertically aligned nanopores. The present invention provides methods of aligning nanopores in a polymeric film. The present invention also provides composite materials and methods of fabricating composite materials containing vertically aligned nanopores.
B01D 69/02 - Membranes semi-perméables destinées aux procédés ou aux appareils de séparation, caractérisées par leur forme, leur structure ou leurs propriétésProcédés spécialement adaptés à leur fabrication caractérisées par leurs propriétés
B01D 71/40 - Polymères d'acides non saturés ou de leurs dérivés, p. ex. sels, amides, imides, nitriles, anhydrides, esters
B01D 71/70 - Polymères contenant, dans la chaîne principale, uniquement du silicium, avec ou sans soufre, azote, oxygène ou carbone
B05D 1/00 - Procédés pour appliquer des liquides ou d'autres matériaux fluides aux surfaces
B05D 3/00 - Traitement préalable des surfaces sur lesquelles des liquides ou d'autres matériaux fluides doivent être appliquésTraitement ultérieur des revêtements appliqués, p. ex. traitement intermédiaire d'un revêtement déjà appliqué, pour préparer les applications ultérieures de liquides ou d'autres matériaux fluides
B05D 3/04 - Traitement préalable des surfaces sur lesquelles des liquides ou d'autres matériaux fluides doivent être appliquésTraitement ultérieur des revêtements appliqués, p. ex. traitement intermédiaire d'un revêtement déjà appliqué, pour préparer les applications ultérieures de liquides ou d'autres matériaux fluides par exposition à des gaz
B05D 3/06 - Traitement préalable des surfaces sur lesquelles des liquides ou d'autres matériaux fluides doivent être appliquésTraitement ultérieur des revêtements appliqués, p. ex. traitement intermédiaire d'un revêtement déjà appliqué, pour préparer les applications ultérieures de liquides ou d'autres matériaux fluides par exposition à des rayonnements
B32B 17/10 - Produits stratifiés composés essentiellement d'une feuille de verre ou de fibres de verre, de scorie ou d'une substance similaire comprenant du verre comme seul composant ou comme composant principal d'une couche adjacente à une autre couche d'une substance spécifique de résine synthétique
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
B32B 27/28 - Produits stratifiés composés essentiellement de résine synthétique comprenant des copolymères de résines synthétiques non complètement couverts par les sous-groupes suivants
5.
HERBAL COMPOSITION PHY906 AND ITS USE IN CHEMOTHERAPY
This invention provides herbal compositions useful for increasing the therapeutic index of chemotherapeutic compounds. This invention also provides methods useful for improving the quality of life of an individual undergoing chemotherapy. Furthermore, this invention improves the treatment of disease by increasing the therapeutic index of chemotherapy drugs by administering the herbal composition PHY906 to a mammal undergoing such chemotherapy.
A61K 31/4412 - Pyridines non condenséesLeurs dérivés hydrogénés ayant des groupes oxo liés directement à l'hétérocycle
A61K 31/7068 - Composés ayant des radicaux saccharide et des hétérocycles ayant l'azote comme hétéro-atome d'un cycle, p. ex. nucléosides, nucléotides contenant des cycles à six chaînons avec l'azote comme hétéro-atome d'un cycle contenant des pyrimidines condensées ou non-condensées ayant des groupes oxo liés directement au cycle pyrimidine, p. ex. cytidine, acide cytidylique
Described is an active layer having a first surface region and a bulk region, the active layer comprising a small molecule component and a polymer component, wherein the relative concentration of the small molecule component is lower in the first surface than in the bulk region. Also described is a method of producing a surface-modified active layer comprising the steps of providing a pristine active layer comprising a small molecule component and a polymer component; applying an adhesive to the exposed surface of the pristine active layer to produce an adhesive-bound active layer; and removing the adhesive from the adhesive-bound active layer, and a method of producing electrical energy from sunlight, such as sunlight deposited over bodies of water.
H10K 30/30 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire comprenant des hétérojonctions de masse, p. ex. des réseaux interpénétrés de domaines de matériaux donneurs et accepteurs
H01L 31/18 - Procédés ou appareils spécialement adaptés à la fabrication ou au traitement de ces dispositifs ou de leurs parties constitutives
H10K 30/20 - Dispositifs organiques sensibles au rayonnement infrarouge, à la lumière, au rayonnement électromagnétique de plus courte longueur d'onde ou au rayonnement corpusculaire comprenant des jonctions organiques-organiques, p. ex. des jonctions donneur-accepteur
A61K 31/7064 - Composés ayant des radicaux saccharide et des hétérocycles ayant l'azote comme hétéro-atome d'un cycle, p. ex. nucléosides, nucléotides contenant des cycles à six chaînons avec l'azote comme hétéro-atome d'un cycle contenant des pyrimidines condensées ou non-condensées
8.
METHODS FOR SELECTIVELY REDUCING IMMUNOGENICITY IN A TRANSPLANT
The present invention relates to methods for reducing or eliminating reactive T cells from a transplant or a part thereof prior to transplantation. The present invention also relates to methods for reducing immunogenicity in a transplant or a part thereof prior to transplantation. The present invention further relates to transplants obtained by the described methods and apoptotic agent treated transplants for use in reducing or preventing inflammatory conditions such as graft-versus-host disease. Specifically, the methods can be used to reduce graft versus host disease following transplantation.
A61K 35/12 - Substances provenant de mammifèresCompositions comprenant des tissus ou des cellules non spécifiésCompositions comprenant des cellules souches non embryonnairesCellules génétiquement modifiées
A61P 37/06 - Immunosuppresseurs, p. ex. médicaments pour le traitement du rejet de greffe
C12N 13/00 - Traitement de micro-organismes ou d'enzymes par énergie électrique ou ondulatoire, p. ex. par magnétisme, par des ondes sonores
9.
HOLOGRAPHIC QUANTUM COMPUTING WITH COMPACT QUANTUM COMPUTERS
Systems and methods for implementing holographic quantum circuits on compact quantum computing systems are provided. Compact quantum computing systems include systems having fewer physical qubits than the number of quantum modes to be instantiated during execution of the quantum circuit. Techniques described herein may be used to perform boson sampling techniques, including with application to molecular docking simulations.
Disclosed herein is a method of treating cancer in a subject in need thereof. The method comprises determining a first level of a first cancer-specific antigen in a cancer sample of the subject; determining a second level of a second cancer-specific antigen in the cancer sample; and administering to the subject a first antibody-drug conjugate (ADC) targeting the first cancer-specific antigen or a second ADC targeting the second cancer-specific antigen based on the levels of the two cancer-specific antigens. Also disclosed herein is a method of constructing a cancer antigen level standard, which can be used in the selection of ADCs.
A61K 47/68 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p. ex. les supports ou les additifs inertesAgents 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 anticorps, une immunoglobuline ou son fragment, p. ex. un fragment Fc
G01N 33/574 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour le cancer
G01N 33/577 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet faisant intervenir des anticorps monoclonaux
A61K 39/395 - AnticorpsImmunoglobulinesImmunsérum, p. ex. sérum antilymphocitaire
11.
Genetically Modified Non-Human Animals And Methods Of Use Thereof
Institute for Research in Biomedicine (IRB) (Suisse)
Inventeur(s)
Murphy, Andrew J.
Stevens, Sean
Rathinam, Chozhavendan
Eynon, Elizabeth
Manz, Markus
Flavell, Richard
Yancopoulos, George D.
Abrégé
Genetically modified mice comprising a nucleic acid sequence encoding a human M-CSF protein are provided. Also provided are genetically modified mice comprising a nucleic acid sequence encoding a human M-CSF protein that have been engrafted with human cells such as human hematopoietic cells, and methods for making such engrafted mice. These mice find use in a number of applications, such as in modeling human immune disease and pathogen infection; in in vivo screens for agents that modulate hematopoietic cell development and/or activity, e.g. in a healthy or a diseased state; in in vivo screens for agents that are toxic to hematopoietic cells; in in vivo screens for agents that prevent against, mitigate, or reverse the toxic effects of toxic agents on hematopoietic cells; in in vivo screens of human hematopoietic cells from an individual to predict the responsiveness of an individual to a disease therapy, etc.
C12N 15/85 - Vecteurs ou systèmes d'expression spécialement adaptés aux hôtes eucaryotes pour cellules animales
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
13.
METHODS AND COMPOSITIONS FOR IDENTIFICATION OF DIAGNOSTICALLY AND THERAPEUTICALLY RELEVANT PROTEINS
The present disclosure generally relates to compositions, methods, and kits for the identification of diagnostically and therapeutically relevant proteins. In some instances, the identification of the diagnostically and therapeutically relevant proteins can be used to aid in treatment of a subject in need thereof.
A61K 31/205 - Sels d'addition d'acides organiques avec des aminesSels d'ammonium quaternaire internes, p. ex. bétaïne, carnitine
C12Q 1/6804 - Analyse d’acides nucléiques utilisant des immunogènes
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C12N 15/11 - Fragments d'ADN ou d'ARNLeurs formes modifiées
The present disclosure relates to the introduction of expression constructs encoding different gene products such as proteins or nucleic acids at defined ratios into host cell lines containing multiple dock sites for insertion of the nucleic acid construct, and to the production of proteins that require expression of at least two gene products.
C07K 16/00 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux
C12N 5/00 - Cellules non différenciées humaines, animales ou végétales, p. ex. lignées cellulairesTissusLeur culture ou conservationMilieux de culture à cet effet
C12N 5/10 - Cellules modifiées par l'introduction de matériel génétique étranger, p. ex. cellules transformées par des virus
15.
COMPOSITIONS AND METHODS FOR TARGETED UBIQUITINATION OF THE VOLTAGE-GATED SODIUM CHANNEL NAV1.8
Compositions and methods for targeted ubiquitination of the voltage-gated sodium channel Nav1.8. The compositions include a bifunctional molecule that includes two bioactive domains, a first bioactive domain for selective binding to Nav1.8 channels and a second bioactive domain for which can be has the activity of (i) catalyzing a ubiquitination reaction to tag the channel for internalization and degradation, (ii) recruitment and binding of a ubiquitin ligase which then catalyzes a ubiquitination reaction to tag the channel for internalization and degradation or (iii) l recruitment of the fusion protein to lysosomes. The bifunctional molecule includes a HECT domain from NEDD4 ubiquitin ligase and includes a myosin tail domain (MTD) from clathrin linker-1 (SCLT-1), functional fragments or variants thereof, provide the two bioactive domains. The compositions are administered to a subject in need thereof, in an effective amount to treat acute chronic pain.
C07K 14/435 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
16.
METHODS OF DETECTING VIRAL OR BACTERIAL INFECTIONS
In one aspect, the invention provides a method for detecting a viral-only or a bacterial-associated respiratory infection in a patient, the method comprising analyzing a respiratory sample to determine levels of at least two respiratory virus infection-associated molecules, at least two bacterial respiratory infection-associated molecules, and comparing the levels of the respiratory virus infection-associated molecules and/or the levels of the bacterial respiratory infection-associated molecules with a predetermined reference level.
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
17.
METHODS OF TREATING, AMELIORATING, AND/OR PREVENTING STRESS-RELATED DISORDER
In one aspect, described herein is a method of treating, ameliorating, and/or preventing a stress-related disorder in a subject in need thereof. In certain embodiments, the method includes administering to the subject a therapeutically effective amount of a α1A-adrenergic receptor subtype selective inhibitor.
A61K 31/145 - Amines, p. ex. amantadine ayant des atomes de soufre, p. ex. thiurames (N-C(S)-S-C(S)-N ou N-C(S)-S-S-C(S)-N)Sulfinylamines (-N=SO)Sulfonylamines (-N=SO2)
18.
PASSIVELY ADAPTIVE LEGGED ROBOT WITH DIFFERENTIALS AND NON-BACKDRIVABLE PRISMATIC LEGS
A legged robot system has a medial body with first and second ends, slidably and rotatably attached to a lateral body with first and second ends via a locomotion mechanism configured to provide at least first and second degrees of freedom of movement for the lateral body relative to the medial body, a plurality of prismatic legs extending downward from positions on the lateral or medial bodies, each leg having a drive mechanism for extending the leg, wherein the first leg provides a third degree of freedom relative to its position on the lateral or medial body, and the second leg provides a fourth degree of freedom relative to its position on the lateral or medial body, and a differential mechanism connecting the first and second legs providing a fifth degree of freedom of movement for the first and second leg relative to each other.
B62D 57/032 - Véhicules caractérisés par des moyens de propulsion ou de prise avec le sol autres que les roues ou les chenilles, seuls ou en complément aux roues ou aux chenilles avec moyens de propulsion en prise avec le sol, p. ex. par jambes mécaniques avec une base de support et des jambes soulevées alternativement ou dans un ordre déterminéVéhicules caractérisés par des moyens de propulsion ou de prise avec le sol autres que les roues ou les chenilles, seuls ou en complément aux roues ou aux chenilles avec moyens de propulsion en prise avec le sol, p. ex. par jambes mécaniques avec des pieds ou des patins soulevés alternativement ou dans un ordre déterminé
B25J 9/10 - Manipulateurs à commande programmée caractérisés par des moyens pour régler la position des éléments manipulateurs
19.
MODIFIED BOTTLEBRUSH BLOCK COPOLYMERS WITH SELECTIVE TISSUE UPTAKE
A method to precisely tailor the surface topography of polymeric nanoparticles having bound thereto polyalkylene oxide and to improve their systemic circulation and diseased tissue accumulation, based on tuning the architecture of shape-persistent amphiphilic bottlebrush block copolymer (BBCP) building blocks and inclusion of small molecule chemical modifications, has been developed. It was demonstrated that nanoparticle formation and surface topography can be controlled by systematically changing structural parameters of BBCP architecture. The surface topography of PEGylated nanoparticles (nanoparticles having PEO or PEG covalently bound thereto) and the presence of hydrophobic small molecule modifications, cationic small molecule modifications, and/or small molecule modifications containing a positively ionizable atom significantly affects their biological performance.
A fabric capacitive strain sensor integrated into everyday clothing to measure human motions. The sensor is made of thin layers of breathable fabrics and exhibits high strains, excellent cyclic stability, and high water vapor transmission rates, which allows for sweat evaporation. The sensor's functionality is evaluated under conditions similar to those experienced on the surface of the human body (35° C. and 90±2% relative humidity) and after washing with fabric detergent. The fabric sensor shows stable capacitance at excitation frequencies up to 1 MHz.
H05K 1/03 - Emploi de matériaux pour réaliser le substrat
D03D 1/00 - Tissus conçus pour faire des articles particuliers
G06F 3/01 - Dispositions d'entrée ou dispositions d'entrée et de sortie combinées pour l'interaction entre l'utilisateur et le calculateur
H05K 3/02 - Appareils ou procédés pour la fabrication de circuits imprimés dans lesquels le matériau conducteur est appliqué à la surface du support isolant et est ensuite enlevé de zones déterminées de la surface, non destinées à servir de conducteurs de courant ou d'éléments de blindage
The present invention provides compositions and methods comprising an activator of interleukin-18 (IL-18) activity for use in therapeutic and non-therapeutic applications. The activator provides IL-18 signaling activity even in the presence of an inhibitory molecule 5 such as IL-18 binding protein (IL-18BP).
A61K 35/17 - LymphocytesLymphocytes BLymphocytes TCellules tueuses naturellesLymphocytes activés par un interféron ou une cytokine
A61K 35/768 - Virus oncolytiques non prévus dans les groupes
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61K 47/64 - Conjugués médicament-peptide, médicament-protéine ou médicament-acide polyaminé, c.-à-d. l’agent de modification étant un peptide, une protéine ou un acide polyaminé lié par covalence ou complexé à un agent thérapeutiquement actif
Systems and methods for performing fault tolerant quantum operations for the 4-legged cat code are provided. The quantum systems include an ancilla qubit dispersively coupled to a first logical qubit. and the quantum system may be operated at least in part by: generating and applying a first drive waveform to the ancilla qubit. the first drive waveform comprising a first comb of 7t-pulses having selective frequencies corresponding to a first selection of even and odd cavity resonance frequencies of the first logical qubit: and reading out a state of the ancilla qubit.
G06N 10/40 - Réalisations ou architectures physiques de processeurs ou de composants quantiques pour la manipulation de qubits, p. ex. couplage ou commande de qubit
G06N 10/70 - Correction, détection ou prévention d’erreur quantique, p. ex. codes de surface ou distillation d’état magique
23.
TITANIUM:SAPPHIRE (TI:SA) WAFERS, INTEGRATED TI:SA LASERS, AND METHODS OF FORMING THE SAME
Provided herein are a method of preparing a Titanium:Sapphire (Ti:Sa) wafer and a photonic circuit integrated (PIC) Titanium:Sapphire (Ti:Sa) laser. The method includes depositing a titanium layer on a top surface of a first sapphire substrate; positioning a second sapphire substrate on the titanium layer, forming a face-to-face configuration with the titanium layer between the first and second sapphire substrates; annealing the first and second sapphire substrates in the face-to-face configuration, forming an annealed substrate; and polishing the annealed substrate, forming a polished substrate. The PIC-Ti:Sa laser includes a substrate; a waveguide formed on the substrate, the waveguide including a microring portion; a Ti:Sa layer formed over the microring portion of the waveguide, the Ti:Sa layer and the microring portion of the waveguide forming a microring cavity; and a laser source coupled to the waveguide. Also provided herein are methods of forming a photonic circuit integrated mode-locked Ti:Sa laser.
G02B 6/42 - Couplage de guides de lumière avec des éléments opto-électroniques
H01S 3/08 - Structure ou forme des résonateurs optiques ou de leurs composants
H01S 3/0941 - Procédés ou appareils pour l'excitation, p. ex. pompage utilisant le pompage optique par de la lumière cohérente produite par un laser à semi-conducteur, p. ex. par une diode laser
24.
ANTIBODIES HAVING PAN-ANTIVIRAL ACTIVITY AND METHODS THEREOF
Described herein are antibodies having pan-antiviral activity. In certain embodiments, the antibodies recognize glycosylation patterns specific to viral proteins, but not found on host proteins. Also described herein are methods of preventing, treating, and/or ameliorating viral infections using the antibodies of the disclosure.
The invention relates to methods of evaluating the quality of a batch of an herbal composition, the method comprising subjecting a test batch of the herbal composition to one or more biological analysis methods and comparing the results derived from the test batch to the results of a known batch of herbal composition which has a known in vivo effect.
Described herein is an mRNA molecule including a 5'-cap analog, a 5'-untranslated region (5'-UTR), and a coding sequence. The translational enhancer sequence, when combined with the 5'-cap analog, increases a translational efficiency of the mRNA. Also described herein is a method of modulating a translational efficiency of an mRNA molecule based on the construction of the mRNA molecule herein, as well as a method of expressing a polypeptide or a protein using the mRNA molecule herein.
An ultra-high vacuum instrument, comprising a vacuum chamber, a sample storage stage, a non-evaporable getter and/or ion pump connected to the vacuum chamber to reduce the ambient pressure in the vacuum chamber, and at least one vacuum port including connection hardware adapted to connect to a sputtering gun for cleaning a sample surface or an evaporator for supplying material to grow a film on a sample. The sample storage stage, in some embodiments, includes a first sample parking position, a heating element adapted to apply heat to a sample loaded in the first sample parking position, one or more second sample parking positions, and a thermal insulating plate positioned to insulate the second sample parking positions from heat generated by the heating element.
H01J 37/20 - Moyens de support ou de mise en position de l'objet ou du matériauMoyens de réglage de diaphragmes ou de lentilles associées au support
H01J 41/12 - Tubes à décharge pour l'évacuation par diffusion d'ions, p. ex. pompes ioniques, pompes ioniques à getter
H01J 7/18 - Moyens d'absorption ou d'adsorption du gaz, p. ex. par getter
H01J 19/70 - Moyens pour produire ou conserver le vide, p. ex. au moyen d'un getter
H01J 41/16 - Tubes à décharge pour l'évacuation par diffusion d'ions, p. ex. pompes ioniques, pompes ioniques à getter avec ionisation au moyen de cathodes thermo-ioniques en utilisant des getters
Topical formulations have been developed which have been demonstrated to reduce ultraviolet ("UV")-induced cyclobutane pyrimidine dimer ("CPD") formation in a human clinical trial. The formulation includes all natural, non-toxic compounds which can be utilized in sunscreens, cosmetics and hair conditioners to protect from ultraviolet radiation. A preferred embodiment of the formulation contains 10% Ferulic Acid, 10% Diosmin, 5% Cytisine and 5% Resveratrol. A method of screening for compounds that are safe and effective to reduce UV-induced CPD formation also has been developed.
A61K 8/49 - Cosmétiques ou préparations similaires pour la toilette caractérisés par la composition contenant des composés organiques contenant des composés hétérocycliques
A61Q 17/04 - Préparations topiques pour faire écran au soleil ou aux radiationsPréparations topiques pour bronzer
G01N 21/25 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes
G01N 21/33 - CouleurPropriétés spectrales, c.-à-d. comparaison de l'effet du matériau sur la lumière pour plusieurs longueurs d'ondes ou plusieurs bandes de longueurs d'ondes différentes en recherchant l'effet relatif du matériau pour les longueurs d'ondes caractéristiques d'éléments ou de molécules spécifiques, p. ex. spectrométrie d'absorption atomique en utilisant la lumière ultraviolette
29.
METHODS AND COMPOSITIONS FOR PROLONGED RENALASE AGONIST ACTIVITY
Administration of recombinant or biologically-isolated renalase has been shown to treat certain diseases and conditions. Stable synthetic peptides exhibiting renalase agonist activity are highly desirable. Disclosed are compositions comprising modified renalase agonist peptides that display increased in vitro and/or in vivo half-life, and methods for their use in treating diseases such as ischemic and toxic organ injury.
An electrolytic device, photoelectrode, and method for inducing an electrochemical reduction of a feed gas, comprising an anode and a hybrid cathode, the hybrid cathode comprising a cathode, a microporous layer disposed on one side of the cathode; a cathode catalyst positioned on the surface of the microporous layer, a gas channel fluidly connected to the microporous layer, containing a quantity of a feed gas, an electrolyte channel fluidly connected to the cathode catalyst containing a quantity of electrolyte, wherein the hybrid cathode is configured to induce an electrochemical reaction in the feed gas to produce methanol, and wherein the cathode catalyst comprises a compound represented by General Formula (I).
C25B 11/04 - ÉlectrodesLeur fabrication non prévue ailleurs caractérisées par le matériau
C25B 11/051 - Électrodes comportant des électro-catalyseurs sur un substrat ou un support
C25B 11/091 - Électrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé d’au moins un élément catalytique et d’au moins un composé catalytiqueÉlectrodes comportant des électro-catalyseurs sur un substrat ou un support caractérisées par le matériau électro-catalytique formé de plusieurs éléments catalytiques ou composés catalytiques
C25B 11/02 - ÉlectrodesLeur fabrication non prévue ailleurs caractérisées par la configuration ou la forme
31.
COMPOSITIONS AND METHODS FOR TREATING AUTOIMMUNE SKIN DISEASES
Methods of treating autoimmune skin diseases and disorders are provided. The methods typically include administrating to a subject with an autoimmune skin disease or disorder an effective amount of a hypoxia-inducible factor-1 (HIF-1) inhibitor. In preferred embodiments, the autoimmune disease is mediated at least in-part by T cells, particularly skin-infiltrating T cells. In some embodiments, the subject has cutaneous lupus (e.g., discoid cutaneous lupus, subacute cutaneous lupus, acute cutaneous lupus), pemphigus, pemphigoid, epidermolysis bullosa acquisita, vitiligo, lichen planus, lichen sclerosus, dermatomyositis, alopecia areata, or Sjögren's syndrome. HIF-1 inhibitors and pharmaceutical compositions including the same for use in the disclosed methods are also provided. The HIF-1 inhibitor can be, for example, a small molecule, functional nucleic acid, or inhibitory polypeptide or protein. The pharmaceutical composition can be formulated to suitable for the type and mode of administration, e.g., systemically or locally to skin effected by the autoimmune disease.
A computer-implemented method of increasing appointment attendance comprises providing a processor and a non-transitory memory including computer program code for one or more programs, the memory and the computer program code configured to, with the at least one processor, perform steps comprising obtaining an appointment data structure, comprising an attendee and a corresponding appointment for the attendee, obtaining a set of population data, obtaining a set of appointment data, obtaining a set of external data, obtaining environmental data, inferring, using the population data, the appointment data, the external data, and the environmental data in a machine learning algorithm, a probability that the attendee will attend the appointment, and when the probability of attendance is below a threshold, performing a mitigation step to increase the probability that the attendee will attend the appointment. A system for increasing appointment attendance and a non-transitory computer-readable medium containing computing instructions are also described.
G16H 40/20 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion ou l’administration de ressources ou d’établissements de soins de santé, p. ex. pour la gestion du personnel hospitalier ou de salles d’opération
33.
MACHINE LEARNING SYSTEM AND METHODS FOR INCREASING APPOINTMENT COMPLIANCE
A computer-implemented method of increasing likelihood of appointment completion comprises providing at least one processor; and at least one non-transitory memory including computer program code, configured to perform steps comprising obtaining an appointment data structure comprising an attendee and a corresponding appointment for the attendee, obtaining data comprising at least one of a set of population data, a set of appointment data, a set of external data, or environmental data, wherein the data comprises at least two different formats, standardizing the at least two different formats of data, inferring, using the standardized data in a machine learning algorithm by the at least one processor and the at least one non-transitory memory, a probability that the attendee will complete the appointment, and when the probability of completion is below a threshold, performing a mitigation step to increase the probability that the attendee will complete the appointment.
G16H 40/20 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour la gestion ou l’administration de ressources ou d’établissements de soins de santé, p. ex. pour la gestion du personnel hospitalier ou de salles d’opération
G16H 20/00 - 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
G16H 80/00 - TIC spécialement adaptées pour faciliter la communication entre les professionnels de la santé ou les patients, p. ex. pour le diagnostic collaboratif, la thérapie collaborative ou la surveillance collaborative de l’état de santé
34.
IMPROVED SELECTIVE JAK2 INHIBITORS AND METHODS OF USE
The compounds of Formula I described herein regulate activity of JAK2 by specifically binding to the JAK2 pseudokinase domain, JH2, and are useful as therapeutic agents in the treatment or amelioration of myeloproliferative disorders. Also provided herein are methods of treating myeloproliferative disorders, and methods of making compounds of Formula I.
C07D 401/12 - Composés hétérocycliques contenant plusieurs hétérocycles comportant des atomes d'azote comme uniques hétéro-atomes du cycle, au moins un cycle étant un cycle à six chaînons avec un unique atome d'azote contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
A61K 31/422 - Oxazoles non condensés et contenant d'autres hétérocycles
A61K 31/4439 - Pyridines non condenséesLeurs 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 31/519 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime condensées en ortho ou en péri avec des hétérocycles
A61K 31/5377 - 1,4-Oxazines, p. ex. morpholine non condensées et contenant d'autres hétérocycles, p. ex. timolol
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
C07D 413/12 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes d'azote et d'oxygène comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne contenant des hétéro-atomes comme chaînons
The invention provides microglial cell comprising cortical organoid cultures, methods of generating the same and methods of use thereof for identifying therapeutic agents.
G01N 33/50 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique
36.
TECHNIQUE FOR PREPARING A FAULT-TOLERANT CLUSTER STATE
Quantum systems and techniques are described to generate fault tolerant cluster states for use in quantum computation, quantum networking, and other applications. The systems and techniques include initializing states in first qubits and generating initial resource states by performing first Pauli product measurements on sets of X-type and/or Z-type qubits of the first qubits, the initial resource states comprising qubit cluster states comprising at least three qubits. The final cluster state may then be generated by fusing two or more initial resource states, the fusing comprising performing second Pauli product measurements between qubits of two or more of the initial resource states.
G06N 10/40 - Réalisations ou architectures physiques de processeurs ou de composants quantiques pour la manipulation de qubits, p. ex. couplage ou commande de qubit
37.
DERMATOLOGIC TOPICAL APPLICATIONS OF ROR GAMMA AND ROR GAMMA-T INHIBITORS FOR THE PREVENTION OF SKIN CANCER DEVELOPMENT
Described herein are methods and compositions useful to reduce (partially/inhibit or completely—prevent) skin cancer development in an individual in need thereof.
Described herein is a probe for monitoring specific RNA splicing events, with utility for identifying molecular modulators of RNA splicing. The probe includes a nucleic acid, a first fluorescent element attached to a first end of the nucleic acid, and a second fluorescent element attached to a second end of the nucleic acid. The fluorescence signal of the probe changes when the probe hybridizes with either a pre-splicing RNA molecule or a splicing product. Also described herein is a method of monitoring RNA splicing and a method of screening of modulators of RNA splicing using the probe.
C12Q 1/6818 - Tests d’hybridation caractérisés par les moyens de détection impliquant l’interaction de plusieurs marqueurs, p. ex. transfert d’énergie de résonance
C12Q 1/6895 - Produits d’acides nucléiques utilisés dans l’analyse d’acides nucléiques, p. ex. amorces ou sondes pour la détection ou l’identification d’organismes pour les plantes, les champignons ou les algues
THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (USA)
YALE UNIVERSITY (USA)
Inventeur(s)
Jin, Jian
Xiong, Yan
Park, Kwang-Su
Velez, Julia
Liu, Jing
Chen, Xian
Song, Juan
Xie, Ling
Sheehy, Ryan N.
Jiang, Yonghui
Wang, Sung-Eun
Abrégé
Described is small molecule N-(l-isopropylpiperidin-4-yl)-6-methoxy-2-morpholino-7- (3-(pyrrolidin-l-yl)propoxy)quinolin-4-amine)) (MS 1262) that inhibits methyltransferases G9a/GLP. This inhibitor can be used for the treatment of patients with G9a/GLP related diseases such as Alzheimer's Disease and Prader-Willi Syndrome.
A61K 31/5377 - 1,4-Oxazines, p. ex. morpholine non condensées et contenant d'autres hétérocycles, p. ex. timolol
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
40.
METHODS FOR IDENTIFYING CARDIOVASCULAR DISEASE FROM RETINAL SCANS
It has been established that the presence of RIPLs is associated with higher prevalence of stroke, and especially in patients with atrial fibrillation. Enhanced methods for the detection and quantitation of retinal ischemic perivascular lesions (RIPLs) from commonly used OCT scans which are widely used in optometry and ophthalmology clinics are described. Systems and methods to characterize disease state and risk of stroke based on the identification and quantitation of RIPLs in the eyes of patients having atrial fibrillation have been developed. Methods of using information obtained according to the described methods to guide patient stratification for anticoagulation therapy are provided. Methods of identifying RIPLs from OCT scans are provided.
A61B 3/00 - Appareils pour l'examen optique des yeuxAppareils pour l'examen clinique des yeux
A61B 3/10 - Appareils pour l'examen optique des yeuxAppareils pour l'examen clinique des yeux du type à mesure objective, c.-à-d. instruments pour l'examen des yeux indépendamment des perceptions ou des réactions du patient
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 3/12 - Appareils pour l'examen optique des yeuxAppareils pour l'examen clinique des yeux du type à mesure objective, c.-à-d. instruments pour l'examen des yeux indépendamment des perceptions ou des réactions du patient pour examiner le fond de l'œil, p. ex. ophtalmoscopes
41.
COLIBACTIN DERIVATIVES AND METHODS OF TREATING, AMELIORATING, AND/OR PREVENTING CANCER
Described herein is a stable colibactin derivative, or a salt, solvate, isotopically labelled derivative, stereoisomer, tautomer, or geometric isomer thereof, or any mixtures thereof. Also described herein is a method of alkylating a DNA molecule, a method of forming a DNA interstrand cross-link (ICL), as well as a method of preventing, treating, and/or ameliorating cancer.
C07D 417/14 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre et d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant au moins trois hétérocycles
A61K 31/403 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à cinq chaînons avec un azote comme seul hétéro-atome d'un cycle, p. ex. sulpiride, succinimide, tolmétine, buflomédil condensés avec des carbocycles, p. ex. carbazole
A61K 31/427 - Thiazoles non condensés et contenant d'autres hétérocycles
C07D 403/14 - Composés hétérocycliques contenant plusieurs hétérocycles, comportant des atomes d'azote comme uniques hétéro-atomes du cycle, non prévus par le groupe contenant au moins trois hétérocycles
42.
METHODS USING WNT AND SHH AGONISTS TO STIMULATE HAIR FOLLICLE GROWTH
Dkk1Dkk1+ progenitors transiently amplify to become quiescent dermal condensate cells by the spatiotemporal patterning of Wnt/β-catenin and sonic hedgehog ("SHH") signaling gradients. Together, they deterministically coordinate a rapid transition from proliferation to quiescence, cell fate specification, and morphogenesis. This is useful for screening to discover compounds that can be administered to hair follicles to stimulate hair growth (new hair follicles) and restore hair follicle size. These agonists of Wnt and SHH are formulated for application to skin to grow hair.
A61K 31/4436 - Pyridines non condenséesLeurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un hétérocycle avec le soufre comme hétéro-atome du cycle
A61P 17/14 - Médicaments pour le traitement des troubles dermatologiques pour le traitement de la calvitie ou de l'alopécie
A61K 8/00 - Cosmétiques ou préparations similaires pour la toilette
A61K 31/506 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime non condensées et contenant d'autres hétérocycles
A61Q 7/00 - Préparations pour modifier la pousse des cheveux ou des poils
G01N 33/58 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des substances marquées
43.
DEVICE AND METHOD FOR POST EXTUBATION DYSPHAGIA, ANTIBACTERIAL THERAPY, AND DETECTION AND DRAINAGE OF PHARYNGEAL SECRETIONS
A drainage device includes an elongate flexible conduit comprising a proximal end opening, a distal end opening and a lumen disposed therebetween. A multi-layer distal portion coaxially surrounding the lumen and having a porous outer surface layer, a porous interior layer and an intermediate absorbent layer therebetween. A drainage system and a device and method for treating dysphagia are also disclosed.
44.
METHODS FOR SENSITIZING DRUG-RESISTANT CANCER CELLS
The present invention is directed to methods of sensitizing tyrosine kinase inhibitor (TKI)-resistant cancer cells in a subject using a SWI/SNF complex modulator.
Described herein is a method of reversing or preventing a formation or enlargement of an axonal spheroid. The method includes introducing into a neuron affected by formation or enlargement of the axonal spheroid a compound that downregulates PLD3 expression level or activity. Also described herein is a method of treating or preventing a neurodegenerative condition in a subject in need thereof. The method includes administering to the subject a compound that downregulates PLD3 expression level or activity in a neuron cell affected by the neurodegenerative condition. Further described herein is a pharmaceutical composition for treating a neurodegenerative condition in a subject. The pharmaceutical composition includes a compound that downregulates PDL3 expression level or activity in a neuron cell affected by the neurodegenerative condition; and a pharmaceutically acceptable carrier.
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
A61P 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 current disclosure includes a modular vaccine platform. Also included are monkeypox vaccines that protect against pathogenic monkeypox species, as well as their variants. The vaccines typically include a modified mRNA encoding at least one immunogen, such as a viral envelope protein, cell surface binding protein, or a biologically effective/significant fragment thereof. The mRNA can be encapsulated into lipid nanoparticles or other carriers and formulated as pharmaceutical compositions that can be used to generate an immune response to pathogens, including monkeypox virus, in a subject.
Methods of isolating and sequencing aberrant expansion-specific RNA sequences using antisense oligonucleotides (ASO) specific for repeat-containing RNAs have been established. The methods isolate repeat-containing RNAs from RNA using hybridization probes specific for repeat-containing sequences. Typically, RNA capture is performed by preferential hybridization of repeat-containing RNAs to a multiplicity of immobilized probes. The methods isolate expansion-specific RNAs and determine the sequences of aberrant splice variants associated with diseases and disorders. In other forms, the methods identify small molecules that selectively target the pathological splice variant transcripts. In some forms, the methods provide expansion-specific ASOs that specifically target and eliminate the pathological splice variant transcripts in vivo. Compositions of ASOs that specifically target and eliminate the pathological splice variant transcripts are also provided.
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 1/6897 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques faisant intervenir des gènes rapporteurs liés de façon fonctionnelle à des promoteurs
48.
CHEMOTHERAPEUTIC BIOADHESIVE PARTICLES WITH IMMUNOSTIMULATORY MOLECULES FOR CANCER TREATMENT
A bioadhesive nanoparticle (BNP) for long-lasting local drug delivery to treat cancer was developed. The bioadhesive nanoparticles (BNP) are composed of biodegradable polymer such as poly(lactic acid)-hyperbranched polyglycerol (PLA-HPG), encapsulating a chemotherapeutic such as camptothecin (CPT). Nanoparticles (NPs) of PLA-HPG are non-adhesive NPs (NNPs), which are stealthy in their native state, but conversion of the vicinal diols of HPG to aldehydes confers the ability to form strong covalent bonds with amine-rich surfaces. The formulation is administered in combination with immunostimulatory molecules such as CPG and shows unexpectedly better killing of cancer cells.
A61K 31/4745 - QuinoléinesIsoquinoléines condensées en ortho ou en péri avec des systèmes hétérocycliques condensées avec des systèmes cycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. phénanthrolines
A61K 31/711 - Acides désoxyribonucléiques naturels, c.-à-d. contenant uniquement des 2'-désoxyriboses liés à l'adénine, la guanine, la cytosine ou la thymine et ayant des liaisons 3'-5' phosphodiester
A61K 47/54 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p. ex. les supports ou les additifs inertesAgents 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 47/69 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p. ex. les supports ou les additifs inertesAgents 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 le conjugué étant caractérisé par sa forme physique ou sa forme galénique, p. ex. émulsion, particule, complexe d’inclusion, stent ou kit
Various semiconductor structures containing buried tunnel junctions or aperture regions are described. Further disclosed are methods for preparing and using such semiconductor structures which can be used, for example, in optoelectronic devices, such as vertical cavity surface emitting lasers (VCSELs), which can emit at long wavelengths.
H01S 5/183 - Lasers à émission de surface [lasers SE], p. ex. comportant à la fois des cavités horizontales et verticales comportant uniquement des cavités verticales, p. ex. lasers à émission de surface à cavité verticale [VCSEL]
50.
BOTTLEBRUSH BLOCK COPOLYMER-LIPID FOR THE FORMATION OF LIPID NANOPARTICLES WITH ROUGH SURFACE TOPOGRAPHY
A61K 9/127 - Vecteurs à bicouches synthétiques, p. ex. liposomes ou liposomes comportant du cholestérol en tant qu’unique agent tensioactif non phosphatidylique
C08G 61/08 - Composés macromoléculaires contenant uniquement des atomes de carbone dans la chaîne principale de la molécule, p. ex. polyxylylènes uniquement des atomes de carbone aliphatiques préparés par ouverture du cycle des composés carbocycliques des composés carbocycliques contenant une ou plusieurs doubles liaisons carbone-carbone dans le cycle
51.
REMOVAL OF AQUEOUS POLY AND PERFLUOROALKYL SUBSTANCES BY COVALENT TRANSFORMATION TO INSOLUBLE FLUORINATED ESTER
Poly arid perfluoroalkyl substances (PFAS) are toxic, ubiquitous contaminants in the environment along with drinking and waste water systems. Current treatment approaches struggle to effectively treat PEAS molecules without generating large amounts of toxic waste or requiring large energy and/or material inputs. With addition of alcohol such as decanol alone, PFAS such as water-soluble perfluorooctanoic acid (PFOA), can be transformed into a water-insoluble, fluorinated ester(s) that precipitate out of solution, facilitating self-removal. Highly hydrophobic fluorinated tails allow for esterification to proceed in water without the addition of any surfactant.
C02F 1/54 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par floculation ou précipitation d'impuretés en suspension utilisant des produits organiques
C02F 101/36 - Composés organiques contenant des atomes d'halogène
52.
METHODS AND COMPOSITIONS FOR TREATING RESPIRATORY DISORDERS
The present disclosure generally relates methods and compositions comprising VEGF-D, which methods and compositions can be used in the treatment of respiratory disorders. In some instances, the methods and compositions can be used for treating acute lung injury (ALI) or acute respiratory distress syndrome (ARDS).
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
A61P 11/00 - Médicaments pour le traitement des troubles du système respiratoire
C07K 14/475 - Facteurs de croissanceRégulateurs de croissance
53.
MACHINE LEARNING METHOD FOR ADAPTIVE TRIAL ENRICHMENT
Provided herein are methods of training an algorithm for adaptive predictive enrichment of a randomized controlled trial (RCT). The method includes providing an RCT with at least one primary outcome; defining an interim analysis timepoint; at the interim analysis timepoint, defining individualized estimates of the effects of a studied intervention for the primary outcome, as compared to a control arm, through iterative analysis; and training a machine-learning algorithm to identify one or more signatures of individualized treatment response in a treatment group as compared to a control group; where the one or more signatures of individualized treatment response are used to recommend predictive enrichment for subsequent RCT enrollment. Also provided herein is a method of adaptive predictive enrichment of a RCT including applying the algorithm trained above.
G16H 10/20 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des essais ou des questionnaires cliniques électroniques
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
G16H 50/70 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour extraire des données médicales, p. ex. pour analyser les cas antérieurs d’autres patients
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
The present invention provides cationic polymeric nanoparticles, and nanoparticle formulations thereof. The invention also provides methods for preparing cationic polymeric nanoparticles, and methods of treating diseases, reducing tumor growth, and increasing uptake of a therapeutic agent by a tumor cell in a subject in need thereof.
A61K 31/495 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec deux azote comme seuls hétéro-atomes d'un cycle, p. ex. pipérazine
55.
Identification and Treatment of Cancers Associated with RASGRF1 Gene Fusions
The disclosure provides compositions and methods for identifying a cancer associated with an RASGRF1 gene fusion in a subject. The disclosure also includes methods of treating a subject who has been pre-selected by detecting an RASGRF1 gene fusion in a sample obtained from the subject.
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
56.
TECHNIQUES FOR QUANTUM ERROR CORRECTION USING MULTIMODE GRID STATES AND RELATED SYSTEMS AND METHODS
Techniques are described for implementing a class of multimode bosonic codes that protect against errors within an ancilla qubit coupled to a bosonic system, that can be realized experimentally. A logical qubit state is represented by the states of multiple different modes of one or more bosonic systems, which may include multiple modes of a single bosonic system and/or single modes from multiple bosonic systems. Techniques for correcting errors are also described. In particular, a series of operations are described that autonomously detect and correct errors by repeatedly performing a sequence of operations that are each applied to the multiple bosonic modes and/or to the ancilla qubit that is coupled to each of the bosonic modes. The codes allow ancilla errors to propagate to the modes of the bosonic system as correctable errors, where they can be corrected, instead of presenting as logical errors in the ancilla qubit.
G06N 10/70 - Correction, détection ou prévention d’erreur quantique, p. ex. codes de surface ou distillation d’état magique
G06N 10/40 - Réalisations ou architectures physiques de processeurs ou de composants quantiques pour la manipulation de qubits, p. ex. couplage ou commande de qubit
Provided herein are methods for communicating data between nodes in a computer system and distributed systems of computer architectures. The methods include generating a hash based upon a data set, communicating the hash to one or more nodes, comparing the communicated hash to stored hashes at the one or more nodes, and communicating the data set when matching hashes are detected. The system includes two or more processing elements configured to communicate data according to the methods above.
Provided is an adsorbent for removing perfluoroalkyl and polyfluoroalkyl substances from an aqueous solution, including perfluoro-octanoic acid (PFOA), perfluoro-octane sulfonate (PFOS), shorter-chained perfluoroalkyl and polyfluoroalkyl substances, and combinations of foregoing. The adsorbent includes iron oxide nanocrystals, wherein the absorbent has an adsorption capacity for PFOA of at least 5000 mg/g or an adsorption capacity for PFOS of at least 25,000 mg/g. Also provided are methods of removing contaminants from an aqueous solution, wherein the contaminants include perfluoroalkyl and polyfluoroalkyl substances.
60.
METHODS FOR THE TREATMENT AND PREVENTION OF NON-VIRAL TICK-BORNE DISEASES AND SYMPTOMS THEREOF OF
Methods and compositions for treating or preventing non-viral tick-borne diseases and symptoms thereof by administering a long half-life 8-aminoquinoline, such as tafenoquine, are disclosed. Kits including a means for testing for a non-viral tick-borne disease and/or symptoms thereof and a long half-life 8-aminoquinoline, such as tafenoquine, are disclosed.
The present invention provides methods for bioprinting collagen and extracellular matrix-based bioinks, and articles such as engineered tissues, comprising the bioinks. In other aspects, the present invention relates to a bioprinting system including a 3D bioprinter with a nozzle, at least one bioink, a support bath solution, wherein the support bath solution comprises PEG (polyethylene glycol) and agarose.
Benaroya Research Institute at Virginia Mason (USA)
Yale University (USA)
Inventeur(s)
Leon, Francisco
Herold, Kevan C.
Long, Sarah Alice
Linsley, Peter S.
Abrégé
Provided herein, in one aspect, is a method of preventing or delaying the onset of clinical type 1 diabetes (T1D), comprising: providing a non-diabetic subject who is at risk for T1D; administering a prophylactically effective amount of an anti-CD3 antibody to the non-diabetic subject; and determining, prior to or after the administering step, that the non-diabetic subject has more than about 5% to more than about 10% TIGIT+KLRG1+CD8+ T-cells in all CD3+ T-cells, which is indicative of successful prevention or delay of the onset of clinical T1D.
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 39/00 - Préparations médicinales contenant des antigènes ou des anticorps
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p. ex. antidiabétiques
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
Provided are digitally-implemented methods of treating a mental health issue in a subject. The methods include digitally delivering a standardized assessment to the subject; analyzing data collected from the standardized assessment; identifying an evidence-based treatment pathway based upon the analysis of the data; and administering the evidence-based treatment pathway to the subject.
G16H 20/70 - 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 thérapies mentales, p. ex. la thérapie psychologique ou le training autogène
G16H 50/30 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le calcul des indices de santéTIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour l’évaluation des risques pour la santé d’une personne
G16H 50/20 - TIC spécialement adaptées au diagnostic médical, à la simulation médicale ou à l’extraction de données médicalesTIC spécialement adaptées à la détection, au suivi ou à la modélisation d’épidémies ou de pandémies pour le diagnostic assisté par ordinateur, p. ex. basé sur des systèmes experts médicaux
G16H 10/20 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des essais ou des questionnaires cliniques électroniques
G16H 40/67 - TIC spécialement adaptées à la gestion ou à l’administration de ressources ou d’établissements de santéTIC spécialement adaptées à la gestion ou au fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement d’équipement ou de dispositifs médicaux pour le fonctionnement à distance
A61B 5/16 - Dispositifs pour la psychotechnieTest des temps de réaction
Aspects of the present invention relate to a system including a transformer encoder with a compression layer, a transformer decoder with an expansion layer, the transformer encoder configured to transform one or more inputs into a control latent vector, a noise injection element configured to add noise to the control latent vector to create a noisy latent vector, a weighting element configured to add one or more weightings to the control latent vector to create an exact latent vector, and the transformer decoder configured to transform the noisy latent vector and exact latent vector into an output.
G16C 20/70 - Apprentissage automatique, exploration de données ou chimiométrie
G06F 30/28 - Optimisation, vérification ou simulation de l’objet conçu utilisant la dynamique des fluides, p. ex. les équations de Navier-Stokes ou la dynamique des fluides numérique [DFN]
65.
METHODS OF IDENTIFYING CIS-REGULATORY ELEMENTS OF TRANSLATION
Described herein is method of identifying cis-regulatory element of translation. The method includes: translating a plurality of mRNA molecules, each comprising a potential cis-regulatory element, with ribosomes to obtain a mixture; generating from the initial mixture an enriched mixture comprising mRNA molecules being translated, the ribosomes, and partial translation products being produced by the ribosomes from the mRNA molecules, according to affinity of the partial translation products to a binding partner thereof; sequencing the mRNA molecules present in the enriched mixture; determining an abundance of each mRNA molecule present in the enriched mixture; and identifying cis-regulatory elements of translation based on the determined abundance of each of the plurality of mRNA molecules. Also described herein is a method of determining translational efficiency of an mRNA molecule that includes similar steps.
66.
METHOD OF PREDICTION OF LIGAND-PROTEIN BINDING AFFINITIES USING META-MODELS
Provided herein are methods of developing a meta-modeling framework for ligand-protein binding affinity prediction by integrating empirical scoring function-based docking and deep learning-based regression outputs through linear and non-linear machine learning models. Thus, empirical docking models and deep learning models were used as base models data. By taking predictions from those base models, machine learning regression models were developed as meta-models. These meta-models significantly improve binding affinity prediction over individual base models and achieve comparable performance to other structure-based deep learning models.
G16B 15/30 - Ciblage de médicament à l’aide de données structurellesPrévision d’amarrage ou de liaison moléculaire
G06N 3/0985 - Optimisation d’hyperparamètresMeta-apprentissageApprendre à apprendre
G16B 40/00 - TIC spécialement adaptées aux biostatistiquesTIC spécialement adaptées à l’apprentissage automatique ou à l’exploration de données liées à la bio-informatique, p. ex. extraction de connaissances ou détection de motifs
Provided herein are methods of training and building algorithms to predict stroke etiology. The method of training an algorithm to predict stroke etiology includes processing electronic health records (EHRs) in a derivation dataset, the processing including extracting clinical variables from the EHRs by detecting concept unique identifiers (CUIs) through natural language processing (NLP), and extracting other covariates from the EHRs through regular expression, wherein the clinical variables and other covariates form a training dataset; training two or more base models with the training set to form two or more trained base models, the base models selected from the group including Random Forests (RF), XGBoost (XGB), support vector classifier (SVC), and logistic regression (LR); refining the two or more trained base models using hyperparameters to form two or more refined base models; and building an ensemble model with the two or more refined base models. Also provided herein are articles and methods of predicting ischemic stroke etiology using the trained algorithm.
A61B 5/00 - Mesure servant à établir un diagnostic Identification des individus
A61B 5/318 - Modalités électriques se rapportant au cœur, p. ex. électrocardiographie [ECG]
G16H 10/40 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients pour des données relatives aux analyses de laboratoire, p. ex. pour des analyses d’échantillon de patient
G06F 18/214 - Génération de motifs d'entraînementProcédés de Bootstrapping, p. ex. ”bagging” ou ”boosting”
68.
COMPOUNDS AND METHODS FOR TREATING CANCERS THAT ARE MGMT DEFICIENT REGARDLESS OF MMR STATUS
Disclosed are compounds and methods of treating, ameliorating, and/or preventing cancers, including cancers that are MGMT deficient regardless of their MMR status, and particularly compounds and methods of treating, ameliorating, and/or preventing cancers that are both MGMT and MMR deficient or that are MGMT deficient and resistant to treatment with temozolomide.
A61K 31/4188 - 1,3-Diazoles condensés avec des systèmes hétérocycliques, p. ex. biotine, sorbinil
A61K 31/427 - Thiazoles non condensés et contenant d'autres hétérocycles
A61K 31/444 - Pyridines non condenséesLeurs dérivés hydrogénés contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p. ex. amrinone
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
PC1-CTT polypeptides for the treatment of Autosomal Dominant Polycystic Kidney Disease (ADPKD) are provided and can be or include PC1-CTT (SEQ ID NO:1) or a functional fragment or variant thereof. In some embodiments, the PC1-CTT polypeptide is a fusion protein or conjugate further including a functional element such as a protein transduction domain, fusogenic polypeptide, targeting signal, or expression and/or purification tag. Nucleic acids encoding the disclosed PC1-CTT polypeptides and other therapeutic proteins are also provided. In some embodiments, the nucleic acid encodes a TOP or TOP-like motif. The nucleic acids can be RNA or DNA, and can be, for example, a vector such as a plasmid or viral vector, or an mRNA. Methods of treatment are provided and typically include administering a subject in need thereof an effective amount of a disclosed polypeptide or nucleic acid.
C07K 14/47 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains provenant de vertébrés provenant de mammifères
A61K 38/00 - Préparations médicinales contenant des peptides
A61K 48/00 - Préparations médicinales contenant du matériel génétique qui est introduit dans des cellules du corps vivant pour traiter des maladies génétiquesThérapie génique
A61P 13/12 - Médicaments pour le traitement des troubles du système urinaire des reins
70.
Physics-based algorithm to universally standardize routinely obtained clinical T2-weighted images
An imaging method calculates T2 maps using only data from a T2w image scan. The imaging system is used in conjunction with an MRI system that includes a magnet housing, a superconducting magnet, shim coils, RF coils, receiver coils, a patient support, and measurement circuitry producing data used to reconstruct images displayed on a display. The measurement circuitry integrates either expanding-constrained alternating minimization for parameter mapping or expanding-constrained alternating minimization for parameter mapping with projected gradient descent.
A61B 5/055 - Détection, mesure ou enregistrement pour établir un diagnostic au moyen de courants électriques ou de champs magnétiquesMesure utilisant des micro-ondes ou des ondes radio faisant intervenir la résonance magnétique nucléaire [RMN] ou électronique [RME], p. ex. formation d'images par résonance magnétique
Described herein is a non-natural mRNA molecule, which includes a non-natural cisregulatory element that modulates the translational efficiency of the mRNA molecule. Also described herein is a method for modulating mRNA translational efficiency.
72.
SYSTEM AND METHOD FOR INTEGRATED LIFESTYLE MEDICINE
A system for integrated lifestyle medicine tracking and digital therapy comprises a central computing system comprises a device interface subsystem, a user data interface subsystem, a data visualization engine, and a set of instructions, which when executed by the processor, perform steps comprising collecting a first data stream from the at least one sensor via the device interface subsystem, collecting a first user-reported data stream from the at least one user via the user data interface subsystem, calculating a probability of at least one lifestyle risk factor from the first data stream and the first user-reported data stream, and presenting the user with at least one intervention to mitigate the at least one lifestyle risk factor. A method for integrated lifestyle medicine tracking and digital therapy is also disclosed.
G16H 10/00 - TIC spécialement adaptées au maniement ou au traitement des données médicales ou de soins de santé relatives aux patients
G16H 20/00 - 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
The present invention relates to fiber jamming systems capable of tuning tensile stiffness of soft systems within seconds without the use of high voltage or temperature changes. The systems employ segmented fibrils of interspersed segments of stretchable and non-stretchable materials. Applying a vacuum to the fibrils in an enclosed volume elicits a large interfacial shear resistance to tensile displacement. In the absence of a vacuum, the fibrils are free to stretch and bend in any direction.
D01F 8/14 - Filaments, ou similaires, faits par l’homme, conjugués, c.-à-d. à plusieurs composantsLeur fabrication à partir de polymères synthétiques avec au moins un polyester comme constituant
A scanning electron microscopy (SEM) system performs subvoxel microscopy with a probe and detector. The probe directs incoming probe electrons at a sample with an energy and a direction. The detector detects electrons scattered by the sample and generates a two-dimensional energy profile map of the detected electrons. The system may determine subvoxel information including features of the sample smaller than a size of the probe using the energy and direction and the two-dimensional energy profile map. The system may determine three-dimensional subvoxel information of the sample. The system may be a focused ion beam scanning electron microscopy (FIB-SEM) system with an emitter directing a FIB at the sample to separate layers thereof. For each of multiple layers, the system may obtain the energy and direction and generate the two-dimensional energy profile map. The system may generate three-dimensional subvoxel volume information of the sample thicker than individual layers.
75.
Protein Capture Membrane and Method of Use Thereof
In one aspect, the invention provides a protein capture membrane comprising a first side and a second side and a plurality of interstices extending contiguously from the first side to the second side, wherein the interstices are coated with a protein-reactive coating; and the porous substrate comprises nanoporous alumina or porous glass. In another aspect the invention provides a method of detecting a protein of interest in a plurality of proteins.
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
B01D 57/02 - Séparation, autre que la séparation de solides, non entièrement couverte par un seul groupe ou sous-classe, p. ex. par électrophorèse
B01D 69/02 - Membranes semi-perméables destinées aux procédés ou aux appareils de séparation, caractérisées par leur forme, leur structure ou leurs propriétésProcédés spécialement adaptés à leur fabrication caractérisées par leurs propriétés
B01D 69/10 - Membranes sur supportSupports pour membranes
76.
COMPOSITIONS AND METHODS OF DETERMINING LUPUS NEPHRITIS CLASS
It has been determined that differential methylation at CpG loci can be used to determine the severity of lupus nephritis (LN). Thus, differentially methylated CpG loci (also referred to herein as biomarkers), as well as methods of detecting methylation at the biomarkers are provided, as are their use to determine the severity of LN and inform treatment. In particular, the differential methylation is useful in distinguishing patients with class II LN from patients suffering from LN of classes III - VI and thereby determining whether the patient should be given immunosuppressants.
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
Described herein are methods of modulating mRNA translational efficiencies with translational enhancers or silencers that affects ribosomal retention. Also described herein are mRNA molecules including translational enhancers or silencers, as well as modified nucleobases. Also described herein are methods of constructing an mRNA molecule for producing a therapeutic peptide or a therapeutic protein with the identified enhancers.
78.
EGFR PROTEOLYSIS TARGETING CHIMERIC MOLECULES AND ASSOCIATED METHODS OF USE
The present invention relates to bifunctional compounds, which find utility to degrade and (inhibit) TBK1. In particular, the present invention is directed to compounds, which contain on one end an E3 ubiquitin ligase binding moiety which binds to an E3 ubiquitin ligase and on the other end a moiety which binds TBK1 such that TBK1 is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of TBK1. The present invention exhibits a broad range of pharmacological activities associated with compounds according to the present invention, consistent with the degradation/inhibition of TBK1.
A61K 47/54 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p. ex. les supports ou les additifs inertesAgents 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 31/427 - Thiazoles non condensés et contenant d'autres hétérocycles
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 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
A61K 31/506 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime non condensées et contenant d'autres hétérocycles
A61K 31/517 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime condensées en ortho ou en péri avec des systèmes carbocycliques, p. ex. quinazoline, périmidine
A61K 31/519 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime condensées en ortho ou en péri avec des hétérocycles
A61K 31/55 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à sept chaînons, p. ex. azélastine, pentylènetétrazole
A61K 31/551 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à sept chaînons, p. ex. azélastine, pentylènetétrazole ayant deux atomes d'azote comme hétéro-atomes d'un cycle, p. ex. clozapine, dilazèpe
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
A61K 47/55 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p. ex. les supports ou les additifs inertesAgents 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 l’agent de modification étant aussi un agent pharmacologiquement ou thérapeutiquement actif, c.-à-d. le conjugué entier étant un co-médicament, p. ex. un dimère, un oligomère ou un polymère de composés pharmacologiquement ou thérapeutiquement actifs
The present invention provides compositions and methods of preparing airway cells. In one aspect, an epithelial airway cell derived from an induced pluripotent stem (iPS) cell characterized by expression of airway cell surface markers and an ability to proliferate is described. In another aspect, methods of differentiating an iPS into an epithelial airway cell is provided. Engineered lungs, methods of making such engineered 10 lungs comprising the epithelial airway cells and treating respiratory disorders are also disclosed.
Fusion proteins including (a) a mast cell intracellular signaling domain; and (b) an amino acid sequence that is heterologous to the mast cell intracellular signaling domain are provided. In some embodiments, (a) includes the intracellular domain of IgE receptor (FcεRI), a cytokine receptor (c- KIT), a G-protein-coupled receptor, or a toll-like receptor expressed in mast cells, or functional fragment or variant thereof. In some embodiments, the amino acid sequence of (a) includes an ITAM sequence. In preferred embodiments, the fusion proteins are chimeric antigen receptors (referred to as "CAR-mast"), that include a transmembrane domain and an extracellular domain that targets an antigen. Nucleic acids encoding the fusion proteins, and mast cells including or expressing the nucleic acids and/or fusion proteins are also provided, as are methods of the using the same to treat diseases and disorders characterized by expression of the antigen.
The invention provides a system for hypothermic, restoration and preservation of organs in a mammal. In certain aspects, the system is capable of preserving organs, maintaining cellular integrity and cellular function for hours postmortem or after global ischemia. The invention also provides synthetic organ perfusate formulations, including a novel perfusate autologous blood mixture, which is able to reduce reperfusion injury, stimulate recovery from hypoxia, metabolically support the energy needs of organs and prevent rigor mortis.
Examples described herein provide a computer-implemented method that includes receiving a noninvasive transabdominal fetal electroencephalography (TA-fEEG) signal associated with a pregnant subject. The method further includes reducing unwanted noise in the TA-fEEG signal using a first machine learning model. The method further includes reconstructing a fetal electroencephalography (fEEG) signal from the TA-fEEG signal using a second machine learning model.
G06F 18/2134 - Extraction de caractéristiques, p. ex. en transformant l'espace des caractéristiquesSynthétisationsMappages, p. ex. procédés de sous-espace basée sur des critères de séparation, p. ex. analyse en composantes indépendantes
The present disclosure provides methods of making and methods of using IL-18 mimic polypeptides for use in therapeutic and non-therapeutic applications. The synthetic IL-18 mimics an increase IL-18R signaling activity even in the presence of an inhibitory molecule such as IL-18BP.
THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (USA)
YALE UNIVERSITY (USA)
GOVERNMENT OF THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE SECRETARY OF COMMERCE (USA)
Inventeur(s)
Diddams, Scott A.
Quinlan, Franklyn J.
Liu, Yifan
Kelleher, Megan L.
Mclemore, Charles A.
Rakich, Peter Thomas
Jin, Naijun
Abrégé
A vacuum-gap optical cavity includes a spacer having a first spacer surface and a second spacer surface, a first mirror having a first reflective coating formed on a first substrate, and a second mirror having a second reflective coating formed on a second substrate. The spacer forms a cavity region that extends between a first aperture at the first spacer surface and a second aperture at the second spacer surface. The first mirror is bonded to the first spacer surface such that the first reflective coating overlaps the first aperture and such that the first mirror completely covers the first aperture. The second mirror is bonded to the second spacer surface such that the second reflective coating overlaps the second aperture and such that the second mirror completely covers the second aperture. The cavity region is maintained under vacuum without active pumping.
H01S 3/08 - Structure ou forme des résonateurs optiques ou de leurs composants
H01S 5/10 - Structure ou forme du résonateur optique
G02B 6/293 - Moyens de couplage optique ayant des bus de données, c.-à-d. plusieurs guides d'ondes interconnectés et assurant un système bidirectionnel par nature en mélangeant et divisant les signaux avec des moyens de sélection de la longueur d'onde
H01S 3/13 - Stabilisation de paramètres de sortie de laser, p. ex. fréquence ou amplitude
H01S 5/06 - Dispositions pour commander les paramètres de sortie du laser, p. ex. en agissant sur le milieu actif
A61K 31/711 - Acides désoxyribonucléiques naturels, c.-à-d. contenant uniquement des 2'-désoxyriboses liés à l'adénine, la guanine, la cytosine ou la thymine et ayant des liaisons 3'-5' phosphodiester
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
86.
Cell-Penetrating Peptides and Methods of Use Thereof
In various aspects and embodiments the invention provides compositions and methods for facilitating cell penetration of a cargo molecule. In another aspect, the invention provides a method of preventing viral infection in a subject in need thereof, the method comprising providing to the subject a therapeutically effective amount of a polypeptide comprising a cell-penetrating peptide and a retromer binding site.
The description relates to imide-based compounds, including bifunctional compounds comprising the same, which find utility as modulators of targeted ubiquitination, especially inhibitors of a variety of polypeptides and other proteins which are degraded and/or otherwise inhibited by bifunctional compounds according to the present invention. In particular, the description provides compounds, which contain on one end a ligand which binds to the cereblon E3 ubiquitin ligase and on the other end a moiety which binds a target protein such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of that protein. Compounds can be synthesized that exhibit a broad range of pharmacological activities consistent with the degradation/inhibition of targeted polypeptides of nearly any type.
C07D 261/08 - Composés hétérocycliques contenant des cycles oxazole-1, 2 ou oxazole-1, 2 hydrogéné non condensés avec d'autres cycles comportant plusieurs liaisons doubles entre chaînons cycliques ou entre chaînons cycliques et chaînons non cycliques avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone du cycle
88.
METHODS OF ACQUIRING MICROSCOPIC IMAGES OF BIOLOGICAL SAMPLES
Described herein is a method of acquiring a microscopic image of a biological sample. In certain embodiments, the method includes at least one of the following: the method including: embedding the biological sample in a first swellable hydrogel; expanding the first swellable hydrogel and the biological sample embedded therein to obtain a first expanded biological sample; embedding the first expanded biological sample in a second swellable hydrogel; labeling a DNA molecule in a chromatin in the biological sample with a first dye; expanding the second swellable hydrogel and the first expanded biological sample embedded therein to obtain a second expanded biological sample; acquiring the microscopic image of the second expanded biological sample with a light microscopy technology. Also described is a method of evaluating the effect of a treatment of a biological sample using the imaging method.
G01N 33/483 - Analyse physique de matériau biologique
G01N 33/58 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des substances marquées
C12Q 1/6809 - Méthodes de détermination ou d’identification des acides nucléiques faisant intervenir la détection différentielle
This invention relates to compositions comprising physiologic dendritic cells and at least one mRNA. The invention further relates to compositions comprising physiologic dendritic cells and at least one mRNA for use in therapeutic treatment.
This invention relates to compositions comprising physiologic dendritic cells and at least one mRNA. The invention further relates to compositions comprising physiologic dendritic cells and at least one mRNA for use in vaccination.
Antibodies, chimeric antigen receptors (CARs) and other molecules that specifically bind ENPP3 are provided. Host cells, such as immune cells, including the molecules, antibodies, fusion proteins, CARs, nucleic acids encoding them, are also provided. In some forms, the cells are CAR immune cells. In some forms, the CAR immune cells maintain the ability to kill ENPP3+ cancer cells after multiple stimulations. Pharmaceutical compositions including the antibodies, CARs or T cells are also provided. In some forms, the molecule or antibody includes drugs conjugated thereto, has antibody-dependent cell-mediated cytotoxicity (ADCC) activity, complement-dependent cytotoxicity activity (CDC), and/or is a bi-specific engager optionally a T cell engager or NK cell engager. Methods of using the described molecules to treat ENPP3+ cancers are also described.
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
C07K 16/40 - Immunoglobulines, p. ex. anticorps monoclonaux ou polyclonaux contre des enzymes
92.
COMPOSITIONS AND METHODS FOR TREATING POST-TRAUMATIC STRESS DISORDER
B.G. Negev Technologies and Applications Ltd. (Israël)
Colorado School of Mines (USA)
Inventeur(s)
Gilron, Jack
Elimelech, Menachem
Cath, Tzahi
Abrégé
Described herein is a reverse osmosis system, comprising: a feed source input, a high pressure feed pump fluidly connected to the feed source input, a reverse osmosis (RO) cascade fluidly connected to the high pressure feed pump; wherein the RO cascade comprises at least one low salt rejection reverse osmosis (LSRRO) stage including a LSRRO membrane and a seawater reverse osmosis (SWRO) stage including a SWRO membrane fluidly connected to the at least one LSRRO stage.
Described herein is a reverse osmosis system, comprising: a feed source input, a high pressure feed pump fluidly connected to the feed source input, a reverse osmosis (RO) cascade fluidly connected to the high pressure feed pump; wherein the RO cascade comprises at least one low salt rejection reverse osmosis (LSRRO) stage including a LSRRO membrane and a seawater reverse osmosis (SWRO) stage including a SWRO membrane fluidly connected to the at least one LSRRO stage.
Also described herein is a reverse osmosis method, comprising: providing the reverse osmosis system of claim 1, inputting a high salinity fluid into the feed source input, increasing the pressure of the high salinity fluid via the high pressure feed pump, performing reverse osmosis via the RO cascade, and collecting at least one of a concentrate and a permeate.
C02F 1/44 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par dialyse, osmose ou osmose inverse
C02F 1/469 - Traitement de l'eau, des eaux résiduaires ou des eaux d'égout par des procédés électrochimiques par séparation électrochimique, p. ex. par électro-osmose, électrodialyse, électrophorèse
C02F 103/06 - Eau souterraine contaminée ou eau de lessivage
C02F 103/08 - Eau de mer, p. ex. pour le dessalement
94.
SPECIFIC THERAPEUTIC MEDICAL MARIJUANA DOSES FOR STRESS AND PAIN
In various aspects and embodiments the invention provides a method of treating pain, stress and anxiety in a subject in need thereof, wherein the method comprises administering to the subject in need thereof a pharmaceutical composition comprising cannabidiol (CBD) and tetrahydrocannabinol (THC) at a ratio between about 3:1 and about 6:1 CBD:THC.
Provided herein are a method of parallelizing zero-knowledge (ZK) protocols, an apparatus for parallelizing zero-knowledge (ZK) protocols, and an apparatus for proving zero-knowledge (ZK) protocols. The method includes providing a ZK framework; calculating local and communication costs for each program instruction of a ZK statement; automatically partitioning the ZK statement according to the calculation; and distributing the partitioned ZK statement to a corresponding number of computing cores for parallel proving or verification. The apparatus for parallelizing zero-knowledge (ZK) protocols includes a processor and a memory unit configured to implement the method. The apparatus for proving zero-knowledge (ZK) protocols includes at least two processors, a memory unit, a communication interface, and a ZK statement parallelized according to the method distributed among the at least two processors. Also provided herein is a non-transitory computer readable storage medium storing computer-executable instructions for performing the method.
H04L 9/32 - Dispositions pour les communications secrètes ou protégéesProtocoles réseaux de sécurité comprenant des moyens pour vérifier l'identité ou l'autorisation d'un utilisateur du système
G06F 9/28 - Augmentation de la vitesse de fonctionnement, p. ex. en utilisant plusieurs dispositifs de microcommande fonctionnant en parallèle
G06Q 20/38 - Protocoles de paiementArchitectures, schémas ou protocoles de paiement leurs détails
96.
FIELD-PROGRAMMABLE ISING MACHINE AND METHOD OF USING
A programmably reconfigurable Ising machine. In embodiments, the programmably reconfigurable Ising machine includes a plurality of spin circuits and a reconfigurable routing network. Each spin circuit includes a spin generator and a set of reconfigurable coupling blocks operatively connected to the spin generator. In embodiments, each reconfigurable coupling block includes a coupling switch operatively connected to the spin generator, a variable coupling unit operatively connected to the coupling switch, and a pin operably connected to the variable coupling unit. In embodiments, the coupling switch and the variable coupling unit are connected to memory and are configurable based on a configuration stored in the memory. In embodiments, the reconfigurable routing network is configured to selectively operatively connect two or more spin circuit of the programmably reconfigurable Ising machine via reconfigurable coupling blocks. Connected spin circuits are interdependent.
THE UNITED STATES GOVERNMENT AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS (USA)
Inventeur(s)
Krystal, John H.
Yoon, Gihyun
Petrakis, Ismene L.
Abrégé
The present application provides pharmaceutical compositions and methods for treating diseases or disorders. The pharmaceutical composition comprises N-methyl-D-aspartate receptor modulator and μ-opioid receptor modulator. The present application also discloses formulations, dosing and administration routes for the pharmaceutical composition. Diseases can be treated by the pharmaceutical composition are also described.
Methods and compositions for treating or preventing non-viral tick-borne diseases and symptoms thereof by administering a long half-life 8-aminoquinoline, such as tafenoquine, are disclosed. Kits including a means for testing for a non-viral tick-borne disease and/or symptoms thereof and a long half-life 8-aminoquinoline, such as tafenoquine, are disclosed.
A61K 31/335 - Composés hétérocycliques ayant l'oxygène comme seul hétéro-atome d'un cycle, p. ex. fungichromine
A61K 31/495 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec deux azote comme seuls hétéro-atomes d'un cycle, p. ex. pipérazine
A61K 31/4706 - 4-Aminoquinoléines8-Aminoquinoléines, p. ex. chloroquine, primaquine
In various aspects and embodiments the invention provides a method of treating cancer in a subject in need thereof, the method comprising administering to the subject a pharmaceutical composition comprising an effective amount of a cytoskeletal tension regulator and an effective amount of a polypeptide having 80% or greater sequence identity to SEQ ID NO: 1 Fas Ligand (FasL).
A61K 31/551 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à sept chaînons, p. ex. azélastine, pentylènetétrazole ayant deux atomes d'azote comme hétéro-atomes d'un cycle, p. ex. clozapine, dilazèpe
A61K 31/472 - Isoquinoléines non condensées, p. ex. papavérine
A61K 31/4745 - QuinoléinesIsoquinoléines condensées en ortho ou en péri avec des systèmes hétérocycliques condensées avec des systèmes cycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. phénanthrolines
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
100.
pH LOW INSERTION PEPTIDE TARGETED DELIVERY OF POTENT CYTOTOXIC COMPOUNDS
University of Rhode Island Board of Trustees (USA)
YALE UNIVERSITY (USA)
Inventeur(s)
Reshetnyak, Yana K.
Andreev, Oleg A.
Moshnikova, Anna
Engelman, Donald M.
Abrégé
The invention features a composition comprising a potent cytotoxic compound and a pHILIP® peptide, where, e.g., the cytotoxic compound cannot be used alone due to a lack of targeting. pHILIP® peptide targets cytotoxic compounds to acidic diseased tissue, translocates cytotoxic compounds across plasma membranes into the cytosols of cells in acidic diseased tissues and induces cell death predominantly in the targeted acidic diseased tissue.
A61K 47/64 - Conjugués médicament-peptide, médicament-protéine ou médicament-acide polyaminé, c.-à-d. l’agent de modification étant un peptide, une protéine ou un acide polyaminé lié par covalence ou complexé à un agent thérapeutiquement actif
A61K 9/00 - Préparations médicinales caractérisées par un aspect particulier
A61K 31/4745 - QuinoléinesIsoquinoléines condensées en ortho ou en péri avec des systèmes hétérocycliques condensées avec des systèmes cycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. phénanthrolines
A61K 31/5386 - 1,4-Oxazines, p. ex. morpholine condensées en spiro ou formant une partie de systèmes cycliques pontés
A61K 31/7036 - Composés ayant des radicaux saccharide liés à des composés non-saccharide par des liaisons glycosidiques liés à un composé carbocyclique, p. ex. phloridzine ayant au moins un groupe amino lié directement au carbocycle, p. ex. streptomycine, gentamycine, amikacine, validamycine, fortimicines
A61K 47/60 - Préparations médicinales caractérisées par les ingrédients non actifs utilisés, p. ex. les supports ou les additifs inertesAgents 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