CNRS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSA INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
Inventeur(s)
Domingo, Pascale
Vervisch, Luc
Barnaud, Camille
Dodier, Eric
Ghazal, Ghassan
Nguyen, Phuc Danh
Sert, Dominique
Abrégé
The invention relates to a double wall lance for injecting reducing agent and oxygen through a tuyere comprising: a. an inner tube (5) for injecting reducing agent (2), b. an outer tube (6) for injecting oxygen (3) which surrounds the inner tube (5), c. an end part (7, 7a,7b,7c) closing the lance (1) and having: - a front face (11a,11b,11c) having a diameter D and comprising: i. a reducing agent outlet hole (8a,8b,8c), ii. a front face periphery (9a,9b,9c) comprising a plurality of main oxygen outlet holes (10a,10b,10c), - a cap (12a,12b,12c) surrounding the end part (7,7a,7b,7c) and extending over a length L starting from the front face (11a,11b,11c) of the end part (7, 7a,7b,7c) to a free end edge (14a,14b,14c), wherein the length L of the cap (12a,12b,12c) represents more than 21,3% of the diameter D of the front face (11a,11b,11c). The invention also relates to a method to inject hot reducing gas into a blast furnace through a tuyere (4) using such double wall lance.
INSTITUT NATIONAL POLYTECHNIQUE DE TOULOUSE (France)
UNIVERSITÉ TOULOUSE III - PAUL SABATIER (France)
INSA ROUEN NORMANDIE (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Bourgeois, Florent
Gurdjos, Célia
Cyr, Martin
Estel, Lionel
Abrégé
The present invention relates to a method for recycling concrete waste from construction and/or deconstruction, comprising at least one step of microwave processing of concrete blocks, at least one step of mechanical processing, and optionally at least one step of carbonation of the concrete fines and the recycled concrete aggregates obtained by the steps of microwave processing of concrete blocks and mechanical processing.
B09B 3/50 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant un rayonnement, p. ex. des ondes électromagnétiques
C07D 207/323 - Composés hétérocycliques contenant des cycles à cinq chaînons, non condensés avec d'autres cycles, ne comportant qu'un atome d'azote comme unique hétéro-atome du cycle avec uniquement des atomes d'hydrogène ou de carbone liés directement à l'atome d'azote du cycle comportant deux 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 avec uniquement des atomes d'hydrogène ou des radicaux ne contenant que des atomes d'hydrogène et de carbone, liés directement à l'atome d'azote du cycle
C07C 41/18 - Préparation d'éthers par des réactions ne formant pas de liaisons sur l'oxygène de la fonction éther
C07C 67/28 - Préparation d'esters d'acides carboxyliques par modification de la partie hydroxyle de l'ester sans introduction d'un groupe ester
C07C 67/30 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester
C07D 209/08 - IndolesIndoles hydrogénés avec uniquement des atomes d'hydrogène ou des radicaux ne contenant que des atomes d'hydrogène et de carbone, liés directement aux atomes de carbone de l'hétérocycle
C07D 277/64 - Benzothiazoles avec uniquement des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués liés en position 2
C07D 307/79 - Benzo [b] furannesBenzo [b] furannes hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone de l'hétérocycle
C07D 333/54 - Benzo [b] thiophènesBenzo [b] thiophènes hydrogénés avec uniquement des atomes d'hydrogène, des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués, liés directement aux atomes de carbone de l'hétérocycle
C07C 1/32 - Préparation d'hydrocarbures à partir d'un ou plusieurs composés, aucun d'eux n'étant un hydrocarbure à partir de composés renfermant des hétéro-atomes autres que l'oxygène ou les halogènes, ou en addition à ceux-ci
C07C 17/361 - Préparation d'hydrocarbures halogénés par des réactions comportant une diminution du nombre d'atomes de carbone
C07C 67/317 - Préparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par élimination d'hydrogène ou de groupes fonctionnelsPréparation d'esters d'acides carboxyliques par modification de la partie acide de l'ester sans introduction d'un groupe ester par hydrogénolyse de groupes fonctionnels
C07D 277/64 - Benzothiazoles avec uniquement des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués liés en position 2
C07D 277/68 - Benzothiazoles avec des hétéro-atomes ou avec des atomes de carbone comportant trois liaisons à des hétéro-atomes, avec au plus une liaison à un halogène, p. ex. radicaux ester ou nitrile, liés directement en position 2
C07D 277/74 - Atomes de soufre substitués par des atomes de carbone
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
Inventeur(s)
Besset, Tatiana
Castanheiro, Thomas
Nobile, Enzo
Arribat, Mathieu
Abrégé
222 with a compound RH, R being a hydrocarbon group, comprising optionally at least one heteroatom, for obtaining a compound having the formula R-C(=S)-F.
C07D 277/64 - Benzothiazoles avec uniquement des radicaux hydrocarbonés ou des radicaux hydrocarbonés substitués liés en position 2
C01B 32/70 - Composés contenant du carbone et du soufre, p. ex. thiophosgène
C07C 333/08 - Acides monothiocarbamiquesLeurs dérivés ayant des atomes d'azote de groupes thiocarbamiques liés à des atomes de carbone de cycles aromatiques à six chaînons
C07F 7/08 - Composés comportant une ou plusieurs liaisons C—Si
6.
USE OF EZH2 INHIBITORS FOR THE TREATMENT OF AORTIC VALVE STENOSIS
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Fraineau, Sylvain
Perzo, Nicolas
Abrégé
Aortic valve stenosis (AS) also called also called Calcific aortic valve disease (CAVD), is the most frequent valvular heart disease in Europe and affects more than 1 in 4 people over 65 years old. AS progression from fibrotic thickening to valvular leaflets calcification leads to heart failure development and eventually to death within 2 to 5 years after symptoms occurrence. The inventors now show that EZH2 inhibition with GSK-126 and GSK-343 directly regulates monocyte and M1 toward M2 macrophage differentiation, reducing VIC deactivation and osteoblastic transition and thus represents an attractive therapeutic target to prevent AS progression. Therefore, the present invention relates to use of EZH2 inhibitors for the treatment of aortic valve stenosis.
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
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
7.
USE OF AN ACID WHEY TO STIMULATE THE GERMINATION OF A PLANT POLLEN GRAIN
The invention relates to the use of an acid whey to stimulate the germination of a plant pollen grain and/or to stimulate the elongation of the pollen tube of said pollen grain. According to another aspect, the invention relates to a method for stimulating the germination of a plant pollen grain and/or for stimulating the elongation of the pollen tube of said pollen grain, in which an acid whey is applied to the plant in an amount sufficient to stimulate the germination of the pollen grain and/or to stimulate the elongation of the pollen tube of said pollen grain. According to a final aspect, the invention relates to a composition comprising (i) an acid whey and (ii) a brown seaweed extract.
A01N 63/10 - Animaux Substances produites par des animaux ou obtenues à partir de ceux-ci
A01P 21/00 - Régulateurs de croissance des végétaux
8.
MEASUREMENT SYSTEM COMPRISING A SPECTROMETRY DEVICE WITH AN ION CYCLOTRON RESONANCE MASS SPECTROMETER AND AN ELECTRONIC DEVICE FOR CLASSIFYING A SET OF PRODUCTS AMONG A PLURALITY OF CLASSES
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
TOTALENERGIES ONETECH (France)
Inventeur(s)
Mendes Siqueira, Anna Luiza
Lacroix-Andrivet, Oscar
Afonso, Carlos
Abrégé
The invention relates to a measurement system (10) comprising: - a spectrometry device (12) comprising an ionisation source (14), a separation module (16) and a detector (18) capable of measuring an ion flow from the sample, the spectrometry device (12) being an ion cyclotron resonance mass spectrometer; and - an electronic device (20) for classifying a set of products among a plurality of classes, the device comprising a module (22) for acquiring a respective mass spectrum for each of the products of the set; a module (24) for determining, from each mass spectrum, a group of one or more compounds included in the product associated with the respective mass spectrum; a module (26) for generating a table comprising, for each of the products of the set, a value of the intensity of the ion flow for each compound present in the product; a module (28) for assigning, to each product of the set, a respective class from among the plurality of classes by applying a multivariate statistical algorithm to the generated table.
G16C 20/20 - Identification d’entités moléculaires, de leurs parties ou de compositions chimiques
H01J 49/00 - Spectromètres pour particules ou tubes séparateurs de particules
G01N 27/62 - Recherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques en recherchant l'ionisation des gaz, p. ex. des aérosolsRecherche ou analyse des matériaux par l'emploi de moyens électriques, électrochimiques ou magnétiques en recherchant les décharges électriques, p. ex. l'émission cathodique
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (France)
Inventeur(s)
Prado, Soizic
Pavesi, Coralie
Xavier, Franck
Abrégé
The present invention relates to a compound of formula (I) or (I'): A-X (I) A-L-B (I') wherein A and B are each independently a radical of the following formula (II) : The present invention also relates to the use of a compound of formula (I) or (I') as a colouring agent, in particular as a red colouring agent. The present invention also relates to a cosmetic, a pharmaceutical composition or a food product comprising at least one compound of formula (I) or (I').
C09B 23/01 - Colorants méthiniques ou polyméthiniques, p. ex. du type cyanine caractérisés par la chaîne méthinique
A23L 5/00 - Préparation ou traitement des aliments ou produits alimentaires en généralAliments ou produits alimentaires ainsi obtenusLeurs matériaux
C09B 23/10 - Colorants méthiniques ou polyméthiniques, p. ex. du type cyanine caractérisés par la chaîne méthinique contenant un nombre pair de groupes CH
INSTITUT NATIONAL UNIVERSITAIRE JEAN-FRANCOIS CHAMPOLLION (France)
UNIVERSITE TOULOUSE III - PAUL SABATIER (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
Inventeur(s)
Benmoussa, Khaddouj
Bonnafe, Elsa
Coste, Agnès
Leprince, Jérôme
Pipy, Bernard
Treilhou, Michel
Abrégé
The present invention relates to an isolated peptide consisting of a sequence of 3 to 39 amino acids derived from the amino acid sequence SEQ ID NO: 1, said peptide having a sequence of amino acids selected from the group consisting of:
a) sequences of 3 to 39 amino acids comprising at least the residues 6 to 8 of SEQ ID NO: 1, and
b) sequences of 3 to 39 amino acids having at least 70% identity with said sequence in a).
C07K 14/435 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Adriouch, Sahil
Lemarcis, Théo
Tardif- San Martin, Virginie
Abrégé
Co-signaling immunotherapy, via immune checkpoint inhibitors (ICIs), such as ipilimumab (anti-CTLA-4) or nivolumab (anti-PD-1), has revolutionized cancer treatment. However, reinvigorating tumor-infiltrating T cell cytotoxicity has revealed cardiac toxicity in a subset of patients. The inventors found lower transcriptomic expression of CTLA-4 in eccentric hypertrophic cardiomyopathy model, associated with higher cardiac total IgG amount and less B cell infiltration, compared to concentric hypertrophic cardiomyopathy. The present invention relates to a method of treating dilated cardiomyopathy (DCM) in a subject in need thereof comprising a step of administering to said subject a therapeutically effective amount of a cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) molecule.
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 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
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
A61P 9/04 - Agents inotropes, c.-à-d. stimulants de la contraction cardiaqueMédicaments pour le traitement de l'insuffisance cardiaque
12.
METHODS AND PHARMACEUTICAL COMPOSITIONS COMPRISING D1-LIKE DOPAMINE RECEPTOR AGONIST FOR THE TREATMENT OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY DISEASE
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Bellien, Jérémy
Guerrot, Dominique
Abrégé
Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary disease affecting 1 in 1,000 to 1 in 2,500 individuals worldwide. The inventor's study performed in 6 patients with ADPKD supports the hypothesis that the stimulation of the dopaminergic system, in particular D1-like family of dopamine receptors, may improve endothelial function by restoring cilia length and mechanotransductory capacity. The inventors carefully assess whether the deficiency in endothelial polycystin-1 and cilia promotes or potentiates both cardiovascular and renal alterations, to explore the mechanisms involved, and to propose and test new pharmacological approaches, in particular targeting the dopaminergic system, to prevent complications of ADPKD. The present invention relates to a method of treating autosomal dominant polycystic kidney disease (ADPKD) in a subject in need thereof comprising a step of administering said subject with a therapeutically effective amount of a D1-like family of dopamine receptors agonist through a continuous systemic delivery.
A61K 31/381 - Composés hétérocycliques ayant le soufre comme hétéro-atome d'un cycle ayant des cycles à cinq chaînons
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
A61P 13/12 - Médicaments pour le traitement des troubles du système urinaire des reins
13.
METHOD FOR RECYCLING CONCRETE CONSTRUCTION AND/OR DEMOLITION WASTE
INSTITUT NATIONAL POLYTECHNIQUE DE TOULOUSE (France)
UNIVERSITÉ TOULOUSE III - PAUL SABATIER (France)
INSA ROUEN NORMANDIE (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Bourgeois, Florent
Cyr, Martin
Estel, Lionel
Gurdjos, Célia
Abrégé
The present invention relates to a method for recycling concrete waste from construction and/or deconstruction, comprising at least one step of microwave processing of concrete blocks, at least one step of mechanical processing, and at least one step of carbonation of recycled concrete aggregates and/or recycled concrete fines; the invention also relates to a recycling installation for carrying out the recycling method and to recycled concrete aggregates obtained by the steps of microwave processing of concrete blocks and mechanical processing.
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE LILLE (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
INSTITUT PASTEUR DE LILLE (France)
UNIVERSITÉ DE LILLE (France)
Inventeur(s)
Pinet, Florence
Mulder, Paul
Abrégé
Exacerbation of heart failure, better known as acute decompensated heart failure (HF), is characterized by dyspnea, edema and fatigue, and is a growing medical problem. The inventors demonstrated that transient O-GlcNAcase inhibition would be suitable for the treatment of acute decompensated heart failure. In particular they used two recently developed models mimicking acute decompensation of heart failure patients, and deciphered mechanisms susceptible to be involved in this cardiovascular protection, with a focus on post-translational cardiac protein modifications and metabolic remodeling. Accordingly, the present invention relates to the use of O-GlcNAcase inhibitors for the treatment of acute decompensated heart failure.
INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
Inventeur(s)
Bellien, Jérémy
Durand, Eric
Richard, Vincent
Abrégé
Aortic valve stenosis (AS), is the most frequent valvular heart disease in Europe and affects more than 1 in 4 people over 65 years old. AS progression from fibrotic thickening to valvular leaflets calcification leads to heart failure development and eventually to death within 2 to 5 years after symptoms occurrence. The inventors now show that endothelin receptor type B (ETB) activation with an agonist decreased the calcium content of VIC. Therefore, the present invention relates to the use of endothelin receptor type B (ETB) agonists for the treatment of aortic valve stenosis.
A61K 38/00 - Préparations médicinales contenant des peptides
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
16.
PRODUCTION OF THERAPEUTIC ANTIBODIES BY THE MICROALGAE PHAEODACTYLUM TRICORNUTUM
Phaeodactylum tricornutumPhaeodactylum tricornutum, as well as optimized culture conditions of said microalgae cells. Altogether, the present invention provides new systems for producing high amounts of monoclonal antibodies, functional fragments or derivatives thereof, in microalgae.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSA ROUEN NORMANDIE (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventeur(s)
Balieu, Sébastien
Renard, Pierre-Yves
Montero-Hadjadje, Maité
Vitale, Nicolas
Cocq, Aurélien
Schlichter, Antoine
Ferlet, Rémy
Haefele, Alexandre
Riachy, Lina
Wolf, Alexander
Abrégé
The present invention relates to the field of glycerophospholipids (GPL) usable for biological studies. In particular, the invention relates to novel GPL compounds comprising at least one reactive function not interfering with the biological processes, to their process of preparation and to their uses in different applications.
G01N 33/00 - Recherche ou analyse des matériaux par des méthodes spécifiques non couvertes par les groupes
C07F 9/6561 - Composés hétérocycliques, p. ex. contenant du phosphore comme hétéro-atome du cycle contenant des systèmes de plusieurs hétérocycles déterminants condensés entre eux ou condensés avec un carbocycle ou un système carbocyclique commun, avec ou sans autres hétérocycles non condensés
C07F 9/117 - Esters des acides phosphoriques avec des alcools cycloaliphatiques
C07F 9/655 - Composés hétérocycliques, p. ex. contenant du phosphore comme hétéro-atome du cycle comportant des atomes d'oxygène, avec ou sans atomes de soufre, de sélénium ou de tellure, comme uniques hétéro-atomes du cycle
18.
DEVICE FOR RECOVERING MAGNETIC GRAINS FROM SINTERED MAGNETS OR PLASTIC MAGNETS
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Inventeur(s)
Le Breton, Jean-Marie
Maat, Nicolas
Aymonier, Cyril
Abrégé
The invention concerns a method and a device for retrieving, from an object A, elements G present in a matrix M, characterized in that it comprises at least the following steps: bringing said abject A into contact with a dense fluid Fd with a molar mass greater than 2 g mol−1 under temperature T1 and pressure P1 conditions suitable for transforming the intergranular phase and for releasing the elements G, (302), modifying the temperature T2 and/or pressure P2 values to stop the reaction transforming the intergranular phase, (303), and recovering the elements G separated front the matrix M (304).
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p. ex. des rognures, pour produire des métaux non ferreux ou leurs composés
C22B 59/00 - Obtention des métaux des terres rares
H01F 41/02 - Appareils ou procédés spécialement adaptés à la fabrication ou à l'assemblage des aimants, des inductances ou des transformateursAppareils ou procédés spécialement adaptés à la fabrication des matériaux caractérisés par leurs propriétés magnétiques pour la fabrication de noyaux, bobines ou aimants
B09B 3/80 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant une étape d'extraction
H01F 1/057 - Alliages caractérisés par leur composition contenant des métaux des terres rares et des métaux de transition magnétiques, p. ex. SmCo5 et des éléments IIIa, p. ex. Nd2Fe14B
19.
CARBALDEHYDE OXIMES AS BUTYRYLCHOLINESTERASE REACTIVATORS
ÉTAT FRANÇAIS REPRÉSENTÉ PAR LA DIRECTION CENTRALE DU SERVICE DE SANTÉ DES ARMÉES (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUÉES DE ROUEN (France)
Inventeur(s)
Probst, Nicolas
Braïki, Anissa
Dubois-Geoffroy, Pierre
Jean, Ludovic
Renard, Pierre-Yves
Dias, José
Nachon, Florian
Abrégé
Compounds are used in the reactivation of butyrylcholinesterase. Such compounds are useful in the treatment or prevention of intoxication with at least one organophosphorus nerve agent. Pharmaceutical compositions and kits include the compounds, and compounds per se.
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 31/4709 - Quinoléines non condensées contenant d'autres hétérocycles
A61K 31/4545 - Pipéridines non condensées, p. ex. pipérocaïne contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p. ex. pipampérone, anabasine
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
A61K 31/506 - PyrimidinesPyrimidines hydrogénées, p. ex. triméthoprime non condensées et contenant d'autres hétérocycles
A61K 31/5377 - 1,4-Oxazines, p. ex. morpholine non condensées et contenant d'autres hétérocycles, p. ex. timolol
A61K 31/437 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques le système hétérocyclique contenant un cycle à cinq chaînons ayant l'azote comme hétéro-atome du cycle, p. ex. indolizine, bêta-carboline
A61K 31/4375 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec un azote comme seul hétéro-atome d'un cycle condensés en ortho ou en péri avec des systèmes hétérocycliques le système hétérocyclique contenant un cycle à six chaînons ayant l'azote comme hétéro-atome du cycle, p. ex. quinolizines, naphtyridines, berbérine, vincamine
20.
METHODS FOR DETECTING THE PRESENCE OF CORONAVIRUS-SPECIFIC ANTIBODIES IN A SUBJECT
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
Inventeur(s)
Boyer, Olivier
Drouot, Laurent
Abrégé
Coronaviridae is a family of enveloped, positive-sense, single-stranded RNA viruses. The viral genome is 26-32 kilobases in length. In late December 2019, a new betacoronavirus SARS-CoV-2 has emerged in Wuhan China. The World Health Organization has named the severe pneumonia caused by this new coronavirus COVID-19 (for Corona Virus Disease 2019, WHO, 2020). To fight against the COVID-19 pandemic in a long term, in addition to the containment measures implemented in many countries, reliable diagnostic methods are highly desirable. In particular, the development and availability of tests for the detection and quantification of anti-SARS-CoV-2 antibodies in subjects with COVID-19 is of strong diagnostic interest. The present fulfils this need. In particular, the inventors developed an 15 Adressable Laser Beads ImmunoAssay (ALBIA) method based on the use of particles conjugated with a coronaviral polypeptides (S1,S2, S2′, N, PL-Pro). More particularly, the inventors show that detection and titration of anti-SARS-CoV-2 Spike S1 IgG and IgM antibodies are feasible by said method.
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
21.
USE OF TREM-1 FOR PREDICTING AND PREVENTING POSTOPERATIVE COMPLICATIONS AFTER CARDIAC SURGERY WITH CARDIOPULMONARY BY-PASS
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
SORBONNE UNIVERSITÉ (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
UNIVERSITÉ PARIS CITÉ (France)
Inventeur(s)
Ait-Oufella, Hafid
Clavier, Thomas
Abrégé
Cardiopulmonary by-pass (CBP) during cardiac surgery leads to deleterious systemic inflammatory response. In a prospective cohort of 46 patients older than 18 years and eligible for non-urgent cardiac surgery with CPB, measurement of sTREM-1 in the plasma was performed immediately after the onset of anesthesia (H0) and 2 and 24 hours after CBP. After CBP, sTREM-1 significantly increased at H2 and at H24 (p<0.001). Based on both baseline sTREM-1 levels and variations, 3 patterns of patients were identified. Profile 1 group with high baseline sTREM-1 levels as well as high increase, developed more severe organ failure after CBP with higher norepinephrine dose at H24, higher SOFA score and more frequently AKI at both H24 and H48. Finally, acute atrial fibrillation at H24 was more frequent in profile 1 when compared to profile 2/3. Profile 1 group had longer ICU and hospital length of stay (LOS). In conclusion, early sTREM-1 variations after cardiac surgery identified a group of patients at high risk for post-operative AKI and prolonged length of stay. Thus sTREM-1 represents a relevant biomarker and biotarget in cardiac surgery with CBP.
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
22.
USE OF BRANCHED CHAIN FATTY ACIDS (BCFAS) FOR THE TREATMENT OF INTESTINAL INFLAMMATION
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Ribet, David
Dechelotte, Pierre
Ezzine, Chaima
Abrégé
The gut microbiota produces a wide variety of metabolites, which interact with intestinal cells by modulating either gene transcription or post-translational modifications of gut proteins. The effect of gut commensal bacteria on SUMOylation, an essential ubiquitin-like modification in intestinal physiology, remains however unknown. Here, the inventors show that branched chain fatty acids (BCFAs) increase protein SUMOylation in different intestinal cell lines. They demonstrated that the hyperSUMOylation induced by BCFAs inhibits the activation of the NF-κB pathway by blocking the degradation of the inhibitory factor ΙκBα in response to TNFα. This results in a decrease in pro-inflammatory cytokines expression as well as a decrease in intestinal epithelial permeability in response to TNFα. Accordingly, the present invention relates to the use of Branched Chain Fatty Acids (BCFAs) for the treatment of diseases associated with intestinal inflammation such as Inflammatory Bowel Diseases and Irritable Bowel Syndrome.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Fraineau, Sylvain
Perzo, Nicolas
Abrégé
Aortic valve stenosis (AS) also called also called Calcific aortic valve disease (CAVD), is the most frequent valvular heart disease in Europe and affects more than 1 in 4 people over 65 years old. AS progression from fibrotic thickening to valvular leaflets calcification leads to heart failure development and eventually to death within 2 to 5 years after symptoms occurrence. The inventors now show that EZH2 inhibition with GSK-126 and GSK-343 directly regulates monocyte and Ml toward M2 macrophage differentiation, reducing VIC deactivation and osteoblastic transition and thus represents an attractive therapeutic target to prevent AS progression. Therefore, the present invention relates to use of EZH2 inhibitors for the treatment of aortic valve stenosis.
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
A61K 31/5377 - 1,4-Oxazines, p. ex. morpholine non condensées et contenant d'autres hétérocycles, p. ex. timolol
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
INSTITUT NATIONAL DES SCIENCES APPLIQUÉES DE ROUEN (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
ECOLE NATIONALE SUPERIEURE D'INGENIEURS DE CAEN (France)
UNIVERSITE DE CAEN NORMANDIE (France)
Inventeur(s)
Ayadi, Firas
Nachbaur, Virginie
Pralong, Valérie
Abrégé
The present invention is in the field of the extraction of lithium from a material comprising lithium and at least another metal. In particular, the invention concerns a process of extraction of lithium at least, from a material comprising lithium and at least another metal.
The invention relates to the use of an acid whey to stimulate the germination of a plant pollen grain and/or to stimulate the elongation of the pollen tube of said pollen grain. According to another aspect, the invention relates to a method for stimulating the germination of a plant pollen grain and/or for stimulating the elongation of the pollen tube of said pollen grain, in which an acid whey is applied to the plant in an amount sufficient to stimulate the germination of the pollen grain and/or to stimulate the elongation of the pollen tube of said pollen grain. According to a final aspect, the invention relates to a composition comprising (i) an acid whey and (ii) a brown seaweed extract.
The invention relates to the use of an acid whey to stimulate the germination of a plant pollen grain and/or to stimulate the elongation of the pollen tube of said pollen grain. According to another aspect, the invention relates to a method for stimulating the germination of a plant pollen grain and/or for stimulating the elongation of the pollen tube of said pollen grain, in which an acid whey is applied to the plant in an amount sufficient to stimulate the germination of the pollen grain and/or to stimulate the elongation of the pollen tube of said pollen grain. According to a final aspect, the invention relates to a composition comprising (i) an acid whey and (ii) a brown seaweed extract.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
ECOLE NORMALE SUPERIEURE DE LYON (France)
UNIVERSITE CLAUDE BERNARD LYON 1 (France)
Inventeur(s)
Gerard, Stéphane
Bouillon, Jean-Philippe
Bentaher, Abderrazzaq
Henon, Eric
Jacquot, Jacky
Sapi, Janos
Velard, Frédéric
Abrégé
The invention relates to compounds of Formula I:
The invention relates to compounds of Formula I:
The invention relates to compounds of Formula I:
or pharmaceutically acceptable solvates thereof, as well as their use in the treatment and/or prevention of diseases or conditions associated with a dysfunction of CFTR channel activity, in particular cystic fibrosis.
A61K 31/501 - PyridazinesPyridazines hydrogénées non condensées et contenant d'autres hétérocycles
A61K 45/06 - Mélanges d'ingrédients actifs sans caractérisation chimique, p. ex. composés antiphlogistiques et pour le cœur
C07D 409/06 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant uniquement des atomes de carbone aliphatiques
C07D 401/04 - 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 liaison directe de chaînon cyclique à chaînon cyclique
28.
NEW CYCLODEXTRIN DIMERS AND THEIR USES THEREOF AS CHEMICAL SCAVENGERS
Centre national de la recherche scientifique (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Université de Rouen-Normandie (France)
Frat Français représenté par le Délégué Général pour I'Armement (France)
Inventeur(s)
Estour, François
Bosco, Michaël
Abrégé
This invention concerns a compound having the following formula (I):
This invention concerns a compound having the following formula (I):
wherein either R1 is a —Y-Nu group and R2 is H, or R1 is H and R2 is a —Y-Nu group and H, wherein Y is, inter alia, —O—(CH2)m—, and m is 1, 2, or 3.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT D'OPTIQUE THEORIQUE ET APPLIQUEE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUTE NATIONAL DE LA SANTE ET DE LA RECHERCE MEDICALE (France)
Inventeur(s)
Feyeux, Maxime
Alessandri, Kevin
Lecourtois, Magalie
Miguel, Laetitia
Nassoy, Pierre
Rovelet Lecrux, Anne
Abrégé
The present invention relates to a method for in-vitro production of mammalian neurons expressing the 6 isoforms of the Tau protein (2N4R, 1N4R, 0N4R, 2N3R, 1N3R, 0N3R), comprising a step of neuronal differentiation, in which cellular microcompartments are cultivated for a period of 5 weeks to 100 weeks, each one comprising a hollow hydro gel capsule surrounding post-mitotic neuronal cells and an extracellular matrix, the neuronal differentiation step being carried out in a bioreactor, the cellular microcompartments being kept in suspension in an enclosure of the bioreactor containing a neuronal differentiation medium.
Centre national de la recherche scientifique (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
MDB TEXINOV (France)
Inventeur(s)
Estour, François
Cornelio, Benedetta
Vandesteene, Marie
Ferreira, Isabelle
Abrégé
The present invention relates to a method for modifying a textile yarn or fabric by immobilising a cyclodextrin derivative on said yarn or fabric, said process comprising a step (a) of contacting said textile yarn or fabric with said cyclodextrin derivative and with a bridging agent such as 1,2,3,4-butanetetracarboxylic acid, optionally in the presence of a catalyst such as cyanamide,
The present invention relates to a method for modifying a textile yarn or fabric by immobilising a cyclodextrin derivative on said yarn or fabric, said process comprising a step (a) of contacting said textile yarn or fabric with said cyclodextrin derivative and with a bridging agent such as 1,2,3,4-butanetetracarboxylic acid, optionally in the presence of a catalyst such as cyanamide,
to obtain a textile yarn or fabric on which the cyclodextrin derivative of formula (I) is immobilised.
A62D 3/33 - Procédés pour rendre les substances chimiques nuisibles inoffensives ou moins nuisibles en effectuant un changement chimique dans les substances par réaction avec des agents chimiques par fixation chimique de la substance nuisible, p. ex. par chélation ou complexation
POLYSILOXANE POLYMER COMPOSITIONS INCLUDING A PHTHALOCYANINE RING OR A PORPHYRIN RING, THEIR PREPARATION PROCESS AND THEIR USE AS STATIONARY PHASES IN HIGH TEMPERATURE GAS CHROMATOGRAPHY
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
SORBONNE UNIVERSITÉ (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Giusti, Pierre
Piparo, Marco
Jousset, Gaëlle
Maniquet, Adrien
Cardinael, Pascal
Tintas, Mihaela-Liliana
Mallet, Jean-Maurice
Abrégé
121232322-O-], where Ar is selected from 1,4- disubstituted benzene, 4,4'- disubstituted 1,1'- biphenyl and 4,4'- disubstituted phenoxybenzene. These copolymers are particularly suited for forming stationary phases for gas chromatography, especially high-temperature gas chromatography.
C08G 77/16 - Polysiloxanes contenant du silicium lié à des groupes contenant de l'oxygène à des groupes hydroxyle
C08G 77/20 - Polysiloxanes contenant du silicium lié à des groupes aliphatiques non saturés
C08G 77/26 - Polysiloxanes contenant du silicium lié à des groupes organiques contenant des atomes autres que le carbone, l'hydrogène et l'oxygène groupes contenant de l'azote
C08G 77/00 - Composés macromoléculaires obtenus par des réactions créant dans la chaîne principale de la macromolécule une liaison contenant du silicium, avec ou sans soufre, azote, oxygène ou carbone
C09D 183/08 - Polysiloxanes contenant du silicium lié à des groupes organiques contenant des atomes autres que le carbone, l'hydrogène et l'oxygène
Institut National de la Sante et de la Recherche Medicale (INSERM) (France)
Universite de Rouen Normandie (France)
Inventeur(s)
Grumolato, Luca
Abrégé
The instant invention relates to a method for labeling endonuclease-treated cells, comprising the steps of a) providing cells or a composition comprising cells; b) bringing into contact said cells or said composition with: —at least one endonuclease suitable for targeting a genomic region of interest in said cells, or a vector suitable for expressing said endonuclease in said cells; —at least one first nucleic acid suitable for introducing one or more silent mutation(s) in said genomic region by homology-directed repair (HDR), and optionally one or more non-silent mutation(s); and —at least one second nucleic acid suitable for introducing one or more silent mutation(s) in said genomic region by homology-directed repair (HDR), but distinct from the silent mutations of the first nucleic acid; thereby labeling endonuclease-treated cells.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCH MÉDICALE) (France)
Inventeur(s)
Ruminy, Philippe
Marchand, Vinciane
Abdel Sater, Ahmad
Viailly, Pierre-Julien
Lanic, Marie Delphine
Jardin, Fabrice
Lae, Marick
Viennot, Mathieu
Abrégé
The invention concerns a method for diagnosing a cancer in a subject, comprising a step of RT-MLPA on a biological sample obtained from the subject, in which the RT-MLPA step is carried out using at least one pair of probes comprising at least one probe chosen among the probes with SEQ ID NO: 1 to 13, and/or the probes with SEQ ID NO: 96 to 99, and/or the probes with SEQ ID NO: 866 to 938, and/or the probes with SEQ ID NO: 940 to 1104, and/or SEQ ID NO: 211 to 1312, and/or the probes with SEQ ID NO: 96 to 99, and/or the probes with SEQ ID NO: 1105 to 1107 and/or the probe with SEQ ID NO: 939 and/or the probes with SEQ ID NO: 1108 to 1123, each of the probes being fused, at at least one end, with a priming sequence, and at least one of the probes of the pair comprising a molecular barcode sequence.
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
34.
USE OF MICROALGAL EXOPOLYSACCHARIDES AS TEXTURIZING AGENTS
A61Q 5/00 - Préparations pour les soins des cheveux
A61Q 19/00 - Préparations pour les soins de la peau
A61K 8/9711 - Phaeophycota ou Phaeophyta [algues brunes], p. ex. Fucus
35.
NOVEL DEPOLYMERIZED EXOPOLYSACCHARIDES, DERIVED FROM MICROALGAE, METHOD FOR PREPARING SAME, AND USES THEREOF IN COSMETICS FOR DELAYING THE EFFECTS OF SKIN AGEING
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
Inventeur(s)
Goncalves, Olivier
Pruvost, Jérémy
Massé, Anthony
Decamp, Antoine
Probert, Ian
Maugard, Thierry
Arnaudin, Ingrid
Bridiau, Nicolas
Toucheteau, Claire
Le Cerf, Didier
Picton, Luc
Dulong, Virginie
Rihouey, Christophe
Gaignard, Clément
Laroche, Céline
Pierre, Guillaume
Delattre, Cédric
Dubessay, Pascal
Michaud, Philippe
Abrégé
The present application relates to novel depolymerized exopolysaccharides derived from microalgae, the method for obtaining same from microalgae, and their use for increasing the production of collagen and/or hyaluronic acid, in order to delay the effects of skin ageing.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Vella, Angela
Houard, Jonathan
Hideur, Ammar
Arnoldi, Laurent
Rigutti, Lorenzo
Abrégé
A tomographic atom probe includes an analysis chamber intended to analyze a sample of material in the form of a nanotip mounted on an anti-vibration support, the nanotip being brought to a temperature of between 0 kelvin and ambient temperature, the nanotip being biased at an adjustable voltage of between 1 kV and 15 kV, the analysis chamber comprising a position-sensitive and time of flight-sensitive ion detector. The atom probe comprises a generator for generating high-peak-intensity single-cycle ultrashort terahertz pulses, the analysis chamber comprising optical means for focusing the terahertz pulses, the focusing of the terahertz pulses causing the atoms of the nanotip to evaporate through the field effect without thermal effects. The terahertz pulses are generated by a femtosecond pulsed laser emitting very high-power ultrashort optical pulses at a high rate.
The present invention relates to a natriuretic peptide selected from the group made up of (i) osteocrin, an osteocrin propeptide of osteocrin derivative, (ii) a lebetin, a lebetin fragment, or a lebetin or lebetin fragment derivative, and (iii) an ANP peptide, ANP propeptide or ANP peptide derivative, for the use thereof in a method for therapeutically treating a bacterial infection associated with a bacterial biofilm in a subject, wherein said natriuretic peptide disperses the bacterial biofilm. In a particular embodiment, the natriuretic peptide is used in combination with an antibiotic.
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 31/407 - 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 systèmes hétérocycliques, p. ex. kétorolac, physostigmine
A61K 31/496 - Pipérazines non condensées contenant d'autres hétérocycles, p. ex. rifampine, thiothixène ou sparfloxacine
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE(INSERM) (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
CENTRE HENRI BECQUEREL (France)
Inventeur(s)
Ruminy, Philippe
Marchand, Vinciane
Bobée, Victor
Jardin, Fabrice
Abrégé
An accurate gene expression based classifier, and the associated assay, which can participate to the establishment a lymphoma diagnosis and to the evaluation of individual prognosis markers are provided. Through its use, one may distinguish subtypes of lymphomas such as ABC DLBCL, GCB DLBCL, PMBL, FL, MCL, SLL and MZL from one another.
G16B 25/10 - Profilage de l’expression de gènes ou de protéinesEstimation ou normalisation de ratio d’expression
C12N 15/10 - Procédés pour l'isolement, la préparation ou la purification d'ADN ou d'ARN
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
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Vurpillot, François
Larde, Rodrigue
Klaes, Benjamin
Da Costa, Gérald
Abrégé
A method for imaging a material to atomic scale by means of a field-ion microscope having a vacuum chamber configured to accommodate the material prepared in the form of a tip and an imaging gas, and an ion detector is provided. The method includes application of a DC electrical potential (VDC) and of a pulsed electrical potential, of which the maximum pulse value is denoted Vimp, so that the tip erodes for a potential value equal to VDC+Vimp; acquisition, by the detector between at least two pulses of the pulsed potential, of series of at least two ion images of the impacts of the ions repelled by the tip onto the detector; and calculation of a quantity characteristic of a trend of the erosion of the tip based on the series of ion images acquired and the adjustment, between each series of images, of the values of VDC and of Vimp such that the quantity characteristic of the trend and the ratio VDC/Vimp remain constant.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Boyer, Olivier
Lemieux, Alexandre
Golinski, Marie-Laure
Joly, Pascal
Abrégé
Pemphigus is a group of rare autoimmune diseases that causes blistering of the skin and mucous membranes, and includes pemphigus vulgaris (PV) and pemphigus foliaceus (PF). Patients with pemphigus have various combinations of autoantibodies to keratinocyte muscarinic acetylcholine receptor subtype M3 (CHRM3), the secretory pathway Ca 2+ /Mn 2+ -ATPase 10 isoform 1 (SPCA1), and desmocollin 3 (DSC3). However, there is still a need to characterize these autoantibodies and optimize their detection for diagnosis and disease monitoring. The inventors now developed an ALBIA for the 3 proteins and successfully detected and quantified the presence of auto-antibodies directed against each of these antigens in pemphigus patients. Furthermore, they showed that detection and quantification of anti-SPCA1 and/or anti-CHRM3 15 were also associated to a risk of relapse in the first year following the treatment using rituximab as a first-line agent. The present invention thus relates to methods for detecting the presence of said pemphigus-specific autoantibodies.
G01N 33/564 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour complexes immunologiques préexistants ou maladies auto-immunes
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
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Anouar, Youssef
Pothion, Hugo
Marie, Jean-Paul
Guerout, Nicolas
Lihrmann, Isabelle
Abrégé
Peripheral nerve injury (PNI) is frequent and many patients suffer lifelong disabilities in severe cases. Now, the inventors tested in a facial nerve regeneration model the therapeutic effect of a short mimetic peptide, named PSELT, which derives from SELENOT, an essential thioredoxinlike selenoprotein endowed with neuroprotective and antioxidant activities. The effects observed were compared to those found after an end-to-end suture used as a gold standard treatment. In addition, PSELT was used in presence or absence of transplanted, nestin-positive boundary cap-derived stem cells (BCSC) to assess the effect of the peptide in combination with a cell therapy. The analyses revealed that PSELT-treated animals exhibit a better motor recovery in terms of protraction amplitude and velocity of vibrissae compared to control and end-sutured animals. Moreover, administration of PSELT following injury enhanced muscle innervation, axonal elongation and myelination of newly formed nerve fibers. PSELT displayed a better therapeutic effect than xenotransplantation of BCSC. When PSELT was used in the presence of BCSC, no additional beneficial effect was observed in comparison to PSELT treatment alone. Accordingly, the present invention relates to use of PSELT for the treatment of nerve injuries.
JANSSEN SCIENCES IRELAND UNLIMITED COMPANY (Irlande)
UNIVERSITE DE ROUEN NORMANDIE (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Inventeur(s)
Beigelman, Leonid
Guillemont, Jérôme Émile Georges
Piettre, Serge
Brioche, Julien
Sunchu, Prabhakar
Abrégé
The present disclosure relates to ethylene-bridged nucleic acid (ENA) compounds, which may find use in therapy and/or prophylaxis. These ENA compounds may also find use as building blocks for preparing oligonucleotides, said oligonucleotides also finding use in therapy and/or prophylaxis. These compounds may be mono- or oligonucleotide derivatives comprising at least one of the following fragment: Formula (IV), wherein R1166 alkyl moiety.
C07H 19/00 - Composés contenant un hétérocycle partageant un hétéro-atome du cycle avec un radical saccharideNucléosidesMononucléotidesLeurs anhydro-dérivés
C07H 21/00 - Composés contenant au moins deux unités mononucléotide comportant chacune des groupes phosphate ou polyphosphate distincts liés aux radicaux saccharide des groupes nucléoside, p. ex. acides nucléiques
ÉTAT FRANÇAIS REPRÉSENTÉ PAR LA DIRECTION CENTRALE DU SERVICE DE SANTÉ DES ARMÉES (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUÉES DE ROUEN (France)
Inventeur(s)
Probst, Nicolas
Braïki, Anissa
Dubois-Geoffroy, Pierre
Jean, Ludovic
Renard, Pierre-Yves
Dias, José
Nachon, Florian
Abrégé
The present invention relates to compounds for their use in the reactivation of butyrylcholinesterase. Such compounds are useful in the treatment or prevention of the intoxication with at least one organophosphorus nerve agent. The invention also relates to pharmaceutical compositions and kits comprising said compounds, and compounds per se.
C07D 401/06 - 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 carbonée contenant uniquement des atomes de carbone aliphatiques
C07D 401/14 - 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 au moins trois hétérocycles
C07D 409/06 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant uniquement des atomes de carbone aliphatiques
C07D 417/06 - 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 deux hétérocycles liés par une chaîne carbonée contenant uniquement des atomes de carbone aliphatiques
A61K 31/44 - Pyridines non condenséesLeurs dérivés hydrogénés
ETAT FRANCAIS REPRESENTE PAR LA DIRECTION CENTRALE DU SERVICE DE SANTE DES ARMEES (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
Inventeur(s)
Probst, Nicolas
Braiki, Anissa
Dubois-Geoffroy, Pierre
Jean, Ludovic
Renard, Pierre-Yves
Dias, Jose
Nachon, Florian
Abrégé
The present invention relates to compounds for their use in the reactivation of butyrylcholinesterase. Such compounds are useful in the treatment or prevention of the intoxication with at least one organophosphorus nerve agent. The invention also relates to pharmaceutical compositions and kits comprising said compounds, and compounds per se.
C07D 401/06 - 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 carbonée contenant uniquement des atomes de carbone aliphatiques
C07D 401/14 - 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 au moins trois hétérocycles
C07D 409/06 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant uniquement des atomes de carbone aliphatiques
C07D 417/06 - 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 deux hétérocycles liés par une chaîne carbonée contenant uniquement des atomes de carbone aliphatiques
45.
METHOD FOR DETERMINING AND PREDICTING THE OXIDATION SENSITIVITY OF A BITUMEN
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Inventeur(s)
Lacroix-Andrivet, Oscar
Hubert-Roux, Marie
Afonso, Carlos
Mendes Siqueira, Anna Luiza
Delayens, Franck
Abrégé
The invention relates to a method for analysing the ageing stability of a bituminous binder, comprising: • a) analysing the bituminous binder by means of negative ion mode electrospray ionisation mass spectrometry and measuring the relative abundance of oxygenated compounds and non-oxygenated compounds comprising at least one nitrogen atom; • b) carrying out accelerated ageing of the bituminous binder; • c) analysing the bituminous binder, aged according to step b), after different time periods by means of negative ion mode electrospray ionisation mass spectrometry and measuring the relative abundance of oxygenated compounds and non-oxygenated compounds comprising at least one nitrogen atom; • d) comparing the measurements of the relative abundances of oxygenated compounds and non-oxygenated compounds comprising at least one nitrogen atom obtained in step a) and in step c).
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE REIMS CHAMPAGNE-ARDENNE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE REIMS (France)
Inventeur(s)
Bellien, Jérémy
Djerada, Zoubir
Abrégé
The growing prevalence of obesity and type 2 diabetes complicates risk and clinical management by potentiating and/or exacerbating hypertension, hyperlipidemia, atherosclerosis and cardiomyopathy, leading to increasing use of the term “cardiometabolic disease” (CMD) to encompass the many facets of this complex syndrome. The inventors assessed the role of the soluble epoxide hydrolase (she) phosphatase domain in metabolism and cardiovascular system, by generating sEH phosphatase knock-in (KI) animals (rats). They unexpectedly revealed that inhibition of the phosphatase domain of sEH improves cardiac systolic function, decreases body weight and increases insulin sensitivity. Moreover under high fat diet, the animals have a decreased body weight gain, were protected against the development of insulin resistance, hepatic steatosis and cardiac hypertrophy. Inhibition of the phosphatase domain of sEH thus represents a new pharmacological target in the treatment of cardiometabolic diseases.
A61K 31/421 - 1,3-Oxazoles, p. ex. pémoline, triméthadione
A61K 31/255 - Esters, p. ex. nitroglycérine, sélénocyanates d'acides oxygénés du soufre ou de leurs thio-analogues
A61K 31/198 - Alpha-amino-acides, p. ex. alanine ou acide édétique [EDTA]
A61K 31/407 - 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 systèmes hétérocycliques, p. ex. kétorolac, physostigmine
A61K 31/41 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à cinq chaînons avec plusieurs hétéro-atomes cycliques, l'un au moins étant l'azote, p. ex. tétrazole
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p. ex. antidiabétiques
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
47.
METHODS AND TOPICAL PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF SKIN MICROVASCULAR DYSFUNCTION
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ GRENOBLE ALPES (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE GRENOBLE (France)
Inventeur(s)
Bellien, Jérémy
Bounoure, Frédéric
Skiba, Mohamed
Savina, Yann
Roustit, Matthieu
Cracowski, Jean-Luc
Abrégé
Microvascular dysfunction remains a major contributor to the development of skin complications. The inventors assessed the impact of the local inhibition of soluble epoxide hydrolase (sEH), which metabolizes vasodilator and anti-inflammatory epoxyeicosanoids, on the diabetic skin microvascular dysfunction. The inventors have therefore developed some formulations of sEH inhibitors (GSK2256294 and t-AUCB) for topical administration. In particular, they show that an aqueous gel containing 400 mg/L t-AUCB dissolved in 50% dimethy lsulfo xide (DMSO) allowed a stable and continuous diffusion of t-AUCB from 2 hours after application on skin pig ears to over a period of 24 h. Compared to a control gel, the gel with t-AUCB did not significantly modify the basal skin blood flow but improved the altered hyperemic response of db/db mice 2 hours after application. The results show that the topical administration of a sEH inhibitor improves the skin microcirculatory function, representing a promising pharmacological approach to prevent the development of skin complications especially in diabetic patients.
A61K 31/17 - Amides, p. ex. acides hydroxamiques ayant le groupe N-C(O)-N ou N-C(S)-N, p. ex. urée, thiourée, carmustine
A61K 31/197 - Acides carboxyliques, p. ex. acide valproïque ayant un groupe amino les groupes amino et carboxyle étant liés à la même chaîne carbone acyclique, p. ex. acide gamma-aminobutyrique [GABA], bêta-alanine, acide epsilon-aminocaproïque ou acide pantothénique
A61K 31/4468 - Pipéridines non condensées, p. ex. pipérocaïne ayant un atome d'azote lié directement en position 4, p. ex. clébopride, fentanyl
A61K 31/53 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec trois azote comme seuls hétéro-atomes d'un cycle, p. ex. chlorazanil, mélamine
A61P 17/00 - Médicaments pour le traitement des troubles dermatologiques
A61P 9/14 - VasoprotecteursAntihémorroïdauxMédicaments pour le traitement des varicesStabilisateurs capillaires
A61P 3/10 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose de l'hyperglycémie, p. ex. antidiabétiques
48.
METHODS FOR DETECTING THE PRESENCE OF CORONAVIRUS-SPECIFIC ANTIBODIES IN A SUBJECT
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
Inventeur(s)
Boyer, Olivier
Drouot, Laurent
Abrégé
Coronaviridae is a family of enveloped, positive-sense, single-stranded RNA viruses. The viral genome is 26–32 kilobases in length. In late December 2019, a new betacoronavirus SARS-CoV-2 has emerged in Wuhan China. The World Health Organization has named the severe pneumonia caused by this new coronavirus COVID-19 (for Corona Virus Disease 2019, WHO, 2020). To fight against the COVID-19 pandemic in a long term, in addition to the containment measures implemented in many countries, reliable diagnostic methods are highly desirable. In particular, the development and availability of tests for the detection and quantification of anti-SARS-CoV-2 antibodies in subjects with COVID-19 is of strong diagnostic interest. The present fulfils this need. In particular, the inventors developed an 15 Adressable Laser Beads ImmunoAssay (ALBIA) method based on the use of particles conjugated with a coronaviral polypeptides (S1,S2, S2', N, PL-Pro). More particularly, the inventors show that detection and titration of anti-SARS-Cov-2 Spike S1 IgG and IgM antibodies are feasible by said method.
G01N 33/569 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour micro-organismes, p. ex. protozoaires, bactéries, virus
49.
PROCESS OF EXTRACTION OF LITHIUM FROM A MATERIAL COMPRISING LITHIUM AND AT LEAST ANOTHER METAL
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
ECOLE NATIONALE SUPERIEURE D'INGENIEURS DE CAEN (France)
UNIVERSITE DE CAEN NORMANDIE (France)
Inventeur(s)
Ayadi, Firas
Nachbaur, Virginie
Pralong, Valerie
Abrégé
The present invention is in the field of the extraction of lithium from a material comprising lithium and at least another metal. In particular, the invention concerns a process of extraction of lithium at least, from a material comprising lithium and at least another metal.
INSTITUT NATIONAL DES SCIENCES APPLIQUÉES DE ROUEN (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
ECOLE NATIONALE SUPERIEURE D'INGENIEURS DE CAEN (France)
UNIVERSITE DE CAEN NORMANDIE (France)
Inventeur(s)
Ayadi, Firas
Nachbaur, Virginie
Pralong, Valérie
Abrégé
The present invention is in the field of the extraction of lithium from a material comprising lithium and at least another metal. In particular, the invention concerns a process of extraction of lithium at least, from a material comprising lithium and at least another metal.
The present invention relates to a device for spectroscopic measurements, in particular X-ray diffraction (XRD), temperature-resolved second harmonic generation (TR-SHG) or infrared (IR) measurements, which prevents the formation of condensation (dew) or ice (frost) when carrying out spectroscopic measurements in sub-ambient temperature conditions and to a method of spectroscopic measurements with said device.
G01N 21/35 - 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 infrarouge
G01N 23/20033 - Porte-échantillons ou leurs supports pourvus de moyens de commande de la température ou de chauffage
G01N 23/207 - Diffractométrie, p. ex. en utilisant une sonde en position centrale et un ou plusieurs détecteurs déplaçables en positions circonférentielles
52.
N2-ARYLMETHYL-4-HALOALKYL-PYRIDAZIN-3-ONE CFTR MODULATORS FOR THE TREATMENT OF CYSTIC FIBROSIS
INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (C.N.R.S.) (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
ECOLE NORMALE SUPERIEURE DE LYON (France)
UNIVERSITE CLAUDE BERNARD LYON 1 (UCBL) (France)
Inventeur(s)
Gerard, Stephane
Bouillon, Jean-Philippe
Bentaher, Abderrazzaq
Henon, Eric
Jacquot, Jacky
Sapi, Janos
Velard, Frederic
Abrégé
The invention relates to compounds of formula I (I) or pharmaceutically acceptable solvates thereof, as well as their use in the treatment and/or prevention of diseases or conditions associated with a dysfunction of CFTR channel activity, particularly cystic fibrosis.
A61K 31/501 - PyridazinesPyridazines hydrogénées non condensées et contenant d'autres hétérocycles
A61P 11/00 - Médicaments pour le traitement des troubles du système respiratoire
C07D 409/06 - Composés hétérocycliques contenant plusieurs hétérocycles, au moins un cycle comportant des atomes de soufre comme uniques hétéro-atomes du cycle contenant deux hétérocycles liés par une chaîne carbonée contenant uniquement des atomes de carbone aliphatiques
53.
N2-ARYLMETHYL-4-HALOALKYL-PYRIDAZIN-3-ONE CFTR MODULATORS FOR THE TREATMENT OF CYSTIC FIBROSIS
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
Inventeur(s)
Gerard, Stéphane
Bouillon, Jean-Philippe
Bentaher, Abderrazzaq
Henon, Eric
Jacquot, Jacky
Sapi, Janos
Velard, Frédéric
Abrégé
The invention relates to compounds of formula I (I) or pharmaceutically acceptable solvates thereof, as well as their use in the treatment and/or prevention of diseases or conditions associated with a dysfunction of CFTR channel activity, particularly cystic fibrosis.
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
INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
UNIVERSITE DE PICARDIE JULES VERNE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
CENTRE HOSPITALIER UNIVERSITAIRE D'AMIENS (France)
Inventeur(s)
Bellien, Jeremy
Six, Isabelle
Mentaverri, Romuald
Kamel, Said
Abrégé
The inventors demonstrate that the phosphatase and hydrolase domains of soluble epoxide hydrolase (sEH) regulate the cardiovascular calcification process and revealed that inhibition of the phosphatase domain of sEH could represent a new pharmacological target in the prevention of cardiovascular calcification. The present invention thus relates to a therapeutically effective amount of an inhibitor of phosphatase activity of soluble epoxide hydrolase for use in a method of treating cardiovascular calcification in a subject in need thereof.
A61K 31/41 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à cinq chaînons avec plusieurs hétéro-atomes cycliques, l'un au moins étant l'azote, p. ex. tétrazole
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
A61K 31/198 - Alpha-amino-acides, p. ex. alanine ou acide édétique [EDTA]
C12Q 1/42 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir une hydrolase une phosphatase
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
MDB TEXINOV (France)
Inventeur(s)
Estour, François
Cornelio, Benedetta
Vandesteene, Marie
Ferreira, Isabelle
Abrégé
The present invention relates to a method for modifying a yarn or a textile fabric by immobilising a cyclodextrin derivative on the yarn or fabric, the method comprising a step (a) of contacting the yarn or textile fabric with the cyclodextrin derivative and a coupling agent such as 1,2,3,4-butanetetracarboxylic acid, optionally in the presence of a catalyst such as cyanamide, in order to obtain a yarn or textile fabric on which the cyclodextrin derivative of formula (I) is immobilised.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Vella, Angela
Houard, Jonathan
Hideur, Ammar
Arnoldi, Laurent
Rigutti, Lorenzo
Abrégé
The invention relates to a tomographic atom probe comprising an analysis chamber (20) intended for analysing a sample (E) of material in the form of a nanotip mounted on an anti-vibration support (21), the nanotip being brought to a temperature between 0 Kelvin and room temperature, the nanotip being polarised at an adjustable voltage between 1 kV and 15 kV, the analysis chamber comprising an ion detector (27) sensitive to position and time of flight. The atom probe according to the invention comprises a generator (10) of ultrashort monocycle terahertz pulses with high peak intensity, the analysis chamber comprising optical means (26) for focusing said terahertz pulses, the focusing of the terahertz pulses leading to the evaporation of the atoms of the nanotip by field effect without thermal effects. The terahertz pulses are generated by a femtosecond pulsed laser emitting ultrashort optical pulses of very high power at a high rate.
The present invention relates to a natriuretic peptide selected from the group made up of (i) osteocrin, an osteocrin propeptide or osteocrin derivative, (ii) a lebetin, a lebetin fragment, or a lebetin or lebetin fragment derivative, and (iii) an ANP peptide, ANP propeptide or ANP peptide derivative, for the use thereof in a method for therapeutically treating a bacterial infection associated with a bacterial biofilm in a subject, wherein said natriuretic peptide disperses the bacterial biofilm. In a particular embodiment, the natriuretic peptide is used in combination with an antibiotic.
A61L 2/16 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des substances chimiques
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
59.
OSTEOCRIN, LEBETIN OR ANP FOR DESTROYING BACTERIAL BIOFILMS
The present invention relates to a natriuretic peptide selected from the group made up of (i) osteocrin, an osteocrin propeptide or osteocrin derivative, (ii) a lebetin, a lebetin fragment, or a lebetin or lebetin fragment derivative, and (iii) an ANP peptide, ANP propeptide or ANP peptide derivative, for the use thereof in a method for therapeutically treating a bacterial infection associated with a bacterial biofilm in a subject, wherein said natriuretic peptide disperses the bacterial biofilm. In a particular embodiment, the natriuretic peptide is used in combination with an antibiotic.
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61L 2/16 - Procédés ou appareils de désinfection ou de stérilisation de matériaux ou d'objets autres que les denrées alimentaires ou les lentilles de contactAccessoires à cet effet utilisant des substances chimiques
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT D'OPTIQUE THEORIQUE ET APPLIQUEE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
Inventeur(s)
Feyeux, Maxime
Alessandri, Kevin
Lecourtois, Magalie
Miguel, Laetitia
Nassoy, Pierre
Rovelet Lecrux, Anne
Abrégé
The present invention relates to a method for in-vitro production of mammalian neurons expressing the 6 isoforms of the Tau protein (2N4R, 1N4R, 0N4R, 2N3R, 1N3R, 0N3R), comprising a step of neuronal differentiation, in which cellular microcompartments are cultivated for a period of 5 weeks to 100 weeks, each one comprising a hollow hydrogel capsule surrounding post-mitotic neuronal cells and an extracellular matrix, the neuronal differentiation step being carried out in a bioreactor, the cellular microcompartments being kept in suspension in an enclosure of the bioreactor containing a neuronal differentiation medium.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
CENTRE HENRI BECQUEREL (France)
Inventeur(s)
Ruminy, Philippe
Marchand, Vinciane
Bobee, Victor
Jardin, Fabrice
Abrégé
Classification of B-Cell non-Hodgkin Lymphomas An accurate gene expression based classifier, and the associated assay, which can participate to the establishment a lymphoma diagnosis and to the evaluation of individual prognosis markers are provided. Through the use of the invention, one may distinguish subtypes of lymphomas such as ABC DLBCL, GCB DLBCL, PMBL, FL, MCL, SLL and MZL from one another.
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
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
CENTRE HENRI BECQUEREL (France)
Inventeur(s)
Ruminy, Philippe
Marchand, Vinciane
Bobée, Victor
Jardin, Fabrice
Abrégé
Classification of B-Cell non-Hodgkin Lymphomas An accurate gene expression based classifier, and the associated assay, which can participate to the establishment a lymphoma diagnosis and to the evaluation of individual prognosis markers are provided. Through the use of the invention, one may distinguish subtypes of lymphomas such as ABC DLBCL, GCB DLBCL, PMBL, FL, MCL, SLL and MZL from one another.
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
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 31/635 - Composés contenant des groupes para-N-benzènesulfonyl-N-, p. ex. sulfanilamide, p-nitrobenzènesulfonohydrazide contenant un hétérocycle, p. ex. sulfadiazine
A61P 3/00 - Médicaments pour le traitement des troubles du métabolisme
A61P 9/00 - Médicaments pour le traitement des troubles du système cardiovasculaire
A61P 25/00 - Médicaments pour le traitement des troubles du système nerveux
A61P 17/02 - Médicaments pour le traitement des troubles dermatologiques pour traiter les blessures, les ulcères, les brûlures, les cicatrices, les cheloïdes, ou similaires
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE CAEN NORMANDIE (France)
CENTRE HOSPITALIER RÉGIONAL UNIVERSITAIRE DE CAEN (France)
ETABLISSEMENT FRANÇAIS DU SANG (EFS) (France)
Inventeur(s)
Latouche, Jean-Baptiste
Toutirais, Olivier
Couture, Alexandre
Le Mauff Quester, Brigitte
Abrégé
CD4 T cell help is essential to promote robust cytotoxic T cell responses and could be harnessed to improve outcomes of cancer immunotherapy. To induce CD4+ T cell responses, the inventors have developed artificial antigen presenting cells (AAPCs) that derived from a mouse fibroblast cell line genetically modified to express a single human leukocyte antigen class II molecule (HLA-DR), the human CD80 costimulation as well as CD54 and CD58 adhesion molecules and that constitutively express an antigen (Ag) in peptide or protein forms in different compartments involved in the major histocompatibility complex class II Ag presentation pathway. In particular, the inventors show that the AAPC expressing the Ag peptide in the endoplasmic reticulum (ER) or protein at the plasma membrane were more potent than Epstein-Barr virus (EBV)-transformed B cells to present epitopes to specific CD4+ T- cells. Interestingly, AAPC targeting the Ag peptide in the ER was more efficient than peptide-pulsed AAPC or autologous APC to amplify memory Ag-specific CD4+ T cells that harbor a Th1 profile and express granzyme B. So, the AAPC system is a reliable and standardized tool to generate a high number of Ag-specific CD4+ with effector functions useful for a cancer adoptive immunotherapy. Thus, the present invention relates to an artificial antigen presenting cell that constitutively expresses an antigen along with a HLA-class II molecule and uses thereof in particular for amplifying and/or activating a population of antigen-specific CD4+ T cells.
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (France)
ECOLE NATIONALE SUPERIEURE D'INGENIEURS DE CAEN (France)
Inventeur(s)
Reboul, Vincent
Franck, Xavier
Glachet, Thomas
Marzag, Hamid
Abrégé
The present invention concerns a novel method for synthesising diazirines, that may or may not be enriched in nitrogen-15, from amino acids or imines, via a one-pot synthesis method, comprising the reaction of the starting amino acid or imine with ammonia, which may or may not be enriched in nitrogen-15, and a hypervalent iodine oxidant. The present invention also relates to a method for synthesising ammonia enriched in nitrogen-15. The invention also concerns certain diazirines of formula (I) likely to be obtained by the claimed synthesis method, and also refers to the 15N2-diazirines of formula (I'). The claimed diazirines can be used in photoaffinity labelling. The 15N2-diazirines can also be used in hyperpolarisation, in particular in the medical imaging field.
C07D 229/02 - Composés hétérocycliques contenant des cycles de moins de cinq chaînons contenant deux atomes d'azote comme uniques hétéro-atomes du cycle contenant des cycles à trois chaînons
67.
NOVEL PATHWAY FOR THE SYNTHESIS OF DIAZIRINES, THAT MAY OR MAY NOT BE ENRICHED IN NITROGEN-15
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN (INSA) (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (France)
ECOLE NATIONALE SUPERIEURE D'INGENIEURS DE CAEN (France)
Inventeur(s)
Reboul, Vincent
Franck, Xavier
Glachet, Thomas
Marzag, Hamid
Abrégé
The present invention concerns a novel method for synthesising diazirines, that may or may not be enriched in nitrogen-15, from amino acids or imines, via a one-pot synthesis method, comprising the reaction of the starting amino acid or imine with ammonia, which may or may not be enriched in nitrogen-15, and a hypervalent iodine oxidant. The present invention also relates to a method for synthesising ammonia enriched in nitrogen-15. The invention also concerns certain diazirines of formula (I) likely to be obtained by the claimed synthesis method, and also refers to the 1522-diazirines of formula (I'). The claimed diazirines can be used in photoaffinity labelling. The 1522-diazirines can also be used in hyperpolarisation, in particular in the medical imaging field.
C07D 229/02 - Composés hétérocycliques contenant des cycles de moins de cinq chaînons contenant deux atomes d'azote comme uniques hétéro-atomes du cycle contenant des cycles à trois chaînons
INSERM (INSTITUT DE LA SANTE ET DE LA RECHERCHE MEDICALE) (France)
Inventeur(s)
Ruminy, Philippe
Marchand, Vinciane
Abdel Sater, Ahmad
Viailly, Pierre-Julien
Lanic, Marie Delphine
Jardin, Fabrice
Lae, Marick
Viennot, Mathieu
Abrégé
The invention concerns a method for diagnosing a cancer in a subject, comprising a step of RT-MLPA on a biological sample obtained from the subject, in which the RT-MLPA step is carried out using at least one pair of probes comprising at least one probe chosen among the probes with SEQ ID NO: 1 to 13, and/or the probes with SEQ ID NO: 96 to 99, and/or the probes with SEQ ID NO: 866 to 938, and/or the probes with SEQ ID NO: 940 to 1104, and/or SEQ ID NO: 211 to 1312, and/or the probes with SEQ ID NO: 96 to 99, and/or the probes with SEQ ID NO: 1105 to 1107 and/or the probe with SEQ ID NO: 939 and/or the probes with SEQ ID NO: 1108 to 1123, each of the probes being fused, at at least one end, with a priming sequence, and at least one of the probes of the pair comprising a molecular barcode sequence.
C12Q 1/6853 - Réactions d’amplification d’acides nucléiques utilisant des amorces ou des matrices modifiées
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
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
Inventeur(s)
Ruminy, Philippe
Marchand, Vinciane
Abdel Sater, Ahmad
Viailly, Pierre-Julien
Lanic, Marie Delphine
Jardin, Fabrice
Lae, Marick
Viennot, Mathieu
Abrégé
The invention concerns a method for diagnosing a cancer in a subject, comprising a step of RT-MLPA on a biological sample obtained from the subject, in which the RT-MLPA step is carried out using at least one pair of probes comprising at least one probe chosen among the probes with SEQ ID NO: 1 to 13, and/or the probes with SEQ ID NO: 96 to 99, and/or the probes with SEQ ID NO: 866 to 938, and/or the probes with SEQ ID NO: 940 to 1104, and/or SEQ ID NO: 211 to 1312, and/or the probes with SEQ ID NO: 96 to 99, and/or the probes with SEQ ID NO: 1105 to 1107 and/or the probe with SEQ ID NO: 939 and/or the probes with SEQ ID NO: 1108 to 1123, each of the probes being fused, at at least one end, with a priming sequence, and at least one of the probes of the pair comprising a molecular barcode sequence.
C12Q 1/6853 - Réactions d’amplification d’acides nucléiques utilisant des amorces ou des matrices modifiées
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
70.
METHODS AND TOPICAL PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF SKIN MICROVASCULAR DYSFUNCTION
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ GRENOBLE ALPES (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE GRENOBLE (France)
Inventeur(s)
Bellien, Jérémy
Bounoure, Frédéric
Skiba, Mohamed
Savina, Yann
Roustit, Matthieu
Cracowski, Jean-Luc
Abrégé
ttttt-AUCB did not significantly modify the basal skin blood flow but improved the altered hyperemic response of db/db mice 2 hours after application. The results show that the topical administration of a sEH inhibitor improves the skin microcirculatory function, representing a promising pharmacological approach to prevent the development of skin complications especially in diabetic patients.
A61K 31/53 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à six chaînons avec trois azote comme seuls hétéro-atomes d'un cycle, p. ex. chlorazanil, mélamine
A61K 31/17 - Amides, p. ex. acides hydroxamiques ayant le groupe N-C(O)-N ou N-C(S)-N, p. ex. urée, thiourée, carmustine
A61K 31/445 - Pipéridines non condensées, p. ex. pipérocaïne
A61P 17/02 - Médicaments pour le traitement des troubles dermatologiques pour traiter les blessures, les ulcères, les brûlures, les cicatrices, les cheloïdes, ou similaires
A61P 9/00 - Médicaments pour le traitement des troubles du système cardiovasculaire
71.
USE OF INHIBITORS OF PHOSPHATASE ACTIVITY OF SOLUBLE EPOXIDE FOR THE TREATMENT OF CARDIOMETABOLIC DISEASES
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ DE REIMS CHAMPAGNE-ARDENNE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE REIMS (France)
Inventeur(s)
Bellien, Jérémy
Djerada, Zoubir
Abrégé
The growing prevalence of obesity and type 2 diabetes complicates risk and clinical management by potentiating and/or exacerbating hypertension, hyperlipidemia, atherosclerosis and cardiomyopathy, leading to increasing use of the term "cardiometabolic disease" (CMD) to encompass the many facets of this complex syndrome. The inventors assessed the role of the soluble epoxide hydrolase (she) phosphatase domain in metabolism and cardiovascular system, by generating sEH phosphatase knock-in (KI) animals (rats). They unexpectedly revealed that inhibition of the phosphatase domain of sEH improves cardiac systolic function, decreases body weight and increases insulin sensitivity. Moreover under high fat diet, the animals have a decreased body weight gain, were protected against the development of insulin resistance, hepatic steatosis and cardiac hypertrophy. Inhibition of the phosphatase domain of sEH thus represents a new pharmacological target in the treatment of cardiometabolic diseases.
A61P 3/08 - Médicaments pour le traitement des troubles du métabolisme de l'homéostase du glucose
A61P 9/00 - Médicaments pour le traitement des troubles du système cardiovasculaire
A61K 31/198 - Alpha-amino-acides, p. ex. alanine ou acide édétique [EDTA]
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 31/41 - Composés hétérocycliques ayant l'azote comme hétéro-atome d'un cycle, p. ex. guanéthidine ou rifamycines ayant des cycles à cinq chaînons avec plusieurs hétéro-atomes cycliques, l'un au moins étant l'azote, p. ex. tétrazole
A61K 31/421 - 1,3-Oxazoles, p. ex. pémoline, triméthadione
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES-ROUEN (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Hideur, Ammar
Haboucha, Adil
Bultel, Arnaud
Idlahcen, Said
Godin, Thomas
Abrégé
A laser source for emitting a group of pulses, includes a primary laser source suitable for emitting at least one primary laser pulse; at least one interferometer suitable for forming, from the primary laser pulse, a plurality of secondary laser pulses, each interferometer comprising at least one delay line allowing two secondary laser pulses to be temporally separated, by a delay comprised between 50 ps and 10 ns; and a single-mode amplifying optical fiber intended to receive the secondary laser pulses, in order to form as output a group of spatially superposed pulses.
H01S 3/10 - Commande de l'intensité, de la fréquence, de la phase, de la polarisation ou de la direction du rayonnement, p. ex. commutation, ouverture de porte, modulation ou démodulation
H01S 3/00 - Lasers, c.-à-d. dispositifs utilisant l'émission stimulée de rayonnement électromagnétique dans la gamme de l’infrarouge, du visible ou de l’ultraviolet
H01S 3/23 - Agencement de plusieurs lasers non prévu dans les groupes , p. ex. agencement en série de deux milieux actifs séparés
H01S 3/094 - Procédés ou appareils pour l'excitation, p. ex. pompage utilisant le pompage optique par de la lumière cohérente
C07K 14/435 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
74.
Austenitic alloy with high aluminum content and associated design process
Centre National de la Recherche Scientifique (France)
Institut National des Sciences Appliquées Rouen Normandie (France)
Inventeur(s)
Couvrat, Mathieu
Facco, Antoine
Pareige, Cristelle
Abrégé
An austenitic alloy based on nickel, chromium and iron, and having a high aluminum content, intended for use at a given operating temperature (Ts) between 900° C. and 1200° C., the alloy comprising the following elements, in weight percent: chromium between 20% and 32%, nickel between 30% and 60%, aluminum between 3.5% and 6%, carbon between 0.4% and 0.7%, titanium between 0.05% and 0.3%, niobium and/or tantalum between 0.6% and 2%, an element, composed of at least one rare earth and/or hafnium, between 0.002% and 0.1%, silicon between 0 and 0.5%, manganese between 0 and 0.5%, tungsten between 0 and 2%, and iron as the balance of the elements in the alloy. The alloy has less than 1% by volume of an intermetallic B2-NiAl phase and less than 1% by volume of an alpha prime phase rich in chromium, after subjecting the alloy to an operating temperature (Ts).
C22C 19/05 - Alliages à base de nickel ou de cobalt, seuls ou ensemble à base de nickel avec du chrome
C22F 1/10 - Modification de la structure physique des métaux ou alliages non ferreux par traitement thermique ou par travail à chaud ou à froid du nickel ou du cobalt ou de leurs alliages
C22C 38/44 - Alliages ferreux, p. ex. aciers alliés contenant du chrome et du nickel et du molybdène ou du tungstène
C22C 38/48 - Alliages ferreux, p. ex. aciers alliés contenant du chrome et du nickel et du niobium ou du tantale
C22C 38/50 - Alliages ferreux, p. ex. aciers alliés contenant du chrome et du nickel et du titane ou du zirconium
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
Inventeur(s)
Gonzalez, Bruno
Marret, Stéphane
Bekri, Soumeya
Laquerriere, Annie
Lecointre, Maryline
Leger, Cécile
Abrégé
The invention relates to a placental growth factor (PlGF) as a drug for use in the prevention and/or treatment of a neurological disorder, particularly a neurodevelopmental disorder. Such disorders are particularly linked to a cortical impairment in subjects having been exposed to alcohol in utero. The present invention also relates to a pharmaceutical composition or to a product comprising PlGF for the same therapeutic uses.
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
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
A61P 25/32 - Médicaments pour le traitement des troubles du système nerveux des états d'abus ou de dépendance à l'alcool
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
76.
ANTI-FROSTING AND ANTI-DEW DEVICE FOR SPECTROSCOPIC MEASUREMENTS
The present invention relates to a device for spectroscopic measurements, in particular X-ray diffraction (XRD), temperature-resolved second harmonic generation (TR-SHG) or infrared (IR) measurements, which prevents the formation of condensation (dew) or ice (frost) when carrying out spectroscopic measurements in sub-ambient temperature conditions and to a method of spectroscopic measurements with said device.
The present invention relates to a device for spectroscopic measurements, in particular X-ray diffraction (XRD), temperature-resolved second harmonic generation (TR-SHG) or infrared (IR) measurements, which prevents the formation of condensation (dew) or ice (frost) when carrying out spectroscopic measurements in sub-ambient temperature conditions and to a method of spectroscopic measurements with said device.
Embodiments of the present disclosure relate to an isolated peptide consisting of a sequence of 3 to 39 amino acids derived from the amino acid sequence SEQ ID NO: 1, said peptide having a sequence of amino acids selected from the group consisting of: a) sequences of 3 to 39 amino acids comprising at least the residues 6 to 8 of SEQ ID NO: 1, and b) sequences of 3 to 39 amino acids having at least 70% identity with said sequence in a).
C07K 7/06 - Peptides linéaires ne contenant que des liaisons peptidiques normales ayant de 5 à 11 amino-acides
C07K 7/08 - Peptides linéaires ne contenant que des liaisons peptidiques normales ayant de 12 à 20 amino-acides
A61K 38/00 - Préparations médicinales contenant des peptides
C07K 14/435 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
ECOLE POLYTECHNIQUE (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
Inventeur(s)
Roca I Cabarrocas, Pere
Chen, Wanghua
Duguay, Sébastien
Pareige, Philippe
Azrak, Edy, Edward
Abrégé
The present invention relates to an alloy structure comprising germanium (Ge) and tin (Sn), characterised in that it takes the form of a filament having a diameter of less than 200 nanometers, referred to as a nanofilament, and in that the alloy contains at least 10% tin (Sn) in atomic percent (at%); and to a method for preparing such a structure, and uses thereof.
C30B 23/00 - Croissance des monocristaux par condensation d'un matériau évaporé ou sublimé
C30B 29/46 - Composés contenant du soufre, du sélénium ou du tellure
C30B 29/60 - Monocristaux ou matériaux polycristallins homogènes de structure déterminée caractérisés par leurs matériaux ou par leur forme caractérisés par la forme
80.
Method and system for recovering magnetic grains from sintered magnets or plastic magnets
C22B 7/00 - Mise en œuvre de matériaux autres que des minerais, p. ex. des rognures, pour produire des métaux non ferreux ou leurs composés
C22B 59/00 - Obtention des métaux des terres rares
H01F 41/02 - Appareils ou procédés spécialement adaptés à la fabrication ou à l'assemblage des aimants, des inductances ou des transformateursAppareils ou procédés spécialement adaptés à la fabrication des matériaux caractérisés par leurs propriétés magnétiques pour la fabrication de noyaux, bobines ou aimants
B09B 3/80 - Destruction de déchets solides ou transformation de déchets solides en quelque chose d'utile ou d'inoffensif impliquant une étape d'extraction
H01F 1/057 - Alliages caractérisés par leur composition contenant des métaux des terres rares et des métaux de transition magnétiques, p. ex. SmCo5 et des éléments IIIa, p. ex. Nd2Fe14B
81.
METHODS AND KITS FOR DETERMINING WHETHER A SUBJECT HAS OR IS AT RISK OF HAVING OF AN AUTOIMMUNE MYOPATHY
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITÉ PARIS DESCARTES (France)
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (France)
ASSISTANCE PUBLIQUE-HÔPITAUX DE PARIS (APHP) (France)
Inventeur(s)
Boyer, Olivier
Drouot, Laurent
Jouen, Fabienne
Chan-Tchi-Song, Philippe
Boitard, Christian
Bourdenet, Gwladys
Abrégé
Autoimmune myopathy (AIM) represents a group of severe inflammatory diseases. Around 60% of patients with AIM have myositis-specific auto-antibodies (aAbs). Thus, the search for aAbs has substantially improved their diagnosis and may also inform on their prognosis, notably when there is an associated risk of cancer. Accordingly, the discovery of 10 new aAbs will help to improve the diagnosis of AIM. The present invention fulfils the need. In a cohort of 671 patients suffering from patients suffering from AIM, the inventors show that a minor percentage of them were positive for the present of MDH2 aAbs. No patient was found positive for this Ab in other autoimmune diseases. Accordingly, detection of anti-MDH2 aAbs would be suitable for the diagnosis of AIM.15
G01N 33/564 - Tests immunologiquesTests faisant intervenir la formation de liaisons biospécifiquesMatériaux à cet effet pour complexes immunologiques préexistants ou maladies auto-immunes
82.
METHODS AND PHARMACEUTICAL COMPOSITIONS FOR PROVIDING CARDIOPROTECTION IN SUBJECTS WHO EXPERIENCED A MYOCARDIAL INFARCTION
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
UNIVERSITÀ DELLA CALABRIA (Italie)
Inventeur(s)
Anouar, Youssef
Angelone, Tommaso
Boukhzar, Loubna
Rocca, Carmine
Abrégé
Myocardial infarction occurs when the blood supply to part of the heart is interrupted causing some heart cells to die. The immediate goal is to restore blood flow to the patient as quickly as possible. However, a significant delay in restoring blood flow leads to a second condition known as ischemia-reperfusion injury that can develop gradually after an ischemic event and may cause irreversible damage to tissues. Successful cardioprotection is limited by a relatively small number of therapeutic targets. The present invention fulfils this need. The inventors indeed showed that a Selenoprotein T (SelT) derived peptide, SelT43-52 (PSELT), is effective against ischemia/reperfusion (I/R) injury.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
ICAHN SCHOOL OF MEDECINE OF MOUNT SINAI (USA)
Inventeur(s)
Grumolato, Luca
Guernet, Alexis
Aaronson, Stuart
Anouar, Youssef
Abrégé
The invention relates to methods for preventing or treating resistance to EGFR inhibitors in cancer patients. More particularly, after performing a screen for small molecules potentially capable of countering cancer resistance to EGFR TKI, inventors identified the multikinase inhibitor sorafenib, which has the property, in combination with EGFR TKI, to prevent the enrichment of tumor cells containing mutations responsible for NSCLC resistance to first and third generation EGFR TKI. These data indicate that this multikinase inhibitor can prevent resistance to several generations of EGFR TKI. These in vitro data were confirmed in an in vivo xenograft mouse model of NSCLC. Finally these data were reproduced in cancer cells using SC-1, a sorafenib analogue. Accordingly, the invention relates to a method of preventing and/or treating cancer resistance to treatment with an epidermal growth factor receptor (EGFR) inhibitor in a subject in need thereof comprising administering to the subject sorafenib drug or sorafenib analogue, alone or in combination with an EGFR inhibitor.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICAL (INSERM) (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Grumolato, Luca
Abrégé
Provided herein are methods and kits for labeling endonuclease-treated cells. The methods comprise: contacting the cells to be labelled with at least one endonuclease suitable for targeting a genomic region of interest, and first and second nucleic acids suitable for introducing one or more silent (or optionally non-silent) mutation(s) in the genomic region by homology-directed repair (HDR). The mutation(s) introduced by the first nucleic acid differ from the mutation(s) introduced by the second nucleic acid.
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Inventeur(s)
Le Breton, Jean-Marie
Maât, Nicolas
Nachbaur, Virginie
Abrégé
Disclosed is a method and system for recovering at least rare earth elements from within an object A consisting of at least one first rare earth portion or a mixture of rare earth elements and a second metal portion. The method includes a solvothermal treatment step that places the object in contact with a fluid for causing at least one rare earth portion and/or mixture of rare earth elements and the metal portion to oxidize in order to separate same, the value of the reaction temperature Tr is selected according to the nature of the object, the reaction following a R-M→R(X)x+M(X)y scheme, where R is the rare earth element or a mixture of rare earth elements, M is the transition metal, and (X) is a group which depends on the fluid used.
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
UNIVERSITÉ DE PICARDIE JULES VERNE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
CENTRE HOSPITALIER UNIVERSITAIRE D'AMIENS (France)
Inventeur(s)
Bellien, Jérémy
Six, Isabelle
Mentaverri, Romuald
Kamel, Saïd
Abrégé
The inventors demonstrate that the phosphatase and hydrolase domains of soluble expoxide hydrolase (sEH) regulate the cardiovascular calcification process and revealed that inhibition of the phosphatase domain of sEH could represent a new pharmacological target in the prevention of cardiovascular calcification. The present invention thus relates to a therapeutically effective amount of an inhibitor of phosphatase activity of soluble epoxide hydrolase for use in a method of treating cardiovascular calcification in a subject in need thereof.
A61K 31/00 - Préparations médicinales contenant des ingrédients actifs organiques
A61K 31/198 - Alpha-amino-acides, p. ex. alanine ou acide édétique [EDTA]
A61K 31/255 - Esters, p. ex. nitroglycérine, sélénocyanates d'acides oxygénés du soufre ou de leurs thio-analogues
C12Q 1/42 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir une hydrolase une phosphatase
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
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUÉES - ROUEN (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Hideur, Ammar
Haboucha, Adil
Bultel, Arnaud
Idlahcen, Said
Godin, Thomas
Abrégé
According to one aspect, the present description relates to a laser source for emitting a group of pulses, comprising: a primary laser source (22) that is suitable for emitting at least one primary laser pulse; at least one interferometer (24) that is suitable for forming, from said primary laser pulse, a plurality of secondary lases pulses, each interferometer comprising at least one delay line allowing two secondary laser pulses to be temporally separated by a delay comprised between 50 ps and 10 ns; and a single-mode amplifying optical fibre that is intended to receive the secondary laser pulses, in order to form, as output, a group of pulses that are spatially superposed.
H01S 3/00 - Lasers, c.-à-d. dispositifs utilisant l'émission stimulée de rayonnement électromagnétique dans la gamme de l’infrarouge, du visible ou de l’ultraviolet
H01S 3/094 - Procédés ou appareils pour l'excitation, p. ex. pompage utilisant le pompage optique par de la lumière cohérente
H01S 3/10 - Commande de l'intensité, de la fréquence, de la phase, de la polarisation ou de la direction du rayonnement, p. ex. commutation, ouverture de porte, modulation ou démodulation
G01N 21/71 - Systèmes dans lesquels le matériau analysé est excité de façon à ce qu'il émette de la lumière ou qu'il produise un changement de la longueur d'onde de la lumière incidente excité thermiquement
H01S 3/23 - Agencement de plusieurs lasers non prévu dans les groupes , p. ex. agencement en série de deux milieux actifs séparés
G01J 3/42 - Spectrométrie d'absorptionSpectrométrie à double faisceauSpectrométrie par scintillementSpectrométrie par réflexion
INSTITUT NATIONAL UNIVERSITAIRE JEAN-FRANCOIS CHAMPOLLION (France)
UNIVERSITE TOULOUSE III - PAUL SABATIER (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
Inventeur(s)
Benmoussa, Khaddouj
Bonnafe, Elsa
Coste, Agnes
Leprince, Jerome
Pipy, Bernard
Treilhou, Michel
Abrégé
The invention relates to an isolated peptide consisting of a sequence of 3 to 39 amino acids derived from the amino acid sequence SEQ ID NO : 1, said peptide having an amino acid sequence selected from the group consisting of: a) the sequences of 3 to 39 amino acids comprising at least the residues 6 to 8 of SEQ ID NO : 1; and b) the sequences of 3 to 39 amino acids that are at least 70% identical to said sequence in a).
C07K 5/083 - Tripeptides la chaîne latérale du premier amino-acide étant acyclique, p. ex. Gly, Ala
C07K 7/06 - Peptides linéaires ne contenant que des liaisons peptidiques normales ayant de 5 à 11 amino-acides
C07K 7/08 - Peptides linéaires ne contenant que des liaisons peptidiques normales ayant de 12 à 20 amino-acides
C07K 14/435 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
INSTITUT NATIONAL UNIVERSITAIRE JEAN-FRANCOIS CHAMPOLLION (France)
UNIVERSITE TOULOUSE III - PAUL SABATIER (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
Inventeur(s)
Benmoussa, Khaddouj
Bonnafe, Elsa
Coste, Agnès
Leprince, Jérôme
Pipy, Bernard
Treilhou, Michel
Abrégé
The invention relates to an isolated peptide consisting of a sequence of 3 to 39 amino acids derived from the amino acid sequence SEQ ID NO : 1, said peptide having an amino acid sequence selected from the group consisting of: a) the sequences of 3 to 39 amino acids comprising at least the residues 6 to 8 of SEQ ID NO : 1; and b) the sequences of 3 to 39 amino acids that are at least 70% identical to said sequence in a).
C07K 5/103 - Tétrapeptides la chaîne latérale du premier amino-acide étant acyclique, p. ex. Gly, Ala
C07K 7/06 - Peptides linéaires ne contenant que des liaisons peptidiques normales ayant de 5 à 11 amino-acides
C07K 7/08 - Peptides linéaires ne contenant que des liaisons peptidiques normales ayant de 12 à 20 amino-acides
C07K 14/435 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
C07K 5/083 - Tripeptides la chaîne latérale du premier amino-acide étant acyclique, p. ex. Gly, Ala
Centre Hospitalier Universitaire De Rouen (France)
Universite de Rouen Normandie (France)
Institut National De La Sante Et De La Recherche Medicale (INSERM) (France)
Inventeur(s)
Gonzalez, Bruno José
Marret, Stéphane
Lecuyer, Matthieu Jean Alexandre
Laquerriere, Annie
Bekri, Soumeya
Lesueur, Céline
Jegou, Sylvie Marguerite Alberte
Marcorelles, Pascale Yvonne Joséphine
Abrégé
The present invention provides a method for the diagnosis of disorders caused by foetal alcohol syndrome, said method comprising the assaying of PLGF (placental growth factor).
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
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
91.
PLACENTAL GROWTH FACTOR FOR THE TREATMENT OF FETAL ALCOHOL SYNDROME DISORDERS (FASD)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
Inventeur(s)
Gonzales, Bruno José
Marret, Stéphane
Lecuyer, Matthieu Jean Alexandre
Laquerriere, Annie
Bekri, Soumeya
Lesueur, Céline
Jegou, Sylvie Marguerite Alberte
Marcorelles, Pascale Yvonne Joséphine
Abrégé
The invention relates to a placental growth factor (PlGF) to be used as a drug in the prevention and/or treatment of fetal alcohol syndrome disorders (FASD) selected from the group comprising fetal alcohol syndrome (FAS), cerebrovascular disease, and growth retardation in a subject exposed to alcohol in utero. The invention also relates to a pharmaceutical composition or a product comprising the PlGF for the same therapeutic uses.
A61K 38/18 - Facteurs de croissanceRégulateurs de croissance
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
A61P 43/00 - Médicaments pour des utilisations spécifiques, non prévus dans les groupes
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
A61P 25/32 - Médicaments pour le traitement des troubles du système nerveux des états d'abus ou de dépendance à l'alcool
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
92.
METHOD AND SYSTEM FOR RECOVERING MAGNETIC GRAINS FROM SINTERED MAGNETS OR PLASTIC MAGNETS
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Inventeur(s)
Maât, Nicolas
Aymonier, Cyril
Le Breton, Jean-Marie
Abrégé
The invention concerns a method and a device for retrieving, from an object A, elements G present in a matrix M, characterised in that it comprises at least the following steps: bringing said object A into contact with a dense fluid Fd with a molar mass greater than 2 g mol-1 under temperature T1 and pressure P1 conditions suitable for transforming the intergranular phase and for releasing the elements G, (302), modifying the temperature T2 and/or pressure P2 values to stop the reaction transforming the intergranular phase, (303), and recovering the elements G separated from the matrix M (304).
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
UNIVERSITÉ PARIS DIDEROT - PARIS 7 (France)
Inventeur(s)
Tan, Yossan-Var
Abad Rabat, Catalina
Voisin, Thierry
Couvineau, Alain
Abrégé
The present invention relates to methods and pharmaceutical compositions for the treatment of autoimmune inflammatory diseases. The inventors showed that orexin receptor antagonists have anti-inflammatory properties. Indeed, these compounds are antagonist for OX1R-mediated calcium mobilization but a full agonist for OX1R-mediated mitochondrial apoptosis, which is the mechanism involved in the improvement of resolution of inflammation observed in the models of colitis, multiple sclerosis and pancreatitis. In particular, the present invention relates to a method of treating an autoimmune inflammatory disease in a subject in need thereof comprising administering to the subject a therapeutically effective amount of at least one OX1R antagonist.
A61K 31/4545 - Pipéridines non condensées, p. ex. pipérocaïne contenant d'autres systèmes hétérocycliques contenant un cycle à six chaînons avec l'azote comme hétéro-atome du cycle, p. ex. pipampérone, anabasine
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
A61P 1/04 - Médicaments pour le traitement des troubles du tractus alimentaire ou de l'appareil digestif des ulcères, des gastrites ou des œsophagites par reflux, p. ex. antiacides, antisécrétoires, protecteurs de la muqueuse
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
09 - Appareils et instruments scientifiques et électriques
41 - Éducation, divertissements, activités sportives et culturelles
42 - Services scientifiques, technologiques et industriels, recherche et conception
Produits et services
Scientific, nautical, surveying, photographic, cinematographic, optical, weighing, measuring, signalling, checking (supervision), life-saving and teaching apparatus and instruments; Apparatus and instruments for conducting, switching, transforming, accumulating, regulating or controlling electricity; Apparatus for recording, transmission or reproduction of sound or images; Magnetic data carriers, recording discs, optical discs; Data processing and computer apparatus; Computer software (recorded programs); Peripherals adapted for use with computers; Detectors; Electric wires; Relays, electric; Diagnostic apparatus, not for medical purposes; Smart cards [integrated circuit cards]; Material testing instruments and machines; Furniture especially made for laboratories; Laboratory equipment, namely apparatus for chromatography, electrical apparatus for monitoring clinical trials, Diagnostic apparatus, not for medical purposes; Electronic publications, downloadable; Interactive multimedia computer game programs; games software downloadable to mobile phones, tablets and other electronic mobile devices; software for use on mobile phones, tablets and other electronic mobile devices; apps featuring computer games; mobile phone apps. Education, Tuition, Tuition, Publication of texts relating to teaching, Production of training films; Publishing of computer software and management software intended for schools, universities and training centres; Publishing of computer software and databases for teaching activities, training management or administration of schools, universities and training centres, publishing of computer software for the storage, processing and transmission of data; Publishing of computer software for computer network management; Online training and educational services; Providing tutoring online (education or providing of training); Publication of texts, other than publicity texts, newspapers, periodicals and all kinds of audio and/or visual media and multimedia carriers (interactive discs, audio-digital CD-ROMs, DVDs); Publication of electronic books and journals on-line; Micropublishing; Correspondence courses, courses given as part of seminars, work placements, conferences or forums; Arranging of exhibitions for cultural or educational purposes; Arranging and conducting of colloquiums, conferences and congresses; Organisation of competitions and games (education or entertainment); Game services provided on-line from a computer network; Production of television and radio programs; television entertainment; Production of films and shows, photographic reports; Leisure services. Engineering evaluations and appraisals in the fields of science and technology; Scientific and technical research; Engineering services; Scientific laboratories; designing prototypes; Material testing; Conducting technical project studies; Scientific, technical and mechanical research; Design and development of computer hardware and software; Research and development for others; Design, installation, maintenance, updating and rental of computer software; Computer programming; Computer system analysis; Computer system design; Consultancy in the field of computers; Software as a service [SaaS]; Server hosting; Energy auditing; Publication of multimedia programs and computerisation of text, still or moving images and musical or non-musical sound for interactive or non-interactive use, namely computer programming.
95.
METHOD OF AMPLIFYING A POPULATION OF ANTIGEN-SPECIFIC MEMORY CD4+ T CELLS USING ARTIFICIAL PRESENTING CELLS EXPRESSING HLA CLASS II MOLECULES
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ DE ROUEN-NORMANDIE (France)
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
ETABLISSEMENT FRANÇAIS DU SANG (EFS) (France)
UNIVERSITÉ DE CAEN NORMANDIE (France)
CENTRE HOSPITALIER RÉGIONAL UNIVERSITAIRE DE CAEN (France)
Inventeur(s)
Latouche, Jean-Baptiste
Le Mauff Quester, Brigitte
Toutirais, Olivier
Abrégé
The present invention relates to method of amplifying a population of antigen-specific memory CD4+ T cells using artificial presenting cells expressing HLA class II molecules. In particular, the present invention relates to a method of amplifying a population of antigen- specific memory CD4+ T cells comprising the steps of i) providing a population of artificial antigen presenting cells consisting host cells that are genetically modified to stably express at least one MHC class II molecule along with at least one accessory molecule ii) loading the population of artificial antigen presenting cells of step i) with an amount of at least one antigen of interest and iii) coculturing the suitable population of a T cells with the population of artificial antigen presenting cells of step ii).
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (France)
UNIVERSITE DE ROUEN-NORMANDIE (France)
INSTITUT NATIONAL DES SCIENCES APPLIQUEES DE ROUEN NORMANDIE (France)
Inventeur(s)
Le Breton, Jean-Marie
Maât, Nicolas
Nachbaur, Virginie
Abrégé
The invention relates to a method and system for recovering at least rare earth elements from within an object A consisting of at least one first rare earth portion or a mixture of rare earth elements and a second metal portion. The invention is characterized in that it comprises a solvothermal treatment step that places the object in contact with a fluid for causing at least one rare earth portion and/or mixture of rare earth elements and the metal portion to oxidize in order to separate same, the value of the reaction temperature Tr is selected according to the nature of the object, the reaction following a R-M→ R(X)x+M(X)y scheme, where R is the rare earth element or a mixture of rare earth elements, M is the transition metal, and (X) is a group which depends on the fluid used.
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
Inventeur(s)
Grumolato, Luca
Abrégé
The instant invention relates to a method for labeling endonuclease-treated cells, comprising the steps of: a) providing cells or a composition comprising cells; b) bringing into contact said cells or said composition with: - at least one endonuclease suitable for targeting a genomic region of interest in said cells, or a vector suitable for expressing said endonuclease in said cells; - at least one first nucleic acid suitable for introducing one or more silent mutation(s) in said genomic region by homology-directed repair (HDR), and optionally one or more non-silent mutation(s); and - at least one second nucleic acid suitable for introducing one or more silent mutation(s) in said genomic region by homology-directed repair (HDR), but distinct from the silent mutations of the first nucleic acid; thereby labeling endonuclease-treated cells.
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques
98.
METHODS AND PHARMACEUTICAL COMPOSITIONS FOR THE TREATMENT OF AUTOIMMUNE INFLAMMATORY DISEASES
INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) (France)
UNIVERSITÉ PARIS DIDEROT - PARIS 7 (France)
UNIVERSITÉ DE ROUEN NORMANDIE (France)
Inventeur(s)
Tan, Yossan-Var
Abad-Rabat, Catalina
Couvineau, Alain
Voisin, Thierry
Abrégé
The present invention relates to methods and pharmaceutical compositions for the treatment of autoimmune inflammatory disease. In particular, the present invention relates to a method of treating an autoimmune inflammatory disease in a subject in need thereof comprising administering to the subject a therapeutically effective amount of at least one OX1R agonist.
A61K 38/17 - Peptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'animauxPeptides ayant plus de 20 amino-acidesGastrinesSomatostatinesMélanotropinesLeurs dérivés provenant d'humains
CENTRE HOSPITALIER UNIVERSITAIRE DE ROUEN (France)
UNIVERSITE DE ROUEN NORMANDIE (France)
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE (INSERM) (France)
Inventeur(s)
Gonzales, Bruno José
Marret, Stéphane
Lecuyer, Matthieu Jean Alexandre
Laquerriere, Annie
Bekri, Soumeya
Lesueur, Céline
Jegou, Sylvie Marguerite Alberte
Marcorelles, Pascale Yvonne Joséphine
Abrégé
The present invention provides a method for the diagnosis of disorders caused by foetal alcohol syndrome, said method comprising the assaying of PLGF (placental growth factor).
G01N 33/68 - Analyse chimique de matériau biologique, p. ex. de sang ou d'urineTest par des méthodes faisant intervenir la formation de liaisons biospécifiques par ligandsTest immunologique faisant intervenir des protéines, peptides ou amino-acides
C12Q 1/68 - Procédés de mesure ou de test faisant intervenir des enzymes, des acides nucléiques ou des micro-organismesCompositions à cet effetProcédés pour préparer ces compositions faisant intervenir des acides nucléiques