未登录Basal-like breast cancer subtype is characterized by deregulated glutamine metabolism and is sensitive to GLS inhibition
Henry, Christophe; Lampa, Michael; He, Timothy; Ospina, Beatriz; Zhang, Bailin; Deng, Gejing; Barberis, Claude; Hoffmann, Dietmar; Pollard, Jack; Francisco, Adrian; Arlt, Heike; Reeves, Jason; Murtie, Joshua; Winter, Christopher; Richon, Victoria; Cheng, Hong; Garcia-Echeverria, Carlos; Wiederschain, Dmitri; Srinivasan, Lakshmi
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收藏Identification of a single residue responsible for agonist selectivity in the oxytocin-vasopressin receptors
Chini, B; Mouillac, B; Ala, Y; Balestre, MN; TrumppKallmeyer, S; Hoflack, J; Elands, J; Hibert, M; Manning, M; Jard, S; Barberis, C
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收藏Discovery and development of a new class of potent, selective, orally active oxytocin receptor antagonists
Quattropani, A; Dorbais, J; Covini, D; Pittet, PA; Colovray, V; Thomas, RJ; Coxhead, R; Halazy, S; Scheer, A; Missotten, M; Ayala, G; Bradshaw, C; De Raemy-Schenk, AM; Nichols, A; Cirillo, R; Tos, EG; Giachetti, C; Golzio, L; Marinelli, P; Church, DJ; Barberis, C; Chollet, A; Schwarz, MK
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收藏The discovery of novel vasopressin V1b receptor ligands for pharmacological, functional and structural investigations
Guillon, G; Derick, S; Pena, A; Cheng, LL; Stoev, S; Seyer, R; Morgat, JL; Barberis, C; Serradeil-Le Gal, C; Wagnon, J; Manning, M
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收藏Pharmacology of (2S,4Z)-N-[(2S)-2-hydroxy-2-phenylethyl]-4(methoxyimino)-1-[(2′-methyl[1,1′-biphenyl]-4-yl)carbonyl]-2-pyrrolidinecarboxamide, a new potent and selective nonpeptide antagonist of the oxytocin receptor
Cirillo, R; Tos, EG; Schwarz, MK; Quattropani, A; Scheer, A; Missotten, M; Dorbais, J; Nichols, A; Borrelli, F; Giachetti, C; Golzio, L; Marinelli, P; Thomas, RJ; Chevillard, C; Laurent, F; Portet, K; Barberis, C; Chollet, A
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收藏A functional genomic study to identify differential gene expression in the preterm and term human myometrium
Charpigny, G; Leroy, MJ; Breuiller-Fouché, A; Tanfin, Z; Mhaouty-Kodja, S; Robin, P; Leiber, D; Cohen-Tannoudji, J; Cabrol, D; Barberis, C; Germain, G
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收藏Direct identification of human oxytocin receptor-binding domains using a photoactivatable cyclic peptide antagonist -: Comparison with the human V1a vasopressin receptor
Breton, C; Chellil, H; Kabbaj-Benmansour, M; Carnazzi, E; Seyer, R; Phalipou, S; Morin, D; Durroux, T; Zingg, H; Barberis, C; Mouillac, B
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收藏Two aromatic residues regulate the response of the human oxytocin receptor to the partial agonist arginine vasopressin
Chini, B; Mouillac, B; Balestre, MN; TrumppKallmeyer, S; Hoflack, J; Hibert, M; Andriolo, M; Pupier, S; Jard, S; Barberis, C
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