10 results for author:"Beau I." in Literature citations
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| The human cytomegalovirus protein TRS1 inhibits autophagy via its interaction with Beclin 1. Chaumorcel M., Lussignol M., Mouna L., Cavignac Y., Fahie K., Cotte-Laffitte J., Geballe A., Brune W., Beau I., Codogno P. et al. J. Virol. 86:2571-2584(2012) · UniProtKB (2) |
| Overview of macroautophagy regulation in mammalian cells. Mehrpour M., Esclatine A., Beau I., Codogno P. Cell Res. 20:748-762(2010) · Mapped (12) |
| Ovarian hyperstimulation syndrome (OHSS) due to mutations in the follicle-stimulating hormone receptor. Rodien P., Beau I., Vasseur C. Ann. Endocrinol. (Paris) 71:206-209(2010) · Mapped (5) |
| Lost to translation: when autophagy targets mature ribosomes. Beau I., Esclatine A., Codogno P. Trends Cell Biol. 18:311-314(2008) · Mapped (2) |
| Biological function of mutant forms of JAGGED1 proteins in Alagille syndrome: inhibitory effect on Notch signaling. Boyer-Di Ponio J., Wright-Crosnier C., Groyer-Picard M.T., Driancourt C., Beau I., Hadchouel M., Meunier-Rotival M. Hum. Mol. Genet. 16:2683-2692(2007) · Mapped (5) |
| A chorionic gonadotropin-sensitive mutation in the follicle-stimulating hormone receptor as a cause of familial gestational spontaneous ovarian hyperstimulation syndrome. Vasseur C., Rodien P., Beau I., Desroches A., Gerard C., de Poncheville L., Chaplot S., Savagner F., Croue A., Mathieu E. et al. N. Engl. J. Med. 349:753-759(2003) · UniProtKB (1) |
| Delayed puberty and primary amenorrhea associated with a novel mutation of the human follicle-stimulating hormone receptor: clinical, histological, and molecular studies. Meduri G., Touraine P., Beau I., Lahuna O., Desroches A., Vacher-Lavenu M.C., Kuttenn F., Misrahi M. J. Clin. Endocrinol. Metab. 88:3491-3498(2003) · UniProtKB (1) |
| New natural inactivating mutations of the follicle-stimulating hormone receptor: correlations between receptor function and phenotype. Touraine P., Beau I., Gougeon A., Meduri G., Desroches A., Pichard C., Detoeuf M., Paniel B., Prieur M., Zorn J.-R. et al. Mol. Endocrinol. 13:1844-1854(1999) · UniProtKB (1) |
| A novel phenotype related to partial loss of function mutations of the follicle stimulating hormone receptor. Beau I., Touraine P., Meduri G., Gougeon A., Desroches A., Matuchansky C., Milgrom E., Kuttenn F., Misrahi M. J. Clin. Invest. 102:1352-1359(1998) · UniProtKB (1) |
| Comparison of immunocytochemical and molecular features with the phenotype in a case of incomplete male pseudohermaphroditism associated with a mutation of the luteinizing hormone receptor. Misrahi M., Meduri G., Pissard S., Bouvattier C., Beau I., Loosfelt H., Jolivet A., Rappaport R., Milgrom E., Bougneres P. J. Clin. Endocrinol. Metab. 82:2159-2165(1997) · UniProtKB (1) |