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85,117 results

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MRAP2 regulates energy homeostasis by promoting primary cilia localization of MC4R.
Bernard A, Ojeda Naharros I, Yue X, Mifsud F, Blake A, Bourgain-Guglielmetti F, Ciprin J, Zhang S, McDaid E, Kim K, Nachury MV, Reiter JF, Vaisse C. Bernard A, et al. Among authors: zhang s. JCI Insight. 2023 Jan 24;8(2):e155900. doi: 10.1172/jci.insight.155900. JCI Insight. 2023. PMID: 36692018 Free PMC article.
The human MC4R promoter: characterization and role in obesity.
Lubrano-Berthelier C, Cavazos M, Le Stunff C, Haas K, Shapiro A, Zhang S, Bougneres P, Vaisse C. Lubrano-Berthelier C, et al. Among authors: zhang s. Diabetes. 2003 Dec;52(12):2996-3000. doi: 10.2337/diabetes.52.12.2996. Diabetes. 2003. PMID: 14633862
Molecular genetics of human obesity-associated MC4R mutations.
Lubrano-Berthelier C, Cavazos M, Dubern B, Shapiro A, Stunff CL, Zhang S, Picart F, Govaerts C, Froguel P, Bougneres P, Clement K, Vaisse C. Lubrano-Berthelier C, et al. Among authors: zhang s. Ann N Y Acad Sci. 2003 Jun;994:49-57. doi: 10.1111/j.1749-6632.2003.tb03161.x. Ann N Y Acad Sci. 2003. PMID: 12851297 Review.
Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case-control study.
Calton MA, Ersoy BA, Zhang S, Kane JP, Malloy MJ, Pullinger CR, Bromberg Y, Pennacchio LA, Dent R, McPherson R, Ahituv N, Vaisse C. Calton MA, et al. Among authors: zhang s. Hum Mol Genet. 2009 Mar 15;18(6):1140-7. doi: 10.1093/hmg/ddn431. Epub 2008 Dec 17. Hum Mol Genet. 2009. PMID: 19091795 Free PMC article.
Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eating.
Lubrano-Berthelier C, Dubern B, Lacorte JM, Picard F, Shapiro A, Zhang S, Bertrais S, Hercberg S, Basdevant A, Clement K, Vaisse C. Lubrano-Berthelier C, et al. Among authors: zhang s. J Clin Endocrinol Metab. 2006 May;91(5):1811-8. doi: 10.1210/jc.2005-1411. Epub 2006 Feb 28. J Clin Endocrinol Metab. 2006. PMID: 16507637
High prevalence of glucose-6-phosphate dehydrogenase deficiency without gene mutation suggests a novel genetic mechanism predisposing to ketosis-prone diabetes.
Sobngwi E, Gautier JF, Kevorkian JP, Villette JM, Riveline JP, Zhang S, Vexiau P, Leal SM, Vaisse C, Mauvais-Jarvis F. Sobngwi E, et al. Among authors: zhang s. J Clin Endocrinol Metab. 2005 Aug;90(8):4446-51. doi: 10.1210/jc.2004-2545. Epub 2005 May 24. J Clin Endocrinol Metab. 2005. PMID: 15914531 Free PMC article.
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