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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. 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
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. 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.
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. Diabetes. 2003 Dec;52(12):2996-3000. doi: 10.2337/diabetes.52.12.2996. Diabetes. 2003. PMID: 14633862
Mutational analysis of the pro-opiomelanocortin gene in French obese children led to the identification of a novel deleterious heterozygous mutation located in the alpha-melanocyte stimulating hormone domain.
Dubern B, Lubrano-Berthelier C, Mencarelli M, Ersoy B, Frelut ML, Bouglé D, Costes B, Simon C, Tounian P, Vaisse C, Clement K. Dubern B, et al. Among authors: lubrano berthelier c. Pediatr Res. 2008 Feb;63(2):211-6. doi: 10.1203/PDR.0b013e31815ed62b. Pediatr Res. 2008. PMID: 18091355
[Genetics of human obesity].
Lubrano-Berthelier C, Clément K. Lubrano-Berthelier C, et al. Rev Med Interne. 2005 Oct;26(10):802-11. doi: 10.1016/j.revmed.2005.03.017. Rev Med Interne. 2005. PMID: 15927311 Review. French.
13 results