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Christian Vaisse

Showing results (21-30 of 48) with videos related to

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Clinical Endocrinology|January 28, 2009
Identification, characterization and rescue of a novel vasopressin-2 receptor mutation causing nephrogenic diabetes insipidusSayali A Ranadive, Baran Ersoy, Helene Favre, et al.
The Journal of Clinical Endocrinology and Metabolism|September 4, 2008
Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC geneKarine Clément, Béatrice Dubern, Monica Mencarelli, et al.
Human Molecular Genetics|December 25, 2002
Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutationsCecile Lubrano-Berthelier, Emmanuelle Durand, Beatrice Dubern, et al.
Science (New York, N.Y.)|December 15, 2018
CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiencyNavneet Matharu, Sawitree Rattanasopha, Serena Tamura, et al.
Plos One|October 17, 2015
The Association of Serum Leptin with Mortality in Older AdultsSuruchi Mishra, Tamara B Harris, Wen-Chi Hsueh, et al.
Nature Genetics|January 10, 2018
Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesityJacqueline E Siljee, Yi Wang, Adelaide A Bernard, et al.
The Journal of Clinical Endocrinology and Metabolism|March 2, 2006
Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eatingCecile Lubrano-Berthelier, Beatrice Dubern, Jean-Marc Lacorte, et al.
Nature Medicine|July 2, 2002
Elevated plasma ghrelin levels in Prader Willi syndromeDavid E Cummings, Karine Clement, Jonathan Q Purnell, et al.
Cell Reports|June 15, 2017
Acute Lesioning and Rapid Repair of Hypothalamic Neurons outside the Blood-Brain BarrierErnie Yulyaningsih, Ivan A Rudenko, Martin Valdearcos, et al.
Pediatric Research|December 20, 2007
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 domainBeatrice Dubern, Cecile Lubrano-Berthelier, Monica Mencarelli, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
Clinical Endocrinology|January 28, 2009
Identification, characterization and rescue of a novel vasopressin-2 receptor mutation causing nephrogenic diabetes insipidusSayali A Ranadive, Baran Ersoy, Helene Favre, et al.
The Journal of Clinical Endocrinology and Metabolism|September 4, 2008
Unexpected endocrine features and normal pigmentation in a young adult patient carrying a novel homozygous mutation in the POMC geneKarine Clément, Béatrice Dubern, Monica Mencarelli, et al.
Human Molecular Genetics|December 25, 2002
Intracellular retention is a common characteristic of childhood obesity-associated MC4R mutationsCecile Lubrano-Berthelier, Emmanuelle Durand, Beatrice Dubern, et al.
Science (New York, N.Y.)|December 15, 2018
CRISPR-mediated activation of a promoter or enhancer rescues obesity caused by haploinsufficiencyNavneet Matharu, Sawitree Rattanasopha, Serena Tamura, et al.
Plos One|October 17, 2015
The Association of Serum Leptin with Mortality in Older AdultsSuruchi Mishra, Tamara B Harris, Wen-Chi Hsueh, et al.
Nature Genetics|January 10, 2018
Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesityJacqueline E Siljee, Yi Wang, Adelaide A Bernard, et al.
The Journal of Clinical Endocrinology and Metabolism|March 2, 2006
Melanocortin 4 receptor mutations in a large cohort of severely obese adults: prevalence, functional classification, genotype-phenotype relationship, and lack of association with binge eatingCecile Lubrano-Berthelier, Beatrice Dubern, Jean-Marc Lacorte, et al.
Nature Medicine|July 2, 2002
Elevated plasma ghrelin levels in Prader Willi syndromeDavid E Cummings, Karine Clement, Jonathan Q Purnell, et al.
Cell Reports|June 15, 2017
Acute Lesioning and Rapid Repair of Hypothalamic Neurons outside the Blood-Brain BarrierErnie Yulyaningsih, Ivan A Rudenko, Martin Valdearcos, et al.
Pediatric Research|December 20, 2007
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 domainBeatrice Dubern, Cecile Lubrano-Berthelier, Monica Mencarelli, et al.
Pageof 5