R01 DK-60540/DK/NIDDK NIH HHS/United States[Grants and Funding] - Search Results

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Year	Number of Results
2004	2
2005	1
2024	0

Page 1

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. 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.

Constitutive activity of the melanocortin-4 receptor is maintained by its N-terminal domain and plays a role in energy homeostasis in humans.

Srinivasan S, Lubrano-Berthelier C, Govaerts C, Picard F, Santiago P, Conklin BR, Vaisse C. Srinivasan S, et al. J Clin Invest. 2004 Oct;114(8):1158-64. doi: 10.1172/JCI21927. J Clin Invest. 2004. PMID: 15489963 Free PMC article.

A homozygous null mutation delineates the role of the melanocortin-4 receptor in humans.

Lubrano-Berthelier C, Le Stunff C, Bougnères P, Vaisse C. Lubrano-Berthelier C, et al. J Clin Endocrinol Metab. 2004 May;89(5):2028-32. doi: 10.1210/jc.2003-031993. J Clin Endocrinol Metab. 2004. PMID: 15126516

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