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Diabetes|December 17, 2009
Insulin gene mutations resulting in early-onset diabetes: marked differences in clinical presentation, metabolic status, and pathogenic effect through endoplasmic reticulum retentionGargi Meur, Albane Simon, Nasret Harun, et al.
Journal of Medical Genetics|February 4, 2022
Dominant negative mutation in oxalate transporter SLC26A6 associated with enteric hyperoxaluria and nephrolithiasisNicolas Cornière, R Brent Thomson, Stéphanie Thauvin, et al.
Cellular and Molecular Life Sciences : CMLS|March 20, 2020
The Map3k12 (Dlk)/JNK3 signaling pathway is required for pancreatic beta-cell proliferation during postnatal developmentMathie Tenenbaum, Valérie Plaisance, Raphael Boutry, et al.
Nucleic Acids Research|June 26, 2012
Dynamic hydroxymethylation of deoxyribonucleic acid marks differentiation-associated enhancersAurélien A Sérandour, Stéphane Avner, Frédérik Oger, et al.
The American Journal of Clinical Nutrition|December 25, 2009
TCF7L2 rs7903146-macronutrient interaction in obese individuals' responses to a 10-wk randomized hypoenergetic dietKatrine Grau, Stephane Cauchi, Claus Holst, et al.
Obesity (Silver Spring, Md.)|January 16, 2010
Analysis of the SIM1 contribution to polygenic obesity in the French populationMaya Ghoussaini, Fanny Stutzmann, Cyril Couturier, et al.
American Journal of Human Genetics|June 30, 2009
Loss-of-function mutation in the dioxygenase-encoding FTO gene causes severe growth retardation and multiple malformationsSarah Boissel, Orit Reish, Karine Proulx, et al.
Obesity (Silver Spring, Md.)|July 16, 2011
Association of sirtuin 1 (SIRT1) gene SNPs and transcript expression levels with severe obesityStephen J Clark, Mario Falchi, Bob Olsson, et al.
Cell Reports|February 3, 2021
Chromatin 3D interaction analysis of the STARD10 locus unveils FCHSD2 as a regulator of insulin secretionMing Hu, Inês Cebola, Gaelle Carrat, et al.
Cell Reports. Medicine|September 2, 2023
High morbidity and mortality in children with untreated congenital deficiency of leptin or its receptorSadia Saeed, Roohia Khanam, Qasim M Janjua, et al.
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