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Diabetes|January 3, 2012
Heterozygous mutations causing partial prohormone convertase 1 deficiency contribute to human obesityJohn W M Creemers, Hélène Choquet, Pieter Stijnen, et al.
Diabetes|August 21, 2010
Evaluation of A2BP1 as an obesity geneLijun Ma, Robert L Hanson, Michael T Traurig, et al.
Obesity (Silver Spring, Md.)|October 24, 2009
The imprinted gene neuronatin is regulated by metabolic status and associated with obesityNiels Vrang, David Meyre, Phillippe Froguel, et al.
Diabetes|October 17, 2009
Prevalence of loss-of-function FTO mutations in lean and obese individualsDavid Meyre, Karine Proulx, Hiroko Kawagoe-Takaki, et al.
Nature|February 13, 2007
A genome-wide association study identifies novel risk loci for type 2 diabetesRobert Sladek, Ghislain Rocheleau, Johan Rung, et al.
Science (New York, N.Y.)|May 3, 2008
A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levelsNabila Bouatia-Naji, Ghislain Rocheleau, Leentje Van Lommel, et al.
The Journal of Clinical Investigation|June 20, 2013
Loss-of-function mutations in SIM1 contribute to obesity and Prader-Willi-like featuresAmélie Bonnefond, Anne Raimondo, Fanny Stutzmann, et al.
Diabetes|August 5, 2009
Genetic variant in HK1 is associated with a proanemic state and A1C but not other glycemic control-related traitsAmélie Bonnefond, Martine Vaxillaire, Yann Labrune, et al.
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