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Obesity Research|October 22, 2003
Role of the DGAT gene C79T single-nucleotide polymorphism in French obese subjectsSylvie Kipfer Coudreau, Patrick Tounian, Geneviève Bonhomme, et al.
International Journal of Obesity (2005)|March 14, 2026
Inversed impaired osteogenic activity in children with severe obesity due to MC4R deficiency compared to LEP and LEPR deficiencyQasim M Janjua, Roohia Khanam, Sadia Saeed, et al.
Science (New York, N.Y.)|January 16, 2007
Comment on "A common genetic variant is associated with adult and childhood obesity"Christian Dina, David Meyre, Chantal Samson, et al.
BMC Medical Genetics|March 24, 2005
Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French populationMaya Ghoussaini, David Meyre, Stéphane Lobbens, et al.
Pediatric Diabetes|January 11, 2011
Familial mild hyperglycemia associated with a novel ABCC8-V84I mutation within three generationsLucie Gonsorcikova, Martine Vaxillaire, Stepanka Pruhova, et al.
Human Genetics|September 29, 2005
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1Helmut Grasberger, Martine Vaxillaire, Silvana Pannain, et al.
Plos One|September 17, 2013
Meal frequencies modify the effect of common genetic variants on body mass index in adolescents of the northern Finland birth cohort 1986Anne Jääskeläinen, Ursula Schwab, Marjukka Kolehmainen, et al.
Iscience|August 17, 2021
Signatures of TSPAN8 variants associated with human metabolic regulation and diseasesTisham De, Angela Goncalves, Doug Speed, et al.
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