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Diabetologia|March 19, 2017
The case for too little melatonin signalling in increased diabetes riskAmélie Bonnefond, Philippe FroguelCell Metabolism|February 3, 2015
Rare and common genetic events in type 2 diabetes: what should biologists know?Amélie Bonnefond, Philippe FroguelThe HUGO Journal|December 2, 2011
Implications of copy number variation in people with chromosomal abnormalities: potential for greater variation in copy number state may contribute to variability of phenotypeAdam J de Smith, Anne L Trewick, Alexandra I F BlakemoreBioinformatics (Oxford, England)|May 7, 2011
famCNV: copy number variant association for quantitative traits in familiesHariklia Eleftherohorinou, Johanna C Andersson-Assarsson, Robin G Walters, et al.Human Molecular Genetics|August 2, 2007
Array CGH analysis of copy number variation identifies 1284 new genes variant in healthy white males: implications for association studies of complex diseasesAdam J de Smith, Anya Tsalenko, Nick Sampas, et al.American Journal of Physiology. Endocrinology and Metabolism|July 12, 2002
Genetic approaches to the molecular understanding of type 2 diabetesMark I McCarthy, Philippe FroguelBiochemical and Biophysical Research Communications|March 27, 2007
Preadipocyte response and impairment of differentiation in an inflammatory environmentOdile Poulain-Godefroy, Philippe FroguelDiabetes|September 28, 2005
Common polymorphisms in the USF1 gene are not associated with type 2 diabetes in French CaucasiansFernando Gibson, Serge Hercberg, Philippe FroguelMolecular Psychiatry|September 5, 2024
Obesity: exploring its connection to brain function through genetic and genomic perspectivesSadia Saeed, Amélie Bonnefond, Philippe FroguelCurrent Diabetes Reports|August 7, 2019
How Recent Advances in Genomics Improve Precision Diagnosis and Personalized Care of Maturity-Onset Diabetes of the YoungMartine Vaxillaire, Philippe Froguel, Amélie BonnefondPageof 53