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Nature|January 7, 2014
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico, Amy L Williams, Suzanne B R Jacobs, et al.
Cell|July 1, 2017
Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct MechanismsVictor Rusu, Eitan Hoch, Josep M Mercader, et al.
European Journal of Endocrinology|November 27, 2018
The SLC16A11 risk haplotype is associated with decreased insulin action, higher transaminases and large-size adipocytesPaloma Almeda-Valdes, Donaji V Gómez Velasco, Olimpia Arellano Campos, et al.
Cell Genomics|July 26, 2023
Discovering cellular programs of intrinsic and extrinsic drivers of metabolic traits using LipocyteProfilerSamantha Laber, Sophie Strobel, Josep M Mercader, et al.
Nature Genetics|March 4, 2014
Loss-of-function mutations in SLC30A8 protect against type 2 diabetesJason Flannick, Gudmar Thorleifsson, Nicola L Beer, et al.
Diabetes|August 26, 2017
A Loss-of-Function Splice Acceptor Variant in IGF2 Is Protective for Type 2 DiabetesJosep M Mercader, Rachel G Liao, Avery D Bell, et al.
Nature Genetics|June 25, 2013
Genome-wide meta-analysis identifies new susceptibility loci for migraineVerneri Anttila, Bendik S Winsvold, Padhraig Gormley, et al.
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