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Cell Reports|February 12, 2026
RAB3GAP2 is a regulator of skeletal muscle endothelial cell proliferation and associated with capillary-to-fiber ratioKristoffer Ström, Nikolay Oskolkov, Tugce Karaderi, et al.
Plos Genetics|August 1, 2014
Distribution and medical impact of loss-of-function variants in the Finnish founder populationElaine T Lim, Peter Würtz, Aki S Havulinna, et al.
Human Molecular Genetics|November 26, 2009
Genetic evidence that raised sex hormone binding globulin (SHBG) levels reduce the risk of type 2 diabetesJohn R B Perry, Michael N Weedon, Claudia Langenberg, et al.
Nature Genetics|January 31, 2017
Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular riskHelen R Warren, Evangelos Evangelou, Claudia P Cabrera, et al.
American Journal of Human Genetics|January 22, 2013
Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminusGea Beunders, Els Voorhoeve, Christelle Golzio, et al.
American Journal of Human Genetics|January 24, 2023
Loci for insulin processing and secretion provide insight into type 2 diabetes riskK Alaine Broadaway, Xianyong Yin, Alice Williamson, et al.
Human Molecular Genetics|February 27, 2022
Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetesNatalia Pervjakova, Gunn-Helen Moen, Maria-Carolina Borges, et al.
Nature Communications|January 10, 2018
Large-scale GWAS identifies multiple loci for hand grip strength providing biological insights into muscular fitnessSara M Willems, Daniel J Wright, Felix R Day, et al.
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