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Nature Communications|September 17, 2014
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in EuropeansNicholas J Timpson, Klaudia Walter, Josine L Min, et al.Cellular and Molecular Life Sciences : CMLS|April 10, 2021
Immune cells lacking Y chromosome show dysregulation of autosomal gene expressionJan P Dumanski, Jonatan Halvardson, Hanna Davies, et al.The Journal of Clinical Investigation|March 24, 2015
Identification and validation of N-acetyltransferase 2 as an insulin sensitivity geneJoshua W Knowles, Weijia Xie, Zhongyang Zhang, et al.Nature Genetics|November 15, 2016
Integrative genomic analysis implicates limited peripheral adipose storage capacity in the pathogenesis of human insulin resistanceLuca A Lotta, Pawan Gulati, Felix R Day, et al.Human Molecular Genetics|February 27, 2018
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM studyTanya M Teslovich, Daniel Seung Kim, Xianyong Yin, et al.The Journal of Clinical Endocrinology and Metabolism|December 7, 2021
Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat DistributionMine Koprulu, Yajie Zhao, Eleanor Wheeler, et al.The Lancet. Diabetes & Endocrinology|June 29, 2023
Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort studyAna P M Canton, Flávia R Tinano, Leonardo Guasti, et al.Cell|July 3, 2024
Loss of transient receptor potential channel 5 causes obesity and postpartum depressionYongxiang Li, Tessa M Cacciottolo, Na Yin, et al.Science (New York, N.Y.)|March 6, 2025
Canine genome-wide association study identifies DENND1B as an obesity gene in dogs and humansNatalie J Wallis, Alyce McClellan, Alexander Mörseburg, et al.Nature|September 11, 2024
Genetic links between ovarian ageing, cancer risk and de novo mutation ratesStasa Stankovic, Saleh Shekari, Qin Qin Huang, et al.Pageof 44