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Science Translational Medicine|January 14, 2021
Kidney disease genetic risk variants alter lysosomal beta-mannosidase (MANBA) expression and disease severityXiangchen Gu, Hongliu Yang, Xin Sheng, et al.
Nature Genetics|January 18, 2006
Variant of transcription factor 7-like 2 (TCF7L2) gene confers risk of type 2 diabetesStruan F A Grant, Gudmar Thorleifsson, Inga Reynisdottir, et al.
JACC. Basic to Translational Science|November 13, 2024
Proteome-Wide Genetic Investigation of Large Artery StiffnessMarie-Joe Dib, Joe David Azzo, Lei Zhao, et al.
Journal of the American Heart Association|August 29, 2024
Prognostic Significance and Biologic Associations of Senescence-Associated Secretory Phenotype Biomarkers in Heart FailureOday Salman, Payman Zamani, Lei Zhao, et al.
Human Molecular Genetics|June 9, 2016
Neuronal deficiency of ARV1 causes an autosomal recessive epileptic encephalopathyElizabeth E Palmer, Kelsey E Jarrett, Rani K Sachdev, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2013
Implementing genomic medicine in the clinic: the future is hereTeri A Manolio, Rex L Chisholm, Brad Ozenberger, et al.
The Lancet. Diabetes & Endocrinology|April 15, 2017
Apolipoprotein(a) isoform size, lipoprotein(a) concentration, and coronary artery disease: a mendelian randomisation analysisDanish Saleheen, Philip C Haycock, Wei Zhao, et al.
Circulation|April 25, 2024
SPTLC3 Is Essential for Complex I Activity and Contributes to Ischemic CardiomyopathyAnna Kovilakath, Adolfo G Mauro, Yolander A Valentine, et al.
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