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The Journal of Clinical Investigation|April 3, 2012
Activation of ER stress and mTORC1 suppresses hepatic sortilin-1 levels in obese miceDing Ai, Juan M Baez, Hongfeng Jiang, et al.
JAMA|November 16, 2024
Evaluating Performance and Agreement of Coronary Heart Disease Polygenic Risk ScoresSarah A Abramowitz, Kristin Boulier, Karl Keat, et al.
Circulation. Genomic and Precision Medicine|February 10, 2022
Coronary Artery Disease Risk of Familial Hypercholesterolemia Genetic Variants Independent of Clinically Observed Longitudinal Cholesterol ExposureShoa L Clarke, Catherine Tcheandjieu, Austin T Hilliard, et al.
Implementation Science Communications|December 2, 2024
A qualitative study of perceptions of the care pathway for familial hypercholesterolemia: screening, diagnosis, treatment, and family cascade screeningAmy R Pettit, Tamar Klaiman, Rebecca Connelly Kersting, et al.
Cell Reports. Medicine|December 13, 2022
Exome-wide association analysis of CT imaging-derived hepatic fat in a medical biobankJoseph Park, Matthew T MacLean, Anastasia M Lucas, et al.
Science Advances|November 7, 2019
Myeloid Tribbles 1 induces early atherosclerosis via enhanced foam cell expansionJessica M Johnston, Adrienn Angyal, Robert C Bauer, et al.
Med (New York, N.Y.)|May 22, 2024
The common p.Ile291Val variant of ERLIN1 enhances TM6SF2 function and is associated with protection against MASLDMiriam Daphne Rendel, Cecilia Vitali, Kate Townsend Creasy, et al.
Plos Genetics|February 4, 2015
Systematic cell-based phenotyping of missense alleles empowers rare variant association studies: a case for LDLR and myocardial infarctionAenne S Thormaehlen, Christian Schuberth, Hong-Hee Won, et al.
Circulation. Genomic and Precision Medicine|April 1, 2026
Friend of GATA2 Variant Ser657Gly Is Associated With Coronary Microvascular DiseaseMarie A Guerraty, S Shefali Verma, Yi-An Ko, et al.
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