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Antimicrobial Agents and Chemotherapy|March 6, 2024
BPR3P0128, a non-nucleoside RNA-dependent RNA polymerase inhibitor, inhibits SARS-CoV-2 variants of concern and exerts synergistic antiviral activity in combination with remdesivirWen-Fang Tang, Yu-Hsiu Chang, Cheng-Chin Lin, et al.Frontiers in Immunology|January 9, 2023
Methotrexate inhibition of SARS-CoV-2 entry, infection and inflammation revealed by bioinformatics approach and a hamster modelYun-Ti Chen, Yu-Hsiu Chang, Nikhil Pathak, et al.Diabetes|September 28, 2017
Genetically Determined Plasma Lipid Levels and Risk of Diabetic Retinopathy: A Mendelian Randomization StudyLucia Sobrin, Yong He Chong, Qiao Fan, et al.Human Molecular Genetics|April 21, 2017
Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid lociNiha Zubair, Mariaelisa Graff, Jose Luis Ambite, et al.Nature Methods|December 31, 2025
cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regionsEric Van Buren, Yi Zhang, Xihao Li, et al.Human Genetics|April 10, 2017
Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established lociLindsay Fernández-Rhodes, Jian Gong, Jeffrey Haessler, et al.Biorxiv : the Preprint Server for Biology|November 14, 2023
A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studiesXihao Li, Han Chen, Margaret Sunitha Selvaraj, et al.Plos Genetics|April 5, 2013
Trans-ethnic fine-mapping of lipid loci identifies population-specific signals and allelic heterogeneity that increases the trait variance explainedYing Wu, Lindsay L Waite, Anne U Jackson, et al.Nature Genetics|May 23, 2017
Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanismsJoanna M M Howson, Wei Zhao, Daniel R Barnes, et al.BMC Genomics|February 20, 2022
Rare coding variants in RCN3 are associated with blood pressureKaren Y He, Tanika N Kelly, Heming Wang, et al.Pageof 21