Dynamic Regulation of SARS-Cov-2 Binding and Cell Entry Mechanisms in Remodeled Human Ventricular Myocardium.
第一作者:
Michael R,Bristow
第一单位:
Division of Cardiology, University of Colorado, Denver/Anschutz Medical Campus, Aurora, Colorado.;ARCA Biopharma, Westminster, Colorado.;University of Colorado Cardiovascular Institute Pharmacogenomics, Aurora, Colorado.
作者:
关键词
ACE, angiotensin converting enzymeACE2, angiotensin converting enzyme 2ARB, angiotensin receptor blockerBNP, B-type natriuretic peptideCOVID-19, coronavirus disease-2019EmBx, endomyocardial biopsiesF/NDC, nonischemic dilated cardiomyopathy with heart failureHFrEF, heart failure with reduced (<0.50) left ventricular ejection fractionIQR, interquartile rangeLOCF, last observation carried forwardLV, left ventricle (ventricular)LVEF, left ventricular ejection fractionNF, nonfailingNR, nonresponderPCR, polymerase chain reactionR, responderRAS, renin-angiotensin systemRGD, arginine-glycine-aspartic acidRNA-Seq, ribonucleic acid sequencingRV, right ventricle (ventricular)SARS-CoV-2, severe acute respiratory syndrome-coronavirus-2angiotensin converting enzyme 2coronavirus disease 2019integrinsmRNA, messenger ribonucleic acidproteasesventricular remodeling
DOI
10.1016/j.jacbts.2020.06.007
PMID
32838074
发布时间
2020-11-24
- 浏览2
JACC. Basic to translational science
2020年5卷9期
871-883页
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