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JACC. Basic to Translational Science|June 10, 2017
Cardiac Myosin Binding Protein-C Autoantibodies are Potential Early Indicators of Cardiac Dysfunction and Patient Outcome in Acute Coronary SyndromeThomas L Lynch, Diederik W D Kuster, Beverly Gonzalez, et al.
Science (New York, N.Y.)|January 15, 2026
Deep-learning analysis of 3D microarchitectural remodeling in hypertrophic cardiomyopathyEric Q Wei, Martin Beyer, Kemar J Brown, et al.
The Journal of Clinical Investigation|February 11, 2014
5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathyDanos C Christodoulou, Hiroko Wakimoto, Kenji Onoue, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 18, 2022
An ancient founder mutation located between ROBO1 and ROBO2 is responsible for increased microtia risk in Amerindigenous populationsDaniel Quiat, Seong Won Kim, Qi Zhang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
The Journal of Clinical Investigation|June 3, 2024
Increased endothelial sclerostin caused by elevated DSCAM mediates multiple trisomy 21 phenotypesDavid M McKean, Qi Zhang, Priyanka Narayan, et al.
The Journal of Clinical Investigation|January 2, 2025
Cardiac fibroblast BAG3 regulates TGFBR2 signaling and fibrosis in dilated cardiomyopathyBryan Z Wang, Margaretha Aj Morsink, Seong Won Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 19, 2022
Damaging variants in FOXI3 cause microtia and craniofacial microsomiaDaniel Quiat, Andrew T Timberlake, Justin J Curran, et al.
The New England Journal of Medicine|February 17, 2012
Truncations of titin causing dilated cardiomyopathyDaniel S Herman, Lien Lam, Matthew R G Taylor, et al.
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