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Human Genetics|May 29, 2016
De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathyPamela A Long, Michael T Zimmermann, Maengjo Kim, et al.
Circulation. Genomic and Precision Medicine|December 29, 2022
Genome-Wide Association and Inheritance-Based Analyses Implicate Unconventional Myosin Genes in Hypoplastic Left Heart SyndromeJeanne L Theis, Sarah-Dana H Shatila, Zachary C Fogarty, et al.
Circulation|January 30, 2002
Metavinculin mutations alter actin interaction in dilated cardiomyopathyTimothy M Olson, Susanne Illenberger, Nina Y Kishimoto, et al.
Circulation. Cardiovascular Genetics|January 14, 2015
Cardiac transcriptome and dilated cardiomyopathy genes in zebrafishYu-Huan Shih, Yuji Zhang, Yonghe Ding, et al.
The American Journal of Cardiology|March 13, 2018
Idiopathic Restrictive Cardiomyopathy in Children and Young AdultsHeather N Anderson, Frank Cetta, David J Driscoll, et al.
Journal of the American College of Cardiology|September 5, 2009
A human atrial natriuretic peptide gene mutation reveals a novel peptide with enhanced blood pressure-lowering, renal-enhancing, and aldosterone-suppressing actionsPaul M McKie, Alessandro Cataliotti, Brenda K Huntley, et al.
Molecular Genetics and Metabolism|October 21, 2005
Identification of a metavinculin missense mutation, R975W, associated with both hypertrophic and dilated cardiomyopathyVlad C Vasile, Melissa L Will, Steve R Ommen, et al.
International Journal of Molecular Sciences|June 2, 2021
TFEB Overexpression, Not mTOR Inhibition, Ameliorates RagCS75Y CardiomyopathyMaengjo Kim, Linghui Lu, Alexey V Dvornikov, et al.
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