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Circulation Research|October 12, 2017
Distinct Cellular Basis for Early Cardiac Arrhythmias, the Cardinal Manifestation of Arrhythmogenic Cardiomyopathy, and the Skin Phenotype of Cardiocutaneous SyndromesJennifer Karmouch, Qiong Q Zhou, Christina Y Miyake, et al.
Circulation. Cardiovascular Genetics|June 7, 2011
Molecular genetic and functional characterization implicate muscle-restricted coiled-coil gene (MURC) as a causal gene for familial dilated cardiomyopathyGabriela Rodriguez, Tomomi Ueyama, Takehiro Ogata, et al.
Circulation|March 4, 2009
Resolution of established cardiac hypertrophy and fibrosis and prevention of systolic dysfunction in a transgenic rabbit model of human cardiomyopathy through thiol-sensitive mechanismsRaffaella Lombardi, Gabriela Rodriguez, Suet Nee Chen, et al.
The Journal of Cardiovascular Aging|July 27, 2022
Deletion of the <i>Lmna</i> gene in fibroblasts causes senescence-associated dilated cardiomyopathy by activating the double-stranded DNA damage response and induction of senescence-associated secretory phenotypeLeila Rouhi, Gaelle Auguste, Qiong Zhou, et al.
Circulation Research|February 12, 2019
Genomic Reorganization of Lamin-Associated Domains in Cardiac Myocytes Is Associated With Differential Gene Expression and DNA Methylation in Human Dilated CardiomyopathySirisha M Cheedipudi, Scot J Matkovich, Cristian Coarfa, et al.
European Journal of Clinical Investigation|May 28, 2011
Determinants of plasma vitamin D levels in patients with acute coronary syndromesGabriella Rodriguez, Aijing Z Starr, Grazyna Z Czernuszewicz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 26, 2014
Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in GenomicsBruce R Korf, Anna B Berry, Melvin Limson, et al.
Cardiovascular Research|July 28, 2019
Exercise restores dysregulated gene expression in a mouse model of arrhythmogenic cardiomyopathySirisha M Cheedipudi, Jinzhu Hu, Siyang Fan, et al.
Human Gene Therapy|April 12, 2018
A Calsequestrin Cis-Regulatory Motif Coupled to a Cardiac Troponin T Promoter Improves Cardiac Adeno-Associated Virus Serotype 9 Transduction SpecificityKyle Chamberlain, Jalish M Riyad, Tyrone Garnett, et al.
Cardiovascular Research|June 16, 2021
The EP300/TP53 pathway, a suppressor of the Hippo and canonical WNT pathways, is activated in human hearts with arrhythmogenic cardiomyopathy in the absence of overt heart failureLeila Rouhi, Siyang Fan, Sirisha M Cheedipudi, et al.
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