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The Journal of Cardiovascular Aging|August 27, 2021
Pharmacological suppression of the WNT signaling pathway attenuates age-dependent expression of the phenotype in a mouse model of arrhythmogenic cardiomyopathySirisha M Cheedipudi, Siyang Fan, Leila Rouhi, et al.
Journal of the American College of Cardiology|February 21, 2006
Antifibrotic effects of antioxidant N-acetylcysteine in a mouse model of human hypertrophic cardiomyopathy mutationAli J Marian, Vinitha Senthil, Suet N Chen, et al.
The Journal of Cardiovascular Aging|August 14, 2023
Cytosolic DNA sensing protein pathway is activated in human hearts with dilated cardiomyopathyLeila Rouhi, Sirisha M Cheedipudi, Benjamin Cathcart, et al.
Circulation Research|July 30, 2016
Knockdown of Plakophilin 2 Downregulates miR-184 Through CpG Hypermethylation and Suppression of the E2F1 Pathway and Leads to Enhanced Adipogenesis In VitroPriyatansh Gurha, Xiaofan Chen, Raffaella Lombardi, et al.
European Journal of Clinical Investigation|December 16, 2010
Metabolomic distinction and insights into the pathogenesis of human primary dilated cardiomyopathyDanny Alexander, Raffaella Lombardi, Gabriela Rodriguez, et al.
BMC Cardiovascular Disorders|January 29, 2009
The 9p21 susceptibility locus for coronary artery disease and the severity of coronary atherosclerosisSuet Nee Chen, Christie M Ballantyne, Antonio M Gotto, et al.
Cardiovascular Research|September 19, 2012
Pathogenesis of hypertrophic cardiomyopathy caused by myozenin 2 mutations is independent of calcineurin activityAlessandra Ruggiero, Suet Nee Chen, Raffaella Lombardi, et al.
The Journal of Cardiovascular Aging|November 18, 2021
A combinatorial oligogenic basis for the phenotypic plasticity between late-onset dilated and arrhythmogenic cardiomyopathy in a single familyKimia Pourebrahim, John Garrity Marian, Yanli Tan, et al.
Circulation Research|February 23, 2017
A Potential Oligogenic Etiology of Hypertrophic Cardiomyopathy: A Classic Single-Gene DisorderLili Li, Matthew Neil Bainbridge, Yanli Tan, et al.
BMC Medical Genetics|March 4, 2017
Identification of established arrhythmogenic right ventricular cardiomyopathy mutation in a patient with the contrasting phenotype of hypertrophic cardiomyopathyMatthew Neil Bainbridge, Lili Li, Yanli Tan, et al.
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