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The Journal of Clinical Investigation|June 3, 2020
BET bromodomain inhibition attenuates cardiac phenotype in myocyte-specific lamin A/C-deficient miceGaelle Auguste, Leila Rouhi, Scot J Matkovich, et al.
The Journal of Cardiovascular Aging|February 23, 2023
PANoptosis is a prominent feature of desmoplakin cardiomyopathyMelis Olcum, Leila Rouhi, Siyang Fan, et al.
Cardiovascular Research|August 25, 2023
Genetic inactivation of β-catenin is salubrious, whereas its activation is deleterious in desmoplakin cardiomyopathyMelis Olcum, Siyang Fan, Leila Rouhi, et al.
The Journal of Clinical Investigation|July 11, 2006
Suppression of canonical Wnt/beta-catenin signaling by nuclear plakoglobin recapitulates phenotype of arrhythmogenic right ventricular cardiomyopathyEduardo Garcia-Gras, Raffaella Lombardi, Michael J Giocondo, et al.
Human Molecular Genetics|July 27, 2007
Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathyE Warwick Daw, Suet Nee Chen, Grazyna Czernuszewicz, et al.
Journal of the American Heart Association|January 25, 2015
Arrhythmogenic cardiomyopathy in a patient with a rare loss-of-function KCNQ1 mutationQinmei Xiong, Qing Cao, Qiongqiong Zhou, et al.
Circulation Research|April 11, 2009
Genetic fate mapping identifies second heart field progenitor cells as a source of adipocytes in arrhythmogenic right ventricular cardiomyopathyRaffaella Lombardi, Jinjiang Dong, Gabriela Rodriguez, et al.
JCI Insight|July 3, 2025
Cardiomyocyte cytosolic nuclear self-DNA contributes to the pathogenesis of desmoplakin cardiomyopathyWeiyue Wang, Benjamin Cathcart, Quoc D Nguyen, et al.
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