Understanding how certain mutations in contractile protein genes are able to alter the function of the heart
A high-throughput screening identifies ZNF418 as a novel regulator of the ubiquitin-proteasome system and autophagy-lysosomal pathway. Autophagy. 2021; 17(10):3124-3139.
Ube2v1 Positively Regulates Protein Aggregation by Modulating Ubiquitin Proteasome System Performance Partially Through K63 Ubiquitination. Circulation Research. 2020; 126(7):907-922.
Myofibroblast-Specific TGFβ Receptor II Signaling in the Fibrotic Response to Cardiac Myosin Binding Protein C-Induced Cardiomyopathy. Circulation Research. 2018; 123(12):1285-1297.
Hypertrophic cardiomyopathy R403Q mutation in rabbit β-myosin reduces contractile function at the molecular and myofibrillar levels. Proceedings of the National Academy of Sciences of the United States of America. 2018; 115(44):11238-11243.
Cardiac Fibrosis in Proteotoxic Cardiac Disease is Dependent Upon Myofibroblast TGF -β Signaling. Journal of the American Heart Association. 2018; 7(20):e010013.
Abstract 265: TGF Beta Signaling and Fibrosis in cMyBP-C-dependent Cardiac Disease. Circulation Research. 2018; 123(Suppl_1).
MMI-0100 Inhibits Cardiac Fibrosis in a Mouse Model Overexpressing Cardiac Myosin Binding Protein C. Journal of the American Heart Association. 2017; 6(9).
An Unbiased High-Throughput Screen to Identify Novel Effectors That Impact on Cardiomyocyte Aggregate Levels. Circulation Research. 2017; 121(6):604-616.
In vivo definition of cardiac myosin-binding protein C's critical interactions with myosin. Pflugers Archiv European Journal of Physiology. 2016; 468(10):1685-1695.
UBC9-Mediated Sumoylation Favorably Impacts Cardiac Function in Compromised Hearts. Circulation Research. 2016; 118(12):1894-1905.