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Molecular Effects of Familial Hypertrophic Cardiomyopathy-Related Mutations in the TNT1 Domain of cTnT

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Year: 2012
Type: article
Source: Journal of Molecular Biology
DOI: 10.1016/j.jmb.2012.05.008
Authors: Edward P. Manning, Jil C. Tardiff, Steven D. Schwartz
Institutions: Albert Einstein College of Medicine, University of Arizona
Language: English

Topic: Cardiomyopathy and Myosin Studies
Subfield: Cardiology and Cardiovascular Medicine
Field: Medicine
Domain: Health Sciences
SDG: Good health and well-being

Open Access status: green

Funders: National Institutes of Health, National Heart, Lung, and Blood Institute, National Institute of General Medical Sciences
Awards: G1438367337, G1514960581, G1842308918, Protein Dynamics in Enzymatic Catalysis, G3981344285, The interaction of myosin and the thin filament: how mutations cause allosteric dysfunction and their connection to genetic cardiomyopathy, Medical Scientist Training Program, G9000234506, Integrative Approach to Divergent Remodeling in Thin Filament Cardiomyopathies
OpenAlex ID: W2114744788
FWCI: 2.47
Cites: 68
Cited by: 35
Related to: 10
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