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Molecular mechanisms of genetic damages of the myocardium in cardiomyopathy
Author(s) -
A.G. Hasanov,
T.V. Bershova,
Е. Н. Басаргина,
Bakanov Mi
Publication year - 2010
Publication title -
biomeditsinskaya khimiya
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.192
H-Index - 15
eISSN - 2310-6972
pISSN - 2310-6905
DOI - 10.18097/pbmc20105603319
Subject(s) - hypertrophic cardiomyopathy , extracellular matrix , cardiomyopathy , dilated cardiomyopathy , cytoskeleton , extracellular , medicine , chemistry , microbiology and biotechnology , cardiology , heart failure , cell , biology , biochemistry
The review highlighted problems of reorganization of myocardical contractile and cytoskeletal proteins in cardiomyopathy (CM). The role of the genetic factors coding contractile proteins, proteins of thin and thick filaments, and also extracellular matrix proteins in processes of formation and development of hypertrophic (HCM) and dilated (DCM) cardiomyopathy are analyzed. The mechanisms responsible for the changes in cardiac proteins on regulation involved into force generation, its transfer, recycling ATP, impairments in transmembranal signals, that finally lead to cardiac cell dysfunction determining various manifestations of CM are considered.

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