Zobrazeno 1 - 4
of 4
pro vyhledávání: '"O. E. Karpicheva"'
Publikováno v:
Cell and Tissue Biology. 17:169-178
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7cc977cbee06f1d730858fc63299cca8
https://doi.org/10.1134/s1990519x23020025
https://doi.org/10.1134/s1990519x23020025
Autor:
O. E. Karpicheva
Publikováno v:
Journal of Evolutionary Biochemistry and Physiology. 57:646-665
Congenital myopathies are a group of clinically and genetically heterogeneous diseases, which are united by primary lesions of skeletal muscles and are characterized by progressive muscle weakness and hypotension, as well as morphological changes in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5547e8bbb428f02e59ebb63f793c9338
https://doi.org/10.1134/s0022093021030133
https://doi.org/10.1134/s0022093021030133
Molecular Mechanisms of Skeletal Muscle Dysfunction in the Early Stages of Human Congenital Myopathy
Autor:
Y. S. Borovikov, O. E. Karpicheva
Publikováno v:
Журнал эволюционной биохимии и физиологии. 56:768-768
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f316d65af08e07b472bd015fd26ca638
https://doi.org/10.31857/s0044452920071924
https://doi.org/10.31857/s0044452920071924
Publikováno v:
Rossiiskii fiziologicheskii zhurnal imeni I.M. Sechenova. 99(1)
Pathogenesis of most myopathies including inherited hypertrophic (HCM) and dilated (DCM) cardiomyopathies is based on modification of structural state of contractile proteins induced by point mutations, such as mutations in alpha-tropomyosin (TM). To
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b69d3087695d7fb8bd2baebad67c2d42
https://pubmed.ncbi.nlm.nih.gov/23659058
https://pubmed.ncbi.nlm.nih.gov/23659058