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pro vyhledávání: '"Clara A. Michell"'
Autor:
Jose R. Pinto, Tiago Veltri, Maicon Landim-Vieira, Michelle S. Parvatiyar, David Gonzalez-Martinez, Karissa M. Dieseldorff Jones, Clara A. Michell, David Dweck, Andrew P. Landstrom, P. Bryant Chase
Publikováno v:
Frontiers in Physiology, Vol 8 (2017)
Mutations in TNNC1—the gene encoding cardiac troponin C (cTnC)—that have been associated with hypertrophic cardiomyopathy (HCM) and cardiac dysfunction may also affect Ca2+-regulation and function of slow skeletal muscle since the same gene is ex
Externí odkaz:
https://doaj.org/article/de0f01d82986440e8a1a28beedc74a76
Autor:
David Gonzalez-Martinez, Karissa M. Dieseldorff Jones, Maicon Landim-Vieira, Michelle S. Parvatiyar, Jose R. Pinto, Andrew P. Landstrom, P. Bryant Chase, Clara A. Michell, Tiago Veltri, David Dweck
Publikováno v:
Frontiers in Physiology
Frontiers in Physiology, Vol 8 (2017)
Frontiers in Physiology, Vol 8 (2017)
Mutations in TNNC1—the gene encoding cardiac troponin C (cTnC)—that have been associated with hypertrophic cardiomyopathy (HCM) and cardiac dysfunction may also affect Ca2+-regulation and function of slow skeletal muscle since the same gene is ex
Publikováno v:
Archives of biochemistry and biophysics. 601
Higher affinity for TnI explains how troponin C (TnC) carrying a causative hypertrophic cardiomyopathy mutation, TnC(A8V), sensitizes muscle cells to Ca(2+). Muscle fibers reconstituted with TnC(A8V) require ∼2.3-fold less [Ca(2+)] to achieve 50% m
Publikováno v:
Biophysical Journal. 108(2):593a-594a
Mutations in cardiac troponin C (cTnC) have been linked to hypertrophic cardiomyopathy (HCM) in humans. The cTnC subunit of the troponin complex is expressed in both slow skeletal and cardiac muscle. The cTnC HCM mutations A8V, C84Y and D145E increas