लोड हो रहा है...

Impact of familial hypertrophic cardiomyopathy-linked mutations in the NH(2) terminus of the RLC on β-myosin cross-bridge mechanics

Familial hypertrophic cardiomyopathy (HCM) is associated with mutations in sarcomeric proteins, including the myosin regulatory light chain (RLC). Here we studied the impact of three HCM mutations located in the NH(2) terminus of the RLC on the molecular mechanism of β-myosin heavy chain (MHC) cross...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:J Appl Physiol (1985)
मुख्य लेखकों: Farman, Gerrie P., Muthu, Priya, Kazmierczak, Katarzyna, Szczesna-Cordary, Danuta, Moore, Jeffrey R.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Physiological Society 2014
विषय:
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC4269682/
https://ncbi.nlm.nih.gov/pubmed/25324513
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/japplphysiol.00798.2014
टैग : टैग जोड़ें
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!