Pathogenic properties of the N-terminal region of cardiac myosin binding protein-C in vitro (Q28265173)

2

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Xiang Ji

3

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Nagalingam R Sundaresan

4

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Mahesh P Gupta

5

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Pieter P de Tombe

6

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Sakthivel Sadayappan

Journal of Muscle Research & Cell Motility

7

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language of work or name

English

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publication date

May 2012

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published in

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volume

33

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issue

1

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page(s)

17-30

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cites work

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Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C

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Unique single molecule binding of cardiac myosin binding protein-C to actin and phosphorylation-dependent inhibition of actomyosin motility requires 17 amino acids of the motif domain

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Cardiac myosin binding protein-C is a potential diagnostic biomarker for myocardial infarction.

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29 September 2017

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29 September 2017

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2 June 2018

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Activation of myocardial contraction by the N-terminal domains of myosin binding protein-C.

2 June 2018

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Inhibition of histone deacetylation blocks cardiac hypertrophy induced by angiotensin II infusion and aortic banding

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Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling.

21 January 2018

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Variety is the splice of life

21 January 2018

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Independent FHC-related cardiac troponin T mutations exhibit specific alterations in myocellular contractility and calcium kinetics

21 January 2018

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PubMed

https://pubmed.ncbi.nlm.nih.gov/22527638

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Myosin-Binding Protein C Phosphorylation, Myofibril Structure, and Contractile Function During Low-Flow Ischemia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22527638

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

cAPK-phosphorylation controls the interaction of the regulatory domain of cardiac myosin binding protein C with myosin-S2 in an on-off fashion

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22527638