The Molecular Mechanisms of Mutations in Actin and Myosin that Cause Inherited Myopathy-Reference-Cited by-同舟云学术

The Molecular Mechanisms of Mutations in Actin and Myosin that Cause Inherited Myopathy

Published:2018-07-11 Issue:7 Volume:19 Page:2020
ISSN:1422-0067
Container-title:International Journal of Molecular Sciences
language:en
Short-container-title:IJMS

Author:

Marston Steven^ORCID

Funder

British Heart Foundation

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

Link

http://www.mdpi.com/1422-0067/19/7/2020/pdf

Reference114 articles.

1. A systematic nomenclature for mammalian tropomyosin isoforms

2. Molecular genetics of actin function

3. Myosinopathies: pathology and mechanisms

4. Mutations and polymorphisms of the skeletal muscle Î±-actin gene (ACTA1)

5. Modulation of Thin Filament Activation by Breakdown or Isoform Switching of Thin Filament Proteins

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