N232S, G741R and D778G β‐cardiac myosin mutants, implicated in familial hypertrophic cardiomyopathy, do not disrupt myofibrillar organisation in cultured myotubes
- 12 December 2000
- journal article
- Published by Wiley in FEBS Letters
- Vol. 486 (3) , 325-327
- https://doi.org/10.1016/s0014-5793(00)02237-7
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Evidence for differential post-translational modifications of slow myosin heavy chain during murine skeletal muscle development.Journal of Muscle Research and Cell Motility, 2000
- Familial Hypertrophic CardiomyopathyCirculation Research, 1998
- Point Mutations in Human β Cardiac Myosin Heavy Chain Have Differential Effects on Sarcomeric Structure and Assembly: An ATP Binding Site Change Disrupts Both Thick and Thin Filaments, Whereas Hypertrophic Cardiomyopathy Mutations Display Normal AssemblyThe Journal of cell biology, 1997
- Myogenic cells express multiple myosin isoformsJournal of Muscle Research and Cell Motility, 1997
- Functions of the myosin ATP and actin binding sites are required for C. elegans thick filament assemblyCell, 1990