Molecular Mechanisms of the Deregulation of Muscle Contraction Induced by the R90P Mutation in Tpm3.12 and the Weakening of This Effect by BDM and W7

Point mutations in the genes encoding the skeletal muscle isoforms of tropomyosin can cause a range of muscle diseases. The amino acid substitution of Arg for Pro residue in the 90th position (R90P) in γ-tropomyosin (Tpm3.12) is associated with congenital fiber type disproportion and muscle weakness...

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Detalles Bibliográficos
Autores principales: Borovikov, Yurii S., Andreeva, Daria D., Avrova, Stanislava V., Sirenko, Vladimir V., Simonyan, Armen O., Redwood, Charles S., Karpicheva, Olga E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231546/
https://www.ncbi.nlm.nih.gov/pubmed/34204776
http://dx.doi.org/10.3390/ijms22126318

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8231546/
https://www.ncbi.nlm.nih.gov/pubmed/34204776
http://dx.doi.org/10.3390/ijms22126318

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