Effects of myopathy-causing mutations R91P and R245G in the TPM3 gene on structural and functional properties of slow skeletal muscle tropomyosin
Author:
Funder
Russian Science Foundation
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference28 articles.
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1. Molecular cloning of TPM3 gene in qinchuan cattle and its effect on myoblast proliferation and differentiation;Animal Biotechnology;2024-05-22
2. Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional properties of slow skeletal muscle tropomyosin γβ-heterodimer;Archives of Biochemistry and Biophysics;2024-02
3. Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy;Skeletal Muscle;2023-11-07
4. Comparative Genomics Identifies the Evolutionarily Conserved Gene TPM3 as a Target of eca-miR-1 Involved in the Skeletal Muscle Development of Donkeys;International Journal of Molecular Sciences;2023-10-22
5. Myopathy-Causing Mutation <i>R91P</i> in the <i>TPM3</i> Gene Drastically Impairs Structural and Functional Properties of Slow Skeletal Muscle Tropomyosin Γβ-Heterodimer;2023
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