Expression and biological activity of Baculovirus generated wild-type human slow α tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference20 articles.
1. A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy
2. The molecular basis for tropomyosin isoform diversity
3. Altered actin and troponin binding of amino-terminal variants of chicken striated muscle alpha-tropomyosin expressed in Escherichia coli.
4. Requirement of amino-terminal modification for striated muscle alpha-tropomyosin function.
5. High-Level Production of Functional Muscle α-Tropomyosin in Pichia pastoris
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1. Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy;Skeletal Muscle;2023-11-07
2. Mechanisms of disturbance of the contractile function of slow skeletal muscles induced by myopathic mutations in the tropomyosinTPM3gene;The FASEB Journal;2020-08-14
3. Molecular Mechanisms of Pathologies of Skeletal and Cardiac Muscles Caused by Point Mutations in the Tropomyosin Genes;Biochemistry (Moscow);2020-01
4. Functional outcomes of structural peculiarities of striated muscle tropomyosin;Journal of Muscle Research and Cell Motility;2019-09-18
5. Molecular Defects in Cardiac Myofilament Ca2+-Regulation Due to Cardiomyopathy-Linked Mutations Can Be Reversed by Small Molecules Binding to Troponin;Frontiers in Physiology;2018-03-27
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