Congenital myopathy‐related mutations in tropomyosin disrupt regulatory function through altered actin affinity and tropomodulin binding-Reference-Cited by-同舟云学术

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Congenital myopathy‐related mutations in tropomyosin disrupt regulatory function through altered actin affinity and tropomodulin binding

Published:2019-03-05 Issue:10 Volume:286 Page:1877-1893
ISSN:1742-464X
Container-title:The FEBS Journal
language:en
Short-container-title:FEBS J

Author:

Moraczewska Joanna¹,Robaszkiewicz Katarzyna¹,Śliwinska Małgorzata¹,Czajkowska Marta¹,Ly Thu²,Kostyukova Alla²,Wen Han³,Zheng Wenjun³

Affiliation:

1. Department of Biochemistry and Cell Biology Faculty of Natural Sciences Kazimierz Wielki University Bydgoszcz Poland

2. Voiland School of Chemical Engineering and Bioengineering University of Washington Pullman WA USA

3. Department of Physics University at Buffalo SUNY NY USA

Funder

Narodowe Centrum Nauki

National Institutes of Health

Publisher

Wiley

Subject

Cell Biology,Molecular Biology,Biochemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/febs.14787

Reference63 articles.

1. Architecture and function in the muscle sarcomere

2. Changes in the Cross-Striations of Muscle during Contraction and Stretch and their Structural Interpretation

3. Fifty years of muscle and the sliding filament hypothesis

4. Structural Changes in Muscle During Contraction: Interference Microscopy of Living Muscle Fibres

5. Tropomyosin: Function Follows Structure

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Congenital myopathies: pathophysiological mechanisms and promising therapies;Journal of Translational Medicine;2024-09-02

2. Functional and Structural Properties of Cytoplasmic Tropomyosin Isoforms Tpm1.8 and Tpm1.9;International Journal of Molecular Sciences;2024-06-22

3. Troponin and a Myopathy-Linked Mutation in TPM3 Inhibit Cofilin-2-Induced Thin Filament Depolymerization;International Journal of Molecular Sciences;2023-11-17

4. A Novel Variant in TPM3 Causing Muscle Weakness and Concomitant Hypercontractile Phenotype;International Journal of Molecular Sciences;2023-11-09

5. Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy;Skeletal Muscle;2023-11-07

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