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For: Borovikov YS, Karpicheva OE, Simonyan AO, Avrova SV, Rogozovets EA, Sirenko VV, Redwood CS. The Primary Causes of Muscle Dysfunction Associated with the Point Mutations in Tpm3.12; Conformational Analysis of Mutant Proteins as a Tool for Classification of Myopathies. Int J Mol Sci 2018;19:E3975. [PMID: 30544720 DOI: 10.3390/ijms19123975] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
1 Matyushenko AM, Levitsky DI. Molecular Mechanisms of Pathologies of Skeletal and Cardiac Muscles Caused by Point Mutations in the Tropomyosin Genes. Biochemistry (Mosc) 2020;85:S20-33. [PMID: 32087052 DOI: 10.1134/S0006297920140023] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
2 Karpicheva OE, Simonyan AO, Rysev NA, Redwood CS, Borovikov YS. Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln147Pro Tropomyosin. Int J Mol Sci 2020;21:E7590. [PMID: 33066566 DOI: 10.3390/ijms21207590] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 1.5] [Reference Citation Analysis]
3 Borovikov YS, Simonyan AO, Avrova SV, Sirenko VV, Redwood CS, Karpicheva OE. Molecular Mechanisms of Muscle Weakness Associated with E173A Mutation in Tpm3.12. Troponin Ca2+ Sensitivity Inhibitor W7 Can Reduce the Damaging Effect of This Mutation. Int J Mol Sci 2020;21:E4421. [PMID: 32580284 DOI: 10.3390/ijms21124421] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
4 Squire J. Special Issue: The Actin-Myosin Interaction in Muscle: Background and Overview. Int J Mol Sci 2019;20:E5715. [PMID: 31739584 DOI: 10.3390/ijms20225715] [Cited by in Crossref: 7] [Cited by in F6Publishing: 7] [Article Influence: 2.3] [Reference Citation Analysis]
5 Potulska-Chromik A, Jędrzejowska M, Gos M, Rosiak E, Kierdaszuk B, Maruszak A, Opuchlik A, Zekanowski C, Fichna JP. Pathogenic Mutations and Putative Phenotype-Affecting Variants in Polish Myofibrillar Myopathy Patients. J Clin Med 2021;10:914. [PMID: 33652732 DOI: 10.3390/jcm10050914] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
6 Gonchar AD, Kopylova GV, Kochurova AM, Berg VY, Shchepkin DV, Koubasova NA, Tsaturyan AK, Kleymenov SY, Matyushenko AM, Levitsky DI. Effects of myopathy-causing mutations R91P and R245G in the TPM3 gene on structural and functional properties of slow skeletal muscle tropomyosin. Biochem Biophys Res Commun 2021;534:8-13. [PMID: 33307294 DOI: 10.1016/j.bbrc.2020.11.103] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
7 Kopylova GV, Matyushenko AM, Koubassova NA, Shchepkin DV, Bershitsky SY, Levitsky DI, Tsaturyan AK. Functional outcomes of structural peculiarities of striated muscle tropomyosin. J Muscle Res Cell Motil 2020;41:55-70. [DOI: 10.1007/s10974-019-09552-8] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
8 Borovikov YS, Andreeva DD, Avrova SV, Sirenko VV, Simonyan AO, Redwood CS, Karpicheva OE. 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. Int J Mol Sci 2021;22:6318. [PMID: 34204776 DOI: 10.3390/ijms22126318] [Reference Citation Analysis]
9 Borovikov YS, Karpicheva OE, Avrova SV, Simonyan AO, Sirenko VV, Redwood CS. The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2. Biochem Biophys Res Commun 2020;523:258-62. [PMID: 31864708 DOI: 10.1016/j.bbrc.2019.12.061] [Cited by in Crossref: 5] [Cited by in F6Publishing: 3] [Article Influence: 1.7] [Reference Citation Analysis]