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137 related items for PubMed ID: 32087052

  • 1. Molecular Mechanisms of Pathologies of Skeletal and Cardiac Muscles Caused by Point Mutations in the Tropomyosin Genes.
    Matyushenko AM, Levitsky DI.
    Biochemistry (Mosc); 2020 Jan; 85(Suppl 1):S20-S33. PubMed ID: 32087052
    [Abstract] [Full Text] [Related]

  • 2. Structural and functional properties of αβ-heterodimers of tropomyosin with myopathic mutations Q147P and K49del in the β-chain.
    Matyushenko AM, Shchepkin DV, Susorov DS, Nefedova VV, Kopylova GV, Berg VY, Kleymenov SY, Levitsky DI.
    Biochem Biophys Res Commun; 2019 Jan 15; 508(3):934-939. PubMed ID: 30545627
    [Abstract] [Full Text] [Related]

  • 3. Effects of myopathy-causing mutations R91P and R245G in the TPM3 gene on structural and functional properties of slow skeletal muscle tropomyosin.
    Gonchar AD, Kopylova GV, Kochurova AM, Berg VY, Shchepkin DV, Koubasova NA, Tsaturyan AK, Kleymenov SY, Matyushenko AM, Levitsky DI.
    Biochem Biophys Res Commun; 2021 Jan 01; 534():8-13. PubMed ID: 33307294
    [Abstract] [Full Text] [Related]

  • 4. Mechanisms of disturbance of the contractile function of slow skeletal muscles induced by myopathic mutations in the tropomyosin TPM3 gene.
    Matyushenko AM, Nefedova VV, Shchepkin DV, Kopylova GV, Berg VY, Pivovarova AV, Kleymenov SY, Bershitsky SY, Levitsky DI.
    FASEB J; 2020 Oct 01; 34(10):13507-13520. PubMed ID: 32797717
    [Abstract] [Full Text] [Related]

  • 5. The effects of cardiomyopathy-associated mutations in the head-to-tail overlap junction of α-tropomyosin on its properties and interaction with actin.
    Matyushenko AM, Koubassova NA, Shchepkin DV, Kopylova GV, Nabiev SR, Nikitina LV, Bershitsky SY, Levitsky DI, Tsaturyan AK.
    Int J Biol Macromol; 2019 Mar 15; 125():1266-1274. PubMed ID: 30240712
    [Abstract] [Full Text] [Related]

  • 6. Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional properties of slow skeletal muscle tropomyosin γβ-heterodimer.
    Gonchar AD, Koubassova NA, Kopylova GV, Kochurova AM, Nefedova VV, Yampolskaya DS, Shchepkin DV, Bershitsky SY, Tsaturyan AK, Matyushenko AM, Levitsky DI.
    Arch Biochem Biophys; 2024 Feb 15; 752():109881. PubMed ID: 38185233
    [Abstract] [Full Text] [Related]

  • 7. Myopathic mutations in the β-chain of tropomyosin differently affect the structural and functional properties of ββ- and αβ-dimers.
    Bershitsky SY, Logvinova DS, Shchepkin DV, Kopylova GV, Matyushenko AM.
    FASEB J; 2019 Feb 15; 33(2):1963-1971. PubMed ID: 30199282
    [Abstract] [Full Text] [Related]

  • 8. Mutations in repeating structural motifs of tropomyosin cause gain of function in skeletal muscle myopathy patients.
    Marston S, Memo M, Messer A, Papadaki M, Nowak K, McNamara E, Ong R, El-Mezgueldi M, Li X, Lehman W.
    Hum Mol Genet; 2013 Dec 15; 22(24):4978-87. PubMed ID: 23886664
    [Abstract] [Full Text] [Related]

  • 9. Functional role of the core gap in the middle part of tropomyosin.
    Matyushenko AM, Shchepkin DV, Kopylova GV, Bershitsky SY, Koubassova NA, Tsaturyan AK, Levitsky DI.
    FEBS J; 2018 Mar 15; 285(5):871-886. PubMed ID: 29278453
    [Abstract] [Full Text] [Related]

  • 10. 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.
    Borovikov YS, Karpicheva OE, Simonyan AO, Avrova SV, Rogozovets EA, Sirenko VV, Redwood CS.
    Int J Mol Sci; 2018 Dec 10; 19(12):. PubMed ID: 30544720
    [Abstract] [Full Text] [Related]

  • 11. Effect of Interchain Disulfide Crosslinking in the Tropomyosin Molecule on Actin-Myosin Interaction in the Atrial Myocardium.
    Shchepkin DV, Matyushenko AM, Bershitsky SY, Kopylova GV.
    Bull Exp Biol Med; 2019 May 10; 167(1):65-68. PubMed ID: 31177460
    [Abstract] [Full Text] [Related]

  • 12. Structural and Functional Effects of Cardiomyopathy-Causing Mutations in the Troponin T-Binding Region of Cardiac Tropomyosin.
    Matyushenko AM, Shchepkin DV, Kopylova GV, Popruga KE, Artemova NV, Pivovarova AV, Bershitsky SY, Levitsky DI.
    Biochemistry; 2017 Jan 10; 56(1):250-259. PubMed ID: 27983818
    [Abstract] [Full Text] [Related]

  • 13. Thermal unfolding of homodimers and heterodimers of different skeletal-muscle isoforms of tropomyosin.
    Matyushenko AM, Kleymenov SY, Susorov DS, Levitsky DI.
    Biophys Chem; 2018 Dec 10; 243():1-7. PubMed ID: 30265962
    [Abstract] [Full Text] [Related]

  • 14. Tropomyosin: double helix from the protein world.
    Nevzorov IA, Levitsky DI.
    Biochemistry (Mosc); 2011 Dec 10; 76(13):1507-27. PubMed ID: 22339601
    [Abstract] [Full Text] [Related]

  • 15. Unique functional properties of slow skeletal muscle tropomyosin.
    Matyushenko AM, Shchepkin DV, Kopylova GV, Bershitsky SY, Levitsky DI.
    Biochimie; 2020 Jul 10; 174():1-8. PubMed ID: 32224097
    [Abstract] [Full Text] [Related]

  • 16. Cardiomyopathy Mutation Alters End-to-End Junction of Tropomyosin and Reduces Calcium Sensitivity.
    Sundar S, Rynkiewicz MJ, Ghosh A, Lehman W, Moore JR.
    Biophys J; 2020 Jan 21; 118(2):303-312. PubMed ID: 31882250
    [Abstract] [Full Text] [Related]

  • 17. Effect of Cardiomyopathic Mutations in Tropomyosin on Calcium Regulation of the Actin-Myosin Interaction in Skeletal Muscle.
    Kopylova GV, Shchepkin DV, Borovkov DI, Matyushenko AM.
    Bull Exp Biol Med; 2016 Nov 21; 162(1):42-44. PubMed ID: 27878731
    [Abstract] [Full Text] [Related]

  • 18. Impact of A134 and E218 Amino Acid Residues of Tropomyosin on Its Flexibility and Function.
    Marchenko MA, Nefedova VV, Yampolskaya DS, Kopylova GV, Shchepkin DV, Bershitsky SY, Koubassova NA, Tsaturyan AK, Levitsky DI, Matyushenko AM.
    Int J Mol Sci; 2020 Nov 18; 21(22):. PubMed ID: 33218166
    [Abstract] [Full Text] [Related]

  • 19. Impaired tropomyosin-troponin interactions reduce activation of the actin thin filament.
    Robaszkiewicz K, Ostrowska Z, Cyranka-Czaja A, Moraczewska J.
    Biochim Biophys Acta; 2015 May 18; 1854(5):381-90. PubMed ID: 25603119
    [Abstract] [Full Text] [Related]

  • 20. Skeletal muscle myopathy mutations at the actin tropomyosin interface that cause gain- or loss-of-function.
    Memo M, Marston S.
    J Muscle Res Cell Motil; 2013 Aug 18; 34(3-4):165-9. PubMed ID: 23719967
    [Abstract] [Full Text] [Related]

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