390 related articles for article (PubMed ID: 26708479)
1. Myopathy-causing Q147P TPM2 mutation shifts tropomyosin strands further towards the open position and increases the proportion of strong-binding cross-bridges during the ATPase cycle.
Karpicheva OE; Simonyan AO; Kuleva NV; Redwood CS; Borovikov YS
Biochim Biophys Acta; 2016 Mar; 1864(3):260-267. PubMed ID: 26708479
[TBL] [Abstract][Full Text] [Related]
2. Aberrant movement of β-tropomyosin associated with congenital myopathy causes defective response of myosin heads and actin during the ATPase cycle.
Borovikov YS; Avrova SV; Rysev NA; Sirenko VV; Simonyan AO; Chernev AA; Karpicheva OE; Piers A; Redwood CS
Arch Biochem Biophys; 2015 Jul; 577-578():11-23. PubMed ID: 25978979
[TBL] [Abstract][Full Text] [Related]
3. The primary cause of muscle disfunction associated with substitutions E240K and R244G in tropomyosin is aberrant behavior of tropomyosin and response of actin and myosin during ATPase cycle.
Simonyan AO; Sirenko VV; Karpicheva OE; Robaszkiewicz K; Śliwinska M; Moraczewska J; Krutetskaya ZI; Borovikov YS
Arch Biochem Biophys; 2018 Apr; 644():17-28. PubMed ID: 29510086
[TBL] [Abstract][Full Text] [Related]
4. Molecular Mechanisms of Deregulation of Muscle Contractility Caused by the R168H Mutation in TPM3 and Its Attenuation by Therapeutic Agents.
Karpicheva OE; Avrova SV; Bogdanov AL; Sirenko VV; Redwood CS; Borovikov YS
Int J Mol Sci; 2023 Mar; 24(6):. PubMed ID: 36982903
[TBL] [Abstract][Full Text] [Related]
5. 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; 19(12):. PubMed ID: 30544720
[TBL] [Abstract][Full Text] [Related]
6. The reason for the low Ca
Avrova SV; Karpicheva OE; Rysev NA; Simonyan AO; Sirenko VV; Redwood CS; Borovikov YS
Biochem Biophys Res Commun; 2018 Jul; 502(2):209-214. PubMed ID: 29792862
[TBL] [Abstract][Full Text] [Related]
7. Gly126Arg substitution causes anomalous behaviour of α-skeletal and β-smooth tropomyosins during the ATPase cycle.
Rysev NA; Nevzorov IA; Avrova SV; Karpicheva OE; Redwood CS; Levitsky DI; Borovikov YS
Arch Biochem Biophys; 2014 Feb; 543():57-66. PubMed ID: 24374033
[TBL] [Abstract][Full Text] [Related]
8. The reason for a high Ca
Borovikov YS; Simonyan AO; Karpicheva OE; Avrova SV; Rysev NA; Sirenko VV; Piers A; Redwood CS
Biochem Biophys Res Commun; 2017 Dec; 494(3-4):681-686. PubMed ID: 29097206
[TBL] [Abstract][Full Text] [Related]
9. The E117K mutation in β-tropomyosin disturbs concerted conformational changes of actomyosin in muscle fibers.
Karpicheva OE; Redwood CS; Borovikov YS
Arch Biochem Biophys; 2014 May; 549():12-6. PubMed ID: 24657080
[TBL] [Abstract][Full Text] [Related]
10. The effect of the dilated cardiomyopathy-causing Glu40Lys TPM1 mutation on actin-myosin interactions during the ATPase cycle.
Borovikov YS; Avrova SV; Karpicheva OE; Robinson P; Redwood CS
Biochem Biophys Res Commun; 2011 Aug; 411(3):496-500. PubMed ID: 21741356
[TBL] [Abstract][Full Text] [Related]
11. Hypertrophic cardiomyopathy-causing Asp175asn and Glu180gly Tpm1 mutations shift tropomyosin strands further towards the open position during the ATPase cycle.
Borovikov YS; Rysev NA; Karpicheva OE; Redwood CS
Biochem Biophys Res Commun; 2011 Apr; 407(1):197-201. PubMed ID: 21376702
[TBL] [Abstract][Full Text] [Related]
12. Abnormal movement of tropomyosin and response of myosin heads and actin during the ATPase cycle caused by the Arg167His, Arg167Gly and Lys168Glu mutations in TPM1 gene.
Borovikov YS; Rysev NA; Chernev AA; Avrova SV; Karpicheva OE; Borys D; Śliwińska M; Moraczewska J
Arch Biochem Biophys; 2016 Sep; 606():157-66. PubMed ID: 27480605
[TBL] [Abstract][Full Text] [Related]
13. Molecular mechanisms of deregulation of the thin filament associated with the R167H and K168E substitutions in tropomyosin Tpm1.1.
Borovikov YS; Rysev NA; Avrova SV; Karpicheva OE; Borys D; Moraczewska J
Arch Biochem Biophys; 2017 Jan; 614():28-40. PubMed ID: 27956029
[TBL] [Abstract][Full Text] [Related]
14. The nemaline myopathy-causing E117K mutation in β-tropomyosin reduces thin filament activation.
Karpicheva OE; Robinson P; Piers A; Borovikov YS; Redwood CS
Arch Biochem Biophys; 2013 Aug; 536(1):25-30. PubMed ID: 23689010
[TBL] [Abstract][Full Text] [Related]
15. Looking for Targets to Restore the Contractile Function in Congenital Myopathy Caused by Gln
Karpicheva OE; Simonyan AO; Rysev NA; Redwood CS; Borovikov YS
Int J Mol Sci; 2020 Oct; 21(20):. PubMed ID: 33066566
[TBL] [Abstract][Full Text] [Related]
16. The effect of the Asp175Asn and Glu180Gly TPM1 mutations on actin-myosin interaction during the ATPase cycle.
Rysev NA; Karpicheva OE; Redwood CS; Borovikov YS
Biochim Biophys Acta; 2012 Feb; 1824(2):366-73. PubMed ID: 22155441
[TBL] [Abstract][Full Text] [Related]
17. Molecular mechanisms of dysfunction of muscle fibres associated with Glu139 deletion in TPM2 gene.
Borovikov YS; Rysev NA; Karpicheva OE; Sirenko VV; Avrova SV; Piers A; Redwood CS
Sci Rep; 2017 Dec; 7(1):16797. PubMed ID: 29196649
[TBL] [Abstract][Full Text] [Related]
18. Comparison of Ca2+-dependent effects of caldesmon-tropomyosin-calmodulin and troponin-tropomyosin complexes on the structure of F-actin in ghost fibers and its interaction with myosin heads.
Dobrowolski Z; Borovikov YS; Nowak E; Gałazkiewicz B; Dabrowska R
Biochim Biophys Acta; 1988 Sep; 956(2):140-50. PubMed ID: 3167066
[TBL] [Abstract][Full Text] [Related]
19. Functional effects of congenital myopathy-related mutations in gamma-tropomyosin gene.
Robaszkiewicz K; Dudek E; Kasprzak AA; Moraczewska J
Biochim Biophys Acta; 2012 Oct; 1822(10):1562-9. PubMed ID: 22749829
[TBL] [Abstract][Full Text] [Related]
20. 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.
Borovikov YS; Andreeva DD; Avrova SV; Sirenko VV; Simonyan AO; Redwood CS; Karpicheva OE
Int J Mol Sci; 2021 Jun; 22(12):. PubMed ID: 34204776
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
