237 related articles for article (PubMed ID: 22798622)
21. Mechanochemical consequences of myopathy-linked mutations in Tpm2.2 on striated muscle contractility.
Küçükdogru R; Franz P; Worch R; Robaszkiewicz K; Siatkowska M; Tsiavaliaris G; Moraczewska J
FASEB J; 2024 Jan; 38(1):e23400. PubMed ID: 38156416
[TBL] [Abstract][Full Text] [Related]
22. Alteration of tropomyosin function and folding by a nemaline myopathy-causing mutation.
Moraczewska J; Greenfield NJ; Liu Y; Hitchcock-DeGregori SE
Biophys J; 2000 Dec; 79(6):3217-25. PubMed ID: 11106625
[TBL] [Abstract][Full Text] [Related]
23. Mutation-specific effects on thin filament length in thin filament myopathy.
Winter JM; Joureau B; Lee EJ; Kiss B; Yuen M; Gupta VA; Pappas CT; Gregorio CC; Stienen GJ; Edvardson S; Wallgren-Pettersson C; Lehtokari VL; Pelin K; Malfatti E; Romero NB; Engelen BG; Voermans NC; Donkervoort S; Bönnemann CG; Clarke NF; Beggs AH; Granzier H; Ottenheijm CA
Ann Neurol; 2016 Jun; 79(6):959-69. PubMed ID: 27074222
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Disease severity and thin filament regulation in M9R TPM3 nemaline myopathy.
Ilkovski B; Mokbel N; Lewis RA; Walker K; Nowak KJ; Domazetovska A; Laing NG; Fowler VM; North KN; Cooper ST
J Neuropathol Exp Neurol; 2008 Sep; 67(9):867-77. PubMed ID: 18716557
[TBL] [Abstract][Full Text] [Related]
26. 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; 1854(5):381-90. PubMed ID: 25603119
[TBL] [Abstract][Full Text] [Related]
27. Nebulin stiffens the thin filament and augments cross-bridge interaction in skeletal muscle.
Kiss B; Lee EJ; Ma W; Li FW; Tonino P; Mijailovich SM; Irving TC; Granzier HL
Proc Natl Acad Sci U S A; 2018 Oct; 115(41):10369-10374. PubMed ID: 30249654
[TBL] [Abstract][Full Text] [Related]
28. 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; 34(3-4):165-9. PubMed ID: 23719967
[TBL] [Abstract][Full Text] [Related]
29. Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia.
Wallgren-Pettersson C; Jokela M; Lehtokari VL; Tyynismaa H; Sainio MT; Ylikallio E; Tynninen O; Pelin K; Auranen M
Neuromuscul Disord; 2024 Feb; 35():29-32. PubMed ID: 38219297
[TBL] [Abstract][Full Text] [Related]
30. A Novel Variant in
Robaszkiewicz K; Siatkowska M; Wadman RI; Kamsteeg EJ; Chen Z; Merve A; Parton M; Bugiardini E; de Bie C; Moraczewska J
Int J Mol Sci; 2023 Nov; 24(22):. PubMed ID: 38003336
[TBL] [Abstract][Full Text] [Related]
31. An alphaTropomyosin mutation alters dimer preference in nemaline myopathy.
Corbett MA; Akkari PA; Domazetovska A; Cooper ST; North KN; Laing NG; Gunning PW; Hardeman EC
Ann Neurol; 2005 Jan; 57(1):42-9. PubMed ID: 15562513
[TBL] [Abstract][Full Text] [Related]
32. Novel deletion of lysine 7 expands the clinical, histopathological and genetic spectrum of TPM2-related myopathies.
Davidson AE; Siddiqui FM; Lopez MA; Lunt P; Carlson HA; Moore BE; Love S; Born DE; Roper H; Majumdar A; Jayadev S; Underhill HR; Smith CO; von der Hagen M; Hubner A; Jardine P; Merrison A; Curtis E; Cullup T; Jungbluth H; Cox MO; Winder TL; Abdel Salam H; Li JZ; Moore SA; Dowling JJ
Brain; 2013 Feb; 136(Pt 2):508-21. PubMed ID: 23413262
[TBL] [Abstract][Full Text] [Related]
33. Cardiomyopathic tropomyosin mutations that increase thin filament Ca2+ sensitivity and tropomyosin N-domain flexibility.
Heller MJ; Nili M; Homsher E; Tobacman LS
J Biol Chem; 2003 Oct; 278(43):41742-8. PubMed ID: 12900417
[TBL] [Abstract][Full Text] [Related]
34. Molecular Mechanisms of Muscle Weakness Associated with E173A Mutation in Tpm3.12. Troponin Ca
Borovikov YS; Simonyan AO; Avrova SV; Sirenko VV; Redwood CS; Karpicheva OE
Int J Mol Sci; 2020 Jun; 21(12):. PubMed ID: 32580284
[TBL] [Abstract][Full Text] [Related]
35. Regulation of contraction in striated muscle.
Gordon AM; Homsher E; Regnier M
Physiol Rev; 2000 Apr; 80(2):853-924. PubMed ID: 10747208
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. Cap disease due to mutation of the beta-tropomyosin gene (TPM2).
Clarke NF; Domazetovska A; Waddell L; Kornberg A; McLean C; North KN
Neuromuscul Disord; 2009 May; 19(5):348-51. PubMed ID: 19345583
[TBL] [Abstract][Full Text] [Related]
39. Three-dimensional reconstruction of thin filaments containing mutant tropomyosin.
Rosol M; Lehman W; Craig R; Landis C; Butters C; Tobacman LS
Biophys J; 2000 Feb; 78(2):908-17. PubMed ID: 10653803
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
