287 related articles for article (PubMed ID: 31270709)
1. Thin filament dysfunctions caused by mutations in tropomyosin Tpm3.12 and Tpm1.1.
Moraczewska J
J Muscle Res Cell Motil; 2020 Mar; 41(1):39-53. PubMed ID: 31270709
[TBL] [Abstract][Full Text] [Related]
2. Congenital myopathy-related mutations in tropomyosin disrupt regulatory function through altered actin affinity and tropomodulin binding.
Moraczewska J; Robaszkiewicz K; Śliwinska M; Czajkowska M; Ly T; Kostyukova A; Wen H; Zheng W
FEBS J; 2019 May; 286(10):1877-1893. PubMed ID: 30768849
[TBL] [Abstract][Full Text] [Related]
3. The cardiomyopathy-associated K15N mutation in tropomyosin alters actin filament pointed end dynamics.
Colpan M; Ly T; Grover S; Tolkatchev D; Kostyukova AS
Arch Biochem Biophys; 2017 Sep; 630():18-26. PubMed ID: 28732641
[TBL] [Abstract][Full Text] [Related]
4. Regulation of Actin Filament Length by Muscle Isoforms of Tropomyosin and Cofilin.
Robaszkiewicz K; Śliwinska M; Moraczewska J
Int J Mol Sci; 2020 Jun; 21(12):. PubMed ID: 32560136
[TBL] [Abstract][Full Text] [Related]
5. Tropomyosin Isoforms Specify Functionally Distinct Actin Filament Populations In Vitro.
Gateva G; Kremneva E; Reindl T; Kotila T; Kogan K; Gressin L; Gunning PW; Manstein DJ; Michelot A; Lappalainen P
Curr Biol; 2017 Mar; 27(5):705-713. PubMed ID: 28216317
[TBL] [Abstract][Full Text] [Related]
6. Tropomyosin isoforms differentially modulate the regulation of actin filament polymerization and depolymerization by cofilins.
Robaszkiewicz K; Ostrowska Z; Marchlewicz K; Moraczewska J
FEBS J; 2016 Feb; 283(4):723-37. PubMed ID: 26663234
[TBL] [Abstract][Full Text] [Related]
7. Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms.
Ochala J; Gokhin DS; Pénisson-Besnier I; Quijano-Roy S; Monnier N; Lunardi J; Romero NB; Fowler VM
Hum Mol Genet; 2012 Oct; 21(20):4473-85. PubMed ID: 22798622
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. HCM and DCM cardiomyopathy-linked α-tropomyosin mutations influence off-state stability and crossbridge interaction on thin filaments.
Farman GP; Rynkiewicz MJ; Orzechowski M; Lehman W; Moore JR
Arch Biochem Biophys; 2018 Jun; 647():84-92. PubMed ID: 29626422
[TBL] [Abstract][Full Text] [Related]
10. Structural destabilization of tropomyosin induced by the cardiomyopathy-linked mutation R21H.
Ly T; Krieger I; Tolkatchev D; Krone C; Moural T; Samatey FA; Kang C; Kostyukova AS
Protein Sci; 2018 Feb; 27(2):498-508. PubMed ID: 29105867
[TBL] [Abstract][Full Text] [Related]
11. Regulation of actin filament turnover by cofilin-1 and cytoplasmic tropomyosin isoforms.
Ostrowska Z; Robaszkiewicz K; Moraczewska J
Biochim Biophys Acta Proteins Proteom; 2017 Jan; 1865(1):88-98. PubMed ID: 27693909
[TBL] [Abstract][Full Text] [Related]
12. Effects of cardiomyopathy-linked mutations K15N and R21H in tropomyosin on thin-filament regulation and pointed-end dynamics.
Ly T; Pappas CT; Johnson D; Schlecht W; Colpan M; Galkin VE; Gregorio CC; Dong WJ; Kostyukova AS
Mol Biol Cell; 2019 Jan; 30(2):268-281. PubMed ID: 30462572
[TBL] [Abstract][Full Text] [Related]
13. A comparison of muscle thin filament models obtained from electron microscopy reconstructions and low-angle X-ray fibre diagrams from non-overlap muscle.
Poole KJ; Lorenz M; Evans G; Rosenbaum G; Pirani A; Craig R; Tobacman LS; Lehman W; Holmes KC
J Struct Biol; 2006 Aug; 155(2):273-84. PubMed ID: 16793285
[TBL] [Abstract][Full Text] [Related]
14. Leiomodin creates a leaky cap at the pointed end of actin-thin filaments.
Tolkatchev D; Smith GE; Schultz LE; Colpan M; Helms GL; Cort JR; Gregorio CC; Kostyukova AS
PLoS Biol; 2020 Sep; 18(9):e3000848. PubMed ID: 32898131
[TBL] [Abstract][Full Text] [Related]
15. Cooperativity of myosin interaction with thin filaments is enhanced by stabilizing substitutions in tropomyosin.
Shchepkin DV; Nabiev SR; Kopylova GV; Matyushenko AM; Levitsky DI; Bershitsky SY; Tsaturyan AK
J Muscle Res Cell Motil; 2017 Apr; 38(2):183-191. PubMed ID: 28540577
[TBL] [Abstract][Full Text] [Related]
16. A new twist on tropomyosin binding to actin filaments: perspectives on thin filament function, assembly and biomechanics.
Lehman W; Rynkiewicz MJ; Moore JR
J Muscle Res Cell Motil; 2020 Mar; 41(1):23-38. PubMed ID: 30771202
[TBL] [Abstract][Full Text] [Related]
17. Distinct sites in tropomyosin specify shared and isoform-specific regulation of myosins II and V.
Barua B; Sckolnick M; White HD; Trybus KM; Hitchcock-DeGregori SE
Cytoskeleton (Hoboken); 2018 Apr; 75(4):150-163. PubMed ID: 29500902
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Mini-thin filaments regulated by troponin-tropomyosin.
Gong H; Hatch V; Ali L; Lehman W; Craig R; Tobacman LS
Proc Natl Acad Sci U S A; 2005 Jan; 102(3):656-61. PubMed ID: 15644437
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]