These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

235 related articles for article (PubMed ID: 22798622)

  • 41. Filament compliance influences cooperative activation of thin filaments and the dynamics of force production in skeletal muscle.
    Tanner BC; Daniel TL; Regnier M
    PLoS Comput Biol; 2012; 8(5):e1002506. PubMed ID: 22589710
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Novel TPM3 mutation in a family with cap myopathy and review of the literature.
    Schreckenbach T; Schröder JM; Voit T; Abicht A; Neuen-Jacob E; Roos A; Bulst S; Kuhl C; Schulz JB; Weis J; Claeys KG
    Neuromuscul Disord; 2014 Feb; 24(2):117-24. PubMed ID: 24239060
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. 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]  

  • 46. 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]  

  • 47. Mutations in actin subdomain 3 that impair thin filament regulation by troponin and tropomyosin.
    Korman VL; Tobacman LS
    J Biol Chem; 1999 Aug; 274(32):22191-6. PubMed ID: 10428784
    [TBL] [Abstract][Full Text] [Related]  

  • 48. 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]  

  • 49. 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]  

  • 50. The molecular mechanism of muscle dysfunction associated with the R133W mutation in Tpm2.2.
    Borovikov YS; Karpicheva OE; Avrova SV; Simonyan AO; Sirenko VV; Redwood CS
    Biochem Biophys Res Commun; 2020 Feb; 523(1):258-262. PubMed ID: 31864708
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Expression and biological activity of Baculovirus generated wild-type human slow alpha tropomyosin and the Met9Arg mutant responsible for a dominant form of nemaline myopathy.
    Akkari PA; Song Y; Hitchcock-DeGregori S; Blechynden L; Laing N
    Biochem Biophys Res Commun; 2002 Aug; 296(2):300-4. PubMed ID: 12163017
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Biochemical Comparison of Tpm1.1 (α) and Tpm2.2 (β) Tropomyosins from Rabbit Skeletal Muscle.
    Lohmeier-Vogel EM; Heeley DH
    Biochemistry; 2016 Mar; 55(9):1418-27. PubMed ID: 26863527
    [TBL] [Abstract][Full Text] [Related]  

  • 53. 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]  

  • 54. 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; 34(10):13507-13520. PubMed ID: 32797717
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Skeletal muscle disease due to mutations in tropomyosin, troponin and cofilin.
    Clarke NF
    Adv Exp Med Biol; 2008; 642():40-54. PubMed ID: 19181092
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Disrupted myosin cross-bridge cycling kinetics triggers muscle weakness in nebulin-related myopathy.
    Ochala J; Lehtokari VL; Iwamoto H; Li M; Feng HZ; Jin JP; Yagi N; Wallgren-Pettersson C; Pénisson-Besnier I; Larsson L
    FASEB J; 2011 Jun; 25(6):1903-13. PubMed ID: 21350120
    [TBL] [Abstract][Full Text] [Related]  

  • 58. L-Carnitine ameliorates congenital myopathy in a tropomyosin 3 de novo mutation transgenic zebrafish.
    Hsu PJ; Wang HD; Tseng YC; Pan SW; Sampurna BP; Jong YJ; Yuh CH
    J Biomed Sci; 2021 Jan; 28(1):8. PubMed ID: 33435938
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Opposite effects of myosin subfragment 1 on binding of cardiac troponin and tropomyosin to the thin filament.
    Cassell M; Tobacman LS
    J Biol Chem; 1996 May; 271(22):12867-72. PubMed ID: 8662810
    [TBL] [Abstract][Full Text] [Related]  

  • 60. 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; 534():8-13. PubMed ID: 33307294
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.