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 *

155 related articles for article (PubMed ID: 11060294)

  • 1. Abnormal contractile function in transgenic mice expressing a familial hypertrophic cardiomyopathy-linked troponin T (I79N) mutation.
    Miller T; Szczesna D; Housmans PR; Zhao J; de Freitas F; Gomes AV; Culbreath L; McCue J; Wang Y; Xu Y; Kerrick WG; Potter JD
    J Biol Chem; 2001 Feb; 276(6):3743-55. PubMed ID: 11060294
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Inotropic stimulation induces cardiac dysfunction in transgenic mice expressing a troponin T (I79N) mutation linked to familial hypertrophic cardiomyopathy.
    Knollmann BC; Blatt SA; Horton K; de Freitas F; Miller T; Bell M; Housmans PR; Weissman NJ; Morad M; Potter JD
    J Biol Chem; 2001 Mar; 276(13):10039-48. PubMed ID: 11113119
    [TBL] [Abstract][Full Text] [Related]  

  • 3. F110I and R278C troponin T mutations that cause familial hypertrophic cardiomyopathy affect muscle contraction in transgenic mice and reconstituted human cardiac fibers.
    Hernandez OM; Szczesna-Cordary D; Knollmann BC; Miller T; Bell M; Zhao J; Sirenko SG; Diaz Z; Guzman G; Xu Y; Wang Y; Kerrick WG; Potter JD
    J Biol Chem; 2005 Nov; 280(44):37183-94. PubMed ID: 16115869
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Differential effect of troponin T mutations on the inotropic responsiveness of mouse hearts--role of myofilament Ca2+ sensitivity increase.
    Sirenko SG; Potter JD; Knollmann BC
    J Physiol; 2006 Aug; 575(Pt 1):201-13. PubMed ID: 16777946
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cardiomyopathy-related mutation (A30V) in mouse cardiac troponin T divergently alters the magnitude of stretch activation in α- and β-myosin heavy chain fibers.
    Mickelson AV; Gollapudi SK; Chandra M
    Am J Physiol Heart Circ Physiol; 2017 Jan; 312(1):H141-H149. PubMed ID: 27769999
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Familial hypertrophic cardiomyopathy-linked mutant troponin T causes stress-induced ventricular tachycardia and Ca2+-dependent action potential remodeling.
    Knollmann BC; Kirchhof P; Sirenko SG; Degen H; Greene AE; Schober T; Mackow JC; Fabritz L; Potter JD; Morad M
    Circ Res; 2003 Mar; 92(4):428-36. PubMed ID: 12600890
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hypertrophic cardiomyopathy-linked mutation in troponin T causes myofibrillar disarray and pro-arrhythmic action potential changes in human iPSC cardiomyocytes.
    Wang L; Kim K; Parikh S; Cadar AG; Bersell KR; He H; Pinto JR; Kryshtal DO; Knollmann BC
    J Mol Cell Cardiol; 2018 Jan; 114():320-327. PubMed ID: 29217433
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Pathogenic troponin T mutants with opposing effects on myofilament Ca
    Dieseldorff Jones KM; Koh Y; Weller RS; Turna RS; Ahmad F; Huke S; Knollmann BC; Pinto JR; Hwang HS
    Arch Biochem Biophys; 2019 Jan; 661():125-131. PubMed ID: 30445044
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy.
    Szczesna D; Zhang R; Zhao J; Jones M; Guzman G; Potter JD
    J Biol Chem; 2000 Jan; 275(1):624-30. PubMed ID: 10617660
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Analysis of the molecular pathogenesis of cardiomyopathy-causing cTnT mutants I79N, ΔE96, and ΔK210.
    Bai F; Caster HM; Pinto JR; Kawai M
    Biophys J; 2013 May; 104(9):1979-88. PubMed ID: 23663841
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a contractile deficit in adult cardiac myocytes expressing hypertrophic cardiomyopathy-associated mutant troponin T proteins.
    Rust EM; Albayya FP; Metzger JM
    J Clin Invest; 1999 May; 103(10):1459-67. PubMed ID: 10330428
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional consequences of the human cardiac troponin I hypertrophic cardiomyopathy mutation R145G in transgenic mice.
    Wen Y; Pinto JR; Gomes AV; Xu Y; Wang Y; Wang Y; Potter JD; Kerrick WG
    J Biol Chem; 2008 Jul; 283(29):20484-94. PubMed ID: 18430738
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prolonged Ca2+ and force transients in myosin RLC transgenic mouse fibers expressing malignant and benign FHC mutations.
    Wang Y; Xu Y; Kerrick WG; Wang Y; Guzman G; Diaz-Perez Z; Szczesna-Cordary D
    J Mol Biol; 2006 Aug; 361(2):286-99. PubMed ID: 16837010
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Delineation of Molecular Pathways Involved in Cardiomyopathies Caused by Troponin T Mutations.
    Gilda JE; Lai X; Witzmann FA; Gomes AV
    Mol Cell Proteomics; 2016 Jun; 15(6):1962-81. PubMed ID: 27022107
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Rat cardiac troponin T mutation (F72L)-mediated impact on thin filament cooperativity is divergently modulated by α- and β-myosin heavy chain isoforms.
    Chandra V; Gollapudi SK; Chandra M
    Am J Physiol Heart Circ Physiol; 2015 Oct; 309(8):H1260-70. PubMed ID: 26342069
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Familial hypertrophic cardiomyopathy mutations from different functional regions of troponin T result in different effects on the pH and Ca2+ sensitivity of cardiac muscle contraction.
    Harada K; Potter JD
    J Biol Chem; 2004 Apr; 279(15):14488-95. PubMed ID: 14722098
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pathogenesis of Hypertrophic Cardiomyopathy is Mutation Rather Than Disease Specific: A Comparison of the Cardiac Troponin T E163R and R92Q Mouse Models.
    Ferrantini C; Coppini R; Pioner JM; Gentile F; Tosi B; Mazzoni L; Scellini B; Piroddi N; Laurino A; Santini L; Spinelli V; Sacconi L; De Tombe P; Moore R; Tardiff J; Mugelli A; Olivotto I; Cerbai E; Tesi C; Poggesi C
    J Am Heart Assoc; 2017 Jul; 6(7):. PubMed ID: 28735292
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Alterations of tension-dependent ATP utilization in a transgenic rat model of hypertrophic cardiomyopathy.
    Frey N; Brixius K; Schwinger RH; Benis T; Karpowski A; Lorenzen HP; Luedde M; Katus HA; Franz WM
    J Biol Chem; 2006 Oct; 281(40):29575-82. PubMed ID: 16882671
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Cardiac troponin T isoforms affect the Ca2+ sensitivity and inhibition of force development. Insights into the role of troponin T isoforms in the heart.
    Gomes AV; Guzman G; Zhao J; Potter JD
    J Biol Chem; 2002 Sep; 277(38):35341-9. PubMed ID: 12093807
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypertrophic cardiomyopathy mutation in cardiac troponin T (R95H) attenuates length-dependent activation in guinea pig cardiac muscle fibers.
    Mickelson AV; Chandra M
    Am J Physiol Heart Circ Physiol; 2017 Dec; 313(6):H1180-H1189. PubMed ID: 28842439
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.