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236 related items for PubMed ID: 15994854

  • 1. Increase in tension-dependent ATP consumption induced by cardiac troponin T mutation.
    Chandra M, Tschirgi ML, Tardiff JC.
    Am J Physiol Heart Circ Physiol; 2005 Nov; 289(5):H2112-9. PubMed ID: 15994854
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  • 2. Cardiac troponin T mutations: correlation between the type of mutation and the nature of myofilament dysfunction in transgenic mice.
    Montgomery DE, Tardiff JC, Chandra M.
    J Physiol; 2001 Oct 15; 536(Pt 2):583-92. PubMed ID: 11600691
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  • 3. Independent FHC-related cardiac troponin T mutations exhibit specific alterations in myocellular contractility and calcium kinetics.
    Haim TE, Dowell C, Diamanti T, Scheuer J, Tardiff JC.
    J Mol Cell Cardiol; 2007 Jun 15; 42(6):1098-110. PubMed ID: 17490679
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  • 4. Ca(2+) activation of myofilaments from transgenic mouse hearts expressing R92Q mutant cardiac troponin T.
    Chandra M, Rundell VL, Tardiff JC, Leinwand LA, De Tombe PP, Solaro RJ.
    Am J Physiol Heart Circ Physiol; 2001 Feb 15; 280(2):H705-13. PubMed ID: 11158969
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  • 5. Temporal and mutation-specific alterations in Ca2+ homeostasis differentially determine the progression of cTnT-related cardiomyopathies in murine models.
    Guinto PJ, Haim TE, Dowell-Martino CC, Sibinga N, Tardiff JC.
    Am J Physiol Heart Circ Physiol; 2009 Aug 15; 297(2):H614-26. PubMed ID: 19502551
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  • 10. Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.
    Morimoto S, Lu QW, Harada K, Takahashi-Yanaga F, Minakami R, Ohta M, Sasaguri T, Ohtsuki I.
    Proc Natl Acad Sci U S A; 2002 Jan 22; 99(2):913-8. PubMed ID: 11773635
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  • 11. Dilated cardiomyopathy mutation (R174W) in troponin T attenuates the length-mediated increase in cross-bridge recruitment and myofilament Ca2+ sensitivity.
    Reda SM, Chandra M.
    Am J Physiol Heart Circ Physiol; 2019 Sep 01; 317(3):H648-H657. PubMed ID: 31373515
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  • 12. Cardiac myosin heavy chain isoform exchange alters the phenotype of cTnT-related cardiomyopathies in mouse hearts.
    Rice R, Guinto P, Dowell-Martino C, He H, Hoyer K, Krenz M, Robbins J, Ingwall JS, Tardiff JC.
    J Mol Cell Cardiol; 2010 May 01; 48(5):979-88. PubMed ID: 20004663
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  • 14. 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 09; 279(15):14488-95. PubMed ID: 14722098
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  • 15. Identification of a functionally critical protein kinase C phosphorylation residue of cardiac troponin T.
    Sumandea MP, Pyle WG, Kobayashi T, de Tombe PP, Solaro RJ.
    J Biol Chem; 2003 Sep 12; 278(37):35135-44. PubMed ID: 12832403
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  • 18. Impact of cardiac troponin T N-terminal deletion and phosphorylation on myofilament function.
    Sumandea MP, Vahebi S, Sumandea CA, Garcia-Cazarin ML, Staidle J, Homsher E.
    Biochemistry; 2009 Aug 18; 48(32):7722-31. PubMed ID: 19586048
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  • 19. Myosin regulatory light chain E22K mutation results in decreased cardiac intracellular calcium and force transients.
    Szczesna-Cordary D, Jones M, Moore JR, Watt J, Kerrick WG, Xu Y, Wang Y, Wagg C, Lopaschuk GD.
    FASEB J; 2007 Dec 18; 21(14):3974-85. PubMed ID: 17606808
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  • 20. Chronic Calmodulin-Kinase II Activation Drives Disease Progression in Mutation-Specific Hypertrophic Cardiomyopathy.
    Lehman SJ, Tal-Grinspan L, Lynn ML, Strom J, Benitez GE, Anderson ME, Tardiff JC.
    Circulation; 2019 Mar 19; 139(12):1517-1529. PubMed ID: 30586744
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