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PUBMED FOR HANDHELDS

Journal Abstract Search


198 related items for PubMed ID: 17606808

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  • 2. The E22K mutation of myosin RLC that causes familial hypertrophic cardiomyopathy increases calcium sensitivity of force and ATPase in transgenic mice.
    Szczesna-Cordary D, Guzman G, Zhao J, Hernandez O, Wei J, Diaz-Perez Z.
    J Cell Sci; 2005 Aug 15; 118(Pt 16):3675-83. PubMed ID: 16076902
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  • 3. Malignant familial hypertrophic cardiomyopathy D166V mutation in the ventricular myosin regulatory light chain causes profound effects in skinned and intact papillary muscle fibers from transgenic mice.
    Kerrick WG, Kazmierczak K, Xu Y, Wang Y, Szczesna-Cordary D.
    FASEB J; 2009 Mar 15; 23(3):855-65. PubMed ID: 18987303
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  • 4. E22K mutation of RLC that causes familial hypertrophic cardiomyopathy in heterozygous mouse myocardium: effect on cross-bridge kinetics.
    Dumka D, Talent J, Akopova I, Guzman G, Szczesna-Cordary D, Borejdo J.
    Am J Physiol Heart Circ Physiol; 2006 Nov 15; 291(5):H2098-106. PubMed ID: 16751284
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  • 5. 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 11; 361(2):286-99. PubMed ID: 16837010
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  • 7. Myosin regulatory light chain mutation found in hypertrophic cardiomyopathy patients increases isometric force production in transgenic mice.
    Kazmierczak K, Muthu P, Huang W, Jones M, Wang Y, Szczesna-Cordary D.
    Biochem J; 2012 Feb 15; 442(1):95-103. PubMed ID: 22091967
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  • 12. Phosphomimetic-mediated in vitro rescue of hypertrophic cardiomyopathy linked to R58Q mutation in myosin regulatory light chain.
    Yadav S, Kazmierczak K, Liang J, Sitbon YH, Szczesna-Cordary D.
    FEBS J; 2019 Jan 15; 286(1):151-168. PubMed ID: 30430732
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  • 15. Constitutive phosphorylation of cardiac myosin regulatory light chain prevents development of hypertrophic cardiomyopathy in mice.
    Yuan CC, Muthu P, Kazmierczak K, Liang J, Huang W, Irving TC, Kanashiro-Takeuchi RM, Hare JM, Szczesna-Cordary D.
    Proc Natl Acad Sci U S A; 2015 Jul 28; 112(30):E4138-46. PubMed ID: 26124132
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  • 16. Cross-bridge kinetics in myofibrils containing familial hypertrophic cardiomyopathy R58Q mutation in the regulatory light chain of myosin.
    Mettikolla P, Calander N, Luchowski R, Gryczynski I, Gryczynski Z, Zhao J, Szczesna-Cordary D, Borejdo J.
    J Theor Biol; 2011 Sep 07; 284(1):71-81. PubMed ID: 21723297
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  • 20. 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 04; 280(44):37183-94. PubMed ID: 16115869
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