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Journal Abstract Search

181 related items for PubMed ID: 26906074

  • 21. Differences in molecular phenotype in mouse and human hypertrophic cardiomyopathy.
    Vakrou S, Liu Y, Zhu L, Greenland GV, Simsek B, Hebl VB, Guan Y, Woldemichael K, Talbot CC, Aon MA, Fukunaga R, Abraham MR.
    Sci Rep; 2021 Jun 23; 11(1):13163. PubMed ID: 34162896
    [Abstract] [Full Text] [Related]

  • 22. 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
    [Abstract] [Full Text] [Related]

  • 23. Regulatory light chain mutations associated with cardiomyopathy affect myosin mechanics and kinetics.
    Greenberg MJ, Watt JD, Jones M, Kazmierczak K, Szczesna-Cordary D, Moore JR.
    J Mol Cell Cardiol; 2009 Jan 07; 46(1):108-15. PubMed ID: 18929571
    [Abstract] [Full Text] [Related]

  • 24. Induced Pluripotent Stem Cell-Derived Cardiomyocytes from a Patient with MYL2-R58Q-Mediated Apical Hypertrophic Cardiomyopathy Show Hypertrophy, Myofibrillar Disarray, and Calcium Perturbations.
    Zhou W, Bos JM, Ye D, Tester DJ, Hrstka S, Maleszewski JJ, Ommen SR, Nishimura RA, Schaff HV, Kim CS, Ackerman MJ.
    J Cardiovasc Transl Res; 2019 Oct 07; 12(5):394-403. PubMed ID: 30796699
    [Abstract] [Full Text] [Related]

  • 25. Different expressivity of a ventricular essential myosin light chain gene Ala57Gly mutation in familial hypertrophic cardiomyopathy.
    Lee W, Hwang TH, Kimura A, Park SW, Satoh M, Nishi H, Harada H, Toyama J, Park JE.
    Am Heart J; 2001 Feb 07; 141(2):184-9. PubMed ID: 11174330
    [Abstract] [Full Text] [Related]

  • 26. Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy.
    Kabaeva ZT, Perrot A, Wolter B, Dietz R, Cardim N, Correia JM, Schulte HD, Aldashev AA, Mirrakhimov MM, Osterziel KJ.
    Eur J Hum Genet; 2002 Nov 07; 10(11):741-8. PubMed ID: 12404107
    [Abstract] [Full Text] [Related]

  • 27. Functional comparison of phosphomimetic S15D and T160D mutants of myosin regulatory light chain exchanged in cardiac muscle preparations of HCM and WT mice.
    Kazmierczak K, Liang J, Gomez-Guevara M, Szczesna-Cordary D.
    Front Cardiovasc Med; 2022 Nov 07; 9():988066. PubMed ID: 36204565
    [Abstract] [Full Text] [Related]

  • 28. Single molecule kinetics in the familial hypertrophic cardiomyopathy D166V mutant mouse heart.
    Muthu P, Mettikolla P, Calander N, Luchowski R, Gryczynski I, Gryczynski Z, Szczesna-Cordary D, Borejdo J.
    J Mol Cell Cardiol; 2010 May 07; 48(5):989-98. PubMed ID: 19914255
    [Abstract] [Full Text] [Related]

  • 29. Transgenic rabbits expressing mutant essential light chain do not develop hypertrophic cardiomyopathy.
    James J, Zhang Y, Wright K, Witt S, Glascock E, Osinska H, Klevitsky R, Martin L, Yager K, Sanbe A, Robbins J.
    J Mol Cell Cardiol; 2002 Jul 07; 34(7):873-82. PubMed ID: 12099725
    [Abstract] [Full Text] [Related]

  • 30. 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 07; 21(14):3974-85. PubMed ID: 17606808
    [Abstract] [Full Text] [Related]

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  • 32. 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
    [Abstract] [Full Text] [Related]

  • 33. Molecular mechanisms of cardiomyopathy phenotypes associated with myosin light chain mutations.
    Huang W, Szczesna-Cordary D.
    J Muscle Res Cell Motil; 2015 Dec 15; 36(6):433-45. PubMed ID: 26385864
    [Abstract] [Full Text] [Related]

  • 34. Impact of familial hypertrophic cardiomyopathy-linked mutations in the NH2 terminus of the RLC on β-myosin cross-bridge mechanics.
    Farman GP, Muthu P, Kazmierczak K, Szczesna-Cordary D, Moore JR.
    J Appl Physiol (1985); 2014 Dec 15; 117(12):1471-7. PubMed ID: 25324513
    [Abstract] [Full Text] [Related]

  • 35. In vivo analysis of an essential myosin light chain mutation linked to familial hypertrophic cardiomyopathy.
    Sanbe A, Nelson D, Gulick J, Setser E, Osinska H, Wang X, Hewett TE, Klevitsky R, Hayes E, Warshaw DM, Robbins J.
    Circ Res; 2000 Aug 18; 87(4):296-302. PubMed ID: 10948063
    [Abstract] [Full Text] [Related]

  • 36. Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation.
    Szczesna D, Ghosh D, Li Q, Gomes AV, Guzman G, Arana C, Zhi G, Stull JT, Potter JD.
    J Biol Chem; 2001 Mar 09; 276(10):7086-92. PubMed ID: 11102452
    [Abstract] [Full Text] [Related]

  • 37. 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
    [Abstract] [Full Text] [Related]

  • 38. 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
    [Abstract] [Full Text] [Related]

  • 39. A gradient of myosin regulatory light-chain phosphorylation across the ventricular wall supports cardiac torsion.
    Davis JS, Hassanzadeh S, Winitsky S, Wen H, Aletras A, Epstein ND.
    Cold Spring Harb Symp Quant Biol; 2002 Nov 15; 67():345-52. PubMed ID: 12858559
    [No Abstract] [Full Text] [Related]

  • 40. Effect of a myosin regulatory light chain mutation K104E on actin-myosin interactions.
    Duggal D, Nagwekar J, Rich R, Huang W, Midde K, Fudala R, Das H, Gryczynski I, Szczesna-Cordary D, Borejdo J.
    Am J Physiol Heart Circ Physiol; 2015 May 15; 308(10):H1248-57. PubMed ID: 25770245
    [Abstract] [Full Text] [Related]

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