| | Functional analysis of the mutations in the human cardiac beta-myosin that are responsible for familial hypertrophic cardiomyopathy. Implication for the clinical outcome. M Sata and M Ikebe PMCID: PMC507754 | | Is Cited by the Following Articles in this Archive: | The R403Q Myosin Mutation Implicated in Familial Hypertrophic Cardiomyopathy Causes Disorder at the Actomyosin Interface Niels Volkmann, HongJun Lui, Larnele Hazelwood, Kathleen M. Trybus, Susan Lowey, and Dorit Hanein PMCID: PMC2040505 Myosin Dynamics on the Millisecond Time Scale Thomas P. Burghardt, Jimmy Yan Hu, and Katalin Ajtai PMCID: PMC2505346 Published in final edited form as: Biophys Chem. 2007 December; 131(1-3): 15–28. Published online 2007 September 11. doi: 10.1016/j.bpc.2007.08.008. Biological, Biochemical and Kinetic Effects of Mutations of the Cardiomyopathy-loop of Dictyostelium Myosin II: Importance of Ala400 Xiong Liu, Shi Shu, Mihály Kovács, and Edward D. Korn PMCID: PMC1201472 Published in final edited form as: J Biol Chem. 2005 July 22; 280(29): 26974–26983. Published online 2005 May 16. doi: 10.1074/jbc.M504453200. Heterologous expression of wild-type and mutant β-cardiac myosin changes the contractile kinetics of cultured mouse myotubes Gaynor Miller, Joanne Maycock, Ed White, Michelle Peckham, and Sarah Calaghan PMCID: PMC2342801 Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy Jil C. Tardiff, Timothy E. Hewett, Bradley M. Palmer, Charlotte Olsson, Stephen M. Factor, Russell L. Moore, Jeffrey Robbins, and Leslie A. Leinwand PMCID: PMC408522 Altered cardiac excitation–contraction coupling in mutant mice with familial hypertrophic cardiomyopathy Wei Dong Gao, Nestor Gustavo Pérez, Christine E. Seidman, Jonathan G. Seidman, and Eduardo Marbán PMCID: PMC408123 IgG subclass reactivity to human cardiac myosin in cardiomyopathy patients is indicative of a Th1-like autoimmune disease P Skyllouriotis, M Skyllouriotis-Lazarou, S Natter, R Steiner, S Spitzauer, S Kapiotis, P Valent, A M Hirschl, S E Guber, G Laufer, G Wollenek, E Wolner, M Wimmer, and R Valenta PMCID: PMC1905170 Neonatal cardiomyopathy in mice homozygous for the Arg403Gln mutation in the α cardiac myosin heavy chain gene Diane Fatkin, Michael E. Christe, Orlando Aristizabal, Bradley K. McConnell, Shardha Srinivasan, Frederick J. Schoen, Christine E. Seidman, Daniel H. Turnbull, and J.G. Seidman PMCID: PMC407864 Functional analysis of myosin mutations that cause familial hypertrophic cardiomyopathy. O Roopnarine and L A Leinwand PMCID: PMC1299973 Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: Insights into disease pathogenesis and troponin function H. Lee Sweeney, Huisheng S. Feng, Zhaouhui Yang, and Hugh Watkins PMCID: PMC24386 Dominant-negative effect of a mutant cardiac troponin T on cardiac structure and function in transgenic mice. L Oberst, G Zhao, J T Park, R Brugada, L H Michael, M L Entman, R Roberts, and A J Marian PMCID: PMC508999 A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy. J C Tardiff, S M Factor, B D Tompkins, T E Hewett, B M Palmer, R L Moore, S Schwartz, J Robbins, and L A Leinwand PMCID: PMC508871 | |
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