Restrictive cardiomyopathy mutations result in prolonged relaxation rates and increased calcium sensitivity compared to hypertrophic cardiomyopathy mutations in cardiac troponin I

被引：0
|
作者：
Davis, JM [1 ]
Edwards, T [1 ]
Wen, HT [1 ]
Metzger, JM [1 ]
机构：
[1] Univ Michigan, Ann Arbor, MI 48109 USA
来源：
BIOPHYSICAL JOURNAL | 2005年 / 88卷 / 01期
关键词：
D O I：
暂无
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
引用
收藏
页码：123A / 123A
页数：1
相关论文
共 50 条
  • [21] Familial hypertrophic cardiomyopathy associated with cardiac β-myosin heavy chain and troponin i mutations
    Frazier, Aisha
    Judge, Daniel P.
    Schulman, Steven P.
    Johnson, Nicole
    Holmes, Kathryn W.
    Murphy, Anne M.
    [J]. PEDIATRIC CARDIOLOGY, 2008, 29 (04) : 846 - 850
  • [22] Effects of hypertrophic cardiomyopathy mutations in troponin I on contractility of skinned cardiac muscle fibres
    Burton, DJ
    Redwood, CS
    Watkins, H
    Ashley, C
    [J]. BIOPHYSICAL JOURNAL, 2002, 82 (01) : 388A - 389A
  • [23] Functional and structural consequences of troponin I mutations associated with restrictive cardiomyopathy
    Yumoto, F
    Lu, QW
    Morimoto, S
    Nagata, K
    Tanokura, M
    Ohtsuki, I
    [J]. BIOPHYSICAL JOURNAL, 2005, 88 (01) : 316A - 316A
  • [24] Functional Effects of Two Troponin I Mutations Linked to Restrictive Cardiomyopathy
    Dewey, Shannamar
    Chen, Josephine
    Susan Nguyen
    Xu, Qian
    Gomes, Aldrin V.
    [J]. BIOPHYSICAL JOURNAL, 2010, 98 (03) : 356A - 357A
  • [25] Computational simulation of hypertrophic cardiomyopathy mutations in Troponin I:: Influence of increased myofilament calcium sensitivity on isometric force, ATPase and [Ca2+]i
    Kataoka, Aya
    Hemmer, Carolyn
    Chase, P. Bryant
    [J]. JOURNAL OF BIOMECHANICS, 2007, 40 (09) : 2044 - 2052
  • [26] Cardiac troponin T mutations result in allele-specific phenotypes in a mouse model for hypertrophic cardiomyopathy
    Tardiff, JC
    Hewett, TE
    Palmer, BM
    Olsson, C
    Factor, SM
    Moore, RL
    Robbins, J
    Leinwand, LA
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (04): : 469 - 481
  • [27] An In Silico Analysis of Troponin I Mutations in Hypertrophic Cardiomyopathy of Indian Origin
    Ramachandran, Gayatri
    Kumar, Manoj
    Rani, Deepa Selvi
    Annanthapur, Venkateshwari
    Calambur, Narasimhan
    Nallari, Pratibha
    Kaur, Punit
    [J]. PLOS ONE, 2013, 8 (08):
  • [28] Physiological effects of cardiac troponin I mutations associated with adult onset familial hypertrophic cardiomyopathy
    Gomes, AV
    Zhao, JJ
    Gendlina, E
    Lopez, I
    Potter, JD
    [J]. BIOPHYSICAL JOURNAL, 2003, 84 (02) : 569A - 569A
  • [29] Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy
    Mogensen, J
    Murphy, RT
    Kubo, T
    Bahl, A
    Moon, JC
    Klausen, IC
    Elliott, PM
    McKenna, WJ
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 44 (12) : 2315 - 2325
  • [30] Cellular and molecular aspects of familial hypertrophic cardiomyopathy caused by mutations in the cardiac troponin I gene
    Gomes, AV
    Potter, JD
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2004, 263 (01) : 99 - 114
12345