CLINICAL IMPLICATIONS OF CARDIAC TROPONIN-T MUTATIONS THAT CAUSE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY

被引:0
|
作者
WATKINS, HC
MACRAE, CA
THIERFELDER, L
MCKENNA, WJ
SEIDMAN, JG
SEIDMAN, CE
机构
[1] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[2] ST GEORGE HOSP,SCH MED,LONDON,ENGLAND
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:442 / 442
页数:1
相关论文
共 50 条
  • [1] MODE OF ACTION OF CARDIAC TROPONIN-T MUTATIONS IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
    WATKINS, HC
    MACRAE, CA
    THIERFELDER, L
    MCKENNA, WJ
    SEIDMAN, JG
    SEIDMAN, CE
    CIRCULATION, 1994, 90 (04) : 520 - 520
  • [2] ALPHA-TROPOMYOSIN AND CARDIAC TROPONIN-T MUTATIONS CAUSE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - A DISEASE OF THE SARCOMERE
    THIERFELDER, L
    WATKINS, H
    MACRAE, C
    LAMAS, R
    MCKENNA, W
    VOSBERG, HP
    SEIDMAN, JG
    SEIDMAN, CE
    CELL, 1994, 77 (05) : 701 - 712
  • [3] Computational characterization of mutations in cardiac troponin T known to cause familial hypertrophic cardiomyopathy
    Cuinto, Pia J.
    Manning, Edward P.
    Schwartz, Steven D.
    Tardiff, Jil C.
    JOURNAL OF THEORETICAL & COMPUTATIONAL CHEMISTRY, 2007, 6 (03): : 413 - 419
  • [4] Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy
    Szczesna, D
    Zhang, R
    Zhao, JJ
    Jones, M
    Guzman, G
    Potter, JD
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (01) : 624 - 630
  • [5] Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy
    Knollmann, BC
    Potter, JD
    TRENDS IN CARDIOVASCULAR MEDICINE, 2001, 11 (05) : 206 - 212
  • [6] MUTATIONS IN THE GENES FOR CARDIAC TROPONIN-T AND ALPHA-TROPOMYOSIN IN HYPERTROPHIC CARDIOMYOPATHY
    WATKINS, H
    MCKENNA, WJ
    THIERFELDER, L
    SUK, HJ
    ANAN, R
    ODONOGHUE, A
    SPIRITO, P
    MATSUMORI, A
    MORAVEC, CS
    SEIDMAN, JG
    SEIDMAN, CE
    NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (16): : 1058 - 1064
  • [7] Homozygous mutation in cardiac troponin T: Implications for familial hypertrophic cardiomyopathy
    Ho, CY
    Lever, HM
    Farver, CM
    DeSanctis, R
    Seidman, JG
    Seidman, CE
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2000, 35 (02) : 201A - 201A
  • [8] Functional analysis of the mutations in cardiac troponin I which cause familial hypertrophic cardiomyopathy
    Elliott, K
    Watkins, H
    Redwood, C
    BIOPHYSICAL JOURNAL, 1999, 76 (01) : A281 - A281
  • [9] CLINICAL IMPLICATIONS OF CARDIAC ALPHA-TROPOMYOSIN GENE-MUTATIONS THAT CAUSE FAMILIAL HYPERTROPHIC CARDIOMYOPATHY
    TAKIHARA, KY
    TANIGUCHI, CN
    MATSUI, H
    NAGATA, S
    KISHIMOTO, T
    CIRCULATION, 1995, 92 (08) : 3759 - 3759
  • [10] ACCUMULATION OF THE ABNORMALITY OF CARDIAC BETA-MYOSIN HEAVY-CHAIN AND CARDIAC TROPONIN-T GENES IN FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - IS CARDIAC TROPONIN-T GENE A DISEASE GENE
    OZAWA, T
    KIMURA, M
    FURUTANI, M
    FURUTANI, Y
    ARAI, S
    IMAMURA, SI
    TAKAO, A
    HOSODA, S
    MATSUOKA, R
    CIRCULATION, 1995, 92 (08) : 2241 - 2241