Pathogenesis of inherited forms of dilated cardiomyopathy.

被引:32
作者
Graham, RM [1 ]
Owens, WA [1 ]
机构
[1] Victor Chang Cardiac Res Inst, Darlinghurst, NSW 2010, Australia
关键词
D O I
10.1056/NEJM199912023412309
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:1759 / 1762
页数:4
相关论文
共 15 条
[1]   Enteroviral protease 2A cleaves dystrophin: Evidence of cytoskeletal disruption in an acquired cardiomyopathy [J].
Badorff, C ;
Lee, GH ;
Lamphear, BJ ;
Martone, ME ;
Campbell, KP ;
Rhoads, RE ;
Knowlton, KU .
NATURE MEDICINE, 1999, 5 (03) :320-326
[2]   IDENTIFICATION OF A NOVEL X-LINKED GENE RESPONSIBLE FOR EMERY-DREIFUSS MUSCULAR-DYSTROPHY [J].
BIONE, S ;
MAESTRINI, E ;
RIVELLA, S ;
MANCINI, M ;
REGIS, S ;
ROMEO, G ;
TONIOLO, D .
NATURE GENETICS, 1994, 8 (04) :323-327
[3]   Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy [J].
Bonne, G ;
Di Barletta, MR ;
Varnous, S ;
Bécane, HM ;
Hammouda, EH ;
Merlini, L ;
Muntoni, F ;
Greenberg, CR ;
Gary, F ;
Urtizberea, JA ;
Duboc, D ;
Fardeau, M ;
Toniolo, D ;
Schwartz, K .
NATURE GENETICS, 1999, 21 (03) :285-288
[4]   3 MUSCULAR-DYSTROPHIES - LOSS OF CYTOSKELETON EXTRACELLULAR-MATRIX LINKAGE [J].
CAMPBELL, KP .
CELL, 1995, 80 (05) :675-679
[5]   Complexity in simplicity: monogenic disorders and complex cardiomyopathies [J].
Chen, J ;
Chien, KR .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (11) :1483-1485
[6]   IDIOPATHIC DILATED CARDIOMYOPATHY [J].
DEC, GW ;
FUSTER, V .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (23) :1564-1575
[7]   Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. [J].
Fatkin, D ;
MacRae, C ;
Sasaki, T ;
Wolff, MR ;
Porcu, M ;
Frenneaux, M ;
Atherton, J ;
Vidaillet, HJ ;
Spudich, S ;
De Girolami, U ;
Seidman, JG ;
Seidman, CE ;
Muntoni, F ;
Muehle, G ;
Johnson, W ;
McDonough, B .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (23) :1715-1724
[8]   A functional enhancer suppresses silencing of a transgene and prevents its localization close to centromeric heterochromatin [J].
Francastel, C ;
Walters, MC ;
Groudine, M ;
Martin, DIK .
CELL, 1999, 99 (03) :259-269
[9]   A MOLECULAR-BASIS FOR FAMILIAL HYPERTROPHIC CARDIOMYOPATHY - A BETA-CARDIAC MYOSIN HEAVY-CHAIN GENE MISSENSE MUTATION [J].
GEISTERFERLOWRANCE, AAT ;
KASS, S ;
TANIGAWA, G ;
VOSBERG, HP ;
MCKENNA, W ;
SEIDMAN, CE ;
SEIDMAN, JG .
CELL, 1990, 62 (05) :999-1006
[10]  
Melacini P, 1999, MUSCLE NERVE, V22, P473, DOI 10.1002/(SICI)1097-4598(199904)22:4<473::AID-MUS8>3.0.CO