-
1
-
-
0023130164
-
Hypertrophic cardiomyopathy: Interrelations of clinical manifestations, pathophysiology, and therapy
-
Maron BJ, Bonow RO, Cannon RO III. Hypertrophic cardiomyopathy: interrelations of clinical manifestations, pathophysiology, and therapy. N Engl J Med. 316:1987;780-789.
-
(1987)
N Engl J Med
, vol.316
, pp. 780-789
-
-
Maron, B.J.1
Bonow, R.O.2
Cannon R.O. III3
-
2
-
-
0030057106
-
Sudden death in young competitive athletes: Clinical, demographic, and pathological profiles
-
Maron BJ, Shirani J, Poliac LC. Sudden death in young competitive athletes: clinical, demographic, and pathological profiles. JAMA. 276:1996;199-204.
-
(1996)
JAMA
, vol.276
, pp. 199-204
-
-
Maron, B.J.1
Shirani, J.2
Poliac, L.C.3
-
4
-
-
18744433901
-
α-Cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
-
Mogensen J, Klausen IC, Pedersen AK. α-Cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. J Clin Invest. 103:1999;R39-R43.
-
(1999)
J Clin Invest
, vol.103
, pp. 39-R43
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
-
5
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscles
-
Poetter K, Jiang H, Hassanzadeh S. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscles. Nature Genet. 13:1996;63-69.
-
(1996)
Nature Genet
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.2
Hassanzadeh, S.3
-
6
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura A, Harada H, Park J-E. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nature Genet. 16:1997;379-382.
-
(1997)
Nature Genet
, vol.16
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park J-E3
-
7
-
-
0029143611
-
Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3
-
MacRae CA, Ghaisas N, Kass S. Familial hypertrophic cardiomyopathy with Wolff-Parkinson-White syndrome maps to a locus on chromosome 7q3. J Clin Invest. 96:1995;1216-1220.
-
(1995)
J Clin Invest
, vol.96
, pp. 1216-1220
-
-
MacRae, C.A.1
Ghaisas, N.2
Kass, S.3
-
8
-
-
0027194702
-
Three-dimensional structure of myosin subfragment-1: A molecular motor
-
Rayment I, Rypniewski WR, Schmidt-Bäse K. Three-dimensional structure of myosin subfragment-1: a molecular motor. Science. 261:1993;50-56.
-
(1993)
Science
, vol.261
, pp. 50-56
-
-
Rayment, I.1
Rypniewski, W.R.2
Schmidt-Bäse, K.3
-
9
-
-
0031055854
-
Organization and sequence of human cardiac myosin binding protein C gene (MyBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy
-
Carrier L, Bonne G, Bahrend E. Organization and sequence of human cardiac myosin binding protein C gene (MyBPC3) and identification of mutations predicted to produce truncated proteins in familial hypertrophic cardiomyopathy. Circ Res. 80:1997;427-434.
-
(1997)
Circ Res
, vol.80
, pp. 427-434
-
-
Carrier, L.1
Bonne, G.2
Bahrend, E.3
-
10
-
-
0029029027
-
Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: A modulator of cardiac contraction?
-
Gautel M, Suffardi O, Freiburg A. Phosphorylation switches specific for the cardiac isoform of myosin binding protein-C: a modulator of cardiac contraction? EMBO J. 14:1995;1952-1960.
-
(1995)
EMBO J
, vol.14
, pp. 1952-1960
-
-
Gautel, M.1
Suffardi, O.2
Freiburg, A.3
-
11
-
-
0024097541
-
Myosin heavy-chain mutations that disrupt caeonorhabditis elegans thick filament assembly
-
Bejsovec A, Anderson P. Myosin heavy-chain mutations that disrupt caeonorhabditis elegans thick filament assembly. Genes Dev. 2:1988;1307-1317.
-
(1988)
Genes Dev
, vol.2
, pp. 1307-1317
-
-
Bejsovec, A.1
Anderson, P.2
-
12
-
-
0028967729
-
Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy
-
Lankford EB, Epstein ND, Fananapazir L. Abnormal contractile properties of muscle fibers expressing beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy. J Clin Invest. 95:1995;1409-1414.
-
(1995)
J Clin Invest
, vol.95
, pp. 1409-1414
-
-
Lankford, E.B.1
Epstein, N.D.2
Fananapazir, L.3
-
13
-
-
0027980111
-
Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction
-
Sweeney HL, Straceski AJ, Leinwand LA. Heterologous expression of a cardiomyopathic myosin that is defective in its actin interaction. J Biol Chem. 269:1994;1603-1605.
-
(1994)
J Biol Chem
, vol.269
, pp. 1603-1605
-
-
Sweeney, H.L.1
Straceski, A.J.2
Leinwand, L.A.3
-
14
-
-
0027302431
-
Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy
-
Cuda G, Fananapazir L, Zhu W. Skeletal muscle expression and abnormal function of β-myosin in hypertrophic cardiomyopathy. J Clin Invest. 91:1993;2861-2865.
-
(1993)
J Clin Invest
, vol.91
, pp. 2861-2865
-
-
Cuda, G.1
Fananapazir, L.2
Zhu, W.3
-
15
-
-
0029804760
-
Expression and functional assessement of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy
-
Watkins H, Seidman CE, Seidman JG. Expression and functional assessement of a truncated cardiac troponin T that causes hypertrophic cardiomyopathy. J Clin Invest. 98:1996;2456-2461.
-
(1996)
J Clin Invest
, vol.98
, pp. 2456-2461
-
-
Watkins, H.1
Seidman, C.E.2
Seidman, J.G.3
-
17
-
-
0029029473
-
Expression of the mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes
-
Marian AJ, Yu Q-T, Mann D. Expression of the mutation causing hypertrophic cardiomyopathy disrupts sarcomere assembly in adult feline cardiac myocytes. Circ Res. 77:1995;98-106.
-
(1995)
Circ Res
, vol.77
, pp. 98-106
-
-
Marian, A.J.1
Yu Q-T2
Mann, D.3
-
19
-
-
0031030298
-
Electrophysiological abnormalities and arrhythmias in α-MHC mutant familial hypertrophic cardiomyopathy mice
-
Berul CI, Christe M, Aronovitz MJ. Electrophysiological abnormalities and arrhythmias in α-MHC mutant familial hypertrophic cardiomyopathy mice. J Clin Invest. 99:1997;570-576.
-
(1997)
J Clin Invest
, vol.99
, pp. 570-576
-
-
Berul, C.I.1
Christe, M.2
Aronovitz, M.J.3
-
20
-
-
0029807438
-
Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy
-
Vikstrom KL, Factor SM, Leinwand LA. Mice expressing mutant myosin heavy chains are a model for familial hypertrophic cardiomyopathy. Mol Med. 2:1996;556-567.
-
(1996)
Mol Med
, vol.2
, pp. 556-567
-
-
Vikstrom, K.L.1
Factor, S.M.2
Leinwand, L.A.3
-
21
-
-
0032526155
-
A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy
-
Tardiff JC, Factor SM, Tompkins BD. A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy. J Clin Invest. 101:1998;2800-2811.
-
(1998)
J Clin Invest
, vol.101
, pp. 2800-2811
-
-
Tardiff, J.C.1
Factor, S.M.2
Tompkins, B.D.3
-
22
-
-
0024617347
-
Genetic dissection of Drosophila myofibril formation; Effects of actin and myosin heavy chain null alleles
-
Beall C, Sepanski MA, Fyrberg EA. Genetic dissection of Drosophila myofibril formation; effects of actin and myosin heavy chain null alleles. Genes Deve. 3:1989;131-140.
-
(1989)
Genes Deve
, vol.3
, pp. 131-140
-
-
Beall, C.1
Sepanski, M.A.2
Fyrberg, E.A.3
-
23
-
-
0025604603
-
Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities
-
Fyrberg E, Fyberg CC, Beall C. Drosophila melanogaster troponin-T mutations engender three distinct syndromes of myofibrillar abnormalities. J Mol Biol. 216:1990;657-675.
-
(1990)
J Mol Biol
, vol.216
, pp. 657-675
-
-
Fyrberg, E.1
Fyberg, C.C.2
Beall, C.3
-
24
-
-
10244221064
-
Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart
-
Jones WK, Grupp IL, Doetschman T. Ablation of the murine alpha myosin heavy chain gene leads to dosage effects and functional deficits in the heart. J Clin Invest. 98:1996;1906-1917.
-
(1996)
J Clin Invest
, vol.98
, pp. 1906-1917
-
-
Jones, W.K.1
Grupp, I.L.2
Doetschman, T.3
-
25
-
-
0030611676
-
Expression of a mutant (Arg92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility
-
Marian AJ, Zhao G, Seta Y, Roberts R, Yu Q-T. Expression of a mutant (Arg92Gln) human cardiac troponin T, known to cause hypertrophic cardiomyopathy, impairs adult cardiac myocyte contractility. Circ Res. 81:1997;76-85.
-
(1997)
Circ Res
, vol.81
, pp. 76-85
-
-
Marian, A.J.1
Zhao, G.2
Seta, Y.3
Roberts, R.4
Yu Q-T5
-
26
-
-
0030899032
-
Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants: Molecular force level of mutant myosins may have a prognostic implication
-
Fujita H, Sugura S, Momomura S. Characterization of mutant myosins of Dictyostelium discoideum equivalent to human familial hypertrophic cardiomyopathy mutants: molecular force level of mutant myosins may have a prognostic implication. J Clin Invest. 99:1997;1010-1015.
-
(1997)
J Clin Invest
, vol.99
, pp. 1010-1015
-
-
Fujita, H.1
Sugura, S.2
Momomura, S.3
-
27
-
-
0029993918
-
Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy
-
Lin D, Bobkova A, Homsher E. Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy. J Clin Invest. 97:1996;2842-2848.
-
(1996)
J Clin Invest
, vol.97
, pp. 2842-2848
-
-
Lin, D.1
Bobkova, A.2
Homsher, E.3
-
28
-
-
0031883848
-
A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity
-
Bottinelli R, Coviello DA, Redwood CS. A mutant tropomyosin that causes hypertrophic cardiomyopathy is expressed in vivo and associated with an increased calcium sensitivity. Circ Res. 82:1998;106-115.
-
(1998)
Circ Res
, vol.82
, pp. 106-115
-
-
Bottinelli, R.1
Coviello, D.A.2
Redwood, C.S.3
-
30
-
-
0031873371
-
2+-sensitizing effects of the mutations at lle-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy
-
2+-sensitizing effects of the mutations at lle-79 and Arg-92 of troponin T in hypertrophic cardiomyopathy. Am J Physiol. 275:1998;C200-7.
-
(1998)
Am J Physiol
, vol.275
, pp. 200-7
-
-
Morimoto, S.1
Yanaga, F.2
Minakami, R.3
-
31
-
-
0031597427
-
AT1 Receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy
-
Osterop AP, Kofflard MJ, Sandjuijl LA. AT1 Receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy. Hypertension. 32:1998;825-830.
-
(1998)
Hypertension
, vol.32
, pp. 825-830
-
-
Osterop, A.P.1
Kofflard, M.J.2
Sandjuijl, L.A.3
-
32
-
-
0031301663
-
Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy
-
Brugada R, Kelsey W, Lechin M. Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy. J Invest Med. 45:1997;542-551.
-
(1997)
J Invest Med
, vol.45
, pp. 542-551
-
-
Brugada, R.1
Kelsey, W.2
Lechin, M.3
-
33
-
-
0027425610
-
Angiotensin converting enzyme polymorphism is associated with hypertrophic cardiomyopathy as well as sudden cardiac death
-
Marian AJ, Yu Q-T, Workman R. Angiotensin converting enzyme polymorphism is associated with hypertrophic cardiomyopathy as well as sudden cardiac death. Lancet. 342:1993;1073-1074.
-
(1993)
Lancet
, vol.342
, pp. 1073-1074
-
-
Marian, A.J.1
Yu Q-T2
Workman, R.3
-
34
-
-
0029149023
-
Angiotensin-I converting enzyme genotypes influence the phenotypic expression of hypertrophic cardiomyopathy
-
Lechin M, Quiñones M, Omran A. Angiotensin-I converting enzyme genotypes influence the phenotypic expression of hypertrophic cardiomyopathy. Circulation. 92:1995;1808-1812.
-
(1995)
Circulation
, vol.92
, pp. 1808-1812
-
-
Lechin, M.1
Quiñones, M.2
Omran, A.3
-
35
-
-
0040873512
-
A molecular basis for familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
Geisterfer-Lowrance AAT, Kass S, Tanigawa G. A molecular basis for familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell. 77:1994;701-712.
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Geisterfer-Lowrance, A.A.T.1
Kass, S.2
Tanigawa, G.3
-
36
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
Watkins H, McKenna WJ, Thierfelder L. Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy. N Engl J Med. 332:1995;1058-1064.
-
(1995)
N Engl J Med
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
-
37
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins H, Rosenzweig A, Hwang DS. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N Eng J Med. 326:1992;1108-1114.
-
(1992)
N Eng J Med
, vol.326
, pp. 1108-1114
-
-
Watkins, H.1
Rosenzweig, A.2
Hwang, D.S.3
-
38
-
-
0026629472
-
Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the β-myosin heavy chain gene
-
Epstein ND, Cohn GM, Cyran F. Differences in clinical expression of hypertrophic cardiomyopathy associated with two distinct mutations in the β-myosin heavy chain gene. Circulation. 86:1992;345-352.
-
(1992)
Circulation
, vol.86
, pp. 345-352
-
-
Epstein, N.D.1
Cohn, G.M.2
Cyran, F.3
-
39
-
-
0028935226
-
Sudden cardiac death in hypertrophic cardiomyopathy: Variability in phenotypic expression of β-myosin heavy chain mutations
-
Marian AJ, Mares A, Kelly DP. Sudden cardiac death in hypertrophic cardiomyopathy: variability in phenotypic expression of β-myosin heavy chain mutations. Eur Heart J. 16:1995;368-376.
-
(1995)
Eur Heart J
, vol.16
, pp. 368-376
-
-
Marian, A.J.1
Mares, A.2
Kelly, D.P.3
-
40
-
-
0030905987
-
An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: Description of clinical features of the family members
-
Conte MR, Morello M, Mangiardi L. An ARG403GLN β-myosin heavy chain gene mutation identified in an Italian family with hypertrophic cardiomyopathy: description of clinical features of the family members. Eur Heart J. 18:1997;1033-1037.
-
(1997)
Eur Heart J
, vol.18
, pp. 1033-1037
-
-
Conte, M.R.1
Morello, M.2
Mangiardi, L.3
-
41
-
-
0027954269
-
Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy
-
Anan R, Greve G, Thierfelder L. Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy. J Clin Invest. 93:1994;280-285.
-
(1994)
J Clin Invest
, vol.93
, pp. 280-285
-
-
Anan, R.1
Greve, G.2
Thierfelder, L.3
-
42
-
-
0031933491
-
Molecular genetic basis of hypertrophic cardiomyopathy: Genetic markers for sudden cardiac death
-
Marian AJ, Roberts R. Molecular genetic basis of hypertrophic cardiomyopathy: genetic markers for sudden cardiac death. J Cardiovasc Electrophysiol. 9:1998;88-99.
-
(1998)
J Cardiovasc Electrophysiol
, vol.9
, pp. 88-99
-
-
Marian, A.J.1
Roberts, R.2
-
43
-
-
0024522202
-
Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population
-
Spirito P, Chiarella F, Carratino L. Clinical course and prognosis of hypertrophic cardiomyopathy in an outpatient population. N Engl J Med. 320:1989;749-755.
-
(1989)
N Engl J Med
, vol.320
, pp. 749-755
-
-
Spirito, P.1
Chiarella, F.2
Carratino, L.3
-
44
-
-
0028140230
-
Genotype-phenotype correlations in hypertrophic cardiomyopathy: Insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations
-
Fananazapir L, Epstein ND. Genotype-phenotype correlations in hypertrophic cardiomyopathy: insights provided by comparisons of kindreds with distinct and identical β-myosin heavy chain gene mutations. Circulation. 89:1994;22-32.
-
(1994)
Circulation
, vol.89
, pp. 22-32
-
-
Fananazapir, L.1
Epstein, N.D.2
-
45
-
-
0031114657
-
Prognostic significance of β-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy
-
Abchee A, Marian AJ. Prognostic significance of β-myosin heavy chain mutations is reflective of their hypertrophic expressivity in patients with hypertrophic cardiomyopathy. J Invest Med. 45:1997;191-196.
-
(1997)
J Invest Med
, vol.45
, pp. 191-196
-
-
Abchee, A.1
Marian, A.J.2
-
46
-
-
0029014579
-
Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac β myosin heavy chain gene mutations
-
Posen BM, Moolman JC, Corfield VA. Clinical and prognostic evaluation of familial hypertrophic cardiomyopathy in two South African families with different cardiac β myosin heavy chain gene mutations. Br Heart J. 74:1995;40-46.
-
(1995)
Br Heart J
, vol.74
, pp. 40-46
-
-
Posen, B.M.1
Moolman, J.C.2
Corfield, V.A.3
-
47
-
-
0027138216
-
Familial hypertrophic cardiomyopathy: Microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene
-
Dausse E, Komajda M, Fetler L. Familial hypertrophic cardiomyopathy: microsatellite haplotyping and identification of a hot spot for mutations in the β-myosin heavy chain gene. J Clin Invest. 92:1993;2807-2813.
-
(1993)
J Clin Invest
, vol.92
, pp. 2807-2813
-
-
Dausse, E.1
Komajda, M.2
Fetler, L.3
-
48
-
-
0031891357
-
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy: A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes
-
Charron P, Dubourg O, Desnos M. Genotype-phenotype correlations in familial hypertrophic cardiomyopathy: a comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes. Eur Heart J. 19:1998;139-145.
-
(1998)
Eur Heart J
, vol.19
, pp. 139-145
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
-
49
-
-
0028178083
-
α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: A disease of the sarcomere
-
Thierfelder L, Watkins H, MacRae C. α-Tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell. 77:1994;701-712.
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
-
51
-
-
0031080070
-
Novel missense mutation in cardiac troponin T gene found in a Japanese patient with hypertrophic cardiomyopathy
-
Nakajima-Taniguchi C, Matsui H, Fujio Y. Novel missense mutation in cardiac troponin T gene found in a Japanese patient with hypertrophic cardiomyopathy. J Mol Cell Cardiol. 29:1997;839-843.
-
(1997)
J Mol Cell Cardiol
, vol.29
, pp. 839-843
-
-
Nakajima-Taniguchi, C.1
Matsui, H.2
Fujio, Y.3
-
52
-
-
8044244822
-
Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy
-
Forissier J-F, Carrier L, Farza H. Codon 102 of the cardiac troponin T gene is a putative hot spot for mutations in familial hypertrophic cardiomyopathy. Circulation. 94:1996;3069-3073.
-
(1996)
Circulation
, vol.94
, pp. 3069-3073
-
-
Forissier J-F1
Carrier, L.2
Farza, H.3
-
53
-
-
0032483037
-
Patients with familial hypertrophic cardiomyopathy caused by a Phe 110lle missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis
-
Anan R, Shono H, Kisanuki A. Patients with familial hypertrophic cardiomyopathy caused by a Phe 110lle missense mutation in the cardiac troponin T gene have variable cardiac morphologies and a favorable prognosis. Circulation. 98:1998;391-397.
-
(1998)
Circulation
, vol.98
, pp. 391-397
-
-
Anan, R.1
Shono, H.2
Kisanuki, A.3
-
54
-
-
0027161005
-
Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11
-
Carrier L, Hengstenberg C, Beckmann JS. Mapping of a novel gene for familial hypertrophic cardiomyopathy to chromosome 11. Nature Genet. 4:1993;311-313.
-
(1993)
Nature Genet
, vol.4
, pp. 311-313
-
-
Carrier, L.1
Hengstenberg, C.2
Beckmann, J.S.3
-
55
-
-
0028886136
-
Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy
-
Bonne G, Carrier L, Bercovici J. Cardiac myosin binding protein-C gene splice acceptor site mutation is associated with familial hypertrophic cardiomyopathy. Nature Genet. 11:1995;438-440.
-
(1995)
Nature Genet
, vol.11
, pp. 438-440
-
-
Bonne, G.1
Carrier, L.2
Bercovici, J.3
-
56
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins H, Conner D, Thierfelder L. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nature Genet. 11:1995;434-437.
-
(1995)
Nature Genet
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
-
57
-
-
0032580520
-
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
-
Nimura H, Bachinski LL, Sangwatanaroj S. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N Engl J Med. 338:1998;1248-1257.
-
(1998)
N Engl J Med
, vol.338
, pp. 1248-1257
-
-
Nimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
-
58
-
-
0032499634
-
Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene
-
Charron P, Dubourg O, Desnos M. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin-binding protein C gene. Circulation. 97:1998;2230-2236.
-
(1998)
Circulation
, vol.97
, pp. 2230-2236
-
-
Charron, P.1
Dubourg, O.2
Desnos, M.3
-
59
-
-
0027180678
-
A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2
-
Thierfelder L, MacRae C, Watkins H. A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2. Proc Natl Acad Sci U S A. 90:1993;6270-6274.
-
(1993)
Proc Natl Acad Sci U S a
, vol.90
, pp. 6270-6274
-
-
Thierfelder, L.1
MacRae, C.2
Watkins, H.3
-
60
-
-
0029794498
-
Clinical implications of hypertrophic cardiomyopathy associated with mutations in the α-tropomyosin gene
-
Yamauchi-Takihara K, Nakajima-Taniguchi C, Matsui H. Clinical implications of hypertrophic cardiomyopathy associated with mutations in the α-tropomyosin gene. Heart. 76:1996;63-65.
-
(1996)
Heart
, vol.76
, pp. 63-65
-
-
Yamauchi-Takihara, K.1
Nakajima-Taniguchi, C.2
Matsui, H.3
-
61
-
-
0031042881
-
Clinical features of hypertophic cardiomyopathy caused by mutation of a 'hot spot' in the alpha-tropomyosin gene
-
Coviello DA, Maron BJ, Spirito P. Clinical features of hypertophic cardiomyopathy caused by mutation of a 'hot spot' in the alpha-tropomyosin gene. J Am Coll Cardiol. 29:1997;635-640.
-
(1997)
J Am Coll Cardiol
, vol.29
, pp. 635-640
-
-
Coviello, D.A.1
Maron, B.J.2
Spirito, P.3
-
62
-
-
15644366960
-
Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy
-
Flavigny J, Richard P, Isnard R. Identification of two novel mutations in the ventricular regulatory myosin light chain gene (MYL2) associated with familial and classical forms of hypertrophic cardiomyopathy. J Mol Med. 76:1998;208-214.
-
(1998)
J Mol Med
, vol.76
, pp. 208-214
-
-
Flavigny, J.1
Richard, P.2
Isnard, R.3
-
63
-
-
0003062898
-
Gene mutations that cause familial hypertrophic cardiomyopathy
-
E. Haber. New York: Scientific American
-
Seidman CE, Seidman JG. Gene mutations that cause familial hypertrophic cardiomyopathy. Haber E. Molecular cardiovascular medicine. 1995;193-209 Scientific American, New York.
-
(1995)
Molecular Cardiovascular Medicine
, pp. 193-209
-
-
Seidman, C.E.1
Seidman, J.G.2
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