-
1
-
-
0032578962
-
Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23
-
Ahmad F, Li D, Karibe A, Gonzalez O, Tapscott T, et al. 1998. Localization of a gene responsible for arrhythmogenic right ventricular dysplasia to chromosome 3p23. Circulation 98:2791-95
-
(1998)
Circulation
, vol.98
, pp. 2791-2795
-
-
Ahmad, F.1
Li, D.2
Karibe, A.3
Gonzalez, O.4
Tapscott, T.5
-
2
-
-
0036167225
-
Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy
-
Arad M, Benson DW, Perez-Atayde AR, McKenna WJ, Sparks EA, et al. 2002. Constitutively active AMP kinase mutations cause glycogen storage disease mimicking hypertrophic cardiomyopathy. J. Clin. Invest. 109:357-62
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 357-362
-
-
Arad, M.1
Benson, D.W.2
Perez-Atayde, A.R.3
McKenna, W.J.4
Sparks, E.A.5
-
3
-
-
19944434362
-
Glycogen storage diseases presenting as hypertrophic cardiomyopathy
-
Arad M, Maron BJ, Gorham JM, Johnson WH, Saul JP, et al. 2005. Glycogen storage diseases presenting as hypertrophic cardiomyopathy. N. Engl. J. Med. 352:362-72
-
(2005)
N. Engl. J. Med.
, vol.352
, pp. 362-372
-
-
Arad, M.1
Maron, B.J.2
Gorham, J.M.3
Johnson, W.H.4
Saul, J.P.5
-
4
-
-
0037782349
-
Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy
-
Arad M, Moskowitz IP, Patel VV, Ahmad F, Perez-Atayde AR, et al. 2003. Transgenic mice overexpressing mutant PRKAG2 define the cause of Wolff-Parkinson-White syndrome in glycogen storage cardiomyopathy. Circulation 107:2850-56
-
(2003)
Circulation
, vol.107
, pp. 2850-2856
-
-
Arad, M.1
Moskowitz, I.P.2
Patel, V.V.3
Ahmad, F.4
Perez-Atayde, A.R.5
-
5
-
-
2542559620
-
Dystrophin disruption in enterovirus-induced myocarditis and dilated cardiomyopathy: From bench to bedside
-
Badorff C, Knowlton KU. 2004. Dystrophin disruption in enterovirus-induced myocarditis and dilated cardiomyopathy: from bench to bedside. Med. Microbiol. Immunol. (Berlin) 193:121-26
-
(2004)
Med. Microbiol. Immunol. (Berlin)
, vol.193
, pp. 121-126
-
-
Badorff, C.1
Knowlton, K.U.2
-
6
-
-
2142765298
-
X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): An update
-
Barth PG, Valianpour F, Bowen VM, Lam J, Duran M, et al. 2004. X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update. Am. J. Med. Genet. 126A:349-54
-
(2004)
Am. J. Med. Genet.
, vol.126 A
, pp. 349-354
-
-
Barth, P.G.1
Valianpour, F.2
Bowen, V.M.3
Lam, J.4
Duran, M.5
-
7
-
-
0032939409
-
Cardiovascular causes of sudden death in young individuals including athletes
-
Basso C, Corrado D, Thiene G. 1999. Cardiovascular causes of sudden death in young individuals including athletes. Cardial. Rev. 7:127-35
-
(1999)
Cardial. Rev.
, vol.7
, pp. 127-135
-
-
Basso, C.1
Corrado, D.2
Thiene, G.3
-
8
-
-
0029787576
-
Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis?
-
see comments
-
Basso C, Thiene G, Corrado D, Angelini A, Nava A, Valente M. 1996. Arrhythmogenic right ventricular cardiomyopathy. Dysplasia, dystrophy, or myocarditis? [see comments]. Circulation 94:983-91
-
(1996)
Circulation
, vol.94
, pp. 983-991
-
-
Basso, C.1
Thiene, G.2
Corrado, D.3
Angelini, A.4
Nava, A.5
Valente, M.6
-
9
-
-
0034154911
-
Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome Iq42-43
-
Bauce B, Nava A, Rampazzo A, Daliento L, Muriago M, et al. 2000. Familial effort polymorphic ventricular arrhythmias in arrhythmogenic right ventricular cardiomyopathy map to chromosome Iq42-43. Am. J. Cardiol. 85:573-79
-
(2000)
Am. J. Cardiol.
, vol.85
, pp. 573-579
-
-
Bauce, B.1
Nava, A.2
Rampazzo, A.3
Daliento, L.4
Muriago, M.5
-
10
-
-
0037125396
-
Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: Early diagnosis of asymptomatic carriers
-
Bauce B, Rampazzo A, Basso C, Bagattin A, Daliento L, et al. 2002. Screening for ryanodine receptor type 2 mutations in families with effort-induced polymorphic ventricular arrhythmias and sudden death: early diagnosis of asymptomatic carriers. J. Am. Coll. Cardiol. 40:341-49
-
(2002)
J. Am. Coll. Cardiol.
, vol.40
, pp. 341-349
-
-
Bauce, B.1
Rampazzo, A.2
Basso, C.3
Bagattin, A.4
Daliento, L.5
-
11
-
-
12144290256
-
ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating
-
Bienengraeber M, Olson TM, Selivanov VA, Kathmann EC, O'Cochlain F, et al. 2004. ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating. Nat. Genet. 36:382-87
-
(2004)
Nat. Genet.
, vol.36
, pp. 382-387
-
-
Bienengraeber, M.1
Olson, T.M.2
Selivanov, V.A.3
Kathmann, E.C.4
O'Cochlain, F.5
-
12
-
-
0032834144
-
Pathological features of glycogen storage disease type II highlighted in the knockout mouse model
-
Bijvoet AG, Van Hirtum H, Vermey M, Van Leenen D, Van Der Ploeg AT, et al. 1999. Pathological features of glycogen storage disease type II highlighted in the knockout mouse model. J. Pathol. 189:416-24
-
(1999)
J. Pathol.
, vol.189
, pp. 416-424
-
-
Bijvoet, A.G.1
Van Hirtum, H.2
Vermey, M.3
Van Leenen, D.4
Van Der Ploeg, A.T.5
-
13
-
-
0033851629
-
Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha-tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay
-
Bing W, Knott A, Redwood C, Esposito G, Purcell I, et al. 2000. Effect of hypertrophic cardiomyopathy mutations in human cardiac muscle alpha-tropomyosin (Asp175Asn and Glu180Gly) on the regulatory properties of human cardiac troponin determined by in vitro motility assay. J. Mol. Cell. Cardiol. 32:1489-98
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, pp. 1489-1498
-
-
Bing, W.1
Knott, A.2
Redwood, C.3
Esposito, G.4
Purcell, I.5
-
14
-
-
0035872209
-
Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: Evidence for the central role of energy compromise in disease pathogenesis
-
Blair E, Redwood C, Ashrafian H, Oliveira M, Broxholme J, et al. 2001. Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis. Hum. Mol. Genet. 10:1215-20
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 1215-1220
-
-
Blair, E.1
Redwood, C.2
Ashrafian, H.3
Oliveira, M.4
Broxholme, J.5
-
15
-
-
0037155048
-
Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy
-
Blair E, Redwood C, de Jesus Oliveira M, Moolman-Smook JC, Brink P, et al. 2002. Mutations of the light meromyosin domain of the beta-myosin heavy chain rod in hypertrophic cardiomyopathy. Circ. Res. 90:263-69
-
(2002)
Circ. Res.
, vol.90
, pp. 263-269
-
-
Blair, E.1
Redwood, C.2
De Jesus Oliveira, M.3
Moolman-Smook, J.C.4
Brink, P.5
-
16
-
-
0033525753
-
Altered crossbridge kinetics in the alphaMHC-403/+ mouse model of familial hypertrophic cardiomyopathy
-
Blanchard E, Seidman C, Seidman JG, LeWinter M, Maughan D. 1999. Altered crossbridge kinetics in the alphaMHC-403/+ mouse model of familial hypertrophic cardiomyopathy. Circ. Res. 84:475-83
-
(1999)
Circ. Res.
, vol.84
, pp. 475-483
-
-
Blanchard, E.1
Seidman, C.2
Seidman, J.G.3
LeWinter, M.4
Maughan, D.5
-
17
-
-
0032977685
-
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy
-
Bonne G, Di Barletta MR, Varnous S, Becane HM, Hammouda EH, et al. 1999. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat. Genet. 21:285-88
-
(1999)
Nat. Genet.
, vol.21
, pp. 285-288
-
-
Bonne, G.1
Di Barletta, M.R.2
Varnous, S.3
Becane, H.M.4
Hammouda, E.H.5
-
18
-
-
0029784361
-
Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23
-
Bowles KR, Gajarski R, Porter P, Goytia V, Bachinski L, et al. 1996. Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23. J. Clin. Invest. 98:1355-60
-
(1996)
J. Clin. Invest.
, vol.98
, pp. 1355-1360
-
-
Bowles, K.R.1
Gajarski, R.2
Porter, P.3
Goytia, V.4
Bachinski, L.5
-
19
-
-
0001862643
-
Dilated cardiomyopathy
-
ed. Willerson JT, JN Cohn. New York: Churchill Livingstone
-
Bozkurt B, Mann DL. 2000. Dilated cardiomyopathy. In Cardiovascular Medicine, ed. Willerson JT, JN Cohn, pp. 1034-53. New York: Churchill Livingstone
-
(2000)
Cardiovascular Medicine
, pp. 1034-1053
-
-
Bozkurt, B.1
Mann, D.L.2
-
20
-
-
0035077977
-
Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases
-
Brega A, Narula J, Arbustini E. 2001. Functional, structural, and genetic mitochondrial abnormalities in myocardial diseases. J. Nucl. Cardiol. 8:89-97
-
(2001)
J. Nucl. Cardiol.
, vol.8
, pp. 89-97
-
-
Brega, A.1
Narula, J.2
Arbustini, E.3
-
21
-
-
0028962264
-
Gene for progressive familial heart block type I maps to chromosome 19q13
-
Brink PA, Ferreira A, Moolman JC, Weymar HW, van der Merwe PL, Corfield VA. 1995. Gene for progressive familial heart block type I maps to chromosome 19q13. Circulation 91:1633-40
-
(1995)
Circulation
, vol.91
, pp. 1633-1640
-
-
Brink, P.A.1
Ferreira, A.2
Moolman, J.C.3
Weymar, H.W.4
Van Der Merwe, P.L.5
Corfield, V.A.6
-
22
-
-
0031301663
-
Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy
-
Brugada R, Kelsey W, Lechin M, Zhao G, Yu QT, et al. 1997. Role of candidate modifier genes on the phenotypic expression of hypertrophy in patients with hypertrophic cardiomyopathy. J. Invest. Med. 45:542-51
-
(1997)
J. Invest. Med.
, vol.45
, pp. 542-551
-
-
Brugada, R.1
Kelsey, W.2
Lechin, M.3
Zhao, G.4
Yu, Q.T.5
-
23
-
-
0035015261
-
Ca(2+) activation of myofilaments from transgenic mouse hearts expressing R92Q mutant cardiac troponin T
-
Chandra M, Rundell VL, Tardiff JC, Leinwand LA, De Tombe PP, Solaro RJ. 2001. Ca(2+) activation of myofilaments from transgenic mouse hearts expressing R92Q mutant cardiac troponin T. Am. J. Physiol. Heart Circ. Physiol. 280:H705-H13
-
(2001)
Am. J. Physiol. Heart Circ. Physiol.
, vol.280
-
-
Chandra, M.1
Rundell, V.L.2
Tardiff, J.C.3
Leinwand, L.A.4
De Tombe, P.P.5
Solaro, R.J.6
-
24
-
-
4544358659
-
Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development
-
Chang S, McKinsey TA, Zhang CL, Richardson JA, Hill JA, Olson EN. 2004. Histone deacetylases 5 and 9 govern responsiveness of the heart to a subset of stress signals and play redundant roles in heart development. Mol. Cell. Biol. 24:8467-76
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 8467-8476
-
-
Chang, S.1
McKinsey, T.A.2
Zhang, C.L.3
Richardson, J.A.4
Hill, J.A.5
Olson, E.N.6
-
25
-
-
0032568477
-
Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21
-
Coonar AS, Protonotarios N, Tsatsopoulou A, Needham EW, Houlston RS, et al. 1998. Gene for arrhythmogenic right ventricular cardiomyopathy with diffuse nonepidermolytic palmoplantar keratoderma and woolly hair (Naxos disease) maps to 17q21. Circulation 97:2049-58
-
(1998)
Circulation
, vol.97
, pp. 2049-2058
-
-
Coonar, A.S.1
Protonotarios, N.2
Tsatsopoulou, A.3
Needham, E.W.4
Houlston, R.S.5
-
26
-
-
0033588050
-
Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: A novel mechanism for cardiomyopathy and muscular dystrophy
-
Coral-Vazquez R, Cohn RD, Moore SA, Hill JA, Weiss RM, et al. 1999. Disruption of the sarcoglycan-sarcospan complex in vascular smooth muscle: a novel mechanism for cardiomyopathy and muscular dystrophy. Cell 98:465-74
-
(1999)
Cell
, vol.98
, pp. 465-474
-
-
Coral-Vazquez, R.1
Cohn, R.D.2
Moore, S.A.3
Hill, J.A.4
Weiss, R.M.5
-
28
-
-
0030712343
-
Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: A multicenter study
-
Corrado D, Basso C, Thiene G, McKenna WJ, Davies MJ, et al. 1997. Spectrum of clinicopathologic manifestations of arrhythmogenic right ventricular cardiomyopathy/dysplasia: a multicenter study. J. Am. Coll. Cardiol. 30:1512-20
-
(1997)
J. Am. Coll. Cardiol.
, vol.30
, pp. 1512-1520
-
-
Corrado, D.1
Basso, C.2
Thiene, G.3
McKenna, W.J.4
Davies, M.J.5
-
29
-
-
16944366521
-
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies
-
D'Adamo P, Fassone L, Gedeon A, Janssen EA, Bione S, et al. 1997. The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. Am. J. Hum. Genet. 61:862-67
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 862-867
-
-
D'Adamo, P.1
Fassone, L.2
Gedeon, A.3
Janssen, E.A.4
Bione, S.5
-
30
-
-
0036401384
-
Novel mutations in sarcomeric protein genes in dilated cardiomyopathy
-
Daehmlow S, Erdmann J, Knueppel T, Gille C, Froemmel C, et al. 2002. Novel mutations in sarcomeric protein genes in dilated cardiomyopathy. Biochem. Biophys. Res. Commun. 298:116-20
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.298
, pp. 116-120
-
-
Daehmlow, S.1
Erdmann, J.2
Knueppel, T.3
Gille, C.4
Froemmel, C.5
-
31
-
-
0028116218
-
Idiopathic dilated cardiomyopathy
-
Dec GW, Fuster V. 1994. Idiopathic dilated cardiomyopathy. N. Engl J. Med. 331:1564-75
-
(1994)
N. Engl J. Med.
, vol.331
, pp. 1564-1575
-
-
Dec, G.W.1
Fuster, V.2
-
32
-
-
0035672057
-
Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy
-
Deinum J, van Gool JM, Kofflard MJ, ten Gate FJ, Danser AH. 2001. Angiotensin II type 2 receptors and cardiac hypertrophy in women with hypertrophic cardiomyopathy. Hypertension 38:1278-81
-
(2001)
Hypertension
, vol.38
, pp. 1278-1281
-
-
Deinum, J.1
Van Gool, J.M.2
Kofflard, M.J.3
Ten Gate, F.J.4
Danser, A.H.5
-
33
-
-
0035807934
-
Effects of phosphorylation and mutation R145G on human cardiac troponin I function
-
Deng Y, Schmidtmann A, Redlich A, Westerdorf B, Jaquet K, Thieleczek R. 2001. Effects of phosphorylation and mutation R145G on human cardiac troponin I function. Biochemistry 40:14593-602
-
(2001)
Biochemistry
, vol.40
, pp. 14593-14602
-
-
Deng, Y.1
Schmidtmann, A.2
Redlich, A.3
Westerdorf, B.4
Jaquet, K.5
Thieleczek, R.6
-
34
-
-
0344837383
-
The influence of age on gender-specific differences in the left ventricular cavity size and contractility in patients with hypertrophic cardiomyopathy
-
discussion 6-7
-
Dimitrow PP, Czarnecka D, Kawecka-Jaszcz K, Dubiel JS. 2003. The influence of age on gender-specific differences in the left ventricular cavity size and contractility in patients with hypertrophic cardiomyopathy. Int. J. Cardiol. 88:11-16; discussion 6-7
-
(2003)
Int. J. Cardiol.
, vol.88
, pp. 11-16
-
-
Dimitrow, P.P.1
Czarnecka, D.2
Kawecka-Jaszcz, K.3
Dubiel, J.S.4
-
35
-
-
2942729737
-
Sex-based comparison of survival in referred patients with hypertrophic cardiomyopathy
-
Dimitrow PP, Czarnecka D, Kawecka-Jaszcz K, Dubiel JS. 2004. Sex-based comparison of survival in referred patients with hypertrophic cardiomyopathy. Am. J. Med. 117:65-66
-
(2004)
Am. J. Med.
, vol.117
, pp. 65-66
-
-
Dimitrow, P.P.1
Czarnecka, D.2
Kawecka-Jaszcz, K.3
Dubiel, J.S.4
-
36
-
-
0028336811
-
Lysosomal glycogen storage with normal acid maltase: A familial study with successful heart transplant
-
Dworzak F, Casazza F, Mora M, De Maria R, Gronda E, et al. 1994. Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplant. Neuromuscul. Disord. 4:243-47
-
(1994)
Neuromuscul. Disord.
, vol.4
, pp. 243-247
-
-
Dworzak, F.1
Casazza, F.2
Mora, M.3
De Maria, R.4
Gronda, E.5
-
37
-
-
0034698086
-
Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy
-
Elliott K, Watkins H, Redwood CS. 2000. Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy. J. Biol. Chem. 275:22069-74
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 22069-22074
-
-
Elliott, K.1
Watkins, H.2
Redwood, C.S.3
-
38
-
-
0034323679
-
Genetic variants in the promoter (g983G > T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy
-
Erdmann J, Hassfeld S, Kallisch H, Fleck E, Regitz-Zagrose V. 2000. Genetic variants in the promoter (g983G > T) and coding region (A92T) of the human cardiotrophin-1 gene (CTF1) in patients with dilated cardiomyopathy. Hum. Mutat. 16:448
-
(2000)
Hum. Mutat.
, vol.16
, pp. 448
-
-
Erdmann, J.1
Hassfeld, S.2
Kallisch, H.3
Fleck, E.4
Regitz-Zagrose, V.5
-
39
-
-
0028140230
-
Genotype-phenotype correlations in hypertrophic cardiomyopathy: Insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations
-
Fananapazir L, Epstein ND. 1994. Genotype-phenotype correlations in hypertrophic cardiomyopathy: insights provided by comparisons of kindreds with distinct and identical beta-myosin heavy chain gene mutations. Circulation 89:22-32
-
(1994)
Circulation
, vol.89
, pp. 22-32
-
-
Fananapazir, L.1
Epstein, N.D.2
-
40
-
-
0033518282
-
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease
-
Fatkin D, MacRae C, Sasaki T, Wolff MR, Porcu M, et al. 1999. Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. N. Engl. J. Med. 341:1715-24
-
(1999)
N. Engl. J. Med.
, vol.341
, pp. 1715-1724
-
-
Fatkin, D.1
MacRae, C.2
Sasaki, T.3
Wolff, M.R.4
Porcu, M.5
-
41
-
-
0033653534
-
An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy
-
Fatkin D, McConnell BK, Mudd JO, Semsarian C, Moskowitz IG, et al. 2000. An abnormal Ca(2+) response in mutant sarcomere protein-mediated familial hypertrophic cardiomyopathy. J. Clin. Invest. 106:1351-59
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 1351-1359
-
-
Fatkin, D.1
McConnell, B.K.2
Mudd, J.O.3
Semsarian, C.4
Moskowitz, I.G.5
-
42
-
-
0034643399
-
Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy
-
Felker GM, Thompson RE, Hare JM, Hruban RH, Clemetson DE, et al. 2000. Underlying causes and long-term survival in patients with initially unexplained cardiomyopathy. N. Engl. J. Med. 342:1077-84
-
(2000)
N. Engl. J. Med.
, vol.342
, pp. 1077-1084
-
-
Felker, G.M.1
Thompson, R.E.2
Hare, J.M.3
Hruban, R.H.4
Clemetson, D.E.5
-
43
-
-
0031882910
-
Cardiac arrest and sudden death in competitive athletes with arrhythmogenic right ventricular dysplasia
-
Furlanello F, Bertoldi A, Dallago M, Furlanello C, Fernando F, et al. 1998. Cardiac arrest and sudden death in competitive athletes with arrhythmogenic right ventricular dysplasia. Pacing Clin. Electrophysiol. 21:331-35
-
(1998)
Pacing Clin. Electrophysiol.
, vol.21
, pp. 331-335
-
-
Furlanello, F.1
Bertoldi, A.2
Dallago, M.3
Furlanello, C.4
Fernando, F.5
-
44
-
-
0030067394
-
A mouse model of familial hypertrophic cardiomyopathy
-
Geisterfer-Lowrance AA, Christe M, Conner DA, Ingwall JS, Schoen FJ, et al. 1996. A mouse model of familial hypertrophic cardiomyopathy. Science 272:731-34
-
(1996)
Science
, vol.272
, pp. 731-734
-
-
Geisterfer-Lowrance, A.A.1
Christe, M.2
Conner, D.A.3
Ingwall, J.S.4
Schoen, F.J.5
-
45
-
-
0025040392
-
A molecular basis for familial hypertrophic cardiomyopathy: A beta cardiac myosin heavy chain gene missense mutation
-
Geisterfer-Lowrance AA, Kass S, Tanigawa G, Vosberg HP, McKenna W, et al. 1990. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation. Cell 62:999-1006
-
(1990)
Cell
, vol.62
, pp. 999-1006
-
-
Geisterfer-Lowrance, A.A.1
Kass, S.2
Tanigawa, G.3
Vosberg, H.P.4
McKenna, W.5
-
46
-
-
0036478897
-
Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy
-
Gerull B, Gramlich M, Atherton J, McNabb M, Trombitas K, et al. 2002. Mutations of TTN, encoding the giant muscle filament titin, cause familial dilated cardiomyopathy. Nat. Genet. 30:201-4
-
(2002)
Nat. Genet.
, vol.30
, pp. 201-204
-
-
Gerull, B.1
Gramlich, M.2
Atherton, J.3
McNabb, M.4
Trombitas, K.5
-
47
-
-
11444264507
-
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
-
Gerull B, Heuser A, Wichter T, Paul M, Basson CT, et al. 2004. Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy. Nat. Genet. 36:1162-64
-
(2004)
Nat. Genet.
, vol.36
, pp. 1162-1164
-
-
Gerull, B.1
Heuser, A.2
Wichter, T.3
Paul, M.4
Basson, C.T.5
-
48
-
-
17344373157
-
Missense mutations in desmin associated with familial cardiac and skeletal myopathy
-
Goldfarb LG, Park KY, Cervenakova L, Gorokhova S, Lee HS, et al. 1998. Missense mutations in desmin associated with familial cardiac and skeletal myopathy. Nat. Genet. 19:402-3
-
(1998)
Nat. Genet.
, vol.19
, pp. 402-403
-
-
Goldfarb, L.G.1
Park, K.Y.2
Cervenakova, L.3
Gorokhova, S.4
Lee, H.S.5
-
49
-
-
0035859215
-
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome
-
Gollob MH, Green MS, Tang AS, Gollob T, Karibe A, et al. 2001. Identification of a gene responsible for familial Wolff-Parkinson-White syndrome. N. Engl. J. Med. 344:1823-31
-
(2001)
N. Engl. J. Med.
, vol.344
, pp. 1823-1831
-
-
Gollob, M.H.1
Green, M.S.2
Tang, A.S.3
Gollob, T.4
Karibe, A.5
-
50
-
-
0034568948
-
Are desmosomes more than tethers for intermediate filaments?
-
Green KJ, Gaudry CA. 2000. Are desmosomes more than tethers for intermediate filaments? Nat. Rev. Mol. Cell Biol. 1:208-16
-
(2000)
Nat. Rev. Mol. Cell Biol.
, vol.1
, pp. 208-216
-
-
Green, K.J.1
Gaudry, C.A.2
-
51
-
-
0031951537
-
Frequency and phenotypes of familial dilated cardiomyopathy
-
Grunig E, Tasman JA, Kucherer H, Franz W, Kubler W, Katus HA. 1998. Frequency and phenotypes of familial dilated cardiomyopathy. J. Am. Coll. Cardiol. 31:186-94
-
(1998)
J. Am. Coll. Cardiol.
, vol.31
, pp. 186-194
-
-
Grunig, E.1
Tasman, J.A.2
Kucherer, H.3
Franz, W.4
Kubler, W.5
Katus, H.A.6
-
52
-
-
85047687537
-
Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human
-
Haghighi K, Kolokathis F, Pater L, Lynch RA, Asahi M, et al. 2003. Human phospholamban null results in lethal dilated cardiomyopathy revealing a critical difference between mouse and human. J. Clin. Invest. 111:869-76
-
(2003)
J. Clin. Invest.
, vol.111
, pp. 869-876
-
-
Haghighi, K.1
Kolokathis, F.2
Pater, L.3
Lynch, R.A.4
Asahi, M.5
-
53
-
-
0034646607
-
Plakoglobin regulates the expression of the anti-apoptotic protein BCL-2
-
Hakimelahi S, Parker HR, Gilchrist AJ, Barry M, Li Z, et al. 2000. Plakoglobin regulates the expression of the anti-apoptotic protein BCL-2. J. Biol. Chem. 275:10905-11
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 10905-10911
-
-
Hakimelahi, S.1
Parker, H.R.2
Gilchrist, A.J.3
Barry, M.4
Li, Z.5
-
54
-
-
0035816114
-
An activating mutation in the gammal subunit of the AMP-activated protein kinase
-
Hamilton SR, Stapleton D, O'Donnell JB Jr, Kung JT, Dalal R, et al. 2001. An activating mutation in the gammal subunit of the AMP-activated protein kinase. FEBS Lett. 500:163-68
-
(2001)
FEBS Lett.
, vol.500
, pp. 163-168
-
-
Hamilton, S.R.1
Stapleton, D.2
O'Donnell Jr., J.B.3
Kung, J.T.4
Dalal, R.5
-
55
-
-
2442417687
-
Familial hypertrophic cardiomyopathy mutations from different functional regions of troponin T result in different effects on the pH and Ca2+ sensitivity of cardiac muscle contraction
-
Harada K, Potter JD. 2004. Familial hypertrophic cardiomyopathy mutations from different functional regions of troponin T result in different effects on the pH and Ca2+ sensitivity of cardiac muscle contraction. J. Biol. Chem. 279:14488-95
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 14488-14495
-
-
Harada, K.1
Potter, J.D.2
-
56
-
-
0034055642
-
Functional consequences of the deletion mutation deltaGluloO in human cardiac troponin T
-
Harada K, Takahashi-Yanaga F, Minakami R, Morimoto S, Ohtsuki I. 2000. Functional consequences of the deletion mutation deltaGluloO in human cardiac troponin T. J. Biochem. (Tokyo) 127:263-68
-
(2000)
J. Biochem. (Tokyo)
, vol.127
, pp. 263-268
-
-
Harada, K.1
Takahashi-Yanaga, F.2
Minakami, R.3
Morimoto, S.4
Ohtsuki, I.5
-
57
-
-
0142149180
-
Cardiomyopathic tropomyosin mutations that increase thin filament Ca2+ sensitivity and tropomyosin N-domain flexibility
-
Heller MJ, Nili M, Homsher E, Tobacman LS. 2003. Cardiomyopathic tropomyosin mutations that increase thin filament Ca2+ sensitivity and tropomyosin N-domain flexibility. J. Biol. Chem. 278:41742-48
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 41742-41748
-
-
Heller, M.J.1
Nili, M.2
Homsher, E.3
Tobacman, L.S.4
-
58
-
-
0034680324
-
Homozygous mutation in cardiac troponin T: Implications for hypertrophic cardiomyopathy
-
Ho CY, Lever HM, DeSanctis R, Farver CF, Seidman JG, Seidman CE. 2000. Homozygous mutation in cardiac troponin T: implications for hypertrophic cardiomyopathy. Circulation 102:1950-55
-
(2000)
Circulation
, vol.102
, pp. 1950-1955
-
-
Ho, C.Y.1
Lever, H.M.2
DeSanctis, R.3
Farver, C.F.4
Seidman, J.G.5
Seidman, C.E.6
-
59
-
-
0037446942
-
Cellular remodeling in heart failure disrupts K(ATP) channel-dependent stress tolerance
-
Hodgson DM, Zingman LV, Kane GC, Perez-Terzic C, Bienengraeber M, et al. 2003. Cellular remodeling in heart failure disrupts K(ATP) channel-dependent stress tolerance. EMBO J. 22:1732-42
-
(2003)
EMBO J.
, vol.22
, pp. 1732-1742
-
-
Hodgson, D.M.1
Zingman, L.V.2
Kane, G.C.3
Perez-Terzic, C.4
Bienengraeber, M.5
-
60
-
-
0035378612
-
First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy
-
Hoffmann B, Schmidt-Traub H, Perrot A, Osterziel KJ, Gessner R. 2001. First mutation in cardiac troponin C, L29Q, in a patient with hypertrophic cardiomyopathy. Hum. Mutat. 17:524
-
(2001)
Hum. Mutat.
, vol.17
, pp. 524
-
-
Hoffmann, B.1
Schmidt-Traub, H.2
Perrot, A.3
Osterziel, K.J.4
Gessner, R.5
-
61
-
-
0034444119
-
Postulated role of inter-domain interaction within the ryanodine receptor in Ca(2+) channel regulation
-
Ikemoto N, Yamamoto T. 2000. Postulated role of inter-domain interaction within the ryanodine receptor in Ca(2+) channel regulation. Trends Cardiovasc. Med. 10:310-16
-
(2000)
Trends Cardiovasc. Med.
, vol.10
, pp. 310-316
-
-
Ikemoto, N.1
Yamamoto, T.2
-
62
-
-
2642567777
-
Fetal and neonatal cardiac tumors
-
Isaacs H Jr. 2004. Fetal and neonatal cardiac tumors. Pediatr. Cardiol. 25:252-73
-
(2004)
Pediatr. Cardiol.
, vol.25
, pp. 252-273
-
-
Isaacs Jr., H.1
-
63
-
-
0010543360
-
Identification of a new locus for autosomal dominant dilated cardiomyopathy on chromosome 9q22-q31
-
Jha S, Kao A, Desai S, St. John Sutton MG, Jessup M, Keating MT. 2001. Identification of a new locus for autosomal dominant dilated cardiomyopathy on chromosome 9q22-q31. Circulation 104:11-135
-
(2001)
Circulation
, vol.104
, pp. 11-135
-
-
Jha, S.1
Kao, A.2
Desai, S.3
St. John Sutton, M.G.4
Jessup, M.5
Keating, M.T.6
-
64
-
-
0033358083
-
Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22
-
Jung M, Poepping I, Perrot A, Ellmer AE, Wienker TF, et al. 1999. Investigation of a family with autosomal dominant dilated cardiomyopathy defines a novel locus on chromosome 2q14-q22. Am. J. Hum. Genet. 65:1068-77
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 1068-1077
-
-
Jung, M.1
Poepping, I.2
Perrot, A.3
Ellmer, A.E.4
Wienker, T.F.5
-
65
-
-
0034619996
-
Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy
-
Kamisago M, Sharma SD, DePalma SR, Solomon S, Sharma P, et al. 2000. Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. N. Engl. J. Med. 343:1688-96
-
(2000)
N. Engl. J. Med.
, vol.343
, pp. 1688-1696
-
-
Kamisago, M.1
Sharma, S.D.2
DePalma, S.R.3
Solomon, S.4
Sharma, P.5
-
66
-
-
0346507496
-
Cardiac remodeling and contractile function in acid alpha-glucosidase knockout mice
-
Kamphoven JH, Stubenitsky R, Reuser AJ, Van Der Ploeg AT, Verdouw PD, Duncker DJ. 2001. Cardiac remodeling and contractile function in acid alpha-glucosidase knockout mice. Physiol. Genomics 5:l71-79
-
(2001)
Physiol. Genomics
, vol.5
-
-
Kamphoven, J.H.1
Stubenitsky, R.2
Reuser, A.J.3
Van Der Ploeg, A.T.4
Verdouw, P.D.5
Duncker, D.J.6
-
67
-
-
0028145745
-
A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1
-
Kass S, MacRae C, Graber HL, Sparks EA, McNamara D, et al. 1994. A gene defect that causes conduction system disease and dilated cardiomyopathy maps to chromosome 1p1-1q1. Nature (Genetics) 7:546-51
-
(1994)
Nature (Genetics)
, vol.7
, pp. 546-551
-
-
Kass, S.1
MacRae, C.2
Graber, H.L.3
Sparks, E.A.4
McNamara, D.5
-
68
-
-
0032973130
-
Dealing with energy demand: The AMP-activated protein kinase
-
Kemp BE, Mitchelhill KI, Stapleton D, Michell BJ, Chen ZP, Witters LA. 1999. Dealing with energy demand: the AMP-activated protein kinase. Trends Biochem. Sci. 24:22-25
-
(1999)
Trends Biochem. Sci.
, vol.24
, pp. 22-25
-
-
Kemp, B.E.1
Mitchelhill, K.I.2
Stapleton, D.3
Michell, B.J.4
Chen, Z.P.5
Witters, L.A.6
-
69
-
-
0030765610
-
Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy
-
Kimura A, Harada H, Park JE, Nishi H, Satoh M, et al. 1997. Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy. Nat. Genet. 16:379-82
-
(1997)
Nat. Genet.
, vol.16
, pp. 379-382
-
-
Kimura, A.1
Harada, H.2
Park, J.E.3
Nishi, H.4
Satoh, M.5
-
70
-
-
0037184992
-
The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy
-
Knoll R, Hoshijima M, Hoffman HM, Person V, Lorenzen-Schmidt I, et al. 2002. The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy. Cell 111:943-55
-
(2002)
Cell
, vol.111
, pp. 943-955
-
-
Knoll, R.1
Hoshijima, M.2
Hoffman, H.M.3
Person, V.4
Lorenzen-Schmidt, I.5
-
71
-
-
2442639087
-
Effects of protein kinase C dependent phosphorylation and a familial hypertrophic cardiomyopathy-related mutation of cardiac troponin I on structural transition of troponin C and myofilament activation
-
Kobayashi T, Dong WJ, Burkart EM, Cheung HC, Solaro RJ. 2004. Effects of protein kinase C dependent phosphorylation and a familial hypertrophic cardiomyopathy-related mutation of cardiac troponin I on structural transition of troponin C and myofilament activation. Biochemistry 43:5996-6004
-
(2004)
Biochemistry
, vol.43
, pp. 5996-6004
-
-
Kobayashi, T.1
Dong, W.J.2
Burkart, E.M.3
Cheung, H.C.4
Solaro, R.J.5
-
72
-
-
17544393835
-
Familial hypertrophic cardiomyopathy mutations in troponin I (K183D, G203S, K206Q) enhance filament sliding
-
Kohler J, Chen Y, Brenner B, Gordon AM, Kraft T, et al. 2003. Familial hypertrophic cardiomyopathy mutations in troponin I (K183D, G203S, K206Q) enhance filament sliding. Physiol. Genomics 14:117-28
-
(2003)
Physiol. Genomics
, vol.14
, pp. 117-128
-
-
Kohler, J.1
Chen, Y.2
Brenner, B.3
Gordon, A.M.4
Kraft, T.5
-
73
-
-
0029151478
-
Linkage of familial dilated cardiomyopathy to chromosome 9
-
Krajinovic M, Pinamonti B, Sinagra G, Vatta M, Severini GM, et al. 1995. Linkage of familial dilated cardiomyopathy to chromosome 9. Am. J. Hum. Genet. 57:846-52
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 846-852
-
-
Krajinovic, M.1
Pinamonti, B.2
Sinagra, G.3
Vatta, M.4
Severini, G.M.5
-
74
-
-
0035969990
-
Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia
-
Laitinen PJ, Brown KM, Piippo K, Swan H, Devaney JM, et al. 2001. Mutations of the cardiac ryanodine receptor (RyR2) gene in familial polymorphic ventricular tachycardia. Circulation 103:485-90
-
(2001)
Circulation
, vol.103
, pp. 485-490
-
-
Laitinen, P.J.1
Brown, K.M.2
Piippo, K.3
Swan, H.4
Devaney, J.M.5
-
75
-
-
1542317663
-
Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction
-
Lammerding J, Schulze PC, Takahashi T, Kozlov S, Sullivan T, et al. 2004. Lamin A/C deficiency causes defective nuclear mechanics and mechanotransduction. J. Clin. Invest. 113:370-78
-
(2004)
J. Clin. Invest.
, vol.113
, pp. 370-378
-
-
Lammerding, J.1
Schulze, P.C.2
Takahashi, T.3
Kozlov, S.4
Sullivan, T.5
-
76
-
-
0037023758
-
Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy
-
Lang R, Gomes AV, Zhao J, Housmans PR, Miller T, Potter JD. 2002. Functional analysis of a troponin I (R145G) mutation associated with familial hypertrophic cardiomyopathy. J. Biol. Chem. 277:11670-78
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 11670-11678
-
-
Lang, R.1
Gomes, A.V.2
Zhao, J.3
Housmans, P.R.4
Miller, T.5
Potter, J.D.6
-
77
-
-
0038029754
-
Impact of genetic polymorphisms on heart failure prognosis
-
Le Corvoisier P, Park HY, Carlson KM, Donahue MP, Marchuk DA, Rockman HA. 2003. Impact of genetic polymorphisms on heart failure prognosis. Arch. Mal. Coeur. Vaiss. 96:197-206
-
(2003)
Arch. Mal. Coeur. Vaiss.
, vol.96
, pp. 197-206
-
-
Le Corvoisier, P.1
Park, H.Y.2
Carlson, K.M.3
Donahue, M.P.4
Marchuk, D.A.5
Rockman, H.A.6
-
78
-
-
0029149023
-
Angiotensin I converting enzyme genotypes and left ventricular hypertrophy in patients with hypertrophic cardiomyopathy
-
Lechin M, Yu QT, Roberts R, Quinones MA, Marian AJ. 1995. Angiotensin I converting enzyme genotypes and left ventricular hypertrophy in patients with hypertrophic cardiomyopathy. Circulation 92:1808-12
-
(1995)
Circulation
, vol.92
, pp. 1808-1812
-
-
Lechin, M.1
Yu, Q.T.2
Roberts, R.3
Quinones, M.A.4
Marian, A.J.5
-
80
-
-
0033910196
-
The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14
-
Li D, Ahmad F, Gardner MJ, Weilbaecher D, Hill R, et al. 2000. The locus of a novel gene responsible for arrhythmogenic right-ventricular dysplasia characterized by early onset and high penetrance maps to chromosome 10p12-p14. Am. J. Hum. Genet. 66:148-56
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 148-156
-
-
Li, D.1
Ahmad, F.2
Gardner, M.J.3
Weilbaecher, D.4
Hill, R.5
-
82
-
-
7644233594
-
Molecular genetics and genomics of heart failure
-
Liew CC, Dzau VJ. 2004. Molecular genetics and genomics of heart failure. Nat. Rev. Genet. 5:811-25
-
(2004)
Nat. Rev. Genet.
, vol.5
, pp. 811-825
-
-
Liew, C.C.1
Dzau, V.J.2
-
83
-
-
0035852766
-
Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy
-
Lim DS, Lutucuta S, Bachireddy P, Youker K, Evans A, et al. 2001. Angiotensin II blockade reverses myocardial fibrosis in a transgenic mouse model of human hypertrophic cardiomyopathy. Circulation 103:789-91
-
(2001)
Circulation
, vol.103
, pp. 789-791
-
-
Lim, D.S.1
Lutucuta, S.2
Bachireddy, P.3
Youker, K.4
Evans, A.5
-
84
-
-
0037058826
-
Lifetime risk for developing congestive heart failure: The Framingham Heart Study
-
Lloyd-Jones DM, Larson MG, Leip EP, Beiser A, D'Agostino RB, et al. 2002. Lifetime risk for developing congestive heart failure: the Framingham Heart Study. Circulation 106:3068-72
-
(2002)
Circulation
, vol.106
, pp. 3068-3072
-
-
Lloyd-Jones, D.M.1
Larson, M.G.2
Leip, E.P.3
Beiser, A.4
D'Agostino, R.B.5
-
85
-
-
0344924880
-
Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization
-
Lu QW, Morimoto S, Harada K, Du CK, Takahashi-Yanaga F, et al. 2003. Cardiac troponin T mutation R141W found in dilated cardiomyopathy stabilizes the troponin T-tropomyosin interaction and causes a Ca2+ desensitization. J. Mol. Cell. Cardiol. 35:1421-27
-
(2003)
J. Mol. Cell. Cardiol.
, vol.35
, pp. 1421-1427
-
-
Lu, Q.W.1
Morimoto, S.2
Harada, K.3
Du, C.K.4
Takahashi-Yanaga, F.5
-
86
-
-
0038464639
-
Phospholamban: A crucial regulator of cardiac contractility
-
MacLennan DH, Kranias EG. 2003. Phospholamban: a crucial regulator of cardiac contractility. Nat. Rev. Mol. Cell. Biol. 4:566-77
-
(2003)
Nat. Rev. Mol. Cell. Biol.
, vol.4
, pp. 566-577
-
-
MacLennan, D.H.1
Kranias, E.G.2
-
87
-
-
0027425610
-
Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death
-
Marian AJ, Yu QT, Workman R, Greve G, Roberts R. 1993. Angiotensin-converting enzyme polymorphism in hypertrophic cardiomyopathy and sudden cardiac death. Lancet 342:1085-86
-
(1993)
Lancet
, vol.342
, pp. 1085-1086
-
-
Marian, A.J.1
Yu, Q.T.2
Workman, R.3
Greve, G.4
Roberts, R.5
-
88
-
-
0034060699
-
Evidence of functional ryanodine receptor involved in apoptosis of prostate cancer (LNCaP) cells
-
Mariot P, Prevarskaya N, Roudbaraki MM, Le Bourhis X, Van Coppenolle F, et al. 2000. Evidence of functional ryanodine receptor involved in apoptosis of prostate cancer (LNCaP) cells. Prostate 43:205-14
-
(2000)
Prostate
, vol.43
, pp. 205-214
-
-
Mariot, P.1
Prevarskaya, N.2
Roudbaraki, M.M.3
Le Bourhis, X.4
Van Coppenolle, F.5
-
89
-
-
0037070514
-
Hypertrophic cardiocmyopathy: A systematic review
-
Maron BJ. 2002. Hypertrophic cardiocmyopathy: a systematic review. JAMA 287:1308-20
-
(2002)
JAMA
, vol.287
, pp. 1308-1320
-
-
Maron, B.J.1
-
90
-
-
0037454174
-
Relationship of race to sudden cardiac death in competitive athletes with hypertrophic cardiomyopathy
-
Maron BJ, Carney KP, Lever HM, Lewis JF, Barac I, et al. 2003. Relationship of race to sudden cardiac death in competitive athletes with hypertrophic cardiomyopathy. J. Am. Coll. Cardiol. 41:974-80
-
(2003)
J. Am. Coll. Cardiol.
, vol.41
, pp. 974-980
-
-
Maron, B.J.1
Carney, K.P.2
Lever, H.M.3
Lewis, J.F.4
Barac, I.5
-
91
-
-
0034702926
-
Epidemiology of hypertrophic cardiomyopathy-related death: Revisited in a large non-referral-based patient population
-
Maron BJ, Olivotto I, Spirito P, Casey SA, Bellone P, et al. 2000. Epidemiology of hypertrophic cardiomyopathy-related death: revisited in a large non-referral-based patient population. Circulation 102:858-64
-
(2000)
Circulation
, vol.102
, pp. 858-864
-
-
Maron, B.J.1
Olivotto, I.2
Spirito, P.3
Casey, S.A.4
Bellone, P.5
-
92
-
-
0034640113
-
PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): Defective regulation in failing hearts
-
Marx SO, Reiken S, Hisamatsu Y, Jayaraman T, Burkhoff D, et al. 2000. PKA phosphorylation dissociates FKBP12.6 from the calcium release channel (ryanodine receptor): defective regulation in failing hearts. Cell 101:365-76
-
(2000)
Cell
, vol.101
, pp. 365-376
-
-
Marx, S.O.1
Reiken, S.2
Hisamatsu, Y.3
Jayaraman, T.4
Burkhoff, D.5
-
93
-
-
0021331062
-
Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patients
-
Matsuishi T, Yoshino M, Terasawa K, Nonaka I. 1984. Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patients. Arch. Neurol. 41:47-52
-
(1984)
Arch. Neurol.
, vol.41
, pp. 47-52
-
-
Matsuishi, T.1
Yoshino, M.2
Terasawa, K.3
Nonaka, I.4
-
94
-
-
1642402966
-
Cardiac histone acetylation - Therapeutic opportunities abound
-
McKinsey TA, Olson EN. 2004. Cardiac histone acetylation-therapeutic opportunities abound. Trends Genet. 20:206-13
-
(2004)
Trends Genet.
, vol.20
, pp. 206-213
-
-
McKinsey, T.A.1
Olson, E.N.2
-
95
-
-
0034679297
-
Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease)
-
McKoy G, Protonotarios N, Crosby A, Tsatsopoulou A, Anastasakis A, et al. 2000. Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease). Lancet 355:2119-24
-
(2000)
Lancet
, vol.355
, pp. 2119-2124
-
-
McKoy, G.1
Protonotarios, N.2
Crosby, A.3
Tsatsopoulou, A.4
Anastasakis, A.5
-
97
-
-
0032701867
-
Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q
-
Melberg A, Oldfors A, Blomstrom-Lundqvist C, Stalberg E, Carlsson B, et al. 1999. Autosomal dominant myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy linked to chromosome 10q. Ann. Neurol. 46:684-92
-
(1999)
Ann. Neurol.
, vol.46
, pp. 684-692
-
-
Melberg, A.1
Oldfors, A.2
Blomstrom-Lundqvist, C.3
Stalberg, E.4
Carlsson, B.5
-
98
-
-
0030882270
-
Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23
-
Messina DN, Speer MC, Pericak-Vance MA, McNally EM. 1997. Linkage of familial dilated cardiomyopathy with conduction defect and muscular dystrophy to chromosome 6q23. Am. J. Hum. Genet. 61:909-17
-
(1997)
Am. J. Hum. Genet.
, vol.61
, pp. 909-917
-
-
Messina, D.N.1
Speer, M.C.2
Pericak-Vance, M.A.3
McNally, E.M.4
-
99
-
-
0032751723
-
Direct, convergent hypersensitivity of calcium-activated force generation produced by hypertrophic cardiomyopathy mutant alpha-tropomyosins in adult cardiac myocytes
-
Michele DE, Albayya FP, Metzger JM. 1999. Direct, convergent hypersensitivity of calcium-activated force generation produced by hypertrophic cardiomyopathy mutant alpha-tropomyosins in adult cardiac myocytes. Nat. Med. 5:1413-17
-
(1999)
Nat. Med.
, vol.5
, pp. 1413-1417
-
-
Michele, D.E.1
Albayya, F.P.2
Metzger, J.M.3
-
100
-
-
0034685949
-
A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle
-
Milan D, Jeon JT, Looft C, Amarger V, Robic A, et al. 2000. A mutation in PRKAG3 associated with excess glycogen content in pig skeletal muscle. Science 288:1248-51
-
(2000)
Science
, vol.288
, pp. 1248-1251
-
-
Milan, D.1
Jeon, J.T.2
Looft, C.3
Amarger, V.4
Robic, A.5
-
102
-
-
0035830841
-
Abnormal contractile function in transgenic mice expressing a familial hypertrophic cardiomyopathy-linked troponinT (I79N) mutation
-
Miller T, Szczesna D, Housmans PR, Zhao J, de Freitas F, et al. 2001. Abnormal contractile function in transgenic mice expressing a familial hypertrophic cardiomyopathy-linked troponinT (I79N) mutation. J. Biol. Chem. 276:3743-55
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 3743-3755
-
-
Miller, T.1
Szczesna, D.2
Housmans, P.R.3
Zhao, J.4
De Freitas, F.5
-
103
-
-
0033615645
-
Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy
-
Minamisawa S, Hoshijima M, Chu G, Ward CA, Frank K, et al. 1999. Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy. Cell 99:313-22
-
(1999)
Cell
, vol.99
, pp. 313-322
-
-
Minamisawa, S.1
Hoshijima, M.2
Chu, G.3
Ward, C.A.4
Frank, K.5
-
104
-
-
18744433901
-
Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy
-
Mogensen J, Klausen IC, Pedersen AK, Egeblad H, Bross P, et al. 1999. Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy. J. Clin. Invest. 103:R39-43
-
(1999)
J. Clin. Invest.
, vol.103
-
-
Mogensen, J.1
Klausen, I.C.2
Pedersen, A.K.3
Egeblad, H.4
Bross, P.5
-
105
-
-
0037238265
-
Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations
-
Mogensen J, Kubo T, Duque M, Uribe W, Shaw A, et al. 2003. Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations. J. Clin. Invest. 111:209-16
-
(2003)
J. Clin. Invest.
, vol.111
, pp. 209-216
-
-
Mogensen, J.1
Kubo, T.2
Duque, M.3
Uribe, W.4
Shaw, A.5
-
106
-
-
0037154179
-
Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy
-
Morimoto S, Lu QW, Harada K, Takahashi-Yanaga F, Minakami R, et al. 2002. Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy. Proc. Natl. Acad. Sci. USA 99:913-18
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 913-918
-
-
Morimoto, S.1
Lu, Q.W.2
Harada, K.3
Takahashi-Yanaga, F.4
Minakami, R.5
-
107
-
-
0034702027
-
Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B)
-
Muchir A, Bonne G, van der Kooi AJ, van Meegen M, Baas F, et al. 2000. Identification of mutations in the gene encoding lamins A/C in autosomal dominant limb girdle muscular dystrophy with atrioventricular conduction disturbances (LGMD1B). Hum. Mol. Genet. 9:1453-59
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 1453-1459
-
-
Muchir, A.1
Bonne, G.2
Van Der Kooi, A.J.3
Van Meegen, M.4
Baas, F.5
-
108
-
-
4644222709
-
Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations
-
Muchir A, Medioni J, Laluc M, Massart C, Arimura T, et al. 2004. Nuclear envelope alterations in fibroblasts from patients with muscular dystrophy, cardiomyopathy, and partial lipodystrophy carrying lamin A/C gene mutations. Muscle Nerve 30:444-50
-
(2004)
Muscle Nerve
, vol.30
, pp. 444-450
-
-
Muchir, A.1
Medioni, J.2
Laluc, M.3
Massart, C.4
Arimura, T.5
-
109
-
-
0033951027
-
Follow-up of patients with arrhythmogenic right ventricular cardiomyopathy dysplasia
-
Munclinger MJ, Patel JJ, Mitha AS. 2000. Follow-up of patients with arrhythmogenic right ventricular cardiomyopathy dysplasia. S. Afr. Med. J. 90:61-68
-
(2000)
S. Afr. Med. J.
, vol.90
, pp. 61-68
-
-
Munclinger, M.J.1
Patel, J.J.2
Mitha, A.S.3
-
110
-
-
0035838393
-
Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy
-
Nagueh SF, Bachinski LL, Meyer D, Hill R, Zoghbi WA, et al. 2001. Tissue Doppler imaging consistently detects myocardial abnormalities in patients with hypertrophic cardiomyopathy and provides a novel means for an early diagnosis before and independently of hypertrophy. Circulation 104:128-30
-
(2001)
Circulation
, vol.104
, pp. 128-130
-
-
Nagueh, S.F.1
Bachinski, L.L.2
Meyer, D.3
Hill, R.4
Zoghbi, W.A.5
-
111
-
-
0041663643
-
Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease
-
Nagueh SF, McFalls J, Meyer D, Hill R, Zoghbi WA, et al. 2003. Tissue Doppler imaging predicts the development of hypertrophic cardiomyopathy in subjects with subclinical disease. Circulation 108:395-98
-
(2003)
Circulation
, vol.108
, pp. 395-398
-
-
Nagueh, S.F.1
McFalls, J.2
Meyer, D.3
Hill, R.4
Zoghbi, W.A.5
-
112
-
-
0033662201
-
Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy
-
Nava A, Bauce B, Basso C, Muriago M, Rampazzo A, et al. 2000. Clinical profile and long-term follow-up of 37 families with arrhythmogenic right ventricular cardiomyopathy. J. Am. Coll. Cardiol. 36:2226-33
-
(2000)
J. Am. Coll. Cardiol.
, vol.36
, pp. 2226-2233
-
-
Nava, A.1
Bauce, B.2
Basso, C.3
Muriago, M.4
Rampazzo, A.5
-
113
-
-
0032580520
-
Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy
-
Niimura H, Bachinski LL, Sangwatanaroj S, Watkins H, Chudley AE, et al. 1998. Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy. N. Engl. J. Med. 338:1248-57
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 1248-1257
-
-
Niimura, H.1
Bachinski, L.L.2
Sangwatanaroj, S.3
Watkins, H.4
Chudley, A.E.5
-
114
-
-
0037192339
-
Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly
-
Niimura H, Patton KK, McKenna WJ, Soults J, Maron BJ, et al. 2002. Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly. Circulation 105:446-51
-
(2002)
Circulation
, vol.105
, pp. 446-451
-
-
Niimura, H.1
Patton, K.K.2
McKenna, W.J.3
Soults, J.4
Maron, B.J.5
-
115
-
-
11144355499
-
Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice
-
Nikolova V, Leimena C, McMahon AC, Tan JC, Chandar S, et al. 2004. Defects in nuclear structure and function promote dilated cardiomyopathy in lamin A/C-deficient mice. J. Clin. Invest. 113:357-69
-
(2004)
J. Clin. Invest.
, vol.113
, pp. 357-369
-
-
Nikolova, V.1
Leimena, C.2
McMahon, A.C.3
Tan, J.C.4
Chandar, S.5
-
116
-
-
0034326902
-
Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma
-
Norgett EE, Hatsell SJ, Carvajal-Huerta L, Cabezas JC, Common J, et al. 2000. Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma. Hum. Mol. Genet. 9:2761-66
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2761-2766
-
-
Norgett, E.E.1
Hatsell, S.J.2
Carvajal-Huerta, L.3
Cabezas, J.C.4
Common, J.5
-
117
-
-
0042161933
-
Sizing up the heart: Development redux in disease
-
Olson EN, Schneider MD. 2003. Sizing up the heart: development redux in disease. Genes Dev. 17:1937-56
-
(2003)
Genes Dev.
, vol.17
, pp. 1937-1956
-
-
Olson, E.N.1
Schneider, M.D.2
-
118
-
-
0033799445
-
Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy
-
Olson TM, Doan TP, Kishimoto NY, Whitby FG, Ackerman MJ, Fananapazir L. 2000. Inherited and de novo mutations in the cardiac actin gene cause hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 32:1687-94
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, pp. 1687-1694
-
-
Olson, T.M.1
Doan, T.P.2
Kishimoto, N.Y.3
Whitby, F.G.4
Ackerman, M.J.5
Fananapazir, L.6
-
119
-
-
0037192309
-
Metavinculin mutations alter actin interaction in dilated cardiomyopathy
-
Olson TM, Illenberger S, Kishimoto NY, Huttelmaier S, Keating MT, Jockusch BM. 2002. Metavinculin mutations alter actin interaction in dilated cardiomyopathy. Circulation 105:431-37
-
(2002)
Circulation
, vol.105
, pp. 431-437
-
-
Olson, T.M.1
Illenberger, S.2
Kishimoto, N.Y.3
Huttelmaier, S.4
Keating, M.T.5
Jockusch, B.M.6
-
120
-
-
0030031004
-
Mapping a cardiomyopathy locus to chromosome 3p22-p25
-
Olson TM, Keating MT. 1996. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J. Clin. Invest. 97:528-32
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 528-532
-
-
Olson, T.M.1
Keating, M.T.2
-
121
-
-
0034971165
-
Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy
-
Olson TM, Kishimoto NY, Whitby FG, Michels W. 2001. Mutations that alter the surface charge of alpha-tropomyosin are associated with dilated cardiomyopathy. J. Mol. Cell Cardiol. 33:723-32
-
(2001)
J. Mol. Cell Cardiol.
, vol.33
, pp. 723-732
-
-
Olson, T.M.1
Kishimoto, N.Y.2
Whitby, F.G.3
Michels, W.4
-
122
-
-
0032076955
-
Actin mutations in dilated cardiomyopathy, a heritable form of heart failure
-
Olson TM, Michels VV, Thibodeau SN, Tai YS, Keating MT. 1998. Actin mutations in dilated cardiomyopathy, a heritable form of heart failure. Science 280:750-52
-
(1998)
Science
, vol.280
, pp. 750-752
-
-
Olson, T.M.1
Michels, V.V.2
Thibodeau, S.N.3
Tai, Y.S.4
Keating, M.T.5
-
124
-
-
0030922569
-
Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy
-
Ortiz-Lopez R, Li H, Su J, Goytia V, Towbin JA. 1997. Evidence for a dystrophin missense mutation as a cause of X-linked dilated cardiomyopathy. Circulation 95:2434-40
-
(1997)
Circulation
, vol.95
, pp. 2434-2440
-
-
Ortiz-Lopez, R.1
Li, H.2
Su, J.3
Goytia, V.4
Towbin, J.A.5
-
125
-
-
0036178004
-
Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: A study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene
-
Ortlepp JR, Vosberg HP, Reith S, Ohme F, Mahon NG, et al. 2002. Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene. Heart 87:270-75
-
(2002)
Heart
, vol.87
, pp. 270-275
-
-
Ortlepp, J.R.1
Vosberg, H.P.2
Reith, S.3
Ohme, F.4
Mahon, N.G.5
-
126
-
-
0031597427
-
AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy
-
Osterop AP, Kofflard MJ, Sandkuijl LA, ten Cate FJ, Krams R, et al. 1998. AT1 receptor A/C1166 polymorphism contributes to cardiac hypertrophy in subjects with hypertrophic cardiomyopathy. Hypertension 32:825-30
-
(1998)
Hypertension
, vol.32
, pp. 825-830
-
-
Osterop, A.P.1
Kofflard, M.J.2
Sandkuijl, L.A.3
Ten Cate, F.J.4
Krams, R.5
-
127
-
-
3042621438
-
Differential cross-bridge kinetics of FHC myosin mutations R403Q and R453C in heterozygous mouse myocardium
-
Palmer BM, Fishbaugher DE, Schmitt JP, Wang Y, Alpert NR, et al. 2004. Differential cross-bridge kinetics of FHC myosin mutations R403Q and R453C in heterozygous mouse myocardium. Am. J. Physiol. Heart Circ. Physiol. 287:H91-H99
-
(2004)
Am. J. Physiol. Heart Circ. Physiol.
, vol.287
-
-
Palmer, B.M.1
Fishbaugher, D.E.2
Schmitt, J.P.3
Wang, Y.4
Alpert, N.R.5
-
128
-
-
0034502439
-
Variants of trophic factors and expression of cardiac hypertrophy in patients with hypertrophic cardiomyopathy
-
Patel R, Lim DS, Reddy D, Nagueh SF, Lutucuta S, et al. 2000. Variants of trophic factors and expression of cardiac hypertrophy in patients with hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 32:2369-77
-
(2000)
J. Mol. Cell. Cardiol.
, vol.32
, pp. 2369-2377
-
-
Patel, R.1
Lim, D.S.2
Reddy, D.3
Nagueh, S.F.4
Lutucuta, S.5
-
129
-
-
0035902491
-
Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy
-
Patel R, Nagueh SF, Tsybouleva N, Abdellatif M, Lutucuta S, et al. 2001. Simvastatin induces regression of cardiac hypertrophy and fibrosis and improves cardiac function in a transgenic rabbit model of human hypertrophic cardiomyopathy. Circulation 104:317-24
-
(2001)
Circulation
, vol.104
, pp. 317-324
-
-
Patel, R.1
Nagueh, S.F.2
Tsybouleva, N.3
Abdellatif, M.4
Lutucuta, S.5
-
130
-
-
0032759099
-
Risk stratification of sudden cardiac death and malignant ventricular arrhythmias in right ventricular dysplasia-cardiomyopathy
-
Peters S, Peters H, Thierfelder L. 1999. Risk stratification of sudden cardiac death and malignant ventricular arrhythmias in right ventricular dysplasia-cardiomyopathy. Int. J. Cardiol. 71:243-50
-
(1999)
Int. J. Cardiol.
, vol.71
, pp. 243-250
-
-
Peters, S.1
Peters, H.2
Thierfelder, L.3
-
131
-
-
15844400653
-
Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle
-
Poetter K, Jiang H, Hassanzadeh S, Master SR, Chang A, et al. 1996. Mutations in either the essential or regulatory light chains of myosin are associated with a rare myopathy in human heart and skeletal muscle. Nat. Genet. 13:63-69
-
(1996)
Nat. Genet.
, vol.13
, pp. 63-69
-
-
Poetter, K.1
Jiang, H.2
Hassanzadeh, S.3
Master, S.R.4
Chang, A.5
-
132
-
-
25844445982
-
-
note
-
Deleted in proof
-
-
-
-
133
-
-
0035793341
-
Overexpression of FK506-binding protein FKBP 12.6 in cardiomyocytes reduces ryanodine receptor-mediated Ca(2+) leak from the sarcoplasmic reticulum and increases contractility
-
Prestle J, Janssen PM, Janssen AP, Zeitz O, Lehnart SE, et al. 2001. Overexpression of FK506-binding protein FKBP 12.6 in cardiomyocytes reduces ryanodine receptor-mediated Ca(2+) leak from the sarcoplasmic reticulum and increases contractility. Circ. Res. 88:188-94
-
(2001)
Circ. Res.
, vol.88
, pp. 188-194
-
-
Prestle, J.1
Janssen, P.M.2
Janssen, A.P.3
Zeitz, O.4
Lehnart, S.E.5
-
134
-
-
0025368411
-
Mechanisms underlying early and delayed after depolarizations induced by catecholamines
-
Priori SG, Corr PB. 1990. Mechanisms underlying early and delayed after depolarizations induced by catecholamines. Am. J. Physiol. 258:H1796-H805
-
(1990)
Am. J. Physiol.
, vol.258
-
-
Priori, S.G.1
Corr, P.B.2
-
135
-
-
0035895322
-
Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia
-
Priori SG, Napolitano C, Tiso N, Memmi M, Vignati G, et al. 2001. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 103:196-200
-
(2001)
Circulation
, vol.103
, pp. 196-200
-
-
Priori, S.G.1
Napolitano, C.2
Tiso, N.3
Memmi, M.4
Vignati, G.5
-
136
-
-
0036853028
-
Glycogen stored in skeletal but not in cardiac muscle in acid alpha-glucosidase mutant (Pompe) mice is highly resistant to transgene-encoded human enzyme
-
Raben N, Jatkar T, Lee A, Lu N, Dwivedi S, et al. 2002. Glycogen stored in skeletal but not in cardiac muscle in acid alpha-glucosidase mutant (Pompe) mice is highly resistant to transgene-encoded human enzyme. Mol. Ther. 6:601-8
-
(2002)
Mol. Ther.
, vol.6
, pp. 601-608
-
-
Raben, N.1
Jatkar, T.2
Lee, A.3
Lu, N.4
Dwivedi, S.5
-
137
-
-
0028243281
-
The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24
-
Rampazzo A, Nava A, Danieli GA, Buja G, Daliento L, et al. 1994. The gene for arrhythmogenic right ventricular cardiomyopathy maps to chromosome 14q23-q24. Hum. Mol. Genet. 3:959-62
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 959-962
-
-
Rampazzo, A.1
Nava, A.2
Danieli, G.A.3
Buja, G.4
Daliento, L.5
-
138
-
-
0028807911
-
A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43
-
Rampazzo A, Nava A, Erne P, Eberhard M, Vian E, et al. 1995. A new locus for arrhythmogenic right ventricular cardiomyopathy (ARVD2) maps to chromosome 1q42-q43. Hum. Mol. Genet. 4:2151-54
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 2151-2154
-
-
Rampazzo, A.1
Nava, A.2
Erne, P.3
Eberhard, M.4
Vian, E.5
-
139
-
-
18644363134
-
Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy
-
Rampazzo A, Nava A, Malacrida S, Beffagna G, Bauce B, et al. 2002. Mutation in human desmoplakin domain binding to plakoglobin causes a dominant form of arrhythmogenic right ventricular cardiomyopathy. Am. J. Hum. Genet. 71:1200-6
-
(2002)
Am. J. Hum. Genet.
, vol.71
, pp. 1200-1206
-
-
Rampazzo, A.1
Nava, A.2
Malacrida, S.3
Beffagna, G.4
Bauce, B.5
-
140
-
-
0030724006
-
ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm
-
Rampazzo A, Nava A, Miorin M, Fonderico P, Pope B, et al. 1997. ARVD4, a new locus for arrhythmogenic right ventricular cardiomyopathy, maps to chromosome 2 long arm. Genomics 45:259-63
-
(1997)
Genomics
, vol.45
, pp. 259-263
-
-
Rampazzo, A.1
Nava, A.2
Miorin, M.3
Fonderico, P.4
Pope, B.5
-
141
-
-
0029024879
-
Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy
-
Rayment I, Holden HM, Sellers JR, Fananapazir L, Epstein ND. 1995. Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy. Proc. Natl. Acad. Sci. USA 92:3864-68
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 3864-3868
-
-
Rayment, I.1
Holden, H.M.2
Sellers, J.R.3
Fananapazir, L.4
Epstein, N.D.5
-
142
-
-
0034625768
-
Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein
-
Redwood C, Lohmann K, Bing W, Esposito GM, Elliott K, et al. 2000. Investigation of a truncated cardiac troponin T that causes familial hypertrophic cardiomyopathy: Ca(2+) regulatory properties of reconstituted thin filaments depend on the ratio of mutant to wild-type protein. Circ. Res. 86:1146-52
-
(2000)
Circ. Res.
, vol.86
, pp. 1146-1152
-
-
Redwood, C.1
Lohmann, K.2
Bing, W.3
Esposito, G.M.4
Elliott, K.5
-
143
-
-
0033214976
-
Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy
-
Redwood CS, Moolman-Smook JC, Watkins H. 1999. Properties of mutant contractile proteins that cause hypertrophic cardiomyopathy. Cardiovasc. Res. 44:20-36
-
(1999)
Cardiovasc. Res.
, vol.44
, pp. 20-36
-
-
Redwood, C.S.1
Moolman-Smook, J.C.2
Watkins, H.3
-
144
-
-
0037630018
-
Hypertrophic cardiomyopathy: Distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy
-
Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, et al. 2003. Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy. Circulation 107:2227-32
-
(2003)
Circulation
, vol.107
, pp. 2227-2232
-
-
Richard, P.1
Charron, P.2
Carrier, L.3
Ledeuil, C.4
Cheav, T.5
-
145
-
-
0033005768
-
Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy
-
Richard P, Isnard R, Carrier L, Dubourg O, Donatien Y, et al. 1999. Double heterozygosity for mutations in the beta-myosin heavy chain and in the cardiac myosin binding protein C genes in a family with hypertrophic cardiomyopathy. J. Med. Genet. 36:542-45
-
(1999)
J. Med. Genet.
, vol.36
, pp. 542-545
-
-
Richard, P.1
Isnard, R.2
Carrier, L.3
Dubourg, O.4
Donatien, Y.5
-
146
-
-
0035940383
-
New concepts in hypertrophic cardiomyopathies, part I
-
Roberts R, Sigwart U. 2001. New concepts in hypertrophic cardiomyopathies, part I. Circulation 104:2113-16
-
(2001)
Circulation
, vol.104
, pp. 2113-2116
-
-
Roberts, R.1
Sigwart, U.2
-
147
-
-
0035975966
-
New concepts in hypertrophic cardiomyopathies, part II
-
Roberts R, Sigwart U. 2001. New concepts in hypertrophic cardiomyopathies, part II. Circulation 104:2249-52
-
(2001)
Circulation
, vol.104
, pp. 2249-2252
-
-
Roberts, R.1
Sigwart, U.2
-
148
-
-
0037174918
-
Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy
-
Robinson P, Mirza M, Knott A, Abdulrazzak H, Willott R, et al. 2002. Alterations in thin filament regulation induced by a human cardiac troponin T mutant that causes dilated cardiomyopathy are distinct from those induced by troponin T mutants that cause hypertrophic cardiomyopathy. J. Biol. Chem. 277:40710-16
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 40710-40716
-
-
Robinson, P.1
Mirza, M.2
Knott, A.3
Abdulrazzak, H.4
Willott, R.5
-
149
-
-
0037379827
-
Mechanical defects of muscle fibers with myosin light chain mutants that cause cardiomyopathy
-
Roopnarine O. 2003. Mechanical defects of muscle fibers with myosin light chain mutants that cause cardiomyopathy. Biophys. J. 84:2440-49
-
(2003)
Biophys. J.
, vol.84
, pp. 2440-2449
-
-
Roopnarine, O.1
-
150
-
-
3042711961
-
Desmin-related cardiomyopathy in transgenic mice: A cardiac amyloidosis
-
Sanbe A, Osinska H, Saffitz JE, Glabe CG, Kayed R, et al. 2004. Desmin-related cardiomyopathy in transgenic mice: a cardiac amyloidosis. Proc. Natl. Acad. Sci. USA 101:10132-36
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 10132-10136
-
-
Sanbe, A.1
Osinska, H.2
Saffitz, J.E.3
Glabe, C.G.4
Kayed, R.5
-
151
-
-
0033610050
-
Structural analysis of the titin gene in hypertrophic cardiomyopathy: Identification of a novel disease gene
-
Satoh M, Takahashi M, Sakamoto T, Hiroe M, Marumo F, Kimura A. 1999. Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene. Biochem. Biophys. Res. Commun. 262:411-17
-
(1999)
Biochem. Biophys. Res. Commun.
, vol.262
, pp. 411-417
-
-
Satoh, M.1
Takahashi, M.2
Sakamoto, T.3
Hiroe, M.4
Marumo, F.5
Kimura, A.6
-
152
-
-
0037470512
-
Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban
-
Schmitt JP, Kamisago M, Asahi M, Li GH, Ahmad F, et al. 2003. Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban. Science 299:1410-13
-
(2003)
Science
, vol.299
, pp. 1410-1413
-
-
Schmitt, J.P.1
Kamisago, M.2
Asahi, M.3
Li, G.H.4
Ahmad, F.5
-
153
-
-
0343183359
-
Dilated cardiomyopathy and sensorineural hearing loss: A heritable syndrome that maps to 6q23-24
-
Schonberger J, Levy H, Grunig E, Sangwatanaroj S, Fatkin D, et al. 2000. Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24. Circulation 101:1812-18
-
(2000)
Circulation
, vol.101
, pp. 1812-1818
-
-
Schonberger, J.1
Levy, H.2
Grunig, E.3
Sangwatanaroj, S.4
Fatkin, D.5
-
154
-
-
0002445752
-
Hypertrophic cardiomyopathy
-
ed. CR Scriver, AL Beaudet, NS Sly, D Valle, B Childs, K Kinzler, B Vogelstein. New York: McGraw-Hill
-
Seidman CE, Seidman JG. 2001. Hypertrophic cardiomyopathy. In The Metabolic and Molecular Basis of Inherited Disease, ed. CR Scriver, AL Beaudet, NS Sly, D Valle, B Childs, K Kinzler, B Vogelstein, pp. 5433-50. New York: McGraw-Hill
-
(2001)
The Metabolic and Molecular Basis of Inherited Disease
, pp. 5433-5450
-
-
Seidman, C.E.1
Seidman, J.G.2
-
155
-
-
0035936792
-
The genetic basis for cardiomyopathy: From mutation identification to mechanistic paradigms
-
Seidman JG, Seidman C. 2001. The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms. Cell 104:557-67
-
(2001)
Cell
, vol.104
, pp. 557-567
-
-
Seidman, J.G.1
Seidman, C.2
-
157
-
-
0036117921
-
The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model
-
Semsarian C, Ahmad I, Giewat M, Georgakopoulos D, Schmitt JP, et al. 2002. The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model. J. Clin. Invest. 109:1013-20
-
(2002)
J. Clin. Invest.
, vol.109
, pp. 1013-1020
-
-
Semsarian, C.1
Ahmad, I.2
Giewat, M.3
Georgakopoulos, D.4
Schmitt, J.P.5
-
158
-
-
0035201270
-
A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy
-
Semsarian C, Healey MJ, Fatkin D, Giewat M, Duffy C, et al. 2001. A polymorphic modifier gene alters the hypertrophic response in a murine model of familial hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 33:2055-60
-
(2001)
J. Mol. Cell. Cardiol.
, vol.33
, pp. 2055-2060
-
-
Semsarian, C.1
Healey, M.J.2
Fatkin, D.3
Giewat, M.4
Duffy, C.5
-
159
-
-
0030050430
-
A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14
-
Severini GM, Krajinovic M, Pinamonti B, Sinagra G, Fioretti P, et al. 1996. A new locus for arrhythmogenic right ventricular dysplasia on the long arm of chromosome 14. Genomics 31:193-200
-
(1996)
Genomics
, vol.31
, pp. 193-200
-
-
Severini, G.M.1
Krajinovic, M.2
Pinamonti, B.3
Sinagra, G.4
Fioretti, P.5
-
160
-
-
0033951216
-
LMNA, encoding lamin A/C, is mutated in partial lipodystrophy
-
Shackleton S, Lloyd DJ, Jackson SN, Evans R, Niermeijer MF, et al. 2000. LMNA, encoding lamin A/C, is mutated in partial lipodystrophy. Nat. Genet. 24:153-56
-
(2000)
Nat. Genet.
, vol.24
, pp. 153-156
-
-
Shackleton, S.1
Lloyd, D.J.2
Jackson, S.N.3
Evans, R.4
Niermeijer, M.F.5
-
161
-
-
0001875649
-
Right ventricular dysplasia: A need for precise pathological definition for interpretation of sudden death
-
Shen WK, Edwards WD, Hammill SC, Gersh BJ. 1994. Right ventricular dysplasia: a need for precise pathological definition for interpretation of
-
(1994)
J. Am. Coll. Cardiol.
, vol.23
, pp. 34
-
-
Shen, W.K.1
Edwards, W.D.2
Hammill, S.C.3
Gersh, B.J.4
-
162
-
-
0033514986
-
Familial dilated cardiomyopathy locus maps to chromosome 2q31
-
Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, et al. 1999. Familial dilated cardiomyopathy locus maps to chromosome 2q31. Circulation 99:1022-26
-
(1999)
Circulation
, vol.99
, pp. 1022-1026
-
-
Siu, B.L.1
Niimura, H.2
Osborne, J.A.3
Fatkin, D.4
MacRae, C.5
-
163
-
-
0032523194
-
Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy
-
Spindler M, Saupe KW, Christe ME, Sweeney HL, Seidman CE, et al. 1998. Diastolic dysfunction and altered energetics in the alphaMHC403/+ mouse model of familial hypertrophic cardiomyopathy. J. Clin. Invest. 101:1775-83
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 1775-1783
-
-
Spindler, M.1
Saupe, K.W.2
Christe, M.E.3
Sweeney, H.L.4
Seidman, C.E.5
-
164
-
-
0037221669
-
Heart failure and the aging population: An increasing burden in the 21st century?
-
Stewart S, MacIntyre K, Capewell S, McMurray JJ. 2003. Heart failure and the aging population: an increasing burden in the 21st century? Heart 89:49-53
-
(2003)
Heart
, vol.89
, pp. 49-53
-
-
Stewart, S.1
MacIntyre, K.2
Capewell, S.3
McMurray, J.J.4
-
165
-
-
0033405388
-
Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
-
Swan H, Piippo K, Viitasalo M, Heikkila P, Paavonen T, et al. 1999. Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts. J. Am. Coll. Cardiol. 34:2035-42
-
(1999)
J. Am. Coll. Cardiol.
, vol.34
, pp. 2035-2042
-
-
Swan, H.1
Piippo, K.2
Viitasalo, M.3
Heikkila, P.4
Paavonen, T.5
-
166
-
-
0035168177
-
A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16
-
Sylvius N, Tesson F, Gayet C, Charron P, Benaiche A, et al. 2001. A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16. Am. J. Hum. Genet. 68:241-46
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 241-246
-
-
Sylvius, N.1
Tesson, F.2
Gayet, C.3
Charron, P.4
Benaiche, A.5
-
167
-
-
0035831430
-
Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation
-
Szczesna D, Ghosh D, Li Q, Gomes AV, Guzman G, et al. 2001. Familial hypertrophic cardiomyopathy mutations in the regulatory light chains of myosin affect their structure, Ca2+ binding, and phosphorylation. J. Biol. Chem. 276:7086-92
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 7086-7092
-
-
Szczesna, D.1
Ghosh, D.2
Li, Q.3
Gomes, A.V.4
Guzman, G.5
-
168
-
-
0034614419
-
Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy
-
Szczesna D, Zhang R, Zhao J, Jones M, Guzman G, Potter JD. 2000. Altered regulation of cardiac muscle contraction by troponin T mutations that cause familial hypertrophic cardiomyopathy. J. Biol. Chem. 275:624-30
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 624-630
-
-
Szczesna, D.1
Zhang, R.2
Zhao, J.3
Jones, M.4
Guzman, G.5
Potter, J.D.6
-
169
-
-
0032982536
-
Undetected cardiac lesions cause unexpected sudden cardiac death during occasional sport activity. A report of 80 cases
-
Tabib A, Miras A, Taniere P, Loire R. 1999. Undetected cardiac lesions cause unexpected sudden cardiac death during occasional sport activity. A report of 80 cases. Eur. Heart J. 20:900-3
-
(1999)
Eur. Heart J.
, vol.20
, pp. 900-903
-
-
Tabib, A.1
Miras, A.2
Taniere, P.3
Loire, R.4
-
170
-
-
0035695803
-
Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy
-
Takahashi-Yanaga F, Morimoto S, Harada K, Minakami R, Shiraishi F, et al. 2001. Functional consequences of the mutations in human cardiac troponin I gene found in familial hypertrophic cardiomyopathy. J. Mol. Cell. Cardiol. 33:2095-107
-
(2001)
J. Mol. Cell. Cardiol.
, vol.33
, pp. 2095-2107
-
-
Takahashi-Yanaga, F.1
Morimoto, S.2
Harada, K.3
Minakami, R.4
Shiraishi, F.5
-
171
-
-
0031080069
-
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation
-
Tesson F, Dufour C, Moolman JC, Carrier L, al-Mahdawi S, et al. 1997. The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation. J. Mol. Cell. Cardiol. 29:831-38
-
(1997)
J. Mol. Cell. Cardiol.
, vol.29
, pp. 831-838
-
-
Tesson, F.1
Dufour, C.2
Moolman, J.C.3
Carrier, L.4
Al-Mahdawi, S.5
-
172
-
-
0028178083
-
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, et al. 1994. Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. Cell 77:701-12
-
(1994)
Cell
, vol.77
, pp. 701-712
-
-
Thierfelder, L.1
Watkins, H.2
MacRae, C.3
Lamas, R.4
McKenna, W.5
-
173
-
-
0035253502
-
Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)
-
Tiso N, Stephan DA, Nava A, Bagattin A, Devaney JM, et al. 2001. Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2). Hum. Mol. Genet. 10:189-94
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 189-194
-
-
Tiso, N.1
Stephan, D.A.2
Nava, A.3
Bagattin, A.4
Devaney, J.M.5
-
174
-
-
0027193330
-
X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus
-
Towbin IA, Hejtmancik IF, Brink P, Gelb B, Zhu XM, et al. 1993. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation 87:1854-65
-
(1993)
Circulation
, vol.87
, pp. 1854-1865
-
-
Towbin, I.A.1
Hejtmancik, I.F.2
Brink, P.3
Gelb, B.4
Zhu, X.M.5
-
175
-
-
0033818186
-
Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy
-
Tsubata S, Bowles KR, Vatta M, Zintz C, Titus I, et al. 2000. Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy. J. Clin. Invest. 106:655-62
-
(2000)
J. Clin. Invest.
, vol.106
, pp. 655-662
-
-
Tsubata, S.1
Bowles, K.R.2
Vatta, M.3
Zintz, C.4
Titus, I.5
-
176
-
-
0034646743
-
Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophice cardiomyopathy
-
Tyska MJ, Hayes E, Giewat M, Seidman CE, Seidman IG, Warshaw DM. 2000. Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophice cardiomyopathy. Circ. Res. 86:737-44
-
(2000)
Circ. Res.
, vol.86
, pp. 737-744
-
-
Tyska, M.J.1
Hayes, E.2
Giewat, M.3
Seidman, C.E.4
Seidman, I.G.5
Warshaw, D.M.6
-
177
-
-
0344873698
-
Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction
-
Vatta M, Mohapatra B, Jimenez S, Sanchez X, Faulkner G, et al. 2003. Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction. J. Am. Coll. Cardiol. 42:2014-27
-
(2003)
J. Am. Coll. Cardiol.
, vol.42
, pp. 2014-2027
-
-
Vatta, M.1
Mohapatra, B.2
Jimenez, S.3
Sanchez, X.4
Faulkner, G.5
-
178
-
-
0142180165
-
Different functional properties of troponin T mutants that cause dilated cardiomyopathy
-
Venkatraman G, Harada K, Gomes AV, Kerrick WG, Potter JD. 2003. Different functional properties of troponin T mutants that cause dilated cardiomyopathy. J. Biol. Chem. 278:41670-76
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 41670-41676
-
-
Venkatraman, G.1
Harada, K.2
Gomes, A.V.3
Kerrick, W.G.4
Potter, J.D.5
-
179
-
-
0028844204
-
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy
-
Watkins H, Conner D, Thierfelder L, Jarcho JA, MacRae C, et al. 1995. Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy. Nat. Genet. 11:434-37
-
(1995)
Nat. Genet.
, vol.11
, pp. 434-437
-
-
Watkins, H.1
Conner, D.2
Thierfelder, L.3
Jarcho, J.A.4
MacRae, C.5
-
180
-
-
0028902929
-
Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy
-
Watkins H, McKenna WJ, Thierfelder L, Suk HJ, Anan R, et al. 1995. Mutations in the genes for cardiac troponin T and α-tropomyosin in hypertrophic cardiomyopathy. N. Engl. J. Med. 332:1058-64
-
(1995)
N. Engl. J. Med.
, vol.332
, pp. 1058-1064
-
-
Watkins, H.1
McKenna, W.J.2
Thierfelder, L.3
Suk, H.J.4
Anan, R.5
-
181
-
-
0026573969
-
Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy
-
Watkins H, Rosenzweig A, Hwang D, Levi T, McKenna W, et al. 1992. Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy. N. Engl. J. Med. 326:1108-14
-
(1992)
N. Engl. J. Med.
, vol.326
, pp. 1108-1114
-
-
Watkins, H.1
Rosenzweig, A.2
Hwang, D.3
Levi, T.4
McKenna, W.5
-
182
-
-
0037144655
-
Myofilament calcium sensitivity and cardiac disease: Insights from troponin I isoforms and mutants
-
Westfall MV, Borton AR, Albayya FP, Metzger IM. 2002. Myofilament calcium sensitivity and cardiac disease: insights from troponin I isoforms and mutants. Circ. Res. 91:525-31
-
(2002)
Circ. Res.
, vol.91
, pp. 525-531
-
-
Westfall, M.V.1
Borton, A.R.2
Albayya, F.P.3
Metzger, I.M.4
-
183
-
-
0041707843
-
Glucose metabolism and energy homeostasis in mouse hearts overexpressing dominant negative alpha2 subunit of AMP-activated protein kinase
-
Xing Y, Musi N, Fujii N, Zou L, Luptak I, et al. 2003. Glucose metabolism and energy homeostasis in mouse hearts overexpressing dominant negative alpha2 subunit of AMP-activated protein kinase. J. Biol. Chem. 278:28372-77
-
(2003)
J. Biol. Chem.
, vol.278
, pp. 28372-28377
-
-
Xing, Y.1
Musi, N.2
Fujii, N.3
Zou, L.4
Luptak, I.5
-
184
-
-
0036344498
-
Dystrophin deficiency markedly increases enterovirus-induced cardiomyopathy: A genetic predisposition to viral heart disease
-
Xiong D, Lee GH, Badorff C, Dorner A, Lee S, et al. 2002. Dystrophin deficiency markedly increases enterovirus-induced cardiomyopathy: a genetic predisposition to viral heart disease. Nat. Med. 8:872-77
-
(2002)
Nat. Med.
, vol.8
, pp. 872-877
-
-
Xiong, D.1
Lee, G.H.2
Badorff, C.3
Dorner, A.4
Lee, S.5
-
185
-
-
0033679195
-
Morphological patterns of death by myocytes in arrhythmogenic right ventricular dysplasia
-
Yamamoto S, Tsyplenkova VG, James TN. 2000. Morphological patterns of death by myocytes in arrhythmogenic right ventricular dysplasia. Am. J. Med. Sci. 320:310-19
-
(2000)
Am. J. Med. Sci.
, vol.320
, pp. 310-319
-
-
Yamamoto, S.1
Tsyplenkova, V.G.2
James, T.N.3
-
186
-
-
0034687593
-
Decreased SLIM1 expression and increased gelsolin expression in failing human hearts measured by high-density oligonucleotide arrays
-
Yang J, Moravec CS, Sussman MA, DiPaola NR, Fu D, et al. 2000. Decreased SLIM1 expression and increased gelsolin expression in failing human hearts measured by high-density oligonucleotide arrays. Circulation 102:3046-52
-
(2000)
Circulation
, vol.102
, pp. 3046-3052
-
-
Yang, J.1
Moravec, C.S.2
Sussman, M.A.3
DiPaola, N.R.4
Fu, D.5
-
187
-
-
0037162697
-
Class II histone deacetylases act as signal-responsive repressers of cardiac hypertrophy
-
Zhang CL, McKinsey TA, Chang S, Antos CL, Hill JA, Olson EN. 2002. Class II histone deacetylases act as signal-responsive repressers of cardiac hypertrophy. Cell 110:479-88
-
(2002)
Cell
, vol.110
, pp. 479-488
-
-
Zhang, C.L.1
McKinsey, T.A.2
Chang, S.3
Antos, C.L.4
Hill, J.A.5
Olson, E.N.6
-
188
-
-
0035044156
-
Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy
-
Zhang J, Kumar A, Stalker HJ, Virdi G, Ferrans VI, et al. 2001. Clinical and molecular studies of a large family with desmin-associated restrictive cardiomyopathy. Clin. Genet. 59:248-56
-
(2001)
Clin. Genet.
, vol.59
, pp. 248-256
-
-
Zhang, J.1
Kumar, A.2
Stalker, H.J.3
Virdi, G.4
Ferrans, V.I.5
-
189
-
-
0036789964
-
Kir6.2 is required for adaptation to stress
-
Zingman LV, Hodgson DM, Bast PH, Kane GC, Perez-Terzic C, et al. 2002. Kir6.2 is required for adaptation to stress. Proc. Natl. Acad. Sci. USA 99:13278-83
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 13278-13283
-
-
Zingman, L.V.1
Hodgson, D.M.2
Bast, P.H.3
Kane, G.C.4
Perez-Terzic, C.5
|