-
1
-
-
0028905566
-
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
-
Wang, Q., et al. 1995. SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome. Cell. 80:805-811.
-
(1995)
Cell
, vol.80
, pp. 805-811
-
-
Wang, Q.1
-
2
-
-
0032546384
-
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
-
Chen, Q., et al. 1998 Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature. 392:293-296.
-
(1998)
Nature
, vol.392
, pp. 293-296
-
-
Chen, Q.1
-
3
-
-
0035931932
-
A sodium-channel mutation causes isolated cardiac conduction disease
-
Tan, H.L., et al. 2001. A sodium-channel mutation causes isolated cardiac conduction disease. Nature. 409:1043-1047.
-
(2001)
Nature
, vol.409
, pp. 1043-1047
-
-
Tan, H.L.1
-
4
-
-
0032741905
-
Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent
-
Dumaine, R., et al. 1999. Ionic mechanisms responsible for the electrocardiographic phenotype of the Brugada syndrome are temperature dependent. Circ. Res. 85:803-809.
-
(1999)
Circ. Res.
, vol.85
, pp. 803-809
-
-
Dumaine, R.1
-
5
-
-
0034640093
-
Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel
-
Veldkamp, M.W., et al. 2000. Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel. Circ. Res. 86:E91-E97.
-
(2000)
Circ. Res.
, vol.86
-
-
Veldkamp, M.W.1
-
6
-
-
0034644530
-
Enhanced Na(+) channel intermediate inactivation in Brugada syndrome
-
Wang, D.W., Makita, N., Kitabatake, A., Balser, J.R., and George, A.L., Jr. 2000. Enhanced Na(+) channel intermediate inactivation in Brugada syndrome. Circ. Res. 87:E37-E43.
-
(2000)
Circ. Res.
, vol.87
-
-
Wang, D.W.1
Makita, N.2
Kitabatake, A.3
Balser, J.R.4
George A.L., Jr.5
-
7
-
-
0033379061
-
Transmural dispersion of repolarization and arrhythmogenicity: The Brugada syndrome versus the long QT syndrome
-
Antzelevitch, C., Yan, G.X., and Shimizu, W. 1999. Transmural dispersion of repolarization and arrhythmogenicity: the Brugada syndrome versus the long QT syndrome. J. Electrocardiol. 32(Suppl):158-165.
-
(1999)
J. Electrocardiol.
, vol.32
, Issue.SUPPL.
, pp. 158-165
-
-
Antzelevitch, C.1
Yan, G.X.2
Shimizu, W.3
-
8
-
-
0033537470
-
"Brugada" syndrome: Clinical data and suggested pathophysiological mechanism
-
Alings, M., and Wilde, A. 1999. "Brugada" syndrome: clinical data and suggested pathophysiological mechanism. Circulation 99:666-673.
-
(1999)
Circulation
, vol.99
, pp. 666-673
-
-
Alings, M.1
Wilde, A.2
-
9
-
-
0037154288
-
Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block
-
Wang, D.W., Viswanathan, P.C., Balser, J.R., George, A.L., Jr., and Benson, D.W. 2002. Clinical, genetic, and biophysical characterization of SCN5A mutations associated with atrioventricular conduction block. Circulation. 105:341-346.
-
(2002)
Circulation
, vol.105
, pp. 341-346
-
-
Wang, D.W.1
Viswanathan, P.C.2
Balser, J.R.3
George A.L., Jr.4
Benson, D.W.5
-
10
-
-
0037065845
-
Clinical and molecular heterogeneity in the Brugada syndrome: A novel gene locus on chromosome 3
-
Weiss, R., et al. 2002. Clinical and molecular heterogeneity in the Brugada syndrome: a novel gene locus on chromosome 3. Circulation. 105:707-713.
-
(2002)
Circulation
, vol.105
, pp. 707-713
-
-
Weiss, R.1
-
11
-
-
0031678410
-
Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis
-
Hull, J., and Thomson, A.H. 1998. Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis. Thorax. 53:1018-1021.
-
(1998)
Thorax
, vol.53
, pp. 1018-1021
-
-
Hull, J.1
Thomson, A.H.2
-
12
-
-
0032461761
-
Apolipoprotein E and Alzheimer's disease. The tip of the susceptibility iceberg
-
Roses, A.D. 1998. Apolipoprotein E and Alzheimer's disease. The tip of the susceptibility iceberg. Ann. NY Acad. Sci. 855:738-743.
-
(1998)
Ann. NY Acad. Sci.
, vol.855
, pp. 738-743
-
-
Roses, A.D.1
-
13
-
-
0034718159
-
The role of apolipoprotein E in Alzheimer's disease: Pharmacogenomic target selection
-
Saunders, A.M., et al. 2000. The role of apolipoprotein E in Alzheimer's disease: pharmacogenomic target selection. Biochim. Biophys. Acta. 1502:85-94.
-
(2000)
Biochim. Biophys. Acta
, vol.1502
, pp. 85-94
-
-
Saunders, A.M.1
-
14
-
-
0033808326
-
Pharmacogenetics and the treatment of cardiovascular disease
-
Wilkins, M.R., Roses, A.D., and Clifford, C.P. 2000. Pharmacogenetics and the treatment of cardiovascular disease. Heart. 84:353-354.
-
(2000)
Heart
, vol.84
, pp. 353-354
-
-
Wilkins, M.R.1
Roses, A.D.2
Clifford, C.P.3
-
15
-
-
18544383162
-
Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia
-
Splawski, I., et al. 2002. Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia. Science. 297:1333-1336.
-
(2002)
Science
, vol.297
, pp. 1333-1336
-
-
Splawski, I.1
-
16
-
-
0037161355
-
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes
-
Yang, P., et al. 2002. Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes. Circulation. 105:1943-1948.
-
(2002)
Circulation
, vol.105
, pp. 1943-1948
-
-
Yang, P.1
-
18
-
-
0033533990
-
A single Na(+) channel mutation causing both long-QT and Brugada syndromes
-
Bezzina, C.R., et al. 1999. A single Na(+) channel mutation causing both long-QT and Brugada syndromes. Circ. Res. 85:1206-1213.
-
(1999)
Circ. Res.
, vol.85
, pp. 1206-1213
-
-
Bezzina, C.R.1
-
19
-
-
0031745967
-
Autoimmune-associated congenital heart block: Demographics, mortality, morbidity and recurrence rates obtained from a national neonatal lupus registry
-
Buyon, J.P. 1998. Autoimmune-associated congenital heart block: demographics, mortality, morbidity and recurrence rates obtained from a national neonatal lupus registry. J. Am. Coll. Cardiol. 31:1658-1666.
-
(1998)
J. Am. Coll. Cardiol.
, vol.31
, pp. 1658-1666
-
-
Buyon, J.P.1
-
20
-
-
0035903135
-
Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes
-
Rivolta, I., et al. 2001. Inherited Brugada and long QT-3 syndrome mutations of a single residue of the cardiac sodium channel confer distinct channel and clinical phenotypes. J. Biol. Chem. 276:30623-30630.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 30623-30630
-
-
Rivolta, I.1
-
21
-
-
0035806895
-
Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes
-
Viswanathan, P.C., et al. 2001. Gating-dependent mechanisms for flecainide action in SCN5A-linked arrhythmia syndromes. Circulation. 104:1200-1205.
-
(2001)
Circulation
, vol.104
, pp. 1200-1205
-
-
Viswanathan, P.C.1
-
22
-
-
0030031004
-
Mapping a cardiomyopathy locus to chromosome 3p22-p25
-
Olson, T.M., and Keating, M.T. 1996. Mapping a cardiomyopathy locus to chromosome 3p22-p25. J. Clin. Invest. 97:528-532.
-
(1996)
J. Clin. Invest.
, vol.97
, pp. 528-532
-
-
Olson, T.M.1
Keating, M.T.2
-
23
-
-
0037123990
-
Differential distribution of cardiac ion channel expression as a basis for regional specialization in electrical function
-
Schram, G., Pourrier, M., Melnyk, P., and Nattel, S. 2002. Differential distribution of cardiac ion channel expression as a basis for regional specialization in electrical function. Circ. Res. 90:939-950.
-
(2002)
Circ. Res.
, vol.90
, pp. 939-950
-
-
Schram, G.1
Pourrier, M.2
Melnyk, P.3
Nattel, S.4
-
24
-
-
0033514263
-
Low penetrance in the long-QT syndrome: Clinical impact
-
Priori, S.G., Napolitano, C., and Schwartz, P.J. 1999. Low penetrance in the long-QT syndrome: clinical impact. Circulation. 99:529-533.
-
(1999)
Circulation
, vol.99
, pp. 529-533
-
-
Priori, S.G.1
Napolitano, C.2
Schwartz, P.J.3
-
25
-
-
0034890305
-
The heart SNPs a beat: Polymorphisms in candidate genes for cardiovascular disease
-
Daley, G.Q., and Cargill, M. 2001. The heart SNPs a beat: polymorphisms in candidate genes for cardiovascular disease. Trends Cardiovasc. Med. 11:60-66.
-
(2001)
Trends Cardiovasc. Med.
, vol.11
, pp. 60-66
-
-
Daley, G.Q.1
Cargill, M.2
-
26
-
-
0033809489
-
Genetic susceptibility to cardiovascular diseases
-
Roses, A.D. 2000. Genetic susceptibility to cardiovascular diseases. Am. Heart J. 140:S45-S47.
-
(2000)
Am. Heart J.
, vol.140
-
-
Roses, A.D.1
-
27
-
-
0034660560
-
Pharmacogenetics and the practice of medicine
-
Roses, A.D. 2000. Pharmacogenetics and the practice of medicine. Nature. 405:857-865.
-
(2000)
Nature
, vol.405
, pp. 857-865
-
-
Roses, A.D.1
-
28
-
-
0003425462
-
A common polymorphism associated with antibiotic-induced cardiac arrhythmia
-
Sesti, F., et al. 2000. A common polymorphism associated with antibiotic-induced cardiac arrhythmia. Proc. Natl. Acad. Sci. USA. 97:10613-10618.
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 10613-10618
-
-
Sesti, F.1
|