-
1
-
-
0036087310
-
Inherited sodium Mhannelepathies: Models for acquired arrhythmias?
-
Balser JR: Inherited sodium Mhannelepathies: models for acquired arrhythmias? Am J Physiol Heart Circ Physiol 2002; 282: H1175-H1180.
-
(2002)
Am J Physiol Heart Circ Physiol
, vol.282
-
-
Balser, J.R.1
-
3
-
-
0028908741
-
Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21
-
George Jr AL, Varkony TA, Drabkin HA et al: Assignment of the human heart tetrodotoxin-resistant voltage-gated Na+ channel alpha-subunit gene (SCN5A) to band 3p21. Cytogenet Cell Genet 1995; 68: 67-70.
-
(1995)
Cytogenet Cell Genet
, vol.68
, pp. 67-70
-
-
George Jr, A.L.1
Varkony, T.A.2
Drabkin, H.A.3
-
4
-
-
0029116230
-
Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia
-
Wang Q, Shen, J, Li Z et al: Cardiac sodium channel mutations in patients with long QT syndrome, an inherited cardiac arrhythmia. Hum Mol Genet 1995; 4: 1603-4607.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1603-4607
-
-
Wang, Q.1
Shen, J.2
Li, Z.3
-
5
-
-
0035931932
-
A sodium-channel mutation causes isolated cardiac conduction disease
-
Tan HL, Bink-Boelkens MT, Bezzini CR et al. A sodium-channel mutation causes isolated cardiac conduction disease. Nature 2001; 409: 1043-1047.
-
(2001)
Nature
, vol.409
, pp. 1043-1047
-
-
Tan, H.L.1
Bink-Boelkens, M.T.2
Bezzini, C.R.3
-
6
-
-
0242317397
-
Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCNSA)
-
Benson DW, Wang DW, Dyment M et al. Congenital sick sinus syndrome caused by recessive mutations in the cardiac sodium channel gene (SCNSA). J Clin Invest 2003; 112: 1019-1028.
-
(2003)
J Clin Invest
, vol.112
, pp. 1019-1028
-
-
Benson, D.W.1
Wang, D.W.2
Dyment, M.3
-
7
-
-
12544251104
-
SCN5A - a mechanistic link between inherited cardiomyopathies and a predisposition to arrhythmias?
-
Adler E, Fuster V: SCN5A - a mechanistic link between inherited cardiomyopathies and a predisposition to arrhythmias? JAMA 2005; 293: 491-493.
-
(2005)
JAMA
, vol.293
, pp. 491-493
-
-
Adler, E.1
Fuster, V.2
-
8
-
-
0032546384
-
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
-
Chen Q, Kirsch GE, Zhang D et al: Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 1998; 392: 293-296.
-
(1998)
Nature
, vol.392
, pp. 293-296
-
-
Chen, Q.1
Kirsch, G.E.2
Zhang, D.3
-
9
-
-
33644665708
-
Oxidative mediated lipid peroxidation recapitulates proarrhythmic effects on cardiac sodium channels
-
Fukuda K, Davies SS, Nakajima T et al: Oxidative mediated lipid peroxidation recapitulates proarrhythmic effects on cardiac sodium channels. Circ Res 2005; 97: 1262-1269.
-
(2005)
Circ Res
, vol.97
, pp. 1262-1269
-
-
Fukuda, K.1
Davies, S.S.2
Nakajima, T.3
-
10
-
-
0031015477
-
Electrophysiologic effects of acute myocardial ischemia. A mechanistic investigation of action potential conduction and conduction failure
-
Shaw RM, Rudy Y. Electrophysiologic effects of acute myocardial ischemia. A mechanistic investigation of action potential conduction and conduction failure. Circ Res 1997; 80: 124-138.
-
(1997)
Circ Res
, vol.80
, pp. 124-138
-
-
Shaw, R.M.1
Rudy, Y.2
-
11
-
-
0024321898
-
Preliminary report: Effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction
-
The Cardiac Arrhythmia Suppression Trial (CAST) Investigators
-
The Cardiac Arrhythmia Suppression Trial (CAST) Investigators: Preliminary report: Effect of encainide and flecainide on mortality in a randomized trial of arrhythmia suppression after myocardial infarction. N Engl J Med 1989; 321: 406-412.
-
(1989)
N Engl J Med
, vol.321
, pp. 406-412
-
-
-
12
-
-
0028898776
-
Electrophysiological effects of flecainide on anisotropic conduction and reentry in infarcted canine hearts
-
Coromilas J, Saltman AE, Waldecker B, Dillon SM, Wit AL: Electrophysiological effects of flecainide on anisotropic conduction and reentry in infarcted canine hearts. Circulation 1995; 91: 2245-2263.
-
(1995)
Circulation
, vol.91
, pp. 2245-2263
-
-
Coromilas, J.1
Saltman, A.E.2
Waldecker, B.3
Dillon, S.M.4
Wit, A.L.5
-
13
-
-
2442698830
-
Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis
-
Antzelevitch C: Cellular basis and mechanism underlying normal and abnormal myocardial repolarization and arrhythmogenesis. Ann Med 2004; 36 (Suppl 1): 5-14.
-
(2004)
Ann Med
, vol.36
, Issue.SUPPL. 1
, pp. 5-14
-
-
Antzelevitch, C.1
-
14
-
-
0027530585
-
Flecainide-induced arrhythmia in canine ventricular epicardlum. Phase 2 reentry?
-
Krishnan SC, Antzelevitch C: Flecainide-induced arrhythmia in canine ventricular epicardlum. Phase 2 reentry? Circulation 1993; 87 562-572.
-
(1993)
Circulation
, vol.87
, pp. 562-572
-
-
Krishnan, S.C.1
Antzelevitch, C.2
-
15
-
-
0027425976
-
Differences in the electrophysiological response of canine ventricular epicardium and endocardium to ischemia. Role of the transient outward current
-
Lukas A, Antzelevitch C: Differences in the electrophysiological response of canine ventricular epicardium and endocardium to ischemia. Role of the transient outward current. Circulation 1993; 88: 2903-2915.
-
(1993)
Circulation
, vol.88
, pp. 2903-2915
-
-
Lukas, A.1
Antzelevitch, C.2
-
16
-
-
0035933766
-
Novel mechanism for Brugada syndrome: Defective surface localization of an SCN5A mutant (R1432G)
-
Baroudi G, Pouliot V, Denjoy I, Guicheney P, Shrier A, Chahine M: Novel mechanism for Brugada syndrome: Defective surface localization of an SCN5A mutant (R1432G). Circ Res 2001; 88: E78-E83.
-
(2001)
Circ Res
, vol.88
-
-
Baroudi, G.1
Pouliot, V.2
Denjoy, I.3
Guicheney, P.4
Shrier, A.5
Chahine, M.6
-
17
-
-
2342523271
-
Human genomics and its impact on arrhythmias
-
Roden DM: Human genomics and its impact on arrhythmias. Trends Cardiovasc Med 2004; 14: 112-116.
-
(2004)
Trends Cardiovasc Med
, vol.14
, pp. 112-116
-
-
Roden, D.M.1
-
19
-
-
8844270153
-
Prediction of similarly acting cis-regulatory modules by subsequence profiling and comparative genomics in Drosophila melanogaster and D. pseudo-obscura
-
Grad YH, Roth FP, Halfon MS, Church GM: Prediction of similarly acting cis-regulatory modules by subsequence profiling and comparative genomics in Drosophila melanogaster and D. pseudo-obscura. Bioinformatics 2004; 20: 2738-2750.
-
(2004)
Bioinformatics
, vol.20
, pp. 2738-2750
-
-
Grad, Y.H.1
Roth, F.P.2
Halfon, M.S.3
Church, G.M.4
-
20
-
-
0037108159
-
The RNA polymerase II core promoter: A key component in the regulation of gene expression
-
Butler JE, Kadonaga JT. The RNA polymerase II core promoter: A key component in the regulation of gene expression. Genes Dev 2002; 16: 2583-2592.
-
(2002)
Genes Dev
, vol.16
, pp. 2583-2592
-
-
Butler, J.E.1
Kadonaga, J.T.2
-
21
-
-
0043269205
-
The RNA polymerase II core promoter
-
Smale ST, Kadonaga JT: The RNA polymerase II core promoter. Annu Rev Biochem 2003; 72: 449-479.
-
(2003)
Annu Rev Biochem
, vol.72
, pp. 449-479
-
-
Smale, S.T.1
Kadonaga, J.T.2
-
22
-
-
0042359360
-
Functional analysis of human promoter polymorphisms
-
Hoogendoorn B, Coleman SL, Guy CA et al: Functional analysis of human promoter polymorphisms. Hum Mol Genet 2003; 12: 2249-2254.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2249-2254
-
-
Hoogendoorn, B.1
Coleman, S.L.2
Guy, C.A.3
-
23
-
-
0346096549
-
Cloning and initial characterization of the human cardiac sodium channel (SCNSA) promoter
-
Yang P, Kupershmidt S, Roden DM: Cloning and initial characterization of the human cardiac sodium channel (SCNSA) promoter. Cardiovasc Res 2004; 61: 56-65.
-
(2004)
Cardiovasc Res
, vol.61
, pp. 56-65
-
-
Yang, P.1
Kupershmidt, S.2
Roden, D.M.3
-
24
-
-
33644872001
-
Common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction
-
Bezzina CR, Shimizu W, Yang P et al: Common sodium channel promoter haplotype in Asian subjects underlies variability in cardiac conduction. Circulation 2006; 113: 338-344.
-
(2006)
Circulation
, vol.113
, pp. 338-344
-
-
Bezzina, C.R.1
Shimizu, W.2
Yang, P.3
-
25
-
-
0032502026
-
Right bundle-branch block and ST-segment elevation in leads V1 through V3: A marker for sudden death in patients without demonstrable structural heart disease
-
Brugada J, Brugada R, Brugada P: Right bundle-branch block and ST-segment elevation in leads V1 through V3: A marker for sudden death in patients without demonstrable structural heart disease. Circulation 1998; 97: 457-460.
-
(1998)
Circulation
, vol.97
, pp. 457-460
-
-
Brugada, J.1
Brugada, R.2
Brugada, P.3
-
26
-
-
0026466921
-
Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. A multicenter report
-
Brugada P, Brugada J: Right bundle branch block, persistent ST segment elevation and sudden cardiac death: A distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol 1992; 20: 1391- 1396.
-
(1992)
J Am Coll Cardiol
, vol.20
, pp. 1391-1396
-
-
Brugada, P.1
Brugada, J.2
-
27
-
-
20144386917
-
Common variants in myocardial ion channel genes modify the QT interval in the general population: Results from the KORA study
-
Pfeufer A, Jalilzadeh S, Perz S et al: Common variants in myocardial ion channel genes modify the QT interval in the general population: Results from the KORA study. Circ Res 2005; 96: 693-701.
-
(2005)
Circ Res
, vol.96
, pp. 693-701
-
-
Pfeufer, A.1
Jalilzadeh, S.2
Perz, S.3
-
28
-
-
0032429154
-
A DNA polymorphism discovery resource for research on human genetic variation
-
Collins FS, Brooks LD, Chakravarti A: A DNA polymorphism discovery resource for research on human genetic variation. Genome Res 1998; 8: 1229-1231.
-
(1998)
Genome Res
, vol.8
, pp. 1229-1231
-
-
Collins, F.S.1
Brooks, L.D.2
Chakravarti, A.3
-
29
-
-
0025871535
-
Four letters in theAgenetic alphabet: A frozen evolutionary optimum?
-
Szathmary E: Four letters in theAgenetic alphabet: a frozen evolutionary optimum? Proc Biol Sci 1991; 245: 91-99.
-
(1991)
Proc Biol Sci
, vol.245
, pp. 91-99
-
-
Szathmary, E.1
-
30
-
-
0035102884
-
A novel polymorphism in the promoter of the RAGE gene is associated with non-small cell lung cancer
-
Schenk S, Schraml P, Bendik I, Ludwig CU: A novel polymorphism in the promoter of the RAGE gene is associated with non-small cell lung cancer. Lung Cancer 2001; 32: 7-12.
-
(2001)
Lung Cancer
, vol.32
, pp. 7-12
-
-
Schenk, S.1
Schraml, P.2
Bendik, I.3
Ludwig, C.U.4
-
31
-
-
0037624040
-
Influence of life stress on depression: Moderation by a polymorphism in the 5-HTT gene
-
Caspi A, Sugden K, Moffitt TE et al: Influence of life stress on depression: Moderation by a polymorphism in the 5-HTT gene. Science 2003; 301: 386-389.
-
(2003)
Science
, vol.301
, pp. 386-389
-
-
Caspi, A.1
Sugden, K.2
Moffitt, T.E.3
-
32
-
-
0006463359
-
Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region
-
Lesch KP, Bengel D, Heils A et al: Association of anxiety-related traits with a polymorphism in the serotonin transporter gene regulatory region. Science 1996; 274: 1527-1531.
-
(1996)
Science
, vol.274
, pp. 1527-1531
-
-
Lesch, K.P.1
Bengel, D.2
Heils, A.3
-
34
-
-
0028141063
-
Molecular cloning and functional analysis of the promoter of rat skeletal muscle voltage-sensitive sodium channel subtype 2 (rSkM2): Evidence for muscle-specific nuclear protein binding to the core promoter
-
Sheng ZH, Zhang H, Barchi RL, Kallen RG: Molecular cloning and functional analysis of the promoter of rat skeletal muscle voltage-sensitive sodium channel subtype 2 (rSkM2): Evidence for muscle-specific nuclear protein binding to the core promoter. DNA Cell Biol 1994; 13: 9-23.
-
(1994)
DNA Cell Biol
, vol.13
, pp. 9-23
-
-
Sheng, Z.H.1
Zhang, H.2
Barchi, R.L.3
Kallen, R.G.4
-
35
-
-
0033951051
-
Substantially reduced risk of cancer of the aerodigestive tract in subjects with variant - 463A of the myeloperoxidase gene
-
Cascorbi I, Henning S, Brockmoller J et al: Substantially reduced risk of cancer of the aerodigestive tract in subjects with variant - 463A of the myeloperoxidase gene. Cancer Res 2000; 60: 644-649.
-
(2000)
Cancer Res
, vol.60
, pp. 644-649
-
-
Cascorbi, I.1
Henning, S.2
Brockmoller, J.3
-
36
-
-
17744393639
-
Characterization of new mutations in the coding sequence and 5′-untranslated region of the human prostacyclin synthase gene (CYP8A1)
-
Chevalier D, Cauffiez C, Bernard C et al: Characterization of new mutations in the coding sequence and 5′-untranslated region of the human prostacyclin synthase gene (CYP8A1). Hum Genet 2001; 108 148-155.
-
(2001)
Hum Genet
, vol.108
, pp. 148-155
-
-
Chevalier, D.1
Cauffiez, C.2
Bernard, C.3
-
37
-
-
0036801821
-
Characterization of thrombomodulin gene mutations of the 5′-regulatory region
-
Nakazawa F, Koyama T, Shibamiya A, Hirosawa S: Characterization of thrombomodulin gene mutations of the 5′-regulatory region. Atherosclerosis 2002; 164: 385-387.
-
(2002)
Atherosclerosis
, vol.164
, pp. 385-387
-
-
Nakazawa, F.1
Koyama, T.2
Shibamiya, A.3
Hirosawa, S.4
-
38
-
-
0029999154
-
An Alu element in the myeloperoxidase promoter contains a composite SP1-thyroid hormone-retinoic acid response element
-
Piedrafita FJ, Molander RB, Vansant G, Orlova EA, Pfahl M, Reynolds WF: An Alu element in the myeloperoxidase promoter contains a composite SP1-thyroid hormone-retinoic acid response element. J Biol Chem 1996; 271: 14412-14420.
-
(1996)
J Biol Chem
, vol.271
, pp. 14412-14420
-
-
Piedrafita, F.J.1
Molander, R.B.2
Vansant, G.3
Orlova, E.A.4
Pfahl, M.5
Reynolds, W.F.6
-
39
-
-
21444443478
-
MatInspector and beyond: Promoter analysis based on transcription factor binding sites
-
Cartharius K, Frech K, Grote K et al: MatInspector and beyond: promoter analysis based on transcription factor binding sites. Bioinformatics 2005; 21: 2933-2942.
-
(2005)
Bioinformatics
, vol.21
, pp. 2933-2942
-
-
Cartharius, K.1
Frech, K.2
Grote, K.3
-
40
-
-
0028971143
-
MatInd and MatInspector: New fast and versatile tools for detection of consensus matches in nucleotide sequence data
-
Quandt K, Frech K, Karas H, Wingender E, Werner T: MatInd and MatInspector: New fast and versatile tools for detection of consensus matches in nucleotide sequence data. Nucleic Acids Res 1995; 23 4878-4884.
-
(1995)
Nucleic Acids Res
, vol.23
, pp. 4878-4884
-
-
Quandt, K.1
Frech, K.2
Karas, H.3
Wingender, E.4
Werner, T.5
-
41
-
-
0030064803
-
The mouse zic gene family. Homologues of the Drosophila pair-rule gene odd-paired
-
Aruga. J, Nagai T, Tokuyama T et al: The mouse zic gene family. Homologues of the Drosophila pair-rule gene odd-paired. J Biol Chem 1996; 271: 1043-1047.
-
(1996)
J Biol Chem
, vol.271
, pp. 1043-1047
-
-
Aruga, J.1
Nagai, T.2
Tokuyama, T.3
-
42
-
-
0028179671
-
Odd-paired: A zinc finger pair-rule protein required for the timely activation of engrailed and wingless in Drosophila embryos
-
BenedyA MJ, Mullen JR, DiNardo S: Odd-paired: a zinc finger pair-rule protein required for the timely activation of engrailed and wingless in Drosophila embryos. Genes Dev 1994; 8: 105-117.
-
(1994)
Genes Dev
, vol.8
, pp. 105-117
-
-
BenedyA, M.J.1
Mullen, J.R.2
DiNardo, S.3
|