-
1
-
-
0028124225
-
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1
-
Browne, D.L., S.T. Gancher, J.G. Nutt et al. 1994. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1. Nature Genet. 8: 136-140.
-
(1994)
Nature Genet.
, vol.8
, pp. 136-140
-
-
Browne, D.L.1
Gancher, S.T.2
Nutt, J.G.3
-
2
-
-
0029120561
-
Identification of two new KCNA1 mutations in episodic ataxia/myokymia families
-
Browne, D.L., E.R.P. Brunt, R.C. Griggs et al. 1995. Identification of two new KCNA1 mutations in episodic ataxia/myokymia families. Human Mol. Genet. 4: 1671-1672.
-
(1995)
Human Mol. Genet.
, vol.4
, pp. 1671-1672
-
-
Browne, D.L.1
Brunt, E.R.P.2
Griggs, R.C.3
-
3
-
-
0029958199
-
Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1
-
Comu, S., M. Giuliani & V. Narayanan. 1996. Episodic ataxia and myokymia syndrome: A new mutation of potassium channel gene Kv1.1. Am. Neurolog. Assoc. 40: 684-687.
-
(1996)
Am. Neurolog. Assoc.
, vol.40
, pp. 684-687
-
-
Comu, S.1
Giuliani, M.2
Narayanan, V.3
-
4
-
-
0028905566
-
SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
-
Wang, Q., J. Shen, I. Splawski 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
Shen, J.2
Splawski, I.3
-
5
-
-
9044240040
-
Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
-
Wang, Q., M.E. Curran, I. Splawski et al. 1996. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nature Genet. 12: 17-23.
-
(1996)
Nature Genet.
, vol.12
, pp. 17-23
-
-
Wang, Q.1
Curran, M.E.2
Splawski, I.3
-
6
-
-
0028914969
-
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
-
Curran, M.E., I. Splawski, K.W. Timothy et al. 1995. A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome. Cell 80: 795-804.
-
(1995)
Cell
, vol.80
, pp. 795-804
-
-
Curran, M.E.1
Splawski, I.2
Timothy, K.W.3
-
7
-
-
0030918946
-
Molecular basis of the long-QT syndrome associated with deafness
-
Splawski, I., K.W. Timothy, G.M. Vincent et al. 1997. Molecular basis of the long-QT syndrome associated with deafness. N. Engl. J. Med. 336: 1562-1567.
-
(1997)
N. Engl. J. Med.
, vol.336
, pp. 1562-1567
-
-
Splawski, I.1
Timothy, K.W.2
Vincent, G.M.3
-
9
-
-
9844261701
-
IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome
-
Tyson, J., L. Traneebjaerg, S. Bellman et al. 1997. IsK and KvLQT1: Mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndrome. Hum. Mol. Genet. 6: 2179-2185.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 2179-2185
-
-
Tyson, J.1
Traneebjaerg, L.2
Bellman, S.3
-
10
-
-
0029840732
-
KVLQT1 mutations in three families with familial or sporadic long QT syndrome
-
Russell, M.W., M. Dick II, F.S. Collins et al. 1996. KVLQT1 mutations in three families with familial or sporadic long QT syndrome. Hum. Molec. Genet. 5: 1319-1324.
-
(1996)
Hum. Molec. Genet.
, vol.5
, pp. 1319-1324
-
-
Russell, M.W.1
Dick M. II2
Collins, F.S.3
-
12
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert, C., B.C. Schroeder, C. Kubisch et al. 1997. A potassium channel mutation in neonatal human epilepsy. Science 279: 403-406.
-
(1997)
Science
, vol.279
, pp. 403-406
-
-
Biervert, C.1
Schroeder, B.C.2
Kubisch, C.3
-
13
-
-
0031974209
-
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
-
Charlier, C., N.A. Singh, S.G. Ryan et al. 1998. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family. Nat. Genet. 18: 6-8.
-
(1998)
Nat. Genet.
, vol.18
, pp. 6-8
-
-
Charlier, C.1
Singh, N.A.2
Ryan, S.G.3
-
14
-
-
0029115971
-
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
-
Patil, N., D.R. Cox, D. Bhat et al. 1995. A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nature Genet. 11: 126-129.
-
(1995)
Nature Genet.
, vol.11
, pp. 126-129
-
-
Patil, N.1
Cox, D.R.2
Bhat, D.3
-
15
-
-
0029847602
-
Multiple mechanisms in the long QT syndrome: Current knowledge, gaps, and future directions
-
Roden, D.M., R. Lazzara, M. Rosen et al. 1996. Multiple mechanisms in the long QT syndrome: current knowledge, gaps, and future directions. Circulation 94: 1996-2012.
-
(1996)
Circulation
, vol.94
, pp. 1996-2012
-
-
Roden, D.M.1
Lazzara, R.2
Rosen, M.3
-
16
-
-
0013881809
-
La tachycardic ventriculaire a deaux foyers opposes variables
-
Dessertenne, F. 1966. La tachycardic ventriculaire a deaux foyers opposes variables. Arch. Mal. Coeur. Vaiss. 59: 263-272.
-
(1966)
Arch. Mal. Coeur. Vaiss.
, vol.59
, pp. 263-272
-
-
Dessertenne, F.1
-
17
-
-
0029835964
-
The electrophysiological mechanism of ventricular arrhythmias in the long QT syndrome
-
El-Sherif, N., E.B. Caref, H. Yin et al. 1996. The electrophysiological mechanism of ventricular arrhythmias in the long QT syndrome. Circ. Res. 79: 474-492.
-
(1996)
Circ. Res.
, vol.79
, pp. 474-492
-
-
El-Sherif, N.1
Caref, E.B.2
Yin, H.3
-
18
-
-
0029097799
-
Molecular mechanism for an inherited cardiac arrhythmia
-
Bennett, P.B., K. Yazawa, N. Makita et al. 1995. Molecular mechanism for an inherited cardiac arrhythmia. Nature 376: 683-685.
-
(1995)
Nature
, vol.376
, pp. 683-685
-
-
Bennett, P.B.1
Yazawa, K.2
Makita, N.3
-
19
-
-
0027257852
-
Delayed rectifier outward current and repolarization in human atrial myocytes
-
Wang, Z., B. Fermini & S. Nattel. 1993. Delayed rectifier outward current and repolarization in human atrial myocytes. Circ. Res. 73: 276-285.
-
(1993)
Circ. Res.
, vol.73
, pp. 276-285
-
-
Wang, Z.1
Fermini, B.2
Nattel, S.3
-
20
-
-
0028020442
-
Rapid and slow components of delayed rectifier currents in human atrial myocytes
-
Wang, Z., B. Fermini & S. Nattel. 1994. Rapid and slow components of delayed rectifier currents in human atrial myocytes. Cardiovasc. Res. 28: 1540-1546.
-
(1994)
Cardiovasc. Res.
, vol.28
, pp. 1540-1546
-
-
Wang, Z.1
Fermini, B.2
Nattel, S.3
-
21
-
-
0029997391
-
+ current in human ventricular myocytes
-
+ current in human ventricular myocytes. Circ. Res. 78: 689-696.
-
(1996)
Circ. Res.
, vol.78
, pp. 689-696
-
-
Li, G.-R.1
Feng, J.2
Yue, L.3
-
22
-
-
0026640423
-
+ current in cardiac myocytes by dofetilide
-
+ current in cardiac myocytes by dofetilide. J. Pharmacol. Exp. Ther. 262: 809-817.
-
(1992)
J. Pharmacol. Exp. Ther.
, vol.262
, pp. 809-817
-
-
Carmeliet, E.1
-
23
-
-
0027429933
-
+ current by almokalant in rabbit ventricular myocytes
-
+ current by almokalant in rabbit ventricular myocytes. Circ. Res. 73: 857-868.
-
(1993)
Circ. Res.
, vol.73
, pp. 857-868
-
-
Carmeliet, E.1
-
24
-
-
0025351245
-
+ current: Differential sensitivity to block by class III antiarrhythmic agents
-
+ current: Differential sensitivity to block by class III antiarrhythmic agents. J. Gen. Physiol. 96: 195-215.
-
(1990)
J. Gen. Physiol.
, vol.96
, pp. 195-215
-
-
Sanguinetti, M.C.1
Jurkiewicz, N.K.2
-
25
-
-
0028171307
-
+ current, by the diuretic agent indapamide in guinea pig myocytes
-
+ current, by the diuretic agent indapamide in guinea pig myocytes. Circ. Res. 75: 879-886.
-
(1994)
Circ. Res.
, vol.75
, pp. 879-886
-
-
Turgeon, J.1
Daleau, P.2
Bennett, P.B.3
-
27
-
-
0027376226
-
+ current similar to Kv1.5 cloned channel currents
-
+ current similar to Kv1.5 cloned channel currents. Circ. Res. 73: 1061-1076.
-
(1993)
Circ. Res.
, vol.73
, pp. 1061-1076
-
-
Wang, Z.1
Fermini, B.2
Nattel, S.3
-
28
-
-
0028292927
-
A family of potassium channel genes related to eag in Drosophila and mammals
-
Warmke, J.W. & B. Ganetzky. 1994. A family of potassium channel genes related to eag in Drosophila and mammals. Proc. Natl. Acad. Sci. USA 91: 3438-3442.
-
(1994)
Proc. Natl. Acad. Sci. USA
, vol.91
, pp. 3438-3442
-
-
Warmke, J.W.1
Ganetzky, B.2
-
30
-
-
0029007356
-
HERG, A human inward rectifier in the voltage-gated potassium channel family
-
Trudeau, M., J.W. Warmke, B. Ganetzky et al. 1995. HERG, A human inward rectifier in the voltage-gated potassium channel family. Science 269: 92-95.
-
(1995)
Science
, vol.269
, pp. 92-95
-
-
Trudeau, M.1
Warmke, J.W.2
Ganetzky, B.3
-
32
-
-
0030025308
-
The inward rectification mechanism of the HERG cardiac potassium channel
-
Smith, P.L., T. Baukrowitz & G. Yellen. 1996. The inward rectification mechanism of the HERG cardiac potassium channel. Nature 379: 833-836.
-
(1996)
Nature
, vol.379
, pp. 833-836
-
-
Smith, P.L.1
Baukrowitz, T.2
Yellen, G.3
-
37
-
-
0029942250
-
High affinity open channel block by dofetilide of HERG expressed in a human cell line
-
Snyders, D.J. & A. Chaudhary. 1996. High affinity open channel block by dofetilide of HERG expressed in a human cell line. Molec. Pharmacol. 49: 949-955.
-
(1996)
Molec. Pharmacol.
, vol.49
, pp. 949-955
-
-
Snyders, D.J.1
Chaudhary, A.2
-
41
-
-
0030890712
-
KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias
-
Yang, W.P., P.C. Levesque, W.A. Little et al. 1997. KvLQT1, a voltage-gated potassium channel responsible for human cardiac arrhythmias. Proc. Natl. Acad. Sci. USA 94: 4017-4021.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 4017-4021
-
-
Yang, W.P.1
Levesque, P.C.2
Little, W.A.3
-
42
-
-
0030799943
-
+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
-
+ channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias. EMBO J. 16: 5472-5479.
-
(1997)
EMBO J.
, vol.16
, pp. 5472-5479
-
-
Chouabe, C.1
Neyroud, N.2
Guichney, P.3
-
43
-
-
0029034215
-
Subunit composition of minK potassium channels
-
Wang, K.-W. & S.A.N. Goldstein. 1995. Subunit composition of minK potassium channels. Neuron 14: 1303-1309.
-
(1995)
Neuron
, vol.14
, pp. 1303-1309
-
-
Wang, K.-W.1
Goldstein, S.A.N.2
-
47
-
-
0030614462
-
The human Δ1261 mutation of the HERG potassium channel results in a truncated protein that contains a subunit interaction domain and decreases the channel expression
-
Li, X., J. Xu & M. Li. 1997. The human Δ1261 mutation of the HERG potassium channel results in a truncated protein that contains a subunit interaction domain and decreases the channel expression. J. Biol. Chem. 272: 705-708.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 705-708
-
-
Li, X.1
Xu, J.2
Li, M.3
-
48
-
-
0030054878
-
Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel
-
493.3
-
Schonherr, R. & S.H. Heinemann. 1996. Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel. J. Physiol. 493.3: 635-642.
-
(1996)
J. Physiol.
, pp. 635-642
-
-
Schonherr, R.1
Heinemann, S.H.2
-
49
-
-
0030012835
-
Missense mutation in the pore region of HERG causes familial long QT syndrome
-
Benson, D.W., C.A. MacRae, M.R. Vesely et al. 1996. Missense mutation in the pore region of HERG causes familial long QT syndrome. Circulation 93: 1791-1795.
-
(1996)
Circulation
, vol.93
, pp. 1791-1795
-
-
Benson, D.W.1
MacRae, C.A.2
Vesely, M.R.3
-
50
-
-
0029793031
-
Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome
-
Satler, C.A., E.P. Walsh, M.R. Vesely et al. 1996. Novel missense mutation in the cyclic nucleotide-binding domain of HERG causes long QT syndrome. Am. J. Med. Genet. 65: 27-35.
-
(1996)
Am. J. Med. Genet.
, vol.65
, pp. 27-35
-
-
Satler, C.A.1
Walsh, E.P.2
Vesely, M.R.3
-
51
-
-
0029831629
-
Genetically defined therapy of inherited long QT syndrome: Correction of abnormal repolarization by potassium
-
Compton, S., R. Lux, M. Ramsey et al. 1996. Genetically defined therapy of inherited long QT syndrome: Correction of abnormal repolarization by potassium. Circulation 94: 1018-1022.
-
(1996)
Circulation
, vol.94
, pp. 1018-1022
-
-
Compton, S.1
Lux, R.2
Ramsey, M.3
-
52
-
-
0030796370
-
Dominant-negative KVLQT1 mutations underlie the LQT1 form of long QT syndrome
-
Shalaby, F.Y., P.C. Levesque, W.-P. Yang et al. 1997. Dominant-negative KVLQT1 mutations underlie the LQT1 form of long QT syndrome. Circulation 96: 1733-1736.
-
(1997)
Circulation
, vol.96
, pp. 1733-1736
-
-
Shalaby, F.Y.1
Levesque, P.C.2
Yang, W.-P.3
-
53
-
-
0031054075
-
A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome
-
Neyroud, N., F. Tesson, I. Denjoy et al. 1997. A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome. Nature Genet. 15: 186-189.
-
(1997)
Nature Genet.
, vol.15
, pp. 186-189
-
-
Neyroud, N.1
Tesson, F.2
Denjoy, I.3
-
54
-
-
0031278313
-
KCNEI mutations cause Jervell and Lange-Nielsen syndrome
-
Schulze-Bahr E., Q. Wang, H. Wedekind et al. 1997. KCNEI mutations cause Jervell and Lange-Nielsen syndrome. Nature Genet. 17: 267-268.
-
(1997)
Nature Genet.
, vol.17
, pp. 267-268
-
-
Schulze-Bahr, E.1
Wang, Q.2
Wedekind, H.3
-
55
-
-
0031936234
-
Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of the long-QT syndrome
-
Duggal, P., M.R. Vesely, D. Wattanasirichaigoon et al. 1998. Mutation of the gene for IsK associated with both Jervell and Lange-Nielsen and Romano-Ward forms of the long-QT syndrome. Circulation 97: 142-146.
-
(1998)
Circulation
, vol.97
, pp. 142-146
-
-
Duggal, P.1
Vesely, M.R.2
Wattanasirichaigoon, D.3
|