메뉴 건너뛰기




Volumn 868, Issue , 1999, Pages 406-413

Dysfunction of delayed rectifier potassium channels in an inherited cardiac arrhythmia

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; MUTANT PROTEIN; POTASSIUM CHANNEL; POTASSIUM ION;

EID: 0032970148     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.1999.tb11302.x     Document Type: Conference Paper
Times cited : (75)

References (55)
  • 1
    • 0028124225 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • + 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 scopus 로고
    • + 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 scopus 로고
    • + 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 scopus 로고
    • + 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 scopus 로고
    • + 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 scopus 로고
    • + 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 scopus 로고
    • 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • + 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 scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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 scopus 로고    scopus 로고
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.