-
1
-
-
13544257263
-
Transient gene expression in suspension HEK-293 cells: Application to large-scale protein production
-
DOI 10.1021/bp049830x
-
Baldi L, Muller N, Picasso S, Jacquet R, Girard P, Thanh HP, Derow E, Wurm FM (2005) Transient gene expression in suspension HEK-293 cells: application to large-scale protein production. Biotechnol Prog 21(1):148-153. doi:10.1021/bp049830x (Pubitemid 40218483)
-
(2005)
Biotechnology Progress
, vol.21
, Issue.1
, pp. 148-153
-
-
Baldi, L.1
Muller, N.2
Picasso, S.3
Jacquet, R.4
Girard, P.5
Huy, P.T.6
Derow, E.7
Wurm, F.M.8
-
2
-
-
0033564055
-
Activation and inactivation of the voltage-gated sodium channel: Role of segment S5 revealed by a novel hyperkalemic periodic paralysis mutation
-
Bendahhou S, Cummins TR, Tawil R, Waxman SG, Ptacek LJ (1999) Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalemic periodic paralysis mutation. The Journal of neuroscience : the official journal of the Society for Neuroscience 19(12):4762-4771
-
(1999)
The Journal of Neuroscience: The Official Journal of the Society for Neuroscience
, vol.19
, Issue.12
, pp. 4762-4771
-
-
Bendahhou, S.1
Cummins, T.R.2
Tawil, R.3
Waxman, S.G.4
Ptacek, L.J.5
-
3
-
-
0033842533
-
A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation
-
Bendahhou S, Cummins TR, Hahn AF, Langlois S, Waxman SG, Ptacek LJ (2000) A double mutation in families with periodic paralysis defines new aspects of sodium channel slow inactivation. J Clin Investig 106(3):431-438 (Pubitemid 30655643)
-
(2000)
Journal of Clinical Investigation
, vol.106
, Issue.3
, pp. 431-438
-
-
Bendahhou, S.1
Cummins, T.R.2
Hahn, A.F.3
Langlois, S.4
Waxman, S.G.5
Ptacek, L.J.6
-
4
-
-
84891919244
-
Mechanisms of a Human Skeletal Myotonia Produced by Mutation in the C-Terminus of NaV1.4: Is Ca(2 +) Regulation Defective?
-
Biswas S, Disilvestre DA, Dong P, Tomaselli GF (2013) Mechanisms of a Human Skeletal Myotonia Produced by Mutation in the C-Terminus of NaV1.4: is Ca(2 +) Regulation Defective? PLoS ONE 8(12):e81063
-
(2013)
PLoS ONE
, vol.8
, Issue.12
-
-
Biswas, S.1
Disilvestre, D.A.2
Dong, P.3
Tomaselli, G.F.4
-
5
-
-
0030998386
-
From mutation to myotonia in sodium channel disorders
-
Cannon SC (1997) From mutation to myotonia in sodium channel disorders. Neuromuscular disorders : NMD 7(4):241-249
-
(1997)
Neuromuscular Disorders: NMD
, vol.7
, Issue.4
, pp. 241-249
-
-
Cannon, S.C.1
-
6
-
-
0027409755
-
Functional expression of sodium channel mutations identified in families with periodic paralysis
-
DOI 10.1016/0896-6273(93)90321-H
-
Cannon SC, Strittmatter SM (1993) Functional expression of sodium channel mutations identified in families with periodic paralysis. Neuron 10(2):317-326 (Pubitemid 23079552)
-
(1993)
Neuron
, vol.10
, Issue.2
, pp. 317-326
-
-
Cannon, S.C.1
Strittmatter, S.M.2
-
7
-
-
0027236264
-
Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels
-
Cannon SC, Brown RH Jr, Corey DP (1993) Theoretical reconstruction of myotonia and paralysis caused by incomplete inactivation of sodium channels. Biophys J 65(1):270-288 (Pubitemid 23206060)
-
(1993)
Biophysical Journal
, vol.65
, Issue.1
, pp. 270-288
-
-
Cannon, S.C.1
Brown Jr., R.H.2
Corey, D.P.3
-
8
-
-
0028288443
-
Functional expression and properties of the human skeletal muscle sodium channel
-
Chahine M, Bennett PB, George AL Jr, Horn R (1994) Functional expression and properties of the human skeletal muscle sodium channel. Pflugers Arch 427(1-2):136-142 (Pubitemid 24131564)
-
(1994)
Pflugers Archiv European Journal of Physiology
, vol.427
, Issue.1-2
, pp. 136-142
-
-
Chahine, M.1
Bennett, P.B.2
George Jr., A.L.3
Horn, R.4
-
9
-
-
0036327041
-
Normokalemic periodic paralysis revisited: Does it exist?
-
DOI 10.1002/ana.10257
-
Chinnery PF, Walls TJ, Hanna MG, Bates D, Fawcett PR (2002) Normokalemic periodic paralysis revisited: does it exist? Annals of neurology 52(2):251-252 (Pubitemid 34810612)
-
(2002)
Annals of Neurology
, vol.52
, Issue.2
, pp. 251-252
-
-
Chinnery, P.F.1
Walls, T.J.2
Hanna, M.G.3
Bates, D.4
Fawcett, P.R.W.5
-
10
-
-
0029976727
-
Impaired slow inactivation in mutant sodium channels
-
Cummins TR, Sigworth FJ (1996) Impaired slow inactivation in mutant sodium channels. Biophys J 71(1):227-236 (Pubitemid 26227309)
-
(1996)
Biophysical Journal
, vol.71
, Issue.1
, pp. 227-236
-
-
Cummins, T.R.1
Sigworth, F.J.2
-
11
-
-
4644363063
-
The detection of a novel mutation by screening SCN4A gene in normokalemic periodic paralysis(write in Chinese)
-
Guo XH, Wu WP, Zhang YH, Zhu K (2004) The detection of a novel mutation by screening SCN4A gene in normokalemic periodic paralysis(write in Chinese). Chin J Neurol 37(3):199-202
-
(2004)
Chin J Neurol
, vol.37
, Issue.3
, pp. 199-202
-
-
Guo, X.H.1
Wu, W.P.2
Zhang, Y.H.3
Zhu, K.4
-
12
-
-
0029926886
-
Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker
-
DOI 10.1085/jgp.107.5.559
-
Hayward LJ, Brown RH Jr, Cannon SC (1996) Inactivation defects caused by myotonia-associated mutations in the sodium channel III-IV linker. J Gen Physiol 107(5):559-576 (Pubitemid 26140797)
-
(1996)
Journal of General Physiology
, vol.107
, Issue.5
, pp. 559-576
-
-
Hayward, L.J.1
Brown Jr., R.H.2
Cannon, S.C.3
-
13
-
-
0031052231
-
Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis
-
Hayward LJ, Brown RH Jr, Cannon SC (1997) Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis. Biophys J 72(3):1204-1219 (Pubitemid 27113644)
-
(1997)
Biophysical Journal
, vol.72
, Issue.3
, pp. 1204-1219
-
-
Hayward, L.J.1
Brown Jr., R.H.2
Cannon, S.C.3
-
14
-
-
0033594335
-
Defective slow inactivation of sodium channels contributes to familial periodic paralysis
-
Hayward LJ, Sandoval GM, Cannon SC (1999) Defective slow inactivation of sodium channels contributes to familial periodic paralysis. Neurology 52(7):1447-1453 (Pubitemid 29190539)
-
(1999)
Neurology
, vol.52
, Issue.7
, pp. 1447-1453
-
-
Hayward, L.J.1
Sandoval, G.M.2
Cannon, S.C.3
-
15
-
-
0040565182
-
Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current
-
Jurkat-Rott K, Mitrovic N, Hang C, Kouzmekine A, Iaizzo P, Herzog J, Lerche H, Nicole S, Vale-Santos J, Chauveau D, Fontaine B, Lehmann-Horn F (2000) Voltage-sensor sodium channel mutations cause hypokalemic periodic paralysis type 2 by enhanced inactivation and reduced current. Proc Natl Acad Sci USA 97(17):9549-9554 (Pubitemid 30650813)
-
(2000)
Proceedings of the National Academy of Sciences of the United States of America
, vol.97
, Issue.17
, pp. 9549-9554
-
-
Jurkat-Rott, K.1
Mitrovic, N.2
Hang, C.3
Kouzmekine, A.4
Iaizzo, P.5
Herzog, J.6
Lerche, H.7
Nicole, S.8
Vale-Santos, J.9
Chauveau, D.10
Fontaine, B.11
Lehmann-Horn, F.12
-
16
-
-
0030885219
-
Sodium channel inactivation is altered by substitution of voltage sensor positive charges
-
DOI 10.1085/jgp.110.4.403
-
Kontis KJ, Goldin AL (1997) Sodium channel inactivation is altered by substitution of voltage sensor positive charges. The Journal of general physiology 110(4):403-413 (Pubitemid 27431178)
-
(1997)
Journal of General Physiology
, vol.110
, Issue.4
, pp. 403-413
-
-
Kontis, K.J.1
Goldin, A.L.2
-
17
-
-
0036211354
-
Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalemic periodic paralysis type II
-
Kuzmenkin A, Muncan V, Jurkat-Rott K, Hang C, Lerche H, Lehmann-Horn F, Mitrovic N (2002) Enhanced inactivation and pH sensitivity of Na(+) channel mutations causing hypokalemic periodic paralysis type II. Brain : a journal of neurology 125(Pt 4):835-843
-
(2002)
Brain: A Journal of Neurology
, vol.125
, Issue.PART 4
, pp. 835-843
-
-
Kuzmenkin, A.1
Muncan, V.2
Jurkat-Rott, K.3
Hang, C.4
Lerche, H.5
Lehmann-Horn, F.6
Mitrovic, N.7
-
18
-
-
0032823307
-
Voltage-gated ion channels and hereditary disease
-
Lehmann-Horn F, Jurkat-Rott K (1999) Voltage-gated ion channels and hereditary disease. Physiol Rev 79(4):1317-1372 (Pubitemid 29473318)
-
(1999)
Physiological Reviews
, vol.79
, Issue.4
, pp. 1317-1372
-
-
Lehmann-Horn, F.1
Jurkat-Rott, K.2
-
19
-
-
0027248018
-
Non-dystrophic myotonias and periodic paralyses. A European Neuromuscular Center Workshop held 4-6 October 1992, Ulm, Germany
-
Lehmann-Horn F, Rudel R, Ricker K (1993) Non-dystrophic myotonias and periodic paralyses. A European Neuromuscular Center Workshop held 4-6 October 1992, Ulm, Germany. Neuromuscular disorders : NMD 3 (2):161-168
-
(1993)
Neuromuscular Disorders: NMD
, vol.3
, Issue.2
, pp. 161-168
-
-
Lehmann-Horn, F.1
Rudel, R.2
Ricker, K.3
-
20
-
-
0026439086
-
Amino acid residues required for fast Na(+)-channel inactivation: Charge neutralizations and deletions in the III-IV linker
-
Patton DE, West JW, Catterall WA, Goldin AL (1992) Amino acid residues required for fast Na(+)-channel inactivation: charge neutralizations and deletions in the III-IV linker. Proc Natl Acad Sci USA 89(22):10905-10909
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, Issue.22
, pp. 10905-10909
-
-
Patton, D.E.1
West, J.W.2
Catterall, W.A.3
Goldin, A.L.4
-
21
-
-
0009859210
-
A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride
-
Poskanzer DC, Kerr DN (1961) A third type of periodic paralysis, with normokalemia and favourable response to sodium chloride. The American journal of medicine 31:328-342
-
(1961)
The American Journal of Medicine
, vol.31
, pp. 328-342
-
-
Poskanzer, D.C.1
Kerr, D.N.2
-
22
-
-
0001969634
-
Ion channel disorders of muscle
-
Karpati GHJD, Griggs RC (eds) Cambridge University Press, Cambridge
-
Ptacek LJBS (2001) Ion channel disorders of muscle. In: Karpati GHJD, Griggs RC (eds) Disorders of voluntary muscle, 7th edn. Cambridge University Press, Cambridge, pp 604-635
-
(2001)
Disorders of Voluntary Muscle, 7th Edn.
, pp. 604-635
-
-
Ptacek, L.J.B.S.1
-
23
-
-
0028379446
-
Slow Na + channel inactivation must be disrupted to evoke prolonged depolarization-induced paralysis
-
Ruff RL (1994) Slow Na + channel inactivation must be disrupted to evoke prolonged depolarization-induced paralysis. Biophys J 66(2 Pt 1):542
-
(1994)
Biophys J
, vol.66
, Issue.2 PART 1
, pp. 542
-
-
Ruff, R.L.1
-
24
-
-
0023903168
-
Slow sodium channel inactivation in mammalian muscle: A possible role in regulating excitability
-
Ruff RL, Simoncini L, Stuhmer W (1988) Slow sodium channel inactivation in mammalian muscle: a possible role in regulating excitability. Muscle Nerve 11(5):502-510
-
(1988)
Muscle Nerve
, vol.11
, Issue.5
, pp. 502-510
-
-
Ruff, R.L.1
Simoncini, L.2
Stuhmer, W.3
-
25
-
-
58149395036
-
Depolarization-activated gating pore current conducted by mutant sodium channels in potassium-sensitive normokalemic periodic paralysis
-
Sokolov S, Scheuer T, Catterall WA (2008) Depolarization-activated gating pore current conducted by mutant sodium channels in potassium-sensitive normokalemic periodic paralysis. Proc Natl Acad Sci USA 105(50):19980-19985
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, Issue.50
, pp. 19980-19985
-
-
Sokolov, S.1
Scheuer, T.2
Catterall, W.A.3
-
26
-
-
0034554770
-
The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation
-
Struyk AF, Scoggan KA, Bulman DE, Cannon SC (2000) The human skeletal muscle Na channel mutation R669H associated with hypokalemic periodic paralysis enhances slow inactivation. The Journal of neuroscience : the official journal of the Society for Neuroscience 20(23):8610-8617
-
(2000)
The Journal of Neuroscience: The Official Journal of the Society for Neuroscience
, vol.20
, Issue.23
, pp. 8610-8617
-
-
Struyk, A.F.1
Scoggan, K.A.2
Bulman, D.E.3
Cannon, S.C.4
-
27
-
-
53549107219
-
Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: Saturation of ion flux and implications for disease pathogenesis
-
Struyk AF, Markin VS, Francis D, Cannon SC (2008) Gating pore currents in DIIS4 mutations of NaV1.4 associated with periodic paralysis: saturation of ion flux and implications for disease pathogenesis. The Journal of general physiology 132(4):447-464
-
(2008)
The Journal of General Physiology
, vol.132
, Issue.4
, pp. 447-464
-
-
Struyk, A.F.1
Markin, V.S.2
Francis, D.3
Cannon, S.C.4
-
28
-
-
10444273389
-
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
-
Vicart S, Sternberg D, Fournier E, Ochsner F, Laforet P, Kuntzer T, Eymard B, Hainque B, Fontaine B (2004) New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis. Neurology 63(11):2120-2127 (Pubitemid 39636261)
-
(2004)
Neurology
, vol.63
, Issue.11
, pp. 2120-2127
-
-
Vicart, S.1
Sternberg, D.2
Fournier, E.3
Ochsner, F.4
Laforet, P.5
Kuntzer, T.6
Eymard, B.7
Hainque, B.8
Fontaine, B.9
-
29
-
-
0342547301
-
A mutation in segment I-S6 alters slow inactivation of sodium channels
-
Wang SY, Wang GK (1997) A mutation in segment I-S6 alters slow inactivation of sodium channels. Biophys J 72(4):1633-1640
-
(1997)
Biophys J
, vol.72
, Issue.4
, pp. 1633-1640
-
-
Wang, S.Y.1
Wang, G.K.2
-
30
-
-
0026483172
-
A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation
-
West JW, Patton DE, Scheuer T, Wang Y, Goldin AL, Catterall WA (1992) A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation. Proc Natl Acad Sci USA 89(22):10910-10914
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, Issue.22
, pp. 10910-10914
-
-
West, J.W.1
Patton, D.E.2
Scheuer, T.3
Wang, Y.4
Goldin, A.L.5
Catterall, W.A.6
-
31
-
-
0142107369
-
+ channels expressed in mammalian cell lines and Xenopus oocytes
-
DOI 10.1016/S1056-8719(03)00041-8
-
Witchel HJ, Milnes JT, Mitcheson JS, Hancox JC (2002) Troubleshooting problems with in vitro screening of drugs for QT interval prolongation using HERG K + channels expressed in mammalian cell lines and Xenopus oocytes. J Pharmacol Toxicol Methods 48(2):65-80 (Pubitemid 37288933)
-
(2002)
Journal of Pharmacological and Toxicological Methods
, vol.48
, Issue.2
, pp. 65-80
-
-
Witchel, H.J.1
Milnes, J.T.2
Mitcheson, J.S.3
Hancox, J.C.4
-
32
-
-
46149083720
-
Mutations of sodium channel alpha-subunit genes in Chinese patients with normokalemic periodic paralysis
-
DOI 10.1007/s10571-007-9231-4
-
Xiuhai G, Weiping W, Ke Z, Hongbin W, Yiling S, MaoYanling (2008) Mutations of sodium channel alpha-subunit genes in Chinese patients with normokalemic periodic paralysis. Cell Mol Neurobiol 28(5):653-661 (Pubitemid 351905071)
-
(2008)
Cellular and Molecular Neurobiology
, vol.28
, Issue.5
, pp. 653-661
-
-
Xiuhai, G.1
Weiping, W.2
Ke, Z.3
Hongbin, W.4
Yiling, S.5
Maoyanling6
|