-
1
-
-
0028263694
-
Auxiliary subunits of voltage-gated ion channels
-
L.L. Isom K.S. De Jongh W.A. Catterall Auxiliary subunits of voltage-gated ion channels Neuron 12 1994 1183 1194
-
(1994)
Neuron
, vol.12
, pp. 1183-1194
-
-
Isom, L.L.1
De Jongh, K.S.2
Catterall, W.A.3
-
2
-
-
0026610268
-
Voltage-sensitive Ca2+ channels
-
2+ channels J Biol Chem 267 1992 1403 1406
-
(1992)
J Biol Chem
, vol.267
, pp. 1403-1406
-
-
Miller, R.J.1
-
3
-
-
0028575955
-
Diversité moléculaire des canaux calciques: du gène à la fonction
-
J. Nargeot P. Charnet Diversité moléculaire des canaux calciques: du gène à la fonction Medécine/sciences 10 1994 1293 1308
-
(1994)
Medécine/sciences
, vol.10
, pp. 1293-1308
-
-
Nargeot, J.1
Charnet, P.2
-
4
-
-
0023654028
-
The voltage-sensitive sodium channel from rabbit skeletal muscle: Chemical characterization of subunits
-
R.H. Roberts R.L. Barchi The voltage-sensitive sodium channel from rabbit skeletal muscle: Chemical characterization of subunits J Biol Chem 262 1987 2298 2303
-
(1987)
J Biol Chem
, vol.262
, pp. 2298-2303
-
-
Roberts, R.H.1
Barchi, R.L.2
-
5
-
-
0024280869
-
Structure and function of voltage-sensitive ion channel
-
W.A. Catterall Structure and function of voltage-sensitive ion channel Science 242 1988 50 61
-
(1988)
Science
, vol.242
, pp. 50-61
-
-
Catterall, W.A.1
-
6
-
-
0023730471
-
The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel
-
K.P. Campbell A.T. Leung A.H. Sharp The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel Trends Neurosci 11 1988 425 430
-
(1988)
Trends Neurosci
, vol.11
, pp. 425-430
-
-
Campbell, K.P.1
Leung, A.T.2
Sharp, A.H.3
-
7
-
-
0028222121
-
An Escherichia coli homologue of eukaryotic potassium channel
-
R. Milkman An Escherichia coli homologue of eukaryotic potassium channel Proc Natl Acad Sci USA 91 1994 3510 3514
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3510-3514
-
-
Milkman, R.1
-
8
-
-
0027370976
-
Structure and fonction of voltage-gated ion channels
-
W.A. Catterall Structure and fonction of voltage-gated ion channels Trends Neurosci 16 1993 500 506
-
(1993)
Trends Neurosci
, vol.16
, pp. 500-506
-
-
Catterall, W.A.1
-
9
-
-
0025334586
-
Pursuing the structure and function of voltage-gated channels
-
H.R. Guy F. Conti Pursuing the structure and function of voltage-gated channels Trends Neurosci 13 1990 201 206
-
(1990)
Trends Neurosci
, vol.13
, pp. 201-206
-
-
Guy, H.R.1
Conti, F.2
-
10
-
-
0021123234
-
Primary structure of electrophorus electricus sodium channel deduced from cDNA sequence
-
M. Noda S. Shimizu T. Tanabe T. Takai T. Kayano T. Ikeda H. Takahashi H. Nakayama Y. Kanaoka K. Minamino K. Kangawa H. Matsuo M.A. Raftery T. Hirose S. Ianayama H. Hayashida T. Miyata S. Numa Primary structure of electrophorus electricus sodium channel deduced from cDNA sequence Nature 312 1984 121 127
-
(1984)
Nature
, vol.312
, pp. 121-127
-
-
Noda, M.1
Shimizu, S.2
Tanabe, T.3
Takai, T.4
Kayano, T.5
Ikeda, T.6
Takahashi, H.7
Nakayama, H.8
Kanaoka, Y.9
Minamino, K.10
Kangawa, K.11
Matsuo, H.12
Raftery, M.A.13
Hirose, T.14
Ianayama, S.15
Hayashida, H.16
Miyata, T.17
Numa, S.18
-
12
-
-
0021280174
-
Purification of the calcium antagonist receptor of the voltage-sensitive calcium channel from skeletal muscle transverse tubules
-
B.M. Curtis W.A. Catterall Purification of the calcium antagonist receptor of the voltage-sensitive calcium channel from skeletal muscle transverse tubules Biochemistry 23 1894 2113 2118
-
(1894)
Biochemistry
, vol.23
, pp. 2113-2118
-
-
Curtis, B.M.1
Catterall, W.A.2
-
13
-
-
0023261936
-
Primary structure of the receptor for calcium channel blockers from skeletal muscle
-
T. Tanabe H. Takeshima A. Mikami V. Flockerzi H. Takahashi K. Kangawa M. Kojima H. Matsuo T. Hirose S. Numa Primary structure of the receptor for calcium channel blockers from skeletal muscle Nature 328 1987 313 318
-
(1987)
Nature
, vol.328
, pp. 313-318
-
-
Tanabe, T.1
Takeshima, H.2
Mikami, A.3
Flockerzi, V.4
Takahashi, H.5
Kangawa, K.6
Kojima, M.7
Matsuo, H.8
Hirose, T.9
Numa, S.10
-
14
-
-
0024432331
-
Primary structure of the β subunit of the DHP-sensitive calcium channel from skeletal muscle
-
P. Ruth A. Röhrkasten M. Biel E. Bosse S. Regulla H.E. Meyer V. Flockerzi F. Hofmann Primary structure of the β subunit of the DHP-sensitive calcium channel from skeletal muscle Science 245 1989 1115 1118
-
(1989)
Science
, vol.245
, pp. 1115-1118
-
-
Ruth, P.1
Röhrkasten, A.2
Biel, M.3
Bosse, E.4
Regulla, S.5
Meyer, H.E.6
Flockerzi, V.7
Hofmann, F.8
-
15
-
-
0023753747
-
Sequence and expression of mRNAs encoding the α1 and α2 subunits of a DHP-sensitive calcium channel
-
S.B. Ellis M.E. Williams N.R. Ways R. Brenner A.H. Sharp A.T. Leung K.P. Campbell E. McKenna W.J. Koch A. Hui A. Schwartz M.M. Harpold Sequence and expression of mRNAs encoding the α 1 and α 2 subunits of a DHP-sensitive calcium channel Science 241 1988 1661 1664
-
(1988)
Science
, vol.241
, pp. 1661-1664
-
-
Ellis, S.B.1
Williams, M.E.2
Ways, N.R.3
Brenner, R.4
Sharp, A.H.5
Leung, A.T.6
Campbell, K.P.7
McKenna, E.8
Koch, W.J.9
Hui, A.10
Schwartz, A.11
Harpold, M.M.12
-
17
-
-
0025346565
-
The cDNA and deduced amino acid sequence of the γ subunit of the L-type calcium channel from rabbit skeletal muscle
-
E. Bosse S. Regulla M. Biel P. Ruth H.E. Meyer V. Flockerzi F. Hofmann The cDNA and deduced amino acid sequence of the γ subunit of the L-type calcium channel from rabbit skeletal muscle FEBS Lett 267 1990 153 156
-
(1990)
FEBS Lett
, vol.267
, pp. 153-156
-
-
Bosse, E.1
Regulla, S.2
Biel, M.3
Ruth, P.4
Meyer, H.E.5
Flockerzi, V.6
Hofmann, F.7
-
18
-
-
0024328801
-
Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel
-
A. Mikami K. Imoto T. Tanabe T. Niidome Y. Mori H. Takeshima S. Narumiya S. Numa Primary structure and functional expression of the cardiac dihydropyridine-sensitive calcium channel Nature 340 1989 230 233
-
(1989)
Nature
, vol.340
, pp. 230-233
-
-
Mikami, A.1
Imoto, K.2
Tanabe, T.3
Niidome, T.4
Mori, Y.5
Takeshima, H.6
Narumiya, S.7
Numa, S.8
-
19
-
-
0025183557
-
Primary structure and functional expression of a high-voltage-activated calcium channel from rabbit lung
-
M. Biel P. Ruth E. Bosse R. Hullin W. Stühmer V. Flockerzi F. Hofmann Primary structure and functional expression of a high-voltage-activated calcium channel from rabbit lung FEBS Lett 269 1990 409 412
-
(1990)
FEBS Lett
, vol.269
, pp. 409-412
-
-
Biel, M.1
Ruth, P.2
Bosse, E.3
Hullin, R.4
Stühmer, W.5
Flockerzi, V.6
Hofmann, F.7
-
20
-
-
0025775195
-
Primary structure and functional expression from complementary DNA of a brain calcium channel
-
Y. Mori T. Friedrich M.-S. Kim A. Mikami J. Nakai P. Ruth E. Bosse F. Hofmann V. Flockerzi T. Furuichi K. Mikoshiba K. Imoto T. Tanabe S. Numa Primary structure and functional expression from complementary DNA of a brain calcium channel Nature 350 1991 398 402
-
(1991)
Nature
, vol.350
, pp. 398-402
-
-
Mori, Y.1
Friedrich, T.2
Kim, M.-S.3
Mikami, A.4
Nakai, J.5
Ruth, P.6
Bosse, E.7
Hofmann, F.8
Flockerzi, V.9
Furuichi, T.10
Mikoshiba, K.11
Imoto, K.12
Tanabe, T.13
Numa, S.14
-
21
-
-
0024406855
-
Induction of calcium currents by the expression of the α1-subunit of the dihydropyridine receptor from skeletal muscle
-
E. Perez-Reyes H.S. Kim A.E. Lacerda W. Horne X. Wei D. Rampe K.P. Campbell A.M. Brown L. Birnbaumer Induction of calcium currents by the expression of the α 1-subunit of the dihydropyridine receptor from skeletal muscle Nature 340 1989 233 236
-
(1989)
Nature
, vol.340
, pp. 233-236
-
-
Perez-Reyes, E.1
Kim, H.S.2
Lacerda, A.E.3
Horne, W.4
Wei, X.5
Rampe, D.6
Campbell, K.P.7
Brown, A.M.8
Birnbaumer, L.9
-
22
-
-
0004306789
-
Molecular insights into regulation of L-type Ca channel function
-
P. Lory G. Varadi A. Schwartz Molecular insights into regulation of L-type Ca channel function News Physiol Sci 6 1991 277 281
-
(1991)
News Physiol Sci
, vol.6
, pp. 277-281
-
-
Lory, P.1
Varadi, G.2
Schwartz, A.3
-
23
-
-
0026572622
-
Heterologous expression of calcium channels
-
J. Nargeot N. Dascal H.A. Lester Heterologous expression of calcium channels J Membr Biol 126 1992 97 108
-
(1992)
J Membr Biol
, vol.126
, pp. 97-108
-
-
Nargeot, J.1
Dascal, N.2
Lester, H.A.3
-
25
-
-
0025912386
-
Acceleration of activation and inactivation by the β subunit of the skeletal muscle calcium channel
-
G. Varadi P. Lory D. Schultz M. Varadi A. Schwartz Acceleration of activation and inactivation by the β subunit of the skeletal muscle calcium channel Nature 352 1991 159 162
-
(1991)
Nature
, vol.352
, pp. 159-162
-
-
Varadi, G.1
Lory, P.2
Schultz, D.3
Varadi, M.4
Schwartz, A.5
-
27
-
-
0026604614
-
Structure and functional expression of α1, α2 and β subunits of a novel human neuronal calcium channel subtype
-
M.E. Williams D.H. Feldman A.F. McCue R. Brenner G. Velicelebi S.B. Ellis M.M. Harpold Structure and functional expression of α 1, α 2 and β subunits of a novel human neuronal calcium channel subtype Neuron 8 1992 71 84
-
(1992)
Neuron
, vol.8
, pp. 71-84
-
-
Williams, M.E.1
Feldman, D.H.2
McCue, A.F.3
Brenner, R.4
Velicelebi, G.5
Ellis, S.B.6
Harpold, M.M.7
-
28
-
-
0025822691
-
Normalization of current kinetics by interaction between the α1 and β subunits of the skeletal muscle dihydropyridine-sensitive Ca2+ channel
-
2+ channel Nature 352 1991 527 530
-
(1991)
Nature
, vol.352
, pp. 527-530
-
-
Lacerda, A.E.1
Kim, H.S.2
Ruth, P.3
Perez-Reyes, E.4
Flockerzi, V.5
Hofmann, F.6
Birnbaumer, L.7
Brown, A.M.8
-
29
-
-
0027420840
-
Stable co-expression of calcium channel α1, β, and α2/δ subunits in a somatic cell line
-
A. Welling E. Bosse A. Cavalié R. Bottlender A. Ludwig W. Nastainczyk V. Flockerzi F. Hofmann Stable co-expression of calcium channel α 1, β , and α 2/δ subunits in a somatic cell line J Physiol 471 1993 749 765
-
(1993)
J Physiol
, vol.471
, pp. 749-765
-
-
Welling, A.1
Bosse, E.2
Cavalié, A.3
Bottlender, R.4
Ludwig, A.5
Nastainczyk, W.6
Flockerzi, V.7
Hofmann, F.8
-
30
-
-
0342760063
-
Structure and function of skeletal muscle and cardiac dihydropyridine receptors
-
T. Tanabe Structure and function of skeletal muscle and cardiac dihydropyridine receptors Handbook of Membrane Channels (Chapt 11) 1994 177 186
-
(1994)
, pp. 177-186
-
-
Tanabe, T.1
-
31
-
-
0025330510
-
Muscular dysgenesis in mice: a model system for studying excitation-contraction coupling
-
B.A. Adams K.G. Beam Muscular dysgenesis in mice: a model system for studying excitation-contraction coupling FASEB J 4 1990 2809 2816
-
(1990)
FASEB J
, vol.4
, pp. 2809-2816
-
-
Adams, B.A.1
Beam, K.G.2
-
32
-
-
0025345444
-
Muscular dysgenesis: A model system for studying skeletal muscle development
-
J.A. Powell Muscular dysgenesis: A model system for studying skeletal muscle development FASEB J 4 1990 2798 2808
-
(1990)
FASEB J
, vol.4
, pp. 2798-2808
-
-
Powell, J.A.1
-
33
-
-
0023723765
-
Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA
-
T. Tanabe K.G. Beam J.A. Powell S. Numa Restoration of excitation-contraction coupling and slow calcium current in dysgenic muscle by dihydropyridine receptor complementary DNA Nature 336 1988 134 139
-
(1988)
Nature
, vol.336
, pp. 134-139
-
-
Tanabe, T.1
Beam, K.G.2
Powell, J.A.3
Numa, S.4
-
34
-
-
0025288735
-
Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling
-
T. Tanabe K.G. Beam B.A. Adams T. Niidome S. Numa Regions of the skeletal muscle dihydropyridine receptor critical for excitation-contraction coupling Nature 346 1990 567 569
-
(1990)
Nature
, vol.346
, pp. 567-569
-
-
Tanabe, T.1
Beam, K.G.2
Adams, B.A.3
Niidome, T.4
Numa, S.5
-
35
-
-
0025887092
-
Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics
-
T. Tanabe B.A. Adams S. Numa K.G. Beam Repeat I of the dihydropyridine receptor is critical in determining calcium channel activation kinetics Nature 352 1991 800 803
-
(1991)
Nature
, vol.352
, pp. 800-803
-
-
Tanabe, T.1
Adams, B.A.2
Numa, S.3
Beam, K.G.4
-
36
-
-
0028063942
-
Critical roles of the S3 segment and the S3-S4 linker of repeat I in activation of L-type calcium channels
-
J. Nakai B.A. Adams K. Imoto K.G. Beam Critical roles of the S3 segment and the S3-S4 linker of repeat I in activation of L-type calcium channels Proc Natl Acad Sci USA 91 1994 1014 1018
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 1014-1018
-
-
Nakai, J.1
Adams, B.A.2
Imoto, K.3
Beam, K.G.4
-
37
-
-
0027430335
-
Molecular localization of ion selectivity sites within the pore of a human L-type cardiac calcium channel
-
S. Tang G. Mikala A. Bahinski A. Yatani G. Varadi A. Schwartz Molecular localization of ion selectivity sites within the pore of a human L-type cardiac calcium channel J Biol Chem 268 1993 13026 13029
-
(1993)
J Biol Chem
, vol.268
, pp. 13026-13029
-
-
Tang, S.1
Mikala, G.2
Bahinski, A.3
Yatani, A.4
Varadi, G.5
Schwartz, A.6
-
39
-
-
0026517122
-
Calcium channel characteristics conferred on the sodium channel by single mutations
-
S.H. Heinemann H. Terlau W. Stühmer K. Imoto S. Numa Calcium channel characteristics conferred on the sodium channel by single mutations Nature 356 1992 441 443
-
(1992)
Nature
, vol.356
, pp. 441-443
-
-
Heinemann, S.H.1
Terlau, H.2
Stühmer, W.3
Imoto, K.4
Numa, S.5
-
40
-
-
0027731815
-
Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action
-
S. Tang A. Yatani A. Bahinski Y. Mori A. Schwartz Molecular localization of regions in the L-type calcium channel critical for dihydropyridine action Neuron 11 1993 1013 1021
-
(1993)
Neuron
, vol.11
, pp. 1013-1021
-
-
Tang, S.1
Yatani, A.2
Bahinski, A.3
Mori, Y.4
Schwartz, A.5
-
41
-
-
0028080195
-
Molecular determinants of voltage-dependent inactivation in calcium channels
-
J.-F. Zhang P.T. Ellinor R.W. Aldrich R.W. Tsien Molecular determinants of voltage-dependent inactivation in calcium channels Nature 372 1994 97 100
-
(1994)
Nature
, vol.372
, pp. 97-100
-
-
Zhang, J.-F.1
Ellinor, P.T.2
Aldrich, R.W.3
Tsien, R.W.4
-
42
-
-
0028179146
-
Calcium channel β-subunit binds to a conserved motif in the I-II cytoplasmic linker of the α1-subunit
-
M. Pragnell M. De Waard Y. Mori T. Tanabe T.P. Snutch K.P. Campbell Calcium channel β -subunit binds to a conserved motif in the I-II cytoplasmic linker of the α 1-subunit Nature 368 1994 67 70
-
(1994)
Nature
, vol.368
, pp. 67-70
-
-
Pragnell, M.1
De Waard, M.2
Mori, Y.3
Tanabe, T.4
Snutch, T.P.5
Campbell, K.P.6
-
43
-
-
0027662214
-
Structure, function and expression of voltage-dependent sodium channels
-
R.G. Kallen S.A. Cohen R.L. Barchi Structure, function and expression of voltage-dependent sodium channels Mol Neur 7 1993 383 428
-
(1993)
Mol Neur
, vol.7
, pp. 383-428
-
-
Kallen, R.G.1
Cohen, S.A.2
Barchi, R.L.3
-
44
-
-
0024692740
-
Primary structures and functionnal expression of mammalian skeletal muscle sodium channel
-
J.S. Trimmer S.S. Cooperman S.A. Tomiko J. Zhou S.M. Crean M.B. Boyle R.G. Kallen Z. Sheng R.L. Barchi F.J. Sigworth R.H. Goodman W.S. Agnew G. Mandel Primary structures and functionnal expression of mammalian skeletal muscle sodium channel Neuron 3 1989 33 49
-
(1989)
Neuron
, vol.3
, pp. 33-49
-
-
Trimmer, J.S.1
Cooperman, S.S.2
Tomiko, S.A.3
Zhou, J.4
Crean, S.M.5
Boyle, M.B.6
Kallen, R.G.7
Sheng, Z.8
Barchi, R.L.9
Sigworth, F.J.10
Goodman, R.H.11
Agnew, W.S.12
Mandel, G.13
-
47
-
-
0022442442
-
Messenger RNA coding for only the α subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes
-
A.L. Goldin T. Snutch H. Lübbert A. Dowsett J. Marshall V. Auld W. Downey L.C. Fritz H.A. Lester R. Dunn W.A. Catterall N. Davidson Messenger RNA coding for only the α subunit of the rat brain Na channel is sufficient for expression of functional channels in Xenopus oocytes Proc Natl Acad Sci USA 83 1986 7503 7507
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 7503-7507
-
-
Goldin, A.L.1
Snutch, T.2
Lübbert, H.3
Dowsett, A.4
Marshall, J.5
Auld, V.6
Downey, W.7
Fritz, L.C.8
Lester, H.A.9
Dunn, R.10
Catterall, W.A.11
Davidson, N.12
-
48
-
-
0024368695
-
Structural parts involved in activation and inactivation of the sodium channel
-
W. Stühmer F. Conti H. Suzuki X. Wang M. Noda N. Yahagi H. Kubo S. Numa Structural parts involved in activation and inactivation of the sodium channel Science 339 1989 597 603
-
(1989)
Science
, vol.339
, pp. 597-603
-
-
Stühmer, W.1
Conti, F.2
Suzuki, H.3
Wang, X.4
Noda, M.5
Yahagi, N.6
Kubo, H.7
Numa, S.8
-
49
-
-
0023784649
-
Identification of an intracellular peptide segment involved in sodium channel inactivation
-
P.M. Vassilev T. Scheuer W.A. Catterall Identification of an intracellular peptide segment involved in sodium channel inactivation Science 241 1988 1658 1661
-
(1988)
Science
, vol.241
, pp. 1658-1661
-
-
Vassilev, P.M.1
Scheuer, T.2
Catterall, W.A.3
-
51
-
-
0010444052
-
Familial periodic paralysis and its transition into spinal muscular atrophy
-
A. Biemond A.P. Daniels Familial periodic paralysis and its transition into spinal muscular atrophy Brain 57 1934 91 95
-
(1934)
Brain
, vol.57
, pp. 91-95
-
-
Biemond, A.1
Daniels, A.P.2
-
52
-
-
84933468777
-
Periodic paralysis
-
J.H. Talbott Periodic paralysis Medicine 20 1941 85 96
-
(1941)
Medicine
, vol.20
, pp. 85-96
-
-
Talbott, J.H.1
-
53
-
-
0002105117
-
Periodic paralysis
-
O.J.S. Buruna J.J. Schipperheyn Periodic paralysis P.J. Vinken G.W. Bruyn Handbook of Clinical Neurology 41 1979 North Holland Publishing Company Amsterdam 147 174
-
(1979)
, pp. 147-174
-
-
Buruna, O.J.S.1
Schipperheyn, J.J.2
-
54
-
-
0000869249
-
Periodic paralysis and paramyotonia congenita
-
F. Lehmann-Horn A.G. Engel K. Ricker R. Rüdel Periodic paralysis and paramyotonia congenita A.G. Engel C. Franzini-Armstrong Myology 2 1992 McGraw-Hill New York 1303 1334 2nd ed
-
(1992)
, pp. 1303-1334
-
-
Lehmann-Horn, F.1
Engel, A.G.2
Ricker, K.3
Rüdel, R.4
-
55
-
-
0028361074
-
Mapping of hypokalaemic periodic paralysis (HypoPP) to chromosome 1q31-q32 in three European families
-
B. Fontaine J.M. Vale Santos K. Jurkat-Rott J. Reboul E. Plassart C.S. Rime A. Elbaz R. Heine J. Guimaraes J. Weissenbach N. Baumann M. Fardeau F. Lehmann-Horn Mapping of hypokalaemic periodic paralysis (HypoPP) to chromosome 1q31-q32 in three European families Nature Genet 6 1994 267 272
-
(1994)
Nature Genet
, vol.6
, pp. 267-272
-
-
Fontaine, B.1
Vale Santos, J.M.2
Jurkat-Rott, K.3
Reboul, J.4
Plassart, E.5
Rime, C.S.6
Elbaz, A.7
Heine, R.8
Guimaraes, J.9
Weissenbach, J.10
Baumann, N.11
Fardeau, M.12
Lehmann-Horn, F.13
-
56
-
-
0028854326
-
Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): Genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 Caucasian families
-
A. Elbaz J. Vale-Santos K. Jurkat-Rott P. Lapie R.A. Ophoff B. Bady T.P. Links C. Puissan A. Villa N. Monnier G.W. Padberg K. Abe N. Feingold J. Guimaraes A.R. Wintzen J.H. Van Der Hoeven J.M. Saudubray J.P. Grunfeld G. Lenoir H. Nivet B. Echenne R.R. Frants M. Fardeau F. Lehmann-Horn B. Fontaine Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): Genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 Caucasian families Am J Hum Genet 56 1995 374 380
-
(1995)
Am J Hum Genet
, vol.56
, pp. 374-380
-
-
Elbaz, A.1
Vale-Santos, J.2
Jurkat-Rott, K.3
Lapie, P.4
Ophoff, R.A.5
Bady, B.6
Links, T.P.7
Puissan, C.8
Villa, A.9
Monnier, N.10
Padberg, G.W.11
Abe, K.12
Feingold, N.13
Guimaraes, J.14
Wintzen, A.R.15
Van Der Hoeven, J.H.16
Saudubray, J.M.17
Grunfeld, J.P.18
Lenoir, G.19
Nivet, H.20
Echenne, B.21
Frants, R.R.22
Fardeau, M.23
Lehmann-Horn, F.24
Fontaine, B.25
more..
-
58
-
-
0002571690
-
Periodic paralysis
-
A.G. Engel Periodic paralysis A.G. Engel C. Franzini-Armstrong Myology 2 1986 McGraw-Hill New York 1843 1870
-
(1986)
, pp. 1843-1870
-
-
Engel, A.G.1
-
60
-
-
34250554520
-
Weitere Mitteilung über die paroxysmale, familiärer Lähmung
-
S. Goldflam Weitere Mitteilung über die paroxysmale, familiärer Lähmung Dtsch Z Nervenheilk 7 1895 1 31
-
(1895)
Dtsch Z Nervenheilk
, vol.7
, pp. 1-31
-
-
Goldflam, S.1
-
62
-
-
0014818105
-
Acetazolamide treatment of hypokalemic periodic paralysis
-
R.C. Griggs W.K. Engel J.S. Resnick Acetazolamide treatment of hypokalemic periodic paralysis Ann Int Med 73 1970 39 48
-
(1970)
Ann Int Med
, vol.73
, pp. 39-48
-
-
Griggs, R.C.1
Engel, W.K.2
Resnick, J.S.3
-
63
-
-
0021368321
-
Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane paramaters
-
R. Rüdel F. Lehmann-Horn K. Ricker G. Küther Hypokalemic periodic paralysis: in vitro investigation of muscle fiber membrane paramaters Muscle Nerve 7 1984 110 120
-
(1984)
Muscle Nerve
, vol.7
, pp. 110-120
-
-
Rüdel, R.1
Lehmann-Horn, F.2
Ricker, K.3
Küther, G.4
-
65
-
-
0026475503
-
Exclusion of linkage between hypokalemic periodic paralysis (Hokpp) and three candidate loci
-
W.L. Casley M. Allon H.K. Cousin S.S. Ting M.A. Crackower L. Hashimoto F. Cornelis J.S. Beckmann A.J. Hudson G.C. Ebers Exclusion of linkage between hypokalemic periodic paralysis (Hokpp) and three candidate loci Genomics 14 1992 493 494
-
(1992)
Genomics
, vol.14
, pp. 493-494
-
-
Casley, W.L.1
Allon, M.2
Cousin, H.K.3
Ting, S.S.4
Crackower, M.A.5
Hashimoto, L.6
Cornelis, F.7
Beckmann, J.S.8
Hudson, A.J.9
Ebers, G.C.10
-
66
-
-
0028234647
-
Dihydropyridine receptor mutations cause hypokalemic periodic paralysis
-
L.J. Ptacek R. Tawil R.C. Griggs A.G. Engel R.B. Layzer H. Kwiecinski P.G. McManis L. Santiago M. Moore G. Fouad P. Bradley M.F. Leppert Dihydropyridine receptor mutations cause hypokalemic periodic paralysis Cell 77 1994 863 868
-
(1994)
Cell
, vol.77
, pp. 863-868
-
-
Ptacek, L.J.1
Tawil, R.2
Griggs, R.C.3
Engel, A.G.4
Layzer, R.B.5
Kwiecinski, H.6
McManis, P.G.7
Santiago, L.8
Moore, M.9
Fouad, G.10
Bradley, P.11
Leppert, M.F.12
-
67
-
-
0027965420
-
A calcium channel mutation causing hypokalemic periodic paralysis
-
K. Jurkat-Rott F. Lehmann-Horn A. Elbaz R. Heine R.G. Gregg K. Hogan P.A. Powers P. Lapie J.E. Vale-Santos J. Weissenbach B. Fontaine A calcium channel mutation causing hypokalemic periodic paralysis Hum Mol Genet 3 1994 1415 1419
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1415-1419
-
-
Jurkat-Rott, K.1
Lehmann-Horn, F.2
Elbaz, A.3
Heine, R.4
Gregg, R.G.5
Hogan, K.6
Powers, P.A.7
Lapie, P.8
Vale-Santos, J.E.9
Weissenbach, J.10
Fontaine, B.11
-
68
-
-
0028007559
-
Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP)
-
E. Plassart A. Elbaz J. Vale-Santos J. Reboul P. Lapie D. Chauveau K. Jurkat-Rott J. Guimaraes J.M. Saudubray J. Weissenbach F. Lehmann-Horn B. Fontaine Genetic heterogeneity in hypokalemic periodic paralysis (hypoPP) Hum Genet 94 1994 551 556
-
(1994)
Hum Genet
, vol.94
, pp. 551-556
-
-
Plassart, E.1
Elbaz, A.2
Vale-Santos, J.3
Reboul, J.4
Lapie, P.5
Chauveau, D.6
Jurkat-Rott, K.7
Guimaraes, J.8
Saudubray, J.M.9
Weissenbach, J.10
Lehmann-Horn, F.11
Fontaine, B.12
-
69
-
-
0027064887
-
A single nucleotide deletion in the skeletal muscle-specific calcium channel transcript of muscular dysgenesis (mdg) mice
-
N. Chaudhari A single nucleotide deletion in the skeletal muscle-specific calcium channel transcript of muscular dysgenesis (mdg) mice J Biol Chem 267 1992 25636 25639
-
(1992)
J Biol Chem
, vol.267
, pp. 25636-25639
-
-
Chaudhari, N.1
-
71
-
-
0022542027
-
Regulation of active Na+-K+ transport in skeletal muscle
-
+ transport in skeletal muscle Physiol Rev 66 1986 542 580
-
(1986)
Physiol Rev
, vol.66
, pp. 542-580
-
-
Clausen, T.1
-
72
-
-
77951421715
-
Adynamia episodica hereditaria
-
I. Gamstorp Adynamia episodica hereditaria Acta Paediatr 45 Suppl 108 1956 1 126
-
(1956)
Acta Paediatr
, vol.45
, Issue.Suppl 108
, pp. 1-126
-
-
Gamstorp, I.1
-
73
-
-
0001008501
-
Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia
-
F.H. Tyler F.E. Stephens F.D. Gunn G.T. Perkoff Clinical manifestations and inheritance of a type of periodic paralysis without hypopotassemia J Clin Invest 30 1951 492 502
-
(1951)
J Clin Invest
, vol.30
, pp. 492-502
-
-
Tyler, F.H.1
Stephens, F.E.2
Gunn, F.D.3
Perkoff, G.T.4
-
74
-
-
0028221445
-
Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: Phenotype to genotype correlations and demonstration of the predominance of two mutations
-
E. Plassart J. Reboul C.S. Rime D. Recan P. Millasseau B. Eymard J. Pelletier C. Thomas F. Chapon C. Desnuelle C. Confavreux B. Bady J. Martin G. Lenoir G. Serratrice M. Fardeau B. Fontaine Mutations in the muscle sodium channel gene (SCN4A) in 13 French families with hyperkalemic periodic paralysis and paramyotonia congenita: Phenotype to genotype correlations and demonstration of the predominance of two mutations Eur J Hum Genet 2 1994 110 124
-
(1994)
Eur J Hum Genet
, vol.2
, pp. 110-124
-
-
Plassart, E.1
Reboul, J.2
Rime, C.S.3
Recan, D.4
Millasseau, P.5
Eymard, B.6
Pelletier, J.7
Thomas, C.8
Chapon, F.9
Desnuelle, C.10
Confavreux, C.11
Bady, B.12
Martin, J.13
Lenoir, G.14
Serratrice, G.15
Fardeau, M.16
Fontaine, B.17
-
75
-
-
0025062007
-
Progressive myopathy in hyperkalemic periodic paralysis
-
W.G. Bradley R. Taylor D.R. Rice I. Hausmanowa-Petrusewicz L.S. Adelman M. Jenkison H. Jedrzejowska H. Drac W.N. Pendleburry Progressive myopathy in hyperkalemic periodic paralysis Arch Neurol 47 1990 1013 1017
-
(1990)
Arch Neurol
, vol.47
, pp. 1013-1017
-
-
Bradley, W.G.1
Taylor, R.2
Rice, D.R.3
Hausmanowa-Petrusewicz, I.4
Adelman, L.S.5
Jenkison, M.6
Jedrzejowska, H.7
Drac, H.8
Pendleburry, W.N.9
-
76
-
-
0022445799
-
Adynamia episodica and paralysis periodica paramyotonica
-
K. Ricker R. Rohkamm R. Bohlen Adynamia episodica and paralysis periodica paramyotonica Neurology 36 1986 682 686
-
(1986)
Neurology
, vol.36
, pp. 682-686
-
-
Ricker, K.1
Rohkamm, R.2
Bohlen, R.3
-
77
-
-
0025021977
-
Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family
-
S.M. Desilva R.H. Kunu J.W. Griffin D.R. Cornblath S. Chavoustie Paramyotonia congenita or hyperkalemic periodic paralysis? Clinical and electrophysiological features of each entity in one family Muscle Nerve 13 1990 21 26
-
(1990)
Muscle Nerve
, vol.13
, pp. 21-26
-
-
Desilva, S.M.1
Kunu, R.H.2
Griffin, J.W.3
Cornblath, D.R.4
Chavoustie, S.5
-
78
-
-
0000092558
-
Über eine familiäre, durch 6 generationen verfolgbare form congenitaler paramyotonie
-
A. Eulenburg Über eine familiäre, durch 6 generationen verfolgbare form congenitaler paramyotonie Neurologishes Zentralblatt 5 1886 265 272
-
(1886)
Neurologishes Zentralblatt
, vol.5
, pp. 265-272
-
-
Eulenburg, A.1
-
79
-
-
0026705098
-
The skeletal muscle chloride channel in dominant and recessive human myotonia
-
M.C. Koch K. Steinmeyer C. Lorenz K. Ricker F. Wolf M. Otto B. Zoll F. Lehmann-Horn K. Grzeschik J. Thomas The skeletal muscle chloride channel in dominant and recessive human myotonia Science 257 1992 797 800
-
(1992)
Science
, vol.257
, pp. 797-800
-
-
Koch, M.C.1
Steinmeyer, K.2
Lorenz, C.3
Ricker, K.4
Wolf, F.5
Otto, M.6
Zoll, B.7
Lehmann-Horn, F.8
Grzeschik, K.9
Thomas, J.10
-
81
-
-
0023140306
-
Adynamia episodica hereditaria with myotonia: A non-inactivating sodium current and the effect of extracellular pH
-
F. Lehmann-Horn G. Küther K. Ricker P. Grafe K. Ballanyi R. Rüdel Adynamia episodica hereditaria with myotonia: A non-inactivating sodium current and the effect of extracellular pH Muscle Nerve 10 1987 363 374
-
(1987)
Muscle Nerve
, vol.10
, pp. 363-374
-
-
Lehmann-Horn, F.1
Küther, G.2
Ricker, K.3
Grafe, P.4
Ballanyi, K.5
Rüdel, R.6
-
82
-
-
0025649547
-
Hyperkalemic periodic paralysis and the adult muscle sodium channel α-subunit gene
-
B. Fontaine T.S. Khurana E.P. Hoffman G.A.P. Bruns J.L. Haines J.A. Trofatter M.P. Hanson J. Rich H. McFarlane D.M. Yasek D. Romano J.F. Gusella R.H. Brown Jr Hyperkalemic periodic paralysis and the adult muscle sodium channel α -subunit gene Science 250 1990 1000 1002
-
(1990)
Science
, vol.250
, pp. 1000-1002
-
-
Fontaine, B.1
Khurana, T.S.2
Hoffman, E.P.3
Bruns, G.A.P.4
Haines, J.L.5
Trofatter, J.A.6
Hanson, M.P.7
Rich, J.8
McFarlane, H.9
Yasek, D.M.10
Romano, D.11
Gusella, J.F.12
Brown, R.H.13
-
84
-
-
0026094556
-
Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17
-
M.C. Koch K. Ricker M. Otto T. Grimm K. Bender B. Zoll P.S. Harper F. Lehmann-Horn R. Rüdel E.P. Hoffman Linkage data suggesting allelic heterogeneity for paramyotonia congenita and hyperkalemic periodic paralysis on chromosome 17 Hum Genet 88 1991 71 74
-
(1991)
Hum Genet
, vol.88
, pp. 71-74
-
-
Koch, M.C.1
Ricker, K.2
Otto, M.3
Grimm, T.4
Bender, K.5
Zoll, B.6
Harper, P.S.7
Lehmann-Horn, F.8
Rüdel, R.9
Hoffman, E.P.10
-
85
-
-
0025872004
-
Paramyotonia Congenita and Hyperkalemic Periodic Paralysis are linked to the adult muscle sodium channel gene
-
G.C. Ebers A.L. George R.L. Barchi S.S. Ting-Pasador R.G. Kallen G.M. Lathrop J.S. Beckman A.F. Hahn W.F. Brown R.D. Campbell A.J. Hudson Paramyotonia Congenita and Hyperkalemic Periodic Paralysis are linked to the adult muscle sodium channel gene Ann Neurol 30 1991 810 816
-
(1991)
Ann Neurol
, vol.30
, pp. 810-816
-
-
Ebers, G.C.1
George, A.L.2
Barchi, R.L.3
Ting-Pasador, S.S.4
Kallen, R.G.5
Lathrop, G.M.6
Beckman, J.S.7
Hahn, A.F.8
Brown, W.F.9
Campbell, R.D.10
Hudson, A.J.11
-
86
-
-
0025790174
-
Identification of a mutation in the gene causing hyperkalemic periodic paralysis
-
L.J. Ptàcek A.L. George R.C. Griggs R. Tawil R.G. Kallen R.L. Barchi M. Robertson M.F. Leppert Identification of a mutation in the gene causing hyperkalemic periodic paralysis Cell 67 1991 1021 1027
-
(1991)
Cell
, vol.67
, pp. 1021-1027
-
-
Ptàcek, L.J.1
George, A.L.2
Griggs, R.C.3
Tawil, R.4
Kallen, R.G.5
Barchi, R.L.6
Robertson, M.7
Leppert, M.F.8
-
88
-
-
0026937757
-
Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel
-
A.I. McClatchey D. McKenna-Yasek D. Cros H.G. Worthen R.W. Kuncl S.M. Desilva D.R. Cornblath J.F. Gusella R.H. Brown Jr Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel Nature Genet 2 1992 148 152
-
(1992)
Nature Genet
, vol.2
, pp. 148-152
-
-
McClatchey, A.I.1
McKenna-Yasek, D.2
Cros, D.3
Worthen, H.G.4
Kuncl, R.W.5
Desilva, S.M.6
Cornblath, D.R.7
Gusella, J.F.8
Brown, R.H.9
-
89
-
-
0026516209
-
Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita
-
A.I. McClatchey P. Van Den Berg M.A. Pericak-Vance W. Raskind C. Verellen D. McKenna-Yasek K. Rao J.L. Haines T. Bird R.H. Brown Jr J.F. Gusella Temperature-sensitive mutations in the III-IV cytoplasmic loop region of the skeletal muscle sodium channel gene in paramyotonia congenita Cell 68 1992 769 774
-
(1992)
Cell
, vol.68
, pp. 769-774
-
-
McClatchey, A.I.1
Van Den Berg, P.2
Pericak-Vance, M.A.3
Raskind, W.4
Verellen, C.5
McKenna-Yasek, D.6
Rao, K.7
Haines, J.L.8
Bird, T.9
Brown, R.H.10
Gusella, J.F.11
-
91
-
-
0027237778
-
A novel SCN4A mutation causing myotonia aggravated by cold and potassium
-
R. Heine U. Pika F. Lehmann-Horn A novel SCN4A mutation causing myotonia aggravated by cold and potassium Hum Mol Genet 2 1993 1349 1353
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1349-1353
-
-
Heine, R.1
Pika, U.2
Lehmann-Horn, F.3
-
92
-
-
0027522103
-
Human sodium channel myotonia: Slowed channel inactivation due to substitution for a glycine within the III-IV linker
-
H. Lerche R. Heine U. Pika A.L. George Jr N. Mitrovic M. Browatzki T. Weib M. Rivet-Bastide C. Franke M. Lomonaco K. Ricker F. Lehmann-Horn Human sodium channel myotonia: Slowed channel inactivation due to substitution for a glycine within the III-IV linker J Physiol 470 1993 13 22
-
(1993)
J Physiol
, vol.470
, pp. 13-22
-
-
Lerche, H.1
Heine, R.2
Pika, U.3
George, A.L.4
Mitrovic, N.5
Browatzki, M.6
Weib, T.7
Rivet-Bastide, M.8
Franke, C.9
Lomonaco, M.10
Ricker, K.11
Lehmann-Horn, F.12
-
93
-
-
0027468893
-
Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis
-
J.L. Ptacek L. Gouw H. Kwiecinski P. McManis J.R. Mendell R.J. Barohn A.L. George R.L. Barchi M. Robertson M.F. Leppert Sodium channel mutations in paramyotonia congenita and hyperkalemic periodic paralysis Ann Neurol 33 1993 300 307
-
(1993)
Ann Neurol
, vol.33
, pp. 300-307
-
-
Ptacek, J.L.1
Gouw, L.2
Kwiecinski, H.3
McManis, P.4
Mendell, J.R.5
Barohn, R.J.6
George, A.L.7
Barchi, R.L.8
Robertson, M.9
Leppert, M.F.10
-
94
-
-
0027248018
-
Workshop report: Non-dystrophic myotonias and periodic paralyses
-
F. Lehmann-Horn R. Rüdel K. Ricker Workshop report: Non-dystrophic myotonias and periodic paralyses Neuromusc Disord 3 1993 161 168
-
(1993)
Neuromusc Disord
, vol.3
, pp. 161-168
-
-
Lehmann-Horn, F.1
Rüdel, R.2
Ricker, K.3
-
95
-
-
0027991026
-
Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis
-
L.J. Ptacek R. Tawil R.C. Griggs G. Meola P. McManis R.J. Barohn J.R. Mendell C. Harris R. Spitzer F. Santiago M.F. Leppert Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis Neurology 44 1994 1500 1503
-
(1994)
Neurology
, vol.44
, pp. 1500-1503
-
-
Ptacek, L.J.1
Tawil, R.2
Griggs, R.C.3
Meola, G.4
McManis, P.5
Barohn, R.J.6
Mendell, J.R.7
Harris, C.8
Spitzer, R.9
Santiago, F.10
Leppert, M.F.11
-
96
-
-
0027460755
-
hyperkalemic periodic paralysis: Rapid molecular diagnosis and relationship of genotype to phenotype in 12 families
-
W.G. Feero J. Wang F. Barany J. Zhou S.M. Todorovic R. Convit G. Galloway I. Hausmanowa-Petrusewicz A. Fidzianska K. Arahata H.B. Wesel C. Wadelius H.G. Marks P. Hartlage H. Hayakawa E.P. Hoffman hyperkalemic periodic paralysis: Rapid molecular diagnosis and relationship of genotype to phenotype in 12 families Neurology 43 1993 668 673
-
(1993)
Neurology
, vol.43
, pp. 668-673
-
-
Feero, W.G.1
Wang, J.2
Barany, F.3
Zhou, J.4
Todorovic, S.M.5
Convit, R.6
Galloway, G.7
Hausmanowa-Petrusewicz, I.8
Fidzianska, A.9
Arahata, K.10
Wesel, H.B.11
Wadelius, C.12
Marks, H.G.13
Hartlage, P.14
Hayakawa, H.15
Hoffman, E.P.16
-
97
-
-
0027521859
-
Molecular genetic and genetic correlations in sodium channelopathies: Lack of founder effect and evidence for a second gene
-
J. Wang J. Zhou S.M. Todorovic W.G. Feero F. Barany R. Conwit I. Hausmanowa-Petrusewicz A. Fidzianska K. Arahata H.B. Wessel A. Sillen H.G. Marks P. Hartlage G. Galloway K. Ricker F. Lehmann-Horn H. Hayakawa E.P. Hoffman Molecular genetic and genetic correlations in sodium channelopathies: Lack of founder effect and evidence for a second gene Am J Hum Genet 52 1993 1074 1084
-
(1993)
Am J Hum Genet
, vol.52
, pp. 1074-1084
-
-
Wang, J.1
Zhou, J.2
Todorovic, S.M.3
Feero, W.G.4
Barany, F.5
Conwit, R.6
Hausmanowa-Petrusewicz, I.7
Fidzianska, A.8
Arahata, K.9
Wessel, H.B.10
Sillen, A.11
Marks, H.G.12
Hartlage, P.13
Galloway, G.14
Ricker, K.15
Lehmann-Horn, F.16
Hayakawa, H.17
Hoffman, E.P.18
-
98
-
-
0028361821
-
Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families
-
C. Meyer-Kleine M. Otto B. Zoll M.C. Koch Molecular and genetic characterisation of German families with paramyotonia congenita and demonstration of founder effect in the Ravensberg families Hum Genet 93 1994 707 710
-
(1994)
Hum Genet
, vol.93
, pp. 707-710
-
-
Meyer-Kleine, C.1
Otto, M.2
Zoll, B.3
Koch, M.C.4
-
99
-
-
0028061597
-
Myotonia fluctans. A third type of muscle sodium channel disease
-
K. Ricker R. Moxley III R. Heine F. Lehmann-Horn Myotonia fluctans. A third type of muscle sodium channel disease Arch Neurol 51 1994 1095 1102
-
(1994)
Arch Neurol
, vol.51
, pp. 1095-1102
-
-
Ricker, K.1
Moxley, R.2
Heine, R.3
Lehmann-Horn, F.4
-
102
-
-
0027409755
-
Functional expression of sodium channel mutations identified in families with periodic paralysis
-
S.C. Cannon S.M. Strittmatter Functional expression of sodium channel mutations identified in families with periodic paralysis Neuron 10 1993 317 326
-
(1993)
Neuron
, vol.10
, pp. 317-326
-
-
Cannon, S.C.1
Strittmatter, S.M.2
-
104
-
-
0028326016
-
Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation
-
M. Chahine A.L. George Jr M. Zhou W. Sun S. Ji R.L. Barchi R. Horn Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation Neuron 12 1994 281 294
-
(1994)
Neuron
, vol.12
, pp. 281-294
-
-
Chahine, M.1
George, A.L.2
Zhou, M.3
Sun, W.4
Ji, S.5
Barchi, R.L.6
Horn, R.7
-
105
-
-
0028128744
-
K+-aggravated myotonia: Destabilization of the inactivated state of the human muscle Na+ channel by the V1589M mutation
-
+ channel by the V1589M mutation J Physiol 478 1994 395 402
-
(1994)
J Physiol
, vol.478
, pp. 395-402
-
-
Mitrovich, N.1
George, A.L.2
Heine, R.3
Wagner, S.4
Pika, U.5
Hartlaub, U.6
Zhou, M.7
Lerche, H.8
Fahlke, C.H.9
Lehmann-Horn, F.10
-
106
-
-
0025774566
-
A sodium channel defect in hyperkalemic periodic paralysis: Potassium-induced failure of inactivation
-
S.C. Cannon R.H. Brown D.P. Corey A sodium channel defect in hyperkalemic periodic paralysis: Potassium-induced failure of inactivation Neuron 6 1991 619 626
-
(1991)
Neuron
, vol.6
, pp. 619-626
-
-
Cannon, S.C.1
Brown, R.H.2
Corey, D.P.3
|