-
1
-
-
0029560754
-
Episodic ataxia results from voltage-dependent potassium channels with altered functions
-
Adelman JP, Bond CT, Pessia M, Maylie J Episodic ataxia results from voltage-dependent potassium channels with altered functions. Neuron 1995, 15:1449-1454.
-
(1995)
Neuron
, vol.15
, pp. 1449-1454
-
-
Adelman, J.P.1
Bond, C.T.2
Pessia, M.3
Maylie, J.4
-
2
-
-
0034954467
-
Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man
-
Alekov AK, et al. Enhanced inactivation and acceleration of activation of the sodium channel associated with epilepsy in man. Eur J Neurosci 2001, 13:2171-2176.
-
(2001)
Eur J Neurosci
, vol.13
, pp. 2171-2176
-
-
Alekov, A.K.1
-
3
-
-
0035030766
-
First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene
-
Baulac S, et al. First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene. Nat Genet 2001, 28:46-48.
-
(2001)
Nat Genet
, vol.28
, pp. 46-48
-
-
Baulac, S.1
-
4
-
-
0036663012
-
Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans
-
Bianchi MT, Song L, Zhang H, Macdonald RL Two different mechanisms of disinhibition produced by GABAA receptor mutations linked to epilepsy in humans. J Neurosci 2002, 22:5321-5327.
-
(2002)
J Neurosci
, vol.22
, pp. 5321-5327
-
-
Bianchi, M.T.1
Song, L.2
Zhang, H.3
Macdonald, R.L.4
-
5
-
-
0032536030
-
A potassium channel mutation in neonatal human epilepsy
-
Biervert C, et al. A potassium channel mutation in neonatal human epilepsy. Science 1998, 279:403-406.
-
(1998)
Science
, vol.279
, pp. 403-406
-
-
Biervert, C.1
-
6
-
-
0028124225
-
Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 [see comments]
-
Browne DL, et al. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1 [see comments]. Nat Genet 1994, 8:136-140.
-
(1994)
Nat Genet
, vol.8
, pp. 136-140
-
-
Browne, D.L.1
-
7
-
-
0029962877
-
A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors
-
Brune W, et al. A GLRA1 null mutation in recessive hyperekplexia challenges the functional role of glycine receptors. Am J Hum Genet 1996, 58:989-997.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 989-997
-
-
Brune, W.1
-
8
-
-
0028029561
-
A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death
-
Buckwalter MS, et al. A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. Hum Mol Genet 1994, 3:2025-2030.
-
(1994)
Hum Mol Genet
, vol.3
, pp. 2025-2030
-
-
Buckwalter, M.S.1
-
9
-
-
0031974209
-
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family [see comments]
-
Charlier C, et al. A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family [see comments]. Nat Genet 1998, 18:53-55.
-
(1998)
Nat Genet
, vol.18
, pp. 53-55
-
-
Charlier, C.1
-
10
-
-
0034987073
-
De novo mutations in the sodium-channel gene scn la cause severe myoclonic epilepsy of infancy
-
Claes L, et al. De novo mutations in the sodium-channel gene scn la cause severe myoclonic epilepsy of infancy. Am J Hum Genet 2001, 68:1327-1332.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1327-1332
-
-
Claes, L.1
-
11
-
-
18544364797
-
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy
-
Cossette P, et al. Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy. Nat Genet 2002, 31:184-189.
-
(2002)
Nat Genet
, vol.31
, pp. 184-189
-
-
Cossette, P.1
-
12
-
-
0033763090
-
The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy
-
De Fusco M, et al. The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy. Nat Genet 2000, 26:275-276.
-
(2000)
Nat Genet
, vol.26
, pp. 275-276
-
-
De Fusco, M.1
-
13
-
-
0035834007
-
Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel
-
Dedek K, et al. Myokymia and neonatal epilepsy caused by a mutation in the voltage sensor of the KCNQ2 K+ channel. Proc Natl Acad Sci U S A 2001, 98:12272-12277.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 12272-12277
-
-
Dedek, K.1
-
14
-
-
0034115766
-
Topiramate as an inhibitor of carbonic anhydrase isoenzymes
-
Dodgson SJ, Shank RP, Maryanoff BE Topiramate as an inhibitor of carbonic anhydrase isoenzymes. Epilepsia 2000, 41:S35-S39.
-
(2000)
Epilepsia
, vol.41
-
-
Dodgson, S.J.1
Shank, R.P.2
Maryanoff, B.E.3
-
15
-
-
0037310734
-
Spreading acidification and depression in the cerebellar cortex
-
Ebner TJ, Chen G Spreading acidification and depression in the cerebellar cortex. Neuroscientist 2003, 9:37-45.
-
(2003)
Neuroscientist
, vol.9
, pp. 37-45
-
-
Ebner, T.J.1
Chen, G.2
-
16
-
-
0033910736
-
Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia
-
Escayg A, et al. Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia. Am J Hum Genet 2000, 66:1531-1539.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1531-1539
-
-
Escayg, A.1
-
17
-
-
0034069651
-
Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 [In Process Citation]
-
Escayg A, et al. Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2 [In Process Citation]. Nat Genet 2000, 24:343-345.
-
(2000)
Nat Genet
, vol.24
, pp. 343-345
-
-
Escayg, A.1
-
18
-
-
0033797135
-
Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability [In Process Citation]
-
Funson LH, et al. Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability [In Process Citation]. Ann Neurol 2000, 48:647-656.
-
(2000)
Ann Neurol
, vol.48
, pp. 647-656
-
-
Funson, L.H.1
-
19
-
-
0030584085
-
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
-
Fletcher CF, et al. Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell 1996, 87:607-617.
-
(1996)
Cell
, vol.87
, pp. 607-617
-
-
Fletcher, C.F.1
-
20
-
-
20244386070
-
Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity
-
Fletcher CF, et al. Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity. FASEB J 2001, 15:1288-1290.
-
(2001)
FASEB J
, vol.15
, pp. 1288-1290
-
-
Fletcher, C.F.1
-
21
-
-
0032872916
-
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
-
Friend KL, et al. Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM. Hum Genet 1999, 105:261-265.
-
(1999)
Hum Genet
, vol.105
, pp. 261-265
-
-
Friend, K.L.1
-
22
-
-
0035089729
-
Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2
-
Guida S, et al. Complete loss of P/Q calcium channel activity caused by a CACNA1A missense mutation carried by patients with episodic ataxia type 2. Am J Hum Genet 2001, 68:759-764.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 759-764
-
-
Guida, S.1
-
23
-
-
0034727607
-
Acetazolamide treatment for migraine aura status
-
Haan J, Sluis P, Sluis LH, Ferrari MD Acetazolamide treatment for migraine aura status. Neurology 2000, 55:1588-1589.
-
(2000)
Neurology
, vol.55
, pp. 1588-1589
-
-
Haan, J.1
Sluis, P.2
Sluis, L.H.3
Ferrari, M.D.4
-
24
-
-
0033103648
-
Functional consequences of mutations in the human alpha 1A calcium channel subunit linked to familial hemiplegic migraine
-
Hans M, et al. Functional consequences of mutations in the human alpha 1A calcium channel subunit linked to familial hemiplegic migraine. J Neurosci 1999, 19:1610-1619.
-
(1999)
J Neurosci
, vol.19
, pp. 1610-1619
-
-
Hans, M.1
-
25
-
-
0344091562
-
Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies
-
Haug K, et al. Mutations in CLCN2 encoding a voltage-gated chloride channel are associated with idiopathic generalized epilepsies. Nat Genet 2003, 33:527-532.
-
(2003)
Nat Genet
, vol.33
, pp. 527-532
-
-
Haug, K.1
-
26
-
-
0037077834
-
Sodium-channel defects in benign familial neonatal-infantile seizures
-
Heron SE, et al. Sodium-channel defects in benign familial neonatal-infantile seizures. Lancet 2002, 360:851-852.
-
(2002)
Lancet
, vol.360
, pp. 851-852
-
-
Heron, S.E.1
-
27
-
-
0345074135
-
A mouse model of episodic ataxia type-1
-
Herson PS, et al. A mouse model of episodic ataxia type-1. Nat Neurosci 2003, 6:378-383.
-
(2003)
Nat Neurosci
, vol.6
, pp. 378-383
-
-
Herson, P.S.1
-
28
-
-
0035954366
-
Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells
-
Ishikawa K, et al. Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells. Neurology 2001, 56:1753-1756.
-
(2001)
Neurology
, vol.56
, pp. 1753-1756
-
-
Ishikawa, K.1
-
29
-
-
0035828406
-
Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel
-
Jouvenceau A, et al. Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel. Lancet 2001, 358:801-807.
-
(2001)
Lancet
, vol.358
, pp. 801-807
-
-
Jouvenceau, A.1
-
30
-
-
0033593005
-
Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit
-
Jun K, et al. Ablation of P/Q-type Ca(2+) channel currents, altered synaptic transmission, and progressive ataxia in mice lacking the alpha(1A)-subunit. Proc Natl Acad Sci U S A 1999, 96:15245-15250.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 15245-15250
-
-
Jun, K.1
-
31
-
-
0032489525
-
Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics
-
Kraus RL, et al. Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics. J Biol Chem 1998, 273:5586-5590.
-
(1998)
J Biol Chem
, vol.273
, pp. 5586-5590
-
-
Kraus, R.L.1
-
32
-
-
0036260284
-
The neuronal channelopathies
-
Kullmann DM The neuronal channelopathies. Brain 2002, 125:1177-1195.
-
(2002)
Brain
, vol.125
, pp. 1177-1195
-
-
Kullmann, D.M.1
-
33
-
-
0035139497
-
The inherited episodic ataxias: how well do we understand the disease mechanisms?
-
Kullmann DM, Rea R, Spauschus A, Jouvenceau A The inherited episodic ataxias: how well do we understand the disease mechanisms?. Neuroscientist 2001, 7:80-88.
-
(2001)
Neuroscientist
, vol.7
, pp. 80-88
-
-
Kullmann, D.M.1
Rea, R.2
Spauschus, A.3
Jouvenceau, A.4
-
34
-
-
0028016521
-
Decreased agonist affinity and chloride conductance of mutant glycine receptors associated with human hereditary hyperekplexia
-
Langosch D, et al. Decreased agonist affinity and chloride conductance of mutant glycine receptors associated with human hereditary hyperekplexia. EMBO J 1994, 13:4223-4228.
-
(1994)
EMBO J
, vol.13
, pp. 4223-4228
-
-
Langosch, D.1
-
35
-
-
0032832304
-
A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions
-
Lerche H, et al. A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions. Ann Neurol 1999, 46:305-312.
-
(1999)
Ann Neurol
, vol.46
, pp. 305-312
-
-
Lerche, H.1
-
36
-
-
0032520102
-
Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes
-
Lewis TM, et al. Properties of human glycine receptors containing the hyperekplexia mutation alpha1(K276E), expressed in Xenopus oocytes. J Physiol 1998, 507:25-40.
-
(1998)
J Physiol
, vol.507
, pp. 25-40
-
-
Lewis, T.M.1
-
37
-
-
0032526434
-
Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner
-
Lorenzon NM, Lutz CM, Frankel WN, Beam KG Altered calcium channel currents in Purkinje cells of the neurological mutant mouse leaner. J Neurosci 1998, 18:4482-4489.
-
(1998)
J Neurosci
, vol.18
, pp. 4482-4489
-
-
Lorenzon, N.M.1
Lutz, C.M.2
Frankel, W.N.3
Beam, K.G.4
-
38
-
-
0037071896
-
Molecular basis of an inherited epilepsy
-
Lossin C, et al. Molecular basis of an inherited epilepsy. Neuron 2002, 34:877-884.
-
(2002)
Neuron
, vol.34
, pp. 877-884
-
-
Lossin, C.1
-
39
-
-
0033916576
-
Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine
-
Main MJ, et al. Modulation of KCNQ2/3 potassium channels by the novel anticonvulsant retigabine. Mol Pharmacol 2000, 58:253-262.
-
(2000)
Mol Pharmacol
, vol.58
, pp. 253-262
-
-
Main, M.J.1
-
40
-
-
4243341823
-
Direct alteration of the P/Q-type Ca2+ channel property by polyglutamine expansion in spinocerebellar ataxia 6
-
Matsuyama Z, et al. Direct alteration of the P/Q-type Ca2+ channel property by polyglutamine expansion in spinocerebellar ataxia 6. J Neurosci 1999, 19:RC14.
-
(1999)
J Neurosci
, vol.19
-
-
Matsuyama, Z.1
-
41
-
-
16044370232
-
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4
-
Ophoff RA, et al. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4. Cell 1996, 87:543-552.
-
(1996)
Cell
, vol.87
, pp. 543-552
-
-
Ophoff, R.A.1
-
42
-
-
0035163074
-
CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy
-
Phillips HA, et al. CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy. Am J Hum Genet 2001, 68:225-231.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 225-231
-
-
Phillips, H.A.1
-
43
-
-
0004529124
-
Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepine
-
Picard F, Bertrand S, Steinlein OK, Bertrand D Mutated nicotinic receptors responsible for autosomal dominant nocturnal frontal lobe epilepsy are more sensitive to carbamazepine. Epilepsia 1999, 40:1198-1209.
-
(1999)
Epilepsia
, vol.40
, pp. 1198-1209
-
-
Picard, F.1
Bertrand, S.2
Steinlein, O.K.3
Bertrand, D.4
-
44
-
-
0035576276
-
Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6
-
Piedras-Renteria ES, et al. Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6. J Neurosci 2001, 21:9185-9193.
-
(2001)
J Neurosci
, vol.21
, pp. 9185-9193
-
-
Piedras-Renteria, E.S.1
-
45
-
-
0036400556
-
Variable K+ channel subunit dysfunction in inherited mutations of KCNA1
-
Rea R, et al. Variable K+ channel subunit dysfunction in inherited mutations of KCNA1. J Physiol 2002, 538:5-23.
-
(2002)
J Physiol
, vol.538
, pp. 5-23
-
-
Rea, R.1
-
46
-
-
0036977495
-
Functional characterisation of compound heterozygosity for GlyR 1 mutations in the startle disease hyperekplexia
-
Rea R, et al. Functional characterisation of compound heterozygosity for GlyR 1 mutations in the startle disease hyperekplexia. Eur J Neurosci 2002, 16:186-196.
-
(2002)
Eur J Neurosci
, vol.16
, pp. 186-196
-
-
Rea, R.1
-
47
-
-
0034279182
-
The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes
-
Restituito S, et al. The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes. J Neurosci 2000, 20:6394-6403.
-
(2000)
J Neurosci
, vol.20
, pp. 6394-6403
-
-
Restituito, S.1
-
48
-
-
0032542232
-
Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy
-
Schroeder BC, Kubisch C, Stein V, Jentsch TJ Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy. Nature 1998, 396:687-690.
-
(1998)
Nature
, vol.396
, pp. 687-690
-
-
Schroeder, B.C.1
Kubisch, C.2
Stein, V.3
Jentsch, T.J.4
-
49
-
-
0027330927
-
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia
-
Shiang R, et al. Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexia. Nat Genet 1993, 5:351-358.
-
(1993)
Nat Genet
, vol.5
, pp. 351-358
-
-
Shiang, R.1
-
50
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns [see comments]
-
Singh NA, et al. A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns [see comments]. Nat Genet 1998, 18:25-29.
-
(1998)
Nat Genet
, vol.18
, pp. 25-29
-
-
Singh, N.A.1
-
51
-
-
0028980028
-
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
-
Steinlein OK, et al. A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nat Genet 1995, 11:201-203.
-
(1995)
Nat Genet
, vol.11
, pp. 201-203
-
-
Steinlein, O.K.1
-
52
-
-
14344277590
-
A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction
-
Sugawara T, et al. A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction. Proc Natl Acad Sci U S A 2001, 98:6384-6389.
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 6384-6389
-
-
Sugawara, T.1
-
53
-
-
0036279411
-
Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
-
Terwindt G, et al. Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine. Arch Neurol 2002, 59:1016-1018.
-
(2002)
Arch Neurol
, vol.59
, pp. 1016-1018
-
-
Terwindt, G.1
-
54
-
-
0036792027
-
Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons
-
Tottene A, et al. Familial hemiplegic migraine mutations increase Ca(2+) influx through single human CaV2.1 channels and decrease maximal CaV2.1 current density in neurons. Proc Natl Acad Sci U S A 2002, 99:13284-13289.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 13284-13289
-
-
Tottene, A.1
-
55
-
-
0035033520
-
Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures
-
Wallace RH, et al. Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures. Nat Genet 2001, 28:49-52.
-
(2001)
Nat Genet
, vol.28
, pp. 49-52
-
-
Wallace, R.H.1
-
56
-
-
17344367657
-
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1, subunit gene SCN1B
-
Wallace RH, et al. Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1, subunit gene SCN1B. Nat Genet 1998, 19:366-370.
-
(1998)
Nat Genet
, vol.19
, pp. 366-370
-
-
Wallace, R.H.1
-
57
-
-
0032483972
-
KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel
-
Wang HS, et al. KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel. Science 1998, 282:1890-1893.
-
(1998)
Science
, vol.282
, pp. 1890-1893
-
-
Wang, H.S.1
-
58
-
-
0036510532
-
Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia
-
Wappl E, et al. Functional consequences of P/Q-type Ca2+ channel Cav2.1 missense mutations associated with episodic ataxia type 2 and progressive ataxia. J Biol Chem 2002, 277:6960-6966.
-
(2002)
J Biol Chem
, vol.277
, pp. 6960-6966
-
-
Wappl, E.1
-
59
-
-
0033862433
-
Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels
-
Wickenden AD, et al. Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels. Mol Pharmacol 2000, 58:591-600.
-
(2000)
Mol Pharmacol
, vol.58
, pp. 591-600
-
-
Wickenden, A.D.1
-
60
-
-
0033561477
-
Specific alteration of spontaneous GABAergic inhibition in cerebellar Purkinje cells in mice lacking the potassium channel Kv1.1
-
Zhang CL, Messing A, Chiu SY Specific alteration of spontaneous GABAergic inhibition in cerebellar Purkinje cells in mice lacking the potassium channel Kv1.1. J Neurosci 1999, 19:2852-2864.
-
(1999)
J Neurosci
, vol.19
, pp. 2852-2864
-
-
Zhang, C.L.1
Messing, A.2
Chiu, S.Y.3
-
61
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel
-
Zhuchenko O, et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel. Nat Genet 1997, 15:62-69.
-
(1997)
Nat Genet
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
|