-
1
-
-
84970378029
-
Glycine receptors: Molecular heterogeneity and implications for disease
-
(1995)
Neuroscientist
, vol.1
, pp. 130-141
-
-
Becker, C.-M.1
-
2
-
-
0002541568
-
Glycine receptors
-
Stephenson FA, Turner AJ, editors. Amino acid neurotransmission. London: Portland
-
(1998)
, pp. 93-112
-
-
Becker, C.-M.1
Langosch, D.2
-
7
-
-
0024317220
-
Proposal for revised classification of epilepsies and epileptic syndromes
-
(1989)
Epilepsia
, vol.30
, pp. 389-399
-
-
-
8
-
-
0030886101
-
Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice
-
(1997)
Cell
, vol.91
, pp. 139-148
-
-
Cox, G.A.1
Lutz, C.M.2
Yang, C.L.3
Biemesderfer, D.4
Bronson, R.T.5
Fu, A.6
Aronson, P.S.7
Noebels, J.L.8
Frankel, W.N.9
-
9
-
-
0034069651
-
+2
-
(2000)
Nat Genet
, vol.24
, pp. 343-345
-
-
Escayg, A.1
MacDonald, B.T.2
Meisler, M.H.3
Baulac, S.4
Huberfeld, G.5
An-Gourfinkel, I.6
Brice, A.7
LeGuern, E.8
Moulard, B.9
Chaigne, D.10
Buresi, C.11
Malafosse, A.12
-
10
-
-
0030584085
-
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
-
(1996)
Cell
, vol.87
, pp. 607-617
-
-
Fletcher, C.F.1
Lutz, C.M.2
O'Sullivan, T.N.3
Shaughnessy J.D., Jr.4
Hawkes, R.5
Frankel, W.N.6
Copeland, N.G.7
Jenkins, N.A.8
-
11
-
-
0025095280
-
Alpha subunit variants of the human glycine receptor: Primary structures, functional expression and chromosomal localization of the corresponding genes
-
(1990)
Embo J
, vol.9
, pp. 771-776
-
-
Grenningloh, G.1
Schmieden, V.2
Schofield, P.R.3
Seeburg, P.H.4
Siddique, T.5
Mohandas, T.K.6
Becker, C.M.7
Betz, H.8
-
12
-
-
0030049370
-
The human glycine receptor beta subunit: Primary structure, functional characterisation and chromosomal localisation of the human and murine genes
-
(1996)
Mol Brain Res
, vol.35
, pp. 211-219
-
-
Handford, C.A.1
Lynch, J.W.2
Baker, E.3
Webb, G.C.4
Ford, J.H.5
Sutherland, G.R.6
Schofield, P.R.7
-
15
-
-
0031024530
-
The idiopathic generalized epilepsies of adolescence with childhood and juvenile age of onset
-
(1997)
Epilepsia
, vol.38
, pp. 4-11
-
-
Janz, D.1
-
17
-
-
17344365408
-
2+ channel gamma subunit
-
(1998)
Nat Genet
, vol.19
, pp. 340-347
-
-
Lefts, V.A.1
Felix, R.2
Biddlecome, G.H.3
Arikkath, J.4
Mahaffey, C.L.5
Valenzuela, A.6
Bartlett II, F.S.7
Mori, Y.8
Campbell, K.P.9
Frankel, W.N.10
-
18
-
-
0001944123
-
Childhood absence epilepsy
-
Roger J, Dravet C, Bureau M, Dreifuss FE, Perret A, Wolf P, editors. London: John Libbey
-
(1992)
Epileptic syndromes in infancy, childhood and adolescence, 2nd ed.
, pp. 135-150
-
-
Loiseau, P.1
-
19
-
-
0344352488
-
The human glycine receptor beta subunit gene (GLRB): Structure, refined chromosomal localization, and population polymorphism
-
(1998)
Genomics
, vol.50
, pp. 341-345
-
-
Milani, N.1
Mülhardt, C.2
Weber, R.G.3
Lichter, P.4
Kioschis, P.5
Poustka, A.6
Becker, C.M.7
-
20
-
-
0027996651
-
The spastic mouse: Aberrant splicing of glycine receptor beta subunit mRNA caused by intronic insertion of L1 element
-
(1994)
Neuron
, vol.13
, pp. 1003-1015
-
-
Mülhardt, C.1
Fischer, M.2
Gass, P.3
Simon Chazottes, D.4
Guenet, J.L.5
Kuhse, J.6
Betz, H.7
Becker, C.M.8
-
21
-
-
0032584597
-
The human glycine receptor subunit alpha3. Glra3 gene structure, chromosomal localization, and functional characterization of alternative transcripts
-
(1998)
J Biol Chem
, vol.273
, pp. 19708-19714
-
-
Nikolic, Z.1
Laube, B.2
Weber, R.G.3
Lichter, P.4
Kioschis, P.5
Poustka, A.6
Mülhardt, C.7
Becker, C.M.8
-
23
-
-
0032542897
-
What's wrong with Bonferroni adjustments
-
(1998)
BMJ
, vol.316
, pp. 1236-1238
-
-
Perneger, T.V.1
-
25
-
-
0030116489
-
The genetics of idiopathic generalized epilepsy: Implications for the understanding of its aetiology
-
(1996)
Mol Med Today
, vol.2
, pp. 173-180
-
-
Sander, T.1
-
26
-
-
0032914247
-
Association analysis of sequence variants of GABAA alpha6, beta2, and gamma2 gene cluster and alcohol dependence
-
(1999)
Alcohol Clin Exp Res
, vol.23
, pp. 427-431
-
-
Sander, T.1
Ball, D.2
Murray, R.3
Patel, J.4
Samochowiec, J.5
Winterer, G.6
Rommelspacher, H.7
Schmidt, L.G.8
Loh, E.W.9
-
29
-
-
17344372328
-
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
-
(1998)
Nat Genet
, vol.18
, pp. 25-29
-
-
Singh, N.A.1
Charlier, C.2
Stauffer, D.3
DuPont, B.R.4
Leach, R.J.5
Melis, R.6
Ronen, G.M.7
Bjerre, I.8
Quattlebaum, T.9
Murphy, J.V.10
McHarg, M.L.11
Gagnon, D.12
Rosales, T.O.13
Peiffer, A.14
Anderson, V.E.15
Leppert, M.16
-
30
-
-
0028980028
-
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
-
(1995)
Nat Genet
, vol.11
, pp. 201-203
-
-
Steinlein, O.K.1
Mulley, J.C.2
Propping, P.3
Wallace, R.H.4
Phillips, H.A.5
Sutherland, G.R.6
Scheffer, I.E.7
Berkovic, S.F.8
-
31
-
-
17344367657
-
+-channel betal subunit gene SCN1B
-
(1998)
Nat Genet
, vol.19
, pp. 366-370
-
-
Wallace, R.H.1
Wang, D.W.2
Singh, R.3
Scheffer, I.E.4
George A.L., Jr.5
Phillips, H.A.6
Saar, K.7
Reis, A.8
Johnson, E.W.9
Sutherland, G.R.10
Berkovic, S.F.11
Mulley, J.C.12
-
32
-
-
0001433373
-
Juvenile absence epilepsy
-
Roger J, Dravet C, Bureau M, Dreifuss FE, Perret A, Wolf P, editors. London: John Libbey
-
(1992)
Epileptic syndromes in infancy, childhood and adolescence, 2nd ed.
, pp. 307-312
-
-
Wolf, P.1
|