-
1
-
-
0024317220
-
Proposal for revised classification of epilepsies and epileptic syndromes
-
Commission on Classification and Terminology of the International League against Epilepsy: Proposal for revised classification of epilepsies and epileptic syndromes. Epilepsia 1989, 30:389-399.
-
(1989)
Epilepsia
, vol.30
, pp. 389-399
-
-
-
2
-
-
0030886101
-
Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice
-
Cox GA, Lutz CM, Yang CL, Biemesderfer D, Bronson RT, Fu A, Aronson PS, Noebels JL, Frankel WN: Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice. Cell 1997, 91:139-148.
-
(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
-
3
-
-
0030070426
-
Targeting epilepsy genes
-
Noebels JL: Targeting epilepsy genes. Neuron 1996, 16:241-244.
-
(1996)
Neuron
, vol.16
, pp. 241-244
-
-
Noebels, J.L.1
-
4
-
-
0001229109
-
Experimental models of epilepsy
-
Edited by Kotagal P. San Diego: Academic Press; in press
-
Seyfried TN, Todorova M: Experimental models of epilepsy. In The Epilepsies: Etiologies and Prevention. Edited by Kotagal P. San Diego: Academic Press; 1998: in press.
-
(1998)
The Epilepsies: Etiologies and Prevention
-
-
Seyfried, T.N.1
Todorova, M.2
-
7
-
-
0025320647
-
The regulation and modulation of pH in the nervous system
-
Chesler M: The regulation and modulation of pH in the nervous system. Prog Neurobiol 1990, 34:401-427.
-
(1990)
Prog Neurobiol
, vol.34
, pp. 401-427
-
-
Chesler, M.1
-
8
-
-
0029858552
-
Acidosis of rat dorsal vagal neurons in situ during spontaneous and evoked activity
-
Trapp S, Luckermann M, Brooks PA, Ballanyi K: Acidosis of rat dorsal vagal neurons in situ during spontaneous and evoked activity. J Physiol 1996, 496:695-710.
-
(1996)
J Physiol
, vol.496
, pp. 695-710
-
-
Trapp, S.1
Luckermann, M.2
Brooks, P.A.3
Ballanyi, K.4
-
9
-
-
0002677849
-
Thalamocortical anatomy and physiology
-
Edited by Engel J, Pedley TA. Philadelphia: Lippincott-Raven Publishers
-
Coulter DA: Thalamocortical anatomy and physiology. In Epilepsy: A Comprehensive Textbook. Edited by Engel J, Pedley TA. Philadelphia: Lippincott-Raven Publishers; 1997: 341-351.
-
(1997)
Epilepsy: A Comprehensive Textbook
, pp. 341-351
-
-
Coulter, D.A.1
-
10
-
-
0023219522
-
How hyperventilation alters the electroencephalogram: A review of controversial viewpoints emphasizing neurophysiological mechanisms
-
Patel VM, Maulsby RL: How hyperventilation alters the electroencephalogram: a review of controversial viewpoints emphasizing neurophysiological mechanisms. J Clin Neurophysiol 1987, 4:101-120.
-
(1987)
J Clin Neurophysiol
, vol.4
, pp. 101-120
-
-
Patel, V.M.1
Maulsby, R.L.2
-
11
-
-
0030719487
-
Knock-out mice reveal a critical antiepileptic role for neuropeptide Y
-
Baraban SC, Hollopeter G, Erickson JG, Schwartzkroin PA, Palmiter RD: Knock-out mice reveal a critical antiepileptic role for neuropeptide Y. J Neurosci 1997, 17:8927-8936.
-
(1997)
J Neurosci
, vol.17
, pp. 8927-8936
-
-
Baraban, S.C.1
Hollopeter, G.2
Erickson, J.G.3
Schwartzkroin, P.A.4
Palmiter, R.D.5
-
12
-
-
0029024135
-
Essential functions of synapsins I and II in synaptic vesicle regulation
-
Rosahl TW, Spillane D, Missler M, Herz J, Selig DK, Wolff JR, Hammer RE, Malenka RC, Sudhof TC: Essential functions of synapsins I and II in synaptic vesicle regulation. Nature 1995, 375:488-493.
-
(1995)
Nature
, vol.375
, pp. 488-493
-
-
Rosahl, T.W.1
Spillane, D.2
Missler, M.3
Herz, J.4
Selig, D.K.5
Wolff, J.R.6
Hammer, R.E.7
Malenka, R.C.8
Sudhof, T.C.9
-
13
-
-
0030812843
-
Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1
-
Tanaka K, Watase K, Manabe T, Yamada K, Watanabe M, Takahashi K, Iwama H, Nishikawa T, Ichihara N, Kikuchi T, et al.: Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1. Science 1997, 276:1699-1702.
-
(1997)
Science
, vol.276
, pp. 1699-1702
-
-
Tanaka, K.1
Watase, K.2
Manabe, T.3
Yamada, K.4
Watanabe, M.5
Takahashi, K.6
Iwama, H.7
Nishikawa, T.8
Ichihara, N.9
Kikuchi, T.10
-
14
-
-
12644290240
-
Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior
-
Homanics GE, DeLorey TM, Firestone LL, Quinlan JJ, Handforth A, Harrison NL, Krasowski MD, Rick CE, Korpi ER, Makela R, et al.: Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior. Proc Natl Acad Sci USA 1997, 94:4143-4148.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 4143-4148
-
-
Homanics, G.E.1
DeLorey, T.M.2
Firestone, L.L.3
Quinlan, J.J.4
Handforth, A.5
Harrison, N.L.6
Krasowski, M.D.7
Rick, C.E.8
Korpi, E.R.9
Makela, R.10
-
15
-
-
0001472222
-
Epilepsy in mice lacking GABAA-receptor delta (δ) subunits
-
Olsen RW, DeLorey TM, Handforth A, Ferguson C, Mihalek RM, Homanics GE: Epilepsy in mice lacking GABAA-receptor delta (δ) subunits. Epilepsia 1997, 38(Suppl 8):123.
-
(1997)
Epilepsia
, vol.38
, Issue.8 SUPPL.
, pp. 123
-
-
Olsen, R.W.1
DeLorey, T.M.2
Handforth, A.3
Ferguson, C.4
Mihalek, R.M.5
Homanics, G.E.6
-
16
-
-
0029610443
-
Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice
-
Brusa R, Zimmerman F, Koh DS, Feldmeyer D, Gass P, Seeburg PH, Sprengel R: Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice. Science 1995, 270:1677-1680.
-
(1995)
Science
, vol.270
, pp. 1677-1680
-
-
Brusa, R.1
Zimmerman, F.2
Koh, D.S.3
Feldmeyer, D.4
Gass, P.5
Seeburg, P.H.6
Sprengel, R.7
-
17
-
-
0028909857
-
Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors
-
Tecott RH, Sun LM, Akana SF, Strack AM, Lowenstein DH, Dallman MF, Julius D: Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors. Nature 1995 374:542-546.
-
(1995)
Nature
, vol.374
, pp. 542-546
-
-
Tecott, R.H.1
Sun, L.M.2
Akana, S.F.3
Strack, A.M.4
Lowenstein, D.H.5
Dallman, M.F.6
Julius, D.7
-
18
-
-
13144280992
-
Mice lacking the delayed rectifier potassium channel MKV1.1
-
Smart SL, Messing A, Chiu SY, Schwartzkroin P, Tempel B: Mice lacking the delayed rectifier potassium channel MKV1.1. Soc Neurosci Abstr 1995, 21:1824.
-
(1995)
Soc Neurosci Abstr
, vol.21
, pp. 1824
-
-
Smart, S.L.1
Messing, A.2
Chiu, S.Y.3
Schwartzkroin, P.4
Tempel, B.5
-
19
-
-
0029115971
-
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation
-
Patil N, Cox DR, Bhat D, Faham M, Myers RM, Peterson AS: A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation. Nat Genet 1995, 11:126-129.
-
(1995)
Nat Genet
, vol.11
, pp. 126-129
-
-
Patil, N.1
Cox, D.R.2
Bhat, D.3
Faham, M.4
Myers, R.M.5
Peterson, A.S.6
-
20
-
-
0030584085
-
Absence epilepsy in tottering mutant mice is associated with calcium channel defects
-
Fletcher CF, Lutz CM, O'Sullivan TN, Shaughnessy JD, Hawkes R, Frankel WN, Copeland NG, Jenkins NA: 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
Lutz, C.M.2
O'Sullivan, T.N.3
Shaughnessy, J.D.4
Hawkes, R.5
Frankel, W.N.6
Copeland, N.G.7
Jenkins, N.A.8
-
21
-
-
0030614535
-
2+ channel β subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (Ih) mouse
-
2+ channel β subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (Ih) mouse. Cell 1997, 88:1-20.
-
(1997)
Cell
, vol.88
, pp. 1-20
-
-
Burgess, D.L.1
Jones, J.M.2
Meisler, M.H.3
Noebels, J.L.4
-
23
-
-
13344250473
-
Ataxia and epileptic seizures in mice lacking type 1 inositol, 1,4,5-trisphosphate receptor
-
Matsumoto M, Nakagawa T, Inoue T, Nagata E, Tanaka K, Takano H, Minowa O, Kuno J, Sakakibara S, Yamada M, et al.: Ataxia and epileptic seizures in mice lacking type 1 inositol, 1,4,5-trisphosphate receptor. Nature 1996 379:168-171.
-
(1996)
Nature
, vol.379
, pp. 168-171
-
-
Matsumoto, M.1
Nakagawa, T.2
Inoue, T.3
Nagata, E.4
Tanaka, K.5
Takano, H.6
Minowa, O.7
Kuno, J.8
Sakakibara, S.9
Yamada, M.10
-
24
-
-
0028866034
-
Overexpression of the neural growth-associated protein GAP-43 induces nerve sprouting in the adult nervous system of transgenic mice
-
Aigner L, Arber S, Kapfhammer JP, Laux T, Schneider C, Botteri F, Brenner HR, Caroni P: Overexpression of the neural growth-associated protein GAP-43 induces nerve sprouting in the adult nervous system of transgenic mice. Cell 1995, 83:269-278.
-
(1995)
Cell
, vol.83
, pp. 269-278
-
-
Aigner, L.1
Arber, S.2
Kapfhammer, J.P.3
Laux, T.4
Schneider, C.5
Botteri, F.6
Brenner, H.R.7
Caroni, P.8
-
25
-
-
0031018336
-
Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality
-
Chae T, Kwon YT, Bronson R, Dikkes P, Li E, Tsai LH: Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality. Neuron 1997, 18:29-42.
-
(1997)
Neuron
, vol.18
, pp. 29-42
-
-
Chae, T.1
Kwon, Y.T.2
Bronson, R.3
Dikkes, P.4
Li, E.5
Tsai, L.H.6
-
26
-
-
0029820548
-
Epilepsy and brain abnormalities in mice lacking the Otx1 gene
-
Acampora D, Mazan S, Avantaggiato V, Barone P, Tuorto F, Lallemand Y, Brulet P, Simeone A: Epilepsy and brain abnormalities in mice lacking the Otx1 gene. Nat Genet 1996, 14:218-222.
-
(1996)
Nat Genet
, vol.14
, pp. 218-222
-
-
Acampora, D.1
Mazan, S.2
Avantaggiato, V.3
Barone, P.4
Tuorto, F.5
Lallemand, Y.6
Brulet, P.7
Simeone, A.8
-
27
-
-
0029159814
-
Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice
-
Toth M, Grimsby J, Buzsaki G, Donovan GP: Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice. Nat Genet 1995, 11:71-75.
-
(1995)
Nat Genet
, vol.11
, pp. 71-75
-
-
Toth, M.1
Grimsby, J.2
Buzsaki, G.3
Donovan, G.P.4
-
28
-
-
4243390911
-
Genetic sphingolipid activator protein (SAP) deficiencies in human and a "knockout" mouse
-
Fujita N, Suzuki K, Vanier MT, Popko B, Maeda N, Klein A, Sandhoff K, Nakayasu H, Sukuki K: Genetic sphingolipid activator protein (SAP) deficiencies in human and a "knockout" mouse. J Neurochem 1996, 66(Suppl 1):S1.
-
(1996)
J Neurochem
, vol.66
, Issue.1 SUPPL.
-
-
Fujita, N.1
Suzuki, K.2
Vanier, M.T.3
Popko, B.4
Maeda, N.5
Klein, A.6
Sandhoff, K.7
Nakayasu, H.8
Sukuki, K.9
-
29
-
-
0029115393
-
Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6
-
Waymire KG, Mahuren JD, Jaje M, Guilarte TR, Coburn SP, MacGregor GR: Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6. Nat Genet 1995, 11:45-51.
-
(1995)
Nat Genet
, vol.11
, pp. 45-51
-
-
Waymire, K.G.1
Mahuren, J.D.2
Jaje, M.3
Guilarte, T.R.4
Coburn, S.P.5
MacGregor, G.R.6
-
30
-
-
16044373842
-
Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice
-
Mangiarini L, Sathasivam K, Seller M, Cozens B, Harper A, Hetherington C, Lawton M, Trottier Y, Lehrach H, Davies SW, Bates GP: Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice. Cell 87:493-506.
-
Cell
, vol.87
, pp. 493-506
-
-
Mangiarini, L.1
Sathasivam, K.2
Seller, M.3
Cozens, B.4
Harper, A.5
Hetherington, C.6
Lawton, M.7
Trottier, Y.8
Lehrach, H.9
Davies, S.W.10
Bates, G.P.11
-
31
-
-
0030995490
-
Deficiency of a protein-repair enzyme results in the accumulation of altered proteins, retardation of growth, and fatal seizures in mice
-
Kim E, Lowenson JD, MacLaren CD, Clarke S, Young SG: Deficiency of a protein-repair enzyme results in the accumulation of altered proteins, retardation of growth, and fatal seizures in mice. Proc Natl Acad Sci USA 1997, 94:6132-6137.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 6132-6137
-
-
Kim, E.1
Lowenson, J.D.2
MacLaren, C.D.3
Clarke, S.4
Young, S.G.5
-
32
-
-
16144368388
-
Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis
-
Sango K, McDonald MP, Crawley JN, Mack ML, Tifft CJ, Skop E, Starr CM, Hoffman A, Sandhoff K, Suzuki K, Proia RL: Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis. Nat Genet 1996, 14:348-352.
-
(1996)
Nat Genet
, vol.14
, pp. 348-352
-
-
Sango, K.1
McDonald, M.P.2
Crawley, J.N.3
Mack, M.L.4
Tifft, C.J.5
Skop, E.6
Starr, C.M.7
Hoffman, A.8
Sandhoff, K.9
Suzuki, K.10
Proia, R.L.11
-
33
-
-
0022889377
-
Jimpy mutant mouse: A 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing
-
Nave KA, Lai C, Bloom FE, Milner RJ: Jimpy mutant mouse: a 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing. Proc Natl Acad Sci USA 1986, 83:9264-9268.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 9264-9268
-
-
Nave, K.A.1
Lai, C.2
Bloom, F.E.3
Milner, R.J.4
-
34
-
-
0031469707
-
Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse
-
Ordway JM, Tallaksen-Greene S, Gutekunst CA, Bernstein EM, Cearley JA, Wiener HW, Dure LS, Lindsey R, Hersch SM, Jope RS, et al.: Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse. Cell 1997, 91:753-763.
-
(1997)
Cell
, vol.91
, pp. 753-763
-
-
Ordway, J.M.1
Tallaksen-Greene, S.2
Gutekunst, C.A.3
Bernstein, E.M.4
Cearley, J.A.5
Wiener, H.W.6
Dure, L.S.7
Lindsey, R.8
Hersch, S.M.9
Jope, R.S.10
|