-
1
-
-
58849127003
-
Abnormal network activity in a targeted genetic model of human double cortex
-
Ackman, J. B., Aniksztejn, L., Crepel, V., Becq, H., Pelle-grino, C., Cardoso, C., Ben-Ari, Y., and Represa, A. (2009). Abnormal network activity in a targeted genetic model of human double cortex. J. Neurosci. 29, 313-327.
-
(2009)
J. Neurosci.
, vol.29
, pp. 313-327
-
-
Ackman, J.B.1
Aniksztejn, L.2
Crepel, V.3
Becq, H.4
Pelle-grino, C.5
Cardoso, C.6
Ben-Ari, Y.7
Represa, A.8
-
2
-
-
0032189771
-
Regional and cellular patterns of reelin mRNA expression in the fore-brain of the developing and adult mouse
-
Alcantara, S., Ruiz, M., D'Arcangelo, G., Ezan, F., De Lecea, L., Curran, T., Sotelo, C., and Soriano, E. (1998). Regional and cellular patterns of reelin mRNA expression in the fore-brain of the developing and adult mouse. J. Neurosci. 18, 7779-7799.
-
(1998)
J. Neurosci.
, vol.18
, pp. 7779-7799
-
-
Alcantara, S.1
Ruiz, M.2
D'Arcangelo, G.3
Ezan, F.4
De Lecea, L.5
Curran, T.6
Sotelo, C.7
Soriano, E.8
-
3
-
-
81055153389
-
Therapeutic value of prenatal rapamycin treatment in a mouse brain model of tuberous sclerosis complex
-
Anderl, S., Freeland, M., Kwiatkowski, D. J., and Goto, J. (2011). Therapeutic value of prenatal rapamycin treatment in a mouse brain model of tuberous sclerosis complex. Hum. Mol. Genet. 20, 4597-4604.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 4597-4604
-
-
Anderl, S.1
Freeland, M.2
Kwiatkowski, D.J.3
Goto, J.4
-
4
-
-
0030698872
-
Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes
-
Anderson, S. A., Eisenstat, D. D., Shi, L., and Rubenstein, J. L. (1997). Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science 278, 474-476.
-
(1997)
Science
, vol.278
, pp. 474-476
-
-
Anderson, S.A.1
Eisenstat, D.D.2
Shi, L.3
Rubenstein, J.L.4
-
5
-
-
63849196530
-
Intrahippocampal infusion of botulinum neurotoxin E (BoNT/E) reduces spontaneous recurrent seizures in a mouse model of mesial temporal lobe epilepsy
-
Antonucci, F., Bozzi, Y., and Caleo, M. (2009). Intrahippocampal infusion of botulinum neurotoxin E (BoNT/E) reduces spontaneous recurrent seizures in a mouse model of mesial temporal lobe epilepsy. Epilepsia 50, 963-966.
-
(2009)
Epilepsia
, vol.50
, pp. 963-966
-
-
Antonucci, F.1
Bozzi, Y.2
Caleo, M.3
-
6
-
-
41149084007
-
Botulinum neuro-toxin E (BoNT/E) reduces CA1 neuron loss and granule cell dispersion, with no effects on chronic seizures, in a mouse model of temporal lobe epilepsy
-
Antonucci, F., Di Garbo, A., Novelli, E., Manno, I., Sartucci, F., Bozzi, Y., and Caleo, M. (2008). Botulinum neuro-toxin E (BoNT/E) reduces CA1 neuron loss and granule cell dispersion, with no effects on chronic seizures, in a mouse model of temporal lobe epilepsy. Exp. Neurol. 210, 388-401.
-
(2008)
Exp. Neurol.
, vol.210
, pp. 388-401
-
-
Antonucci, F.1
Di Garbo, A.2
Novelli, E.3
Manno, I.4
Sartucci, F.5
Bozzi, Y.6
Caleo, M.7
-
7
-
-
0035013909
-
Functional and physical coupling of voltage-sensitive calcium channels with exocytotic proteins: ramifications for the secretion mechanism
-
Atlas, D. (2001). Functional and physical coupling of voltage-sensitive calcium channels with exocytotic proteins: ramifications for the secretion mechanism. J. Neurochem. 77, 972-985.
-
(2001)
J. Neurochem.
, vol.77
, pp. 972-985
-
-
Atlas, D.1
-
8
-
-
0042011519
-
Cellular biology of epilepto-genesis
-
Avanzini, G., and Franceschetti, S. (2003). Cellular biology of epilepto-genesis. Lancet Neurol. 2, 33-42.
-
(2003)
Lancet Neurol
, vol.2
, pp. 33-42
-
-
Avanzini, G.1
Franceschetti, S.2
-
9
-
-
34249800070
-
Epilepto-genic channelopathies: experimental models of human pathologies
-
Avanzini, G., Franceschetti, S., and Mantegazza, M. (2007). Epilepto-genic channelopathies: experimental models of human pathologies. Epilepsia 48(Suppl. 2), 51-64.
-
(2007)
Epilepsia
, vol.48
, Issue.SUPPL. 2
, pp. 51-64
-
-
Avanzini, G.1
Franceschetti, S.2
Mantegazza, M.3
-
10
-
-
0344395644
-
RNAi reveals doublecortin is required for radial migration in rat neocortex
-
Bai, J., Ramos, R. L., Ackman, J. B., Thomas, A. M., Lee, R. V., and Loturco, J. J. (2003). RNAi reveals doublecortin is required for radial migration in rat neocortex. Nat. Neurosci. 6, 1277-1283.
-
(2003)
Nat. Neurosci.
, vol.6
, pp. 1277-1283
-
-
Bai, J.1
Ramos, R.L.2
Ackman, J.B.3
Thomas, A.M.4
Lee, R.V.5
Loturco, J.J.6
-
11
-
-
37149056344
-
Lack of synapsin I reduces the readily releasable pool of synaptic vesicles at central inhibitory synapses
-
Baldelli, P., Fassio, A., Valtorta, F., and Benfenati, E (2007). Lack of synapsin I reduces the readily releasable pool of synaptic vesicles at central inhibitory synapses. J. Neu-rosci. 27, 13520-13531.
-
(2007)
J. Neu-rosci.
, vol.27
, pp. 13520-13531
-
-
Baldelli, P.1
Fassio, A.2
Valtorta, F.3
Benfenati, E.4
-
12
-
-
32144433872
-
A developmental and genetic classification for malformations of cortical development
-
Barkovich, A. J., Kuzniecky R. I., Jackson, G. D., Guerrini, R., and Dobyns, W. B. (2005). A developmental and genetic classification for malformations of cortical development. Neurology 65, 1873-1887.
-
(2005)
Neurology
, vol.65
, pp. 1873-1887
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Jackson, G.D.3
Guerrini, R.4
Dobyns, W.B.5
-
13
-
-
33750684965
-
Effects of seizures on developmental processes in the immature brain
-
Ben-Ari, Y., and Holmes, G. L. (2006). Effects of seizures on developmental processes in the immature brain. Lancet Neurol. 5,1055-1063.
-
(2006)
Lancet Neurol
, vol.5
, pp. 1055-1063
-
-
Ben-Ari, Y.1
Holmes, G.L.2
-
14
-
-
0026706939
-
Synaptic vesicle-associated Ca2+/calmodulin-dependent protein kinase II is a binding protein for synapsin I
-
Benfenati, F., Valtorta, F., Ruben-stein, J. L., Gorelick, F. S., Greengard, P., and Czernik, A. J. (1992). Synaptic vesicle-associated Ca2+/calmodulin-dependent protein kinase II is a binding protein for synapsin I. Nature 359, 417-420.
-
(1992)
Nature
, vol.359
, pp. 417-420
-
-
Benfenati, F.1
Valtorta, F.2
Ruben-stein, J.L.3
Gorelick, F.S.4
Greengard, P.5
Czernik, A.J.6
-
15
-
-
0033969699
-
Critical periods during sensory development
-
Berardi, N., Pizzorusso, T., and Maf-fei, L. (2000). Critical periods during sensory development. Curr. Opin. Neurobiol. 10,138-145.
-
(2000)
Curr. Opin. Neurobiol.
, vol.10
, pp. 138-145
-
-
Berardi, N.1
Pizzorusso, T.2
Maf-fei, L.3
-
16
-
-
23644451209
-
Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a
-
Bergren, S. K., Chen, S., Galecki, A., and Kearney, J. A. (2005). Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a. Mamm. Genome 16, 683-690.
-
(2005)
Mamm. Genome
, vol.16
, pp. 683-690
-
-
Bergren, S.K.1
Chen, S.2
Galecki, A.3
Kearney, J.A.4
-
17
-
-
67651183610
-
Fine mapping of an epilepsy modifier gene on mouse chromosome 19
-
Bergren, S. K., Rutter, E. D., and Kearney, J. A. (2009). Fine mapping of an epilepsy modifier gene on mouse chromosome 19. Mamm. Genome 20, 359-366.
-
(2009)
Mamm. Genome
, vol.20
, pp. 359-366
-
-
Bergren, S.K.1
Rutter, E.D.2
Kearney, J.A.3
-
18
-
-
23744437313
-
Phosphorylation of synapsin I by cAMP-dependent protein kinase controls synaptic vesicle dynamics in developing neurons
-
Bonanomi, D., Menegon, A., Miccio, A., Ferrari, G., Corradi, A., Kao, H. T., Benfenati, F., and Valtorta, E (2005).Phosphorylation of synapsin I by cAMP-dependent protein kinase controls synaptic vesicle dynamics in developing neurons. J. Neurosci. 25, 7299-7308.
-
(2005)
J. Neurosci.
, vol.25
, pp. 7299-7308
-
-
Bonanomi, D.1
Menegon, A.2
Miccio, A.3
Ferrari, G.4
Corradi, A.5
Kao, H.T.6
Benfenati, F.7
Valtorta, E.8
-
19
-
-
66149098514
-
Defects in cell polarity underlie TSC and ADPKD-associated cystogenesis
-
Bonnet, C. S., Aldred, M., von Ruh-land, C., Harris, R., Sandford, R., and Cheadle, J. P. (2009). Defects in cell polarity underlie TSC and ADPKD-associated cystogenesis. Hum. Mol. Genet. 18,2166-2176.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2166-2176
-
-
Bonnet, C.S.1
Aldred, M.2
von Ruh-land, C.3
Harris, R.4
Sandford, R.5
Cheadle, J.P.6
-
20
-
-
34249054919
-
Heterogeneity of glu-tamatergic and GABAergic release machinery in cerebral cortex
-
Bragina, L., Candiracci, C., Barbaresi, P., Giovedi, S., Benfenati, F., and Conti, E (2007). Heterogeneity of glu-tamatergic and GABAergic release machinery in cerebral cortex. Neu-roscience 146, 1829-1840.
-
(2007)
Neu-roscience
, vol.146
, pp. 1829-1840
-
-
Bragina, L.1
Candiracci, C.2
Barbaresi, P.3
Giovedi, S.4
Benfenati, F.5
Conti, E.6
-
21
-
-
79951531485
-
Rapamycin suppresses mossy fiber sprouting but not seizure frequency in a mouse model of temporal lobe epilepsy
-
Buckmaster, P. S., and Lew, E H. (2011). Rapamycin suppresses mossy fiber sprouting but not seizure frequency in a mouse model of temporal lobe epilepsy. J. Neurosci. 31, 2337-2347.
-
(2011)
J. Neurosci.
, vol.31
, pp. 2337-2347
-
-
Buckmaster, P.S.1
Lew, E.H.2
-
22
-
-
14344276586
-
Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization
-
Cahana, A., Escamez, T., Nowakowski, R. S., Hayes, N. L., Giacobini, M., von Holst, A., Shmueli, O., Sapir, T., McConnell, S. K., Wurst, W., Martinez, S., and Reiner, O. (2001). Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization. Proc. Natl. Acad. Sci. U.S.A. 98, 6429-6434.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 6429-6434
-
-
Cahana, A.1
Escamez, T.2
Nowakowski, R.S.3
Hayes, N.L.4
Giacobini, M.5
von Holst, A.6
Shmueli, O.7
Sapir, T.8
McConnell, S.K.9
Wurst, W.10
Martinez, S.11
Reiner, O.12
-
23
-
-
70350451970
-
Epilepsy: synapses stuck in childhood
-
Caleo, M. (2009). Epilepsy: synapses stuck in childhood. Nat. Med. 15, 1126-1127.
-
(2009)
Nat. Med.
, vol.15
, pp. 1126-1127
-
-
Caleo, M.1
-
24
-
-
34247513103
-
Transient synaptic silencing of developing striate cortex has persistent effects on visual function and plasticity
-
Caleo, M., Restani, L., Gianfranceschi, L., Costantin, L., Rossi, C., Rossetto, O., Montecucco, C., and Maffei, L. (2007). Transient synaptic silencing of developing striate cortex has persistent effects on visual function and plasticity. J. Neurosci. 27,4530-4540.
-
(2007)
J. Neurosci.
, vol.27
, pp. 4530-4540
-
-
Caleo, M.1
Restani, L.2
Gianfranceschi, L.3
Costantin, L.4
Rossi, C.5
Rossetto, O.6
Montecucco, C.7
Maffei, L.8
-
25
-
-
77956363288
-
Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice
-
Chabrol, E., Navarro, V., Provenzano, G., Cohen, I., Dinocourt, C., Rivaud-Péchoux, S., Fricker, D., Baulac, M., Miles, R., Leguern, E., and Baulac, S. (2010). Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice. Brain 133, 2749-2762.
-
(2010)
Brain
, vol.133
, pp. 2749-2762
-
-
Chabrol, E.1
Navarro, V.2
Provenzano, G.3
Cohen, I.4
Dinocourt, C.5
Rivaud-Péchoux, S.6
Fricker, D.7
Baulac, M.8
Miles, R.9
Leguern, E.10
Baulac, S.11
-
26
-
-
66549107350
-
Opposite changes in glutamatergic and GABAergic transmission underlie the diffuse hyperexcitability of synapsin I-deficient cortical networks
-
Chiappalone, M., Casagrande, S., Tedesco, M., Valtorta, F., Baldelli, P., Martinoia, S., and Benfenati, E (2009). Opposite changes in glutamatergic and GABAergic transmission underlie the diffuse hyperexcitability of synapsin I-deficient cortical networks. Cereb. Cortex 19, 1422-1439.
-
(2009)
Cereb. Cortex
, vol.19
, pp. 1422-1439
-
-
Chiappalone, M.1
Casagrande, S.2
Tedesco, M.3
Valtorta, F.4
Baldelli, P.5
Martinoia, S.6
Benfenati, E.7
-
27
-
-
0029022960
-
Impairment of axonal development and of synaptogenesis in hippocam-pal neurons of synapsin I-deficient mice
-
Chin, L. S., Li, L., Ferreira, A., Kosik, K. S., and Greengard, P. (1995). Impairment of axonal development and of synaptogenesis in hippocam-pal neurons of synapsin I-deficient mice. Proc. Natl. Acad. Sci. U.S.A. 92, 9230-9234.
-
(1995)
Proc. Natl. Acad. Sci. U. S. A.
, vol.92
, pp. 9230-9234
-
-
Chin, L.S.1
Li, L.2
Ferreira, A.3
Kosik, K.S.4
Greengard, P.5
-
28
-
-
34250188057
-
Dlx transcription factors promote migration through repression of axon and dendrite growth
-
Cobos, I., Borello, U., and Rubenstein, J. L. (2007). Dlx transcription factors promote migration through repression of axon and dendrite growth. Neuron 54, 873-888.
-
(2007)
Neuron
, vol.54
, pp. 873-888
-
-
Cobos, I.1
Borello, U.2
Rubenstein, J.L.3
-
29
-
-
13244253699
-
The vertebrate ortholog of Aristaless is regulated by Dlx genes in the developing f orebrain
-
Cobos, I., Broccoli, V., and Rubenstein, J. L. (2005a). The vertebrate ortholog of Aristaless is regulated by Dlx genes in the developing f orebrain. J. Comp. Neurol. 483, 292-303.
-
(2005)
J. Comp. Neurol.
, vol.483
, pp. 292-303
-
-
Cobos, I.1
Broccoli, V.2
Rubenstein, J.L.3
-
30
-
-
23044437148
-
Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy
-
Cobos, I., Calcagnotto, M. E., Vilaythong, A. J., Thwin, M. T., Noebels, J. L., Baraban, S. C., and Rubenstein, J. L. (2005b). Mice lacking Dlx1 show subtype-specific loss of interneurons, reduced inhibition and epilepsy. Nat. Neurosci. 8, 1059-1068.
-
(2005)
Nat. Neurosci.
, vol.8
, pp. 1059-1068
-
-
Cobos, I.1
Calcagnotto, M.E.2
Vilaythong, A.J.3
Thwin, M.T.4
Noebels, J.L.5
Baraban, S.C.6
Rubenstein, J.L.7
-
31
-
-
0345256499
-
Genetic animal models for absence epilepsy: a review of the WAG/Rij strain of rats
-
Coenen, A. M., and Van Luijtelaar, E. L. (2003). Genetic animal models for absence epilepsy: a review of the WAG/Rij strain of rats. Behav. Genet. 33, 635-655.
-
(2003)
Behav. Genet.
, vol.33
, pp. 635-655
-
-
Coenen, A.M.1
Van Luijtelaar, E.L.2
-
32
-
-
34247474911
-
Inactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous gen-italia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation
-
Colombo, E., Collombat, P., Colasante, G., Bianchi, M., Long, J., Mansouri, A., Rubenstein, J. L., and Broccoli, V. (2007). Inactivation of Arx, the murine ortholog of the X-linked lissencephaly with ambiguous gen-italia gene, leads to severe disorganization of the ventral telencephalon with impaired neuronal migration and differentiation. J. Neurosci. 27, 4786-4798.
-
(2007)
J. Neurosci.
, vol.27
, pp. 4786-4798
-
-
Colombo, E.1
Collombat, P.2
Colasante, G.3
Bianchi, M.4
Long, J.5
Mansouri, A.6
Rubenstein, J.L.7
Broccoli, V.8
-
33
-
-
6944226376
-
Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and fore-brain GABAergic neurons
-
Colombo, E., Galli, R., Cossu, G., Gecz, J., and Broccoli, V. (2004). Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and fore-brain GABAergic neurons. Dev. Dyn. 231,631-639.
-
(2004)
Dev. Dyn.
, vol.231
, pp. 631-639
-
-
Colombo, E.1
Galli, R.2
Cossu, G.3
Gecz, J.4
Broccoli, V.5
-
34
-
-
77955286449
-
Endogenous SNAP-25 regulates native voltage-gated calcium channels in glutamatergic neurons
-
Condliffe, S. B., Corradini, I., Pozzi, D., Verderio, C., and Matteoli, M. (2010). Endogenous SNAP-25 regulates native voltage-gated calcium channels in glutamatergic neurons. J. Biol. Chem. 285,24968-24976.
-
(2010)
J. Biol. Chem
, vol.285
, pp. 24968-24976
-
-
Condliffe, S.B.1
Corradini, I.2
Pozzi, D.3
Verderio, C.4
Matteoli, M.5
-
35
-
-
39949084146
-
A mechanism for inside-out lamination in the neocortex
-
Cooper, J. A. (2008). A mechanism for inside-out lamination in the neocortex. Trends Neurosci. 31, 113-119.
-
(2008)
Trends Neurosci
, vol.31
, pp. 113-119
-
-
Cooper, J.A.1
-
36
-
-
0036758617
-
Doublecortin is required in mice for lamination of the hippocampus but not the neocortex
-
Corbo, J. C., Deuel, T. A., Long, J. M., Laporte, P., Tsai, E., Wynshaw-Boris, A., and Walsh, C. A. (2002). Doublecortin is required in mice for lamination of the hippocampus but not the neocortex. J. Neurosci. 22, 7548-7557.
-
(2002)
J. Neurosci.
, vol.22
, pp. 7548-7557
-
-
Corbo, J.C.1
Deuel, T.A.2
Long, J.M.3
Laporte, P.4
Tsai, E.5
Wynshaw-Boris, A.6
Walsh, C.A.7
-
37
-
-
0033592991
-
Abnormal neurotransmis-sion in mice lacking synaptic vesicle protein 2A (SV2A)
-
Crowder, K. M., Gunther, J. M., Jones, T. A., Hale, B. D., Zhang, H. Z., Peterson, M. R., Scheller, R. H., Chavkin, C., and Bajjalieh, S. M. (1999). Abnormal neurotransmis-sion in mice lacking synaptic vesicle protein 2A (SV2A). Proc. Natl. Acad. Sci. U.S.A. 96, 15268-15273.
-
(1999)
Proc. Natl. Acad. Sci. U. S. A.
, vol.96
, pp. 15268-15273
-
-
Crowder, K.M.1
Gunther, J.M.2
Jones, T.A.3
Hale, B.D.4
Zhang, H.Z.5
Peterson, M.R.6
Scheller, R.H.7
Chavkin, C.8
Bajjalieh, S.M.9
-
38
-
-
30844465706
-
Reelin mouse mutants as models of cortical development disorders
-
D'Arcangelo, G. (2006). Reelin mouse mutants as models of cortical development disorders. Epilepsy Behav. 8, 81-90.
-
(2006)
Epilepsy Behav
, vol.8
, pp. 81-90
-
-
D'Arcangelo, G.1
-
39
-
-
0032031914
-
Reeler: new tales on an old mutant mouse
-
D'Arcangelo, G., and Curran, T. (1998). Reeler: new tales on an old mutant mouse. Bioessays 20,235-244.
-
(1998)
Bioessays
, vol.20
, pp. 235-244
-
-
D'Arcangelo, G.1
Curran, T.2
-
40
-
-
0033763090
-
The nico-tinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy
-
De Fusco, M., Becchetti, A., Patrig-nani,A.,Annesi, G.,Gambardella,A., Quattrone, A., Ballabio, A., Wanke, E., and Casari, G. (2000). The nico-tinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy. Nat. Genet. 26, 275-276.
-
(2000)
Nat. Genet.
, vol.26
, pp. 275-276
-
-
De Fusco, M.1
Becchetti, A.2
Patrig-nani, A.3
Annesi, G.4
Gambardella, A.5
Quattrone, A.6
Ballabio, A.7
Wanke, E.8
Casari, G.9
-
41
-
-
79955467659
-
Neuronal activity is required for the development of specific cortical interneuron subtypes
-
De Marco García, N. V., Karayannis, T., and Fishell, G. (2011). Neuronal activity is required for the development of specific cortical interneuron subtypes. Nature 472, 351-355.
-
(2011)
Nature
, vol.472
, pp. 351-355
-
-
De Marco García, N.V.1
Karayannis, T.2
Fishell, G.3
-
42
-
-
17444444915
-
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar hetero-topia and lissencephaly syndrome
-
des Portes, V., Pinard, J. M., Billuart, P., Vinet, M. C., Koulakoff, A., Carrie, A., Gelot, A., Dupuis, E., Motte, J., Berwald-Netter, Y., Catala, M., Kahn, A., Beldjord, C., and Chelly,J. (1998). A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar hetero-topia and lissencephaly syndrome. Cell 92,51-61.
-
(1998)
Cell
, vol.92
, pp. 51-61
-
-
des Portes, V.1
Pinard, J.M.2
Billuart, P.3
Vinet, M.C.4
Koulakoff, A.5
Carrie, A.6
Gelot, A.7
Dupuis, E.8
Motte, J.9
Berwald-Netter, Y.10
Catala, M.11
Kahn, A.12
Beldjord, C.13
Chelly, J.14
-
43
-
-
29544450409
-
Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth
-
Deuel, T. A., Liu, J. S., Corbo, J. C., Yoo, S. Y., Rorke-Adams, L. B., and Walsh, C. A. (2006). Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth. Neuron 49, 41-53.
-
(2006)
Neuron
, vol.49
, pp. 41-53
-
-
Deuel, T.A.1
Liu, J.S.2
Corbo, J.C.3
Yoo, S.Y.4
Rorke-Adams, L.B.5
Walsh, C.A.6
-
44
-
-
40149100452
-
Is exposure to enriched environment beneficial for functional post-lesional recovery in temporal lobe epilepsy? Neurosci
-
Dhanushkodi, A., and Shetty, A. K. (2008). Is exposure to enriched environment beneficial for functional post-lesional recovery in temporal lobe epilepsy? Neurosci. Biobehav. Rev. 32, 657-674.
-
(2008)
Biobehav. Rev.
, vol.32
, pp. 657-674
-
-
Dhanushkodi, A.1
Shetty, A.K.2
-
45
-
-
79952762804
-
Impaired reelin processing and secretion by Cajal-Retzius cells contributes to granule cell dispersion in a mouse model of temporal lobe epilepsy
-
Duveau, V., Madhusudan, A., Caleo, M., Knuesel, I., and Fritschy, J. M. (2010). Impaired reelin processing and secretion by Cajal-Retzius cells contributes to granule cell dispersion in a mouse model of temporal lobe epilepsy. Hippocampus 21, 935-944.
-
(2010)
Hippocampus
, vol.21
, pp. 935-944
-
-
Duveau, V.1
Madhusudan, A.2
Caleo, M.3
Knuesel, I.4
Fritschy, J.M.5
-
46
-
-
49149088555
-
Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis
-
Ehninger, D., Han, S., Shilyansky, C., Zhou, Y., Li, W., Kwiatkowski, D. J., Ramesh, V., and Silva, A. J. (2008). Reversal of learning deficits in a Tsc2+/- mouse model of tuberous sclerosis. Nat. Med. 14, 843-848.
-
(2008)
Nat. Med.
, vol.14
, pp. 843-848
-
-
Ehninger, D.1
Han, S.2
Shilyansky, C.3
Zhou, Y.4
Li, W.5
Kwiatkowski, D.J.6
Ramesh, V.7
Silva, A.J.8
-
47
-
-
0028011961
-
Functional postnatal development of the rat primary visual cortex and the role of visual experience: dark rearing and monocular deprivation
-
Fagiolini, M., Pizzorusso, T., Berardi, N., Domenici, L., and Maffei, L. (1994). Functional postnatal development of the rat primary visual cortex and the role of visual experience: dark rearing and monocular deprivation. Vision Res. 34, 709-720.
-
(1994)
Vision Res
, vol.34
, pp. 709-720
-
-
Fagiolini, M.1
Pizzorusso, T.2
Berardi, N.3
Domenici, L.4
Maffei, L.5
-
48
-
-
79953296435
-
Single-cell Tsc1 knockout during corticogene-sis generates tuber-like lesions and reduces seizure threshold in mice
-
Feliciano, D. M., Su, T., Lopez, J., Platel, J. C., and Bordey, A. (2011). Single-cell Tsc1 knockout during corticogene-sis generates tuber-like lesions and reduces seizure threshold in mice. J. Clin. Invest. 121,1596-1607.
-
(2011)
J. Clin. Invest
, vol.121
, pp. 1596-1607
-
-
Feliciano, D.M.1
Su, T.2
Lopez, J.3
Platel, J.C.4
Bordey, A.5
-
49
-
-
33845959978
-
Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis
-
Feng, Y., Chen, M. H., Moskowitz, I. P., Mendonza, A. M., Vidali, L., Nakamura, F., Kwiatkowski, D. J., and Walsh, C. A. (2006). Filamin A (FLNA) is required for cell-cell contact in vascular development and cardiac morphogenesis. Proc. Natl. Acad. Sci. U.S.A. 103, 19836-19841.
-
(2006)
Proc. Natl. Acad. Sci. U. S. A
, vol.103
, pp. 19836-19841
-
-
Feng, Y.1
Chen, M.H.2
Moskowitz, I.P.3
Mendonza, A.M.4
Vidali, L.5
Nakamura, F.6
Kwiatkowski, D.J.7
Walsh, C.A.8
-
50
-
-
0035282457
-
Synaptotagmin I functions as a calcium regulator of release probability
-
Fernandez-Chacon, R., Konigstorfer, A., Gerber, S. H., Garcia, J., Matos, M. F., Stevens, C. F., Brose, N., Rizo, J., Rosenmund, C., and Sudhof, T. C. (2001). Synaptotagmin I functions as a calcium regulator of release probability. Nature 410,41-49.
-
(2001)
Nature
, vol.410
, pp. 41-49
-
-
Fernandez-Chacon, R.1
Konigstorfer, A.2
Gerber, S.H.3
Garcia, J.4
Matos, M.F.5
Stevens, C.F.6
Brose, N.7
Rizo, J.8
Rosenmund, C.9
Sudhof, T.C.10
-
51
-
-
46249115465
-
Perspectives on the developmental origins of cortical interneuron diversity
-
discussion 35-44, 96-28
-
Fishell, G. (2007). Perspectives on the developmental origins of cortical interneuron diversity. Novartis Found. Symp. 288,21-35; discussion 35-44, 96-28.
-
(2007)
Novartis Found. Symp.
, vol.288
, pp. 21-35
-
-
Fishell, G.1
-
52
-
-
38749105842
-
Pyramidal neurons grow up and change their mind
-
Fishell, G., and Hanashima, C. (2008). Pyramidal neurons grow up and change their mind. Neuron 57, 333-338.
-
(2008)
Neuron
, vol.57
, pp. 333-338
-
-
Fishell, G.1
Hanashima, C.2
-
53
-
-
33644827461
-
Rapamycin causes regression of astrocytomas in tuberous sclerosis complex
-
Franz, D. N., Leonard, J., Tudor, C., Chuck, G., Care, M., Sethuraman, G., Dinopoulos, A., Thomas, G., and Crone, K. R. (2006). Rapamycin causes regression of astrocytomas in tuberous sclerosis complex. Ann. Neurol. 59, 490-498.
-
(2006)
Ann. Neurol.
, vol.59
, pp. 490-498
-
-
Franz, D.N.1
Leonard, J.2
Tudor, C.3
Chuck, G.4
Care, M.5
Sethuraman, G.6
Dinopoulos, A.7
Thomas, G.8
Crone, K.R.9
-
54
-
-
45949106524
-
Cell-autonomous roles of ARX in cell proliferation and neu-ronal migration during corticogene-sis
-
Friocourt, G., Kanatani, S., Tabata, H., Yozu, M., Takahashi, T., Antypa, M., Raguenes, O., Chelly, J., Ferec, C., Nakajima, K., and Parnavelas, J. G. (2008). Cell-autonomous roles of ARX in cell proliferation and neu-ronal migration during corticogene-sis. J. Neurosci. 28, 5794-5805.
-
(2008)
J. Neurosci.
, vol.28
, pp. 5794-5805
-
-
Friocourt, G.1
Kanatani, S.2
Tabata, H.3
Yozu, M.4
Takahashi, T.5
Antypa, M.6
Raguenes, O.7
Chelly, J.8
Ferec, C.9
Nakajima, K.10
Parnavelas, J.G.11
-
55
-
-
34147109177
-
Both doublecortin and doublecortin-like kinase play a role in cortical interneuron migration
-
Friocourt, G., Liu, J. S., Antypa, M., Rakic, S., Walsh, C. A., and Parnavelas, J. G. (2007). Both doublecortin and doublecortin-like kinase play a role in cortical interneuron migration. J. Neurosci. 27, 3875-3883.
-
(2007)
J. Neurosci.
, vol.27
, pp. 3875-3883
-
-
Friocourt, G.1
Liu, J.S.2
Antypa, M.3
Rakic, S.4
Walsh, C.A.5
Parnavelas, J.G.6
-
56
-
-
77953376969
-
Mutations in ARX result in several defects involving GABAergic neurons
-
doi: 10.3389/fncel.2010.00004
-
Friocourt, G., and Parnavelas, J. G. (2010). Mutations in ARX result in several defects involving GABAergic neurons. Front. Cell. Neurosci. 4:4. doi: 10.3389/fncel.2010.00004
-
(2010)
Front. Cell. Neurosci.
, vol.4
, pp. 4
-
-
Friocourt, G.1
Parnavelas, J.G.2
-
57
-
-
33644786915
-
The role of ARX in cortical development
-
Friocourt, G., Poirier, K., Rakic, S., Parnavelas, J. G., and Chelly, J. (2006). The role of ARX in cortical development. Eur. J. Neurosci. 23, 869-876.
-
(2006)
Eur. J. Neurosci.
, vol.23
, pp. 869-876
-
-
Friocourt, G.1
Poirier, K.2
Rakic, S.3
Parnavelas, J.G.4
Chelly, J.5
-
58
-
-
77956010349
-
Role for Reelin in stabilizing cortical architecture
-
Frotscher, M. (2010). Role for Reelin in stabilizing cortical architecture. Trends Neurosci. 33,407-414.
-
(2010)
Trends Neurosci
, vol.33
, pp. 407-414
-
-
Frotscher, M.1
-
59
-
-
33749038646
-
Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission
-
Fukata, Y., Adesnik, H., Iwanaga, T., Bredt, D. S., Nicoll, R. A., and Fukata, M. (2006). Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission. Science 313, 1792-1795.
-
(2006)
Science
, vol.313
, pp. 1792-1795
-
-
Fukata, Y.1
Adesnik, H.2
Iwanaga, T.3
Bredt, D.S.4
Nicoll, R.A.5
Fukata, M.6
-
60
-
-
77649259534
-
Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy
-
Fukata, Y., Lovero, K. L., Iwanaga, T., Watanabe, A., Yokoi, N., Tabuchi, K., Shigemoto, R., Nicoll, R. A., and Fukata, M. (2010). Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy. Proc. Natl. Acad. Sci. U.S.A. 107, 3799-3804.
-
(2010)
Proc. Natl. Acad. Sci. U. S. A.
, vol.107
, pp. 3799-3804
-
-
Fukata, Y.1
Lovero, K.L.2
Iwanaga, T.3
Watanabe, A.4
Yokoi, N.5
Tabuchi, K.6
Shigemoto, R.7
Nicoll, R.A.8
Fukata, M.9
-
61
-
-
53849108827
-
Strange bedfellows: Reelin and Notch signaling interact to regulate cell migration in the developing neocortex
-
Gaiano, N. (2008). Strange bedfellows: Reelin and Notch signaling interact to regulate cell migration in the developing neocortex. Neuron 60, 189-191.
-
(2008)
Neuron
, vol.60
, pp. 189-191
-
-
Gaiano, N.1
-
62
-
-
77955578706
-
Mutations affecting GABAergic signaling in seizures and epilepsy
-
Galanopoulou, A. S. (2010). Mutations affecting GABAergic signaling in seizures and epilepsy. Pflugers Arch. 460,505-523.
-
(2010)
Pflugers Arch
, vol.460
, pp. 505-523
-
-
Galanopoulou, A.S.1
-
63
-
-
0034656110
-
Blockade of neuronal activity during hip-pocampal development produces a chronic focal epilepsy in the rat
-
Galvan, C. D., Hrachovy, R. A., Smith, K. L., and Swann, J. W (2000). Blockade of neuronal activity during hip-pocampal development produces a chronic focal epilepsy in the rat. J. Neurosci. 20,2904-2916.
-
(2000)
J. Neurosci.
, vol.20
, pp. 2904-2916
-
-
Galvan, C.D.1
Hrachovy, R.A.2
Smith, K.L.3
Swann, J.W.4
-
64
-
-
1542407037
-
Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy
-
Garcia, C. C., Blair, H. J., Seager, M., Coulthard, A., Tennant, S., Buddles, M., Curtis, A., and Goodship, J. A. (2004). Identification of a mutation in synapsin I, a synaptic vesicle protein, in a family with epilepsy. J. Med. Genet. 41,183-186.
-
(2004)
J. Med. Genet.
, vol.41
, pp. 183-186
-
-
Garcia, C.C.1
Blair, H.J.2
Seager, M.3
Coulthard, A.4
Tennant, S.5
Buddles, M.6
Curtis, A.7
Goodship, J.A.8
-
65
-
-
10644264473
-
Different presynaptic roles of synapsins at excitatory and inhibitory synapses
-
Gitler, D., Takagishi, Y., Feng, J., Ren, Y., Rodriguiz, R. M., Wetsel, W. C., Greengard, P., and Augustine, G. J. (2004). Different presynaptic roles of synapsins at excitatory and inhibitory synapses. J. Neurosci. 24, 11368-11380.
-
(2004)
J. Neurosci.
, vol.24
, pp. 11368-11380
-
-
Gitler, D.1
Takagishi, Y.2
Feng, J.3
Ren, Y.4
Rodriguiz, R.M.5
Wetsel, W.C.6
Greengard, P.7
Augustine, G.J.8
-
66
-
-
36448957653
-
Masking epilepsy by combining two epilepsy genes
-
Glasscock, E., Qian, J., Yoo, J. W., and Noebels, J. L. (2007). Masking epilepsy by combining two epilepsy genes. Nat. Neurosci. 10, 1554-1558.
-
(2007)
Nat. Neurosci.
, vol.10
, pp. 1554-1558
-
-
Glasscock, E.1
Qian, J.2
Yoo, J.W.3
Noebels, J.L.4
-
67
-
-
0032498306
-
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
Gleeson, J. G., Allen, K. M., Fox, J. W., Lamperti, E. D., Berkovic, S., Schef-fer, I., Cooper, E. C., Dobyns, W B., Minnerath, S. R., Ross, M. E., and Walsh, C. A. (1998). Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 92, 63-72.
-
(1998)
Cell
, vol.92
, pp. 63-72
-
-
Gleeson, J.G.1
Allen, K.M.2
Fox, J.W.3
Lamperti, E.D.4
Berkovic, S.5
Schef-fer, I.6
Cooper, E.C.7
Dobyns, W.B.8
Minnerath, S.R.9
Ross, M.E.10
Walsh, C.A.11
-
68
-
-
0034255316
-
Neuronal migration disorders: from genetic diseases to developmental mechanisms
-
Gleeson, J. G., and Walsh, C. A. (2000). Neuronal migration disorders: from genetic diseases to developmental mechanisms. Trends Neurosci. 23, 352-359.
-
(2000)
Trends Neurosci
, vol.23
, pp. 352-359
-
-
Gleeson, J.G.1
Walsh, C.A.2
-
69
-
-
1842330268
-
Axonal remodeling during postnatal maturation of CA3 hippocampal pyramidal neurons
-
Gomez-Di Cesare, C. M., Smith, K. L., Rice, F. L., and Swann, J. W. (1997). Axonal remodeling during postnatal maturation of CA3 hippocampal pyramidal neurons. J. Comp. Neurol. 384,165-180.
-
(1997)
J. Comp. Neurol.
, vol.384
, pp. 165-180
-
-
Gomez-Di Cesare, C.M.1
Smith, K.L.2
Rice, F.L.3
Swann, J.W.4
-
70
-
-
33847198932
-
Reelin regulates neuronal progenitor migration in intact and epileptic hippocampus
-
Gong, C., Wang, T. W., Huang, H. S., and Parent, J. M. (2007). Reelin regulates neuronal progenitor migration in intact and epileptic hippocampus. J. Neurosci. 27, 1803-1811.
-
(2007)
J. Neurosci.
, vol.27
, pp. 1803-1811
-
-
Gong, C.1
Wang, T.W.2
Huang, H.S.3
Parent, J.M.4
-
71
-
-
37849049287
-
Cognitive deficits in Tsc1((/() mice in the absence of cerebral lesions and seizures
-
Goorden, S. M. I., van Woerden, G. M., van der Weerd, L., Cheadle, J. P., and Elgersma, Y (2007). Cognitive deficits in Tsc1((/() mice in the absence of cerebral lesions and seizures. Ann. Neurol. 62, 648-655.
-
(2007)
Ann. Neurol.
, vol.62
, pp. 648-655
-
-
Goorden, S.M.I.1
van Woerden, G.M.2
van der Weerd, L.3
Cheadle, J.P.4
Elgersma, Y.5
-
72
-
-
33747594579
-
Genetic malformations of cortical development
-
Guerrini, R., and Marini, C. (2006). Genetic malformations of cortical development. Exp. Brain Res. 173, 322-333.
-
(2006)
Exp. Brain Res.
, vol.173
, pp. 322-333
-
-
Guerrini, R.1
Marini, C.2
-
73
-
-
77951207235
-
Neuronal migration disorders
-
Guerrini, R., and Parrini, E. (2010). Neuronal migration disorders. Neu-robiol. Dis. 38, 154-166.
-
(2010)
Neu-robiol. Dis.
, vol.38
, pp. 154-166
-
-
Guerrini, R.1
Parrini, E.2
-
74
-
-
33644750857
-
Molecular mechanisms of cortical differentiation
-
Guillemot, F., Molnar, Z., Tarabykin, V., and Stoykova, A. (2006). Molecular mechanisms of cortical differentiation. Eur. J. Neurosci. 23, 857-868.
-
(2006)
Eur. J. Neurosci.
, vol.23
, pp. 857-868
-
-
Guillemot, F.1
Molnar, Z.2
Tarabykin, V.3
Stoykova, A.4
-
75
-
-
0037101624
-
Role for reelin in the development of granule cell dispersion in temporal lobe epilepsy
-
Haas, C. A., Dudeck, O., Kirsch, M., Huszka, C., Kann, G., Pollak, S., Zentner, J., and Frotscher, M. (2002). Role for reelin in the development of granule cell dispersion in temporal lobe epilepsy. J. Neurosci. 22, 5797-5802.
-
(2002)
J. Neurosci.
, vol.22
, pp. 5797-5802
-
-
Haas, C.A.1
Dudeck, O.2
Kirsch, M.3
Huszka, C.4
Kann, G.5
Pollak, S.6
Zentner, J.7
Frotscher, M.8
-
76
-
-
77249154019
-
Reelin deficiency causes granule cell dispersion in epilepsy. Exp
-
Haas, C. A., and Frotscher, M. (2010). Reelin deficiency causes granule cell dispersion in epilepsy. Exp. Brain Res. 200, 141-149.
-
(2010)
Brain Res
, vol.200
, pp. 141-149
-
-
Haas, C.A.1
Frotscher, M.2
-
77
-
-
32544437651
-
Layer positioning of late-born cortical interneurons is dependent on Reelin but not p35 signaling
-
Hammond, V., So, E., Gunnersen, J.,Val-canis, H., Kalloniatis, M., and Tan, S. S. (2006). Layer positioning of late-born cortical interneurons is dependent on Reelin but not p35 signaling. J. Neurosci. 26,1646-1655.
-
(2006)
J. Neurosci.
, vol.26
, pp. 1646-1655
-
-
Hammond, V.1
So, E.2
Gunnersen, J.3
Val-canis, H.4
Kalloniatis, M.5
Tan, S.S.6
-
78
-
-
77950076985
-
Neurogenic radial glia in the outer subventricu-lar zone of human neocortex
-
Hansen, D. V., Lui, J. H., Parker, P. R., and Kriegstein, A. R. (2010). Neurogenic radial glia in the outer subventricu-lar zone of human neocortex. Nature 464, 554-561.
-
(2010)
Nature
, vol.464
, pp. 554-561
-
-
Hansen, D.V.1
Lui, J.H.2
Parker, P.R.3
Kriegstein, A.R.4
-
79
-
-
53849138043
-
Interaction between Reelin and Notch signaling regulates neuronal migration in the cerebral cortex
-
Hashimoto-Torii, K., Torii, M., Sark-isian, M. R., Bartley, C. M., Shen, J., Radtke, F., Gridley, T., Sestan, N., and Rakic,P. (2008). Interaction between Reelin and Notch signaling regulates neuronal migration in the cerebral cortex. Neuron 60,273-284.
-
(2008)
Neuron
, vol.60
, pp. 273-284
-
-
Hashimoto-Torii, K.1
Torii, M.2
Sark-isian, M.R.3
Bartley, C.M.4
Shen, J.5
Radtke, F.6
Gridley, T.7
Sestan, N.8
Rakic, P.9
-
80
-
-
33646849420
-
Reelin deficiency and displacement of mature neurons, but not neurogenesis, underlie the formation of granule cell dispersion in the epileptic hippocampus
-
Heinrich, C., Nitta, N., Flubacher, A., Muller, M., Fahrner, A., Kirsch, M., Freiman, T., Suzuki, F., Depaulis, A., Frotscher, M., and Haas, C. A. (2006). Reelin deficiency and displacement of mature neurons, but not neurogenesis, underlie the formation of granule cell dispersion in the epileptic hippocampus. J. Neurosci. 26,4701-4713.
-
(2006)
J. Neurosci.
, vol.26
, pp. 4701-4713
-
-
Heinrich, C.1
Nitta, N.2
Flubacher, A.3
Muller, M.4
Fahrner, A.5
Kirsch, M.6
Freiman, T.7
Suzuki, F.8
Depaulis, A.9
Frotscher, M.10
Haas, C.A.11
-
81
-
-
0028340242
-
Deletion map of the coloboma (Cm) locus on mouse chromosome 2
-
Hess, E. J., Collins, K. A., Copeland, N. G., Jenkins, N. A., and Wilson, M. C. (1994). Deletion map of the coloboma (Cm) locus on mouse chromosome 2. Genomics21, 257-261.
-
(1994)
Genomics
, vol.21
, pp. 257-261
-
-
Hess, E.J.1
Collins, K.A.2
Copeland, N.G.3
Jenkins, N.A.4
Wilson, M.C.5
-
82
-
-
0026642183
-
Spontaneous locomotor hyperactivity in a mouse mutant with a deletion including the Snap gene on chromosome 2
-
Hess, E. J., Jinnah, H. A., Kozak, C. A., and Wilson, M. C. (1992). Spontaneous locomotor hyperactivity in a mouse mutant with a deletion including the Snap gene on chromosome 2. J. Neurosci. 12, 2865-2874.
-
(1992)
J. Neurosci.
, vol.12
, pp. 2865-2874
-
-
Hess, E.J.1
Jinnah, H.A.2
Kozak, C.A.3
Wilson, M.C.4
-
83
-
-
34247164656
-
Tuberous sclerosis complex and epilepsy: recent developments and future challenges
-
Holmes, G. L., and Stafstrom, C. E. (2007). Tuberous sclerosis complex and epilepsy: recent developments and future challenges. Epilepsia 48, 617-630.
-
(2007)
Epilepsia
, vol.48
, pp. 617-630
-
-
Holmes, G.L.1
Stafstrom, C.E.2
-
84
-
-
79959889039
-
Regulation of cortical neuron migration by the Reelin signaling pathway
-
Honda, T., Kobayashi, K., Mikoshiba, K., and Nakajima, K. (2011). Regulation of cortical neuron migration by the Reelin signaling pathway. Neu-rochem. Res. 36,1270-1279.
-
(2011)
Neu-rochem. Res.
, vol.36
, pp. 1270-1279
-
-
Honda, T.1
Kobayashi, K.2
Mikoshiba, K.3
Nakajima, K.4
-
85
-
-
77955845741
-
Pharmacological inhibition of the mammalian target of rapamycin pathway suppresses acquired epilepsy
-
Huang, X., Zhang, H., Yang, J., Wu, J., Mcmahon, J., Lin, Y., Cao, Z., Gruen-thal, M., and Huang, Y (2010). Pharmacological inhibition of the mammalian target of rapamycin pathway suppresses acquired epilepsy. Neuro-biol. Dis. 40,193-199.
-
(2010)
Neuro-biol. Dis.
, vol.40
, pp. 193-199
-
-
Huang, X.1
Zhang, H.2
Yang, J.3
Wu, J.4
Mcmahon, J.5
Lin, Y.6
Cao, Z.7
Gruen-thal, M.8
Huang, Y.9
-
86
-
-
0037459076
-
Membrane fusion
-
Jahn, R., Lang, T., and Sudhof, T. C. (2003). Membrane fusion. Cell 112, 519-533.
-
(2003)
Cell
, vol.112
, pp. 519-533
-
-
Jahn, R.1
Lang, T.2
Sudhof, T.C.3
-
87
-
-
0033398955
-
SV2A and SV2B function as redundant Ca2+ regulators in neurotransmitter release
-
Janz, R., Goda, Y., Geppert, M., Missler, M., and Sudhof, T. C. (1999). SV2A and SV2B function as redundant Ca2+ regulators in neurotransmitter release. Neuron 24,1003-1016.
-
(1999)
Neuron
, vol.24
, pp. 1003-1016
-
-
Janz, R.1
Goda, Y.2
Geppert, M.3
Missler, M.4
Sudhof, T.C.5
-
88
-
-
27944450100
-
Hamartin and tuberin: working together for tumour suppression
-
Jozwiak, J. (2006). Hamartin and tuberin: working together for tumour suppression. Int. J. Cancer 118,1-5.
-
(2006)
Int. J. Cancer
, vol.118
, pp. 1-5
-
-
Jozwiak, J.1
-
89
-
-
18544376557
-
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
-
Kalachikov, S., Evgrafov, O., Ross, B., Winawer, M., Barker-Cummings, C., Martinelli Boneschi, F., Choi, C., Morozov, P., Das, K., Teplitskaya, E., Yu, A., Cayanis, E., Penchaszadeh, G., Kottmann, A. H., Pedley, T. A., Hauser, W A., Ottman, R., and Gilliam, T. C. (2002). Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat. Genet. 30, 335-341.
-
(2002)
Nat. Genet.
, vol.30
, pp. 335-341
-
-
Kalachikov, S.1
Evgrafov, O.2
Ross, B.3
Winawer, M.4
Barker-Cummings, C.5
Martinelli Boneschi, F.6
Choi, C.7
Morozov, P.8
Das, K.9
Teplitskaya, E.10
Yu, A.11
Cayanis, E.12
Penchaszadeh, G.13
Kottmann, A.H.14
Pedley, T.A.15
Hauser, W.A.16
Ottman, R.17
Gilliam, T.C.18
-
90
-
-
0029963657
-
Synaptic activity and the construction of cortical circuits
-
Katz, L. C., and Shatz, C. J. (1996). Synaptic activity and the construction of cortical circuits. Science 274, 1133-1138.
-
(1996)
Science
, vol.274
, pp. 1133-1138
-
-
Katz, L.C.1
Shatz, C.J.2
-
91
-
-
0035863416
-
A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities
-
Kearney, J. A., Plummer, N. W., Smith, M. R., Kapur, J., Cummins, T. R., Waxman, S. G., Goldin, A. L., and Meisler, M. H. (2001). A gain-of-function mutation in the sodium channel gene Scn2a results in seizures and behavioral abnormalities. Neuroscience 102, 307-317.
-
(2001)
Neuroscience
, vol.102
, pp. 307-317
-
-
Kearney, J.A.1
Plummer, N.W.2
Smith, M.R.3
Kapur, J.4
Cummins, T.R.5
Waxman, S.G.6
Goldin, A.L.7
Meisler, M.H.8
-
92
-
-
33846037932
-
Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans
-
Keays, D. A., Tian, G., Poirier, K., Huang, G.-J., Siebold, C., Cleak, J., Oliver, P. L., Fray, M., Harvey, R. J., Molnar, Z., Pinon, M. C., Dear, N., Valdar, W., Brown, S. D. M., Davies, K. E., Rawl-ins, J. N.P., Cowan, N. J., Nolan, P., Chelly, J., and Flint, J. (2007). Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans. Cell 128, 45-57.
-
(2007)
Cell
, vol.128
, pp. 45-57
-
-
Keays, D.A.1
Tian, G.2
Poirier, K.3
Huang, G.-J.4
Siebold, C.5
Cleak, J.6
Oliver, P.L.7
Fray, M.8
Harvey, R.J.9
Molnar, Z.10
Pinon, M.C.11
Dear, N.12
Valdar, W.13
Brown, S.D.M.14
Davies, K.E.15
Rawl-ins, J.N.P.16
Cowan, N.J.17
Nolan, P.18
Chelly, J.19
Flint, J.20
more..
-
93
-
-
36549009913
-
Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly
-
Kerjan, G., and Gleeson, J. G. (2007). Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly. Trends Genet. 23, 623-630.
-
(2007)
Trends Genet
, vol.23
, pp. 623-630
-
-
Kerjan, G.1
Gleeson, J.G.2
-
94
-
-
58149352587
-
Moving neurons back into place
-
Kerjan, G., and Gleeson, J. G. (2009). Moving neurons back into place. Nat. Med. 15, 17-18.
-
(2009)
Nat. Med.
, vol.15
, pp. 17-18
-
-
Kerjan, G.1
Gleeson, J.G.2
-
95
-
-
70350755706
-
Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice
-
Kitamura, K., Itou, Y., Yanazawa, M., Ohsawa, M., Suzuki-Migishima, R., Umeki, Y., Hohjoh, H., Yanagawa, Y., Shinba, T., Itoh, M., Nakamura, K., and Goto, Y. (2009). Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice. Hum. Mol. Genet. 18, 3708-3724.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 3708-3724
-
-
Kitamura, K.1
Itou, Y.2
Yanazawa, M.3
Ohsawa, M.4
Suzuki-Migishima, R.5
Umeki, Y.6
Hohjoh, H.7
Yanagawa, Y.8
Shinba, T.9
Itoh, M.10
Nakamura, K.11
Goto, Y.12
-
96
-
-
0036844387
-
Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal gen-italia in humans
-
Kitamura, K., Yanazawa, M., Sugiyama, N., Miura, H., Iizuka-Kogo, A., Kusaka, M., Omichi, K., Suzuki, R., Kato-Fukui, Y., Kamiirisa, K., Mat-suo, M., Kamijo, S., Kasahara, M., Yoshioka, H., Ogata, T., Fukuda, T., Kondo, I., Kato, M., Dobyns, W. B., Yokoyama, M., and Morohashi, K. (2002). Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal gen-italia in humans. Nat. Genet. 32, 359-369.
-
(2002)
Nat. Genet.
, vol.32
, pp. 359-369
-
-
Kitamura, K.1
Yanazawa, M.2
Sugiyama, N.3
Miura, H.4
Iizuka-Kogo, A.5
Kusaka, M.6
Omichi, K.7
Suzuki, R.8
Kato-Fukui, Y.9
Kamiirisa, K.10
Mat-suo, M.11
Kamijo, S.12
Kasahara, M.13
Yoshioka, H.14
Ogata, T.15
Fukuda, T.16
Kondo, I.17
Kato, M.18
Dobyns, W.B.19
Yokoyama, M.20
Morohashi, K.21
more..
-
97
-
-
0035902509
-
A germ-line Tsc1 mutation causes tumor development and embryonic lethality that are similar, but not identical to, those caused by Tsc2 mutation in mice
-
Kobayashi, T., Minowa, O., Sugitani, Y., Takai, S., Mitani, H., Kobayashi, E., Noda, T., and Hino, O. (2001). A germ-line Tsc1 mutation causes tumor development and embryonic lethality that are similar, but not identical to, those caused by Tsc2 mutation in mice. Proc. Natl. Acad. Sci. U.S.A. 98, 8762-8767.
-
(2001)
Proc. Natl. Acad. Sci. U. S. A.
, vol.98
, pp. 8762-8767
-
-
Kobayashi, T.1
Minowa, O.2
Sugitani, Y.3
Takai, S.4
Mitani, H.5
Kobayashi, E.6
Noda, T.7
Hino, O.8
-
98
-
-
29544446945
-
Doublecortin-like kinase functions with doublecortin to mediate fiber tract decussation and neuronal migration
-
Koizumi, H., Tanaka, T., and Glee-son, J. G. (2006). Doublecortin-like kinase functions with doublecortin to mediate fiber tract decussation and neuronal migration. Neuron 49, 55-66.
-
(2006)
Neuron
, vol.49
, pp. 55-66
-
-
Koizumi, H.1
Tanaka, T.2
Glee-son, J.G.3
-
99
-
-
33750375788
-
Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion
-
Kriegstein, A., Noctor, S., and Martinez-Cerdeno, V. (2006). Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion. Nat. Rev. Neurosci. 7,883-890.
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 883-890
-
-
Kriegstein, A.1
Noctor, S.2
Martinez-Cerdeno, V.3
-
100
-
-
3042638932
-
Patterns of neuronal migration in the embryonic cortex
-
Kriegstein, A. R., and Noctor, S. C. (2004). Patterns of neuronal migration in the embryonic cortex. Trends Neurosci. 27, 392-399.
-
(2004)
Trends Neurosci
, vol.27
, pp. 392-399
-
-
Kriegstein, A.R.1
Noctor, S.C.2
-
101
-
-
77954520146
-
Neurological channelopathies
-
Kullmann, D. M. (2010). Neurological channelopathies. Annu. Rev. Neurosci. 33, 151-172.
-
(2010)
Annu. Rev. Neurosci.
, vol.33
, pp. 151-172
-
-
Kullmann, D.M.1
-
102
-
-
77957825588
-
Spontaneous epileptic manifestations in a DCX knockdown model of human double cortex
-
Lapray, D., Popova, I. Y., Kindler, J., Jor-quera, I., Becq, H., Manent, J. B., Luhmann, H. J., and Represa, A. (2010). Spontaneous epileptic manifestations in a DCX knockdown model of human double cortex. Cereb. Cortex 20,2694-2701.
-
(2010)
Cereb. Cortex
, vol.20
, pp. 2694-2701
-
-
Lapray, D.1
Popova, I.Y.2
Kindler, J.3
Jor-quera, I.4
Becq, H.5
Manent, J.B.6
Luhmann, H.J.7
Represa, A.8
-
103
-
-
0032941179
-
Benign familial neonatal epilepsy with mutations in two potassium channel genes
-
Leppert, M., and Singh, N. (1999). Benign familial neonatal epilepsy with mutations in two potassium channel genes. Curr. Opin. Neurol. 12, 143-147.
-
(1999)
Curr. Opin. Neurol.
, vol.12
, pp. 143-147
-
-
Leppert, M.1
Singh, N.2
-
104
-
-
58349091226
-
The DLX1 and DLX2 genes and susceptibility to autism spectrum disorders
-
Liu, X., Novosedlik, N., Wang, A., Hudson, M. L., Cohen, I. L., Chudley, A. E., Forster-Gibson, C. J., Lewis, S. M. E., and Holden, J. J. A. (2009). The DLX1 and DLX2 genes and susceptibility to autism spectrum disorders. Eur. J. Hum. Genet. 17, 228-235.
-
(2009)
Eur. J. Hum. Genet
, vol.17
, pp. 228-235
-
-
Liu, X.1
Novosedlik, N.2
Wang, A.3
Hudson, M.L.4
Cohen, I.L.5
Chudley, A.E.6
Forster-Gibson, C.J.7
Lewis, S.M.E.8
Holden, J.J.A.9
-
105
-
-
79959924122
-
Development and evolution of the human neocortex
-
Lui, J. H., Hansen, D. V., and Kriegstein, A. R. (2011). Development and evolution of the human neocortex. Cell 146,18-36.
-
(2011)
Cell
, vol.146
, pp. 18-36
-
-
Lui, J.H.1
Hansen, D.V.2
Kriegstein, A.R.3
-
106
-
-
58149250332
-
Are cortical tubers epileptogenic? Evidence from electrocorticography
-
Major, P., Rakowski, S., Simon, M. V., Cheng, M. L., Eskandar, E., Baron, J., Leeman, B. A., Frosch, M. P., and Thiele, E. A. (2009). Are cortical tubers epileptogenic? Evidence from electrocorticography. Epilepsia 50,147-154.
-
(2009)
Epilepsia
, vol.50
, pp. 147-154
-
-
Major, P.1
Rakowski, S.2
Simon, M.V.3
Cheng, M.L.4
Eskandar, E.5
Baron, J.6
Leeman, B.A.7
Frosch, M.P.8
Thiele, E.A.9
-
107
-
-
0037421992
-
Neuronal or glial progeny: regional differences in radial glia fate
-
Malatesta, P., Hack, M. A., Hartfuss, E., Kettenmann, H., Klinkert,W.,Kirch-hoff, F., and Gotz, M. (2003). Neuronal or glial progeny: regional differences in radial glia fate. Neuron 37,751-764.
-
(2003)
Neuron
, vol.37
, pp. 751-764
-
-
Malatesta, P.1
Hack, M.A.2
Hartfuss, E.3
Kettenmann, H.4
Klinkert, W.5
Kirch-hoff, F.6
Gotz, M.7
-
108
-
-
18644370431
-
A noncanonical release of GABA and glutamate modulates neuronal migration
-
Manent, J. B., Demarque, M., Jor-quera, I., Pellegrino, C., Ben-Ari, Y., Aniksztejn, L., and Represa, A. (2005). A noncanonical release of GABA and glutamate modulates neuronal migration. J. Neurosci. 25, 4755-4765.
-
(2005)
J. Neurosci.
, vol.25
, pp. 4755-4765
-
-
Manent, J.B.1
Demarque, M.2
Jor-quera, I.3
Pellegrino, C.4
Ben-Ari, Y.5
Aniksztejn, L.6
Represa, A.7
-
109
-
-
33745260448
-
Glutamate acting on AMPA but not NMDA receptors modulates the migration of hippocam-pal interneurons
-
Manent, J. B., Jorquera, I., Ben-Ari, Y., Aniksztejn, L., and Represa, A. (2006). Glutamate acting on AMPA but not NMDA receptors modulates the migration of hippocam-pal interneurons. J. Neurosci. 26, 5901-5909.
-
(2006)
J. Neurosci.
, vol.26
, pp. 5901-5909
-
-
Manent, J.B.1
Jorquera, I.2
Ben-Ari, Y.3
Aniksztejn, L.4
Represa, A.5
-
110
-
-
38549100026
-
Antiepileptic drugs and brain maturation: fetal exposure to lamotrigine generates cortical malformations in rats
-
Manent, J. B., Jorquera, I., Franco, V., Ben-Ari, Y., Perucca, E., and Represa, A. (2008). Antiepileptic drugs and brain maturation: fetal exposure to lamotrigine generates cortical malformations in rats. Epilepsy Res. 78, 131-139.
-
(2008)
Epilepsy Res
, vol.78
, pp. 131-139
-
-
Manent, J.B.1
Jorquera, I.2
Franco, V.3
Ben-Ari, Y.4
Perucca, E.5
Represa, A.6
-
111
-
-
34247145936
-
Fetal exposure to GABA-acting antiepileptic drugs generates hippocampal and cortical dysplasias
-
Manent, J. B., Jorquera, I., Mazzuc-chelli, I., Depaulis, A., Perucca, E., Ben-Ari, Y., and Represa, A. (2007). Fetal exposure to GABA-acting antiepileptic drugs generates hippocampal and cortical dysplasias. Epilepsia 48, 684-693.
-
(2007)
Epilepsia
, vol.48
, pp. 684-693
-
-
Manent, J.B.1
Jorquera, I.2
Mazzuc-chelli, I.3
Depaulis, A.4
Perucca, E.5
Ben-Ari, Y.6
Represa, A.7
-
112
-
-
34249087739
-
Neurotransmitters and brain maturation: early paracrine actions of GABA and glutamate modulate neuronal migration
-
Manent, J. B., and Represa, A. (2007). Neurotransmitters and brain maturation: early paracrine actions of GABA and glutamate modulate neuronal migration. Neuroscientist 13, 268-279.
-
(2007)
Neuroscientist
, vol.13
, pp. 268-279
-
-
Manent, J.B.1
Represa, A.2
-
113
-
-
58149343267
-
Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder
-
Manent, J. B., Wang, Y., Chang, Y., Paramasivam, M., and Loturco, J. J. (2009). Dcx reexpression reduces subcortical band heterotopia and seizure threshold in an animal model of neuronal migration disorder. Nat. Med. 15,84-90.
-
(2009)
Nat. Med.
, vol.15
, pp. 84-90
-
-
Manent, J.B.1
Wang, Y.2
Chang, Y.3
Paramasivam, M.4
Loturco, J.J.5
-
114
-
-
80052549646
-
Environmental enrichment reduces spontaneous seizures in the Q54 transgenic mouse model of temporal lobe epilepsy
-
Manno, I., Macchi, F., Caleo, M., and Bozzi, Y (2011). Environmental enrichment reduces spontaneous seizures in the Q54 transgenic mouse model of temporal lobe epilepsy. Epilepsia52,e113-e117.
-
(2011)
Epilepsia
-
-
Manno, I.1
Macchi, F.2
Caleo, M.3
Bozzi, Y.4
-
115
-
-
77949300922
-
Voltage-gated sodium channels as therapeutic targets in epilepsy and other neurological disorders
-
Mantegazza, M., Curia, G., Biagini, G., Ragsdale, D. S., and Avoli, M. (2010). Voltage-gated sodium channels as therapeutic targets in epilepsy and other neurological disorders. Lancet Neurol. 9,413-424.
-
(2010)
Lancet Neurol
, vol.9
, pp. 413-424
-
-
Mantegazza, M.1
Curia, G.2
Biagini, G.3
Ragsdale, D.S.4
Avoli, M.5
-
116
-
-
79957591321
-
What disorders of cortical development tell us about the cortex: one plus one does not always make two
-
Manzini, M. C., and Walsh, C. A. (2011). What disorders of cortical development tell us about the cortex: one plus one does not always make two. Curr. Opin. Genet. Dev. 21, 333-339.
-
(2011)
Curr. Opin. Genet. Dev.
, vol.21
, pp. 333-339
-
-
Manzini, M.C.1
Walsh, C.A.2
-
118
-
-
67649391197
-
Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females
-
Marsh, E., Fulp, C., Gomez, E., Nasral-lah, I., Minarcik, J., Sudi, J., Christian, S. L., Mancini, G., Labosky, P., Dobyns, W., Brooks-Kayal, A., and Golden, J. A. (2009). Targeted loss of Arx results in a developmental epilepsy mouse model and recapitulates the human phenotype in heterozygous females. Brain 132, 1563-1576.
-
(2009)
Brain
, vol.132
, pp. 1563-1576
-
-
Marsh, E.1
Fulp, C.2
Gomez, E.3
Nasral-lah, I.4
Minarcik, J.5
Sudi, J.6
Christian, S.L.7
Mancini, G.8
Labosky, P.9
Dobyns, W.10
Brooks-Kayal, A.11
Golden, J.A.12
-
119
-
-
77951248599
-
Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAer-gic) interneuron abnormalities
-
Martin, M. S., Dutt, K., Papale, L. A., Dubé, C. M., Dutton, S. B., de Haan, G., Shankar, A., Tufik, S., Meisler, M. H., Baram, T. Z., Goldin, A. L., and Escayg, A. (2010). Altered function of the SCN1A voltage-gated sodium channel leads to gamma-aminobutyric acid-ergic (GABAer-gic) interneuron abnormalities. J. Biol. Chem. 285, 9823-9834.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 9823-9834
-
-
Martin, M.S.1
Dutt, K.2
Papale, L.A.3
Dubé, C.M.4
Dutton, S.B.5
de Haan, G.6
Shankar, A.7
Tufik, S.8
Meisler, M.H.9
Baram, T.Z.10
Goldin, A.L.11
Escayg, A.12
-
120
-
-
0035145745
-
Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia
-
Matsumoto, N., Leventer, R. J., Kuc, J. A., Mewborn, S. K., Dudlicek, L. L., Ramocki, M. B., Pilz, D. T., Mills, P. L., Das, S., Ross, M. E., Ledbetter, D. H., and Dobyns, W.B. (2001). Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia. Eur. J. Hum. Genet. 9, 5-12.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 5-12
-
-
Matsumoto, N.1
Leventer, R.J.2
Kuc, J.A.3
Mewborn, S.K.4
Dudlicek, L.L.5
Ramocki, M.B.6
Pilz, D.T.7
Mills, P.L.8
Das, S.9
Ross, M.E.10
Ledbetter, D.H.11
Dobyns, W.B.12
-
121
-
-
77954514571
-
Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects
-
Meisler, M. H., O'Brien, J. E., and Sharkey,L.M. (2010). Sodium channel gene family: epilepsy mutations, gene interactions and modifier effects.J. Physiol. 588,1841-1848.
-
(2010)
J. Physiol.
, vol.588
, pp. 1841-1848
-
-
Meisler, M.H.1
O'Brien, J.E.2
Sharkey, L.M.3
-
122
-
-
76149146046
-
Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons
-
Miyoshi, G., Hjerling-Leffler, J., Karayannis, T., Sousa, V. H., Butt, S. J., Battiste, J., Johnson, J. E., Machold, R. P., and Fishell, G. (2010). Genetic fate mapping reveals that the caudal ganglionic eminence produces a large and diverse population of superficial cortical interneurons. J. Neurosci. 30,1582-1594.
-
(2010)
J. Neurosci.
, vol.30
, pp. 1582-1594
-
-
Miyoshi, G.1
Hjerling-Leffler, J.2
Karayannis, T.3
Sousa, V.H.4
Butt, S.J.5
Battiste, J.6
Johnson, J.E.7
Machold, R.P.8
Fishell, G.9
-
123
-
-
34249084013
-
Neuronal subtype specification in the cerebral cortex
-
Molyneaux, B. J., Arlotta, P., Menezes, J. R., and Macklis, J. D. (2007). Neuronal subtype specification in the cerebral cortex. Nat. Rev. Neurosci. 8, 427-437.
-
(2007)
Nat. Rev. Neurosci.
, vol.8
, pp. 427-437
-
-
Molyneaux, B.J.1
Arlotta, P.2
Menezes, J.R.3
Macklis, J.D.4
-
124
-
-
64249118425
-
Rapamycin reduces seizure frequency in tuberous sclerosis complex
-
Muncy, J., Butler, I. J., and Koenig, M. K. (2009). Rapamycin reduces seizure frequency in tuberous sclerosis complex. J. Child Neurol. 24, 477.
-
(2009)
J. Child Neurol.
, vol.24
, pp. 477
-
-
Muncy, J.1
Butler, I.J.2
Koenig, M.K.3
-
125
-
-
0042357395
-
The biology of epilepsy genes
-
Noebels, J. L. (2003). The biology of epilepsy genes. Annu. Rev. Neurosci. 26, 599-625.
-
(2003)
Annu. Rev. Neurosci.
, vol.26
, pp. 599-625
-
-
Noebels, J.L.1
-
126
-
-
49649090865
-
Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus
-
doi:10.1371/journal.pone.0002473
-
Nosten-Bertrand, M., Kappeler, C., Dinocourt, C., Denis, C., Germain, J., Phan Dinh Tuy, F., Verstraeten, S., Alvarez, C., Metin, C., Chelly, J., Giros, B., Miles, R., Depaulis, A., and Francis, F. (2008). Epilepsy in Dcx knockout mice associated with discrete lamination defects and enhanced excitability in the hippocampus. PLoS ONE 3, e2473. doi:10.1371/journal.pone.0002473
-
(2008)
PLoS ONE
, vol.3
-
-
Nosten-Bertrand, M.1
Kappeler, C.2
Dinocourt, C.3
Denis, C.4
Germain, J.5
Phan Dinh Tuy, F.6
Verstraeten, S.7
Alvarez, C.8
Metin, C.9
Chelly, J.10
Giros, B.11
Miles, R.12
Depaulis, A.13
Francis, F.14
-
127
-
-
62649142705
-
Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy
-
Oakley, J. C., Kalume, F., Yu, F. H., Scheuer, T., and Catterall, W. A. (2009). Temperature- and age-dependent seizures in a mouse model of severe myoclonic epilepsy in infancy. Proc. Natl. Acad. Sci. U.S.A. 106, 3994-3999.
-
(2009)
Proc. Natl. Acad. Sci. U.S.A.
, vol.106
, pp. 3994-3999
-
-
Oakley, J.C.1
Kalume, F.2
Yu, F.H.3
Scheuer, T.4
Catterall, W.A.5
-
128
-
-
34249791771
-
Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation
-
Ogiwara, I., Miyamoto, H., Morita, N., Atapour, N., Mazaki, E., Inoue, I., Takeuchi, T., Itohara, S., Yanagawa, Y., Obata, K., Furuichi, T., Hensch, T. K., and Yamakawa K. (2007). Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation. J. Neurosci. 27, 5903-5914.
-
(2007)
J. Neurosci.
, vol.27
, pp. 5903-5914
-
-
Ogiwara, I.1
Miyamoto, H.2
Morita, N.3
Atapour, N.4
Mazaki, E.5
Inoue, I.6
Takeuchi, T.7
Itohara, S.8
Yanagawa, Y.9
Obata, K.10
Furuichi, T.11
Hensch, T.K.12
Yamakawa, K.13
-
129
-
-
0029917555
-
Common and distinct fusion proteins in axonal growth and transmitter release
-
Osen-Sand, A., Staple, J. K., Naldi, E., Schiavo, G., Rossetto, O., Petit-pierre, S., Malgaroli, A., Monte-cucco, C., and Catsicas, S. (1996). Common and distinct fusion proteins in axonal growth and transmitter release. J. Comp. Neurol. 367, 222-234.
-
(1996)
J. Comp. Neurol.
, vol.367
, pp. 222-234
-
-
Osen-Sand, A.1
Staple, J.K.2
Naldi, E.3
Schiavo, G.4
Rossetto, O.5
Petit-pierre, S.6
Malgaroli, A.7
Monte-cucco, C.8
Catsicas, S.9
-
130
-
-
33645318989
-
Reeler homozy-gous mice exhibit enhanced susceptibility to epileptiform activity
-
Patrylo, P. R., Browning, R. A., and Cranick, S. (2006). Reeler homozy-gous mice exhibit enhanced susceptibility to epileptiform activity. Epilepsia 47, 257-266.
-
(2006)
Epilepsia
, vol.47
, pp. 257-266
-
-
Patrylo, P.R.1
Browning, R.A.2
Cranick, S.3
-
131
-
-
0001490738
-
Is epilepsy a progressive disorder? Prospects for new therapeutic approaches in temporal-lobe epilepsy
-
Pitkanen, A., and Sutula, T. P. (2002). Is epilepsy a progressive disorder? Prospects for new therapeutic approaches in temporal-lobe epilepsy. Lancet Neurol. 1,173-181.
-
(2002)
Lancet Neurol
, vol.1
, pp. 173-181
-
-
Pitkanen, A.1
Sutula, T.P.2
-
132
-
-
33745968073
-
Layer acquisition by cortical GABAergic interneurons is independent of Reelin signaling
-
Pla, R., Borrell, V., Flames, N., and Marín, O. (2006). Layer acquisition by cortical GABAergic interneurons is independent of Reelin signaling. J. Neurosci. 26, 6924-6934.
-
(2006)
J. Neurosci.
, vol.26
, pp. 6924-6934
-
-
Pla, R.1
Borrell, V.2
Flames, N.3
Marín, O.4
-
133
-
-
38349133919
-
Activity-dependent phosphorylation of Ser187 is required for SNAP-25-negative modulation of neuronal voltage-gated calcium channels
-
Pozzi, D., Condliffe, S., Bozzi, Y., Chikhladze, M., Grumelli, C., Proux-Gillardeaux, V., Takahashi, M., Franceschetti, S., Verderio, C., and Matteoli, M. (2008). Activity-dependent phosphorylation of Ser187 is required for SNAP-25-negative modulation of neuronal voltage-gated calcium channels. Proc. Natl. Acad. Sci. U.S.A. 105, 323-328.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 323-328
-
-
Pozzi, D.1
Condliffe, S.2
Bozzi, Y.3
Chikhladze, M.4
Grumelli, C.5
Proux-Gillardeaux, V.6
Takahashi, M.7
Franceschetti, S.8
Verderio, C.9
Matteoli, M.10
-
134
-
-
0031018055
-
Coloboma hyperactive mutant mice exhibit regional and transmitter-specific deficits in neurotransmis-sion
-
Raber, J., Mehta, P. P., Kreifeldt, M., Parsons, L. H., Weiss, F., Bloom, F. E., and Wilson, M. C. (1997). Coloboma hyperactive mutant mice exhibit regional and transmitter-specific deficits in neurotransmis-sion. J. Neurochem. 68,176-186.
-
(1997)
J. Neurochem.
, vol.68
, pp. 176-186
-
-
Raber, J.1
Mehta, P.P.2
Kreifeldt, M.3
Parsons, L.H.4
Weiss, F.5
Bloom, F.E.6
Wilson, M.C.7
-
135
-
-
79958184395
-
A pulse rapamycin therapy for infantile spasms and associated cognitive decline
-
Raffo, E., Coppola, A., Ono, T.,Briggs, S. W., and Galanopoulou, A. S. (2011). A pulse rapamycin therapy for infantile spasms and associated cognitive decline. Neurobiol Dis. 43, 322-329.
-
(2011)
Neurobiol Dis
, vol.43
, pp. 322-329
-
-
Raffo, E.1
Coppola, A.2
Ono, T.3
Briggs, S.W.4
Galanopoulou, A.S.5
-
136
-
-
35048888932
-
The radial edifice of cortical architecture: from neuronal silhouettes to genetic engineering
-
Rakic, P. (2007). The radial edifice of cortical architecture: from neuronal silhouettes to genetic engineering. Brain Res. Rev. 55, 204-219.
-
(2007)
Brain Res. Rev
, vol.55
, pp. 204-219
-
-
Rakic, P.1
-
137
-
-
0029024135
-
Essential functions of synapsins I and II in synap-tic vesicle regulation
-
Rosahl, T. W., Spillane, D., Missler, M., Herz, J., Selig, D. K., Wolff, J. R., Hammer, R. E., Malenka, R. C., and Sudhof, T. C. (1995). Essential functions of synapsins I and II in synap-tic vesicle regulation. Nature 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
-
138
-
-
0033642929
-
Intrinsic and extrinsic control of cortical development
-
discussion 75-82, 109-113
-
Rubenstein, J. L. (2000). Intrinsic and extrinsic control of cortical development. Novartis Found. Symp. 228, 67-75; discussion 75-82,109-113.
-
(2000)
Novartis Found. Symp.
, vol.228
, pp. 67-75
-
-
Rubenstein, J.L.1
-
139
-
-
79952668314
-
Annual research review: development of the cerebral cortex: implications for neurodevelopmental disorders
-
Rubenstein, J. L. (2011). Annual research review: development of the cerebral cortex: implications for neurodevelopmental disorders. J. Child Psychol Psychiatry 52, 339-355.
-
(2011)
J. Child Psychol Psychiatry
, vol.52
, pp. 339-355
-
-
Rubenstein, J.L.1
-
140
-
-
63349100105
-
Enrich the environment to empower the brain
-
Sale, A., Berardi, N., and Maffei, L. (2009). Enrich the environment to empower the brain. Trends Neurosci. 32, 233-239.
-
(2009)
Trends Neurosci
, vol.32
, pp. 233-239
-
-
Sale, A.1
Berardi, N.2
Maffei, L.3
-
141
-
-
33749515473
-
Effects in neocortical neurons of mutations of the Na(v)1, 2 Na+ channel causing benign familial neonatal-infantile seizures
-
Scalmani, P., Rusconi, R., Armatura, E., Zara, F., Avanzini, G., Franceschetti, S., and Mantegazza, M. (2006). Effects in neocortical neurons of mutations of the Na(v)1.2 Na+ channel causing benign familial neonatal-infantile seizures. J Neurosci 26, 10100-10109.
-
(2006)
J Neurosci
, vol.26
, pp. 10100-10109
-
-
Scalmani, P.1
Rusconi, R.2
Armatura, E.3
Zara, F.4
Avanzini, G.5
Franceschetti, S.6
Mantegazza, M.7
-
142
-
-
0030943313
-
Generalized epilepsy with febrile seizures plus: a genetic disorder with heterogeneous clinical phenotypes
-
Scheffer, I. E., and Berkovic, S. E (1997). Generalized epilepsy with febrile seizures plus: a genetic disorder with heterogeneous clinical phenotypes. Brain 120,479-490.
-
(1997)
Brain
, vol.120
, pp. 479-490
-
-
Scheffer, I.E.1
Berkovic, S.E.2
-
143
-
-
0035798088
-
SNARE function analyzed in synap-tobrevin/VAMP knockout mice
-
Schoch, S., Deak, F., Konigstorfer, A., Mozhayeva, M., Sara, Y., Sudhof, T. C., and Kavalali, E. T. (2001). SNARE function analyzed in synap-tobrevin/VAMP knockout mice. Science 294,1117-1122.
-
(2001)
Science
, vol.294
, pp. 1117-1122
-
-
Schoch, S.1
Deak, F.2
Konigstorfer, A.3
Mozhayeva, M.4
Sara, Y.5
Sudhof, T.C.6
Kavalali, E.T.7
-
144
-
-
33344456574
-
The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1
-
Schulte, U., Thumfart, J. O., Klocker, N., Sailer, C. A., Bildl, W., Bin-iossek, M., Dehn, D., Deller, T., Eble, S., Abbass, K., Wangler, T., Knaus, H. G., and Fakler, B. (2006). The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1. Neuron 49, 697-706.
-
(2006)
Neuron
, vol.49
, pp. 697-706
-
-
Schulte, U.1
Thumfart, J.O.2
Klocker, N.3
Sailer, C.A.4
Bildl, W.5
Bin-iossek, M.6
Dehn, D.7
Deller, T.8
Eble, S.9
Abbass, K.10
Wangler, T.11
Knaus, H.G.12
Fakler, B.13
-
145
-
-
0037022308
-
The SNARE protein SNAP-25 is linked to fast calcium triggering of exocytosis
-
Sorensen, J. B., Matti, U., Wei, S. H., Nehring, R. B., Voets, T., Ashery, U., Binz, T., Neher, E., and Rettig, J. (2002). The SNARE protein SNAP-25 is linked to fast calcium triggering of exocytosis. Proc. Natl. Acad. Sci. U.S.A. 99, 1627-1632.
-
(2002)
Proc. Natl. Acad. Sci. U. S. A
, vol.99
, pp. 1627-1632
-
-
Sorensen, J.B.1
Matti, U.2
Wei, S.H.3
Nehring, R.B.4
Voets, T.5
Ashery, U.6
Binz, T.7
Neher, E.8
Rettig, J.9
-
146
-
-
79954525041
-
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation
-
Striano, P., Busolin, G., Santulli, L., Leonardi, E., Coppola, A., Vitiello, L., Rigon, L., Michelucci, R., Tosatto, S. C.,Striano,S.,andNobile, C. (2011). Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation. Neurology 76, 1173-1176.
-
(2011)
Neurology
, vol.76
, pp. 1173-1176
-
-
Striano, P.1
Busolin, G.2
Santulli, L.3
Leonardi, E.4
Coppola, A.5
Vitiello, L.6
Rigon, L.7
Michelucci, R.8
Tosatto, S.C.9
Striano, S.10
Nobile, C.11
-
147
-
-
0036337338
-
Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression
-
Stuhmer, T., Anderson, S. A., Ekker, M., and Rubenstein, J. L. (2002). Ectopic expression of the Dlx genes induces glutamic acid decarboxylase and Dlx expression. Development 129,245-252.
-
(2002)
Development
, vol.129
, pp. 245-252
-
-
Stuhmer, T.1
Anderson, S.A.2
Ekker, M.3
Rubenstein, J.L.4
-
148
-
-
80155189536
-
Inhibition of the mammalian target of rapamycin blocks epilepsy progression in NS-Pten conditional knockout mice
-
Sunnen, C. N., Brewster, A. L., Lugo, J. N., Vanegas, F., Turcios, E., Mukhi, S., Parghi, D., D'Arcangelo, G., and Anderson, A. E. (2011). Inhibition of the mammalian target of rapamycin blocks epilepsy progression in NS-Pten conditional knockout mice. Epilepsia 52, 2065-2075.
-
(2011)
Epilepsia
, vol.52
, pp. 2065-2075
-
-
Sunnen, C.N.1
Brewster, A.L.2
Lugo, J.N.3
Vanegas, F.4
Turcios, E.5
Mukhi, S.6
Parghi, D.7
D'Arcangelo, G.8
Anderson, A.E.9
-
149
-
-
0021382826
-
Penicillin-induced epilepto-genesis in immature rat CA3 hip-pocampal pyramidal cells
-
Swann, J. W., and Brady, R. J. (1984). Penicillin-induced epilepto-genesis in immature rat CA3 hip-pocampal pyramidal cells. Brain Res. 314,243-254.
-
(1984)
Brain Res
, vol.314
, pp. 243-254
-
-
Swann, J.W.1
Brady, R.J.2
-
150
-
-
79960963398
-
A blueprint for the spa-tiotemporal origins of mouse hip-pocampal interneuron diversity
-
Tricoire, L, Pelkey, K. A., Erkkila, B. E., Jeffries, B. W., Yuan, X., and McBain, C.J. (2011). A blueprint for the spa-tiotemporal origins of mouse hip-pocampal interneuron diversity. J. Neurosci. 31,10948-10970.
-
(2011)
J. Neurosci.
, vol.31
, pp. 10948-10970
-
-
Tricoire, L.1
Pelkey, K.A.2
Erkkila, B.E.3
Jeffries, B.W.4
Yuan, X.5
McBain, C.J.6
-
151
-
-
0028946378
-
Selective increase in T-type calcium conductance of retic-ular thalamic neurons in a rat model of absence epilepsy
-
Tsakiridou, E., Bertollini, L., De Curtis, M., Avanzini, G., and Pape, H. C. (1995). Selective increase in T-type calcium conductance of retic-ular thalamic neurons in a rat model of absence epilepsy. J. Neurosci. 15, 3110-3117.
-
(1995)
J. Neurosci.
, vol.15
, pp. 3110-3117
-
-
Tsakiridou, E.1
Bertollini, L.2
De Curtis, M.3
Avanzini, G.4
Pape, H.C.5
-
152
-
-
0037030466
-
Het-erozygosity for the tuberous sclerosis complex (TSC) gene products results in increased astrocyte numbers and decreased p27-Kip 1 expression in TSC2+/- cells
-
Uhlmann, E. J., Apicelli, A. J., Baldwin, R. L., Burke, S. P., Bajenaru, M. L., Onda, H., Kwiatkowski, D., and Gutmann, D. H. (2002). Het-erozygosity for the tuberous sclerosis complex (TSC) gene products results in increased astrocyte numbers and decreased p27-Kip 1 expression in TSC2+/- cells. Oncogene 21, 4050-4059.
-
(2002)
Oncogene
, vol.21
, pp. 4050-4059
-
-
Uhlmann, E.J.1
Apicelli, A.J.2
Baldwin, R.L.3
Burke, S.P.4
Bajenaru, M.L.5
Onda, H.6
Kwiatkowski, D.7
Gutmann, D.H.8
-
153
-
-
0028895773
-
Accelerated structural maturation induced by synapsin I at developing neuromuscular synapses of Xenopus laevis
-
Valtorta, F., Iezzi, N., Benfenati, F., Lu, B., Poo, M. M., and Greengard, P. (1995). Accelerated structural maturation induced by synapsin I at developing neuromuscular synapses of Xenopus laevis. Eur. J. Neurosci. 7, 261-270.
-
(1995)
Eur. J. Neurosci.
, vol.7
, pp. 261-270
-
-
Valtorta, F.1
Iezzi, N.2
Benfenati, F.3
Lu, B.4
Poo, M.M.5
Greengard, P.6
-
154
-
-
10744223345
-
SNAP-25 modulation of calcium dynamics underlies differences in GABAergic and glutamater-gic responsiveness to depolarization
-
Verderio, C., Pozzi, D., Pravettoni, E., Inverardi, F., Schenk, U., Coco, S., Proux-Gillardeaux, V., Galli, T., Ros-setto, O., Frassoni, C., and Matteoli, M. (2004). SNAP-25 modulation of calcium dynamics underlies differences in GABAergic and glutamater-gic responsiveness to depolarization. Neuron 41, 599-610.
-
(2004)
Neuron
, vol.41
, pp. 599-610
-
-
Verderio, C.1
Pozzi, D.2
Pravettoni, E.3
Inverardi, F.4
Schenk, U.5
Coco, S.6
Proux-Gillardeaux, V.7
Galli, T.8
Ros-setto, O.9
Frassoni, C.10
Matteoli, M.11
-
155
-
-
77950989444
-
Dlx5 and Dlx6 regulate the development of parvalbumin-expressing cortical interneurons
-
Wang, Y., Dye, C. A., Sohal, V., Long, J. E., Estrada, R. C., Roztocil, T., Lufkin, T., Deisseroth, K., Baraban, S. C., and Rubenstein, J. L. (2010). Dlx5 and Dlx6 regulate the development of parvalbumin-expressing cortical interneurons.J. Neurosci. 30, 5334-5345.
-
(2010)
J. Neurosci.
, vol.30
, pp. 5334-5345
-
-
Wang, Y.1
Dye, C.A.2
Sohal, V.3
Long, J.E.4
Estrada, R.C.5
Roztocil, T.6
Lufkin, T.7
Deisseroth, K.8
Baraban, S.C.9
Rubenstein, J.L.10
-
156
-
-
63149114250
-
Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse
-
Way, S. W., McKenna, J. III, Mietzsch, U., Reith, R. M., Wu, H. C., and Gam-bello, M. J. (2009). Loss of Tsc2 in radial glia models the brain pathology of tuberous sclerosis complex in the mouse. Hum. Mol. Genet. 18, 1252-1265.
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 1252-1265
-
-
Way, S.W.1
McKenna III, J.2
Mietzsch, U.3
Reith, R.M.4
Wu, H.C.5
Gam-bello, M.J.6
-
157
-
-
0035115120
-
Selective alterations in glutamate and GABA receptor subunit mRNA expression in dysplastic neurons and giant cells of cortical tubers
-
White, R., Hua, Y., Scheithauer, B., Lynch, D. R., Henske, E. P., and Crino, P. B. (2001). Selective alterations in glutamate and GABA receptor subunit mRNA expression in dysplastic neurons and giant cells of cortical tubers. Ann. Neurol. 49, 67-78.
-
(2001)
Ann. Neurol.
, vol.49
, pp. 67-78
-
-
White, R.1
Hua, Y.2
Scheithauer, B.3
Lynch, D.R.4
Henske, E.P.5
Crino, P.B.6
-
158
-
-
0033962487
-
Coloboma mouse mutant as an animal model of hyper-kinesis and attention deficit hyper-activity disorder
-
Wilson, M. C. (2000). Coloboma mouse mutant as an animal model of hyper-kinesis and attention deficit hyper-activity disorder. Neurosci. Biobehav. Rev. 24, 51-57.
-
(2000)
Neurosci. Biobehav. Rev.
, vol.24
, pp. 51-57
-
-
Wilson, M.C.1
-
159
-
-
33747614577
-
The origin and specification of cortical interneurons
-
Wonders, C. P., and Anderson, S. A. (2006). The origin and specification of cortical interneurons. Nat. Rev. Neurosci. 7, 687-696.
-
(2006)
Nat. Rev. Neurosci.
, vol.7
, pp. 687-696
-
-
Wonders, C.P.1
Anderson, S.A.2
-
160
-
-
33847698162
-
Abnormal laminar position and dendrite development of interneurons in the reeler forebrain
-
Yabut, O., Renfro, A., Niu, S., Swann, J. W., Marín, O., and D'Arcangelo, G. (2007). Abnormal laminar position and dendrite development of interneurons in the reeler forebrain. Brain Res. 1140,75-83.
-
(2007)
Brain Res
, vol.1140
, pp. 75-83
-
-
Yabut, O.1
Renfro, A.2
Niu, S.3
Swann, J.W.4
Marín, O.5
D'Arcangelo, G.6
-
161
-
-
33748115786
-
Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy
-
Yu, F. H., Mantegazza, M., Westenbroek, R. E., Robbins, C. A., Kalume, F., Burton, K. A., Spain, W. J., Mcknight, G. S., Scheuer, T., and Catterall, W A. (2006). Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy. Nat. Neurosci. 9, 1142-1149.
-
(2006)
Nat. Neurosci.
, vol.9
, pp. 1142-1149
-
-
Yu, F.H.1
Mantegazza, M.2
Westenbroek, R.E.3
Robbins, C.A.4
Kalume, F.5
Burton, K.A.6
Spain, W.J.7
Mcknight, G.S.8
Scheuer, T.9
Catterall, W.A.10
-
162
-
-
77952477811
-
Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyper-excitability
-
Yu, Y. E., Wen, L., Silva, J., Li, Z., Head, K., Sossey-Alaoui, K., Pao, A., Mei, L., and Cowell, J. K. (2010). Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyper-excitability. Hum. Mol. Genet. 19, 1702-1711.
-
(2010)
Hum. Mol. Genet.
, vol.19
, pp. 1702-1711
-
-
Yu, Y.E.1
Wen, L.2
Silva, J.3
Li, Z.4
Head, K.5
Sossey-Alaoui, K.6
Pao, A.7
Mei, L.8
Cowell, J.K.9
-
163
-
-
34247892266
-
Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation
-
Zaki, M., Shehab, M., El-Aleem, A. A., Abdel-Salam, G., Koeller, H. B., Ilkin, Y., Ross, M. E., Dobyns, W B., and Gleeson, J. G. (2007). Identification of a novel recessive RELN mutation using a homozygous balanced reciprocal translocation. Am. J. Med. Genet. A 143A, 939-944.
-
(2007)
Am. J. Med. Genet. A
, vol.143 A
, pp. 939-944
-
-
Zaki, M.1
Shehab, M.2
El-Aleem, A.A.3
Abdel-Salam, G.4
Koeller, H.B.5
Ilkin, Y.6
Ross, M.E.7
Dobyns, W.B.8
Gleeson, J.G.9
-
164
-
-
66149169973
-
The mammalian target of rapamycin signaling pathway mediates epileptogenesis in a model of temporal lobe epilepsy
-
Zeng, L. H., Rensing, N. R., and Wong, M. (2009). The mammalian target of rapamycin signaling pathway mediates epileptogenesis in a model of temporal lobe epilepsy. J. Neurosci. 29,6964-6972.
-
(2009)
J. Neurosci.
, vol.29
, pp. 6964-6972
-
-
Zeng, L.H.1
Rensing, N.R.2
Wong, M.3
-
165
-
-
78651064535
-
Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex
-
Zeng, L. H., Rensing, N. R., Zhang, B., Gutmann, D. H., Gambello, M. J., and Wong, M. (2011). Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex. Hum. Mol. Genet. 20,445-454.
-
(2011)
Hum. Mol. Genet.
, vol.20
, pp. 445-454
-
-
Zeng, L.H.1
Rensing, N.R.2
Zhang, B.3
Gutmann, D.H.4
Gambello, M.J.5
Wong, M.6
-
166
-
-
42949140259
-
Rapamycin prevents epilepsy in a mouse model of tuberous sclerosis complex
-
Zeng, L. H., Xu, L., Gutmann, D. H., and Wong, M. (2008). Rapamycin prevents epilepsy in a mouse model of tuberous sclerosis complex. Ann. Neurol. 63, 444-453.
-
(2008)
Ann. Neurol.
, vol.63
, pp. 444-453
-
-
Zeng, L.H.1
Xu, L.2
Gutmann, D.H.3
Wong, M.4
-
167
-
-
2642536944
-
Elevated thalamic low-voltage-activated currents precede the onset of absence epilepsy in the SNAP25-deficient mouse mutant coloboma
-
Zhang, Y., Vilaythong, A. P., Yoshor, D., and Noebels, J. L. (2004). Elevated thalamic low-voltage-activated currents precede the onset of absence epilepsy in the SNAP25-deficient mouse mutant coloboma. J. Neurosci. 24, 5239-5248.
-
(2004)
J. Neurosci.
, vol.24
, pp. 5239-5248
-
-
Zhang, Y.1
Vilaythong, A.P.2
Yoshor, D.3
Noebels, J.L.4
-
168
-
-
70350494929
-
Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy
-
Zhou, Y D., Lee, S., Jin, Z., Wright, M., Smith, S. E., and Anderson, M. P. (2009). Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy. Nat. Med. 15, 1208-1214.
-
(2009)
Nat. Med.
, vol.15
, pp. 1208-1214
-
-
Zhou, Y.D.1
Lee, S.2
Jin, Z.3
Wright, M.4
Smith, S.E.5
Anderson, M.P.6
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