-
2
-
-
0020164149
-
Neocortical histogenesis in normal and reeler mice: A developmental study based upon [H]thymidine autoradiography
-
(1982)
Brain Res
, vol.256
, pp. 293-302
-
-
Caviness, V.S.1
-
3
-
-
0022528327
-
Effects of ethanol on the generation and migration of cerebral cortical neurons
-
(1986)
Science
, vol.233
, pp. 1308-1311
-
-
Miller, M.W.1
-
7
-
-
0033136701
-
Genetic malformation of the cerebral cortex
-
(1999)
Neuron
, vol.23
, pp. 19-29
-
-
Walsh, C.A.1
-
8
-
-
0015244631
-
Guidance of neurons migrating to the fetal monkey neocortex
-
(1971)
Brain Res
, vol.33
, pp. 471-476
-
-
Rakic, P.1
-
9
-
-
0023785808
-
Specification of cerebral cortical areas
-
(1988)
Science
, vol.241
, pp. 170-176
-
-
Rakic, P.1
-
23
-
-
0032143437
-
BDNF regulates reelin expression and Cajal-Retzius cell development in the cerebral cortex
-
(1998)
Neuron
, vol.21
, pp. 305-315
-
-
Ringstedt, T.1
Linnarsson, S.2
Wagner, J.3
Lendhal, U.4
Kokaia, Z.5
Arenas, E.6
Ernfors, P.7
Ibanez, C.F.8
-
24
-
-
0032422555
-
Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia
-
(1998)
Neuron
, vol.21
, pp. 1315-1325
-
-
Fox, J.W.1
Lamperti, E.D.2
Eksioglu, Y.Z.3
Hong, S.E.4
Feng, Y.5
Graham, D.A.6
Scheffer, I.E.7
Dobyns, W.B.8
Hirsch, B.A.9
Radtke, R.A.10
Berkovic, S.F.11
Huttenlocher, P.R.12
Walsh, C.A.13
-
29
-
-
0031848149
-
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
-
(1998)
Nature Genet
, vol.19
, pp. 333-339
-
-
Hirotsune, S.1
Fleck, M.W.2
Gambello, M.J.3
Bix, G.J.4
Chen, A.5
Clark, G.D.6
Ledbetter, D.H.7
McBain, C.J.8
Wynshaw-Boris, A.9
-
31
-
-
0002606769
-
The role of the subplate in the development of the mammalian telencephalon
-
Peters A, Jones EG (eds) Development and Maturation of Cerebral Cortex. Plenum, New York
-
(1988)
, pp. 35-58
-
-
Shatz, C.J.1
Chun, L.L.M.2
Luskin, M.B.3
-
33
-
-
17444444915
-
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
-
(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
-
34
-
-
0032498306
-
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
(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
Scheffer, I.6
Cooper, E.C.7
Dobyns, W.B.8
Minnerath, S.R.9
Ross, M.E.10
Walsh, C.A.11
-
35
-
-
0033153135
-
Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons
-
(1999)
Neuron
, vol.23
, pp. 247-256
-
-
Francis, F.1
Koulakoff, A.2
Boucher, D.3
Chafey, P.4
Schaar, B.5
Vinet, M.C.6
Friocourt, G.7
McConnell, N.8
Reiner, O.9
Kahn, A.10
McConnell, S.K.11
Berwald-Netter, Y.12
Denoulet, P.13
Chelly, J.14
-
37
-
-
7844223263
-
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
-
(1998)
Hum Mol Genet
, vol.7
, pp. 2029-2037
-
-
Pilz, D.T.1
Matsumoto, N.2
Minnerath, S.3
Mills, P.4
Gleeson, J.G.5
Allen, K.M.6
Walsh, C.A.7
Barkovich, J.A.8
Dobyns, W.B.9
Ledbetter, D.H.10
Ross, M.E.11
-
38
-
-
0030797143
-
A genetic animal model of human neocortical heterotopia associated with seizures
-
(1997)
J Neurosci
, vol.17
, pp. 6236-6242
-
-
Lee, K.S.1
Schotter, F.2
Collins, J.L.3
Lanzino, G.4
Couture, D.5
Ran, A.6
Hiramatsu, K.I.7
Goto, Y.8
Hong, S.C.9
Caner, H.10
Yamamoto, H.11
Chen, Z.F.12
Bertram, E.13
Berr, S.14
Omary, R.15
Scrable, H.16
Jackson, T.17
Goble, J.18
Eisenman, L.19
-
39
-
-
16944361876
-
Peroxisome deficiency induces abnormal brain development and intrauterine growth retardation in Zellweger mice
-
(1997)
Nature Genet
, vol.17
, pp. 49-57
-
-
Baes, M.1
Gressens, P.2
Baumgart, E.3
Casteels, M.4
Fransen, M.5
Carmeliet, P.6
Evrard, P.7
Fahimi, D.8
Declercq, P.E.9
Collen, D.10
Van Veldhoven, P.P.11
Mannaerts, G.P.12
-
40
-
-
0030830906
-
Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder
-
(1997)
J Cell Biol
, vol.139
, pp. 1293-1305
-
-
Faust, P.L.1
Hatten, M.E.2
-
41
-
-
0033840419
-
Neuronal migration in Zellweger mice is secondary to glutamate receptor dysfunction
-
(2000)
Ann Neurol
, vol.48
, pp. 336-343
-
-
Gressens, P.1
Baes, M.2
Leroux, P.3
Lombet, A.4
Van Veldhoven, P.5
Janssen, A.6
Vamecq, J.7
Marret, S.8
Evrard, P.9
-
46
-
-
0029609458
-
Prenatal cocaine exposure adversely affects development of the primate cerebral cortex
-
(1995)
Synapse
, vol.21
, pp. 332-341
-
-
Lidow, M.S.1
|