-
2
-
-
0028294425
-
The subplate, a transient neocortical structure: Its role in the development of connections between thalamus and cortex
-
Allendoerfer K.L., Shatz C.J. The subplate, a transient neocortical structure: Its role in the development of connections between thalamus and cortex. Annu. Rev. Neurosci. 17:1994;185-218.
-
(1994)
Annu. Rev. Neurosci.
, vol.17
, pp. 185-218
-
-
Allendoerfer, K.L.1
Shatz, C.J.2
-
3
-
-
0030827595
-
Role of GGF/neuregulin signaling in interactions between migrating neurons and radial glia in the developing cerebral cortex
-
Anton E.S., Marchionni M.A., Lee K.F., Rakic P. Role of GGF/neuregulin signaling in interactions between migrating neurons and radial glia in the developing cerebral cortex. Development. 124:1997;3501-3510.
-
(1997)
Development
, vol.124
, pp. 3501-3510
-
-
Anton, E.S.1
Marchionni, M.A.2
Lee, K.F.3
Rakic, P.4
-
4
-
-
0031149411
-
Widespread neuronal ectopia associated with secondary defects in cerebrocortical chondroitin sulfate proteoglycans and basal lamina in MARCKS-deficient mice
-
Blackshear P.J., Silver J., Nairn A.C., Sulik K.K., Squier M.V., Stumpo D.J., Tuttle J.S. Widespread neuronal ectopia associated with secondary defects in cerebrocortical chondroitin sulfate proteoglycans and basal lamina in MARCKS-deficient mice. Exp. Neurol. 145:1997;46-61.
-
(1997)
Exp. Neurol.
, vol.145
, pp. 46-61
-
-
Blackshear, P.J.1
Silver, J.2
Nairn, A.C.3
Sulik, K.K.4
Squier, M.V.5
Stumpo, D.J.6
Tuttle, J.S.7
-
5
-
-
0030065606
-
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
-
Brunelli S., Faiella A., Capra V., Nigro V., Simeone A., Cama A., Boncinelli E. Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly. Nat. Genet. 12:1996;94-96.
-
(1996)
Nat. Genet.
, vol.12
, pp. 94-96
-
-
Brunelli, S.1
Faiella, A.2
Capra, V.3
Nigro, V.4
Simeone, A.5
Cama, A.6
Boncinelli, E.7
-
6
-
-
0031453499
-
Determination of the migratory capacity of embryonic cortical cells lacking the transcription factor Pax-6
-
Caric D., Gooday D., Hill R.E., McConnell S.K., Price D.J. Determination of the migratory capacity of embryonic cortical cells lacking the transcription factor Pax-6. Development. 124:1997;5087-5096.
-
(1997)
Development
, vol.124
, pp. 5087-5096
-
-
Caric, D.1
Gooday, D.2
Hill, R.E.3
McConnell, S.K.4
Price, D.J.5
-
7
-
-
0031018336
-
Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality
-
Chae T., Kwon Y.T., Bronson R., Dikkes P., Li E., Tsai L.H. Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality. Neuron. 18:1997;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
-
8
-
-
0031470554
-
Neuronal death in the hippocampus is promoted by plasmin-catalyzed degradation of laminin
-
Chen Z.L., Strickland S. Neuronal death in the hippocampus is promoted by plasmin-catalyzed degradation of laminin. Cell. 91:1997;917-925.
-
(1997)
Cell
, vol.91
, pp. 917-925
-
-
Chen, Z.L.1
Strickland, S.2
-
9
-
-
0028940096
-
Protein related to extracellular matrix proteins deleted in the mouse mutant reeler
-
D'Arcangelo G., Miao G.G., Chen S.-C., Soares H.D., Morgan J.I., Curran T.A. Protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature. 374:1995;719-723.
-
(1995)
Nature
, vol.374
, pp. 719-723
-
-
D'Arcangelo, G.1
Miao, G.G.2
Chen, S.-C.3
Soares, H.D.4
Morgan, J.I.5
Curran, T.A.6
-
10
-
-
0031031005
-
Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody
-
D'Arcangelo G., Nakajima K., Miyata T., Ogawa M., Mikoshiba K., Curran T. Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody. J. Neurosci. 17:1997;23-31.
-
(1997)
J. Neurosci.
, vol.17
, pp. 23-31
-
-
D'Arcangelo, G.1
Nakajima, K.2
Miyata, T.3
Ogawa, M.4
Mikoshiba, K.5
Curran, T.6
-
11
-
-
0027945831
-
The role of neurotrophins in the developing nervous system
-
Davies A.M. The role of neurotrophins in the developing nervous system. J. Neurobiol. 25:1994;1334-1348.
-
(1994)
J. Neurobiol.
, vol.25
, pp. 1334-1348
-
-
Davies, A.M.1
-
12
-
-
17444444915
-
Novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia 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., Chelly J.A. Novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell. 92:1998;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.A.14
-
13
-
-
0027486966
-
Lissencephaly: A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13
-
Dobyns W.B., Reiner O., Carrozzo R., Ledbetter D.H. Lissencephaly: A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. J. Am. Med. Assoc. 270:1993;2838-2842.
-
(1993)
J. Am. Med. Assoc.
, vol.270
, pp. 2838-2842
-
-
Dobyns, W.B.1
Reiner, O.2
Carrozzo, R.3
Ledbetter, D.H.4
-
14
-
-
0030027091
-
Periventricular heterotopia: An X-linked dominant epilepsy locus causing aberrant cerebral cortical development
-
Eksioglu Y.Z., Scheffer I.E., Cardenas P., Knoll J., DiMario F., Ramsby G., Berg M., Kamuro K., Berkovic S.F., Duyk G.M., Parisi J., Huttenlocher P.R., Walsh C.A. Periventricular heterotopia: An X-linked dominant epilepsy locus causing aberrant cerebral cortical development. Neuron. 16:1996;77-87.
-
(1996)
Neuron
, vol.16
, pp. 77-87
-
-
Eksioglu, Y.Z.1
Scheffer, I.E.2
Cardenas, P.3
Knoll, J.4
DiMario, F.5
Ramsby, G.6
Berg, M.7
Kamuro, K.8
Berkovic, S.F.9
Duyk, G.M.10
Parisi, J.11
Huttenlocher, P.R.12
Walsh, C.A.13
-
15
-
-
0025990092
-
Astrotactin provides a receptor system for CNS neuronal migration
-
Fishell G., Hatten M.E. Astrotactin provides a receptor system for CNS neuronal migration. Development. 113:1991;755-765.
-
(1991)
Development
, vol.113
, pp. 755-765
-
-
Fishell, G.1
Hatten, M.E.2
-
16
-
-
0027401223
-
The fates of cells in the developing cerebral cortex of normal and methylazoxymethanol acetate-lesioned mice
-
Gillies K., Price D.J. The fates of cells in the developing cerebral cortex of normal and methylazoxymethanol acetate-lesioned mice. Eur. J. Neurosci. 5:1993;73-84.
-
(1993)
Eur. J. Neurosci.
, vol.5
, pp. 73-84
-
-
Gillies, K.1
Price, D.J.2
-
17
-
-
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., Scheffer I., Cooper E.C., Dobyns W.B., Minnerath S.R., Ross M.E., Walsh C.A. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell. 92:1998;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
Scheffer, I.6
Cooper, E.C.7
Dobyns, W.B.8
Minnerath, S.R.9
Ross, M.E.10
Walsh, C.A.11
-
18
-
-
0028289473
-
Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients
-
Green A.J., Smith M., Yates J.R.W. Loss of heterozygosity on chromosome 16p13.3 in hamartomas from tuberous sclerosis patients. Nat. Genet. 6:1994;193-196.
-
(1994)
Nat. Genet.
, vol.6
, pp. 193-196
-
-
Green, A.J.1
Smith, M.2
Yates, J.R.W.3
-
19
-
-
0027470214
-
Multiple restricted lineages in the embryonic rat cerebral cortex
-
Grove E.A., Williams B.P., Li D.-Q., Hajihosseini M., Friedrich A., Price J. Multiple restricted lineages in the embryonic rat cerebral cortex. Development. 117:1993;553-561.
-
(1993)
Development
, vol.117
, pp. 553-561
-
-
Grove, E.A.1
Williams, B.P.2
Li, D.-Q.3
Hajihosseini, M.4
Friedrich, A.5
Price, J.6
-
20
-
-
0000534849
-
Congenital malformations
-
D.L. Graham, & P.L. Lantos. London: E. Arnold
-
Harding B.N., Copp A.J. Congenital malformations. Graham D.L., Lantos P.L. Greenfield's Neuropathology. 1997;397-533 E. Arnold, London.
-
(1997)
Greenfield's Neuropathology
, pp. 397-533
-
-
Harding, B.N.1
Copp, A.J.2
-
21
-
-
0028023599
-
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor
-
Hattori M., Adachi H., Tsujimoto M., Arai H., Inoue K. Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor. Nature. 370:1994;216-218.
-
(1994)
Nature
, vol.370
, pp. 216-218
-
-
Hattori, M.1
Adachi, H.2
Tsujimoto, M.3
Arai, H.4
Inoue, K.5
-
22
-
-
0031848149
-
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
-
Hirotsune S., Fleck M.W., Gambello M.J., Bix G.J., Chen A., Clark G.D., Ledbetter D.H., McBain C.J., Wynshaw-Boris A. Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat. Genet. 19:1998;333-339.
-
(1998)
Nat. 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
-
23
-
-
0030704354
-
Neuronal position in the developing brain is regulated by mouse disabled-1
-
Howell B.W., Hawkes R., Soriano P., Cooper J.A. Neuronal position in the developing brain is regulated by mouse disabled-1. Nature. 389:1997;733-737.
-
(1997)
Nature
, vol.389
, pp. 733-737
-
-
Howell, B.W.1
Hawkes, R.2
Soriano, P.3
Cooper, J.A.4
-
24
-
-
0030947095
-
Programmed cell death in animal development
-
Jacobson M.D., Weil M., Raff M.C. Programmed cell death in animal development. Cell. 88:1997;347-354.
-
(1997)
Cell
, vol.88
, pp. 347-354
-
-
Jacobson, M.D.1
Weil, M.2
Raff, M.C.3
-
25
-
-
0023024017
-
Genetics of human cancer
-
Knudson A.J. Genetics of human cancer. Annu. Rev. Genet. 20:1986;231-251.
-
(1986)
Annu. Rev. Genet.
, vol.20
, pp. 231-251
-
-
Knudson, A.J.1
-
26
-
-
0029956641
-
Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice
-
Kuida K., Zheng T.S., Na S.Q., Kuan C.Y., Yang D., Karasuyama H., Rakic P., Flavell R.A. Decreased apoptosis in the brain and premature lethality in CPP32-deficient mice. Nature. 384:1996;368-372.
-
(1996)
Nature
, vol.384
, pp. 368-372
-
-
Kuida, K.1
Zheng, T.S.2
Na, S.Q.3
Kuan, C.Y.4
Yang, D.5
Karasuyama, H.6
Rakic, P.7
Flavell, R.A.8
-
27
-
-
0030972375
-
The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and the milk-ejection reflex
-
Labosky P.A., Winnier G.E., Jetton T.L., Hargett L., Ryan A.K., Rosenfeld M.G., Parlow A.F., Hogan B.L.M. The winged helix gene, Mf3, is required for normal development of the diencephalon and midbrain, postnatal growth and the milk-ejection reflex. Development. 124:1997;1263-1274.
-
(1997)
Development
, vol.124
, pp. 1263-1274
-
-
Labosky, P.A.1
Winnier, G.E.2
Jetton, T.L.3
Hargett, L.4
Ryan, A.K.5
Rosenfeld, M.G.6
Parlow, A.F.7
Hogan, B.L.M.8
-
28
-
-
0028895055
-
Mouse Otx2 functions in the formation and patterning of rostral head
-
Matsuo I., Kuratani S., Kimura C., Takeda N., Aizawa S. Mouse Otx2 functions in the formation and patterning of rostral head. Genes Dev. 9:1995;2646-2658.
-
(1995)
Genes Dev.
, vol.9
, pp. 2646-2658
-
-
Matsuo, I.1
Kuratani, S.2
Kimura, C.3
Takeda, N.4
Aizawa, S.5
-
29
-
-
0025952778
-
Cell cycle dependence of laminar determination in developing neocortex
-
McConnell S.K., Kaznowski C.E. Cell cycle dependence of laminar determination in developing neocortex. Science. 254:1991;282-285.
-
(1991)
Science
, vol.254
, pp. 282-285
-
-
McConnell, S.K.1
Kaznowski, C.E.2
-
30
-
-
0030894092
-
Stem cells in the central nervous system
-
McKay R. Stem cells in the central nervous system. Science. 276:1997;66-71.
-
(1997)
Science
, vol.276
, pp. 66-71
-
-
McKay, R.1
-
31
-
-
0029789652
-
Distribution of a reeler gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogeneic antibody CR-50 on normal and reeler mice
-
Miyata T., Nakajima K., Aruga J., Takahashi S., Ikenaka K., Mikoshiba K., Ogawa M. Distribution of a reeler gene-related antigen in the developing cerebellum: An immunohistochemical study with an allogeneic antibody CR-50 on normal and reeler mice. J. Comp. Neurol. 372:1996;215-228.
-
(1996)
J. Comp. Neurol.
, vol.372
, pp. 215-228
-
-
Miyata, T.1
Nakajima, K.2
Aruga, J.3
Takahashi, S.4
Ikenaka, K.5
Mikoshiba, K.6
Ogawa, M.7
-
32
-
-
0029768093
-
Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death
-
Ohshima T., Ward J.M., Huh C.G., Longenecker G., Veeranna, Pant H.C., Brady R.O., Martin L.J., Kulkarni A.B. Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death. Proc. Natl. Acad. Sci. USA. 93:1996;11173-11178.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 11173-11178
-
-
Ohshima, T.1
Ward, J.M.2
Huh, C.G.3
Longenecker, G.4
Veeranna5
Pant, H.C.6
Brady, R.O.7
Martin, L.J.8
Kulkarni, A.B.9
-
33
-
-
0030767662
-
Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development
-
Porter F.D., Drago J., Xu Y., Cheema S.S., Wassif C., Huang S.P., Lee E., Grinberg A., Massalas J.S., Bodine D., Alt F., Westphal H. Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development. Development. 124:1997;2935-2944.
-
(1997)
Development
, vol.124
, pp. 2935-2944
-
-
Porter, F.D.1
Drago, J.2
Xu, Y.3
Cheema, S.S.4
Wassif, C.5
Huang, S.P.6
Lee, E.7
Grinberg, A.8
Massalas, J.S.9
Bodine, D.10
Alt, F.11
Westphal, H.12
-
34
-
-
0031031331
-
Fates of the earliest generated cells in the developing murine neocortex
-
Price D.J., Aslam S., Tasker L., Gillies K. Fates of the earliest generated cells in the developing murine neocortex. J. Comp. Neurol. 377:1997;414-422.
-
(1997)
J. Comp. Neurol.
, vol.377
, pp. 414-422
-
-
Price, D.J.1
Aslam, S.2
Tasker, L.3
Gillies, K.4
-
35
-
-
0028808204
-
Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain
-
Qiu M.S., Bulfone A., Martinez S., Meneses J.J., Shimamura K., Pedersen R.A., Rubenstein J.L.R. Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain. Genes Dev. 9:1995;2523-2538.
-
(1995)
Genes Dev.
, vol.9
, pp. 2523-2538
-
-
Qiu, M.S.1
Bulfone, A.2
Martinez, S.3
Meneses, J.J.4
Shimamura, K.5
Pedersen, R.A.6
Rubenstein, J.L.R.7
-
36
-
-
0015340401
-
Mode of cell migration to the superficial layers of fetal monkey neocortex
-
Rakic P. Mode of cell migration to the superficial layers of fetal monkey neocortex. J. Comp. Neurol. 145:1972;61-84.
-
(1972)
J. Comp. Neurol.
, vol.145
, pp. 61-84
-
-
Rakic, P.1
-
37
-
-
0028110454
-
Subependymal heterotopia: A distinct neuronal migration disorder associated with epilepsy
-
Raymond A.A., Fish D.R., Stevens J.M., Sisodiya S.M., Alsanjari N., Shorvon S.D. Subependymal heterotopia: a distinct neuronal migration disorder associated with epilepsy. J. Neurol. Neurosurg. Psychiatry. 57:1994;1195-1202.
-
(1994)
J. Neurol. Neurosurg. Psychiatry
, vol.57
, pp. 1195-1202
-
-
Raymond, A.A.1
Fish, D.R.2
Stevens, J.M.3
Sisodiya, S.M.4
Alsanjari, N.5
Shorvon, S.D.6
-
38
-
-
0027176708
-
Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats
-
Reiner O., Carrozzo R., Shen Y., Wehnert M., Faustinella F., Dobyns W.B., Caskey C.T., Ledbetter D.H. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature. 364:1993;717-721.
-
(1993)
Nature
, vol.364
, pp. 717-721
-
-
Reiner, O.1
Carrozzo, R.2
Shen, Y.3
Wehnert, M.4
Faustinella, F.5
Dobyns, W.B.6
Caskey, C.T.7
Ledbetter, D.H.8
-
39
-
-
0031658384
-
Disabled-1 acts downstream of Reelin in a signaling pathway that controls laminar organization in the mammalian brain
-
Rice D.S., Sheldon M., D'Arcangelo G., Nakajima K., Goldowitz D., Curran T. Disabled-1 acts downstream of Reelin in a signaling pathway that controls laminar organization in the mammalian brain. Development. 125:1998;3719-3729.
-
(1998)
Development
, vol.125
, pp. 3719-3729
-
-
Rice, D.S.1
Sheldon, M.2
D'Arcangelo, G.3
Nakajima, K.4
Goldowitz, D.5
Curran, T.6
-
40
-
-
0030750450
-
Neuregulin and erbB receptors play a critical role in neuronal migration
-
Rio C., Rieff H.I., Qi P.M., Corfas G. Neuregulin and erbB receptors play a critical role in neuronal migration. Neuron. 19:1997;39-50.
-
(1997)
Neuron
, vol.19
, pp. 39-50
-
-
Rio, C.1
Rieff, H.I.2
Qi, P.M.3
Corfas, G.4
-
41
-
-
0028156614
-
The role of disordered genetic control of neurogenesis in the pathogenesis of migration disorders
-
Rorke L.B. The role of disordered genetic control of neurogenesis in the pathogenesis of migration disorders. J. Neuropathol. Exp. Neurol. 53:1994;105-117.
-
(1994)
J. Neuropathol. Exp. Neurol.
, vol.53
, pp. 105-117
-
-
Rorke, L.B.1
-
42
-
-
0030702084
-
Caspases: Intracellular signaling by proteolysis
-
Salvesen G.S., Dixit V.M. Caspases: Intracellular signaling by proteolysis. Cell. 91:1997;443-446.
-
(1997)
Cell
, vol.91
, pp. 443-446
-
-
Salvesen, G.S.1
Dixit, V.M.2
-
43
-
-
0027279692
-
Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus
-
Schmahl W., Knoedlseder M., Favor J., Davidson D. Defects of neuronal migration and the pathogenesis of cortical malformations are associated with Small eye (Sey) in the mouse, a point mutation at the Pax-6-locus. Acta Neuropathol. (Berl.). 86:1993;126-135.
-
(1993)
Acta Neuropathol. (Berl.)
, vol.86
, pp. 126-135
-
-
Schmahl, W.1
Knoedlseder, M.2
Favor, J.3
Davidson, D.4
-
44
-
-
0027957253
-
Disruption of neuronal migration in the neocortex of the dreher mutant mouse
-
Sekiguchi M., Abe H., Shimai K., Huang G., Inoue T., Nowakowski R.S. Disruption of neuronal migration in the neocortex of the dreher mutant mouse. Dev. Brain Res. 77:1994;37-43.
-
(1994)
Dev. Brain Res.
, vol.77
, pp. 37-43
-
-
Sekiguchi, M.1
Abe, H.2
Shimai, K.3
Huang, G.4
Inoue, T.5
Nowakowski, R.S.6
-
45
-
-
0030717493
-
Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice
-
Sheldon M., Rice D.S., D'Arcangelo G., Yoneshima H., Nakajima K., Mikoshiba K., Howell B.W., Cooper J.A., Goldowitz D., Curran T. Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice. Nature. 389:1997;730-733.
-
(1997)
Nature
, vol.389
, pp. 730-733
-
-
Sheldon, M.1
Rice, D.S.2
D'Arcangelo, G.3
Yoneshima, H.4
Nakajima, K.5
Mikoshiba, K.6
Howell, B.W.7
Cooper, J.A.8
Goldowitz, D.9
Curran, T.10
-
46
-
-
0015846291
-
Neuronal migration, with special reference to developing human brain: A review
-
Sidman R.L., Rakic P. Neuronal migration, with special reference to developing human brain: a review. Brain Res. 62:1973;1-35.
-
(1973)
Brain Res.
, vol.62
, pp. 1-35
-
-
Sidman, R.L.1
Rakic, P.2
-
47
-
-
17944401056
-
Altered forebrain and hindbrain development in mice mutant for the Gsh-2 homeobox gene
-
Szucsik J.C., Witte D.P., Li H., Pixley S.K., Small K.M., Potter S.S. Altered forebrain and hindbrain development in mice mutant for the Gsh-2 homeobox gene. Dev. Biol. 191:1997;230-242.
-
(1997)
Dev. Biol.
, vol.191
, pp. 230-242
-
-
Szucsik, J.C.1
Witte, D.P.2
Li, H.3
Pixley, S.K.4
Small, K.M.5
Potter, S.S.6
-
49
-
-
0026573837
-
Morphological substrates of infantile spasms: Studies based on surgically resected cerebral tissue
-
Vinters H.V., Fisher R.S., Cornford M.E., Mah V., Secor D.L., De Rosa M.J., Comair Y.G., Peacock W.J., Shields W.D. Morphological substrates of infantile spasms: studies based on surgically resected cerebral tissue. Childs's Nerv. Syst. 8:1992;8-17.
-
(1992)
Childs's Nerv. Syst.
, vol.8
, pp. 8-17
-
-
Vinters, H.V.1
Fisher, R.S.2
Cornford, M.E.3
Mah, V.4
Secor, D.L.5
De Rosa, M.J.6
Comair, Y.G.7
Peacock, W.J.8
Shields, W.D.9
-
50
-
-
0030034606
-
Subplate neurons - Missing link in brain injury of the premature infant
-
Volpe J.J. Subplate neurons - missing link in brain injury of the premature infant. Pediatrics. 97:1996;112-113.
-
(1996)
Pediatrics
, vol.97
, pp. 112-113
-
-
Volpe, J.J.1
-
51
-
-
0030868450
-
Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse
-
Ware M.L., Fox J.W., González J.L., Davis N.M., De Rouvroit C.L., Russo C.J., Chua S.C. Jr., Goffinet A.M., Walsh C.A. Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse. Neuron. 19:1997;239-249.
-
(1997)
Neuron
, vol.19
, pp. 239-249
-
-
Ware, M.L.1
Fox, J.W.2
González, J.L.3
Davis, N.M.4
De Rouvroit, C.L.5
Russo, C.J.6
Chua S.C., Jr.7
Goffinet, A.M.8
Walsh, C.A.9
-
52
-
-
0031017511
-
Emx1 and Emx2 functions in development of dorsal telencephalon
-
Yoshida M., Suda Y., Matsuo I., Miyamoto N., Takeda N., Kuratani S., Aizawa S. Emx1 and Emx2 functions in development of dorsal telencephalon. Development. 124:1997;101-111.
-
(1997)
Development
, vol.124
, pp. 101-111
-
-
Yoshida, M.1
Suda, Y.2
Matsuo, I.3
Miyamoto, N.4
Takeda, N.5
Kuratani, S.6
Aizawa, S.7
-
53
-
-
0029947209
-
CNS gene encoding astrotactin, which supports neuronal migration along glial fibers
-
Zheng C., Heintz N., Hatten M.E. CNS gene encoding astrotactin, which supports neuronal migration along glial fibers. Science. 272:1996;417-419.
-
(1996)
Science
, vol.272
, pp. 417-419
-
-
Zheng, C.1
Heintz, N.2
Hatten, M.E.3
|