-
1
-
-
0024319579
-
The lissencephaly syndromes
-
Aicardi, J. 1989. The lissencephaly syndromes. Int Pediatr 4:118-126.
-
(1989)
Int Pediatr
, vol.4
, pp. 118-126
-
-
Aicardi, J.1
-
2
-
-
0344334400
-
Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse
-
Angevine JB, Sidman RL. 1961. Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse. Nature 192:766-768.
-
(1961)
Nature
, vol.192
, pp. 766-768
-
-
Angevine, J.B.1
Sidman, R.L.2
-
3
-
-
0004270170
-
-
New York: Greene Publishing Associates and Wiley-Interscience
-
Ausubel FM, Brent R, Kingston RE, Moore DD, Seidman JG, Smith JA, Struhl K. 1992. Current protocols in molecular biology. New York: Greene Publishing Associates and Wiley-Interscience.
-
(1992)
Current Protocols in Molecular Biology
-
-
Ausubel, F.M.1
Brent, R.2
Kingston, R.E.3
Moore, D.D.4
Seidman, J.G.5
Smith, J.A.6
Struhl, K.7
-
4
-
-
0023122493
-
Disorders of neuronal migration
-
Barth PG. 1987. Disorders of neuronal migration. Can J Neurol Sci 14:1-16.
-
(1987)
Can J Neurol Sci
, vol.14
, pp. 1-16
-
-
Barth, P.G.1
-
5
-
-
0027173483
-
JunB differs from c-Jun in its DNA-binding and dimerization domains, and represses c-Jun by formation of inactive heterodimers
-
Deng T, Karin M. 1993. JunB differs from c-Jun in its DNA-binding and dimerization domains, and represses c-Jun by formation of inactive heterodimers. Genes Dev 7:479-490.
-
(1993)
Genes Dev
, vol.7
, pp. 479-490
-
-
Deng, T.1
Karin, M.2
-
6
-
-
16944367121
-
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): Evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22
-
des Portes V, Pinard J M, Smadja D, Motte J, Boespflug-Tanguy O, Moutard M L, Desguerre I, Billuart P, Carrie A, Bienvenu T, Vinet M C, Bachner L, Beldjord C, Dulac O, Kahn A, Ponsot G, Chelly J. 1997. Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22. J Med Genet 34:177-183.
-
(1997)
J Med Genet
, vol.34
, pp. 177-183
-
-
Des Portes, V.1
Pinard, J.M.2
Smadja, D.3
Motte, J.4
Boespflug-Tanguy, O.5
Moutard, M.L.6
Desguerre, I.7
Billuart, P.8
Carrie, A.9
Bienvenu, T.10
Vinet, M.C.11
Bachner, L.12
Beldjord, C.13
Dulac, O.14
Kahn, A.15
Ponsot, G.16
Chelly, J.17
-
7
-
-
17444444915
-
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar hetrotropia 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 M7 Kahn A, Beldjord C, Chelly J. 1998. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar hetrotropia 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
-
8
-
-
0033153135
-
Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating neurons
-
Francis F, Koulakoff A, Chafey P, Vinet M C, Schaar B, Boucher D, Billuart P, Reiner O, Kahn A, Denoulet P, McConnell SK, Berwald-Netter Y, Chelly J. 1999. Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating neurons. Neuron 23:247-256.
-
(1999)
Neuron
, vol.23
, pp. 247-256
-
-
Francis, F.1
Koulakoff, A.2
Chafey, P.3
Vinet, M.C.4
Schaar, B.5
Boucher, D.6
Billuart, P.7
Reiner, O.8
Kahn, A.9
Denoulet, P.10
McConnell, S.K.11
Berwald-Netter, Y.12
Chelly, J.13
-
9
-
-
0032498306
-
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
Gleeson JG, Allen KM, Fox JW, Lamperti ED, Berkovic S, Scheffer I, Cooper EC, Dobyns WB, Minnerath SR, Ross ME, Walsh CA. 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
Scheffer, I.6
Cooper, E.C.7
Dobyns, W.B.8
Minnerath, S.R.9
Ross, M.E.10
Walsh, C.A.11
-
10
-
-
0019351935
-
SV40-transformed simian cells support the replication of early SV40 mutants
-
Gluzman Y. 1981. SV40-transformed simian cells support the replication of early SV40 mutants. Cell 23:175-182.
-
(1981)
Cell
, vol.23
, pp. 175-182
-
-
Gluzman, Y.1
-
11
-
-
0029871290
-
Structural basis for the autoinhibition of calcium/calmodulin-dependent protein kinase I
-
Goldberg J, Nairn AC, Kutiyan J. 1996. Structural basis for the autoinhibition of calcium/calmodulin-dependent protein kinase I. Cell 84:875-887.
-
(1996)
Cell
, vol.84
, pp. 875-887
-
-
Goldberg, J.1
Nairn, A.C.2
Kutiyan, J.3
-
12
-
-
0033105173
-
Expression of doublecortin correlates with neuronal migration and pattern formation in diverse regions of the developing chick brain
-
Hannan AJ, Henke RC, Seeto GS, Capes-Davis A, Dunn J, Jeffrey PL. 1999. Expression of doublecortin correlates with neuronal migration and pattern formation in diverse regions of the developing chick brain. J Neurosci Res 55:650-657.
-
(1999)
J Neurosci Res
, vol.55
, pp. 650-657
-
-
Hannan, A.J.1
Henke, R.C.2
Seeto, G.S.3
Capes-Davis, A.4
Dunn, J.5
Jeffrey, P.L.6
-
13
-
-
0002977846
-
Gray matter heterotopia
-
Guerrini R, Andermann F, Canapicchiet R, Roger J, Zilfkin R, Pfanner P. editors. Phiadelphia: Lippincott-Raven.
-
Harding B. 1996. Gray matter heterotopia. In: Guerrini R, Andermann F, Canapicchiet R, Roger J, Zilfkin R, Pfanner P. editors. Dysplasias of cerebral Ccortex and epilepsy. Phiadelphia: Lippincott-Raven. p. 81-88.
-
(1996)
Dysplasias of Cerebral Ccortex and Epilepsy
, pp. 81-88
-
-
Harding, B.1
-
14
-
-
0028023599
-
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor
-
Hattori M, Adachi H, Tsujimoto M, Arai N, Inoue K. 1994. Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor. Nature 370:216-218.
-
(1994)
Nature
, vol.370
, pp. 216-218
-
-
Hattori, M.1
Adachi, H.2
Tsujimoto, M.3
Arai, N.4
Inoue, K.5
-
15
-
-
15144347935
-
Hippocampal plasticity involves extensive gene induction and multiple cellular mechanisms
-
Hevroni D, Rattner A, Bundman M, Lederfein D, Gabarah A, Mangelus M, Silverman MA, Kedar H, Naor C, Kornuc M, Hanoch T, Seger R, Theill LE, Nedivi E, Richter-Levin G, Citri Y. 1998. Hippocampal plasticity involves extensive gene induction and multiple cellular mechanisms. J Mol Neurosci 10:75-98.
-
(1998)
J Mol Neurosci
, vol.10
, pp. 75-98
-
-
Hevroni, D.1
Rattner, A.2
Bundman, M.3
Lederfein, D.4
Gabarah, A.5
Mangelus, M.6
Silverman, M.A.7
Kedar, H.8
Naor, C.9
Kornuc, M.10
Hanoch, T.11
Seger, R.12
Theill, L.E.13
Nedivi, E.14
Richter-Levin, G.15
Citri, Y.16
-
16
-
-
0031848149
-
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality
-
Hirotsune S, Fleck MW, Gambello MJ, Bix GJ, Chen A, Clark GD, Ledbetter DH, McBain CJ, Wynshaw-Boris A. 1998. Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat Genet 19:333-339.
-
(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
-
17
-
-
0032832998
-
Doublecortin, a stabilizer of microtubules
-
Horesh D, Sapir T, Francis F, Grayer Wolf S, Elbaum M, Chelly J, Reiner O. 1999. Doublecortin, a stabilizer of microtubules. Hum Mol Genet 8:1599-1610.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1599-1610
-
-
Horesh, D.1
Sapir, T.2
Francis, F.3
Grayer Wolf, S.4
Elbaum, M.5
Chelly, J.6
Reiner, O.7
-
19
-
-
0031040866
-
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome
-
Lo Nigro CL, Chong CS, Smith AC, Dobyns WB, Carrozzo R, Ledbetter DH. 1997. Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome. Hum Mol Genet 6:157-164.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 157-164
-
-
Lo Nigro, C.L.1
Chong, C.S.2
Smith, A.C.3
Dobyns, W.B.4
Carrozzo, R.5
Ledbetter, D.H.6
-
21
-
-
0033104802
-
Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS)
-
Matsumoto N, Pilz DT, Ledbetter DH. 1999. Genomic structure, chromosomal mapping, and expression pattern of human DCAMKL1 (KIAA0369), a homologue of DCX (XLIS). Genomics 56:179-183.
-
(1999)
Genomics
, vol.56
, pp. 179-183
-
-
Matsumoto, N.1
Pilz, D.T.2
Ledbetter, D.H.3
-
22
-
-
0028858680
-
Constructing the cerebral cortex: Neurogenesis and fate determination
-
McConnell SK. 1995. Constructing the cerebral cortex: neurogenesis and fate determination. Neuron 15:761-768.
-
(1995)
Neuron
, vol.15
, pp. 761-768
-
-
McConnell, S.K.1
-
23
-
-
0031589004
-
Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro
-
Nagase T, Ishikawa K, Nakajima D, Ohira M, Seki N, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O. 1997. Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro. DNA Res 4:141-150.
-
(1997)
DNA Res
, vol.4
, pp. 141-150
-
-
Nagase, T.1
Ishikawa, K.2
Nakajima, D.3
Ohira, M.4
Seki, N.5
Miyajima, N.6
Tanaka, A.7
Kotani, H.8
Nomura, N.9
Ohara, O.10
-
24
-
-
0027183404
-
Numerous candidate plasticity-related genes revealed by differential cDNA cloning
-
Nedivi E, Hevroni D, Naot D, Israeli D, Citri Y. 1993. Numerous candidate plasticity-related genes revealed by differential cDNA cloning. Nature 363:718-722.
-
(1993)
Nature
, vol.363
, pp. 718-722
-
-
Nedivi, E.1
Hevroni, D.2
Naot, D.3
Israeli, D.4
Citri, Y.5
-
25
-
-
0029692152
-
In situ hybridization analysis of chick embryos in whole mount and tissue sections
-
Orlando, FL: Academic Press
-
Nieto MA, Patel K, Wilkinson D. 1996. In situ hybridization analysis of chick embryos in whole mount and tissue sections. Methods in Cell Biology, Orlando, FL: Academic Press, p. 219-235.
-
(1996)
Methods in Cell Biology
, pp. 219-235
-
-
Nieto, M.A.1
Patel, K.2
Wilkinson, D.3
-
26
-
-
0031588576
-
Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA encoding relatively large proteins
-
Ohara O, Nagase T, Ishikawa K, Nakajima D, Ohira M, Seki N, Nomura N. 1997. Construction and characterization of human brain cDNA libraries suitable for analysis of cDNA encoding relatively large proteins. DNA Res 4:53-59.
-
(1997)
DNA Res
, vol.4
, pp. 53-59
-
-
Ohara, O.1
Nagase, T.2
Ishikawa, K.3
Nakajima, D.4
Ohira, M.5
Seki, N.6
Nomura, N.7
-
27
-
-
0031613727
-
Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to doublecortin
-
Omori Y, Suzuki M, Ozaki K, Harada Y, Nakamura Y, Takahashi E, Fujiwara T. 1998. Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to doublecortin. J Hum Genet 43:169-77.
-
(1998)
J Hum Genet
, vol.43
, pp. 169-177
-
-
Omori, Y.1
Suzuki, M.2
Ozaki, K.3
Harada, Y.4
Nakamura, Y.5
Takahashi, E.6
Fujiwara, T.7
-
28
-
-
0015965793
-
Neurons in Rhesus monkey visual cortex: Systematic relation between time of origin and eventual disposition
-
Rakic P. 1974. Neurons in Rhesus monkey visual cortex: systematic relation between time of origin and eventual disposition. Science 183:425-427.
-
(1974)
Science
, vol.183
, pp. 425-427
-
-
Rakic, P.1
-
29
-
-
0032057722
-
Abnormal cortical development; towards elucidation of the LIS1 gene product function
-
Reiner O, Sapir T. 1998. Abnormal cortical development; towards elucidation of the LIS1 gene product function. Int J Mol Medicine 1:849-853.
-
(1998)
Int J Mol Medicine
, vol.1
, pp. 849-853
-
-
Reiner, O.1
Sapir, T.2
-
30
-
-
0027176708
-
Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats
-
Reiner O, Carrozzo R, Shen Y, Whenert M, Faustinella F, Dobyns WB, Caskey CT, Ledbetter DH. 1993. Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats. Nature 364:717-721.
-
(1993)
Nature
, vol.364
, pp. 717-721
-
-
Reiner, O.1
Carrozzo, R.2
Shen, Y.3
Whenert, M.4
Faustinella, F.5
Dobyns, W.B.6
Caskey, C.T.7
Ledbetter, D.H.8
-
31
-
-
0029013985
-
Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration
-
Reiner O, Albrecht U, Gordon M, Chianese KA, Wong C, Sapir T, Siracusa LD, Buchberg AM, Caskey CT, Eichele G. 1995. Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration. J Neurosci 15:3730-3738.
-
(1995)
J Neurosci
, vol.15
, pp. 3730-3738
-
-
Reiner, O.1
Albrecht, U.2
Gordon, M.3
Chianese, K.A.4
Wong, C.5
Sapir, T.6
Siracusa, L.D.7
Buchberg, A.M.8
Caskey, C.T.9
Eichele, G.10
-
32
-
-
8244247118
-
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): A gene causing neuronal migration defects in human brain
-
Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motte J, Mira AP, Scheffer I, Berkovic S, Scaravilli F, King RA, Ledbetter DH, Schlessinger D, Dobyns WB, Walsh CA. 1997. Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain. Hum Mol Genet 6:555-562.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 555-562
-
-
Ross, M.E.1
Allen, K.M.2
Srivastava, A.K.3
Featherstone, T.4
Gleeson, J.G.5
Hirsch, B.6
Harding, B.N.7
Andermann, E.8
Abdullah, R.9
Berg, M.10
Czapansky-Bielman, D.11
Flanders, D.J.12
Guerrini, R.13
Motte, J.14
Mira, A.P.15
Scheffer, I.16
Berkovic, S.17
Scaravilli, F.18
King, R.A.19
Ledbetter, D.H.20
Schlessinger, D.21
Dobyns, W.B.22
Walsh, C.A.23
more..
-
33
-
-
0030695246
-
Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit
-
Sapir T, Elbaum M, Reiner O. 1997. Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit. EMBO J 16:6977-6984.
-
(1997)
EMBO J
, vol.16
, pp. 6977-6984
-
-
Sapir, T.1
Elbaum, M.2
Reiner, O.3
-
34
-
-
0027198033
-
Ependymal abnormalities in lissencephaly/pachgyria
-
Sarnat HB, Darwish HZ, Barth PG, Trevenen CL, Pinto A, Kotagal S, Shishikura K, Osawa M, Korobkin R. 1993. Ependymal abnormalities in lissencephaly/pachgyria. J Neuropathol Exp Neurol 52:525-541.
-
(1993)
J Neuropathol Exp Neurol
, vol.52
, pp. 525-541
-
-
Sarnat, H.B.1
Darwish, H.Z.2
Barth, P.G.3
Trevenen, C.L.4
Pinto, A.5
Kotagal, S.6
Shishikura, K.7
Osawa, M.8
Korobkin, R.9
-
35
-
-
0033613840
-
CPG16, a novel protein serine/threonine kinase downstream of cAMP-dependent protein kinase
-
Silverman M.A, Benard O. Jaaro H, Rattner A, Citri Y, Seger R. 1999. CPG16, a novel protein serine/threonine kinase downstream of cAMP-dependent protein kinase. J Biol Chem 274:2631-2636.
-
(1999)
J Biol Chem
, vol.274
, pp. 2631-2636
-
-
Silverman, M.A.1
Benard, O.2
Jaaro, H.3
Rattner, A.4
Citri, Y.5
Seger, R.6
-
36
-
-
0033557797
-
DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX)
-
Sossey-Alaoui K, Srivastava AK. 1999. DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX). Genomics 56:121-126.
-
(1999)
Genomics
, vol.56
, pp. 121-126
-
-
Sossey-Alaoui, K.1
Srivastava, A.K.2
-
37
-
-
0033035849
-
Kainate-elicited seizures induce mRNA encoding a CaMK-related peptide: A putative modulator of kinase activity in rat hippocampus
-
Vreugdenhil E, Datson N, Engels B, de Jong J, van Koningsbruggen S, Schaaf M, de Kloet ER. 1999. Kainate-elicited seizures induce mRNA encoding a CaMK-related peptide: a putative modulator of kinase activity in rat hippocampus. J Neurobiol 39:41-50.
-
(1999)
J Neurobiol
, vol.39
, pp. 41-50
-
-
Vreugdenhil, E.1
Datson, N.2
Engels, B.3
De Jong, J.4
Van Koningsbruggen, S.5
Schaaf, M.6
De Kloet, E.R.7
|