GoldenJA. Cell migration and cerebral cortical development. Neuropathol Appl Neurobiol2001;27:22–28.
2.
KatoMDobynsWB. Lissencephaly and the molecular basis of neuronal migration. Hum Mol Genet2003;12:R89–R96.
3.
Wynshaw-BorisAGambelloMJ. LIS1 and dynein motor function in neuronal migration and development. Genes Dev2001;15:639–651.
4.
PilzDTMatsumotoNMinnerathS. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet1998;7:2029–2037.
5.
ReinerOCarrozzoRShenY. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats. Nature1993;364:717–721.
6.
AumaisJPTunsteadJRMcNeilRS. NudC associates with Lis1 and the dynein motor at the leading pole of neurons. J Neurosci2001;21:RC187.
7.
SasakiSShionoyaAIshidaM. A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system. Neuron2000;28:681–696.
8.
GeiserJRSchottEJKingsburyTJ. Saccharomyces cerevisiae genes required in the absence of the CIN8-encoded spindle motor act in functionally diverse mitotic pathways. Mol Biol Cell1997;8:1035–1050.
9.
XiangXOsmaniAHOsmaniSA. NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration. Mol Biol Cell1995;6:297–310.
10.
ReinerOBar-AmISapirT. LIS2, gene and pseudogene, homologous to LIS1 (lissencephaly 1), located on the short and long arms of chromosome 2. Genomics1995;30:251–256.
11.
LeiYWarriorR. The Drosophila Lissencephaly1 (DLis1) gene is required for nuclear migration. Dev Biol2000;226:57–72.
12.
LiuZStewardRLuoL. Drosophila Lis1 is required for neuroblast proliferation, dendritic elaboration and axonal transport. Nat Cell Biol2000;2:776–783.
13.
ReinerOAlbrechtUGordonM. Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration. J Neurosci1995;15:3730–3738.
14.
HattoriMAdachiHTsujimotoM. Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase (corrected). Nature1994;370:216–218.
TokuokaSMIshiiSKawamuraN. Involvement of platelet-activating factor and LIS1 in neuronal migration. Eur J Neurosci2003;18:563–570.
17.
KoizumiHYamaguchiNHattoriM. Targeted disruption of intracellular type I platelet activating factor-acetylhydrolase catalytic subunits causes severe impairment in spermatogenesis. J Biol Chem2003;278:12489–12494.
18.
WillinsDALiuBXiangX. Mutations in the heavy chain of cytoplasmic dynein suppress the nudF nuclear migration mutation of Aspergillus nidulans. Mol Gen Genet1997;255:194–200.
19.
SwanANguyenTSuterB. Drosophila Lissencephaly-1 functions with Bic-D and dynein in oocyte determination and nuclear positioning. Nat Cell Biol1999;1:444–449.
20.
McGrailMGepnerJSilvanovichA. Regulation of cytoplasmic dynein function in vivo by the Drosophila Glued complex. J Cell Biol1995;131:411–425.
21.
FaulknerNEDujardinDLTaiCY. A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function. Nature Cell Biol2000;2:784–791.
22.
NiethammerMSmithDSAyalaR. NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein. Neuron2000;28:697–711.
23.
LeeWLOberleJRCooperJA. The role of the lissencephaly protein Pac1 during nuclear migration in budding yeast. J Cell Biol2003;160:355–364.
24.
CahanaAEscamezTNowakowskiRS. Targeted mutagenesis of Lis1 disrupts cortical development and LIS1 homodimerization. Proc Natl Acad Sci U S A2001;98:6429–6434.
25.
GambelloMJDarlingDLYinglingJ. Multiple dose-dependent effects of Lis1 on cerebral cortical development. J Neurosci2003;23:1719–1729.
26.
HirotsuneSFleckMWGambelloMJ. Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality. Nat Genet1998;19:333–339.
27.
FleckMWHirotsuneSGambelloMJ. Hippocampal abnormalities and enhanced excitability in a murine model of human lissencephaly. J Neurosci2000;20:2439–2450.
28.
KholmanskikhSSDobrinJSWynshaw-BorisA. Disregulated RhoGTPases and actin cytoskeleton contribute to the migration defect in Lis1-deficient neurons. J Neurosci2003;23:8673–8681.
29.
HoffmannBZuoWLiuA. The LIS1-related protein NUDF of Aspergillus nidulans and its interaction partner NUDE bind directly to specific subunits of dynein and dynactin and to alpha- and gamma-tubulin. J Biol Chem2001;276:38877–38884.
30.
SasakiSShionoyaAIshidaM. A LIS/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system. Neuron2000;28:681–696.
31.
CardosoCLeventerRJWardHL. Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3. Am J Hum Genet2003;72:918–930.
32.
Toyo-okaKShionoyaAGambelloMJ. 14–3–3Epsilon is important for neuronal migration by binding to NUDEL: a molecular explanation for Miller-Dieker syndrome. Nat Genet2003;34:274–285.
33.
CorboJCDeuelTALongJM. Doublecortin is required in mice for lamination of the hippocampus but not the neocortex. J Neurosci2002;22:7548–7557.
34.
GleesonJG. Classical lissencephaly and double cortex (subcortical band heterotopia): LIS1 and doublecortin. Curr Opin Neurol2000;13:121–125.
35.
BaiJRamosRLAckmanJB. RNAi reveals doublecortin is required for radial migration in rat neocortex. Nat Neurosci2003;6:1277–1283.
36.
HoreshDSapirTFrancisF. Doublecortin, a stabilizer of microtubules. Hum Mol Genet1999;8:1599–1610.
37.
GleesonJGLinPTFlanaganLA. Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons. Neuron1999;23:257–271.
38.
RakicP. Principles of neural cell migration. Experientia1990;46:882–891.
39.
AlterMLieboJDesnickSO. The behavior of the reeler neurological mutant mouse. Neurology1968;18:289.
40.
CavinessV. Neocortical histogenesis in normal and reeler mice: a developmental study based upon [3H]thymidine autoradiography. Dev Brain Res1982;4:293–302.
41.
HongSEShugartYYHuangDT. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations. Nat Genet2000;26:93–96.
42.
D'ArcangeloGMiaoGGChenSC. A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature1995;374:719–723.
43.
D'ArcangeloGNakajimaKMiyataT. Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody. J Neurosci1997;17:23–31.
44.
OgawaMMiyataTNakajimaK. The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons. Neuron1995;14:899–912.
45.
BairdDHBaptistaCAWangLC. Specificity of a target cell-derived stop signal for afferent axonal growth. J Neurobiol1992;23:579–591.
46.
TrommsdorffMGotthardtMHiesbergerT. Reeler/disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2. Cell1999;97:689–701.
47.
HiesbergerTTrommsdorffMHowellBW. Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation. Neuron1999;24:481–489.
48.
D'ArcangeloGHomayouniRKeshvaraL. Reelin is a ligand for lipoprotein receptors. Neuron1999;24:471–479.
49.
DulabonLOlsonECTaglientiMG. Reelin binds α3β1-integrin and inhibits neuronal migration. Neuron2000;27:33–44.
50.
SenzakiKOgawaMYagiT. Proteins of the CNR family are multiple receptors for Reelin. Cell1999;99:635–647.
51.
GuptaATsaiLHWynshaw-BorisA. Life is a journey: a genetic look at neocortical development. Nat Rev Genet2002;3:342–355.
52.
OhiraRZhangYGuoW. Human ARX gene: genomic characterization and expression. Mol Genet Metab2002;77:179.
53.
MiuraHYanazawaMKatoK. Expression of a novel aristaless related homeobox gene ‘Arx’ in the vertebrate telencephalon, diencephalon and floor plate. Mech Dev1997;65:99–109.
54.
BienvenuTPoirierKFriocourtG. ARX, a novel Prd-class-homeobox gene highly expressed in the telencephalon, is mutated in X-linked mental retardation. Hum Mol Genet2002;11:981–991.
55.
KatoMDasSPetrasK. Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation. Hum Mutat2004;23:147–159.
56.
KitamuraKYanazawaMSugiyamaN. Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans. Nat Genet2002;32:359–369.
57.
SherrEH. The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes. Curr Opin Pediatr2003;15:567–571.
58.
UyanikGAignerLMartinP. ARX mutations in X-linked lissencephaly with abnormal genitalia. Neurology2003;61:232–235.
59.
ChaeTKwonYTBronsonR. Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality. Neuron1997;18:29–42.
60.
DhavanRTsaiLH. A decade of CDK5. Nat Rev Mol Cell Biol2001;2:749–759.
61.
BoulderC. Embryonic vertebrate central nervous system: revised terminology. Anat Rec1970;166:257–261.
62.
RakicP. Neuronal migration and contact guidance in primate telencephalon. Postgrad Med J1978;54. Suppl. 1:25–40.
63.
MarinORubensteinJL. Cell migration in the forebrain. Annu Rev Neurosci2003;26:441–483.
64.
AdamsNCTomodaTCooperM. Mice that lack astrotactin have slowed neuronal migration. Development2002;129:965–972.
65.
FishellGHattenM. Astrotactin provides a receptor system for CNS neuronal migration. Development1991;113:755–765.
66.
AntonESMarchionniMALeeKF. Role of GGF/neuregulin signaling in interactions between migrating neurons and radial glia in the developing cerebral cortex. Development1997;124:3501–3510.
67.
RioCRieffHIQiP. Neuregulin and erbB receptors play a critical role in neuronal migration. Neuron1997;19:39–50.
68.
OnoKToasiewiczHMagnusonT. N-CAM mutation inhibits tangential neuronal migration and is phenocopied by enzymatic removal of polysialic acid. Neuron1994;13:595–609.
AndersonSAEisenstatDDShiL. Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes. Science1997;278:474–476.
78.
MillerMW. The migration and neurochemical differentiation of gamma-aminobutyric acid (GABA)-immunoreactive neurons in rat visual cortex as demonstrated by a combined immunocytochemical-autoradiographic technique. Brain Res1986;393:41–46.
79.
McManusMFNasrallahIMPancoastMM. Lis1 is necessary for normal non-radial migration of inhibitory interneurons. Am J Pathol2004;165:775–784.
80.
PancoastMMDobynsWBGoldenJA. Interneuron deficits in patients with the Miller-Dieker syndrome. Acta Neuropathol Berl2005;109:400–404
81.
SchuurmansCGuillemotF. Molecular mechanisms underlying cell fate specification in the developing telencephalon. Curr Opin Neurobiol2002;12:26–34.
82.
MarinOYaronABagriA. Sorting of striatal and cortical interneurons regulated by semaphorin-neuropilin interactions. Science2001;293:872–875.