doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
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Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growthComparative aspects of cerebral cortical developmentGenes and brain malformations associated with abnormal neuron positioningAxonal transport: cargo-specific mechanisms of motility and regulationDoublecortin knockout mice show normal hippocampal-dependent memory despite CA3 lamination defectsMolecular Basis for Specific Regulation of Neuronal Kinesin-3 Motors by Doublecortin Family ProteinsGenetic Basis of Brain MalformationsBeta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdownSynergistic effects of MAP2 and MAP1B knockout in neuronal migration, dendritic outgrowth, and microtubule organizationEndogenous versus exogenous markers of adult neurogenesis in canaries and other birds: advantages and disadvantagesExpression of reelin, its receptors and its intracellular signaling protein, Disabled1 in the canary brain: relationships with the song control system.The microtubule-associated protein doublecortin is broadly expressed in the telencephalon of adult canariesDoublecortin recognizes the 13-protofilament microtubule cooperatively and tracks microtubule endsDoublecortin (DCX) mediates endocytosis of neurofascin independently of microtubule binding.Doublecortin associates with microtubules preferentially in regions of the axon displaying actin-rich protrusive structuresAnalysis of adult neurogenesis: evidence for a prominent "non-neurogenic" DCX-protein pool in rodent brain.Adapting for endocytosis: roles for endocytic sorting adaptors in directing neural development.Doublecortin (Dcx) family proteins regulate filamentous actin structure in developing neurons.Advanced microscopic imaging methods to investigate cortical development and the etiology of mental retardation.Neuronal migration, cerebral cortical development, and cerebral cortical anomalies.Multisite phosphorylation of doublecortin by cyclin-dependent kinase 5.The genetics of lissencephaly.Doublecortin kinase-2, a novel doublecortin-related protein kinase associated with terminal segments of axons and dendrites.Retinoic acid reduces human neuroblastoma cell migration and invasiveness: effects on DCX, LIS1, neurofilaments-68 and vimentin expression.Doublecortin may play a role in defining chondrocyte phenotype.Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division.Septin 14 is involved in cortical neuronal migration via interaction with Septin 4.Fibroblast growth factor 2 enhances striatal and nigral neurogenesis in the acute 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's diseaseThe neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changesSomatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypesEpilepsy and genetic malformations of the cerebral cortex.Clinical and molecular basis of classical lissencephaly: Mutations in the LIS1 gene (PAFAH1B1).The contribution of αβ-tubulin curvature to microtubule dynamics.From genes to behavior in developmental dyslexia.Evidence that Doublecortin is dispensable for the development of adult born neurons in mice.An isoform-specific SnoN1-FOXO1 repressor complex controls neuronal morphogenesis and positioning in the mammalian brainOrganelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout miceMorphological and functional aspects of progenitors perturbed in cortical malformations.Hippocampal plasticity after a vagus nerve injury in the rat.Cellular dynamics of neuronal migration in the hippocampus.
P2860
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P2860
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
description
1998 nî lūn-bûn
@nan
1998 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@ast
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@en
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@nl
type
label
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@ast
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@en
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@nl
prefLabel
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@ast
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@en
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@nl
P2093
P356
P1476
doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)
@en
P2093
I Desguerre
J M Pinard
L C Meiners
M L Moutard
P304
P356
10.1093/HMG/7.7.1063
P407
P577
1998-07-01T00:00:00Z