doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH) - Wikidata - awgldk - TriplyDB

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

http://www.wikidata.org/entity/Q28273011

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Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth Comparative aspects of cerebral cortical development Genes and brain malformations associated with abnormal neuron positioning Axonal transport: cargo-specific mechanisms of motility and regulation Doublecortin knockout mice show normal hippocampal-dependent memory despite CA3 lamination defects Molecular Basis for Specific Regulation of Neuronal Kinesin-3 Motors by Doublecortin Family Proteins Genetic Basis of Brain Malformations Beta tubulin isoforms are not interchangeable for rescuing impaired radial migration due to Tubb3 knockdown Synergistic effects of MAP2 and MAP1B knockout in neuronal migration, dendritic outgrowth, and microtubule organization Endogenous versus exogenous markers of adult neurogenesis in canaries and other birds: advantages and disadvantages Expression 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 canaries Doublecortin recognizes the 13-protofilament microtubule cooperatively and tracks microtubule ends Doublecortin (DCX) mediates endocytosis of neurofascin independently of microtubule binding.Doublecortin associates with microtubules preferentially in regions of the axon displaying actin-rich protrusive structures Analysis 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 disease The neuropathology of autism: defects of neurogenesis and neuronal migration, and dysplastic changes Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes Epilepsy 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 brain Organelle and cellular abnormalities associated with hippocampal heterotopia in neonatal doublecortin knockout mice Morphological 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.

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P2860

doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

http://www.wikidata.org/entity/Q28273011

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

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1998年論文

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1998年論文

@zh-hant

1998年論文

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1998年論文

@zh-mo

1998年論文

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1998年论文

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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)

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Human Molecular Genetics

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doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH)

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P2093

B Echenne

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7

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7

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Cherif Beldjord

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13666644

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