(Q28201327)

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ORCID Public Data File 2021

author name string

Yi-Xin Wu

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Anindita Sen

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Vann Bennett

Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein

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language of work or name

English

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publication date

15 September 2002

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published in

Journal of Neuroscience

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volume

22

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issue

18

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page(s)

7948-58

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7948-7958

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cites work

1 reference

12 December 2020

A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome

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12 December 2020

Altered distribution of dopaminergic neurons in the brain of L1 null mice

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12 December 2020

Tyrosine phosphorylation at a site highly conserved in the L1 family of cell adhesion molecules abolishes ankyrin binding and increases lateral mobility of neurofascin

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12 December 2020

The expression and posttranslational modification of a neuron-specific beta-tubulin isotype during chick embryogenesis

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12 December 2020

LIS1 and dynein motor function in neuronal migration and development

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12 December 2020

LIS1: cellular function of a disease-causing gene

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12 December 2020

The L1 family of neural cell adhesion molecules: old proteins performing new tricks

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12 December 2020

Neuroglian-mediated cell adhesion induces assembly of the membrane skeleton at cell contact sites

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12 December 2020

KIAA0369, doublecortin-like kinase, is expressed during brain development

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12 December 2020

Long-distance neuronal migration in the adult mammalian brain

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12 December 2020

NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration

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12 December 2020

Interaction between LIS1 and doublecortin, two lissencephaly gene products

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12 December 2020

Errors in corticospinal axon guidance in mice lacking the neural cell adhesion molecule L1.

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12 December 2020

Immunohistochemical localization of neurocan and L1 in the formation of thalamocortical pathway of developing rats

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12 December 2020

Molecular composition of the node of Ranvier: identification of ankyrin-binding cell adhesion molecules neurofascin (mucin+/third FNIII domain-) and NrCAM at nodal axon segments

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12 December 2020

Ankyrin-binding activity of nervous system cell adhesion molecules expressed in adult brain.

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12 December 2020

Doublecortin mutations cluster in evolutionarily conserved functional domains

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12 December 2020

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

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12 December 2020

Doublecortin interacts with mu subunits of clathrin adaptor complexes in the developing nervous system

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12 December 2020

Direct evidence for homotypic, glia-independent neuronal migration

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12 December 2020

Patient mutations in doublecortin define a repeated tubulin-binding domain

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12 December 2020

Genotype-phenotype correlation in L1 associated diseases

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12 December 2020

Cytoplasmic domain mutations of the L1 cell adhesion molecule reduce L1-ankyrin interactions.

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12 December 2020

Structural and functional evolution of the L1 family: are four adhesion molecules better than one?

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12 December 2020

Structural requirements for association of neurofascin with ankyrin

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12 December 2020

Abnormalities in neuronal process extension, hippocampal development, and the ventricular system of L1 knockout mice

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12 December 2020

Doublecortin is a developmentally regulated, microtubule-associated protein expressed in migrating and differentiating neurons

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12 December 2020

Neural cell recognition molecule L1: from cell biology to human hereditary brain malformations

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12 December 2020

Chain migration of neuronal precursors.

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12 December 2020

Drosophila neuroglian: a member of the immunoglobulin superfamily with extensive homology to the vertebrate neural adhesion molecule L1.

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12 December 2020

DCAMKL1 encodes a protein kinase with homology to doublecortin that regulates microtubule polymerization

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12 December 2020

Doublecortin expression in the adult rat telencephalon

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12 December 2020

Disruption of the mouse L1 gene leads to malformations of the nervous system

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12 December 2020

CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1.

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12 December 2020

LAD-1, the Caenorhabditis elegans L1CAM homologue, participates in embryonic and gonadal morphogenesis and is a substrate for fibroblast growth factor receptor pathway-dependent phosphotyrosine-based signaling

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12 December 2020

FIGQY phosphorylation defines discrete populations of L1 cell adhesion molecules at sites of cell-cell contact and in migrating neurons

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12 December 2020

Ankyrin binding activity shared by the neurofascin/L1/NrCAM family of nervous system cell adhesion molecules

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12 December 2020

Spindle positioning during the asymmetric first cell division of Caenorhabditis elegans embryos.

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12 December 2020

Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit.

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12 December 2020

Nuclear migration, nucleokinesis and lissencephaly

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12 December 2020

The phosphorylation state of the FIGQY tyrosine of neurofascin determines ankyrin-binding activity and patterns of cell segregation

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12 December 2020

Doublecortin, a stabilizer of microtubules

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12 December 2020

Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons

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12 December 2020

10.1523/JNEUROSCI.22-18-07948.2002

Identifiers

DOI

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OpenCitations bibliographic resource ID

956578

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

956578

PMC publication ID

6758080

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PubMed publication ID

12223548

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