(Q33976255)

30 July 2017

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title

Neuronal migration disorders: from genetic diseases to developmental mechanisms (English)

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30 July 2017

Gleeson JG

1

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30 July 2017

Walsh CA

series ordinal

2

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30 July 2017

publication date

1 August 2000

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30 July 2017

published in

Trends in Neurosciences

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30 July 2017

volume

23

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30 July 2017

issue

8

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30 July 2017

page(s)

352-359

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Mode of cell migration to the superficial layers of fetal monkey neocortex

30 July 2017

cites work

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7 January 2021

Widespread Dispersion of Neuronal Clones Across Functional Regions of the Cerebral Cortex

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7 January 2021

Diverse migratory pathways in the developing cerebral cortex

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7 January 2021

Interneuron Migration from Basal Forebrain to Neocortex: Dependence on Dlx Genes

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7 January 2021

Dual origin of the mammalian neocortex and evolution of the cortical plate

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7 January 2021

Autoradiographic study of cell migration during histogenesis of cerebral cortex in the mouse

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7 January 2021

Cell lineage and patterns of migration in the developing cortex.

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7 January 2021

Time of origin or corresponding cell classes in the cerebral cortex of normal and reeler mutant mice: an autoradiographic analysis

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7 January 2021

Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patients

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7 January 2021

Epilepsy and anomalies of neuronal migration: MRI and clinical aspects

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7 January 2021

Periventricular Heterotopia: An X-Linked Dominant Epilepsy Locus Causing Aberrant Cerebral Cortical Development

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7 January 2021

Gray matter heterotopias: MR characteristics and correlation with developmental and neurologic manifestations

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7 January 2021

Periventricular heterotopia and epilepsy

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7 January 2021

Seizure onset from periventricular nodular heterotopias: depth-electrode study

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7 January 2021

Periventricular and subcortical nodular heterotopia. A study of 33 patients

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7 January 2021

Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.

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7 January 2021

Filamin binds to the cytoplasmic domain of the beta1-integrin. Identification of amino acids responsible for this interaction

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

The small GTPase RalA targets filamin to induce filopodia

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

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7 January 2021

Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene.

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7 January 2021

X-linked female band heterotopia-male lissencephaly syndrome

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase [corrected]

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Platelet activating factor: a biologically active phosphoglyceride

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Platelet-activating factor produces neuronal growth cone collapse

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https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Neuronal cytoskeletal alterations evoked by a platelet-activating factor (PAF) analogue

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Doublecortin, a stabilizer of microtubules

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Birthdate and Cell Marker Analysis of Scrambler: A Novel Mutation Affecting Cortical Development with a Reeler-Like Phenotype

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Events governing organization of postmigratory neurons: studies on brain development in normal and reeler mice.

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

The reeler gene-associated antigen on Cajal-Retzius neurons is a crucial molecule for laminar organization of cortical neurons.

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Patterns of cell and fiber distribution in the neocortex of the reeler mutant mouse

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Reelin is a secreted glycoprotein recognized by the CR-50 monoclonal antibody.

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

A novel neurological mutant mouse, yotari, which exhibits reeler-like phenotype but expresses CR-50 antigen/Reelin

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Aberrant Splicing of a Mouse disabled Homolog, mdab1, in the scrambler Mouse

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Neuronal position in the developing brain is regulated by mouse disabled-1

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Reelin-induced tyrosine [corrected] phosphorylation of disabled 1 during neuronal positioning

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

The disabled 1 phosphotyrosine-binding domain binds to the internalization signals of transmembrane glycoproteins and to phospholipids

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Reeler/Disabled-like disruption of neuronal migration in knockout mice lacking the VLDL receptor and ApoE receptor 2

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Reelin is a ligand for lipoprotein receptors

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Proteins of the CNR family are multiple receptors for Reelin

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Cyclin-dependent kinase 5-deficient mice demonstrate novel developmental arrest in cerebral cortex

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

A novel disruption of cortical development inp35?/? mice distinct fromreeler

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

A family of human cdc2-related protein kinases

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

p35 is a neural-specific regulatory subunit of cyclin-dependent kinase 5

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

A brain-specific activator of cyclin-dependent kinase 5.

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

An Isoform of the Neuronal Cyclin-dependent Kinase 5 (Cdk5) Activator

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

cdc2-like kinase from rat spinal cord specifically phosphorylates KSPXK motifs in neurofilament proteins: isolation and characterization

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Phosphorylation of the high molecular weight neurofilament protein (NF-H) by Cdk5 and p35

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Phosphorylation of human high molecular weight neurofilament protein (hNF-H) by neuronal cyclin-dependent kinase 5 (cdk5)

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Evidence for cdk5 as a Major Activity Phosphorylating Tau Protein in Porcine Brain Extract1

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Abnormal Alzheimer-like phosphorylation of tau-protein by cyclin-dependent kinases cdk2 and cdk5

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Potentiation of GSK-3-catalyzed Alzheimer-like phosphorylation of human tau by cdk5.

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Phosphorylation by Neuronal cdc2-like Protein Kinase Promotes Dimerization of Tau Protein in Vitro

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

The cdk5/p35 kinase is essential for neurite outgrowth during neuronal differentiation

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Walker-Warburg syndrome: Neurologic features and muscle membrane structure

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Essential role of alpha 6 integrins in cortical and retinal lamination

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Presenilin-1 deficiency leads to loss of Cajal-Retzius neurons and cortical dysplasia similar to human type 2 lissencephaly

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

Dual role of Cajal-Retzius cells and reelin in cortical development

1 reference

https://api.crossref.org/works/10.1016/S0166-2236(00)01607-6

7 January 2021

10.1016/S0166-2236(00)01607-6

Identifiers

DOI

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30 July 2017

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