(Q30671553)

26 June 2017

1 reference

title

Neuronal migration, cerebral cortical development, and cerebral cortical anomalies (English)

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26 June 2017

Daniela Pilz

1

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26 June 2017

Neil Stoodley

series ordinal

2

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26 June 2017

Jeffrey A Golden

series ordinal

3

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26 June 2017

publication date

1 January 2002

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Journal of Neuropathology & Experimental Neurology

26 June 2017

published in

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26 June 2017

volume

61

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26 June 2017

issue

1

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26 June 2017

page(s)

1-11

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Mechanisms of glial-guided neuronal migration in vitro and in vivo

26 June 2017

cites work

1 reference

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Principles of neural cell migration

21 January 2018

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

21 January 2018

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Neuregulin and erbB receptors play a critical role in neuronal migration

21 January 2018

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Structure, expression, and function of Ng-CAM, a member of the immunoglobulin superfamily involved in neuron-neuron and neuron-glia adhesion

21 January 2018

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Cell adhesion molecule L1 guides cell migration in primary reaggregation cultures of mouse cerebellar cells

21 January 2018

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Antibodies that recognize astrotactin block granule neuron binding to astroglia

21 January 2018

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CNS gene encoding astrotactin, which supports neuronal migration along glial fibers

21 January 2018

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Tenascin promotes cerebellar granule cell migration and neurite outgrowth by different domains in the fibronectin type III repeats

21 January 2018

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Retrovirally introduced antisense integrin RNA inhibits neuroblast migration in vivo

21 January 2018

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Architectonic map of neocortex of the normal mouse

21 January 2018

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21 January 2018

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

21 January 2018

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Central nervous system neuronal migration

21 January 2018

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A new view of early cortical development

21 January 2018

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Proteins of the CNR family are multiple receptors for Reelin

21 January 2018

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

21 January 2018

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Reelin is a ligand for lipoprotein receptors

21 January 2018

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

21 January 2018

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https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Reelin binds alpha3beta1 integrin and inhibits neuronal migration.

21 January 2018

1 reference

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

21 January 2018

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Mouse disabled (mDab1): a Src binding protein implicated in neuronal development

21 January 2018

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Cellular functions regulated by Src family kinases

21 January 2018

1 reference

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Knockouts of Src-family kinases: stiff bones, wimpy T cells, and bad memories.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Src family kinases are required for integrin but not PDGFR signal transduction.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Cables links Cdk5 and c-Abl and facilitates Cdk5 tyrosine phosphorylation, kinase upregulation, and neurite outgrowth

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Targeted disruption of the cyclin-dependent kinase 5 gene results in abnormal corticogenesis, neuronal pathology and perinatal death

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Expression of constitutively active alpha-PAK reveals effects of the kinase on actin and focal complexes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

The role of cytoplasmic dynein in the human brain developmental disease lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Interaction of the p62 subunit of dynactin with Arp1 and the cortical actin cytoskeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

LIS1 regulates CNS lamination by interacting with mNudE, a central component of the centrosome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein

21 January 2018

1 reference

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A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Direct association of LIS1, the lissencephaly gene product, with a mammalian homologue of a fungal nuclear distribution protein, rNUDE

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

LIS1 and dynein motor function in neuronal migration and development

21 January 2018

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A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Actin-binding protein promotes the bipolar and perpendicular branching of actin filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Human endothelial actin-binding protein (ABP-280, nonmuscle filamin): a molecular leaf spring

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

The architecture of actin filaments and the ultrastructural location of actin-binding protein in the periphery of lung macrophages

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Mechanisms of actin rearrangements mediating platelet activation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

The small GTPase RalA targets filamin to induce filopodia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Commissural fibers may guide cholinergic neuronal migration in developing rat cervical spinal cord

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Interneuron migration from basal forebrain to neocortex: dependence on Dlx genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Separate progenitors for radial and tangential cell dispersion during development of the cerebral neocortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Cell migration from the ganglionic eminences is required for the development of hippocampal GABAergic interneurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

An olfactory sensory map develops in the absence of normal projection neurons or GABAergic interneurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Cellular and molecular guidance of GABAergic neuronal migration from an extracortical origin to the neocortex

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

A classification scheme for malformations of cortical development

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Lissencephaly and other malformations of cortical development: 1995 update

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Omphalocele in Miller-Dieker syndrome: expanding the phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Fluorescence in situ hybridization analysis with LIS1 specific probes reveals a high deletion mutation rate in isolated lissencephaly sequence.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Another Arab patient with overlap of Váradi-Papp/Opitz trigonocephaly syndromes?

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Diagnostic criteria for Walker-Warburg syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Development of the cortical dysplasia of type II lissencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Incidence and distribution of neomembranes of dura mater

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Clinical and genetic distinction between Walker-Warburg syndrome and muscle-eye-brain disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Clinical spectrum and genetic studies of Fukuyama congenital muscular dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Periventricular heterotopia and epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Familial periventricular nodular heterotopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

Periventricular heterotopia may result from radial glial fiber disruption.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

The p35/Cdk5 kinase is a neuron-specific Rac effector that inhibits Pak1 activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F61.1.1

21 January 2018

Identifiers

DOI

10.1093/JNEN/61.1.1

1 reference

26 June 2017

1 reference