(Q33748771)

29 July 2017

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title

Genes that regulate neuronal migration in the cerebral cortex (English)

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29 July 2017

Allen KM

1

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29 July 2017

Walsh CA

series ordinal

2

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29 July 2017

language of work or name

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1 September 1999

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29 July 2017

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29 July 2017

volume

36

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29 July 2017

issue

2-3

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29 July 2017

page(s)

143-154

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The agyria-pachygyria complex: a spectrum of cortical malformations.

29 July 2017

cites work

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7 January 2021

The place of neuronal migration abnormalities in child neurology.

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7 January 2021

A YAC contig in Xq22.3-q23, from DXS287 to DXS8088, spanning the brain-specific genes doublecortin (DCX) and PAK3.

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7 January 2021

Malformations of neocortical development: magnetic resonance imaging correlates.

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7 January 2021

Band heterotopia: Correlation of outcome with magnetic resonance imaging parameters

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7 January 2021

Neocortical histogenesis in normal and reeler mice: a developmental study based upon [3H]thymidine autoradiography.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Enhancement of hippocampal excitatory synaptic transmission by platelet-activating factor

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7 January 2021

Platelet-activating factor produces neuronal growth cone collapse

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7 January 2021

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7 January 2021

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7 January 2021

Temporal and spatial patterns of expression of p35, a regulatory subunit of cyclin-dependent kinase 5, in the nervous system of the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Causal heterogeneity in isolated lissencephaly

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

X-linked malformations of neuronal migration

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Two new mutants, ‘trembler’ and ‘reeler’, with neurological actions in the house mouse (Mus musculus L.)

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Neuropathologic findings in cortical resections (including hemispherectomies) performed for the treatment of intractable childhood epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Dispersion of neural progenitors within the germinal zones of the forebrain

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Folding of proteins with WD-repeats: comparison of six members of the WD-repeat superfamily to the G protein beta subunit

1 reference

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7 January 2021

Drosophila abl tyrosine kinase in embryonic CNS axons: a role in axonogenesis is revealed through dosage-sensitive interactions with disabled

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Dosage-sensitive modifiers of Drosophila abl tyrosine kinase function: prospero, a regulator of axonal outgrowth, and disabled, a novel tyrosine kinase substrate.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

Characterization of mutations in the gene doublecortin in patients with double cortex syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

Cerebellar disorganization characteristic of reeler in scrambler mutant mice despite presence of reelin.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

Microdysgenesis in resected temporal neocortex: Incidence and clinical significance in focal epilepsy

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

The reeler gene encodes a protein with an EGF-like motif expressed by pioneer neurons

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Brain acetylhydrolase that inactivates platelet-activating factor is a G-protein-like trimer

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Rapid and efficient construction of yeast artificial chromosome contigs in the mouse genome with interspersed repetitive sequence PCR (IRS-PCR): generation of a 5-cM, > 5 megabase contig on mouse chromosome 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Expression of the LIS-1 gene product in brain anomalies with a migration disorder

1 reference

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7 January 2021

Neuroregulatory and neuropathological actions of the ether-phospholipid platelet-activating factor

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https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Magnetic resonance imaging in developmental disorders of the cerebral cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

A novel disruption of cortical development in p35(-/-) mice distinct from reeler

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

The density of dystopic neurons in the white matter of the gyrus frontalis inferior in epilepsies

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Diverse migratory pathways in the developing cerebral cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Neurons in rhesus monkey visual cortex: systematic relation between time of origin and eventual disposition

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Principles of neural cell migration

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy. Clinical, EEG and neuroimaging features in 100 adult patie

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

Radial mosaicism and tangential cell dispersion both contribute to mouse neocortical development

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Morphological substrates of infantile spasms: studies based on surgically resected cerebral tissue

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Clonal dispersion in proliferative layers of developing cerebral cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

7 January 2021

Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0920-1211%2899%2900048-0

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%2FS0920-1211%2899%2900048-0

7 January 2021

10.1016/S0920-1211(99)00048-0

Identifiers

DOI

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29 July 2017

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