(Q24314944)

GOA release 2020-03-11

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P Billuart

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V des Portes

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J M Pinard

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M C Vinet

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A Koulakoff

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A Carrié

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A Gelot

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E Dupuis

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J Motte

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Y Berwald-Netter

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M Catala

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A Kahn

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J Chelly

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

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language of work or name

English

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publication date

9 January 1998

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51-61

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cites work

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

The subplate, a transient neocortical structure: its role in the development of connections between thalamus and cortex

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Identification and characterization of the gene causing type 1 spinocerebellar ataxia

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Activation of protein kinase C decreases phosphorylation of c-Jun at sites that negatively regulate its DNA-binding activity

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Illegitimate transcription: transcription of any gene in any cell type

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

X-linked malformations of neuronal migration

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https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

7 January 2021

Structure in lissencephaly determined by immunohistochemical staining

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Adhesion in cell migration

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Contact and adhesive specificities in the associations, migrations, and targeting of cells and axons

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Protein kinase recognition sequence motifs

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Selective role of N-type calcium channels in neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Modulation of neuronal migration by NMDA receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Magnetic resonance imaging in childhood intractable partial epilepsies: pathologic correlations

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

A simple method for displaying the hydropathic character of a protein

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Spacing and orientation of bipartite DNA-binding motifs as potential functional determinants for POU domain factors

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

7 January 2021

Cell lineage in the cerebral cortex of the mouse studied in vivo and in vitro with a recombinant retrovirus

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Cytoplasmic mRNA-protein interactions in eukaryotic gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Constructing the cerebral cortex: Neurogenesis and fate determination

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Prediction of the coding sequences of unidentified human genes. VII. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Diffuse cortical dysplasia, or the 'double cortex' syndrome: the clinical and epileptic spectrum in 10 patients

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Specification of cerebral cortical areas

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Cortical development: View from neurological mutants two decades later

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

7 January 2021

Activation of c-Src in cells bearing v-Crk and its suppression by Csk

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

cDNA cloning of human N-Oct3, a nervous-system specific POU domain transcription factor binding to the octamer DNA motif

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

A Gene Map of the Human Genome

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

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%2FS0092-8674%2800%2980898-3

7 January 2021

Cloning, characterization, and expression of a novel GDP dissociation inhibitor isoform from skeletal muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Catalytic specificity of protein-tyrosine kinases is critical for selective signalling

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021

Genome maps 7. The human transcript map. Wall chart

1 reference

https://api.crossref.org/works/10.1016%2FS0092-8674%2800%2980898-3

7 January 2021