(Q24314944)

GOA release 2020-03-11

author

Cherif Beldjord

13

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Pierre Billuart

object named as

P Billuart

3

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author name string

V des Portes

1

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J M Pinard

2

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M C Vinet

4

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A Koulakoff

5

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A Carrié

6

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A Gelot

7

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E Dupuis

8

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J Motte

9

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Y Berwald-Netter

10

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M Catala

11

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A Kahn

12

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J Chelly

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

14

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language of work or name

English

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publication date

9 January 1998

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published in

Cell

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volume

92

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page(s)

51-61

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issue

1

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cites work

1 reference

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Identification and characterization of the gene causing type 1 spinocerebellar ataxia.

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7 January 2021

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

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7 January 2021

Illegitimate transcription: transcription of any gene in any cell type

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7 January 2021

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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

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7 January 2021

X-linked malformations of neuronal migration

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7 January 2021

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Structure in lissencephaly determined by immunohistochemical staining.

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7 January 2021

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

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7 January 2021

Adhesion in cell migration

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7 January 2021

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

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7 January 2021

Protein kinase recognition sequence motifs

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7 January 2021

Selective role of N-type calcium channels in neuronal migration

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7 January 2021

Modulation of neuronal migration by NMDA receptors.

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Magnetic resonance imaging in childhood intractable partial epilepsies: pathologic correlations.

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7 January 2021

A simple method for displaying the hydropathic character of a protein

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7 January 2021

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

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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

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7 January 2021

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

1 reference

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7 January 2021

Cytoplasmic mRNA-protein interactions in eukaryotic gene expression

1 reference

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7 January 2021

Constructing the cerebral cortex: neurogenesis and fate determination

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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

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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7 January 2021

Specification of cerebral cortical areas

1 reference

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7 January 2021

Cortical development: view from neurological mutants two decades later

1 reference

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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

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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

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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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

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7 January 2021

A Gene Map of the Human Genome

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7 January 2021

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

1 reference

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7 January 2021

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

1 reference

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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

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7 January 2021

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

1 reference

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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

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7 January 2021