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rdf:type |
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lifeskim:mentions |
umls-concept:C0017337,
umls-concept:C0205314,
umls-concept:C0265219,
umls-concept:C0679622,
umls-concept:C0927232,
umls-concept:C1314939,
umls-concept:C1326504,
umls-concept:C1514873,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C2681930
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pubmed:issue |
1
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pubmed:dateCreated |
1998-3-16
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pubmed:databankReference |
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pubmed:abstractText |
X-SCLH/LIS syndrome is a neuronal migration disorder with disruption of the six-layered neocortex. It consists of subcortical laminar heterotopia (SCLH, band heterotopia, or double cortex) in females and lissencephaly (LIS) in males, leading to epilepsy and cognitive impairment. We report the characterization of a novel CNS gene encoding a 40 kDa predicted protein that we named Doublecortin and the identification of mutations in four unrelated X-SCLH/LIS cases. The predicted protein shares significant homology with the N-terminal segment of a protein containing a protein kinase domain at its C-terminal part. This novel gene is highly expressed during brain development, mainly in fetal neurons including precursors. The complete disorganization observed in lissencephaly and heterotopia thus seems to reflect a failure of early events associated with neuron dispersion.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0092-8674
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pubmed:author |
pubmed-author:BeldjordCC,
pubmed-author:Berwald-NetterYY,
pubmed-author:BilluartPP,
pubmed-author:CarriéAA,
pubmed-author:CatalaMM,
pubmed-author:ChellyJJ,
pubmed-author:DupuisEE,
pubmed-author:GelotAA,
pubmed-author:KahnAA,
pubmed-author:KoulakoffAA,
pubmed-author:MottoDD,
pubmed-author:PinardJ MJM,
pubmed-author:VinetM CMC,
pubmed-author:des PortesVV
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pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
92
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
51-61
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9489699-Adolescent,
pubmed-meshheading:9489699-Amino Acid Sequence,
pubmed-meshheading:9489699-Base Sequence,
pubmed-meshheading:9489699-Cell Movement,
pubmed-meshheading:9489699-Central Nervous System,
pubmed-meshheading:9489699-Cerebral Cortex,
pubmed-meshheading:9489699-Child, Preschool,
pubmed-meshheading:9489699-Chromosome Mapping,
pubmed-meshheading:9489699-Chromosomes, Artificial, Yeast,
pubmed-meshheading:9489699-DNA, Complementary,
pubmed-meshheading:9489699-Epilepsy,
pubmed-meshheading:9489699-Family Health,
pubmed-meshheading:9489699-Female,
pubmed-meshheading:9489699-Gene Expression,
pubmed-meshheading:9489699-Genes,
pubmed-meshheading:9489699-Humans,
pubmed-meshheading:9489699-Male,
pubmed-meshheading:9489699-Microtubule-Associated Proteins,
pubmed-meshheading:9489699-Molecular Sequence Data,
pubmed-meshheading:9489699-Mutation,
pubmed-meshheading:9489699-Neurons,
pubmed-meshheading:9489699-Neuropeptides,
pubmed-meshheading:9489699-Pedigree,
pubmed-meshheading:9489699-Peptides,
pubmed-meshheading:9489699-Sequence Homology, Amino Acid,
pubmed-meshheading:9489699-Sequence Tagged Sites,
pubmed-meshheading:9489699-Sex Chromosome Aberrations,
pubmed-meshheading:9489699-Syndrome,
pubmed-meshheading:9489699-Transcription, Genetic,
pubmed-meshheading:9489699-X Chromosome
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pubmed:year |
1998
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pubmed:articleTitle |
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.
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pubmed:affiliation |
INSERM U129-ICGM, Faculté de Médecine Cochin, Paris, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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