Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome.
about
Induced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Neurobiology of social behavior abnormalities in autism and Williams syndromeUsing transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeCattle genome-wide analysis reveals genetic signatures in trypanotolerant N'Dama.Essential role of the N-terminal region of TFII-I in viability and behavior.Intracisternal Gtf2i Gene Therapy Ameliorates Deficits in Cognition and Synaptic Plasticity of a Mouse Model of Williams-Beuren SyndromeNegative autoregulation of GTF2IRD1 in Williams-Beuren syndrome via a novel DNA binding mechanismReduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice.Rearrangements of the Williams-Beuren syndrome locus: molecular basis and implications for speech and language development.An atypical 7q11.23 deletion in a normal IQ Williams-Beuren syndrome patient.Challenges in clinical diagnosis of williams-beuren syndrome in sub-saharan africans: case reports from cameroon.Sleep in children with Williams SyndromeThe contribution of CLIP2 haploinsufficiency to the clinical manifestations of the Williams-Beuren syndrome.William's syndrome: gene expression is related to parental origin and regional coordinate control.Identification of the TFII-I family target genes in the vertebrate genome.Smaller and larger deletions of the Williams Beuren syndrome region implicate genes involved in mild facial phenotype, epilepsy and autistic traits.A genome-wide linkage and association scan reveals novel loci for autism.Autism spectrum disorders: the quest for genetic syndromes.Modeling Williams syndrome with induced pluripotent stem cells.Williams syndrome: a genetic deletion disorder presenting clues to the biology of sociability and clinical challenges of hypersociability.Molecular and phenotypic characterization of atypical Williams-Beuren syndrome.The contribution of GTF2I haploinsufficiency to Williams syndrome.Haploinsufficiency of Gtf2i, a gene deleted in Williams Syndrome, leads to increases in social interactions.Performance on tasks of visuospatial memory and ability: A cross-sectional study in 330 adolescents aged 11 to 20.Rare genomic rearrangement in a boy with Williams-Beuren syndrome associated to XYY syndrome and intriguing behavior.
P2860
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P2860
Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
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2006年学术文章
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2006年学术文章
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2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
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2006年學術文章
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2006年學術文章
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name
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@en
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@nl
type
label
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@en
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@nl
prefLabel
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@en
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@nl
P2093
P1476
Contribution of CYLN2 and GTF2 ...... symptoms in Williams Syndrome.
@en
P2093
De Zeeuw CI
Govaerts LC
Hoogenraad CC
Jansweijer MC
Koekkoek SK
Lagers-van Haselen GC
Thorgeirsson SS
P304
P356
10.1016/J.NBD.2006.12.009
P577
2006-12-20T00:00:00Z