Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
about
Genome annotation of a 1.5 Mb region of human chromosome 6q23 encompassing a quantitative trait locus for fetal hemoglobin expression in adultsInduced chromosome deletions cause hypersociability and other features of Williams-Beuren syndrome in mice.Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligaseHotspots of mammalian chromosomal evolutionMulti-species sequence comparison reveals dynamic evolution of the elastin gene that has involved purifying selection and lineage-specific insertions/deletionsHuman-zebrafish non-coding conserved elements act in vivo to regulate transcriptionUsing transcription modules to identify expression clusters perturbed in Williams-Beuren syndromeInduced chromosome deletion in a Williams-Beuren syndrome mouse model causes cardiovascular abnormalities.Loss of WSTF results in spontaneous fluctuations of heterochromatin formation and resolution, combined with substantial changes to gene expression.Parallel construction of orthologous sequence-ready clone contig maps in multiple speciesNeural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.Expression of the transcription factor, TFII-I, during post-implantation mouse embryonic development.Identification and characterization of multi-species conserved sequencesGene expression of NMDA receptor subunits in the cerebellum of elderly patients with schizophreniaAn Alu transposition model for the origin and expansion of human segmental duplications.Conserved and non-conserved enhancers direct tissue specific transcription in ancient germ layer specific developmental control genesA physical map of the mouse genome.Autistic disorder in patients with Williams-Beuren syndrome: a reconsideration of the Williams-Beuren syndrome phenotype.GALA, a database for genomic sequence alignments and annotationsCovariation in frequencies of substitution, deletion, transposition, and recombination during eutherian evolutionGenetic modifiers of cardiovascular phenotype caused by elastin haploinsufficiency act by extrinsic noncomplementation.Conserved non-genic sequences - an unexpected feature of mammalian genomes.Connection between elastin haploinsufficiency and increased cell proliferation in patients with supravalvular aortic stenosis and Williams-Beuren syndromeAn intermediate grade of finished genomic sequence suitable for comparative analyses.The representation of semantic knowledge in a child with Williams syndrome.Mutational mechanisms of Williams-Beuren syndrome deletions.More than the sum of its parts: new mouse models for dissecting the genetic complexities of Williams-Beuren syndrome.Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.Age-associated memory changes in adults with williams syndrome.Numerous potentially functional but non-genic conserved sequences on human chromosome 21
P2860
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P2860
Generation and comparative analysis of approximately 3.3 Mb of mouse genomic sequence orthologous to the region of human chromosome 7q11.23 implicated in Williams syndrome.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Generation and comparative ana ...... plicated in Williams syndrome.
@ast
Generation and comparative ana ...... plicated in Williams syndrome.
@en
type
label
Generation and comparative ana ...... plicated in Williams syndrome.
@ast
Generation and comparative ana ...... plicated in Williams syndrome.
@en
prefLabel
Generation and comparative ana ...... plicated in Williams syndrome.
@ast
Generation and comparative ana ...... plicated in Williams syndrome.
@en
P2093
P2860
P50
P356
P1433
P1476
Generation and comparative ana ...... plicated in Williams syndrome.
@en
P2093
Gerard G Bouffard
Jacquelyn R Idol
James W Thomas
Jeffrey W Touchman
Jennifer C McDowell
Johannah L Doyle
Nicole L Dietrich
Pamela J Thomas
Robert W Blakesley
Scott Schwartz
P2860
P356
10.1101/GR.214802
P577
2002-01-01T00:00:00Z