Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome
about
Repression of TFII-I-dependent transcription by nuclear exclusionCharacterization and gene structure of a novel retinoblastoma-protein-associated protein similar to the transcription regulator TFII-IPhysical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASxbeta.Alternatively spliced isoforms of TFII-I. Complex formation, nuclear translocation, and differential gene regulationWilliams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23Characterization of general transcription factor 3, a transcription factor involved in slow muscle-specific gene expressionThe SUMO ubiquitin-protein isopeptide ligase family member Miz1/PIASxbeta /Siz2 is a transcriptional cofactor for TFII-IVascular endothelial growth factor receptor-2: counter-regulation by the transcription factors, TFII-I and TFII-IRD1Isolation and characterization of BEN, a member of the TFII-I family of DNA-binding proteins containing distinct helix-loop-helix domainsThe role of a Williams-Beuren syndrome-associated helix-loop-helix domain-containing transcription factor in activin/nodal signalingThe nuclear localization pattern and interaction partners of GTF2IRD1 demonstrate a role in chromatin regulationRegulation of alternative splicing of Gtf2ird1 and its impact on slow muscle promoter activity.Structure-function analysis of TFII-I. Roles of the N-terminal end, basic region, and I-repeats.Regulation of immunoglobulin promoter activity by TFII-I class transcription factors.Molecular dissection of DNA sequences and factors involved in slow muscle-specific transcription.Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndromeA physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome--deletion region at 7q11.23Gene expression profiles--a new dynamic and functional dimension to the exploration of learning and memory.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.Social Cognition in Williams Syndrome: Relations between Performance on the Social Attribution Task and Cognitive and Behavioral CharacteristicsGTF2IRD2 is located in the Williams-Beuren syndrome critical region 7q11.23 and encodes a protein with two TFII-I-like helix-loop-helix repeatsGenetic mapping of brain plasticity across development in Williams syndrome: ERP markers of face and language processing.Determination and functional analysis of the consensus binding site for TFII-I family member BEN, implicated in Williams-Beuren syndrome.Gene expression profiles during long-term memory consolidation.Outcome in adult life for people with Williams syndrome-- results from a survey of 239 families.GTF2IRD1 regulates transcription by binding an evolutionarily conserved DNA motif 'GUCE'.
P2860
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P2860
Identification of a putative transcription factor gene (WBSCR11) that is commonly deleted in Williams-Beuren syndrome
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Identification of a putative t ...... ed in Williams-Beuren syndrome
@ast
Identification of a putative t ...... ed in Williams-Beuren syndrome
@en
Identification of a putative t ...... ed in Williams-Beuren syndrome
@nl
type
label
Identification of a putative t ...... ed in Williams-Beuren syndrome
@ast
Identification of a putative t ...... ed in Williams-Beuren syndrome
@en
Identification of a putative t ...... ed in Williams-Beuren syndrome
@nl
prefLabel
Identification of a putative t ...... ed in Williams-Beuren syndrome
@ast
Identification of a putative t ...... ed in Williams-Beuren syndrome
@en
Identification of a putative t ...... ed in Williams-Beuren syndrome
@nl
P2093
P356
P1433
P1476
Identification of a putative t ...... ed in Williams-Beuren syndrome
@en
P2093
P304
P356
10.1006/GENO.1999.5784
P407
P577
1999-04-01T00:00:00Z