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注意：仅列出部分参考文献，下载原文获取全部文献信息。Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development
Badam Enkhmandakh et al.
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Reduced fear and aggression and altered serotonin metabolism in Gtf2ird1-targeted mice
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Determination and functional analysis of the consensus binding site for TFII-I family member BEN, implicated in Williams-Beuren Syndrome
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Recruitment of coregulator complexes to the β-globin gene locus by TFII-I and upstream stimulatory factor
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Dominance of SOX9 function over RUNX2 during skeletogenesis
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Opposing functions of TFII-I spliced lsoforms in growth factor-induced gene expression
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HES1 cooperates with pRb to activate RUNX2-dependent transcription
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TFII-I down-regulates a subset of estrogen-responsive genes through its interaction with an initiator element and estrogen receptor α
Y Ogura et al.
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Antagonistic regulation of beta-globin gene expression by helix-loop-helix proteins USF and TFII-I
Valerie J. Crusselle-Davis et al.
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Inhibition of TFII-I-dependent cell cycle regulation by p53
ZP Desgranges et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
GTF2IRD1 in craniofacial development of humans and mice
M Tassabehji et al.
SCIENCE (2005)
Transcriptional regulation of the Grp78 promoter by endoplasmic reticulum stress - Role of TFII-I and its tyrosine phosphorylation
M Hong et al.
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Comparison of TFII-I gene family members deleted in Williams-Beuren syndrome
TA Hinsley et al.
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Inhibitor of DNA binding/differentiation helix-loop-helix proteins mediate bone morphogenetic protein-induced osteoblast differentiation of mesenchymal stem cells
Y Peng et al.
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Runx2 induces osteoblast and chondrocyte differentiation and enhances their migration by coupling with PI3K-Akt signaling
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Nomenclature for Runt-related (RUNX) proteins
AJ van Wijnen et al.
ONCOGENE (2004)
GTF21 hemizygosity implicated in mental retardation in Williams syndrome: Genotype-phenotype analysis of five families with deletions in the Williams syndrome region
CA Morris et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2003)
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF21 on Chromosome 7q11.23
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Unusual cognitive and behavioural profile in a Williams syndrome patient with atypical 7q11.23 deletion
C Gagliardi et al.
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Physical and functional interactions of histone deacetylase 3 with TFII-I family proteins and PIASαβ
MI Tussié-Luna et al.
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c-Src-dependent transcriptional activation of TFII-I
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Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method
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Biochemistry and biology of the inducible multifunctional transcription factor TFII-1
AL Roy
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The retinoblastoma protein acts as a transcriptional coactivator required for osteogenic differentiation
DM Thomas et al.
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