GTF2I gene

Known as: DIWS, SPIN, BAP135 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1997-2017
051019972017

Papers overview

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2014
2014
We analyzed 28 thymic epithelial tumors (TETs) using next-generation sequencing and identified a missense mutation (chromosome 7… (More)
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2012
2012
Duplication (dup7q11.23) and deletion (Williams syndrome) of chromosomal region 7q11.23 cause neurodevelopmental disorders with… (More)
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2011
2011
Identifying genes involved in social behavior is important for autism research. Williams-Beuren syndrome (WBS) is a developmental… (More)
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2009
2009
Genetic contributions to human cognition and behavior are clear but difficult to define. Williams syndrome (WS) provides a unique… (More)
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2009
2009
GTF2I and GTF2IRD1 encoding the multifunctional transcription factors TFII-I and BEN are clustered at the 7q11.23 region… (More)
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2007
2007
Williams syndrome is a rare congenital disorder involving the cardiovascular system, mental retardation, distinctive facial… (More)
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2005
2005
A hallmark of general transcription factor 3 (GTF3) is the presence of multiple GTF2I-like repeats that were suggested to mediate… (More)
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1998
1998
We have cloned and characterized Gtf2i, the mouse homolog of human GTF2I (general transcription factor II-I), which encodes BAP… (More)
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1998
1998
Williams-Beuren syndrome (WBS) is a neurodevelopmental disorder with multisystemic manifestations caused by heterozygosity for a… (More)
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1997
1997
Bruton's tyrosine kinase (Btk) is essential for B cell activation, but downstream targets of Btk have not been defined. We now… (More)
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