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BAZ1B gene

Known as: Williams-Beuren syndrome chromosome region 9, WBSCR9, BROMODOMAIN ADJACENT TO ZINC FINGER DOMAIN, 1B 
National Institutes of Health

Papers overview

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Highly Cited
2016
Highly Cited
2016
Summary Metabolic activity is intimately linked to T cell fate and function. Using high-resolution mass spectrometry, we… Expand
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Highly Cited
2013
Highly Cited
2013
Elevated serum urate concentrations can cause gout, a prevalent and painful inflammatory arthritis. By combining data from >140… Expand
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Highly Cited
2011
Highly Cited
2011
Among mammalian sirtuins, SIRT7 is the only enzyme residing in nucleoli where ribosomal DNA is transcribed. Recent reports… Expand
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Highly Cited
2009
Highly Cited
2009
DNA double-stranded breaks present a serious challenge for eukaryotic cells. The inability to repair breaks leads to genomic… Expand
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Highly Cited
2009
Highly Cited
2009
A number of nuclear complexes modify chromatin structure and operate as functional units. However, the in vivo role of each… Expand
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Highly Cited
2004
Highly Cited
2004
Chromatin states have to be faithfully duplicated during DNA replication to maintain cell identity. It is unclear whether or how… Expand
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Highly Cited
2003
Highly Cited
2003
We identified a human multiprotein complex (WINAC) that directly interacts with the vitamin D receptor (VDR) through the Williams… Expand
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Highly Cited
2002
Highly Cited
2002
The Williams Syndrome Transcription Factor (WSTF), the product of the WBSCR9 gene, is invariably deleted in the… Expand
Highly Cited
2002
Highly Cited
2002
We previously characterized major components of mitotic chromosomes assembled in Xenopus laevis egg extracts and collectively… Expand
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Highly Cited
1998
Highly Cited
1998
Williams syndrome (WS) is a developmental disorder caused by deletion of multiple genes at chromosome 7q11.23. Here, we report… Expand