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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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2016
2016
Williams syndrome (WS) is a neurodevelopmental disorder caused by a genomic deletion of ∼28 genes that results in a cognitive and… Expand
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Highly Cited
2014
Highly Cited
2014
Metabolic syndrome (MetS) has become a health and financial burden worldwide. The MetS definition captures clustering of risk… Expand
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2014
2014
The artificial WSTF PHD_EL5 RING finger was designed via “α-helical region substitution”, and its structural model for the… 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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2010
2010
Williams–Beuren syndrome (WBS; OMIM no. 194050) is a multisystemic neurodevelopmental disorder caused by a hemizygous deletion of… Expand
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Highly Cited
2009
Highly Cited
2009
Blood lipids are important cardiovascular disease (CVD) risk factors with both genetic and environmental determinants. The… 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
2002
Highly Cited
2002
The Williams Syndrome Transcription Factor (WSTF), the product of the WBSCR9 gene, is invariably deleted in the… Expand
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