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ZNF274 gene

Known as: ZNF274B, ZSCAN51, ZNF274 
 
National Institutes of Health

Papers overview

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2018
2018
Prader-Willi syndrome (PWS) is characterized by neonatal hypotonia, developmental delay and hyperphagia/obesity and is caused by… Expand
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2016
2016
ABSTRACT ATRX is a SWI/SNF chromatin remodeler proposed to govern genomic stability through the regulation of repetitive… Expand
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Highly Cited
2010
Highly Cited
2010
Only a small percentage of human transcription factors (e.g. those associated with a specific differentiation program) are… Expand
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2000
2000
A human cDNA encoding a novel zinc-finger protein, ZNF274, was identified by the "nuclear transportation trap" method (Ueki, N… Expand
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