ZNF274 gene

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

Topic mentions per year

Topic mentions per year

2000-2018
0120002018

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… (More)
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2016
2016
ATRX is a SWI/SNF chromatin remodeler proposed to govern genomic stability through the regulation of repetitive sequences, such… (More)
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2014
2014
Prader-Willi syndrome (PWS), a disorder of genomic imprinting, is characterized by neonatal hypotonia, hypogonadism, small hands… (More)
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Highly Cited
2013
Highly Cited
2013
Nonalcoholic fatty liver disease (NAFLD) is the most common chronic liver disorder in industrialized countries. Liver samples… (More)
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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… (More)
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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… (More)
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