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ZFP57 gene

Known as: ZNF698, ZFP57, bA145L22.2 
 
National Institutes of Health

Papers overview

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2016
2016
ZFP57 maintains genomic imprinting in mouse embryos and ES cells. To test its roles during iPS reprogramming,we derived iPS… Expand
Review
2016
Review
2016
Imprinted genes are an exceptional cluster of genes which are expressed in a parent-of-origin dependent fashion. This allele… Expand
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2015
2015
Significance Abnormal heart development is a common birth defect. Genomic imprinting is absolutely essential for mammalian… Expand
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2014
2014
Several common biological properties between cancer cells and embryonic stem (ES) cells suggest the possibility that some genes… Expand
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Review
2013
Review
2013
DNA methylation is an epigenetic mark that is essential for the development of mammals; it is frequently altered in diseases… Expand
Highly Cited
2011
Highly Cited
2011
Summary The maintenance of H3K9 and DNA methylation at imprinting control regions (ICRs) during early embryogenesis is key to the… Expand
Highly Cited
2011
Highly Cited
2011
Background: ZFP57 is a maternal-zygotic effect gene that maintains genomic imprinting in mouse embryos. Results: KAP1 facilitates… Expand
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2009
2009
Silver-Russell syndrome (SRS) describes a uniform malformation syndrome characterized by intrauterine and postnatal growth… Expand
2009
2009
One known genetic mechanism for transient neonatal diabetes is loss of methylation at 6q24. The etiology of prune belly sequence… Expand
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