KCNQ1OT1 protein, human

Known as: NCRNA00012, KvDMR1 protein, human, Long QT Intronic Transcript 1 
KCNQ1 opposite strand/antisense transcript 1 (~92 kb) is encoded by the human KCNQ1OT1 gene. This non-coding RNA plays a role in epigenetic processes… (More)
National Institutes of Health

Papers overview

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Highly Cited
2009
Highly Cited
2009
Long noncoding RNAs are implicated in a number of regulatory functions in eukaryotic genomes. The paternally expressed long… (More)
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Highly Cited
2008
Highly Cited
2008
Recent investigations have implicated long antisense noncoding RNAs in the epigenetic regulation of chromosomal domains. Here we… (More)
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Highly Cited
2006
Highly Cited
2006
Infection of mammalian hosts with Leishmania amazonensis depends on the remarkable ability of these parasites to replicate within… (More)
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2006
2006
The human chromosome region 11p15.5 contains a number of maternally and paternally imprinted genes, and the LIT1/KCNQ1OT1 locus… (More)
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Highly Cited
2006
Highly Cited
2006
The mouse Kcnq1 imprinted domain is located on distal chromosome 7 and contains several imprinted genes that are paternally… (More)
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Highly Cited
2003
Highly Cited
2003
Recent data in humans and animals suggest that assisted reproductive technology (ART) might affect the epigenetics of early… (More)
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Highly Cited
2002
Highly Cited
2002
Beckwith-Wiedemann syndrome (BWS) presents with visceromegaly, macroglossia, tumor predisposition and other congenital… (More)
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Highly Cited
2002
Highly Cited
2002
Beckwith-Wiedemann syndrome (BWS) is a congenital cancer-predisposition syndrome associated with embryonal cancers, macroglossia… (More)
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Highly Cited
2001
Highly Cited
2001
Dysregulation of imprinted genes on human chromosome 11p15 has been implicated in Beckwith-Wiedemann syndrome (BWS), an… (More)
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Highly Cited
2001
Highly Cited
2001
Beckwith-Wiedemann syndrome (BWS) is an overgrowth malformation syndrome that maps to human chromosome 11p15.5, a region that… (More)
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