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KCNQ1OT1 wt Allele

Known as: Non-Protein Coding RNA 12 Gene, NCRNA00012, KCNQ1 Opposite Strand/Antisense Transcript 1 (Non-Protein Coding) wt Allele 
Human KCNQ1OT1 wild-type allele is located in the vicinity of 11p15 and is approximately 92 kb in length. This allele, which encodes KCNQ1 opposite… 
National Institutes of Health

Related topics

Related topics

3 relations
11p15Epigenetic ProcessTranscriptional Regulation

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
DNA methylation status of imprinted H19 and KvDMR1 genes in human placentas after conception using assisted reproductive technology.
Background Assisted reproductive technologies (ARTs), such as in vitro fertilization (IVF) and intracytoplasmic sperm injection… 
2014
2014
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by intracytoplasmic sperm injection and in vitro fertilization and embryo transfer.
2013
2013
Abnormal methylation of KCNQ1OT1 and differential methylation of H19 imprinting control regions in human ICSI embryos.
Summary To evaluate the integrity of genomic imprinting in embryos that failed to develop normally following intracytoplasmic… 
2011
2011
Evaluation of DNA methylation status at differentially methylated regions in IVF-conceived newborn twins.
2011
2011
The heterogeneity of hyperinsulinaemic hypoglycaemia in 19 patients with Beckwith-Wiedemann syndrome due to KvDMR1 hypomethylation
Abstract Beckwith-Wiedemann syndrome (BWS) is an overgrowth syndrome caused by multiple epigenetic and genetic changes affecting… 
Highly Cited
2010
Highly Cited
2010
Aberrant CpG methylation of the imprinting control region KvDMR1 detected in assisted reproductive technology-produced calves and pathogenesis of large offspring syndrome.
Review
2009
Review
2009
Beckwith–Wiedemann syndrome associated with congenital hypothyroidism in a preterm neonate: a case report and literature review
This report describes for the first time the association of Beckwith–Wiedemann syndrome (BWS) and hypothyroidism in a 25 weeks… 
Highly Cited
2005
Highly Cited
2005
Lsh controls silencing of the imprinted Cdkn1c gene
Epigenetic regulation, such as DNA methylation plays an important role in the control of imprinting. Lsh, a member of the SNF2… 
2003
2003
Silencing of CDKN 1 C ( p 57 KIP 2 ) is associated with hypomethylation at KvDMR 1 in Beckwith – Wiedemann syndrome
Context: Beckwith–Wiedemann syndrome (BWS) arises by several genetic and epigenetic mechanisms affecting the balance of imprinted… 
2001
2001
Loss of Imprinting of Long QT Intronic Transcript 1 in Colorectal Cancer
Loss of imprinting (LOI) of the insulin-like growth factor 2 (IGF2) and H19 genes on human chromosome 11 has been found not only… 
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