LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.
about
ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role in Beckwith-Wiedemann syndrome.Induction of p57(KIP2) expression by p73beta.In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT geneIdentification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting controlAn antisense RNA regulates the bidirectional silencing property of the Kcnq1 imprinting control regionThe non-coding RNAs as riboregulatorsRegulatory long non-coding RNAs and neuronal disordersEpigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defectsSilencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndromeAn imprinted transcript, antisense to Nesp, adds complexity to the cluster of imprinted genes at the mouse Gnas locusA pathway from chromosome transfer to engineering resulting in human and mouse artificial chromosomes for a variety of applications to bio-medical challengesLong Intergenic Non-Coding RNAs: Novel Drivers of Human Lymphocyte DifferentiationFrequent loss of imprinting of IGF2 and MEST in lung adenocarcinomaThe DM domain protein DMRT1 is a dose-sensitive regulator of fetal germ cell proliferation and pluripotencyLoss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndromeUM 9(5)h and UM 9(5)p, human and porcine noncoding transcripts with preferential expression in the cerebellum.Antisense transcripts with FANTOM2 clone set and their implications for gene regulation.The importance of imprinting in the human placenta.Disclosing hidden transcripts: mouse natural sense-antisense transcripts tend to be poly(A) negative and nuclear localizedImprinted genes as potential genetic and epigenetic toxicologic targetsNo evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age.Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.RNA traffic control of chromatin complexes.Spatial, temporal and interindividual epigenetic variation of functionally important DNA methylation patterns.Shaping the Genome with Non-Coding RNAsAddition of H19 'loss of methylation testing' for Beckwith-Wiedemann syndrome (BWS) increases the diagnostic yield.Epigenetic variation during the adult lifespan: cross-sectional and longitudinal data on monozygotic twin pairs.Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer.Low frequency of imprinting defects in ICSI children born small for gestational age.DNA methylation in genomic imprinting, development, and disease.Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers.Stability of genomic imprinting in human induced pluripotent stem cells.Imprinting disorders: non-Mendelian mechanisms affecting growth.Involvement of long non-coding RNA in colorectal cancer: From benchtop to bedside (Review)The silence RNA keeps: cis mechanisms of RNA mediated epigenetic silencing in mammals.Depletion of Kcnq1ot1 non-coding RNA does not affect imprinting maintenance in stem cells.Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome.Oppositely imprinted genes p57(Kip2) and igf2 interact in a mouse model for Beckwith-Wiedemann syndrome.
P2860
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P2860
LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.
description
1999 nî lūn-bûn
@nan
1999 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հուլիսին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@ast
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@en
type
label
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@ast
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@en
prefLabel
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@ast
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@en
P2093
P356
P1476
LIT1, an imprinted antisense R ...... using monochromosomal hybrids.
@en
P2093
A P Feinberg
M A Yoshida
M Oshimura
T C Schulz
P304
P356
10.1093/HMG/8.7.1209
P577
1999-07-01T00:00:00Z