Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region (Q35806688)

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scientific article published on December 2002

Language	Label	Description	Also known as
English	Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region	scientific article published on December 2002

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scholarly article

1 reference

Europe PubMed Central

10 August 2017

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region (English)

1 reference

Europe PubMed Central

10 August 2017

DNA methylation

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author name string

Hitomi Yatsuki

1

1 reference

Europe PubMed Central

10 August 2017

Keiichiro Joh

2

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Europe PubMed Central

10 August 2017

Ken Higashimoto

3

1 reference

Europe PubMed Central

10 August 2017

Hidenobu Soejima

4

1 reference

Europe PubMed Central

10 August 2017

Yuji Arai

5

1 reference

Europe PubMed Central

10 August 2017

Youdong Wang

6

1 reference

Europe PubMed Central

10 August 2017

Izuho Hatada

7

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Europe PubMed Central

10 August 2017

Yayoi Obata

8

1 reference

Europe PubMed Central

10 August 2017

Hiroko Morisaki

9

1 reference

Europe PubMed Central

10 August 2017

Zhongming Zhang

10

1 reference

Europe PubMed Central

10 August 2017

Tetsuji Nakagawachi

11

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Europe PubMed Central

10 August 2017

Yuji Satoh

12

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Europe PubMed Central

10 August 2017

Tsunehiro Mukai

13

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Europe PubMed Central

10 August 2017

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publication date

1 December 2002

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Europe PubMed Central

10 August 2017

Genome Research

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Europe PubMed Central

10 August 2017

12

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Europe PubMed Central

10 August 2017

12

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Europe PubMed Central

10 August 2017

1860-1870

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Europe PubMed Central

10 August 2017

A differentially methylated imprinting control region within the Kcnq1 locus harbors a methylation-sensitive chromatin insulator

1 reference

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Disruption of an imprinted gene cluster by a targeted chromosomal translocation in mice

1 reference

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Establishment and maintenance of DNA methylation patterns in mouse Ndn: implications for maintenance of imprinting in target genes of the imprinting center.

1 reference

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X-chromosome inactivation: counting, choice and initiation

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Genomic imprinting: parental influence on the genome

1 reference

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Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain

1 reference

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Sequence and functional comparison in the Beckwith-Wiedemann region: implications for a novel imprinting centre and extended imprinting

1 reference

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Imprinting: focusing on the center

1 reference

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Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome

1 reference

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11 July 2018

Sequence conservation and variability of imprinting in the Beckwith-Wiedemann syndrome gene cluster in human and mouse

1 reference

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Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse an

1 reference

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Beckwith-Wiedemann syndrome: imprinting in clusters revisited

1 reference

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A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=187562

11 July 2018

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

1 reference

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11 July 2018

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting

1 reference

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In vivo nuclease hypersensitivity studies reveal multiple sites of parental origin-dependent differential chromatin conformation in the 150 kb SNRPN transcription unit

1 reference

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Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

1 reference

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Chromatin conformation of the H19 epigenetic mark.

1 reference

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A novel gene, ITM, located between p57KIP2 and IPL, is imprinted in mice

1 reference

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Urea improves efficiency of bisulphite-mediated sequencing of 5'-methylcytosine in genomic DNA

1 reference

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Syntenic organization of the mouse distal chromosome 7 imprinting cluster and the Beckwith-Wiedemann syndrome region in chromosome 11p15.5.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=187562

11 July 2018

Multiple mechanisms regulate imprinting of the mouse distal chromosome 7 gene cluster

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=187562

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IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes

1 reference

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11 July 2018

Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=187562

11 July 2018

The IPL gene on chromosome 11p15.5 is imprinted in humans and mice and is similar to TDAG51, implicated in Fas expression and apoptosis

1 reference

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Low frequency of p57KIP2 mutation in Beckwith-Wiedemann syndrome

1 reference

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Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors

1 reference

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Structure of the imprinted mouse Snrpn gene and establishment of its parental-specific methylation pattern

1 reference

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Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=187562

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An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

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Dynamic methylation adjustment and counting as part of imprinting mechanisms

1 reference

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Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse

1 reference

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DNA methylation and gene expression

1 reference

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Dnmt3L and the establishment of maternal genomic imprints.

1 reference

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Imprinting and the epigenetic asymmetry between parental genomes.

1 reference

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Distant cis-elements regulate imprinted expression of the mouse p57( Kip2) (Cdkn1c) gene: implications for the human disorder, Beckwith--Wiedemann syndrome.

1 reference

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1 reference

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Bisulfite sequencing in preimplantation embryos: DNA methylation profile of the upstream region of the mouse imprinted H19 gene.

1 reference

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Imprinting of mouse Kvlqt1 is developmentally regulated.

1 reference

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Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19.

1 reference

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Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

1 reference

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A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

1 reference

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Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome

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1 reference

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12 December 2020

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10.1101/GR.110702

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Europe PubMed Central

10 August 2017

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Europe PubMed Central

10 August 2017

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Europe PubMed Central

10 August 2017

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