Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer (Q34303935)

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English	Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer	scientific article

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scholarly article

1 reference

Europe PubMed Central

1 August 2017

Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer (English)

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Europe PubMed Central

1 August 2017

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author name string

Hidenobu Soejima

1

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Europe PubMed Central

1 August 2017

Tetsuji Nakagawachi

2

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Europe PubMed Central

1 August 2017

Wei Zhao

3

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Europe PubMed Central

1 August 2017

Ken Higashimoto

4

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Europe PubMed Central

1 August 2017

Takeshi Urano

5

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Europe PubMed Central

1 August 2017

Shiroh Matsukura

6

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Europe PubMed Central

1 August 2017

Yoshihiko Kitajima

7

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Europe PubMed Central

1 August 2017

Makoto Takeuchi

8

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Europe PubMed Central

1 August 2017

Masahiro Nakayama

9

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Europe PubMed Central

1 August 2017

Mitsuo Oshimura

10

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Europe PubMed Central

1 August 2017

Kohji Miyazaki

11

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Europe PubMed Central

1 August 2017

Keiichiro Joh

12

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Europe PubMed Central

1 August 2017

Tsunehiro Mukai

13

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1 August 2017

language of work or name

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publication date

1 May 2004

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Europe PubMed Central

1 August 2017

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Europe PubMed Central

1 August 2017

23

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1 August 2017

25

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1 August 2017

4380-4388

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Europe PubMed Central

1 August 2017

https://scigraph.springernature.com/pub.10.1038/sj.onc.1207576

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Aberrant patterns of DNA methylation, chromatin formation and gene expression in cancer

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Three tumor-suppressor regions on chromosome 11p identified by high-resolution deletion mapping in human non-small-cell lung cancer

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Silencing of CDKN1C (p57KIP2) is associated with hypomethylation at KvDMR1 in Beckwith-Wiedemann syndrome

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Insulator and silencer sequences in the imprinted region of human chromosome 11p15.5.

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

The two-domain hypothesis in Beckwith-Wiedemann syndrome

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

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

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

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

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Translating the Histone Code

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Cancer epigenetics comes of age

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Inactivation of p57KIP2 by regional promoter hypermethylation and histone deacetylation in human tumors

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Methylation of histone H3 lysine 9 creates a binding site for HP1 proteins

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 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

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Aberrant DNA methylation of p57(KIP2) gene in the promoter region in lymphoid malignancies of B-cell phenotype

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

A differentially methylated region within the gene Kcnq1 functions as an imprinted promoter and silencer.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Decreased expression of p57(KIP2)mRNA in human bladder cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Gain of imprinting at chromosome 11p15: A pathogenetic mechanism identified in human hepatocarcinomas

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Characterization of 21 newly established esophageal cancer cell lines

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

The non-coding Air RNA is required for silencing autosomal imprinted genes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

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://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Methylation of histone H3 at lysine 4 is highly conserved and correlates with transcriptionally active nuclei in Tetrahymena

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

The language of covalent histone modifications

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Characterization of the human p57KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Suppression of cell transformation by the cyclin-dependent kinase inhibitor p57KIP2 requires binding to proliferating cell nuclear antigen

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Tumor development in the Beckwith-Wiedemann syndrome is associated with a variety of constitutional molecular 11p15 alterations including imprinting defects of KCNQ1OT1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

COBRA: a sensitive and quantitative DNA methylation assay

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

21 January 2018

Increased tumour risk for BWS patients correlates with aberrant H19 and not KCNQ1OT1 methylation: occurrence of KCNQ1OT1 hypomethylation in familial cases of BWS

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of methylation at chromosome 11p15.5 is common in human adult tumors

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation and expression of the p27KIP1 and p57KIP2 genes in human gastric cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

7 January 2021

based on heuristic

inferred from DOI database lookup

Bidirectional silencing and DNA methylation-sensitive methylation-spreading properties of the Kcnq1 imprinting control region map to the same regions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

7 January 2021

based on heuristic

inferred from DOI database lookup

Hot-stop PCR: a simple and general assay for linear quantitation of allele ratios

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1207576

7 January 2021

based on heuristic

inferred from DOI database lookup

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10.1038/SJ.ONC.1207576

1 reference

Europe PubMed Central

1 August 2017

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1 reference

Europe PubMed Central

1 August 2017

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