(Q80799580)

English

Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations

scientific article published on 15 August 2007

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scholarly article

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Japanese and North American/European patients with Beckwith-Wiedemann syndrome have different frequencies of some epigenetic and genetic alterations (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Beckwith-Wiedemann syndrome

1 reference

based on heuristic

inferred from title

Hidenobu Soejima

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

author name string

Kensaku Sasaki

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Ken Higashimoto

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Hitomi Yatsuki

4

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Hirofumi Ohashi

5

1 reference

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3 January 2020

Shinya Yakabe

6

1 reference

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3 January 2020

Keiichiro Joh

7

1 reference

Europe PubMed Central

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3 January 2020

Norio Niikawa

8

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

Tsunehiro Mukai

9

1 reference

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3 January 2020

publication date

15 August 2007

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3 January 2020

European Journal of Human Genetics

1 reference

Europe PubMed Central

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3 January 2020

15

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3 January 2020

12

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3 January 2020

1205-1210

1 reference

Europe PubMed Central

PubMed publication ID

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3 January 2020

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201912

0 references

Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Risk of cancer during the first four years of life in children from The Beckwith-Wiedemann Syndrome Registry

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

New p57KIP2 mutations in Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Microdeletions in the human H19 DMR result in loss of IGF2 imprinting and Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Mechanisms causing imprinting defects in familial Beckwith–Wiedemann syndrome with Wilms' tumour

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

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.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Tumor risk in Beckwith-Wiedemann syndrome: A review and meta-analysis.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenetic differences between Wilms' tumours in white and east-Asian children.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Epigenotyping as a tool for the prediction of tumor risk and tumor type in patients with Beckwith-Wiedemann syndrome (BWS)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201912

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201912

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:17700627%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

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