(Q36927144)

English

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region

scientific article published on 06 July 2006

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

17 August 2017

The epigenetic imprinting defect of patients with Beckwith-Wiedemann syndrome born after assisted reproductive technology is not restricted to the 11p15 region (English)

1 reference

Europe PubMed Central

17 August 2017

0 references

Beckwith-Wiedemann syndrome

1 reference

based on heuristic

inferred from title

author name string

S Rossignol

1

1 reference

Europe PubMed Central

17 August 2017

V Steunou

2

1 reference

Europe PubMed Central

17 August 2017

C Chalas

3

1 reference

Europe PubMed Central

17 August 2017

A Kerjean

4

1 reference

Europe PubMed Central

17 August 2017

M Rigolet

5

1 reference

Europe PubMed Central

17 August 2017

E Viegas-Pequignot

6

1 reference

Europe PubMed Central

17 August 2017

P Jouannet

7

1 reference

Europe PubMed Central

17 August 2017

Y Le Bouc

8

1 reference

Europe PubMed Central

17 August 2017

C Gicquel

9

1 reference

Europe PubMed Central

17 August 2017

language of work or name

0 references

publication date

6 July 2006

1 reference

Europe PubMed Central

17 August 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

17 August 2017

43

1 reference

Europe PubMed Central

17 August 2017

12

1 reference

Europe PubMed Central

17 August 2017

902-907

1 reference

Europe PubMed Central

17 August 2017

ZAC, LIT1 (KCNQ1OT1) and p57KIP2 (CDKN1C) are in an imprinted gene network that may play a role 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=2563199

29 September 2017

Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

DNMT3B mutations and DNA methylation defect define two types of ICF syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Beckwith-Wiedemann syndrome and IVF: a case-control study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Imprinting errors and developmental asymmetry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

In vitro fertilization may increase the risk of Beckwith-Wiedemann syndrome related to the abnormal imprinting of the KCN1OT gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Beckwith-Wiedemann syndrome and assisted reproduction technology (ART)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Association of in vitro fertilization with Beckwith-Wiedemann syndrome and epigenetic alterations of LIT1 and H19

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Intracytoplasmic sperm injection may increase the risk of imprinting defects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Bisulfite genomic sequencing: systematic investigation of critical experimental parameters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Genomic imprinting: parental influence on the genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Establishment of the paternal methylation imprint of the human H19 and MEST/PEG1 genes during spermatogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Conservation of a maternal-specific methylation signal at the human IGF2R locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

29 September 2017

Stochastic imprinting in the progeny of Dnmt3L-/- females.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Selective loss of imprinting in the placenta following preimplantation development in culture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Gene-specific timing and epigenetic memory in oocyte imprinting.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Epigenetic abnormalities of the mannose-6-phosphate/IGF2 receptor gene are uncommon in human overgrowth syndromes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Methylation imprints of the imprint control region of the SNRPN-gene in human gametes and preimplantation embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Another case of imprinting defect in a girl with Angelman syndrome who was conceived by intracytoplasmic semen injection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 September 2018

Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2563199

4 December 2018

Epigenetic mark sequence of the H19 gene in human sperm

1 reference

https://pubmed.ncbi.nlm.nih.gov/16825435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discordant KCNQ1OT1 imprinting in sets of monozygotic twins discordant for Beckwith-Wiedemann syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16825435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional Polymorphism in the Parental Imprinting of the Human IGF2R Gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/16825435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic change in IGF2R is associated with fetal overgrowth after sheep embryo culture

1 reference

https://pubmed.ncbi.nlm.nih.gov/16825435

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.2006.042135

1 reference

Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

17 August 2017

1 reference

Europe PubMed Central

17 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q36927144&oldid=2166866093"