(Q36471719)

English

IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

14 August 2017

IGF2/H19 hypomethylation is tissue, cell, and CpG site dependent and not correlated with body asymmetry in adolescents with Silver-Russell syndrome (English)

1 reference

Europe PubMed Central

14 August 2017

1 reference

based on heuristic

inferred from title

Silver-Russell syndrome

1 reference

based on heuristic

inferred from title

author name string

Kai Kannenberg

1

1 reference

Europe PubMed Central

14 August 2017

Karin Weber

2

1 reference

Europe PubMed Central

14 August 2017

Cathrin Binder

3

1 reference

Europe PubMed Central

14 August 2017

Christina Urban

4

1 reference

Europe PubMed Central

14 August 2017

Hans-Joachim Kirschner

5

1 reference

Europe PubMed Central

14 August 2017

Gerhard Binder

6

1 reference

Europe PubMed Central

14 August 2017

publication date

18 September 2012

1 reference

Europe PubMed Central

14 August 2017

Clinical Epigenetics

1 reference

Europe PubMed Central

14 August 2017

4

1 reference

Europe PubMed Central

14 August 2017

1

1 reference

Europe PubMed Central

14 August 2017

15

1 reference

Europe PubMed Central

14 August 2017

copyright license

Creative Commons Attribution 2.0 Generic

18 September 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

https://scigraph.springernature.com/pub.10.1186/1868-7083-4-15

0 references

Increased incidence of aberrant DNA methylation within diverse imprinted gene loci outside of IGF2/H19 in Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Silver-Russell syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Specific age-associated DNA methylation changes in human dermal fibroblasts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

The importance of imprinting in the human placenta.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

CTCF binding at the H19 imprinting control region mediates maternally inherited higher-order chromatin conformation to restrict enhancer access to Igf2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Methylation-specific MLPA (MS-MLPA): simultaneous detection of CpG methylation and copy number changes of up to 40 sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

MLPA and MAPH: new techniques for detection of gene deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Placental-specific IGF-II is a major modulator of placental and fetal growth.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

CTCF mediates methylation-sensitive enhancer-blocking activity at the H19/Igf2 locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Methylation of a CTCF-dependent boundary controls imprinted expression of the Igf2 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Growth and symptoms in Silver-Russell syndrome: review on the basis of 386 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Role for DNA methylation in genomic imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

The structure and expression of a novel gene activated in early mouse embryogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Use of an aqueous soluble tetrazolium/formazan assay for cell growth assays in culture

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Parental imprinting of the mouse H19 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

The product of the H19 gene may function as an RNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

30 September 2017

Disruption of insulin-like growth factor 2 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=3523983

28 June 2018

A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

28 June 2018

Embryological and molecular investigations of parental imprinting on mouse chromosome 7.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

28 June 2018

An update of the Swedish reference standards for weight, length and head circumference at birth for given gestational age (1977-1981).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

28 June 2018

Effect of long-term growth hormone treatment on final height of children with Russell-Silver syndrome.

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

Epimutation of the telomeric imprinting center region on chromosome 11p15 in Silver-Russell syndrome.

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

Maternal-specific footprints at putative CTCF sites in the H19 imprinting control region give evidence for insulator function.

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 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://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

CTCF binding at the insulin-like growth factor-II (IGF2)/H19 imprinting control region is insufficient to regulate IGF2/H19 expression in human tissues

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

21 September 2018

Clinically distinct epigenetic subgroups in Silver-Russell syndrome: the degree of H19 hypomethylation associates with phenotype severity and genital and skeletal anomalies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

21 September 2018

Molecular and clinical findings and their correlations in Silver-Russell syndrome: implications for a positive role of IGF2 in growth determination and differential imprinting regulation of the IGF2-H19 domain in bodies and placentas.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3523983

21 September 2018

Post-receptor IGF1 insensitivity restricted to the MAPK pathway in a Silver–Russell syndrome patient with hypomethylation at the imprinting control region on chromosome 11

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

The insulin–like growth factor type–2 receptor gene is imprinted in the mouse but not in humans

1 reference

https://api.crossref.org/works/10.1186%2F1868-7083-4-15

21 January 2018

Monitoring of cellular senescence by DNA-methylation at specific CpG sites

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental disomy 7 in Silver-Russell syndrome and primordial growth retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The endocrine phenotype in silver-russell syndrome is defined by the underlying epigenetic alteration

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Silver-Russell syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth hormone treatment does not alter lower limb asymmetry in children with Russell-Silver syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

IGF-II serum levels are normal in children with Silver-Russell syndrome who frequently carry epimutations at the IGF2 locus.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of methylation at paternal and maternal imprinted loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/22989232

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1868-7083-4-15

1 reference

Europe PubMed Central

14 August 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

14 August 2017

1 reference

Europe PubMed Central

14 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=Q36471719&oldid=1800397803"