IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance. (Q34285924)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

title

IGF2/H19 hypomethylation in a patient with very low birthweight, preocious pubarche and insulin resistance (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

1 reference

1 reference

1 reference

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Jorg Tost

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

Lourdes Ibáñez

1 reference

ORCID Public Data File 2021

Rinki Murphy

series ordinal

1

object named as

Rinki Murphy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

author name string

Andrew Hattersley

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

publication date

30 May 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

volume

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

page(s)

42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

Epigenetic signatures of Silver-Russell syndrome.

2 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Clinical spectrum of premature pubarche: links to metabolic syndrome and ovarian hyperandrogenism

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Somatically acquired hypomethylation of IGF2 in breast and colorectal cancer

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Distinct methylation changes at the IGF2-H19 locus in congenital growth disorders and cancer.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Hypomethylation of the H19 gene causes not only Silver-Russell syndrome (SRS) but also isolated asymmetry or an SRS-like phenotype

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Loss of imprinting of IGF2: a common epigenetic modifier of intestinal tumor risk

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

The role of the growth hormone/insulin-like growth factor axis in tumor growth and progression: Lessons from animal models

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Is maternal duplication of 11p15 associated with Silver-Russell syndrome?

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3459807

Interaction between differentially methylated regions partitions the imprinted genes Igf2 and H19 into parent-specific chromatin loops

6 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Altered gene expression and methylation of the human chromosome 11 imprinted region in small for gestational age (SGA) placentae.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Antagonism between DNA hypermethylation and enhancer-blocking activity at the H19 DMD is uncovered by CpG mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Severe intrauterine growth retardation and atypical diabetes associated with a translocation breakpoint disrupting regulation of the insulin-like growth factor 2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Insulin sensitization for girls with precocious pubarche and with risk for polycystic ovary syndrome: effects of prepubertal initiation and postpubertal discontinuation of metformin treatment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

The Exeter Family Study of Childhood Health (EFSOCH): study protocol and methodology

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Insulin sensitization early after menarche prevents progression from precocious pubarche to polycystic ovary syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Broad clinical spectrum in Silver-Russell syndrome and consequences for genetic testing in growth retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Searching for genomic variants in IGF2 and CDKN1C in Silver-Russell syndrome patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-42

Duplications of chromosome 11p15 of maternal origin result in a phenotype that includes growth retardation

21 January 2018

1 reference

12 December 2020

[Secular growth changes. Weight, height and body mass index values in infant, children, adolescent and young adults from Barcelona population]

1 reference

12 December 2020

(Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation?

1 reference

12 December 2020

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

12 December 2020

DNA methylation analysis by pyrosequencing

1 reference

12 December 2020

IGF2/H19 hypomethylation in Silver-Russell syndrome and isolated hemihypoplasia

1 reference

12 December 2020

Hypermethylation of the IGF2 differentially methylated region 2 is a specific event in insulinomas leading to loss-of-imprinting and overexpression

1 reference

12 December 2020

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

12 December 2020

Loss of IGF2 imprinting: a potential marker of colorectal cancer risk

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-13-42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

2 February 2020

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json

2 February 2020

PubMed publication ID

22646060

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22646060%20AND%20SRC:MED&resulttype=core&format=json