(Q49112560)

English

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.

scientific article published on 8 July 2008

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

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 (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Silver-Russell syndrome

1 reference

based on heuristic

inferred from title

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

15

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

13

object named as

Reiko Horikawa

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Kazuki Yamazawa

1

object named as

Kazuki Yamazawa

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

10

object named as

Seiji Mizuno

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

3

object named as

Toshiro Nagai

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Tomonobu Hasegawa

7

object named as

Tomonobu Hasegawa

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

11

object named as

Yoko Miyoshi

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

4

object named as

Tatsuro Kondoh

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Kentaro Matsuoka

14

object named as

Kentaro Matsuoka

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

Kazumichi Onigata

5

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Katsuhiro Maeyama

6

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Yukihiro Hasegawa

8

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Toshio Yamazaki

9

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Shinichiro Miyagawa

12

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

publication date

8 July 2008

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

Journal of Molecular Medicine

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

86

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1171-1181

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

10

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18607558%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

https://scigraph.springernature.com/pub.10.1007/s00109-008-0377-4

0 references

Maternal uniparental disomy 14 dissection of the phenotype with respect to rare autosomal recessively inherited traits, trisomy mosaicism, and genomic imprinting

1 reference

https://api.crossref.org/works/10.1007%2FS00109-008-0377-4

21 January 2018

Accurate quantification of DNA methylation using combined bisulfite restriction analysis coupled with the Agilent 2100 Bioanalyzer platform

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An enhancer deletion affects both H19 and Igf2 expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dissociation of IGF2 and H19 imprinting in human brain

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Placental-specific insulin-like growth factor 2 (Igf2) regulates the diffusional exchange characteristics of the mouse placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated placental expression of the imprinted PHLDA2 gene is associated with low birth weight

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Promoter-specific IGF2 imprinting status and its plasticity during human liver development

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spatial and temporal patterns of expression of messenger RNA for insulin-like growth factors and their binding proteins in the placenta of man and laboratory animals.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinted genes in the placenta--a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Symmetric and asymmetric DNA methylation in the human IGF2-H19 imprinted region

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential regulation of imprinting in the murine embryo and placenta by the Dlk1-Dio3 imprinting control region

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disruption of imprinting caused by deletion of the H19 gene region in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth effects of uniparental disomies and the conflict theory of genomic imprinting

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence for evolutionarily conserved secondary structure in the H19 tumor suppressor RNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Uniparental disomy: clinical indications for testing in growth retardation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Epigenetic mutations in 11p15 in Silver-Russell syndrome are restricted to the telomeric imprinting domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Limited evolutionary conservation of imprinting in the human placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection and measurement of PCR bias in quantitative methylation analysis of bisulphite-treated DNA.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Placental hypoplasia in maternal uniparental disomy for chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tumour-suppressor activity of H19 RNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinted genes, placental development and fetal growth

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of the H19 differentially methylated domain results in loss of imprinted expression of H19 and Igf2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

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/18607558

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/18607558

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/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic imprinting in the placenta

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regions

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/18607558

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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=Q49112560&oldid=1753558888"