(Q36820044)

English

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2.

scientific article published on November 1997

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scholarly article

1 reference

Europe PubMed Central

16 August 2017

Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. (English)

1 reference

Europe PubMed Central

16 August 2017

1 reference

based on heuristic

inferred from title

5

1 reference

Europe PubMed Central

16 August 2017

7

1 reference

Europe PubMed Central

16 August 2017

author name string

Moore T

1

1 reference

Europe PubMed Central

16 August 2017

Constancia M

2

1 reference

Europe PubMed Central

16 August 2017

Zubair M

3

1 reference

Europe PubMed Central

16 August 2017

Bailleul B

4

1 reference

Europe PubMed Central

16 August 2017

Sasaki H

6

1 reference

Europe PubMed Central

16 August 2017

language of work or name

0 references

publication date

1 November 1997

1 reference

Europe PubMed Central

16 August 2017

number of pages

6

1 reference

based on heuristic

inferred from page(s)

Proceedings of the National Academy of Sciences of the United States of America

1 reference

Europe PubMed Central

16 August 2017

94

1 reference

Europe PubMed Central

16 August 2017

12509-12514

1 reference

Europe PubMed Central

16 August 2017

23

1 reference

Europe PubMed Central

16 August 2017

Genomic regions regulating imprinting and insulin-like growth factor-II promoter 3 activity in transgenics: novel enhancer and silencer elements.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Switch from monoallelic to biallelic human IGF2 promoter methylation during aging and carcinogenesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Parental allele specific methylation of the human insulin-like growth factor II gene 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=25020

29 September 2017

DNA methylation and genomic imprinting

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Allele-specific methylation and expression of an imprinted U2af1-rs1 (SP2) gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Identification of a novel paternally expressed gene in the Prader-Willi syndrome region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

The ontogeny of allele-specific methylation associated with imprinted genes in the mouse.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Coordinate developmental regulation of high and low molecular weight mRNAs for rat insulin-like growth factor II.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

The product of the mouse Xist gene is a 15 kb inactive X-specific transcript containing no conserved ORF and located in the nucleus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Formation of methylation patterns in the mammalian genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

29 September 2017

Discriminating translation of insulin-like growth factor-II (IGF-II) during mouse embryogenesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

27 June 2018

Regulation of genomic imprinting by gametic and embryonic processes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

27 June 2018

Developmental control of allelic methylation in the imprinted mouse Igf2 and H19 genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

27 June 2018

Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

27 June 2018

Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=25020

27 June 2018

Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

A paternal-specific methylation imprint marks the alleles of the mouse H19 gene.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Nucleotide sequence of a 28-kb mouse genomic region comprising the imprinted Igf2 gene.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Genomic deletion of an imprint maintenance element abolishes imprinting of both insulin-like growth factor II and H19.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

The minisatellite in the diabetes susceptibility locus IDDM2 regulates insulin transcription.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription.

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Epigenetic mechanisms underlying the imprinting of the mouse H19 gene

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Characteristics of imprinted genes

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Genome imprinting phenomena on mouse chromosome 7

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.94.23.12509

21 January 2018

Identifiers

10.1073/PNAS.94.23.12509

1 reference

Europe PubMed Central

16 August 2017

1997PNAS...9412509M

0 references

1 reference

Europe PubMed Central

16 August 2017

1 reference

Europe PubMed Central

16 August 2017

ResearchGate publication ID

0 references

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