(Q52094982)

English

Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis.

scientific article published in December 2003

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scholarly article

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Imprinted methylation profiles for proximal mouse chromosomes 11 and 7 as revealed by methylation-sensitive representational difference analysis. (English)

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

5

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

author name string

David Monk

1

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Rachel Smith

2

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Philippe Arnaud

3

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Michael A Preece

4

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Colin V Beechey

6

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Jo Peters

7

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

Gudrun E Moore

9

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

publication date

1 December 2003

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

number of pages

12

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based on heuristic

inferred from page(s)

Mammalian Genome

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

14

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

805-816

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Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

12

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

https://scigraph.springernature.com/pub.10.1007/s00335-003-2287-7

0 references

Genetics of silver-russell syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Time of initiation and site of action of the mouse chromosome 11 imprinting effects

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomy.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grb10: A new substrate of the insulin-like growth factor I receptor

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cluster of oppositely imprinted transcripts at the Gnas locus in the distal imprinting region of mouse chromosome 2

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of imprinted loci by methylation: use of methylation-sensitive representational difference analysis (Me-RDA).

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

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/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DDC and COBL, flanking the imprinted GRB10 gene on 7p12, are biallelically expressed

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Methylation-sensitive binding of transcription factor YY1 to an insulator sequence within the paternally expressed imprinted gene, Peg3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microarray expression profiling of tissues from mice with uniparental duplications of chromosomes 7 and 11 to identify imprinted genes.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

No evidence for mosaicism in Silver-Russell syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic imprinting: parental influence on the genome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA methylation and genomic imprinting

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Regulation of maternal behavior and offspring growth by paternally expressed Peg3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of 7p11.2-p13, including GRB10, in Silver-Russell syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of imprinted loci by methylation-sensitive representational difference analysis: application to mouse distal chromosome 2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms of genomic imprinting

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of imprinting in U2AFBPL, a human homologue of the imprinted mouse gene U2afbp-rs

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Genome-Wide Screen for Normally Methylated Human CpG Islands That Can Identify Novel Imprinted Genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conflicting reports of imprinting status of human GRB10 in developing brain: how reliable are somatic cell hybrids for predicting allelic origin of expression?

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Discovery of a novel, paternally expressed ubiquitin-specific processing protease gene through comparative analysis of an imprinted region of mouse chromosome 7 and human chromosome 19q13.4

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cells.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A protein related to splicing factor U2AF35 that interacts with U2AF65 and SR proteins in splicing of pre-mRNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Binding of SH2 containing proteins to the insulin receptor: a new way for modulating insulin signalling.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinting of PEG3, the human homologue of a mouse gene involved in nurturing behavior

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal uniparental disomy 7 in Silver-Russell syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Zim1, a maternally expressed mouse Kruppel-type zinc-finger gene located in proximal chromosome 7.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interaction of a GRB-IR splice variant (a human GRB10 homolog) with the insulin and insulin-like growth factor I receptors. Evidence for a role in mitogenic signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinting of human GRB10 and its mutations in two patients with Russell-Silver syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Conserved methylation imprints in the human and mouse GRB10 genes with divergent allelic expression suggests differential reading of the same mark

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mouse U2af1-rs1 is a neomorphic imprinted gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Natural History of the Silver-Russell Syndrome: A Longitudinal Study of Thirty-nine Cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Assignment of growth factor receptor-bound protein 10 (GRB10) to human chromosome 7p11.2-p12

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grb10 interacts differentially with the insulin receptor, insulin-like growth factor I receptor, and epidermal growth factor receptor via the Grb10 Src homology 2 (SH2) domain and a second novel domain located between the pleckstrin homology [...]

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal repression of the human GRB10 gene in the developing central nervous system; evaluation of the role for GRB10 in Silver-Russell syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of novel imprinted genes in a genome-wide screen for maternal methylation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence against GRB10 as the gene responsible for Silver-Russell syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Duplication of 7p12.1-p13, including GRB10 and IGFBP1, in a mother and daughter with features of Silver-Russell syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of a redefined proximal mouse chromosome 11 imprinting region and U2afbp-rs/U2af1-rs1 expression.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Exon sharing of a novel human zinc-finger gene, ZIM2, and paternally expressed gene 3 (PEG3)

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of the Meg1/Grb10 imprinted gene on mouse proximal chromosome 11, a candidate for the Silver-Russell syndrome gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Inactive allele-specific methylation and chromatin structure of the imprinted gene U2af1-rs1 on mouse chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grb10 proteins in insulin-like growth factor and insulin receptor signaling (review).

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinting regulation of the murine Meg1/Grb10 and human GRB10 genes; roles of brain-specific promoters and mouse-specific CTCF-binding sites.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential activity of maternally and paternally derived chromosome regions in mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mechanisms leading to uniparental disomy and their clinical consequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peg3 imprinted gene on proximal chromosome 7 encodes for a zinc finger protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genome imprinting phenomena on mouse chromosome 7

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosome 7p disruptions in Silver Russell syndrome: delineating an imprinted candidate gene region.

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An analysis of the distribution of hetero- and isodisomic regions of chromosome 7 in five mUPD7 Silver-Russell syndrome probands

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of Silver-Russell syndrome: a clinical and molecular genetic study and new diagnostic criteria

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Imprinting and evolution of two Kruppel-type zinc-finger genes, ZIM3 and ZNF264, located in the PEG3/USP29 imprinted domain

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A genome-wide screen for normally methylated human CpG islands that can identify novel imprinted genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/14724735

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00335-003-2287-7

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

1 reference

Europe PubMed Central

22 April 2018

http://europepmc.org/abstract/MED/14724735

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