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Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome.
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1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
title
Transactivation of Igf2 in a mouse model of Beckwith-Wiedemann syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author
Wolf Reik
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Wendy Dean
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Gavin Kelsey
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Nicholas Allen
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
author name string
Sun FL
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
language of work or name
English
0 references
publication date
1 October 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
published in
Nature
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
volume
389
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
issue
6653
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
page(s)
809-815
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
exact match
https://scigraph.springernature.com/pub.10.1038/39797
0 references
cites work
A growth-deficiency phenotype in heterozygous mice carrying an insulin-like growth factor II gene disrupted by targeting.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of the mouse insulin-like growth factor II gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting in clusters: lessons from Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An enhancer deletion affects both H19 and Igf2 expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of imprinting caused by deletion of the H19 gene region in mice
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Deletion of the H19 transcription unit reveals the existence of a putative imprinting control element
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting: potentially active chromatin of the repressed maternal allele of the mouse insulin-like growth factor II (Igf2) gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic regions regulating imprinting and insulin-like growth factor-II promoter 3 activity in transgenics: novel enhancer and silencer elements.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic imprinting and gene activation in cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mammary cancer in transgenic mice expressing insulin-like growth factor II (IGF-II)
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A second signal supplied by insulin-like growth factor II in oncogene-induced tumorigenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting of IGF2 and H19: lack of reciprocity in sporadic Beckwith-Wiedemann syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting mutations in the Beckwith-Wiedemann syndrome suggested by altered imprinting pattern in the IGF2-H19 domain.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting mutation in the Beckwith-Wiedemann syndrome leads to biallelic IGF2 expression through an H19-independent pathway
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Altered cell differentiation and proliferation in mice lacking p57KIP2 indicates a role in Beckwith–Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Ablation of the CDK inhibitor p57Kip2 results in increased apoptosis and delayed differentiation during mouse development.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of the imprinted IGF2/cation-independent mannose 6-phosphate receptor results in fetal overgrowth and perinatal lethality
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Regulation of embryonic growth and lysosomal targeting by the imprinted Igf2/Mpr gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mouse mutants lacking the type 2 IGF receptor (IGF2R) are rescued from perinatal lethality in Igf2 and Igf1r null backgrounds.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Embryological and molecular investigations of parental imprinting on mouse chromosome 7.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of an Igf-2 transgene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mosaic uniparental disomy in Beckwith-Wiedemann syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic overgrowth associated with overexpression of insulin-like growth factor II.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dynamic methylation adjustment and counting as part of imprinting mechanisms
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aberrant methylation of an imprinted gene U2af1-rs1(SP2) caused by its own transgene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Xist has properties of the X-chromosome inactivation centre
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Nucleotide sequence of a 28-kb mouse genomic region comprising the imprinted Igf2 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Evolution of Insulin-Like Growth Factor II: Characterization of the Mouse IGF-II Gene and Identification of Two Pseudo-Exons
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Efficientin vitrosynthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2F39797
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/39797
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
Dimensions Publication ID
1029474313
0 references
PubMed ID
9349812
1 reference
stated in
Europe PubMed Central
PubMed ID
9349812
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9349812%20AND%20SRC:MED&resulttype=core&format=json
retrieved
7 November 2019
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