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English
Imprinting moves to the centre
scientific article published on 01 October 1996
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
title
Imprinting moves to the centre
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
author
Anne Ferguson-Smith
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
publication date
1 October 1996
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
volume
14
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
page(s)
119-121
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng1096-119
0 references
cites work
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
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%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple genetic loci within 11p15 defined by Beckwith-Wiedemann syndrome rearrangement breakpoints and subchromosomal transferable fragments
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
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%2FNG1096-119
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%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
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%2FNG1096-119
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%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic imprinting: control of gene expression by epigenetic inheritance
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Inherited microdeletions in the Angelman and Prader-Willi syndromes define an imprinting centre on human chromosome 15.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Biallelic expression of imprinted genes in the mouse germ line: implications for erasure, establishment, and mechanisms of genomic imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG1096-119
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG1096-119
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
PubMed publication ID
8841173
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8841173
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8841173%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
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