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Genomic imprinting and gene activation in cancer
scientific article published on 01 June 1993
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
title
Genomic imprinting and gene activation in cancer
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
author
Andrew P. Feinberg
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
publication date
1 June 1993
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
volume
4
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
page(s)
110-113
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng0693-110
0 references
cites work
Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
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%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal imprinting of the mouse Snrpn gene and conserved linkage homology with the human Prader-Willi syndrome region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A candidate mouse model for Prader-Willi syndrome which shows an absence of Snrpn expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The mouse insulin-like growth factor type-2 receptor is imprinted and closely linked to the Tme locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of the mouse H19 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic loss of chromosome 1p36 in neuroblastoma is of preferential maternal origin and correlates with N-myc amplification
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preferential amplification of the paternal allele of the N-myc gene in human neuroblastomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Expression of recessive alleles by chromosomal mechanisms in retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Somatic deletion and duplication of genes on chromosome 11 in Wilms' tumours.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of a Harvey ras allele in sporadic Wilms' tumour
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genome imprinting, cellular mosaicism and carcinogenesis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental origin of chromosomes involved in the translocation t(9;22).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Carcinogenesis. Is imprinting to blame?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parthenogenic Origin of Benign Ovarian Teratomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader-Willi syndrome critical region
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Uniparental paternal disomy in a genetic cancer-predisposing syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Dads and disomy and disease
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
IGF2 is parentally imprinted during human embryogenesis and in the Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental genomic imprinting of the human IGF2 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Relaxation of imprinted genes in human cancer.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
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%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Insulin-like growth factor II-mediated proliferation of human neuroblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental imprinting of the human H19 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Zinc finger point mutations within the WT1 gene in Wilms tumor patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tumor cell growth arrest caused by subchromosomal transferable DNA fragments from chromosome 11
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mosaicism in normal tissues of Wilms' tumour patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Genomic imprinting and carcinogenesis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Trans-sensing hypothesis for origin of Beckwith-Wiedemann syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hypomethylation distinguishes genes of some human cancers from their normal counterparts
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental-origin-specific epigenetic modification of the mouse H19 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Maternal-specific methylation of the imprinted mouse Igf2r locus identifies the expressed locus as carrying the imprinting signal.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preferential mutation of paternally derived RB gene as the initial event in sporadic osteosarcoma.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Parental origin of mutations of the retinoblastoma gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Preferential germline mutation of the paternal allele in retinoblastoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG0693-110
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG0693-110
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
PubMed ID
8348145
1 reference
stated in
Europe PubMed Central
PubMed ID
8348145
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8348145%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 October 2019
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