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Infrequent mutation of theWT1 gene in 77 Wilms' tumors
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
title
Infrequent mutation of the WT1 gene in 77 Wilms' Tumors
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
author
Manfred Gessler
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Craig Peters
series ordinal
7
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
author name string
König A
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Arden K
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Grundy P
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Orkin S
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Sallan S
series ordinal
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Ruyle S
series ordinal
8
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Mandell J
series ordinal
9
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
Li F
series ordinal
10
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
publication date
1 January 1994
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
published in
Human Mutation
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
volume
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
issue
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
page(s)
212-222
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
cites work
Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
21 January 2018
Nephrogenic rests, nephroblastomatosis, and the pathogenesis of Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
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/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous somatic Wt1 point mutations in sporadic unilateral Wilms tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Abnormalities of chromosomes 1 and 11 in Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Suppression of tumorigenicity in Wilms tumor by the p15.5-p14 region of chromosome 11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Aniridia-Wilms’ tumor association: evidence for specific deletion of 11p13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A physical map around the WAGR complex on the short arm of chromosome 11
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The genomic organization and expression of the WT1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous inactivation of WT1 in a Wilms' tumor associated with the WAGR syndrome.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A single base pair polymorphism in the WT1 gene detected by single-strand conformation polymorphism analysis.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An internal deletion within an 11p13 zinc finger gene contributes to the development of Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Tumor-specific loss of 11p15.5 alleles in del11p13 Wilms tumor and in familial adrenocortical carcinoma
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Lack of linkage of familial Wilms' tumour to chromosomal band 11 p13
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
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/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Transcriptional repression mediated by the WT1 Wilms tumor gene product
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
WT1 mutations contribute to abnormal genital system development and hereditary Wilms' tumour
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Direct pulsed field gel electrophoresis of Wilms' tumors shows that dna deletions in 11 p 13 are rare
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Familial predisposition to Wilms tumor does not segregate with the WT1 gene.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Sensitivity of Single-Strand Conformation Polymorphism Analysis for the Detection of Single Base Substitutions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetics and molecular genetics of Wilms' tumor of childhood
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
PCR detection of an insertion/deletion polymorphism in intron 1 of the HRAS1 locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Smallest region of overlap in Wilms tumor deletions uniquely implicates an 11p13 zinc finger gene as the disease locus
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2FHUMU.1380030307
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1002/HUMU.1380030307
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
PubMed publication ID
8019557
1 reference
stated in
Europe PubMed Central
PubMed publication ID
8019557
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8019557%20AND%20SRC:MED&resulttype=core&format=json
retrieved
23 October 2019
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