Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q71580257)
Watch
English
Genotype/phenotype correlations in Wilms' tumor
scientific article published on 01 November 1996
In more languages
edit
Statements
instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
title
Genotype/phenotype correlations in Wilms' tumor
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
main subject
phenotype
1 reference
based on heuristic
inferred from title
author name string
Huff V
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
publication date
1 November 1996
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
published in
Pediatric Blood Cancer
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
volume
27
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
issue
5
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
page(s)
408-414
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
cites work
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Non-11p constitutional chromosome abnormalities in Wilms' tumor patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Wilms' tumor in the Li-Fraumeni cancer family syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Familial primary hyperparathyroidism complicated with Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
The cytogenetics of Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Abnormalities of chromosomes 1 and 11 in Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Cytogenetic changes in Wilms' tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Infrequency of ras, p53, WT1, or RB gene alterations in Wilms tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Anaplastic Wilms' tumour, a subtype displaying poor prognosis, harbours p53 gene mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Binding of the Wilms' tumor locus zinc finger protein to the EGR-1 consensus sequence
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Transcriptional repression mediated by the WT1 Wilms tumor gene product
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Infrequent mutation of theWT1 gene in 77 Wilms' tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Epigenetic lesions at the H19 locus in Wilms' tumour patients
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Loss of imprinting of IGF2 is linked to reduced expression and abnormal methylation of H19 in Wilms' tumour
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
The genomic organization and expression of the WT1 gene
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Inactivation of WT1 in nephrogenic rests, genetic precursors to Wilms' tumour
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Low frequency of mutations in the WT1 coding region in Wilms' tumor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Fine structure analysis of the WT1 gene in sporadic Wilms tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
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%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
A point mutation found in the WT1 gene in a sporadic Wilms' tumor without genitourinary abnormalities is identical with the most frequent point mutation in Denys-Drash syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Denys-Drash syndrome: relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
WT1 mutations in patients with Denys-Drash syndrome: a novel mutation in exon 8 and paternal allele origin
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Evidence that WT1 mutations in Denys — Drash syndrome patients may act in a dominant-negative fashion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
A novel mutation of the WT1 gene (a tumor suppressor gene for Wilms' tumor) in a patient with Denys-Drash syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Further evidence that imbalance of WT1 isoforms may be involved in Denys – Drash syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys-Drash syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
WT1 mutations associated with incomplete Denys-Drash syndrome define a domain predicted to behave in a dominant-negative fashion
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1002%2F%28SICI%291096-911X%28199611%2927%3A5%3C408%3A%3AAID-MPO4%3E3.0.CO%3B2-Q
retrieved
21 January 2018
Identifiers
DOI
10.1002/(SICI)1096-911X(199611)27:5<408::AID-MPO4>3.0.CO;2-Q
0 references
PubMed ID
8827067
1 reference
stated in
Europe PubMed Central
PubMed ID
8827067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8827067%20AND%20SRC:MED&resulttype=core&format=json
retrieved
19 October 2019
Sitelinks
Wikipedia
(0 entries)
edit
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit