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Allelic imbalance at chromosome 1q21 in Wilms tumor
scientific article published on 01 August 1997
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
title
Allelic imbalance at chromosome 1q21 in Wilms tumor
(English)
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
main subject
nephroblastoma
1 reference
based on heuristic
inferred from title
author
Melissa Little
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
author name string
M H Law
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
E Algar
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
publication date
1 August 1997
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
published in
Cancer Genetics and Cytogenetics
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
volume
97
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
page(s)
54-59
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
cites work
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/10.1016%2FS0165-4608%2896%2900342-1
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/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A clinical overview of WT1 gene mutations
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
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/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelotyping in Wilms Tumors Identifies a Putative Third Tumor Suppressor Gene on Chromosome 11
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
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/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Cytogenetic changes in Wilms' tumors
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The WT1 Wilms tumor gene product: a developmentally regulated transcription factor in the kidney that functions as a tumor suppressor
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA recognition by splicing variants of the Wilms' tumor suppressor, WT1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Modulation of DNA binding specificity by alternative splicing of the Wilms tumor wt1 gene transcript
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
+P5 (D1S3309E), a novel target binding site for the Wilms' tumour suppressor 1 (WT1) gene, maps to human chromosome 1q21-->22.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Homozygous intragenic deletion in the WT1 gene in a sporadic Wilms' tumour associated with high levels of expression of a truncated transcript
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A second-generation linkage map of the human genome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A PCR-based linkage map of human chromosome 1.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The 1993-94 Généthon human genetic linkage map
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequent loss of chromosome arm 1p DNA in parathyroid adenomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Differences in patterns of allelic loss between two common types of adult cancer, breast and colon carcinoma, and Wilms' tumor of childhood
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 1 aberrations in cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Allelic imbalance on chromosome 1 in human breast cancer. I. Minisatellite and RFLP analysis
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Human and mouse chromosomal mapping of the myeloid cell leukemia-1 gene: MCL1 maps to human chromosome 1q21, a region that is frequently altered in preneoplastic and neoplastic disease.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutional duplication 1q in acute myeloid leukemia
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Constitutive fragile sites and cancer.
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spontaneous chromosome aberrations in Fanconi's anemia patients are located at fragile sites and acute myeloid leukemia breakpoints
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-4608%2896%2900342-1
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0165-4608(96)00342-1
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
PubMed publication ID
9242218
1 reference
stated in
Europe PubMed Central
PubMed publication ID
9242218
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9242218%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 November 2019
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