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English
Mutation of the ST7 tumor suppressor gene on 7q31.1 is rare in breast, ovarian and colorectal cancers
scientific article published on 01 December 2001
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
title
Mutation of the ST7 tumor suppressor gene on 7q31.1 is rare in breast, ovarian and colorectal cancers
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
author
Ian G. Campbell
series ordinal
5
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
author name string
Thomas NA
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
Choong DY
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
Jokubaitis VJ
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
Neville PJ
series ordinal
4
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
publication date
1 December 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
published in
Nature Genetics
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
volume
29
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
issue
4
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
page(s)
379-380
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/ng784
0 references
cites work
Frequent loss of heterozygosity in the region of the D7S523 locus in advanced ovarian cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a 1300 kilobase deletion unit on chromosome 7q31.3 in invasive epithelial ovarian carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
(C-A)n microsatellite repeat D7S522 is the most commonly deleted region in human primary breast cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Chromosome 7 suppresses indefinite division of nontumorigenic immortalized human fibroblast cell lines KMST-6 and SUSM-1
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Definitive functional evidence for a tumor suppressor gene on human chromosome 7q31.1 neighboring the Fra7G site
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutational and functional analyses reveal that ST7 is a highly conserved tumor-suppressor gene on human chromosome 7q31
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of a novel gene on chromosome 7q31 that is interrupted by a translocation breakpoint in an autistic individual
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FNG784
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/NG784
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
PubMed ID
11726923
1 reference
stated in
Europe PubMed Central
PubMed ID
11726923
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11726923%20AND%20SRC:MED&resulttype=core&format=json
retrieved
4 December 2019
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