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APC gene: database of germline and somatic mutations in human tumors and cell lines
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
title
APC gene: database of germline and somatic mutations in human tumors and cell lines
(English)
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
main subject
database
0 references
author
Pierre Laurent-Puig
series ordinal
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Christophe Beroud
series ordinal
2
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
Thierry Soussi
series ordinal
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
language of work or name
English
0 references
publication date
1 January 1998
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
published in
Nucleic Acids Research
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
volume
26
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
issue
1
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
page(s)
269-270
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
cites work
Familial colorectal cancer in Ashkenazim due to a hypermutable tract in APC.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Somatic mutation of the APC gene in gastric cancer: frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mutations of the APC (adenomatous polyposis coli) gene
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mutations of the APC gene occur during early stages of gastric adenoma development.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Phenotypic variability of familial adenomatous polyposis in 11 unrelated families with identical APC gene mutation
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Novel germline APC gene mutation in a large familial adenomatous polyposis kindred displaying variable phenotypes
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Attenuated familial adenomatous polyposis due to a mutation in the 3' part of the APC gene. A clue for understanding the function of the APC protein
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Somatic mutations of the APC gene in sporadic hepatoblastomas
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Lessons from hereditary colorectal cancer
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Germline mutations in the 3' part of APC exon 15 do not result in truncated proteins and are associated with attenuated adenomatous polyposis coli.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Familial infiltrative fibromatosis (desmoid tumours) (MIM135290) caused by a recurrent 3' APC gene mutation.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
APC gene alterations in Barrett's metaplasia are implicated at an early stage in the carcinogenesis of esophageal adenocarcinoma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Germline versus somatic mutations of the APC gene: evidence for mechanistic differences
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Mutation analysis of the p53, APC, and p16 genes in the Barrett's oesophagus, dysplasia, and adenocarcinoma
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
The adenomatous polyposis coli (APC) tumor suppressor
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Alleles of the APC gene: an attenuated form of familial polyposis
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Restriction of ocular fundus lesions to a specific subgroup of APC mutations in adenomatous polyposis coli patients.
1 reference
stated in
PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/9399850
retrieved
12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1093/NAR/26.1.269
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
DBLP publication ID
journals/nar/Laurent-PuigBS98
1 reference
stated in
DBLP Dataset 2021-01-02
retrieved
28 January 2021
PMC publication ID
147178
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
PubMed publication ID
9399850
1 reference
stated in
Europe PubMed Central
PMC publication ID
147178
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9399850%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 November 2019
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