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p53 and APC gene mutations: software and databases
scientific article
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
title
p53 and APC gene mutations: software and databases
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
main subject
software
0 references
author name string
Béroud C
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
Soussi T
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
language of work or name
English
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publication date
1 January 1997
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
published in
Nucleic Acids Research
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
volume
25
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
issue
1
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
page(s)
138
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
cites work
APC mutations in colorectal tumors with mismatch repair deficiency
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
7 July 2018
Deletions and insertions in the p53 tumor suppressor gene in human cancers: confirmation of the DNA polymerase slippage/misalignment model.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
7 July 2018
p53 gene mutation: software and database.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
7 July 2018
Software and database for the analysis of mutations in the human FBN1 gene
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
7 July 2018
APC gene: database of germline and somatic mutations in human tumors and cell lines
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
7 July 2018
Severe Gardner syndrome in families with mutations restricted to a specific region of the APC gene.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
7 July 2018
Familial adenomatous polyposis: desmoid tumours and lack of ophthalmic lesions (CHRPE) associated with APC mutations beyond codon 1444.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=146392
retrieved
26 October 2018
Identifiers
DOI
10.1093/NAR/25.1.138
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
DBLP publication ID
journals/nar/BeroudS97
1 reference
stated in
DBLP Dataset 2021-01-02
retrieved
28 January 2021
PMCID
146392
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
PubMed ID
9016523
1 reference
stated in
Europe PubMed Central
PubMed ID
9016523
retrieved
3 August 2017
ResearchGate publication ID
14191675
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