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English
MSH-6: extending the reliability of immunohistochemistry as a screening tool in Muir–Torre syndrome
scientific article published on 7 December 2007
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
title
MSH-6: extending the reliability of immunohistochemistry as a screening tool in Muir-Torre syndrome
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
main subject
immunohistochemistry
1 reference
based on heuristic
inferred from title
author
Meera Mahalingam
series ordinal
3
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
author name string
Vishes Chhibber
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Karen Dresser
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
publication date
7 December 2007
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
published in
Modern Pathology
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
volume
21
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
issue
2
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
page(s)
159-164
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
exact match
https://scigraph.springernature.com/pub.10.1038/modpathol.3800997
0 references
cites work
Multiple primary carcinomata of the colon, duodenum, and larynx associated with kerato-acanthomata of the face
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Multiple sebaceous tumors
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
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Different phenotypes in Muir-Torre syndrome: clinical and biomolecular characterization in two Italian families
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and Hyperplasias
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Frequency of hereditary nonpolyposis colorectal carcinoma (Lynch syndromes I and II)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Microsatellite instability and immunostaining for MSH-2 and MLH-1 in cutaneous and internal tumors from patients with the Muir-Torre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An individual with Muir-Torre syndrome found to have a pathogenic MSH6 gene mutation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MSH6 mutation in Muir-Torre syndrome: could this be a rare finding?
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mutation in the mismatch repair gene Msh6 causes cancer susceptibility
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
An illustrative case of Muir-Torre syndrome: contribution of immunohistochemical analysis in identifying indicator sebaceous lesions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
The Muir-Torre syndrome: a 25-year retrospect
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary nonpolyposis colorectal cancer and related conditions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
DNA mismatch repair and the significance of a sebaceous skin tumor for visceral cancer prevention
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Loss of DNA mismatch repair proteins in skin tumors from patients with Muir-Torre syndrome and MSH2 or MLH1 germline mutations: establishment of immunohistochemical analysis as a screening test
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Mismatch repair proteins expression and microsatellite instability in skin lesions with sebaceous differentiation: a study in different clinical subgroups with and without extracutaneous cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
MLH1 promoter hypermethylation is associated with the microsatellite instability phenotype in sporadic endometrial carcinomas
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Hereditary cancer: two hits revisited
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
"Second hit" in sebaceous tumors from Muir-Torre patients with germline mutations in MSH2: allele loss is not the preferred mode of inactivation
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Widespread microsatellite instability in sebaceous tumours of patients with the Muir-Torre syndrome
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Muir-Torre phenotype has a frequency of DNA mismatch-repair-gene mutations similar to that in hereditary nonpolyposis colorectal cancer families defined by the Amsterdam criteria
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1038%2FMODPATHOL.3800997
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1038/MODPATHOL.3800997
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
Dimensions Publication ID
1051591945
0 references
PubMed ID
18065960
1 reference
stated in
Europe PubMed Central
PubMed ID
18065960
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18065960%20AND%20SRC:MED&resulttype=core&format=json
retrieved
29 December 2019
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