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English
Mutator genes and mosaicism in colorectal cancer
scientific article published on February 1996
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instance of
scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
review article
1 reference
stated in
Europe PubMed Central
title
Mutator genes and mosaicism in colorectal cancer
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
main subject
colorectal cancer
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based on heuristic
inferred from title
author
Malcolm G. Dunlop
series ordinal
1
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stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
language of work or name
English
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based on heuristic
inferred from title
publication date
1 February 1996
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stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
published in
Current Opinion in Genetics & Development
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stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
volume
6
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stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
issue
1
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stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
page(s)
76-81
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stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
cites work
Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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The barrier to recombination between Escherichia coli and Salmonella typhimurium is disrupted in mismatch-repair mutants.
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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Mechanisms of DNA-mismatch correction
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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Isolation of an hMSH2-p160 Heterodimer That Restores DNA Mismatch Repair to Tumor Cells
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Mutations of GTBP in genetically unstable cells
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7 January 2021
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Binding of mismatched microsatellite DNA sequences by the human MSH2 protein
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer.
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Mutation of a mutL homolog in hereditary colon cancer
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Mutations of two PMS homologues in hereditary nonpolyposis colon cancer
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Dual requirement in yeast DNA mismatch repair for MLH1 and PMS1, two homologs of the bacterial mutL gene
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Genetic instability occurs in the majority of young patients with colorectal cancer
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Screening for large bowel neoplasms in individuals with a family history of colorectal cancer
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Hypermutability and mismatch repair deficiency in RER+ tumor cells
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7 January 2021
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Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis
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reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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Inactivation of the mouse Msh2 gene results in mismatch repair deficiency, methylation tolerance, hyperrecombination, and predisposition to cancer
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Dynamic mutations: a new class of mutations causing human disease
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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Mismatch repair deficiency in phenotypically normal human cells
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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Somatic mosaicism in sperm is associated with intergenerational (CAG)n changes in Huntington disease.
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Instability of short tandem repeats (microsatellites) in human cancers.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Clues to the pathogenesis of familial colorectal cancer
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Microsatellite instability in cancer of the proximal colon
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Spontaneous mutations at aprt locus in a mammalian cell line defective in mismatch recognition
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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Genomic instability in repeated sequences is an early somatic event in colorectal tumorigenesis that persists after transformation
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Inactivation of the type II TGF-beta receptor in colon cancer cells with microsatellite instability
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
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Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
DNA sequence analysis of spontaneous mutations at the aprt locus of hamster cells
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
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A genetic model for colorectal tumorigenesis
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic mosaicism in normal tissues of Wilms' tumour patients
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
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A somatic mutation in the adenomatous polyposis coli (APC) gene in peripheral blood cells--implications for predictive diagnosis.
1 reference
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Crossref
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https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
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Mandibular osteomas in sporadic colorectal carcinoma. A genetic marker.
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
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Phenotypic variation in hereditary nonpolyposis colon cancer syndrome. Association with infiltrative fibromatosis (desmoid tumor)
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0959-437X%2896%2990014-3
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7 January 2021
based on heuristic
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Identifiers
DOI
10.1016/S0959-437X(96)90014-3
1 reference
stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
PubMed ID
8791479
1 reference
stated in
Europe PubMed Central
PubMed ID
8791479
retrieved
26 September 2017
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