(Q55034846)

16 June 2018

title

Loss or somatic mutations of hMSH2 occur in hereditary nonpolyposis colorectal cancers with hMSH2 germline mutations. (English)

1 reference

16 June 2018

author name string

S L Lu

1

1 reference

16 June 2018

Y Akiyama

2

1 reference

16 June 2018

H Nagasaki

3

1 reference

16 June 2018

T Nomizu

4

1 reference

16 June 2018

E Ikeda

5

1 reference

16 June 2018

S Baba

6

1 reference

16 June 2018

K Ushio

7

1 reference

16 June 2018

T Iwama

8

1 reference

16 June 2018

K Maruyama

9

1 reference

16 June 2018

Y Yuasa

10

1 reference

16 June 2018

publication date

1 March 1996

1 reference

16 June 2018

number of pages

9

1 reference

Japanese Journal of Cancer Research

inferred from page(s)

published in

1 reference

16 June 2018

volume

87

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16 June 2018

issue

3

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16 June 2018

page(s)

279-287

1 reference

16 June 2018

Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesis

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Microsatellite instability in cancer of the proximal colon

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Clues to the pathogenesis of familial colorectal cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Genetic mapping of a locus predisposing to human colorectal cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Genetics, natural history, tumor spectrum, and pathology of hereditary nonpolyposis colorectal cancer: an updated review

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Hypermutability and mismatch repair deficiency in RER+ tumor cells

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Optimization of nonradioisotopic single strand conformation polymorphism analysis with a conventional minislab gel electrophoresis apparatus

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Defective mismatch repair in extracts of colorectal and endometrial cancer cell lines exhibiting microsatellite instability

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Mutation of a mutL homolog in hereditary colon cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Colon cancer and DNA repair: have mismatches met their match?

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for msh2 mutations

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Genetic instability occurs in the majority of young patients with colorectal cancer

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Mutation and cancer: statistical study of retinoblastoma

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

A second-generation linkage map of the human genome

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Germ-line mutations of the APC gene in 53 familial adenomatous polyposis patients

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

A general method for isolation of high molecular weight DNA from eukaryotes

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Molecular diagnosis of familial adenomatous polyposis.

16 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5921088

Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancer

13 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1996.TB00218.X

A frequent hMSH2 mutation in hereditary non-polyposis colon cancer syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1996.TB00218.X

Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1111%2FJ.1349-7006.1996.TB00218.X

Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients

21 January 2018

1 reference

12 December 2020

Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome

1 reference

12 December 2020

All in the (cancer) family

1 reference

12 December 2020

Hereditary nonpolyposis colorectal cancer (lynch syndromes I and II). I. Clinical description of resource

1 reference

12 December 2020

DNA alterations in cells from hereditary non-polyposis colorectal cancer patients

1 reference

12 December 2020

Accumulation of multiple mutations in tumour suppressor genes during colorectal tumorigenesis in HNPCC patients

1 reference

12 December 2020

Mutations in the BRCA1 gene in families with early-onset breast and ovarian cancer

1 reference

12 December 2020

10.1111/J.1349-7006.1996.TB00218.X

Identifiers

DOI

1 reference

16 June 2018

PMC publication ID

5921088

1 reference

16 June 2018

PubMed publication ID

8613431

1 reference

16 June 2018