Genotyping possible polymorphic variants of human mismatch repair genes in healthy Korean individuals and sporadic colorectal cancer patients. (Q54703701)

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scientific article published in January 2004

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English	Genotyping possible polymorphic variants of human mismatch repair genes in healthy Korean individuals and sporadic colorectal cancer patients.	scientific article published in January 2004

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Genotyping possible polymorphic variants of human mismatch repair genes in healthy Korean individuals and sporadic colorectal cancer patients. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

colorectal cancer

1 reference

based on heuristic

inferred from title

DNA mismatch repair

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based on heuristic

inferred from title

10

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

author name string

Jin C Kim

1

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Seon A Roh

2

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Kum H Koo

3

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

In H Ka

4

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Hee C Kim

5

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Chang S Yu

6

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Kang H Lee

7

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Jung S Kim

8

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Han I Lee

9

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

publication date

1 January 2004

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Familial Cancer

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

3

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

2

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

129-137

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

The colon cancer burden of genetically defined hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability and the role of hMSH2 in sporadic colorectalcancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promises and perils of individual and population risk estimation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single-nucleotide polymorphisms in the public domain: how useful are they?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A DNA polymorphism discovery resource for research on human genetic variation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Novel Missense Mutation in the DNA Mismatch Repair Gene hMLH1 Present among East Asians but Not among Europeans

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Large-scale discovery and genotyping of single-nucleotide polymorphisms in the mouse

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide polymorphisms as tools in human genetics

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary predisposition to cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: structure-based assessment of amino acid variation

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

SNP and mutation discovery using base-specific cleavage and MALDI-TOF mass spectrometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of germline mutations of hMLH1, hMSH2, hPMS1, hPMS2, and hMSH6 genes in 75 French kindreds with nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genomic DNA-based hMSH2 and hMLH1 mutation screening in 32 Eastern United States hereditary nonpolyposis colorectal cancer pedigrees

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High-throughput genotyping with single nucleotide polymorphisms

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability and alterations in the hMSH2 gene in human ovarian cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

hMLH1 and hMSH2 mutations in families with familial clustering of gastric cancer and hereditary non-polyposis colorectal cancer.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of mismatch repair genes, hMLH1 and hMSH2, in sporadic endometrial carcinomas with microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A polymorphism in the hMSH2 gene (gIVS12-6T>C) associated with non-Hodgkin lymphomas

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline HNPCC gene variants have little influence on the risk for sporadic colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequence analysis of the mismatch repair gene hMSH6 in the germline of patients with familial and sporadic colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotyping single nucleotide polymorphisms by mass spectrometry.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Unbalanced germ-line expression of hMLH1 and hMSH2 alleles in hereditary nonpolyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutational analysis of the hMLH1 gene using an automated two-dimensional DNA typing system

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germ-line msh6 mutations in colorectal cancer families

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Missense mutations in hMLH1 associated with colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An integrated system for high throughput TaqManTM based SNP genotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Single nucleotide polymorphism libraries: why and how are we building them?

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms and colorectal tumor risk

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial endometrial cancer in female carriers of MSH6 germline mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic instability in human ovarian cancer cell lines.

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary nonpolyposis colorectal cancer: frequent occurrence of large genomic deletions in MSH2 and MLH1 genes

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Denaturing gradient gel electrophoresis (DGGE): a rapid and sensitive technique to screen nucleotide sequence variation in populations

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An intronic germline transition in the HNPCC gene hMSH2 is associated with sporadic colorectal cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of clinicopathologic characteristics and genetic alterations between microsatellite instability-positive and microsatellite instability-negative sporadic colorectal carcinomas in patients younger than 40 years old

1 reference

https://pubmed.ncbi.nlm.nih.gov/15340264

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1023/B:FAME.0000039919.66461.8F

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 June 2018

http://europepmc.org/abstract/MED/15340264

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