×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
8261515
1993
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.
7874129
1994
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
CausalMutation
CLINVAR
Detection of new mutations in six out of 10 Swiss HNPCC families by genomic sequencing of the hMSH2 and hMLH1 genes.
8592341
1995
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
CausalMutation
CLINVAR
Genetic instability occurs in the majority of young patients with colorectal cancer.
7585065
1995
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer.
8872463
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Germline mutations of hMLH1 and hMSH2 genes in Korean hereditary nonpolyposis colorectal cancer.
8797773
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Microsatellite instability and the role of hMSH2 in sporadic colorectalcancer.
8700523
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Hereditary nonpolyposis colorectal cancer (HNPCC): eight novel germline mutations in hMSH2 or hMLH1 genes.
9298827
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Frequent somatic mutations of hMSH3 with reference to microsatellite instability in hereditary nonpolyposis colorectal cancers.
9240418
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Use of SSCP analysis to identify germline mutations in HNPCC families fulfilling the Amsterdam criteria.
9048925
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Identification of concurrent germ-line mutations in hMSH2 and/or hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.
9419403
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.
9311737
1997
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
CausalMutation
CLINVAR
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
9718327
1998
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Novel germline mutations of hMSH2 in a patient with hereditary nonpolyposis colorectal cancer (HNPCC) and in a patient with six primary cancers.
9621522
1998
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Germline mutations of hMLH1 and hMSH2 genes in patients with suspected hereditary nonpolyposis colorectal cancer and sporadic early-onset colorectal cancer.
9559627
1998
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
9718327
1998
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Novel hMLH1 and hMSH2 germline mutations in African Americans with colorectal cancer.
10386556
1999
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Influence of selection criteria on mutation detection in patients with hereditary nonpolyposis colorectal cancer.
10375096
1999
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening.
10528862
1999
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Functional analysis of human MutSalpha and MutSbeta complexes in yeast.
9889267
1999
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Four novel MSH2 / MLH1 gene mutations in portuguese HNPCC families.
10612836
2000
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Population-based molecular detection of hereditary nonpolyposis colorectal cancer.
10829038
2000
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2.
10573010
2000
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
CLINVAR
Novel germline mutation (300-305delAGTTGA) in the human MSH2 gene in hereditary non-polyposis colorectal cancer (HNPCC).
10874318
2000
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
Colorectal cancer, hereditary nonpolyposis, type 1
0.600
GeneticVariation
UNIPROT
Enhanced detection of deleterious and other germline mutations of hMSH2 and hMLH1 in Japanese hereditary nonpolyposis colorectal cancer kindreds.
10777691
2000