×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
Biomarker
group
MGD
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
Biomarker
group
MGD
×
Entrez Id:
4072
Gene Symbol:
EPCAM
EPCAM
0.410
GeneticVariation
group
CLINVAR
×
Entrez Id:
1495
Gene Symbol:
CTNNA1
CTNNA1
0.300
Biomarker
group
CLINGEN
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
[A method of study for stomatological materials].
1061282
1976
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
0.640
CausalMutation
group
CLINVAR
Review of the basic principles of drug action.
2440087
1986
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
Immunosuppression. Binding by design.
1710317
1991
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Oxidative metabolism in reperfused myocardium.
1756143
1991
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
CausalMutation
group
CLINVAR
"""Central arousal"" and sexual responsiveness in the snail, Helix aspersa."
2059188
1991
×
Entrez Id:
80204
Gene Symbol:
FBXO11
FBXO11
0.100
CausalMutation
group
CLINVAR
"""Central arousal"" and sexual responsiveness in the snail, Helix aspersa."
2059188
1991
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
8261515
1993
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
Biomarker
group
CLINGEN
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
8261515
1993
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
8062247
1994
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
GeneticVariation
group
CLINVAR
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
8062247
1994
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
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
0.900
GeneticVariation
group
CLINVAR
Genetic instability in human ovarian cancer cell lines.
7937795
1994
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Mutation of a mutL homolog in hereditary colon cancer.
8128251
1994
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
0.640
Biomarker
group
CLINGEN
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
8072530
1994
×
Entrez Id:
2052
Gene Symbol:
EPHX1
EPHX1
0.300
Biomarker
group
CLINGEN
Human microsomal epoxide hydrolase: genetic polymorphism and functional expression in vitro of amino acid variants.
7516776
1994
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Germ line mutations of hMSH2 and hMLH1 genes in Japanese families with hereditary nonpolyposis colorectal cancer (HNPCC): usefulness of DNA analysis for screening and diagnosis of HNPCC patients.
8581513
1995
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
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
0.900
CausalMutation
group
CLINVAR
Genetic instability occurs in the majority of young patients with colorectal cancer.
7585065
1995
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.
7726159
1995
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families.
8521398
1995
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Alternative splicing of MLH1 messenger RNA in human normal cells.
7728749
1995