×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
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:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer.
7557107
1995
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)
7757073
1995
×
Entrez Id:
5395
Gene Symbol:
PMS2
PMS2
0.640
CausalMutation
group
CLINVAR
Mismatch repair deficiency in phenotypically normal human cells.
7632227
1995
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
Biomarker
group
CLINGEN
GTBP, a 160-kilodalton protein essential for mismatch-binding activity in human cells.
7604265
1995
×
Entrez Id:
2956
Gene Symbol:
MSH6
MSH6
0.640
Biomarker
group
CLINGEN
Isolation of an hMSH2-p160 heterodimer that restores DNA mismatch repair to tumor cells.
7604264
1995
×
Entrez Id:
324
Gene Symbol:
APC
APC
0.300
Biomarker
group
CTD_human
The molecular basis of Turcot's syndrome.
7661930
1995
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
RNA-based mutation screening in hereditary nonpolyposis colorectal cancer.
8808596
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.
8574961
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations.
8566964
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
Biomarker
group
CLINGEN
Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient mice.
8706033
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
Genetic heterogeneity and unmapped genes for colorectal cancer.
8640829
1996
×
Entrez Id:
4436
Gene Symbol:
MSH2
MSH2
0.900
CausalMutation
group
CLINVAR
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
0.900
CausalMutation
group
CLINVAR
DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.
8776590
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Genetic counseling in a Navajo hereditary nonpolyposis colorectal cancer kindred.
8630936
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.
8574961
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Germline mutations of hMLH1 and hMSH2 genes in Korean hereditary nonpolyposis colorectal cancer.
8797773
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
GeneticVariation
group
CLINVAR
CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations.
8566964
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
GeneticVariation
group
CLINVAR
DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.
8776590
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome.
8880570
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.
8776590
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome.
8646682
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
GeneticVariation
group
CLINVAR
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.
8574961
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancer.
8872463
1996
×
Entrez Id:
4292
Gene Symbol:
MLH1
MLH1
0.700
CausalMutation
group
CLINVAR
Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16.
8571956
1996