|
| 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: |
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: |
5395 |
| Gene Symbol: |
PMS2 |
PMS2
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Review of the basic principles of drug action.
|
2440087 |
1986 |
|
| 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: |
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: |
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: |
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: |
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: |
5395 |
| Gene Symbol: |
PMS2 |
PMS2
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Mismatch repair deficiency in phenotypically normal human cells.
|
7632227 |
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 |
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 |
Alternative splicing of MLH1 messenger RNA in human normal cells.
|
7728749 |
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: |
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: |
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: |
5395 |
| Gene Symbol: |
PMS2 |
PMS2
|
0.640 |
Biomarker
|
group |
CLINGEN |
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
|
8072530 |
1994 |