Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
Biomarker
|
group |
MGD |
|
|
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation
|
group |
CLINVAR |
Immunosuppression. Binding by design.
|
1710317 |
1991 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Genetic instability occurs in the majority of young patients with colorectal cancer.
|
7585065 |
1995 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis.
|
7726159 |
1995 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
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 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation
|
group |
CLINVAR |
Genetic instability in human ovarian cancer cell lines.
|
7937795 |
1994 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
|
8062247 |
1994 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
GeneticVariation
|
group |
CLINVAR |
hMSH2 mutations in hereditary nonpolyposis colorectal cancer kindreds.
|
8062247 |
1994 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
|
8261515 |
1993 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
Biomarker
|
group |
CLINGEN |
Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer.
|
8261515 |
1993 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations.
|
8566964 |
1996 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients.
|
8574961 |
1996 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
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 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
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 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Genetic heterogeneity and unmapped genes for colorectal cancer.
|
8640829 |
1996 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
Biomarker
|
group |
CLINGEN |
Spontaneous intestinal carcinomas and skin neoplasms in Msh2-deficient mice.
|
8706033 |
1996 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer.
|
8776590 |
1996 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
RNA-based mutation screening in hereditary nonpolyposis colorectal cancer.
|
8808596 |
1996 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
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 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.
|
9222765 |
1997 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations.
|
9311737 |
1997 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer.
|
9506527 |
1998 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Systematic analysis of hMSH2 and hMLH1 in young colon cancer patients and controls.
|
9718327 |
1998 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Interactions of human hMSH2 with hMSH3 and hMSH2 with hMSH6: examination of mutations found in hereditary nonpolyposis colorectal cancer.
|
9774676 |
1998 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.900 |
CausalMutation
|
group |
CLINVAR |
Microsatellite instability and mutation of DNA mismatch repair genes in gliomas.
|
9777949 |
1998 |