Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Review of the basic principles of drug action.
|
2440087 |
1986 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Mismatch repair deficiency in phenotypically normal human cells.
|
7632227 |
1995 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
CLINGEN |
Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
|
8072530 |
1994 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
A naturally occurring hPMS2 mutation can confer a dominant negative mutator phenotype.
|
9488480 |
1998 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer.
|
10037723 |
1999 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
GeneticVariation
|
group |
CLINVAR |
The interaction of the human MutL homologues in hereditary nonpolyposis colon cancer.
|
10037723 |
1999 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene.
|
10763829 |
2000 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Structure and function of the N-terminal 40 kDa fragment of human PMS2: a monomeric GHL ATPase.
|
11574484 |
2001 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
CLINGEN |
Functional analysis of MLH1 mutations linked to hereditary nonpolyposis colon cancer.
|
11793442 |
2002 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Contribution of human mlh1 and pms2 ATPase activities to DNA mismatch repair.
|
11897781 |
2002 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Variation in the extent of microsatellite instability in human cell lines with defects in different mismatch repair genes.
|
12714694 |
2003 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
CTD_human |
Hereditary non-polyposis colorectal cancer and the role of hPMS2 and hEXO1 mutations.
|
14756672 |
2004 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
LHGDN |
Microsatellite instability, immunohistochemistry, and additional PMS2 staining in suspected hereditary nonpolyposis colorectal cancer.
|
14871975 |
2004 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome.
|
15077197 |
2004 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
CLINGEN |
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
|
15872200 |
2005 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
|
15872200 |
2005 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer.
|
15887099 |
2005 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
CLINGEN |
Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer.
|
15887124 |
2005 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
Biomarker
|
group |
CTD_human |
Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer.
|
15887124 |
2005 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.
|
16144131 |
2005 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
GeneticVariation
|
group |
CLINVAR |
Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair.
|
16338176 |
2006 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Truncation of the C-terminus of human MLH1 blocks intracellular stabilization of PMS2 and disrupts DNA mismatch repair.
|
16338176 |
2006 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
GeneticVariation
|
group |
LHGDN |
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
|
16472587 |
2006 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
|
16472587 |
2006 |
Hereditary Nonpolyposis Colorectal Neoplasms
|
0.640 |
CausalMutation
|
group |
CLINVAR |
PMS2 mutations in childhood cancer.
|
16507833 |
2006 |