Pages that link to "Q57200626"
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The following pages link to MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis (Q57200626):
Displaying 50 items.
- Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. (Q24539206) (← links)
- Promoter methylation and immunohistochemical expression of hMLH1 and hMSH2 in sporadic colorectal cancer: a study from India (Q28303580) (← links)
- Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma (Q29615026) (← links)
- The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population (Q33343083) (← links)
- Genetic susceptibility to non-polyposis colorectal cancer (Q33764029) (← links)
- Mutated gene-specific phenotypes of dinucleotide repeat instability in human colorectal carcinoma cell lines deficient in DNA mismatch repair (Q33861772) (← links)
- DNA mismatch repair and cancer (Q34164892) (← links)
- DNA mismatch repair defects: role in colorectal carcinogenesis (Q34568596) (← links)
- Prevalence of pathological germline mutations of hMLH1 and hMSH2 genes in colorectal cancer (Q34633911) (← links)
- Rapid design of denaturing gradient-based two-dimensional electrophoretic gene mutational scanning tests (Q34666570) (← links)
- The molecular and genetic basis of colon cancer (Q35037873) (← links)
- Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing (Q35594437) (← links)
- Microsatellite instability and high content of activated cytotoxic lymphocytes identify colon cancer patients with a favorable prognosis (Q35746560) (← links)
- Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancers (Q35810106) (← links)
- Is surveillance of the small bowel indicated for Lynch syndrome families? (Q35954134) (← links)
- Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient with a constitutional PMS2 deficiency (Q36069679) (← links)
- Mutation and methylation of hMLH1 in gastric carcinomas with microsatellite instability (Q36178601) (← links)
- Human mismatch repair protein hMutLα is required to repair short slipped-DNAs of trinucleotide repeats (Q36451916) (← links)
- Epigenetic phenotypes distinguish microsatellite-stable and -unstable colorectal cancers (Q36549885) (← links)
- Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer (Q36609603) (← links)
- MSH6 germline mutations in early-onset colorectal cancer patients without family history of the disease (Q36611645) (← links)
- Mutation profiles of synchronous colorectal cancers from a patient with Lynch syndrome suggest distinct oncogenic pathways (Q36936956) (← links)
- Differences and evolution of the methods for the assessment of microsatellite instability (Q37235042) (← links)
- Endometrial cancer as a familial tumor: pathology and molecular carcinogenesis (review). (Q37236178) (← links)
- Thyroid cancer in a patient with a germline MSH2 mutation. Case report and review of the Lynch syndrome expanding tumour spectrum (Q37326213) (← links)
- Molecular and clinical characteristics of MSH6 variants: an analysis of 25 index carriers of a germline variant (Q37360286) (← links)
- Assessment of in silico protein sequence analysis in the clinical classification of variants in cancer risk genes (Q37746632) (← links)
- A meta‐analysis of the prevalence of somatic mutations in the hMLH1 and hMSH2 genes in colorectal cancer (Q37944383) (← links)
- Modeling and Global Optimization of DNA separation. (Q38843850) (← links)
- Improved mutation detection in GC-rich DNA fragments by combined DGGE and CDGE. (Q39728473) (← links)
- RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems (Q40882961) (← links)
- First report of a de novo germline mutation in the MLH1 gene (Q40976567) (← links)
- Microsatellite instability and mismatch repair gene inactivation in sporadic pancreatic and colon tumours (Q42112990) (← links)
- Functional characterization of MLH1 missense variants identified in Lynch syndrome patients. (Q42833087) (← links)
- A novel MSH2 germline mutation in a Druze HNPCC family (Q44095031) (← links)
- Association of colonic and endometrial carcinomas in Portuguese families with hereditary nonpolyposis colorectal carcinoma significantly increases the probability of detecting a pathogenic mutation in mismatch repair genes, primarily the MSH2 gene. (Q47278309) (← links)
- Comprehensive functional assessment of MLH1 variants of unknown significance (Q47449157) (← links)
- MSI-L gastric carcinomas share the hMLH1 methylation status of MSI-H carcinomas but not their clinicopathological profile (Q48386704) (← links)
- Mutator phenotypes of common polymorphisms and missense mutations in MSH2. (Q54360036) (← links)
- Genotyping possible polymorphic variants of human mismatch repair genes in healthy Korean individuals and sporadic colorectal cancer patients. (Q54703701) (← links)
- BAT-26 identifies sporadic colorectal cancers with mutator phenotype: a correlative study with clinico-pathological features and mutations in mismatch repair genes. (Q55033193) (← links)
- Two-Dimensional DNA Fingerprinting (Q57569300) (← links)
- Germline and somatic mutations in hMSH6 and hMSH3 in gastrointestinal cancers of the microsatellite mutator phenotype (Q57978009) (← links)
- (Q58006160) (redirect page) (← links)
- Clinical Definition of Hereditary Non-polyposis Colorectal Cancer: A Search for the Impossible? (Q58006247) (← links)
- (Q58079187) (redirect page) (← links)
- Microsatellite instability induced by hydrogen peroxide in Escherichia coli (Q58493764) (← links)
- Causes of microsatellite instability in colorectal tumors (Q58862209) (← links)
- Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein (Q59273299) (← links)
- Methylation pattern of different regions of theMLH1 promoter and silencing of gene expression in hereditary and sporadic colorectal cancer (Q61196002) (← links)