Pages that link to "Q57200636"
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The following pages link to DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer (Q57200636):
Displaying 50 items.
- Association of hereditary nonpolyposis colorectal cancer-related tumors displaying low microsatellite instability with MSH6 germline mutations. (Q24539206) (← links)
- Inherited colorectal cancer syndromes (Q24628009) (← links)
- Mutations predisposing to hereditary nonpolyposis colorectal cancer (Q28235642) (← links)
- Alterations of copy number of methylation pattern in mismatch repair genes by methylation specific-multiplex ligation-dependent probe amplification in cases of colon cancer (Q28298882) (← links)
- Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer (Q28394400) (← links)
- Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes (Q31804977) (← links)
- The instability within: problems in current analyses of microsatellite instability (Q31833517) (← links)
- Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma: a novel approach (Q33270665) (← links)
- The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population (Q33343083) (← links)
- Gastrointestinal polyposis syndromes (Q33599177) (← links)
- Public health perspectives on testing for colorectal cancer susceptibility genes (Q33644845) (← links)
- The clinical and molecular genetic approach to Duchenne and Becker muscular dystrophy: an updated protocol (Q33679539) (← links)
- Some aspects of molecular diagnostics in Lynch syndrome (Q33722604) (← links)
- Economic and Practical Factors in Diagnosing HNPCC Using Clinical Criteria, Immunohistochemistry and Microsatellite Instability Analysis (Q33732330) (← 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)
- Pedigree and genetic analysis of a novel mutation carrier patient suffering from hereditary nonpolyposis colorectal cancer (Q34013141) (← links)
- Little evidence for involvement of MLH3 in colorectal cancer predisposition (Q34204951) (← links)
- Hereditary non-polyposis colorectal cancer syndrome: combined risk of gastrointestinal and gynaecological cancer (Q34316225) (← links)
- Identification of a splicing enhancer in MLH1 using COMPARE, a new assay for determination of relative RNA splicing efficiencies (Q34446453) (← links)
- Genetic testing for high-risk colon cancer patients (Q34533915) (← links)
- DNA mismatch repair defects: role in colorectal carcinogenesis (Q34568596) (← links)
- A novel c. 204 Ile68Met germline variant in exon 2 of the mutL homolog 1 gene in a colorectal cancer patient. (Q34584251) (← 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)
- Linkage disequilibrium mapping in isolated populations: the example of Finland revisited (Q34754002) (← links)
- Review article: genetic testing and counselling for hereditary colorectal cancer (Q34975833) (← links)
- Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management (Q34977063) (← links)
- CLINICAL MANAGEMENT OF FAMILIES WITH HEREDITARY COLORECTAL CANCER SYNDROMES. (Q35087269) (← links)
- Evaluation of a counselling protocol for predictive genetic testing for hereditary non-polyposis colorectal cancer (Q35434003) (← links)
- Diagnosis and Management of Hereditary Non-Polyposis Colon Cancer (Q35551054) (← links)
- Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing (Q35594437) (← links)
- Endometrial and colorectal tumors from patients with hereditary nonpolyposis colon cancer display different patterns of microsatellite instability (Q35747961) (← links)
- Tracing cell fates in human colorectal tumors from somatic microsatellite mutations: evidence of adenomas with stem cell architecture (Q35753529) (← links)
- Microsatellite instability in adenomas as a marker for hereditary nonpolyposis colorectal cancer (Q35788009) (← links)
- Genetic and epigenetic modification of MLH1 accounts for a major share of microsatellite-unstable colorectal cancers (Q35810106) (← links)
- Ultraviolet radiation and skin cancer: molecular mechanisms (Q36034693) (← links)
- Hereditary non-polyposis colon cancer (Q36198294) (← links)
- Recently identified colon cancer predispositions: MYH and MSH6 mutations (Q36484887) (← links)
- Epigenetic phenotypes distinguish microsatellite-stable and -unstable colorectal cancers (Q36549885) (← links)
- Germline MSH6 mutations are more prevalent in endometrial cancer patient cohorts than hereditary non polyposis colorectal cancer cohorts (Q36677899) (← links)
- Update on Lynch syndrome genomics (Q36990046) (← links)
- Genetic diagnosis strategy of hereditary non-polyposis colorectal cancer (Q37122495) (← links)
- Genomic instability and carcinogenesis: an update. (Q37514904) (← links)
- Genetic counseling considerations in the evaluation of families for Lynch syndrome--a review (Q37798758) (← links)
- Epigenetic mechanisms in the pathogenesis of Lynch syndrome. (Q38180152) (← links)
- Three new mutations in hereditary nonpolyposis colorectal cancer (Lynch syndrome II) in Uruguay (Q40597964) (← links)
- hMLH1 and hMSH2 gene mutations are present in radial growth-phase cutaneous malignant melanoma cell lines and can be induced further by ultraviolet-B irradiation (Q40600852) (← links)
- Mosaic AZF deletions and susceptibility to testicular tumors (Q40727010) (← links)
- RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems (Q40882961) (← links)