Pages that link to "Q46118451"

The following pages link to The MLH1 D132H variant is associated with susceptibility to sporadic colorectal cancer (Q46118451):

Displaying 39 items.

• Microsatellite instability in colorectal cancer (Q24627393) (← links)
• Comparisons of substitution, insertion and deletion probes for resequencing and mutational analysis using oligonucleotide microarrays (Q24792059) (← links)
• Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesis (Q25257401) (← links)
• Identification and dissection of a complex DNA repair sensitivity phenotype in Baker's yeast (Q27940380) (← links)
• Mismatch repair polymorphisms and colorectal polyps: hMLH1-93G>A variant modifies risk associated with smoking (Q28219035) (← links)
• The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population (Q33343083) (← links)
• Incompatibilities involving yeast mismatch repair genes: a role for genetic modifiers and implications for disease penetrance and variation in genomic mutation rates (Q33345237) (← links)
• Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions (Q33739955) (← links)
• The biochemical basis of microsatellite instability and abnormal immunohistochemistry and clinical behavior in Lynch syndrome: from bench to bedside (Q33762979) (← links)
• Racial differences in MLH1 and MSH2 mutation: an analysis of yellow race and white race based on the InSiGHT database (Q33770899) (← links)
• Hereditary Non-Polyposis Colorectal Cancer: the rise and fall of a confusing term (Q33866105) (← links)
• Mismatch repair polymorphisms and risk of colon cancer, tumour microsatellite instability and interactions with lifestyle factors (Q33990340) (← links)
• Application of molecular diagnostics for the detection of Lynch syndrome (Q34088809) (← links)
• Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study (Q34102606) (← links)
• A novel and rapid method of determining the effect of unclassified MLH1 genetic variants on differential allelic expression (Q34239761) (← links)
• The incidence of Lynch syndrome (Q34560535) (← links)
• Mutations in the MutSalpha interaction interface of MLH1 can abolish DNA mismatch repair (Q35537125) (← links)
• Genetic predisposition to colorectal cancer (Q35930688) (← links)
• Strategies for mapping and cloning quantitative trait genes in rodents (Q36085684) (← links)
• Evolution of the nomenclature for the hereditary colorectal cancer syndromes (Q36246478) (← links)
• Use of microsatellite instability and immunohistochemistry testing for the identification of individuals at risk for Lynch syndrome (Q36246500) (← links)
• Lynch syndrome (hereditary non-polyposis colorectal cancer): current concepts and approaches to management (Q36259687) (← links)
• What are SNPs and haplotypes and how will they help us manage the prevention of adult cancer? (Q36284693) (← links)
• A novel germline MLH1 mutation causing Lynch Syndrome in patients from the Republic of Macedonia (Q36375623) (← links)
• DNA mismatch repair and Lynch syndrome (Q36527421) (← links)
• Pharmacogenomics of colorectal cancer prevention and treatment (Q36597059) (← links)
• Comprehensive molecular analysis of mismatch repair gene defects in suspected Lynch syndrome (hereditary nonpolyposis colorectal cancer) cases (Q37385768) (← links)
• A promoter polymorphism in the hMLH1 gene (-93G/A) associated with sporadic colorectal cancer (Q37407287) (← links)
• Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas (Q37619454) (← links)
• The recent progress of the mechanism and regulation of tumor necrosis in colorectal cancer (Q38533166) (← links)
• Evaluation of CADD Scores in Curated Mismatch Repair Gene Variants Yields a Model for Clinical Validation and Prioritization (Q41076527) (← links)
• Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management (Q42616545) (← links)
• Association between Mismatch-repair Genetic variation and the Risk of Multiple Primary Cancers: A Meta-Analysis (Q44177099) (← links)
• Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR). (Q44498341) (← links)
• Polymorphism of MSH2 Gly322Asp and MLH1 -93G>A in non-familial colon cancer - a case-controlled study (Q47144676) (← links)
• MLH1 -93G>A promoter polymorphism and the risk of microsatellite-unstable colorectal cancer (Q50692777) (← links)
• Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer (Q57569926) (← links)
• Identification of Muir-Torre syndrome among patients with sebaceous tumors and keratoacanthomas (Q61198638) (← links)
• UniProt genomic mapping for deciphering functional effects of missense variants. (Q64970700) (← links)