Pages that link to "Q24671692"

The following pages link to Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis (Q24671692):

Displaying 32 items.

• Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds (Q24535557) (← links)
• The association between genetic variants in hMLH1 and hMSH2 and the development of sporadic colorectal cancer in the Danish population (Q33343083) (← links)
• Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation. (Q33677624) (← links)
• Microsatellite instability in early onset and familial colorectal cancer. (Q33678081) (← links)
• Psychological distress in applicants for predictive DNA testing for autosomal dominant, heritable, late onset disorders. The Rotterdam/Leiden Genetics Workgroup. (Q33678811) (← links)
• Predicting adaptation to presymptomatic DNA testing for late onset disorders: who will experience distress? Rotterdam Leiden Genetics Workgroup (Q33681277) (← links)
• Germline MLH1 and MSH2 mutational spectrum including frequent large genomic aberrations in Hungarian hereditary non-polyposis colorectal cancer families: implications for genetic testing (Q34100062) (← links)
• Muir-Torre Phenotype Has a Frequency of DNA Mismatch-Repair-Gene Mutations Similar to That in Hereditary Nonpolyposis Colorectal Cancer Families Defined by the Amsterdam Criteria (Q34386209) (← links)
• Clinicopathological and molecular genetic analysis of HNPCC in China (Q35011402) (← links)
• Hereditary non-polyposis colorectal cancer: clinical and molecular evidence for a new entity of hereditary colorectal cancer (Q35597944) (← links)
• Conventional and tissue microarray immunohistochemical expression analysis of mismatch repair in hereditary colorectal tumors (Q35748966) (← links)
• Majority of hMLH1 mutations responsible for hereditary nonpolyposis colorectal cancer cluster at the exonic region 15-16 (Q35881396) (← links)
• RNA-based mutation screening in hereditary nonpolyposis colorectal cancer (Q35882089) (← links)
• Hereditary desmoid disease due to a frameshift mutation at codon 1924 of the APC gene (Q35882235) (← links)
• Genetic detection of Chinese hereditary nonpolyposis colorectal cancer. (Q36474384) (← links)
• Lynch or Not Lynch? Is that Always a Question? (Q37994931) (← links)
• The genetics of inherited colon cancer (Q40849233) (← links)
• DNA mismatch repair gene mutations in human cancer (Q41561505) (← links)
• Mutation screening of MSH2 and MLH1 mRNA in hereditary non-polyposis colon cancer syndrome (Q42026314) (← links)
• Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations (Q42037545) (← links)
• Prediction‐based threading of the hMSH2 DNA mismatch repair protein (Q45988031) (← links)
• Does mutation of transforming growth factor-beta type II receptor gene play an important role in colorectal polyps? (Q46778172) (← links)
• A Comparison Between Denaturing Gradient Gel Electrophoresis and Denaturing High Performance Liquid Chromatography in Detecting Mutations in Genes Associated with Hereditary Non-Polyposis Colorectal Cancer (HNPCC) and the Identification of 9 New Mut (Q49466011) (← links)
• Cumulative incidence of colorectal and extracolonic cancers in MLH1 and MSH2 mutation carriers of hereditary nonpolyposis colorectal cancer (Q50854368) (← links)
• Is MSH2 a breast cancer susceptibility gene? (Q53227682) (← links)
• Genotyping possible polymorphic variants of human mismatch repair genes in healthy Korean individuals and sporadic colorectal cancer patients. (Q54703701) (← links)
• Loss or somatic mutations of hMSH2 occur in hereditary nonpolyposis colorectal cancers with hMSH2 germline mutations. (Q55034846) (← links)
• CpG dinucleotides in the hMSH2 and hMLH1 genes are hotspots for HNPCC mutations. (Q55066383) (← links)
• Does the occurrence of certain rare cancers indicate an inherited cancer susceptibility? (Q59159730) (← links)
• Identification and surveillance of 19 Lynch syndrome families in southern Italy: report of six novel germline mutations and a common founder mutation (Q60023148) (← links)
• Reduction in hMSH2 mRNA levels by premature translation termination: implications for mutation screening in hereditary nonpolyposis colorectal cancer (Q74610810) (← links)
• Germline mutations of the hMLH1 and hMSH2 mismatch repair genes in Belgian hereditary nonpolyposis colon cancer (HNPCC) patients (Q83879718) (← links)