Pages that link to "Q28246320"

The following pages link to Molecular basis of HNPCC: mutations of MMR genes (Q28246320):

Displaying 44 items.

• Hereditary nonpolyposis colorectal cancer in 95 families: differences and similarities between mutation-positive and mutation-negative kindreds (Q24535557) (← links)
• Early steps in the DNA base excision/single-strand interruption repair pathway in mammalian cells (Q24650179) (← links)
• N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha (Q24679608) (← links)
• Connecting the Dots: From DNA Damage and Repair to Aging (Q26750854) (← links)
• Crystal structure of Δ-[Ru(bpy)2dppz]2+ bound to mismatched DNA reveals side-by-side metalloinsertion and intercalation (Q27670885) (← links)
• Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma (Q29615026) (← links)
• Investigation on the role of nsSNPs in HNPCC genes--a bioinformatics approach. (Q30376403) (← links)
• Efficiency of Base Excision Repair of Oxidative DNA Damage and Its Impact on the Risk of Colorectal Cancer in the Polish Population (Q30396620) (← links)
• Challenges and pitfalls in HNPCC screening by microsatellite analysis and immunohistochemistry (Q33208352) (← links)
• Stabilization of mismatch repair gene PMS2 by glycogen synthase kinase 3beta is implicated in the treatment of cervical carcinoma (Q33533641) (← links)
• Somatic hypermethylation of MSH2 is a frequent event in Lynch Syndrome colorectal cancers (Q33795280) (← links)
• Immunohistochemical expression of mismatch repair genes: a screening tool for predicting mutator phenotype in liver fluke infection-associated intrahepatic cholangiocarcinoma (Q33866403) (← links)
• The molecular genetics of colorectal cancer (Q34027887) (← links)
• Establishing a cancer genetics programme in Asia - the singapore experience (Q34253892) (← 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)
• Guidance on gastrointestinal surveillance for hereditary non-polyposis colorectal cancer, familial adenomatous polypolis, juvenile polyposis, and Peutz-Jeghers syndrome (Q34526950) (← links)
• DNA mismatch-specific targeting and hypersensitivity of mismatch-repair-deficient cells to bulky rhodium(III) intercalators (Q34572718) (← links)
• Meta-analysis of different test indicators: Helicobacter pylori infection and the risk of colorectal cancer. (Q34592456) (← links)
• Elevated levels of somatic mutation in a manifesting BRCA1 mutation carrier (Q34994680) (← links)
• The role of hypermethylation of the hMLH1 promoter region in HNPCC versus MSI+ sporadic colorectal cancers (Q35435480) (← links)
• Mechanisms of inactivation of mismatch repair genes in human colorectal cancer cell lines: the predominant role of hMLH1. (Q35619996) (← links)
• Assay validation for identification of hereditary nonpolyposis colon cancer-causing mutations in mismatch repair genes MLH1, MSH2, and MSH6 (Q35836701) (← links)
• Hereditary nonpolyposis colorectal cancer (Lynch syndrome): criteria for identification and management (Q36060735) (← links)
• Mutation and methylation of hMLH1 in gastric carcinomas with microsatellite instability (Q36178601) (← links)
• Sebaceous neoplasia and Torre-Muir syndrome. (Q36248563) (← links)
• Mutational targets in colorectal cancer cells with microsatellite instability. (Q36417805) (← links)
• hMSH2 is the most commonly mutated MMR gene in a cohort of Greek HNPCC patients (Q36616145) (← links)
• Methylation of hMLH1 promoter correlates with the gene silencing with a region-specific manner in colorectal cancer (Q36644067) (← links)
• Activity (transcription) of the genes for MLH1, MSH2 and p53 in sporadic colorectal tumours with micro-satellite instability (Q36694101) (← links)
• Oligonucleotide-directed mutagenesis screen to identify pathogenic Lynch syndrome-associated MSH2 DNA mismatch repair gene variants (Q36821500) (← links)
• Molecular Genetics of Colorectal Cancer: An Overview (Q37004224) (← links)
• Deficiencies in Chfr and Mlh1 synergistically enhance tumor susceptibility in mice. (Q37328459) (← links)
• DNA mismatch binding and antiproliferative activity of rhodium metalloinsertors (Q38357043) (← links)
• Haematuria in association with Lynch syndrome (Q38679590) (← links)
• Selective cytotoxicity of rhodium metalloinsertors in mismatch repair-deficient cells (Q39439511) (← links)
• Deletion Mutations in an Australian Series of HNPCC Patients (Q39574011) (← links)
• hMSH2 expression is driven by AP1-dependent regulation through phorbol-ester exposure (Q39936198) (← 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)
• Impact of 226C>T MSH2 gene mutation on cancer phenotypes in two HNPCC-associated highly-consanguineous families from Kuwait: emphasis on premarital genetic testing (Q57729078) (← links)
• Advances in Identification of Susceptibility Gene Defects of Hereditary Colorectal Cancer (Q61809717) (← links)
• [Prophylactic surgery for hereditary non-polyposis colorectal cancer] (Q81489426) (← links)
• Familial/inherited cancer syndrome: a focus on the highly consanguineous Arab population (Q89559254) (← links)
• Chromothripsis and DNA Repair Disorders (Q89919958) (← links)
• HDAC6 regulates DNA damage response via deacetylating MLH1 (Q91633487) (← links)