https://ogma.newcastle.edu.au/vital/access/ /manager/Index ${session.getAttribute("locale")} 5 Frequency of the common MYH mutations (G382D and Y165C) in MMR mutation positive and negative HNPCC patients https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:35 Wed 11 Apr 2018 16:59:08 AEST ]]> Deletion mutations in an Australian series of HNPCC patients https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:458 Wed 11 Apr 2018 15:11:16 AEST ]]> Mutation analysis of the MYH gene in an Australian series of colorectal polyposis patients with or without germline APC mutations https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:375 Thu 25 Jul 2013 09:10:05 AEST ]]> The -149C>T SNP within the ΔDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer https://ogma.newcastle.edu.au/vital/access/ /manager/Repository/uon:5537 T polymorphism located within the promoter region of the ΔDNMT3B gene has recently been reported to be associated with a significant increase to the risk of early onset CRC. In this study we determined the ΔDNMT3B genotype in 404 confirmed HNPCC participants (total of 194 CRC cases) from Australia (203) and Poland (201). Front the total number of participants there were 194 diagnosed cases of CRC and 210 healthy MMR gene Mutation carriers. The study was undertaken to assess whether the reported effect observed in a previous study of 146 HNPCC patients is consistent in a larger separate and unrelated participant cohort. Through the statistical tests of Kaplan-Meier survival analysis and Cox hazard regression models we did not observe any significant association between the ΔDNMT3B C>T SNP and early onset CRC in HNPCC patients.]]> Sat 24 Mar 2018 07:46:39 AEDT ]]>