About this item
- Title
- Endometrial Cancer and Copy Number Variation
- Content partner
- University of Otago
- Collection
- Otago University Research Archive
- Description
Endometrial cancer is the most common gynaecological cancer in New Zealand and the incidence is increasing as the population ages. Genetic predictors of endometrial cancer risk that allow early detection of the disease are important for prevention and improved management strategies. Mutations in the mismatch repair (MMR) genes MLH1, MSH2, MSH6, PMS1 and PMS2 are known to confer increased risk in a proportion of endometrial cancer cases, and the mutation spectrum includes copy number variants ...
- Format
- Research paper
- Research format
- Scholarly text / Thesis
- Thesis level
- Masters
- Date created
- 2013
- Creator
- Moir-Meyer, Gemma
- URL
- https://hdl.handle.net/10523/4170
- Related subjects
- copy number variation / CNV / loading / CNV load / mismatch repair pathway / candidate gene / MSH2 / MSH6 / MUTYH / RPA3 / TGFBR3 / genome wide association study / GWAS / PennCNV / CNV frequency / rare CNVs / common CNVs / deletion / duplication / copy number gain / copy number loss / endometrial cancer
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Report this itemDigitalNZ brings together more than 30 million items from institutions so that they are easy to find and use. This information is the best information we could find on this item. This item was added on 05 February 2015, and updated 28 February 2025.
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