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dc.contributor.author Kirkpatrick, Robert Daniel en_US
dc.date.accessioned 2007-05-18T12:16:56Z
dc.date.available 2007-05-18T12:16:56Z
dc.date.issued 1999-09-01T00:00:00Z en_US
dc.identifier.uri http://hdl.handle.net/1993/1683
dc.description.abstract DNA damage represents a threat to the livelihood of a cell or organism. This damage must be dealt with in an efficient manner to prevent cell death, or in higher organisms, neoplasia. The study of DNA repair in yeast has been greatly aided by the discovery of radiation-sensitive mutants and their corresponding ' RAD' genes. A loss of function of these 'RAD' or related genes compromises the cell's ability to repair DNA damage. One of the most effective pathways for repairing DNA damage is nucleotide excision repair. Within this pathway, the 'RAD23' gene product plays a crucial, albeit poorly understood role. In this study, three Rad23p-interacting proteins were investigated in order to better understand the role of Rad23p itself. Two of the three proteins investigated were found to be important to cell viability while the remaining protein appeared to be functionally disposable. None of the proteins were found to play a role in DNA repair using the methods in this thesis, suggesting that their interaction with Rad23p is not biologically significant. Alternatively, these genes may be involved with 'RAD23 ' in cellular processes unrelated to DNA repair. en_US
dc.format.extent 6398100 bytes
dc.format.extent 184 bytes
dc.format.mimetype application/pdf
dc.format.mimetype text/plain
dc.language en en_US
dc.language.iso en_US
dc.rights info:eu-repo/semantics/openAccess
dc.title Interactions of the DNA repair protein Rad23 in the yeast two-hybrid system en_US
dc.type info:eu-repo/semantics/masterThesis
dc.degree.discipline Human Genetics en_US
dc.degree.level Master of Science (M.Sc.) en_US


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