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http://arks.princeton.edu/ark:/88435/dsp01qf85nd734Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.advisor | Notterman, Daniel A. | - |
| dc.contributor.author | Wetlinski, Catherine | - |
| dc.date.accessioned | 2016-07-08T14:46:46Z | - |
| dc.date.available | 2016-07-08T14:46:46Z | - |
| dc.date.created | 2016-04-22 | - |
| dc.date.issued | 2016-07-08 | - |
| dc.identifier.uri | http://arks.princeton.edu/ark:/88435/dsp01qf85nd734 | - |
| dc.description.abstract | In this thesis, I set out to examine fertility as a late effect of pediatric cancer therapy. I determine why fertility is an inadequate measure of the reproductive fitness of adult cancer survivors and explore the causes of deficits in fertility after pediatric cancer therapy. I focus mainly on the male germ cell line, exploring various sperm genomic damages that occur as a result of chemotherapy and/or radiotherapy in childhood and adolescence. Although sperm chromosome aneuploidy presents as a consequence of pediatric cancer therapy, I worry more with sperm DNA fragmentation, which includes single-strand and double-strand DNA breaks, which are genotoxic and have the ability to be transmitted to offspring. I find, however, that although DNA-impaired spermatozoa may fertilize an egg, it is unlikely for these damages to remain in the embryo or for the embryo to remain. | en_US |
| dc.format.extent | 75 pages | * |
| dc.language.iso | en_US | en_US |
| dc.title | GERM CELL GENOTOXICITY THE LASTING EFFECTS OF PEDIATRIC CANCER THERAPY | en_US |
| dc.type | Princeton University Senior Theses | - |
| pu.date.classyear | 2016 | en_US |
| pu.department | Molecular Biology | en_US |
| pu.pdf.coverpage | SeniorThesisCoverPage | - |
| Appears in Collections: | Molecular Biology, 1954-2020 | |
Files in This Item:
| File | Size | Format | |
|---|---|---|---|
| WetlinskiCatherine_Thesis.pdf | 354.7 kB | Adobe PDF | Request a copy |
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