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Please use this identifier to cite or link to this item: http://arks.princeton.edu/ark:/88435/dsp01qf85nd734
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dc.contributor.advisorNotterman, Daniel A.-
dc.contributor.authorWetlinski, Catherine-
dc.date.accessioned2016-07-08T14:46:46Z-
dc.date.available2016-07-08T14:46:46Z-
dc.date.created2016-04-22-
dc.date.issued2016-07-08-
dc.identifier.urihttp://arks.princeton.edu/ark:/88435/dsp01qf85nd734-
dc.description.abstractIn 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.extent75 pages*
dc.language.isoen_USen_US
dc.titleGERM CELL GENOTOXICITY THE LASTING EFFECTS OF PEDIATRIC CANCER THERAPYen_US
dc.typePrinceton University Senior Theses-
pu.date.classyear2016en_US
pu.departmentMolecular Biologyen_US
pu.pdf.coverpageSeniorThesisCoverPage-
Appears in Collections:Molecular Biology, 1954-2020

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