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School of Biological Sciences
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Gene expression profiling supports the hypothesis that human ovarian surface epithelia are multipotent and capable of serving as ovarian cancer initiating cells
Evidence that p53-mediated cell-cycle-arrest inhibits chemotherapeutic treatment of ovarian carcinomas
LTR retrotransposons and the evolution of dosage compensation in Drosophila
Identification of candidate methylation-responsive genes in ovarian cancer
Epigenetic changes within the promoter region of the HLA-G gene in ovarian tumors