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This data provides the basis for further research to delineate the role of novel genes in XRT-induced CNS injury. JAK3 will be studied as a potential neuro-protective target from XRT injury.The possibility of damaging the central nervous system (CNS) is a major problem in clinical radiation treatment (XRT). Using cDNA microarray, we studied global gene expression in mouse brain within 24 h following clinically relevant doses of XRT.Early response of mouse brain to XRT is a complex process that involves dose- and time-dependent expression of hundreds of genes and modulates different molecular functions and pathways. Genes involved in signal transduction, metabolism, structural proteins, transcription, and cell cycle were modulated by XRT in mouse brain. Using real time PCR, we confirmed changes in expression of DNA fragmentation factor, beta subunit, nuclease sensitive element binding protein 1, Janus kinase3 (JAK3), and Telomeric repeat binding factor 1. Upregulation of JAK3 expression was demonstrated by immunohistochemistry.
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Early gene expression profile in mouse brain after exposure to clinically relevant doses of ionizing radiation.
2005
in English
0494073853 9780494073858
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Source: Masters Abstracts International, Volume: 44-02, page: 0779.
Thesis (M.Sc.)--University of Toronto, 2005.
Electronic version licensed for access by U. of T. users.
GERSTEIN MICROTEXT copy on microfiche (2 microfiches).
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