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dc.contributor.authorDrake, Kennethen_US
dc.date.accessioned2008-08-08T02:31:05Z
dc.date.available2008-08-08T02:31:05Z
dc.date.issued2008-08-08T02:31:05Z
dc.date.submittedDecember 2007en_US
dc.identifier.otherDISS-1996en_US
dc.identifier.urihttp://hdl.handle.net/10106/912
dc.description.abstractRalbp1 is a multi-specific transporter of glutathione conjugates as well as unconjugated amphiphilic toxins. Because glutathione conjugates are major metabolites of toxic lipid peroxidation products generated as a consequence of oxidant and radiant stress, the hypothesis is put forth that the function of Ralbp1 in-vivo and in vitro should be to protect organisms from chemical stress by removing toxic chemicals. Studies described in this dissertation were designed to prove this hypothesis. We tested the hypothesis by examining whether the inhibition or augmentation of Ralbp1 would sensitize or protect cells and whole animals from the toxic effects of chemicals and radiation. These studies establish that Ralbp1 is a primary determinant of resistance to chemical stressors by the direct transport of these toxins.en_US
dc.description.sponsorshipAwasthi, Sanjayen_US
dc.language.isoENen_US
dc.publisherChemistry & Biochemistryen_US
dc.titleRalbp1 In Stress Resistanceen_US
dc.typePh.D.en_US
dc.contributor.committeeChairAwasthi, Sanjayen_US
dc.degree.departmentChemistry & Biochemistryen_US
dc.degree.disciplineChemistry & Biochemistryen_US
dc.degree.grantorUniversity of Texas at Arlingtonen_US
dc.degree.leveldoctoralen_US
dc.degree.namePh.D.en_US


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