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You searched for +publisher:"University of Kansas" +contributor:("Klaassen, Curtis D."). Showing records 1 – 12 of 12 total matches.

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University of Kansas

1. Zhang, Youcai. CHARACTERIZATION OF ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A1 (OATP1A1) IN THE BILE ACID HOMEOSTASIS OF MICE.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2011, University of Kansas

 Organic anion transporting polypeptides (human: OATPs; all other species: Oatps; gene symbol: SLCO/Slco) are sodium-independent transport systems that mediate the transmembrane transport of a wide… (more)

Subjects/Keywords: Toxicology; Bile acids; Cholestasis; Intestinal bacteria; Organic anion transporting polypeptide

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APA (6th Edition):

Zhang, Y. (2011). CHARACTERIZATION OF ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A1 (OATP1A1) IN THE BILE ACID HOMEOSTASIS OF MICE. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7930

Chicago Manual of Style (16th Edition):

Zhang, Youcai. “CHARACTERIZATION OF ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A1 (OATP1A1) IN THE BILE ACID HOMEOSTASIS OF MICE.” 2011. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/7930.

MLA Handbook (7th Edition):

Zhang, Youcai. “CHARACTERIZATION OF ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A1 (OATP1A1) IN THE BILE ACID HOMEOSTASIS OF MICE.” 2011. Web. 24 Apr 2019.

Vancouver:

Zhang Y. CHARACTERIZATION OF ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A1 (OATP1A1) IN THE BILE ACID HOMEOSTASIS OF MICE. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/7930.

Council of Science Editors:

Zhang Y. CHARACTERIZATION OF ORGANIC ANION TRANSPORTING POLYPEPTIDE 1A1 (OATP1A1) IN THE BILE ACID HOMEOSTASIS OF MICE. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/7930


University of Kansas

2. Saito, Chieko. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Acetaminophen (APAP) is a widely used analgesic, which is safe at therapeutic levels. APAP is mainly conjugated with glucuronic acid and sulfate to form water-soluble,… (more)

Subjects/Keywords: Health sciences; Toxicology; Acetaminophen; C-jun n-terminal kinase; Glutathione; Metallothionein; N-acetylcysteine

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APA (6th Edition):

Saito, C. (2010). PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6369

Chicago Manual of Style (16th Edition):

Saito, Chieko. “PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/6369.

MLA Handbook (7th Edition):

Saito, Chieko. “PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY.” 2010. Web. 24 Apr 2019.

Vancouver:

Saito C. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/6369.

Council of Science Editors:

Saito C. PROTECTIVE STRATEGIES AGAINST ACETAMINOPHEN INDUCED HEPATOTOXICITY. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6369


University of Kansas

3. Weaver, Yi Miao. STRUCTURAL REQUIREMENTS OF ORGANIC ANION TRANSPORTING POLYPEPTIDE MEDIATED TRANSPORT.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 The organic anion transporting polypeptides (human: OATP; other: Oatp) form a mammalian transporter superfamily that mediates the transport of structurally unrelated compounds across the cell… (more)

Subjects/Keywords: Health sciences; Pharmacology; Biology; Physiology; Oatp; Organic anion; Perfluoronated carboxylates; Pfca; Structure; Transporters

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APA (6th Edition):

Weaver, Y. M. (2010). STRUCTURAL REQUIREMENTS OF ORGANIC ANION TRANSPORTING POLYPEPTIDE MEDIATED TRANSPORT. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7394

Chicago Manual of Style (16th Edition):

Weaver, Yi Miao. “STRUCTURAL REQUIREMENTS OF ORGANIC ANION TRANSPORTING POLYPEPTIDE MEDIATED TRANSPORT.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/7394.

MLA Handbook (7th Edition):

Weaver, Yi Miao. “STRUCTURAL REQUIREMENTS OF ORGANIC ANION TRANSPORTING POLYPEPTIDE MEDIATED TRANSPORT.” 2010. Web. 24 Apr 2019.

Vancouver:

Weaver YM. STRUCTURAL REQUIREMENTS OF ORGANIC ANION TRANSPORTING POLYPEPTIDE MEDIATED TRANSPORT. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/7394.

Council of Science Editors:

Weaver YM. STRUCTURAL REQUIREMENTS OF ORGANIC ANION TRANSPORTING POLYPEPTIDE MEDIATED TRANSPORT. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7394


University of Kansas

4. Cui, Yue. DEVELOPMENTAL REGULATION OF THE DRUG-PROCESSING GENOME IN MOUSE LIVER.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Despite the recent progress in understanding the expression patterns and regulatory mechanisms of drug-processing genes, namely phase-I and -II drug metabolizing enzymes and transporters in… (more)

Subjects/Keywords: Health sciences; Toxicology; Pharmacology; Molecular biology; Bile acids; Drug metabolism; Epigenetics; Liver development; Nuclear receptors; Transporters

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APA (6th Edition):

Cui, Y. (2010). DEVELOPMENTAL REGULATION OF THE DRUG-PROCESSING GENOME IN MOUSE LIVER. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/6777

Chicago Manual of Style (16th Edition):

Cui, Yue. “DEVELOPMENTAL REGULATION OF THE DRUG-PROCESSING GENOME IN MOUSE LIVER.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/6777.

MLA Handbook (7th Edition):

Cui, Yue. “DEVELOPMENTAL REGULATION OF THE DRUG-PROCESSING GENOME IN MOUSE LIVER.” 2010. Web. 24 Apr 2019.

Vancouver:

Cui Y. DEVELOPMENTAL REGULATION OF THE DRUG-PROCESSING GENOME IN MOUSE LIVER. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/6777.

Council of Science Editors:

Cui Y. DEVELOPMENTAL REGULATION OF THE DRUG-PROCESSING GENOME IN MOUSE LIVER. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/6777


University of Kansas

5. Fu, Zidong. Regulation of Xenobiotic and Bile Acid Metabolism by the Anti-aging Intervention Calorie Restriction in Mice.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2013, University of Kansas

 Calorie restriction (CR), defined as reduced calorie intake without causing malnutrition, is the best-known intervention to increase life span and slow aging-related diseases in various… (more)

Subjects/Keywords: Toxicology; Pharmacology; Animal sciences; aging; bile acids; calorie restriction; xenobiotic metabolism and detoxification

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APA (6th Edition):

Fu, Z. (2013). Regulation of Xenobiotic and Bile Acid Metabolism by the Anti-aging Intervention Calorie Restriction in Mice. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/19597

Chicago Manual of Style (16th Edition):

Fu, Zidong. “Regulation of Xenobiotic and Bile Acid Metabolism by the Anti-aging Intervention Calorie Restriction in Mice.” 2013. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/19597.

MLA Handbook (7th Edition):

Fu, Zidong. “Regulation of Xenobiotic and Bile Acid Metabolism by the Anti-aging Intervention Calorie Restriction in Mice.” 2013. Web. 24 Apr 2019.

Vancouver:

Fu Z. Regulation of Xenobiotic and Bile Acid Metabolism by the Anti-aging Intervention Calorie Restriction in Mice. [Internet] [Doctoral dissertation]. University of Kansas; 2013. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/19597.

Council of Science Editors:

Fu Z. Regulation of Xenobiotic and Bile Acid Metabolism by the Anti-aging Intervention Calorie Restriction in Mice. [Doctoral Dissertation]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/19597


University of Kansas

6. Selwyn Samraj, Felcy Pavithra. Alterations in bile acid homeostasis and drug metabolism in germ-free mice.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2014, University of Kansas

 "We may be born 100% human but will die 90% bacterial – a truly complex organism!" (Goodacre, 2007). This statement reflects the fact that there are… (more)

Subjects/Keywords: Toxicology; Physiology; Bile acid; Drug metabolism; Germ-free mice

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APA (6th Edition):

Selwyn Samraj, F. P. (2014). Alterations in bile acid homeostasis and drug metabolism in germ-free mice. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/23957

Chicago Manual of Style (16th Edition):

Selwyn Samraj, Felcy Pavithra. “Alterations in bile acid homeostasis and drug metabolism in germ-free mice.” 2014. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/23957.

MLA Handbook (7th Edition):

Selwyn Samraj, Felcy Pavithra. “Alterations in bile acid homeostasis and drug metabolism in germ-free mice.” 2014. Web. 24 Apr 2019.

Vancouver:

Selwyn Samraj FP. Alterations in bile acid homeostasis and drug metabolism in germ-free mice. [Internet] [Doctoral dissertation]. University of Kansas; 2014. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/23957.

Council of Science Editors:

Selwyn Samraj FP. Alterations in bile acid homeostasis and drug metabolism in germ-free mice. [Doctoral Dissertation]. University of Kansas; 2014. Available from: http://hdl.handle.net/1808/23957


University of Kansas

7. Pacyniak, Erik Kristofer. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 Polybrominated diphenyl ethers (PBDEs) were introduced in the late 1970's as additive flame retardants incorporated into textiles, electronics, plastics and furniture. Although 2,2',3,3',4,4',5,5',6,6'-decabromodiphenyl ether (BDE209)… (more)

Subjects/Keywords: Toxicology; Constitutive androstane receptor; Nuclear receptors; Organic anion transporting polypeptide; Polybrominated diphenyl ethers; Pregnane x receptor

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APA (6th Edition):

Pacyniak, E. K. (2010). Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7717

Chicago Manual of Style (16th Edition):

Pacyniak, Erik Kristofer. “Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/7717.

MLA Handbook (7th Edition):

Pacyniak, Erik Kristofer. “Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver.” 2010. Web. 24 Apr 2019.

Vancouver:

Pacyniak EK. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/7717.

Council of Science Editors:

Pacyniak EK. Molecular Mechanism of Polybrominated Diphenyl Ether Disposition in the Liver. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7717


University of Kansas

8. Wang, Pan. Computational Molecular Modeling Studies of the Interactions of Estrogens with Their Receptors and Intracellular Estrogen Binding Protein PDIp.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 The endogenous estrogens are vitally-important female sex hormones with diverse biological functions. Disruption of their actions contributes to the pathogenesis of a number of disease… (more)

Subjects/Keywords: Pharmacology; Antiestrogen; Estrogen; Estrogen receptor; Molecular docking; Molecular modeling; Pdip

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APA (6th Edition):

Wang, P. (2010). Computational Molecular Modeling Studies of the Interactions of Estrogens with Their Receptors and Intracellular Estrogen Binding Protein PDIp. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7432

Chicago Manual of Style (16th Edition):

Wang, Pan. “Computational Molecular Modeling Studies of the Interactions of Estrogens with Their Receptors and Intracellular Estrogen Binding Protein PDIp.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/7432.

MLA Handbook (7th Edition):

Wang, Pan. “Computational Molecular Modeling Studies of the Interactions of Estrogens with Their Receptors and Intracellular Estrogen Binding Protein PDIp.” 2010. Web. 24 Apr 2019.

Vancouver:

Wang P. Computational Molecular Modeling Studies of the Interactions of Estrogens with Their Receptors and Intracellular Estrogen Binding Protein PDIp. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/7432.

Council of Science Editors:

Wang P. Computational Molecular Modeling Studies of the Interactions of Estrogens with Their Receptors and Intracellular Estrogen Binding Protein PDIp. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7432


University of Kansas

9. Song, Peizhen. EFFECT OF BILE ACID FEEDING AND SEQUESTRATION ON LIVER BILE ACID COMPOSITION AND GENE REGULATION IN MICE.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2010, University of Kansas

 The dissertation investigates the non-hepatotoxic doses of five bile acids (BAs) in the feed of mice, as well as adaptations in the expression of genes… (more)

Subjects/Keywords: Toxicology; Pathology; Bile acids; Cholestyramine resin; Cyp7a1; Cyp8b1; Fgf15; Fxr

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APA (6th Edition):

Song, P. (2010). EFFECT OF BILE ACID FEEDING AND SEQUESTRATION ON LIVER BILE ACID COMPOSITION AND GENE REGULATION IN MICE. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7756

Chicago Manual of Style (16th Edition):

Song, Peizhen. “EFFECT OF BILE ACID FEEDING AND SEQUESTRATION ON LIVER BILE ACID COMPOSITION AND GENE REGULATION IN MICE.” 2010. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/7756.

MLA Handbook (7th Edition):

Song, Peizhen. “EFFECT OF BILE ACID FEEDING AND SEQUESTRATION ON LIVER BILE ACID COMPOSITION AND GENE REGULATION IN MICE.” 2010. Web. 24 Apr 2019.

Vancouver:

Song P. EFFECT OF BILE ACID FEEDING AND SEQUESTRATION ON LIVER BILE ACID COMPOSITION AND GENE REGULATION IN MICE. [Internet] [Doctoral dissertation]. University of Kansas; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/7756.

Council of Science Editors:

Song P. EFFECT OF BILE ACID FEEDING AND SEQUESTRATION ON LIVER BILE ACID COMPOSITION AND GENE REGULATION IN MICE. [Doctoral Dissertation]. University of Kansas; 2010. Available from: http://hdl.handle.net/1808/7756

10. Wu, Kai Connie. THE ROLE OF NRF2 IN PREVENTING OXIDATIVE/ELECTROPHILIC STRESS-INDUCED LIVER INJURY.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2012, University of Kansas

 Redox maintenance is critical for all biological species. Amplification of mechanisms that reduces oxidative/electrophilic stress promotes health and extends life. Nuclear factor, erythroid derived 2,… (more)

Subjects/Keywords: Toxicology; High throughput screening; Liver; Microarray; Nrf2; Oxidative stress

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APA (6th Edition):

Wu, K. C. (2012). THE ROLE OF NRF2 IN PREVENTING OXIDATIVE/ELECTROPHILIC STRESS-INDUCED LIVER INJURY. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/10289

Chicago Manual of Style (16th Edition):

Wu, Kai Connie. “THE ROLE OF NRF2 IN PREVENTING OXIDATIVE/ELECTROPHILIC STRESS-INDUCED LIVER INJURY.” 2012. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/10289.

MLA Handbook (7th Edition):

Wu, Kai Connie. “THE ROLE OF NRF2 IN PREVENTING OXIDATIVE/ELECTROPHILIC STRESS-INDUCED LIVER INJURY.” 2012. Web. 24 Apr 2019.

Vancouver:

Wu KC. THE ROLE OF NRF2 IN PREVENTING OXIDATIVE/ELECTROPHILIC STRESS-INDUCED LIVER INJURY. [Internet] [Doctoral dissertation]. University of Kansas; 2012. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/10289.

Council of Science Editors:

Wu KC. THE ROLE OF NRF2 IN PREVENTING OXIDATIVE/ELECTROPHILIC STRESS-INDUCED LIVER INJURY. [Doctoral Dissertation]. University of Kansas; 2012. Available from: http://hdl.handle.net/1808/10289

11. Hart, Steven N. NEW APPROACHES IN UNDERSTANDING DRUG METABOLISM.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2011, University of Kansas

 Limitations in technology, such as DNA sequencing and appropriate model systems, have made it difficult to understand the genetic and non-genetic factors that influence the… (more)

Subjects/Keywords: Pharmacology; Genetics

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APA (6th Edition):

Hart, S. N. (2011). NEW APPROACHES IN UNDERSTANDING DRUG METABOLISM. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/7921

Chicago Manual of Style (16th Edition):

Hart, Steven N. “NEW APPROACHES IN UNDERSTANDING DRUG METABOLISM.” 2011. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/7921.

MLA Handbook (7th Edition):

Hart, Steven N. “NEW APPROACHES IN UNDERSTANDING DRUG METABOLISM.” 2011. Web. 24 Apr 2019.

Vancouver:

Hart SN. NEW APPROACHES IN UNDERSTANDING DRUG METABOLISM. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/7921.

Council of Science Editors:

Hart SN. NEW APPROACHES IN UNDERSTANDING DRUG METABOLISM. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/7921


University of Kansas

12. Reisman, Scott Aaron. PHARMACOLOGIC AND TRANSGENIC ACTIVATION OF NUCLEAR FACTOR-ERYTHROID 2-RELATED FACTOR 2 (NRF2) ALTERS KINETICS AND TOXICODYNAMICS OF XENOBIOTICS.

Degree: PhD, Pharmacology, Toxicology & Therapeutics, 2008, University of Kansas

 Nuclear factor erythroid 2-related factor 2 (Nrf2) is a transcription factor, which, upon translocation into the nucleus, is capable of inducing a variety of cytoprotective… (more)

Subjects/Keywords: Health sciences; Toxicology; Pharmacology; Acetaminophen; Electrophilic stress; Glutathione-s-transferases; Nad(p)h:quinone oxidoreductase; Nrf2; Oxidative stress

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APA (6th Edition):

Reisman, S. A. (2008). PHARMACOLOGIC AND TRANSGENIC ACTIVATION OF NUCLEAR FACTOR-ERYTHROID 2-RELATED FACTOR 2 (NRF2) ALTERS KINETICS AND TOXICODYNAMICS OF XENOBIOTICS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/4325

Chicago Manual of Style (16th Edition):

Reisman, Scott Aaron. “PHARMACOLOGIC AND TRANSGENIC ACTIVATION OF NUCLEAR FACTOR-ERYTHROID 2-RELATED FACTOR 2 (NRF2) ALTERS KINETICS AND TOXICODYNAMICS OF XENOBIOTICS.” 2008. Doctoral Dissertation, University of Kansas. Accessed April 24, 2019. http://hdl.handle.net/1808/4325.

MLA Handbook (7th Edition):

Reisman, Scott Aaron. “PHARMACOLOGIC AND TRANSGENIC ACTIVATION OF NUCLEAR FACTOR-ERYTHROID 2-RELATED FACTOR 2 (NRF2) ALTERS KINETICS AND TOXICODYNAMICS OF XENOBIOTICS.” 2008. Web. 24 Apr 2019.

Vancouver:

Reisman SA. PHARMACOLOGIC AND TRANSGENIC ACTIVATION OF NUCLEAR FACTOR-ERYTHROID 2-RELATED FACTOR 2 (NRF2) ALTERS KINETICS AND TOXICODYNAMICS OF XENOBIOTICS. [Internet] [Doctoral dissertation]. University of Kansas; 2008. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1808/4325.

Council of Science Editors:

Reisman SA. PHARMACOLOGIC AND TRANSGENIC ACTIVATION OF NUCLEAR FACTOR-ERYTHROID 2-RELATED FACTOR 2 (NRF2) ALTERS KINETICS AND TOXICODYNAMICS OF XENOBIOTICS. [Doctoral Dissertation]. University of Kansas; 2008. Available from: http://hdl.handle.net/1808/4325

.