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You searched for subject:(Drug metabolism). Showing records 1 – 30 of 318 total matches.

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University of Manchester

1. Sall, Carolina. In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions:Towards a Physiologically-Based Pharmacokinetic Model.

Degree: 2013, University of Manchester

 Repaglinide is currently recommended as an in vivo CYP2C8 probe by the U.S. Food and Drug Administration (FDA), but the kinetic characterisation and enzymes involved… (more)

Subjects/Keywords: repaglinide; drug metabolism

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Sall, C. (2013). In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions:Towards a Physiologically-Based Pharmacokinetic Model. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201277

Chicago Manual of Style (16th Edition):

Sall, Carolina. “In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions:Towards a Physiologically-Based Pharmacokinetic Model.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 18, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201277.

MLA Handbook (7th Edition):

Sall, Carolina. “In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions:Towards a Physiologically-Based Pharmacokinetic Model.” 2013. Web. 18 Jan 2021.

Vancouver:

Sall C. In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions:Towards a Physiologically-Based Pharmacokinetic Model. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Jan 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201277.

Council of Science Editors:

Sall C. In Vitro-In Vivo Assessment of Repaglinide Metabolism and Drug-Drug Interactions:Towards a Physiologically-Based Pharmacokinetic Model. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201277


University of Manchester

2. Wood, Francesca Leanne. Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance.

Degree: 2016, University of Manchester

 As a critical parameter in pharmacokinetics, prediction of clearance is an integral aspect of drug discovery programmes. Since the liver is the major site of… (more)

Subjects/Keywords: hepatocytes; hepatic clearance; drug metabolism

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APA (6th Edition):

Wood, F. L. (2016). Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576

Chicago Manual of Style (16th Edition):

Wood, Francesca Leanne. “Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance.” 2016. Doctoral Dissertation, University of Manchester. Accessed January 18, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576.

MLA Handbook (7th Edition):

Wood, Francesca Leanne. “Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance.” 2016. Web. 18 Jan 2021.

Vancouver:

Wood FL. Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Jan 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576.

Council of Science Editors:

Wood FL. Optimisation of In Vitro Methodology for Drug Metabolism Studies to Improve Prediction of Hepatic Drug Clearance. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301576


University of Toronto

3. Utgikar, Rucha. Down-regulation of Cytochrome P450 2C8 by 3-methylcholanthrene in Human Hepatocellualar Carcinoma Cell Lines.

Degree: 2012, University of Toronto

3-Methylcholanthrene (MC) is a model polycyclic aromatic hydrocarbon that induces cytochrome P450 1A1 (CYP1A1) expression. This laboratory has shown previously that aromatic hydrocarbons, which are… (more)

Subjects/Keywords: drug metabolism; CYP2C8; 0419

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APA (6th Edition):

Utgikar, R. (2012). Down-regulation of Cytochrome P450 2C8 by 3-methylcholanthrene in Human Hepatocellualar Carcinoma Cell Lines. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32636

Chicago Manual of Style (16th Edition):

Utgikar, Rucha. “Down-regulation of Cytochrome P450 2C8 by 3-methylcholanthrene in Human Hepatocellualar Carcinoma Cell Lines.” 2012. Masters Thesis, University of Toronto. Accessed January 18, 2021. http://hdl.handle.net/1807/32636.

MLA Handbook (7th Edition):

Utgikar, Rucha. “Down-regulation of Cytochrome P450 2C8 by 3-methylcholanthrene in Human Hepatocellualar Carcinoma Cell Lines.” 2012. Web. 18 Jan 2021.

Vancouver:

Utgikar R. Down-regulation of Cytochrome P450 2C8 by 3-methylcholanthrene in Human Hepatocellualar Carcinoma Cell Lines. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1807/32636.

Council of Science Editors:

Utgikar R. Down-regulation of Cytochrome P450 2C8 by 3-methylcholanthrene in Human Hepatocellualar Carcinoma Cell Lines. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32636

4. Koppel, Nitzan. Characterization of a widely distributed cardiac drug-inactivating enzyme from the human gut bacterium Eggerthella lenta.

Degree: PhD, 2018, Harvard University

 The human body is colonized by trillions of microorganisms that are increasingly implicated in modulating human health and disease. In particular, the human gut microbiota… (more)

Subjects/Keywords: Gut microbiota; drug metabolism; biochemistry

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APA (6th Edition):

Koppel, N. (2018). Characterization of a widely distributed cardiac drug-inactivating enzyme from the human gut bacterium Eggerthella lenta. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41129160

Chicago Manual of Style (16th Edition):

Koppel, Nitzan. “Characterization of a widely distributed cardiac drug-inactivating enzyme from the human gut bacterium Eggerthella lenta.” 2018. Doctoral Dissertation, Harvard University. Accessed January 18, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41129160.

MLA Handbook (7th Edition):

Koppel, Nitzan. “Characterization of a widely distributed cardiac drug-inactivating enzyme from the human gut bacterium Eggerthella lenta.” 2018. Web. 18 Jan 2021.

Vancouver:

Koppel N. Characterization of a widely distributed cardiac drug-inactivating enzyme from the human gut bacterium Eggerthella lenta. [Internet] [Doctoral dissertation]. Harvard University; 2018. [cited 2021 Jan 18]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41129160.

Council of Science Editors:

Koppel N. Characterization of a widely distributed cardiac drug-inactivating enzyme from the human gut bacterium Eggerthella lenta. [Doctoral Dissertation]. Harvard University; 2018. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41129160


University of Manchester

5. Sall, Carolina. In vitro-in vivo assessment of repaglinide metabolism and drug-drug interactions : towards a physiologically-based pharmacokinetic model.

Degree: PhD, 2013, University of Manchester

 Repaglinide is currently recommended as an in vivo CYP2C8 probe by the U.S. Food and Drug Administration (FDA), but the kinetic characterisation and enzymes involved… (more)

Subjects/Keywords: 610; repaglinide; drug metabolism

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APA (6th Edition):

Sall, C. (2013). In vitro-in vivo assessment of repaglinide metabolism and drug-drug interactions : towards a physiologically-based pharmacokinetic model. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/in-vitroin-vivo-assessment-of-repaglinide-metabolism-and-drugdrug-interactionstowards-a-physiologicallybased-pharmacokinetic-model(1b8eca49-bc68-484e-b921-2e324b4c5f00).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756781

Chicago Manual of Style (16th Edition):

Sall, Carolina. “In vitro-in vivo assessment of repaglinide metabolism and drug-drug interactions : towards a physiologically-based pharmacokinetic model.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 18, 2021. https://www.research.manchester.ac.uk/portal/en/theses/in-vitroin-vivo-assessment-of-repaglinide-metabolism-and-drugdrug-interactionstowards-a-physiologicallybased-pharmacokinetic-model(1b8eca49-bc68-484e-b921-2e324b4c5f00).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756781.

MLA Handbook (7th Edition):

Sall, Carolina. “In vitro-in vivo assessment of repaglinide metabolism and drug-drug interactions : towards a physiologically-based pharmacokinetic model.” 2013. Web. 18 Jan 2021.

Vancouver:

Sall C. In vitro-in vivo assessment of repaglinide metabolism and drug-drug interactions : towards a physiologically-based pharmacokinetic model. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Jan 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/in-vitroin-vivo-assessment-of-repaglinide-metabolism-and-drugdrug-interactionstowards-a-physiologicallybased-pharmacokinetic-model(1b8eca49-bc68-484e-b921-2e324b4c5f00).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756781.

Council of Science Editors:

Sall C. In vitro-in vivo assessment of repaglinide metabolism and drug-drug interactions : towards a physiologically-based pharmacokinetic model. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/in-vitroin-vivo-assessment-of-repaglinide-metabolism-and-drugdrug-interactionstowards-a-physiologicallybased-pharmacokinetic-model(1b8eca49-bc68-484e-b921-2e324b4c5f00).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.756781


Rice University

6. Mitchell, Nicole Elyse. Machine Learning-Based Prediction of Sites of Metabolism in Drugs: Exploring Feature Extraction Methods on Molecular Graphs.

Degree: MS, Engineering, 2020, Rice University

Drug metabolism studies are a critical component of the drug design process. Metabolism of some drugs can lead to diminished therapeutic efficacy or even toxicity.… (more)

Subjects/Keywords: machine learning; drug metabolism

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APA (6th Edition):

Mitchell, N. E. (2020). Machine Learning-Based Prediction of Sites of Metabolism in Drugs: Exploring Feature Extraction Methods on Molecular Graphs. (Masters Thesis). Rice University. Retrieved from http://hdl.handle.net/1911/108430

Chicago Manual of Style (16th Edition):

Mitchell, Nicole Elyse. “Machine Learning-Based Prediction of Sites of Metabolism in Drugs: Exploring Feature Extraction Methods on Molecular Graphs.” 2020. Masters Thesis, Rice University. Accessed January 18, 2021. http://hdl.handle.net/1911/108430.

MLA Handbook (7th Edition):

Mitchell, Nicole Elyse. “Machine Learning-Based Prediction of Sites of Metabolism in Drugs: Exploring Feature Extraction Methods on Molecular Graphs.” 2020. Web. 18 Jan 2021.

Vancouver:

Mitchell NE. Machine Learning-Based Prediction of Sites of Metabolism in Drugs: Exploring Feature Extraction Methods on Molecular Graphs. [Internet] [Masters thesis]. Rice University; 2020. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1911/108430.

Council of Science Editors:

Mitchell NE. Machine Learning-Based Prediction of Sites of Metabolism in Drugs: Exploring Feature Extraction Methods on Molecular Graphs. [Masters Thesis]. Rice University; 2020. Available from: http://hdl.handle.net/1911/108430


University of Arizona

7. Fan, Xiaoyu. Function and Regulation of Intestinal Cytochrome P450 .

Degree: 2019, University of Arizona

 The overall goal of this thesis was to study the function and regulation of intestinal P450s. The central hypothesis is that disease state and environmental… (more)

Subjects/Keywords: Drug metabolism; Intestinal P450s

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APA (6th Edition):

Fan, X. (2019). Function and Regulation of Intestinal Cytochrome P450 . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/634254

Chicago Manual of Style (16th Edition):

Fan, Xiaoyu. “Function and Regulation of Intestinal Cytochrome P450 .” 2019. Doctoral Dissertation, University of Arizona. Accessed January 18, 2021. http://hdl.handle.net/10150/634254.

MLA Handbook (7th Edition):

Fan, Xiaoyu. “Function and Regulation of Intestinal Cytochrome P450 .” 2019. Web. 18 Jan 2021.

Vancouver:

Fan X. Function and Regulation of Intestinal Cytochrome P450 . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10150/634254.

Council of Science Editors:

Fan X. Function and Regulation of Intestinal Cytochrome P450 . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/634254


University of Toronto

8. Novalen, Maria. Investigation of a Metabolic Pathway Leading to an Idiosyncratic Drug Reaction: Is the Sulfate of 12-Hydroxynevirapine Responsible for the Skin Rash in Brown Norway rats?.

Degree: 2010, University of Toronto

An animal model of nevirapine (NVP)-induced skin rash was used to test the hypothesis that sulfonation of 12-OH NVP, a metabolite of NVP proven essential… (more)

Subjects/Keywords: nevirapine; drug metabolism; adverse drug reactions; idiosyncratic drug reactions; 0383

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APA (6th Edition):

Novalen, M. (2010). Investigation of a Metabolic Pathway Leading to an Idiosyncratic Drug Reaction: Is the Sulfate of 12-Hydroxynevirapine Responsible for the Skin Rash in Brown Norway rats?. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25882

Chicago Manual of Style (16th Edition):

Novalen, Maria. “Investigation of a Metabolic Pathway Leading to an Idiosyncratic Drug Reaction: Is the Sulfate of 12-Hydroxynevirapine Responsible for the Skin Rash in Brown Norway rats?.” 2010. Masters Thesis, University of Toronto. Accessed January 18, 2021. http://hdl.handle.net/1807/25882.

MLA Handbook (7th Edition):

Novalen, Maria. “Investigation of a Metabolic Pathway Leading to an Idiosyncratic Drug Reaction: Is the Sulfate of 12-Hydroxynevirapine Responsible for the Skin Rash in Brown Norway rats?.” 2010. Web. 18 Jan 2021.

Vancouver:

Novalen M. Investigation of a Metabolic Pathway Leading to an Idiosyncratic Drug Reaction: Is the Sulfate of 12-Hydroxynevirapine Responsible for the Skin Rash in Brown Norway rats?. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1807/25882.

Council of Science Editors:

Novalen M. Investigation of a Metabolic Pathway Leading to an Idiosyncratic Drug Reaction: Is the Sulfate of 12-Hydroxynevirapine Responsible for the Skin Rash in Brown Norway rats?. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25882


Vanderbilt University

9. Baglia, Michelle Lynn. Germline and Somatic Variation in Genes Involved in Metabolism of Chemotherapy Drugs and Breast Cancer Outcomes.

Degree: PhD, Epidemiology, 2016, Vanderbilt University

 Triple-negative breast cancer (TNBC), which is characterized by minimal or lack of expression of estrogen receptors and progesterone receptors, and the absence of overexpression of… (more)

Subjects/Keywords: chemotherapy; drug metabolism; survival; breast cancer

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APA (6th Edition):

Baglia, M. L. (2016). Germline and Somatic Variation in Genes Involved in Metabolism of Chemotherapy Drugs and Breast Cancer Outcomes. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10714

Chicago Manual of Style (16th Edition):

Baglia, Michelle Lynn. “Germline and Somatic Variation in Genes Involved in Metabolism of Chemotherapy Drugs and Breast Cancer Outcomes.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 18, 2021. http://hdl.handle.net/1803/10714.

MLA Handbook (7th Edition):

Baglia, Michelle Lynn. “Germline and Somatic Variation in Genes Involved in Metabolism of Chemotherapy Drugs and Breast Cancer Outcomes.” 2016. Web. 18 Jan 2021.

Vancouver:

Baglia ML. Germline and Somatic Variation in Genes Involved in Metabolism of Chemotherapy Drugs and Breast Cancer Outcomes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1803/10714.

Council of Science Editors:

Baglia ML. Germline and Somatic Variation in Genes Involved in Metabolism of Chemotherapy Drugs and Breast Cancer Outcomes. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/10714


Texas A&M University

10. Liu, Zhen. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.

Degree: PhD, Chemistry, 2013, Texas A&M University

 Mycobacterium tuberculosis (M. tuberculosis) contains a wide array of genes responsible for the synthesis and secretion of a variety of bioactive lipids. The genes represent… (more)

Subjects/Keywords: Structural biology; Enzymology; Drug discovery; Lipid metabolism

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APA (6th Edition):

Liu, Z. (2013). Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151650

Chicago Manual of Style (16th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Doctoral Dissertation, Texas A&M University. Accessed January 18, 2021. http://hdl.handle.net/1969.1/151650.

MLA Handbook (7th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Web. 18 Jan 2021.

Vancouver:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1969.1/151650.

Council of Science Editors:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151650


Texas A&M University

11. Huang, Hsiao-Ling. Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis.

Degree: PhD, Chemistry, 2016, Texas A&M University

 As the world population battles drug-resistant tuberculosis (TB), there is an urgent need for novel anti-tubercular drugs. This dissertation documents the studies of glyoxylate shunt… (more)

Subjects/Keywords: Drug Discovery; Structural Biology; Carbon Metabolism; Tuberculosis

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APA (6th Edition):

Huang, H. (2016). Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174220

Chicago Manual of Style (16th Edition):

Huang, Hsiao-Ling. “Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis.” 2016. Doctoral Dissertation, Texas A&M University. Accessed January 18, 2021. http://hdl.handle.net/1969.1/174220.

MLA Handbook (7th Edition):

Huang, Hsiao-Ling. “Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis.” 2016. Web. 18 Jan 2021.

Vancouver:

Huang H. Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1969.1/174220.

Council of Science Editors:

Huang H. Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/174220


University of Manchester

12. Cantu Reinhard, Fabian Gilberto. A Computational Chemistry Approach to Cytochrome P450 Metabolism.

Degree: 2018, University of Manchester

 Drugs and other xenobiotic compounds exhibit different transformations upon entering the human body, most often starting with an oxidative reaction involving P450 enzymes. Hence, the… (more)

Subjects/Keywords: DFT; P450; Computational Chemistry; Drug Metabolism

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APA (6th Edition):

Cantu Reinhard, F. G. (2018). A Computational Chemistry Approach to Cytochrome P450 Metabolism. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301

Chicago Manual of Style (16th Edition):

Cantu Reinhard, Fabian Gilberto. “A Computational Chemistry Approach to Cytochrome P450 Metabolism.” 2018. Doctoral Dissertation, University of Manchester. Accessed January 18, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301.

MLA Handbook (7th Edition):

Cantu Reinhard, Fabian Gilberto. “A Computational Chemistry Approach to Cytochrome P450 Metabolism.” 2018. Web. 18 Jan 2021.

Vancouver:

Cantu Reinhard FG. A Computational Chemistry Approach to Cytochrome P450 Metabolism. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Jan 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301.

Council of Science Editors:

Cantu Reinhard FG. A Computational Chemistry Approach to Cytochrome P450 Metabolism. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317301


UCLA

13. Van Valkenburgh, Juno. Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes.

Degree: Chemistry, 2019, UCLA

 In chapter 1, strategies toward the asymmetric synthesis of a deoxycytidine kinase (dCK) inhibitor are presented. Small molecule dCK inhibitors are potential cancer therapeutics: in… (more)

Subjects/Keywords: Chemistry; cancer therapies; drug design; nucleotide metabolism

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APA (6th Edition):

Van Valkenburgh, J. (2019). Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6hs572xd

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Van Valkenburgh, Juno. “Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes.” 2019. Thesis, UCLA. Accessed January 18, 2021. http://www.escholarship.org/uc/item/6hs572xd.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Van Valkenburgh, Juno. “Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes.” 2019. Web. 18 Jan 2021.

Vancouver:

Van Valkenburgh J. Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes. [Internet] [Thesis]. UCLA; 2019. [cited 2021 Jan 18]. Available from: http://www.escholarship.org/uc/item/6hs572xd.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Van Valkenburgh J. Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes. [Thesis]. UCLA; 2019. Available from: http://www.escholarship.org/uc/item/6hs572xd

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Ottawa

14. Tayyabi, Ehsen. Gone Fishing: Synthesis and Design of a Superparamagnetic Nanobait for Trapping Reactive Metabolites In Vivo.

Degree: 2018, University of Ottawa

 Adverse drug reactions are common causes of medical injuries. Drug-induced hepatotoxicity remains one of the leading causes of emergency room visits, FDA non-approval, and drug(more)

Subjects/Keywords: Molecular Imaging; Chemical Biology; MRI; Drug Metabolism

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APA (6th Edition):

Tayyabi, E. (2018). Gone Fishing: Synthesis and Design of a Superparamagnetic Nanobait for Trapping Reactive Metabolites In Vivo. (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37338

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tayyabi, Ehsen. “Gone Fishing: Synthesis and Design of a Superparamagnetic Nanobait for Trapping Reactive Metabolites In Vivo. ” 2018. Thesis, University of Ottawa. Accessed January 18, 2021. http://hdl.handle.net/10393/37338.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tayyabi, Ehsen. “Gone Fishing: Synthesis and Design of a Superparamagnetic Nanobait for Trapping Reactive Metabolites In Vivo. ” 2018. Web. 18 Jan 2021.

Vancouver:

Tayyabi E. Gone Fishing: Synthesis and Design of a Superparamagnetic Nanobait for Trapping Reactive Metabolites In Vivo. [Internet] [Thesis]. University of Ottawa; 2018. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10393/37338.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tayyabi E. Gone Fishing: Synthesis and Design of a Superparamagnetic Nanobait for Trapping Reactive Metabolites In Vivo. [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37338

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Adelaide

15. Gourlay, Geoffrey Keith. Pyridine nucleotide involvement in rat hepatic microsomal drug metabolism.

Degree: 1976, University of Adelaide

Subjects/Keywords: Drug metabolism.; Coenzymes.

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APA (6th Edition):

Gourlay, G. K. (1976). Pyridine nucleotide involvement in rat hepatic microsomal drug metabolism. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/20177

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Gourlay, Geoffrey Keith. “Pyridine nucleotide involvement in rat hepatic microsomal drug metabolism.” 1976. Thesis, University of Adelaide. Accessed January 18, 2021. http://hdl.handle.net/2440/20177.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Gourlay, Geoffrey Keith. “Pyridine nucleotide involvement in rat hepatic microsomal drug metabolism.” 1976. Web. 18 Jan 2021.

Vancouver:

Gourlay GK. Pyridine nucleotide involvement in rat hepatic microsomal drug metabolism. [Internet] [Thesis]. University of Adelaide; 1976. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/2440/20177.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Gourlay GK. Pyridine nucleotide involvement in rat hepatic microsomal drug metabolism. [Thesis]. University of Adelaide; 1976. Available from: http://hdl.handle.net/2440/20177

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Illinois – Chicago

16. Huang, Ke. In vitro Investigation of Metabolism, Bioactivation, and Botanical-Drug Interactions of Licorice.

Degree: 2017, University of Illinois – Chicago

 The dried roots of licorice have been consumed for the past 6000 years as a flavoring and sweetening agent in the western world and in… (more)

Subjects/Keywords: Licorice; Glabridin; Metabolism; Metabolic Activation; Drug Inhibition

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APA (6th Edition):

Huang, K. (2017). In vitro Investigation of Metabolism, Bioactivation, and Botanical-Drug Interactions of Licorice. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/21723

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Huang, Ke. “In vitro Investigation of Metabolism, Bioactivation, and Botanical-Drug Interactions of Licorice.” 2017. Thesis, University of Illinois – Chicago. Accessed January 18, 2021. http://hdl.handle.net/10027/21723.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Huang, Ke. “In vitro Investigation of Metabolism, Bioactivation, and Botanical-Drug Interactions of Licorice.” 2017. Web. 18 Jan 2021.

Vancouver:

Huang K. In vitro Investigation of Metabolism, Bioactivation, and Botanical-Drug Interactions of Licorice. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/10027/21723.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Huang K. In vitro Investigation of Metabolism, Bioactivation, and Botanical-Drug Interactions of Licorice. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/21723

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Manchester

17. Wood, Francesca. Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance.

Degree: PhD, 2016, University of Manchester

 As a critical parameter in pharmacokinetics, prediction of clearance is an integral aspect of drug discovery programmes. Since the liver is the major site of… (more)

Subjects/Keywords: 610; drug metabolism; hepatocytes; hepatic clearance

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Wood, F. (2016). Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443

Chicago Manual of Style (16th Edition):

Wood, Francesca. “Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance.” 2016. Doctoral Dissertation, University of Manchester. Accessed January 18, 2021. https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443.

MLA Handbook (7th Edition):

Wood, Francesca. “Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance.” 2016. Web. 18 Jan 2021.

Vancouver:

Wood F. Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2021 Jan 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443.

Council of Science Editors:

Wood F. Optimisation of in vitro methodology for drug metabolism studies to improve prediction of hepatic drug clearance. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/optimisation-of-in-vitro-methodology-for-drug-metabolism-studies-to-improve-prediction-of-hepatic-drug-clearance(0786531a-2e10-48a7-9b35-e2e7e1935338).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764443


University of Bath

18. Makwana, Amit. Studies on the N-dealkylation of codeine by Candida tropicalis.

Degree: PhD, 1990, University of Bath

Subjects/Keywords: 615.1; Drug metabolism

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APA (6th Edition):

Makwana, A. (1990). Studies on the N-dealkylation of codeine by Candida tropicalis. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-ndealkylation-of-codeine-by-candida-tropicalis(fbd61dc3-4cc3-4dc5-b10d-9fdc70a5aeae).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278237

Chicago Manual of Style (16th Edition):

Makwana, Amit. “Studies on the N-dealkylation of codeine by Candida tropicalis.” 1990. Doctoral Dissertation, University of Bath. Accessed January 18, 2021. https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-ndealkylation-of-codeine-by-candida-tropicalis(fbd61dc3-4cc3-4dc5-b10d-9fdc70a5aeae).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278237.

MLA Handbook (7th Edition):

Makwana, Amit. “Studies on the N-dealkylation of codeine by Candida tropicalis.” 1990. Web. 18 Jan 2021.

Vancouver:

Makwana A. Studies on the N-dealkylation of codeine by Candida tropicalis. [Internet] [Doctoral dissertation]. University of Bath; 1990. [cited 2021 Jan 18]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-ndealkylation-of-codeine-by-candida-tropicalis(fbd61dc3-4cc3-4dc5-b10d-9fdc70a5aeae).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278237.

Council of Science Editors:

Makwana A. Studies on the N-dealkylation of codeine by Candida tropicalis. [Doctoral Dissertation]. University of Bath; 1990. Available from: https://researchportal.bath.ac.uk/en/studentthesis/studies-on-the-ndealkylation-of-codeine-by-candida-tropicalis(fbd61dc3-4cc3-4dc5-b10d-9fdc70a5aeae).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.278237


University of the Western Cape

19. Ntshongontshi, Nomaphelo. Cytochrome P450-3A4/copper-poly(propylene imine)- polypyrrole star co-polymer Nanobiosensor system for delavirdine – a non-nucleoside reverse transcriptase inhibitor HIV drug .

Degree: 2014, University of the Western Cape

 HIV and AIDS are among the world's pandemics that pose serious concern to almost every individual in the world. With the current level of availability… (more)

Subjects/Keywords: Biosensor; Delavirdine drug; Metabolism; Cyclic voltammetry (CV)

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APA (6th Edition):

Ntshongontshi, N. (2014). Cytochrome P450-3A4/copper-poly(propylene imine)- polypyrrole star co-polymer Nanobiosensor system for delavirdine – a non-nucleoside reverse transcriptase inhibitor HIV drug . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4446

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ntshongontshi, Nomaphelo. “Cytochrome P450-3A4/copper-poly(propylene imine)- polypyrrole star co-polymer Nanobiosensor system for delavirdine – a non-nucleoside reverse transcriptase inhibitor HIV drug .” 2014. Thesis, University of the Western Cape. Accessed January 18, 2021. http://hdl.handle.net/11394/4446.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ntshongontshi, Nomaphelo. “Cytochrome P450-3A4/copper-poly(propylene imine)- polypyrrole star co-polymer Nanobiosensor system for delavirdine – a non-nucleoside reverse transcriptase inhibitor HIV drug .” 2014. Web. 18 Jan 2021.

Vancouver:

Ntshongontshi N. Cytochrome P450-3A4/copper-poly(propylene imine)- polypyrrole star co-polymer Nanobiosensor system for delavirdine – a non-nucleoside reverse transcriptase inhibitor HIV drug . [Internet] [Thesis]. University of the Western Cape; 2014. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/11394/4446.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ntshongontshi N. Cytochrome P450-3A4/copper-poly(propylene imine)- polypyrrole star co-polymer Nanobiosensor system for delavirdine – a non-nucleoside reverse transcriptase inhibitor HIV drug . [Thesis]. University of the Western Cape; 2014. Available from: http://hdl.handle.net/11394/4446

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Washington University in St. Louis

20. Guggisberg, Ann Marie. Discovery and characterization of a novel class of metabolic regulators in the malaria parasite Plasmodium falciparum.

Degree: PhD, Biology & Biomedical Sciences (Molecular Genetics & Genomics), 2016, Washington University in St. Louis

 The malaria parasite, Plasmodium falciparum, infects hundreds of millions of people per year and causes hundreds of thousands of deaths. Within the host red blood… (more)

Subjects/Keywords: drug resistance, malaria, metabolism, parasitology; Biology

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APA (6th Edition):

Guggisberg, A. M. (2016). Discovery and characterization of a novel class of metabolic regulators in the malaria parasite Plasmodium falciparum. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/989

Chicago Manual of Style (16th Edition):

Guggisberg, Ann Marie. “Discovery and characterization of a novel class of metabolic regulators in the malaria parasite Plasmodium falciparum.” 2016. Doctoral Dissertation, Washington University in St. Louis. Accessed January 18, 2021. https://openscholarship.wustl.edu/art_sci_etds/989.

MLA Handbook (7th Edition):

Guggisberg, Ann Marie. “Discovery and characterization of a novel class of metabolic regulators in the malaria parasite Plasmodium falciparum.” 2016. Web. 18 Jan 2021.

Vancouver:

Guggisberg AM. Discovery and characterization of a novel class of metabolic regulators in the malaria parasite Plasmodium falciparum. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2016. [cited 2021 Jan 18]. Available from: https://openscholarship.wustl.edu/art_sci_etds/989.

Council of Science Editors:

Guggisberg AM. Discovery and characterization of a novel class of metabolic regulators in the malaria parasite Plasmodium falciparum. [Doctoral Dissertation]. Washington University in St. Louis; 2016. Available from: https://openscholarship.wustl.edu/art_sci_etds/989

21. Berg, Aad. Cytochrome P-450-Substrate Interaction and Hepatic Drug Metabolism in the Mouse.

Degree: Department of Radiation Oncology, 1977, Erasmus University Medical Center

 textabstractA drug which has entered the circulation, may be eliminated as such by the kidney and excreted in the urine. This depends on the lipid-solubility… (more)

Subjects/Keywords: drug metabolism; mouse

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APA (6th Edition):

Berg, A. (1977). Cytochrome P-450-Substrate Interaction and Hepatic Drug Metabolism in the Mouse. (Doctoral Dissertation). Erasmus University Medical Center. Retrieved from http://hdl.handle.net/1765/26191

Chicago Manual of Style (16th Edition):

Berg, Aad. “Cytochrome P-450-Substrate Interaction and Hepatic Drug Metabolism in the Mouse.” 1977. Doctoral Dissertation, Erasmus University Medical Center. Accessed January 18, 2021. http://hdl.handle.net/1765/26191.

MLA Handbook (7th Edition):

Berg, Aad. “Cytochrome P-450-Substrate Interaction and Hepatic Drug Metabolism in the Mouse.” 1977. Web. 18 Jan 2021.

Vancouver:

Berg A. Cytochrome P-450-Substrate Interaction and Hepatic Drug Metabolism in the Mouse. [Internet] [Doctoral dissertation]. Erasmus University Medical Center; 1977. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1765/26191.

Council of Science Editors:

Berg A. Cytochrome P-450-Substrate Interaction and Hepatic Drug Metabolism in the Mouse. [Doctoral Dissertation]. Erasmus University Medical Center; 1977. Available from: http://hdl.handle.net/1765/26191


University of Bath

22. Fordyce, Karen. Aspects of genetic and environmental control of phase II metabolism.

Degree: PhD, 1987, University of Bath

Subjects/Keywords: 615.1; Drug metabolism

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APA (6th Edition):

Fordyce, K. (1987). Aspects of genetic and environmental control of phase II metabolism. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/aspects-of-genetic-and-environmental-control-of-phase-ii-metabolism(06cc680c-9bad-407e-b21c-9817681f55ed).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375338

Chicago Manual of Style (16th Edition):

Fordyce, Karen. “Aspects of genetic and environmental control of phase II metabolism.” 1987. Doctoral Dissertation, University of Bath. Accessed January 18, 2021. https://researchportal.bath.ac.uk/en/studentthesis/aspects-of-genetic-and-environmental-control-of-phase-ii-metabolism(06cc680c-9bad-407e-b21c-9817681f55ed).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375338.

MLA Handbook (7th Edition):

Fordyce, Karen. “Aspects of genetic and environmental control of phase II metabolism.” 1987. Web. 18 Jan 2021.

Vancouver:

Fordyce K. Aspects of genetic and environmental control of phase II metabolism. [Internet] [Doctoral dissertation]. University of Bath; 1987. [cited 2021 Jan 18]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/aspects-of-genetic-and-environmental-control-of-phase-ii-metabolism(06cc680c-9bad-407e-b21c-9817681f55ed).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375338.

Council of Science Editors:

Fordyce K. Aspects of genetic and environmental control of phase II metabolism. [Doctoral Dissertation]. University of Bath; 1987. Available from: https://researchportal.bath.ac.uk/en/studentthesis/aspects-of-genetic-and-environmental-control-of-phase-ii-metabolism(06cc680c-9bad-407e-b21c-9817681f55ed).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.375338


University of Manchester

23. Cantu Guerra, Fabian. A computational chemistry approach to cytochrome P450 metabolism.

Degree: PhD, 2018, University of Manchester

 Drugs and other xenobiotic compounds exhibit different transformations upon entering the human body, most often starting with an oxidative reaction involving P450 enzymes. Hence, the… (more)

Subjects/Keywords: DFT; P450; Computational Chemistry; Drug Metabolism

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APA (6th Edition):

Cantu Guerra, F. (2018). A computational chemistry approach to cytochrome P450 metabolism. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-computational-chemistry-approach-to-cytochrome-p450-metabolism(e42a5d4b-ead5-4687-950e-5f63d6093f1e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799271

Chicago Manual of Style (16th Edition):

Cantu Guerra, Fabian. “A computational chemistry approach to cytochrome P450 metabolism.” 2018. Doctoral Dissertation, University of Manchester. Accessed January 18, 2021. https://www.research.manchester.ac.uk/portal/en/theses/a-computational-chemistry-approach-to-cytochrome-p450-metabolism(e42a5d4b-ead5-4687-950e-5f63d6093f1e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799271.

MLA Handbook (7th Edition):

Cantu Guerra, Fabian. “A computational chemistry approach to cytochrome P450 metabolism.” 2018. Web. 18 Jan 2021.

Vancouver:

Cantu Guerra F. A computational chemistry approach to cytochrome P450 metabolism. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Jan 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-computational-chemistry-approach-to-cytochrome-p450-metabolism(e42a5d4b-ead5-4687-950e-5f63d6093f1e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799271.

Council of Science Editors:

Cantu Guerra F. A computational chemistry approach to cytochrome P450 metabolism. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-computational-chemistry-approach-to-cytochrome-p450-metabolism(e42a5d4b-ead5-4687-950e-5f63d6093f1e).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799271


University of Sydney

24. Painter, Arran Blake. Altered drug metabolism and clearance pathways in cancer cachexia .

Degree: 2014, University of Sydney

 Cancer cachexia, a syndrome of lean and adipose tissue loss in cancer patients, is associated with reduced quality of life, poor survival outcomes and increased… (more)

Subjects/Keywords: Cancer; cachexia; inflammation; drug metabolism; transport

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APA (6th Edition):

Painter, A. B. (2014). Altered drug metabolism and clearance pathways in cancer cachexia . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/12269

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Painter, Arran Blake. “Altered drug metabolism and clearance pathways in cancer cachexia .” 2014. Thesis, University of Sydney. Accessed January 18, 2021. http://hdl.handle.net/2123/12269.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Painter, Arran Blake. “Altered drug metabolism and clearance pathways in cancer cachexia .” 2014. Web. 18 Jan 2021.

Vancouver:

Painter AB. Altered drug metabolism and clearance pathways in cancer cachexia . [Internet] [Thesis]. University of Sydney; 2014. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/2123/12269.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Painter AB. Altered drug metabolism and clearance pathways in cancer cachexia . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/12269

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Vanderbilt University

25. Crouch, Rachel Denise. Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics.

Degree: PhD, Pharmacology, 2016, Vanderbilt University

 Unacceptable pharmacokinetics (PK) relating to aldehyde oxidase (AO) metabolism have resulted in clinical failure of several promising drug candidates, yet reliable and standardized methods to… (more)

Subjects/Keywords: aldehyde oxidase; allometric scaling; drug metabolism; pharmacokinetics; drug interaction

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APA (6th Edition):

Crouch, R. D. (2016). Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14636

Chicago Manual of Style (16th Edition):

Crouch, Rachel Denise. “Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 18, 2021. http://hdl.handle.net/1803/14636.

MLA Handbook (7th Edition):

Crouch, Rachel Denise. “Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics.” 2016. Web. 18 Jan 2021.

Vancouver:

Crouch RD. Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1803/14636.

Council of Science Editors:

Crouch RD. Aldehyde Oxidase Drug Metabolism: Evaluation of Drug Interaction Potential and Allometric Scaling Methods to Predict Human Pharmacokinetics. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14636


University of Toronto

26. Huang, Yiying. Characterizing the Expression and Localization of Drug Transporters and Metabolic Enzymes in the testes of Uninfected and HIV-1 Infected, Treated Subjects – Potential Contribution to an HIV-1 Sanctuary.

Degree: 2015, University of Toronto

Previous studies have reported that HIV-1 is capable of both acute and persistent infection in the testes. The naturally restrictive environment in the testes, due… (more)

Subjects/Keywords: Drug Metabolism; Drug Transporters; HIV; Sanctuary Site; Testes; 0572

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APA (6th Edition):

Huang, Y. (2015). Characterizing the Expression and Localization of Drug Transporters and Metabolic Enzymes in the testes of Uninfected and HIV-1 Infected, Treated Subjects – Potential Contribution to an HIV-1 Sanctuary. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70405

Chicago Manual of Style (16th Edition):

Huang, Yiying. “Characterizing the Expression and Localization of Drug Transporters and Metabolic Enzymes in the testes of Uninfected and HIV-1 Infected, Treated Subjects – Potential Contribution to an HIV-1 Sanctuary.” 2015. Masters Thesis, University of Toronto. Accessed January 18, 2021. http://hdl.handle.net/1807/70405.

MLA Handbook (7th Edition):

Huang, Yiying. “Characterizing the Expression and Localization of Drug Transporters and Metabolic Enzymes in the testes of Uninfected and HIV-1 Infected, Treated Subjects – Potential Contribution to an HIV-1 Sanctuary.” 2015. Web. 18 Jan 2021.

Vancouver:

Huang Y. Characterizing the Expression and Localization of Drug Transporters and Metabolic Enzymes in the testes of Uninfected and HIV-1 Infected, Treated Subjects – Potential Contribution to an HIV-1 Sanctuary. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1807/70405.

Council of Science Editors:

Huang Y. Characterizing the Expression and Localization of Drug Transporters and Metabolic Enzymes in the testes of Uninfected and HIV-1 Infected, Treated Subjects – Potential Contribution to an HIV-1 Sanctuary. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70405


Universiteit Utrecht

27. Waterschoot, R.A.B. van. Interplay between CYP3A and drug transporters.

Degree: 2009, Universiteit Utrecht

 Cytochrome P450 3A (CYP3A) and P-glycoprotein (P-gp/MDR1) are two important detoxifying systems that protect us against many potentially harmful xenobiotics but their activity also strongly… (more)

Subjects/Keywords: Farmacie; Intestinal and hepatic drug metabolism; drug transport; drug toxicity; pharmacokinetics CYP3A; P-glycoprotein; MRP2

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APA (6th Edition):

Waterschoot, R. A. B. v. (2009). Interplay between CYP3A and drug transporters. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/35859

Chicago Manual of Style (16th Edition):

Waterschoot, R A B van. “Interplay between CYP3A and drug transporters.” 2009. Doctoral Dissertation, Universiteit Utrecht. Accessed January 18, 2021. http://dspace.library.uu.nl:8080/handle/1874/35859.

MLA Handbook (7th Edition):

Waterschoot, R A B van. “Interplay between CYP3A and drug transporters.” 2009. Web. 18 Jan 2021.

Vancouver:

Waterschoot RABv. Interplay between CYP3A and drug transporters. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2009. [cited 2021 Jan 18]. Available from: http://dspace.library.uu.nl:8080/handle/1874/35859.

Council of Science Editors:

Waterschoot RABv. Interplay between CYP3A and drug transporters. [Doctoral Dissertation]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/35859


University of California – San Francisco

28. Hosey, Chelsea Mariah. Predicting Drug Disposition by Integrating In Vitro and In Silico Methodology.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2016, University of California – San Francisco

 The safety and efficacy of drugs depend upon appropriate dosing of drugs made possible by understanding the dispositional profile a drug will follow. A drug’s… (more)

Subjects/Keywords: Pharmaceutical sciences; Biliary Elimination; Biopharmaceutics Drug Disposition Classification System; Drug Disposition; Drug Elimination; Metabolism; Transporters

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Hosey, C. M. (2016). Predicting Drug Disposition by Integrating In Vitro and In Silico Methodology. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/5ds3q196

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hosey, Chelsea Mariah. “Predicting Drug Disposition by Integrating In Vitro and In Silico Methodology.” 2016. Thesis, University of California – San Francisco. Accessed January 18, 2021. http://www.escholarship.org/uc/item/5ds3q196.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hosey, Chelsea Mariah. “Predicting Drug Disposition by Integrating In Vitro and In Silico Methodology.” 2016. Web. 18 Jan 2021.

Vancouver:

Hosey CM. Predicting Drug Disposition by Integrating In Vitro and In Silico Methodology. [Internet] [Thesis]. University of California – San Francisco; 2016. [cited 2021 Jan 18]. Available from: http://www.escholarship.org/uc/item/5ds3q196.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hosey CM. Predicting Drug Disposition by Integrating In Vitro and In Silico Methodology. [Thesis]. University of California – San Francisco; 2016. Available from: http://www.escholarship.org/uc/item/5ds3q196

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Toronto

29. Crosby, Michael. Regulation of Hepatic CYP3A4 by 3-Methylcholanthrene in Humanized PXR-CAR-CYP3A4/3A7 Mice.

Degree: 2017, University of Toronto

Polycyclic aromatic hydrocarbons (PAHs) are environmental pollutants that activate the aryl hydrocarbon receptor, triggering many biological effects typified by induction of cytochrome P450 1A1 (CYP1A1).… (more)

Subjects/Keywords: aryl hydrocarbon receptor; Cyp3a11; drug metabolism; drug metabolizing enzyme; P450; polycyclic aromatic hydrocarbon; 0419

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Crosby, M. (2017). Regulation of Hepatic CYP3A4 by 3-Methylcholanthrene in Humanized PXR-CAR-CYP3A4/3A7 Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79379

Chicago Manual of Style (16th Edition):

Crosby, Michael. “Regulation of Hepatic CYP3A4 by 3-Methylcholanthrene in Humanized PXR-CAR-CYP3A4/3A7 Mice.” 2017. Masters Thesis, University of Toronto. Accessed January 18, 2021. http://hdl.handle.net/1807/79379.

MLA Handbook (7th Edition):

Crosby, Michael. “Regulation of Hepatic CYP3A4 by 3-Methylcholanthrene in Humanized PXR-CAR-CYP3A4/3A7 Mice.” 2017. Web. 18 Jan 2021.

Vancouver:

Crosby M. Regulation of Hepatic CYP3A4 by 3-Methylcholanthrene in Humanized PXR-CAR-CYP3A4/3A7 Mice. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1807/79379.

Council of Science Editors:

Crosby M. Regulation of Hepatic CYP3A4 by 3-Methylcholanthrene in Humanized PXR-CAR-CYP3A4/3A7 Mice. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79379


University of Washington

30. Seguin, Ryan Patrick. Non-Dissociative Sequential Metabolism of Enoxacin to a Metabolic Intermediate Complex with Cytochrome P450 1A2.

Degree: PhD, 2017, University of Washington

 Cytochrome P450 enzymes constitute a superfamily of isoforms which accelerate the removal of foreign compounds from the body through oxidative biotransformation to generate polar metabolites… (more)

Subjects/Keywords: Cytochrome P450; Drug-Drug Interactions; Drug Metabolism; Enoxacin; Fluoroquinolone; Mechanism-Based Inhibition; Pharmaceutical sciences; Medicinal chemistry

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Seguin, R. P. (2017). Non-Dissociative Sequential Metabolism of Enoxacin to a Metabolic Intermediate Complex with Cytochrome P450 1A2. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/40646

Chicago Manual of Style (16th Edition):

Seguin, Ryan Patrick. “Non-Dissociative Sequential Metabolism of Enoxacin to a Metabolic Intermediate Complex with Cytochrome P450 1A2.” 2017. Doctoral Dissertation, University of Washington. Accessed January 18, 2021. http://hdl.handle.net/1773/40646.

MLA Handbook (7th Edition):

Seguin, Ryan Patrick. “Non-Dissociative Sequential Metabolism of Enoxacin to a Metabolic Intermediate Complex with Cytochrome P450 1A2.” 2017. Web. 18 Jan 2021.

Vancouver:

Seguin RP. Non-Dissociative Sequential Metabolism of Enoxacin to a Metabolic Intermediate Complex with Cytochrome P450 1A2. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2021 Jan 18]. Available from: http://hdl.handle.net/1773/40646.

Council of Science Editors:

Seguin RP. Non-Dissociative Sequential Metabolism of Enoxacin to a Metabolic Intermediate Complex with Cytochrome P450 1A2. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/40646

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