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You searched for +publisher:"University of Southern California" +contributor:("Louie, Stan"). Showing records 1 – 19 of 19 total matches.

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University of Southern California

1. Zhu, Min. Total synthesis of specialized pro-resolving lipid mediators and their analogs.

Degree: PhD, Chemistry, 2013, University of Southern California

 This dissertation reports research on the total synthesis of a series of DHA-derived specialized pro-resolving mediators (SPMs), which can be divided into four projects corresponding… (more)

Subjects/Keywords: total synthesis; lipid mediator

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APA (6th Edition):

Zhu, M. (2013). Total synthesis of specialized pro-resolving lipid mediators and their analogs. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7519

Chicago Manual of Style (16th Edition):

Zhu, Min. “Total synthesis of specialized pro-resolving lipid mediators and their analogs.” 2013. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7519.

MLA Handbook (7th Edition):

Zhu, Min. “Total synthesis of specialized pro-resolving lipid mediators and their analogs.” 2013. Web. 08 Mar 2021.

Vancouver:

Zhu M. Total synthesis of specialized pro-resolving lipid mediators and their analogs. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7519.

Council of Science Editors:

Zhu M. Total synthesis of specialized pro-resolving lipid mediators and their analogs. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/353055/rec/7519


University of Southern California

2. Liu, Siyu. Pharmacodynamics impact of etravirine disposition into breast milk in relation to HIV replication in this milk.

Degree: MS, Pharmaceutical Sciences, 2016, University of Southern California

 Mother‐to‐child transmission (MTCT) through breastfeeding continues to be a major concern for the transmission of HIV infection among children in developing countries. The transmission usually… (more)

Subjects/Keywords: etravirine; MTCT; breast milk; HAART; HIV

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APA (6th Edition):

Liu, S. (2016). Pharmacodynamics impact of etravirine disposition into breast milk in relation to HIV replication in this milk. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381738/rec/5015

Chicago Manual of Style (16th Edition):

Liu, Siyu. “Pharmacodynamics impact of etravirine disposition into breast milk in relation to HIV replication in this milk.” 2016. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381738/rec/5015.

MLA Handbook (7th Edition):

Liu, Siyu. “Pharmacodynamics impact of etravirine disposition into breast milk in relation to HIV replication in this milk.” 2016. Web. 08 Mar 2021.

Vancouver:

Liu S. Pharmacodynamics impact of etravirine disposition into breast milk in relation to HIV replication in this milk. [Internet] [Masters thesis]. University of Southern California; 2016. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381738/rec/5015.

Council of Science Editors:

Liu S. Pharmacodynamics impact of etravirine disposition into breast milk in relation to HIV replication in this milk. [Masters Thesis]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381738/rec/5015


University of Southern California

3. Finaldi, Anne-Marie. Studies on lipid mediators, and on potential modulators of GRP78.

Degree: PhD, Chemistry, 2014, University of Southern California

 The research presented within this dissertation is a compilation of three projects with the underlying theme of designing and synthesizing relevant molecules for biological studies.… (more)

Subjects/Keywords: lipid mediators; docosahexaenoic acid; resolvins; protectins; inflammation; cancer; GRP78

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APA (6th Edition):

Finaldi, A. (2014). Studies on lipid mediators, and on potential modulators of GRP78. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343800/rec/6176

Chicago Manual of Style (16th Edition):

Finaldi, Anne-Marie. “Studies on lipid mediators, and on potential modulators of GRP78.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343800/rec/6176.

MLA Handbook (7th Edition):

Finaldi, Anne-Marie. “Studies on lipid mediators, and on potential modulators of GRP78.” 2014. Web. 08 Mar 2021.

Vancouver:

Finaldi A. Studies on lipid mediators, and on potential modulators of GRP78. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343800/rec/6176.

Council of Science Editors:

Finaldi A. Studies on lipid mediators, and on potential modulators of GRP78. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/343800/rec/6176


University of Southern California

4. Sharda, Nidhi. Blockade of CXCR2 as a novel approach for cancer chemotherapy.

Degree: MS, Pharmaceutical Sciences, 2012, University of Southern California

 There is interplay between the malignant tumor cells and their non-malignant counterparts found in the microenvironment. This active bi-directional cross-talk between cancer cells and normal… (more)

Subjects/Keywords: CXCR2; IL8; Cancer; chemotherapy; inflammation; angiogenesis

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APA (6th Edition):

Sharda, N. (2012). Blockade of CXCR2 as a novel approach for cancer chemotherapy. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/36653/rec/1143

Chicago Manual of Style (16th Edition):

Sharda, Nidhi. “Blockade of CXCR2 as a novel approach for cancer chemotherapy.” 2012. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/36653/rec/1143.

MLA Handbook (7th Edition):

Sharda, Nidhi. “Blockade of CXCR2 as a novel approach for cancer chemotherapy.” 2012. Web. 08 Mar 2021.

Vancouver:

Sharda N. Blockade of CXCR2 as a novel approach for cancer chemotherapy. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/36653/rec/1143.

Council of Science Editors:

Sharda N. Blockade of CXCR2 as a novel approach for cancer chemotherapy. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/36653/rec/1143


University of Southern California

5. Sanchez, Tino Wilson. Design and discovery of small molecules inhibiting the interaction of cellular LEDGF/p75 and HIV-1 integrase.

Degree: PhD, Pharmaceutical Sciences, 2012, University of Southern California

 Cellular transcription co-activator p75, also known as lens epithelial-derived growth factor (LEDGF/p75), plays an essential role in HIV-1 IN-led integration of viral DNA into the… (more)

Subjects/Keywords: HIV; AIDS; therapeutics; virus; antiviral; drug design; integrase; host factor; LEDGF; chaperone; pharmaceutical sciences; pharmacophore; small molecules

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APA (6th Edition):

Sanchez, T. W. (2012). Design and discovery of small molecules inhibiting the interaction of cellular LEDGF/p75 and HIV-1 integrase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8559/rec/1858

Chicago Manual of Style (16th Edition):

Sanchez, Tino Wilson. “Design and discovery of small molecules inhibiting the interaction of cellular LEDGF/p75 and HIV-1 integrase.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8559/rec/1858.

MLA Handbook (7th Edition):

Sanchez, Tino Wilson. “Design and discovery of small molecules inhibiting the interaction of cellular LEDGF/p75 and HIV-1 integrase.” 2012. Web. 08 Mar 2021.

Vancouver:

Sanchez TW. Design and discovery of small molecules inhibiting the interaction of cellular LEDGF/p75 and HIV-1 integrase. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8559/rec/1858.

Council of Science Editors:

Sanchez TW. Design and discovery of small molecules inhibiting the interaction of cellular LEDGF/p75 and HIV-1 integrase. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8559/rec/1858


University of Southern California

6. Winkler, Jeremy W. The total synthesis of novel lipid mediators and their role in inflammation.

Degree: PhD, Chemistry, 2014, University of Southern California

 This body of work is about the design, synthesis and activity of a new and exciting class of compounds made from Docosahexaenoic Acid (DHA) termed… (more)

Subjects/Keywords: chemistry; organic chemistry; inflammation; lipid; omega-3; resolvin; neuroprotectin

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APA (6th Edition):

Winkler, J. W. (2014). The total synthesis of novel lipid mediators and their role in inflammation. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356236/rec/7364

Chicago Manual of Style (16th Edition):

Winkler, Jeremy W. “The total synthesis of novel lipid mediators and their role in inflammation.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356236/rec/7364.

MLA Handbook (7th Edition):

Winkler, Jeremy W. “The total synthesis of novel lipid mediators and their role in inflammation.” 2014. Web. 08 Mar 2021.

Vancouver:

Winkler JW. The total synthesis of novel lipid mediators and their role in inflammation. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356236/rec/7364.

Council of Science Editors:

Winkler JW. The total synthesis of novel lipid mediators and their role in inflammation. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356236/rec/7364


University of Southern California

7. Gaffney, Kevin J. Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators.

Degree: PhD, Chemistry, 2015, University of Southern California

 This dissertation details my efforts towards the design and development of novel small molecules anti-cancer agents including joint efforts with a host of colleagues and… (more)

Subjects/Keywords: medicinal chemistry

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APA (6th Edition):

Gaffney, K. J. (2015). Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556

Chicago Manual of Style (16th Edition):

Gaffney, Kevin J. “Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556.

MLA Handbook (7th Edition):

Gaffney, Kevin J. “Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators.” 2015. Web. 08 Mar 2021.

Vancouver:

Gaffney KJ. Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556.

Council of Science Editors:

Gaffney KJ. Adventures in medicinal chemistry: design and synthesis of small molecule biological modulators. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/303233/rec/556


University of Southern California

8. Bateman, Leslie Anne. Using chemistry to reveal the consequences of post translational modifications in cancer.

Degree: PhD, Chemistry, 2014, University of Southern California

 Post translational modifications (PTMs), including glycosylation and acetylation, have a wide variety of implications in cells. My goal was to explore the molecular consequences of… (more)

Subjects/Keywords: post translational modifications; chemical biology; cancer metabolism; chemical probes; O‐GlcNAc; glycosylation; acetylation

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APA (6th Edition):

Bateman, L. A. (2014). Using chemistry to reveal the consequences of post translational modifications in cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/438440/rec/7750

Chicago Manual of Style (16th Edition):

Bateman, Leslie Anne. “Using chemistry to reveal the consequences of post translational modifications in cancer.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/438440/rec/7750.

MLA Handbook (7th Edition):

Bateman, Leslie Anne. “Using chemistry to reveal the consequences of post translational modifications in cancer.” 2014. Web. 08 Mar 2021.

Vancouver:

Bateman LA. Using chemistry to reveal the consequences of post translational modifications in cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/438440/rec/7750.

Council of Science Editors:

Bateman LA. Using chemistry to reveal the consequences of post translational modifications in cancer. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/438440/rec/7750


University of Southern California

9. Sainz, Marcos A. Design, synthesis, and biological evaluation of novel therapeutics for cancer.

Degree: PhD, Chemistry, 2015, University of Southern California

 This dissertation details my efforts towards the design, synthesis and biological evaluation of novel, small molecule anti-cancer agents. This was accomplished with a joint collaboration… (more)

Subjects/Keywords: organic chemistry; synthesis; medicinal chemistry; dUTPase; PNA; bortezomib; MEF2

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APA (6th Edition):

Sainz, M. A. (2015). Design, synthesis, and biological evaluation of novel therapeutics for cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/518515/rec/1877

Chicago Manual of Style (16th Edition):

Sainz, Marcos A. “Design, synthesis, and biological evaluation of novel therapeutics for cancer.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/518515/rec/1877.

MLA Handbook (7th Edition):

Sainz, Marcos A. “Design, synthesis, and biological evaluation of novel therapeutics for cancer.” 2015. Web. 08 Mar 2021.

Vancouver:

Sainz MA. Design, synthesis, and biological evaluation of novel therapeutics for cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/518515/rec/1877.

Council of Science Editors:

Sainz MA. Design, synthesis, and biological evaluation of novel therapeutics for cancer. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/518515/rec/1877


University of Southern California

10. Russell, Jared. The impact of ritonavir on HIV therapy: balancing efficacy and toxicity.

Degree: PhD, Pharmaceutical Sciences, 2012, University of Southern California

 Objective: The aim of this dissertation is to evaluate the impact of ritonavir (RTV) on HIV therapy. We examine both beneficial and harmful outcomes caused… (more)

Subjects/Keywords: ABCC2; ABCC4; HIV; kidney dysfunction; ritonavir; tenofovir

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APA (6th Edition):

Russell, J. (2012). The impact of ritonavir on HIV therapy: balancing efficacy and toxicity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/205177/rec/6839

Chicago Manual of Style (16th Edition):

Russell, Jared. “The impact of ritonavir on HIV therapy: balancing efficacy and toxicity.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/205177/rec/6839.

MLA Handbook (7th Edition):

Russell, Jared. “The impact of ritonavir on HIV therapy: balancing efficacy and toxicity.” 2012. Web. 08 Mar 2021.

Vancouver:

Russell J. The impact of ritonavir on HIV therapy: balancing efficacy and toxicity. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/205177/rec/6839.

Council of Science Editors:

Russell J. The impact of ritonavir on HIV therapy: balancing efficacy and toxicity. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/205177/rec/6839


University of Southern California

11. Jadhav, Sachin Suresh. Impact of an angiotensin analogue in treating thermal and combined radiation injuries.

Degree: PhD, Pharmacy / Pharmaceutical Sciences, 2014, University of Southern California

 Background: In recent years there has been a growing concern regarding the use of nuclear weapons by terrorists. Such incidents in the past have shown… (more)

Subjects/Keywords: combined radiation injury; radiation; renin-angiotensin system; wound healing

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APA (6th Edition):

Jadhav, S. S. (2014). Impact of an angiotensin analogue in treating thermal and combined radiation injuries. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/379350/rec/3371

Chicago Manual of Style (16th Edition):

Jadhav, Sachin Suresh. “Impact of an angiotensin analogue in treating thermal and combined radiation injuries.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/379350/rec/3371.

MLA Handbook (7th Edition):

Jadhav, Sachin Suresh. “Impact of an angiotensin analogue in treating thermal and combined radiation injuries.” 2014. Web. 08 Mar 2021.

Vancouver:

Jadhav SS. Impact of an angiotensin analogue in treating thermal and combined radiation injuries. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/379350/rec/3371.

Council of Science Editors:

Jadhav SS. Impact of an angiotensin analogue in treating thermal and combined radiation injuries. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/379350/rec/3371


University of Southern California

12. Serrao, Erik. Novel modes of HIV-1 integrase inhibition.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Southern California

 Though highly active cocktails of antiretroviral drugs have been developed to potently knock down HIV-1 viral load, drug resistance mutations have contributed to the continued… (more)

Subjects/Keywords: HIV-1; integrase; LEDGF/p75; Hsp90; protein-protein interaction; virus-host interaction

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APA (6th Edition):

Serrao, E. (2013). Novel modes of HIV-1 integrase inhibition. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472

Chicago Manual of Style (16th Edition):

Serrao, Erik. “Novel modes of HIV-1 integrase inhibition.” 2013. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472.

MLA Handbook (7th Edition):

Serrao, Erik. “Novel modes of HIV-1 integrase inhibition.” 2013. Web. 08 Mar 2021.

Vancouver:

Serrao E. Novel modes of HIV-1 integrase inhibition. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472.

Council of Science Editors:

Serrao E. Novel modes of HIV-1 integrase inhibition. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472


University of Southern California

13. Mordwinkin, Nicholas Michael. The peptide angiotensin-(1-7) as a novel treatment for complications induced by type 2 diabetes mellitus.

Degree: PhD, Pharmaceutical Sciences, 2012, University of Southern California

 The aim of this dissertation is to evaluate the impact of type 2 diabetes mellitus on oxidative stress and inflammation in the bone marrow and… (more)

Subjects/Keywords: diabetes; angiotensin; oxidative stress; inflammation; immune dysfunction; progenitor cells; stem cells; endothelial dysfunction; cardiovascular disease; bone marrow

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APA (6th Edition):

Mordwinkin, N. M. (2012). The peptide angiotensin-(1-7) as a novel treatment for complications induced by type 2 diabetes mellitus. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/9565/rec/7068

Chicago Manual of Style (16th Edition):

Mordwinkin, Nicholas Michael. “The peptide angiotensin-(1-7) as a novel treatment for complications induced by type 2 diabetes mellitus.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/9565/rec/7068.

MLA Handbook (7th Edition):

Mordwinkin, Nicholas Michael. “The peptide angiotensin-(1-7) as a novel treatment for complications induced by type 2 diabetes mellitus.” 2012. Web. 08 Mar 2021.

Vancouver:

Mordwinkin NM. The peptide angiotensin-(1-7) as a novel treatment for complications induced by type 2 diabetes mellitus. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/9565/rec/7068.

Council of Science Editors:

Mordwinkin NM. The peptide angiotensin-(1-7) as a novel treatment for complications induced by type 2 diabetes mellitus. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/9565/rec/7068


University of Southern California

14. Sharma, Natasha. Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism.

Degree: PhD, Pharmaceutical Sciences, 2013, University of Southern California

 The ability of autophagy to support cancer cells under the conditions of metabolic, chemotherapeutic and endoplasmic reticulum stress (ERS) has led to its emergence as… (more)

Subjects/Keywords: autophagy; mefloquine; cancer; metabolism

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APA (6th Edition):

Sharma, N. (2013). Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3503

Chicago Manual of Style (16th Edition):

Sharma, Natasha. “Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism.” 2013. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3503.

MLA Handbook (7th Edition):

Sharma, Natasha. “Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism.” 2013. Web. 08 Mar 2021.

Vancouver:

Sharma N. Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3503.

Council of Science Editors:

Sharma N. Inhibition of tumor cell growth by mefloquine via multimechanistic effects involving increased cellular stress, inhibition of autophagy, and impairment of cellular energy metabolism. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/252066/rec/3503


University of Southern California

15. Jadhav, Sachin Suresh. Effects of combined thermal and radiation injury on the renin-angiotensin system.

Degree: MS, Pharmaceutical Sciences, 2010, University of Southern California

 The renin angiotensin system (RAS) plays an important role in wound repair. However, little is known pertaining to RAS expression in response to thermal and… (more)

Subjects/Keywords: radiation; angiotensin; wound healing; gene expression; immunohistochemistry; apoptosis

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APA (6th Edition):

Jadhav, S. S. (2010). Effects of combined thermal and radiation injury on the renin-angiotensin system. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/308059/rec/2213

Chicago Manual of Style (16th Edition):

Jadhav, Sachin Suresh. “Effects of combined thermal and radiation injury on the renin-angiotensin system.” 2010. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/308059/rec/2213.

MLA Handbook (7th Edition):

Jadhav, Sachin Suresh. “Effects of combined thermal and radiation injury on the renin-angiotensin system.” 2010. Web. 08 Mar 2021.

Vancouver:

Jadhav SS. Effects of combined thermal and radiation injury on the renin-angiotensin system. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/308059/rec/2213.

Council of Science Editors:

Jadhav SS. Effects of combined thermal and radiation injury on the renin-angiotensin system. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/308059/rec/2213


University of Southern California

16. Liu, Shanshan. Factors impacting drug disposition and clinical outcomes: age, hepatic metabolism, renal elimination and pharmacogentetics.

Degree: PhD, Pharmaceutical Sciences, 2009, University of Southern California

 Objective: This dissertation aims to evaluate factors impacting drug disposition and clinical outcomes.; Methods: Pharmacokinetic studies were conducted for gemcitabine in urothelial cancer, paclitaxel in… (more)

Subjects/Keywords: drug disposition; age; hepatic metabolism; renal elimination; pharmacogenetics

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

APA (6th Edition):

Liu, S. (2009). Factors impacting drug disposition and clinical outcomes: age, hepatic metabolism, renal elimination and pharmacogentetics. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248933/rec/2726

Chicago Manual of Style (16th Edition):

Liu, Shanshan. “Factors impacting drug disposition and clinical outcomes: age, hepatic metabolism, renal elimination and pharmacogentetics.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248933/rec/2726.

MLA Handbook (7th Edition):

Liu, Shanshan. “Factors impacting drug disposition and clinical outcomes: age, hepatic metabolism, renal elimination and pharmacogentetics.” 2009. Web. 08 Mar 2021.

Vancouver:

Liu S. Factors impacting drug disposition and clinical outcomes: age, hepatic metabolism, renal elimination and pharmacogentetics. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248933/rec/2726.

Council of Science Editors:

Liu S. Factors impacting drug disposition and clinical outcomes: age, hepatic metabolism, renal elimination and pharmacogentetics. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248933/rec/2726


University of Southern California

17. Lin, Hsin-Yen. Plasma levels of paclitaxel in the elderly. Effect of liver and renal function.

Degree: MS, Pharmaceutical Sciences, 2008, University of Southern California

 The percentage of elderly people in society will increase significantly in the next 20 years. Because this population will have some reduction in their liver… (more)

Subjects/Keywords: paclitaxel; age; liver; renal

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

APA (6th Edition):

Lin, H. (2008). Plasma levels of paclitaxel in the elderly. Effect of liver and renal function. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/141725/rec/5068

Chicago Manual of Style (16th Edition):

Lin, Hsin-Yen. “Plasma levels of paclitaxel in the elderly. Effect of liver and renal function.” 2008. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/141725/rec/5068.

MLA Handbook (7th Edition):

Lin, Hsin-Yen. “Plasma levels of paclitaxel in the elderly. Effect of liver and renal function.” 2008. Web. 08 Mar 2021.

Vancouver:

Lin H. Plasma levels of paclitaxel in the elderly. Effect of liver and renal function. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/141725/rec/5068.

Council of Science Editors:

Lin H. Plasma levels of paclitaxel in the elderly. Effect of liver and renal function. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/141725/rec/5068


University of Southern California

18. Golden, Encouse B. Utilizing chemotherapies to alter the balance between life and death in the ER stress response of cancer.

Degree: PhD, Pathobiology, 2009, University of Southern California

 When the protein load is lower than the endoplasmic reticulum (ER) folding capacity, the ER master regulator, GRP78, suppresses ER unfolded protein response (UPR) signaling… (more)

Subjects/Keywords: endoplasmic reticulum stress; celecoxib; chloroquine; green tea; epigallocatechin gallate; bortezomib; proteasome; autophagy; glioblastoma; breast cancer; multiple myeloma

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

APA (6th Edition):

Golden, E. B. (2009). Utilizing chemotherapies to alter the balance between life and death in the ER stress response of cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183258/rec/7791

Chicago Manual of Style (16th Edition):

Golden, Encouse B. “Utilizing chemotherapies to alter the balance between life and death in the ER stress response of cancer.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183258/rec/7791.

MLA Handbook (7th Edition):

Golden, Encouse B. “Utilizing chemotherapies to alter the balance between life and death in the ER stress response of cancer.” 2009. Web. 08 Mar 2021.

Vancouver:

Golden EB. Utilizing chemotherapies to alter the balance between life and death in the ER stress response of cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183258/rec/7791.

Council of Science Editors:

Golden EB. Utilizing chemotherapies to alter the balance between life and death in the ER stress response of cancer. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183258/rec/7791


University of Southern California

19. Bi, Lucun. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.

Degree: PhD, Pharmaceutical Sciences, 2008, University of Southern California

 High level of virologic failure was observed in HIV patients receiving combinations of tenofovir (TFV), lamivudine (3TC) combined with either abacavir (ABC) or didanosine (ddI).… (more)

Subjects/Keywords: nucleoside analog; NRTI; intracellular drug-drug interaction; efflux transporters; MRP2; MRP4; cellular adaptive response; ddNTP; TFV; ABC; ddI; endogenous nucleotide pools; PNP

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

APA (6th Edition):

Bi, L. (2008). Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609

Chicago Manual of Style (16th Edition):

Bi, Lucun. “Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609.

MLA Handbook (7th Edition):

Bi, Lucun. “Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine.” 2008. Web. 08 Mar 2021.

Vancouver:

Bi L. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609.

Council of Science Editors:

Bi L. Intracellular drug-drug interaction between nucleoside analogs leads to early virologic failure in HIV patients receiving triple nucleoside combinations of tenofovir, lamivudine and abacavir or didanosine. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/47592/rec/3609

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