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You searched for +publisher:"University of Southern California" +contributor:("Beringer, Paul"). Showing records 1 – 4 of 4 total matches.

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University of Southern California

1. Agnello, Melissa. Biological impact of fluoroquinolone resistance in Pseudomonas aeruginosa.

Degree: PhD, Clinical and Experimental Therapeutics, 2015, University of Southern California

 Pseudomonas aeruginosa (Pa) is an important Gram‐negative pathogen in the hospital setting. Pa causes severe disease in susceptible patients, such as those in the intensive… (more)

Subjects/Keywords: Pseudomonas aeruginosa; fluoroquinolones; antibiotic resistance; fitness

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APA (6th Edition):

Agnello, M. (2015). Biological impact of fluoroquinolone resistance in Pseudomonas aeruginosa. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/600617/rec/1116

Chicago Manual of Style (16th Edition):

Agnello, Melissa. “Biological impact of fluoroquinolone resistance in Pseudomonas aeruginosa.” 2015. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/600617/rec/1116.

MLA Handbook (7th Edition):

Agnello, Melissa. “Biological impact of fluoroquinolone resistance in Pseudomonas aeruginosa.” 2015. Web. 18 Apr 2021.

Vancouver:

Agnello M. Biological impact of fluoroquinolone resistance in Pseudomonas aeruginosa. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/600617/rec/1116.

Council of Science Editors:

Agnello M. Biological impact of fluoroquinolone resistance in Pseudomonas aeruginosa. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/600617/rec/1116


University of Southern California

2. Brill, Dab. Image-driven pharmacokinetics of tropoelastin nanoparticles.

Degree: MS, Molecular Pharmacology and Toxicology, 2015, University of Southern California

 Clinical pharmacokinetics (PK) primarily measures the concentration of drugs in the blood. For nanomedicines it may be more relevant to determine concentration within a target… (more)

Subjects/Keywords: pharmacokinetics; image-driven; positron emission tomography; molecular imaging; biodistribution

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APA (6th Edition):

Brill, D. (2015). Image-driven pharmacokinetics of tropoelastin nanoparticles. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3353

Chicago Manual of Style (16th Edition):

Brill, Dab. “Image-driven pharmacokinetics of tropoelastin nanoparticles.” 2015. Masters Thesis, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3353.

MLA Handbook (7th Edition):

Brill, Dab. “Image-driven pharmacokinetics of tropoelastin nanoparticles.” 2015. Web. 18 Apr 2021.

Vancouver:

Brill D. Image-driven pharmacokinetics of tropoelastin nanoparticles. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3353.

Council of Science Editors:

Brill D. Image-driven pharmacokinetics of tropoelastin nanoparticles. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3353


University of Southern California

3. Ha, Helen Nen. Identification of small-molecules targeting CXCR2 function and signaling.

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

 Chemokine receptor, CXCR2, and its ligands are an essential component of the immune system that mediates the trafficking of neutrophils to sites of infection. It… (more)

Subjects/Keywords: CXCR2; CXCL8; inflammation

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APA (6th Edition):

Ha, H. N. (2013). Identification of small-molecules targeting CXCR2 function and signaling. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/308809/rec/3324

Chicago Manual of Style (16th Edition):

Ha, Helen Nen. “Identification of small-molecules targeting CXCR2 function and signaling.” 2013. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/308809/rec/3324.

MLA Handbook (7th Edition):

Ha, Helen Nen. “Identification of small-molecules targeting CXCR2 function and signaling.” 2013. Web. 18 Apr 2021.

Vancouver:

Ha HN. Identification of small-molecules targeting CXCR2 function and signaling. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/308809/rec/3324.

Council of Science Editors:

Ha HN. Identification of small-molecules targeting CXCR2 function and signaling. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/308809/rec/3324


University of Southern California

4. Wang, Jian. ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients.

Degree: PhD, Molecular Pharmacology & Toxicology, 2009, University of Southern California

 Tacrolimus and mycophenolic acid (MPA) are commonly used in clinic to prevent rejection in transplant recipients. The influence of ABCB1 polymorphisms on tacrolimus dosing has… (more)

Subjects/Keywords: pharmacogenetics; ABCB1; IMPDH; transplantation; polymorphism

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

APA (6th Edition):

Wang, J. (2009). ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458

Chicago Manual of Style (16th Edition):

Wang, Jian. “ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients.” 2009. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458.

MLA Handbook (7th Edition):

Wang, Jian. “ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients.” 2009. Web. 18 Apr 2021.

Vancouver:

Wang J. ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458.

Council of Science Editors:

Wang J. ABCB1 and IMPDH functional and genetic contributions to tacrolimus and mycophenolic acid therapy in transplant patients. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/535363/rec/458

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