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You searched for +publisher:"University of Southern California" +contributor:("Wang, Clay C. C."). Showing records 1 – 20 of 20 total matches.

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University of Southern California

1. Chen, Yu-Sheng. Production and characterization of proinsulin-transferrin fusion protein.

Degree: MS, Pharmaceutical Sciences, 2011, University of Southern California

 A transferrin-based fusion protein, proinsulin-transferrin (ProIns-Tf) had been constructed using recombinant protein technology in our laboratory. Based on the in vitro preliminary results, ProIns-Tf reduced… (more)

Subjects/Keywords: bifunctional fusion protein; his-tag; insulin; proinsulin; protein purification; transferrin

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APA (6th Edition):

Chen, Y. (2011). Production and characterization of proinsulin-transferrin fusion protein. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258

Chicago Manual of Style (16th Edition):

Chen, Yu-Sheng. “Production and characterization of proinsulin-transferrin fusion protein.” 2011. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258.

MLA Handbook (7th Edition):

Chen, Yu-Sheng. “Production and characterization of proinsulin-transferrin fusion protein.” 2011. Web. 08 Mar 2021.

Vancouver:

Chen Y. Production and characterization of proinsulin-transferrin fusion protein. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258.

Council of Science Editors:

Chen Y. Production and characterization of proinsulin-transferrin fusion protein. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/627825/rec/5258


University of Southern California

2. Jain, Sofina M. Fungal polyketides  – Review of recent findings.

Degree: MS, Pharmacy / Pharmaceutical Sciences, 2011, University of Southern California

 Fungal polyketides are a group of bioactive compounds which have found use in humans as anti-cholesterol, anti-cancer and antibiotic agents. These are synthesized by a… (more)

Subjects/Keywords: fungal polyketides; HR-PKS; NR-PKS; PT domain; SAT domain; TE domain

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APA (6th Edition):

Jain, S. M. (2011). Fungal polyketides  – Review of recent findings. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/469726/rec/2951

Chicago Manual of Style (16th Edition):

Jain, Sofina M. “Fungal polyketides  – Review of recent findings.” 2011. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/469726/rec/2951.

MLA Handbook (7th Edition):

Jain, Sofina M. “Fungal polyketides  – Review of recent findings.” 2011. Web. 08 Mar 2021.

Vancouver:

Jain SM. Fungal polyketides  – Review of recent findings. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/469726/rec/2951.

Council of Science Editors:

Jain SM. Fungal polyketides  – Review of recent findings. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/469726/rec/2951


University of Southern California

3. Sanchez, James F. The study of the Aspergillus nidulans metabolome in the post-genomic era.

Degree: PhD, Pharmaceutical Sciences, 2011, University of Southern California

 Filamentous fungi have long been recognized to be a rich source of bioactive secondary metabolites. The genomic sequencing of several species of Aspergillus, however, has… (more)

Subjects/Keywords: Aspergillus nidulans; secondary metabolites; genetic deletion analysis; F9775; xanthones; prenylations

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APA (6th Edition):

Sanchez, J. F. (2011). The study of the Aspergillus nidulans metabolome in the post-genomic era. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/630777/rec/7334

Chicago Manual of Style (16th Edition):

Sanchez, James F. “The study of the Aspergillus nidulans metabolome in the post-genomic era.” 2011. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/630777/rec/7334.

MLA Handbook (7th Edition):

Sanchez, James F. “The study of the Aspergillus nidulans metabolome in the post-genomic era.” 2011. Web. 08 Mar 2021.

Vancouver:

Sanchez JF. The study of the Aspergillus nidulans metabolome in the post-genomic era. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/630777/rec/7334.

Council of Science Editors:

Sanchez JF. The study of the Aspergillus nidulans metabolome in the post-genomic era. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/630777/rec/7334


University of Southern California

4. Janson, Matthew Austin. Genotoxic impurity analysis in pharmaceuticals.

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

 This review paper covers the analytical methods used to monitor genotoxic impurities. Specifically, the impurities discussed here contain hydrazine, nitro, arylamine or aldehyde functional groups… (more)

Subjects/Keywords: genotoxic; impurity; pharmaceutical; analysis; review

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APA (6th Edition):

Janson, M. A. (2009). Genotoxic impurity analysis in pharmaceuticals. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253144/rec/3026

Chicago Manual of Style (16th Edition):

Janson, Matthew Austin. “Genotoxic impurity analysis in pharmaceuticals.” 2009. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253144/rec/3026.

MLA Handbook (7th Edition):

Janson, Matthew Austin. “Genotoxic impurity analysis in pharmaceuticals.” 2009. Web. 08 Mar 2021.

Vancouver:

Janson MA. Genotoxic impurity analysis in pharmaceuticals. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253144/rec/3026.

Council of Science Editors:

Janson MA. Genotoxic impurity analysis in pharmaceuticals. [Masters Thesis]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253144/rec/3026


University of Southern California

5. Lin, Alexander. Isolation of secondary metabolites from Aspergillus nidulans.

Degree: MS, Biochemistry & Molecular Biology, 2009, University of Southern California

 The sequencing of fungal genomes has shown that there are many more secondary metabolism pathways than previously thought. Using a variety of genetic approaches, the… (more)

Subjects/Keywords: secondary metabolites; Aspergillus nidulans; austinol; dehydroaustinol; asperfuranone; ergosterol

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APA (6th Edition):

Lin, A. (2009). Isolation of secondary metabolites from Aspergillus nidulans. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266532/rec/3670

Chicago Manual of Style (16th Edition):

Lin, Alexander. “Isolation of secondary metabolites from Aspergillus nidulans.” 2009. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266532/rec/3670.

MLA Handbook (7th Edition):

Lin, Alexander. “Isolation of secondary metabolites from Aspergillus nidulans.” 2009. Web. 08 Mar 2021.

Vancouver:

Lin A. Isolation of secondary metabolites from Aspergillus nidulans. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266532/rec/3670.

Council of Science Editors:

Lin A. Isolation of secondary metabolites from Aspergillus nidulans. [Masters Thesis]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/266532/rec/3670


University of Southern California

6. Albayram, Onder. Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations.

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

 Single nucleotide polymorphisms (SNPs) might be at the basis of both the relationship between genetic diversification influencing drug metabolism (pharmacokinetic approach) or drug targets (pharmacodynamic… (more)

Subjects/Keywords: schizophrenia; pharmacogenetics; molecular diagnosis

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APA (6th Edition):

Albayram, O. (2008). Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193716/rec/4192

Chicago Manual of Style (16th Edition):

Albayram, Onder. “Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations.” 2008. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193716/rec/4192.

MLA Handbook (7th Edition):

Albayram, Onder. “Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations.” 2008. Web. 08 Mar 2021.

Vancouver:

Albayram O. Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193716/rec/4192.

Council of Science Editors:

Albayram O. Molecular genetic mechanisms of schizophrenia and pharmacogenetic characterizations. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/193716/rec/4192


University of Southern California

7. Sanchez, Tino Wilson. Discovery of new HIV-1 integrase inhibitors.

Degree: MS, Pharmacy / Pharmaceutical Sciences, 2007, University of Southern California

 We identified 49 novel HIV-1 IN inhibitors with a wide inhibitory profile. Furan and sulfonamide based inhibitors were tested in vitro against HIV-1 IN. Their… (more)

Subjects/Keywords: integrase; HIV

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APA (6th Edition):

Sanchez, T. W. (2007). Discovery of new HIV-1 integrase inhibitors. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484210/rec/2028

Chicago Manual of Style (16th Edition):

Sanchez, Tino Wilson. “Discovery of new HIV-1 integrase inhibitors.” 2007. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484210/rec/2028.

MLA Handbook (7th Edition):

Sanchez, Tino Wilson. “Discovery of new HIV-1 integrase inhibitors.” 2007. Web. 08 Mar 2021.

Vancouver:

Sanchez TW. Discovery of new HIV-1 integrase inhibitors. [Internet] [Masters thesis]. University of Southern California; 2007. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484210/rec/2028.

Council of Science Editors:

Sanchez TW. Discovery of new HIV-1 integrase inhibitors. [Masters Thesis]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484210/rec/2028


University of Southern California

8. Lo, Hsien-Chun. Secondary metabolites of Aspergillus nidulans.

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

 The complete sequencing of genomes of several Aspergillus species, including A. nidulans, revealed that these fungal species have a potential to produce a surprising large… (more)

Subjects/Keywords: secondary metabolites; Aspergillus nidulans

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APA (6th Edition):

Lo, H. (2008). Secondary metabolites of Aspergillus nidulans. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/57384/rec/5741

Chicago Manual of Style (16th Edition):

Lo, Hsien-Chun. “Secondary metabolites of Aspergillus nidulans.” 2008. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/57384/rec/5741.

MLA Handbook (7th Edition):

Lo, Hsien-Chun. “Secondary metabolites of Aspergillus nidulans.” 2008. Web. 08 Mar 2021.

Vancouver:

Lo H. Secondary metabolites of Aspergillus nidulans. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/57384/rec/5741.

Council of Science Editors:

Lo H. Secondary metabolites of Aspergillus nidulans. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/57384/rec/5741


University of Southern California

9. Lee, Hsin-Fang. Preparation and characterization of Tf-G-CSF fusion protein.

Degree: MS, Molecular Pharmacology & Toxicology, 2008, University of Southern California

 In this study, Tf-H42-G-CSF fusion protein was engineered for investigating the effects of H4 helical linker 's on the fusion protein expression and the sequence… (more)

Subjects/Keywords: transferrin; G-CSF; fusion protein

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APA (6th Edition):

Lee, H. (2008). Preparation and characterization of Tf-G-CSF fusion protein. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189

Chicago Manual of Style (16th Edition):

Lee, Hsin-Fang. “Preparation and characterization of Tf-G-CSF fusion protein.” 2008. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189.

MLA Handbook (7th Edition):

Lee, Hsin-Fang. “Preparation and characterization of Tf-G-CSF fusion protein.” 2008. Web. 08 Mar 2021.

Vancouver:

Lee H. Preparation and characterization of Tf-G-CSF fusion protein. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189.

Council of Science Editors:

Lee H. Preparation and characterization of Tf-G-CSF fusion protein. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/89126/rec/5189


University of Southern California

10. Ren, Ling. Comparison of cellular uptake of arginine-rich cell-penetrating peptides.

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

 In this study, five arginine-rich peptides YGR6, YGR6E6, YG(RE)6, YGR6G6 and YG(RG)6 were engineered for investigating the roles of positive charges and sequence of cationic… (more)

Subjects/Keywords: cell-penetrating peptide; arginine rich; transduction; endocytosis; drug delivery

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APA (6th Edition):

Ren, L. (2009). Comparison of cellular uptake of arginine-rich cell-penetrating peptides. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/235676/rec/1511

Chicago Manual of Style (16th Edition):

Ren, Ling. “Comparison of cellular uptake of arginine-rich cell-penetrating peptides.” 2009. Masters Thesis, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/235676/rec/1511.

MLA Handbook (7th Edition):

Ren, Ling. “Comparison of cellular uptake of arginine-rich cell-penetrating peptides.” 2009. Web. 08 Mar 2021.

Vancouver:

Ren L. Comparison of cellular uptake of arginine-rich cell-penetrating peptides. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/235676/rec/1511.

Council of Science Editors:

Ren L. Comparison of cellular uptake of arginine-rich cell-penetrating peptides. [Masters Thesis]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/235676/rec/1511


University of Southern California

11. Kim, Kyunghwan. Identification of two negative regulators of p53: H1.2 complex and VprBP.

Degree: PhD, Biochemistry & Molecular Biology, 2010, University of Southern California

 p53 is a transcription factor which regulates the cell cycle, DNA repair and apoptosis in response to DNA damage. Even though the mechanisms of p53… (more)

Subjects/Keywords: p53; linker histone; VprBP; chromatin; transcription; histone; acetylation; cancer

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APA (6th Edition):

Kim, K. (2010). Identification of two negative regulators of p53: H1.2 complex and VprBP. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310646/rec/3327

Chicago Manual of Style (16th Edition):

Kim, Kyunghwan. “Identification of two negative regulators of p53: H1.2 complex and VprBP.” 2010. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310646/rec/3327.

MLA Handbook (7th Edition):

Kim, Kyunghwan. “Identification of two negative regulators of p53: H1.2 complex and VprBP.” 2010. Web. 08 Mar 2021.

Vancouver:

Kim K. Identification of two negative regulators of p53: H1.2 complex and VprBP. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310646/rec/3327.

Council of Science Editors:

Kim K. Identification of two negative regulators of p53: H1.2 complex and VprBP. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/310646/rec/3327


University of Southern California

12. Praseuth, Alex. Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds.

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

 Nonribosomal peptides (NRPs) are synthesized by modular mega–enzyme called NRP synthetase (NRPS) that catalyze a peptide bond forming reaction using natural amino acid as substrate.… (more)

Subjects/Keywords: NRPS

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APA (6th Edition):

Praseuth, A. (2008). Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85841/rec/928

Chicago Manual of Style (16th Edition):

Praseuth, Alex. “Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85841/rec/928.

MLA Handbook (7th Edition):

Praseuth, Alex. “Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds.” 2008. Web. 08 Mar 2021.

Vancouver:

Praseuth A. Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85841/rec/928.

Council of Science Editors:

Praseuth A. Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85841/rec/928


University of Southern California

13. Al-Mawsawi, Laith Qassim. Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design.

Degree: PhD, Pharmaceutical Sciences, 2007, University of Southern California

 HIV-1 integrase (IN) is an essential enzyme for viral replication and the subject of extensive pharmacological research aimed at designing clinically suitable drugs for the… (more)

Subjects/Keywords: HIV; integrase; protein structure and function; inhibitor; drug design

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APA (6th Edition):

Al-Mawsawi, L. Q. (2007). Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/579616/rec/2026

Chicago Manual of Style (16th Edition):

Al-Mawsawi, Laith Qassim. “Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design.” 2007. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/579616/rec/2026.

MLA Handbook (7th Edition):

Al-Mawsawi, Laith Qassim. “Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design.” 2007. Web. 08 Mar 2021.

Vancouver:

Al-Mawsawi LQ. Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/579616/rec/2026.

Council of Science Editors:

Al-Mawsawi LQ. Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design. [Doctoral Dissertation]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/579616/rec/2026


University of Southern California

14. Zawahir, Faathma. Targeting human base excision repair as a novel strategy in cancer therapeutics.

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

 APE1 is an attractive target for the rational design of small-molecule inhibitors in the field of oncological therapeutic research. It is an essential enzyme in… (more)

Subjects/Keywords: APE1; DNA repair; cancer therapeutics

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APA (6th Edition):

Zawahir, F. (2009). Targeting human base excision repair as a novel strategy in cancer therapeutics. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248516/rec/6327

Chicago Manual of Style (16th Edition):

Zawahir, Faathma. “Targeting human base excision repair as a novel strategy in cancer therapeutics.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248516/rec/6327.

MLA Handbook (7th Edition):

Zawahir, Faathma. “Targeting human base excision repair as a novel strategy in cancer therapeutics.” 2009. Web. 08 Mar 2021.

Vancouver:

Zawahir F. Targeting human base excision repair as a novel strategy in cancer therapeutics. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248516/rec/6327.

Council of Science Editors:

Zawahir F. Targeting human base excision repair as a novel strategy in cancer therapeutics. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248516/rec/6327


University of Southern California

15. 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 (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


University of Southern California

16. Barnes, Maureen P. Cytochrome c cationic oligopeptide conjugates: their cellular uptake, intracellular processing and biological activity.

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

 Peptides characterized as protein transduction domain peptides (PTD) or membrane transduction peptides (MTP) have recently attracted attention as a novel approach for the efficient intracellular… (more)

Subjects/Keywords: Barnes

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APA (6th Edition):

Barnes, M. P. (2009). Cytochrome c cationic oligopeptide conjugates: their cellular uptake, intracellular processing and biological activity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/161201/rec/1751

Chicago Manual of Style (16th Edition):

Barnes, Maureen P. “Cytochrome c cationic oligopeptide conjugates: their cellular uptake, intracellular processing and biological activity.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/161201/rec/1751.

MLA Handbook (7th Edition):

Barnes, Maureen P. “Cytochrome c cationic oligopeptide conjugates: their cellular uptake, intracellular processing and biological activity.” 2009. Web. 08 Mar 2021.

Vancouver:

Barnes MP. Cytochrome c cationic oligopeptide conjugates: their cellular uptake, intracellular processing and biological activity. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/161201/rec/1751.

Council of Science Editors:

Barnes MP. Cytochrome c cationic oligopeptide conjugates: their cellular uptake, intracellular processing and biological activity. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/161201/rec/1751


University of Southern California

17. Li, Angela Ying-Jian. Molecular analysis of high mobility group A2 (HMGA2) oncogenic function.

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

 HMGA2 is located on chromosome 12q13-15, which is frequently amplified or subjected to chromosomal rearrangements in human cancers. However, the multitudinous tumorigenic roles of HMGA2… (more)

Subjects/Keywords: HMGA2; NHEJ; DNA-PK; DSBs; hTERT; telomere

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APA (6th Edition):

Li, A. Y. (2008). Molecular analysis of high mobility group A2 (HMGA2) oncogenic function. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176

Chicago Manual of Style (16th Edition):

Li, Angela Ying-Jian. “Molecular analysis of high mobility group A2 (HMGA2) oncogenic function.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176.

MLA Handbook (7th Edition):

Li, Angela Ying-Jian. “Molecular analysis of high mobility group A2 (HMGA2) oncogenic function.” 2008. Web. 08 Mar 2021.

Vancouver:

Li AY. Molecular analysis of high mobility group A2 (HMGA2) oncogenic function. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176.

Council of Science Editors:

Li AY. Molecular analysis of high mobility group A2 (HMGA2) oncogenic function. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86635/rec/4176


University of Southern California

18. Tsai, Albert G. Molecular mechanisms of recurrent chromosomal translocations in human leukemias and lymphomas.

Degree: PhD, Biochemistry & Molecular Biology, 2008, University of Southern California

 The bcl-2 translocation, t(14;18)(q32;q21), is found in about 50% of all non-Hodgkin 's lymphomas, and the bcl-1 translocation, t(11;14)(q13;q32), in >90% of mantle cell lymphomas,… (more)

Subjects/Keywords: chromosomal translocation; chromosomal rearrangement; DNA double-strand break repair; non-Hodgkin'; s lymphoma

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

APA (6th Edition):

Tsai, A. G. (2008). Molecular mechanisms of recurrent chromosomal translocations in human leukemias and lymphomas. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/196021/rec/4201

Chicago Manual of Style (16th Edition):

Tsai, Albert G. “Molecular mechanisms of recurrent chromosomal translocations in human leukemias and lymphomas.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/196021/rec/4201.

MLA Handbook (7th Edition):

Tsai, Albert G. “Molecular mechanisms of recurrent chromosomal translocations in human leukemias and lymphomas.” 2008. Web. 08 Mar 2021.

Vancouver:

Tsai AG. Molecular mechanisms of recurrent chromosomal translocations in human leukemias and lymphomas. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/196021/rec/4201.

Council of Science Editors:

Tsai AG. Molecular mechanisms of recurrent chromosomal translocations in human leukemias and lymphomas. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/196021/rec/4201


University of Southern California

19. Evans, Eunbyul. The characterization of SNAREs and rabs in lacrimal gland acinar cells.

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

 The lacrimal gland secretes tear proteins and fluid to help maintain a healthy ocular surface. Dry eye diseases are often characterized by decreased secretory function… (more)

Subjects/Keywords: SNAREs; rab gtpases; pIgR; rab3D; vesicle trafficking; acinar cells

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APA (6th Edition):

Evans, E. (2008). The characterization of SNAREs and rabs in lacrimal gland acinar cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/197418/rec/6506

Chicago Manual of Style (16th Edition):

Evans, Eunbyul. “The characterization of SNAREs and rabs in lacrimal gland acinar cells.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/197418/rec/6506.

MLA Handbook (7th Edition):

Evans, Eunbyul. “The characterization of SNAREs and rabs in lacrimal gland acinar cells.” 2008. Web. 08 Mar 2021.

Vancouver:

Evans E. The characterization of SNAREs and rabs in lacrimal gland acinar cells. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/197418/rec/6506.

Council of Science Editors:

Evans E. The characterization of SNAREs and rabs in lacrimal gland acinar cells. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/197418/rec/6506


University of Southern California

20. Yuan, Liyun. Reversible lipidization of peptide and protein drugs for prolonging the plasma half-lives and passive liver targeting.

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

 The interest in developing peptide and protein drugs has been shadowed by their short elimination half-life and impermeability through biological membranes. Pegylation is widely attempted… (more)

Subjects/Keywords: reversible lipidization; octreotide; interferon-alpha; plasma half-lives; liver targeting

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

APA (6th Edition):

Yuan, L. (2009). Reversible lipidization of peptide and protein drugs for prolonging the plasma half-lives and passive liver targeting. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/593072/rec/5583

Chicago Manual of Style (16th Edition):

Yuan, Liyun. “Reversible lipidization of peptide and protein drugs for prolonging the plasma half-lives and passive liver targeting.” 2009. Doctoral Dissertation, University of Southern California. Accessed March 08, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/593072/rec/5583.

MLA Handbook (7th Edition):

Yuan, Liyun. “Reversible lipidization of peptide and protein drugs for prolonging the plasma half-lives and passive liver targeting.” 2009. Web. 08 Mar 2021.

Vancouver:

Yuan L. Reversible lipidization of peptide and protein drugs for prolonging the plasma half-lives and passive liver targeting. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2021 Mar 08]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/593072/rec/5583.

Council of Science Editors:

Yuan L. Reversible lipidization of peptide and protein drugs for prolonging the plasma half-lives and passive liver targeting. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/593072/rec/5583

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