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You searched for +publisher:"University of Southern California" +contributor:("Roberts, Richard W."). Showing records 1 – 22 of 22 total matches.

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University of Southern California

1. Fiacco, Stephen V. Directed evolution provides stable, cell permeable, efficacious, and orally bioavailable peptidomimetics.

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

 Peptides have poor bioavailability and natural sequences cannot readily be converted into drug-like molecules. This is due in large part to protease degradation and difficulties… (more)

Subjects/Keywords: cyclic; bioavailibility

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APA (6th Edition):

Fiacco, S. V. (2014). Directed evolution provides stable, cell permeable, efficacious, and orally bioavailable peptidomimetics. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/39276/rec/2013

Chicago Manual of Style (16th Edition):

Fiacco, Stephen V. “Directed evolution provides stable, cell permeable, efficacious, and orally bioavailable peptidomimetics.” 2014. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/39276/rec/2013.

MLA Handbook (7th Edition):

Fiacco, Stephen V. “Directed evolution provides stable, cell permeable, efficacious, and orally bioavailable peptidomimetics.” 2014. Web. 21 Feb 2019.

Vancouver:

Fiacco SV. Directed evolution provides stable, cell permeable, efficacious, and orally bioavailable peptidomimetics. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/39276/rec/2013.

Council of Science Editors:

Fiacco SV. Directed evolution provides stable, cell permeable, efficacious, and orally bioavailable peptidomimetics. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/39276/rec/2013


University of Southern California

2. Lo, Hsien-Chun. Molecular genetic mining of the secondary metabolome in Aspergillus nidulans.

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

 Natural products (secondary metabolites) are an abundant source of bioactive compounds. These small molecules play substantial roles in modern drug development. Aspergillus, a member of… (more)

Subjects/Keywords: Secondary metabolites; Natural product

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APA (6th Edition):

Lo, H. (2012). Molecular genetic mining of the secondary metabolome in Aspergillus nidulans. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186

Chicago Manual of Style (16th Edition):

Lo, Hsien-Chun. “Molecular genetic mining of the secondary metabolome in Aspergillus nidulans.” 2012. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186.

MLA Handbook (7th Edition):

Lo, Hsien-Chun. “Molecular genetic mining of the secondary metabolome in Aspergillus nidulans.” 2012. Web. 21 Feb 2019.

Vancouver:

Lo H. Molecular genetic mining of the secondary metabolome in Aspergillus nidulans. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186.

Council of Science Editors:

Lo H. Molecular genetic mining of the secondary metabolome in Aspergillus nidulans. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/64711/rec/4186


University of Southern California

3. Thompson, Bryant. Predictable microfluidic mixing using discrete element microfluidics.

Degree: MS, Biomedical Engineering, 2015, University of Southern California

 A novel microfluidic platform has been developed which utilizes a library of standardized, modular components manufactured using stereolithography. Large‐scale 3‐dimensional assemblies that were previously difficult… (more)

Subjects/Keywords: microfluidics; modular microfluidics; 3D‐printed microfluidics; SLA

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APA (6th Edition):

Thompson, B. (2015). Predictable microfluidic mixing using discrete element microfluidics. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/601219/rec/5172

Chicago Manual of Style (16th Edition):

Thompson, Bryant. “Predictable microfluidic mixing using discrete element microfluidics.” 2015. Masters Thesis, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/601219/rec/5172.

MLA Handbook (7th Edition):

Thompson, Bryant. “Predictable microfluidic mixing using discrete element microfluidics.” 2015. Web. 21 Feb 2019.

Vancouver:

Thompson B. Predictable microfluidic mixing using discrete element microfluidics. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/601219/rec/5172.

Council of Science Editors:

Thompson B. Predictable microfluidic mixing using discrete element microfluidics. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/601219/rec/5172


University of Southern California

4. 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/7325

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 February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/630777/rec/7325.

MLA Handbook (7th Edition):

Sanchez, James F. “The study of the Aspergillus nidulans metabolome in the post-genomic era.” 2011. Web. 21 Feb 2019.

Vancouver:

Sanchez JF. The study of the Aspergillus nidulans metabolome in the post-genomic era. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/630777/rec/7325.

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/7325


University of Southern California

5. Schroeder, Christi A. Quantifying aspects of DNA damage.

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

 The exposure of deoxyribonucleic acid, DNA, to radiation is known to result in damage, which can lead to variety of biological consequences including disruptions in… (more)

Subjects/Keywords: DNA photodamage; DNA ionization

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APA (6th Edition):

Schroeder, C. A. (2013). Quantifying aspects of DNA damage. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/676733/rec/5342

Chicago Manual of Style (16th Edition):

Schroeder, Christi A. “Quantifying aspects of DNA damage.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/676733/rec/5342.

MLA Handbook (7th Edition):

Schroeder, Christi A. “Quantifying aspects of DNA damage.” 2013. Web. 21 Feb 2019.

Vancouver:

Schroeder CA. Quantifying aspects of DNA damage. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/676733/rec/5342.

Council of Science Editors:

Schroeder CA. Quantifying aspects of DNA damage. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/676733/rec/5342


University of Southern California

6. Howell, Shannon Marie. Directed evolution of high affinity, cyclic, protease resistant peptides using mRNA display.

Degree: PhD, Chemistry, 2016, University of Southern California

 Protein‐protein interaction networks are involved in a large number of cellular processes. The binding of two or more proteins in a cell can have a… (more)

Subjects/Keywords: mRNA display; peptides; evolution; selection; protease resistance; proteins

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APA (6th Edition):

Howell, S. M. (2016). Directed evolution of high affinity, cyclic, protease resistant peptides using mRNA display. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/432342/rec/2012

Chicago Manual of Style (16th Edition):

Howell, Shannon Marie. “Directed evolution of high affinity, cyclic, protease resistant peptides using mRNA display.” 2016. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/432342/rec/2012.

MLA Handbook (7th Edition):

Howell, Shannon Marie. “Directed evolution of high affinity, cyclic, protease resistant peptides using mRNA display.” 2016. Web. 21 Feb 2019.

Vancouver:

Howell SM. Directed evolution of high affinity, cyclic, protease resistant peptides using mRNA display. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/432342/rec/2012.

Council of Science Editors:

Howell SM. Directed evolution of high affinity, cyclic, protease resistant peptides using mRNA display. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/432342/rec/2012


University of Southern California

7. Somoza, Amber Dorothy. Application of biological and chemical approaches to generate new and diverse fungal natural products.

Degree: PhD, Chemistry, 2012, University of Southern California

 Filamentous fungi are prolific producers of bioactive secondary metabolites. Recent genome sequencing reveals fungi harbor more secondary metabolites than are currently known. Exploration of fungal… (more)

Subjects/Keywords: Aspergillus; fungi; secondary metabolites; genetic engineering; biosynthesis

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APA (6th Edition):

Somoza, A. D. (2012). Application of biological and chemical approaches to generate new and diverse fungal natural products. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/85291/rec/850

Chicago Manual of Style (16th Edition):

Somoza, Amber Dorothy. “Application of biological and chemical approaches to generate new and diverse fungal natural products.” 2012. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/85291/rec/850.

MLA Handbook (7th Edition):

Somoza, Amber Dorothy. “Application of biological and chemical approaches to generate new and diverse fungal natural products.” 2012. Web. 21 Feb 2019.

Vancouver:

Somoza AD. Application of biological and chemical approaches to generate new and diverse fungal natural products. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/85291/rec/850.

Council of Science Editors:

Somoza AD. Application of biological and chemical approaches to generate new and diverse fungal natural products. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/85291/rec/850


University of Southern California

8. Junge, Jason Alexander. Emergent visualization technology: evolution of PSD95.FingR.

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

 In vitro protein evolution through mRNA display is a powerful method whereby new proteins with interesting properties can be developed as tools to assist in… (more)

Subjects/Keywords: intrabody; mRNA display; PSD95; FingR; in vitro evolution

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APA (6th Edition):

Junge, J. A. (2013). Emergent visualization technology: evolution of PSD95.FingR. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/358906/rec/2300

Chicago Manual of Style (16th Edition):

Junge, Jason Alexander. “Emergent visualization technology: evolution of PSD95.FingR.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/358906/rec/2300.

MLA Handbook (7th Edition):

Junge, Jason Alexander. “Emergent visualization technology: evolution of PSD95.FingR.” 2013. Web. 21 Feb 2019.

Vancouver:

Junge JA. Emergent visualization technology: evolution of PSD95.FingR. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/358906/rec/2300.

Council of Science Editors:

Junge JA. Emergent visualization technology: evolution of PSD95.FingR. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/358906/rec/2300


University of Southern California

9. Oertell, Keriann Michelle. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.

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

 A β,γ-bridging oxygen substituted dNTP toolkit comprising a variety of steric and electrostatic properties has been synthesized and used to investigate DNA polymerase β. Surprisingly,… (more)

Subjects/Keywords: kinetics; fidelity; polymerase

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APA (6th Edition):

Oertell, K. M. (2013). DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071

Chicago Manual of Style (16th Edition):

Oertell, Keriann Michelle. “DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071.

MLA Handbook (7th Edition):

Oertell, Keriann Michelle. “DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.” 2013. Web. 21 Feb 2019.

Vancouver:

Oertell KM. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071.

Council of Science Editors:

Oertell KM. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071


University of Southern California

10. Hu, Biliang. Lentiviral vaccine engineering towards enhanced safety and efficiency.

Degree: PhD, Chemical Engineering, 2013, University of Southern California

 Extensive understanding of the lentivirus biology has evolved the design of lentivector (LV) for therapeutic gene delivery, and transformed lentivector to one of the most… (more)

Subjects/Keywords: cancer immunotherapy; CD8 T cell; dendritic cell; lentivector; transgene integration; tumor microenvironment

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APA (6th Edition):

Hu, B. (2013). Lentiviral vaccine engineering towards enhanced safety and efficiency. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795

Chicago Manual of Style (16th Edition):

Hu, Biliang. “Lentiviral vaccine engineering towards enhanced safety and efficiency.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795.

MLA Handbook (7th Edition):

Hu, Biliang. “Lentiviral vaccine engineering towards enhanced safety and efficiency.” 2013. Web. 21 Feb 2019.

Vancouver:

Hu B. Lentiviral vaccine engineering towards enhanced safety and efficiency. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795.

Council of Science Editors:

Hu B. Lentiviral vaccine engineering towards enhanced safety and efficiency. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/219102/rec/3795


University of Southern California

11. Jayathilaka, Nimanthi. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2012, University of Southern California

 Enzymes that modify epigenetic status provide attractive targets for therapy in various diseases including cardiac hypertrophy, cancer, neurodegenerative diseases, and immune dysfunction. The therapeutic development… (more)

Subjects/Keywords: histone deacetylases (HDAC); HDAC inhibitors; myocyte enhancer factor 2 (MEF2); transcription regulation

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APA (6th Edition):

Jayathilaka, N. (2012). Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496

Chicago Manual of Style (16th Edition):

Jayathilaka, Nimanthi. “Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.” 2012. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496.

MLA Handbook (7th Edition):

Jayathilaka, Nimanthi. “Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.” 2012. Web. 21 Feb 2019.

Vancouver:

Jayathilaka N. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496.

Council of Science Editors:

Jayathilaka N. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3496


University of Southern California

12. Praseuth, Mike B. Examinations of secondary metabolites and their production in fungi and bacteria.

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

 Fungi are known to produce a wide variety of secondary metabolites with biological activities that are commercially used as pharmaceutical agents (e.g. lovastatin and penicillin).… (more)

Subjects/Keywords: fungi; Aspergillus; nidulans; Niger; carbonarius; Escherichia coli; polyketide synthases

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APA (6th Edition):

Praseuth, M. B. (2013). Examinations of secondary metabolites and their production in fungi and bacteria. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/243435/rec/2567

Chicago Manual of Style (16th Edition):

Praseuth, Mike B. “Examinations of secondary metabolites and their production in fungi and bacteria.” 2013. Masters Thesis, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/243435/rec/2567.

MLA Handbook (7th Edition):

Praseuth, Mike B. “Examinations of secondary metabolites and their production in fungi and bacteria.” 2013. Web. 21 Feb 2019.

Vancouver:

Praseuth MB. Examinations of secondary metabolites and their production in fungi and bacteria. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/243435/rec/2567.

Council of Science Editors:

Praseuth MB. Examinations of secondary metabolites and their production in fungi and bacteria. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/243435/rec/2567


University of Southern California

13. Al-Bassam, Sarmad. A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons.

Degree: PhD, Molecular Biology, 2013, University of Southern California

 In neurons transmembrane proteins are targeted to dendrites in vesicles that traffic solely within the somatodendritic compartment. How these vesicles are retained within the somatodendritic… (more)

Subjects/Keywords: polarized trafficking; dissociated neurons; vesicle transport; axon tnitial segment; FKBP; conditional aggregation domain; shield-1; pulse-chase

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APA (6th Edition):

Al-Bassam, S. (2013). A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287

Chicago Manual of Style (16th Edition):

Al-Bassam, Sarmad. “A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287.

MLA Handbook (7th Edition):

Al-Bassam, Sarmad. “A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons.” 2013. Web. 21 Feb 2019.

Vancouver:

Al-Bassam S. A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287.

Council of Science Editors:

Al-Bassam S. A novel pulse-chase paradigm to visualize the trafficking of transport vesicles in neurons. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/225948/rec/287


University of Southern California

14. Hung, Kuo-Chan. Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2014, University of Southern California

 mRNA display is an in vitro selection technique that can evolve novel ligands to modulating protein-protein interactions and regulate crucial biological functions. Previous efforts have… (more)

Subjects/Keywords: mRNA display; in vitro selection technique; G protein-coupled receptors; β 2AR; DC-SIGN; cancer vaccine; Dendritic cells; fibronectin scaffold

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APA (6th Edition):

Hung, K. (2014). Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1910

Chicago Manual of Style (16th Edition):

Hung, Kuo-Chan. “Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN.” 2014. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1910.

MLA Handbook (7th Edition):

Hung, Kuo-Chan. “Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN.” 2014. Web. 21 Feb 2019.

Vancouver:

Hung K. Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1910.

Council of Science Editors:

Hung K. Developing peptide and antibody-mimetic ligands for the cell surface receptors β2AR and DC-SIGN. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/59567/rec/1910


University of Southern California

15. Mora, Rudy J. Genetically-encoded probes for visualizing protein trafficking dynamics in living neurons.

Degree: PhD, Neuroscience, 2012, University of Southern California

 Here I describe the development of genetically-encoded probes for visualizing the trafficking of neuronal proteins in living cells. The probes are derived from a diverse… (more)

Subjects/Keywords: probe; calcium; traffic; neuron; CaMKII

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APA (6th Edition):

Mora, R. J. (2012). Genetically-encoded probes for visualizing protein trafficking dynamics in living neurons. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8143/rec/3010

Chicago Manual of Style (16th Edition):

Mora, Rudy J. “Genetically-encoded probes for visualizing protein trafficking dynamics in living neurons.” 2012. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8143/rec/3010.

MLA Handbook (7th Edition):

Mora, Rudy J. “Genetically-encoded probes for visualizing protein trafficking dynamics in living neurons.” 2012. Web. 21 Feb 2019.

Vancouver:

Mora RJ. Genetically-encoded probes for visualizing protein trafficking dynamics in living neurons. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8143/rec/3010.

Council of Science Editors:

Mora RJ. Genetically-encoded probes for visualizing protein trafficking dynamics in living neurons. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/8143/rec/3010


University of Southern California

16. Jalali-Yazdi, Farzad. Generation and characterization of peptide theranostics by mRNA display.

Degree: PhD, Chemical Engineering, 2017, University of Southern California

 We explore the effectiveness of peptides as therapeutic reagents in chapters 2-4 of this work. In Chapter 2 we show successful inhibition of hepatitis C… (more)

Subjects/Keywords: peptide; mRNA display; hepatitis C virus; protein engineering; affinity

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

APA (6th Edition):

Jalali-Yazdi, F. (2017). Generation and characterization of peptide theranostics by mRNA display. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/605269/rec/2983

Chicago Manual of Style (16th Edition):

Jalali-Yazdi, Farzad. “Generation and characterization of peptide theranostics by mRNA display.” 2017. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/605269/rec/2983.

MLA Handbook (7th Edition):

Jalali-Yazdi, Farzad. “Generation and characterization of peptide theranostics by mRNA display.” 2017. Web. 21 Feb 2019.

Vancouver:

Jalali-Yazdi F. Generation and characterization of peptide theranostics by mRNA display. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/605269/rec/2983.

Council of Science Editors:

Jalali-Yazdi F. Generation and characterization of peptide theranostics by mRNA display. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/605269/rec/2983


University of Southern California

17. Noridomi, Kaori. Structural studies of nicotinic acetylcholine receptors and their regulatory complexes.

Degree: PhD, Chemistry, 2017, University of Southern California

 Nicotinic acetylcholine receptors (nAChRs) play a key role in neuronal communication by sending electric signals upon binding of neurotransmitters, acetylcholines. nAChRs relate closely to various… (more)

Subjects/Keywords: nicotinic acetylcholine receptors; crystal structure; crystallography; myasthenia gravis

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APA (6th Edition):

Noridomi, K. (2017). Structural studies of nicotinic acetylcholine receptors and their regulatory complexes. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117

Chicago Manual of Style (16th Edition):

Noridomi, Kaori. “Structural studies of nicotinic acetylcholine receptors and their regulatory complexes.” 2017. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117.

MLA Handbook (7th Edition):

Noridomi, Kaori. “Structural studies of nicotinic acetylcholine receptors and their regulatory complexes.” 2017. Web. 21 Feb 2019.

Vancouver:

Noridomi K. Structural studies of nicotinic acetylcholine receptors and their regulatory complexes. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117.

Council of Science Editors:

Noridomi K. Structural studies of nicotinic acetylcholine receptors and their regulatory complexes. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/632077/rec/6117


University of Southern California

18. Maker, Ashley Julia. Developing improved silica materials and devices for integrated optics applications.

Degree: PhD, Chemical Engineering, 2014, University of Southern California

 Due to their favorable optical and material properties, silica-based materials and devices have found many important applications throughout science and engineering, especially in sensing, communications,… (more)

Subjects/Keywords: sol-gel silica materials; high index films and coatings; rare earth lasers; optical sensors; integrated optics; toroid microcavities; optical resonators; waveguides

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APA (6th Edition):

Maker, A. J. (2014). Developing improved silica materials and devices for integrated optics applications. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419619/rec/1907

Chicago Manual of Style (16th Edition):

Maker, Ashley Julia. “Developing improved silica materials and devices for integrated optics applications.” 2014. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419619/rec/1907.

MLA Handbook (7th Edition):

Maker, Ashley Julia. “Developing improved silica materials and devices for integrated optics applications.” 2014. Web. 21 Feb 2019.

Vancouver:

Maker AJ. Developing improved silica materials and devices for integrated optics applications. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419619/rec/1907.

Council of Science Editors:

Maker AJ. Developing improved silica materials and devices for integrated optics applications. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/419619/rec/1907


University of Southern California

19. Chow, Cheryl-Emiliane T. Microbe to microbe: monthly microbial community dynamics and interactions at the San Pedro Ocean Time-series.

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

 Our ability to define and quantify individual microbe-microbe interactions with traditional community ecology principles is still in development yet these relationships are key to understanding… (more)

Subjects/Keywords: microbial ecology; marine microbiology; bacteria; virus; time-series; association networks

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APA (6th Edition):

Chow, C. T. (2013). Microbe to microbe: monthly microbial community dynamics and interactions at the San Pedro Ocean Time-series. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/69109/rec/4060

Chicago Manual of Style (16th Edition):

Chow, Cheryl-Emiliane T. “Microbe to microbe: monthly microbial community dynamics and interactions at the San Pedro Ocean Time-series.” 2013. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/69109/rec/4060.

MLA Handbook (7th Edition):

Chow, Cheryl-Emiliane T. “Microbe to microbe: monthly microbial community dynamics and interactions at the San Pedro Ocean Time-series.” 2013. Web. 21 Feb 2019.

Vancouver:

Chow CT. Microbe to microbe: monthly microbial community dynamics and interactions at the San Pedro Ocean Time-series. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/69109/rec/4060.

Council of Science Editors:

Chow CT. Microbe to microbe: monthly microbial community dynamics and interactions at the San Pedro Ocean Time-series. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/69109/rec/4060


University of Southern California

20. Le Ny, Anne-Laure M. Photocontrol of DNA compaction using light-responsive surfactants.

Degree: PhD, Chemical Engineering, 2008, University of Southern California

 DNA condensation in vitro has been of interest for many years as a model of naturally occurring DNA packaging (e.g. chromatin, sperm head and virus… (more)

Subjects/Keywords: DNA; compaction; surfactant; expansion; dynamics; vesicles

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

APA (6th Edition):

Le Ny, A. M. (2008). Photocontrol of DNA compaction using light-responsive surfactants. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/62851/rec/5032

Chicago Manual of Style (16th Edition):

Le Ny, Anne-Laure M. “Photocontrol of DNA compaction using light-responsive surfactants.” 2008. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/62851/rec/5032.

MLA Handbook (7th Edition):

Le Ny, Anne-Laure M. “Photocontrol of DNA compaction using light-responsive surfactants.” 2008. Web. 21 Feb 2019.

Vancouver:

Le Ny AM. Photocontrol of DNA compaction using light-responsive surfactants. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/62851/rec/5032.

Council of Science Editors:

Le Ny AM. Photocontrol of DNA compaction using light-responsive surfactants. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/62851/rec/5032


University of Southern California

21. Hamill, Andrea C. Photocontrol of protein conformation through the use of photoresponsive surfactants, investigated by small angle neutron scattering.

Degree: PhD, Chemical Engineering, 2008, University of Southern California

 A photoresponsive surfactant, azoTAB, is used to control protein structure. When azoTAB is combined with a protein, illumination with visible and UV light can be… (more)

Subjects/Keywords: protein; surfactant; small angle neutron scattering

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

APA (6th Edition):

Hamill, A. C. (2008). Photocontrol of protein conformation through the use of photoresponsive surfactants, investigated by small angle neutron scattering. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24126/rec/5034

Chicago Manual of Style (16th Edition):

Hamill, Andrea C. “Photocontrol of protein conformation through the use of photoresponsive surfactants, investigated by small angle neutron scattering.” 2008. Doctoral Dissertation, University of Southern California. Accessed February 21, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24126/rec/5034.

MLA Handbook (7th Edition):

Hamill, Andrea C. “Photocontrol of protein conformation through the use of photoresponsive surfactants, investigated by small angle neutron scattering.” 2008. Web. 21 Feb 2019.

Vancouver:

Hamill AC. Photocontrol of protein conformation through the use of photoresponsive surfactants, investigated by small angle neutron scattering. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2019 Feb 21]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24126/rec/5034.

Council of Science Editors:

Hamill AC. Photocontrol of protein conformation through the use of photoresponsive surfactants, investigated by small angle neutron scattering. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/24126/rec/5034


University of Southern California

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

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 February 21, 2019. 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. 21 Feb 2019.

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 2019 Feb 21]. 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

.