Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"University of Southern California" +contributor:("Shen, Wei-Chiang"). Showing records 1 – 30 of 55 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

▼ Search Limiters


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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 Mar 2021.

Vancouver:

Chen Y. Production and characterization of proinsulin-transferrin fusion protein. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2021 Mar 05]. 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. Ma, Tao. Expression and purification of different elastin like polypeptides (ELPs) constructs for therapeutic applications.

Degree: MS, Pharmaceutical Sciences, 2015, University of Southern California

 There are many rationales for modifying recombinant proteins by using polymers, which include: i) altering permeability/diffusion via controlling their hydrodynamic radius; ii) modulating mediators of… (more)

Subjects/Keywords: elastin like polypeptides; ELPs; lacritin; protein expression; scaling-up of protein purification; endotoxin removal

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ma, T. (2015). Expression and purification of different elastin like polypeptides (ELPs) constructs for therapeutic applications. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/592829/rec/2687

Chicago Manual of Style (16th Edition):

Ma, Tao. “Expression and purification of different elastin like polypeptides (ELPs) constructs for therapeutic applications.” 2015. Masters Thesis, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/592829/rec/2687.

MLA Handbook (7th Edition):

Ma, Tao. “Expression and purification of different elastin like polypeptides (ELPs) constructs for therapeutic applications.” 2015. Web. 05 Mar 2021.

Vancouver:

Ma T. Expression and purification of different elastin like polypeptides (ELPs) constructs for therapeutic applications. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/592829/rec/2687.

Council of Science Editors:

Ma T. Expression and purification of different elastin like polypeptides (ELPs) constructs for therapeutic applications. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/592829/rec/2687


University of Southern California

3. Agarwal, Amit Rajendra. Metabolic shift in lung alveolar cell mitochondria after exposure to environmental toxicants.

Degree: PhD, Molecular Pharmacology and Toxicology, 2014, University of Southern California

 Cigarette smoking (CS) leads to alteration in cellular redox status, a hallmark in the pathogenesis of chronic obstructive pulmonary disease (COPD). The current study was… (more)

Subjects/Keywords: alveolar cells; mitochondria; pulmonary surfactant; acrolein; respiration; oxidative stress; GAPDH

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Agarwal, A. R. (2014). Metabolic shift in lung alveolar cell mitochondria after exposure to environmental toxicants. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/348237/rec/4054

Chicago Manual of Style (16th Edition):

Agarwal, Amit Rajendra. “Metabolic shift in lung alveolar cell mitochondria after exposure to environmental toxicants.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/348237/rec/4054.

MLA Handbook (7th Edition):

Agarwal, Amit Rajendra. “Metabolic shift in lung alveolar cell mitochondria after exposure to environmental toxicants.” 2014. Web. 05 Mar 2021.

Vancouver:

Agarwal AR. Metabolic shift in lung alveolar cell mitochondria after exposure to environmental toxicants. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/348237/rec/4054.

Council of Science Editors:

Agarwal AR. Metabolic shift in lung alveolar cell mitochondria after exposure to environmental toxicants. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/348237/rec/4054


University of Southern California

4. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 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 05]. 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

5. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 Mar 2021.

Vancouver:

Jain SM. Fungal polyketides  – Review of recent findings. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2021 Mar 05]. 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

6. Qiu, Xinru. pH-sensitive cytotoxicity of a cell penetrating peptide fused with a histidine-glutamate co-oligopeptide.

Degree: MS, Pharmaceutical Sciences, 2015, University of Southern California

 With the growth of research and biotechnology, more proteins and peptides have been developed as potential therapeutics. Due to their high cell surface binding and… (more)

Subjects/Keywords: pH-sensitive; cytotoxicity; cell penetrating peptide; acidic tumor microenvironment

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Qiu, X. (2015). pH-sensitive cytotoxicity of a cell penetrating peptide fused with a histidine-glutamate co-oligopeptide. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/553016/rec/5013

Chicago Manual of Style (16th Edition):

Qiu, Xinru. “pH-sensitive cytotoxicity of a cell penetrating peptide fused with a histidine-glutamate co-oligopeptide.” 2015. Masters Thesis, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/553016/rec/5013.

MLA Handbook (7th Edition):

Qiu, Xinru. “pH-sensitive cytotoxicity of a cell penetrating peptide fused with a histidine-glutamate co-oligopeptide.” 2015. Web. 05 Mar 2021.

Vancouver:

Qiu X. pH-sensitive cytotoxicity of a cell penetrating peptide fused with a histidine-glutamate co-oligopeptide. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/553016/rec/5013.

Council of Science Editors:

Qiu X. pH-sensitive cytotoxicity of a cell penetrating peptide fused with a histidine-glutamate co-oligopeptide. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/553016/rec/5013


University of Southern California

7. Chen, Yi-Hsun. Computer modeling of protein-peptide interface solvation.

Degree: MS, Pharmaceutical Sciences, 2014, University of Southern California

 Water is important in the formation of bimolecular complexes by forming hydrogen bonds to other neighboring water molecules. The formation of hydrogen bond networks could… (more)

Subjects/Keywords: computational calculation; computer modeling; protein-peptide complex; solvation; WATGEN; Abl-SH3 domain

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, Y. (2014). Computer modeling of protein-peptide interface solvation. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515488/rec/1558

Chicago Manual of Style (16th Edition):

Chen, Yi-Hsun. “Computer modeling of protein-peptide interface solvation.” 2014. Masters Thesis, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515488/rec/1558.

MLA Handbook (7th Edition):

Chen, Yi-Hsun. “Computer modeling of protein-peptide interface solvation.” 2014. Web. 05 Mar 2021.

Vancouver:

Chen Y. Computer modeling of protein-peptide interface solvation. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515488/rec/1558.

Council of Science Editors:

Chen Y. Computer modeling of protein-peptide interface solvation. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515488/rec/1558


University of Southern California

8. Jiang, Tianyi. Energy metabolism and inflammation in brain aging: significance of age-dependent astrocyte metabolic-redox profile.

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

 Aging is risk factor for diseases in both peripheral and central nervous system. Studies in this dissertation are aimed at investigating brain aging in the… (more)

Subjects/Keywords: brain aging; lipoic acid; mitochondria; insulin signaling; JNK signaling; PGC1α

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jiang, T. (2015). Energy metabolism and inflammation in brain aging: significance of age-dependent astrocyte metabolic-redox profile. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/433414/rec/2355

Chicago Manual of Style (16th Edition):

Jiang, Tianyi. “Energy metabolism and inflammation in brain aging: significance of age-dependent astrocyte metabolic-redox profile.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/433414/rec/2355.

MLA Handbook (7th Edition):

Jiang, Tianyi. “Energy metabolism and inflammation in brain aging: significance of age-dependent astrocyte metabolic-redox profile.” 2015. Web. 05 Mar 2021.

Vancouver:

Jiang T. Energy metabolism and inflammation in brain aging: significance of age-dependent astrocyte metabolic-redox profile. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/433414/rec/2355.

Council of Science Editors:

Jiang T. Energy metabolism and inflammation in brain aging: significance of age-dependent astrocyte metabolic-redox profile. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/433414/rec/2355


University of Southern California

9. Sun, Shuting. Fluorescent imaging probes of nitrogen-containing bone active drugs: design, synthesis and applications.

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

 Bisphosphonates (BPs) are therapeutic agents for treatment of bone disorders such as osteoporosis and Paget’s disease. Several nitrogen-containing bisphosphonates (N-BPs) and phosphonocarboxylate (PC) analogues also… (more)

Subjects/Keywords: bisphosphonates; BPs; imaging probes; fluorescent imaging; fluorescent bisphosphonates; nitrogen-containing bisphosphonates; N-BPs; risedronate; zoledronate; minodronate; phosphonocarboxylate; osteoporosis; osteonecrosis of the jaw; ONJ; drug distribution; otosclerosis; cochlear imaging; cancer imaging; click chemistry; azido bisphosphonate

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sun, S. (2015). Fluorescent imaging probes of nitrogen-containing bone active drugs: design, synthesis and applications. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/337307/rec/2853

Chicago Manual of Style (16th Edition):

Sun, Shuting. “Fluorescent imaging probes of nitrogen-containing bone active drugs: design, synthesis and applications.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/337307/rec/2853.

MLA Handbook (7th Edition):

Sun, Shuting. “Fluorescent imaging probes of nitrogen-containing bone active drugs: design, synthesis and applications.” 2015. Web. 05 Mar 2021.

Vancouver:

Sun S. Fluorescent imaging probes of nitrogen-containing bone active drugs: design, synthesis and applications. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/337307/rec/2853.

Council of Science Editors:

Sun S. Fluorescent imaging probes of nitrogen-containing bone active drugs: design, synthesis and applications. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/337307/rec/2853


University of Southern California

10. Wang, Hsuan-Yao. Comparison of the pharmacokinetic profiles between monomeric and oligomeric transferrin.

Degree: MS, Pharmaceutical Sciences, 2014, University of Southern California

 Transferrin, a protein responsible for transporting ferric ion, has been utilized in therapeutic development with the characteristics of inducing endocytosis and transcytosis. Several protein therapeutic… (more)

Subjects/Keywords: transferrin; oligomer; pharmacokinetics; drug delivery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, H. (2014). Comparison of the pharmacokinetic profiles between monomeric and oligomeric transferrin. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/407009/rec/1521

Chicago Manual of Style (16th Edition):

Wang, Hsuan-Yao. “Comparison of the pharmacokinetic profiles between monomeric and oligomeric transferrin.” 2014. Masters Thesis, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/407009/rec/1521.

MLA Handbook (7th Edition):

Wang, Hsuan-Yao. “Comparison of the pharmacokinetic profiles between monomeric and oligomeric transferrin.” 2014. Web. 05 Mar 2021.

Vancouver:

Wang H. Comparison of the pharmacokinetic profiles between monomeric and oligomeric transferrin. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/407009/rec/1521.

Council of Science Editors:

Wang H. Comparison of the pharmacokinetic profiles between monomeric and oligomeric transferrin. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/407009/rec/1521


University of Southern California

11. Zhou, Jie. A novel in-cell lethality-based molecular screening system using a split barnase.

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

 We have developed a cell-based reporter assay using the cytotoxic ribonuclease barnase aimed at identifying new protein-protein inhibitors. Barnase is an extensively well-characterized N1/T1 ribonuclease,… (more)

Subjects/Keywords: Barnase; lethality; screening system; protein interaction inhibitor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhou, J. (2012). A novel in-cell lethality-based molecular screening system using a split barnase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80406/rec/284

Chicago Manual of Style (16th Edition):

Zhou, Jie. “A novel in-cell lethality-based molecular screening system using a split barnase.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80406/rec/284.

MLA Handbook (7th Edition):

Zhou, Jie. “A novel in-cell lethality-based molecular screening system using a split barnase.” 2012. Web. 05 Mar 2021.

Vancouver:

Zhou J. A novel in-cell lethality-based molecular screening system using a split barnase. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80406/rec/284.

Council of Science Editors:

Zhou J. A novel in-cell lethality-based molecular screening system using a split barnase. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/80406/rec/284


University of Southern California

12. Sancheti, Harshkumar. Age dependent modulation of synaptic plasticity and insulin mimetic effect of lipoic acid on a 3xTg-AD mouse model of Alzheimer's disease: implications as a therapeutic/nutraceutical agent.

Degree: PhD, Molecular Pharmacology and Toxicology, 2016, University of Southern California

 Alzheimer’s disease is a type of dementia that causes problems with memory, thinking and behavior. Currently, there are no approved drugs to treat Alzheimer’s disease;… (more)

Subjects/Keywords: Alzheimer'; s disease; triple transgenic mice (3xTg-AD); lipoic acid; brain; glucose uptake; glucose metabolism; PI3K/Akt; IRS; glutamate; hypometabolism; hypermetabolism; synaptic plasticity; long term potentiation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sancheti, H. (2016). Age dependent modulation of synaptic plasticity and insulin mimetic effect of lipoic acid on a 3xTg-AD mouse model of Alzheimer's disease: implications as a therapeutic/nutraceutical agent. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/376878/rec/577

Chicago Manual of Style (16th Edition):

Sancheti, Harshkumar. “Age dependent modulation of synaptic plasticity and insulin mimetic effect of lipoic acid on a 3xTg-AD mouse model of Alzheimer's disease: implications as a therapeutic/nutraceutical agent.” 2016. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/376878/rec/577.

MLA Handbook (7th Edition):

Sancheti, Harshkumar. “Age dependent modulation of synaptic plasticity and insulin mimetic effect of lipoic acid on a 3xTg-AD mouse model of Alzheimer's disease: implications as a therapeutic/nutraceutical agent.” 2016. Web. 05 Mar 2021.

Vancouver:

Sancheti H. Age dependent modulation of synaptic plasticity and insulin mimetic effect of lipoic acid on a 3xTg-AD mouse model of Alzheimer's disease: implications as a therapeutic/nutraceutical agent. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/376878/rec/577.

Council of Science Editors:

Sancheti H. Age dependent modulation of synaptic plasticity and insulin mimetic effect of lipoic acid on a 3xTg-AD mouse model of Alzheimer's disease: implications as a therapeutic/nutraceutical agent. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/376878/rec/577


University of Southern California

13. Shah, Manali. Protein aggregation: current scenario and recent developments.

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

 Aggregation of proteins is the major topic of discussion and debate in the biopharmaceutical industry. Various chemical and physical properties of proteins have been studied… (more)

Subjects/Keywords: protein; aggregation; degenerative diseases; protein aggregates; aggregation detection techniques; protein aggregation diseases; mechanisms of protein aggregation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shah, M. (2012). Protein aggregation: current scenario and recent developments. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300

Chicago Manual of Style (16th Edition):

Shah, Manali. “Protein aggregation: current scenario and recent developments.” 2012. Masters Thesis, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300.

MLA Handbook (7th Edition):

Shah, Manali. “Protein aggregation: current scenario and recent developments.” 2012. Web. 05 Mar 2021.

Vancouver:

Shah M. Protein aggregation: current scenario and recent developments. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300.

Council of Science Editors:

Shah M. Protein aggregation: current scenario and recent developments. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/41391/rec/5300


University of Southern California

14. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 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 05]. 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

15. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 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 05]. 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

16. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 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 05]. 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

17. Contreras, Janette. Analysis of endocytic and trafficking pathways of potential candidates for drug delivery in HeLa and lacrimal gland acinar cells.

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

 When identifying potential candidates for drug delivery or biomedical diagnostic tools, it is of utmost importance to delineate, as best as possible, their uptake and… (more)

Subjects/Keywords: endocytosis; HeLa; lacrimal gland; trafficking; cyclotides; Adenovirus; nanoparticles

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Contreras, J. (2012). Analysis of endocytic and trafficking pathways of potential candidates for drug delivery in HeLa and lacrimal gland acinar cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/201066/rec/805

Chicago Manual of Style (16th Edition):

Contreras, Janette. “Analysis of endocytic and trafficking pathways of potential candidates for drug delivery in HeLa and lacrimal gland acinar cells.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/201066/rec/805.

MLA Handbook (7th Edition):

Contreras, Janette. “Analysis of endocytic and trafficking pathways of potential candidates for drug delivery in HeLa and lacrimal gland acinar cells.” 2012. Web. 05 Mar 2021.

Vancouver:

Contreras J. Analysis of endocytic and trafficking pathways of potential candidates for drug delivery in HeLa and lacrimal gland acinar cells. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/201066/rec/805.

Council of Science Editors:

Contreras J. Analysis of endocytic and trafficking pathways of potential candidates for drug delivery in HeLa and lacrimal gland acinar cells. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/201066/rec/805


University of Southern California

18. Hsueh, Aaron Pang-Yu. Trafficking of targeted elastin‐like polypeptide nanoparticles in the lacrimal gland.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Southern California

 Rapid clearance from the tears presents a formidable obstacle to the delivery of peptide drugs to the eye surface. This impedes therapies for ocular infections,… (more)

Subjects/Keywords: Coxsackievirus and adenovirus receptor; elastin‐like polypeptide; immune‐mediated inflammation; intercellular adhesion molecule-1; knob; multifunctional nanoparticle; transcytosis; lacrimal gland

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hsueh, A. P. (2017). Trafficking of targeted elastin‐like polypeptide nanoparticles in the lacrimal gland. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/602725/rec/7558

Chicago Manual of Style (16th Edition):

Hsueh, Aaron Pang-Yu. “Trafficking of targeted elastin‐like polypeptide nanoparticles in the lacrimal gland.” 2017. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/602725/rec/7558.

MLA Handbook (7th Edition):

Hsueh, Aaron Pang-Yu. “Trafficking of targeted elastin‐like polypeptide nanoparticles in the lacrimal gland.” 2017. Web. 05 Mar 2021.

Vancouver:

Hsueh AP. Trafficking of targeted elastin‐like polypeptide nanoparticles in the lacrimal gland. [Internet] [Doctoral dissertation]. University of Southern California; 2017. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/602725/rec/7558.

Council of Science Editors:

Hsueh AP. Trafficking of targeted elastin‐like polypeptide nanoparticles in the lacrimal gland. [Doctoral Dissertation]. University of Southern California; 2017. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/602725/rec/7558


University of Southern California

19. Wang, Yan. Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.

Degree: PhD, Molecular Pharmacology and Toxicology, 2013, University of Southern California

 Long-acting insulin (INS) analogues that exhibit prolonged time-action profiles and liver-specificity are currently in great demand for diabetes treatment. Native INS and its protein precursor… (more)

Subjects/Keywords: transferrin; insulin; proinsulin; prodrug activation; recombinant fusion protein; diabetes

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, Y. (2013). Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274

Chicago Manual of Style (16th Edition):

Wang, Yan. “Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.” 2013. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274.

MLA Handbook (7th Edition):

Wang, Yan. “Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.” 2013. Web. 05 Mar 2021.

Vancouver:

Wang Y. Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274.

Council of Science Editors:

Wang Y. Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5274


University of Southern California

20. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 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 05]. 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

21. Shi, Pu. Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide.

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

 Chapter 1: Cytotoxicity, low water solubility, rapid clearance from circulation, and off‐target side‐effects are common drawbacks of conventional small‐molecule drugs. To overcome these shortcomings, many… (more)

Subjects/Keywords: drug delivery; elastin-like polypeptide; nanoparticle; tumor targeting

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shi, P. (2014). Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559

Chicago Manual of Style (16th Edition):

Shi, Pu. “Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide.” 2014. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559.

MLA Handbook (7th Edition):

Shi, Pu. “Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide.” 2014. Web. 05 Mar 2021.

Vancouver:

Shi P. Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559.

Council of Science Editors:

Shi P. Integrin-mediated targeting of protein polymer nanoparticles carrying a cytostatic macrolide. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/453262/rec/3559


University of Southern California

22. Chen, Xiaoying. Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics.

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

 Recombinant fusion proteins have become an important class of biomolecules since the invention of recombinant DNA technology. As an indispensable component of recombinant fusion proteins,… (more)

Subjects/Keywords: linker; fusion protein; transferrin; pharmacokinetics; pharmacodynamics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, X. (2011). Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837

Chicago Manual of Style (16th Edition):

Chen, Xiaoying. “Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics.” 2011. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837.

MLA Handbook (7th Edition):

Chen, Xiaoying. “Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics.” 2011. Web. 05 Mar 2021.

Vancouver:

Chen X. Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837.

Council of Science Editors:

Chen X. Linkers in transferrin fusion proteins: effects on pharmacokinetics and pharmacodynamics. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/637770/rec/3837


University of Southern California

23. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 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 05]. 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

24. Fei, Likun. Cell penetrating peptide-based drug delivery system for targeting mildly acidic pH.

Degree: PhD, Pharmaceutical Sciences, 2015, University of Southern California

 Properties of different arginine‐rich peptides, including net charge and charge distribution, were evaluated for their influence on surface binding, internalization, and intracellular localization. The peptides… (more)

Subjects/Keywords: cell penetrating peptide; drug delivery; pH‐sensitive activation; recombinant protein; tumor‐targeting

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Fei, L. (2015). Cell penetrating peptide-based drug delivery system for targeting mildly acidic pH. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381331/rec/1264

Chicago Manual of Style (16th Edition):

Fei, Likun. “Cell penetrating peptide-based drug delivery system for targeting mildly acidic pH.” 2015. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381331/rec/1264.

MLA Handbook (7th Edition):

Fei, Likun. “Cell penetrating peptide-based drug delivery system for targeting mildly acidic pH.” 2015. Web. 05 Mar 2021.

Vancouver:

Fei L. Cell penetrating peptide-based drug delivery system for targeting mildly acidic pH. [Internet] [Doctoral dissertation]. University of Southern California; 2015. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381331/rec/1264.

Council of Science Editors:

Fei L. Cell penetrating peptide-based drug delivery system for targeting mildly acidic pH. [Doctoral Dissertation]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381331/rec/1264


University of Southern California

25. Kenien, Randall N. Comparison of cationic and amphipathic cell penetrating peptides in the internalization and intracellular localization of cytochrome c conjugates.

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

 In this project, we evaluated the cellular uptake, cytosolic and nuclear transport, and apoptotic function of cytochrome c following conjugation with the amphipathic peptide MAP,… (more)

Subjects/Keywords: cell penetrating peptide; model amphipathic peptide; oligoarginine; cytochrome c; cytosolic and nuclear delivery; subcellular delivery; apoptosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kenien, R. N. (2012). Comparison of cationic and amphipathic cell penetrating peptides in the internalization and intracellular localization of cytochrome c conjugates. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/204128/rec/1510

Chicago Manual of Style (16th Edition):

Kenien, Randall N. “Comparison of cationic and amphipathic cell penetrating peptides in the internalization and intracellular localization of cytochrome c conjugates.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/204128/rec/1510.

MLA Handbook (7th Edition):

Kenien, Randall N. “Comparison of cationic and amphipathic cell penetrating peptides in the internalization and intracellular localization of cytochrome c conjugates.” 2012. Web. 05 Mar 2021.

Vancouver:

Kenien RN. Comparison of cationic and amphipathic cell penetrating peptides in the internalization and intracellular localization of cytochrome c conjugates. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/204128/rec/1510.

Council of Science Editors:

Kenien RN. Comparison of cationic and amphipathic cell penetrating peptides in the internalization and intracellular localization of cytochrome c conjugates. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/204128/rec/1510


University of Southern California

26. Mo, Robert H. Cell penetrating peptide-based polyplexes for sirRNA delivery.

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

 In this dissertation, a novel cell penetrating peptide (CPP)-based polyplex was developed and evaluated for small interfering RNA (siRNA) delivery and efficacy. The design resolved… (more)

Subjects/Keywords: cell penetrating peptides; membrane transduction domains; siRNA delivery; polyplex; model amphipathic peptide; oligoarginine; polyarginine; amphipathic; cationic; autophagy; autophagosomes; siRNA

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mo, R. H. (2012). Cell penetrating peptide-based polyplexes for sirRNA delivery. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/22203/rec/1265

Chicago Manual of Style (16th Edition):

Mo, Robert H. “Cell penetrating peptide-based polyplexes for sirRNA delivery.” 2012. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/22203/rec/1265.

MLA Handbook (7th Edition):

Mo, Robert H. “Cell penetrating peptide-based polyplexes for sirRNA delivery.” 2012. Web. 05 Mar 2021.

Vancouver:

Mo RH. Cell penetrating peptide-based polyplexes for sirRNA delivery. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/22203/rec/1265.

Council of Science Editors:

Mo RH. Cell penetrating peptide-based polyplexes for sirRNA delivery. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/22203/rec/1265


University of Southern California

27. Williams, Melissa Marie. Nucleoside phosphonate prodrugs: synthesis and antiviral activity.

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

 Acyclic nucleoside phosphonates, ANPs, are a drug class with broad-spectrum activity against DNA and RNA viruses. However, limitations with ANP efficacy include: low cell membrane… (more)

Subjects/Keywords: acyclic nucleoside phosphonates; prodrugs; tyrosinamide; lipophilic promoiety

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Williams, M. M. (2016). Nucleoside phosphonate prodrugs: synthesis and antiviral activity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/529681/rec/4481

Chicago Manual of Style (16th Edition):

Williams, Melissa Marie. “Nucleoside phosphonate prodrugs: synthesis and antiviral activity.” 2016. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/529681/rec/4481.

MLA Handbook (7th Edition):

Williams, Melissa Marie. “Nucleoside phosphonate prodrugs: synthesis and antiviral activity.” 2016. Web. 05 Mar 2021.

Vancouver:

Williams MM. Nucleoside phosphonate prodrugs: synthesis and antiviral activity. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/529681/rec/4481.

Council of Science Editors:

Williams MM. Nucleoside phosphonate prodrugs: synthesis and antiviral activity. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/529681/rec/4481


University of Southern California

28. 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

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 05, 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. 05 Mar 2021.

Vancouver:

Janson MA. Genotoxic impurity analysis in pharmaceuticals. [Internet] [Masters thesis]. University of Southern California; 2009. [cited 2021 Mar 05]. 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

29. Agarwal, Amit. Effect of cigarette smoke on redox regulation in chronic obstructive pulmonary disease.

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

 Chronic obstructive pulmonary disease (COPD) is a persistent obstruction of airways in the lungs due to the narrowing of the passage ways. Cigarette smoking is… (more)

Subjects/Keywords: cigarette smoke; redox

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Agarwal, A. (2010). Effect of cigarette smoke on redox regulation in chronic obstructive pulmonary disease. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/378889/rec/2175

Chicago Manual of Style (16th Edition):

Agarwal, Amit. “Effect of cigarette smoke on redox regulation in chronic obstructive pulmonary disease.” 2010. Masters Thesis, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/378889/rec/2175.

MLA Handbook (7th Edition):

Agarwal, Amit. “Effect of cigarette smoke on redox regulation in chronic obstructive pulmonary disease.” 2010. Web. 05 Mar 2021.

Vancouver:

Agarwal A. Effect of cigarette smoke on redox regulation in chronic obstructive pulmonary disease. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/378889/rec/2175.

Council of Science Editors:

Agarwal A. Effect of cigarette smoke on redox regulation in chronic obstructive pulmonary disease. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/378889/rec/2175


University of Southern California

30. Amet, Nurmamet. Human growth hormone-transferrin recombinant fusion protein for oral delivery.

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

 Protein drug delivery is limited to needle injection associating with pain, inconvenience, and non- compliance. Therefore, protein drug with oral dosage form is preferred. We… (more)

Subjects/Keywords: fusion protein; oral delivery; helical linker; protein drug; human growth hormone; transferrin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Amet, N. (2008). Human growth hormone-transferrin recombinant fusion protein for oral delivery. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109040/rec/3279

Chicago Manual of Style (16th Edition):

Amet, Nurmamet. “Human growth hormone-transferrin recombinant fusion protein for oral delivery.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 05, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109040/rec/3279.

MLA Handbook (7th Edition):

Amet, Nurmamet. “Human growth hormone-transferrin recombinant fusion protein for oral delivery.” 2008. Web. 05 Mar 2021.

Vancouver:

Amet N. Human growth hormone-transferrin recombinant fusion protein for oral delivery. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2021 Mar 05]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109040/rec/3279.

Council of Science Editors:

Amet N. Human growth hormone-transferrin recombinant fusion protein for oral delivery. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109040/rec/3279

[1] [2]

.