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You searched for +publisher:"University of Southern California" +contributor:("Haworth, Ian S."). Showing records 1 – 30 of 50 total matches.

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University of Southern California

1. Aletomeh, Yasaman. Pancreatic cancer: a review on biology, genetics and therapeutics.

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

 Pancreatic cancer is the fourth leading cause of cancer death in the United States and remains a major unsolved health problem in the 21st century.… (more)

Subjects/Keywords: pancreatic cancer; cancer biology; genetics; therapeutics

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APA (6th Edition):

Aletomeh, Y. (2014). Pancreatic cancer: a review on biology, genetics and therapeutics. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/516607/rec/4901

Chicago Manual of Style (16th Edition):

Aletomeh, Yasaman. “Pancreatic cancer: a review on biology, genetics and therapeutics.” 2014. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/516607/rec/4901.

MLA Handbook (7th Edition):

Aletomeh, Yasaman. “Pancreatic cancer: a review on biology, genetics and therapeutics.” 2014. Web. 12 Dec 2019.

Vancouver:

Aletomeh Y. Pancreatic cancer: a review on biology, genetics and therapeutics. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/516607/rec/4901.

Council of Science Editors:

Aletomeh Y. Pancreatic cancer: a review on biology, genetics and therapeutics. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/516607/rec/4901


University of Southern California

2. 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

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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/1555

Chicago Manual of Style (16th Edition):

Chen, Yi-Hsun. “Computer modeling of protein-peptide interface solvation.” 2014. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515488/rec/1555.

MLA Handbook (7th Edition):

Chen, Yi-Hsun. “Computer modeling of protein-peptide interface solvation.” 2014. Web. 12 Dec 2019.

Vancouver:

Chen Y. Computer modeling of protein-peptide interface solvation. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/515488/rec/1555.

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/1555


University of Southern California

3. Chen, Po-Han. The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b.

Degree: MS, Biochemistry & Molecular Biology, 2011, University of Southern California

 Mehtyl-CpG binding domain protein 2 and 3 (MBD2 and MBD3) contain methyl-CpG binding domains (MBD) and belong to a family of MBD proteins. Methyl-CpG binding… (more)

Subjects/Keywords: MBD protein; methyl-CpG

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APA (6th Edition):

Chen, P. (2011). The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6927

Chicago Manual of Style (16th Edition):

Chen, Po-Han. “The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b.” 2011. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6927.

MLA Handbook (7th Edition):

Chen, Po-Han. “The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b.” 2011. Web. 12 Dec 2019.

Vancouver:

Chen P. The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6927.

Council of Science Editors:

Chen P. The kinetic study of engineered MBD domain interactions with methylated DNA: insight into binding of methylated DNA by MBD2b. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/278087/rec/6927


University of Southern California

4. Sutch, Brian Thomas. Computational prediction and analysis of protein-RNA interfaces.

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

 Protein-RNA complexes play a central role in many biological processes, including translation, mRNA stabilization, ribosome formation, and viral packaging. The investigation of short nucleic acid… (more)

Subjects/Keywords: protein-RNA; interface solvation; aptamer

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APA (6th Edition):

Sutch, B. T. (2010). Computational prediction and analysis of protein-RNA interfaces. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/385424/rec/1549

Chicago Manual of Style (16th Edition):

Sutch, Brian Thomas. “Computational prediction and analysis of protein-RNA interfaces.” 2010. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/385424/rec/1549.

MLA Handbook (7th Edition):

Sutch, Brian Thomas. “Computational prediction and analysis of protein-RNA interfaces.” 2010. Web. 12 Dec 2019.

Vancouver:

Sutch BT. Computational prediction and analysis of protein-RNA interfaces. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/385424/rec/1549.

Council of Science Editors:

Sutch BT. Computational prediction and analysis of protein-RNA interfaces. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/385424/rec/1549


University of Southern California

5. Xu, Meng. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.

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

 The hetero-hexamer of the eukaryotic minichromosome maintenance (MCM) proteins plays an essential role in replication of genomic DNA. The ring-shaped Mcm2-7 hexamers comprising one of… (more)

Subjects/Keywords: helicase; cell cycle proteins; DNA-binding proteins; recombinant proteins; protein binding; protein oligomerization; schizosaccharomyces pombe; Escherichiai coli; simian virus 40

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APA (6th Edition):

Xu, M. (2012). Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106

Chicago Manual of Style (16th Edition):

Xu, Meng. “Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.” 2012. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106.

MLA Handbook (7th Edition):

Xu, Meng. “Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication.” 2012. Web. 12 Dec 2019.

Vancouver:

Xu M. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106.

Council of Science Editors:

Xu M. Biochemical characterization and structural analysis of two hexameric helicases for eukaryotic DNA replication. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/112770/rec/1106


University of Southern California

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

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

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

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

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APA (6th Edition):

Brill, D. (2015). Image-driven pharmacokinetics of tropoelastin nanoparticles. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3347

Chicago Manual of Style (16th Edition):

Brill, Dab. “Image-driven pharmacokinetics of tropoelastin nanoparticles.” 2015. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3347.

MLA Handbook (7th Edition):

Brill, Dab. “Image-driven pharmacokinetics of tropoelastin nanoparticles.” 2015. Web. 12 Dec 2019.

Vancouver:

Brill D. Image-driven pharmacokinetics of tropoelastin nanoparticles. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3347.

Council of Science Editors:

Brill D. Image-driven pharmacokinetics of tropoelastin nanoparticles. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/582705/rec/3347


University of Southern California

7. Grant, Gian Paola Gacho. Motions and conformations of nucleic acids studied using site-directed spin labeling.

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

 Deoxyribonucleic acid (DNA) and ribonucleic acid (RNA) play crucial roles in life. They carry and transmit genetic information, regulate and maintain gene expression, and in… (more)

Subjects/Keywords: site-directed spin labeling; DNA; RNA; structure; dynamics; EPR

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APA (6th Edition):

Grant, G. P. G. (2009). Motions and conformations of nucleic acids studied using site-directed spin labeling. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225

Chicago Manual of Style (16th Edition):

Grant, Gian Paola Gacho. “Motions and conformations of nucleic acids studied using site-directed spin labeling.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225.

MLA Handbook (7th Edition):

Grant, Gian Paola Gacho. “Motions and conformations of nucleic acids studied using site-directed spin labeling.” 2009. Web. 12 Dec 2019.

Vancouver:

Grant GPG. Motions and conformations of nucleic acids studied using site-directed spin labeling. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225.

Council of Science Editors:

Grant GPG. Motions and conformations of nucleic acids studied using site-directed spin labeling. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253948/rec/4225


University of Southern California

8. Rivera, Christopher Andrew. Ultrafast spectroscopic interrogation and simulation of excited states and reactive surfaces.

Degree: PhD, Chemistry (Chemical Physics), 2011, University of Southern California

 Making a movie of a chemical reaction requires intricate knowledge of both the chemical actors and the environment. Furthermore, the subtleties of the reactive surfaces… (more)

Subjects/Keywords: molecular dynamics; photodissociation; pump-probe; spectroscopy; time-resolved; ultrafast

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APA (6th Edition):

Rivera, C. A. (2011). Ultrafast spectroscopic interrogation and simulation of excited states and reactive surfaces. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/433284/rec/7646

Chicago Manual of Style (16th Edition):

Rivera, Christopher Andrew. “Ultrafast spectroscopic interrogation and simulation of excited states and reactive surfaces.” 2011. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/433284/rec/7646.

MLA Handbook (7th Edition):

Rivera, Christopher Andrew. “Ultrafast spectroscopic interrogation and simulation of excited states and reactive surfaces.” 2011. Web. 12 Dec 2019.

Vancouver:

Rivera CA. Ultrafast spectroscopic interrogation and simulation of excited states and reactive surfaces. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/433284/rec/7646.

Council of Science Editors:

Rivera CA. Ultrafast spectroscopic interrogation and simulation of excited states and reactive surfaces. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/433284/rec/7646


University of Southern California

9. Karver, Mark R. Toward a new (Au)ra of gold-based therapeutics: thio-reactive probes in autoimmunity.

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

 Gold(I) compounds have been used in the United States for nearly 80 years for the treatment of rheumatoid arthritis (RA). The advancement of gold-based therapeutics… (more)

Subjects/Keywords: gold; phosphine; rheumatoid arthritis; auranofin; protein tyrosine phosphatase

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APA (6th Edition):

Karver, M. R. (2009). Toward a new (Au)ra of gold-based therapeutics: thio-reactive probes in autoimmunity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/567713/rec/7511

Chicago Manual of Style (16th Edition):

Karver, Mark R. “Toward a new (Au)ra of gold-based therapeutics: thio-reactive probes in autoimmunity.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/567713/rec/7511.

MLA Handbook (7th Edition):

Karver, Mark R. “Toward a new (Au)ra of gold-based therapeutics: thio-reactive probes in autoimmunity.” 2009. Web. 12 Dec 2019.

Vancouver:

Karver MR. Toward a new (Au)ra of gold-based therapeutics: thio-reactive probes in autoimmunity. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/567713/rec/7511.

Council of Science Editors:

Karver MR. Toward a new (Au)ra of gold-based therapeutics: thio-reactive probes in autoimmunity. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/567713/rec/7511


University of Southern California

10. Nagatani, Gerald Kenji. Biochemical modifications and regulation of the gastric H,K-ATPase.

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

 The α/β heterodimeric gastric H,K-ATPase is the enzyme responsible for gastric HCl secretion by the parietal cell. It is an integral membrane protein of the… (more)

Subjects/Keywords: H,K-ATPase; proton pump; parietal cell; tubulovesicles; phosphoinositides; ubiquitin; ubiquitination; glutathione; glutathiolation

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APA (6th Edition):

Nagatani, G. K. (2009). Biochemical modifications and regulation of the gastric H,K-ATPase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/224408/rec/1107

Chicago Manual of Style (16th Edition):

Nagatani, Gerald Kenji. “Biochemical modifications and regulation of the gastric H,K-ATPase.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/224408/rec/1107.

MLA Handbook (7th Edition):

Nagatani, Gerald Kenji. “Biochemical modifications and regulation of the gastric H,K-ATPase.” 2009. Web. 12 Dec 2019.

Vancouver:

Nagatani GK. Biochemical modifications and regulation of the gastric H,K-ATPase. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/224408/rec/1107.

Council of Science Editors:

Nagatani GK. Biochemical modifications and regulation of the gastric H,K-ATPase. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/224408/rec/1107


University of Southern California

11. Chamberlain, Brian Thomas. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.

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

 A variety of triphosphate analogs that replace a natural phosphate anhydride P-O-P linkage with a phosphonate P-CXY-P moiety have been synthesized for the characterization of… (more)

Subjects/Keywords: bisphosphonates; organoazides; nucleotides; polymerase

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APA (6th Edition):

Chamberlain, B. T. (2012). Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837

Chicago Manual of Style (16th Edition):

Chamberlain, Brian Thomas. “Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.” 2012. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837.

MLA Handbook (7th Edition):

Chamberlain, Brian Thomas. “Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.” 2012. Web. 12 Dec 2019.

Vancouver:

Chamberlain BT. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837.

Council of Science Editors:

Chamberlain BT. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837


University of Southern California

12. Bedrood, Sahar. Structural features and modifiers of islet amyloid polypeptide: implications for type II diabetes mellitus.

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

 Protein misfolding is a common motif in a number of human diseases, including Alzheimer disease, Parkinson disease and type II diabetes mellitus (TTDM). In TTDM,… (more)

Subjects/Keywords: IAPP; islet amyloid polypeptide; amyloid; protein misfolding; type II diabetes mellitus; amyloid structure; curcumin; annexin V

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APA (6th Edition):

Bedrood, S. (2009). Structural features and modifiers of islet amyloid polypeptide: implications for type II diabetes mellitus. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/243190/rec/6114

Chicago Manual of Style (16th Edition):

Bedrood, Sahar. “Structural features and modifiers of islet amyloid polypeptide: implications for type II diabetes mellitus.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/243190/rec/6114.

MLA Handbook (7th Edition):

Bedrood, Sahar. “Structural features and modifiers of islet amyloid polypeptide: implications for type II diabetes mellitus.” 2009. Web. 12 Dec 2019.

Vancouver:

Bedrood S. Structural features and modifiers of islet amyloid polypeptide: implications for type II diabetes mellitus. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/243190/rec/6114.

Council of Science Editors:

Bedrood S. Structural features and modifiers of islet amyloid polypeptide: implications for type II diabetes mellitus. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/243190/rec/6114


University of Southern California

13. Sankar, Saranya. Discovery of small molecules for brain cancer treatment.

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

 Brain tumor claimed the lives of 14,080 people in United States in the past year. Gliomas are one of the most malignant and deadly forms… (more)

Subjects/Keywords: brain cancer; tumor; PDI; glioblastomas

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APA (6th Edition):

Sankar, S. (2014). Discovery of small molecules for brain cancer treatment. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/383014/rec/2030

Chicago Manual of Style (16th Edition):

Sankar, Saranya. “Discovery of small molecules for brain cancer treatment.” 2014. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/383014/rec/2030.

MLA Handbook (7th Edition):

Sankar, Saranya. “Discovery of small molecules for brain cancer treatment.” 2014. Web. 12 Dec 2019.

Vancouver:

Sankar S. Discovery of small molecules for brain cancer treatment. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/383014/rec/2030.

Council of Science Editors:

Sankar S. Discovery of small molecules for brain cancer treatment. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/383014/rec/2030


University of Southern California

14. Rychkova, Anna. Exploring the nature of the translocon-assisted protein insertion.

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

 The main subject of the current dissertation is related to the fundamental question of membrane protein folding. Membrane proteins represent an important class of proteins… (more)

Subjects/Keywords: apparent free energy; coarse grained model; membrane proteins; signal peptide; topology; translocon

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APA (6th Edition):

Rychkova, A. (2013). Exploring the nature of the translocon-assisted protein insertion. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/297485/rec/2670

Chicago Manual of Style (16th Edition):

Rychkova, Anna. “Exploring the nature of the translocon-assisted protein insertion.” 2013. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/297485/rec/2670.

MLA Handbook (7th Edition):

Rychkova, Anna. “Exploring the nature of the translocon-assisted protein insertion.” 2013. Web. 12 Dec 2019.

Vancouver:

Rychkova A. Exploring the nature of the translocon-assisted protein insertion. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/297485/rec/2670.

Council of Science Editors:

Rychkova A. Exploring the nature of the translocon-assisted protein insertion. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/297485/rec/2670


University of Southern California

15. Shah, Anuri N. The effect of familial mutants of Parkinson's disease on membrane remodeling.

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

 The pathological hallmark of Parkinson’s disease (PD) is the presence of Lewy bodies or cell inclusions in neurons, comprising an amyloid protein known as alpha… (more)

Subjects/Keywords: Parkinson'; s; alpha synuclein; membrane remodeling; mutants

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APA (6th Edition):

Shah, A. N. (2013). The effect of familial mutants of Parkinson's disease on membrane remodeling. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/344785/rec/6595

Chicago Manual of Style (16th Edition):

Shah, Anuri N. “The effect of familial mutants of Parkinson's disease on membrane remodeling.” 2013. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/344785/rec/6595.

MLA Handbook (7th Edition):

Shah, Anuri N. “The effect of familial mutants of Parkinson's disease on membrane remodeling.” 2013. Web. 12 Dec 2019.

Vancouver:

Shah AN. The effect of familial mutants of Parkinson's disease on membrane remodeling. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/344785/rec/6595.

Council of Science Editors:

Shah AN. The effect of familial mutants of Parkinson's disease on membrane remodeling. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/344785/rec/6595


University of Southern California

16. Krylov, Ivan S. Synthesis, structural analysis and in vitro antiviral activities of novel cyclic and acyclic (S)-HPMPA and (S)-HPMPC tyrosinamide prodrugs.

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

 Acyclic nucleoside phosphonates (ANPs), in particular (S) HPMPC (Cidofovir, Vistide®) and (S) HPMPA are highly potent broad spectrum antiviral agents. Unfortunately, unfavorable Absorption, Distribution, Metabolism… (more)

Subjects/Keywords: acyclic nucleoside phosphonates; antiviral; cidofovir; prodrugs; (S)-HPMPA; tyrosinamide; amino acid

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APA (6th Edition):

Krylov, I. S. (2013). Synthesis, structural analysis and in vitro antiviral activities of novel cyclic and acyclic (S)-HPMPA and (S)-HPMPC tyrosinamide prodrugs. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/109157/rec/6290

Chicago Manual of Style (16th Edition):

Krylov, Ivan S. “Synthesis, structural analysis and in vitro antiviral activities of novel cyclic and acyclic (S)-HPMPA and (S)-HPMPC tyrosinamide prodrugs.” 2013. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/109157/rec/6290.

MLA Handbook (7th Edition):

Krylov, Ivan S. “Synthesis, structural analysis and in vitro antiviral activities of novel cyclic and acyclic (S)-HPMPA and (S)-HPMPC tyrosinamide prodrugs.” 2013. Web. 12 Dec 2019.

Vancouver:

Krylov IS. Synthesis, structural analysis and in vitro antiviral activities of novel cyclic and acyclic (S)-HPMPA and (S)-HPMPC tyrosinamide prodrugs. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/109157/rec/6290.

Council of Science Editors:

Krylov IS. Synthesis, structural analysis and in vitro antiviral activities of novel cyclic and acyclic (S)-HPMPA and (S)-HPMPC tyrosinamide prodrugs. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/109157/rec/6290


University of Southern California

17. Upton, Thomas George. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.

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

 A stereoelectronically varied series of alpha-substituted methylenebisphosphonic acids (X,Y = H, F, Cl, Br, CH3) was synthesized and used to prepare corresponding dNTP beta,y-CXY and… (more)

Subjects/Keywords: DNA polymerase beta; bisphosphonates; titrations; fluorination; trifluoromethylation; halogenation; nucleotide analogues; stereoselectivity; autodock; docking; inhibitor design; HIV reverse transcriptase; polymerase kinetics

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APA (6th Edition):

Upton, T. G. (2009). Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859

Chicago Manual of Style (16th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859.

MLA Handbook (7th Edition):

Upton, Thomas George. “Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function.” 2009. Web. 12 Dec 2019.

Vancouver:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859.

Council of Science Editors:

Upton TG. Design and synthesis of a series of methylenebisphosphonates: a nucleotide analogue toolkit to probe nucleic acid polymerase structure and function. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/109922/rec/1859


University of Southern California

18. Kuo, Chihhao. Cellular uptake of cyclic cystine knotted cyclotides from Momordica cochinchinesis family.

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

 Cyclotides are miniproteins that consist of a cyclic backbone strengthened with three internal disulfide bonds and the compact tertiary structure grants cyclotides with exceptional stability.… (more)

Subjects/Keywords: cyclotide; cyclic cystine knot; Momordica cochinchinesis trypsin inhibitor; drug delivery

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APA (6th Edition):

Kuo, C. (2010). Cellular uptake of cyclic cystine knotted cyclotides from Momordica cochinchinesis family. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/391361/rec/1268

Chicago Manual of Style (16th Edition):

Kuo, Chihhao. “Cellular uptake of cyclic cystine knotted cyclotides from Momordica cochinchinesis family.” 2010. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/391361/rec/1268.

MLA Handbook (7th Edition):

Kuo, Chihhao. “Cellular uptake of cyclic cystine knotted cyclotides from Momordica cochinchinesis family.” 2010. Web. 12 Dec 2019.

Vancouver:

Kuo C. Cellular uptake of cyclic cystine knotted cyclotides from Momordica cochinchinesis family. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/391361/rec/1268.

Council of Science Editors:

Kuo C. Cellular uptake of cyclic cystine knotted cyclotides from Momordica cochinchinesis family. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/391361/rec/1268


University of Southern California

19. Peterson, Larryn Wrisa. Peptidomimetic prodrugs of cidofovir: design, synthesis, transport, mechanism of activation, and antiviral activity.

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

 Cidofovir and its equivalently potent cyclic form are possible therapies for a broad spectrum of viral infections, but are limited in this role by low… (more)

Subjects/Keywords: cidofovir; cyclic cidofovir; antiviral; prodrugs; hPEPT1; oral bioavailability; beta-elimination; human cytomegalovirus

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APA (6th Edition):

Peterson, L. W. (2009). Peptidomimetic prodrugs of cidofovir: design, synthesis, transport, mechanism of activation, and antiviral activity. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/188027/rec/4964

Chicago Manual of Style (16th Edition):

Peterson, Larryn Wrisa. “Peptidomimetic prodrugs of cidofovir: design, synthesis, transport, mechanism of activation, and antiviral activity.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/188027/rec/4964.

MLA Handbook (7th Edition):

Peterson, Larryn Wrisa. “Peptidomimetic prodrugs of cidofovir: design, synthesis, transport, mechanism of activation, and antiviral activity.” 2009. Web. 12 Dec 2019.

Vancouver:

Peterson LW. Peptidomimetic prodrugs of cidofovir: design, synthesis, transport, mechanism of activation, and antiviral activity. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/188027/rec/4964.

Council of Science Editors:

Peterson LW. Peptidomimetic prodrugs of cidofovir: design, synthesis, transport, mechanism of activation, and antiviral activity. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/188027/rec/4964


University of Southern California

20. Zhou, Bo. Structural and biochemical studies of large T antigen: the SV40 replicative helicase.

Degree: PhD, Molecular Biology, 2012, University of Southern California

 Simian Virus 40 (SV40) replication has long been regarded as a useful model system in circumventing the complexity of studying the eukaryotic DNA replication process.… (more)

Subjects/Keywords: large T antigen; helicase; DNA polymerase; Primase; DNA replication; crystallography

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APA (6th Edition):

Zhou, B. (2012). Structural and biochemical studies of large T antigen: the SV40 replicative helicase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106

Chicago Manual of Style (16th Edition):

Zhou, Bo. “Structural and biochemical studies of large T antigen: the SV40 replicative helicase.” 2012. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106.

MLA Handbook (7th Edition):

Zhou, Bo. “Structural and biochemical studies of large T antigen: the SV40 replicative helicase.” 2012. Web. 12 Dec 2019.

Vancouver:

Zhou B. Structural and biochemical studies of large T antigen: the SV40 replicative helicase. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106.

Council of Science Editors:

Zhou B. Structural and biochemical studies of large T antigen: the SV40 replicative helicase. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6106


University of Southern California

21. Raut, Anuja. Mechanism of action of rapamycin and its applications in aging, cancer therapy and metabolism.

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

 Rapamycin is a potent immunosuppressive macrolide which binds to FK506 binding protein (FKBP12), the cytosolic receptor to rapamycin. The FKBP12-Rapamycin complex binds to and allosterically… (more)

Subjects/Keywords: rapamycin; mTOR; immunosuppressant; pharmacology

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APA (6th Edition):

Raut, A. (2014). Mechanism of action of rapamycin and its applications in aging, cancer therapy and metabolism. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385332/rec/4002

Chicago Manual of Style (16th Edition):

Raut, Anuja. “Mechanism of action of rapamycin and its applications in aging, cancer therapy and metabolism.” 2014. Masters Thesis, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385332/rec/4002.

MLA Handbook (7th Edition):

Raut, Anuja. “Mechanism of action of rapamycin and its applications in aging, cancer therapy and metabolism.” 2014. Web. 12 Dec 2019.

Vancouver:

Raut A. Mechanism of action of rapamycin and its applications in aging, cancer therapy and metabolism. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385332/rec/4002.

Council of Science Editors:

Raut A. Mechanism of action of rapamycin and its applications in aging, cancer therapy and metabolism. [Masters Thesis]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/385332/rec/4002


University of Southern California

22. Li, Yiyu. Algorithm development for modeling protein assemblies.

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

 Amyloid fibrils are associated with over 40 human diseases. For example, fibrils of human islet amyloid polypeptide (hIAPP), α-synuclein, and amyloid-β are pathological hallmarks of… (more)

Subjects/Keywords: algorithm; MFIBRIL; molecular modeling; protein assemblies; human islet amyloid polypeptide (hIAPP)

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APA (6th Edition):

Li, Y. (2013). Algorithm development for modeling protein assemblies. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/234407/rec/602

Chicago Manual of Style (16th Edition):

Li, Yiyu. “Algorithm development for modeling protein assemblies.” 2013. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/234407/rec/602.

MLA Handbook (7th Edition):

Li, Yiyu. “Algorithm development for modeling protein assemblies.” 2013. Web. 12 Dec 2019.

Vancouver:

Li Y. Algorithm development for modeling protein assemblies. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/234407/rec/602.

Council of Science Editors:

Li Y. Algorithm development for modeling protein assemblies. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/234407/rec/602


University of Southern California

23. Bala, Joy Lynn Fabile. Synthesis of fluorescent conjugates of risedronate and related analogues for bone imaging.

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

 Bisphosphonates are structural analogues of pyrophosphate with increased hydrolytic stability. The P-C-P backbone of BPs gives rise to two additional side chains, which can be… (more)

Subjects/Keywords: bisphosphonate

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APA (6th Edition):

Bala, J. L. F. (2009). Synthesis of fluorescent conjugates of risedronate and related analogues for bone imaging. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183651/rec/6280

Chicago Manual of Style (16th Edition):

Bala, Joy Lynn Fabile. “Synthesis of fluorescent conjugates of risedronate and related analogues for bone imaging.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183651/rec/6280.

MLA Handbook (7th Edition):

Bala, Joy Lynn Fabile. “Synthesis of fluorescent conjugates of risedronate and related analogues for bone imaging.” 2009. Web. 12 Dec 2019.

Vancouver:

Bala JLF. Synthesis of fluorescent conjugates of risedronate and related analogues for bone imaging. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183651/rec/6280.

Council of Science Editors:

Bala JLF. Synthesis of fluorescent conjugates of risedronate and related analogues for bone imaging. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/183651/rec/6280


University of Southern California

24. Marchelletta, Ronald. Characterization of the class v myosin motor, Myosin 5c, in lacrimal acini.

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

 Lacrimal gland acinar cells (LGACs) are the major contributor to ocular surface proteins extruded into the tear film. It has been suggested that a reduction… (more)

Subjects/Keywords: myosin; unconventional motor; lacrimal acini; intracellular traffic; Myosin 5; actin reorganization

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APA (6th Edition):

Marchelletta, R. (2009). Characterization of the class v myosin motor, Myosin 5c, in lacrimal acini. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/560841/rec/1309

Chicago Manual of Style (16th Edition):

Marchelletta, Ronald. “Characterization of the class v myosin motor, Myosin 5c, in lacrimal acini.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/560841/rec/1309.

MLA Handbook (7th Edition):

Marchelletta, Ronald. “Characterization of the class v myosin motor, Myosin 5c, in lacrimal acini.” 2009. Web. 12 Dec 2019.

Vancouver:

Marchelletta R. Characterization of the class v myosin motor, Myosin 5c, in lacrimal acini. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/560841/rec/1309.

Council of Science Editors:

Marchelletta R. Characterization of the class v myosin motor, Myosin 5c, in lacrimal acini. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/560841/rec/1309


University of Southern California

25. Pathania, Divya. Targeting cellular redox modulations for pancreatic cancer treatment.

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

 Altered cellular bioenergetics and oxidative stress are emerging hallmarks of most cancers including pancreatic cancer. Elevated levels of intrinsic reactive oxygen species (ROS) in tumors… (more)

Subjects/Keywords: oxidative stress; small molecule anticancer drugs; quinazolinediones; triphenylphosphoniums; cellular oxygen consumption rate; reactive oxygen species; pancreatic cancer; chemotherapy induced peripheral neuropathy

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APA (6th Edition):

Pathania, D. (2013). Targeting cellular redox modulations for pancreatic cancer treatment. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314353/rec/6315

Chicago Manual of Style (16th Edition):

Pathania, Divya. “Targeting cellular redox modulations for pancreatic cancer treatment.” 2013. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314353/rec/6315.

MLA Handbook (7th Edition):

Pathania, Divya. “Targeting cellular redox modulations for pancreatic cancer treatment.” 2013. Web. 12 Dec 2019.

Vancouver:

Pathania D. Targeting cellular redox modulations for pancreatic cancer treatment. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314353/rec/6315.

Council of Science Editors:

Pathania D. Targeting cellular redox modulations for pancreatic cancer treatment. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314353/rec/6315


University of Southern California

26. Xu, Liya. Structure-function studies on the mammalian intestinal dipeptide transporter hPEPT1.

Degree: PhD, Neuroscience, 2010, University of Southern California

 Intestinal protein digestion generates a massive variety and quantity of short chain peptides that are later absorbed into small intestinal epithelial cells by the di/tri-peptide… (more)

Subjects/Keywords: hPEPT1; structure-function study; dipeptide transporter; membrane protein; computer modeling

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APA (6th Edition):

Xu, L. (2010). Structure-function studies on the mammalian intestinal dipeptide transporter hPEPT1. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/368654/rec/6128

Chicago Manual of Style (16th Edition):

Xu, Liya. “Structure-function studies on the mammalian intestinal dipeptide transporter hPEPT1.” 2010. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/368654/rec/6128.

MLA Handbook (7th Edition):

Xu, Liya. “Structure-function studies on the mammalian intestinal dipeptide transporter hPEPT1.” 2010. Web. 12 Dec 2019.

Vancouver:

Xu L. Structure-function studies on the mammalian intestinal dipeptide transporter hPEPT1. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/368654/rec/6128.

Council of Science Editors:

Xu L. Structure-function studies on the mammalian intestinal dipeptide transporter hPEPT1. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/368654/rec/6128


University of Southern California

27. 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

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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/5267

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 December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5267.

MLA Handbook (7th Edition):

Wang, Yan. “Proinsulin-transferrin recombinant fusion protein: mechanism of activation and potential application in diabetes treatment.” 2013. Web. 12 Dec 2019.

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 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/91307/rec/5267.

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/5267


University of Southern California

28. Ambroso, Mark Robert. The structure and function of membrane curving proteins on different membrane shapes and their regulation by post-translational modifications.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2016, University of Southern California

 Membrane curvature is an essential biophysical property utilized within cells to execute their most basic functions. Recent advances in this field have shown proteins capable… (more)

Subjects/Keywords: electron paramagnetic resonance; BAR proteins; lysine acetylation

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APA (6th Edition):

Ambroso, M. R. (2016). The structure and function of membrane curving proteins on different membrane shapes and their regulation by post-translational modifications. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/622126/rec/7320

Chicago Manual of Style (16th Edition):

Ambroso, Mark Robert. “The structure and function of membrane curving proteins on different membrane shapes and their regulation by post-translational modifications.” 2016. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/622126/rec/7320.

MLA Handbook (7th Edition):

Ambroso, Mark Robert. “The structure and function of membrane curving proteins on different membrane shapes and their regulation by post-translational modifications.” 2016. Web. 12 Dec 2019.

Vancouver:

Ambroso MR. The structure and function of membrane curving proteins on different membrane shapes and their regulation by post-translational modifications. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/622126/rec/7320.

Council of Science Editors:

Ambroso MR. The structure and function of membrane curving proteins on different membrane shapes and their regulation by post-translational modifications. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/622126/rec/7320


University of Southern California

29. Jao, Christine Chua. Membrane curvature sensors and inducers studied by site-directed spin labeling.

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

 Control and regulation of membrane curvature play important roles in membrane trafficking and remodeling events. These processes are mediated by proteins that can sense and/or… (more)

Subjects/Keywords: membrane; curvature; electron paramagnetic resonance; site-directed spin labeling

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

APA (6th Edition):

Jao, C. C. (2010). Membrane curvature sensors and inducers studied by site-directed spin labeling. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/299240/rec/4034

Chicago Manual of Style (16th Edition):

Jao, Christine Chua. “Membrane curvature sensors and inducers studied by site-directed spin labeling.” 2010. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/299240/rec/4034.

MLA Handbook (7th Edition):

Jao, Christine Chua. “Membrane curvature sensors and inducers studied by site-directed spin labeling.” 2010. Web. 12 Dec 2019.

Vancouver:

Jao CC. Membrane curvature sensors and inducers studied by site-directed spin labeling. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/299240/rec/4034.

Council of Science Editors:

Jao CC. Membrane curvature sensors and inducers studied by site-directed spin labeling. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/299240/rec/4034


University of Southern California

30. Price, Eric Allen. Computational construction and analysis of DNA and RNA.

Degree: PhD, Molecular & Computational Biology, 2009, University of Southern California

 Proper understanding of nucleic acid structure and function is critical as nucleic acids emerge as major targets and therapeutic mediators of physiological changes. Efficient, repeatable,… (more)

Subjects/Keywords: DNA; RNA; computation; computational; biology; construction; analysis; nasdac; nautilis; nasnic; nasnox; natcar; natscape; nitroxide; nucleic acids

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Price, E. A. (2009). Computational construction and analysis of DNA and RNA. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/186383/rec/1540

Chicago Manual of Style (16th Edition):

Price, Eric Allen. “Computational construction and analysis of DNA and RNA.” 2009. Doctoral Dissertation, University of Southern California. Accessed December 12, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/186383/rec/1540.

MLA Handbook (7th Edition):

Price, Eric Allen. “Computational construction and analysis of DNA and RNA.” 2009. Web. 12 Dec 2019.

Vancouver:

Price EA. Computational construction and analysis of DNA and RNA. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Dec 12]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/186383/rec/1540.

Council of Science Editors:

Price EA. Computational construction and analysis of DNA and RNA. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/186383/rec/1540

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