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You searched for +publisher:"University of Southern California" +contributor:("Neamati, Nouri"). Showing records 1 – 27 of 27 total matches.

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University of Southern California

1. Pullanikat, Prasanna. Preparation of novel ligands for rhodium (II) and palladium (II) catalysts and application in the synthesis of palmerolide A and conversion of biomass into formic acid.

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

 This dissertation focuses on the studies toward total synthesis of palmerolide A, preparation of ligands for rhodium catalyzed C-H activation reaction. Preparation of NHC-Pd (II)… (more)

Subjects/Keywords: palmerolide A; (E)-ethyl octa-2,7-dienoate; (R,E)-ethyl 7,8-dihydroxyoct-2-enoate; (R,E)-ethyl 8-((tert-butyldiphenylsilyl)oxy)-7-hydroxyoct-2-enoate; (R,E)-ethyl 8-((tert-butyldiphenylsilyl)oxy)-7-(methoxymethoxy) oct-2-enoate; (R,E)-ethyl 8-hydroxy-7-(methoxymethoxy)oct-2-enoate; (R,E)-ethyl 7-(methoxymethoxy)-8-((methylsulfonyl)oxy)oct-2-enoate; (R,E)-ethyl 8-iodo-7-(methoxymethoxy)oct-2-enoate; (4S,5S)-dimethyl 2,2-dimethyl-1,3-dioxolane -4,5-dicarboxylate; ((4R,5R)-2,2-dimethyl-1,3-dioxolane-4,5-diyl)dimethanol; ((4R,5R)-5-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methanol; ((4R,5R)-5-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolan-4-yl)methyl4-methylbenzene sulfonate; (2R,3R)-2,3-dihydroxy-4-((4-methoxybenzyl)oxy)butyl-4-methylbenzenesulfonate; (R)-2-((4-methoxybenzyl)oxy)-1-((R)-oxiran-2-yl)ethanol; (R)-2-((R)-2-((4-methoxybenzyl)oxy)-1-(methoxy methoxy)ethyl) oxirane; (2R,3R)-1-((4-methoxy benzyl)oxy)-2-(methoxymethoxy)hex-5-yn-3-ol; (4R,5S)-4-(iodomethyl)-5-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-1,3-dioxolane; (R)-1-((4-methoxybenzyl)oxy)but-3-en-2-ol; (R,E)-(8-ethoxy-2-hydroxy-8-oxooct-6-en-1- yl)triphenylphosphonium iodide; hex-5-en-1-yl benzoate; (R)-5,6-dihydroxyhexyl benzoate; (R)-5-((tert-butyldimethylsilyl)oxy)-6-hydroxyhexyl benzoate; (R)-5-((tert-butyldimethylsilyl)oxy)6-oxohexylbenzoate; R, E)-5-((tert-butyldimethylsilyloxy)-7-iodohept-6-en-1-yl benzoate; methyl 2-(2-methyl-1,3-dioxolan-2-yl)acetate; 2-(2-methyl-1,3-dioxolan-2-yl)ethanol; 2-(2-methyl-1,3-dioxolan-2-yl)acetaldehyde; (E)-ethyl 4-(2-methyl-1,3-dioxolan-2-yl)but-2-enoate; (E)-4-(2-methyl-1,3-dioxolan-2-yl)but-2-en-1-ol; ((2R,3R)-3-((2-methyl-1,3-dioxolan-2-yl)methyl)oxiran-2-yl)methanol; (2S,3R)-2-methyl-4-(2-methyl-1,3-dioxolan-2-yl)butane-1,3-diol; (4R,5S)-2-(4-methoxyphenyl)-5-methyl-4-((2-methyl-1,3-dioxolan-2-yl)methyl)-1,3-dioxane; (4R,5S)-2-(4-methoxyphenyl)-5-methyl-4-(2-methylallyl)-1,3-dioxane; (2R,3S)-3-methyl-1-(2-methyl-1,3-dioxolan-2-yl)pent-4-yn-2-ol and (4R,5S)-4-hydroxy-5-methylhept-6-yn-2-one; tert-butyldimethyl(((2R,3S)-3-methyl-1(2-methyl-1,3-dioxolan-2-yl)hex-4-yn-2-yl) oxy) silane; (E)-methyl 5-methylhexa-2,5-dienoate; (E)-5-methylhexa-2,5-dien-1-ol; ((2R,3R)-3-(2-methylallyl)oxiran-2-yl)methanol; (2S,3R)-2,5-dimethylhex-5-ene-1,3-diol; (4R,5S)-2-(4-methoxyphenyl)-5-methyl-4-(2-methylallyl)-1,3-dioxane; (4S,5R,E)-5-((4-methoxybenzyl)oxy)-2,4,7-trimethylocta-2,7-dienal; (2R,3R)-hept-6-yne-1,2,3-triol; methyl 2-((4S,4'R,5R)-2,2,2',2'-tetramethyl [4,4'-bi(1,3- dioxolan)]-5-yl)acetate; 4-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-4 hydroxy-but-2-enoic acid methylester; 4-(2,2-Dimethyl-[1,3]dioxolan-4-yl)-4-hydroxy-but-2-enoic acid methylester; (4S,E)-methyl 4-((tert-butyldiphenylsilyl)oxy)-4-(2,2-dimethyl-1,3-dioxolan-4-yl)but-2-enoate; (S,E)-4-((tert-butyldiphenylsilyl)oxy)-4-((R)-2,2-dimethyl-1,3-dioxo lan-4-yl)but-2-en-1-ol; (S,E)-4-((tert-butyldiphenylsilyl)oxy)-4-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)but-2-enal; 4-((4-methoxybenzyl)oxy)butan-1-ol; 1-((4-iodobutoxy)methyl)-4-methoxybenzene; 1-((4-iodobutoxy)methyl)-4-methoxybenzene; (5S,E)-5-((R)-2,2-dimethyl-1,3-dioxolan-4-yl)8-(4-((4-methoxybenzyl)oxy)butyl)-2,2,10,10,11,11-hexamethyl-3,3-diphenyl-4,9-dioxa-3,10-disiladodec-6-ene; (2R,3S,E)-3-((tert-butyldiphenylsilyl)oxy) 10-((4-methoxybenzyl) oxy)dec-4-ene-1,2,6-triol; (2R,3S,E)-3,6-bis((tert-butyldiphenylsilyl)oxy) 10-((4-methoxybenzyl) oxy)dec-4-ene-1,2-diol; (2R,3S,E)-3,6-bis((tert-butyldiphenylsilyl) oxy)-2-hydroxy-10-((4-methoxybenzyl)oxy)dec-4-en-1 yl benzoate; (2R,3S,E)-3,6-bis((tert-butyldiphenylsilyl)oxy)-10 ((4-methoxybenzyl)oxy)-2-((methylsulfonyl)oxy)dec-4-en-1-ylbenzoate; (8S,E)-5-(4-((4-methoxybenzyl)oxy)butyl)-2,2,11,11-tetramethyl-8-((S)-oxiran-2-yl)-3,3,10,10-tetra-phenyl-4,9-dioxa-3,10-disiladodec-6-ene; (4S,5R)-4-(((4-methoxybenzyl)oxy)methyl)-2,2-dimethyl-5-((phenyl sulfonyl)methyl)-1,3-dioxolane; diazoamide compounds; 1-[4,4-bis-(tert-butyl-dimethyl silanyloxymethyl)-2,2-dimethyloxazolidin-3-yl]2-diazo-ethanone; 1-[4,4-bis-(tert-butyl-dimethylsilanyloxymethyl)-2,2-dimethyloxazolidin-3-yl]-2-diazo-ethanone; 1-(4,4-bis(((tert-butyldimethylsilyl)oxy)methyl)- 2,2-dimethyloxazo- lidin-3-yl)-2-diazoethanone; 1-trifluoromethanesulfonylimidazolidin-2-one ligands; 1-[4,4-bis-(tertbutyldimethylsilanyloxy- methyl)2,2-dimethyl-oxazolidin-3-yl]2-diazo-butane-1,3-dione; 1-[3,3-bis-(tert-butyl-dimethylsilanyloxymethyl)-1-oxa-4- aza-spiro[4.5]dec-4-yl]-2-diazo-ethanone; 1-[3,3-bis-(tert-butyl-dimethyl-silanyloxymethyl)-1-oxa-4-aza-spiro[4.5]dec-4-yl]-2-diazobutane-1,3-dione; trans-1-benzylhexahydro-1H-indol-(3H)-one; N-cyclohexyl-2-diazo-N-phenyl 2-(phenylsulfonyl)acetamide NHC-Pd complex; oxidative degradation; biomass; carbohydrates; glycerol; ethylene glycol; glycolic acid

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APA (6th Edition):

Pullanikat, P. (2012). Preparation of novel ligands for rhodium (II) and palladium (II) catalysts and application in the synthesis of palmerolide A and conversion of biomass into formic acid. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/440514/rec/5201

Chicago Manual of Style (16th Edition):

Pullanikat, Prasanna. “Preparation of novel ligands for rhodium (II) and palladium (II) catalysts and application in the synthesis of palmerolide A and conversion of biomass into formic acid.” 2012. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/440514/rec/5201.

MLA Handbook (7th Edition):

Pullanikat, Prasanna. “Preparation of novel ligands for rhodium (II) and palladium (II) catalysts and application in the synthesis of palmerolide A and conversion of biomass into formic acid.” 2012. Web. 20 Oct 2020.

Vancouver:

Pullanikat P. Preparation of novel ligands for rhodium (II) and palladium (II) catalysts and application in the synthesis of palmerolide A and conversion of biomass into formic acid. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/440514/rec/5201.

Council of Science Editors:

Pullanikat P. Preparation of novel ligands for rhodium (II) and palladium (II) catalysts and application in the synthesis of palmerolide A and conversion of biomass into formic acid. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/440514/rec/5201


University of Southern California

2. 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/2033

Chicago Manual of Style (16th Edition):

Sankar, Saranya. “Discovery of small molecules for brain cancer treatment.” 2014. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/383014/rec/2033.

MLA Handbook (7th Edition):

Sankar, Saranya. “Discovery of small molecules for brain cancer treatment.” 2014. Web. 20 Oct 2020.

Vancouver:

Sankar S. Discovery of small molecules for brain cancer treatment. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/383014/rec/2033.

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/2033


University of Southern California

3. 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/4906

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 October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/516607/rec/4906.

MLA Handbook (7th Edition):

Aletomeh, Yasaman. “Pancreatic cancer: a review on biology, genetics and therapeutics.” 2014. Web. 20 Oct 2020.

Vancouver:

Aletomeh Y. Pancreatic cancer: a review on biology, genetics and therapeutics. [Internet] [Masters thesis]. University of Southern California; 2014. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/516607/rec/4906.

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/4906


University of Southern California

4. Butkevich, Alexey. Multicomponent reactions in the synthesis of nitrogen heterocycles and their application to drug discovery.

Degree: PhD, Chemistry, 2011, University of Southern California

 This dissertation comprises two separate projects, relying on the use of multicomponent reactions as a common theme. The introduction (Chapter 1) briefly overviews the utility… (more)

Subjects/Keywords: multicomponent reaction; Petasis reaction; Ugi reaction; drug discovery; heterocycles; nitrogen heterocycles; chromene; dihydroquinoline; isoindoline; propiolamide; pyrroline; BODIPY; organic synthesis; kinetics; NMR; boronic acid; trifluoroborate; diastereoselective; tocopherol; medicinal chemistry; cancer; APE1; Ref-1

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APA (6th Edition):

Butkevich, A. (2011). Multicomponent reactions in the synthesis of nitrogen heterocycles and their application to drug discovery. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/439727/rec/4264

Chicago Manual of Style (16th Edition):

Butkevich, Alexey. “Multicomponent reactions in the synthesis of nitrogen heterocycles and their application to drug discovery.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/439727/rec/4264.

MLA Handbook (7th Edition):

Butkevich, Alexey. “Multicomponent reactions in the synthesis of nitrogen heterocycles and their application to drug discovery.” 2011. Web. 20 Oct 2020.

Vancouver:

Butkevich A. Multicomponent reactions in the synthesis of nitrogen heterocycles and their application to drug discovery. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/439727/rec/4264.

Council of Science Editors:

Butkevich A. Multicomponent reactions in the synthesis of nitrogen heterocycles and their application to drug discovery. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/439727/rec/4264


University of Southern California

5. Al Safi, Rasha. HIV-1 integrase and human APE1: two DNA-processing enzymes and two druggable targets.

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

 HIV-1 Integrase (IN) and the human apurinic/apyrimidinic endonuclease 1 (APE1) are two DNA-processing enzymes implicated in disease. IN catalyses the insertion of viral DNA into… (more)

Subjects/Keywords: HIV-1; integrase; APE1; cancer

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APA (6th Edition):

Al Safi, R. (2011). HIV-1 integrase and human APE1: two DNA-processing enzymes and two druggable targets. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/427286/rec/3202

Chicago Manual of Style (16th Edition):

Al Safi, Rasha. “HIV-1 integrase and human APE1: two DNA-processing enzymes and two druggable targets.” 2011. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/427286/rec/3202.

MLA Handbook (7th Edition):

Al Safi, Rasha. “HIV-1 integrase and human APE1: two DNA-processing enzymes and two druggable targets.” 2011. Web. 20 Oct 2020.

Vancouver:

Al Safi R. HIV-1 integrase and human APE1: two DNA-processing enzymes and two druggable targets. [Internet] [Masters thesis]. University of Southern California; 2011. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/427286/rec/3202.

Council of Science Editors:

Al Safi R. HIV-1 integrase and human APE1: two DNA-processing enzymes and two druggable targets. [Masters Thesis]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/427286/rec/3202


University of Southern California

6. Qian, Junjie. Discovery of small-molecule compounds targeting TREX1.

Degree: MS, Biochemistry and Molecular Biology, 2012, University of Southern California

 Three prime repair exonuclease 1 (TREX1) plays an important role in human DNA repair. More importantly, it has been recently discovered that the 3’→5’ DNA… (more)

Subjects/Keywords: HIV1; TREX1; Small Molecule Compounds; Inhibitor

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APA (6th Edition):

Qian, J. (2012). Discovery of small-molecule compounds targeting TREX1. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/74180/rec/2034

Chicago Manual of Style (16th Edition):

Qian, Junjie. “Discovery of small-molecule compounds targeting TREX1.” 2012. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/74180/rec/2034.

MLA Handbook (7th Edition):

Qian, Junjie. “Discovery of small-molecule compounds targeting TREX1.” 2012. Web. 20 Oct 2020.

Vancouver:

Qian J. Discovery of small-molecule compounds targeting TREX1. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/74180/rec/2034.

Council of Science Editors:

Qian J. Discovery of small-molecule compounds targeting TREX1. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/74180/rec/2034


University of Southern California

7. 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 October 20, 2020. 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. 20 Oct 2020.

Vancouver:

Li Y. Algorithm development for modeling protein assemblies. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. 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

8. Kim, Hyunjung. Targeting chromatin modification in human cancer: SMYD3 mediated ERα transcription regulation. Cooperative role between H3.3 and HP1ϒ.

Degree: PhD, Genetic, Molecular & Cellular Biology, 2011, University of Southern California

 The genome of eukaryotic cells is composed in nucleoprotein structure called ‘chromatin’. The basic repeating unit of chromatin is nucleosome, which consists of two pairs… (more)

Subjects/Keywords: chromatin; histone; post-translational modification; methyltransferase; histone variant; HP1; H3.3; transcription; gene regulation; estrogen receptor; HSP70

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APA (6th Edition):

Kim, H. (2011). Targeting chromatin modification in human cancer: SMYD3 mediated ERα transcription regulation. Cooperative role between H3.3 and HP1ϒ. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/471093/rec/6325

Chicago Manual of Style (16th Edition):

Kim, Hyunjung. “Targeting chromatin modification in human cancer: SMYD3 mediated ERα transcription regulation. Cooperative role between H3.3 and HP1ϒ.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/471093/rec/6325.

MLA Handbook (7th Edition):

Kim, Hyunjung. “Targeting chromatin modification in human cancer: SMYD3 mediated ERα transcription regulation. Cooperative role between H3.3 and HP1ϒ.” 2011. Web. 20 Oct 2020.

Vancouver:

Kim H. Targeting chromatin modification in human cancer: SMYD3 mediated ERα transcription regulation. Cooperative role between H3.3 and HP1ϒ. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/471093/rec/6325.

Council of Science Editors:

Kim H. Targeting chromatin modification in human cancer: SMYD3 mediated ERα transcription regulation. Cooperative role between H3.3 and HP1ϒ. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/471093/rec/6325


University of Southern California

9. Yu, Yingzhe. Identification of small molecular inhibitors targeting G13D mutant K-ras.

Degree: MS, Biochemistry and Molecular Biology, 2012, University of Southern California

 K-ras mutations can be frequently found in various cancers and are associated with resistance to treatment or poor prognosis. Thus far, however, there is no… (more)

Subjects/Keywords: inhibitors; targeting; G13D mutant K-ras

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APA (6th Edition):

Yu, Y. (2012). Identification of small molecular inhibitors targeting G13D mutant K-ras. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/66766/rec/3323

Chicago Manual of Style (16th Edition):

Yu, Yingzhe. “Identification of small molecular inhibitors targeting G13D mutant K-ras.” 2012. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/66766/rec/3323.

MLA Handbook (7th Edition):

Yu, Yingzhe. “Identification of small molecular inhibitors targeting G13D mutant K-ras.” 2012. Web. 20 Oct 2020.

Vancouver:

Yu Y. Identification of small molecular inhibitors targeting G13D mutant K-ras. [Internet] [Masters thesis]. University of Southern California; 2012. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/66766/rec/3323.

Council of Science Editors:

Yu Y. Identification of small molecular inhibitors targeting G13D mutant K-ras. [Masters Thesis]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/66766/rec/3323


University of Southern California

10. Shabaik, Yumna Hosam. Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy.

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

 Pancreatic cancer is one of the deadliest cancers with a 5-year survival rate of 6%. Therapeutic options against this disease are limited and there is… (more)

Subjects/Keywords: cancer; mitochondria; small molecule; triphenylphosphonium cation

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APA (6th Edition):

Shabaik, Y. H. (2013). Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1956

Chicago Manual of Style (16th Edition):

Shabaik, Yumna Hosam. “Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1956.

MLA Handbook (7th Edition):

Shabaik, Yumna Hosam. “Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy.” 2013. Web. 20 Oct 2020.

Vancouver:

Shabaik YH. Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1956.

Council of Science Editors:

Shabaik YH. Development of novel small molecules targeting mitochondrial and oxidative stress signaling pathways for pancreatic cancer therapy. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/221777/rec/1956


University of Southern California

11. Haworth, Kevin G. Molecular characterization of the HIV-1 Vpu protein and its role in antagonizing the cellular restriction factor BST-2/tetherin both in vitro and in vivo.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2013, University of Southern California

 The cellular restriction factor BST-2/tetherin exerts a late stage anti-viral activity against enveloped viruses, retaining newly formed virions at the cell surface and effectively lowering… (more)

Subjects/Keywords: BST2; tetherin; Vpu; HIV; humanized mice

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APA (6th Edition):

Haworth, K. G. (2013). Molecular characterization of the HIV-1 Vpu protein and its role in antagonizing the cellular restriction factor BST-2/tetherin both in vitro and in vivo. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/295396/rec/4184

Chicago Manual of Style (16th Edition):

Haworth, Kevin G. “Molecular characterization of the HIV-1 Vpu protein and its role in antagonizing the cellular restriction factor BST-2/tetherin both in vitro and in vivo.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/295396/rec/4184.

MLA Handbook (7th Edition):

Haworth, Kevin G. “Molecular characterization of the HIV-1 Vpu protein and its role in antagonizing the cellular restriction factor BST-2/tetherin both in vitro and in vivo.” 2013. Web. 20 Oct 2020.

Vancouver:

Haworth KG. Molecular characterization of the HIV-1 Vpu protein and its role in antagonizing the cellular restriction factor BST-2/tetherin both in vitro and in vivo. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/295396/rec/4184.

Council of Science Editors:

Haworth KG. Molecular characterization of the HIV-1 Vpu protein and its role in antagonizing the cellular restriction factor BST-2/tetherin both in vitro and in vivo. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/295396/rec/4184


University of Southern California

12. Ramkumar, Kavya. Design of novel anticancer agents targeting cellular stress response pathways.

Degree: PhD, Pharmaceutical Sciences, 2016, University of Southern California

 Cancer cells exploit cellular stress response mechanisms, such as the unfolded protein response and oxidative stress response, to cope with unfavorable growth conditions and to… (more)

Subjects/Keywords: anticancer; drug design; GRP78; GSTO1; inhibitor

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APA (6th Edition):

Ramkumar, K. (2016). Design of novel anticancer agents targeting cellular stress response pathways. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/456380/rec/1871

Chicago Manual of Style (16th Edition):

Ramkumar, Kavya. “Design of novel anticancer agents targeting cellular stress response pathways.” 2016. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/456380/rec/1871.

MLA Handbook (7th Edition):

Ramkumar, Kavya. “Design of novel anticancer agents targeting cellular stress response pathways.” 2016. Web. 20 Oct 2020.

Vancouver:

Ramkumar K. Design of novel anticancer agents targeting cellular stress response pathways. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/456380/rec/1871.

Council of Science Editors:

Ramkumar K. Design of novel anticancer agents targeting cellular stress response pathways. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/456380/rec/1871


University of Southern California

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

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

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

Subjects/Keywords: CXCR2; CXCL8; inflammation

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Ha, Helen Nen. “Identification of small-molecules targeting CXCR2 function and signaling.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/308809/rec/3324.

MLA Handbook (7th Edition):

Ha, Helen Nen. “Identification of small-molecules targeting CXCR2 function and signaling.” 2013. Web. 20 Oct 2020.

Vancouver:

Ha HN. Identification of small-molecules targeting CXCR2 function and signaling. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/308809/rec/3324.

Council of Science Editors:

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


University of Southern California

14. Millard, Melissa. Discovery of novel small molecules targeting cancer cell metabolism.

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

 Advanced age is a risk-factor common to most cancers. In coming years, a marked increase in the population aged 65 and over will compound the… (more)

Subjects/Keywords: small molecule anti-cancer agents; pancreatic cancer; breast cancer; mitochondria; cancer cell metabolism; PKM2; pyruvate kinase M2; oncology; cancer therapy

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APA (6th Edition):

Millard, M. (2013). Discovery of novel small molecules targeting cancer cell metabolism. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2030

Chicago Manual of Style (16th Edition):

Millard, Melissa. “Discovery of novel small molecules targeting cancer cell metabolism.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2030.

MLA Handbook (7th Edition):

Millard, Melissa. “Discovery of novel small molecules targeting cancer cell metabolism.” 2013. Web. 20 Oct 2020.

Vancouver:

Millard M. Discovery of novel small molecules targeting cancer cell metabolism. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2030.

Council of Science Editors:

Millard M. Discovery of novel small molecules targeting cancer cell metabolism. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/254502/rec/2030


University of Southern California

15. 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/6324

Chicago Manual of Style (16th Edition):

Pathania, Divya. “Targeting cellular redox modulations for pancreatic cancer treatment.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314353/rec/6324.

MLA Handbook (7th Edition):

Pathania, Divya. “Targeting cellular redox modulations for pancreatic cancer treatment.” 2013. Web. 20 Oct 2020.

Vancouver:

Pathania D. Targeting cellular redox modulations for pancreatic cancer treatment. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314353/rec/6324.

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/6324


University of Southern California

16. Huang, Chiun-Wei. A novel design of integrin α2β1 targeting peptide probe for molecular imaging in prostate cancer.

Degree: PhD, Biomedical Engineering, 2011, University of Southern California

 Prostate cancer is one of the leading causes of cancer-related deaths in the United States and Europe. Despite the fact that prostate-specific antigen (PSA) screening… (more)

Subjects/Keywords: prostate cancer; integrin α 2β 1; PET; molecular imaging

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APA (6th Edition):

Huang, C. (2011). A novel design of integrin α2β1 targeting peptide probe for molecular imaging in prostate cancer. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/432536/rec/283

Chicago Manual of Style (16th Edition):

Huang, Chiun-Wei. “A novel design of integrin α2β1 targeting peptide probe for molecular imaging in prostate cancer.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/432536/rec/283.

MLA Handbook (7th Edition):

Huang, Chiun-Wei. “A novel design of integrin α2β1 targeting peptide probe for molecular imaging in prostate cancer.” 2011. Web. 20 Oct 2020.

Vancouver:

Huang C. A novel design of integrin α2β1 targeting peptide probe for molecular imaging in prostate cancer. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/432536/rec/283.

Council of Science Editors:

Huang C. A novel design of integrin α2β1 targeting peptide probe for molecular imaging in prostate cancer. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/432536/rec/283


University of Southern California

17. Xu, Shili. Discovery of novel small molecules for ovarian cancer treatment.

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

 Ovarian cancer is one of the leading cancers causing women’s death in the United States mainly due to its late diagnosis and resistance to current… (more)

Subjects/Keywords: ovarian cancer; protein disulfide isomerase (PDI); propynoic acid carbamoyl methyl amide (PACMA); PACMA 31; ER stress; unfolded protein response (UPR); glycoprotein 130 (gp130); SC144; small molecule; chemotherapy; drug resistance; inhibitor; quinoxalinhydrazide; xenograft; oral bioavailability; Stat3

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APA (6th Edition):

Xu, S. (2013). Discovery of novel small molecules for ovarian cancer treatment. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2029

Chicago Manual of Style (16th Edition):

Xu, Shili. “Discovery of novel small molecules for ovarian cancer treatment.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2029.

MLA Handbook (7th Edition):

Xu, Shili. “Discovery of novel small molecules for ovarian cancer treatment.” 2013. Web. 20 Oct 2020.

Vancouver:

Xu S. Discovery of novel small molecules for ovarian cancer treatment. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2029.

Council of Science Editors:

Xu S. Discovery of novel small molecules for ovarian cancer treatment. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/242171/rec/2029


University of Southern California

18. Serrao, Erik. Novel modes of HIV-1 integrase inhibition.

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

 Though highly active cocktails of antiretroviral drugs have been developed to potently knock down HIV-1 viral load, drug resistance mutations have contributed to the continued… (more)

Subjects/Keywords: HIV-1; integrase; LEDGF/p75; Hsp90; protein-protein interaction; virus-host interaction

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APA (6th Edition):

Serrao, E. (2013). Novel modes of HIV-1 integrase inhibition. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472

Chicago Manual of Style (16th Edition):

Serrao, Erik. “Novel modes of HIV-1 integrase inhibition.” 2013. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472.

MLA Handbook (7th Edition):

Serrao, Erik. “Novel modes of HIV-1 integrase inhibition.” 2013. Web. 20 Oct 2020.

Vancouver:

Serrao E. Novel modes of HIV-1 integrase inhibition. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472.

Council of Science Editors:

Serrao E. Novel modes of HIV-1 integrase inhibition. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128443/rec/4472


University of Southern California

19. Ramkumar, Kavya. Discovery of novel small-molecule compounds with antiviral and anticancer properties.

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

 HIV-1 integrase (IN) has emerged as an important therapeutic target for anti-HIV drug development. Its uniqueness to the virus and its critical role in the… (more)

Subjects/Keywords: integrase; HIV; cancer; boron; rhodanine; ellipticine

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APA (6th Edition):

Ramkumar, K. (2008). Discovery of novel small-molecule compounds with antiviral and anticancer properties. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/115747/rec/2032

Chicago Manual of Style (16th Edition):

Ramkumar, Kavya. “Discovery of novel small-molecule compounds with antiviral and anticancer properties.” 2008. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/115747/rec/2032.

MLA Handbook (7th Edition):

Ramkumar, Kavya. “Discovery of novel small-molecule compounds with antiviral and anticancer properties.” 2008. Web. 20 Oct 2020.

Vancouver:

Ramkumar K. Discovery of novel small-molecule compounds with antiviral and anticancer properties. [Internet] [Masters thesis]. University of Southern California; 2008. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/115747/rec/2032.

Council of Science Editors:

Ramkumar K. Discovery of novel small-molecule compounds with antiviral and anticancer properties. [Masters Thesis]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/115747/rec/2032


University of Southern California

20. Venkata, Kalyan Chakravarthy Nagulapalli. Palladium mediated methods for the total synthesis of lipid mediators and organoboron compounds.

Degree: PhD, Chemistry, 2008, University of Southern California

 This dissertation deals with synthetic and conformational studies of biologically important compounds.; Chapter 1 is overview of lipid mediators that possess anti-inflammatory and promote resolution.… (more)

Subjects/Keywords: conformational studies of lipoxins; benzolipoxins; organoboron compounds synthesis

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APA (6th Edition):

Venkata, K. C. N. (2008). Palladium mediated methods for the total synthesis of lipid mediators and organoboron compounds. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/143947/rec/4905

Chicago Manual of Style (16th Edition):

Venkata, Kalyan Chakravarthy Nagulapalli. “Palladium mediated methods for the total synthesis of lipid mediators and organoboron compounds.” 2008. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/143947/rec/4905.

MLA Handbook (7th Edition):

Venkata, Kalyan Chakravarthy Nagulapalli. “Palladium mediated methods for the total synthesis of lipid mediators and organoboron compounds.” 2008. Web. 20 Oct 2020.

Vancouver:

Venkata KCN. Palladium mediated methods for the total synthesis of lipid mediators and organoboron compounds. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/143947/rec/4905.

Council of Science Editors:

Venkata KCN. Palladium mediated methods for the total synthesis of lipid mediators and organoboron compounds. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/143947/rec/4905


University of Southern California

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

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

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

Subjects/Keywords: integrase; HIV

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Sanchez, Tino Wilson. “Discovery of new HIV-1 integrase inhibitors.” 2007. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484210/rec/2028.

MLA Handbook (7th Edition):

Sanchez, Tino Wilson. “Discovery of new HIV-1 integrase inhibitors.” 2007. Web. 20 Oct 2020.

Vancouver:

Sanchez TW. Discovery of new HIV-1 integrase inhibitors. [Internet] [Masters thesis]. University of Southern California; 2007. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/484210/rec/2028.

Council of Science Editors:

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


University of Southern California

22. Hadi, Victor. An organic chemistry approach toward the synthesis of valuable biological compounds: synthetic progress toward the Palmerolide A subunits, expeditious enyne coupling via alkynes, and development of the next generation of HIV-1 integrase inhibitors.

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

 A very rare opportunity has been bestowed into me to work in three different facets of organic chemistry: total synthesis, methodology, and medicinal chemistry. While… (more)

Subjects/Keywords: enyne formation; integrase inhibitor; Palmerolide A; pyrazolone

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APA (6th Edition):

Hadi, V. (2010). An organic chemistry approach toward the synthesis of valuable biological compounds: synthetic progress toward the Palmerolide A subunits, expeditious enyne coupling via alkynes, and development of the next generation of HIV-1 integrase inhibitors. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/415548/rec/792

Chicago Manual of Style (16th Edition):

Hadi, Victor. “An organic chemistry approach toward the synthesis of valuable biological compounds: synthetic progress toward the Palmerolide A subunits, expeditious enyne coupling via alkynes, and development of the next generation of HIV-1 integrase inhibitors.” 2010. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/415548/rec/792.

MLA Handbook (7th Edition):

Hadi, Victor. “An organic chemistry approach toward the synthesis of valuable biological compounds: synthetic progress toward the Palmerolide A subunits, expeditious enyne coupling via alkynes, and development of the next generation of HIV-1 integrase inhibitors.” 2010. Web. 20 Oct 2020.

Vancouver:

Hadi V. An organic chemistry approach toward the synthesis of valuable biological compounds: synthetic progress toward the Palmerolide A subunits, expeditious enyne coupling via alkynes, and development of the next generation of HIV-1 integrase inhibitors. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/415548/rec/792.

Council of Science Editors:

Hadi V. An organic chemistry approach toward the synthesis of valuable biological compounds: synthetic progress toward the Palmerolide A subunits, expeditious enyne coupling via alkynes, and development of the next generation of HIV-1 integrase inhibitors. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/415548/rec/792


University of Southern California

23. Liu, Lifei. Gonadal hormone regulation of neurogenesis and therapeutic implications for neurodegenerative diseases.

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

 Discovery of adult neurogenesis shed light on the exciting possibility that stimulation of this process can be applied as a novel regenerative strategy for CNS… (more)

Subjects/Keywords: Alzheimer'; s disease; neurogenesis; regenerative medicine; gonadal hormone; progesterone; allopregnanolone

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APA (6th Edition):

Liu, L. (2009). Gonadal hormone regulation of neurogenesis and therapeutic implications for neurodegenerative diseases. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279040/rec/3082

Chicago Manual of Style (16th Edition):

Liu, Lifei. “Gonadal hormone regulation of neurogenesis and therapeutic implications for neurodegenerative diseases.” 2009. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279040/rec/3082.

MLA Handbook (7th Edition):

Liu, Lifei. “Gonadal hormone regulation of neurogenesis and therapeutic implications for neurodegenerative diseases.” 2009. Web. 20 Oct 2020.

Vancouver:

Liu L. Gonadal hormone regulation of neurogenesis and therapeutic implications for neurodegenerative diseases. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279040/rec/3082.

Council of Science Editors:

Liu L. Gonadal hormone regulation of neurogenesis and therapeutic implications for neurodegenerative diseases. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279040/rec/3082


University of Southern California

24. Pattamatta, Preeti. Discovery of novel small-molecule compounds with anticancer properties.

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

 Cancer has emerged as one of the deadliest diseases in the recent past. According to the current statistics, one in every four deaths in the… (more)

Subjects/Keywords: anticancer; small molecules; drug discovery

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APA (6th Edition):

Pattamatta, P. (2010). Discovery of novel small-molecule compounds with anticancer properties. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2031

Chicago Manual of Style (16th Edition):

Pattamatta, Preeti. “Discovery of novel small-molecule compounds with anticancer properties.” 2010. Masters Thesis, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2031.

MLA Handbook (7th Edition):

Pattamatta, Preeti. “Discovery of novel small-molecule compounds with anticancer properties.” 2010. Web. 20 Oct 2020.

Vancouver:

Pattamatta P. Discovery of novel small-molecule compounds with anticancer properties. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2031.

Council of Science Editors:

Pattamatta P. Discovery of novel small-molecule compounds with anticancer properties. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2031


University of Southern California

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

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

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

Subjects/Keywords: NRPS

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Praseuth, Alex. “Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds.” 2008. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85841/rec/928.

MLA Handbook (7th Edition):

Praseuth, Alex. “Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds.” 2008. Web. 20 Oct 2020.

Vancouver:

Praseuth A. Assembling NRPS modules in e. coli to establish a platform for rational design of biologically active compounds. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85841/rec/928.

Council of Science Editors:

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


University of Southern California

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

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

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Al-Mawsawi, Laith Qassim. “Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design.” 2007. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/579616/rec/2026.

MLA Handbook (7th Edition):

Al-Mawsawi, Laith Qassim. “Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design.” 2007. Web. 20 Oct 2020.

Vancouver:

Al-Mawsawi LQ. Discovery of a novel HIV-1 integrase inhibitor binding site: insight into enzyme structure/function and inhibitor design. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/579616/rec/2026.

Council of Science Editors:

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


University of Southern California

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

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

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

Subjects/Keywords: APE1; DNA repair; cancer therapeutics

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Zawahir, Faathma. “Targeting human base excision repair as a novel strategy in cancer therapeutics.” 2009. Doctoral Dissertation, University of Southern California. Accessed October 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248516/rec/6327.

MLA Handbook (7th Edition):

Zawahir, Faathma. “Targeting human base excision repair as a novel strategy in cancer therapeutics.” 2009. Web. 20 Oct 2020.

Vancouver:

Zawahir F. Targeting human base excision repair as a novel strategy in cancer therapeutics. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Oct 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/248516/rec/6327.

Council of Science Editors:

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

.