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You searched for subject:(Medicinal Chemistry AND Pharmaceutics). Showing records 121 – 150 of 180 total matches.

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121. Playa, Hilaire Colleen. Computer-Aided Drug Design and Discovery, Screening and Synthesis of Small Molecule Inhibitors of Nucleoside Transporters.

Degree: PhD, Pharmaceutical Sciences, 2014, University of Tennessee Health Science Center

  Using prior biological data, pharmacophore models were made for hCNT1, hCNT3, hENT1, and hENT4. The hCNT3 and hCNT1 pharmacophore were used to select compounds… (more)

Subjects/Keywords: SLC29; nucleoside transporters; nucleosides; PMAT; QSAR; SLC28; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Playa, H. C. (2014). Computer-Aided Drug Design and Discovery, Screening and Synthesis of Small Molecule Inhibitors of Nucleoside Transporters. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/398

Chicago Manual of Style (16th Edition):

Playa, Hilaire Colleen. “Computer-Aided Drug Design and Discovery, Screening and Synthesis of Small Molecule Inhibitors of Nucleoside Transporters.” 2014. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/398.

MLA Handbook (7th Edition):

Playa, Hilaire Colleen. “Computer-Aided Drug Design and Discovery, Screening and Synthesis of Small Molecule Inhibitors of Nucleoside Transporters.” 2014. Web. 12 Dec 2019.

Vancouver:

Playa HC. Computer-Aided Drug Design and Discovery, Screening and Synthesis of Small Molecule Inhibitors of Nucleoside Transporters. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2014. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/398.

Council of Science Editors:

Playa HC. Computer-Aided Drug Design and Discovery, Screening and Synthesis of Small Molecule Inhibitors of Nucleoside Transporters. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2014. Available from: https://dc.uthsc.edu/dissertations/398

122. Lin, Zongtao. Synthesis of 20S-Hydroxyvitamin D3 Analogs and Their 1α-Hydroxyl Derivatives as Potent Anti-inflammatory Agents.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Tennessee Health Science Center

 Rheumatoid arthritis (RA) is one of the autoimmune diseases, and is affecting 2.5 million Americans in total. Among the treatment options of RA, 1α,25-dihydroxyvitamin D3… (more)

Subjects/Keywords: 20S-Hydroxyvitamin D3; Analog; Anti-inflammatory; Metabolite; Synthesis; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Lin, Z. (2017). Synthesis of 20S-Hydroxyvitamin D3 Analogs and Their 1α-Hydroxyl Derivatives as Potent Anti-inflammatory Agents. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/435

Chicago Manual of Style (16th Edition):

Lin, Zongtao. “Synthesis of 20S-Hydroxyvitamin D3 Analogs and Their 1α-Hydroxyl Derivatives as Potent Anti-inflammatory Agents.” 2017. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/435.

MLA Handbook (7th Edition):

Lin, Zongtao. “Synthesis of 20S-Hydroxyvitamin D3 Analogs and Their 1α-Hydroxyl Derivatives as Potent Anti-inflammatory Agents.” 2017. Web. 12 Dec 2019.

Vancouver:

Lin Z. Synthesis of 20S-Hydroxyvitamin D3 Analogs and Their 1α-Hydroxyl Derivatives as Potent Anti-inflammatory Agents. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2017. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/435.

Council of Science Editors:

Lin Z. Synthesis of 20S-Hydroxyvitamin D3 Analogs and Their 1α-Hydroxyl Derivatives as Potent Anti-inflammatory Agents. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2017. Available from: https://dc.uthsc.edu/dissertations/435

123. Thomson, Margaret Mary. Age-Associated Expression Patterns of OATP 1B1 and OATP 1B3 and Their Effect on the Disposition of Fexofenadine.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Tennessee Health Science Center

 As part of the drug disposition process (absorption, distribution, metabolism, excretion), an often overlooked aspect is transport. In order for drugs to be metabolized and… (more)

Subjects/Keywords: Drug Transport; Fexofenadine; OATP1B1; OATP1B3; Ontogeny; Pediatrics; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Thomson, M. M. (2017). Age-Associated Expression Patterns of OATP 1B1 and OATP 1B3 and Their Effect on the Disposition of Fexofenadine. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/430

Chicago Manual of Style (16th Edition):

Thomson, Margaret Mary. “Age-Associated Expression Patterns of OATP 1B1 and OATP 1B3 and Their Effect on the Disposition of Fexofenadine.” 2017. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/430.

MLA Handbook (7th Edition):

Thomson, Margaret Mary. “Age-Associated Expression Patterns of OATP 1B1 and OATP 1B3 and Their Effect on the Disposition of Fexofenadine.” 2017. Web. 12 Dec 2019.

Vancouver:

Thomson MM. Age-Associated Expression Patterns of OATP 1B1 and OATP 1B3 and Their Effect on the Disposition of Fexofenadine. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2017. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/430.

Council of Science Editors:

Thomson MM. Age-Associated Expression Patterns of OATP 1B1 and OATP 1B3 and Their Effect on the Disposition of Fexofenadine. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2017. Available from: https://dc.uthsc.edu/dissertations/430

124. Richmond, Oliver H., III. Extraction, Purification and Evaluation of PRMT5-Inhibitory Phytochemical Compounds for the Treatment of Prostate Adenocarcinoma.

Degree: PhD, Biological Science, 2019, Clark University Atlanta

  The development and advancement of prostate cancer is supported by a plethora of genetic and proteomic abnormalities, including events of post-translational modifications. The protein… (more)

Subjects/Keywords: PRMT5; Protein Methyltransferase; Prostate Cancer; Small Molecule Inhibitors; Natural Inhibitors; Alternative and Complementary Medicine; Alternative and Complementary Medicine; Biochemistry; Cancer Biology; Cell Biology; Medicinal Chemistry and Pharmaceutics; Molecular Biology

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APA (6th Edition):

Richmond, Oliver H., I. (2019). Extraction, Purification and Evaluation of PRMT5-Inhibitory Phytochemical Compounds for the Treatment of Prostate Adenocarcinoma. (Doctoral Dissertation). Clark University Atlanta. Retrieved from http://digitalcommons.auctr.edu/cauetds/185

Chicago Manual of Style (16th Edition):

Richmond, Oliver H., III. “Extraction, Purification and Evaluation of PRMT5-Inhibitory Phytochemical Compounds for the Treatment of Prostate Adenocarcinoma.” 2019. Doctoral Dissertation, Clark University Atlanta. Accessed December 12, 2019. http://digitalcommons.auctr.edu/cauetds/185.

MLA Handbook (7th Edition):

Richmond, Oliver H., III. “Extraction, Purification and Evaluation of PRMT5-Inhibitory Phytochemical Compounds for the Treatment of Prostate Adenocarcinoma.” 2019. Web. 12 Dec 2019.

Vancouver:

Richmond, Oliver H. I. Extraction, Purification and Evaluation of PRMT5-Inhibitory Phytochemical Compounds for the Treatment of Prostate Adenocarcinoma. [Internet] [Doctoral dissertation]. Clark University Atlanta; 2019. [cited 2019 Dec 12]. Available from: http://digitalcommons.auctr.edu/cauetds/185.

Council of Science Editors:

Richmond, Oliver H. I. Extraction, Purification and Evaluation of PRMT5-Inhibitory Phytochemical Compounds for the Treatment of Prostate Adenocarcinoma. [Doctoral Dissertation]. Clark University Atlanta; 2019. Available from: http://digitalcommons.auctr.edu/cauetds/185


Wayne State University

125. Conti, Denise Santos. Polymeric Nanocarriers And Their Oral Inhalation Formulations For The Regional Delivery Of Nucleic Acids To The Lungs.

Degree: PhD, Chemical Engineering and Materials Science, 2013, Wayne State University

  Gene therapy has attracted attention in the fields of medicine, pharmacy, and bionanotechnology due to the potential for treating a large number of medically… (more)

Subjects/Keywords: gene therapy; nucleic acids; oral inhalation; polymeric nanocarriers; pressurized metered-dose inhalers; pulmonary epithelium; Chemical Engineering; Medicinal Chemistry and Pharmaceutics; Molecular Biology

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APA (6th Edition):

Conti, D. S. (2013). Polymeric Nanocarriers And Their Oral Inhalation Formulations For The Regional Delivery Of Nucleic Acids To The Lungs. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/756

Chicago Manual of Style (16th Edition):

Conti, Denise Santos. “Polymeric Nanocarriers And Their Oral Inhalation Formulations For The Regional Delivery Of Nucleic Acids To The Lungs.” 2013. Doctoral Dissertation, Wayne State University. Accessed December 12, 2019. https://digitalcommons.wayne.edu/oa_dissertations/756.

MLA Handbook (7th Edition):

Conti, Denise Santos. “Polymeric Nanocarriers And Their Oral Inhalation Formulations For The Regional Delivery Of Nucleic Acids To The Lungs.” 2013. Web. 12 Dec 2019.

Vancouver:

Conti DS. Polymeric Nanocarriers And Their Oral Inhalation Formulations For The Regional Delivery Of Nucleic Acids To The Lungs. [Internet] [Doctoral dissertation]. Wayne State University; 2013. [cited 2019 Dec 12]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/756.

Council of Science Editors:

Conti DS. Polymeric Nanocarriers And Their Oral Inhalation Formulations For The Regional Delivery Of Nucleic Acids To The Lungs. [Doctoral Dissertation]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_dissertations/756


Virginia Commonwealth University

126. Dhapare, Sneha. SALVIANOLIC ACID B FOR PULMONARY DELIVERY TOWARDS REVERSAL OF EMPHYSEMA.

Degree: PhD, Pharmaceutical Sciences, 2017, Virginia Commonwealth University

  A new pathobiologic hypothesis has recently emerged that the alveolar structural destruction and loss in emphysema are caused by the deficiency of vascular endothelial… (more)

Subjects/Keywords: Emphysema; salvianolic acid B; vascular endothelial growth factor (VEGF); cell death; cell proliferation; cell migration; Cell Biology; Medicinal Chemistry and Pharmaceutics; Pharmacology

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APA (6th Edition):

Dhapare, S. (2017). SALVIANOLIC ACID B FOR PULMONARY DELIVERY TOWARDS REVERSAL OF EMPHYSEMA. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/4812

Chicago Manual of Style (16th Edition):

Dhapare, Sneha. “SALVIANOLIC ACID B FOR PULMONARY DELIVERY TOWARDS REVERSAL OF EMPHYSEMA.” 2017. Doctoral Dissertation, Virginia Commonwealth University. Accessed December 12, 2019. https://scholarscompass.vcu.edu/etd/4812.

MLA Handbook (7th Edition):

Dhapare, Sneha. “SALVIANOLIC ACID B FOR PULMONARY DELIVERY TOWARDS REVERSAL OF EMPHYSEMA.” 2017. Web. 12 Dec 2019.

Vancouver:

Dhapare S. SALVIANOLIC ACID B FOR PULMONARY DELIVERY TOWARDS REVERSAL OF EMPHYSEMA. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2017. [cited 2019 Dec 12]. Available from: https://scholarscompass.vcu.edu/etd/4812.

Council of Science Editors:

Dhapare S. SALVIANOLIC ACID B FOR PULMONARY DELIVERY TOWARDS REVERSAL OF EMPHYSEMA. [Doctoral Dissertation]. Virginia Commonwealth University; 2017. Available from: https://scholarscompass.vcu.edu/etd/4812


University of New Mexico

127. Borunda Duque, Teofilo. Evaluating the Aryl Hydrocarbon Receptor as a Target for Pharmacologic Activity of Repurposed Drugs.

Degree: College of Pharmacy, 2018, University of New Mexico

  The discovery of new pharmacologic targets is important for the advancement of pharmacotherapy and identification of new indications for current drugs. The aryl hydrocarbon… (more)

Subjects/Keywords: Chemicals and Drugs; Medicinal Chemistry and Pharmaceutics; Other Chemicals and Drugs; Pharmacology; Pharmacology, Toxicology and Environmental Health; Toxicology; Aryl Hydrocarbon receptor; Drug Repurposing; Pharmacology; Pharmaceutical target

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APA (6th Edition):

Borunda Duque, T. (2018). Evaluating the Aryl Hydrocarbon Receptor as a Target for Pharmacologic Activity of Repurposed Drugs. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/phrm_etds/19

Chicago Manual of Style (16th Edition):

Borunda Duque, Teofilo. “Evaluating the Aryl Hydrocarbon Receptor as a Target for Pharmacologic Activity of Repurposed Drugs.” 2018. Masters Thesis, University of New Mexico. Accessed December 12, 2019. https://digitalrepository.unm.edu/phrm_etds/19.

MLA Handbook (7th Edition):

Borunda Duque, Teofilo. “Evaluating the Aryl Hydrocarbon Receptor as a Target for Pharmacologic Activity of Repurposed Drugs.” 2018. Web. 12 Dec 2019.

Vancouver:

Borunda Duque T. Evaluating the Aryl Hydrocarbon Receptor as a Target for Pharmacologic Activity of Repurposed Drugs. [Internet] [Masters thesis]. University of New Mexico; 2018. [cited 2019 Dec 12]. Available from: https://digitalrepository.unm.edu/phrm_etds/19.

Council of Science Editors:

Borunda Duque T. Evaluating the Aryl Hydrocarbon Receptor as a Target for Pharmacologic Activity of Repurposed Drugs. [Masters Thesis]. University of New Mexico; 2018. Available from: https://digitalrepository.unm.edu/phrm_etds/19

128. D'Cunha, Napoleon. Pioneering a Novel Class of Tetrahydroimidazopyridines with Anti-Proliferative Property Study Against Prostate Cancer.

Degree: PhD, Chemistry, 2016, Clark University Atlanta

  The synthesis of tetrahydroimidazo[1,5-a]pyridine (rIMP) through the transfer hydrogenation of imidazo[1,5-a]pyridine (IMP) was successfully developed. The simple two-step procedure is the most viable and… (more)

Subjects/Keywords: Tetrahydroimidazopyridine; Imidazopyridine; Catalytic Hydrogenation; Reduction by Hydrazine; Anti-Proliferative Property; Prostate Cancer Cells; Heterocyclic Compounds; Laboratory and Basic Science Research; Medicinal Chemistry and Pharmaceutics; Organic Chemicals

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APA (6th Edition):

D'Cunha, N. (2016). Pioneering a Novel Class of Tetrahydroimidazopyridines with Anti-Proliferative Property Study Against Prostate Cancer. (Doctoral Dissertation). Clark University Atlanta. Retrieved from http://digitalcommons.auctr.edu/cauetds/39

Chicago Manual of Style (16th Edition):

D'Cunha, Napoleon. “Pioneering a Novel Class of Tetrahydroimidazopyridines with Anti-Proliferative Property Study Against Prostate Cancer.” 2016. Doctoral Dissertation, Clark University Atlanta. Accessed December 12, 2019. http://digitalcommons.auctr.edu/cauetds/39.

MLA Handbook (7th Edition):

D'Cunha, Napoleon. “Pioneering a Novel Class of Tetrahydroimidazopyridines with Anti-Proliferative Property Study Against Prostate Cancer.” 2016. Web. 12 Dec 2019.

Vancouver:

D'Cunha N. Pioneering a Novel Class of Tetrahydroimidazopyridines with Anti-Proliferative Property Study Against Prostate Cancer. [Internet] [Doctoral dissertation]. Clark University Atlanta; 2016. [cited 2019 Dec 12]. Available from: http://digitalcommons.auctr.edu/cauetds/39.

Council of Science Editors:

D'Cunha N. Pioneering a Novel Class of Tetrahydroimidazopyridines with Anti-Proliferative Property Study Against Prostate Cancer. [Doctoral Dissertation]. Clark University Atlanta; 2016. Available from: http://digitalcommons.auctr.edu/cauetds/39


Northeastern University

129. Patel, Darshna Rajendrakumar. Enhancement of in vitro therapeutic efficacy using combination paclitaxel and ceramide therapy using EGFR targeted biodegradable polymeric nanoparticles in ovarian cancer model.

Degree: MS, School of Pharmacy, 2012, Northeastern University

 Currently, tumor-cell resistance to the chemotherapy is key reason for failure of the clinical treatment of cancer cells; almost all chemotherapeutic strategies used are susceptible… (more)

Subjects/Keywords: biodegradable nanoparticles; ceramide; drug resistance; ovarian cancer; paclitaxel; tumor targeting; Medicinal and Pharmaceutical Chemistry; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Patel, D. R. (2012). Enhancement of in vitro therapeutic efficacy using combination paclitaxel and ceramide therapy using EGFR targeted biodegradable polymeric nanoparticles in ovarian cancer model. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002956

Chicago Manual of Style (16th Edition):

Patel, Darshna Rajendrakumar. “Enhancement of in vitro therapeutic efficacy using combination paclitaxel and ceramide therapy using EGFR targeted biodegradable polymeric nanoparticles in ovarian cancer model.” 2012. Masters Thesis, Northeastern University. Accessed December 12, 2019. http://hdl.handle.net/2047/d20002956.

MLA Handbook (7th Edition):

Patel, Darshna Rajendrakumar. “Enhancement of in vitro therapeutic efficacy using combination paclitaxel and ceramide therapy using EGFR targeted biodegradable polymeric nanoparticles in ovarian cancer model.” 2012. Web. 12 Dec 2019.

Vancouver:

Patel DR. Enhancement of in vitro therapeutic efficacy using combination paclitaxel and ceramide therapy using EGFR targeted biodegradable polymeric nanoparticles in ovarian cancer model. [Internet] [Masters thesis]. Northeastern University; 2012. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2047/d20002956.

Council of Science Editors:

Patel DR. Enhancement of in vitro therapeutic efficacy using combination paclitaxel and ceramide therapy using EGFR targeted biodegradable polymeric nanoparticles in ovarian cancer model. [Masters Thesis]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002956


Northeastern University

130. Xu, Jing. Multimodal therapeutic strategy for pancreatic cancer: EGFR-targeted gelatin-based nanoparticles for combination wild-type p53 gene and cytotoxic drug delivery.

Degree: PhD, School of Pharmacy, 2013, Northeastern University

 Pancreatic adenocarcinoma is the fourth lethal cancer in the United States. Many therapeutic strategies such as the chemotherapy and gene therapy have been applied as… (more)

Subjects/Keywords: Drug Delivery; epidermal growth factor receptor (EGFR) targeting; Gene Therapy; Pancreatic Cancer; Thiolated type B gelatin nanoparticles; wild type p53; Medicinal Chemistry and Pharmaceutics; Pharmacology, Toxicology and Environmental Health

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APA (6th Edition):

Xu, J. (2013). Multimodal therapeutic strategy for pancreatic cancer: EGFR-targeted gelatin-based nanoparticles for combination wild-type p53 gene and cytotoxic drug delivery. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003307

Chicago Manual of Style (16th Edition):

Xu, Jing. “Multimodal therapeutic strategy for pancreatic cancer: EGFR-targeted gelatin-based nanoparticles for combination wild-type p53 gene and cytotoxic drug delivery.” 2013. Doctoral Dissertation, Northeastern University. Accessed December 12, 2019. http://hdl.handle.net/2047/d20003307.

MLA Handbook (7th Edition):

Xu, Jing. “Multimodal therapeutic strategy for pancreatic cancer: EGFR-targeted gelatin-based nanoparticles for combination wild-type p53 gene and cytotoxic drug delivery.” 2013. Web. 12 Dec 2019.

Vancouver:

Xu J. Multimodal therapeutic strategy for pancreatic cancer: EGFR-targeted gelatin-based nanoparticles for combination wild-type p53 gene and cytotoxic drug delivery. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2047/d20003307.

Council of Science Editors:

Xu J. Multimodal therapeutic strategy for pancreatic cancer: EGFR-targeted gelatin-based nanoparticles for combination wild-type p53 gene and cytotoxic drug delivery. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003307


Northeastern University

131. Sharma, Rishi. Design and synthesis of novel cannabinoids with controlled detoxification.

Degree: PhD, School of Pharmacy, 2011, Northeastern University

 Cannabis has been used medicinally and recreationally for several centuries, commonly in the form of the plant's dried leaf/flower ("marijuana"). Δ9- Tetrahydrocannabinol (Δ9-THC) is the… (more)

Subjects/Keywords: Cannabinoids; Controlled Duration of Action; Depot effect; Detoxification; Lipophilicity; Soft drug; Medicinal and Pharmaceutical Chemistry; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Sharma, R. (2011). Design and synthesis of novel cannabinoids with controlled detoxification. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002953

Chicago Manual of Style (16th Edition):

Sharma, Rishi. “Design and synthesis of novel cannabinoids with controlled detoxification.” 2011. Doctoral Dissertation, Northeastern University. Accessed December 12, 2019. http://hdl.handle.net/2047/d20002953.

MLA Handbook (7th Edition):

Sharma, Rishi. “Design and synthesis of novel cannabinoids with controlled detoxification.” 2011. Web. 12 Dec 2019.

Vancouver:

Sharma R. Design and synthesis of novel cannabinoids with controlled detoxification. [Internet] [Doctoral dissertation]. Northeastern University; 2011. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2047/d20002953.

Council of Science Editors:

Sharma R. Design and synthesis of novel cannabinoids with controlled detoxification. [Doctoral Dissertation]. Northeastern University; 2011. Available from: http://hdl.handle.net/2047/d20002953


Northeastern University

132. Apte, Anjali Vasant. Multifunctional nanocarriers for enhanced tumor delivery.

Degree: PhD, School of Pharmacy, 2012, Northeastern University

 A tumor is an abnormally growing mass of cells. Ordinary chemotherapeutic agents used to prevent tumor growth produce more side effects and less than desired… (more)

Subjects/Keywords: cell-penetrating peptide; liposomes and micelles; monoclonal antibody; multifunctional nanocarriers; pH-sensitive polymer; tumor drug delivery; Medicinal and Pharmaceutical Chemistry; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Apte, A. V. (2012). Multifunctional nanocarriers for enhanced tumor delivery. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002948

Chicago Manual of Style (16th Edition):

Apte, Anjali Vasant. “Multifunctional nanocarriers for enhanced tumor delivery.” 2012. Doctoral Dissertation, Northeastern University. Accessed December 12, 2019. http://hdl.handle.net/2047/d20002948.

MLA Handbook (7th Edition):

Apte, Anjali Vasant. “Multifunctional nanocarriers for enhanced tumor delivery.” 2012. Web. 12 Dec 2019.

Vancouver:

Apte AV. Multifunctional nanocarriers for enhanced tumor delivery. [Internet] [Doctoral dissertation]. Northeastern University; 2012. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2047/d20002948.

Council of Science Editors:

Apte AV. Multifunctional nanocarriers for enhanced tumor delivery. [Doctoral Dissertation]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002948


McMaster University

133. Piazza, Justin E. Novel Antipsychotic Drug Carriers: The Development of Nanoparticle and Microgel Drug Carriers for Antipsychotic Delivery in the Treatment of Schizophrenia.

Degree: MSc, 2013, McMaster University

Lectin-functionalized, Poly [oligo(ethylene glycol) methyl ether methacrylate] (POEGMA) loaded with 3(R)-[(2(S)-pyrrolidinylcarbonyl)amino]-2-oxo-1-pyrrolidineacetamide (PAOPA) and poly(ethylene glycol)–block-poly(D,L-lactic-co-glycolic acid) (PEG-PLGA) nanoparticles loaded with haloperidol were prepared with… (more)

Subjects/Keywords: nanoparticle; microgel; antipsychotic; allosteric modulator; PAOPA; Amino Acids, Peptides, and Proteins; Biochemistry; Biomaterials; Cell Biology; Medicinal Chemistry and Pharmaceutics; Molecular and Cellular Neuroscience; Molecular Biology; Nanomedicine; Nervous System Diseases; Pharmaceutics and Drug Design; Polymer Science; Psychiatric and Mental Health; Toxicology; Amino Acids, Peptides, and Proteins

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APA (6th Edition):

Piazza, J. E. (2013). Novel Antipsychotic Drug Carriers: The Development of Nanoparticle and Microgel Drug Carriers for Antipsychotic Delivery in the Treatment of Schizophrenia. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13291

Chicago Manual of Style (16th Edition):

Piazza, Justin E. “Novel Antipsychotic Drug Carriers: The Development of Nanoparticle and Microgel Drug Carriers for Antipsychotic Delivery in the Treatment of Schizophrenia.” 2013. Masters Thesis, McMaster University. Accessed December 12, 2019. http://hdl.handle.net/11375/13291.

MLA Handbook (7th Edition):

Piazza, Justin E. “Novel Antipsychotic Drug Carriers: The Development of Nanoparticle and Microgel Drug Carriers for Antipsychotic Delivery in the Treatment of Schizophrenia.” 2013. Web. 12 Dec 2019.

Vancouver:

Piazza JE. Novel Antipsychotic Drug Carriers: The Development of Nanoparticle and Microgel Drug Carriers for Antipsychotic Delivery in the Treatment of Schizophrenia. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11375/13291.

Council of Science Editors:

Piazza JE. Novel Antipsychotic Drug Carriers: The Development of Nanoparticle and Microgel Drug Carriers for Antipsychotic Delivery in the Treatment of Schizophrenia. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13291


University of Kentucky

134. Al-Darraji, Ahmed Hamish Neamah. AZITHROMYCIN THERAPY REDUCES CARDIAC INFLAMMATION AND MITIGATES ADVERSE CARDIAC REMODELING AFTER MYOCARDIAL INFARCTION.

Degree: 2019, University of Kentucky

 Introduction: Myocardial infarction (MI) remains the leading cause of morbidity and mortality worldwide. Induced by cardiomyocyte death, MI initiates a prolonged and uncontrolled inflammatory response… (more)

Subjects/Keywords: Myocardial infarction; Post-myocardial infarction inflammation; Macrophage; Macrophage polarization; Azithromycin; liposomal azithromycin; Medicinal Chemistry and Pharmaceutics; Pharmaceutics and Drug Design; Pharmacology; Pharmacology, Toxicology and Environmental Health; Pharmacy and Pharmaceutical Sciences; Toxicology

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APA (6th Edition):

Al-Darraji, A. H. N. (2019). AZITHROMYCIN THERAPY REDUCES CARDIAC INFLAMMATION AND MITIGATES ADVERSE CARDIAC REMODELING AFTER MYOCARDIAL INFARCTION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacol_etds/30

Chicago Manual of Style (16th Edition):

Al-Darraji, Ahmed Hamish Neamah. “AZITHROMYCIN THERAPY REDUCES CARDIAC INFLAMMATION AND MITIGATES ADVERSE CARDIAC REMODELING AFTER MYOCARDIAL INFARCTION.” 2019. Doctoral Dissertation, University of Kentucky. Accessed December 12, 2019. https://uknowledge.uky.edu/pharmacol_etds/30.

MLA Handbook (7th Edition):

Al-Darraji, Ahmed Hamish Neamah. “AZITHROMYCIN THERAPY REDUCES CARDIAC INFLAMMATION AND MITIGATES ADVERSE CARDIAC REMODELING AFTER MYOCARDIAL INFARCTION.” 2019. Web. 12 Dec 2019.

Vancouver:

Al-Darraji AHN. AZITHROMYCIN THERAPY REDUCES CARDIAC INFLAMMATION AND MITIGATES ADVERSE CARDIAC REMODELING AFTER MYOCARDIAL INFARCTION. [Internet] [Doctoral dissertation]. University of Kentucky; 2019. [cited 2019 Dec 12]. Available from: https://uknowledge.uky.edu/pharmacol_etds/30.

Council of Science Editors:

Al-Darraji AHN. AZITHROMYCIN THERAPY REDUCES CARDIAC INFLAMMATION AND MITIGATES ADVERSE CARDIAC REMODELING AFTER MYOCARDIAL INFARCTION. [Doctoral Dissertation]. University of Kentucky; 2019. Available from: https://uknowledge.uky.edu/pharmacol_etds/30


University of Kentucky

135. Stamatkin, Christopher W. PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) AS A THERAPEUTIC TARGET IN NSCLC.

Degree: 2014, University of Kentucky

 Deregulated activation of phosphatidylinositol 3-kinase (PI3K) pathway is central to many human malignancies. The functions of this pathway are critical for normal cell metabolism, proliferation,… (more)

Subjects/Keywords: PI3K; NSCLC; drug discovery; targeted therapy; lung cancer; Medical Cell Biology; Medical Genetics; Medical Pharmacology; Medicinal Chemistry and Pharmaceutics; Oncology; Other Pharmacy and Pharmaceutical Sciences; Pharmaceutics and Drug Design; Pharmacology, Toxicology and Environmental Health

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APA (6th Edition):

Stamatkin, C. W. (2014). PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) AS A THERAPEUTIC TARGET IN NSCLC. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/58

Chicago Manual of Style (16th Edition):

Stamatkin, Christopher W. “PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) AS A THERAPEUTIC TARGET IN NSCLC.” 2014. Doctoral Dissertation, University of Kentucky. Accessed December 12, 2019. https://uknowledge.uky.edu/pharmacy_etds/58.

MLA Handbook (7th Edition):

Stamatkin, Christopher W. “PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) AS A THERAPEUTIC TARGET IN NSCLC.” 2014. Web. 12 Dec 2019.

Vancouver:

Stamatkin CW. PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) AS A THERAPEUTIC TARGET IN NSCLC. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2019 Dec 12]. Available from: https://uknowledge.uky.edu/pharmacy_etds/58.

Council of Science Editors:

Stamatkin CW. PHOSPHATIDYLINOSITOL 3-KINASE (PI3K) AS A THERAPEUTIC TARGET IN NSCLC. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: https://uknowledge.uky.edu/pharmacy_etds/58

136. Vankayala, Sai Lakshmana Kumar. Computational Approaches for Structure Based Drug Design and Protein Structure-Function Prediction.

Degree: 2013, University of South Florida

 This dissertation thesis consists of a series of chapters that are interwoven by solving interesting biological problems, employing various computational methodologies. These techniques provide meaningful… (more)

Subjects/Keywords: Biophysics; Cancer; Computational Chemistry; Hydroxyurea; Medicinal Chemistry; Sickle cell disease; Chemistry; Computer Sciences; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Vankayala, S. L. K. (2013). Computational Approaches for Structure Based Drug Design and Protein Structure-Function Prediction. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4601

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Vankayala, Sai Lakshmana Kumar. “Computational Approaches for Structure Based Drug Design and Protein Structure-Function Prediction.” 2013. Thesis, University of South Florida. Accessed December 12, 2019. https://scholarcommons.usf.edu/etd/4601.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Vankayala, Sai Lakshmana Kumar. “Computational Approaches for Structure Based Drug Design and Protein Structure-Function Prediction.” 2013. Web. 12 Dec 2019.

Vancouver:

Vankayala SLK. Computational Approaches for Structure Based Drug Design and Protein Structure-Function Prediction. [Internet] [Thesis]. University of South Florida; 2013. [cited 2019 Dec 12]. Available from: https://scholarcommons.usf.edu/etd/4601.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Vankayala SLK. Computational Approaches for Structure Based Drug Design and Protein Structure-Function Prediction. [Thesis]. University of South Florida; 2013. Available from: https://scholarcommons.usf.edu/etd/4601

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

137. Zeng, Kui. Discovery of Quinic Acid Derivatives as Oral Anti-inflammatory Agents.

Degree: PhD, Pharmaceutical Sciences, 2010, University of Tennessee Health Science Center

  Quinic acid (QA) esters found in hot water extracts of Uncaria tomentosa (a.k.a. Cat’s claw) exert anti-inflammatory activity through mechanisms involving inhibition of the… (more)

Subjects/Keywords: anti-inflammation; orally active drug; quinic acid derivatives; Alternative and Complementary Medicine; Chemicals and Drugs; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Natural Products Chemistry and Pharmacognosy; Pharmaceutical Preparations; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Zeng, K. (2010). Discovery of Quinic Acid Derivatives as Oral Anti-inflammatory Agents. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/314

Chicago Manual of Style (16th Edition):

Zeng, Kui. “Discovery of Quinic Acid Derivatives as Oral Anti-inflammatory Agents.” 2010. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/314.

MLA Handbook (7th Edition):

Zeng, Kui. “Discovery of Quinic Acid Derivatives as Oral Anti-inflammatory Agents.” 2010. Web. 12 Dec 2019.

Vancouver:

Zeng K. Discovery of Quinic Acid Derivatives as Oral Anti-inflammatory Agents. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2010. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/314.

Council of Science Editors:

Zeng K. Discovery of Quinic Acid Derivatives as Oral Anti-inflammatory Agents. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2010. Available from: https://dc.uthsc.edu/dissertations/314

138. Siricilla, Shajila. Discovery of Natural Product-based Antimycobacterial Agents Effective against Non-replicating Bacilli.

Degree: PhD, Pharmaceutical Sciences, 2017, University of Tennessee Health Science Center

  New antimycobacterial molecules that kill non-replicating Mycobacterium tuberculosis (Mtb) were identified by screening libraries of synthetic natural products. De novo screening of a 400-membered… (more)

Subjects/Keywords: MenA inhibitors; Mycobacterium tuberculosis; mycolyl arabinogalactan; Phosphotransferase inhibitors; Pleuromutilin analogs; WecA and MurX inhibitors; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Natural Products Chemistry and Pharmacognosy; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Siricilla, S. (2017). Discovery of Natural Product-based Antimycobacterial Agents Effective against Non-replicating Bacilli. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/434

Chicago Manual of Style (16th Edition):

Siricilla, Shajila. “Discovery of Natural Product-based Antimycobacterial Agents Effective against Non-replicating Bacilli.” 2017. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/434.

MLA Handbook (7th Edition):

Siricilla, Shajila. “Discovery of Natural Product-based Antimycobacterial Agents Effective against Non-replicating Bacilli.” 2017. Web. 12 Dec 2019.

Vancouver:

Siricilla S. Discovery of Natural Product-based Antimycobacterial Agents Effective against Non-replicating Bacilli. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2017. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/434.

Council of Science Editors:

Siricilla S. Discovery of Natural Product-based Antimycobacterial Agents Effective against Non-replicating Bacilli. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2017. Available from: https://dc.uthsc.edu/dissertations/434


Edith Cowan University

139. Klinac, Dragana. The evaluation of midazolam on head injured patients in the prehospital setting.

Degree: 2008, Edith Cowan University

 Midazolam (Hypnovel ®) is the only sedating agent used by paramedics at St John Ambulance Service W.A. in the management of many conditions including seizure… (more)

Subjects/Keywords: Midazolam; Head; Wounds and injuries; Chemotherapy.; Emergency Medicine; Medical Biochemistry; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Klinac, D. (2008). The evaluation of midazolam on head injured patients in the prehospital setting. (Thesis). Edith Cowan University. Retrieved from http://ro.ecu.edu.au/theses/195

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Klinac, Dragana. “The evaluation of midazolam on head injured patients in the prehospital setting.” 2008. Thesis, Edith Cowan University. Accessed December 12, 2019. http://ro.ecu.edu.au/theses/195.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Klinac, Dragana. “The evaluation of midazolam on head injured patients in the prehospital setting.” 2008. Web. 12 Dec 2019.

Vancouver:

Klinac D. The evaluation of midazolam on head injured patients in the prehospital setting. [Internet] [Thesis]. Edith Cowan University; 2008. [cited 2019 Dec 12]. Available from: http://ro.ecu.edu.au/theses/195.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Klinac D. The evaluation of midazolam on head injured patients in the prehospital setting. [Thesis]. Edith Cowan University; 2008. Available from: http://ro.ecu.edu.au/theses/195

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Texas Medical Center

140. Tsao, Ning. Design, Synthesis and Development of Transporter Targeting Agents for Image-guided Therapy and Drug Delivery.

Degree: PhD, 2013, Texas Medical Center

  The purpose of this study was to design, synthesize and develop novel transporter targeting agents for image-guided therapy and drug delivery. Two novel agents,… (more)

Subjects/Keywords: glycopeptide; Imaging probe; PET imaging; SPECT imaging; guanine; theranostics; drug delivery system; Amino Acids, Peptides, and Proteins; Diagnosis; Heterocyclic Compounds; Medicinal Chemistry and Pharmaceutics; Medicine and Health Sciences; Nucleic Acids, Nucleotides, and Nucleosides; Other Analytical, Diagnostic and Therapeutic Techniques and Equipment; Pharmacology; Radiology

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APA (6th Edition):

Tsao, N. (2013). Design, Synthesis and Development of Transporter Targeting Agents for Image-guided Therapy and Drug Delivery. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/350

Chicago Manual of Style (16th Edition):

Tsao, Ning. “Design, Synthesis and Development of Transporter Targeting Agents for Image-guided Therapy and Drug Delivery.” 2013. Doctoral Dissertation, Texas Medical Center. Accessed December 12, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/350.

MLA Handbook (7th Edition):

Tsao, Ning. “Design, Synthesis and Development of Transporter Targeting Agents for Image-guided Therapy and Drug Delivery.” 2013. Web. 12 Dec 2019.

Vancouver:

Tsao N. Design, Synthesis and Development of Transporter Targeting Agents for Image-guided Therapy and Drug Delivery. [Internet] [Doctoral dissertation]. Texas Medical Center; 2013. [cited 2019 Dec 12]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/350.

Council of Science Editors:

Tsao N. Design, Synthesis and Development of Transporter Targeting Agents for Image-guided Therapy and Drug Delivery. [Doctoral Dissertation]. Texas Medical Center; 2013. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/350


Texas Medical Center

141. Chen, Lu. COMPUTATIONAL MODELING OF RNA-SMALL MOLECULE AND RNA-PROTEIN INTERACTIONS.

Degree: PhD, 2015, Texas Medical Center

  The past decade has witnessed an era of RNA biology; despite the considerable discoveries nowadays, challenges still remain when one aims to screen RNA-interacting… (more)

Subjects/Keywords: RNA-small molecule interaction; RNA-protein interaction; molecular docking; virtual screening; NMR; scoring function; molecular dynamics; interface threading; microRNA; Bioinformatics; Biophysics; Medicinal-Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Statistical Models; Structural Biology

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APA (6th Edition):

Chen, L. (2015). COMPUTATIONAL MODELING OF RNA-SMALL MOLECULE AND RNA-PROTEIN INTERACTIONS. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/626

Chicago Manual of Style (16th Edition):

Chen, Lu. “COMPUTATIONAL MODELING OF RNA-SMALL MOLECULE AND RNA-PROTEIN INTERACTIONS.” 2015. Doctoral Dissertation, Texas Medical Center. Accessed December 12, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/626.

MLA Handbook (7th Edition):

Chen, Lu. “COMPUTATIONAL MODELING OF RNA-SMALL MOLECULE AND RNA-PROTEIN INTERACTIONS.” 2015. Web. 12 Dec 2019.

Vancouver:

Chen L. COMPUTATIONAL MODELING OF RNA-SMALL MOLECULE AND RNA-PROTEIN INTERACTIONS. [Internet] [Doctoral dissertation]. Texas Medical Center; 2015. [cited 2019 Dec 12]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/626.

Council of Science Editors:

Chen L. COMPUTATIONAL MODELING OF RNA-SMALL MOLECULE AND RNA-PROTEIN INTERACTIONS. [Doctoral Dissertation]. Texas Medical Center; 2015. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/626


Texas Medical Center

142. Grandjean, Geoffrey, PhD. Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1a Activity and Provides Novel Targets for Inhibiting Tumor Growth.

Degree: PhD, 2015, Texas Medical Center

  Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1α Activity and Provides Novel Targets for Inhibiting Tumor Growth By Geoffrey Grandjean Advisory Professor:… (more)

Subjects/Keywords: HIF-1a; Glycolysis; Small Molecule; Warburg Effect; Metabolism; Hypoxia; Biochemistry; Biology; Cancer Biology; Cell Biology; Enzymes and Coenzymes; Laboratory and Basic Science Research; Medicinal Chemistry and Pharmaceutics; Medicine and Health Sciences; Pharmacology

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APA (6th Edition):

Grandjean, Geoffrey, P. (2015). Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1a Activity and Provides Novel Targets for Inhibiting Tumor Growth. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/643

Chicago Manual of Style (16th Edition):

Grandjean, Geoffrey, PhD. “Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1a Activity and Provides Novel Targets for Inhibiting Tumor Growth.” 2015. Doctoral Dissertation, Texas Medical Center. Accessed December 12, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/643.

MLA Handbook (7th Edition):

Grandjean, Geoffrey, PhD. “Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1a Activity and Provides Novel Targets for Inhibiting Tumor Growth.” 2015. Web. 12 Dec 2019.

Vancouver:

Grandjean, Geoffrey P. Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1a Activity and Provides Novel Targets for Inhibiting Tumor Growth. [Internet] [Doctoral dissertation]. Texas Medical Center; 2015. [cited 2019 Dec 12]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/643.

Council of Science Editors:

Grandjean, Geoffrey P. Normal Glycolytic Enzyme Activity is Critical for Hypoxia Inducible Factor-1a Activity and Provides Novel Targets for Inhibiting Tumor Growth. [Doctoral Dissertation]. Texas Medical Center; 2015. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/643

143. Hanawa-Romero, Emi. Synthesis and Evaluation of A Novel Carbohydrate Template and Analogs Thereof for Potential CNS-active Drugs.

Degree: PhD, Chemistry and Biochemistry, 2017, Seton Hall University

  Central nervous system (CNS) disorders are becoming a major societal problem. Examples of well-known CNS disorders are: neurodegenerative disorders such as Parkinson's, Huntington's and… (more)

Subjects/Keywords: charbohydrates; CNS disorders; SAR study; organic synthesis; carbohydrate drugs; Carbohydrates; Medicinal Chemistry and Pharmaceutics; Organic Chemicals

…2.3. Results: Chemistry 39 2.4. Summary 74 Chapter 3. Evaluation of A Novel… 

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APA (6th Edition):

Hanawa-Romero, E. (2017). Synthesis and Evaluation of A Novel Carbohydrate Template and Analogs Thereof for Potential CNS-active Drugs. (Doctoral Dissertation). Seton Hall University. Retrieved from http://scholarship.shu.edu/dissertations/2279

Chicago Manual of Style (16th Edition):

Hanawa-Romero, Emi. “Synthesis and Evaluation of A Novel Carbohydrate Template and Analogs Thereof for Potential CNS-active Drugs.” 2017. Doctoral Dissertation, Seton Hall University. Accessed December 12, 2019. http://scholarship.shu.edu/dissertations/2279.

MLA Handbook (7th Edition):

Hanawa-Romero, Emi. “Synthesis and Evaluation of A Novel Carbohydrate Template and Analogs Thereof for Potential CNS-active Drugs.” 2017. Web. 12 Dec 2019.

Vancouver:

Hanawa-Romero E. Synthesis and Evaluation of A Novel Carbohydrate Template and Analogs Thereof for Potential CNS-active Drugs. [Internet] [Doctoral dissertation]. Seton Hall University; 2017. [cited 2019 Dec 12]. Available from: http://scholarship.shu.edu/dissertations/2279.

Council of Science Editors:

Hanawa-Romero E. Synthesis and Evaluation of A Novel Carbohydrate Template and Analogs Thereof for Potential CNS-active Drugs. [Doctoral Dissertation]. Seton Hall University; 2017. Available from: http://scholarship.shu.edu/dissertations/2279

144. Kurian, Lathamol A. Submonomer Synthesis and Structure-activity Relationship Studies of Azapeptide Inhibitors of the Insulin Receptor Tyrosine Kinase.

Degree: PhD, Chemistry and Biochemistry, 2014, Seton Hall University

  Azapeptides are a class of peptide mimics (peptidomimetics), which have served as valuable tools for the development of peptide based therapeutic agents. The therapeutic… (more)

Subjects/Keywords: Azapeptide; peptidomimetic; IRTK phosphorylation; IRTK phosphorylation; Amino Acids, Peptides, and Proteins; Biochemistry; Medicinal Chemistry and Pharmaceutics

…APPLICATIONS IN MEDICINAL CHEMISTRY 1.1 ABSTRACT Azapeptides are a class of peptide mimics (… …structural analyses that has enabled their widespread applications in medicinal chemistry. 1.2… …biology, medicinal chemistry and pharmaceutical research. In spite of their potential, peptides… …enable the synthesis of structurally diverse azapeptides for medicinal chemistry applications… …55,56 1.5 MEDICINAL CHEMISTRY APPLICATIONS Azapeptides have been shown to enhance the… 

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APA (6th Edition):

Kurian, L. A. (2014). Submonomer Synthesis and Structure-activity Relationship Studies of Azapeptide Inhibitors of the Insulin Receptor Tyrosine Kinase. (Doctoral Dissertation). Seton Hall University. Retrieved from http://scholarship.shu.edu/dissertations/1991

Chicago Manual of Style (16th Edition):

Kurian, Lathamol A. “Submonomer Synthesis and Structure-activity Relationship Studies of Azapeptide Inhibitors of the Insulin Receptor Tyrosine Kinase.” 2014. Doctoral Dissertation, Seton Hall University. Accessed December 12, 2019. http://scholarship.shu.edu/dissertations/1991.

MLA Handbook (7th Edition):

Kurian, Lathamol A. “Submonomer Synthesis and Structure-activity Relationship Studies of Azapeptide Inhibitors of the Insulin Receptor Tyrosine Kinase.” 2014. Web. 12 Dec 2019.

Vancouver:

Kurian LA. Submonomer Synthesis and Structure-activity Relationship Studies of Azapeptide Inhibitors of the Insulin Receptor Tyrosine Kinase. [Internet] [Doctoral dissertation]. Seton Hall University; 2014. [cited 2019 Dec 12]. Available from: http://scholarship.shu.edu/dissertations/1991.

Council of Science Editors:

Kurian LA. Submonomer Synthesis and Structure-activity Relationship Studies of Azapeptide Inhibitors of the Insulin Receptor Tyrosine Kinase. [Doctoral Dissertation]. Seton Hall University; 2014. Available from: http://scholarship.shu.edu/dissertations/1991

145. Zhu, Rui. Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch.

Degree: PhD, Pharmaceutical Sciences, 2012, University of Tennessee Health Science Center

  Solubility behavior is one of the most challenging aspects for drug commercialization and often the main reason of drug that do not reach to… (more)

Subjects/Keywords: Hassan Almoazen; Ph.D. Gerald M. Rajan; Ph.D. George C. Wood; Ph.D. Arthur D. Straughn; Ph.D; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Zhu, R. (2012). Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/323

Chicago Manual of Style (16th Edition):

Zhu, Rui. “Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch.” 2012. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/323.

MLA Handbook (7th Edition):

Zhu, Rui. “Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch.” 2012. Web. 12 Dec 2019.

Vancouver:

Zhu R. Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2012. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/323.

Council of Science Editors:

Zhu R. Investigation of Enhancement of Furosemide Solubilization with Cyclodextrins and a Novel Octenyl Succinate Anhydride Starch. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2012. Available from: https://dc.uthsc.edu/dissertations/323

146. Wilson, Jason B. Synthesis and Evaluation of Tetramic Acids as Antimicrobial Agents.

Degree: MS, Pharmaceutical Sciences, 2008, University of Tennessee Health Science Center

  As bacterial infectious diseases are a major cause of morbity and mortality throughout the world, and many causative organisms are resistant to currently available… (more)

Subjects/Keywords: Antibiotics; antimicrobials; pyrrolidine; tetramic; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Wilson, J. B. (2008). Synthesis and Evaluation of Tetramic Acids as Antimicrobial Agents. (Thesis). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/367

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wilson, Jason B. “Synthesis and Evaluation of Tetramic Acids as Antimicrobial Agents.” 2008. Thesis, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/367.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wilson, Jason B. “Synthesis and Evaluation of Tetramic Acids as Antimicrobial Agents.” 2008. Web. 12 Dec 2019.

Vancouver:

Wilson JB. Synthesis and Evaluation of Tetramic Acids as Antimicrobial Agents. [Internet] [Thesis]. University of Tennessee Health Science Center; 2008. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/367.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wilson JB. Synthesis and Evaluation of Tetramic Acids as Antimicrobial Agents. [Thesis]. University of Tennessee Health Science Center; 2008. Available from: https://dc.uthsc.edu/dissertations/367

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

147. Wu, Xiaoxin. Hit Identification for PKCζ Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation.

Degree: MS, Pharmaceutical Sciences, 2016, University of Tennessee Health Science Center

  Protein kinase C ζ (PKCζ) is believed to be a promising target for the treatment of some diseases, including inflammatory diseases, obesity and diabetes.… (more)

Subjects/Keywords: JW-1-61A; PKCζ; Structure-based modification; Virtual Screening; Chemical and Pharmacologic Phenomena; Diseases; Endocrine System Diseases; Medical Sciences; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Wu, X. (2016). Hit Identification for PKCζ Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation. (Thesis). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/389

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Wu, Xiaoxin. “Hit Identification for PKCζ Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation.” 2016. Thesis, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/389.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Wu, Xiaoxin. “Hit Identification for PKCζ Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation.” 2016. Web. 12 Dec 2019.

Vancouver:

Wu X. Hit Identification for PKCζ Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation. [Internet] [Thesis]. University of Tennessee Health Science Center; 2016. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/389.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Wu X. Hit Identification for PKCζ Inhibitors: Structure-Based Optimization, Virtual Screening, and Biological Evaluation. [Thesis]. University of Tennessee Health Science Center; 2016. Available from: https://dc.uthsc.edu/dissertations/389

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

148. Whaley, Sarah Garland. Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans.

Degree: PhD, Pharmaceutical Sciences, 2018, University of Tennessee Health Science Center

  Despite the scientific and medical communities’ best efforts, the incidence of fungal infections in susceptible populations continues to rise. The most common cause of… (more)

Subjects/Keywords: antifungal; azole resistance; Candida; Candida albicans; Candida glabrata; fluconazole; Bacterial Infections and Mycoses; Diseases; Medical Biochemistry; Medical Sciences; Medicinal and Pharmaceutical Chemistry; Medicine and Health Sciences; Pharmaceutics and Drug Design; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Whaley, S. G. (2018). Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans. (Doctoral Dissertation). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/453

Chicago Manual of Style (16th Edition):

Whaley, Sarah Garland. “Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans.” 2018. Doctoral Dissertation, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/453.

MLA Handbook (7th Edition):

Whaley, Sarah Garland. “Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans.” 2018. Web. 12 Dec 2019.

Vancouver:

Whaley SG. Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans. [Internet] [Doctoral dissertation]. University of Tennessee Health Science Center; 2018. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/453.

Council of Science Editors:

Whaley SG. Novel Determinants That Influence Azole Susceptibility in Candida glabrata and Candida albicans. [Doctoral Dissertation]. University of Tennessee Health Science Center; 2018. Available from: https://dc.uthsc.edu/dissertations/453


University of Kentucky

149. Holbrook, Selina Y. L. DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC.

Degree: 2018, University of Kentucky

 The extensive and sometimes incorrect and noncompliant use of various types of antimicrobial agents has accelerated the development of antimicrobial resistance (AMR). In fact, AMR… (more)

Subjects/Keywords: aminoglycoside-modifying enzyme (AME); enzyme engineering; substrate promiscuity; enzyme kinetics; minimum inhibitory concentrations (MICs); drug combination; Bacteria; Bacterial Infections and Mycoses; Fungi; Medicinal and Pharmaceutical Chemistry; Microbiology; Pharmaceutics and Drug Design

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

APA (6th Edition):

Holbrook, S. Y. L. (2018). DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/89

Chicago Manual of Style (16th Edition):

Holbrook, Selina Y L. “DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC.” 2018. Doctoral Dissertation, University of Kentucky. Accessed December 12, 2019. https://uknowledge.uky.edu/pharmacy_etds/89.

MLA Handbook (7th Edition):

Holbrook, Selina Y L. “DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC.” 2018. Web. 12 Dec 2019.

Vancouver:

Holbrook SYL. DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC. [Internet] [Doctoral dissertation]. University of Kentucky; 2018. [cited 2019 Dec 12]. Available from: https://uknowledge.uky.edu/pharmacy_etds/89.

Council of Science Editors:

Holbrook SYL. DISCOVERY OF NEW ANTIMICROBIAL OPTIONS AND EVALUATION OF AMINOGLYCOSIDE RESISTANCE ENZYME-ASSOCIATED RESISTANCE EPIDEMIC. [Doctoral Dissertation]. University of Kentucky; 2018. Available from: https://uknowledge.uky.edu/pharmacy_etds/89


Virginia Commonwealth University

150. Park, Sung H. High Affinity Block of ICl,swell by Thiol-Reactive Small Molecules.

Degree: PhD, Physiology and Biophysics, 2016, Virginia Commonwealth University

  Ebselen (Ebs) is considered as a glutathione peroxidase (GPx) mimetic and primarily thought to function by scavenging intracellular reactive oxygen species (ROS). Previous to… (more)

Subjects/Keywords: Ebs; high affinity block of; DI TNC1 astrocytes; thiol-reactive small molecules; Ebs-p-yne; VRAC; Biophysics; Cellular and Molecular Physiology; Medicinal Chemistry and Pharmaceutics; Molecular and Cellular Neuroscience; Neuroscience and Neurobiology; Pharmacology, Toxicology and Environmental Health

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

APA (6th Edition):

Park, S. H. (2016). High Affinity Block of ICl,swell by Thiol-Reactive Small Molecules. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/4433

Chicago Manual of Style (16th Edition):

Park, Sung H. “High Affinity Block of ICl,swell by Thiol-Reactive Small Molecules.” 2016. Doctoral Dissertation, Virginia Commonwealth University. Accessed December 12, 2019. https://scholarscompass.vcu.edu/etd/4433.

MLA Handbook (7th Edition):

Park, Sung H. “High Affinity Block of ICl,swell by Thiol-Reactive Small Molecules.” 2016. Web. 12 Dec 2019.

Vancouver:

Park SH. High Affinity Block of ICl,swell by Thiol-Reactive Small Molecules. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2016. [cited 2019 Dec 12]. Available from: https://scholarscompass.vcu.edu/etd/4433.

Council of Science Editors:

Park SH. High Affinity Block of ICl,swell by Thiol-Reactive Small Molecules. [Doctoral Dissertation]. Virginia Commonwealth University; 2016. Available from: https://scholarscompass.vcu.edu/etd/4433

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