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You searched for subject:(Pharmacy AND Pharmaceutical Sciences). Showing records 1 – 30 of 1113 total matches.

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1. Sivagurunathan, N. Exploration of soil and marine sources for Microbes producing Asparaginase.

Degree: Pharmaceutical Sciences, 2011, Manipal University

A systematic study to explore the soil and marine sources for L-asparaginase producing eukaryotes was carried out. The study included identification of the isolate, optimization… (more)

Subjects/Keywords: Pharmaceutical Sciences; Pharmacy

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APA (6th Edition):

Sivagurunathan, N. (2011). Exploration of soil and marine sources for Microbes producing Asparaginase. (Thesis). Manipal University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/4980

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):

Sivagurunathan, N. “Exploration of soil and marine sources for Microbes producing Asparaginase.” 2011. Thesis, Manipal University. Accessed May 29, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/4980.

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

MLA Handbook (7th Edition):

Sivagurunathan, N. “Exploration of soil and marine sources for Microbes producing Asparaginase.” 2011. Web. 29 May 2020.

Vancouver:

Sivagurunathan N. Exploration of soil and marine sources for Microbes producing Asparaginase. [Internet] [Thesis]. Manipal University; 2011. [cited 2020 May 29]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4980.

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

Council of Science Editors:

Sivagurunathan N. Exploration of soil and marine sources for Microbes producing Asparaginase. [Thesis]. Manipal University; 2011. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4980

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

2. Mallipeddi, Rama. The application of coarse particle ethylcellulose and high molecular weight polyethylene oxide in the production of beads by extrusion-spheronization.

Degree: 2009, University of the Sciences in Philadelphia

  The present investigation evaluated the potential of coarse particle ethylcellulose (CPEC) and high molecular weight polyethylene oxide (PEO) in the production of beads by… (more)

Subjects/Keywords: Chemistry, Pharmaceutical; Health Sciences, Pharmacy

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APA (6th Edition):

Mallipeddi, R. (2009). The application of coarse particle ethylcellulose and high molecular weight polyethylene oxide in the production of beads by extrusion-spheronization. (Thesis). University of the Sciences in Philadelphia. Retrieved from http://pqdtopen.proquest.com/#viewpdf?dispub=3349136

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):

Mallipeddi, Rama. “The application of coarse particle ethylcellulose and high molecular weight polyethylene oxide in the production of beads by extrusion-spheronization.” 2009. Thesis, University of the Sciences in Philadelphia. Accessed May 29, 2020. http://pqdtopen.proquest.com/#viewpdf?dispub=3349136.

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

MLA Handbook (7th Edition):

Mallipeddi, Rama. “The application of coarse particle ethylcellulose and high molecular weight polyethylene oxide in the production of beads by extrusion-spheronization.” 2009. Web. 29 May 2020.

Vancouver:

Mallipeddi R. The application of coarse particle ethylcellulose and high molecular weight polyethylene oxide in the production of beads by extrusion-spheronization. [Internet] [Thesis]. University of the Sciences in Philadelphia; 2009. [cited 2020 May 29]. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3349136.

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

Council of Science Editors:

Mallipeddi R. The application of coarse particle ethylcellulose and high molecular weight polyethylene oxide in the production of beads by extrusion-spheronization. [Thesis]. University of the Sciences in Philadelphia; 2009. Available from: http://pqdtopen.proquest.com/#viewpdf?dispub=3349136

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

3. Kumar, Sunny. Development of a Novel Vaccine Adjuvant and Delivery System for Cancer and Influenza.

Degree: PhD, Pharmaceutical Sciences, 2013, South Dakota State University

  Vaccines often require addition of adjuvants to boost the potency and longevity of antigen specific immune responses. At present, there is a scarcity of… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Kumar, S. (2013). Development of a Novel Vaccine Adjuvant and Delivery System for Cancer and Influenza. (Doctoral Dissertation). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1449

Chicago Manual of Style (16th Edition):

Kumar, Sunny. “Development of a Novel Vaccine Adjuvant and Delivery System for Cancer and Influenza.” 2013. Doctoral Dissertation, South Dakota State University. Accessed May 29, 2020. http://openprairie.sdstate.edu/etd/1449.

MLA Handbook (7th Edition):

Kumar, Sunny. “Development of a Novel Vaccine Adjuvant and Delivery System for Cancer and Influenza.” 2013. Web. 29 May 2020.

Vancouver:

Kumar S. Development of a Novel Vaccine Adjuvant and Delivery System for Cancer and Influenza. [Internet] [Doctoral dissertation]. South Dakota State University; 2013. [cited 2020 May 29]. Available from: http://openprairie.sdstate.edu/etd/1449.

Council of Science Editors:

Kumar S. Development of a Novel Vaccine Adjuvant and Delivery System for Cancer and Influenza. [Doctoral Dissertation]. South Dakota State University; 2013. Available from: http://openprairie.sdstate.edu/etd/1449

4. Lynch, Christophina. Evaluation of Carvedilol and Berberine on Thiol Related Pathways.

Degree: PhD, Pharmaceutical Sciences, 2015, South Dakota State University

  Thiols are an important component of the body’s antioxidant defense mechanism. Thiols are oxidized to disulfides when exposed to free radicals. Disulfides are subsequently… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Lynch, C. (2015). Evaluation of Carvedilol and Berberine on Thiol Related Pathways. (Doctoral Dissertation). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1804

Chicago Manual of Style (16th Edition):

Lynch, Christophina. “Evaluation of Carvedilol and Berberine on Thiol Related Pathways.” 2015. Doctoral Dissertation, South Dakota State University. Accessed May 29, 2020. http://openprairie.sdstate.edu/etd/1804.

MLA Handbook (7th Edition):

Lynch, Christophina. “Evaluation of Carvedilol and Berberine on Thiol Related Pathways.” 2015. Web. 29 May 2020.

Vancouver:

Lynch C. Evaluation of Carvedilol and Berberine on Thiol Related Pathways. [Internet] [Doctoral dissertation]. South Dakota State University; 2015. [cited 2020 May 29]. Available from: http://openprairie.sdstate.edu/etd/1804.

Council of Science Editors:

Lynch C. Evaluation of Carvedilol and Berberine on Thiol Related Pathways. [Doctoral Dissertation]. South Dakota State University; 2015. Available from: http://openprairie.sdstate.edu/etd/1804

5. Kuppast, Bhimanna. Synthesis and Biological Evaluation of Substituted Thiazolo(4,5-d)Pyrimidines and Substituted Pyrimidines as Corticotropin Releasing Factor (CRF) Receptor Antagonists.

Degree: PhD, Pharmaceutical Sciences, 2014, South Dakota State University

  Corticotropin releasing factor (CRF) is a neuropeptide hormone produced from the hypothalamus that coordinates behavioral, endocrine and autonomic functions in stress response and its… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Kuppast, B. (2014). Synthesis and Biological Evaluation of Substituted Thiazolo(4,5-d)Pyrimidines and Substituted Pyrimidines as Corticotropin Releasing Factor (CRF) Receptor Antagonists. (Doctoral Dissertation). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1567

Chicago Manual of Style (16th Edition):

Kuppast, Bhimanna. “Synthesis and Biological Evaluation of Substituted Thiazolo(4,5-d)Pyrimidines and Substituted Pyrimidines as Corticotropin Releasing Factor (CRF) Receptor Antagonists.” 2014. Doctoral Dissertation, South Dakota State University. Accessed May 29, 2020. http://openprairie.sdstate.edu/etd/1567.

MLA Handbook (7th Edition):

Kuppast, Bhimanna. “Synthesis and Biological Evaluation of Substituted Thiazolo(4,5-d)Pyrimidines and Substituted Pyrimidines as Corticotropin Releasing Factor (CRF) Receptor Antagonists.” 2014. Web. 29 May 2020.

Vancouver:

Kuppast B. Synthesis and Biological Evaluation of Substituted Thiazolo(4,5-d)Pyrimidines and Substituted Pyrimidines as Corticotropin Releasing Factor (CRF) Receptor Antagonists. [Internet] [Doctoral dissertation]. South Dakota State University; 2014. [cited 2020 May 29]. Available from: http://openprairie.sdstate.edu/etd/1567.

Council of Science Editors:

Kuppast B. Synthesis and Biological Evaluation of Substituted Thiazolo(4,5-d)Pyrimidines and Substituted Pyrimidines as Corticotropin Releasing Factor (CRF) Receptor Antagonists. [Doctoral Dissertation]. South Dakota State University; 2014. Available from: http://openprairie.sdstate.edu/etd/1567

6. Xie, Jiashu. Evaluation and Applications of a Novel Glutathione Reductase Inhibitor as a Model of Thiol Oxidative Stress in H9C2 Rat Cardiomyocytes.

Degree: PhD, Pharmaceutical Sciences, 2014, South Dakota State University

  Thiol redox state (TRS) refers to the balance between reduced thiols and their corresponding disulfides, and is mainly reflected by the ratio of GSH/GSSG.… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Xie, J. (2014). Evaluation and Applications of a Novel Glutathione Reductase Inhibitor as a Model of Thiol Oxidative Stress in H9C2 Rat Cardiomyocytes. (Doctoral Dissertation). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1604

Chicago Manual of Style (16th Edition):

Xie, Jiashu. “Evaluation and Applications of a Novel Glutathione Reductase Inhibitor as a Model of Thiol Oxidative Stress in H9C2 Rat Cardiomyocytes.” 2014. Doctoral Dissertation, South Dakota State University. Accessed May 29, 2020. http://openprairie.sdstate.edu/etd/1604.

MLA Handbook (7th Edition):

Xie, Jiashu. “Evaluation and Applications of a Novel Glutathione Reductase Inhibitor as a Model of Thiol Oxidative Stress in H9C2 Rat Cardiomyocytes.” 2014. Web. 29 May 2020.

Vancouver:

Xie J. Evaluation and Applications of a Novel Glutathione Reductase Inhibitor as a Model of Thiol Oxidative Stress in H9C2 Rat Cardiomyocytes. [Internet] [Doctoral dissertation]. South Dakota State University; 2014. [cited 2020 May 29]. Available from: http://openprairie.sdstate.edu/etd/1604.

Council of Science Editors:

Xie J. Evaluation and Applications of a Novel Glutathione Reductase Inhibitor as a Model of Thiol Oxidative Stress in H9C2 Rat Cardiomyocytes. [Doctoral Dissertation]. South Dakota State University; 2014. Available from: http://openprairie.sdstate.edu/etd/1604

7. England, Christopher Gene, 1988-. Study of novel nanoparticle transport and drug release for cancer treatment.

Degree: PhD, 2014, University of Louisville

  Nano-scale particles sized 10—400 nm administered systemically preferentially extravasate from tumor vasculature due to the enhanced permeability and retention effect. Therapeutic success remains elusive,… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

England, Christopher Gene, 1. (2014). Study of novel nanoparticle transport and drug release for cancer treatment. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1712 ; https://ir.library.louisville.edu/etd/1712

Chicago Manual of Style (16th Edition):

England, Christopher Gene, 1988-. “Study of novel nanoparticle transport and drug release for cancer treatment.” 2014. Doctoral Dissertation, University of Louisville. Accessed May 29, 2020. 10.18297/etd/1712 ; https://ir.library.louisville.edu/etd/1712.

MLA Handbook (7th Edition):

England, Christopher Gene, 1988-. “Study of novel nanoparticle transport and drug release for cancer treatment.” 2014. Web. 29 May 2020.

Vancouver:

England, Christopher Gene 1. Study of novel nanoparticle transport and drug release for cancer treatment. [Internet] [Doctoral dissertation]. University of Louisville; 2014. [cited 2020 May 29]. Available from: 10.18297/etd/1712 ; https://ir.library.louisville.edu/etd/1712.

Council of Science Editors:

England, Christopher Gene 1. Study of novel nanoparticle transport and drug release for cancer treatment. [Doctoral Dissertation]. University of Louisville; 2014. Available from: 10.18297/etd/1712 ; https://ir.library.louisville.edu/etd/1712


University of Louisville

8. Shidal, Christopher Paul. Lunasin reduces the melanoma stem cell population in vitro and inhibits tumor proliferation in vivo.

Degree: MS, 2014, University of Louisville

  Lunasin is a 44 amino acid peptide derived from the soybean seed that has been shown to have cancer chemopreventive and chemotherapeutic properties. In… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Shidal, C. P. (2014). Lunasin reduces the melanoma stem cell population in vitro and inhibits tumor proliferation in vivo. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/1765 ; https://ir.library.louisville.edu/etd/1765

Chicago Manual of Style (16th Edition):

Shidal, Christopher Paul. “Lunasin reduces the melanoma stem cell population in vitro and inhibits tumor proliferation in vivo.” 2014. Masters Thesis, University of Louisville. Accessed May 29, 2020. 10.18297/etd/1765 ; https://ir.library.louisville.edu/etd/1765.

MLA Handbook (7th Edition):

Shidal, Christopher Paul. “Lunasin reduces the melanoma stem cell population in vitro and inhibits tumor proliferation in vivo.” 2014. Web. 29 May 2020.

Vancouver:

Shidal CP. Lunasin reduces the melanoma stem cell population in vitro and inhibits tumor proliferation in vivo. [Internet] [Masters thesis]. University of Louisville; 2014. [cited 2020 May 29]. Available from: 10.18297/etd/1765 ; https://ir.library.louisville.edu/etd/1765.

Council of Science Editors:

Shidal CP. Lunasin reduces the melanoma stem cell population in vitro and inhibits tumor proliferation in vivo. [Masters Thesis]. University of Louisville; 2014. Available from: 10.18297/etd/1765 ; https://ir.library.louisville.edu/etd/1765


University of Louisville

9. Kyakulaga, Al Hassan. Withaferin a synergistically enhances the effects of paclitaxel against lung cancer.

Degree: MS, 2017, University of Louisville

  Lung cancer is the leading cause of cancer-related deaths among both men and women in the U.S and worldwide. Today, paclitaxel (PAC) or taxol… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Kyakulaga, A. H. (2017). Withaferin a synergistically enhances the effects of paclitaxel against lung cancer. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/2650 ; https://ir.library.louisville.edu/etd/2650

Chicago Manual of Style (16th Edition):

Kyakulaga, Al Hassan. “Withaferin a synergistically enhances the effects of paclitaxel against lung cancer.” 2017. Masters Thesis, University of Louisville. Accessed May 29, 2020. 10.18297/etd/2650 ; https://ir.library.louisville.edu/etd/2650.

MLA Handbook (7th Edition):

Kyakulaga, Al Hassan. “Withaferin a synergistically enhances the effects of paclitaxel against lung cancer.” 2017. Web. 29 May 2020.

Vancouver:

Kyakulaga AH. Withaferin a synergistically enhances the effects of paclitaxel against lung cancer. [Internet] [Masters thesis]. University of Louisville; 2017. [cited 2020 May 29]. Available from: 10.18297/etd/2650 ; https://ir.library.louisville.edu/etd/2650.

Council of Science Editors:

Kyakulaga AH. Withaferin a synergistically enhances the effects of paclitaxel against lung cancer. [Masters Thesis]. University of Louisville; 2017. Available from: 10.18297/etd/2650 ; https://ir.library.louisville.edu/etd/2650


University of Louisville

10. Cheng, Pei-Hsin. Cyclin E induction and oncolytic replication of E1b-deleted adenoviruses.

Degree: PhD, 2013, University of Louisville

  Virus-mediated oncolysis has been considered as a new and promising cancer therapeutic approach. Although adenoviruses (Ads) with deletion of E1b55K preferentially replicate in cancer… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Cheng, P. (2013). Cyclin E induction and oncolytic replication of E1b-deleted adenoviruses. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/2282 ; https://ir.library.louisville.edu/etd/2282

Chicago Manual of Style (16th Edition):

Cheng, Pei-Hsin. “Cyclin E induction and oncolytic replication of E1b-deleted adenoviruses.” 2013. Doctoral Dissertation, University of Louisville. Accessed May 29, 2020. 10.18297/etd/2282 ; https://ir.library.louisville.edu/etd/2282.

MLA Handbook (7th Edition):

Cheng, Pei-Hsin. “Cyclin E induction and oncolytic replication of E1b-deleted adenoviruses.” 2013. Web. 29 May 2020.

Vancouver:

Cheng P. Cyclin E induction and oncolytic replication of E1b-deleted adenoviruses. [Internet] [Doctoral dissertation]. University of Louisville; 2013. [cited 2020 May 29]. Available from: 10.18297/etd/2282 ; https://ir.library.louisville.edu/etd/2282.

Council of Science Editors:

Cheng P. Cyclin E induction and oncolytic replication of E1b-deleted adenoviruses. [Doctoral Dissertation]. University of Louisville; 2013. Available from: 10.18297/etd/2282 ; https://ir.library.louisville.edu/etd/2282

11. Sabitha M. Chitin nanogels as an effective nanocarrier for the treatment of melanoma via the transdermal route.

Degree: Pharmaceutical Sciences, 2012, Amrita Vishwa Vidyapeetham (University)

The use of nanocarriers is one among the many strategies used for enhancing penetration of drugs in transdermal delivery. The nanogels have the advantage of… (more)

Subjects/Keywords: Pharmaceutical Sciences; Pharmacy; Chitin nanogels

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APA (6th Edition):

M, S. (2012). Chitin nanogels as an effective nanocarrier for the treatment of melanoma via the transdermal route. (Thesis). Amrita Vishwa Vidyapeetham (University). Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/4982

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):

M, Sabitha. “Chitin nanogels as an effective nanocarrier for the treatment of melanoma via the transdermal route.” 2012. Thesis, Amrita Vishwa Vidyapeetham (University). Accessed May 29, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/4982.

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

MLA Handbook (7th Edition):

M, Sabitha. “Chitin nanogels as an effective nanocarrier for the treatment of melanoma via the transdermal route.” 2012. Web. 29 May 2020.

Vancouver:

M S. Chitin nanogels as an effective nanocarrier for the treatment of melanoma via the transdermal route. [Internet] [Thesis]. Amrita Vishwa Vidyapeetham (University); 2012. [cited 2020 May 29]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4982.

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

Council of Science Editors:

M S. Chitin nanogels as an effective nanocarrier for the treatment of melanoma via the transdermal route. [Thesis]. Amrita Vishwa Vidyapeetham (University); 2012. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/4982

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


Loyola University Chicago

12. Gao, Yandi. Identifying Oncogenic Drivers in NSCLC Cells Harboring EGFR Kinase Domain Mutation with Resistance to EGFR TKI and Mesenchymal Phenotype.

Degree: MS, Pharmacology and Experimental Therapeutics, 2014, Loyola University Chicago

  EGFR kinase domain mutant NSCLC cells are exquisitely dependent on mutant EGFR for cell survival and proliferation. Patients with mutant EGFR respond well to… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Gao, Y. (2014). Identifying Oncogenic Drivers in NSCLC Cells Harboring EGFR Kinase Domain Mutation with Resistance to EGFR TKI and Mesenchymal Phenotype. (Thesis). Loyola University Chicago. Retrieved from http://ecommons.luc.edu/luc_theses/2622

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):

Gao, Yandi. “Identifying Oncogenic Drivers in NSCLC Cells Harboring EGFR Kinase Domain Mutation with Resistance to EGFR TKI and Mesenchymal Phenotype.” 2014. Thesis, Loyola University Chicago. Accessed May 29, 2020. http://ecommons.luc.edu/luc_theses/2622.

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

MLA Handbook (7th Edition):

Gao, Yandi. “Identifying Oncogenic Drivers in NSCLC Cells Harboring EGFR Kinase Domain Mutation with Resistance to EGFR TKI and Mesenchymal Phenotype.” 2014. Web. 29 May 2020.

Vancouver:

Gao Y. Identifying Oncogenic Drivers in NSCLC Cells Harboring EGFR Kinase Domain Mutation with Resistance to EGFR TKI and Mesenchymal Phenotype. [Internet] [Thesis]. Loyola University Chicago; 2014. [cited 2020 May 29]. Available from: http://ecommons.luc.edu/luc_theses/2622.

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

Council of Science Editors:

Gao Y. Identifying Oncogenic Drivers in NSCLC Cells Harboring EGFR Kinase Domain Mutation with Resistance to EGFR TKI and Mesenchymal Phenotype. [Thesis]. Loyola University Chicago; 2014. Available from: http://ecommons.luc.edu/luc_theses/2622

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


Eastern Michigan University

13. Niraghatam, Vamsi Vardhan. Regulatory issues concerning the preclinical testing of synthetic peptides.

Degree: MS, Health Sciences, 2018, Eastern Michigan University

  Any new drug or biological product undergoes rigorous testing in animals and humans for review by the United States Food and Drug Administration (FDA)… (more)

Subjects/Keywords: Pharmacology; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Niraghatam, V. V. (2018). Regulatory issues concerning the preclinical testing of synthetic peptides. (Masters Thesis). Eastern Michigan University. Retrieved from https://commons.emich.edu/theses/932

Chicago Manual of Style (16th Edition):

Niraghatam, Vamsi Vardhan. “Regulatory issues concerning the preclinical testing of synthetic peptides.” 2018. Masters Thesis, Eastern Michigan University. Accessed May 29, 2020. https://commons.emich.edu/theses/932.

MLA Handbook (7th Edition):

Niraghatam, Vamsi Vardhan. “Regulatory issues concerning the preclinical testing of synthetic peptides.” 2018. Web. 29 May 2020.

Vancouver:

Niraghatam VV. Regulatory issues concerning the preclinical testing of synthetic peptides. [Internet] [Masters thesis]. Eastern Michigan University; 2018. [cited 2020 May 29]. Available from: https://commons.emich.edu/theses/932.

Council of Science Editors:

Niraghatam VV. Regulatory issues concerning the preclinical testing of synthetic peptides. [Masters Thesis]. Eastern Michigan University; 2018. Available from: https://commons.emich.edu/theses/932


Loyola University Chicago

14. Buhrmaster, James. Creating a BRET Assay to Monitor the Interaction between β-Arrestin-1 and STAM-1.

Degree: MS, Pharmacology and Experimental Therapeutics, 2017, Loyola University Chicago

  CXCR4 is a chemokine receptor that is overexpressed in multiple disease states, including cancer. Understanding the mechanisms by which cells regulate CXCR4 expression is… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Buhrmaster, J. (2017). Creating a BRET Assay to Monitor the Interaction between β-Arrestin-1 and STAM-1. (Thesis). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_theses/3663

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):

Buhrmaster, James. “Creating a BRET Assay to Monitor the Interaction between β-Arrestin-1 and STAM-1.” 2017. Thesis, Loyola University Chicago. Accessed May 29, 2020. https://ecommons.luc.edu/luc_theses/3663.

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

MLA Handbook (7th Edition):

Buhrmaster, James. “Creating a BRET Assay to Monitor the Interaction between β-Arrestin-1 and STAM-1.” 2017. Web. 29 May 2020.

Vancouver:

Buhrmaster J. Creating a BRET Assay to Monitor the Interaction between β-Arrestin-1 and STAM-1. [Internet] [Thesis]. Loyola University Chicago; 2017. [cited 2020 May 29]. Available from: https://ecommons.luc.edu/luc_theses/3663.

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

Council of Science Editors:

Buhrmaster J. Creating a BRET Assay to Monitor the Interaction between β-Arrestin-1 and STAM-1. [Thesis]. Loyola University Chicago; 2017. Available from: https://ecommons.luc.edu/luc_theses/3663

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


Loyola University Chicago

15. Kouta, Ahmed. Comparative Studies on Biochemical and Pharmacological Profiles of Bovine, Ovine and Porcine Heparins.

Degree: MS, Pharmacology and Experimental Therapeutics, 2017, Loyola University Chicago

  Heparin, a highly sulfated glycosaminoglycan (GAG), is used extensively as an anticoagulant. It consists of repeating disaccharide units, containing iduronic acid (or glucuronic acid)… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Kouta, A. (2017). Comparative Studies on Biochemical and Pharmacological Profiles of Bovine, Ovine and Porcine Heparins. (Thesis). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_theses/3687

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):

Kouta, Ahmed. “Comparative Studies on Biochemical and Pharmacological Profiles of Bovine, Ovine and Porcine Heparins.” 2017. Thesis, Loyola University Chicago. Accessed May 29, 2020. https://ecommons.luc.edu/luc_theses/3687.

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

MLA Handbook (7th Edition):

Kouta, Ahmed. “Comparative Studies on Biochemical and Pharmacological Profiles of Bovine, Ovine and Porcine Heparins.” 2017. Web. 29 May 2020.

Vancouver:

Kouta A. Comparative Studies on Biochemical and Pharmacological Profiles of Bovine, Ovine and Porcine Heparins. [Internet] [Thesis]. Loyola University Chicago; 2017. [cited 2020 May 29]. Available from: https://ecommons.luc.edu/luc_theses/3687.

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

Council of Science Editors:

Kouta A. Comparative Studies on Biochemical and Pharmacological Profiles of Bovine, Ovine and Porcine Heparins. [Thesis]. Loyola University Chicago; 2017. Available from: https://ecommons.luc.edu/luc_theses/3687

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

16. Alharbi, Metab. Evaluation of the Effect of Carvedilol on the Thioredoxin Pathway in H9C2 Rat Cardiomyocytes.

Degree: PhD, Pharmaceutical Sciences, 2019, South Dakota State University

  The thioredoxin (Trx) system is an endogenous antioxidant system that affects cell function and survival through controlling cellular redox status. Trx and TrxR are… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Alharbi, M. (2019). Evaluation of the Effect of Carvedilol on the Thioredoxin Pathway in H9C2 Rat Cardiomyocytes. (Doctoral Dissertation). South Dakota State University. Retrieved from https://openprairie.sdstate.edu/etd/3179

Chicago Manual of Style (16th Edition):

Alharbi, Metab. “Evaluation of the Effect of Carvedilol on the Thioredoxin Pathway in H9C2 Rat Cardiomyocytes.” 2019. Doctoral Dissertation, South Dakota State University. Accessed May 29, 2020. https://openprairie.sdstate.edu/etd/3179.

MLA Handbook (7th Edition):

Alharbi, Metab. “Evaluation of the Effect of Carvedilol on the Thioredoxin Pathway in H9C2 Rat Cardiomyocytes.” 2019. Web. 29 May 2020.

Vancouver:

Alharbi M. Evaluation of the Effect of Carvedilol on the Thioredoxin Pathway in H9C2 Rat Cardiomyocytes. [Internet] [Doctoral dissertation]. South Dakota State University; 2019. [cited 2020 May 29]. Available from: https://openprairie.sdstate.edu/etd/3179.

Council of Science Editors:

Alharbi M. Evaluation of the Effect of Carvedilol on the Thioredoxin Pathway in H9C2 Rat Cardiomyocytes. [Doctoral Dissertation]. South Dakota State University; 2019. Available from: https://openprairie.sdstate.edu/etd/3179


Wayne State University

17. Paritala, Hanumantharao. Enzymology And Medicinal Chemistry Of N5-Carboxyaminoimidazole Ribonucleotide Synthetase : A Novel Antibacterial Target.

Degree: PhD, Pharmaceutical Sciences, 2010, Wayne State University

  N5-Carboxyaminoimidazole ribonucleotide synthetase (N5-CAIR synthetase), a key enzyme in microbial de novo purine biosynthesis, catalyzes the conversion of aminoimidazole ribonucleotide (AIR) to N5-CAIR. To… (more)

Subjects/Keywords: Biochemistry; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Paritala, H. (2010). Enzymology And Medicinal Chemistry Of N5-Carboxyaminoimidazole Ribonucleotide Synthetase : A Novel Antibacterial Target. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/26

Chicago Manual of Style (16th Edition):

Paritala, Hanumantharao. “Enzymology And Medicinal Chemistry Of N5-Carboxyaminoimidazole Ribonucleotide Synthetase : A Novel Antibacterial Target.” 2010. Doctoral Dissertation, Wayne State University. Accessed May 29, 2020. https://digitalcommons.wayne.edu/oa_dissertations/26.

MLA Handbook (7th Edition):

Paritala, Hanumantharao. “Enzymology And Medicinal Chemistry Of N5-Carboxyaminoimidazole Ribonucleotide Synthetase : A Novel Antibacterial Target.” 2010. Web. 29 May 2020.

Vancouver:

Paritala H. Enzymology And Medicinal Chemistry Of N5-Carboxyaminoimidazole Ribonucleotide Synthetase : A Novel Antibacterial Target. [Internet] [Doctoral dissertation]. Wayne State University; 2010. [cited 2020 May 29]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/26.

Council of Science Editors:

Paritala H. Enzymology And Medicinal Chemistry Of N5-Carboxyaminoimidazole Ribonucleotide Synthetase : A Novel Antibacterial Target. [Doctoral Dissertation]. Wayne State University; 2010. Available from: https://digitalcommons.wayne.edu/oa_dissertations/26


University of Louisville

18. Stathem, Morgan L. Building a metabolic bridge between glycolysis and sphingolipid biosynthesis : implications in cancer.

Degree: MS, 2014, University of Louisville

  Cancer therapeutics has seen an emergence and re-emergence of two metabolic fields in recent years, namely bioactive sphingolipids and glycolytic metabolism. Anaerobic glycolysis and… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Stathem, M. L. (2014). Building a metabolic bridge between glycolysis and sphingolipid biosynthesis : implications in cancer. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/1374 ; https://ir.library.louisville.edu/etd/1374

Chicago Manual of Style (16th Edition):

Stathem, Morgan L. “Building a metabolic bridge between glycolysis and sphingolipid biosynthesis : implications in cancer.” 2014. Masters Thesis, University of Louisville. Accessed May 29, 2020. 10.18297/etd/1374 ; https://ir.library.louisville.edu/etd/1374.

MLA Handbook (7th Edition):

Stathem, Morgan L. “Building a metabolic bridge between glycolysis and sphingolipid biosynthesis : implications in cancer.” 2014. Web. 29 May 2020.

Vancouver:

Stathem ML. Building a metabolic bridge between glycolysis and sphingolipid biosynthesis : implications in cancer. [Internet] [Masters thesis]. University of Louisville; 2014. [cited 2020 May 29]. Available from: 10.18297/etd/1374 ; https://ir.library.louisville.edu/etd/1374.

Council of Science Editors:

Stathem ML. Building a metabolic bridge between glycolysis and sphingolipid biosynthesis : implications in cancer. [Masters Thesis]. University of Louisville; 2014. Available from: 10.18297/etd/1374 ; https://ir.library.louisville.edu/etd/1374


Purdue University

19. Chung, Eun Kyoung. Beta-lactam antimicrobial dosing optimization in obese patients compared to non-obese patients using population pharmacokinetic/pharmacodynamic approach.

Degree: PhD, Pharmacy Practice, 2015, Purdue University

  Obesity is a significant global health problem and has been associated with altered pharmacokinetics and pharmacodynamics of many drugs. However, little is known regarding… (more)

Subjects/Keywords: Pharmacology; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Chung, E. K. (2015). Beta-lactam antimicrobial dosing optimization in obese patients compared to non-obese patients using population pharmacokinetic/pharmacodynamic approach. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/441

Chicago Manual of Style (16th Edition):

Chung, Eun Kyoung. “Beta-lactam antimicrobial dosing optimization in obese patients compared to non-obese patients using population pharmacokinetic/pharmacodynamic approach.” 2015. Doctoral Dissertation, Purdue University. Accessed May 29, 2020. https://docs.lib.purdue.edu/open_access_dissertations/441.

MLA Handbook (7th Edition):

Chung, Eun Kyoung. “Beta-lactam antimicrobial dosing optimization in obese patients compared to non-obese patients using population pharmacokinetic/pharmacodynamic approach.” 2015. Web. 29 May 2020.

Vancouver:

Chung EK. Beta-lactam antimicrobial dosing optimization in obese patients compared to non-obese patients using population pharmacokinetic/pharmacodynamic approach. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2020 May 29]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/441.

Council of Science Editors:

Chung EK. Beta-lactam antimicrobial dosing optimization in obese patients compared to non-obese patients using population pharmacokinetic/pharmacodynamic approach. [Doctoral Dissertation]. Purdue University; 2015. Available from: https://docs.lib.purdue.edu/open_access_dissertations/441


University of Iowa

20. Hayes, Michael Patrick. Chemical inhibitors of protein-protein interactions involved in G protein-mediated signaling events as potential therapeutics.

Degree: PhD, Pharmaceutical Sciences and Experimental Therapeutics, 2017, University of Iowa

  G protein-coupled receptors (GPCRs) play a central role in numerous biological processes, from olfaction to vision to neurotransmission and more, leading to their classification… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Hayes, M. P. (2017). Chemical inhibitors of protein-protein interactions involved in G protein-mediated signaling events as potential therapeutics. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5945

Chicago Manual of Style (16th Edition):

Hayes, Michael Patrick. “Chemical inhibitors of protein-protein interactions involved in G protein-mediated signaling events as potential therapeutics.” 2017. Doctoral Dissertation, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/5945.

MLA Handbook (7th Edition):

Hayes, Michael Patrick. “Chemical inhibitors of protein-protein interactions involved in G protein-mediated signaling events as potential therapeutics.” 2017. Web. 29 May 2020.

Vancouver:

Hayes MP. Chemical inhibitors of protein-protein interactions involved in G protein-mediated signaling events as potential therapeutics. [Internet] [Doctoral dissertation]. University of Iowa; 2017. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/5945.

Council of Science Editors:

Hayes MP. Chemical inhibitors of protein-protein interactions involved in G protein-mediated signaling events as potential therapeutics. [Doctoral Dissertation]. University of Iowa; 2017. Available from: https://ir.uiowa.edu/etd/5945


University of Iowa

21. Jiang, Dahai. Application of polymers in nucleic acid delivery.

Degree: PhD, Pharmacy, 2011, University of Iowa

  Gene therapy and immunotherapy are powerful techniques in the treatment of many life threatening diseases. The major challenge in these therapies is to seek… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Jiang, D. (2011). Application of polymers in nucleic acid delivery. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2721

Chicago Manual of Style (16th Edition):

Jiang, Dahai. “Application of polymers in nucleic acid delivery.” 2011. Doctoral Dissertation, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/2721.

MLA Handbook (7th Edition):

Jiang, Dahai. “Application of polymers in nucleic acid delivery.” 2011. Web. 29 May 2020.

Vancouver:

Jiang D. Application of polymers in nucleic acid delivery. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/2721.

Council of Science Editors:

Jiang D. Application of polymers in nucleic acid delivery. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/2721


University of Iowa

22. Azevedo, Eduardo Pereira de. Aldehyde-functionalized chitosan and cellulose:chitosan composites: application as drug carriers and vascular bypass grafts.

Degree: PhD, Pharmacy, 2011, University of Iowa

  In this work, aldehyde-functionalized chitosan was produced by the reaction of chitosan in the solid state with nitrogen oxide gases, generated in situ from… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Azevedo, E. P. d. (2011). Aldehyde-functionalized chitosan and cellulose:chitosan composites: application as drug carriers and vascular bypass grafts. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1119

Chicago Manual of Style (16th Edition):

Azevedo, Eduardo Pereira de. “Aldehyde-functionalized chitosan and cellulose:chitosan composites: application as drug carriers and vascular bypass grafts.” 2011. Doctoral Dissertation, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/1119.

MLA Handbook (7th Edition):

Azevedo, Eduardo Pereira de. “Aldehyde-functionalized chitosan and cellulose:chitosan composites: application as drug carriers and vascular bypass grafts.” 2011. Web. 29 May 2020.

Vancouver:

Azevedo EPd. Aldehyde-functionalized chitosan and cellulose:chitosan composites: application as drug carriers and vascular bypass grafts. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/1119.

Council of Science Editors:

Azevedo EPd. Aldehyde-functionalized chitosan and cellulose:chitosan composites: application as drug carriers and vascular bypass grafts. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/1119


University of Iowa

23. Schenck, Daniel Michael. Submersion and lateral transport behavior of microparticles at a lung surfactant interface on model mucus hydrogels.

Degree: PhD, Pharmaceutical Sciences and Experimental Therapeutics, 2015, University of Iowa

  Barriers to effective pulmonary drug delivery are inherent to the lung physiology and present a challenge when attempting to bypass the natural defenses against… (more)

Subjects/Keywords: publicabstract; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Schenck, D. M. (2015). Submersion and lateral transport behavior of microparticles at a lung surfactant interface on model mucus hydrogels. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2009

Chicago Manual of Style (16th Edition):

Schenck, Daniel Michael. “Submersion and lateral transport behavior of microparticles at a lung surfactant interface on model mucus hydrogels.” 2015. Doctoral Dissertation, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/2009.

MLA Handbook (7th Edition):

Schenck, Daniel Michael. “Submersion and lateral transport behavior of microparticles at a lung surfactant interface on model mucus hydrogels.” 2015. Web. 29 May 2020.

Vancouver:

Schenck DM. Submersion and lateral transport behavior of microparticles at a lung surfactant interface on model mucus hydrogels. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/2009.

Council of Science Editors:

Schenck DM. Submersion and lateral transport behavior of microparticles at a lung surfactant interface on model mucus hydrogels. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/2009


Virginia Commonwealth University

24. Bafail, Duaa. The Effect of Damaged Bases on The End Joining of DNA Double Strand Break Ends.

Degree: MS, Pharmacology & Toxicology, 2014, Virginia Commonwealth University

  DNA double strand breaks (DSBs ) are extremely toxic to cells because they can lead to genomic rearrangements and even cell death. Two main… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Bafail, D. (2014). The Effect of Damaged Bases on The End Joining of DNA Double Strand Break Ends. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/7PA0-RK57 ; https://scholarscompass.vcu.edu/etd/3516

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):

Bafail, Duaa. “The Effect of Damaged Bases on The End Joining of DNA Double Strand Break Ends.” 2014. Thesis, Virginia Commonwealth University. Accessed May 29, 2020. https://doi.org/10.25772/7PA0-RK57 ; https://scholarscompass.vcu.edu/etd/3516.

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

MLA Handbook (7th Edition):

Bafail, Duaa. “The Effect of Damaged Bases on The End Joining of DNA Double Strand Break Ends.” 2014. Web. 29 May 2020.

Vancouver:

Bafail D. The Effect of Damaged Bases on The End Joining of DNA Double Strand Break Ends. [Internet] [Thesis]. Virginia Commonwealth University; 2014. [cited 2020 May 29]. Available from: https://doi.org/10.25772/7PA0-RK57 ; https://scholarscompass.vcu.edu/etd/3516.

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

Council of Science Editors:

Bafail D. The Effect of Damaged Bases on The End Joining of DNA Double Strand Break Ends. [Thesis]. Virginia Commonwealth University; 2014. Available from: https://doi.org/10.25772/7PA0-RK57 ; https://scholarscompass.vcu.edu/etd/3516

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


Virginia Commonwealth University

25. Farthing, Christine. Modulation Of CNS Neurotransmitter Levels And Associated Behaviors In Organic Anion Transporter 1 (Slc22a6) And Organic Anion Transporter 3 (Slc22a8) Knockout Mice.

Degree: PhD, Pharmaceutical Sciences, 2014, Virginia Commonwealth University

  According to the World Health Organization, mental disorders represent the leading cause of disability in the US generating ~58 billion dollars in medical costs… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Farthing, C. (2014). Modulation Of CNS Neurotransmitter Levels And Associated Behaviors In Organic Anion Transporter 1 (Slc22a6) And Organic Anion Transporter 3 (Slc22a8) Knockout Mice. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/501D-JC95 ; https://scholarscompass.vcu.edu/etd/3562

Chicago Manual of Style (16th Edition):

Farthing, Christine. “Modulation Of CNS Neurotransmitter Levels And Associated Behaviors In Organic Anion Transporter 1 (Slc22a6) And Organic Anion Transporter 3 (Slc22a8) Knockout Mice.” 2014. Doctoral Dissertation, Virginia Commonwealth University. Accessed May 29, 2020. https://doi.org/10.25772/501D-JC95 ; https://scholarscompass.vcu.edu/etd/3562.

MLA Handbook (7th Edition):

Farthing, Christine. “Modulation Of CNS Neurotransmitter Levels And Associated Behaviors In Organic Anion Transporter 1 (Slc22a6) And Organic Anion Transporter 3 (Slc22a8) Knockout Mice.” 2014. Web. 29 May 2020.

Vancouver:

Farthing C. Modulation Of CNS Neurotransmitter Levels And Associated Behaviors In Organic Anion Transporter 1 (Slc22a6) And Organic Anion Transporter 3 (Slc22a8) Knockout Mice. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2014. [cited 2020 May 29]. Available from: https://doi.org/10.25772/501D-JC95 ; https://scholarscompass.vcu.edu/etd/3562.

Council of Science Editors:

Farthing C. Modulation Of CNS Neurotransmitter Levels And Associated Behaviors In Organic Anion Transporter 1 (Slc22a6) And Organic Anion Transporter 3 (Slc22a8) Knockout Mice. [Doctoral Dissertation]. Virginia Commonwealth University; 2014. Available from: https://doi.org/10.25772/501D-JC95 ; https://scholarscompass.vcu.edu/etd/3562


Virginia Commonwealth University

26. Zalavadia, Ankit. QUANTITATIVE ANALYSIS OF 5-CHLORO-2-METHOXY-N-[2-(4-SULFAMOYLPHENYL)ETHYL]BENZAMIDE (GLYBURIDE ANALOGUE, GA) IN MOUSE PLASMA AND WHOLE BLOOD USING A MICRO-EXTRACTION AND LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY.

Degree: MS, Pharmaceutical Sciences, 2016, Virginia Commonwealth University

  Pharmacokinetic evaluation of 5-chloro-2-methoxy-N-[2-(4- sulfamoylphenyl)ethyl]benzamide in mouse plasma demanded for a suitable bioanalytical method. No reported bioanalytical method exists to-date that can quantify concentration… (more)

Subjects/Keywords: Other Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Zalavadia, A. (2016). QUANTITATIVE ANALYSIS OF 5-CHLORO-2-METHOXY-N-[2-(4-SULFAMOYLPHENYL)ETHYL]BENZAMIDE (GLYBURIDE ANALOGUE, GA) IN MOUSE PLASMA AND WHOLE BLOOD USING A MICRO-EXTRACTION AND LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/S5W8-0P17 ; https://scholarscompass.vcu.edu/etd/4279

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):

Zalavadia, Ankit. “QUANTITATIVE ANALYSIS OF 5-CHLORO-2-METHOXY-N-[2-(4-SULFAMOYLPHENYL)ETHYL]BENZAMIDE (GLYBURIDE ANALOGUE, GA) IN MOUSE PLASMA AND WHOLE BLOOD USING A MICRO-EXTRACTION AND LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY.” 2016. Thesis, Virginia Commonwealth University. Accessed May 29, 2020. https://doi.org/10.25772/S5W8-0P17 ; https://scholarscompass.vcu.edu/etd/4279.

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

MLA Handbook (7th Edition):

Zalavadia, Ankit. “QUANTITATIVE ANALYSIS OF 5-CHLORO-2-METHOXY-N-[2-(4-SULFAMOYLPHENYL)ETHYL]BENZAMIDE (GLYBURIDE ANALOGUE, GA) IN MOUSE PLASMA AND WHOLE BLOOD USING A MICRO-EXTRACTION AND LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY.” 2016. Web. 29 May 2020.

Vancouver:

Zalavadia A. QUANTITATIVE ANALYSIS OF 5-CHLORO-2-METHOXY-N-[2-(4-SULFAMOYLPHENYL)ETHYL]BENZAMIDE (GLYBURIDE ANALOGUE, GA) IN MOUSE PLASMA AND WHOLE BLOOD USING A MICRO-EXTRACTION AND LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY. [Internet] [Thesis]. Virginia Commonwealth University; 2016. [cited 2020 May 29]. Available from: https://doi.org/10.25772/S5W8-0P17 ; https://scholarscompass.vcu.edu/etd/4279.

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

Council of Science Editors:

Zalavadia A. QUANTITATIVE ANALYSIS OF 5-CHLORO-2-METHOXY-N-[2-(4-SULFAMOYLPHENYL)ETHYL]BENZAMIDE (GLYBURIDE ANALOGUE, GA) IN MOUSE PLASMA AND WHOLE BLOOD USING A MICRO-EXTRACTION AND LIQUID CHROMATOGRAPHY-TANDEM MASS SPECTROMETRY. [Thesis]. Virginia Commonwealth University; 2016. Available from: https://doi.org/10.25772/S5W8-0P17 ; https://scholarscompass.vcu.edu/etd/4279

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


University of New Mexico

27. Ordonez Suarez, Yoselin. Biphasic Effects of Vanadium Sulfate on Cerebrovascular Endothelial Cell Barrier Integrity.

Degree: 2019, University of New Mexico

  The objective of this study was to investigate the biphasic effects of vanadyl sulfate in cerebral vascular endothelial cells with a focus on understanding… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Ordonez Suarez, Y. (2019). Biphasic Effects of Vanadium Sulfate on Cerebrovascular Endothelial Cell Barrier Integrity. (Masters Thesis). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/phrm_etds/22

Chicago Manual of Style (16th Edition):

Ordonez Suarez, Yoselin. “Biphasic Effects of Vanadium Sulfate on Cerebrovascular Endothelial Cell Barrier Integrity.” 2019. Masters Thesis, University of New Mexico. Accessed May 29, 2020. https://digitalrepository.unm.edu/phrm_etds/22.

MLA Handbook (7th Edition):

Ordonez Suarez, Yoselin. “Biphasic Effects of Vanadium Sulfate on Cerebrovascular Endothelial Cell Barrier Integrity.” 2019. Web. 29 May 2020.

Vancouver:

Ordonez Suarez Y. Biphasic Effects of Vanadium Sulfate on Cerebrovascular Endothelial Cell Barrier Integrity. [Internet] [Masters thesis]. University of New Mexico; 2019. [cited 2020 May 29]. Available from: https://digitalrepository.unm.edu/phrm_etds/22.

Council of Science Editors:

Ordonez Suarez Y. Biphasic Effects of Vanadium Sulfate on Cerebrovascular Endothelial Cell Barrier Integrity. [Masters Thesis]. University of New Mexico; 2019. Available from: https://digitalrepository.unm.edu/phrm_etds/22


University of Iowa

28. Zhang, Jinzhou. Preparation and characterization of oxidized cellulose beads by extrusion/spheronization for chemoembolization.

Degree: PhD, Pharmacy, 2013, University of Iowa

  Transarterial chemoembolization (TACE) has been practiced in patients for over 30 years and describes the infusion of chemotherapeutic agents followed by embolic particles. This… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Zhang, J. (2013). Preparation and characterization of oxidized cellulose beads by extrusion/spheronization for chemoembolization. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2028

Chicago Manual of Style (16th Edition):

Zhang, Jinzhou. “Preparation and characterization of oxidized cellulose beads by extrusion/spheronization for chemoembolization.” 2013. Doctoral Dissertation, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/2028.

MLA Handbook (7th Edition):

Zhang, Jinzhou. “Preparation and characterization of oxidized cellulose beads by extrusion/spheronization for chemoembolization.” 2013. Web. 29 May 2020.

Vancouver:

Zhang J. Preparation and characterization of oxidized cellulose beads by extrusion/spheronization for chemoembolization. [Internet] [Doctoral dissertation]. University of Iowa; 2013. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/2028.

Council of Science Editors:

Zhang J. Preparation and characterization of oxidized cellulose beads by extrusion/spheronization for chemoembolization. [Doctoral Dissertation]. University of Iowa; 2013. Available from: https://ir.uiowa.edu/etd/2028


University of Iowa

29. Al Bakri, Wisam Saad Hasan. Characterization of atrazine transport across nasal respiratory and olfactory mucosae.

Degree: MS, Pharmacy, 2014, University of Iowa

  The herbicide atrazine is one of the most commonly used pesticides in United States. Atrazine was banned in the European Union in 2005 because… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Al Bakri, W. S. H. (2014). Characterization of atrazine transport across nasal respiratory and olfactory mucosae. (Masters Thesis). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/4559

Chicago Manual of Style (16th Edition):

Al Bakri, Wisam Saad Hasan. “Characterization of atrazine transport across nasal respiratory and olfactory mucosae.” 2014. Masters Thesis, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/4559.

MLA Handbook (7th Edition):

Al Bakri, Wisam Saad Hasan. “Characterization of atrazine transport across nasal respiratory and olfactory mucosae.” 2014. Web. 29 May 2020.

Vancouver:

Al Bakri WSH. Characterization of atrazine transport across nasal respiratory and olfactory mucosae. [Internet] [Masters thesis]. University of Iowa; 2014. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/4559.

Council of Science Editors:

Al Bakri WSH. Characterization of atrazine transport across nasal respiratory and olfactory mucosae. [Masters Thesis]. University of Iowa; 2014. Available from: https://ir.uiowa.edu/etd/4559


University of Iowa

30. Lin, Chih-Wei. Modeling glucose-insulin kinetics and development of type 2 diabetes in offspring of diabetic parents.

Degree: PhD, Pharmacy, 2011, University of Iowa

  Type 2 diabetes (T2D) has been studied for decades. Many risk factors of T2D have been identified, but few studies were designed to investigate… (more)

Subjects/Keywords: Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Lin, C. (2011). Modeling glucose-insulin kinetics and development of type 2 diabetes in offspring of diabetic parents. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/2741

Chicago Manual of Style (16th Edition):

Lin, Chih-Wei. “Modeling glucose-insulin kinetics and development of type 2 diabetes in offspring of diabetic parents.” 2011. Doctoral Dissertation, University of Iowa. Accessed May 29, 2020. https://ir.uiowa.edu/etd/2741.

MLA Handbook (7th Edition):

Lin, Chih-Wei. “Modeling glucose-insulin kinetics and development of type 2 diabetes in offspring of diabetic parents.” 2011. Web. 29 May 2020.

Vancouver:

Lin C. Modeling glucose-insulin kinetics and development of type 2 diabetes in offspring of diabetic parents. [Internet] [Doctoral dissertation]. University of Iowa; 2011. [cited 2020 May 29]. Available from: https://ir.uiowa.edu/etd/2741.

Council of Science Editors:

Lin C. Modeling glucose-insulin kinetics and development of type 2 diabetes in offspring of diabetic parents. [Doctoral Dissertation]. University of Iowa; 2011. Available from: https://ir.uiowa.edu/etd/2741

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