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You searched for subject:(Drug development). Showing records 1 – 30 of 388 total matches.

[1] [2] [3] [4] [5] … [13]

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Rutgers University

1. Tsai, Pei-Chin, 1984-. Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications.

Degree: PhD, Pharmaceutical Science, 2016, Rutgers University

Three-dimensional (3D) human skin equivalents (HSEs) are in-vitro models that have morphology and function similar to native human skin. Traditionally, drug discovery for lead compounds… (more)

Subjects/Keywords: Drug development

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APA (6th Edition):

Tsai, Pei-Chin, 1. (2016). Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/50236/

Chicago Manual of Style (16th Edition):

Tsai, Pei-Chin, 1984-. “Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications.” 2016. Doctoral Dissertation, Rutgers University. Accessed September 23, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/50236/.

MLA Handbook (7th Edition):

Tsai, Pei-Chin, 1984-. “Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications.” 2016. Web. 23 Sep 2019.

Vancouver:

Tsai, Pei-Chin 1. Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2019 Sep 23]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50236/.

Council of Science Editors:

Tsai, Pei-Chin 1. Development of three dimensional human skin equivalents based on decellularized extracellular matrices and tyrosine-derived polycarbonate polymers for in-vitro drug screening applications. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50236/


University of Utah

2. Guo, Jeremy. Rapid throughput solubility screening assay development and its applications in preformulation;.

Degree: PhD, Pharmaceutics & Pharmaceutical Chemistry;, 2007, University of Utah

Drug solubility is an important physicochemical property for orally administered drugs because it can significantly influence drug dissolution and absorption profiles. Investigative drugs need to… (more)

Subjects/Keywords: Analysis; Drug Development; Drug Solubility

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APA (6th Edition):

Guo, J. (2007). Rapid throughput solubility screening assay development and its applications in preformulation;. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/137/rec/1072

Chicago Manual of Style (16th Edition):

Guo, Jeremy. “Rapid throughput solubility screening assay development and its applications in preformulation;.” 2007. Doctoral Dissertation, University of Utah. Accessed September 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/137/rec/1072.

MLA Handbook (7th Edition):

Guo, Jeremy. “Rapid throughput solubility screening assay development and its applications in preformulation;.” 2007. Web. 23 Sep 2019.

Vancouver:

Guo J. Rapid throughput solubility screening assay development and its applications in preformulation;. [Internet] [Doctoral dissertation]. University of Utah; 2007. [cited 2019 Sep 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/137/rec/1072.

Council of Science Editors:

Guo J. Rapid throughput solubility screening assay development and its applications in preformulation;. [Doctoral Dissertation]. University of Utah; 2007. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd1/id/137/rec/1072


University of Wisconsin – La Cross

3. Ladell, Peter. Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii.

Degree: 2011, University of Wisconsin – La Cross

 Each year, it is estimated that 1.7 million healthcare-acquired infections occur in the United States with 70% of the bacteria causing these infections being resistant… (more)

Subjects/Keywords: Antibiotics; Drug development

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APA (6th Edition):

Ladell, P. (2011). Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii. (Thesis). University of Wisconsin – La Cross. Retrieved from http://digital.library.wisc.edu/1793/54691

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):

Ladell, Peter. “Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii.” 2011. Thesis, University of Wisconsin – La Cross. Accessed September 23, 2019. http://digital.library.wisc.edu/1793/54691.

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

MLA Handbook (7th Edition):

Ladell, Peter. “Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii.” 2011. Web. 23 Sep 2019.

Vancouver:

Ladell P. Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii. [Internet] [Thesis]. University of Wisconsin – La Cross; 2011. [cited 2019 Sep 23]. Available from: http://digital.library.wisc.edu/1793/54691.

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

Council of Science Editors:

Ladell P. Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii. [Thesis]. University of Wisconsin – La Cross; 2011. Available from: http://digital.library.wisc.edu/1793/54691

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


University of Newcastle

4. Cossar, Peter. Inhibiting the NusB-NusE protein-protein interaction - a novel target for antibiotic drug development.

Degree: PhD, 2018, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

The strain of antibiotic resistances on global health has led to a movement away from traditional approaches to… (more)

Subjects/Keywords: antibiotic drug; drug development; NusB-NusE protein

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APA (6th Edition):

Cossar, P. (2018). Inhibiting the NusB-NusE protein-protein interaction - a novel target for antibiotic drug development. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1383709

Chicago Manual of Style (16th Edition):

Cossar, Peter. “Inhibiting the NusB-NusE protein-protein interaction - a novel target for antibiotic drug development.” 2018. Doctoral Dissertation, University of Newcastle. Accessed September 23, 2019. http://hdl.handle.net/1959.13/1383709.

MLA Handbook (7th Edition):

Cossar, Peter. “Inhibiting the NusB-NusE protein-protein interaction - a novel target for antibiotic drug development.” 2018. Web. 23 Sep 2019.

Vancouver:

Cossar P. Inhibiting the NusB-NusE protein-protein interaction - a novel target for antibiotic drug development. [Internet] [Doctoral dissertation]. University of Newcastle; 2018. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1959.13/1383709.

Council of Science Editors:

Cossar P. Inhibiting the NusB-NusE protein-protein interaction - a novel target for antibiotic drug development. [Doctoral Dissertation]. University of Newcastle; 2018. Available from: http://hdl.handle.net/1959.13/1383709


Drexel University

5. Chen, Nan. Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells.

Degree: 2015, Drexel University

Androgen receptor (AR) signaling is the primary driver for prostate cancer progression. Androgen deprivation therapy (ADT) although initially effective, will eventually fail with the development(more)

Subjects/Keywords: Drug development; Drug Design; Biochemical Phenomena

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APA (6th Edition):

Chen, N. (2015). Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7165

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):

Chen, Nan. “Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells.” 2015. Thesis, Drexel University. Accessed September 23, 2019. http://hdl.handle.net/1860/idea:7165.

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

MLA Handbook (7th Edition):

Chen, Nan. “Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells.” 2015. Web. 23 Sep 2019.

Vancouver:

Chen N. Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells. [Internet] [Thesis]. Drexel University; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1860/idea:7165.

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

Council of Science Editors:

Chen N. Small Molecule Sigma1 Modulators Induce the Degradation of Androgen Receptor and Splice Variants in Castration Resistant Prostate Cancer Cells. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:7165

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


Drexel University

6. Falcucci, Romulo Martelli. Neuroprotective properties of novel positive allosteric modulators of EAAT2.

Degree: 2016, Drexel University

Excitatory amino acid transporters (EAATs) play a crucial role in the removal of synaptic glutamate to maintain extracellular concentrations below excitotoxic levels. Glutamate-mediated excitotoxicity has… (more)

Subjects/Keywords: Drug Design; Drug development; Biochemical Phenomena

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APA (6th Edition):

Falcucci, R. M. (2016). Neuroprotective properties of novel positive allosteric modulators of EAAT2. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7166

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):

Falcucci, Romulo Martelli. “Neuroprotective properties of novel positive allosteric modulators of EAAT2.” 2016. Thesis, Drexel University. Accessed September 23, 2019. http://hdl.handle.net/1860/idea:7166.

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

MLA Handbook (7th Edition):

Falcucci, Romulo Martelli. “Neuroprotective properties of novel positive allosteric modulators of EAAT2.” 2016. Web. 23 Sep 2019.

Vancouver:

Falcucci RM. Neuroprotective properties of novel positive allosteric modulators of EAAT2. [Internet] [Thesis]. Drexel University; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1860/idea:7166.

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

Council of Science Editors:

Falcucci RM. Neuroprotective properties of novel positive allosteric modulators of EAAT2. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7166

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


Drexel University

7. Patra, Sayani. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner.

Degree: 2016, Drexel University

Drug addiction is believed to occur, in part, as a result of maladaptive changes in dopaminergic pathways. The extracellular signal-regulated kinase 1/2 (ERK1/2) mitogen-activated protein… (more)

Subjects/Keywords: Biochemical Phenomena; Drug Design; Drug development

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APA (6th Edition):

Patra, S. (2016). Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7168

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):

Patra, Sayani. “Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner.” 2016. Thesis, Drexel University. Accessed September 23, 2019. http://hdl.handle.net/1860/idea:7168.

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

MLA Handbook (7th Edition):

Patra, Sayani. “Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner.” 2016. Web. 23 Sep 2019.

Vancouver:

Patra S. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. [Internet] [Thesis]. Drexel University; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1860/idea:7168.

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

Council of Science Editors:

Patra S. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7168

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


Penn State University

8. Kim, Min-Jung. Partnership Conditions for New Drug Development Based on a Real Option.

Degree: MS, Industrial Engineering, 2009, Penn State University

 The partnership between a big pharmaceutical company which has capital and marketing resources and a biochemical company which possesses intellectual property of a candidate drug(more)

Subjects/Keywords: real option; drug development; partnership

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APA (6th Edition):

Kim, M. (2009). Partnership Conditions for New Drug Development Based on a Real Option. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9673

Chicago Manual of Style (16th Edition):

Kim, Min-Jung. “Partnership Conditions for New Drug Development Based on a Real Option.” 2009. Masters Thesis, Penn State University. Accessed September 23, 2019. https://etda.libraries.psu.edu/catalog/9673.

MLA Handbook (7th Edition):

Kim, Min-Jung. “Partnership Conditions for New Drug Development Based on a Real Option.” 2009. Web. 23 Sep 2019.

Vancouver:

Kim M. Partnership Conditions for New Drug Development Based on a Real Option. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2019 Sep 23]. Available from: https://etda.libraries.psu.edu/catalog/9673.

Council of Science Editors:

Kim M. Partnership Conditions for New Drug Development Based on a Real Option. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9673


Oregon State University

9. Watts, K. Shawn. Steps toward structure-assisted drug design.

Degree: MS, Biochemistry and Biophysics, 2000, Oregon State University

 The three dimensional structure of both a ligand and its cognate receptor are required for the success of structure-assisted drug design. This thesis reports the… (more)

Subjects/Keywords: Drug development

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APA (6th Edition):

Watts, K. S. (2000). Steps toward structure-assisted drug design. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/32743

Chicago Manual of Style (16th Edition):

Watts, K Shawn. “Steps toward structure-assisted drug design.” 2000. Masters Thesis, Oregon State University. Accessed September 23, 2019. http://hdl.handle.net/1957/32743.

MLA Handbook (7th Edition):

Watts, K Shawn. “Steps toward structure-assisted drug design.” 2000. Web. 23 Sep 2019.

Vancouver:

Watts KS. Steps toward structure-assisted drug design. [Internet] [Masters thesis]. Oregon State University; 2000. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1957/32743.

Council of Science Editors:

Watts KS. Steps toward structure-assisted drug design. [Masters Thesis]. Oregon State University; 2000. Available from: http://hdl.handle.net/1957/32743


University of Illinois – Urbana-Champaign

10. Nguyen, Lien Thi Thuy. Design, synthesis, and biological activities of small molecules that target myotonic dystrophy.

Degree: PhD, Chemistry, 2016, University of Illinois – Urbana-Champaign

 Myotonic dystrophy (DM) is a triple-repeat expansion, multi-systemic disease that affects one in eight thousand people worldwide. The cause of the disease is a progressive,… (more)

Subjects/Keywords: Myotonic Dystrophy; Drug development

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APA (6th Edition):

Nguyen, L. T. T. (2016). Design, synthesis, and biological activities of small molecules that target myotonic dystrophy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90730

Chicago Manual of Style (16th Edition):

Nguyen, Lien Thi Thuy. “Design, synthesis, and biological activities of small molecules that target myotonic dystrophy.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed September 23, 2019. http://hdl.handle.net/2142/90730.

MLA Handbook (7th Edition):

Nguyen, Lien Thi Thuy. “Design, synthesis, and biological activities of small molecules that target myotonic dystrophy.” 2016. Web. 23 Sep 2019.

Vancouver:

Nguyen LTT. Design, synthesis, and biological activities of small molecules that target myotonic dystrophy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2142/90730.

Council of Science Editors:

Nguyen LTT. Design, synthesis, and biological activities of small molecules that target myotonic dystrophy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/90730


Rutgers University

11. Wang, Yifan, 1989-. Using multivariate analysis for pharmaceutical drug product development.

Degree: PhD, Chemical and Biochemical Engineering, 2016, Rutgers University

Manufacturing of pharmaceutical products has a prominent role in the healthcare industry. Generally, the ultimate aim of pharmaceutical development is to release to the market… (more)

Subjects/Keywords: Drug development; Multivariate analysis

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APA (6th Edition):

Wang, Yifan, 1. (2016). Using multivariate analysis for pharmaceutical drug product development. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51493/

Chicago Manual of Style (16th Edition):

Wang, Yifan, 1989-. “Using multivariate analysis for pharmaceutical drug product development.” 2016. Doctoral Dissertation, Rutgers University. Accessed September 23, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/51493/.

MLA Handbook (7th Edition):

Wang, Yifan, 1989-. “Using multivariate analysis for pharmaceutical drug product development.” 2016. Web. 23 Sep 2019.

Vancouver:

Wang, Yifan 1. Using multivariate analysis for pharmaceutical drug product development. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2019 Sep 23]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51493/.

Council of Science Editors:

Wang, Yifan 1. Using multivariate analysis for pharmaceutical drug product development. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51493/

12. Visser, Samuel Jacob de. A question based approach to drug development.

Degree: 2003, Centre for Human Drug Research (CHDR), Faculty of Science, Leiden University

 As shown in the previous case study, changing the development plan from phase/time oriented to question based can improve the insights on the information that… (more)

Subjects/Keywords: Drug development; Drug development

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APA (6th Edition):

Visser, S. J. d. (2003). A question based approach to drug development. (Doctoral Dissertation). Centre for Human Drug Research (CHDR), Faculty of Science, Leiden University. Retrieved from http://hdl.handle.net/1887/28222

Chicago Manual of Style (16th Edition):

Visser, Samuel Jacob de. “A question based approach to drug development.” 2003. Doctoral Dissertation, Centre for Human Drug Research (CHDR), Faculty of Science, Leiden University. Accessed September 23, 2019. http://hdl.handle.net/1887/28222.

MLA Handbook (7th Edition):

Visser, Samuel Jacob de. “A question based approach to drug development.” 2003. Web. 23 Sep 2019.

Vancouver:

Visser SJd. A question based approach to drug development. [Internet] [Doctoral dissertation]. Centre for Human Drug Research (CHDR), Faculty of Science, Leiden University; 2003. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1887/28222.

Council of Science Editors:

Visser SJd. A question based approach to drug development. [Doctoral Dissertation]. Centre for Human Drug Research (CHDR), Faculty of Science, Leiden University; 2003. Available from: http://hdl.handle.net/1887/28222


University of KwaZulu-Natal

13. Masupye, Euphenia Mathebule. Evaluation of extemporaneous compounding in tetriary hospital pharmacy in the Polokwane Municipality : a pilot study.

Degree: 2015, University of KwaZulu-Natal

 Background: Some medicines are available in doses that are not suitable for a specific population group and therefore manipulation of the existing medication is undertaken… (more)

Subjects/Keywords: Drug development - hospital pharmacies.; South Africa (Polokwane).; Extemporaneous compounding.; Drug design.; New drug development.

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APA (6th Edition):

Masupye, E. M. (2015). Evaluation of extemporaneous compounding in tetriary hospital pharmacy in the Polokwane Municipality : a pilot study. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/14924

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):

Masupye, Euphenia Mathebule. “Evaluation of extemporaneous compounding in tetriary hospital pharmacy in the Polokwane Municipality : a pilot study.” 2015. Thesis, University of KwaZulu-Natal. Accessed September 23, 2019. http://hdl.handle.net/10413/14924.

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

MLA Handbook (7th Edition):

Masupye, Euphenia Mathebule. “Evaluation of extemporaneous compounding in tetriary hospital pharmacy in the Polokwane Municipality : a pilot study.” 2015. Web. 23 Sep 2019.

Vancouver:

Masupye EM. Evaluation of extemporaneous compounding in tetriary hospital pharmacy in the Polokwane Municipality : a pilot study. [Internet] [Thesis]. University of KwaZulu-Natal; 2015. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/10413/14924.

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

Council of Science Editors:

Masupye EM. Evaluation of extemporaneous compounding in tetriary hospital pharmacy in the Polokwane Municipality : a pilot study. [Thesis]. University of KwaZulu-Natal; 2015. Available from: http://hdl.handle.net/10413/14924

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


University of Arizona

14. Smith, Breland Elise. Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer .

Degree: 2014, University of Arizona

 The research described in this dissertation is focused on the knowledge-based, often in silico assisted design, targeted synthesis, and biological evaluation of small molecules of… (more)

Subjects/Keywords: Medicinal Chemistry; Structure Based Drug Design; Biochemistry; Drug Discovery and Development

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APA (6th Edition):

Smith, B. E. (2014). Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/337213

Chicago Manual of Style (16th Edition):

Smith, Breland Elise. “Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer .” 2014. Doctoral Dissertation, University of Arizona. Accessed September 23, 2019. http://hdl.handle.net/10150/337213.

MLA Handbook (7th Edition):

Smith, Breland Elise. “Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer .” 2014. Web. 23 Sep 2019.

Vancouver:

Smith BE. Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/10150/337213.

Council of Science Editors:

Smith BE. Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/337213


University of KwaZulu-Natal

15. Morris, Lynn. The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection.

Degree: 2011, University of KwaZulu-Natal

 An understanding of how broadly neutralizing activity develops in HIV-1-infected individuals is needed to guide vaccine design and immunization strategies. Here we used a large… (more)

Subjects/Keywords: Vaccines.; Drug development.; HIV infections – Immunology.

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APA (6th Edition):

Morris, L. (2011). The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/7883

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):

Morris, Lynn. “The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection.” 2011. Thesis, University of KwaZulu-Natal. Accessed September 23, 2019. http://hdl.handle.net/10413/7883.

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

MLA Handbook (7th Edition):

Morris, Lynn. “The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection.” 2011. Web. 23 Sep 2019.

Vancouver:

Morris L. The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/10413/7883.

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

Council of Science Editors:

Morris L. The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://hdl.handle.net/10413/7883

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


University of KwaZulu-Natal

16. [No author]. The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection.

Degree: 2011, University of KwaZulu-Natal

 An understanding of how broadly neutralizing activity develops in HIV-1-infected individuals is needed to guide vaccine design and immunization strategies. Here we used a large… (more)

Subjects/Keywords: Vaccines.; Drug development.; HIV infections – Immunology.

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APA (6th Edition):

author], [. (2011). The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. (Thesis). University of KwaZulu-Natal. Retrieved from http://dx.doi.org/10.1128/JVI.00198-11

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):

author], [No. “The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. ” 2011. Thesis, University of KwaZulu-Natal. Accessed September 23, 2019. http://dx.doi.org/10.1128/JVI.00198-11.

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

MLA Handbook (7th Edition):

author], [No. “The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. ” 2011. Web. 23 Sep 2019.

Vancouver:

author] [. The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. [Internet] [Thesis]. University of KwaZulu-Natal; 2011. [cited 2019 Sep 23]. Available from: http://dx.doi.org/10.1128/JVI.00198-11.

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

Council of Science Editors:

author] [. The Neutralization Breadth of HIV-1 Develops Incrementally over Four Years and Is Associated with CD4+ T Cell Decline and High Viral Load during Acute Infection. [Thesis]. University of KwaZulu-Natal; 2011. Available from: http://dx.doi.org/10.1128/JVI.00198-11

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


Victoria University of Wellington

17. Ting, Samuel Z.Y. The Synthesis of Aigialomycin D Analogues.

Degree: 2010, Victoria University of Wellington

 Aigialomycin D is a fungal natural product possessing kinase inhibition properties. It is a member of a class of compounds known as the resorcylic acid… (more)

Subjects/Keywords: Resorcylic acid lactones; Drug development; Lactones

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APA (6th Edition):

Ting, S. Z. Y. (2010). The Synthesis of Aigialomycin D Analogues. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1412

Chicago Manual of Style (16th Edition):

Ting, Samuel Z Y. “The Synthesis of Aigialomycin D Analogues.” 2010. Masters Thesis, Victoria University of Wellington. Accessed September 23, 2019. http://hdl.handle.net/10063/1412.

MLA Handbook (7th Edition):

Ting, Samuel Z Y. “The Synthesis of Aigialomycin D Analogues.” 2010. Web. 23 Sep 2019.

Vancouver:

Ting SZY. The Synthesis of Aigialomycin D Analogues. [Internet] [Masters thesis]. Victoria University of Wellington; 2010. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/10063/1412.

Council of Science Editors:

Ting SZY. The Synthesis of Aigialomycin D Analogues. [Masters Thesis]. Victoria University of Wellington; 2010. Available from: http://hdl.handle.net/10063/1412


University of KwaZulu-Natal

18. [No author]. The impact of antiretroviral treatement scale-up on health systems in South Africa : a qualitative study.

Degree: Development studies, 2008, University of KwaZulu-Natal

 This study investigates the impact of the scale-up of antiretroviral treatment (ART) on the health system in South Africa. It looks at the positive and… (more)

Subjects/Keywords: AIDS (Disease) – Drug therapy.; Development studies.

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APA (6th Edition):

author], [. (2008). The impact of antiretroviral treatement scale-up on health systems in South Africa : a qualitative study. (Thesis). University of KwaZulu-Natal. Retrieved from http://hdl.handle.net/10413/1116

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):

author], [No. “The impact of antiretroviral treatement scale-up on health systems in South Africa : a qualitative study. ” 2008. Thesis, University of KwaZulu-Natal. Accessed September 23, 2019. http://hdl.handle.net/10413/1116.

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

MLA Handbook (7th Edition):

author], [No. “The impact of antiretroviral treatement scale-up on health systems in South Africa : a qualitative study. ” 2008. Web. 23 Sep 2019.

Vancouver:

author] [. The impact of antiretroviral treatement scale-up on health systems in South Africa : a qualitative study. [Internet] [Thesis]. University of KwaZulu-Natal; 2008. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/10413/1116.

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

Council of Science Editors:

author] [. The impact of antiretroviral treatement scale-up on health systems in South Africa : a qualitative study. [Thesis]. University of KwaZulu-Natal; 2008. Available from: http://hdl.handle.net/10413/1116

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


University of Aberdeen

19. Mavridis, Lazaros. High throughput virtual drug screening using spherical harmonic molecular surface representations.

Degree: 2009, University of Aberdeen

 This thesis presents new spherical harmonic (SH) approaches for ligand-based high-throughput virtual screening (HTVS). If it is assumed that small drug molecules may be adequately… (more)

Subjects/Keywords: 615; Drugs : High throughput screening (Drug development)

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

APA (6th Edition):

Mavridis, L. (2009). High throughput virtual drug screening using spherical harmonic molecular surface representations. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25936 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499650

Chicago Manual of Style (16th Edition):

Mavridis, Lazaros. “High throughput virtual drug screening using spherical harmonic molecular surface representations.” 2009. Doctoral Dissertation, University of Aberdeen. Accessed September 23, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25936 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499650.

MLA Handbook (7th Edition):

Mavridis, Lazaros. “High throughput virtual drug screening using spherical harmonic molecular surface representations.” 2009. Web. 23 Sep 2019.

Vancouver:

Mavridis L. High throughput virtual drug screening using spherical harmonic molecular surface representations. [Internet] [Doctoral dissertation]. University of Aberdeen; 2009. [cited 2019 Sep 23]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25936 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499650.

Council of Science Editors:

Mavridis L. High throughput virtual drug screening using spherical harmonic molecular surface representations. [Doctoral Dissertation]. University of Aberdeen; 2009. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=25936 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.499650


Rhodes University

20. Laming, Dustin. Development of a high-throughput bioassay to determine the rate of antimalarial drug action using fluorescent vitality probes.

Degree: Faculty of Science, Biochemistry and Microbiology, 2016, Rhodes University

 Malaria is one of the most prevalent diseases in Africa and the Plasmodium falciparum species is widely accepted as the most virulent, with a fatality… (more)

Subjects/Keywords: Malaria  – Africa; Plasmodium falciparum; Drug development; Fluorescence

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APA (6th Edition):

Laming, D. (2016). Development of a high-throughput bioassay to determine the rate of antimalarial drug action using fluorescent vitality probes. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/64434

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):

Laming, Dustin. “Development of a high-throughput bioassay to determine the rate of antimalarial drug action using fluorescent vitality probes.” 2016. Thesis, Rhodes University. Accessed September 23, 2019. http://hdl.handle.net/10962/64434.

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

MLA Handbook (7th Edition):

Laming, Dustin. “Development of a high-throughput bioassay to determine the rate of antimalarial drug action using fluorescent vitality probes.” 2016. Web. 23 Sep 2019.

Vancouver:

Laming D. Development of a high-throughput bioassay to determine the rate of antimalarial drug action using fluorescent vitality probes. [Internet] [Thesis]. Rhodes University; 2016. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/10962/64434.

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

Council of Science Editors:

Laming D. Development of a high-throughput bioassay to determine the rate of antimalarial drug action using fluorescent vitality probes. [Thesis]. Rhodes University; 2016. Available from: http://hdl.handle.net/10962/64434

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


Case Western Reserve University

21. Mehta, Kalpita Deepak. Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications.

Degree: MSs, Biology, 2010, Case Western Reserve University

Drug screening and profiling in the drug discovery process can be carried out either by using stable transfected or transiently transfected cell lines. Transient expression… (more)

Subjects/Keywords: Cellular Biology; Drug discovery and development

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APA (6th Edition):

Mehta, K. D. (2010). Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1269628794

Chicago Manual of Style (16th Edition):

Mehta, Kalpita Deepak. “Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications.” 2010. Masters Thesis, Case Western Reserve University. Accessed September 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1269628794.

MLA Handbook (7th Edition):

Mehta, Kalpita Deepak. “Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications.” 2010. Web. 23 Sep 2019.

Vancouver:

Mehta KD. Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications. [Internet] [Masters thesis]. Case Western Reserve University; 2010. [cited 2019 Sep 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1269628794.

Council of Science Editors:

Mehta KD. Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications. [Masters Thesis]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1269628794


University of Southern California

22. Yardley, Megan M. Development of ivermectin as a platform for the treatment and/or prevention of alcohol use disorders.

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

 Alcohol use disorders (AUDs) affect over 18 million people in the United States alone, cost over $235 billion, and yet only 8% of this population… (more)

Subjects/Keywords: medications development; alcoholism therapy; drug repositioning

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APA (6th Edition):

Yardley, M. M. (2016). Development of ivermectin as a platform for the treatment and/or prevention of alcohol use disorders. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/444768/rec/1946

Chicago Manual of Style (16th Edition):

Yardley, Megan M. “Development of ivermectin as a platform for the treatment and/or prevention of alcohol use disorders.” 2016. Doctoral Dissertation, University of Southern California. Accessed September 23, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/444768/rec/1946.

MLA Handbook (7th Edition):

Yardley, Megan M. “Development of ivermectin as a platform for the treatment and/or prevention of alcohol use disorders.” 2016. Web. 23 Sep 2019.

Vancouver:

Yardley MM. Development of ivermectin as a platform for the treatment and/or prevention of alcohol use disorders. [Internet] [Doctoral dissertation]. University of Southern California; 2016. [cited 2019 Sep 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/444768/rec/1946.

Council of Science Editors:

Yardley MM. Development of ivermectin as a platform for the treatment and/or prevention of alcohol use disorders. [Doctoral Dissertation]. University of Southern California; 2016. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/444768/rec/1946


University of Sydney

23. Dinarvand, Mojdeh. Discovery and development of novel antibacterials from natural products .

Degree: 2017, University of Sydney

 Methicillin-resistant Staphylococcus aureus (MRSA) is a major human pathogen associated with a variety of moderate to severe infections. The multi-drug resistant nature of this pathogen… (more)

Subjects/Keywords: Drug discovery and development; natural products; Microbiology

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APA (6th Edition):

Dinarvand, M. (2017). Discovery and development of novel antibacterials from natural products . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18569

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):

Dinarvand, Mojdeh. “Discovery and development of novel antibacterials from natural products .” 2017. Thesis, University of Sydney. Accessed September 23, 2019. http://hdl.handle.net/2123/18569.

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

MLA Handbook (7th Edition):

Dinarvand, Mojdeh. “Discovery and development of novel antibacterials from natural products .” 2017. Web. 23 Sep 2019.

Vancouver:

Dinarvand M. Discovery and development of novel antibacterials from natural products . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2123/18569.

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

Council of Science Editors:

Dinarvand M. Discovery and development of novel antibacterials from natural products . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/18569

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


University of Debrecen

24. Sabazade, Shiva. Alzheimers disease drugs used today and under development .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Alzheimer`s disease is the leading cause of dementia worldwide. It’s a neurodegenerative disorder with a multifactorial etiology and a complex pathology. Over the past decades… (more)

Subjects/Keywords: Alzheimer drug development

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APA (6th Edition):

Sabazade, S. (n.d.). Alzheimers disease drugs used today and under development . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/230511

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sabazade, Shiva. “Alzheimers disease drugs used today and under development .” Thesis, University of Debrecen. Accessed September 23, 2019. http://hdl.handle.net/2437/230511.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sabazade, Shiva. “Alzheimers disease drugs used today and under development .” Web. 23 Sep 2019.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Sabazade S. Alzheimers disease drugs used today and under development . [Internet] [Thesis]. University of Debrecen; [cited 2019 Sep 23]. Available from: http://hdl.handle.net/2437/230511.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Sabazade S. Alzheimers disease drugs used today and under development . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/230511

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Oregon State University

25. Mandrell, David. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials.

Degree: MS, Industrial Engineering, 2010, Oregon State University

 The field of nanotechnology has been rapidly developing new materials. These materials have become incorporated into consumer products and the environment after only minimal assessment… (more)

Subjects/Keywords: Automation; High throughput screening (Drug development)

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APA (6th Edition):

Mandrell, D. (2010). Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/16495

Chicago Manual of Style (16th Edition):

Mandrell, David. “Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials.” 2010. Masters Thesis, Oregon State University. Accessed September 23, 2019. http://hdl.handle.net/1957/16495.

MLA Handbook (7th Edition):

Mandrell, David. “Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials.” 2010. Web. 23 Sep 2019.

Vancouver:

Mandrell D. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. [Internet] [Masters thesis]. Oregon State University; 2010. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1957/16495.

Council of Science Editors:

Mandrell D. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. [Masters Thesis]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/16495


IUPUI

26. Cheemakurthi, Usha Deepika. DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN.

Degree: 2010, IUPUI

The main focus of our work is to develop, apply and assess cheminformatics tools and methods. In particular, we focus on the following three areas:… (more)

Subjects/Keywords: Implementation of Tools; Development; Design; Drug Discovery

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

APA (6th Edition):

Cheemakurthi, U. D. (2010). DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2268

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):

Cheemakurthi, Usha Deepika. “DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN.” 2010. Thesis, IUPUI. Accessed September 23, 2019. http://hdl.handle.net/1805/2268.

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

MLA Handbook (7th Edition):

Cheemakurthi, Usha Deepika. “DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN.” 2010. Web. 23 Sep 2019.

Vancouver:

Cheemakurthi UD. DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN. [Internet] [Thesis]. IUPUI; 2010. [cited 2019 Sep 23]. Available from: http://hdl.handle.net/1805/2268.

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

Council of Science Editors:

Cheemakurthi UD. DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN. [Thesis]. IUPUI; 2010. Available from: http://hdl.handle.net/1805/2268

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


University of Wollongong

27. Jafari, Somayeh. Design, Synthesis, and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine That Display Reduced Weight Gain and Metabolic Side Effects.

Degree: PhD, 2012, University of Wollongong

  “Design, Synthesis and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine that Display Reduced Weight Gain and Metabolic Side Effects”Somayeh Jafari University of… (more)

Subjects/Keywords: drug development; Olanzapine; weight gain; antipsychotics

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APA (6th Edition):

Jafari, S. (2012). Design, Synthesis, and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine That Display Reduced Weight Gain and Metabolic Side Effects. (Doctoral Dissertation). University of Wollongong. Retrieved from 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY, 1109 NEUROSCIENCES ; https://ro.uow.edu.au/theses/3582

Chicago Manual of Style (16th Edition):

Jafari, Somayeh. “Design, Synthesis, and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine That Display Reduced Weight Gain and Metabolic Side Effects.” 2012. Doctoral Dissertation, University of Wollongong. Accessed September 23, 2019. 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY, 1109 NEUROSCIENCES ; https://ro.uow.edu.au/theses/3582.

MLA Handbook (7th Edition):

Jafari, Somayeh. “Design, Synthesis, and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine That Display Reduced Weight Gain and Metabolic Side Effects.” 2012. Web. 23 Sep 2019.

Vancouver:

Jafari S. Design, Synthesis, and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine That Display Reduced Weight Gain and Metabolic Side Effects. [Internet] [Doctoral dissertation]. University of Wollongong; 2012. [cited 2019 Sep 23]. Available from: 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY, 1109 NEUROSCIENCES ; https://ro.uow.edu.au/theses/3582.

Council of Science Editors:

Jafari S. Design, Synthesis, and Pharmacological Evaluation of Novel Antipsychotic Drugs Based on Olanzapine That Display Reduced Weight Gain and Metabolic Side Effects. [Doctoral Dissertation]. University of Wollongong; 2012. Available from: 0304 MEDICINAL AND BIOMOLECULAR CHEMISTRY, 1109 NEUROSCIENCES ; https://ro.uow.edu.au/theses/3582


Rutgers University

28. Fang, Fang, 1971-. Methods of evaluation of performance of adaptive designs on treatment effect intervals and methods of designing two-stage winner designs with survival outcomes.

Degree: PhD, Statistics and Biostatistics, 2010, Rutgers University

The accuracy of the treatment effect estimation is crucial to the success of phase 3 studies. The calculation of fixed sample size relies on the… (more)

Subjects/Keywords: Sampling (Statistics); Drugs – Testing; Drug development

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APA (6th Edition):

Fang, Fang, 1. (2010). Methods of evaluation of performance of adaptive designs on treatment effect intervals and methods of designing two-stage winner designs with survival outcomes. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056339

Chicago Manual of Style (16th Edition):

Fang, Fang, 1971-. “Methods of evaluation of performance of adaptive designs on treatment effect intervals and methods of designing two-stage winner designs with survival outcomes.” 2010. Doctoral Dissertation, Rutgers University. Accessed September 23, 2019. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056339.

MLA Handbook (7th Edition):

Fang, Fang, 1971-. “Methods of evaluation of performance of adaptive designs on treatment effect intervals and methods of designing two-stage winner designs with survival outcomes.” 2010. Web. 23 Sep 2019.

Vancouver:

Fang, Fang 1. Methods of evaluation of performance of adaptive designs on treatment effect intervals and methods of designing two-stage winner designs with survival outcomes. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2019 Sep 23]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056339.

Council of Science Editors:

Fang, Fang 1. Methods of evaluation of performance of adaptive designs on treatment effect intervals and methods of designing two-stage winner designs with survival outcomes. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056339


Columbia University

29. Tekle-Smith, Makeda Aislinn. Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development.

Degree: 2019, Columbia University

 In order to provide scalable, efficient and selective routes towards pharmaceutically relevant compounds, we have focused on improving the economical viability and practicality of strained-silane… (more)

Subjects/Keywords: Chemistry, Organic; Drug development; Lewis acids; Chemistry

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

APA (6th Edition):

Tekle-Smith, M. A. (2019). Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/d8-ypj5-jh11

Chicago Manual of Style (16th Edition):

Tekle-Smith, Makeda Aislinn. “Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development.” 2019. Doctoral Dissertation, Columbia University. Accessed September 23, 2019. https://doi.org/10.7916/d8-ypj5-jh11.

MLA Handbook (7th Edition):

Tekle-Smith, Makeda Aislinn. “Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development.” 2019. Web. 23 Sep 2019.

Vancouver:

Tekle-Smith MA. Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2019 Sep 23]. Available from: https://doi.org/10.7916/d8-ypj5-jh11.

Council of Science Editors:

Tekle-Smith MA. Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development. [Doctoral Dissertation]. Columbia University; 2019. Available from: https://doi.org/10.7916/d8-ypj5-jh11


Drexel University

30. Mendoza, Carlie Sunga. Purification and characterization of a Kaposi’s sarcoma-associated herpesvirus latency-associated nuclear antigen DNA-binding domain mutant.

Degree: 2018, Drexel University

Kaposi's sarcoma-associated herpesvirus (KSHV) infection is associated with three human malignancies: Kaposi’s sarcoma (KS), primary effusion lymphoma (PEL), and Multicentric Castleman’s disease (MCD). Latency-associated nuclear… (more)

Subjects/Keywords: Oncology; Cytology; Crystals – Structure; Herpesviruses; Drug development

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

APA (6th Edition):

Mendoza, C. S. (2018). Purification and characterization of a Kaposi’s sarcoma-associated herpesvirus latency-associated nuclear antigen DNA-binding domain mutant. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A7963

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):

Mendoza, Carlie Sunga. “Purification and characterization of a Kaposi’s sarcoma-associated herpesvirus latency-associated nuclear antigen DNA-binding domain mutant.” 2018. Thesis, Drexel University. Accessed September 23, 2019. https://idea.library.drexel.edu/islandora/object/idea%3A7963.

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

MLA Handbook (7th Edition):

Mendoza, Carlie Sunga. “Purification and characterization of a Kaposi’s sarcoma-associated herpesvirus latency-associated nuclear antigen DNA-binding domain mutant.” 2018. Web. 23 Sep 2019.

Vancouver:

Mendoza CS. Purification and characterization of a Kaposi’s sarcoma-associated herpesvirus latency-associated nuclear antigen DNA-binding domain mutant. [Internet] [Thesis]. Drexel University; 2018. [cited 2019 Sep 23]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A7963.

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

Council of Science Editors:

Mendoza CS. Purification and characterization of a Kaposi’s sarcoma-associated herpesvirus latency-associated nuclear antigen DNA-binding domain mutant. [Thesis]. Drexel University; 2018. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A7963

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

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