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You searched for subject:(Drug development). Showing records 1 – 30 of 469 total matches.

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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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Guo J. Rapid throughput solubility screening assay development and its applications in preformulation;. [Internet] [Doctoral dissertation]. University of Utah; 2007. [cited 2021 Jan 16]. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Ladell P. Isolation and characterization of antibiotics produced by the nematode symbiont Xenorhabdus szentirmaii. [Internet] [Thesis]. University of Wisconsin – La Cross; 2011. [cited 2021 Jan 16]. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Patra S. Development of RNAi-based genetic tools to silence MKP3 expression in a cell-specific manner. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Jan 16]. 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


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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Falcucci RM. Neuroprotective properties of novel positive allosteric modulators of EAAT2. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Jan 16]. 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. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


University of Georgia

8. Zheng, Bo. Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation.

Degree: 2014, University of Georgia

 Pharmacokinetics is the science dedicated to the study of rate processes such as absorption, distribution, metabolism, and excretion (ADME) of a drug and the multiple… (more)

Subjects/Keywords: Pharmacokinetics; Natural Product; Drug Development; Drug Discovery

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APA (6th Edition):

Zheng, B. (2014). Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/26206

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):

Zheng, Bo. “Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation.” 2014. Thesis, University of Georgia. Accessed January 16, 2021. http://hdl.handle.net/10724/26206.

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

MLA Handbook (7th Edition):

Zheng, Bo. “Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation.” 2014. Web. 16 Jan 2021.

Vancouver:

Zheng B. Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10724/26206.

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

Council of Science Editors:

Zheng B. Pharmacokinetic evaluation of investigational agents obtained from bioactive marine natural products, chemical synthesis and reformulation. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/26206

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


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 January 16, 2021. http://hdl.handle.net/1957/32743.

MLA Handbook (7th Edition):

Watts, K Shawn. “Steps toward structure-assisted drug design.” 2000. Web. 16 Jan 2021.

Vancouver:

Watts KS. Steps toward structure-assisted drug design. [Internet] [Masters thesis]. Oregon State University; 2000. [cited 2021 Jan 16]. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Wang, Yifan 1. Using multivariate analysis for pharmaceutical drug product development. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2021 Jan 16]. 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 January 16, 2021. http://hdl.handle.net/1887/28222.

MLA Handbook (7th Edition):

Visser, Samuel Jacob de. “A question based approach to drug development.” 2003. Web. 16 Jan 2021.

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 2021 Jan 16]. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


Vanderbilt University

14. Kilchrist, Kameron V. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.

Degree: PhD, Biomedical Engineering, 2019, Vanderbilt University

 Since the FDA approved the first recombinant protein 37 years ago, drug developers have harnessed biologics to treat human disease. Despite tremendous progress in extracellular… (more)

Subjects/Keywords: intracellular drug delivery; drug delivery; endosome disruption; assay development

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APA (6th Edition):

Kilchrist, K. V. (2019). New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15474

Chicago Manual of Style (16th Edition):

Kilchrist, Kameron V. “New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed January 16, 2021. http://hdl.handle.net/1803/15474.

MLA Handbook (7th Edition):

Kilchrist, Kameron V. “New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.” 2019. Web. 16 Jan 2021.

Vancouver:

Kilchrist KV. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1803/15474.

Council of Science Editors:

Kilchrist KV. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/15474


University of Vermont

15. Cornetta, Amanda Rose. Measurement of Changes in Heme Ruffling Caused by the Staphylococcus aureus Heme-Degrading Enzyme, IsdG.

Degree: Chemistry, 2019, University of Vermont

  Staphylococcus aureus is one of the most common causes of infection and has been rapidly developing drug resistance, making the discovery of a new… (more)

Subjects/Keywords: drug development; protein structure; mutagenesis; porphyrin complex; drug-resistance

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APA (6th Edition):

Cornetta, A. R. (2019). Measurement of Changes in Heme Ruffling Caused by the Staphylococcus aureus Heme-Degrading Enzyme, IsdG. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/hcoltheses/280

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):

Cornetta, Amanda Rose. “Measurement of Changes in Heme Ruffling Caused by the Staphylococcus aureus Heme-Degrading Enzyme, IsdG.” 2019. Thesis, University of Vermont. Accessed January 16, 2021. https://scholarworks.uvm.edu/hcoltheses/280.

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

MLA Handbook (7th Edition):

Cornetta, Amanda Rose. “Measurement of Changes in Heme Ruffling Caused by the Staphylococcus aureus Heme-Degrading Enzyme, IsdG.” 2019. Web. 16 Jan 2021.

Vancouver:

Cornetta AR. Measurement of Changes in Heme Ruffling Caused by the Staphylococcus aureus Heme-Degrading Enzyme, IsdG. [Internet] [Thesis]. University of Vermont; 2019. [cited 2021 Jan 16]. Available from: https://scholarworks.uvm.edu/hcoltheses/280.

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

Council of Science Editors:

Cornetta AR. Measurement of Changes in Heme Ruffling Caused by the Staphylococcus aureus Heme-Degrading Enzyme, IsdG. [Thesis]. University of Vermont; 2019. Available from: https://scholarworks.uvm.edu/hcoltheses/280

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


Princeton University

16. Tian, Chang. Therapeutic Nanocarriers for Enhanced Drug Delivery: from Laboratory-Scale Formulation to Clinical-Scale Production .

Degree: PhD, 2020, Princeton University

 This thesis describes studies in the development of therapeutic nanoparticles to achieve enhanced drug delivery, starting from formulation design to scale-up production and processing. Polymeric… (more)

Subjects/Keywords: drug delivery; drug development; Flash NanoPrecipitation; formulation; nanoparticle; scale-up

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APA (6th Edition):

Tian, C. (2020). Therapeutic Nanocarriers for Enhanced Drug Delivery: from Laboratory-Scale Formulation to Clinical-Scale Production . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01w6634668x

Chicago Manual of Style (16th Edition):

Tian, Chang. “Therapeutic Nanocarriers for Enhanced Drug Delivery: from Laboratory-Scale Formulation to Clinical-Scale Production .” 2020. Doctoral Dissertation, Princeton University. Accessed January 16, 2021. http://arks.princeton.edu/ark:/88435/dsp01w6634668x.

MLA Handbook (7th Edition):

Tian, Chang. “Therapeutic Nanocarriers for Enhanced Drug Delivery: from Laboratory-Scale Formulation to Clinical-Scale Production .” 2020. Web. 16 Jan 2021.

Vancouver:

Tian C. Therapeutic Nanocarriers for Enhanced Drug Delivery: from Laboratory-Scale Formulation to Clinical-Scale Production . [Internet] [Doctoral dissertation]. Princeton University; 2020. [cited 2021 Jan 16]. Available from: http://arks.princeton.edu/ark:/88435/dsp01w6634668x.

Council of Science Editors:

Tian C. Therapeutic Nanocarriers for Enhanced Drug Delivery: from Laboratory-Scale Formulation to Clinical-Scale Production . [Doctoral Dissertation]. Princeton University; 2020. Available from: http://arks.princeton.edu/ark:/88435/dsp01w6634668x


University of Arizona

17. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Smith BE. Small Molecule Approaches Toward Therapeutics for Alzheimer's Disease and Colon Cancer . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2021 Jan 16]. 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


Rhodes University

18. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


Drexel University

19. 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 (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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


University of Wollongong

20. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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


Oregon State University

21. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Mandrell D. Automated manipulation of zebrafish embryos for high-throughput toxicology screening of nanomaterials. [Internet] [Masters thesis]. Oregon State University; 2010. [cited 2021 Jan 16]. 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


University of Debrecen

22. 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 January 16, 2021. 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. 16 Jan 2021.

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 2021 Jan 16]. 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.


Columbia University

23. 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 (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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Tekle-Smith MA. Synthetic Innovations Towards the Total Synthesis of Natural Product Derivatives for Drug Development. [Internet] [Doctoral dissertation]. Columbia University; 2019. [cited 2021 Jan 16]. 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


University of Surrey

24. Howe, Katharine. Impact of drug transporter expression on in vitro cellular assays.

Degree: PhD, 2008, University of Surrey

 Membrane transporters are essential for the transfer of hydrophobic molecules across the plasma membrane of cells; therefore active and facilitated transport processes can determine the… (more)

Subjects/Keywords: 615.19; Drug development

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APA (6th Edition):

Howe, K. (2008). Impact of drug transporter expression on in vitro cellular assays. (Doctoral Dissertation). University of Surrey. Retrieved from http://epubs.surrey.ac.uk/855530/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493131

Chicago Manual of Style (16th Edition):

Howe, Katharine. “Impact of drug transporter expression on in vitro cellular assays.” 2008. Doctoral Dissertation, University of Surrey. Accessed January 16, 2021. http://epubs.surrey.ac.uk/855530/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493131.

MLA Handbook (7th Edition):

Howe, Katharine. “Impact of drug transporter expression on in vitro cellular assays.” 2008. Web. 16 Jan 2021.

Vancouver:

Howe K. Impact of drug transporter expression on in vitro cellular assays. [Internet] [Doctoral dissertation]. University of Surrey; 2008. [cited 2021 Jan 16]. Available from: http://epubs.surrey.ac.uk/855530/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493131.

Council of Science Editors:

Howe K. Impact of drug transporter expression on in vitro cellular assays. [Doctoral Dissertation]. University of Surrey; 2008. Available from: http://epubs.surrey.ac.uk/855530/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.493131

25. NC DOCKS at The University of North Carolina at Greensboro; Norris, Lorraine Malek. Approaches towards the biomimetic synthesis of 9-hydroxypinoresinol analogs: a stepping point in the development of a new anti-seizure drug.

Degree: 2013, NC Docks

 A recently isolated natural compound, Petaslignolide A, from the leaves of Petasites japonicas, has shown to be an effective neuroprotecting agent because of its antioxidant… (more)

Subjects/Keywords: Petasites $x Therapeutic use; Drug development

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APA (6th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Norris, L. M. (2013). Approaches towards the biomimetic synthesis of 9-hydroxypinoresinol analogs: a stepping point in the development of a new anti-seizure drug. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Norris_uncg_0154M_11229.pdf

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):

NC DOCKS at The University of North Carolina at Greensboro; Norris, Lorraine Malek. “Approaches towards the biomimetic synthesis of 9-hydroxypinoresinol analogs: a stepping point in the development of a new anti-seizure drug.” 2013. Thesis, NC Docks. Accessed January 16, 2021. http://libres.uncg.edu/ir/uncg/f/Norris_uncg_0154M_11229.pdf.

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

MLA Handbook (7th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Norris, Lorraine Malek. “Approaches towards the biomimetic synthesis of 9-hydroxypinoresinol analogs: a stepping point in the development of a new anti-seizure drug.” 2013. Web. 16 Jan 2021.

Vancouver:

NC DOCKS at The University of North Carolina at Greensboro; Norris LM. Approaches towards the biomimetic synthesis of 9-hydroxypinoresinol analogs: a stepping point in the development of a new anti-seizure drug. [Internet] [Thesis]. NC Docks; 2013. [cited 2021 Jan 16]. Available from: http://libres.uncg.edu/ir/uncg/f/Norris_uncg_0154M_11229.pdf.

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

Council of Science Editors:

NC DOCKS at The University of North Carolina at Greensboro; Norris LM. Approaches towards the biomimetic synthesis of 9-hydroxypinoresinol analogs: a stepping point in the development of a new anti-seizure drug. [Thesis]. NC Docks; 2013. Available from: http://libres.uncg.edu/ir/uncg/f/Norris_uncg_0154M_11229.pdf

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


University of Southern California

26. 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/1949

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 January 16, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/444768/rec/1949.

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. 16 Jan 2021.

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 2021 Jan 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/444768/rec/1949.

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/1949


University of Sydney

27. 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 January 16, 2021. 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. 16 Jan 2021.

Vancouver:

Dinarvand M. Discovery and development of novel antibacterials from natural products . [Internet] [Thesis]. University of Sydney; 2017. [cited 2021 Jan 16]. 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

28. NC DOCKS at The University of North Carolina at Greensboro; Strader, Cherilyn R. Fingolimod (Gilenya; FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite and the creation of a natural products pure compound database and organized storage system.

Degree: 2012, NC Docks

 Fingolimod (Gilenya; FTY720), a synthetic compound based on the fungal secondary metabolite, myriocin (ISP-I), is a potent immunosuppressant that was approved in September 2010 by… (more)

Subjects/Keywords: Multiple Sclerosis $x Treatment; Cheminformatics; Drug development

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APA (6th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Strader, C. R. (2012). Fingolimod (Gilenya; FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite and the creation of a natural products pure compound database and organized storage system. (Thesis). NC Docks. Retrieved from http://libres.uncg.edu/ir/uncg/f/Strader_uncg_0154M_10938.pdf

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):

NC DOCKS at The University of North Carolina at Greensboro; Strader, Cherilyn R. “Fingolimod (Gilenya; FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite and the creation of a natural products pure compound database and organized storage system.” 2012. Thesis, NC Docks. Accessed January 16, 2021. http://libres.uncg.edu/ir/uncg/f/Strader_uncg_0154M_10938.pdf.

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

MLA Handbook (7th Edition):

NC DOCKS at The University of North Carolina at Greensboro; Strader, Cherilyn R. “Fingolimod (Gilenya; FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite and the creation of a natural products pure compound database and organized storage system.” 2012. Web. 16 Jan 2021.

Vancouver:

NC DOCKS at The University of North Carolina at Greensboro; Strader CR. Fingolimod (Gilenya; FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite and the creation of a natural products pure compound database and organized storage system. [Internet] [Thesis]. NC Docks; 2012. [cited 2021 Jan 16]. Available from: http://libres.uncg.edu/ir/uncg/f/Strader_uncg_0154M_10938.pdf.

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

Council of Science Editors:

NC DOCKS at The University of North Carolina at Greensboro; Strader CR. Fingolimod (Gilenya; FTY720): a recently approved multiple sclerosis drug based on a fungal secondary metabolite and the creation of a natural products pure compound database and organized storage system. [Thesis]. NC Docks; 2012. Available from: http://libres.uncg.edu/ir/uncg/f/Strader_uncg_0154M_10938.pdf

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


Rhodes University

29. Adendorff, Matthew Ralph. Marine anti-malarial isonitriles : a synthetic and computational study.

Degree: MS, Faculty of Science, Chemistry, 2010, Rhodes University

 The development of Plasmodium falciparum malarial resistance to the current armoury of anti-malarial drugs requires the development of new treatments to help combat this disease.… (more)

Subjects/Keywords: Isocyanides; Isocyanates; Marine pharmacology; Antimalarials; Antimalarials  – Development; Drug development

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

APA (6th Edition):

Adendorff, M. R. (2010). Marine anti-malarial isonitriles : a synthetic and computational study. (Masters Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1006674

Chicago Manual of Style (16th Edition):

Adendorff, Matthew Ralph. “Marine anti-malarial isonitriles : a synthetic and computational study.” 2010. Masters Thesis, Rhodes University. Accessed January 16, 2021. http://hdl.handle.net/10962/d1006674.

MLA Handbook (7th Edition):

Adendorff, Matthew Ralph. “Marine anti-malarial isonitriles : a synthetic and computational study.” 2010. Web. 16 Jan 2021.

Vancouver:

Adendorff MR. Marine anti-malarial isonitriles : a synthetic and computational study. [Internet] [Masters thesis]. Rhodes University; 2010. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10962/d1006674.

Council of Science Editors:

Adendorff MR. Marine anti-malarial isonitriles : a synthetic and computational study. [Masters Thesis]. Rhodes University; 2010. Available from: http://hdl.handle.net/10962/d1006674


Rhodes University

30. Conibear, Anne Claire. Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials.

Degree: Faculty of Science, Chemistry, 2013, Rhodes University

Malaria continues to be an enormous health-threat in the developing world and the emergence of drug resistance has further compounded the problem. The parasite-specific enzyme,… (more)

Subjects/Keywords: Antimalarials  – Development; Malaria  – Chemotherapy; Drug development; Enzyme kinetics; Phosphate esters

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

APA (6th Edition):

Conibear, A. C. (2013). Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1008282

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):

Conibear, Anne Claire. “Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials.” 2013. Thesis, Rhodes University. Accessed January 16, 2021. http://hdl.handle.net/10962/d1008282.

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

MLA Handbook (7th Edition):

Conibear, Anne Claire. “Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials.” 2013. Web. 16 Jan 2021.

Vancouver:

Conibear AC. Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials. [Internet] [Thesis]. Rhodes University; 2013. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10962/d1008282.

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

Council of Science Editors:

Conibear AC. Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1008282

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

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