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You searched for subject:(Drug Design). Showing records 1 – 30 of 856 total matches.

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University of KwaZulu-Natal

1. Khoza, Leon Joseph. Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain.

Degree: 2020, University of KwaZulu-Natal

 Mental disorders contribute to 13% of the global burden of disease. With major depressive disorder (MDD) expected to be the most significant contributor by 2030,… (more)

Subjects/Keywords: Ketamine.; Drug design.; Drug interaction.; Drug delivery.

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APA (6th Edition):

Khoza, L. J. (2020). Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/19171

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):

Khoza, Leon Joseph. “Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain.” 2020. Thesis, University of KwaZulu-Natal. Accessed April 11, 2021. https://researchspace.ukzn.ac.za/handle/10413/19171.

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

MLA Handbook (7th Edition):

Khoza, Leon Joseph. “Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain.” 2020. Web. 11 Apr 2021.

Vancouver:

Khoza LJ. Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain. [Internet] [Thesis]. University of KwaZulu-Natal; 2020. [cited 2021 Apr 11]. Available from: https://researchspace.ukzn.ac.za/handle/10413/19171.

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

Council of Science Editors:

Khoza LJ. Evaluation of the pharmacodynamic effects of Ketamine on neurotransmitter levels and CREB/BDNF expression in rat brain. [Thesis]. University of KwaZulu-Natal; 2020. Available from: https://researchspace.ukzn.ac.za/handle/10413/19171

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


Drexel University

2. 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 April 11, 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. 11 Apr 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 Apr 11]. 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

3. 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 April 11, 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. 11 Apr 2021.

Vancouver:

Falcucci RM. Neuroprotective properties of novel positive allosteric modulators of EAAT2. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Apr 11]. 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

4. 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 April 11, 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. 11 Apr 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 Apr 11]. 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 Sydney

5. Lin, Hsuan-Yu. The use of computer-aided drug design in small molecule drug discovery .

Degree: 2018, University of Sydney

Drug discovery is one of the most challenging research fields that contributes to the birth of novel drugs for therapeutic use. Due to the complexity… (more)

Subjects/Keywords: computer-aided drug design; drug discovery

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APA (6th Edition):

Lin, H. (2018). The use of computer-aided drug design in small molecule drug discovery . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20236

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):

Lin, Hsuan-Yu. “The use of computer-aided drug design in small molecule drug discovery .” 2018. Thesis, University of Sydney. Accessed April 11, 2021. http://hdl.handle.net/2123/20236.

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

MLA Handbook (7th Edition):

Lin, Hsuan-Yu. “The use of computer-aided drug design in small molecule drug discovery .” 2018. Web. 11 Apr 2021.

Vancouver:

Lin H. The use of computer-aided drug design in small molecule drug discovery . [Internet] [Thesis]. University of Sydney; 2018. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2123/20236.

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

Council of Science Editors:

Lin H. The use of computer-aided drug design in small molecule drug discovery . [Thesis]. University of Sydney; 2018. Available from: http://hdl.handle.net/2123/20236

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


Vanderbilt University

6. Butkiewicz, Mariusz. Advancing Quantitative Structure Activity Relationship Strategies in Ligand-Based Computer-Aided Drug Design.

Degree: PhD, Chemistry, 2014, Vanderbilt University

 Quantitative structure activity relationship (QSAR) modeling using high-throughput screening (HTS) data enables the development of predictive models for in silico screening. A cheminformatics framework termed… (more)

Subjects/Keywords: computer-aided drug design; QSAR

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APA (6th Edition):

Butkiewicz, M. (2014). Advancing Quantitative Structure Activity Relationship Strategies in Ligand-Based Computer-Aided Drug Design. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13619

Chicago Manual of Style (16th Edition):

Butkiewicz, Mariusz. “Advancing Quantitative Structure Activity Relationship Strategies in Ligand-Based Computer-Aided Drug Design.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed April 11, 2021. http://hdl.handle.net/1803/13619.

MLA Handbook (7th Edition):

Butkiewicz, Mariusz. “Advancing Quantitative Structure Activity Relationship Strategies in Ligand-Based Computer-Aided Drug Design.” 2014. Web. 11 Apr 2021.

Vancouver:

Butkiewicz M. Advancing Quantitative Structure Activity Relationship Strategies in Ligand-Based Computer-Aided Drug Design. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1803/13619.

Council of Science Editors:

Butkiewicz M. Advancing Quantitative Structure Activity Relationship Strategies in Ligand-Based Computer-Aided Drug Design. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/13619

7. Duffell, Katie Melissa. Design and characterisation of tool inhibitors of DNA damage response proteins.

Degree: PhD, 2018, University of Sussex

 As a result of the high cost of drug discovery, it is imperative that promising targets with strong disease association are identified and validated before… (more)

Subjects/Keywords: 540; RS0420 Drug design

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APA (6th Edition):

Duffell, K. M. (2018). Design and characterisation of tool inhibitors of DNA damage response proteins. (Doctoral Dissertation). University of Sussex. Retrieved from http://sro.sussex.ac.uk/id/eprint/75256/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742140

Chicago Manual of Style (16th Edition):

Duffell, Katie Melissa. “Design and characterisation of tool inhibitors of DNA damage response proteins.” 2018. Doctoral Dissertation, University of Sussex. Accessed April 11, 2021. http://sro.sussex.ac.uk/id/eprint/75256/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742140.

MLA Handbook (7th Edition):

Duffell, Katie Melissa. “Design and characterisation of tool inhibitors of DNA damage response proteins.” 2018. Web. 11 Apr 2021.

Vancouver:

Duffell KM. Design and characterisation of tool inhibitors of DNA damage response proteins. [Internet] [Doctoral dissertation]. University of Sussex; 2018. [cited 2021 Apr 11]. Available from: http://sro.sussex.ac.uk/id/eprint/75256/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742140.

Council of Science Editors:

Duffell KM. Design and characterisation of tool inhibitors of DNA damage response proteins. [Doctoral Dissertation]. University of Sussex; 2018. Available from: http://sro.sussex.ac.uk/id/eprint/75256/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742140

8. Kundu, Preeti. Inhibition and reaction mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase: A potential target for novel drug design.

Degree: 2020, Victoria University of Wellington; Victoria University of Wellington

 Tuberculosis (TB), which is estimated to affect 2 billion individuals worldwide, is an infection predominately caused by Mycobacterium tuberculosis(M. tuberculosis). Of particular concern is the… (more)

Subjects/Keywords: inhibition; reaction mechanism; drug design

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APA (6th Edition):

Kundu, P. (2020). Inhibition and reaction mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase: A potential target for novel drug design. (Doctoral Dissertation). Victoria University of Wellington; Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8945

Chicago Manual of Style (16th Edition):

Kundu, Preeti. “Inhibition and reaction mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase: A potential target for novel drug design.” 2020. Doctoral Dissertation, Victoria University of Wellington; Victoria University of Wellington. Accessed April 11, 2021. http://hdl.handle.net/10063/8945.

MLA Handbook (7th Edition):

Kundu, Preeti. “Inhibition and reaction mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase: A potential target for novel drug design.” 2020. Web. 11 Apr 2021.

Vancouver:

Kundu P. Inhibition and reaction mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase: A potential target for novel drug design. [Internet] [Doctoral dissertation]. Victoria University of Wellington; Victoria University of Wellington; 2020. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/10063/8945.

Council of Science Editors:

Kundu P. Inhibition and reaction mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase: A potential target for novel drug design. [Doctoral Dissertation]. Victoria University of Wellington; Victoria University of Wellington; 2020. Available from: http://hdl.handle.net/10063/8945


Duquesne University

9. Zhou, Xilin. Synthesis of Bicyclic Thieno[2,3-d]Pyrimidines, Tricyclic Thieno[2,3-d]Pyrimidines and Thieno[3,2-d]Pyrimidines as Classical and Nonclassical Antifolates.

Degree: MS, Medicinal Chemistry, 2012, Duquesne University

 An introduction, background and research progress in the areas of antifolates and antimitotic agents has been reviewed and discussed. Thymidylate synthase (TS), dihydrofolate reductase (DHFR)… (more)

Subjects/Keywords: Antifolate; Drug design; SAR

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APA (6th Edition):

Zhou, X. (2012). Synthesis of Bicyclic Thieno[2,3-d]Pyrimidines, Tricyclic Thieno[2,3-d]Pyrimidines and Thieno[3,2-d]Pyrimidines as Classical and Nonclassical Antifolates. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1413

Chicago Manual of Style (16th Edition):

Zhou, Xilin. “Synthesis of Bicyclic Thieno[2,3-d]Pyrimidines, Tricyclic Thieno[2,3-d]Pyrimidines and Thieno[3,2-d]Pyrimidines as Classical and Nonclassical Antifolates.” 2012. Masters Thesis, Duquesne University. Accessed April 11, 2021. https://dsc.duq.edu/etd/1413.

MLA Handbook (7th Edition):

Zhou, Xilin. “Synthesis of Bicyclic Thieno[2,3-d]Pyrimidines, Tricyclic Thieno[2,3-d]Pyrimidines and Thieno[3,2-d]Pyrimidines as Classical and Nonclassical Antifolates.” 2012. Web. 11 Apr 2021.

Vancouver:

Zhou X. Synthesis of Bicyclic Thieno[2,3-d]Pyrimidines, Tricyclic Thieno[2,3-d]Pyrimidines and Thieno[3,2-d]Pyrimidines as Classical and Nonclassical Antifolates. [Internet] [Masters thesis]. Duquesne University; 2012. [cited 2021 Apr 11]. Available from: https://dsc.duq.edu/etd/1413.

Council of Science Editors:

Zhou X. Synthesis of Bicyclic Thieno[2,3-d]Pyrimidines, Tricyclic Thieno[2,3-d]Pyrimidines and Thieno[3,2-d]Pyrimidines as Classical and Nonclassical Antifolates. [Masters Thesis]. Duquesne University; 2012. Available from: https://dsc.duq.edu/etd/1413


University of Oxford

10. Boyles, Fergus. Developing novel scoring functions for protein-ligand docking using machine learning.

Degree: PhD, 2020, University of Oxford

 Structure-based drug discovery uses information about the structure of a protein to identify novel ligands that bind to the protein. The fundamental problem in structure-based… (more)

Subjects/Keywords: Computer Aided Drug Design

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APA (6th Edition):

Boyles, F. (2020). Developing novel scoring functions for protein-ligand docking using machine learning. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:2255ad26-71dd-4470-a13d-e4f30e8a4a6a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.813607

Chicago Manual of Style (16th Edition):

Boyles, Fergus. “Developing novel scoring functions for protein-ligand docking using machine learning.” 2020. Doctoral Dissertation, University of Oxford. Accessed April 11, 2021. http://ora.ox.ac.uk/objects/uuid:2255ad26-71dd-4470-a13d-e4f30e8a4a6a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.813607.

MLA Handbook (7th Edition):

Boyles, Fergus. “Developing novel scoring functions for protein-ligand docking using machine learning.” 2020. Web. 11 Apr 2021.

Vancouver:

Boyles F. Developing novel scoring functions for protein-ligand docking using machine learning. [Internet] [Doctoral dissertation]. University of Oxford; 2020. [cited 2021 Apr 11]. Available from: http://ora.ox.ac.uk/objects/uuid:2255ad26-71dd-4470-a13d-e4f30e8a4a6a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.813607.

Council of Science Editors:

Boyles F. Developing novel scoring functions for protein-ligand docking using machine learning. [Doctoral Dissertation]. University of Oxford; 2020. Available from: http://ora.ox.ac.uk/objects/uuid:2255ad26-71dd-4470-a13d-e4f30e8a4a6a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.813607


University of KwaZulu-Natal

11. Gill, Atal Anudeep Singh. Synthesis, characterization and application of novel composite nano-materials for the electrochemical detection of MRSA and related drugs.

Degree: 2020, University of KwaZulu-Natal

 This thesis reports the development of electroanalytical methods applicable for detection of MRSA and selected antibacterial drugs; vancomycin and ciprofloxacin. The detection techniques used to… (more)

Subjects/Keywords: Nanomaterials - drug delivery.; Antibacterial drugs - drug design.; Antibiotics - drug delivery.; Antimicrobial resistance - drug development.

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APA (6th Edition):

Gill, A. A. S. (2020). Synthesis, characterization and application of novel composite nano-materials for the electrochemical detection of MRSA and related drugs. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/19004

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):

Gill, Atal Anudeep Singh. “Synthesis, characterization and application of novel composite nano-materials for the electrochemical detection of MRSA and related drugs.” 2020. Thesis, University of KwaZulu-Natal. Accessed April 11, 2021. https://researchspace.ukzn.ac.za/handle/10413/19004.

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

MLA Handbook (7th Edition):

Gill, Atal Anudeep Singh. “Synthesis, characterization and application of novel composite nano-materials for the electrochemical detection of MRSA and related drugs.” 2020. Web. 11 Apr 2021.

Vancouver:

Gill AAS. Synthesis, characterization and application of novel composite nano-materials for the electrochemical detection of MRSA and related drugs. [Internet] [Thesis]. University of KwaZulu-Natal; 2020. [cited 2021 Apr 11]. Available from: https://researchspace.ukzn.ac.za/handle/10413/19004.

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

Council of Science Editors:

Gill AAS. Synthesis, characterization and application of novel composite nano-materials for the electrochemical detection of MRSA and related drugs. [Thesis]. University of KwaZulu-Natal; 2020. Available from: https://researchspace.ukzn.ac.za/handle/10413/19004

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

12. Skarbek, Charles. Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer.

Degree: Docteur es, Pharmacotechnie et biopharmacie, 2017, Université Paris-Saclay (ComUE)

L’ifosfamide (IFO) et le cyclophosphamide (CPM) sont des oxazaphosphorines, prodrogues nécessitant une bioactivation pour être actif. Dans le cas de l’IFO, sa biotransformation conduit à… (more)

Subjects/Keywords: Nanoparticules; Drug design; Ciblage; Nanoparticle; Drug design; Targeting

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APA (6th Edition):

Skarbek, C. (2017). Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2017SACLS247

Chicago Manual of Style (16th Edition):

Skarbek, Charles. “Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer.” 2017. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 11, 2021. http://www.theses.fr/2017SACLS247.

MLA Handbook (7th Edition):

Skarbek, Charles. “Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer.” 2017. Web. 11 Apr 2021.

Vancouver:

Skarbek C. Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2017. [cited 2021 Apr 11]. Available from: http://www.theses.fr/2017SACLS247.

Council of Science Editors:

Skarbek C. Synthèse et évaluation pharmacologique d’analogues préactivés de l’ifosfamide : prodrogues et nanoparticules à visée antitumorale : Synthesis and pharmacological evaluation of preactivated ifosfamide analogs : prodrugs and nanoparticles designed against cancer. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2017. Available from: http://www.theses.fr/2017SACLS247


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 April 11, 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. 11 Apr 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 Apr 11]. 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 Kentucky

14. Hou, Shurong. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.

Degree: 2014, University of Kentucky

 Cocaine is one of the most reinforcing drugs of abuse and has caused serious medical and social problems. There is no FDA-approved medication specific for… (more)

Subjects/Keywords: Protein drug; enzyme therapy; human butyrylcholinesterase; cocaine; drug abuse treatment; Pharmaceutics and Drug Design

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APA (6th Edition):

Hou, S. (2014). HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/38

Chicago Manual of Style (16th Edition):

Hou, Shurong. “HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.” 2014. Doctoral Dissertation, University of Kentucky. Accessed April 11, 2021. https://uknowledge.uky.edu/pharmacy_etds/38.

MLA Handbook (7th Edition):

Hou, Shurong. “HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION.” 2014. Web. 11 Apr 2021.

Vancouver:

Hou S. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2014. [cited 2021 Apr 11]. Available from: https://uknowledge.uky.edu/pharmacy_etds/38.

Council of Science Editors:

Hou S. HUMAN BUTYRYLCHOLINESTERASE MUTANTS FOR COCAINE DETOXIFICATION. [Doctoral Dissertation]. University of Kentucky; 2014. Available from: https://uknowledge.uky.edu/pharmacy_etds/38


Vanderbilt University

15. Sun, Qi. Discovery of K-Ras inhibitors for the treatment of cancer.

Degree: PhD, Biochemistry, 2015, Vanderbilt University

 Ras is a small GTPase that functions as a molecular switch, cycling between inactive (GDP-bound) and active (GTP-bound) states. Mutations in Ras fix the protein… (more)

Subjects/Keywords: Cancer; K-Ras; Fragment-based drug discovery; Structural-based drug design

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APA (6th Edition):

Sun, Q. (2015). Discovery of K-Ras inhibitors for the treatment of cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11334

Chicago Manual of Style (16th Edition):

Sun, Qi. “Discovery of K-Ras inhibitors for the treatment of cancer.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed April 11, 2021. http://hdl.handle.net/1803/11334.

MLA Handbook (7th Edition):

Sun, Qi. “Discovery of K-Ras inhibitors for the treatment of cancer.” 2015. Web. 11 Apr 2021.

Vancouver:

Sun Q. Discovery of K-Ras inhibitors for the treatment of cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1803/11334.

Council of Science Editors:

Sun Q. Discovery of K-Ras inhibitors for the treatment of cancer. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/11334


University of KwaZulu-Natal

16. Ndagi, Umar. Insight into cancer targets and ligand binding landscape using bioinformatics and integrated molecular modeling tools.

Degree: 2017, University of KwaZulu-Natal

 The alarming rate of varying types of cancer diseases in human remains a global burden requiring drastic treatment in which, a prominent method of combating… (more)

Subjects/Keywords: Breast cancer.; Prostate cancer.; Cancer.; Drug design.; Ligands.; Drug resistance.; Bioinformatics.

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APA (6th Edition):

Ndagi, U. (2017). Insight into cancer targets and ligand binding landscape using bioinformatics and integrated molecular modeling tools. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/18521

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):

Ndagi, Umar. “Insight into cancer targets and ligand binding landscape using bioinformatics and integrated molecular modeling tools.” 2017. Thesis, University of KwaZulu-Natal. Accessed April 11, 2021. https://researchspace.ukzn.ac.za/handle/10413/18521.

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

MLA Handbook (7th Edition):

Ndagi, Umar. “Insight into cancer targets and ligand binding landscape using bioinformatics and integrated molecular modeling tools.” 2017. Web. 11 Apr 2021.

Vancouver:

Ndagi U. Insight into cancer targets and ligand binding landscape using bioinformatics and integrated molecular modeling tools. [Internet] [Thesis]. University of KwaZulu-Natal; 2017. [cited 2021 Apr 11]. Available from: https://researchspace.ukzn.ac.za/handle/10413/18521.

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

Council of Science Editors:

Ndagi U. Insight into cancer targets and ligand binding landscape using bioinformatics and integrated molecular modeling tools. [Thesis]. University of KwaZulu-Natal; 2017. Available from: https://researchspace.ukzn.ac.za/handle/10413/18521

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


University of Cambridge

17. Chee, Xavier. Rational Development of New Inhibitors of Lipoteichoic Acid Synthase.

Degree: PhD, 2017, University of Cambridge

 Staphyloccocus aureus is an opportunisitic pathogen that causes soft skin and tissue infections (SSTI) such as endocarditis, osteomyelitis and meningitis. In recent years, the re-emergence… (more)

Subjects/Keywords: Virtual screening; Drug discovery; Antibiotics; Antimicrobial resistance; Computational drug design

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APA (6th Edition):

Chee, X. (2017). Rational Development of New Inhibitors of Lipoteichoic Acid Synthase. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/269766

Chicago Manual of Style (16th Edition):

Chee, Xavier. “Rational Development of New Inhibitors of Lipoteichoic Acid Synthase.” 2017. Doctoral Dissertation, University of Cambridge. Accessed April 11, 2021. https://www.repository.cam.ac.uk/handle/1810/269766.

MLA Handbook (7th Edition):

Chee, Xavier. “Rational Development of New Inhibitors of Lipoteichoic Acid Synthase.” 2017. Web. 11 Apr 2021.

Vancouver:

Chee X. Rational Development of New Inhibitors of Lipoteichoic Acid Synthase. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2021 Apr 11]. Available from: https://www.repository.cam.ac.uk/handle/1810/269766.

Council of Science Editors:

Chee X. Rational Development of New Inhibitors of Lipoteichoic Acid Synthase. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/269766


Eastern Michigan University

18. Weerakoon, Darshani Avanthi. Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1.

Degree: MS, Chemistry, 2014, Eastern Michigan University

  Plasminogen activator inhibitor type-1 (PAI-1) is a member of the serine protease inhibitor (serpin) superfamily. Excessive levels of PAI-1 inhibit urokinase-type plasminogen activator (uPA)… (more)

Subjects/Keywords: Drug design; Drug synthesis; Isatin; Oxindole; PAI-1; Small molecules; Chemistry

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APA (6th Edition):

Weerakoon, D. A. (2014). Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1. (Masters Thesis). Eastern Michigan University. Retrieved from https://commons.emich.edu/theses/705

Chicago Manual of Style (16th Edition):

Weerakoon, Darshani Avanthi. “Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1.” 2014. Masters Thesis, Eastern Michigan University. Accessed April 11, 2021. https://commons.emich.edu/theses/705.

MLA Handbook (7th Edition):

Weerakoon, Darshani Avanthi. “Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1.” 2014. Web. 11 Apr 2021.

Vancouver:

Weerakoon DA. Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1. [Internet] [Masters thesis]. Eastern Michigan University; 2014. [cited 2021 Apr 11]. Available from: https://commons.emich.edu/theses/705.

Council of Science Editors:

Weerakoon DA. Design, synthesis and evaluation of small molecules as inhibitors of plasminogen activator inhibitor-1. [Masters Thesis]. Eastern Michigan University; 2014. Available from: https://commons.emich.edu/theses/705


University of KwaZulu-Natal

19. Shunmugam, Letitia. In silico investigation of hepatitis c virus: a novel perspective into targeted viral inhibition of NS3 helicase, NS 3/4a protease and NS5b RNA dependent RNA polymerase.

Degree: 2019, University of KwaZulu-Natal

 Hepatitis C Virus (HCV) is an escalating global healthcare and economic burden that requires extensive intervention to alleviate its control. Over the years, drug design(more)

Subjects/Keywords: Hepatitis C virus - drug design.; Hepatitis C virus - drug delivery.

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APA (6th Edition):

Shunmugam, L. (2019). In silico investigation of hepatitis c virus: a novel perspective into targeted viral inhibition of NS3 helicase, NS 3/4a protease and NS5b RNA dependent RNA polymerase. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/16623

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):

Shunmugam, Letitia. “In silico investigation of hepatitis c virus: a novel perspective into targeted viral inhibition of NS3 helicase, NS 3/4a protease and NS5b RNA dependent RNA polymerase.” 2019. Thesis, University of KwaZulu-Natal. Accessed April 11, 2021. https://researchspace.ukzn.ac.za/handle/10413/16623.

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

MLA Handbook (7th Edition):

Shunmugam, Letitia. “In silico investigation of hepatitis c virus: a novel perspective into targeted viral inhibition of NS3 helicase, NS 3/4a protease and NS5b RNA dependent RNA polymerase.” 2019. Web. 11 Apr 2021.

Vancouver:

Shunmugam L. In silico investigation of hepatitis c virus: a novel perspective into targeted viral inhibition of NS3 helicase, NS 3/4a protease and NS5b RNA dependent RNA polymerase. [Internet] [Thesis]. University of KwaZulu-Natal; 2019. [cited 2021 Apr 11]. Available from: https://researchspace.ukzn.ac.za/handle/10413/16623.

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

Council of Science Editors:

Shunmugam L. In silico investigation of hepatitis c virus: a novel perspective into targeted viral inhibition of NS3 helicase, NS 3/4a protease and NS5b RNA dependent RNA polymerase. [Thesis]. University of KwaZulu-Natal; 2019. Available from: https://researchspace.ukzn.ac.za/handle/10413/16623

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


University of Arizona

20. 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 April 11, 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. 11 Apr 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 Apr 11]. 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

21. Ståhl, Elin. Drug prevention in large companies .

Degree: Chalmers tekniska högskola / Institutionen för industri- och materialvetenskap, 2020, Chalmers University of Technology

 Eyescanner was a newly founded startup with the vision to develop a new solution for drug testing through scanning of pupil reactions and eye movements.… (more)

Subjects/Keywords: Drug prevention, Work environment, Service blueprint, Enterprise; design, Eyescanner, Drug test

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APA (6th Edition):

Ståhl, E. (2020). Drug prevention in large companies . (Thesis). Chalmers University of Technology. Retrieved from http://hdl.handle.net/20.500.12380/301089

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):

Ståhl, Elin. “Drug prevention in large companies .” 2020. Thesis, Chalmers University of Technology. Accessed April 11, 2021. http://hdl.handle.net/20.500.12380/301089.

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

MLA Handbook (7th Edition):

Ståhl, Elin. “Drug prevention in large companies .” 2020. Web. 11 Apr 2021.

Vancouver:

Ståhl E. Drug prevention in large companies . [Internet] [Thesis]. Chalmers University of Technology; 2020. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/20.500.12380/301089.

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

Council of Science Editors:

Ståhl E. Drug prevention in large companies . [Thesis]. Chalmers University of Technology; 2020. Available from: http://hdl.handle.net/20.500.12380/301089

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


Dalhousie University

22. Ward, Sarah. The Development of Exogenous Anticonvulsants and Endogenous Uracil-Based Antiepileptic Agents.

Degree: MS, Department of Chemistry, 2011, Dalhousie University

 Epilepsy is a common neurological disorder for which the development of new and improved therapies is essential. Thus, the central theme of this thesis pertains… (more)

Subjects/Keywords: Epilepsy; drug design; anticonvulsant; antiepileptogenic; uracil

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APA (6th Edition):

Ward, S. (2011). The Development of Exogenous Anticonvulsants and Endogenous Uracil-Based Antiepileptic Agents. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14244

Chicago Manual of Style (16th Edition):

Ward, Sarah. “The Development of Exogenous Anticonvulsants and Endogenous Uracil-Based Antiepileptic Agents.” 2011. Masters Thesis, Dalhousie University. Accessed April 11, 2021. http://hdl.handle.net/10222/14244.

MLA Handbook (7th Edition):

Ward, Sarah. “The Development of Exogenous Anticonvulsants and Endogenous Uracil-Based Antiepileptic Agents.” 2011. Web. 11 Apr 2021.

Vancouver:

Ward S. The Development of Exogenous Anticonvulsants and Endogenous Uracil-Based Antiepileptic Agents. [Internet] [Masters thesis]. Dalhousie University; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/10222/14244.

Council of Science Editors:

Ward S. The Development of Exogenous Anticonvulsants and Endogenous Uracil-Based Antiepileptic Agents. [Masters Thesis]. Dalhousie University; 2011. Available from: http://hdl.handle.net/10222/14244


University of Utah

23. Simeone, Timothy A. Regulation of allosteric modulation of GABAa receptor function: interaction between recombininant GABAa receptors and the novel anticonvulsant drug topiramate.

Degree: PhD, Neurology;, 2003, University of Utah

 GABA [A] receptors are the main source of fast inhibitory synaptic transmission in the brain, and are therefore of great interest as a target of… (more)

Subjects/Keywords: Pharmacokinetics; Drug Design

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APA (6th Edition):

Simeone, T. A. (2003). Regulation of allosteric modulation of GABAa receptor function: interaction between recombininant GABAa receptors and the novel anticonvulsant drug topiramate. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1738/rec/964

Chicago Manual of Style (16th Edition):

Simeone, Timothy A. “Regulation of allosteric modulation of GABAa receptor function: interaction between recombininant GABAa receptors and the novel anticonvulsant drug topiramate.” 2003. Doctoral Dissertation, University of Utah. Accessed April 11, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1738/rec/964.

MLA Handbook (7th Edition):

Simeone, Timothy A. “Regulation of allosteric modulation of GABAa receptor function: interaction between recombininant GABAa receptors and the novel anticonvulsant drug topiramate.” 2003. Web. 11 Apr 2021.

Vancouver:

Simeone TA. Regulation of allosteric modulation of GABAa receptor function: interaction between recombininant GABAa receptors and the novel anticonvulsant drug topiramate. [Internet] [Doctoral dissertation]. University of Utah; 2003. [cited 2021 Apr 11]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1738/rec/964.

Council of Science Editors:

Simeone TA. Regulation of allosteric modulation of GABAa receptor function: interaction between recombininant GABAa receptors and the novel anticonvulsant drug topiramate. [Doctoral Dissertation]. University of Utah; 2003. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/1738/rec/964


Vanderbilt University

24. Kaufmann, Kristian Wallace. Computational prediction of protein small molecule interfaces using ROSETTA.

Degree: PhD, Chemistry, 2011, Vanderbilt University

 Protein small molecule docking has focused on the modeling of small molecule flexibility and scoring of small molecules binding to fixed protein structures due to… (more)

Subjects/Keywords: homology modeling; virtual screening; drug design

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APA (6th Edition):

Kaufmann, K. W. (2011). Computational prediction of protein small molecule interfaces using ROSETTA. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14473

Chicago Manual of Style (16th Edition):

Kaufmann, Kristian Wallace. “Computational prediction of protein small molecule interfaces using ROSETTA.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed April 11, 2021. http://hdl.handle.net/1803/14473.

MLA Handbook (7th Edition):

Kaufmann, Kristian Wallace. “Computational prediction of protein small molecule interfaces using ROSETTA.” 2011. Web. 11 Apr 2021.

Vancouver:

Kaufmann KW. Computational prediction of protein small molecule interfaces using ROSETTA. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1803/14473.

Council of Science Editors:

Kaufmann KW. Computational prediction of protein small molecule interfaces using ROSETTA. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/14473


Texas Tech University

25. Patkar, Presheet P. Sterol methyltransferase: Probing its drug-target and allosteric properties.

Degree: PhD, Chemistry, 2016, Texas Tech University

 The methylation of cycloartenol by plant 24-SMT (Glycine max) leads to formation of a single product – 24(28)-methylenecycloartenol. This is in stark contrast to the… (more)

Subjects/Keywords: Sterol methyltransferase; SMT; rational drug design; Allostery

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APA (6th Edition):

Patkar, P. P. (2016). Sterol methyltransferase: Probing its drug-target and allosteric properties. (Doctoral Dissertation). Texas Tech University. Retrieved from http://hdl.handle.net/2346/72384

Chicago Manual of Style (16th Edition):

Patkar, Presheet P. “Sterol methyltransferase: Probing its drug-target and allosteric properties.” 2016. Doctoral Dissertation, Texas Tech University. Accessed April 11, 2021. http://hdl.handle.net/2346/72384.

MLA Handbook (7th Edition):

Patkar, Presheet P. “Sterol methyltransferase: Probing its drug-target and allosteric properties.” 2016. Web. 11 Apr 2021.

Vancouver:

Patkar PP. Sterol methyltransferase: Probing its drug-target and allosteric properties. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2346/72384.

Council of Science Editors:

Patkar PP. Sterol methyltransferase: Probing its drug-target and allosteric properties. [Doctoral Dissertation]. Texas Tech University; 2016. Available from: http://hdl.handle.net/2346/72384


UCLA

26. Van Valkenburgh, Juno. Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes.

Degree: Chemistry, 2019, UCLA

 In chapter 1, strategies toward the asymmetric synthesis of a deoxycytidine kinase (dCK) inhibitor are presented. Small molecule dCK inhibitors are potential cancer therapeutics: in… (more)

Subjects/Keywords: Chemistry; cancer therapies; drug design; nucleotide metabolism

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APA (6th Edition):

Van Valkenburgh, J. (2019). Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6hs572xd

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):

Van Valkenburgh, Juno. “Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes.” 2019. Thesis, UCLA. Accessed April 11, 2021. http://www.escholarship.org/uc/item/6hs572xd.

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

MLA Handbook (7th Edition):

Van Valkenburgh, Juno. “Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes.” 2019. Web. 11 Apr 2021.

Vancouver:

Van Valkenburgh J. Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes. [Internet] [Thesis]. UCLA; 2019. [cited 2021 Apr 11]. Available from: http://www.escholarship.org/uc/item/6hs572xd.

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

Council of Science Editors:

Van Valkenburgh J. Development of Small-Molecule Modulators of Nucleotide Metabolism Enzymes. [Thesis]. UCLA; 2019. Available from: http://www.escholarship.org/uc/item/6hs572xd

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


Boston University

27. Villar, Elizabeth A. Study of protein-macrocycle Interactions for lessons in drug design.

Degree: PhD, Chemistry, 2016, Boston University

 Macrocycles (MCs) have become an increasing area of interest for drug design efforts, especially for classically “difficult” targets like protein-protein interactions (PPIs). And although there… (more)

Subjects/Keywords: Chemistry; Drug design; Macrocycle; NEMO; Protein mapping

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APA (6th Edition):

Villar, E. A. (2016). Study of protein-macrocycle Interactions for lessons in drug design. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/19759

Chicago Manual of Style (16th Edition):

Villar, Elizabeth A. “Study of protein-macrocycle Interactions for lessons in drug design.” 2016. Doctoral Dissertation, Boston University. Accessed April 11, 2021. http://hdl.handle.net/2144/19759.

MLA Handbook (7th Edition):

Villar, Elizabeth A. “Study of protein-macrocycle Interactions for lessons in drug design.” 2016. Web. 11 Apr 2021.

Vancouver:

Villar EA. Study of protein-macrocycle Interactions for lessons in drug design. [Internet] [Doctoral dissertation]. Boston University; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/2144/19759.

Council of Science Editors:

Villar EA. Study of protein-macrocycle Interactions for lessons in drug design. [Doctoral Dissertation]. Boston University; 2016. Available from: http://hdl.handle.net/2144/19759


University of Glasgow

28. Forrest, Fiona Ruth Ferguson. Conformational studies on some inhibitors of thermolysin and EC 3.4.24.11.

Degree: PhD, 1987, University of Glasgow

 Molecular modeling is an exciting new approach in the field of drug design. A molecule's activity as a drug is dependent upon its conformation i.e.… (more)

Subjects/Keywords: 615.1; Drug design

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APA (6th Edition):

Forrest, F. R. F. (1987). Conformational studies on some inhibitors of thermolysin and EC 3.4.24.11. (Doctoral Dissertation). University of Glasgow. Retrieved from http://theses.gla.ac.uk/77560/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305787

Chicago Manual of Style (16th Edition):

Forrest, Fiona Ruth Ferguson. “Conformational studies on some inhibitors of thermolysin and EC 3.4.24.11.” 1987. Doctoral Dissertation, University of Glasgow. Accessed April 11, 2021. http://theses.gla.ac.uk/77560/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305787.

MLA Handbook (7th Edition):

Forrest, Fiona Ruth Ferguson. “Conformational studies on some inhibitors of thermolysin and EC 3.4.24.11.” 1987. Web. 11 Apr 2021.

Vancouver:

Forrest FRF. Conformational studies on some inhibitors of thermolysin and EC 3.4.24.11. [Internet] [Doctoral dissertation]. University of Glasgow; 1987. [cited 2021 Apr 11]. Available from: http://theses.gla.ac.uk/77560/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305787.

Council of Science Editors:

Forrest FRF. Conformational studies on some inhibitors of thermolysin and EC 3.4.24.11. [Doctoral Dissertation]. University of Glasgow; 1987. Available from: http://theses.gla.ac.uk/77560/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.305787

29. Gerogiokas, Georgios. Quantitative models of biomolecular hydration thermodynamics.

Degree: PhD, 2015, University of Edinburgh

 This thesis explores the use of cell theory calculations to characterise hydration thermodynamics in small molecules (cations, ions, hydrophobic molecules), proteins and protein-ligand complexes. Cell… (more)

Subjects/Keywords: 615.1; computer aided drug design; hydration thermodynamics

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

APA (6th Edition):

Gerogiokas, G. (2015). Quantitative models of biomolecular hydration thermodynamics. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/14181

Chicago Manual of Style (16th Edition):

Gerogiokas, Georgios. “Quantitative models of biomolecular hydration thermodynamics.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed April 11, 2021. http://hdl.handle.net/1842/14181.

MLA Handbook (7th Edition):

Gerogiokas, Georgios. “Quantitative models of biomolecular hydration thermodynamics.” 2015. Web. 11 Apr 2021.

Vancouver:

Gerogiokas G. Quantitative models of biomolecular hydration thermodynamics. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1842/14181.

Council of Science Editors:

Gerogiokas G. Quantitative models of biomolecular hydration thermodynamics. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/14181


Hong Kong University of Science and Technology

30. Hadiwinoto, Gabriela Daisy CBME. A proof of concept for integrated continuous manufacturing of a pharmaceutical for dry powder inhalation.

Degree: 2017, Hong Kong University of Science and Technology

 The direct administration of drugs to the pulmonary tract offers important advantages for treatment of various local and systemic diseases compared to oral administration. A… (more)

Subjects/Keywords: Drug delivery systems ; Design ; Drugs ; Pulmonary pharmacology

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

APA (6th Edition):

Hadiwinoto, G. D. C. (2017). A proof of concept for integrated continuous manufacturing of a pharmaceutical for dry powder inhalation. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-91124 ; https://doi.org/10.14711/thesis-991012551364603412 ; http://repository.ust.hk/ir/bitstream/1783.1-91124/1/th_redirect.html

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):

Hadiwinoto, Gabriela Daisy CBME. “A proof of concept for integrated continuous manufacturing of a pharmaceutical for dry powder inhalation.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed April 11, 2021. http://repository.ust.hk/ir/Record/1783.1-91124 ; https://doi.org/10.14711/thesis-991012551364603412 ; http://repository.ust.hk/ir/bitstream/1783.1-91124/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Hadiwinoto, Gabriela Daisy CBME. “A proof of concept for integrated continuous manufacturing of a pharmaceutical for dry powder inhalation.” 2017. Web. 11 Apr 2021.

Vancouver:

Hadiwinoto GDC. A proof of concept for integrated continuous manufacturing of a pharmaceutical for dry powder inhalation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2021 Apr 11]. Available from: http://repository.ust.hk/ir/Record/1783.1-91124 ; https://doi.org/10.14711/thesis-991012551364603412 ; http://repository.ust.hk/ir/bitstream/1783.1-91124/1/th_redirect.html.

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

Council of Science Editors:

Hadiwinoto GDC. A proof of concept for integrated continuous manufacturing of a pharmaceutical for dry powder inhalation. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: http://repository.ust.hk/ir/Record/1783.1-91124 ; https://doi.org/10.14711/thesis-991012551364603412 ; http://repository.ust.hk/ir/bitstream/1783.1-91124/1/th_redirect.html

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

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