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You searched for subject:(drug discovery). Showing records 1 – 30 of 488 total matches.

[1] [2] [3] [4] [5] … [17]

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University of Helsinki

1. Subramanian, Vigneshwari. Field-based Proteochemometric Models Derived from 3D Protein Structures: A Novel Approach to Visualize Affinity and Selectivity Features.

Degree: Faculty of Pharmacy, 2016, University of Helsinki

Designing drugs that are selective is crucial in pharmaceutical research to avoid unwanted side effects. To decipher selectivity of drug targets, computational approaches that utilize… (more)

Subjects/Keywords: computational Drug Discovery; computational Drug Discovery

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

APA (6th Edition):

Subramanian, V. (2016). Field-based Proteochemometric Models Derived from 3D Protein Structures: A Novel Approach to Visualize Affinity and Selectivity Features. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/170374

Chicago Manual of Style (16th Edition):

Subramanian, Vigneshwari. “Field-based Proteochemometric Models Derived from 3D Protein Structures: A Novel Approach to Visualize Affinity and Selectivity Features.” 2016. Doctoral Dissertation, University of Helsinki. Accessed November 15, 2019. http://hdl.handle.net/10138/170374.

MLA Handbook (7th Edition):

Subramanian, Vigneshwari. “Field-based Proteochemometric Models Derived from 3D Protein Structures: A Novel Approach to Visualize Affinity and Selectivity Features.” 2016. Web. 15 Nov 2019.

Vancouver:

Subramanian V. Field-based Proteochemometric Models Derived from 3D Protein Structures: A Novel Approach to Visualize Affinity and Selectivity Features. [Internet] [Doctoral dissertation]. University of Helsinki; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10138/170374.

Council of Science Editors:

Subramanian V. Field-based Proteochemometric Models Derived from 3D Protein Structures: A Novel Approach to Visualize Affinity and Selectivity Features. [Doctoral Dissertation]. University of Helsinki; 2016. Available from: http://hdl.handle.net/10138/170374


University of Illinois – Urbana-Champaign

2. No, Joo Hwan. Drug discovery against malaria parasite: drug repositioning strategy.

Degree: PhD, 0319, 2011, University of Illinois – Urbana-Champaign

 Malaria, caused by Plasmodium spp., causes ~1 million deaths each year and there are ever present problems due to drug resistance. In this work, I… (more)

Subjects/Keywords: Drug discovery; Malaria

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APA (6th Edition):

No, J. H. (2011). Drug discovery against malaria parasite: drug repositioning strategy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/26307

Chicago Manual of Style (16th Edition):

No, Joo Hwan. “Drug discovery against malaria parasite: drug repositioning strategy.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 15, 2019. http://hdl.handle.net/2142/26307.

MLA Handbook (7th Edition):

No, Joo Hwan. “Drug discovery against malaria parasite: drug repositioning strategy.” 2011. Web. 15 Nov 2019.

Vancouver:

No JH. Drug discovery against malaria parasite: drug repositioning strategy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2142/26307.

Council of Science Editors:

No JH. Drug discovery against malaria parasite: drug repositioning strategy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/26307


Temple University

3. Hoffman, Benjamin. The Genetics of Cancer in Pharmacological Drug Development.

Degree: PhD, 2011, Temple University

Molecular and Cellular Physiology

The field of cancer therapeutic development has been dominated by two research and discovery paradigms, the cytotoxicity-based or phenotype driven strategy… (more)

Subjects/Keywords: Biology; Cancer; Drug Discovery; Therapeutics

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APA (6th Edition):

Hoffman, B. (2011). The Genetics of Cancer in Pharmacological Drug Development. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,212455

Chicago Manual of Style (16th Edition):

Hoffman, Benjamin. “The Genetics of Cancer in Pharmacological Drug Development.” 2011. Doctoral Dissertation, Temple University. Accessed November 15, 2019. http://digital.library.temple.edu/u?/p245801coll10,212455.

MLA Handbook (7th Edition):

Hoffman, Benjamin. “The Genetics of Cancer in Pharmacological Drug Development.” 2011. Web. 15 Nov 2019.

Vancouver:

Hoffman B. The Genetics of Cancer in Pharmacological Drug Development. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2019 Nov 15]. Available from: http://digital.library.temple.edu/u?/p245801coll10,212455.

Council of Science Editors:

Hoffman B. The Genetics of Cancer in Pharmacological Drug Development. [Doctoral Dissertation]. Temple University; 2011. Available from: http://digital.library.temple.edu/u?/p245801coll10,212455


University of Illinois – Chicago

4. Rush, Michael D. Magnetic Microbead Affinity Selection Screening: Development, Application, and Evaluation.

Degree: 2017, University of Illinois – Chicago

 Contemporary natural product drug discovery relies on bioassay guided fractionation. This technique – while exhaustive – is expensive and time consuming. By introducing mass spectrometry… (more)

Subjects/Keywords: drug discovery; natural products; magmass

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APA (6th Edition):

Rush, M. D. (2017). Magnetic Microbead Affinity Selection Screening: Development, Application, and Evaluation. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22086

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):

Rush, Michael D. “Magnetic Microbead Affinity Selection Screening: Development, Application, and Evaluation.” 2017. Thesis, University of Illinois – Chicago. Accessed November 15, 2019. http://hdl.handle.net/10027/22086.

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

MLA Handbook (7th Edition):

Rush, Michael D. “Magnetic Microbead Affinity Selection Screening: Development, Application, and Evaluation.” 2017. Web. 15 Nov 2019.

Vancouver:

Rush MD. Magnetic Microbead Affinity Selection Screening: Development, Application, and Evaluation. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10027/22086.

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

Council of Science Editors:

Rush MD. Magnetic Microbead Affinity Selection Screening: Development, Application, and Evaluation. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22086

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


Victoria University of Wellington

5. Sampson, Liam D P. High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888.

Degree: 2012, Victoria University of Wellington

 The discovery and characterisation of novel small molecule drug candidates is a medical priority. Recent advances in synthetic organic chemistry allow the de novo production… (more)

Subjects/Keywords: Drug discovery; Chemical genetics; Yeast

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APA (6th Edition):

Sampson, L. D. P. (2012). High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2590

Chicago Manual of Style (16th Edition):

Sampson, Liam D P. “High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888.” 2012. Masters Thesis, Victoria University of Wellington. Accessed November 15, 2019. http://hdl.handle.net/10063/2590.

MLA Handbook (7th Edition):

Sampson, Liam D P. “High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888.” 2012. Web. 15 Nov 2019.

Vancouver:

Sampson LDP. High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888. [Internet] [Masters thesis]. Victoria University of Wellington; 2012. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10063/2590.

Council of Science Editors:

Sampson LDP. High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888. [Masters Thesis]. Victoria University of Wellington; 2012. Available from: http://hdl.handle.net/10063/2590

6. Liu, Yi. EXPLORING NEW USES OF EXISTING DRUGS AGAINST LIVER STAGE MALARIA.

Degree: 2014, Johns Hopkins University

 Malaria, as one of the most lethal infectious diseases, has been causing much morbidity and mortality worldwide for decades. The causative parasites, Plasmodium spp., are… (more)

Subjects/Keywords: Malaria; Liver stage; Drug discovery

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APA (6th Edition):

Liu, Y. (2014). EXPLORING NEW USES OF EXISTING DRUGS AGAINST LIVER STAGE MALARIA. (Thesis). Johns Hopkins University. Retrieved from http://jhir.library.jhu.edu/handle/1774.2/37225

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):

Liu, Yi. “EXPLORING NEW USES OF EXISTING DRUGS AGAINST LIVER STAGE MALARIA.” 2014. Thesis, Johns Hopkins University. Accessed November 15, 2019. http://jhir.library.jhu.edu/handle/1774.2/37225.

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

MLA Handbook (7th Edition):

Liu, Yi. “EXPLORING NEW USES OF EXISTING DRUGS AGAINST LIVER STAGE MALARIA.” 2014. Web. 15 Nov 2019.

Vancouver:

Liu Y. EXPLORING NEW USES OF EXISTING DRUGS AGAINST LIVER STAGE MALARIA. [Internet] [Thesis]. Johns Hopkins University; 2014. [cited 2019 Nov 15]. Available from: http://jhir.library.jhu.edu/handle/1774.2/37225.

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

Council of Science Editors:

Liu Y. EXPLORING NEW USES OF EXISTING DRUGS AGAINST LIVER STAGE MALARIA. [Thesis]. Johns Hopkins University; 2014. Available from: http://jhir.library.jhu.edu/handle/1774.2/37225

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


University of Southern California

7. Pattamatta, Preeti. Discovery of novel small-molecule compounds with anticancer properties.

Degree: MS, Biochemistry & Molecular Biology, 2010, University of Southern California

 Cancer has emerged as one of the deadliest diseases in the recent past. According to the current statistics, one in every four deaths in the… (more)

Subjects/Keywords: anticancer; small molecules; drug discovery

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APA (6th Edition):

Pattamatta, P. (2010). Discovery of novel small-molecule compounds with anticancer properties. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2028

Chicago Manual of Style (16th Edition):

Pattamatta, Preeti. “Discovery of novel small-molecule compounds with anticancer properties.” 2010. Masters Thesis, University of Southern California. Accessed November 15, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2028.

MLA Handbook (7th Edition):

Pattamatta, Preeti. “Discovery of novel small-molecule compounds with anticancer properties.” 2010. Web. 15 Nov 2019.

Vancouver:

Pattamatta P. Discovery of novel small-molecule compounds with anticancer properties. [Internet] [Masters thesis]. University of Southern California; 2010. [cited 2019 Nov 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2028.

Council of Science Editors:

Pattamatta P. Discovery of novel small-molecule compounds with anticancer properties. [Masters Thesis]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/146657/rec/2028


University of St. Andrews

8. Kipandula, Wakisa. Exploring the utilization of Crithidia fasciculata as a model organism to study pathogenic kinetoplastids .

Degree: 2017, University of St. Andrews

 This study aimed to explore the utilization of C. fasciculata as a convenient model organism to study the cell biology and drug discovery vehicle of… (more)

Subjects/Keywords: Drug discovery; Crithidia fasciculata; Kinetoplastids

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APA (6th Edition):

Kipandula, W. (2017). Exploring the utilization of Crithidia fasciculata as a model organism to study pathogenic kinetoplastids . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/12217

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):

Kipandula, Wakisa. “Exploring the utilization of Crithidia fasciculata as a model organism to study pathogenic kinetoplastids .” 2017. Thesis, University of St. Andrews. Accessed November 15, 2019. http://hdl.handle.net/10023/12217.

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

MLA Handbook (7th Edition):

Kipandula, Wakisa. “Exploring the utilization of Crithidia fasciculata as a model organism to study pathogenic kinetoplastids .” 2017. Web. 15 Nov 2019.

Vancouver:

Kipandula W. Exploring the utilization of Crithidia fasciculata as a model organism to study pathogenic kinetoplastids . [Internet] [Thesis]. University of St. Andrews; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10023/12217.

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

Council of Science Editors:

Kipandula W. Exploring the utilization of Crithidia fasciculata as a model organism to study pathogenic kinetoplastids . [Thesis]. University of St. Andrews; 2017. Available from: http://hdl.handle.net/10023/12217

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


University of Cambridge

9. Higueruelo, Alicia Perez. Molecular recognition from atomic interactions : insights into drug discovery.

Degree: PhD, 2012, University of Cambridge

 The failure of the pharmaceutical industry to increase the delivery of new drugs into the market is driving a re-assessment of practices and methods in… (more)

Subjects/Keywords: 572; Drug discovery; Molecular recognition

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APA (6th Edition):

Higueruelo, A. P. (2012). Molecular recognition from atomic interactions : insights into drug discovery. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/244380 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569809

Chicago Manual of Style (16th Edition):

Higueruelo, Alicia Perez. “Molecular recognition from atomic interactions : insights into drug discovery.” 2012. Doctoral Dissertation, University of Cambridge. Accessed November 15, 2019. https://www.repository.cam.ac.uk/handle/1810/244380 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569809.

MLA Handbook (7th Edition):

Higueruelo, Alicia Perez. “Molecular recognition from atomic interactions : insights into drug discovery.” 2012. Web. 15 Nov 2019.

Vancouver:

Higueruelo AP. Molecular recognition from atomic interactions : insights into drug discovery. [Internet] [Doctoral dissertation]. University of Cambridge; 2012. [cited 2019 Nov 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/244380 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569809.

Council of Science Editors:

Higueruelo AP. Molecular recognition from atomic interactions : insights into drug discovery. [Doctoral Dissertation]. University of Cambridge; 2012. Available from: https://www.repository.cam.ac.uk/handle/1810/244380 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.569809


Victoria University of Wellington

10. Miller, Christopher Hamilton. Seleno-amino acids: A novel class of anti-tuberculosis compounds identified through modified culture screening conditions.

Degree: 2013, Victoria University of Wellington

 Tuberculosis continues to be a major world health problem, causing more deaths than any other bacterial disease. Long treatment durations using a complex cocktail of… (more)

Subjects/Keywords: Tuberculosis; Drug discovery; Antitubercular agents

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APA (6th Edition):

Miller, C. H. (2013). Seleno-amino acids: A novel class of anti-tuberculosis compounds identified through modified culture screening conditions. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2819

Chicago Manual of Style (16th Edition):

Miller, Christopher Hamilton. “Seleno-amino acids: A novel class of anti-tuberculosis compounds identified through modified culture screening conditions.” 2013. Doctoral Dissertation, Victoria University of Wellington. Accessed November 15, 2019. http://hdl.handle.net/10063/2819.

MLA Handbook (7th Edition):

Miller, Christopher Hamilton. “Seleno-amino acids: A novel class of anti-tuberculosis compounds identified through modified culture screening conditions.” 2013. Web. 15 Nov 2019.

Vancouver:

Miller CH. Seleno-amino acids: A novel class of anti-tuberculosis compounds identified through modified culture screening conditions. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10063/2819.

Council of Science Editors:

Miller CH. Seleno-amino acids: A novel class of anti-tuberculosis compounds identified through modified culture screening conditions. [Doctoral Dissertation]. Victoria University of Wellington; 2013. Available from: http://hdl.handle.net/10063/2819


University of Illinois – Urbana-Champaign

11. Circello, Benjamin T. Investigations into the biosynthesis and mode of action of the phosphonate antibiotic dehydrophos.

Degree: PhD, 0322, 2011, University of Illinois – Urbana-Champaign

 Dehydrophos is a vinyl phosphonate tripeptide produced by Streptomyces luridus with demonstrated broad spectrum antibiotic activity. Dehydrophos antibiotic activity was determined to be dependent on… (more)

Subjects/Keywords: phosphonate; antibiotic; Streptomyces; drug discovery

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APA (6th Edition):

Circello, B. T. (2011). Investigations into the biosynthesis and mode of action of the phosphonate antibiotic dehydrophos. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/18576

Chicago Manual of Style (16th Edition):

Circello, Benjamin T. “Investigations into the biosynthesis and mode of action of the phosphonate antibiotic dehydrophos.” 2011. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed November 15, 2019. http://hdl.handle.net/2142/18576.

MLA Handbook (7th Edition):

Circello, Benjamin T. “Investigations into the biosynthesis and mode of action of the phosphonate antibiotic dehydrophos.” 2011. Web. 15 Nov 2019.

Vancouver:

Circello BT. Investigations into the biosynthesis and mode of action of the phosphonate antibiotic dehydrophos. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2011. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2142/18576.

Council of Science Editors:

Circello BT. Investigations into the biosynthesis and mode of action of the phosphonate antibiotic dehydrophos. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2011. Available from: http://hdl.handle.net/2142/18576


University of Oklahoma

12. Mattes, Allison. Advancement of Natural Products: Optimization of Instrumentation and Examples of their Application to the Isolation of New Compounds.

Degree: PhD, 2019, University of Oklahoma

 The world of natural products has a long rich history dating back thousands of years and was the origin of medicine as we know it.… (more)

Subjects/Keywords: Natural Products; Drug Discovery; NMR

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APA (6th Edition):

Mattes, A. (2019). Advancement of Natural Products: Optimization of Instrumentation and Examples of their Application to the Isolation of New Compounds. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/320427

Chicago Manual of Style (16th Edition):

Mattes, Allison. “Advancement of Natural Products: Optimization of Instrumentation and Examples of their Application to the Isolation of New Compounds.” 2019. Doctoral Dissertation, University of Oklahoma. Accessed November 15, 2019. http://hdl.handle.net/11244/320427.

MLA Handbook (7th Edition):

Mattes, Allison. “Advancement of Natural Products: Optimization of Instrumentation and Examples of their Application to the Isolation of New Compounds.” 2019. Web. 15 Nov 2019.

Vancouver:

Mattes A. Advancement of Natural Products: Optimization of Instrumentation and Examples of their Application to the Isolation of New Compounds. [Internet] [Doctoral dissertation]. University of Oklahoma; 2019. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/11244/320427.

Council of Science Editors:

Mattes A. Advancement of Natural Products: Optimization of Instrumentation and Examples of their Application to the Isolation of New Compounds. [Doctoral Dissertation]. University of Oklahoma; 2019. Available from: http://hdl.handle.net/11244/320427


University of Sydney

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

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 November 15, 2019. 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. 15 Nov 2019.

Vancouver:

Lin H. The use of computer-aided drug design in small molecule drug discovery . [Internet] [Thesis]. University of Sydney; 2018. [cited 2019 Nov 15]. 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


Texas A&M University

14. Liu, Zhen. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.

Degree: 2013, Texas A&M University

 Mycobacterium tuberculosis (M. tuberculosis) contains a wide array of genes responsible for the synthesis and secretion of a variety of bioactive lipids. The genes represent… (more)

Subjects/Keywords: Structural biology; Enzymology; Drug discovery; Lipid metabolism

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APA (6th Edition):

Liu, Z. (2013). Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151650

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):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Thesis, Texas A&M University. Accessed November 15, 2019. http://hdl.handle.net/1969.1/151650.

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

MLA Handbook (7th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Web. 15 Nov 2019.

Vancouver:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1969.1/151650.

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

Council of Science Editors:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151650

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


University of Illinois – Chicago

15. O hAinmhire, Eoghainin. Identification and Characterization of Potential Drug Targets In Serous Ovarian Cancer.

Degree: 2015, University of Illinois – Chicago

 Ovarian cancer is the most lethal gynecological disease in women in the US. The Cancer Genome Atlas Network identified p53 mutations in 96% of high-grade… (more)

Subjects/Keywords: Ovarian cancer; drug discovery; p53; TGFbeta; PAX8

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APA (6th Edition):

O hAinmhire, E. (2015). Identification and Characterization of Potential Drug Targets In Serous Ovarian Cancer. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19811

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):

O hAinmhire, Eoghainin. “Identification and Characterization of Potential Drug Targets In Serous Ovarian Cancer.” 2015. Thesis, University of Illinois – Chicago. Accessed November 15, 2019. http://hdl.handle.net/10027/19811.

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

MLA Handbook (7th Edition):

O hAinmhire, Eoghainin. “Identification and Characterization of Potential Drug Targets In Serous Ovarian Cancer.” 2015. Web. 15 Nov 2019.

Vancouver:

O hAinmhire E. Identification and Characterization of Potential Drug Targets In Serous Ovarian Cancer. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10027/19811.

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

Council of Science Editors:

O hAinmhire E. Identification and Characterization of Potential Drug Targets In Serous Ovarian Cancer. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19811

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

16. Esakkiammal, P. Bibliometric analysis of research productivity in drug discovery in medicinal plants;.

Degree: 2015, Manonmaniam Sundaranar University

Communication is culture The gamut of science is best captured by the newline newlineconcept of a well articulated science communication system in which newline newlineparticipating… (more)

Subjects/Keywords: Bibliometric analysis; drug discovery; medicinal plants; productivity

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APA (6th Edition):

Esakkiammal, P. (2015). Bibliometric analysis of research productivity in drug discovery in medicinal plants;. (Thesis). Manonmaniam Sundaranar University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/43210

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):

Esakkiammal, P. “Bibliometric analysis of research productivity in drug discovery in medicinal plants;.” 2015. Thesis, Manonmaniam Sundaranar University. Accessed November 15, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/43210.

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

MLA Handbook (7th Edition):

Esakkiammal, P. “Bibliometric analysis of research productivity in drug discovery in medicinal plants;.” 2015. Web. 15 Nov 2019.

Vancouver:

Esakkiammal P. Bibliometric analysis of research productivity in drug discovery in medicinal plants;. [Internet] [Thesis]. Manonmaniam Sundaranar University; 2015. [cited 2019 Nov 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/43210.

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

Council of Science Editors:

Esakkiammal P. Bibliometric analysis of research productivity in drug discovery in medicinal plants;. [Thesis]. Manonmaniam Sundaranar University; 2015. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/43210

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


University of Pretoria

17. Barnard, Bernice. Inhibition of lysine-specific demethylase 1 as an antimalarial target by polyamine analogues.

Degree: MSc, Biochemistry, 2015, University of Pretoria

 According to the World Health Organization, malaria has been classified as one of the three most important infectious diseases in Africa. The number of malaria… (more)

Subjects/Keywords: UCTD; Malaria; Drug discovery; Plasmidium; Pollyamine

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APA (6th Edition):

Barnard, B. (2015). Inhibition of lysine-specific demethylase 1 as an antimalarial target by polyamine analogues. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/46152

Chicago Manual of Style (16th Edition):

Barnard, Bernice. “Inhibition of lysine-specific demethylase 1 as an antimalarial target by polyamine analogues.” 2015. Masters Thesis, University of Pretoria. Accessed November 15, 2019. http://hdl.handle.net/2263/46152.

MLA Handbook (7th Edition):

Barnard, Bernice. “Inhibition of lysine-specific demethylase 1 as an antimalarial target by polyamine analogues.” 2015. Web. 15 Nov 2019.

Vancouver:

Barnard B. Inhibition of lysine-specific demethylase 1 as an antimalarial target by polyamine analogues. [Internet] [Masters thesis]. University of Pretoria; 2015. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2263/46152.

Council of Science Editors:

Barnard B. Inhibition of lysine-specific demethylase 1 as an antimalarial target by polyamine analogues. [Masters Thesis]. University of Pretoria; 2015. Available from: http://hdl.handle.net/2263/46152


University of Kansas

18. Johnson, David Keith. Pocket optimization and its application to identify small-molecule inhibitors of protein-protein interactions.

Degree: PhD, Molecular Biosciences, 2016, University of Kansas

 Because of their ubiquitous nature in many cellular processes, modulating protein-protein interactions offers tremendous therapeutic potential. However, protein-protein interactions remain a difficult class of drug(more)

Subjects/Keywords: Bioinformatics; Computational; Conformational; Discovery; Drug; Selection

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APA (6th Edition):

Johnson, D. K. (2016). Pocket optimization and its application to identify small-molecule inhibitors of protein-protein interactions. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21851

Chicago Manual of Style (16th Edition):

Johnson, David Keith. “Pocket optimization and its application to identify small-molecule inhibitors of protein-protein interactions.” 2016. Doctoral Dissertation, University of Kansas. Accessed November 15, 2019. http://hdl.handle.net/1808/21851.

MLA Handbook (7th Edition):

Johnson, David Keith. “Pocket optimization and its application to identify small-molecule inhibitors of protein-protein interactions.” 2016. Web. 15 Nov 2019.

Vancouver:

Johnson DK. Pocket optimization and its application to identify small-molecule inhibitors of protein-protein interactions. [Internet] [Doctoral dissertation]. University of Kansas; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1808/21851.

Council of Science Editors:

Johnson DK. Pocket optimization and its application to identify small-molecule inhibitors of protein-protein interactions. [Doctoral Dissertation]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/21851


University of Edinburgh

19. Hsin, Kun-Yi. Development and use of databases for ligand-protein interaction studies.

Degree: 2010, University of Edinburgh

 This project applies structure-activity relationship (SAR), structure-based and database mining approaches to study ligand-protein interactions. To support these studies, we have developed a relational database… (more)

Subjects/Keywords: 572.8; ligand-protein interaction; drug discovery; metalloprotein

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APA (6th Edition):

Hsin, K. (2010). Development and use of databases for ligand-protein interaction studies. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/3974

Chicago Manual of Style (16th Edition):

Hsin, Kun-Yi. “Development and use of databases for ligand-protein interaction studies.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed November 15, 2019. http://hdl.handle.net/1842/3974.

MLA Handbook (7th Edition):

Hsin, Kun-Yi. “Development and use of databases for ligand-protein interaction studies.” 2010. Web. 15 Nov 2019.

Vancouver:

Hsin K. Development and use of databases for ligand-protein interaction studies. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1842/3974.

Council of Science Editors:

Hsin K. Development and use of databases for ligand-protein interaction studies. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/3974


Case Western Reserve University

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

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

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

Subjects/Keywords: Cellular Biology; Drug discovery and development

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Mehta, Kalpita Deepak. “Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications.” 2010. Masters Thesis, Case Western Reserve University. Accessed November 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1269628794.

MLA Handbook (7th Edition):

Mehta, Kalpita Deepak. “Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications.” 2010. Web. 15 Nov 2019.

Vancouver:

Mehta KD. Commercialization of Transiently Transfected Cell Lines for High Throughput Drug Screening and Profiling Applications. [Internet] [Masters thesis]. Case Western Reserve University; 2010. [cited 2019 Nov 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1269628794.

Council of Science Editors:

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


University of California – Berkeley

21. Sonoiki, Ebere Irene. Studies to elucidate the molecular targets of two potent antimalarial benzoxaborole compounds in Plasmodium falciparum.

Degree: Infectious Diseases & Immunity, 2014, University of California – Berkeley

 With increasing resistance of malaria parasites to available drugs, there is a great need for new antimalarials, ideally with novel mechanisms of action. We are… (more)

Subjects/Keywords: Public health; Drug discovery; Malaria; Resistance

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APA (6th Edition):

Sonoiki, E. I. (2014). Studies to elucidate the molecular targets of two potent antimalarial benzoxaborole compounds in Plasmodium falciparum. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/4965v7kx

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):

Sonoiki, Ebere Irene. “Studies to elucidate the molecular targets of two potent antimalarial benzoxaborole compounds in Plasmodium falciparum.” 2014. Thesis, University of California – Berkeley. Accessed November 15, 2019. http://www.escholarship.org/uc/item/4965v7kx.

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

MLA Handbook (7th Edition):

Sonoiki, Ebere Irene. “Studies to elucidate the molecular targets of two potent antimalarial benzoxaborole compounds in Plasmodium falciparum.” 2014. Web. 15 Nov 2019.

Vancouver:

Sonoiki EI. Studies to elucidate the molecular targets of two potent antimalarial benzoxaborole compounds in Plasmodium falciparum. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2019 Nov 15]. Available from: http://www.escholarship.org/uc/item/4965v7kx.

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

Council of Science Editors:

Sonoiki EI. Studies to elucidate the molecular targets of two potent antimalarial benzoxaborole compounds in Plasmodium falciparum. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/4965v7kx

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


Texas A&M University

22. Hughes, Ryan C. Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target.

Degree: PhD, Biochemistry, 2016, Texas A&M University

 Current therapies for treatment of mycobacterial infections are adequate when diagnosis and pathology is well defined. Yet more evidence is beginning to accumulate for the… (more)

Subjects/Keywords: Tuberculosis; Drug Discovery; Crystallography; Serine Hydrolase

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APA (6th Edition):

Hughes, R. C. (2016). Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/159056

Chicago Manual of Style (16th Edition):

Hughes, Ryan C. “Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target.” 2016. Doctoral Dissertation, Texas A&M University. Accessed November 15, 2019. http://hdl.handle.net/1969.1/159056.

MLA Handbook (7th Edition):

Hughes, Ryan C. “Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target.” 2016. Web. 15 Nov 2019.

Vancouver:

Hughes RC. Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1969.1/159056.

Council of Science Editors:

Hughes RC. Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/159056


University of Sydney

23. Elias, Nabiha Toni. Design and Synthesis of Peptidic Natural Product Analogues as Anti-infective Drug Leads .

Degree: 2017, University of Sydney

 Natural products, including peptides, offer a rich source of bioactive metabolites commonly exploited for the development of drug therapies. Accordingly, our research endeavors have been… (more)

Subjects/Keywords: natural products; drug discovery; peptides; anti-infectives

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APA (6th Edition):

Elias, N. T. (2017). Design and Synthesis of Peptidic Natural Product Analogues as Anti-infective Drug Leads . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17094

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):

Elias, Nabiha Toni. “Design and Synthesis of Peptidic Natural Product Analogues as Anti-infective Drug Leads .” 2017. Thesis, University of Sydney. Accessed November 15, 2019. http://hdl.handle.net/2123/17094.

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

MLA Handbook (7th Edition):

Elias, Nabiha Toni. “Design and Synthesis of Peptidic Natural Product Analogues as Anti-infective Drug Leads .” 2017. Web. 15 Nov 2019.

Vancouver:

Elias NT. Design and Synthesis of Peptidic Natural Product Analogues as Anti-infective Drug Leads . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2123/17094.

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

Council of Science Editors:

Elias NT. Design and Synthesis of Peptidic Natural Product Analogues as Anti-infective Drug Leads . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17094

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


University of Sydney

24. 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 November 15, 2019. http://hdl.handle.net/2123/18569.

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

MLA Handbook (7th Edition):

Dinarvand, Mojdeh. “Discovery and development of novel antibacterials from natural products .” 2017. Web. 15 Nov 2019.

Vancouver:

Dinarvand M. Discovery and development of novel antibacterials from natural products . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2123/18569.

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

Council of Science Editors:

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

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


University of Manchester

25. Nisbar, Nur Dayana binti. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv.

Degree: 2018, University of Manchester

 Tuberculosis is a disease that kills more people every year than any other infectious disease and is caused by the human pathogen, Mycobacterium tuberculosis (Mtb).… (more)

Subjects/Keywords: Tuberculosis; Cytochrome P450; Fragment-based drug discovery

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APA (6th Edition):

Nisbar, N. D. b. (2018). Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431

Chicago Manual of Style (16th Edition):

Nisbar, Nur Dayana binti. “Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv.” 2018. Doctoral Dissertation, University of Manchester. Accessed November 15, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431.

MLA Handbook (7th Edition):

Nisbar, Nur Dayana binti. “Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv.” 2018. Web. 15 Nov 2019.

Vancouver:

Nisbar NDb. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Nov 15]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431.

Council of Science Editors:

Nisbar NDb. Characterisation of orphan cytochrome P450s from Mycobacterium tuberculosis H37Rv. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:313431


Montana Tech

26. Kearns, Alison King. MECHANISMS AND CYTOTOXIC EFFECTS OF NQO1-DIRECTED LAVENDAMYCIN DERIVATIVES AND MITOCHONDRIA-TARGETED ANTHRACENYL ISOXAZOLE AMIDES AS NOVEL ANTITUMOR AGENTS.

Degree: PhD, 2013, Montana Tech

  Cancer is a common, complex, and oftentimes fatal disease. Despite extensive research in the field of cancer drug discovery, there are still improvements to… (more)

Subjects/Keywords: Antitumor agents; Cancer; Targeted drug discovery

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APA (6th Edition):

Kearns, A. K. (2013). MECHANISMS AND CYTOTOXIC EFFECTS OF NQO1-DIRECTED LAVENDAMYCIN DERIVATIVES AND MITOCHONDRIA-TARGETED ANTHRACENYL ISOXAZOLE AMIDES AS NOVEL ANTITUMOR AGENTS. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/4132

Chicago Manual of Style (16th Edition):

Kearns, Alison King. “MECHANISMS AND CYTOTOXIC EFFECTS OF NQO1-DIRECTED LAVENDAMYCIN DERIVATIVES AND MITOCHONDRIA-TARGETED ANTHRACENYL ISOXAZOLE AMIDES AS NOVEL ANTITUMOR AGENTS.” 2013. Doctoral Dissertation, Montana Tech. Accessed November 15, 2019. https://scholarworks.umt.edu/etd/4132.

MLA Handbook (7th Edition):

Kearns, Alison King. “MECHANISMS AND CYTOTOXIC EFFECTS OF NQO1-DIRECTED LAVENDAMYCIN DERIVATIVES AND MITOCHONDRIA-TARGETED ANTHRACENYL ISOXAZOLE AMIDES AS NOVEL ANTITUMOR AGENTS.” 2013. Web. 15 Nov 2019.

Vancouver:

Kearns AK. MECHANISMS AND CYTOTOXIC EFFECTS OF NQO1-DIRECTED LAVENDAMYCIN DERIVATIVES AND MITOCHONDRIA-TARGETED ANTHRACENYL ISOXAZOLE AMIDES AS NOVEL ANTITUMOR AGENTS. [Internet] [Doctoral dissertation]. Montana Tech; 2013. [cited 2019 Nov 15]. Available from: https://scholarworks.umt.edu/etd/4132.

Council of Science Editors:

Kearns AK. MECHANISMS AND CYTOTOXIC EFFECTS OF NQO1-DIRECTED LAVENDAMYCIN DERIVATIVES AND MITOCHONDRIA-TARGETED ANTHRACENYL ISOXAZOLE AMIDES AS NOVEL ANTITUMOR AGENTS. [Doctoral Dissertation]. Montana Tech; 2013. Available from: https://scholarworks.umt.edu/etd/4132


University of British Columbia

27. McHardy, Lianne M. A study of the mechanism of action of novel inhibitors of tumour cell invasion .

Degree: 2007, University of British Columbia

 Metastasis is the leading cause of death in cancer patients. Tumour invasion and migration are critical aspects of metastatic progression. A forward chemical genetics project… (more)

Subjects/Keywords: Cancer; Drug Discovery

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APA (6th Edition):

McHardy, L. M. (2007). A study of the mechanism of action of novel inhibitors of tumour cell invasion . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/252

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):

McHardy, Lianne M. “A study of the mechanism of action of novel inhibitors of tumour cell invasion .” 2007. Thesis, University of British Columbia. Accessed November 15, 2019. http://hdl.handle.net/2429/252.

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

MLA Handbook (7th Edition):

McHardy, Lianne M. “A study of the mechanism of action of novel inhibitors of tumour cell invasion .” 2007. Web. 15 Nov 2019.

Vancouver:

McHardy LM. A study of the mechanism of action of novel inhibitors of tumour cell invasion . [Internet] [Thesis]. University of British Columbia; 2007. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/2429/252.

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

Council of Science Editors:

McHardy LM. A study of the mechanism of action of novel inhibitors of tumour cell invasion . [Thesis]. University of British Columbia; 2007. Available from: http://hdl.handle.net/2429/252

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


IUPUI

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

Degree: 2010, IUPUI

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Cheemakurthi, Usha Deepika. “DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN.” 2010. Thesis, IUPUI. Accessed November 15, 2019. http://hdl.handle.net/1805/2268.

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

MLA Handbook (7th Edition):

Cheemakurthi, Usha Deepika. “DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN.” 2010. Web. 15 Nov 2019.

Vancouver:

Cheemakurthi UD. DESIGN, DEVELOPMENT AND IMPLEMENTATION OF TOOLS IN. [Internet] [Thesis]. IUPUI; 2010. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1805/2268.

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

Council of Science Editors:

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

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


University of Ottawa

29. Cooke, Donald M. Targeting Connexins to Promote Functional Neural Repair and Regeneration .

Degree: 2013, University of Ottawa

 The connexins are a family of 21 proteins that represent the structural units of intercellular gap junctions and single membrane hemichannels. These channels provide a… (more)

Subjects/Keywords: Gap junctions; Connexins; Pannexins; Drug discovery

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APA (6th Edition):

Cooke, D. M. (2013). Targeting Connexins to Promote Functional Neural Repair and Regeneration . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/24308

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):

Cooke, Donald M. “Targeting Connexins to Promote Functional Neural Repair and Regeneration .” 2013. Thesis, University of Ottawa. Accessed November 15, 2019. http://hdl.handle.net/10393/24308.

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

MLA Handbook (7th Edition):

Cooke, Donald M. “Targeting Connexins to Promote Functional Neural Repair and Regeneration .” 2013. Web. 15 Nov 2019.

Vancouver:

Cooke DM. Targeting Connexins to Promote Functional Neural Repair and Regeneration . [Internet] [Thesis]. University of Ottawa; 2013. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/10393/24308.

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

Council of Science Editors:

Cooke DM. Targeting Connexins to Promote Functional Neural Repair and Regeneration . [Thesis]. University of Ottawa; 2013. Available from: http://hdl.handle.net/10393/24308

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


Texas A&M University

30. Huang, Hsiao-Ling. Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis.

Degree: PhD, Chemistry, 2016, Texas A&M University

 As the world population battles drug-resistant tuberculosis (TB), there is an urgent need for novel anti-tubercular drugs. This dissertation documents the studies of glyoxylate shunt… (more)

Subjects/Keywords: Drug Discovery; Structural Biology; Carbon Metabolism; Tuberculosis

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

APA (6th Edition):

Huang, H. (2016). Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174220

Chicago Manual of Style (16th Edition):

Huang, Hsiao-Ling. “Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis.” 2016. Doctoral Dissertation, Texas A&M University. Accessed November 15, 2019. http://hdl.handle.net/1969.1/174220.

MLA Handbook (7th Edition):

Huang, Hsiao-Ling. “Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis.” 2016. Web. 15 Nov 2019.

Vancouver:

Huang H. Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2019 Nov 15]. Available from: http://hdl.handle.net/1969.1/174220.

Council of Science Editors:

Huang H. Structural and Biochemical Studies of Glyoxylate Shunt Enzymes as Drug Targets of Mycobacterium tuberculosis. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/174220

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