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You searched for subject:(Malaria Chemotherapy). Showing records 1 – 28 of 28 total matches.

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University of Pretoria

1. Roux, Suretha. Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts.

Degree: Biochemistry, 2009, University of Pretoria

Malaria is a global health threat that causes 300 – 500 million clinical cases annually, resulting in approximately 2 million deaths. Chemotherapy and prophylaxis are… (more)

Subjects/Keywords: Enzymes; Novel drugs; Chemotherapy; Malaria; UCTD

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

APA (6th Edition):

Roux, S. (2009). Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/26993

Chicago Manual of Style (16th Edition):

Roux, Suretha. “Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts.” 2009. Masters Thesis, University of Pretoria. Accessed October 14, 2019. http://hdl.handle.net/2263/26993.

MLA Handbook (7th Edition):

Roux, Suretha. “Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts.” 2009. Web. 14 Oct 2019.

Vancouver:

Roux S. Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts. [Internet] [Masters thesis]. University of Pretoria; 2009. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2263/26993.

Council of Science Editors:

Roux S. Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts. [Masters Thesis]. University of Pretoria; 2009. Available from: http://hdl.handle.net/2263/26993


University of Pretoria

2. [No author]. Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts .

Degree: 2009, University of Pretoria

Malaria is a global health threat that causes 300 – 500 million clinical cases annually, resulting in approximately 2 million deaths. Chemotherapy and prophylaxis are… (more)

Subjects/Keywords: Enzymes; Novel drugs; Chemotherapy; Malaria; UCTD

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APA (6th Edition):

author], [. (2009). Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-08042008-142035/

Chicago Manual of Style (16th Edition):

author], [No. “Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts .” 2009. Masters Thesis, University of Pretoria. Accessed October 14, 2019. http://upetd.up.ac.za/thesis/available/etd-08042008-142035/.

MLA Handbook (7th Edition):

author], [No. “Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts .” 2009. Web. 14 Oct 2019.

Vancouver:

author] [. Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts . [Internet] [Masters thesis]. University of Pretoria; 2009. [cited 2019 Oct 14]. Available from: http://upetd.up.ac.za/thesis/available/etd-08042008-142035/.

Council of Science Editors:

author] [. Modulation of functional properties of bi-functional S-Adenosylmethionine decarboxylase / Ornithine decarboxylase of Plasmodium falciparum by structural motifs in parasite-specific inserts . [Masters Thesis]. University of Pretoria; 2009. Available from: http://upetd.up.ac.za/thesis/available/etd-08042008-142035/


Rhodes University

3. Idahosa, Kenudi Christiana. Bayliss-Hillman adducts as scaffolds for the construction of novel compounds with medicinal potential.

Degree: Faculty of Science, Chemistry, 2012, Rhodes University

 This project has focused on exploring the application of Baylis-Hillman (BH) {a.k.a. Morita-Baylis-Hillman (MBH)} scaffolds in the construction of various compounds with medicinal potential. A… (more)

Subjects/Keywords: Antimalarials  – Research; Malaria  – Chemotherapy  – Research; AIDS (Disease)  – Treatment  – Research; AIDS (Disease)  – Chemotherapy  – Research

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APA (6th Edition):

Idahosa, K. C. (2012). Bayliss-Hillman adducts as scaffolds for the construction of novel compounds with medicinal potential. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1006763

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):

Idahosa, Kenudi Christiana. “Bayliss-Hillman adducts as scaffolds for the construction of novel compounds with medicinal potential.” 2012. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1006763.

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

MLA Handbook (7th Edition):

Idahosa, Kenudi Christiana. “Bayliss-Hillman adducts as scaffolds for the construction of novel compounds with medicinal potential.” 2012. Web. 14 Oct 2019.

Vancouver:

Idahosa KC. Bayliss-Hillman adducts as scaffolds for the construction of novel compounds with medicinal potential. [Internet] [Thesis]. Rhodes University; 2012. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1006763.

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

Council of Science Editors:

Idahosa KC. Bayliss-Hillman adducts as scaffolds for the construction of novel compounds with medicinal potential. [Thesis]. Rhodes University; 2012. Available from: http://hdl.handle.net/10962/d1006763

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


Rhodes University

4. Yao, Jia. Synthesis of silver nanoparticles and their role against a thiazolekinase enzyme from Plasmodium falciparum.

Degree: MS, Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2014, Rhodes University

Malaria, a mosquito-borne infectious disease, caused by the protozoan Plasmodium genus, is the greatest health challenges worldwide. The plasmodial vitamin B1 biosynthetic enzyme PfThzK diverges… (more)

Subjects/Keywords: Silver; Nanoparticles; Thiazoles; Plasmodium falciparum; Antimalarials; Malaria  – Chemotherapy

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APA (6th Edition):

Yao, J. (2014). Synthesis of silver nanoparticles and their role against a thiazolekinase enzyme from Plasmodium falciparum. (Masters Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1020894

Chicago Manual of Style (16th Edition):

Yao, Jia. “Synthesis of silver nanoparticles and their role against a thiazolekinase enzyme from Plasmodium falciparum.” 2014. Masters Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1020894.

MLA Handbook (7th Edition):

Yao, Jia. “Synthesis of silver nanoparticles and their role against a thiazolekinase enzyme from Plasmodium falciparum.” 2014. Web. 14 Oct 2019.

Vancouver:

Yao J. Synthesis of silver nanoparticles and their role against a thiazolekinase enzyme from Plasmodium falciparum. [Internet] [Masters thesis]. Rhodes University; 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1020894.

Council of Science Editors:

Yao J. Synthesis of silver nanoparticles and their role against a thiazolekinase enzyme from Plasmodium falciparum. [Masters Thesis]. Rhodes University; 2014. Available from: http://hdl.handle.net/10962/d1020894


Rhodes University

5. Njuguna, Joyce Njoki. Structural analysis of prodomain inhibition of cysteine proteases in plasmodium species.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2012, Rhodes University

 Plasmodium is a genus of parasites causing malaria, a virulent protozoan infection in humans resulting in over a million deaths annually. Treatment of malaria is… (more)

Subjects/Keywords: Plasmodium; Cysteine proteinases; Proteolytic enzymes; Malaria  – Chemotherapy; Antimalarials; Plasmodium falciparum

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APA (6th Edition):

Njuguna, J. N. (2012). Structural analysis of prodomain inhibition of cysteine proteases in plasmodium species. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004081

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):

Njuguna, Joyce Njoki. “Structural analysis of prodomain inhibition of cysteine proteases in plasmodium species.” 2012. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1004081.

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

MLA Handbook (7th Edition):

Njuguna, Joyce Njoki. “Structural analysis of prodomain inhibition of cysteine proteases in plasmodium species.” 2012. Web. 14 Oct 2019.

Vancouver:

Njuguna JN. Structural analysis of prodomain inhibition of cysteine proteases in plasmodium species. [Internet] [Thesis]. Rhodes University; 2012. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1004081.

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

Council of Science Editors:

Njuguna JN. Structural analysis of prodomain inhibition of cysteine proteases in plasmodium species. [Thesis]. Rhodes University; 2012. Available from: http://hdl.handle.net/10962/d1004081

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


Rhodes University

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

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Conibear, Anne Claire. “Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials.” 2013. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1008282.

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

MLA Handbook (7th Edition):

Conibear, Anne Claire. “Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials.” 2013. Web. 14 Oct 2019.

Vancouver:

Conibear AC. Synthesis and evaluation of novel inhibitors of 1-Deoxy-D-xylolose-5-phosphate reductoisomerase as potential antimalarials. [Internet] [Thesis]. Rhodes University; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1008282.

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

Council of Science Editors:

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

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


Michigan State University

7. Divo, Alan Andrew. The mitochondrion of Plasmodium falciparum as a site for chemotherapeutic intervention.

Degree: PhD, Department of Microbiology and Public Health, 1985, Michigan State University

Subjects/Keywords: Plasmodium falciparum; Mitochondria; Malaria; Chemotherapy

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APA (6th Edition):

Divo, A. A. (1985). The mitochondrion of Plasmodium falciparum as a site for chemotherapeutic intervention. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:18005

Chicago Manual of Style (16th Edition):

Divo, Alan Andrew. “The mitochondrion of Plasmodium falciparum as a site for chemotherapeutic intervention.” 1985. Doctoral Dissertation, Michigan State University. Accessed October 14, 2019. http://etd.lib.msu.edu/islandora/object/etd:18005.

MLA Handbook (7th Edition):

Divo, Alan Andrew. “The mitochondrion of Plasmodium falciparum as a site for chemotherapeutic intervention.” 1985. Web. 14 Oct 2019.

Vancouver:

Divo AA. The mitochondrion of Plasmodium falciparum as a site for chemotherapeutic intervention. [Internet] [Doctoral dissertation]. Michigan State University; 1985. [cited 2019 Oct 14]. Available from: http://etd.lib.msu.edu/islandora/object/etd:18005.

Council of Science Editors:

Divo AA. The mitochondrion of Plasmodium falciparum as a site for chemotherapeutic intervention. [Doctoral Dissertation]. Michigan State University; 1985. Available from: http://etd.lib.msu.edu/islandora/object/etd:18005


Rhodes University

8. Kanzi, Aquillah Mumo. Falcipains as malarial drug targets.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2013, Rhodes University

Malaria is an infectious disease caused by parasites of the Plasmodium genus with mortality rates of more than a million annually, hence a major global… (more)

Subjects/Keywords: Malaria; Malaria  – Chemotherapy; Plasmodium falciparum; Antimalarials  – Development; Cysteine proteinases; Cysteine proteinases  – Inhibitors; Papain; Drug development; Bioinformatics

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APA (6th Edition):

Kanzi, A. M. (2013). Falcipains as malarial drug targets. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1003842

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):

Kanzi, Aquillah Mumo. “Falcipains as malarial drug targets.” 2013. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1003842.

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

MLA Handbook (7th Edition):

Kanzi, Aquillah Mumo. “Falcipains as malarial drug targets.” 2013. Web. 14 Oct 2019.

Vancouver:

Kanzi AM. Falcipains as malarial drug targets. [Internet] [Thesis]. Rhodes University; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1003842.

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

Council of Science Editors:

Kanzi AM. Falcipains as malarial drug targets. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1003842

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


Rhodes University

9. Faya, Ngonidzashe. A step forward in defining Hsp90s as potential drug targets for human parasitic diseases.

Degree: MS, Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2014, Rhodes University

 Parasitic diseases remain a health burden affecting more than 500 million people worldwide with malaria having the highest mortality rate. The parasites can be transferred… (more)

Subjects/Keywords: Heat shock proteins  – Research; Malaria  – Chemotherapy  – Research; Antimalarials  – Development  – Research; Parasitic diseases  – Research; Plasmodium

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APA (6th Edition):

Faya, N. (2014). A step forward in defining Hsp90s as potential drug targets for human parasitic diseases. (Masters Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1012993

Chicago Manual of Style (16th Edition):

Faya, Ngonidzashe. “A step forward in defining Hsp90s as potential drug targets for human parasitic diseases.” 2014. Masters Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1012993.

MLA Handbook (7th Edition):

Faya, Ngonidzashe. “A step forward in defining Hsp90s as potential drug targets for human parasitic diseases.” 2014. Web. 14 Oct 2019.

Vancouver:

Faya N. A step forward in defining Hsp90s as potential drug targets for human parasitic diseases. [Internet] [Masters thesis]. Rhodes University; 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1012993.

Council of Science Editors:

Faya N. A step forward in defining Hsp90s as potential drug targets for human parasitic diseases. [Masters Thesis]. Rhodes University; 2014. Available from: http://hdl.handle.net/10962/d1012993


University of Namibia

10. Uusiku, A. Synthesis and characterization of metal complexes 2-Benzoylpyridene and di-2-pyridyl ketone schiff base ligands derived from s-methyldithiocarbazate fragment and its application to biological activity toward P.Falciparum .

Degree: 2015, University of Namibia

 The synthesis, characterization, spectroscopic and biological evaluation of 2-benzoylpyridine-s-methyldithiocarbazate (HL1) and di-2-pyradylketone-s-methyldithiocarbazate (HL2) with selected metal ions of copper (II), zinc (II), cadmium (II), nickel… (more)

Subjects/Keywords: Metal complexes ; Biological activity ; P. Falciparum ; 2-Benzoylpyridine ; Di-2-Pyridyl ; Metal complexes ; Malaria, Chemotherapy

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APA (6th Edition):

Uusiku, A. (2015). Synthesis and characterization of metal complexes 2-Benzoylpyridene and di-2-pyridyl ketone schiff base ligands derived from s-methyldithiocarbazate fragment and its application to biological activity toward P.Falciparum . (Thesis). University of Namibia. Retrieved from http://hdl.handle.net/11070/1689

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):

Uusiku, A. “Synthesis and characterization of metal complexes 2-Benzoylpyridene and di-2-pyridyl ketone schiff base ligands derived from s-methyldithiocarbazate fragment and its application to biological activity toward P.Falciparum .” 2015. Thesis, University of Namibia. Accessed October 14, 2019. http://hdl.handle.net/11070/1689.

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

MLA Handbook (7th Edition):

Uusiku, A. “Synthesis and characterization of metal complexes 2-Benzoylpyridene and di-2-pyridyl ketone schiff base ligands derived from s-methyldithiocarbazate fragment and its application to biological activity toward P.Falciparum .” 2015. Web. 14 Oct 2019.

Vancouver:

Uusiku A. Synthesis and characterization of metal complexes 2-Benzoylpyridene and di-2-pyridyl ketone schiff base ligands derived from s-methyldithiocarbazate fragment and its application to biological activity toward P.Falciparum . [Internet] [Thesis]. University of Namibia; 2015. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/11070/1689.

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

Council of Science Editors:

Uusiku A. Synthesis and characterization of metal complexes 2-Benzoylpyridene and di-2-pyridyl ketone schiff base ligands derived from s-methyldithiocarbazate fragment and its application to biological activity toward P.Falciparum . [Thesis]. University of Namibia; 2015. Available from: http://hdl.handle.net/11070/1689

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


Rhodes University

11. Kroon, Matthys Christoffel. High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2013, Rhodes University

 The papain-like cysteine protease family (C1 proteases) is highly important because of its involvement in research and industrial applications and its role in various human… (more)

Subjects/Keywords: Cysteine proteinases; Cysteine proteinases  – Inhibitors; Papain; Cystatins; Malaria  – Chemotherapy; Homology (Biology); Protein-protein interactions

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APA (6th Edition):

Kroon, M. C. (2013). High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1001619

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):

Kroon, Matthys Christoffel. “High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors.” 2013. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1001619.

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

MLA Handbook (7th Edition):

Kroon, Matthys Christoffel. “High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors.” 2013. Web. 14 Oct 2019.

Vancouver:

Kroon MC. High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors. [Internet] [Thesis]. Rhodes University; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1001619.

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

Council of Science Editors:

Kroon MC. High-throughput modelling and structural investigation of cysteine protease complexes with protein inhibitors. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1001619

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


Rhodes University

12. Mutorwa, Marius Kudumo. Synthesis of novel inhibitors of 1-Deoxy-D-xylulose-5-phosphate reductoisomerase as potential anti-malarial lead compounds.

Degree: Faculty of Science, Chemistry, 2011, Rhodes University

 This research has focused on the development of novel substrate mimics as potential DXR inhibitors of 1-deoxy-D-xylulose-5-phosphate reductoisomerase (DXR), an essential enzyme in the mevalonate-independent… (more)

Subjects/Keywords: Antimalarials  – Development; Plasmodium falciparum; Malaria  – Chemotherapy; Drug development; Lead compounds; Phosphonates; Phosphonic acids; Ligands

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APA (6th Edition):

Mutorwa, M. K. (2011). Synthesis of novel inhibitors of 1-Deoxy-D-xylulose-5-phosphate reductoisomerase as potential anti-malarial lead compounds. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1005037

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):

Mutorwa, Marius Kudumo. “Synthesis of novel inhibitors of 1-Deoxy-D-xylulose-5-phosphate reductoisomerase as potential anti-malarial lead compounds.” 2011. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1005037.

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

MLA Handbook (7th Edition):

Mutorwa, Marius Kudumo. “Synthesis of novel inhibitors of 1-Deoxy-D-xylulose-5-phosphate reductoisomerase as potential anti-malarial lead compounds.” 2011. Web. 14 Oct 2019.

Vancouver:

Mutorwa MK. Synthesis of novel inhibitors of 1-Deoxy-D-xylulose-5-phosphate reductoisomerase as potential anti-malarial lead compounds. [Internet] [Thesis]. Rhodes University; 2011. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1005037.

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

Council of Science Editors:

Mutorwa MK. Synthesis of novel inhibitors of 1-Deoxy-D-xylulose-5-phosphate reductoisomerase as potential anti-malarial lead compounds. [Thesis]. Rhodes University; 2011. Available from: http://hdl.handle.net/10962/d1005037

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


Hong Kong University of Science and Technology

13. Pai, Hendry Hung On. A chemical model for mode of antimalarial action of artemisinin.

Degree: 1998, Hong Kong University of Science and Technology

 Artemisinin 8, an active component in a traditional Chinese herb called qinghao, has been extensively used to treat severe malaria. However, mode of action of… (more)

Subjects/Keywords: Artemisia  – Therapeutic use; Antimalarials; Malaria  – Chemotherapy

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APA (6th Edition):

Pai, H. H. O. (1998). A chemical model for mode of antimalarial action of artemisinin. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b603809 ; http://repository.ust.hk/ir/bitstream/1783.1-3993/1/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):

Pai, Hendry Hung On. “A chemical model for mode of antimalarial action of artemisinin.” 1998. Thesis, Hong Kong University of Science and Technology. Accessed October 14, 2019. https://doi.org/10.14711/thesis-b603809 ; http://repository.ust.hk/ir/bitstream/1783.1-3993/1/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):

Pai, Hendry Hung On. “A chemical model for mode of antimalarial action of artemisinin.” 1998. Web. 14 Oct 2019.

Vancouver:

Pai HHO. A chemical model for mode of antimalarial action of artemisinin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 1998. [cited 2019 Oct 14]. Available from: https://doi.org/10.14711/thesis-b603809 ; http://repository.ust.hk/ir/bitstream/1783.1-3993/1/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:

Pai HHO. A chemical model for mode of antimalarial action of artemisinin. [Thesis]. Hong Kong University of Science and Technology; 1998. Available from: https://doi.org/10.14711/thesis-b603809 ; http://repository.ust.hk/ir/bitstream/1783.1-3993/1/th_redirect.html

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


Hong Kong University of Science and Technology

14. Soo, May Kei. Preparation of qinghaosu derivatives bearing DNA-binding ligands.

Degree: 1999, Hong Kong University of Science and Technology

 For the aim of enhancing cytotoxicity of artemisinin derivatives with the long term aim of developing new cytotoxic anticancer drugs, O- and C-glycosidation chemistry is… (more)

Subjects/Keywords: Artemisia  – Therapeutic use; Antimalarials; Malaria  – Chemotherapy

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APA (6th Edition):

Soo, M. K. (1999). Preparation of qinghaosu derivatives bearing DNA-binding ligands. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b648435 ; http://repository.ust.hk/ir/bitstream/1783.1-3998/1/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):

Soo, May Kei. “Preparation of qinghaosu derivatives bearing DNA-binding ligands.” 1999. Thesis, Hong Kong University of Science and Technology. Accessed October 14, 2019. https://doi.org/10.14711/thesis-b648435 ; http://repository.ust.hk/ir/bitstream/1783.1-3998/1/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):

Soo, May Kei. “Preparation of qinghaosu derivatives bearing DNA-binding ligands.” 1999. Web. 14 Oct 2019.

Vancouver:

Soo MK. Preparation of qinghaosu derivatives bearing DNA-binding ligands. [Internet] [Thesis]. Hong Kong University of Science and Technology; 1999. [cited 2019 Oct 14]. Available from: https://doi.org/10.14711/thesis-b648435 ; http://repository.ust.hk/ir/bitstream/1783.1-3998/1/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:

Soo MK. Preparation of qinghaosu derivatives bearing DNA-binding ligands. [Thesis]. Hong Kong University of Science and Technology; 1999. Available from: https://doi.org/10.14711/thesis-b648435 ; http://repository.ust.hk/ir/bitstream/1783.1-3998/1/th_redirect.html

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


Hong Kong University of Science and Technology

15. Lung, Chung Man. Decomposition of current clinically-used artemisinin derivatives and preparation of polar artemisinin derivatives.

Degree: 2006, Hong Kong University of Science and Technology

 In Chapter 1 of this thesis, decomposition of current clinically-used artemisnins is discussed. Artesunate formulated into rectal capsules undergoes decomposition under the thermal stress testing… (more)

Subjects/Keywords: Artemisia  – Derivatives  – Therapeutic use; Malaria  – Chemotherapy

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APA (6th Edition):

Lung, C. M. (2006). Decomposition of current clinically-used artemisinin derivatives and preparation of polar artemisinin derivatives. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b938098 ; http://repository.ust.hk/ir/bitstream/1783.1-4042/1/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):

Lung, Chung Man. “Decomposition of current clinically-used artemisinin derivatives and preparation of polar artemisinin derivatives.” 2006. Thesis, Hong Kong University of Science and Technology. Accessed October 14, 2019. https://doi.org/10.14711/thesis-b938098 ; http://repository.ust.hk/ir/bitstream/1783.1-4042/1/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):

Lung, Chung Man. “Decomposition of current clinically-used artemisinin derivatives and preparation of polar artemisinin derivatives.” 2006. Web. 14 Oct 2019.

Vancouver:

Lung CM. Decomposition of current clinically-used artemisinin derivatives and preparation of polar artemisinin derivatives. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2006. [cited 2019 Oct 14]. Available from: https://doi.org/10.14711/thesis-b938098 ; http://repository.ust.hk/ir/bitstream/1783.1-4042/1/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:

Lung CM. Decomposition of current clinically-used artemisinin derivatives and preparation of polar artemisinin derivatives. [Thesis]. Hong Kong University of Science and Technology; 2006. Available from: https://doi.org/10.14711/thesis-b938098 ; http://repository.ust.hk/ir/bitstream/1783.1-4042/1/th_redirect.html

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


Rhodes University

16. Mokoena, Fortunate. Malarial drug targets cysteine proteases as hemoglobinases.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology;, 2012, Rhodes University

Malaria has consistently been rated as the worst parasitic disease in the world. This disease affects an estimated 5 billion households annually. Malaria has a… (more)

Subjects/Keywords: Malaria  – Chemotherapy; Antimalarials; Hemoglobin; Proteolytic enzymes; Cysteine proteinases; Plasmodium falciparum; Plasmodium vivax; Papain

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APA (6th Edition):

Mokoena, F. (2012). Malarial drug targets cysteine proteases as hemoglobinases. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004065

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):

Mokoena, Fortunate. “Malarial drug targets cysteine proteases as hemoglobinases.” 2012. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1004065.

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

MLA Handbook (7th Edition):

Mokoena, Fortunate. “Malarial drug targets cysteine proteases as hemoglobinases.” 2012. Web. 14 Oct 2019.

Vancouver:

Mokoena F. Malarial drug targets cysteine proteases as hemoglobinases. [Internet] [Thesis]. Rhodes University; 2012. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1004065.

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

Council of Science Editors:

Mokoena F. Malarial drug targets cysteine proteases as hemoglobinases. [Thesis]. Rhodes University; 2012. Available from: http://hdl.handle.net/10962/d1004065

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


Rhodes University

17. Clitheroe, Crystal-Leigh. In-silico analysis of Plasmodium falciparum Hop protein and its interactions with Hsp70 and Hsp90.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2013, Rhodes University

A lessor understood co-chaperone, the Hsp70/Hsp90 organising protein (Hop), has been found to play an important role in modulating the activity and co-interaction of two… (more)

Subjects/Keywords: Plasmodium falciparum; Heat shock proteins; Molecular chaperones; Homology (Biology); Protein-protein interactions; Malaria  – Chemotherapy

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APA (6th Edition):

Clitheroe, C. (2013). In-silico analysis of Plasmodium falciparum Hop protein and its interactions with Hsp70 and Hsp90. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1003819

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):

Clitheroe, Crystal-Leigh. “In-silico analysis of Plasmodium falciparum Hop protein and its interactions with Hsp70 and Hsp90.” 2013. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1003819.

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

MLA Handbook (7th Edition):

Clitheroe, Crystal-Leigh. “In-silico analysis of Plasmodium falciparum Hop protein and its interactions with Hsp70 and Hsp90.” 2013. Web. 14 Oct 2019.

Vancouver:

Clitheroe C. In-silico analysis of Plasmodium falciparum Hop protein and its interactions with Hsp70 and Hsp90. [Internet] [Thesis]. Rhodes University; 2013. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1003819.

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

Council of Science Editors:

Clitheroe C. In-silico analysis of Plasmodium falciparum Hop protein and its interactions with Hsp70 and Hsp90. [Thesis]. Rhodes University; 2013. Available from: http://hdl.handle.net/10962/d1003819

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


University of Pretoria

18. Manning, Suzanne Kathryn. Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes.

Degree: Biochemistry, 2005, University of Pretoria

Please read the abstract in the section 00front of this document Advisors/Committee Members: Prof A I Louw (advisor).

Subjects/Keywords: Malaria drug resistance research; Plasmodium falciparum microbiology research; Malaria chemotherapy; UCTD

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APA (6th Edition):

Manning, S. (2005). Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/29635

Chicago Manual of Style (16th Edition):

Manning, Suzanne. “Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes.” 2005. Masters Thesis, University of Pretoria. Accessed October 14, 2019. http://hdl.handle.net/2263/29635.

MLA Handbook (7th Edition):

Manning, Suzanne. “Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes.” 2005. Web. 14 Oct 2019.

Vancouver:

Manning S. Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes. [Internet] [Masters thesis]. University of Pretoria; 2005. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/2263/29635.

Council of Science Editors:

Manning S. Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes. [Masters Thesis]. University of Pretoria; 2005. Available from: http://hdl.handle.net/2263/29635


University of Pretoria

19. [No author]. Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes .

Degree: 2005, University of Pretoria

Please read the abstract in the section 00front of this document Advisors/Committee Members: Prof A I Louw (advisor).

Subjects/Keywords: Malaria drug resistance research; Plasmodium falciparum microbiology research; Malaria chemotherapy; UCTD

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APA (6th Edition):

author], [. (2005). Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-11212005-085137/

Chicago Manual of Style (16th Edition):

author], [No. “Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes .” 2005. Masters Thesis, University of Pretoria. Accessed October 14, 2019. http://upetd.up.ac.za/thesis/available/etd-11212005-085137/.

MLA Handbook (7th Edition):

author], [No. “Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes .” 2005. Web. 14 Oct 2019.

Vancouver:

author] [. Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes . [Internet] [Masters thesis]. University of Pretoria; 2005. [cited 2019 Oct 14]. Available from: http://upetd.up.ac.za/thesis/available/etd-11212005-085137/.

Council of Science Editors:

author] [. Molecular characterization of the hexose transporter (PfHT1) of Plasmodium falciparum in Xenopus laevis oocytes . [Masters Thesis]. University of Pretoria; 2005. Available from: http://upetd.up.ac.za/thesis/available/etd-11212005-085137/


Jawaharlal Nehru University

20. Deshpande, Shreekant. Synthesis, biological evaluation and QSAR studies of novel antimalarial agents.

Degree:  – , 2010, Jawaharlal Nehru University

None

Summary and References included

Advisors/Committee Members: Prabhakar, Yenamandra S, Katti, Seturam.

Subjects/Keywords: Malaria chemotherapy; Novel antimalarial agents; Antimalarial agents; Chloroquine; QSAR

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APA (6th Edition):

Deshpande, S. (2010). Synthesis, biological evaluation and QSAR studies of novel antimalarial agents. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/13467

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):

Deshpande, Shreekant. “Synthesis, biological evaluation and QSAR studies of novel antimalarial agents.” 2010. Thesis, Jawaharlal Nehru University. Accessed October 14, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/13467.

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

MLA Handbook (7th Edition):

Deshpande, Shreekant. “Synthesis, biological evaluation and QSAR studies of novel antimalarial agents.” 2010. Web. 14 Oct 2019.

Vancouver:

Deshpande S. Synthesis, biological evaluation and QSAR studies of novel antimalarial agents. [Internet] [Thesis]. Jawaharlal Nehru University; 2010. [cited 2019 Oct 14]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/13467.

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

Council of Science Editors:

Deshpande S. Synthesis, biological evaluation and QSAR studies of novel antimalarial agents. [Thesis]. Jawaharlal Nehru University; 2010. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/13467

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


Rhodes University

21. Njunge, James Mwangi. Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2014, Rhodes University

 Human malaria is an economically important disease caused by single-celled parasites of the Plasmodium genus whose biology displays great evolutionary adaptation to both its mammalian… (more)

Subjects/Keywords: Plasmodium falciparum; Heat shock proteins; Malaria  – Chemotherapy; Protein-protein interactions; Erythrocytes  – Biotechnology; Molecular chaperones; Host-parasite relationships; Mitochondria

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APA (6th Edition):

Njunge, J. M. (2014). Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1013186

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):

Njunge, James Mwangi. “Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70.” 2014. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1013186.

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

MLA Handbook (7th Edition):

Njunge, James Mwangi. “Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70.” 2014. Web. 14 Oct 2019.

Vancouver:

Njunge JM. Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70. [Internet] [Thesis]. Rhodes University; 2014. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1013186.

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

Council of Science Editors:

Njunge JM. Characterization of the Hsp40 partner proteins of Plasmodium falciparum Hsp70. [Thesis]. Rhodes University; 2014. Available from: http://hdl.handle.net/10962/d1013186

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


Rhodes University

22. Goble, Jessica Leigh. The druggable antimalarial target 1-deoxy-D-xylulose-5-phosphate reductoisomerase: purfication, kinetic characterization and inhibition studies.

Degree: Faculty of Science, Biochemistry, Microbiology and Biotechnology, 2011, Rhodes University

 Plasmodium falciparum 1–deoxy–D–xylulose–5 phosphatereductoisomerase (PfDXR) plays a role in isoprenoid biosynthesis in the malaria parasite and is absent in the human host, making this parasite… (more)

Subjects/Keywords: Antimalarials  – Development; Plasmodium falciparum; Drug development; Plasmodium falciparum  – Purification; Plasmodium falciparum  – Inhibitors; Enzyme kinetics; Malaria  – Chemotherapy

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APA (6th Edition):

Goble, J. L. (2011). The druggable antimalarial target 1-deoxy-D-xylulose-5-phosphate reductoisomerase: purfication, kinetic characterization and inhibition studies. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1004008

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):

Goble, Jessica Leigh. “The druggable antimalarial target 1-deoxy-D-xylulose-5-phosphate reductoisomerase: purfication, kinetic characterization and inhibition studies.” 2011. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1004008.

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

MLA Handbook (7th Edition):

Goble, Jessica Leigh. “The druggable antimalarial target 1-deoxy-D-xylulose-5-phosphate reductoisomerase: purfication, kinetic characterization and inhibition studies.” 2011. Web. 14 Oct 2019.

Vancouver:

Goble JL. The druggable antimalarial target 1-deoxy-D-xylulose-5-phosphate reductoisomerase: purfication, kinetic characterization and inhibition studies. [Internet] [Thesis]. Rhodes University; 2011. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1004008.

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

Council of Science Editors:

Goble JL. The druggable antimalarial target 1-deoxy-D-xylulose-5-phosphate reductoisomerase: purfication, kinetic characterization and inhibition studies. [Thesis]. Rhodes University; 2011. Available from: http://hdl.handle.net/10962/d1004008

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


Hong Kong University of Science and Technology

23. Ho, Wing Yan. Studies on molecular mechanism of action and synthesis of new derivatives of the antimalarial drug artemisinin.

Degree: 2004, Hong Kong University of Science and Technology

 The thesis commences with an overview of the history and development of the Chinese peroxidic sesquiterpene qinghaosu or artemisinin, and its conversion into the current… (more)

Subjects/Keywords: Artemisia  – Derivatives  – Therapeutic use; Antimalarials; Malaria  – Chemotherapy

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APA (6th Edition):

Ho, W. Y. (2004). Studies on molecular mechanism of action and synthesis of new derivatives of the antimalarial drug artemisinin. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b843327 ; http://repository.ust.hk/ir/bitstream/1783.1-2236/1/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):

Ho, Wing Yan. “Studies on molecular mechanism of action and synthesis of new derivatives of the antimalarial drug artemisinin.” 2004. Thesis, Hong Kong University of Science and Technology. Accessed October 14, 2019. https://doi.org/10.14711/thesis-b843327 ; http://repository.ust.hk/ir/bitstream/1783.1-2236/1/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):

Ho, Wing Yan. “Studies on molecular mechanism of action and synthesis of new derivatives of the antimalarial drug artemisinin.” 2004. Web. 14 Oct 2019.

Vancouver:

Ho WY. Studies on molecular mechanism of action and synthesis of new derivatives of the antimalarial drug artemisinin. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2004. [cited 2019 Oct 14]. Available from: https://doi.org/10.14711/thesis-b843327 ; http://repository.ust.hk/ir/bitstream/1783.1-2236/1/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:

Ho WY. Studies on molecular mechanism of action and synthesis of new derivatives of the antimalarial drug artemisinin. [Thesis]. Hong Kong University of Science and Technology; 2004. Available from: https://doi.org/10.14711/thesis-b843327 ; http://repository.ust.hk/ir/bitstream/1783.1-2236/1/th_redirect.html

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


Université Montpellier II

24. Wein, Sharon. Propriétés et mécanisme d'action des analogues de choline, une nouvelle classe d'antipaludiques. Etude de l'albitiazolium, candidat clinique. : Properties and mechanism of action of choline analogues, a new class of antimalarials. Study of the clinical candidate albitiazolium.

Degree: Docteur es, Biologie Santé, 2012, Université Montpellier II

Les analogues de choline constituent une nouvelle classe d'antipaludiques qui inhibent la biosynthèse de la phosphatidylcholine (PC) de Plasmodium, parasite responsable du paludisme. Les études… (more)

Subjects/Keywords: Plasmodium; Paludisme; Phospholipides; Chimiothérapie; Analogue de choline; Mécanisme d'action; Plasmodium; Malaria; Phospholipid; Chemotherapy; Choline analogue; Mechanism of action

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APA (6th Edition):

Wein, S. (2012). Propriétés et mécanisme d'action des analogues de choline, une nouvelle classe d'antipaludiques. Etude de l'albitiazolium, candidat clinique. : Properties and mechanism of action of choline analogues, a new class of antimalarials. Study of the clinical candidate albitiazolium. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2012MON20078

Chicago Manual of Style (16th Edition):

Wein, Sharon. “Propriétés et mécanisme d'action des analogues de choline, une nouvelle classe d'antipaludiques. Etude de l'albitiazolium, candidat clinique. : Properties and mechanism of action of choline analogues, a new class of antimalarials. Study of the clinical candidate albitiazolium.” 2012. Doctoral Dissertation, Université Montpellier II. Accessed October 14, 2019. http://www.theses.fr/2012MON20078.

MLA Handbook (7th Edition):

Wein, Sharon. “Propriétés et mécanisme d'action des analogues de choline, une nouvelle classe d'antipaludiques. Etude de l'albitiazolium, candidat clinique. : Properties and mechanism of action of choline analogues, a new class of antimalarials. Study of the clinical candidate albitiazolium.” 2012. Web. 14 Oct 2019.

Vancouver:

Wein S. Propriétés et mécanisme d'action des analogues de choline, une nouvelle classe d'antipaludiques. Etude de l'albitiazolium, candidat clinique. : Properties and mechanism of action of choline analogues, a new class of antimalarials. Study of the clinical candidate albitiazolium. [Internet] [Doctoral dissertation]. Université Montpellier II; 2012. [cited 2019 Oct 14]. Available from: http://www.theses.fr/2012MON20078.

Council of Science Editors:

Wein S. Propriétés et mécanisme d'action des analogues de choline, une nouvelle classe d'antipaludiques. Etude de l'albitiazolium, candidat clinique. : Properties and mechanism of action of choline analogues, a new class of antimalarials. Study of the clinical candidate albitiazolium. [Doctoral Dissertation]. Université Montpellier II; 2012. Available from: http://www.theses.fr/2012MON20078


Rhodes University

25. Hatherley, Rowan. Structural bioinformatics studies and tool development related to drug discovery.

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

 This thesis is divided into two distinct sections which can be combined under the broad umbrella of structural bioinformatics studies related to drug discovery. The… (more)

Subjects/Keywords: Structural bioinformatics; Drug development; Natural products  – Databases; Natural products  – Biotechnology; Sequence alignment (Bioinformatics); Malaria  – Chemotherapy; Heat shock proteins; Plasmodium falciparum

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APA (6th Edition):

Hatherley, R. (2016). Structural bioinformatics studies and tool development related to drug discovery. (Thesis). Rhodes University. Retrieved from http://hdl.handle.net/10962/d1020021

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):

Hatherley, Rowan. “Structural bioinformatics studies and tool development related to drug discovery.” 2016. Thesis, Rhodes University. Accessed October 14, 2019. http://hdl.handle.net/10962/d1020021.

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

MLA Handbook (7th Edition):

Hatherley, Rowan. “Structural bioinformatics studies and tool development related to drug discovery.” 2016. Web. 14 Oct 2019.

Vancouver:

Hatherley R. Structural bioinformatics studies and tool development related to drug discovery. [Internet] [Thesis]. Rhodes University; 2016. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/10962/d1020021.

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

Council of Science Editors:

Hatherley R. Structural bioinformatics studies and tool development related to drug discovery. [Thesis]. Rhodes University; 2016. Available from: http://hdl.handle.net/10962/d1020021

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

26. Horta, Pedro Filipe Castela. Design and synthesis of novel quinolones directed to the Plasmodium falciparum bc1 protein complex.

Degree: 2016, RCAAP

Tese de Doutoramento, Química, Especialização em Química Orgânica, Faculdade de Ciências e Tecnologia, Universidade do Algarve, 2016

Apesar dos intensos esforços para controlo da malária,… (more)

Subjects/Keywords: Malária; Quimioterapia antimalárica; Descoberta de fármacos; Quinolonas; Inibidores do complexo bc1 de P. falciparum; Tautomeria 4-oxo-quinolina/4-hidroxi-quinolina; Malaria; Antimalarial chemotherapy; Drug discovery; Quinolone 3-esters; Inhibitors of P. falciparum bc1 complex; 4-oxo-quinoline/4-hydroxy-quinoline tautomerism; Domínio/Área Científica::Engenharia e Tecnologia::Outras Engenharias e Tecnologias; Domínio/Área Científica::Ciências Naturais::Ciências Químicas

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

APA (6th Edition):

Horta, P. F. C. (2016). Design and synthesis of novel quinolones directed to the Plasmodium falciparum bc1 protein complex. (Thesis). RCAAP. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8685

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):

Horta, Pedro Filipe Castela. “Design and synthesis of novel quinolones directed to the Plasmodium falciparum bc1 protein complex.” 2016. Thesis, RCAAP. Accessed October 14, 2019. https://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8685.

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

MLA Handbook (7th Edition):

Horta, Pedro Filipe Castela. “Design and synthesis of novel quinolones directed to the Plasmodium falciparum bc1 protein complex.” 2016. Web. 14 Oct 2019.

Vancouver:

Horta PFC. Design and synthesis of novel quinolones directed to the Plasmodium falciparum bc1 protein complex. [Internet] [Thesis]. RCAAP; 2016. [cited 2019 Oct 14]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8685.

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

Council of Science Editors:

Horta PFC. Design and synthesis of novel quinolones directed to the Plasmodium falciparum bc1 protein complex. [Thesis]. RCAAP; 2016. Available from: https://www.rcaap.pt/detail.jsp?id=oai:sapientia.ualg.pt:10400.1/8685

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

27. Patil, Vishal. Design and synthesis of small molecule inhibitors of zinc metalloenzymes.

Degree: PhD, Chemistry and Biochemistry, 2011, Georgia Tech

 Histone deacetylases (HDACs) are a class of enzymes that play a crucial role in DNA expression by removing an acetyl group from the ɛ-N-acetyl lysine… (more)

Subjects/Keywords: Bifunctional inhibitors; Isoform selectivity; Spliceosome assembly inhibitors; Leishmania; Malaria; Histone deacetylase inhibitors; Cancer chemotherapy; Zinc binding groups; Metalloenzymes; Enzymes; Metalloproteins

…zincmetalloenzymes. xxiii Pharmacophoric Model of HDACi In the quest of effective chemotherapy, we… …more effective chemotherapy compared to nonselective inhibitors. Molecular docking analysis… …of cancer, leishmania, malaria and other genetic disorders. xxvi CHAPTER 1 INTRODUCTION… …cancer chemotherapy outcome, partly due to reversible cell cycle arrest by HDACi.20 Therefore… …types of cancer than any other class of chemotherapy agents. They act primarily by stabilizing… 

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

APA (6th Edition):

Patil, V. (2011). Design and synthesis of small molecule inhibitors of zinc metalloenzymes. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45859

Chicago Manual of Style (16th Edition):

Patil, Vishal. “Design and synthesis of small molecule inhibitors of zinc metalloenzymes.” 2011. Doctoral Dissertation, Georgia Tech. Accessed October 14, 2019. http://hdl.handle.net/1853/45859.

MLA Handbook (7th Edition):

Patil, Vishal. “Design and synthesis of small molecule inhibitors of zinc metalloenzymes.” 2011. Web. 14 Oct 2019.

Vancouver:

Patil V. Design and synthesis of small molecule inhibitors of zinc metalloenzymes. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2019 Oct 14]. Available from: http://hdl.handle.net/1853/45859.

Council of Science Editors:

Patil V. Design and synthesis of small molecule inhibitors of zinc metalloenzymes. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/45859

28. Silva, Ana Cláudia Melo Pompeu da. Planejamento, síntese e avaliação biológica de derivados quinolínicos potencialmente antimaláricos.

Degree: Mestrado, Insumos Farmacêuticos, 2004, University of São Paulo

A emergência e a disseminação de cepas resistentes aos fármacos antimaláricos disponíveis na quimioterapia têm conduzido à busca por novos agentes potencialmente ativos. Neste sentido,… (more)

Subjects/Keywords: Antimalarials (Evaluation); Antimalarials (Planning); Antimalarials (Synthesis); Antimaláricos (Avaliação); Antimaláricos (Planejamento); Antimaláricos (Síntese); Drugs planning; Malaria (chemotherapy); Malária (Quimioterapia); Mecanismo de ação; Mechanism of action; Planejamento de fármacos; Quinoline; Quinolínico

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

APA (6th Edition):

Silva, A. C. M. P. d. (2004). Planejamento, síntese e avaliação biológica de derivados quinolínicos potencialmente antimaláricos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/9/9138/tde-26022015-173101/ ;

Chicago Manual of Style (16th Edition):

Silva, Ana Cláudia Melo Pompeu da. “Planejamento, síntese e avaliação biológica de derivados quinolínicos potencialmente antimaláricos.” 2004. Masters Thesis, University of São Paulo. Accessed October 14, 2019. http://www.teses.usp.br/teses/disponiveis/9/9138/tde-26022015-173101/ ;.

MLA Handbook (7th Edition):

Silva, Ana Cláudia Melo Pompeu da. “Planejamento, síntese e avaliação biológica de derivados quinolínicos potencialmente antimaláricos.” 2004. Web. 14 Oct 2019.

Vancouver:

Silva ACMPd. Planejamento, síntese e avaliação biológica de derivados quinolínicos potencialmente antimaláricos. [Internet] [Masters thesis]. University of São Paulo; 2004. [cited 2019 Oct 14]. Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-26022015-173101/ ;.

Council of Science Editors:

Silva ACMPd. Planejamento, síntese e avaliação biológica de derivados quinolínicos potencialmente antimaláricos. [Masters Thesis]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/9/9138/tde-26022015-173101/ ;

.