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You searched for +publisher:"University of Pretoria" +contributor:("Birkholtz, Lyn-Marie"). Showing records 1 – 30 of 30 total matches.

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University of Pretoria

1. 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 August 22, 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. 22 Aug 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 Aug 22]. 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 Pretoria

2. Niemand, Jandeli. Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum.

Degree: Biochemistry, 2012, University of Pretoria

 Plasmodium falciparum causes the most severe form of human malaria, and the continual development of resistance of this parasite to current anti-malarial drugs underpins a… (more)

Subjects/Keywords: Human malaria parasite; Plasmodium falciparum; Biosynthetic enzymes; Polyamines; UCTD

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APA (6th Edition):

Niemand, J. (2012). Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/24986

Chicago Manual of Style (16th Edition):

Niemand, Jandeli. “Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum.” 2012. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/24986.

MLA Handbook (7th Edition):

Niemand, Jandeli. “Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum.” 2012. Web. 22 Aug 2019.

Vancouver:

Niemand J. Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2012. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/24986.

Council of Science Editors:

Niemand J. Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2012. Available from: http://hdl.handle.net/2263/24986


University of Pretoria

3. Human, Esmare. Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase.

Degree: Biochemistry, 2008, University of Pretoria

 Malaria is a life-threatening parasitic disease that causes at least 300 million acute illnesses annually, of which at least one million infected humans die, mainly… (more)

Subjects/Keywords: Plasmodium falciparum; Malaria; Functional expression; Dihydrofolate synthase-folypolyglutamate synthase; Disease; UCTD

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APA (6th Edition):

Human, E. (2008). Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25829

Chicago Manual of Style (16th Edition):

Human, Esmare. “Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase.” 2008. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/25829.

MLA Handbook (7th Edition):

Human, Esmare. “Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase.” 2008. Web. 22 Aug 2019.

Vancouver:

Human E. Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase. [Internet] [Masters thesis]. University of Pretoria; 2008. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/25829.

Council of Science Editors:

Human E. Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase. [Masters Thesis]. University of Pretoria; 2008. Available from: http://hdl.handle.net/2263/25829


University of Pretoria

4. Rossouw, Ingrid. Transcriptional and genomic analyses reveal an analogous mechanism for a Piperidinyl-Benzimidazolone analog in Babesia divergens compared to other apicomplexans.

Degree: PhD, Genetics, 2015, University of Pretoria

 Human babesiosis is a rapidly emerging, zoonotic, infectious disease causing potentially lifethreatening malaria-like symptoms in humans. Disease prevalence has escalated over the past 50 years… (more)

Subjects/Keywords: UCTD

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APA (6th Edition):

Rossouw, I. (2015). Transcriptional and genomic analyses reveal an analogous mechanism for a Piperidinyl-Benzimidazolone analog in Babesia divergens compared to other apicomplexans. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/50769

Chicago Manual of Style (16th Edition):

Rossouw, Ingrid. “Transcriptional and genomic analyses reveal an analogous mechanism for a Piperidinyl-Benzimidazolone analog in Babesia divergens compared to other apicomplexans.” 2015. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/50769.

MLA Handbook (7th Edition):

Rossouw, Ingrid. “Transcriptional and genomic analyses reveal an analogous mechanism for a Piperidinyl-Benzimidazolone analog in Babesia divergens compared to other apicomplexans.” 2015. Web. 22 Aug 2019.

Vancouver:

Rossouw I. Transcriptional and genomic analyses reveal an analogous mechanism for a Piperidinyl-Benzimidazolone analog in Babesia divergens compared to other apicomplexans. [Internet] [Doctoral dissertation]. University of Pretoria; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/50769.

Council of Science Editors:

Rossouw I. Transcriptional and genomic analyses reveal an analogous mechanism for a Piperidinyl-Benzimidazolone analog in Babesia divergens compared to other apicomplexans. [Doctoral Dissertation]. University of Pretoria; 2015. Available from: http://hdl.handle.net/2263/50769


University of Pretoria

5. Reeksting, S.B. (Shaun Bernard). Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis.

Degree: Biochemistry, 2009, University of Pretoria

 Malaria, a disease transmitted by female mosquitoes, has plagued the world for many centuries. The disease is associated with high mortality rates, severe poverty, and… (more)

Subjects/Keywords: Malaria parasite; Pfspdsyn inhibitors; Pfodc-adometdc inhibition; Polyamine biosynthesis; UCTD

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APA (6th Edition):

Reeksting, S. B. (. (2009). Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/28508

Chicago Manual of Style (16th Edition):

Reeksting, S B (Shaun. “Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis.” 2009. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/28508.

MLA Handbook (7th Edition):

Reeksting, S B (Shaun. “Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis.” 2009. Web. 22 Aug 2019.

Vancouver:

Reeksting SB(. Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis. [Internet] [Masters thesis]. University of Pretoria; 2009. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/28508.

Council of Science Editors:

Reeksting SB(. Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis. [Masters Thesis]. University of Pretoria; 2009. Available from: http://hdl.handle.net/2263/28508


University of Pretoria

6. Williams, Marni. Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase.

Degree: Biochemistry, 2008, University of Pretoria

 The polyamines putrescine, spermidine and spermine play essential roles in the proliferation and differentiation of most eukaryotic cells. Inhibition of the polyamine pathway is known… (more)

Subjects/Keywords: Eukaryotic cells; Polyamine metabolism; Malaria; Enzymes; UCTD

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APA (6th Edition):

Williams, M. (2008). Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/26979

Chicago Manual of Style (16th Edition):

Williams, Marni. “Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase.” 2008. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/26979.

MLA Handbook (7th Edition):

Williams, Marni. “Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase.” 2008. Web. 22 Aug 2019.

Vancouver:

Williams M. Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase. [Internet] [Masters thesis]. University of Pretoria; 2008. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/26979.

Council of Science Editors:

Williams M. Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase. [Masters Thesis]. University of Pretoria; 2008. Available from: http://hdl.handle.net/2263/26979


University of Pretoria

7. Ismail, Nabila. Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum.

Degree: Biochemistry, 2014, University of Pretoria

 The asexual life cycle of Plasmodium falciparum parasites takes only 48 hours, allowing for rapid replication. The continuous infection, rupturing and re-infection of erythrocytes results… (more)

Subjects/Keywords: Plasmodium falciparum parasites; Infection; Diseases; UCTD

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APA (6th Edition):

Ismail, N. (2014). Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/40345

Chicago Manual of Style (16th Edition):

Ismail, Nabila. “Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum.” 2014. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/40345.

MLA Handbook (7th Edition):

Ismail, Nabila. “Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum.” 2014. Web. 22 Aug 2019.

Vancouver:

Ismail N. Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum. [Internet] [Masters thesis]. University of Pretoria; 2014. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/40345.

Council of Science Editors:

Ismail N. Inhibition of the histone deacetylase family as a drug target in the human malaria parasite, plasmodium falciparum. [Masters Thesis]. University of Pretoria; 2014. Available from: http://hdl.handle.net/2263/40345


University of Pretoria

8. Coertzen, Dina. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.

Degree: PhD, Biochemistry, 2015, University of Pretoria

 Malaria is considered the most prevailing human parasitic disease. Despite various chemotherapeutic interventions being available, the parasite responsible for the most lethal form of malaria,… (more)

Subjects/Keywords: UCTD; S-adenosylmethionine decarboxylase; Plasmodium falciparum; Parasite Specific Inserts; Polyamines

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APA (6th Edition):

Coertzen, D. (2015). Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/46163

Chicago Manual of Style (16th Edition):

Coertzen, Dina. “Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.” 2015. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/46163.

MLA Handbook (7th Edition):

Coertzen, Dina. “Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.” 2015. Web. 22 Aug 2019.

Vancouver:

Coertzen D. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/46163.

Council of Science Editors:

Coertzen D. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2015. Available from: http://hdl.handle.net/2263/46163


University of Pretoria

9. Williams, Marni. Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase .

Degree: 2008, University of Pretoria

 The polyamines putrescine, spermidine and spermine play essential roles in the proliferation and differentiation of most eukaryotic cells. Inhibition of the polyamine pathway is known… (more)

Subjects/Keywords: Eukaryotic cells; Polyamine metabolism; Malaria; Enzymes; UCTD

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

APA (6th Edition):

Williams, M. (2008). Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-08042008-072858/

Chicago Manual of Style (16th Edition):

Williams, Marni. “Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase .” 2008. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://upetd.up.ac.za/thesis/available/etd-08042008-072858/.

MLA Handbook (7th Edition):

Williams, Marni. “Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase .” 2008. Web. 22 Aug 2019.

Vancouver:

Williams M. Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase . [Internet] [Masters thesis]. University of Pretoria; 2008. [cited 2019 Aug 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-08042008-072858/.

Council of Science Editors:

Williams M. Delineation of functional roles of parasite-specific inserts in the malarial S-adenosylmethionine decarboxylase / ornithine decarboxylase . [Masters Thesis]. University of Pretoria; 2008. Available from: http://upetd.up.ac.za/thesis/available/etd-08042008-072858/


University of Pretoria

10. [No author]. Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase .

Degree: 2008, University of Pretoria

 Malaria is a life-threatening parasitic disease that causes at least 300 million acute illnesses annually, of which at least one million infected humans die, mainly… (more)

Subjects/Keywords: Plasmodium falciparum; Malaria; Functional expression; Dihydrofolate synthase-folypolyglutamate synthase; Disease; UCTD

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APA (6th Edition):

author], [. (2008). Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-06252008-093616/

Chicago Manual of Style (16th Edition):

author], [No. “Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase .” 2008. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://upetd.up.ac.za/thesis/available/etd-06252008-093616/.

MLA Handbook (7th Edition):

author], [No. “Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase .” 2008. Web. 22 Aug 2019.

Vancouver:

author] [. Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase . [Internet] [Masters thesis]. University of Pretoria; 2008. [cited 2019 Aug 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-06252008-093616/.

Council of Science Editors:

author] [. Kinetic analysis of a recombinantly expressed Plasmodium falciparum dihydrofolate synthase-folylpolyglutamate synthase . [Masters Thesis]. University of Pretoria; 2008. Available from: http://upetd.up.ac.za/thesis/available/etd-06252008-093616/


University of Pretoria

11. Niemand, Jandeli. Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum .

Degree: 2012, University of Pretoria

 Plasmodium falciparum causes the most severe form of human malaria, and the continual development of resistance of this parasite to current anti-malarial drugs underpins a… (more)

Subjects/Keywords: Human malaria parasite; Plasmodium falciparum; Biosynthetic enzymes; Polyamines; UCTD

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APA (6th Edition):

Niemand, J. (2012). Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-05252012-112525/

Chicago Manual of Style (16th Edition):

Niemand, Jandeli. “Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum .” 2012. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://upetd.up.ac.za/thesis/available/etd-05252012-112525/.

MLA Handbook (7th Edition):

Niemand, Jandeli. “Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum .” 2012. Web. 22 Aug 2019.

Vancouver:

Niemand J. Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum . [Internet] [Doctoral dissertation]. University of Pretoria; 2012. [cited 2019 Aug 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-05252012-112525/.

Council of Science Editors:

Niemand J. Biochemical characterisation of putrescine and spermidine uptake as a potential therapeutic target against the human malaria parasite, Plasmodium falciparum . [Doctoral Dissertation]. University of Pretoria; 2012. Available from: http://upetd.up.ac.za/thesis/available/etd-05252012-112525/


University of Pretoria

12. [No author]. Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis .

Degree: 2009, University of Pretoria

 Malaria, a disease transmitted by female mosquitoes, has plagued the world for many centuries. The disease is associated with high mortality rates, severe poverty, and… (more)

Subjects/Keywords: Malaria parasite; Pfspdsyn inhibitors; Pfodc-adometdc inhibition; Polyamine biosynthesis; UCTD

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

author], [. (2009). Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-10072009-162558/

Chicago Manual of Style (16th Edition):

author], [No. “Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis .” 2009. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://upetd.up.ac.za/thesis/available/etd-10072009-162558/.

MLA Handbook (7th Edition):

author], [No. “Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis .” 2009. Web. 22 Aug 2019.

Vancouver:

author] [. Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis . [Internet] [Masters thesis]. University of Pretoria; 2009. [cited 2019 Aug 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-10072009-162558/.

Council of Science Editors:

author] [. Metabolomic analyses of the malaria parasite after inhibition of polyamine biosynthesis . [Masters Thesis]. University of Pretoria; 2009. Available from: http://upetd.up.ac.za/thesis/available/etd-10072009-162558/


University of Pretoria

13. Williams, Marni. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria is prevalent in over 100 countries which is populated by half of the world’s population and culminates in approximately one million deaths per annum,… (more)

Subjects/Keywords: Protein-protein interactions; Polyamines; Plasmodium falciparum; Malaria; X-ray crystallography; Structure-based drug design; S-adenosylmethionine decarboxylase/ornithine de; UCTD

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

APA (6th Edition):

Williams, M. (2011). Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/26237

Chicago Manual of Style (16th Edition):

Williams, Marni. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.” 2011. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/26237.

MLA Handbook (7th Edition):

Williams, Marni. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.” 2011. Web. 22 Aug 2019.

Vancouver:

Williams M. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/26237.

Council of Science Editors:

Williams M. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/26237


University of Pretoria

14. [No author]. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum .

Degree: 2011, University of Pretoria

 Malaria is prevalent in over 100 countries which is populated by half of the world’s population and culminates in approximately one million deaths per annum,… (more)

Subjects/Keywords: Protein-protein interactions; Polyamines; Plasmodium falciparum; Malaria; X-ray crystallography; Structure-based drug design; S-adenosylmethionine decarboxylase/ornithine de; UCTD

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APA (6th Edition):

author], [. (2011). Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-07122011-104755/

Chicago Manual of Style (16th Edition):

author], [No. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum .” 2011. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://upetd.up.ac.za/thesis/available/etd-07122011-104755/.

MLA Handbook (7th Edition):

author], [No. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum .” 2011. Web. 22 Aug 2019.

Vancouver:

author] [. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum . [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2019 Aug 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-07122011-104755/.

Council of Science Editors:

author] [. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum . [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://upetd.up.ac.za/thesis/available/etd-07122011-104755/


University of Pretoria

15. Rossouw, C.L. (Claire Louise). Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture.

Degree: Biochemistry, 2013, University of Pretoria

 Although conventional two-dimensional (2D) cell culture is convenient for routine work, researchers are turning to three-dimensional (3D) cell culture for more accurate, physiologically representative information… (more)

Subjects/Keywords: Albumin production; Enhanced cell function; Three-dimensional cell culture; Drug metabolism; UCTD

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APA (6th Edition):

Rossouw, C. L. (. L. (2013). Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/24273

Chicago Manual of Style (16th Edition):

Rossouw, C L (Claire Louise). “Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture.” 2013. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/24273.

MLA Handbook (7th Edition):

Rossouw, C L (Claire Louise). “Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture.” 2013. Web. 22 Aug 2019.

Vancouver:

Rossouw CL(L. Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture. [Internet] [Doctoral dissertation]. University of Pretoria; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/24273.

Council of Science Editors:

Rossouw CL(L. Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture. [Doctoral Dissertation]. University of Pretoria; 2013. Available from: http://hdl.handle.net/2263/24273


University of Pretoria

16. Rossouw, C.L. (Claire Louise). Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture .

Degree: 2013, University of Pretoria

 Although conventional two-dimensional (2D) cell culture is convenient for routine work, researchers are turning to three-dimensional (3D) cell culture for more accurate, physiologically representative information… (more)

Subjects/Keywords: Albumin production; Enhanced cell function; Three-dimensional cell culture; Drug metabolism; UCTD

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APA (6th Edition):

Rossouw, C. L. (. L. (2013). Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-05012013-153550/

Chicago Manual of Style (16th Edition):

Rossouw, C L (Claire Louise). “Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture .” 2013. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://upetd.up.ac.za/thesis/available/etd-05012013-153550/.

MLA Handbook (7th Edition):

Rossouw, C L (Claire Louise). “Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture .” 2013. Web. 22 Aug 2019.

Vancouver:

Rossouw CL(L. Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture . [Internet] [Doctoral dissertation]. University of Pretoria; 2013. [cited 2019 Aug 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-05012013-153550/.

Council of Science Editors:

Rossouw CL(L. Development and applications of a novel, thermoresponsive scaffold for three-dimensional cell culture . [Doctoral Dissertation]. University of Pretoria; 2013. Available from: http://upetd.up.ac.za/thesis/available/etd-05012013-153550/

17. Steyn, Denise. Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance.

Degree: Pharmacology, 2016, University of Pretoria

 Introduction: Plasmodium falciparum is the dominant cause of severe malaria in humans, with the highest number of global deaths occurring in Africa and Southeast Asia.… (more)

Subjects/Keywords: Pharmacology; Malaria; UCTD

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APA (6th Edition):

Steyn, D. (2016). Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/51382

Chicago Manual of Style (16th Edition):

Steyn, Denise. “Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance.” 2016. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/51382.

MLA Handbook (7th Edition):

Steyn, Denise. “Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance.” 2016. Web. 22 Aug 2019.

Vancouver:

Steyn D. Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance. [Internet] [Masters thesis]. University of Pretoria; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/51382.

Council of Science Editors:

Steyn D. Mechanisms of potential novel antimalarials and proteomics of Plasmodium falciparum resistance. [Masters Thesis]. University of Pretoria; 2016. Available from: http://hdl.handle.net/2263/51382


University of Pretoria

18. Reeksting, S.B. (Shaun Bernard). Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof.

Degree: Biochemistry, 2013, University of Pretoria

 Malaria is caused by the parasite Plasmodium falciparum and still plagues many parts of the world. To date, efforts to control the spread of the… (more)

Subjects/Keywords: Vitamin b6; PLP; Malaria; Pyridoxal 5'-phosphate; Pdx1; Drug design; Plasmodium falciparum; Therapeutics; UCTD

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APA (6th Edition):

Reeksting, S. B. (. (2013). Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/32965

Chicago Manual of Style (16th Edition):

Reeksting, S B (Shaun. “Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof.” 2013. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/32965.

MLA Handbook (7th Edition):

Reeksting, S B (Shaun. “Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof.” 2013. Web. 22 Aug 2019.

Vancouver:

Reeksting SB(. Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof. [Internet] [Doctoral dissertation]. University of Pretoria; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/32965.

Council of Science Editors:

Reeksting SB(. Targeted inhibition of the Plasmodium falciparum Vitamin B6 producing enzyme Pdx1 and the biochemical and functional consequences thereof. [Doctoral Dissertation]. University of Pretoria; 2013. Available from: http://hdl.handle.net/2263/32965


University of Pretoria

19. Besaans, Ethan Wade. Synthesis structure-activity relationships and biological evaluation of optimised terminally alkylated (bis)urea and (bis)thiourea polyamine analogues as antiplasmodial agents.

Degree: MSc, Biochemistry, 2017, University of Pretoria

 The sustained control and elimination of malaria requires novel approaches to combat the emergence of drug resistance. Plasmodium falciparum causes the most lethal form of… (more)

Subjects/Keywords: UCTD

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APA (6th Edition):

Besaans, E. W. (2017). Synthesis structure-activity relationships and biological evaluation of optimised terminally alkylated (bis)urea and (bis)thiourea polyamine analogues as antiplasmodial agents. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/63227

Chicago Manual of Style (16th Edition):

Besaans, Ethan Wade. “Synthesis structure-activity relationships and biological evaluation of optimised terminally alkylated (bis)urea and (bis)thiourea polyamine analogues as antiplasmodial agents.” 2017. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/63227.

MLA Handbook (7th Edition):

Besaans, Ethan Wade. “Synthesis structure-activity relationships and biological evaluation of optimised terminally alkylated (bis)urea and (bis)thiourea polyamine analogues as antiplasmodial agents.” 2017. Web. 22 Aug 2019.

Vancouver:

Besaans EW. Synthesis structure-activity relationships and biological evaluation of optimised terminally alkylated (bis)urea and (bis)thiourea polyamine analogues as antiplasmodial agents. [Internet] [Masters thesis]. University of Pretoria; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/63227.

Council of Science Editors:

Besaans EW. Synthesis structure-activity relationships and biological evaluation of optimised terminally alkylated (bis)urea and (bis)thiourea polyamine analogues as antiplasmodial agents. [Masters Thesis]. University of Pretoria; 2017. Available from: http://hdl.handle.net/2263/63227


University of Pretoria

20. Naude, Mariska. Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites.

Degree: MSc, Biochemistry, 2018, University of Pretoria

 The Plasmodium falciparum parasite is the causative agent of the most severe form of malaria. The increase in resistance against the majority of antimalarial compounds… (more)

Subjects/Keywords: Plasmodium falciparum; UCTD

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APA (6th Edition):

Naude, M. (2018). Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/67044

Chicago Manual of Style (16th Edition):

Naude, Mariska. “Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites.” 2018. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/67044.

MLA Handbook (7th Edition):

Naude, Mariska. “Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites.” 2018. Web. 22 Aug 2019.

Vancouver:

Naude M. Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites. [Internet] [Masters thesis]. University of Pretoria; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/67044.

Council of Science Editors:

Naude M. Dynamic bioinformatics and isotopic evaluation of the permeome of intraerythrocytic Plasmodium falciparum parasites. [Masters Thesis]. University of Pretoria; 2018. Available from: http://hdl.handle.net/2263/67044


University of Pretoria

21. Von Grüning, Hilde. CRISPR/Cas9 mediated deletion of genes encoding putative cell cycle regulators in Plasmodium falciparum.

Degree: MSc, Biochemistry, 2018, University of Pretoria

 Functional genomic tools can be used to interrogate unique features of parasite biology that could be marked for future intervention strategies. One such unique biological… (more)

Subjects/Keywords: UCTD

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APA (6th Edition):

Von Grüning, H. (2018). CRISPR/Cas9 mediated deletion of genes encoding putative cell cycle regulators in Plasmodium falciparum. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/65954

Chicago Manual of Style (16th Edition):

Von Grüning, Hilde. “CRISPR/Cas9 mediated deletion of genes encoding putative cell cycle regulators in Plasmodium falciparum.” 2018. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/65954.

MLA Handbook (7th Edition):

Von Grüning, Hilde. “CRISPR/Cas9 mediated deletion of genes encoding putative cell cycle regulators in Plasmodium falciparum.” 2018. Web. 22 Aug 2019.

Vancouver:

Von Grüning H. CRISPR/Cas9 mediated deletion of genes encoding putative cell cycle regulators in Plasmodium falciparum. [Internet] [Masters thesis]. University of Pretoria; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/65954.

Council of Science Editors:

Von Grüning H. CRISPR/Cas9 mediated deletion of genes encoding putative cell cycle regulators in Plasmodium falciparum. [Masters Thesis]. University of Pretoria; 2018. Available from: http://hdl.handle.net/2263/65954


University of Pretoria

22. Joshua, Alicia Celeste. Investigating phenotypic differences of Plasmodium falciparum parasites following exposure to classical antimalarial drugs.

Degree: MSc, Biochemistry, 2019, University of Pretoria

 Malaria remains a leading health problem with an estimated 445 000 deaths occurring in 2016 of which the majority of deaths occurred in Africa. Currently,… (more)

Subjects/Keywords: Malaria; Plasmodium falciparum; Phenotype Microarray; Phenomics; UCTD

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APA (6th Edition):

Joshua, A. C. (2019). Investigating phenotypic differences of Plasmodium falciparum parasites following exposure to classical antimalarial drugs. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/68306

Chicago Manual of Style (16th Edition):

Joshua, Alicia Celeste. “Investigating phenotypic differences of Plasmodium falciparum parasites following exposure to classical antimalarial drugs.” 2019. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/68306.

MLA Handbook (7th Edition):

Joshua, Alicia Celeste. “Investigating phenotypic differences of Plasmodium falciparum parasites following exposure to classical antimalarial drugs.” 2019. Web. 22 Aug 2019.

Vancouver:

Joshua AC. Investigating phenotypic differences of Plasmodium falciparum parasites following exposure to classical antimalarial drugs. [Internet] [Masters thesis]. University of Pretoria; 2019. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/68306.

Council of Science Editors:

Joshua AC. Investigating phenotypic differences of Plasmodium falciparum parasites following exposure to classical antimalarial drugs. [Masters Thesis]. University of Pretoria; 2019. Available from: http://hdl.handle.net/2263/68306


University of Pretoria

23. Van der Watt, Mariëtte Elizabeth. Exploring the kinase inhibitor chemical space for novel dual active and gametocyte-focussed antimalarials.

Degree: PhD, Biochemistry, 2019, University of Pretoria

 The success achieved in controlling malaria in recent years [1, 2], has caused a focal shift to elimination of the disease, with renewed interest in… (more)

Subjects/Keywords: UCTD

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APA (6th Edition):

Van der Watt, M. (2019). Exploring the kinase inhibitor chemical space for novel dual active and gametocyte-focussed antimalarials. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/70519

Chicago Manual of Style (16th Edition):

Van der Watt, Mariëtte. “Exploring the kinase inhibitor chemical space for novel dual active and gametocyte-focussed antimalarials.” 2019. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/70519.

MLA Handbook (7th Edition):

Van der Watt, Mariëtte. “Exploring the kinase inhibitor chemical space for novel dual active and gametocyte-focussed antimalarials.” 2019. Web. 22 Aug 2019.

Vancouver:

Van der Watt M. Exploring the kinase inhibitor chemical space for novel dual active and gametocyte-focussed antimalarials. [Internet] [Doctoral dissertation]. University of Pretoria; 2019. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/70519.

Council of Science Editors:

Van der Watt M. Exploring the kinase inhibitor chemical space for novel dual active and gametocyte-focussed antimalarials. [Doctoral Dissertation]. University of Pretoria; 2019. Available from: http://hdl.handle.net/2263/70519


University of Pretoria

24. Matlebjane, Dikeledi M.A. In vitro efficacy assessment of targeted antimalarial drugs synthesized following in silico design.

Degree: MSc, Pharmacology, 2017, University of Pretoria

 Malaria is a major public health problem that affects millions of lives globally. The increased burden of malaria requires new interventions that will address the… (more)

Subjects/Keywords: Malaria; Plasmodium falciparum; In silico design; CDPK; FIKK; Kinase; Bromodomain protein; ATP-binding site; Stage specificity; Kill kinetics

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APA (6th Edition):

Matlebjane, D. M. A. (2017). In vitro efficacy assessment of targeted antimalarial drugs synthesized following in silico design. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/63045

Chicago Manual of Style (16th Edition):

Matlebjane, Dikeledi M A. “In vitro efficacy assessment of targeted antimalarial drugs synthesized following in silico design.” 2017. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/63045.

MLA Handbook (7th Edition):

Matlebjane, Dikeledi M A. “In vitro efficacy assessment of targeted antimalarial drugs synthesized following in silico design.” 2017. Web. 22 Aug 2019.

Vancouver:

Matlebjane DMA. In vitro efficacy assessment of targeted antimalarial drugs synthesized following in silico design. [Internet] [Masters thesis]. University of Pretoria; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/63045.

Council of Science Editors:

Matlebjane DMA. In vitro efficacy assessment of targeted antimalarial drugs synthesized following in silico design. [Masters Thesis]. University of Pretoria; 2017. Available from: http://hdl.handle.net/2263/63045


University of Pretoria

25. Venter, Tarryn Lee. Characterisation of the pre-invasion glycophosphatidylinositol-anchored surface proteins of Plasmodium falciparum merozoites.

Degree: MSc, Pharmacology, 2017, University of Pretoria

 Plasmodium falciparum is a protozoan parasite responsible for causing the most severe form of malaria in humans. This species is responsible for over 90% of… (more)

Subjects/Keywords: Malaria; Plasmodium falciparum; Merozoite; Erythrocyte invasion; Cell culture; MACs isolation; MSF assay; Merozoite invasion assay; SDS-PAGE; Electrophoresis; LC-MS/MS; Proteomics

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APA (6th Edition):

Venter, T. L. (2017). Characterisation of the pre-invasion glycophosphatidylinositol-anchored surface proteins of Plasmodium falciparum merozoites. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/63040

Chicago Manual of Style (16th Edition):

Venter, Tarryn Lee. “Characterisation of the pre-invasion glycophosphatidylinositol-anchored surface proteins of Plasmodium falciparum merozoites.” 2017. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/63040.

MLA Handbook (7th Edition):

Venter, Tarryn Lee. “Characterisation of the pre-invasion glycophosphatidylinositol-anchored surface proteins of Plasmodium falciparum merozoites.” 2017. Web. 22 Aug 2019.

Vancouver:

Venter TL. Characterisation of the pre-invasion glycophosphatidylinositol-anchored surface proteins of Plasmodium falciparum merozoites. [Internet] [Masters thesis]. University of Pretoria; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/63040.

Council of Science Editors:

Venter TL. Characterisation of the pre-invasion glycophosphatidylinositol-anchored surface proteins of Plasmodium falciparum merozoites. [Masters Thesis]. University of Pretoria; 2017. Available from: http://hdl.handle.net/2263/63040


University of Pretoria

26. Clark, Katherine. Transcriptome- and proteome-wide responses to putrescine depletion in the human malaria parasite, Plasmodium falciparum.

Degree: Biochemistry, 2013, University of Pretoria

Please read the abstract in the document attached. Advisors/Committee Members: Birkholtz, Lyn-Marie (advisor), Louw, Abraham Izak (coadvisor).

Subjects/Keywords: UCTD

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APA (6th Edition):

Clark, K. (2013). Transcriptome- and proteome-wide responses to putrescine depletion in the human malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/30795

Chicago Manual of Style (16th Edition):

Clark, Katherine. “Transcriptome- and proteome-wide responses to putrescine depletion in the human malaria parasite, Plasmodium falciparum.” 2013. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/30795.

MLA Handbook (7th Edition):

Clark, Katherine. “Transcriptome- and proteome-wide responses to putrescine depletion in the human malaria parasite, Plasmodium falciparum.” 2013. Web. 22 Aug 2019.

Vancouver:

Clark K. Transcriptome- and proteome-wide responses to putrescine depletion in the human malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/30795.

Council of Science Editors:

Clark K. Transcriptome- and proteome-wide responses to putrescine depletion in the human malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2013. Available from: http://hdl.handle.net/2263/30795


University of Pretoria

27. Coetzee, Nanika. Sexual differentiation of malaria parasites is controlled by unique epigenomic and proteomic cascades as revealed by comparative functional genome analyses.

Degree: PhD, Biochemistry, 2018, University of Pretoria

 There is a continuous and urgent need for novel antimalarial agents with new modes of action due to P. falciparum resistance development against most of… (more)

Subjects/Keywords: UCTD

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APA (6th Edition):

Coetzee, N. (2018). Sexual differentiation of malaria parasites is controlled by unique epigenomic and proteomic cascades as revealed by comparative functional genome analyses. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/65958

Chicago Manual of Style (16th Edition):

Coetzee, Nanika. “Sexual differentiation of malaria parasites is controlled by unique epigenomic and proteomic cascades as revealed by comparative functional genome analyses.” 2018. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/65958.

MLA Handbook (7th Edition):

Coetzee, Nanika. “Sexual differentiation of malaria parasites is controlled by unique epigenomic and proteomic cascades as revealed by comparative functional genome analyses.” 2018. Web. 22 Aug 2019.

Vancouver:

Coetzee N. Sexual differentiation of malaria parasites is controlled by unique epigenomic and proteomic cascades as revealed by comparative functional genome analyses. [Internet] [Doctoral dissertation]. University of Pretoria; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/65958.

Council of Science Editors:

Coetzee N. Sexual differentiation of malaria parasites is controlled by unique epigenomic and proteomic cascades as revealed by comparative functional genome analyses. [Doctoral Dissertation]. University of Pretoria; 2018. Available from: http://hdl.handle.net/2263/65958


University of Pretoria

28. Griffiths, Caron, A. High-content and super-resolution microscopy reveals the dynamic nuclear architecture aand mobile epigenetic marks in Plasmodiumfalciparum.

Degree: Biochemistry, 2013, University of Pretoria

 The malaria-causing parasite Plasmodium falciparum 1s dependent on tightly regulated gene expression for its progression through the intra-erythrocytic life cycle, pathogenesis and establishment of persistent… (more)

Subjects/Keywords: Malaria; Parasite Plasmodium falciparum; Diseases; Var gene; UCTD

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APA (6th Edition):

Griffiths, Caron, A. (2013). High-content and super-resolution microscopy reveals the dynamic nuclear architecture aand mobile epigenetic marks in Plasmodiumfalciparum. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/32818

Chicago Manual of Style (16th Edition):

Griffiths, Caron, A. “High-content and super-resolution microscopy reveals the dynamic nuclear architecture aand mobile epigenetic marks in Plasmodiumfalciparum.” 2013. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/32818.

MLA Handbook (7th Edition):

Griffiths, Caron, A. “High-content and super-resolution microscopy reveals the dynamic nuclear architecture aand mobile epigenetic marks in Plasmodiumfalciparum.” 2013. Web. 22 Aug 2019.

Vancouver:

Griffiths, Caron A. High-content and super-resolution microscopy reveals the dynamic nuclear architecture aand mobile epigenetic marks in Plasmodiumfalciparum. [Internet] [Masters thesis]. University of Pretoria; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/32818.

Council of Science Editors:

Griffiths, Caron A. High-content and super-resolution microscopy reveals the dynamic nuclear architecture aand mobile epigenetic marks in Plasmodiumfalciparum. [Masters Thesis]. University of Pretoria; 2013. Available from: http://hdl.handle.net/2263/32818


University of Pretoria

29. Van Biljon, Riëtte Andelé. Integrative transcriptome and phenome analysis reveals unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites.

Degree: PhD, Biochemistry, 2019, University of Pretoria

 The Plasmodium falciparum parasite, the major causative agent of malaria on the African continent, has evolved numerous cellular adaptations to effectively propagate its species. The… (more)

Subjects/Keywords: UCTD

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APA (6th Edition):

Van Biljon, R. A. (2019). Integrative transcriptome and phenome analysis reveals unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/70517

Chicago Manual of Style (16th Edition):

Van Biljon, Riëtte Andelé. “Integrative transcriptome and phenome analysis reveals unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites.” 2019. Doctoral Dissertation, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/70517.

MLA Handbook (7th Edition):

Van Biljon, Riëtte Andelé. “Integrative transcriptome and phenome analysis reveals unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites.” 2019. Web. 22 Aug 2019.

Vancouver:

Van Biljon RA. Integrative transcriptome and phenome analysis reveals unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites. [Internet] [Doctoral dissertation]. University of Pretoria; 2019. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/70517.

Council of Science Editors:

Van Biljon RA. Integrative transcriptome and phenome analysis reveals unique regulatory cascades controlling the intraerythrocytic asexual and sexual development of human malaria parasites. [Doctoral Dissertation]. University of Pretoria; 2019. Available from: http://hdl.handle.net/2263/70517


University of Pretoria

30. Damadeu Kouemo, Laura. Assessing the in vitro efficacy of in silico designed compounds targeting the malarial Qi site of cytochrome bc1.

Degree: MSc, Pharmacology, 2018, University of Pretoria

 Plasmodium falciparum is the causative agent of the most commonly fatal form of malaria in Africa with annual deaths of more than 300 000. The… (more)

Subjects/Keywords: UCTD; Unrestricted

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APA (6th Edition):

Damadeu Kouemo, L. (2018). Assessing the in vitro efficacy of in silico designed compounds targeting the malarial Qi site of cytochrome bc1. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/67749

Chicago Manual of Style (16th Edition):

Damadeu Kouemo, Laura. “Assessing the in vitro efficacy of in silico designed compounds targeting the malarial Qi site of cytochrome bc1.” 2018. Masters Thesis, University of Pretoria. Accessed August 22, 2019. http://hdl.handle.net/2263/67749.

MLA Handbook (7th Edition):

Damadeu Kouemo, Laura. “Assessing the in vitro efficacy of in silico designed compounds targeting the malarial Qi site of cytochrome bc1.” 2018. Web. 22 Aug 2019.

Vancouver:

Damadeu Kouemo L. Assessing the in vitro efficacy of in silico designed compounds targeting the malarial Qi site of cytochrome bc1. [Internet] [Masters thesis]. University of Pretoria; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2263/67749.

Council of Science Editors:

Damadeu Kouemo L. Assessing the in vitro efficacy of in silico designed compounds targeting the malarial Qi site of cytochrome bc1. [Masters Thesis]. University of Pretoria; 2018. Available from: http://hdl.handle.net/2263/67749

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