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You searched for +publisher:"Victoria University of Wellington" +contributor:("Atkinson, Paul"). Showing records 1 – 10 of 10 total matches.

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Victoria University of Wellington

1. Busby, Bede P. The Chemical Genetic Interactions of Statin Drugs with Their Target Genes in Saccharomyces cerevisiae.

Degree: 2009, Victoria University of Wellington

 Statins, competitive inhibitors of the rate limiting cholesterol/ergosterol enzymes HMG-CoA reductase (HMG1 and HMG2), are the most widely prescribed human therapeutic drugs. They are effective… (more)

Subjects/Keywords: Yeast; Biochemical genetics; Chemical Genetics; Statins

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APA (6th Edition):

Busby, B. P. (2009). The Chemical Genetic Interactions of Statin Drugs with Their Target Genes in Saccharomyces cerevisiae. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1221

Chicago Manual of Style (16th Edition):

Busby, Bede P. “The Chemical Genetic Interactions of Statin Drugs with Their Target Genes in Saccharomyces cerevisiae.” 2009. Masters Thesis, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/1221.

MLA Handbook (7th Edition):

Busby, Bede P. “The Chemical Genetic Interactions of Statin Drugs with Their Target Genes in Saccharomyces cerevisiae.” 2009. Web. 28 Mar 2020.

Vancouver:

Busby BP. The Chemical Genetic Interactions of Statin Drugs with Their Target Genes in Saccharomyces cerevisiae. [Internet] [Masters thesis]. Victoria University of Wellington; 2009. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/1221.

Council of Science Editors:

Busby BP. The Chemical Genetic Interactions of Statin Drugs with Their Target Genes in Saccharomyces cerevisiae. [Masters Thesis]. Victoria University of Wellington; 2009. Available from: http://hdl.handle.net/10063/1221


Victoria University of Wellington

2. Coorey, Namal. A Novel High-Throughput Screening Tool in Saccharomyces Cerevisiae.

Degree: 2012, Victoria University of Wellington

 The elucidation of drug targets and their biological effects can be aided by the identification of yeast deletion mutants that confer hypersensitivity to the drug.… (more)

Subjects/Keywords: Pleiotropic drug resistance; Chemical genetics; DMA

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APA (6th Edition):

Coorey, N. (2012). A Novel High-Throughput Screening Tool in Saccharomyces Cerevisiae. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2750

Chicago Manual of Style (16th Edition):

Coorey, Namal. “A Novel High-Throughput Screening Tool in Saccharomyces Cerevisiae.” 2012. Masters Thesis, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/2750.

MLA Handbook (7th Edition):

Coorey, Namal. “A Novel High-Throughput Screening Tool in Saccharomyces Cerevisiae.” 2012. Web. 28 Mar 2020.

Vancouver:

Coorey N. A Novel High-Throughput Screening Tool in Saccharomyces Cerevisiae. [Internet] [Masters thesis]. Victoria University of Wellington; 2012. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/2750.

Council of Science Editors:

Coorey N. A Novel High-Throughput Screening Tool in Saccharomyces Cerevisiae. [Masters Thesis]. Victoria University of Wellington; 2012. Available from: http://hdl.handle.net/10063/2750


Victoria University of Wellington

3. Quek, Natelle C H. The Characterization of TA-289, a Novel Antifungal from Fusarium sp.

Degree: 2011, Victoria University of Wellington

 Natural products offer vast structural and chemical diversity highly sought after in drug discovery research. Saccharomyces cerevisiae makes an ideal model eukaryotic organism for drug… (more)

Subjects/Keywords: Drug; Oxidative stress; Saccharomyces cerevisiae

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APA (6th Edition):

Quek, N. C. H. (2011). The Characterization of TA-289, a Novel Antifungal from Fusarium sp. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1891

Chicago Manual of Style (16th Edition):

Quek, Natelle C H. “The Characterization of TA-289, a Novel Antifungal from Fusarium sp.” 2011. Masters Thesis, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/1891.

MLA Handbook (7th Edition):

Quek, Natelle C H. “The Characterization of TA-289, a Novel Antifungal from Fusarium sp.” 2011. Web. 28 Mar 2020.

Vancouver:

Quek NCH. The Characterization of TA-289, a Novel Antifungal from Fusarium sp. [Internet] [Masters thesis]. Victoria University of Wellington; 2011. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/1891.

Council of Science Editors:

Quek NCH. The Characterization of TA-289, a Novel Antifungal from Fusarium sp. [Masters Thesis]. Victoria University of Wellington; 2011. Available from: http://hdl.handle.net/10063/1891


Victoria University of Wellington

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

Degree: 2012, Victoria University of Wellington

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

Subjects/Keywords: Drug discovery; Chemical genetics; Yeast

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Sampson, Liam D P. “High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888.” 2012. Masters Thesis, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/2590.

MLA Handbook (7th Edition):

Sampson, Liam D P. “High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888.” 2012. Web. 28 Mar 2020.

Vancouver:

Sampson LDP. High Throughput Drug Discovery in S. Cerevisiae: the Characterisation of FC-592 and FC-888. [Internet] [Masters thesis]. Victoria University of Wellington; 2012. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/2590.

Council of Science Editors:

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


Victoria University of Wellington

5. Yibmantasiri, Ploi. Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae.

Degree: 2012, Victoria University of Wellington

 One of the major problems in biology is to identify genes that are involved in specific processes. Classical genetics and biochemistry, although powerful and informative,… (more)

Subjects/Keywords: Genome-wide screening; Genetic networks; Drug resistance

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APA (6th Edition):

Yibmantasiri, P. (2012). Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/2539

Chicago Manual of Style (16th Edition):

Yibmantasiri, Ploi. “Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae.” 2012. Doctoral Dissertation, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/2539.

MLA Handbook (7th Edition):

Yibmantasiri, Ploi. “Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae.” 2012. Web. 28 Mar 2020.

Vancouver:

Yibmantasiri P. Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2012. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/2539.

Council of Science Editors:

Yibmantasiri P. Genome-Wide Screening and Genetic Networks in Pleiotropic Drug Resistance, Oxidative Stress, and Drug Targets in S. Cerevisiae. [Doctoral Dissertation]. Victoria University of Wellington; 2012. Available from: http://hdl.handle.net/10063/2539


Victoria University of Wellington

6. Molimau-Samasoni, Seeseei. Exploring the Molecular Mechanisms of Action of Samoan Medicinal Plants via Chemical Genetic Analyses.

Degree: 2016, Victoria University of Wellington

 Natural products are a robust source of drug leads, and medicinal plants have been the source of natural products that are important pharmaceuticals in modern… (more)

Subjects/Keywords: Medicinal; Plants; Yeast

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APA (6th Edition):

Molimau-Samasoni, S. (2016). Exploring the Molecular Mechanisms of Action of Samoan Medicinal Plants via Chemical Genetic Analyses. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8787

Chicago Manual of Style (16th Edition):

Molimau-Samasoni, Seeseei. “Exploring the Molecular Mechanisms of Action of Samoan Medicinal Plants via Chemical Genetic Analyses.” 2016. Doctoral Dissertation, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/8787.

MLA Handbook (7th Edition):

Molimau-Samasoni, Seeseei. “Exploring the Molecular Mechanisms of Action of Samoan Medicinal Plants via Chemical Genetic Analyses.” 2016. Web. 28 Mar 2020.

Vancouver:

Molimau-Samasoni S. Exploring the Molecular Mechanisms of Action of Samoan Medicinal Plants via Chemical Genetic Analyses. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2016. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/8787.

Council of Science Editors:

Molimau-Samasoni S. Exploring the Molecular Mechanisms of Action of Samoan Medicinal Plants via Chemical Genetic Analyses. [Doctoral Dissertation]. Victoria University of Wellington; 2016. Available from: http://hdl.handle.net/10063/8787


Victoria University of Wellington

7. Busby, Bede Phillip. Phenotypic implications of genetic interaction networks in Saccharomyces cerevisiae.

Degree: 2015, Victoria University of Wellington

 Gene functions were studied as extensive networks comprising synergistic functional interactions between overlapping pairs of genes. Elucidation of such networks related to drug phenotypes (statins… (more)

Subjects/Keywords: Genetic interaction; Network; Genetics; Saccharomyces cerevisiae; Yeast

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APA (6th Edition):

Busby, B. P. (2015). Phenotypic implications of genetic interaction networks in Saccharomyces cerevisiae. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8756

Chicago Manual of Style (16th Edition):

Busby, Bede Phillip. “Phenotypic implications of genetic interaction networks in Saccharomyces cerevisiae.” 2015. Doctoral Dissertation, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/8756.

MLA Handbook (7th Edition):

Busby, Bede Phillip. “Phenotypic implications of genetic interaction networks in Saccharomyces cerevisiae.” 2015. Web. 28 Mar 2020.

Vancouver:

Busby BP. Phenotypic implications of genetic interaction networks in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2015. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/8756.

Council of Science Editors:

Busby BP. Phenotypic implications of genetic interaction networks in Saccharomyces cerevisiae. [Doctoral Dissertation]. Victoria University of Wellington; 2015. Available from: http://hdl.handle.net/10063/8756


Victoria University of Wellington

8. Roberts, Christina. Investigating the Quantitative Trait Loci Contributing to Individual Variation in Drug Response.

Degree: 2015, Victoria University of Wellington

 Individuals often display a wide variety of phenotypic responses to drug treatment, in terms of both efficacy and side effects. Part of this variation appears… (more)

Subjects/Keywords: BSA; Bulk segregant analysis; QTL; Quantitative trait locus; Drug

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APA (6th Edition):

Roberts, C. (2015). Investigating the Quantitative Trait Loci Contributing to Individual Variation in Drug Response. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/5169

Chicago Manual of Style (16th Edition):

Roberts, Christina. “Investigating the Quantitative Trait Loci Contributing to Individual Variation in Drug Response.” 2015. Doctoral Dissertation, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/5169.

MLA Handbook (7th Edition):

Roberts, Christina. “Investigating the Quantitative Trait Loci Contributing to Individual Variation in Drug Response.” 2015. Web. 28 Mar 2020.

Vancouver:

Roberts C. Investigating the Quantitative Trait Loci Contributing to Individual Variation in Drug Response. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2015. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/5169.

Council of Science Editors:

Roberts C. Investigating the Quantitative Trait Loci Contributing to Individual Variation in Drug Response. [Doctoral Dissertation]. Victoria University of Wellington; 2015. Available from: http://hdl.handle.net/10063/5169

9. Bircham, Peter William. The use of high-throughput microscopy in the characterisation of phenotypes associated with the Unfolded Protein Response in Saccharomyces cerevisiae.

Degree: 2014, Victoria University of Wellington

 Proteins traversing the secretory pathway begin their passage in the endoplasmic reticulum (ER) where they must be correctly folded and processed to pass quality control… (more)

Subjects/Keywords: Yeast; GFP; Green fluorescent protein; Microscopy

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APA (6th Edition):

Bircham, P. W. (2014). The use of high-throughput microscopy in the characterisation of phenotypes associated with the Unfolded Protein Response in Saccharomyces cerevisiae. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/3600

Chicago Manual of Style (16th Edition):

Bircham, Peter William. “The use of high-throughput microscopy in the characterisation of phenotypes associated with the Unfolded Protein Response in Saccharomyces cerevisiae.” 2014. Doctoral Dissertation, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/3600.

MLA Handbook (7th Edition):

Bircham, Peter William. “The use of high-throughput microscopy in the characterisation of phenotypes associated with the Unfolded Protein Response in Saccharomyces cerevisiae.” 2014. Web. 28 Mar 2020.

Vancouver:

Bircham PW. The use of high-throughput microscopy in the characterisation of phenotypes associated with the Unfolded Protein Response in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2014. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/3600.

Council of Science Editors:

Bircham PW. The use of high-throughput microscopy in the characterisation of phenotypes associated with the Unfolded Protein Response in Saccharomyces cerevisiae. [Doctoral Dissertation]. Victoria University of Wellington; 2014. Available from: http://hdl.handle.net/10063/3600

10. Coorey, Namal. Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine.

Degree: 2017, Victoria University of Wellington

 Transition-state structure analogues are among the most powerful chemical inhibitors discovered to date with picomolar efficacy for enzymes. The nucleoside analogue methylthioadenosine-DADMe-immucillin A (MTDIA) is… (more)

Subjects/Keywords: Autophagy; Lipids; Cancer; Methylthioadenosine-DADMe-immucillin A; Forodesine; MTDIA

…Medicine) and synthesised by members of the Ferrier Institute (Victoria University of… …Wellington) (Evans et al., 2004; Evans et al., 2003). Methylthio-DADMeImmucillin A… 

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APA (6th Edition):

Coorey, N. (2017). Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/6906

Chicago Manual of Style (16th Edition):

Coorey, Namal. “Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine.” 2017. Doctoral Dissertation, Victoria University of Wellington. Accessed March 28, 2020. http://hdl.handle.net/10063/6906.

MLA Handbook (7th Edition):

Coorey, Namal. “Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine.” 2017. Web. 28 Mar 2020.

Vancouver:

Coorey N. Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2017. [cited 2020 Mar 28]. Available from: http://hdl.handle.net/10063/6906.

Council of Science Editors:

Coorey N. Elucidating the anti-cancer mechanisms for transition-state structure inhibitors of nucleoside phosphorylases methylthioadenosine-DADMe-immucillin A and forodesine. [Doctoral Dissertation]. Victoria University of Wellington; 2017. Available from: http://hdl.handle.net/10063/6906

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