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You searched for +publisher:"University of Saskatchewan" +contributor:("Lee, Jeremy"). Showing records 1 – 30 of 56 total matches.

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University of Saskatchewan

1. Nienaber, Kurt. X-RAY INDUCED PHOTOREDUCTION OF REDOX ACTIVE METAL IONS.

Degree: 2020, University of Saskatchewan

 The use of synchrotron light sources has provided insights into structure, function, and mechanism of numerous proteins and enzymes. The fields of macromolecular crystallography and… (more)

Subjects/Keywords: X-ray Absorption Spectroscopy; Photoreduction; Copper

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APA (6th Edition):

Nienaber, K. (2020). X-RAY INDUCED PHOTOREDUCTION OF REDOX ACTIVE METAL IONS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12805

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):

Nienaber, Kurt. “X-RAY INDUCED PHOTOREDUCTION OF REDOX ACTIVE METAL IONS.” 2020. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/12805.

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

MLA Handbook (7th Edition):

Nienaber, Kurt. “X-RAY INDUCED PHOTOREDUCTION OF REDOX ACTIVE METAL IONS.” 2020. Web. 21 Oct 2020.

Vancouver:

Nienaber K. X-RAY INDUCED PHOTOREDUCTION OF REDOX ACTIVE METAL IONS. [Internet] [Thesis]. University of Saskatchewan; 2020. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/12805.

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

Council of Science Editors:

Nienaber K. X-RAY INDUCED PHOTOREDUCTION OF REDOX ACTIVE METAL IONS. [Thesis]. University of Saskatchewan; 2020. Available from: http://hdl.handle.net/10388/12805

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


University of Saskatchewan

2. Jakova, Elisabet 1991-. The effects of an AC field on the transport of peptides and other molecules through the α-Hemolysin pore.

Degree: 2016, University of Saskatchewan

 This research is based on superimposing an alternating current (AC) onto a direct current (DC) during the nanopore analysis of various peptides, single-stranded DNA, α-synuclein… (more)

Subjects/Keywords: α-Hemolysin; AC field; α-helical peptide; α-Synuclein; Protein-drug complexes

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APA (6th Edition):

Jakova, E. 1. (2016). The effects of an AC field on the transport of peptides and other molecules through the α-Hemolysin pore. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7322

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):

Jakova, Elisabet 1991-. “The effects of an AC field on the transport of peptides and other molecules through the α-Hemolysin pore.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7322.

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

MLA Handbook (7th Edition):

Jakova, Elisabet 1991-. “The effects of an AC field on the transport of peptides and other molecules through the α-Hemolysin pore.” 2016. Web. 21 Oct 2020.

Vancouver:

Jakova E1. The effects of an AC field on the transport of peptides and other molecules through the α-Hemolysin pore. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7322.

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

Council of Science Editors:

Jakova E1. The effects of an AC field on the transport of peptides and other molecules through the α-Hemolysin pore. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7322

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


University of Saskatchewan

3. Yu, Corey H 1988-. Dynamics and Interactions of Metal-Binding Domains in the Function of Wilson Disease Protein.

Degree: 2017, University of Saskatchewan

 Wilson disease protein (ATP7B) is a P-type ATPase that catalyzes the transport of copper across cell membranes and is critical for maintaining copper homeostasis. ATP7B… (more)

Subjects/Keywords: NMR spectroscopy; ATP7B; nanobody; protein dynamics; cisplatin resistance

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APA (6th Edition):

Yu, C. H. 1. (2017). Dynamics and Interactions of Metal-Binding Domains in the Function of Wilson Disease Protein. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7700

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):

Yu, Corey H 1988-. “Dynamics and Interactions of Metal-Binding Domains in the Function of Wilson Disease Protein.” 2017. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7700.

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

MLA Handbook (7th Edition):

Yu, Corey H 1988-. “Dynamics and Interactions of Metal-Binding Domains in the Function of Wilson Disease Protein.” 2017. Web. 21 Oct 2020.

Vancouver:

Yu CH1. Dynamics and Interactions of Metal-Binding Domains in the Function of Wilson Disease Protein. [Internet] [Thesis]. University of Saskatchewan; 2017. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7700.

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

Council of Science Editors:

Yu CH1. Dynamics and Interactions of Metal-Binding Domains in the Function of Wilson Disease Protein. [Thesis]. University of Saskatchewan; 2017. Available from: http://hdl.handle.net/10388/7700

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


University of Saskatchewan

4. Arrafi, Sifa 1988-. Structural and Functional Characterization of the Tip60 Chromodomain.

Degree: 2016, University of Saskatchewan

 The Tat-interactive protein of 60 kDa (Tip60) is a histone acetyltransferase enzyme that appears to have a wide range of acetylation targets, which include core… (more)

Subjects/Keywords: Tip60; Chromodomain; Histone; X-ray crystallography; ITC; SPR

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APA (6th Edition):

Arrafi, S. 1. (2016). Structural and Functional Characterization of the Tip60 Chromodomain. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7536

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):

Arrafi, Sifa 1988-. “Structural and Functional Characterization of the Tip60 Chromodomain.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7536.

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

MLA Handbook (7th Edition):

Arrafi, Sifa 1988-. “Structural and Functional Characterization of the Tip60 Chromodomain.” 2016. Web. 21 Oct 2020.

Vancouver:

Arrafi S1. Structural and Functional Characterization of the Tip60 Chromodomain. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7536.

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

Council of Science Editors:

Arrafi S1. Structural and Functional Characterization of the Tip60 Chromodomain. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7536

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


University of Saskatchewan

5. Xu, Caishuang 1989-. STRUCTURAL AND FUNCTIONAL STUDIES OF SALMONELLA TYPHIMURIUM EFFECTORS GTGE AND SPVB.

Degree: 2015, University of Saskatchewan

 Salmonella is a genus of Gram-negative bacteria, which is a major cause of foodborne disease. To create a safe intracellular environment for the pathogen within… (more)

Subjects/Keywords: Salmonella; effectors; GtgE; protease, SpvB; ADP-ribosylation; crystallization

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APA (6th Edition):

Xu, C. 1. (2015). STRUCTURAL AND FUNCTIONAL STUDIES OF SALMONELLA TYPHIMURIUM EFFECTORS GTGE AND SPVB. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12610

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):

Xu, Caishuang 1989-. “STRUCTURAL AND FUNCTIONAL STUDIES OF SALMONELLA TYPHIMURIUM EFFECTORS GTGE AND SPVB.” 2015. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/12610.

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

MLA Handbook (7th Edition):

Xu, Caishuang 1989-. “STRUCTURAL AND FUNCTIONAL STUDIES OF SALMONELLA TYPHIMURIUM EFFECTORS GTGE AND SPVB.” 2015. Web. 21 Oct 2020.

Vancouver:

Xu C1. STRUCTURAL AND FUNCTIONAL STUDIES OF SALMONELLA TYPHIMURIUM EFFECTORS GTGE AND SPVB. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/12610.

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

Council of Science Editors:

Xu C1. STRUCTURAL AND FUNCTIONAL STUDIES OF SALMONELLA TYPHIMURIUM EFFECTORS GTGE AND SPVB. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/12610

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


University of Saskatchewan

6. Ye, Shengjian 1988-. THE ROLE OF N-TERMINAL REGIONS IN REGULATING THE LEVEL OF PLANT ICK CYCLIN-DEPENDENT KINASE INHIBITORS.

Degree: 2016, University of Saskatchewan

 Plants have a family of cyclin-dependent kinase (CDK) inhibitors named ICKs (interactor/inhibitor of CDK), which are important cell cycle regulators and can modulate CDK activity… (more)

Subjects/Keywords: Arabidopsis thaliana; cell cycle; CDK inhibitor; protein stability

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APA (6th Edition):

Ye, S. 1. (2016). THE ROLE OF N-TERMINAL REGIONS IN REGULATING THE LEVEL OF PLANT ICK CYCLIN-DEPENDENT KINASE INHIBITORS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12600

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):

Ye, Shengjian 1988-. “THE ROLE OF N-TERMINAL REGIONS IN REGULATING THE LEVEL OF PLANT ICK CYCLIN-DEPENDENT KINASE INHIBITORS.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/12600.

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

MLA Handbook (7th Edition):

Ye, Shengjian 1988-. “THE ROLE OF N-TERMINAL REGIONS IN REGULATING THE LEVEL OF PLANT ICK CYCLIN-DEPENDENT KINASE INHIBITORS.” 2016. Web. 21 Oct 2020.

Vancouver:

Ye S1. THE ROLE OF N-TERMINAL REGIONS IN REGULATING THE LEVEL OF PLANT ICK CYCLIN-DEPENDENT KINASE INHIBITORS. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/12600.

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

Council of Science Editors:

Ye S1. THE ROLE OF N-TERMINAL REGIONS IN REGULATING THE LEVEL OF PLANT ICK CYCLIN-DEPENDENT KINASE INHIBITORS. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/12600

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


University of Saskatchewan

7. Krasniqi, Besnik. Nanopore Sensing Of Peptides And Proteins.

Degree: 2013, University of Saskatchewan

 In recent years the application of single-molecule techniques to probe biomolecules and intermolecular interactions at single-molecule resolution has expanded rapidly. Here, I investigate a series… (more)

Subjects/Keywords: nanopore; nanopore sensing; solid-state pores; alpha-hemolysin; isomers; zeta potential; metal ion binding; protein ligand interactions; Ribonuclease A

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APA (6th Edition):

Krasniqi, B. (2013). Nanopore Sensing Of Peptides And Proteins. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2013-11-1280

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):

Krasniqi, Besnik. “Nanopore Sensing Of Peptides And Proteins.” 2013. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2013-11-1280.

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

MLA Handbook (7th Edition):

Krasniqi, Besnik. “Nanopore Sensing Of Peptides And Proteins.” 2013. Web. 21 Oct 2020.

Vancouver:

Krasniqi B. Nanopore Sensing Of Peptides And Proteins. [Internet] [Thesis]. University of Saskatchewan; 2013. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2013-11-1280.

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

Council of Science Editors:

Krasniqi B. Nanopore Sensing Of Peptides And Proteins. [Thesis]. University of Saskatchewan; 2013. Available from: http://hdl.handle.net/10388/ETD-2013-11-1280

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


University of Saskatchewan

8. Voth, Kevin Andrew 1991-. Structural Biology of Legionella pneumophila Effectors.

Degree: 2019, University of Saskatchewan

 Legionella pneumophila is a Gram-negative intracellular pathogen that causes Legionnaires’ disease and Pontiac fever in elderly or immunocompromised humans. The ability of Legionella to thrive… (more)

Subjects/Keywords: Host-pathogen; effectors

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APA (6th Edition):

Voth, K. A. 1. (2019). Structural Biology of Legionella pneumophila Effectors. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12302

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):

Voth, Kevin Andrew 1991-. “Structural Biology of Legionella pneumophila Effectors.” 2019. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/12302.

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

MLA Handbook (7th Edition):

Voth, Kevin Andrew 1991-. “Structural Biology of Legionella pneumophila Effectors.” 2019. Web. 21 Oct 2020.

Vancouver:

Voth KA1. Structural Biology of Legionella pneumophila Effectors. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/12302.

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

Council of Science Editors:

Voth KA1. Structural Biology of Legionella pneumophila Effectors. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12302

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


University of Saskatchewan

9. Boulet, Aren. Physical interaction and functional studies of human SCO1, a mitochondrial metallochaperone.

Degree: 2014, University of Saskatchewan

 Cytochrome c oxidase (COX) is a multimeric protein complex embedded in the inner mitochondrial membrane that contributes to the electrochemical potential ultimately required for adenosine… (more)

Subjects/Keywords: SCO1; SCO2; COX; Cytochrome c oxidase; Copper

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APA (6th Edition):

Boulet, A. (2014). Physical interaction and functional studies of human SCO1, a mitochondrial metallochaperone. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-04-1468

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):

Boulet, Aren. “Physical interaction and functional studies of human SCO1, a mitochondrial metallochaperone.” 2014. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2014-04-1468.

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

MLA Handbook (7th Edition):

Boulet, Aren. “Physical interaction and functional studies of human SCO1, a mitochondrial metallochaperone.” 2014. Web. 21 Oct 2020.

Vancouver:

Boulet A. Physical interaction and functional studies of human SCO1, a mitochondrial metallochaperone. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2014-04-1468.

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

Council of Science Editors:

Boulet A. Physical interaction and functional studies of human SCO1, a mitochondrial metallochaperone. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-04-1468

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


University of Saskatchewan

10. Christensen, Christopher 1984-. Isolation and Use of the Aeromonas hydrophila Secretin ExeD for Nanopore Analysis.

Degree: 2016, University of Saskatchewan

 Nanopore analysis is a technique for measuring single molecule interactions with an open pore in solution. Current progress in the field is hindered by the… (more)

Subjects/Keywords: Nanopore Analysis; ExeD; Aeromonas hydrophila

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APA (6th Edition):

Christensen, C. 1. (2016). Isolation and Use of the Aeromonas hydrophila Secretin ExeD for Nanopore Analysis. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7517

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):

Christensen, Christopher 1984-. “Isolation and Use of the Aeromonas hydrophila Secretin ExeD for Nanopore Analysis.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7517.

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

MLA Handbook (7th Edition):

Christensen, Christopher 1984-. “Isolation and Use of the Aeromonas hydrophila Secretin ExeD for Nanopore Analysis.” 2016. Web. 21 Oct 2020.

Vancouver:

Christensen C1. Isolation and Use of the Aeromonas hydrophila Secretin ExeD for Nanopore Analysis. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7517.

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

Council of Science Editors:

Christensen C1. Isolation and Use of the Aeromonas hydrophila Secretin ExeD for Nanopore Analysis. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7517

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


University of Saskatchewan

11. Paul, James 1986-. Synthetic lethal interactions of EPHB6 in breast cancer cells.

Degree: 2016, University of Saskatchewan

 Sequencing of tumor genomes has shown that many loss-of-function alterations exist in cancer cells. Some of these alterations are a product of the cancerous progression… (more)

Subjects/Keywords: breast cancer; genetic interaction; synthetic lethality; EPHB6; SRC kinase; KX2-391

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APA (6th Edition):

Paul, J. 1. (2016). Synthetic lethal interactions of EPHB6 in breast cancer cells. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7663

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):

Paul, James 1986-. “Synthetic lethal interactions of EPHB6 in breast cancer cells.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7663.

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

MLA Handbook (7th Edition):

Paul, James 1986-. “Synthetic lethal interactions of EPHB6 in breast cancer cells.” 2016. Web. 21 Oct 2020.

Vancouver:

Paul J1. Synthetic lethal interactions of EPHB6 in breast cancer cells. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7663.

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

Council of Science Editors:

Paul J1. Synthetic lethal interactions of EPHB6 in breast cancer cells. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7663

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


University of Saskatchewan

12. Kulik, Daryna 1988-. Conversion of the ATP synthase subunit c into a hydrophilic pore.

Degree: 2016, University of Saskatchewan

 Nanopore analysis is a very promising technique for many applications, such as the study of intrinsically disordered proteins, folding and misfolding of proteins and DNA… (more)

Subjects/Keywords: Nanopore; nanopore analysis; ATP synthase; c-ring; subunit c; single-molecule analysis

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APA (6th Edition):

Kulik, D. 1. (2016). Conversion of the ATP synthase subunit c into a hydrophilic pore. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7535

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):

Kulik, Daryna 1988-. “Conversion of the ATP synthase subunit c into a hydrophilic pore.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7535.

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

MLA Handbook (7th Edition):

Kulik, Daryna 1988-. “Conversion of the ATP synthase subunit c into a hydrophilic pore.” 2016. Web. 21 Oct 2020.

Vancouver:

Kulik D1. Conversion of the ATP synthase subunit c into a hydrophilic pore. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7535.

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

Council of Science Editors:

Kulik D1. Conversion of the ATP synthase subunit c into a hydrophilic pore. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7535

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


University of Saskatchewan

13. Chen, Yi. Physiological, Behavioral, and Biochemical Responses to Restraint Stress in Cattle.

Degree: 2016, University of Saskatchewan

 Stress has a significant impact on animal health and productivity and public perception of animal stress can influence industry practices. Understanding stress responses in livestock… (more)

Subjects/Keywords: Behavior; Cattle Stress; Cortisol; Glucose; Kinome; Restraint

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APA (6th Edition):

Chen, Y. (2016). Physiological, Behavioral, and Biochemical Responses to Restraint Stress in Cattle. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2016-05-2559

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

Chicago Manual of Style (16th Edition):

Chen, Yi. “Physiological, Behavioral, and Biochemical Responses to Restraint Stress in Cattle.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2016-05-2559.

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

MLA Handbook (7th Edition):

Chen, Yi. “Physiological, Behavioral, and Biochemical Responses to Restraint Stress in Cattle.” 2016. Web. 21 Oct 2020.

Vancouver:

Chen Y. Physiological, Behavioral, and Biochemical Responses to Restraint Stress in Cattle. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2016-05-2559.

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

Council of Science Editors:

Chen Y. Physiological, Behavioral, and Biochemical Responses to Restraint Stress in Cattle. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/ETD-2016-05-2559

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


University of Saskatchewan

14. Wang, Sheng. Studies of E2s Related to Unconventional Ubiquitination in Arabidopsis thaliana.

Degree: 2018, University of Saskatchewan

 Protein ubiquitination, a fundamental protein modification cascade, is catalyzed by three types of enzymes referred to as E1 for ubiquitin (Ub) activation, E2 for Ub… (more)

Subjects/Keywords: Ubiquitination; gametogenesis

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APA (6th Edition):

Wang, S. (2018). Studies of E2s Related to Unconventional Ubiquitination in Arabidopsis thaliana. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11670

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):

Wang, Sheng. “Studies of E2s Related to Unconventional Ubiquitination in Arabidopsis thaliana.” 2018. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/11670.

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

MLA Handbook (7th Edition):

Wang, Sheng. “Studies of E2s Related to Unconventional Ubiquitination in Arabidopsis thaliana.” 2018. Web. 21 Oct 2020.

Vancouver:

Wang S. Studies of E2s Related to Unconventional Ubiquitination in Arabidopsis thaliana. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/11670.

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

Council of Science Editors:

Wang S. Studies of E2s Related to Unconventional Ubiquitination in Arabidopsis thaliana. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/11670

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


University of Saskatchewan

15. Lu, Yin. Single-molecule fluorescence microscopy studies of fluorescent probes in thin films and on nanoparticle surfaces.

Degree: 2011, University of Saskatchewan

 Single-molecule (SM) fluorescence spectroscopy has become a useful and important experimental approach for investigating the optical properties of chemical systems. In this thesis, four subprojects… (more)

Subjects/Keywords: fluorescence; single-molecule; microscopy

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APA (6th Edition):

Lu, Y. (2011). Single-molecule fluorescence microscopy studies of fluorescent probes in thin films and on nanoparticle surfaces. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-01312011-155230

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):

Lu, Yin. “Single-molecule fluorescence microscopy studies of fluorescent probes in thin films and on nanoparticle surfaces.” 2011. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/etd-01312011-155230.

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

MLA Handbook (7th Edition):

Lu, Yin. “Single-molecule fluorescence microscopy studies of fluorescent probes in thin films and on nanoparticle surfaces.” 2011. Web. 21 Oct 2020.

Vancouver:

Lu Y. Single-molecule fluorescence microscopy studies of fluorescent probes in thin films and on nanoparticle surfaces. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/etd-01312011-155230.

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

Council of Science Editors:

Lu Y. Single-molecule fluorescence microscopy studies of fluorescent probes in thin films and on nanoparticle surfaces. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/etd-01312011-155230

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


University of Saskatchewan

16. Knudsen, Kaeli Jean 1994-. A popular antidepressant drug and its metabolite induce toxicity via beta-amyloid and a serotonin transporter-dependent mechanism.

Degree: 2019, University of Saskatchewan

 Depression increases the risk of Alzheimer disease (AD); however, some of this risk might be associated with the type of antidepressant drug used to treat… (more)

Subjects/Keywords: Alzheimer disease; beta-amyloid; C. elegans; cell culture; Fluoxetine; serotonin transporter

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APA (6th Edition):

Knudsen, K. J. 1. (2019). A popular antidepressant drug and its metabolite induce toxicity via beta-amyloid and a serotonin transporter-dependent mechanism. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11773

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):

Knudsen, Kaeli Jean 1994-. “A popular antidepressant drug and its metabolite induce toxicity via beta-amyloid and a serotonin transporter-dependent mechanism.” 2019. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/11773.

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

MLA Handbook (7th Edition):

Knudsen, Kaeli Jean 1994-. “A popular antidepressant drug and its metabolite induce toxicity via beta-amyloid and a serotonin transporter-dependent mechanism.” 2019. Web. 21 Oct 2020.

Vancouver:

Knudsen KJ1. A popular antidepressant drug and its metabolite induce toxicity via beta-amyloid and a serotonin transporter-dependent mechanism. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/11773.

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

Council of Science Editors:

Knudsen KJ1. A popular antidepressant drug and its metabolite induce toxicity via beta-amyloid and a serotonin transporter-dependent mechanism. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/11773

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


University of Saskatchewan

17. Marshall, Jeremy Davin Seiberling. STRUCTURAL ANALYSIS OF THE P85 BH DOMAIN IN COMPLEX WITH BINDING PARTNERS AND EFFECT OF MUTATIONS.

Degree: 2017, University of Saskatchewan

 The phosphatidylinositol 3-kinase (PI3K)/PTEN (phosphatase and tensin homologue deleted on chromosome 10) pathway is activated upon stimulation of receptor tyrosine kinases (RTKs) and regulates downstream… (more)

Subjects/Keywords: p85; crystallography; structural study; cancer; PI3K

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APA (6th Edition):

Marshall, J. D. S. (2017). STRUCTURAL ANALYSIS OF THE P85 BH DOMAIN IN COMPLEX WITH BINDING PARTNERS AND EFFECT OF MUTATIONS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/8321

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):

Marshall, Jeremy Davin Seiberling. “STRUCTURAL ANALYSIS OF THE P85 BH DOMAIN IN COMPLEX WITH BINDING PARTNERS AND EFFECT OF MUTATIONS.” 2017. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/8321.

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

MLA Handbook (7th Edition):

Marshall, Jeremy Davin Seiberling. “STRUCTURAL ANALYSIS OF THE P85 BH DOMAIN IN COMPLEX WITH BINDING PARTNERS AND EFFECT OF MUTATIONS.” 2017. Web. 21 Oct 2020.

Vancouver:

Marshall JDS. STRUCTURAL ANALYSIS OF THE P85 BH DOMAIN IN COMPLEX WITH BINDING PARTNERS AND EFFECT OF MUTATIONS. [Internet] [Thesis]. University of Saskatchewan; 2017. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/8321.

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

Council of Science Editors:

Marshall JDS. STRUCTURAL ANALYSIS OF THE P85 BH DOMAIN IN COMPLEX WITH BINDING PARTNERS AND EFFECT OF MUTATIONS. [Thesis]. University of Saskatchewan; 2017. Available from: http://hdl.handle.net/10388/8321

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


University of Saskatchewan

18. Zhao, Liang. Studies of stored mRNAs during seed aging in Arabidopsis thaliana, Brassica napus and wheat (Triticum aestivum).

Degree: 2019, University of Saskatchewan

 How plant seeds age remains poorly understood and effective tools for monitoring seed aging are lacking. Dry seeds contain various stored mRNAs which are believed… (more)

Subjects/Keywords: Arabidopsis thaliana; real-time quantitative PCR (qPCR); seed aging; seed germination; stored mRNA; long-lived mRNA

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APA (6th Edition):

Zhao, L. (2019). Studies of stored mRNAs during seed aging in Arabidopsis thaliana, Brassica napus and wheat (Triticum aestivum). (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12519

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):

Zhao, Liang. “Studies of stored mRNAs during seed aging in Arabidopsis thaliana, Brassica napus and wheat (Triticum aestivum).” 2019. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/12519.

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

MLA Handbook (7th Edition):

Zhao, Liang. “Studies of stored mRNAs during seed aging in Arabidopsis thaliana, Brassica napus and wheat (Triticum aestivum).” 2019. Web. 21 Oct 2020.

Vancouver:

Zhao L. Studies of stored mRNAs during seed aging in Arabidopsis thaliana, Brassica napus and wheat (Triticum aestivum). [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/12519.

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

Council of Science Editors:

Zhao L. Studies of stored mRNAs during seed aging in Arabidopsis thaliana, Brassica napus and wheat (Triticum aestivum). [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12519

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


University of Saskatchewan

19. Islam, MD Fahmid 1989-. Design, Construction, and Screening of an shRNA Library Targeting Human Circular RNAs.

Degree: 2018, University of Saskatchewan

 Recent advances in next-generation sequencing (NGS) methods and computational analyses have identified a large class of non-polyadenylated RNA molecules. Further, analysis of these RNAs revealed… (more)

Subjects/Keywords: circular RNA; cancer; essentiality; screen; next-generation sequencing

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APA (6th Edition):

Islam, M. F. 1. (2018). Design, Construction, and Screening of an shRNA Library Targeting Human Circular RNAs. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/9235

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):

Islam, MD Fahmid 1989-. “Design, Construction, and Screening of an shRNA Library Targeting Human Circular RNAs.” 2018. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/9235.

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

MLA Handbook (7th Edition):

Islam, MD Fahmid 1989-. “Design, Construction, and Screening of an shRNA Library Targeting Human Circular RNAs.” 2018. Web. 21 Oct 2020.

Vancouver:

Islam MF1. Design, Construction, and Screening of an shRNA Library Targeting Human Circular RNAs. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/9235.

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

Council of Science Editors:

Islam MF1. Design, Construction, and Screening of an shRNA Library Targeting Human Circular RNAs. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/9235

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


University of Saskatchewan

20. Maley, Jason 1974-. Protein Interactions With Nitrogen-Doped Amorphous Carbon Surfaces.

Degree: 2019, University of Saskatchewan

 Amorphous carbon is a very promising material for biocompatible devices. It can be made by a variety of plasma-assisted deposition techniques and is readily doped… (more)

Subjects/Keywords: Amorphous carbon nitride; fullerene-like carbon nitride; surface plasmon resonance; protein-surface interactions

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APA (6th Edition):

Maley, J. 1. (2019). Protein Interactions With Nitrogen-Doped Amorphous Carbon Surfaces. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12201

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):

Maley, Jason 1974-. “Protein Interactions With Nitrogen-Doped Amorphous Carbon Surfaces.” 2019. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/12201.

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

MLA Handbook (7th Edition):

Maley, Jason 1974-. “Protein Interactions With Nitrogen-Doped Amorphous Carbon Surfaces.” 2019. Web. 21 Oct 2020.

Vancouver:

Maley J1. Protein Interactions With Nitrogen-Doped Amorphous Carbon Surfaces. [Internet] [Thesis]. University of Saskatchewan; 2019. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/12201.

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

Council of Science Editors:

Maley J1. Protein Interactions With Nitrogen-Doped Amorphous Carbon Surfaces. [Thesis]. University of Saskatchewan; 2019. Available from: http://hdl.handle.net/10388/12201

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


University of Saskatchewan

21. Arsenault, Ryan. Development and application of genus-specific peptide arrays for kinome analysis.

Degree: 2011, University of Saskatchewan

 Phosphorylation represents a central mechanism to regulate cell function. Protein phosphorylation is catalyzed by a class of enzymes called kinases, the cellular complement of which… (more)

Subjects/Keywords: kinome; peptide array; genus-specific; kinase; prion; PrPC; PrPSc; Mycobacterium avium subsp. paratuberculosis; MAP; mycobacteria; cell signalling; PIIKA

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APA (6th Edition):

Arsenault, R. (2011). Development and application of genus-specific peptide arrays for kinome analysis. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-12-267

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):

Arsenault, Ryan. “Development and application of genus-specific peptide arrays for kinome analysis.” 2011. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2011-12-267.

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

MLA Handbook (7th Edition):

Arsenault, Ryan. “Development and application of genus-specific peptide arrays for kinome analysis.” 2011. Web. 21 Oct 2020.

Vancouver:

Arsenault R. Development and application of genus-specific peptide arrays for kinome analysis. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2011-12-267.

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

Council of Science Editors:

Arsenault R. Development and application of genus-specific peptide arrays for kinome analysis. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-12-267

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

22. Haji, Tahereh. MdfA as a Model for Structural and Functional Characterization of Putative Multidrug Transporters.

Degree: 2012, University of Saskatchewan

 Numerous members of the Major Facilitator Superfamily of membrane transporters are involved in multidrug resistance (MDR) of gram-positive bacteria, such as Staphylococcus aureus (S. aureus).… (more)

Subjects/Keywords: Multidrug Transporters; MdfA; Antibiotic Resistance

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APA (6th Edition):

Haji, T. (2012). MdfA as a Model for Structural and Functional Characterization of Putative Multidrug Transporters. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2012-12-805

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):

Haji, Tahereh. “MdfA as a Model for Structural and Functional Characterization of Putative Multidrug Transporters.” 2012. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2012-12-805.

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

MLA Handbook (7th Edition):

Haji, Tahereh. “MdfA as a Model for Structural and Functional Characterization of Putative Multidrug Transporters.” 2012. Web. 21 Oct 2020.

Vancouver:

Haji T. MdfA as a Model for Structural and Functional Characterization of Putative Multidrug Transporters. [Internet] [Thesis]. University of Saskatchewan; 2012. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2012-12-805.

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

Council of Science Editors:

Haji T. MdfA as a Model for Structural and Functional Characterization of Putative Multidrug Transporters. [Thesis]. University of Saskatchewan; 2012. Available from: http://hdl.handle.net/10388/ETD-2012-12-805

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

23. Ulaganathan, Thirumalai Selvi. Structural studies on enzymes involved in uronic acid polysaccharide degradation.

Degree: 2018, University of Saskatchewan

 Uronates are charged sugars that constitute a major component of glycosaminoglycans (heparin, heparin sulfate, hyaluronan etc.,) and cell wall polysaccharides of plants (pectate/ pectin) and… (more)

Subjects/Keywords: Polysaccharide lyases; hepIII; Ulvan lyases; X-ray crystallography; catalytic mechanism.

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APA (6th Edition):

Ulaganathan, T. S. (2018). Structural studies on enzymes involved in uronic acid polysaccharide degradation. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/9233

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):

Ulaganathan, Thirumalai Selvi. “Structural studies on enzymes involved in uronic acid polysaccharide degradation.” 2018. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/9233.

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

MLA Handbook (7th Edition):

Ulaganathan, Thirumalai Selvi. “Structural studies on enzymes involved in uronic acid polysaccharide degradation.” 2018. Web. 21 Oct 2020.

Vancouver:

Ulaganathan TS. Structural studies on enzymes involved in uronic acid polysaccharide degradation. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/9233.

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

Council of Science Editors:

Ulaganathan TS. Structural studies on enzymes involved in uronic acid polysaccharide degradation. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/9233

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

24. Furber, Levi. Regulation of constitutive platelet-derived growth factor receptor degradation by the 105 kilodalton isoform of ankyrin3.

Degree: 2014, University of Saskatchewan

 Deregulation of platelet-derived growth factor receptor (PDGFR) signaling is a driving event in glioblastoma, promotes tumor progression epithelial to mesenchymal transition (EMT) in multiple cancers,… (more)

Subjects/Keywords: Ankyrin; PDGFR; degradation; endocytosis; dynamin; clathrin; constitutive; shRNA; small molecule inhibitors; signaling; ubiquitin

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APA (6th Edition):

Furber, L. (2014). Regulation of constitutive platelet-derived growth factor receptor degradation by the 105 kilodalton isoform of ankyrin3. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-03-1496

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):

Furber, Levi. “Regulation of constitutive platelet-derived growth factor receptor degradation by the 105 kilodalton isoform of ankyrin3.” 2014. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2014-03-1496.

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

MLA Handbook (7th Edition):

Furber, Levi. “Regulation of constitutive platelet-derived growth factor receptor degradation by the 105 kilodalton isoform of ankyrin3.” 2014. Web. 21 Oct 2020.

Vancouver:

Furber L. Regulation of constitutive platelet-derived growth factor receptor degradation by the 105 kilodalton isoform of ankyrin3. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2014-03-1496.

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

Council of Science Editors:

Furber L. Regulation of constitutive platelet-derived growth factor receptor degradation by the 105 kilodalton isoform of ankyrin3. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-03-1496

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

25. Hedlin, Peter. Design and delivery of a cryptic PrPC epitope for the induction of a PrPSc-specific antibody response.

Degree: 2011, University of Saskatchewan

 Transmissible spongiform encephalopathies (TSEs) represent a unique category of diseases known as protein misfolding diseases. Pathogenesis is dependent on the misfolding of normal cellular prion… (more)

Subjects/Keywords: TSE; CWD; BSE; Prions; Scrapie; Vaccine

University of Saskatchewan Norwegian School of Veterinary Science 57 Characterization of Antibody… …2.4.6 60 Immunoprecipitation 60 2.5 Genotyping of the University of Saskatchewan Sheep… …the Suppliers 62 3.1 Genotyping of the Prnp Gene for University of Saskatchewan Sheep… …11-40. Downloaded from arjournals.annualreviews.org by University of Saskatchewan on 02/11… 

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APA (6th Edition):

Hedlin, P. (2011). Design and delivery of a cryptic PrPC epitope for the induction of a PrPSc-specific antibody response. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-09-167

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):

Hedlin, Peter. “Design and delivery of a cryptic PrPC epitope for the induction of a PrPSc-specific antibody response.” 2011. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2011-09-167.

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

MLA Handbook (7th Edition):

Hedlin, Peter. “Design and delivery of a cryptic PrPC epitope for the induction of a PrPSc-specific antibody response.” 2011. Web. 21 Oct 2020.

Vancouver:

Hedlin P. Design and delivery of a cryptic PrPC epitope for the induction of a PrPSc-specific antibody response. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2011-09-167.

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

Council of Science Editors:

Hedlin P. Design and delivery of a cryptic PrPC epitope for the induction of a PrPSc-specific antibody response. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-09-167

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

26. Pan, Min. functional analyses of variants of human SCO1, a mitochondrial metallochaperone.

Degree: 2013, University of Saskatchewan

 Cytochrome c oxidase (COX) is a multimeric protein complex whose enzymatic activity contributes to the generation of an electrochemical potential required to synthesize adenosine triphosphate… (more)

Subjects/Keywords: Keyword 1; Human SCO1

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APA (6th Edition):

Pan, M. (2013). functional analyses of variants of human SCO1, a mitochondrial metallochaperone. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2013-09-1245

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):

Pan, Min. “functional analyses of variants of human SCO1, a mitochondrial metallochaperone.” 2013. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2013-09-1245.

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

MLA Handbook (7th Edition):

Pan, Min. “functional analyses of variants of human SCO1, a mitochondrial metallochaperone.” 2013. Web. 21 Oct 2020.

Vancouver:

Pan M. functional analyses of variants of human SCO1, a mitochondrial metallochaperone. [Internet] [Thesis]. University of Saskatchewan; 2013. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2013-09-1245.

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

Council of Science Editors:

Pan M. functional analyses of variants of human SCO1, a mitochondrial metallochaperone. [Thesis]. University of Saskatchewan; 2013. Available from: http://hdl.handle.net/10388/ETD-2013-09-1245

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

27. Ding, Hao. The Q motif is involved in DNA binding that affects ATP hydrolysis and unwinding in ChlR1 helicase.

Degree: 2016, University of Saskatchewan

 Helicases are molecular motors that couple the energy of nucleoside triphosphate (NTP) hydrolysis to the unwinding and remodeling of structured DNA or RNA. The conversion… (more)

Subjects/Keywords: Helicase; Q motif

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APA (6th Edition):

Ding, H. (2016). The Q motif is involved in DNA binding that affects ATP hydrolysis and unwinding in ChlR1 helicase. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2016-02-2413

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):

Ding, Hao. “The Q motif is involved in DNA binding that affects ATP hydrolysis and unwinding in ChlR1 helicase.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2016-02-2413.

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

MLA Handbook (7th Edition):

Ding, Hao. “The Q motif is involved in DNA binding that affects ATP hydrolysis and unwinding in ChlR1 helicase.” 2016. Web. 21 Oct 2020.

Vancouver:

Ding H. The Q motif is involved in DNA binding that affects ATP hydrolysis and unwinding in ChlR1 helicase. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2016-02-2413.

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

Council of Science Editors:

Ding H. The Q motif is involved in DNA binding that affects ATP hydrolysis and unwinding in ChlR1 helicase. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/ETD-2016-02-2413

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

28. Pujara, Pareshkumar. CHARACTERIZATION OF PEPTIDE CYCLASE 1 (PCY1), A SERINE PROTEASE-LIKE ENZYME INVOLVED IN CYCLIC PEPTIDE BIOSYNTHESIS IN PLANTS.

Degree: 2013, University of Saskatchewan

 Plants within the Caryophyllaceae, and certain other families, produce cyclic peptides (CPs) which generally consist of 5–12 proteinogenic amino acids. Until recently, very little was… (more)

Subjects/Keywords: Cyclic peptide; Biosynthesis

Page 1

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APA (6th Edition):

Pujara, P. (2013). CHARACTERIZATION OF PEPTIDE CYCLASE 1 (PCY1), A SERINE PROTEASE-LIKE ENZYME INVOLVED IN CYCLIC PEPTIDE BIOSYNTHESIS IN PLANTS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2013-11-1327

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):

Pujara, Pareshkumar. “CHARACTERIZATION OF PEPTIDE CYCLASE 1 (PCY1), A SERINE PROTEASE-LIKE ENZYME INVOLVED IN CYCLIC PEPTIDE BIOSYNTHESIS IN PLANTS.” 2013. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2013-11-1327.

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

MLA Handbook (7th Edition):

Pujara, Pareshkumar. “CHARACTERIZATION OF PEPTIDE CYCLASE 1 (PCY1), A SERINE PROTEASE-LIKE ENZYME INVOLVED IN CYCLIC PEPTIDE BIOSYNTHESIS IN PLANTS.” 2013. Web. 21 Oct 2020.

Vancouver:

Pujara P. CHARACTERIZATION OF PEPTIDE CYCLASE 1 (PCY1), A SERINE PROTEASE-LIKE ENZYME INVOLVED IN CYCLIC PEPTIDE BIOSYNTHESIS IN PLANTS. [Internet] [Thesis]. University of Saskatchewan; 2013. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2013-11-1327.

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

Council of Science Editors:

Pujara P. CHARACTERIZATION OF PEPTIDE CYCLASE 1 (PCY1), A SERINE PROTEASE-LIKE ENZYME INVOLVED IN CYCLIC PEPTIDE BIOSYNTHESIS IN PLANTS. [Thesis]. University of Saskatchewan; 2013. Available from: http://hdl.handle.net/10388/ETD-2013-11-1327

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

29. Choudhary, Pooja. Alternative rownstream roles for Ste2p and an α-arrestin in sacccharomyces cerevisiae mating.

Degree: 2014, University of Saskatchewan

 Ste2p and Ste3p are well-characterized yeast pheromone G-protein Coupled Receptors (GPCR) those are involved in the signaling of mating responses that lead to cell fusion.… (more)

Subjects/Keywords: yeast, pheromone; G-protein coupled receptor; arrestin; site-directed mutagenesis; alternate functionalities; cell cycle; zygote; mating

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

APA (6th Edition):

Choudhary, P. (2014). Alternative rownstream roles for Ste2p and an α-arrestin in sacccharomyces cerevisiae mating. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-11-1813

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):

Choudhary, Pooja. “Alternative rownstream roles for Ste2p and an α-arrestin in sacccharomyces cerevisiae mating.” 2014. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/ETD-2014-11-1813.

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

MLA Handbook (7th Edition):

Choudhary, Pooja. “Alternative rownstream roles for Ste2p and an α-arrestin in sacccharomyces cerevisiae mating.” 2014. Web. 21 Oct 2020.

Vancouver:

Choudhary P. Alternative rownstream roles for Ste2p and an α-arrestin in sacccharomyces cerevisiae mating. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/ETD-2014-11-1813.

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

Council of Science Editors:

Choudhary P. Alternative rownstream roles for Ste2p and an α-arrestin in sacccharomyces cerevisiae mating. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-11-1813

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

30. Ambilwade, Dakshata P 1989-. Structural characterization of components of the flagellar export apparatus from the H. pylori.

Degree: 2016, University of Saskatchewan

 H. pylori is a human gastric pathogen responsible for serious health conditions such as gastritis and peptic ulcers. It requires polar sheathed flagella for initial… (more)

Subjects/Keywords: H. pylori; flagellar export apparatus; FliH; FliI; FliJ.

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

APA (6th Edition):

Ambilwade, D. P. 1. (2016). Structural characterization of components of the flagellar export apparatus from the H. pylori. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7480

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):

Ambilwade, Dakshata P 1989-. “Structural characterization of components of the flagellar export apparatus from the H. pylori.” 2016. Thesis, University of Saskatchewan. Accessed October 21, 2020. http://hdl.handle.net/10388/7480.

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

MLA Handbook (7th Edition):

Ambilwade, Dakshata P 1989-. “Structural characterization of components of the flagellar export apparatus from the H. pylori.” 2016. Web. 21 Oct 2020.

Vancouver:

Ambilwade DP1. Structural characterization of components of the flagellar export apparatus from the H. pylori. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2020 Oct 21]. Available from: http://hdl.handle.net/10388/7480.

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

Council of Science Editors:

Ambilwade DP1. Structural characterization of components of the flagellar export apparatus from the H. pylori. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7480

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

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