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You searched for subject:(0487). Showing records 1 – 30 of 481 total matches.

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University of Toronto

1. Thakkar, Mauli Jitendra. Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding.

Degree: 2015, University of Toronto

Intracellular nickel concentration in Escherichia coli is controlled by a transcription factor called NikR, which represses the nikABCDE operon, encoding a nickel specific transporter. The… (more)

Subjects/Keywords: 0487

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

APA (6th Edition):

Thakkar, M. J. (2015). Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69713

Chicago Manual of Style (16th Edition):

Thakkar, Mauli Jitendra. “Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding.” 2015. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/69713.

MLA Handbook (7th Edition):

Thakkar, Mauli Jitendra. “Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding.” 2015. Web. 23 Sep 2020.

Vancouver:

Thakkar MJ. Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/69713.

Council of Science Editors:

Thakkar MJ. Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69713


University of Toronto

2. Deol, Navdeep. Characterizing the Role of the Pβ Peptide: A Potential Mitochondria to Nuclear Signal in Mitochondrial Quality Control.

Degree: 2016, University of Toronto

The PINK1/Parkin mediated mitophagy pathway is fundamental for maintaining a healthy mitochondrial network. We have previously shown that the mitochondrial rhomboid protease PARL is required… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Deol, N. (2016). Characterizing the Role of the Pβ Peptide: A Potential Mitochondria to Nuclear Signal in Mitochondrial Quality Control. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72690

Chicago Manual of Style (16th Edition):

Deol, Navdeep. “Characterizing the Role of the Pβ Peptide: A Potential Mitochondria to Nuclear Signal in Mitochondrial Quality Control.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/72690.

MLA Handbook (7th Edition):

Deol, Navdeep. “Characterizing the Role of the Pβ Peptide: A Potential Mitochondria to Nuclear Signal in Mitochondrial Quality Control.” 2016. Web. 23 Sep 2020.

Vancouver:

Deol N. Characterizing the Role of the Pβ Peptide: A Potential Mitochondria to Nuclear Signal in Mitochondrial Quality Control. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/72690.

Council of Science Editors:

Deol N. Characterizing the Role of the Pβ Peptide: A Potential Mitochondria to Nuclear Signal in Mitochondrial Quality Control. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72690


University of Toronto

3. Rapp, Chloe Louise. Utilizing Homology Models and Biochemical Analysis to Determine the Structural Consequences of SLC26 Anion Transport Membrane Protein Mutations.

Degree: 2016, University of Toronto

The availability of the crystal structure of a bacterial member of the SLC26 anion transporters has allowed us to create 3-dimensional models of 10 human… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Rapp, C. L. (2016). Utilizing Homology Models and Biochemical Analysis to Determine the Structural Consequences of SLC26 Anion Transport Membrane Protein Mutations. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/75960

Chicago Manual of Style (16th Edition):

Rapp, Chloe Louise. “Utilizing Homology Models and Biochemical Analysis to Determine the Structural Consequences of SLC26 Anion Transport Membrane Protein Mutations.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/75960.

MLA Handbook (7th Edition):

Rapp, Chloe Louise. “Utilizing Homology Models and Biochemical Analysis to Determine the Structural Consequences of SLC26 Anion Transport Membrane Protein Mutations.” 2016. Web. 23 Sep 2020.

Vancouver:

Rapp CL. Utilizing Homology Models and Biochemical Analysis to Determine the Structural Consequences of SLC26 Anion Transport Membrane Protein Mutations. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/75960.

Council of Science Editors:

Rapp CL. Utilizing Homology Models and Biochemical Analysis to Determine the Structural Consequences of SLC26 Anion Transport Membrane Protein Mutations. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/75960


University of Toronto

4. Xia, Fan. A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT.

Degree: 2016, University of Toronto

The uracil-H+ symporter UraA and the uracil phosphoribosyltransferase UPRT are both encoded on the ura operon in E. coli, creating genetic and functional link between… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Xia, F. (2016). A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76147

Chicago Manual of Style (16th Edition):

Xia, Fan. “A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/76147.

MLA Handbook (7th Edition):

Xia, Fan. “A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT.” 2016. Web. 23 Sep 2020.

Vancouver:

Xia F. A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/76147.

Council of Science Editors:

Xia F. A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76147


University of Toronto

5. Xia, Fan. A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT.

Degree: 2016, University of Toronto

The uracil-H+ symporter UraA and the uracil phosphoribosyltransferase UPRT are both encoded on the ura operon in E. coli, creating genetic and functional link between… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Xia, F. (2016). A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76215

Chicago Manual of Style (16th Edition):

Xia, Fan. “A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/76215.

MLA Handbook (7th Edition):

Xia, Fan. “A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT.” 2016. Web. 23 Sep 2020.

Vancouver:

Xia F. A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/76215.

Council of Science Editors:

Xia F. A Uracil Transport Metabolon in E. coli: Interaction between the Membrane Transporter UraA and the Cytosolic Enzyme UPRT. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76215


University of Toronto

6. Tan, Wendy. Characterization of the Mitochondrial Peptide Pβ.

Degree: 2018, University of Toronto

Mitophagy, the degradation of damaged mitochondria, and mitochondrial biogenesis, the formation of new mitochondria, are two critical mitochondrial quality control pathways that maintain a healthy… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Tan, W. (2018). Characterization of the Mitochondrial Peptide Pβ. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89552

Chicago Manual of Style (16th Edition):

Tan, Wendy. “Characterization of the Mitochondrial Peptide Pβ.” 2018. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/89552.

MLA Handbook (7th Edition):

Tan, Wendy. “Characterization of the Mitochondrial Peptide Pβ.” 2018. Web. 23 Sep 2020.

Vancouver:

Tan W. Characterization of the Mitochondrial Peptide Pβ. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/89552.

Council of Science Editors:

Tan W. Characterization of the Mitochondrial Peptide Pβ. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89552


University of Toronto

7. Barras, Eliane. Characterizing the Deubiquitinase USP35.

Degree: 2016, University of Toronto

Mitophagy involves the selective removal of damaged mitochondria by autophagy. Defective mitophagy, resulting in the accumulation of toxic mitochondrial byproducts, leads to cell death; this… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Barras, E. (2016). Characterizing the Deubiquitinase USP35. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91772

Chicago Manual of Style (16th Edition):

Barras, Eliane. “Characterizing the Deubiquitinase USP35.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/91772.

MLA Handbook (7th Edition):

Barras, Eliane. “Characterizing the Deubiquitinase USP35.” 2016. Web. 23 Sep 2020.

Vancouver:

Barras E. Characterizing the Deubiquitinase USP35. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/91772.

Council of Science Editors:

Barras E. Characterizing the Deubiquitinase USP35. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/91772


University of Toronto

8. Hung, Pui Shan (Minnie). Identification of Ploidy Maintenance Genes in Saccharomyces cerevisiae.

Degree: 2016, University of Toronto

In eukaryotes, ploidy maintenance is very important for ensuring genome stability and proper cellular function. Mistakes in the spindle checkpoint, spindle pole body (SPB) duplication… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Hung, P. S. (. (2016). Identification of Ploidy Maintenance Genes in Saccharomyces cerevisiae. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/92779

Chicago Manual of Style (16th Edition):

Hung, Pui Shan (Minnie). “Identification of Ploidy Maintenance Genes in Saccharomyces cerevisiae.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/92779.

MLA Handbook (7th Edition):

Hung, Pui Shan (Minnie). “Identification of Ploidy Maintenance Genes in Saccharomyces cerevisiae.” 2016. Web. 23 Sep 2020.

Vancouver:

Hung PS(. Identification of Ploidy Maintenance Genes in Saccharomyces cerevisiae. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/92779.

Council of Science Editors:

Hung PS(. Identification of Ploidy Maintenance Genes in Saccharomyces cerevisiae. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/92779


University of Toronto

9. Thakkar, Mauli Jitendra. Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding.

Degree: 2015, University of Toronto

Intracellular nickel concentration in Escherichia coli is controlled by a transcription factor called NikR, which represses the nikABCDE operon, encoding a nickel specific transporter. The… (more)

Subjects/Keywords: 0487

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thakkar, M. J. (2015). Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/94468

Chicago Manual of Style (16th Edition):

Thakkar, Mauli Jitendra. “Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding.” 2015. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/94468.

MLA Handbook (7th Edition):

Thakkar, Mauli Jitendra. “Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding.” 2015. Web. 23 Sep 2020.

Vancouver:

Thakkar MJ. Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/94468.

Council of Science Editors:

Thakkar MJ. Engineering a Ni(II)-independent NikR to Determine the Role of the α3-helix in the Mechanism of Ni(II)-activated DNA Binding. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/94468


University of Toronto

10. Correa, Ryan Vincent. Optimization and Applications of Slow-Proton-Exchange (SPE) Nuclear Magnetic Resonance pH Sensors.

Degree: 2018, University of Toronto

The measurement of pH is ubiquitously important in biochemistry, clinical medicine, and industrial processes. There are still improvements to be made in this field, especially… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Correa, R. V. (2018). Optimization and Applications of Slow-Proton-Exchange (SPE) Nuclear Magnetic Resonance pH Sensors. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/101586

Chicago Manual of Style (16th Edition):

Correa, Ryan Vincent. “Optimization and Applications of Slow-Proton-Exchange (SPE) Nuclear Magnetic Resonance pH Sensors.” 2018. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/101586.

MLA Handbook (7th Edition):

Correa, Ryan Vincent. “Optimization and Applications of Slow-Proton-Exchange (SPE) Nuclear Magnetic Resonance pH Sensors.” 2018. Web. 23 Sep 2020.

Vancouver:

Correa RV. Optimization and Applications of Slow-Proton-Exchange (SPE) Nuclear Magnetic Resonance pH Sensors. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/101586.

Council of Science Editors:

Correa RV. Optimization and Applications of Slow-Proton-Exchange (SPE) Nuclear Magnetic Resonance pH Sensors. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/101586


University of Toronto

11. Laframboise, Krystal Annette. Identifying Novel Mechanisms of Genome Maintenance in Saccharomyces cerevisiae using the DNA Damage-inducibility of Ribonucleotide Reductase.

Degree: 2016, University of Toronto

The identification of genome maintenance genes in Saccharomyces cerevisiae has been limited to loss-of-function screens that ignore the consequences of gene overexpression. Here, I assay… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Laframboise, K. A. (2016). Identifying Novel Mechanisms of Genome Maintenance in Saccharomyces cerevisiae using the DNA Damage-inducibility of Ribonucleotide Reductase. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/97207

Chicago Manual of Style (16th Edition):

Laframboise, Krystal Annette. “Identifying Novel Mechanisms of Genome Maintenance in Saccharomyces cerevisiae using the DNA Damage-inducibility of Ribonucleotide Reductase.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/97207.

MLA Handbook (7th Edition):

Laframboise, Krystal Annette. “Identifying Novel Mechanisms of Genome Maintenance in Saccharomyces cerevisiae using the DNA Damage-inducibility of Ribonucleotide Reductase.” 2016. Web. 23 Sep 2020.

Vancouver:

Laframboise KA. Identifying Novel Mechanisms of Genome Maintenance in Saccharomyces cerevisiae using the DNA Damage-inducibility of Ribonucleotide Reductase. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/97207.

Council of Science Editors:

Laframboise KA. Identifying Novel Mechanisms of Genome Maintenance in Saccharomyces cerevisiae using the DNA Damage-inducibility of Ribonucleotide Reductase. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/97207


University of Toronto

12. Baghestani, Zahra. Structure and Role of Chromatin Architecture in the Inactive X Chromosome.

Degree: 2015, University of Toronto

The significant impact of three-dimensional organization of chromatin on gene regulation is well known. Since silencing of the inactive X chromosome (Xi) provides a unique… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Baghestani, Z. (2015). Structure and Role of Chromatin Architecture in the Inactive X Chromosome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/88565

Chicago Manual of Style (16th Edition):

Baghestani, Zahra. “Structure and Role of Chromatin Architecture in the Inactive X Chromosome.” 2015. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/88565.

MLA Handbook (7th Edition):

Baghestani, Zahra. “Structure and Role of Chromatin Architecture in the Inactive X Chromosome.” 2015. Web. 23 Sep 2020.

Vancouver:

Baghestani Z. Structure and Role of Chromatin Architecture in the Inactive X Chromosome. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/88565.

Council of Science Editors:

Baghestani Z. Structure and Role of Chromatin Architecture in the Inactive X Chromosome. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/88565


University of Toronto

13. Baghestani, Zahra. Structure and Role of Chromatin Architecture in the Inactive X Chromosome.

Degree: 2015, University of Toronto

The significant impact of three-dimensional organization of chromatin on gene regulation is well known. Since silencing of the inactive X chromosome (Xi) provides a unique… (more)

Subjects/Keywords: 0487

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Baghestani, Z. (2015). Structure and Role of Chromatin Architecture in the Inactive X Chromosome. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/88755

Chicago Manual of Style (16th Edition):

Baghestani, Zahra. “Structure and Role of Chromatin Architecture in the Inactive X Chromosome.” 2015. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/88755.

MLA Handbook (7th Edition):

Baghestani, Zahra. “Structure and Role of Chromatin Architecture in the Inactive X Chromosome.” 2015. Web. 23 Sep 2020.

Vancouver:

Baghestani Z. Structure and Role of Chromatin Architecture in the Inactive X Chromosome. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/88755.

Council of Science Editors:

Baghestani Z. Structure and Role of Chromatin Architecture in the Inactive X Chromosome. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/88755


University of Toronto

14. Aboualizadeh, Farzaneh. Mapping and Characterization of the Interaction Network of ALK Receptor Tyrosine Kinase using the Mammalian Membrane Two-Hybrid (MaMTH) Assay.

Degree: 2018, University of Toronto

Anaplastic Lymphoma Kinase (ALK) which belongs to the Receptor Tyrosine Kinases (RTKs) play a critical role in development and progression of many type of cancers.… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Aboualizadeh, F. (2018). Mapping and Characterization of the Interaction Network of ALK Receptor Tyrosine Kinase using the Mammalian Membrane Two-Hybrid (MaMTH) Assay. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89488

Chicago Manual of Style (16th Edition):

Aboualizadeh, Farzaneh. “Mapping and Characterization of the Interaction Network of ALK Receptor Tyrosine Kinase using the Mammalian Membrane Two-Hybrid (MaMTH) Assay.” 2018. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/89488.

MLA Handbook (7th Edition):

Aboualizadeh, Farzaneh. “Mapping and Characterization of the Interaction Network of ALK Receptor Tyrosine Kinase using the Mammalian Membrane Two-Hybrid (MaMTH) Assay.” 2018. Web. 23 Sep 2020.

Vancouver:

Aboualizadeh F. Mapping and Characterization of the Interaction Network of ALK Receptor Tyrosine Kinase using the Mammalian Membrane Two-Hybrid (MaMTH) Assay. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/89488.

Council of Science Editors:

Aboualizadeh F. Mapping and Characterization of the Interaction Network of ALK Receptor Tyrosine Kinase using the Mammalian Membrane Two-Hybrid (MaMTH) Assay. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89488


University of Toronto

15. Mak, Stefanie Hei Chi. The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor.

Degree: PhD, 2017, University of Toronto

 Actinorhodin is a blue-pigmented, redox-active secondary metabolite that is produced by the bacterium Streptomyces coelicolor. Although actinorhodin has been used as a model compound for… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Mak, S. H. C. (2017). The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80963

Chicago Manual of Style (16th Edition):

Mak, Stefanie Hei Chi. “The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor.” 2017. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/80963.

MLA Handbook (7th Edition):

Mak, Stefanie Hei Chi. “The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor.” 2017. Web. 23 Sep 2020.

Vancouver:

Mak SHC. The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/80963.

Council of Science Editors:

Mak SHC. The Molecular Action of Actinorhodin, an Antibiotic Produced by Streptomyces coelicolor. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/80963


University of Toronto

16. Wisnovsky, Simon. Investigating the Cellular Effects of Mitochondrial DNA Damage Using Targeted Chemical Probes.

Degree: PhD, 2017, University of Toronto

Mitochondria are compartments within eukaryotic cells that produce energy to power cellular metabolism. Uniquely amongst mammalian organelles, mitochondria contain a small amount of their own… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Wisnovsky, S. (2017). Investigating the Cellular Effects of Mitochondrial DNA Damage Using Targeted Chemical Probes. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/93033

Chicago Manual of Style (16th Edition):

Wisnovsky, Simon. “Investigating the Cellular Effects of Mitochondrial DNA Damage Using Targeted Chemical Probes.” 2017. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/93033.

MLA Handbook (7th Edition):

Wisnovsky, Simon. “Investigating the Cellular Effects of Mitochondrial DNA Damage Using Targeted Chemical Probes.” 2017. Web. 23 Sep 2020.

Vancouver:

Wisnovsky S. Investigating the Cellular Effects of Mitochondrial DNA Damage Using Targeted Chemical Probes. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/93033.

Council of Science Editors:

Wisnovsky S. Investigating the Cellular Effects of Mitochondrial DNA Damage Using Targeted Chemical Probes. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/93033


University of Toronto

17. Marsolais, Alexander John. Regulation of mRNA Stability by the RNA-binding Protein Pumilio during Early Drosophila Embryogenesis.

Degree: PhD, 2015, University of Toronto

The maternal-to-zygotic transition (MZT) is a characteristic phase of early metazoan development where control of embryogenesis transitions from products encoded by the mother to those… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Marsolais, A. J. (2015). Regulation of mRNA Stability by the RNA-binding Protein Pumilio during Early Drosophila Embryogenesis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/82437

Chicago Manual of Style (16th Edition):

Marsolais, Alexander John. “Regulation of mRNA Stability by the RNA-binding Protein Pumilio during Early Drosophila Embryogenesis.” 2015. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/82437.

MLA Handbook (7th Edition):

Marsolais, Alexander John. “Regulation of mRNA Stability by the RNA-binding Protein Pumilio during Early Drosophila Embryogenesis.” 2015. Web. 23 Sep 2020.

Vancouver:

Marsolais AJ. Regulation of mRNA Stability by the RNA-binding Protein Pumilio during Early Drosophila Embryogenesis. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/82437.

Council of Science Editors:

Marsolais AJ. Regulation of mRNA Stability by the RNA-binding Protein Pumilio during Early Drosophila Embryogenesis. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/82437


University of Toronto

18. Wan, Chun Kit. Functional characterization of N6- threonylcarbamoyladenosine biosynthesis by the universally conserved Sua5/YrdC and Kae1/Qri7/YgjD protein families.

Degree: PhD, 2017, University of Toronto

 N6-threonylcarbamoyladenosine (t6A) is a universally conserved tRNA modification found on nearly all tRNA molecules that recognize ANN codons on messenger RNAs. The presence of t6A… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Wan, C. K. (2017). Functional characterization of N6- threonylcarbamoyladenosine biosynthesis by the universally conserved Sua5/YrdC and Kae1/Qri7/YgjD protein families. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80741

Chicago Manual of Style (16th Edition):

Wan, Chun Kit. “Functional characterization of N6- threonylcarbamoyladenosine biosynthesis by the universally conserved Sua5/YrdC and Kae1/Qri7/YgjD protein families.” 2017. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/80741.

MLA Handbook (7th Edition):

Wan, Chun Kit. “Functional characterization of N6- threonylcarbamoyladenosine biosynthesis by the universally conserved Sua5/YrdC and Kae1/Qri7/YgjD protein families.” 2017. Web. 23 Sep 2020.

Vancouver:

Wan CK. Functional characterization of N6- threonylcarbamoyladenosine biosynthesis by the universally conserved Sua5/YrdC and Kae1/Qri7/YgjD protein families. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/80741.

Council of Science Editors:

Wan CK. Functional characterization of N6- threonylcarbamoyladenosine biosynthesis by the universally conserved Sua5/YrdC and Kae1/Qri7/YgjD protein families. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/80741


University of Toronto

19. Li, Zhijie. Structural and Biochemical Characterization of the Mammalian Glycosyltransferases, N-acetylglucosaminyltransferase II and Protein O-fucosyltransferase 1.

Degree: PhD, 2015, University of Toronto

Glycosyltransferases are the enzymes responsible for the biosynthesis of glycans. Each of these enzymes catalyzes the transfer of a sugar moiety from a donor molecule… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Li, Z. (2015). Structural and Biochemical Characterization of the Mammalian Glycosyltransferases, N-acetylglucosaminyltransferase II and Protein O-fucosyltransferase 1. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76678

Chicago Manual of Style (16th Edition):

Li, Zhijie. “Structural and Biochemical Characterization of the Mammalian Glycosyltransferases, N-acetylglucosaminyltransferase II and Protein O-fucosyltransferase 1.” 2015. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/76678.

MLA Handbook (7th Edition):

Li, Zhijie. “Structural and Biochemical Characterization of the Mammalian Glycosyltransferases, N-acetylglucosaminyltransferase II and Protein O-fucosyltransferase 1.” 2015. Web. 23 Sep 2020.

Vancouver:

Li Z. Structural and Biochemical Characterization of the Mammalian Glycosyltransferases, N-acetylglucosaminyltransferase II and Protein O-fucosyltransferase 1. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/76678.

Council of Science Editors:

Li Z. Structural and Biochemical Characterization of the Mammalian Glycosyltransferases, N-acetylglucosaminyltransferase II and Protein O-fucosyltransferase 1. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/76678


University of Toronto

20. Hua, Rong. Communication between the Endoplasmic Reticulum and Peroxisomes in Mammalian Cells.

Degree: PhD, 2017, University of Toronto

 Peroxisomes are important metabolic organelles found in virtually all eukaryotic cells. Since their discovery, peroxisomes have long been seen in close proximity to the endoplasmic… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Hua, R. (2017). Communication between the Endoplasmic Reticulum and Peroxisomes in Mammalian Cells. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/79025

Chicago Manual of Style (16th Edition):

Hua, Rong. “Communication between the Endoplasmic Reticulum and Peroxisomes in Mammalian Cells.” 2017. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/79025.

MLA Handbook (7th Edition):

Hua, Rong. “Communication between the Endoplasmic Reticulum and Peroxisomes in Mammalian Cells.” 2017. Web. 23 Sep 2020.

Vancouver:

Hua R. Communication between the Endoplasmic Reticulum and Peroxisomes in Mammalian Cells. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/79025.

Council of Science Editors:

Hua R. Communication between the Endoplasmic Reticulum and Peroxisomes in Mammalian Cells. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79025


University of Toronto

21. Peek, James. Structural and Biochemical Analysis of the Shikimate Dehydrogenase Family.

Degree: PhD, 2014, University of Toronto

 The shikimate dehydrogenase (SDH) family consists of at least five structurally related, but functionally distinct enzyme classes. The archetypal member of the family, AroE, catalyzes… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Peek, J. (2014). Structural and Biochemical Analysis of the Shikimate Dehydrogenase Family. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68329

Chicago Manual of Style (16th Edition):

Peek, James. “Structural and Biochemical Analysis of the Shikimate Dehydrogenase Family.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/68329.

MLA Handbook (7th Edition):

Peek, James. “Structural and Biochemical Analysis of the Shikimate Dehydrogenase Family.” 2014. Web. 23 Sep 2020.

Vancouver:

Peek J. Structural and Biochemical Analysis of the Shikimate Dehydrogenase Family. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/68329.

Council of Science Editors:

Peek J. Structural and Biochemical Analysis of the Shikimate Dehydrogenase Family. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68329


University of Toronto

22. Cretu, Daniela. Identification and Validation of Candidate Soluble Biomarkers for Psoriatic Arthritis Using Quantitative Proteomics.

Degree: PhD, 2015, University of Toronto

 There is a high prevalence of undiagnosed PsA in psoriasis patients; therefore identifying soluble biomarkers for PsA will help in screening psoriasis patients for appropriate… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Cretu, D. (2015). Identification and Validation of Candidate Soluble Biomarkers for Psoriatic Arthritis Using Quantitative Proteomics. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/70808

Chicago Manual of Style (16th Edition):

Cretu, Daniela. “Identification and Validation of Candidate Soluble Biomarkers for Psoriatic Arthritis Using Quantitative Proteomics.” 2015. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/70808.

MLA Handbook (7th Edition):

Cretu, Daniela. “Identification and Validation of Candidate Soluble Biomarkers for Psoriatic Arthritis Using Quantitative Proteomics.” 2015. Web. 23 Sep 2020.

Vancouver:

Cretu D. Identification and Validation of Candidate Soluble Biomarkers for Psoriatic Arthritis Using Quantitative Proteomics. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/70808.

Council of Science Editors:

Cretu D. Identification and Validation of Candidate Soluble Biomarkers for Psoriatic Arthritis Using Quantitative Proteomics. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70808

23. Mortazavi, Seyedeh Mahshid. Engineering the Escherichia coli NikR Transcription Factor via Mutations in the α3 Helix.

Degree: 2014, University of Toronto

Escherichia coli NikR is a metal-responsive transcription factor that controls nickel uptake by regulating expression of a nickel-specific transporter, NikABCDE. NikR contains a high-affinity nickel-binding… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Mortazavi, S. M. (2014). Engineering the Escherichia coli NikR Transcription Factor via Mutations in the α3 Helix. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/65590

Chicago Manual of Style (16th Edition):

Mortazavi, Seyedeh Mahshid. “Engineering the Escherichia coli NikR Transcription Factor via Mutations in the α3 Helix.” 2014. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/65590.

MLA Handbook (7th Edition):

Mortazavi, Seyedeh Mahshid. “Engineering the Escherichia coli NikR Transcription Factor via Mutations in the α3 Helix.” 2014. Web. 23 Sep 2020.

Vancouver:

Mortazavi SM. Engineering the Escherichia coli NikR Transcription Factor via Mutations in the α3 Helix. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/65590.

Council of Science Editors:

Mortazavi SM. Engineering the Escherichia coli NikR Transcription Factor via Mutations in the α3 Helix. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/65590

24. Duan, Zhuang. Identification and Characterization of Novel Anti-phage Compounds using a High Throughput Approach.

Degree: 2016, University of Toronto

Bacteriophages play important roles in human health. They encode and spread diverse virulence factors, and have been implicated in regulating microbiome symbiosis. In this thesis,… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Duan, Z. (2016). Identification and Characterization of Novel Anti-phage Compounds using a High Throughput Approach. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74672

Chicago Manual of Style (16th Edition):

Duan, Zhuang. “Identification and Characterization of Novel Anti-phage Compounds using a High Throughput Approach.” 2016. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/74672.

MLA Handbook (7th Edition):

Duan, Zhuang. “Identification and Characterization of Novel Anti-phage Compounds using a High Throughput Approach.” 2016. Web. 23 Sep 2020.

Vancouver:

Duan Z. Identification and Characterization of Novel Anti-phage Compounds using a High Throughput Approach. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/74672.

Council of Science Editors:

Duan Z. Identification and Characterization of Novel Anti-phage Compounds using a High Throughput Approach. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/74672


University of Toronto

25. Bruce, Mary Christine. Substrate Specificity and Regulation of Nedd4 proteins.

Degree: 2009, University of Toronto

Nedd4-1 and Nedd4-2 are closely related E3 ubiquitin protein ligases that contain a C2 domain, 3-4 WW domains, and a catalytic ubiquitin ligase HECT domain.… (more)

Subjects/Keywords: 0487

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APA (6th Edition):

Bruce, M. C. (2009). Substrate Specificity and Regulation of Nedd4 proteins. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/17454

Chicago Manual of Style (16th Edition):

Bruce, Mary Christine. “Substrate Specificity and Regulation of Nedd4 proteins.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/17454.

MLA Handbook (7th Edition):

Bruce, Mary Christine. “Substrate Specificity and Regulation of Nedd4 proteins.” 2009. Web. 23 Sep 2020.

Vancouver:

Bruce MC. Substrate Specificity and Regulation of Nedd4 proteins. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/17454.

Council of Science Editors:

Bruce MC. Substrate Specificity and Regulation of Nedd4 proteins. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/17454


University of Toronto

26. Zhao, Boyu. Investigation of the Regulation of the Lysine Decarboxylase LdcI Activity by the Alarmone ppGpp and MoxR Family AAA+ ATPase RavA.

Degree: 2012, University of Toronto

The lysine-dependent acid stress response system in Escherichia coli protects the cells under moderately acidic conditions. It consists of LdcI, the inducible lysine decarboxylase and… (more)

Subjects/Keywords: LdcI; ppGpp; 0487

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APA (6th Edition):

Zhao, B. (2012). Investigation of the Regulation of the Lysine Decarboxylase LdcI Activity by the Alarmone ppGpp and MoxR Family AAA+ ATPase RavA. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33622

Chicago Manual of Style (16th Edition):

Zhao, Boyu. “Investigation of the Regulation of the Lysine Decarboxylase LdcI Activity by the Alarmone ppGpp and MoxR Family AAA+ ATPase RavA.” 2012. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/33622.

MLA Handbook (7th Edition):

Zhao, Boyu. “Investigation of the Regulation of the Lysine Decarboxylase LdcI Activity by the Alarmone ppGpp and MoxR Family AAA+ ATPase RavA.” 2012. Web. 23 Sep 2020.

Vancouver:

Zhao B. Investigation of the Regulation of the Lysine Decarboxylase LdcI Activity by the Alarmone ppGpp and MoxR Family AAA+ ATPase RavA. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/33622.

Council of Science Editors:

Zhao B. Investigation of the Regulation of the Lysine Decarboxylase LdcI Activity by the Alarmone ppGpp and MoxR Family AAA+ ATPase RavA. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33622


University of Toronto

27. Huen, Jennifer. Structural and Functional Characterization of the Essential AAA+ ATPases Rvb1 and Rvb2 of S. cerevisiae.

Degree: 2014, University of Toronto

Rvb1 and Rvb2 are essential proteins of the AAA+ superfamily of ATPases associated with a diversity of cellular activities. The Rvbs are components of several… (more)

Subjects/Keywords: ATPases; DNA; 0487

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APA (6th Edition):

Huen, J. (2014). Structural and Functional Characterization of the Essential AAA+ ATPases Rvb1 and Rvb2 of S. cerevisiae. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/72507

Chicago Manual of Style (16th Edition):

Huen, Jennifer. “Structural and Functional Characterization of the Essential AAA+ ATPases Rvb1 and Rvb2 of S. cerevisiae.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/72507.

MLA Handbook (7th Edition):

Huen, Jennifer. “Structural and Functional Characterization of the Essential AAA+ ATPases Rvb1 and Rvb2 of S. cerevisiae.” 2014. Web. 23 Sep 2020.

Vancouver:

Huen J. Structural and Functional Characterization of the Essential AAA+ ATPases Rvb1 and Rvb2 of S. cerevisiae. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/72507.

Council of Science Editors:

Huen J. Structural and Functional Characterization of the Essential AAA+ ATPases Rvb1 and Rvb2 of S. cerevisiae. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/72507


University of Toronto

28. Wu, Edwin. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.

Degree: 2013, University of Toronto

The ubiquitin-proteasome system regulates protein degradation. Although proteasomes localize in the nucleus of proliferating Saccharomyces cerevisiae, they are sequestered into cytoplasmic proteasome storage granules (PSG)… (more)

Subjects/Keywords: proteasome; ubiquitin; quiescence; 0487

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APA (6th Edition):

Wu, E. (2013). The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43342

Chicago Manual of Style (16th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/43342.

MLA Handbook (7th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Web. 23 Sep 2020.

Vancouver:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/43342.

Council of Science Editors:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43342


University of Toronto

29. Basir, Sahar Ansari. Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA.

Degree: 2013, University of Toronto

Apolipoprotein B (apoB) is a key structural and functional protein of lipoproteins and is synthesized constitutively in the liver. This study investigated the role of… (more)

Subjects/Keywords: apoB; translational control; miRNA; 0487

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APA (6th Edition):

Basir, S. A. (2013). Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42671

Chicago Manual of Style (16th Edition):

Basir, Sahar Ansari. “Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA.” 2013. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/42671.

MLA Handbook (7th Edition):

Basir, Sahar Ansari. “Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA.” 2013. Web. 23 Sep 2020.

Vancouver:

Basir SA. Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/42671.

Council of Science Editors:

Basir SA. Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42671


University of Toronto

30. Ricer, Tyler. The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa.

Degree: 2014, University of Toronto

Pseudomonas aeruginosa is an opportunistic, gram-negative pathogen that is involved in a variety of infections. The bacterium secretes and chemically modifies alginate to form a… (more)

Subjects/Keywords: Biochemistry; X-ray Crystallography; 0487

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APA (6th Edition):

Ricer, T. (2014). The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72547

Chicago Manual of Style (16th Edition):

Ricer, Tyler. “The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa.” 2014. Masters Thesis, University of Toronto. Accessed September 23, 2020. http://hdl.handle.net/1807/72547.

MLA Handbook (7th Edition):

Ricer, Tyler. “The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa.” 2014. Web. 23 Sep 2020.

Vancouver:

Ricer T. The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1807/72547.

Council of Science Editors:

Ricer T. The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/72547

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