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You searched for +publisher:"University of Toronto" +contributor:("Biochemistry"). Showing records 1 – 30 of 272 total matches.

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University of Toronto

1. Christian, Patricia. Investigating the Role of Autophagy in Intracellular Apolipoprotein B Traffic and Very-low-density-lipoprotein Assembly and Secretion.

Degree: 2013, University of Toronto

Apolipoprotein B (apoB) is the main protein of very-low-density lipoprotein (VLDL). As apoB is translated and moves through the secretory pathway, lipids from cytoplasmic lipid… (more)

Subjects/Keywords: Apolipoprotein B; Very-low-density-lipoprotein; Autophagy; Lipophagy; Lipid droplets; 0487

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APA (6th Edition):

Christian, P. (2013). Investigating the Role of Autophagy in Intracellular Apolipoprotein B Traffic and Very-low-density-lipoprotein Assembly and Secretion. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42743

Chicago Manual of Style (16th Edition):

Christian, Patricia. “Investigating the Role of Autophagy in Intracellular Apolipoprotein B Traffic and Very-low-density-lipoprotein Assembly and Secretion.” 2013. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/42743.

MLA Handbook (7th Edition):

Christian, Patricia. “Investigating the Role of Autophagy in Intracellular Apolipoprotein B Traffic and Very-low-density-lipoprotein Assembly and Secretion.” 2013. Web. 07 Mar 2021.

Vancouver:

Christian P. Investigating the Role of Autophagy in Intracellular Apolipoprotein B Traffic and Very-low-density-lipoprotein Assembly and Secretion. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/42743.

Council of Science Editors:

Christian P. Investigating the Role of Autophagy in Intracellular Apolipoprotein B Traffic and Very-low-density-lipoprotein Assembly and Secretion. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42743


University of Toronto

2. 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 March 07, 2021. http://hdl.handle.net/1807/43342.

MLA Handbook (7th Edition):

Wu, Edwin. “The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence.” 2013. Web. 07 Mar 2021.

Vancouver:

Wu E. The Role of Ubiquitin on Yeast Proteasome Dynamics in Quiescence. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Mar 07]. 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

3. 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 March 07, 2021. 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. 07 Mar 2021.

Vancouver:

Basir SA. Role of miRNAs in Translational Control of Human Apolipoprotein B-100 mRNA. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2021 Mar 07]. 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

4. 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 March 07, 2021. http://hdl.handle.net/1807/72547.

MLA Handbook (7th Edition):

Ricer, Tyler. “The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa.” 2014. Web. 07 Mar 2021.

Vancouver:

Ricer T. The Molecular Mechanism of Alginate O-Acetylation in Pseudomonas aeruginosa. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Mar 07]. 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


University of Toronto

5. Judd, Andrew. Investigating Surface Lipoprotein Translocation in Neisseria meningitidis.

Degree: 2014, University of Toronto

Neisseria meningitidis infections are a major cause of bacterial meningitis cases around the world. During an infection, Neisseria meningitidis employs surface lipoproteins in nutrient acquisition… (more)

Subjects/Keywords: Surface Lipoproteins; Neisseria meningitidis; 0487

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APA (6th Edition):

Judd, A. (2014). Investigating Surface Lipoprotein Translocation in Neisseria meningitidis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/71546

Chicago Manual of Style (16th Edition):

Judd, Andrew. “Investigating Surface Lipoprotein Translocation in Neisseria meningitidis.” 2014. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/71546.

MLA Handbook (7th Edition):

Judd, Andrew. “Investigating Surface Lipoprotein Translocation in Neisseria meningitidis.” 2014. Web. 07 Mar 2021.

Vancouver:

Judd A. Investigating Surface Lipoprotein Translocation in Neisseria meningitidis. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/71546.

Council of Science Editors:

Judd A. Investigating Surface Lipoprotein Translocation in Neisseria meningitidis. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/71546


University of Toronto

6. Zhao, Liang. Structural and Functional Characterization of the Yeast R2TP Complex.

Degree: 2014, University of Toronto

Rvb1 and Rvb2, two closely related essential AAA+ helicases, play important roles in various cellular pathways. Our group found that they form a complex with… (more)

Subjects/Keywords: protein; yeast; rvb; EM; purification; SEC; I domain; Liang Zhao; 3D; cryo-EM; AAA+; R2TP

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APA (6th Edition):

Zhao, L. (2014). Structural and Functional Characterization of the Yeast R2TP Complex. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72543

Chicago Manual of Style (16th Edition):

Zhao, Liang. “Structural and Functional Characterization of the Yeast R2TP Complex.” 2014. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/72543.

MLA Handbook (7th Edition):

Zhao, Liang. “Structural and Functional Characterization of the Yeast R2TP Complex.” 2014. Web. 07 Mar 2021.

Vancouver:

Zhao L. Structural and Functional Characterization of the Yeast R2TP Complex. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/72543.

Council of Science Editors:

Zhao L. Structural and Functional Characterization of the Yeast R2TP Complex. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/72543


University of Toronto

7. Fung, Karen Yin Yue. Determining the Role of Cin85 and CD2AP in Septin-mediated Cytokinesis.

Degree: 2014, University of Toronto

Septins are a family of GTP-binding proteins implicated in mammalian cytokinesis. Our lab has shown that the N-terminal region of SEPT9 is critical during the… (more)

Subjects/Keywords: CD2AP; Cin85; mammalian cytokinesis; protein-protein interaction; Septins; 0487

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APA (6th Edition):

Fung, K. Y. Y. (2014). Determining the Role of Cin85 and CD2AP in Septin-mediated Cytokinesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68532

Chicago Manual of Style (16th Edition):

Fung, Karen Yin Yue. “Determining the Role of Cin85 and CD2AP in Septin-mediated Cytokinesis.” 2014. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/68532.

MLA Handbook (7th Edition):

Fung, Karen Yin Yue. “Determining the Role of Cin85 and CD2AP in Septin-mediated Cytokinesis.” 2014. Web. 07 Mar 2021.

Vancouver:

Fung KYY. Determining the Role of Cin85 and CD2AP in Septin-mediated Cytokinesis. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/68532.

Council of Science Editors:

Fung KYY. Determining the Role of Cin85 and CD2AP in Septin-mediated Cytokinesis. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68532


University of Toronto

8. Darowski, Katelyn Dawn. Systematic Analysis of Protein-Protein Interactions Between the ErbB Family of RTKs and a Complete Set of Human Phosphatases.

Degree: 2014, University of Toronto

This thesis has created a resource describing interactions between the ErbB family receptor tyrosine kinases and human phosphatases using the Membrane Yeast Two Hybrid system… (more)

Subjects/Keywords: EGFR; ErbB; ERK1/2; Interactome; Kinase; Phosphatase; 0487

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APA (6th Edition):

Darowski, K. D. (2014). Systematic Analysis of Protein-Protein Interactions Between the ErbB Family of RTKs and a Complete Set of Human Phosphatases. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68540

Chicago Manual of Style (16th Edition):

Darowski, Katelyn Dawn. “Systematic Analysis of Protein-Protein Interactions Between the ErbB Family of RTKs and a Complete Set of Human Phosphatases.” 2014. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/68540.

MLA Handbook (7th Edition):

Darowski, Katelyn Dawn. “Systematic Analysis of Protein-Protein Interactions Between the ErbB Family of RTKs and a Complete Set of Human Phosphatases.” 2014. Web. 07 Mar 2021.

Vancouver:

Darowski KD. Systematic Analysis of Protein-Protein Interactions Between the ErbB Family of RTKs and a Complete Set of Human Phosphatases. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/68540.

Council of Science Editors:

Darowski KD. Systematic Analysis of Protein-Protein Interactions Between the ErbB Family of RTKs and a Complete Set of Human Phosphatases. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68540


University of Toronto

9. Anthony Chen, Kar Ki. Role of FGF Receptors in Rescue of ΔF508-CFTR.

Degree: 2015, University of Toronto

ΔF508-CFTR is the most common mutation causing cystic fibrosis (CF), where it exhibits folding defects and is unable to reach the plasma membrane. To identify… (more)

Subjects/Keywords: cystic fibrosis; FGFR; kinase; ΔF508-CFTR; 0487

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APA (6th Edition):

Anthony Chen, K. K. (2015). Role of FGF Receptors in Rescue of ΔF508-CFTR. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70251

Chicago Manual of Style (16th Edition):

Anthony Chen, Kar Ki. “Role of FGF Receptors in Rescue of ΔF508-CFTR.” 2015. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/70251.

MLA Handbook (7th Edition):

Anthony Chen, Kar Ki. “Role of FGF Receptors in Rescue of ΔF508-CFTR.” 2015. Web. 07 Mar 2021.

Vancouver:

Anthony Chen KK. Role of FGF Receptors in Rescue of ΔF508-CFTR. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/70251.

Council of Science Editors:

Anthony Chen KK. Role of FGF Receptors in Rescue of ΔF508-CFTR. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70251


University of Toronto

10. Manan, Yaseen. Investigating the Structure of MacB, an ABC Transporter Protein.

Degree: 2015, University of Toronto

Despite the need to understand membrane proteins at the molecular level, fewer than 2% of the structures in the PDB are of membrane proteins. Detergents… (more)

Subjects/Keywords: ABC Transporter; Drug; Exporter; MacB; Membrane Proteins; X-Ray Crystallography; 0487

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APA (6th Edition):

Manan, Y. (2015). Investigating the Structure of MacB, an ABC Transporter Protein. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70462

Chicago Manual of Style (16th Edition):

Manan, Yaseen. “Investigating the Structure of MacB, an ABC Transporter Protein.” 2015. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/70462.

MLA Handbook (7th Edition):

Manan, Yaseen. “Investigating the Structure of MacB, an ABC Transporter Protein.” 2015. Web. 07 Mar 2021.

Vancouver:

Manan Y. Investigating the Structure of MacB, an ABC Transporter Protein. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/70462.

Council of Science Editors:

Manan Y. Investigating the Structure of MacB, an ABC Transporter Protein. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70462


University of Toronto

11. Sawicki, Maxime. Inhibition of the FKBP Family of Peptidyl Prolyl Isomerases Induces Abortive Translocation and Degradation of the Cellular Prion Protein.

Degree: 2015, University of Toronto

Prion disorders are a class of neurodegenerative diseases that feature a structural change of the prion protein from its cellular form (PrPC) into its scrapie… (more)

Subjects/Keywords: 0379

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APA (6th Edition):

Sawicki, M. (2015). Inhibition of the FKBP Family of Peptidyl Prolyl Isomerases Induces Abortive Translocation and Degradation of the Cellular Prion Protein. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70648

Chicago Manual of Style (16th Edition):

Sawicki, Maxime. “Inhibition of the FKBP Family of Peptidyl Prolyl Isomerases Induces Abortive Translocation and Degradation of the Cellular Prion Protein.” 2015. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/70648.

MLA Handbook (7th Edition):

Sawicki, Maxime. “Inhibition of the FKBP Family of Peptidyl Prolyl Isomerases Induces Abortive Translocation and Degradation of the Cellular Prion Protein.” 2015. Web. 07 Mar 2021.

Vancouver:

Sawicki M. Inhibition of the FKBP Family of Peptidyl Prolyl Isomerases Induces Abortive Translocation and Degradation of the Cellular Prion Protein. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/70648.

Council of Science Editors:

Sawicki M. Inhibition of the FKBP Family of Peptidyl Prolyl Isomerases Induces Abortive Translocation and Degradation of the Cellular Prion Protein. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70648


University of Toronto

12. Song, Ki Myung. Investigating βPix as a Novel Upstream Regulator of the Hippo Pathway.

Degree: 2015, University of Toronto

The Hippo pathway regulates cell growth and organ size and dysregulation of the pathway leads to cancer. In mammals, the core Hippo pathway consists of… (more)

Subjects/Keywords: Arfgef7; Hippo; Lats; Mst; Yap/Taz; 0487

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APA (6th Edition):

Song, K. M. (2015). Investigating βPix as a Novel Upstream Regulator of the Hippo Pathway. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70682

Chicago Manual of Style (16th Edition):

Song, Ki Myung. “Investigating βPix as a Novel Upstream Regulator of the Hippo Pathway.” 2015. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/70682.

MLA Handbook (7th Edition):

Song, Ki Myung. “Investigating βPix as a Novel Upstream Regulator of the Hippo Pathway.” 2015. Web. 07 Mar 2021.

Vancouver:

Song KM. Investigating βPix as a Novel Upstream Regulator of the Hippo Pathway. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/70682.

Council of Science Editors:

Song KM. Investigating βPix as a Novel Upstream Regulator of the Hippo Pathway. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70682


University of Toronto

13. 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 March 07, 2021. 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. 07 Mar 2021.

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 2021 Mar 07]. 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

14. Safi, Frozan. Drosophila Nedd4-long Reduces Amphiphysin Levels in Muscles and Leads to Impaired T-tubule Formation.

Degree: 2015, University of Toronto

Drosophila Nedd4 (dNedd4) is a HECT ubiquitin ligase with two main splice isoforms: dNedd4 short (dNedd4S) and long (dNedd4Lo). We previously showed that while dNedd4S… (more)

Subjects/Keywords: Amphiphysin; muscle developemt; Nedd4; 0487

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APA (6th Edition):

Safi, F. (2015). Drosophila Nedd4-long Reduces Amphiphysin Levels in Muscles and Leads to Impaired T-tubule Formation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74875

Chicago Manual of Style (16th Edition):

Safi, Frozan. “Drosophila Nedd4-long Reduces Amphiphysin Levels in Muscles and Leads to Impaired T-tubule Formation.” 2015. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/74875.

MLA Handbook (7th Edition):

Safi, Frozan. “Drosophila Nedd4-long Reduces Amphiphysin Levels in Muscles and Leads to Impaired T-tubule Formation.” 2015. Web. 07 Mar 2021.

Vancouver:

Safi F. Drosophila Nedd4-long Reduces Amphiphysin Levels in Muscles and Leads to Impaired T-tubule Formation. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/74875.

Council of Science Editors:

Safi F. Drosophila Nedd4-long Reduces Amphiphysin Levels in Muscles and Leads to Impaired T-tubule Formation. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/74875


University of Toronto

15. Hong, Seo Jung. Characterization of Mammalian ER Quality Control Systems in the Context of Select Human Pathologies.

Degree: 2016, University of Toronto

Quality control (QC) systems in the endoplasmic reticulum (ER) are established by intricate networks of molecular chaperones and foldases, and sophisticated degradative processes such as… (more)

Subjects/Keywords: Endoplasmic reticulum; ERAD; FKBP10; Prion protein; Protein folding; Quality control; 0487

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APA (6th Edition):

Hong, S. J. (2016). Characterization of Mammalian ER Quality Control Systems in the Context of Select Human Pathologies. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74877

Chicago Manual of Style (16th Edition):

Hong, Seo Jung. “Characterization of Mammalian ER Quality Control Systems in the Context of Select Human Pathologies.” 2016. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/74877.

MLA Handbook (7th Edition):

Hong, Seo Jung. “Characterization of Mammalian ER Quality Control Systems in the Context of Select Human Pathologies.” 2016. Web. 07 Mar 2021.

Vancouver:

Hong SJ. Characterization of Mammalian ER Quality Control Systems in the Context of Select Human Pathologies. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/74877.

Council of Science Editors:

Hong SJ. Characterization of Mammalian ER Quality Control Systems in the Context of Select Human Pathologies. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/74877


University of Toronto

16. Chang, Yuan-Heng. Structural Effects of Extracellular Loop Mutations in CFTR Helical Hairpins.

Degree: 2017, University of Toronto

Here we investigate the structural effects of single amino acid replacements in the extracellular (ECL2) loop region using helical hairpin constructs derived from TM3 and… (more)

Subjects/Keywords: CFTR; E217 and Q220; ECL2; Mutations; Structural Effects; TM3/4; 0487

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APA (6th Edition):

Chang, Y. (2017). Structural Effects of Extracellular Loop Mutations in CFTR Helical Hairpins. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76652

Chicago Manual of Style (16th Edition):

Chang, Yuan-Heng. “Structural Effects of Extracellular Loop Mutations in CFTR Helical Hairpins.” 2017. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/76652.

MLA Handbook (7th Edition):

Chang, Yuan-Heng. “Structural Effects of Extracellular Loop Mutations in CFTR Helical Hairpins.” 2017. Web. 07 Mar 2021.

Vancouver:

Chang Y. Structural Effects of Extracellular Loop Mutations in CFTR Helical Hairpins. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/76652.

Council of Science Editors:

Chang Y. Structural Effects of Extracellular Loop Mutations in CFTR Helical Hairpins. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/76652


University of Toronto

17. Orlowicz, Agata. Mechanisms of Vts1-Mediated Repression in S. cerevisiae.

Degree: 2011, University of Toronto

Vts1p is the Saccharomyces cerevisiae member of the Smaug family of post-transcriptional regulators, which is a group of sequence-specific RNA-binding proteins that regulate target mRNA… (more)

Subjects/Keywords: Vts1; post-transcriptional regulation; 0487

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APA (6th Edition):

Orlowicz, A. (2011). Mechanisms of Vts1-Mediated Repression in S. cerevisiae. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29596

Chicago Manual of Style (16th Edition):

Orlowicz, Agata. “Mechanisms of Vts1-Mediated Repression in S. cerevisiae.” 2011. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/29596.

MLA Handbook (7th Edition):

Orlowicz, Agata. “Mechanisms of Vts1-Mediated Repression in S. cerevisiae.” 2011. Web. 07 Mar 2021.

Vancouver:

Orlowicz A. Mechanisms of Vts1-Mediated Repression in S. cerevisiae. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/29596.

Council of Science Editors:

Orlowicz A. Mechanisms of Vts1-Mediated Repression in S. cerevisiae. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29596


University of Toronto

18. Kharbanda, Neha. Engineering the (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) Monomer from its Dimer.

Degree: 2011, University of Toronto

(S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) is a TIM (βα)8 barrel protein found in Archaea and the enzyme catalyzing the first step in the biosynthesis of archaeal… (more)

Subjects/Keywords: Protein Engineering; TIM Barrel evolution; Archaea; GGGPS; Archaeal Membrane Lipid Synthesis; 0487

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APA (6th Edition):

Kharbanda, N. (2011). Engineering the (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) Monomer from its Dimer. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29571

Chicago Manual of Style (16th Edition):

Kharbanda, Neha. “Engineering the (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) Monomer from its Dimer.” 2011. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/29571.

MLA Handbook (7th Edition):

Kharbanda, Neha. “Engineering the (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) Monomer from its Dimer.” 2011. Web. 07 Mar 2021.

Vancouver:

Kharbanda N. Engineering the (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) Monomer from its Dimer. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/29571.

Council of Science Editors:

Kharbanda N. Engineering the (S)-3-O-Geranylgeranylglyceryl Phosphate Synthase (GGGPS) Monomer from its Dimer. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29571


University of Toronto

19. Zholumbetov, Eric. The Role of Septin 5 in Exocytosis.

Degree: 2011, University of Toronto

Septins are an evolutionarily conserved family of proteins that have been implicated in a multitude of cellular processes. Septin 5 is mainly expressed in the… (more)

Subjects/Keywords: Septins; Septin 5; Exocytosis; TIRF; Secretion assay; 0379

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APA (6th Edition):

Zholumbetov, E. (2011). The Role of Septin 5 in Exocytosis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29652

Chicago Manual of Style (16th Edition):

Zholumbetov, Eric. “The Role of Septin 5 in Exocytosis.” 2011. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/29652.

MLA Handbook (7th Edition):

Zholumbetov, Eric. “The Role of Septin 5 in Exocytosis.” 2011. Web. 07 Mar 2021.

Vancouver:

Zholumbetov E. The Role of Septin 5 in Exocytosis. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/29652.

Council of Science Editors:

Zholumbetov E. The Role of Septin 5 in Exocytosis. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29652


University of Toronto

20. Tam, William. Characterization of an Iron-Sulfur Binding Protein in the Tail Tip Complex of Bacteriophage Lambda.

Degree: 2012, University of Toronto

The assembly of λ tail requires the action of 11 gene products which must interact in an organized fashion to assemble infectious tail particles. GpL… (more)

Subjects/Keywords: bacteriophage; lambda; iron-sulfur cluter; protein assembly; 0487; 0307

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APA (6th Edition):

Tam, W. (2012). Characterization of an Iron-Sulfur Binding Protein in the Tail Tip Complex of Bacteriophage Lambda. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42907

Chicago Manual of Style (16th Edition):

Tam, William. “Characterization of an Iron-Sulfur Binding Protein in the Tail Tip Complex of Bacteriophage Lambda.” 2012. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/42907.

MLA Handbook (7th Edition):

Tam, William. “Characterization of an Iron-Sulfur Binding Protein in the Tail Tip Complex of Bacteriophage Lambda.” 2012. Web. 07 Mar 2021.

Vancouver:

Tam W. Characterization of an Iron-Sulfur Binding Protein in the Tail Tip Complex of Bacteriophage Lambda. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/42907.

Council of Science Editors:

Tam W. Characterization of an Iron-Sulfur Binding Protein in the Tail Tip Complex of Bacteriophage Lambda. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/42907


University of Toronto

21. Shi, Peilin. Investigating the Anti-viral Property of Verotoxin and its Receptor Gb3 in Preventing Primary HIV-1 Infection.

Degree: 2011, University of Toronto

Verotoxin produced by Enterohemorrhagic E. coli is comprised of a catalytic A subunit and a receptor Gb3 binding B subunit pentamer. VT causes protein synthesis… (more)

Subjects/Keywords: HIV-1; Verotoxin; glycosphingolipid; Gb3; 0379; 0720; 0307

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APA (6th Edition):

Shi, P. (2011). Investigating the Anti-viral Property of Verotoxin and its Receptor Gb3 in Preventing Primary HIV-1 Infection. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31440

Chicago Manual of Style (16th Edition):

Shi, Peilin. “Investigating the Anti-viral Property of Verotoxin and its Receptor Gb3 in Preventing Primary HIV-1 Infection.” 2011. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/31440.

MLA Handbook (7th Edition):

Shi, Peilin. “Investigating the Anti-viral Property of Verotoxin and its Receptor Gb3 in Preventing Primary HIV-1 Infection.” 2011. Web. 07 Mar 2021.

Vancouver:

Shi P. Investigating the Anti-viral Property of Verotoxin and its Receptor Gb3 in Preventing Primary HIV-1 Infection. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/31440.

Council of Science Editors:

Shi P. Investigating the Anti-viral Property of Verotoxin and its Receptor Gb3 in Preventing Primary HIV-1 Infection. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31440


University of Toronto

22. Puhacz, Michael. Identification and Characterization of the Interaction between VPS33B and SNAREs.

Degree: 2011, University of Toronto

VPS33B is a Sec1/Munc18 protein required for the biogenesis of α-granules in megakaryocytes, which give rise to platelets. Mutations in VPS33B cause arthrogryposis, renal dysfunction… (more)

Subjects/Keywords: SNAREs; Sec1/Munc18; VPS33B; syntaxin-6; megakaryocyte; platelet; 0379

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APA (6th Edition):

Puhacz, M. (2011). Identification and Characterization of the Interaction between VPS33B and SNAREs. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31394

Chicago Manual of Style (16th Edition):

Puhacz, Michael. “Identification and Characterization of the Interaction between VPS33B and SNAREs.” 2011. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/31394.

MLA Handbook (7th Edition):

Puhacz, Michael. “Identification and Characterization of the Interaction between VPS33B and SNAREs.” 2011. Web. 07 Mar 2021.

Vancouver:

Puhacz M. Identification and Characterization of the Interaction between VPS33B and SNAREs. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/31394.

Council of Science Editors:

Puhacz M. Identification and Characterization of the Interaction between VPS33B and SNAREs. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31394


University of Toronto

23. Pour, Navaz Karimian. Insulin Modulates Intracellular Apolipoprotein B mRNA Traffic into RNA Granules/Cytoplasmic P Bodies: Implications in Translational Control.

Degree: 2012, University of Toronto

Apolipoprotein B (ApoB) synthesis is partially regulated at the translational level; however, the molecular mechanisms that govern translational control of apoB mRNA remains largely unknown.… (more)

Subjects/Keywords: Insulin; Apolipoprotein B; P bodies; Polysome; 0306

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APA (6th Edition):

Pour, N. K. (2012). Insulin Modulates Intracellular Apolipoprotein B mRNA Traffic into RNA Granules/Cytoplasmic P Bodies: Implications in Translational Control. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32580

Chicago Manual of Style (16th Edition):

Pour, Navaz Karimian. “Insulin Modulates Intracellular Apolipoprotein B mRNA Traffic into RNA Granules/Cytoplasmic P Bodies: Implications in Translational Control.” 2012. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/32580.

MLA Handbook (7th Edition):

Pour, Navaz Karimian. “Insulin Modulates Intracellular Apolipoprotein B mRNA Traffic into RNA Granules/Cytoplasmic P Bodies: Implications in Translational Control.” 2012. Web. 07 Mar 2021.

Vancouver:

Pour NK. Insulin Modulates Intracellular Apolipoprotein B mRNA Traffic into RNA Granules/Cytoplasmic P Bodies: Implications in Translational Control. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/32580.

Council of Science Editors:

Pour NK. Insulin Modulates Intracellular Apolipoprotein B mRNA Traffic into RNA Granules/Cytoplasmic P Bodies: Implications in Translational Control. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32580


University of Toronto

24. Tuhman-Mushkin, Jana. Structural Studies of Saccharomyces cerevisiae V1-ATPase in the Stationary Phase of Yeast Cell Culture.

Degree: 2012, University of Toronto

Vacuolar-type ATPases (V-ATPases) are ubiquitous membrane-bound protein complexes present in the endo-membrane system of all eukaryotic cells. In eukaryotic cells, the reversible dissociation of the… (more)

Subjects/Keywords: cryo-EM; V-ATPase

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APA (6th Edition):

Tuhman-Mushkin, J. (2012). Structural Studies of Saccharomyces cerevisiae V1-ATPase in the Stationary Phase of Yeast Cell Culture. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32635

Chicago Manual of Style (16th Edition):

Tuhman-Mushkin, Jana. “Structural Studies of Saccharomyces cerevisiae V1-ATPase in the Stationary Phase of Yeast Cell Culture.” 2012. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/32635.

MLA Handbook (7th Edition):

Tuhman-Mushkin, Jana. “Structural Studies of Saccharomyces cerevisiae V1-ATPase in the Stationary Phase of Yeast Cell Culture.” 2012. Web. 07 Mar 2021.

Vancouver:

Tuhman-Mushkin J. Structural Studies of Saccharomyces cerevisiae V1-ATPase in the Stationary Phase of Yeast Cell Culture. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/32635.

Council of Science Editors:

Tuhman-Mushkin J. Structural Studies of Saccharomyces cerevisiae V1-ATPase in the Stationary Phase of Yeast Cell Culture. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32635


University of Toronto

25. 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 March 07, 2021. 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. 07 Mar 2021.

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 2021 Mar 07]. 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

26. Yin, Lois Menglu. Interactions of Cationic Antimicrobial Peptides with Bacterial Membranes and Biofilms.

Degree: 2012, University of Toronto

Cationic antimicrobial peptides (CAPs) offer a viable alternative to conventional antibiotics as they physically disrupt the bacterial membranes, leading to cell lysis and death. However,… (more)

Subjects/Keywords: antimicrobial peptides; biofilms; 0487

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APA (6th Edition):

Yin, L. M. (2012). Interactions of Cationic Antimicrobial Peptides with Bacterial Membranes and Biofilms. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33594

Chicago Manual of Style (16th Edition):

Yin, Lois Menglu. “Interactions of Cationic Antimicrobial Peptides with Bacterial Membranes and Biofilms.” 2012. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/33594.

MLA Handbook (7th Edition):

Yin, Lois Menglu. “Interactions of Cationic Antimicrobial Peptides with Bacterial Membranes and Biofilms.” 2012. Web. 07 Mar 2021.

Vancouver:

Yin LM. Interactions of Cationic Antimicrobial Peptides with Bacterial Membranes and Biofilms. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/33594.

Council of Science Editors:

Yin LM. Interactions of Cationic Antimicrobial Peptides with Bacterial Membranes and Biofilms. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33594


University of Toronto

27. Caplan, David. A Computational Study of Proton Uptake Pathways in Cytochrome c Oxidase.

Degree: 2012, University of Toronto

Cytochrome c oxidase (CcO), the terminal enzyme in the electron transport chain, couples proton pumping to the reduction of dioxygen into water. The coupling mechanism… (more)

Subjects/Keywords: cytochrome c oxidase; proton pumping; molecular simulations; computational biology; 0487

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APA (6th Edition):

Caplan, D. (2012). A Computational Study of Proton Uptake Pathways in Cytochrome c Oxidase. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33352

Chicago Manual of Style (16th Edition):

Caplan, David. “A Computational Study of Proton Uptake Pathways in Cytochrome c Oxidase.” 2012. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/33352.

MLA Handbook (7th Edition):

Caplan, David. “A Computational Study of Proton Uptake Pathways in Cytochrome c Oxidase.” 2012. Web. 07 Mar 2021.

Vancouver:

Caplan D. A Computational Study of Proton Uptake Pathways in Cytochrome c Oxidase. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/33352.

Council of Science Editors:

Caplan D. A Computational Study of Proton Uptake Pathways in Cytochrome c Oxidase. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33352


University of Toronto

28. Pow, Andre. Structural and Functional Characterization of Clp Chaperones and Proteases in the Human Malaria Parasite Plasmodium falciparum.

Degree: 2012, University of Toronto

The Clp chaperones and proteases play a pivotal role in maintaining cellular homeostasis. They are highly conserved across prokaryotes and can also be found in… (more)

Subjects/Keywords: Clp; protease; chaperone; apicoplast; Plasmodium falciparum; PfClp; ATPases; PfClpP; PfClpR

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APA (6th Edition):

Pow, A. (2012). Structural and Functional Characterization of Clp Chaperones and Proteases in the Human Malaria Parasite Plasmodium falciparum. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33493

Chicago Manual of Style (16th Edition):

Pow, Andre. “Structural and Functional Characterization of Clp Chaperones and Proteases in the Human Malaria Parasite Plasmodium falciparum.” 2012. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/33493.

MLA Handbook (7th Edition):

Pow, Andre. “Structural and Functional Characterization of Clp Chaperones and Proteases in the Human Malaria Parasite Plasmodium falciparum.” 2012. Web. 07 Mar 2021.

Vancouver:

Pow A. Structural and Functional Characterization of Clp Chaperones and Proteases in the Human Malaria Parasite Plasmodium falciparum. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/33493.

Council of Science Editors:

Pow A. Structural and Functional Characterization of Clp Chaperones and Proteases in the Human Malaria Parasite Plasmodium falciparum. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33493


University of Toronto

29. 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 March 07, 2021. http://hdl.handle.net/1807/89552.

MLA Handbook (7th Edition):

Tan, Wendy. “Characterization of the Mitochondrial Peptide Pβ.” 2018. Web. 07 Mar 2021.

Vancouver:

Tan W. Characterization of the Mitochondrial Peptide Pβ. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2021 Mar 07]. 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

30. Hossain, Khalid. Novel Tripartite Motif Containing 22 Interactions in the Context of Very Early Onset Inflammatory Bowel Disease.

Degree: 2018, University of Toronto

Genetics predominate in very early onset inflammatory bowel disease (VEOIBD). With poor outcomes and therapeutic response, monogenic causes revealed by whole exome sequencing has potential… (more)

Subjects/Keywords: E3 Ubiquitin Ligase; HDAC1; Inflammatory Bowel Disease; Paediatric; TRIM22; Whole Exome Sequencing; 0379

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APA (6th Edition):

Hossain, K. (2018). Novel Tripartite Motif Containing 22 Interactions in the Context of Very Early Onset Inflammatory Bowel Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91336

Chicago Manual of Style (16th Edition):

Hossain, Khalid. “Novel Tripartite Motif Containing 22 Interactions in the Context of Very Early Onset Inflammatory Bowel Disease.” 2018. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/91336.

MLA Handbook (7th Edition):

Hossain, Khalid. “Novel Tripartite Motif Containing 22 Interactions in the Context of Very Early Onset Inflammatory Bowel Disease.” 2018. Web. 07 Mar 2021.

Vancouver:

Hossain K. Novel Tripartite Motif Containing 22 Interactions in the Context of Very Early Onset Inflammatory Bowel Disease. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/91336.

Council of Science Editors:

Hossain K. Novel Tripartite Motif Containing 22 Interactions in the Context of Very Early Onset Inflammatory Bowel Disease. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91336

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