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You searched for +publisher:"University of Toronto" +contributor:("Gariepy, Jean"). Showing records 1 – 8 of 8 total matches.

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University of Toronto

1. Broad, Amaalia. A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells.

Degree: 2009, University of Toronto

The delivery of biomolecules by cell penetrating peptides (CPPs) is an innovative therapeutic strategy. However delivery efficiency is hindered by the entrapment of CPPs in… (more)

Subjects/Keywords: Drug Delivery; Endosomal Escape; 0491

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APA (6th Edition):

Broad, A. (2009). A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/18890

Chicago Manual of Style (16th Edition):

Broad, Amaalia. “A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells.” 2009. Masters Thesis, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/18890.

MLA Handbook (7th Edition):

Broad, Amaalia. “A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells.” 2009. Web. 24 Apr 2019.

Vancouver:

Broad A. A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/18890.

Council of Science Editors:

Broad A. A Role for ETA(253-412) in Peptide-based Delivery of Therapeutic Molecules into Cells. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/18890


University of Toronto

2. Wei. Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1).

Degree: 2012, University of Toronto

Shiga-like toxin 1 (SLT-1) is produced by Escherichia coli strains like the pathogenic strain O157:H7. These bacterial strains are responsible for worldwide cases of food… (more)

Subjects/Keywords: protein toxin; shiga-like toxin 1; 0307

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APA (6th Edition):

Wei. (2012). Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1). (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32501

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

Wei. “Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1).” 2012. Masters Thesis, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/32501.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

Wei. “Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1).” 2012. Web. 24 Apr 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

Wei. Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1). [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/32501.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

Wei. Identification of Cellular Components Interacting with the Shiga-like Toxin 1 A1 Chain (SLT-1 A1). [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32501

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


University of Toronto

3. Prodeus, Aaron. Targeting IgV-like Domain Immune Checkpoint Receptors with Novel Nucleic Acid and Protein-Based Therapeutics.

Degree: PhD, 2018, University of Toronto

 The immune system is heavily regulated by negative checkpoint pathways; a network of cell signaling events governed by immune inhibitory ligand-receptor interactions. Physiologically, these negative… (more)

Subjects/Keywords: Aptamer; Autoimmunity; Immunomodulation; Immunotherapy; Inflammation; Oncology; 0307

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APA (6th Edition):

Prodeus, A. (2018). Targeting IgV-like Domain Immune Checkpoint Receptors with Novel Nucleic Acid and Protein-Based Therapeutics. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89699

Chicago Manual of Style (16th Edition):

Prodeus, Aaron. “Targeting IgV-like Domain Immune Checkpoint Receptors with Novel Nucleic Acid and Protein-Based Therapeutics.” 2018. Doctoral Dissertation, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/89699.

MLA Handbook (7th Edition):

Prodeus, Aaron. “Targeting IgV-like Domain Immune Checkpoint Receptors with Novel Nucleic Acid and Protein-Based Therapeutics.” 2018. Web. 24 Apr 2019.

Vancouver:

Prodeus A. Targeting IgV-like Domain Immune Checkpoint Receptors with Novel Nucleic Acid and Protein-Based Therapeutics. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/89699.

Council of Science Editors:

Prodeus A. Targeting IgV-like Domain Immune Checkpoint Receptors with Novel Nucleic Acid and Protein-Based Therapeutics. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89699


University of Toronto

4. Latimer, Caitlin. Octaarginine Labelled 30 nm Gold Nanoparticles as Agents for Enhanced Radiotherapy.

Degree: 2013, University of Toronto

Traditional radiation therapy is limited by the radiotoxic effects on surrounding healthy tissues. This project investigated the use of a gold nanoparticle (AuNP) conjugated to… (more)

Subjects/Keywords: gold nanoparticle; radiotherapy; 0760

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APA (6th Edition):

Latimer, C. (2013). Octaarginine Labelled 30 nm Gold Nanoparticles as Agents for Enhanced Radiotherapy. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43000

Chicago Manual of Style (16th Edition):

Latimer, Caitlin. “Octaarginine Labelled 30 nm Gold Nanoparticles as Agents for Enhanced Radiotherapy.” 2013. Masters Thesis, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/43000.

MLA Handbook (7th Edition):

Latimer, Caitlin. “Octaarginine Labelled 30 nm Gold Nanoparticles as Agents for Enhanced Radiotherapy.” 2013. Web. 24 Apr 2019.

Vancouver:

Latimer C. Octaarginine Labelled 30 nm Gold Nanoparticles as Agents for Enhanced Radiotherapy. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/43000.

Council of Science Editors:

Latimer C. Octaarginine Labelled 30 nm Gold Nanoparticles as Agents for Enhanced Radiotherapy. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43000

5. Orava, Erik. Functional DNA Aptamers as Biotherapeutic Molecules.

Degree: 2013, University of Toronto

Aptamers are single-stranded oligonucleotides, DNA or RNA, which can bind to a myriad of targets such as ions, peptides, proteins, drugs, organic and inorganic molecules… (more)

Subjects/Keywords: aptamer; therapeutic; biologic; 0491

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APA (6th Edition):

Orava, E. (2013). Functional DNA Aptamers as Biotherapeutic Molecules. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/43690

Chicago Manual of Style (16th Edition):

Orava, Erik. “Functional DNA Aptamers as Biotherapeutic Molecules.” 2013. Doctoral Dissertation, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/43690.

MLA Handbook (7th Edition):

Orava, Erik. “Functional DNA Aptamers as Biotherapeutic Molecules.” 2013. Web. 24 Apr 2019.

Vancouver:

Orava E. Functional DNA Aptamers as Biotherapeutic Molecules. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/43690.

Council of Science Editors:

Orava E. Functional DNA Aptamers as Biotherapeutic Molecules. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43690

6. Cheung, Melissa. A Ribosome-inactivating Protein Toxin as a Template for Cancer Drug Discovery.

Degree: 2012, University of Toronto

Cancer cells display aberrant receptors on their surface that can serve as targets for the development of directed drug therapies. As such, our group has… (more)

Subjects/Keywords: Biomarker; Cancer; Toxin; Targeted-Therapy; Shiga-like Toxin 1; Combinatorial Library; 0307

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APA (6th Edition):

Cheung, M. (2012). A Ribosome-inactivating Protein Toxin as a Template for Cancer Drug Discovery. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/33952

Chicago Manual of Style (16th Edition):

Cheung, Melissa. “A Ribosome-inactivating Protein Toxin as a Template for Cancer Drug Discovery.” 2012. Doctoral Dissertation, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/33952.

MLA Handbook (7th Edition):

Cheung, Melissa. “A Ribosome-inactivating Protein Toxin as a Template for Cancer Drug Discovery.” 2012. Web. 24 Apr 2019.

Vancouver:

Cheung M. A Ribosome-inactivating Protein Toxin as a Template for Cancer Drug Discovery. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/33952.

Council of Science Editors:

Cheung M. A Ribosome-inactivating Protein Toxin as a Template for Cancer Drug Discovery. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33952

7. McCluskey, Andrew. Shiga-like Toxin 1: Molecular Mechanism of Toxicity and Discovery of Inhibitors.

Degree: 2010, University of Toronto

Ribosome-inactivating proteins (RIPs) such as Shiga-like toxin 1 (SLT-1) halt protein synthesis in eukaryotic cells by depurinating a single adenine base in the sarcin-ricin loop… (more)

Subjects/Keywords: ribosome inactivating protein; toxin; ribosomal stalk; proteomics; 0307

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APA (6th Edition):

McCluskey, A. (2010). Shiga-like Toxin 1: Molecular Mechanism of Toxicity and Discovery of Inhibitors. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32046

Chicago Manual of Style (16th Edition):

McCluskey, Andrew. “Shiga-like Toxin 1: Molecular Mechanism of Toxicity and Discovery of Inhibitors.” 2010. Doctoral Dissertation, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/32046.

MLA Handbook (7th Edition):

McCluskey, Andrew. “Shiga-like Toxin 1: Molecular Mechanism of Toxicity and Discovery of Inhibitors.” 2010. Web. 24 Apr 2019.

Vancouver:

McCluskey A. Shiga-like Toxin 1: Molecular Mechanism of Toxicity and Discovery of Inhibitors. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/32046.

Council of Science Editors:

McCluskey A. Shiga-like Toxin 1: Molecular Mechanism of Toxicity and Discovery of Inhibitors. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32046


University of Toronto

8. Perampalam, Subodini. Cell Targeted Ribosome Inactivating Proteins Derived from Protein Combinatorial Libraries.

Degree: 2008, University of Toronto

Combinatorial protein libraries based on a protein template offer a vast potential for deriving protein variants harboring new receptor specificity while retaining other tem-plate functions… (more)

Subjects/Keywords: Protein libraries; cytotoxicity; anti-cancer agents; shiga like toxin 1; ribosome inactivating protein; 0760

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

APA (6th Edition):

Perampalam, S. (2008). Cell Targeted Ribosome Inactivating Proteins Derived from Protein Combinatorial Libraries. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/11244

Chicago Manual of Style (16th Edition):

Perampalam, Subodini. “Cell Targeted Ribosome Inactivating Proteins Derived from Protein Combinatorial Libraries.” 2008. Doctoral Dissertation, University of Toronto. Accessed April 24, 2019. http://hdl.handle.net/1807/11244.

MLA Handbook (7th Edition):

Perampalam, Subodini. “Cell Targeted Ribosome Inactivating Proteins Derived from Protein Combinatorial Libraries.” 2008. Web. 24 Apr 2019.

Vancouver:

Perampalam S. Cell Targeted Ribosome Inactivating Proteins Derived from Protein Combinatorial Libraries. [Internet] [Doctoral dissertation]. University of Toronto; 2008. [cited 2019 Apr 24]. Available from: http://hdl.handle.net/1807/11244.

Council of Science Editors:

Perampalam S. Cell Targeted Ribosome Inactivating Proteins Derived from Protein Combinatorial Libraries. [Doctoral Dissertation]. University of Toronto; 2008. Available from: http://hdl.handle.net/1807/11244

.