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You searched for subject:(0307). Showing records 1 – 30 of 709 total matches.

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University of Toronto

1. Huang, Tonny Chao. Functional and Structural Characterization Reveals Novel FBXW7 Biology.

Degree: 2018, University of Toronto

This thesis aims to examine aspects of FBXW7 biology, a protein that is frequently mutated in a variety of cancers. The first part of this… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Huang, T. C. (2018). Functional and Structural Characterization Reveals Novel FBXW7 Biology. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91554

Chicago Manual of Style (16th Edition):

Huang, Tonny Chao. “Functional and Structural Characterization Reveals Novel FBXW7 Biology.” 2018. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/91554.

MLA Handbook (7th Edition):

Huang, Tonny Chao. “Functional and Structural Characterization Reveals Novel FBXW7 Biology.” 2018. Web. 27 May 2019.

Vancouver:

Huang TC. Functional and Structural Characterization Reveals Novel FBXW7 Biology. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/91554.

Council of Science Editors:

Huang TC. Functional and Structural Characterization Reveals Novel FBXW7 Biology. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91554


University of Toronto

2. Malek-Gilani, Nakisa. Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming.

Degree: 2016, University of Toronto

Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming By Nakisa Malek-Gilani Master of Science, 2016 Cell and Systems Biology, University of… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Malek-Gilani, N. (2016). Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/82404

Chicago Manual of Style (16th Edition):

Malek-Gilani, Nakisa. “Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming.” 2016. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/82404.

MLA Handbook (7th Edition):

Malek-Gilani, Nakisa. “Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming.” 2016. Web. 27 May 2019.

Vancouver:

Malek-Gilani N. Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/82404.

Council of Science Editors:

Malek-Gilani N. Importance of Cell Specific Transcription Factors in Sox2 Regulation, Conservation and Reprogramming. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/82404


University of Toronto

3. McLaughlin, Megan. Exploration of Peptide Recognition using Directed Evolution of the PDZ Domain Fold.

Degree: 2013, University of Toronto

The PDZ domain family is one of the most abundant peptide recognition modules in metazoan proteomes. Characterization of natural PDZ domains has provided insight into… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

McLaughlin, M. (2013). Exploration of Peptide Recognition using Directed Evolution of the PDZ Domain Fold. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/35648

Chicago Manual of Style (16th Edition):

McLaughlin, Megan. “Exploration of Peptide Recognition using Directed Evolution of the PDZ Domain Fold.” 2013. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/35648.

MLA Handbook (7th Edition):

McLaughlin, Megan. “Exploration of Peptide Recognition using Directed Evolution of the PDZ Domain Fold.” 2013. Web. 27 May 2019.

Vancouver:

McLaughlin M. Exploration of Peptide Recognition using Directed Evolution of the PDZ Domain Fold. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/35648.

Council of Science Editors:

McLaughlin M. Exploration of Peptide Recognition using Directed Evolution of the PDZ Domain Fold. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35648


University of Toronto

4. Williams, Rashida. Generation of Anti-CD133 Human Synthetic Antibodies as Tools for Exploring CD133 Function.

Degree: 2013, University of Toronto

Two synthetic human antibody fragments against the human pentaspan membrane protein CD133 were isolated using a novel selection method involving direct selections on cells coupled… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Williams, R. (2013). Generation of Anti-CD133 Human Synthetic Antibodies as Tools for Exploring CD133 Function. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43333

Chicago Manual of Style (16th Edition):

Williams, Rashida. “Generation of Anti-CD133 Human Synthetic Antibodies as Tools for Exploring CD133 Function.” 2013. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/43333.

MLA Handbook (7th Edition):

Williams, Rashida. “Generation of Anti-CD133 Human Synthetic Antibodies as Tools for Exploring CD133 Function.” 2013. Web. 27 May 2019.

Vancouver:

Williams R. Generation of Anti-CD133 Human Synthetic Antibodies as Tools for Exploring CD133 Function. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/43333.

Council of Science Editors:

Williams R. Generation of Anti-CD133 Human Synthetic Antibodies as Tools for Exploring CD133 Function. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43333


University of Toronto

5. Yang, Weining. Characterizing the Dual Roles of Versican in Angiogenesis and Wound Repair.

Degree: 2014, University of Toronto

While appearing to be disparate processes, wound healing and tumor progression utilize many similar molecular mechanisms. In particular, versican, a chondroitin sulfate proteoglycan is understood… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Yang, W. (2014). Characterizing the Dual Roles of Versican in Angiogenesis and Wound Repair. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67936

Chicago Manual of Style (16th Edition):

Yang, Weining. “Characterizing the Dual Roles of Versican in Angiogenesis and Wound Repair.” 2014. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/67936.

MLA Handbook (7th Edition):

Yang, Weining. “Characterizing the Dual Roles of Versican in Angiogenesis and Wound Repair.” 2014. Web. 27 May 2019.

Vancouver:

Yang W. Characterizing the Dual Roles of Versican in Angiogenesis and Wound Repair. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/67936.

Council of Science Editors:

Yang W. Characterizing the Dual Roles of Versican in Angiogenesis and Wound Repair. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67936


University of Toronto

6. Ling, Harrod. Characterization of the Role of Ubiquitin Protein Ligase E3 Component N-recognin 4 (UBR4) in the Murine Circadian Clock.

Degree: 2014, University of Toronto

Ubiquitination is an important post-translational modification in the molecular clock that regulates degradation of clock proteins through ubiquitin ligases. However, no ubiquitin ligase has been… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Ling, H. (2014). Characterization of the Role of Ubiquitin Protein Ligase E3 Component N-recognin 4 (UBR4) in the Murine Circadian Clock. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/68000

Chicago Manual of Style (16th Edition):

Ling, Harrod. “Characterization of the Role of Ubiquitin Protein Ligase E3 Component N-recognin 4 (UBR4) in the Murine Circadian Clock.” 2014. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/68000.

MLA Handbook (7th Edition):

Ling, Harrod. “Characterization of the Role of Ubiquitin Protein Ligase E3 Component N-recognin 4 (UBR4) in the Murine Circadian Clock.” 2014. Web. 27 May 2019.

Vancouver:

Ling H. Characterization of the Role of Ubiquitin Protein Ligase E3 Component N-recognin 4 (UBR4) in the Murine Circadian Clock. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/68000.

Council of Science Editors:

Ling H. Characterization of the Role of Ubiquitin Protein Ligase E3 Component N-recognin 4 (UBR4) in the Murine Circadian Clock. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68000


University of Toronto

7. Ong, Jamie. The Role of Fgfr2 Isoforms and Frem1 in Craniofacial Development.

Degree: 2015, University of Toronto

OBJECTIVES: 1) To determine whether the Fgfr2W290R mutant results in the generation of additional isoforms and 2) to characterize the spatial and temporal expression of… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Ong, J. (2015). The Role of Fgfr2 Isoforms and Frem1 in Craniofacial Development. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/69671

Chicago Manual of Style (16th Edition):

Ong, Jamie. “The Role of Fgfr2 Isoforms and Frem1 in Craniofacial Development.” 2015. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/69671.

MLA Handbook (7th Edition):

Ong, Jamie. “The Role of Fgfr2 Isoforms and Frem1 in Craniofacial Development.” 2015. Web. 27 May 2019.

Vancouver:

Ong J. The Role of Fgfr2 Isoforms and Frem1 in Craniofacial Development. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/69671.

Council of Science Editors:

Ong J. The Role of Fgfr2 Isoforms and Frem1 in Craniofacial Development. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69671


University of Toronto

8. Chung, Daniel. Perinuclear Tethers License Telomeric DSBs for a Broad Kinesin- and NPC-dependent DNA Repair Process.

Degree: 2015, University of Toronto

DNA double-strand breaks (DSBs) are often targeted to nuclear pore complexes (NPCs) for repair. We show that the Kinesin-14 motor protein complex (Cik1-Kar3) cooperates with… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Chung, D. (2015). Perinuclear Tethers License Telomeric DSBs for a Broad Kinesin- and NPC-dependent DNA Repair Process. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74686

Chicago Manual of Style (16th Edition):

Chung, Daniel. “Perinuclear Tethers License Telomeric DSBs for a Broad Kinesin- and NPC-dependent DNA Repair Process.” 2015. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/74686.

MLA Handbook (7th Edition):

Chung, Daniel. “Perinuclear Tethers License Telomeric DSBs for a Broad Kinesin- and NPC-dependent DNA Repair Process.” 2015. Web. 27 May 2019.

Vancouver:

Chung D. Perinuclear Tethers License Telomeric DSBs for a Broad Kinesin- and NPC-dependent DNA Repair Process. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/74686.

Council of Science Editors:

Chung D. Perinuclear Tethers License Telomeric DSBs for a Broad Kinesin- and NPC-dependent DNA Repair Process. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/74686


University of Toronto

9. Di Clemente, Sarah. The Role of the Src-like Adaptor Protein in the Regulation of GM-CSFR Signaling.

Degree: 2014, University of Toronto

GM-CSF is a cytokine that regulates proliferation and survival of myeloid progenitor cells and stimulates dendritic cell (DC) differentiation. The Src-like adaptor protein (SLAP) has… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Di Clemente, S. (2014). The Role of the Src-like Adaptor Protein in the Regulation of GM-CSFR Signaling. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/74764

Chicago Manual of Style (16th Edition):

Di Clemente, Sarah. “The Role of the Src-like Adaptor Protein in the Regulation of GM-CSFR Signaling.” 2014. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/74764.

MLA Handbook (7th Edition):

Di Clemente, Sarah. “The Role of the Src-like Adaptor Protein in the Regulation of GM-CSFR Signaling.” 2014. Web. 27 May 2019.

Vancouver:

Di Clemente S. The Role of the Src-like Adaptor Protein in the Regulation of GM-CSFR Signaling. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/74764.

Council of Science Editors:

Di Clemente S. The Role of the Src-like Adaptor Protein in the Regulation of GM-CSFR Signaling. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/74764


University of Toronto

10. Tiberia, Erica. Cardiofaciocutaneous Syndrome-Associated BRAF Mutants in Development and Cancer.

Degree: 2017, University of Toronto

Cardiofaciocutaneous syndrome (CFCS) is an autosomal-dominant disorder caused by germ-line mutations in members of the RAS/ERK signaling pathway, most commonly in BRAF. Selected mutations that… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Tiberia, E. (2017). Cardiofaciocutaneous Syndrome-Associated BRAF Mutants in Development and Cancer. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79300

Chicago Manual of Style (16th Edition):

Tiberia, Erica. “Cardiofaciocutaneous Syndrome-Associated BRAF Mutants in Development and Cancer.” 2017. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/79300.

MLA Handbook (7th Edition):

Tiberia, Erica. “Cardiofaciocutaneous Syndrome-Associated BRAF Mutants in Development and Cancer.” 2017. Web. 27 May 2019.

Vancouver:

Tiberia E. Cardiofaciocutaneous Syndrome-Associated BRAF Mutants in Development and Cancer. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/79300.

Council of Science Editors:

Tiberia E. Cardiofaciocutaneous Syndrome-Associated BRAF Mutants in Development and Cancer. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79300


University of Toronto

11. Volpatti, Jonathan. Characterization of a Zebrafish Model of X-linked Centronuclear Myopathy for Therapeutic Drug Development.

Degree: 2017, University of Toronto

X-linked centronuclear myopathy (XLCNM) is a congenital skeletal muscle disorder caused by mutations in MTM1. Despite being associated with a high rate of neonatal mortality… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Volpatti, J. (2017). Characterization of a Zebrafish Model of X-linked Centronuclear Myopathy for Therapeutic Drug Development. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79313

Chicago Manual of Style (16th Edition):

Volpatti, Jonathan. “Characterization of a Zebrafish Model of X-linked Centronuclear Myopathy for Therapeutic Drug Development.” 2017. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/79313.

MLA Handbook (7th Edition):

Volpatti, Jonathan. “Characterization of a Zebrafish Model of X-linked Centronuclear Myopathy for Therapeutic Drug Development.” 2017. Web. 27 May 2019.

Vancouver:

Volpatti J. Characterization of a Zebrafish Model of X-linked Centronuclear Myopathy for Therapeutic Drug Development. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/79313.

Council of Science Editors:

Volpatti J. Characterization of a Zebrafish Model of X-linked Centronuclear Myopathy for Therapeutic Drug Development. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79313


University of Toronto

12. Sabouhanian, Amir-Arsalan. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.

Degree: 2015, University of Toronto

A critical challenge in molecular evolutionary biology is to determine how changes in protein coding sequence correlate with ecology, physiology, or morphology. While statistical approaches… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Sabouhanian, A. (2015). Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/80446

Chicago Manual of Style (16th Edition):

Sabouhanian, Amir-Arsalan. “Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.” 2015. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/80446.

MLA Handbook (7th Edition):

Sabouhanian, Amir-Arsalan. “Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.” 2015. Web. 27 May 2019.

Vancouver:

Sabouhanian A. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/80446.

Council of Science Editors:

Sabouhanian A. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/80446


University of Toronto

13. Sabouhanian, Amir-Arsalan. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.

Degree: 2015, University of Toronto

A critical challenge in molecular evolutionary biology is to determine how changes in protein coding sequence correlate with ecology, physiology, or morphology. While statistical approaches… (more)

Subjects/Keywords: 0307

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sabouhanian, A. (2015). Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/80447

Chicago Manual of Style (16th Edition):

Sabouhanian, Amir-Arsalan. “Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.” 2015. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/80447.

MLA Handbook (7th Edition):

Sabouhanian, Amir-Arsalan. “Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.” 2015. Web. 27 May 2019.

Vancouver:

Sabouhanian A. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/80447.

Council of Science Editors:

Sabouhanian A. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/80447


University of Toronto

14. Hall, Mathew Adam. Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16.

Degree: 2014, University of Toronto

My research seeks to uncover novel mechanisms of cooperation between the insulin and Ras/MAPK signalling cascades. I use Caenorhabditis elegans as a model system and… (more)

Subjects/Keywords: 0307

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

APA (6th Edition):

Hall, M. A. (2014). Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/82644

Chicago Manual of Style (16th Edition):

Hall, Mathew Adam. “Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16.” 2014. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/82644.

MLA Handbook (7th Edition):

Hall, Mathew Adam. “Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16.” 2014. Web. 27 May 2019.

Vancouver:

Hall MA. Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/82644.

Council of Science Editors:

Hall MA. Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/82644


University of Toronto

15. Hall, Mathew Adam. Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16.

Degree: 2014, University of Toronto

My research seeks to uncover novel mechanisms of cooperation between the insulin and Ras/MAPK signalling cascades. I use Caenorhabditis elegans as a model system and… (more)

Subjects/Keywords: 0307

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hall, M. A. (2014). Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/82643

Chicago Manual of Style (16th Edition):

Hall, Mathew Adam. “Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16.” 2014. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/82643.

MLA Handbook (7th Edition):

Hall, Mathew Adam. “Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16.” 2014. Web. 27 May 2019.

Vancouver:

Hall MA. Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/82643.

Council of Science Editors:

Hall MA. Insulin Signaling Promotes Ras/MAPK Cascade Activity by Inhibiting the FOXO Transcription Factor DAF-16. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/82643


University of Toronto

16. Sabouhanian, Amir-Arsalan. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.

Degree: 2015, University of Toronto

A critical challenge in molecular evolutionary biology is to determine how changes in protein coding sequence correlate with ecology, physiology, or morphology. While statistical approaches… (more)

Subjects/Keywords: 0307

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sabouhanian, A. (2015). Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/94525

Chicago Manual of Style (16th Edition):

Sabouhanian, Amir-Arsalan. “Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.” 2015. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/94525.

MLA Handbook (7th Edition):

Sabouhanian, Amir-Arsalan. “Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology.” 2015. Web. 27 May 2019.

Vancouver:

Sabouhanian A. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/94525.

Council of Science Editors:

Sabouhanian A. Correlated Evolution of Teleost Fish Rhodopsin with Habitat: Linking Molecular Changes to Ecology. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/94525


University of Toronto

17. Cote, Atina. In Vivo Analysis of Cruciform Extrusion and Resolution of DNA Palindromes in Eukaryotes.

Degree: 2009, University of Toronto

DNA palindromes are implicated in several examples of gross chromosomal aberrations in the human genome, however, the molecular mechanism(s) that govern palindrome instability are largely… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Cote, A. (2009). In Vivo Analysis of Cruciform Extrusion and Resolution of DNA Palindromes in Eukaryotes. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/17746

Chicago Manual of Style (16th Edition):

Cote, Atina. “In Vivo Analysis of Cruciform Extrusion and Resolution of DNA Palindromes in Eukaryotes.” 2009. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/17746.

MLA Handbook (7th Edition):

Cote, Atina. “In Vivo Analysis of Cruciform Extrusion and Resolution of DNA Palindromes in Eukaryotes.” 2009. Web. 27 May 2019.

Vancouver:

Cote A. In Vivo Analysis of Cruciform Extrusion and Resolution of DNA Palindromes in Eukaryotes. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/17746.

Council of Science Editors:

Cote A. In Vivo Analysis of Cruciform Extrusion and Resolution of DNA Palindromes in Eukaryotes. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/17746


University of Toronto

18. Zhao, Yanling. An Investigation of the Regulation of RNA Polymerase II Transcription.

Degree: PhD, 2015, University of Toronto

 The C-terminal domain (CTD) of the largest RNA polymerase II (RNAPII) subunit, POLR2A, is a platform for modifications specifying the recruitment of factors that regulate… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Zhao, Y. (2015). An Investigation of the Regulation of RNA Polymerase II Transcription. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/71434

Chicago Manual of Style (16th Edition):

Zhao, Yanling. “An Investigation of the Regulation of RNA Polymerase II Transcription.” 2015. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/71434.

MLA Handbook (7th Edition):

Zhao, Yanling. “An Investigation of the Regulation of RNA Polymerase II Transcription.” 2015. Web. 27 May 2019.

Vancouver:

Zhao Y. An Investigation of the Regulation of RNA Polymerase II Transcription. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/71434.

Council of Science Editors:

Zhao Y. An Investigation of the Regulation of RNA Polymerase II Transcription. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/71434


University of Toronto

19. Xiong, Hui Yuan. Inference and Analysis of the Human Splicing Code.

Degree: PhD, 2016, University of Toronto

 We construct and analyse a computational model that predicts the outcome of alternative splicing by recognizing features in RNA sequences. The computational model can be… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Xiong, H. Y. (2016). Inference and Analysis of the Human Splicing Code. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/73219

Chicago Manual of Style (16th Edition):

Xiong, Hui Yuan. “Inference and Analysis of the Human Splicing Code.” 2016. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/73219.

MLA Handbook (7th Edition):

Xiong, Hui Yuan. “Inference and Analysis of the Human Splicing Code.” 2016. Web. 27 May 2019.

Vancouver:

Xiong HY. Inference and Analysis of the Human Splicing Code. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/73219.

Council of Science Editors:

Xiong HY. Inference and Analysis of the Human Splicing Code. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/73219


University of Toronto

20. Malik, Natasha. Investigation of Epstein-Barr Virus-Host Interactions during Latent and Lytic Infection.

Degree: PhD, 2014, University of Toronto

Epstein-Barr virus is a gammaherpesvirus that latently infects more than 90% of the adult population and persists for the life of the host. The viral… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Malik, N. (2014). Investigation of Epstein-Barr Virus-Host Interactions during Latent and Lytic Infection. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/74819

Chicago Manual of Style (16th Edition):

Malik, Natasha. “Investigation of Epstein-Barr Virus-Host Interactions during Latent and Lytic Infection.” 2014. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/74819.

MLA Handbook (7th Edition):

Malik, Natasha. “Investigation of Epstein-Barr Virus-Host Interactions during Latent and Lytic Infection.” 2014. Web. 27 May 2019.

Vancouver:

Malik N. Investigation of Epstein-Barr Virus-Host Interactions during Latent and Lytic Infection. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/74819.

Council of Science Editors:

Malik N. Investigation of Epstein-Barr Virus-Host Interactions during Latent and Lytic Infection. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/74819


University of Toronto

21. Safavian, Darya. An Investigation of the Cellular Responses and the Role of the Exocyst Complex in Early Stages of Pollen-Pistil Interactions in Brassicaceae.

Degree: PhD, 2015, University of Toronto

In Brassicaceae, complex signaling events occur at the early stages of interaction between the pollen grain and the stigmatic surface at the top of the… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Safavian, D. (2015). An Investigation of the Cellular Responses and the Role of the Exocyst Complex in Early Stages of Pollen-Pistil Interactions in Brassicaceae. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/75681

Chicago Manual of Style (16th Edition):

Safavian, Darya. “An Investigation of the Cellular Responses and the Role of the Exocyst Complex in Early Stages of Pollen-Pistil Interactions in Brassicaceae.” 2015. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/75681.

MLA Handbook (7th Edition):

Safavian, Darya. “An Investigation of the Cellular Responses and the Role of the Exocyst Complex in Early Stages of Pollen-Pistil Interactions in Brassicaceae.” 2015. Web. 27 May 2019.

Vancouver:

Safavian D. An Investigation of the Cellular Responses and the Role of the Exocyst Complex in Early Stages of Pollen-Pistil Interactions in Brassicaceae. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/75681.

Council of Science Editors:

Safavian D. An Investigation of the Cellular Responses and the Role of the Exocyst Complex in Early Stages of Pollen-Pistil Interactions in Brassicaceae. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/75681


University of Toronto

22. Amoozadeh, Yasaman. Mechanism of Claudin Regulation in Kidney Tubular Epithelial Cells.

Degree: PhD, 2016, University of Toronto

 Abstract The overall objective of my studies was to gain insight into the role and regulation of claudin family tight junction (TJ) proteins in kidney… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Amoozadeh, Y. (2016). Mechanism of Claudin Regulation in Kidney Tubular Epithelial Cells. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76296

Chicago Manual of Style (16th Edition):

Amoozadeh, Yasaman. “Mechanism of Claudin Regulation in Kidney Tubular Epithelial Cells.” 2016. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/76296.

MLA Handbook (7th Edition):

Amoozadeh, Yasaman. “Mechanism of Claudin Regulation in Kidney Tubular Epithelial Cells.” 2016. Web. 27 May 2019.

Vancouver:

Amoozadeh Y. Mechanism of Claudin Regulation in Kidney Tubular Epithelial Cells. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/76296.

Council of Science Editors:

Amoozadeh Y. Mechanism of Claudin Regulation in Kidney Tubular Epithelial Cells. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76296


University of Toronto

23. Yu, Rosemary. Pre-clinical analysis of fluvastatin as a metastasis-prevention agent in breast cancer.

Degree: PhD, 2017, University of Toronto

Fluvastatin is a member of the statin family of drugs, widely prescribed to lower serum cholesterol. Accumulating evidence from epidemiological, pre-clinical, and clinical studies indicate… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Yu, R. (2017). Pre-clinical analysis of fluvastatin as a metastasis-prevention agent in breast cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/88993

Chicago Manual of Style (16th Edition):

Yu, Rosemary. “Pre-clinical analysis of fluvastatin as a metastasis-prevention agent in breast cancer.” 2017. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/88993.

MLA Handbook (7th Edition):

Yu, Rosemary. “Pre-clinical analysis of fluvastatin as a metastasis-prevention agent in breast cancer.” 2017. Web. 27 May 2019.

Vancouver:

Yu R. Pre-clinical analysis of fluvastatin as a metastasis-prevention agent in breast cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/88993.

Council of Science Editors:

Yu R. Pre-clinical analysis of fluvastatin as a metastasis-prevention agent in breast cancer. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/88993


University of Toronto

24. Sheikh, Taimoor. Genetic, Functional and Clinical Evaluation of MeCP2 Mutations.

Degree: PhD, 2018, University of Toronto

 Rett syndrome (RTT; MIM# 312750) is a neurodevelopmental disorder, the second most common genetic cause of intellectual disability (ID) in girls. Rett incidence (1:10,000-15,000) accounts… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Sheikh, T. (2018). Genetic, Functional and Clinical Evaluation of MeCP2 Mutations. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89761

Chicago Manual of Style (16th Edition):

Sheikh, Taimoor. “Genetic, Functional and Clinical Evaluation of MeCP2 Mutations.” 2018. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/89761.

MLA Handbook (7th Edition):

Sheikh, Taimoor. “Genetic, Functional and Clinical Evaluation of MeCP2 Mutations.” 2018. Web. 27 May 2019.

Vancouver:

Sheikh T. Genetic, Functional and Clinical Evaluation of MeCP2 Mutations. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/89761.

Council of Science Editors:

Sheikh T. Genetic, Functional and Clinical Evaluation of MeCP2 Mutations. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89761


University of Toronto

25. Park, Nicole. ASCL1 directs the neuronal fate of neoplastic cells in glioblastoma.

Degree: PhD, 2018, University of Toronto

 Tumours represent aberrant organogenesis with growth caused by unlimited proliferation and failure of differentiation of malignant precursor cells. I propose that defects in lineage commitment… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Park, N. (2018). ASCL1 directs the neuronal fate of neoplastic cells in glioblastoma. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89781

Chicago Manual of Style (16th Edition):

Park, Nicole. “ASCL1 directs the neuronal fate of neoplastic cells in glioblastoma.” 2018. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/89781.

MLA Handbook (7th Edition):

Park, Nicole. “ASCL1 directs the neuronal fate of neoplastic cells in glioblastoma.” 2018. Web. 27 May 2019.

Vancouver:

Park N. ASCL1 directs the neuronal fate of neoplastic cells in glioblastoma. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/89781.

Council of Science Editors:

Park N. ASCL1 directs the neuronal fate of neoplastic cells in glioblastoma. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89781


University of Toronto

26. D'Ambrosio, Lisa Michelle. Defining the Role of Pds5 in the Maintenance of Sister Chromatid Cohesion.

Degree: PhD, 2015, University of Toronto

 The establishment, maintenance and dissolution of sister chromatid cohesion are sequentially coordinated during the cell cycle to ensure faithful chromosome transmission. This cell cycle-dependent regulation… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

D'Ambrosio, L. M. (2015). Defining the Role of Pds5 in the Maintenance of Sister Chromatid Cohesion. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69247

Chicago Manual of Style (16th Edition):

D'Ambrosio, Lisa Michelle. “Defining the Role of Pds5 in the Maintenance of Sister Chromatid Cohesion.” 2015. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/69247.

MLA Handbook (7th Edition):

D'Ambrosio, Lisa Michelle. “Defining the Role of Pds5 in the Maintenance of Sister Chromatid Cohesion.” 2015. Web. 27 May 2019.

Vancouver:

D'Ambrosio LM. Defining the Role of Pds5 in the Maintenance of Sister Chromatid Cohesion. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/69247.

Council of Science Editors:

D'Ambrosio LM. Defining the Role of Pds5 in the Maintenance of Sister Chromatid Cohesion. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69247


University of Toronto

27. Cardelli, Marco. Estrogen Receptor-related Receptor Gamma (ERRg) is a Regulator of Skeletogenesis.

Degree: PhD, 2015, University of Toronto

 Sex steroids, such as Estrogen, play important roles in physiological and pathological processes, including bone growth and bone homeostasis. Estrogen's effects are mediated through its… (more)

Subjects/Keywords: 0307

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APA (6th Edition):

Cardelli, M. (2015). Estrogen Receptor-related Receptor Gamma (ERRg) is a Regulator of Skeletogenesis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69283

Chicago Manual of Style (16th Edition):

Cardelli, Marco. “Estrogen Receptor-related Receptor Gamma (ERRg) is a Regulator of Skeletogenesis.” 2015. Doctoral Dissertation, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/69283.

MLA Handbook (7th Edition):

Cardelli, Marco. “Estrogen Receptor-related Receptor Gamma (ERRg) is a Regulator of Skeletogenesis.” 2015. Web. 27 May 2019.

Vancouver:

Cardelli M. Estrogen Receptor-related Receptor Gamma (ERRg) is a Regulator of Skeletogenesis. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/69283.

Council of Science Editors:

Cardelli M. Estrogen Receptor-related Receptor Gamma (ERRg) is a Regulator of Skeletogenesis. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69283


University of Toronto

28. Sam, Kevin. Differential Protein Interactions of NMDA Receptor NR2 Subunits.

Degree: 2010, University of Toronto

NMDA-type glutamate receptors (NMDAR) regulate neurotransmission and excitotoxicity. NMDAR signaling is believed to be dependent on NR2 subunit (A-D) composition and interactions with intracellular proteins.… (more)

Subjects/Keywords: 0307; 0317

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APA (6th Edition):

Sam, K. (2010). Differential Protein Interactions of NMDA Receptor NR2 Subunits. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25792

Chicago Manual of Style (16th Edition):

Sam, Kevin. “Differential Protein Interactions of NMDA Receptor NR2 Subunits.” 2010. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/25792.

MLA Handbook (7th Edition):

Sam, Kevin. “Differential Protein Interactions of NMDA Receptor NR2 Subunits.” 2010. Web. 27 May 2019.

Vancouver:

Sam K. Differential Protein Interactions of NMDA Receptor NR2 Subunits. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/25792.

Council of Science Editors:

Sam K. Differential Protein Interactions of NMDA Receptor NR2 Subunits. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25792


University of Toronto

29. Landry, Cameron. Mechanisms of Regulation of Promyelocytic Leukemia (PML) Proteins by Epstein-Barr Nuclear Antigen 1 (EBNA1) and Ubiquitin Specific Protease 7 (USP7).

Degree: 2013, University of Toronto

Promyelocytic leukemia (PML) nuclear bodies (NBs) are important nuclear structures that mediate tumour suppressive and antiviral functions. Epstein-Barr virus (EBV) has evolved mechanisms to disrupt… (more)

Subjects/Keywords: 0307; 0720

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APA (6th Edition):

Landry, C. (2013). Mechanisms of Regulation of Promyelocytic Leukemia (PML) Proteins by Epstein-Barr Nuclear Antigen 1 (EBNA1) and Ubiquitin Specific Protease 7 (USP7). (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70018

Chicago Manual of Style (16th Edition):

Landry, Cameron. “Mechanisms of Regulation of Promyelocytic Leukemia (PML) Proteins by Epstein-Barr Nuclear Antigen 1 (EBNA1) and Ubiquitin Specific Protease 7 (USP7).” 2013. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/70018.

MLA Handbook (7th Edition):

Landry, Cameron. “Mechanisms of Regulation of Promyelocytic Leukemia (PML) Proteins by Epstein-Barr Nuclear Antigen 1 (EBNA1) and Ubiquitin Specific Protease 7 (USP7).” 2013. Web. 27 May 2019.

Vancouver:

Landry C. Mechanisms of Regulation of Promyelocytic Leukemia (PML) Proteins by Epstein-Barr Nuclear Antigen 1 (EBNA1) and Ubiquitin Specific Protease 7 (USP7). [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/70018.

Council of Science Editors:

Landry C. Mechanisms of Regulation of Promyelocytic Leukemia (PML) Proteins by Epstein-Barr Nuclear Antigen 1 (EBNA1) and Ubiquitin Specific Protease 7 (USP7). [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/70018

30. Bromand, Sadat. Superficial Zone Chondrocytes Modulate Polyphosphate Levels In Deep Zone Cartilage Which Correlate with Increased Tissue Formation And Decreased Mineralization By Deep Zone Chondrocytes.

Degree: 2014, University of Toronto

Loss of the superficial zone of articular cartilage is an early change in osteoarthritis and with disease progression the deep zone (DZ) of cartilage shows… (more)

Subjects/Keywords: 0541; 0307

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APA (6th Edition):

Bromand, S. (2014). Superficial Zone Chondrocytes Modulate Polyphosphate Levels In Deep Zone Cartilage Which Correlate with Increased Tissue Formation And Decreased Mineralization By Deep Zone Chondrocytes. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/65620

Chicago Manual of Style (16th Edition):

Bromand, Sadat. “Superficial Zone Chondrocytes Modulate Polyphosphate Levels In Deep Zone Cartilage Which Correlate with Increased Tissue Formation And Decreased Mineralization By Deep Zone Chondrocytes.” 2014. Masters Thesis, University of Toronto. Accessed May 27, 2019. http://hdl.handle.net/1807/65620.

MLA Handbook (7th Edition):

Bromand, Sadat. “Superficial Zone Chondrocytes Modulate Polyphosphate Levels In Deep Zone Cartilage Which Correlate with Increased Tissue Formation And Decreased Mineralization By Deep Zone Chondrocytes.” 2014. Web. 27 May 2019.

Vancouver:

Bromand S. Superficial Zone Chondrocytes Modulate Polyphosphate Levels In Deep Zone Cartilage Which Correlate with Increased Tissue Formation And Decreased Mineralization By Deep Zone Chondrocytes. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2019 May 27]. Available from: http://hdl.handle.net/1807/65620.

Council of Science Editors:

Bromand S. Superficial Zone Chondrocytes Modulate Polyphosphate Levels In Deep Zone Cartilage Which Correlate with Increased Tissue Formation And Decreased Mineralization By Deep Zone Chondrocytes. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/65620

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