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You searched for +publisher:"University of Toronto" +contributor:("Laboratory Medicine and Pathobiology"). Showing records 1 – 30 of 301 total matches.

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1. Kugathasan, Lakshmi. The Protective Role of the Angiopoetin-1 - Tie2 System in Transgenic Models of Pulmonary Arterial Hypertension.

Degree: 2010, University of Toronto

The role of the Angiopoietin-1 (Ang1)-Tie2 pathway in pulmonary arterial hypertension (PAH) is controversial, with one group suggesting that increased Ang1-Tie2 activity may even play… (more)

Subjects/Keywords: pulmonary hypertension; angiopoietin; 0571

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APA (6th Edition):

Kugathasan, L. (2010). The Protective Role of the Angiopoetin-1 - Tie2 System in Transgenic Models of Pulmonary Arterial Hypertension. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/24788

Chicago Manual of Style (16th Edition):

Kugathasan, Lakshmi. “The Protective Role of the Angiopoetin-1 - Tie2 System in Transgenic Models of Pulmonary Arterial Hypertension.” 2010. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/24788.

MLA Handbook (7th Edition):

Kugathasan, Lakshmi. “The Protective Role of the Angiopoetin-1 - Tie2 System in Transgenic Models of Pulmonary Arterial Hypertension.” 2010. Web. 21 Sep 2018.

Vancouver:

Kugathasan L. The Protective Role of the Angiopoetin-1 - Tie2 System in Transgenic Models of Pulmonary Arterial Hypertension. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/24788.

Council of Science Editors:

Kugathasan L. The Protective Role of the Angiopoetin-1 - Tie2 System in Transgenic Models of Pulmonary Arterial Hypertension. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24788

2. Schwock, Joerg. Inhibition of Hsp90 and its Client Kinase FAK has Therapeutic Potential in Squamous Cell Carcinomas of the Uterine Cervix and Oral Cavity.

Degree: 2010, University of Toronto

Heat shock protein 90 (Hsp90) is an essential and conserved chaperone, required for the conformational maturation and stability of many signaling kinases. We hypothesized that… (more)

Subjects/Keywords: Hsp90; focal adhesion kinase; cancer; metastasis; uterine cervix; oral cavity; 0992; 0571

Laboratory Medicine and Pathobiology University of Toronto, Year 2010 Abstract Heat shock protein… …Medicine and Pathobiology University of Toronto © Copyright by Joerg Schwock, 2010 ii… …Geddie (Laboratory Medicine and Pathobiology, Toronto, Ontario) and L.C. Horn (… …West Family Memorial Fund of the University of Toronto to Joerg Schwock (PhD student… …conformity with the requirements for the degree of Doctor of Philosophy Department of Laboratory… 

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APA (6th Edition):

Schwock, J. (2010). Inhibition of Hsp90 and its Client Kinase FAK has Therapeutic Potential in Squamous Cell Carcinomas of the Uterine Cervix and Oral Cavity. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/26517

Chicago Manual of Style (16th Edition):

Schwock, Joerg. “Inhibition of Hsp90 and its Client Kinase FAK has Therapeutic Potential in Squamous Cell Carcinomas of the Uterine Cervix and Oral Cavity.” 2010. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/26517.

MLA Handbook (7th Edition):

Schwock, Joerg. “Inhibition of Hsp90 and its Client Kinase FAK has Therapeutic Potential in Squamous Cell Carcinomas of the Uterine Cervix and Oral Cavity.” 2010. Web. 21 Sep 2018.

Vancouver:

Schwock J. Inhibition of Hsp90 and its Client Kinase FAK has Therapeutic Potential in Squamous Cell Carcinomas of the Uterine Cervix and Oral Cavity. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/26517.

Council of Science Editors:

Schwock J. Inhibition of Hsp90 and its Client Kinase FAK has Therapeutic Potential in Squamous Cell Carcinomas of the Uterine Cervix and Oral Cavity. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/26517

3. Fenili, Daniela. Characterization of Inositol Transporters as a Method for Drug Delivery to the Centra Nervous System.

Degree: 2010, University of Toronto

A challenge in the treatment of central nervous system (CNS) diseases is the transport of drug candidates into the brain. Inositol stereoisomers have show promise… (more)

Subjects/Keywords: Neuroscience; Alzheimer's disease; 0317

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APA (6th Edition):

Fenili, D. (2010). Characterization of Inositol Transporters as a Method for Drug Delivery to the Centra Nervous System. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32934

Chicago Manual of Style (16th Edition):

Fenili, Daniela. “Characterization of Inositol Transporters as a Method for Drug Delivery to the Centra Nervous System.” 2010. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32934.

MLA Handbook (7th Edition):

Fenili, Daniela. “Characterization of Inositol Transporters as a Method for Drug Delivery to the Centra Nervous System.” 2010. Web. 21 Sep 2018.

Vancouver:

Fenili D. Characterization of Inositol Transporters as a Method for Drug Delivery to the Centra Nervous System. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32934.

Council of Science Editors:

Fenili D. Characterization of Inositol Transporters as a Method for Drug Delivery to the Centra Nervous System. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32934

4. Sabatini, Peter Jarrod Bruno. Polarity Control in Migrating Vascular Smooth Muscle Cells: N-cadherin Localization and Function.

Degree: 2009, University of Toronto

Vascular endothelial cell loss initiates directional migration of medial smooth muscle cells into the arterial intima contributing to in-stent restenosis, atherosclerosis and coronary arterial by-pass… (more)

Subjects/Keywords: Vascular Biology; Polarity; N-cadherin; Restenosis; Migration; 0379

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APA (6th Edition):

Sabatini, P. J. B. (2009). Polarity Control in Migrating Vascular Smooth Muscle Cells: N-cadherin Localization and Function. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/19321

Chicago Manual of Style (16th Edition):

Sabatini, Peter Jarrod Bruno. “Polarity Control in Migrating Vascular Smooth Muscle Cells: N-cadherin Localization and Function.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/19321.

MLA Handbook (7th Edition):

Sabatini, Peter Jarrod Bruno. “Polarity Control in Migrating Vascular Smooth Muscle Cells: N-cadherin Localization and Function.” 2009. Web. 21 Sep 2018.

Vancouver:

Sabatini PJB. Polarity Control in Migrating Vascular Smooth Muscle Cells: N-cadherin Localization and Function. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/19321.

Council of Science Editors:

Sabatini PJB. Polarity Control in Migrating Vascular Smooth Muscle Cells: N-cadherin Localization and Function. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/19321

5. Sufan, Roxana Ioana. Molecular Characterization of the von Hippel-Lindau Ubiquitin Ligase.

Degree: 2009, University of Toronto

Marking proteins for degradation by the proteasome is a classical function of ubiquitination. This process of covalent attachment of a chain of ubiquitin molecules to… (more)

Subjects/Keywords: VHL; CCRCC; HIF; Polycythemia; Ubiquitin; NEDD8; Cullin; JAK2; 0307

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APA (6th Edition):

Sufan, R. I. (2009). Molecular Characterization of the von Hippel-Lindau Ubiquitin Ligase. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/26478

Chicago Manual of Style (16th Edition):

Sufan, Roxana Ioana. “Molecular Characterization of the von Hippel-Lindau Ubiquitin Ligase.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/26478.

MLA Handbook (7th Edition):

Sufan, Roxana Ioana. “Molecular Characterization of the von Hippel-Lindau Ubiquitin Ligase.” 2009. Web. 21 Sep 2018.

Vancouver:

Sufan RI. Molecular Characterization of the von Hippel-Lindau Ubiquitin Ligase. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/26478.

Council of Science Editors:

Sufan RI. Molecular Characterization of the von Hippel-Lindau Ubiquitin Ligase. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/26478

6. Hyrcza, Martin Dominik. Gene Expression Changes in Immune Cells During Human Immunodeficiency Virus 1 (HIV-1) Infection.

Degree: 2009, University of Toronto

Human immunodeficiency virus infection is a chronic condition causing significant changes in the immune system, which are reflected in the altered gene expression patterns of… (more)

Subjects/Keywords: HIV; interferon response; gene expression; immune cells; Primary: 0307; Secondary: 0564 & 0982

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APA (6th Edition):

Hyrcza, M. D. (2009). Gene Expression Changes in Immune Cells During Human Immunodeficiency Virus 1 (HIV-1) Infection. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/26459

Chicago Manual of Style (16th Edition):

Hyrcza, Martin Dominik. “Gene Expression Changes in Immune Cells During Human Immunodeficiency Virus 1 (HIV-1) Infection.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/26459.

MLA Handbook (7th Edition):

Hyrcza, Martin Dominik. “Gene Expression Changes in Immune Cells During Human Immunodeficiency Virus 1 (HIV-1) Infection.” 2009. Web. 21 Sep 2018.

Vancouver:

Hyrcza MD. Gene Expression Changes in Immune Cells During Human Immunodeficiency Virus 1 (HIV-1) Infection. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/26459.

Council of Science Editors:

Hyrcza MD. Gene Expression Changes in Immune Cells During Human Immunodeficiency Virus 1 (HIV-1) Infection. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/26459

7. Rosa, Maria Fabiana De. Multidrug Resistance Protein 1 (MDR1) and Glycosphingolipids Biosynthesis: Advantages for Therapeutics.

Degree: 2009, University of Toronto

ABC drug transporter, MDR1, is a drug flippase that moves a variety of hydrophobic molecules from the inner to the outer leaflet of the plasma… (more)

Subjects/Keywords: P-glycoprotein; Multidrug Resistance; glycosphingolipids; Fabry disease; Adamantyl Gb3; 0379; 0419; 0487

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APA (6th Edition):

Rosa, M. F. D. (2009). Multidrug Resistance Protein 1 (MDR1) and Glycosphingolipids Biosynthesis: Advantages for Therapeutics. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/19262

Chicago Manual of Style (16th Edition):

Rosa, Maria Fabiana De. “Multidrug Resistance Protein 1 (MDR1) and Glycosphingolipids Biosynthesis: Advantages for Therapeutics.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/19262.

MLA Handbook (7th Edition):

Rosa, Maria Fabiana De. “Multidrug Resistance Protein 1 (MDR1) and Glycosphingolipids Biosynthesis: Advantages for Therapeutics.” 2009. Web. 21 Sep 2018.

Vancouver:

Rosa MFD. Multidrug Resistance Protein 1 (MDR1) and Glycosphingolipids Biosynthesis: Advantages for Therapeutics. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/19262.

Council of Science Editors:

Rosa MFD. Multidrug Resistance Protein 1 (MDR1) and Glycosphingolipids Biosynthesis: Advantages for Therapeutics. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/19262

8. McLean, Jesse Ryan. Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis.

Degree: 2009, University of Toronto

Peripherin is a type III intermediate filament protein that is predominately expressed in the peripheral nervous system and in subsets of efferent projections in the… (more)

Subjects/Keywords: Amyotrophic Lateral Sclerosis (ALS); Isoforms; alternative translation; aggregation; 0317

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APA (6th Edition):

McLean, J. R. (2009). Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32015

Chicago Manual of Style (16th Edition):

McLean, Jesse Ryan. “Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32015.

MLA Handbook (7th Edition):

McLean, Jesse Ryan. “Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis.” 2009. Web. 21 Sep 2018.

Vancouver:

McLean JR. Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32015.

Council of Science Editors:

McLean JR. Characterization of Peripherin Isoforms in Amyotrophic Lateral Sclerosis. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/32015

9. Eissa, Azza. Characterization of Kallikrein-related Peptidase-8 in Normal Human Epidermis and Psoriasis.

Degree: 2013, University of Toronto

Kallikrein-8 (KLK8) is a relatively-uncharacterized epidermal protease. Although proposed to regulate wound-healing and barrier repair in KLK8-deficient mouse skin, KLK8-catalytic activity was never demonstrated in… (more)

Subjects/Keywords: Kallikrein; Epidermis; Stratum corneum; Psoriasis; 0487; 0307

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APA (6th Edition):

Eissa, A. (2013). Characterization of Kallikrein-related Peptidase-8 in Normal Human Epidermis and Psoriasis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/43602

Chicago Manual of Style (16th Edition):

Eissa, Azza. “Characterization of Kallikrein-related Peptidase-8 in Normal Human Epidermis and Psoriasis.” 2013. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/43602.

MLA Handbook (7th Edition):

Eissa, Azza. “Characterization of Kallikrein-related Peptidase-8 in Normal Human Epidermis and Psoriasis.” 2013. Web. 21 Sep 2018.

Vancouver:

Eissa A. Characterization of Kallikrein-related Peptidase-8 in Normal Human Epidermis and Psoriasis. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/43602.

Council of Science Editors:

Eissa A. Characterization of Kallikrein-related Peptidase-8 in Normal Human Epidermis and Psoriasis. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43602

10. Wang, Jenny Jing. Discovery of a VEGF-A Responsive lincRNA in Human Endothelial Cells with Disease Relevance and Anti-angiogenic Therapeutic Potential in Glioblastoma Multiforme.

Degree: 2014, University of Toronto

Large intergenic RNAs (lincRNA) are involved in numerous cellular processes, including many relevant to normal development and cancer progression. In my doctoral research, we hypothesized… (more)

Subjects/Keywords: lincRNAs; Glioblastoma; 0564; 0992; 0379

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APA (6th Edition):

Wang, J. J. (2014). Discovery of a VEGF-A Responsive lincRNA in Human Endothelial Cells with Disease Relevance and Anti-angiogenic Therapeutic Potential in Glioblastoma Multiforme. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/44140

Chicago Manual of Style (16th Edition):

Wang, Jenny Jing. “Discovery of a VEGF-A Responsive lincRNA in Human Endothelial Cells with Disease Relevance and Anti-angiogenic Therapeutic Potential in Glioblastoma Multiforme.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/44140.

MLA Handbook (7th Edition):

Wang, Jenny Jing. “Discovery of a VEGF-A Responsive lincRNA in Human Endothelial Cells with Disease Relevance and Anti-angiogenic Therapeutic Potential in Glioblastoma Multiforme.” 2014. Web. 21 Sep 2018.

Vancouver:

Wang JJ. Discovery of a VEGF-A Responsive lincRNA in Human Endothelial Cells with Disease Relevance and Anti-angiogenic Therapeutic Potential in Glioblastoma Multiforme. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/44140.

Council of Science Editors:

Wang JJ. Discovery of a VEGF-A Responsive lincRNA in Human Endothelial Cells with Disease Relevance and Anti-angiogenic Therapeutic Potential in Glioblastoma Multiforme. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/44140

11. Kuzmanov, Uros. Characterization of Kallikrein 6 N-glycosylation Patterns and Identification of Sialylated Glycoproteins in Ovarian Cancer.

Degree: 2013, University of Toronto

Ovarian cancer is the leading cause of death among all gynecological disorders. Aberrant glycosylation, or more specifically, increased sialylation of proteins has been observed in… (more)

Subjects/Keywords: glycosylation; ovarian cancer; 0487

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APA (6th Edition):

Kuzmanov, U. (2013). Characterization of Kallikrein 6 N-glycosylation Patterns and Identification of Sialylated Glycoproteins in Ovarian Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/35871

Chicago Manual of Style (16th Edition):

Kuzmanov, Uros. “Characterization of Kallikrein 6 N-glycosylation Patterns and Identification of Sialylated Glycoproteins in Ovarian Cancer.” 2013. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/35871.

MLA Handbook (7th Edition):

Kuzmanov, Uros. “Characterization of Kallikrein 6 N-glycosylation Patterns and Identification of Sialylated Glycoproteins in Ovarian Cancer.” 2013. Web. 21 Sep 2018.

Vancouver:

Kuzmanov U. Characterization of Kallikrein 6 N-glycosylation Patterns and Identification of Sialylated Glycoproteins in Ovarian Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/35871.

Council of Science Editors:

Kuzmanov U. Characterization of Kallikrein 6 N-glycosylation Patterns and Identification of Sialylated Glycoproteins in Ovarian Cancer. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35871

12. Lee, Jooeun. Sensing of Bacterial Peptidoglycan by Peptidoglycan Recognition Molecules.

Degree: 2013, University of Toronto

Peptidoglycan is an essential component of bacteria that provide structure and integrity of the cell. The main goal of this thesis has been to study… (more)

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APA (6th Edition):

Lee, J. (2013). Sensing of Bacterial Peptidoglycan by Peptidoglycan Recognition Molecules. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/35877

Chicago Manual of Style (16th Edition):

Lee, Jooeun. “Sensing of Bacterial Peptidoglycan by Peptidoglycan Recognition Molecules.” 2013. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/35877.

MLA Handbook (7th Edition):

Lee, Jooeun. “Sensing of Bacterial Peptidoglycan by Peptidoglycan Recognition Molecules.” 2013. Web. 21 Sep 2018.

Vancouver:

Lee J. Sensing of Bacterial Peptidoglycan by Peptidoglycan Recognition Molecules. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/35877.

Council of Science Editors:

Lee J. Sensing of Bacterial Peptidoglycan by Peptidoglycan Recognition Molecules. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/35877

13. Organ, Shawna L. c-MET and KRAS: Signalling and Clinical Implications in Colorectal Cancer.

Degree: 2013, University of Toronto

Colorectal cancer (CRC) is the third leading cause of death from cancer in North America. The KRAS gene is mutated in approximately 40-50% of all… (more)

Subjects/Keywords: c-MET; KRAS; 0379

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APA (6th Edition):

Organ, S. L. (2013). c-MET and KRAS: Signalling and Clinical Implications in Colorectal Cancer. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/43691

Chicago Manual of Style (16th Edition):

Organ, Shawna L. “c-MET and KRAS: Signalling and Clinical Implications in Colorectal Cancer.” 2013. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/43691.

MLA Handbook (7th Edition):

Organ, Shawna L. “c-MET and KRAS: Signalling and Clinical Implications in Colorectal Cancer.” 2013. Web. 21 Sep 2018.

Vancouver:

Organ SL. c-MET and KRAS: Signalling and Clinical Implications in Colorectal Cancer. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/43691.

Council of Science Editors:

Organ SL. c-MET and KRAS: Signalling and Clinical Implications in Colorectal Cancer. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43691

14. Oliver, Jordan. Role of Epithelium-specific ETS Transcription Factor-1 in Airway Epithelial Regeneration.

Degree: 2012, University of Toronto

Human epithelium-specific ETS transcription factor-1 (ESE-1), which is also known as E74-like factor-3 (Elf3) in mice, is strongly expressed in lung during fetal development and… (more)

Subjects/Keywords: ESE-1; ETS; transcription factor; airway epithelial injury; airway epithelial regeneration; 0571; 0719; 0383

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APA (6th Edition):

Oliver, J. (2012). Role of Epithelium-specific ETS Transcription Factor-1 in Airway Epithelial Regeneration. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32316

Chicago Manual of Style (16th Edition):

Oliver, Jordan. “Role of Epithelium-specific ETS Transcription Factor-1 in Airway Epithelial Regeneration.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32316.

MLA Handbook (7th Edition):

Oliver, Jordan. “Role of Epithelium-specific ETS Transcription Factor-1 in Airway Epithelial Regeneration.” 2012. Web. 21 Sep 2018.

Vancouver:

Oliver J. Role of Epithelium-specific ETS Transcription Factor-1 in Airway Epithelial Regeneration. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32316.

Council of Science Editors:

Oliver J. Role of Epithelium-specific ETS Transcription Factor-1 in Airway Epithelial Regeneration. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32316

15. Ling, Erick. Notch Pathway Blockade in Human Glioblastoma Stem Cells Defines Heterogeneity and Sensitivity to Neuronal Lineage Commitment.

Degree: 2012, University of Toronto

Glioblastoma is the commonest form of brain neoplasm and among the most malignant forms of cancer. The identification of a subpopulation of self-renewing and multipotent… (more)

Subjects/Keywords: Glioblastoma; Cancer stem cells; Notch signaling; 0992

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APA (6th Edition):

Ling, E. (2012). Notch Pathway Blockade in Human Glioblastoma Stem Cells Defines Heterogeneity and Sensitivity to Neuronal Lineage Commitment. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/44086

Chicago Manual of Style (16th Edition):

Ling, Erick. “Notch Pathway Blockade in Human Glioblastoma Stem Cells Defines Heterogeneity and Sensitivity to Neuronal Lineage Commitment.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/44086.

MLA Handbook (7th Edition):

Ling, Erick. “Notch Pathway Blockade in Human Glioblastoma Stem Cells Defines Heterogeneity and Sensitivity to Neuronal Lineage Commitment.” 2012. Web. 21 Sep 2018.

Vancouver:

Ling E. Notch Pathway Blockade in Human Glioblastoma Stem Cells Defines Heterogeneity and Sensitivity to Neuronal Lineage Commitment. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/44086.

Council of Science Editors:

Ling E. Notch Pathway Blockade in Human Glioblastoma Stem Cells Defines Heterogeneity and Sensitivity to Neuronal Lineage Commitment. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/44086

16. Rubino, Stephen. New Insights into the Regulation of Intestinal Immunity by Nod1 and Nod2.

Degree: 2014, University of Toronto

Nod1 and Nod2 are intracellular pattern recognition receptors that detect specific moieties of peptidoglycan, a critical component of the bacterial cell wall, to initiate host… (more)

Subjects/Keywords: Innate Immunity; Th17; 0982

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APA (6th Edition):

Rubino, S. (2014). New Insights into the Regulation of Intestinal Immunity by Nod1 and Nod2. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/44135

Chicago Manual of Style (16th Edition):

Rubino, Stephen. “New Insights into the Regulation of Intestinal Immunity by Nod1 and Nod2.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/44135.

MLA Handbook (7th Edition):

Rubino, Stephen. “New Insights into the Regulation of Intestinal Immunity by Nod1 and Nod2.” 2014. Web. 21 Sep 2018.

Vancouver:

Rubino S. New Insights into the Regulation of Intestinal Immunity by Nod1 and Nod2. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/44135.

Council of Science Editors:

Rubino S. New Insights into the Regulation of Intestinal Immunity by Nod1 and Nod2. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/44135

17. Baker, Amy. Disruption of Lymphatic Function following Lymph Node Excision and Irradiation: Integrating Natural Compensatory Responses with Potential Therapeutic Approaches to Facilitate Lymph Flow Restoration.

Degree: 2014, University of Toronto

Introduction: The removal or irradiation of one or more lymph nodes during cancer surgery appears to be a significant causative factor in lymphedema development. In… (more)

Subjects/Keywords: Lymphedema; Breast Cancer; Lymphatics; Radiation Therapy; Lymph node; 0571, 0574, 0719, 0564, 0433

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APA (6th Edition):

Baker, A. (2014). Disruption of Lymphatic Function following Lymph Node Excision and Irradiation: Integrating Natural Compensatory Responses with Potential Therapeutic Approaches to Facilitate Lymph Flow Restoration. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69049

Chicago Manual of Style (16th Edition):

Baker, Amy. “Disruption of Lymphatic Function following Lymph Node Excision and Irradiation: Integrating Natural Compensatory Responses with Potential Therapeutic Approaches to Facilitate Lymph Flow Restoration.” 2014. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/69049.

MLA Handbook (7th Edition):

Baker, Amy. “Disruption of Lymphatic Function following Lymph Node Excision and Irradiation: Integrating Natural Compensatory Responses with Potential Therapeutic Approaches to Facilitate Lymph Flow Restoration.” 2014. Web. 21 Sep 2018.

Vancouver:

Baker A. Disruption of Lymphatic Function following Lymph Node Excision and Irradiation: Integrating Natural Compensatory Responses with Potential Therapeutic Approaches to Facilitate Lymph Flow Restoration. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/69049.

Council of Science Editors:

Baker A. Disruption of Lymphatic Function following Lymph Node Excision and Irradiation: Integrating Natural Compensatory Responses with Potential Therapeutic Approaches to Facilitate Lymph Flow Restoration. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/69049

18. Dubuc, Adrian. Mining the Medulloblastoma Genome and Transcriptome.

Degree: 2013, University of Toronto

Medulloblastoma is a devastating disease of the cerebellum, and the most common solid pediatric malignancy of the central nervous system. Recently, transcriptome-wide profiling has dissected… (more)

Subjects/Keywords: medulloblastoma; cancer; brain tumor; epigenetics; genomics; 0992; 0571; 0564

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APA (6th Edition):

Dubuc, A. (2013). Mining the Medulloblastoma Genome and Transcriptome. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/43530

Chicago Manual of Style (16th Edition):

Dubuc, Adrian. “Mining the Medulloblastoma Genome and Transcriptome.” 2013. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/43530.

MLA Handbook (7th Edition):

Dubuc, Adrian. “Mining the Medulloblastoma Genome and Transcriptome.” 2013. Web. 21 Sep 2018.

Vancouver:

Dubuc A. Mining the Medulloblastoma Genome and Transcriptome. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/43530.

Council of Science Editors:

Dubuc A. Mining the Medulloblastoma Genome and Transcriptome. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43530

19. Ciavarra, Giovanni. The Role of the Retinoblastoma Protein Family in Skeletal Myogenesis.

Degree: 2011, University of Toronto

The retinoblastoma tumor suppressor (pRb) is thought to orchestrate terminal differentiation by inhibiting cell proliferation and apoptosis and stimulating lineage-specific transcription factors. In this thesis… (more)

Subjects/Keywords: skeletal myogenesis; muscle; differentiation; retinoblastoma; pRb; autophagy; p107; p130; Rb; cell cycle; 0379; 0307

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APA (6th Edition):

Ciavarra, G. (2011). The Role of the Retinoblastoma Protein Family in Skeletal Myogenesis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/29688

Chicago Manual of Style (16th Edition):

Ciavarra, Giovanni. “The Role of the Retinoblastoma Protein Family in Skeletal Myogenesis.” 2011. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/29688.

MLA Handbook (7th Edition):

Ciavarra, Giovanni. “The Role of the Retinoblastoma Protein Family in Skeletal Myogenesis.” 2011. Web. 21 Sep 2018.

Vancouver:

Ciavarra G. The Role of the Retinoblastoma Protein Family in Skeletal Myogenesis. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/29688.

Council of Science Editors:

Ciavarra G. The Role of the Retinoblastoma Protein Family in Skeletal Myogenesis. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29688

20. Cho, Chan-Kyung Jane. Identification and Verification of Candidate Biomarkers for Down Syndrome and Discovery of Dysregulated Molecular Pathways in Amniocytes by Proteomics Approaches.

Degree: 2012, University of Toronto

Down syndrome (DS), caused by an extra chromosome 21, affects 1 in 750 live births, and is characterized by cognitive impairment as well as several… (more)

Subjects/Keywords: Proteomics; Down syndrome; 0566

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APA (6th Edition):

Cho, C. J. (2012). Identification and Verification of Candidate Biomarkers for Down Syndrome and Discovery of Dysregulated Molecular Pathways in Amniocytes by Proteomics Approaches. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/33873

Chicago Manual of Style (16th Edition):

Cho, Chan-Kyung Jane. “Identification and Verification of Candidate Biomarkers for Down Syndrome and Discovery of Dysregulated Molecular Pathways in Amniocytes by Proteomics Approaches.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/33873.

MLA Handbook (7th Edition):

Cho, Chan-Kyung Jane. “Identification and Verification of Candidate Biomarkers for Down Syndrome and Discovery of Dysregulated Molecular Pathways in Amniocytes by Proteomics Approaches.” 2012. Web. 21 Sep 2018.

Vancouver:

Cho CJ. Identification and Verification of Candidate Biomarkers for Down Syndrome and Discovery of Dysregulated Molecular Pathways in Amniocytes by Proteomics Approaches. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/33873.

Council of Science Editors:

Cho CJ. Identification and Verification of Candidate Biomarkers for Down Syndrome and Discovery of Dysregulated Molecular Pathways in Amniocytes by Proteomics Approaches. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33873

21. Kushwah, Rahul. Vector Specific Tolerance Induction for Airwary Gene Therapy.

Degree: 2011, University of Toronto

The success of adenoviral mediated airway gene therapy is hindered by host immune responses against adenoviral vectors. Helper-dependent adenoviral vectors (HD-Ad) are devoid of viral… (more)

Subjects/Keywords: Dendritic Cells; Tolerance; Adenovirus; Gene Therapy; 0982; 0720; 0369

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APA (6th Edition):

Kushwah, R. (2011). Vector Specific Tolerance Induction for Airwary Gene Therapy. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/31809

Chicago Manual of Style (16th Edition):

Kushwah, Rahul. “Vector Specific Tolerance Induction for Airwary Gene Therapy.” 2011. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/31809.

MLA Handbook (7th Edition):

Kushwah, Rahul. “Vector Specific Tolerance Induction for Airwary Gene Therapy.” 2011. Web. 21 Sep 2018.

Vancouver:

Kushwah R. Vector Specific Tolerance Induction for Airwary Gene Therapy. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/31809.

Council of Science Editors:

Kushwah R. Vector Specific Tolerance Induction for Airwary Gene Therapy. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31809

22. Conroy, Andrea. Biomarkers of Severe Malaria: Complement Activation and Dysregulated Angiogenesis in Placental Malaria and Cerebral Malaria.

Degree: 2011, University of Toronto

Biomarkers measured in the blood can provide information about disease pathophysiology, diagnosis and prognosis. Pronounced proinflammatory responses are characteristic of severe malaria, and excessive activation… (more)

Subjects/Keywords: Malaria; Biomarker; Pregnancy; Complement; Angiogenesis; 0982; 0380; 0766; 0718

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APA (6th Edition):

Conroy, A. (2011). Biomarkers of Severe Malaria: Complement Activation and Dysregulated Angiogenesis in Placental Malaria and Cerebral Malaria. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32064

Chicago Manual of Style (16th Edition):

Conroy, Andrea. “Biomarkers of Severe Malaria: Complement Activation and Dysregulated Angiogenesis in Placental Malaria and Cerebral Malaria.” 2011. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32064.

MLA Handbook (7th Edition):

Conroy, Andrea. “Biomarkers of Severe Malaria: Complement Activation and Dysregulated Angiogenesis in Placental Malaria and Cerebral Malaria.” 2011. Web. 21 Sep 2018.

Vancouver:

Conroy A. Biomarkers of Severe Malaria: Complement Activation and Dysregulated Angiogenesis in Placental Malaria and Cerebral Malaria. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32064.

Council of Science Editors:

Conroy A. Biomarkers of Severe Malaria: Complement Activation and Dysregulated Angiogenesis in Placental Malaria and Cerebral Malaria. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/32064

23. Bikopoulos, George. Novel Molecular Mechanisms Controlling Pancreatic β-cell Function and Hepatic Glucose Homeostasis.

Degree: 2012, University of Toronto

The key defects characteristic of hyperglycemia in T2D include increased hepatic glucose production, a diminution of insulin secretion, and an absolute impairment in peripheral insulin… (more)

Subjects/Keywords: Pancreas; Liver; Transcription; Free fatty acids; 0307

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APA (6th Edition):

Bikopoulos, G. (2012). Novel Molecular Mechanisms Controlling Pancreatic β-cell Function and Hepatic Glucose Homeostasis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/42482

Chicago Manual of Style (16th Edition):

Bikopoulos, George. “Novel Molecular Mechanisms Controlling Pancreatic β-cell Function and Hepatic Glucose Homeostasis.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/42482.

MLA Handbook (7th Edition):

Bikopoulos, George. “Novel Molecular Mechanisms Controlling Pancreatic β-cell Function and Hepatic Glucose Homeostasis.” 2012. Web. 21 Sep 2018.

Vancouver:

Bikopoulos G. Novel Molecular Mechanisms Controlling Pancreatic β-cell Function and Hepatic Glucose Homeostasis. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/42482.

Council of Science Editors:

Bikopoulos G. Novel Molecular Mechanisms Controlling Pancreatic β-cell Function and Hepatic Glucose Homeostasis. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/42482

24. Chow, Man Chi Edith. Destabilization of IL-8 mRNA by Anthrax Lethal Toxin: Demonstration of the Requirement for TTP and Examination of its Cellular Interactions.

Degree: 2012, University of Toronto

Control of mRNA stability is an important aspect in the regulation of gene expression. A well studied signal for rapid transcript decay in mammalian cells… (more)

Subjects/Keywords: Anthrax lethal toxin; mRNA destabilization; Tristetraprolin; 0410; 0307

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APA (6th Edition):

Chow, M. C. E. (2012). Destabilization of IL-8 mRNA by Anthrax Lethal Toxin: Demonstration of the Requirement for TTP and Examination of its Cellular Interactions. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/33880

Chicago Manual of Style (16th Edition):

Chow, Man Chi Edith. “Destabilization of IL-8 mRNA by Anthrax Lethal Toxin: Demonstration of the Requirement for TTP and Examination of its Cellular Interactions.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/33880.

MLA Handbook (7th Edition):

Chow, Man Chi Edith. “Destabilization of IL-8 mRNA by Anthrax Lethal Toxin: Demonstration of the Requirement for TTP and Examination of its Cellular Interactions.” 2012. Web. 21 Sep 2018.

Vancouver:

Chow MCE. Destabilization of IL-8 mRNA by Anthrax Lethal Toxin: Demonstration of the Requirement for TTP and Examination of its Cellular Interactions. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/33880.

Council of Science Editors:

Chow MCE. Destabilization of IL-8 mRNA by Anthrax Lethal Toxin: Demonstration of the Requirement for TTP and Examination of its Cellular Interactions. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33880

25. Emami, Nashmil. Identification and Functional Characterization of a Novel Activation Cascade of the KLK Family in Seminal Plasma.

Degree: 2009, University of Toronto

Proteolytic processes are often mediated by highly orchestrated cascades, through which protease enzymes function coordinately to ensure a stepwise activation. This thesis presents experimental data… (more)

Subjects/Keywords: Proteolytic Cascade; kallikrein-related peptidases; 0307

Pathobiology University of Toronto ©Copyright by Nashmil Emami (2009) Identification and… …Nashmil Emami Doctor of Philosophy 2009 Department of Laboratory Medicine and Pathobiology… …the Degree of Doctor of Philosophy Graduate Department of Laboratory Medicine and… …University of Toronto ABSTRACT Proteolytic processes are often mediated by highly orchestrated… 

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APA (6th Edition):

Emami, N. (2009). Identification and Functional Characterization of a Novel Activation Cascade of the KLK Family in Seminal Plasma. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/17757

Chicago Manual of Style (16th Edition):

Emami, Nashmil. “Identification and Functional Characterization of a Novel Activation Cascade of the KLK Family in Seminal Plasma.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/17757.

MLA Handbook (7th Edition):

Emami, Nashmil. “Identification and Functional Characterization of a Novel Activation Cascade of the KLK Family in Seminal Plasma.” 2009. Web. 21 Sep 2018.

Vancouver:

Emami N. Identification and Functional Characterization of a Novel Activation Cascade of the KLK Family in Seminal Plasma. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/17757.

Council of Science Editors:

Emami N. Identification and Functional Characterization of a Novel Activation Cascade of the KLK Family in Seminal Plasma. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/17757

26. Ward, Ryan. Identification and Characterization of Cancer Stem Cells in Mouse Medulloblastoma and Glioma.

Degree: 2010, University of Toronto

According to the cancer stem cell hypothesis a subpopulation of cells within a tumour has the capacity to sustain its growth. These cells are termed… (more)

Subjects/Keywords: Medulloblastoma; Glioma; Cancer Stem Cell; Mouse Model; 0992

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APA (6th Edition):

Ward, R. (2010). Identification and Characterization of Cancer Stem Cells in Mouse Medulloblastoma and Glioma. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32053

Chicago Manual of Style (16th Edition):

Ward, Ryan. “Identification and Characterization of Cancer Stem Cells in Mouse Medulloblastoma and Glioma.” 2010. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32053.

MLA Handbook (7th Edition):

Ward, Ryan. “Identification and Characterization of Cancer Stem Cells in Mouse Medulloblastoma and Glioma.” 2010. Web. 21 Sep 2018.

Vancouver:

Ward R. Identification and Characterization of Cancer Stem Cells in Mouse Medulloblastoma and Glioma. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32053.

Council of Science Editors:

Ward R. Identification and Characterization of Cancer Stem Cells in Mouse Medulloblastoma and Glioma. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32053

27. Russell, Ryan. Molecular Characterization of the von Hippel-Lindau Tumour Suppressor Protein.

Degree: 2009, University of Toronto

Inheritance of one mutant von Hippel-Lindau (VHL) allele gives rise to the development of the autosomal dominant VHL disease, which affects approximately 1 in 36… (more)

Subjects/Keywords: VHL; Hypoxia; 0307

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APA (6th Edition):

Russell, R. (2009). Molecular Characterization of the von Hippel-Lindau Tumour Suppressor Protein. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32019

Chicago Manual of Style (16th Edition):

Russell, Ryan. “Molecular Characterization of the von Hippel-Lindau Tumour Suppressor Protein.” 2009. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32019.

MLA Handbook (7th Edition):

Russell, Ryan. “Molecular Characterization of the von Hippel-Lindau Tumour Suppressor Protein.” 2009. Web. 21 Sep 2018.

Vancouver:

Russell R. Molecular Characterization of the von Hippel-Lindau Tumour Suppressor Protein. [Internet] [Doctoral dissertation]. University of Toronto; 2009. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32019.

Council of Science Editors:

Russell R. Molecular Characterization of the von Hippel-Lindau Tumour Suppressor Protein. [Doctoral Dissertation]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/32019

28. Torti, Dax. Functional Roles of the SWI/SNF ATPase Brahma Related Gene 1 (BRG1) and Special AT-Rich Binding Protein (SATB1) in Virus Response and Innate Immunity.

Degree: 2012, University of Toronto

The innate immune response is a primary transcriptional defence network activated by interferons (IFNs) α/ β in response to viral infection. A cell must have… (more)

Subjects/Keywords: BRG1; SATB1; Interferon; Innate Immunity; 0307

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APA (6th Edition):

Torti, D. (2012). Functional Roles of the SWI/SNF ATPase Brahma Related Gene 1 (BRG1) and Special AT-Rich Binding Protein (SATB1) in Virus Response and Innate Immunity. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32831

Chicago Manual of Style (16th Edition):

Torti, Dax. “Functional Roles of the SWI/SNF ATPase Brahma Related Gene 1 (BRG1) and Special AT-Rich Binding Protein (SATB1) in Virus Response and Innate Immunity.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/32831.

MLA Handbook (7th Edition):

Torti, Dax. “Functional Roles of the SWI/SNF ATPase Brahma Related Gene 1 (BRG1) and Special AT-Rich Binding Protein (SATB1) in Virus Response and Innate Immunity.” 2012. Web. 21 Sep 2018.

Vancouver:

Torti D. Functional Roles of the SWI/SNF ATPase Brahma Related Gene 1 (BRG1) and Special AT-Rich Binding Protein (SATB1) in Virus Response and Innate Immunity. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/32831.

Council of Science Editors:

Torti D. Functional Roles of the SWI/SNF ATPase Brahma Related Gene 1 (BRG1) and Special AT-Rich Binding Protein (SATB1) in Virus Response and Innate Immunity. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32831

29. Weerasekera, Rasanjala Kumari. The Development of Novel Protein Topology Mapping Strategies using Crosslinking, Cyanogen Bromide Cleavage, and Mass Spectrometry.

Degree: 2011, University of Toronto

Advances in protein topology mapping methods are urgently needed to complement the wealth of interactome data that is presently being generated at a rapid pace.… (more)

Subjects/Keywords: protein structure; mass spectrometry; chemical crosslinking; interface mapping; proteomics; protein topology mapping; cyanogen bromide; interactome; method development; HPLC; 0307

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APA (6th Edition):

Weerasekera, R. K. (2011). The Development of Novel Protein Topology Mapping Strategies using Crosslinking, Cyanogen Bromide Cleavage, and Mass Spectrometry. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/31969

Chicago Manual of Style (16th Edition):

Weerasekera, Rasanjala Kumari. “The Development of Novel Protein Topology Mapping Strategies using Crosslinking, Cyanogen Bromide Cleavage, and Mass Spectrometry.” 2011. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/31969.

MLA Handbook (7th Edition):

Weerasekera, Rasanjala Kumari. “The Development of Novel Protein Topology Mapping Strategies using Crosslinking, Cyanogen Bromide Cleavage, and Mass Spectrometry.” 2011. Web. 21 Sep 2018.

Vancouver:

Weerasekera RK. The Development of Novel Protein Topology Mapping Strategies using Crosslinking, Cyanogen Bromide Cleavage, and Mass Spectrometry. [Internet] [Doctoral dissertation]. University of Toronto; 2011. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/31969.

Council of Science Editors:

Weerasekera RK. The Development of Novel Protein Topology Mapping Strategies using Crosslinking, Cyanogen Bromide Cleavage, and Mass Spectrometry. [Doctoral Dissertation]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31969

30. Pacal, Marek. Coordinating Cell Cycle Exit and Differentiation in the Mammalian Retina and its Dependence on Rb.

Degree: 2012, University of Toronto

Cell cycle exit (“birth”) of retinal progenitor cells (RPCs) is considered a watershed that is preceded by changing levels of cell cycle regulators, and followed… (more)

Subjects/Keywords: Retina; Retinoblastoma cell of origin; Cell cycle exit control; 0307

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APA (6th Edition):

Pacal, M. (2012). Coordinating Cell Cycle Exit and Differentiation in the Mammalian Retina and its Dependence on Rb. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/33857

Chicago Manual of Style (16th Edition):

Pacal, Marek. “Coordinating Cell Cycle Exit and Differentiation in the Mammalian Retina and its Dependence on Rb.” 2012. Doctoral Dissertation, University of Toronto. Accessed September 21, 2018. http://hdl.handle.net/1807/33857.

MLA Handbook (7th Edition):

Pacal, Marek. “Coordinating Cell Cycle Exit and Differentiation in the Mammalian Retina and its Dependence on Rb.” 2012. Web. 21 Sep 2018.

Vancouver:

Pacal M. Coordinating Cell Cycle Exit and Differentiation in the Mammalian Retina and its Dependence on Rb. [Internet] [Doctoral dissertation]. University of Toronto; 2012. [cited 2018 Sep 21]. Available from: http://hdl.handle.net/1807/33857.

Council of Science Editors:

Pacal M. Coordinating Cell Cycle Exit and Differentiation in the Mammalian Retina and its Dependence on Rb. [Doctoral Dissertation]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33857

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