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You searched for subject:(0982). Showing records 1 – 30 of 470 total matches.

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University of Toronto

1. Lee, Korris. Dynamic Regulation of CD8+ T cell Signalling by the Adaptor Protein 3BP2.

Degree: 2014, University of Toronto

AbstractDynamic Regulation of CD8+ T Cells by the Adaptor Protein 3BP2Korris Lee © 2014 MSc Department of Immunology, University of TorontoCD8+ T cells fill an… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Lee, K. (2014). Dynamic Regulation of CD8+ T cell Signalling by the Adaptor Protein 3BP2. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67901

Chicago Manual of Style (16th Edition):

Lee, Korris. “Dynamic Regulation of CD8+ T cell Signalling by the Adaptor Protein 3BP2.” 2014. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/67901.

MLA Handbook (7th Edition):

Lee, Korris. “Dynamic Regulation of CD8+ T cell Signalling by the Adaptor Protein 3BP2.” 2014. Web. 29 Oct 2020.

Vancouver:

Lee K. Dynamic Regulation of CD8+ T cell Signalling by the Adaptor Protein 3BP2. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/67901.

Council of Science Editors:

Lee K. Dynamic Regulation of CD8+ T cell Signalling by the Adaptor Protein 3BP2. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67901


University of Toronto

2. Shiu, Maria. Modulation of T Cell Distribution and Function by High-intensity Interval Training.

Degree: 2016, University of Toronto

High-intensity interval training (HIIT) may disrupt immunity. Regulatory T cells (Tregs) are important in restoring immune homeostasis. This study investigated the impact of acute versus… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Shiu, M. (2016). Modulation of T Cell Distribution and Function by High-intensity Interval Training. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/71708

Chicago Manual of Style (16th Edition):

Shiu, Maria. “Modulation of T Cell Distribution and Function by High-intensity Interval Training.” 2016. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/71708.

MLA Handbook (7th Edition):

Shiu, Maria. “Modulation of T Cell Distribution and Function by High-intensity Interval Training.” 2016. Web. 29 Oct 2020.

Vancouver:

Shiu M. Modulation of T Cell Distribution and Function by High-intensity Interval Training. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/71708.

Council of Science Editors:

Shiu M. Modulation of T Cell Distribution and Function by High-intensity Interval Training. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/71708


University of Toronto

3. Tanic, Milica. Role of Notch Signaling in Human T Cell Activation using Artificial Antigen Presenting Cells.

Degree: 2016, University of Toronto

Adoptive cell transfer of ex vivo-expanded tumor infiltrating lymphocytes (TILs) is an emerging approach for treating cancers. One limitation in this approach is the use… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Tanic, M. (2016). Role of Notch Signaling in Human T Cell Activation using Artificial Antigen Presenting Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76124

Chicago Manual of Style (16th Edition):

Tanic, Milica. “Role of Notch Signaling in Human T Cell Activation using Artificial Antigen Presenting Cells.” 2016. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/76124.

MLA Handbook (7th Edition):

Tanic, Milica. “Role of Notch Signaling in Human T Cell Activation using Artificial Antigen Presenting Cells.” 2016. Web. 29 Oct 2020.

Vancouver:

Tanic M. Role of Notch Signaling in Human T Cell Activation using Artificial Antigen Presenting Cells. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/76124.

Council of Science Editors:

Tanic M. Role of Notch Signaling in Human T Cell Activation using Artificial Antigen Presenting Cells. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76124


University of Toronto

4. Xhiku, Sintia. Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis.

Degree: 2016, University of Toronto

Hematopoietic development of pluripotent stem cells (PSCs) begins with the emergence of hemogenic endothelial (HE) precursors, followed by endothelial-to-hematopoietic transition (EHT). To test the effect… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Xhiku, S. (2016). Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76139

Chicago Manual of Style (16th Edition):

Xhiku, Sintia. “Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis.” 2016. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/76139.

MLA Handbook (7th Edition):

Xhiku, Sintia. “Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis.” 2016. Web. 29 Oct 2020.

Vancouver:

Xhiku S. Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/76139.

Council of Science Editors:

Xhiku S. Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76139


University of Toronto

5. Xhiku, Sintia. Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis.

Degree: 2016, University of Toronto

Hematopoietic development of pluripotent stem cells (PSCs) begins with the emergence of hemogenic endothelial (HE) precursors, followed by endothelial-to-hematopoietic transition (EHT). To test the effect… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Xhiku, S. (2016). Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/76207

Chicago Manual of Style (16th Edition):

Xhiku, Sintia. “Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis.” 2016. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/76207.

MLA Handbook (7th Edition):

Xhiku, Sintia. “Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis.” 2016. Web. 29 Oct 2020.

Vancouver:

Xhiku S. Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/76207.

Council of Science Editors:

Xhiku S. Role of Notch Signaling in Human Pluripotent Stem Cell-derived Hematopoiesis. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76207


University of Toronto

6. Oveisi, Morvarid. DISTINCT NEUTROPHIL RESPONSES TO ORAL COMMENSAL AND PATHOGENIC BIOFILMS.

Degree: 2018, University of Toronto

Periodontal disease, one of the most prevalent inflammatory conditions affecting millions of people each year, is initiated by microbial dysbiosis. The accumulation of bacteria in… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Oveisi, M. (2018). DISTINCT NEUTROPHIL RESPONSES TO ORAL COMMENSAL AND PATHOGENIC BIOFILMS. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/91513

Chicago Manual of Style (16th Edition):

Oveisi, Morvarid. “DISTINCT NEUTROPHIL RESPONSES TO ORAL COMMENSAL AND PATHOGENIC BIOFILMS.” 2018. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/91513.

MLA Handbook (7th Edition):

Oveisi, Morvarid. “DISTINCT NEUTROPHIL RESPONSES TO ORAL COMMENSAL AND PATHOGENIC BIOFILMS.” 2018. Web. 29 Oct 2020.

Vancouver:

Oveisi M. DISTINCT NEUTROPHIL RESPONSES TO ORAL COMMENSAL AND PATHOGENIC BIOFILMS. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/91513.

Council of Science Editors:

Oveisi M. DISTINCT NEUTROPHIL RESPONSES TO ORAL COMMENSAL AND PATHOGENIC BIOFILMS. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/91513


University of Toronto

7. Yam, Jennifer Yuen-Man. Exploring the Role of CCR6/CCL20 Axis in B Cell Migration into the CNS during EAE.

Degree: 2016, University of Toronto

B cells have been implicated in the pathogenesis of multiple sclerosis (MS) but how they migrate into the central nervous system (CNS) is poorly understood.… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Yam, J. Y. (2016). Exploring the Role of CCR6/CCL20 Axis in B Cell Migration into the CNS during EAE. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/92618

Chicago Manual of Style (16th Edition):

Yam, Jennifer Yuen-Man. “Exploring the Role of CCR6/CCL20 Axis in B Cell Migration into the CNS during EAE.” 2016. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/92618.

MLA Handbook (7th Edition):

Yam, Jennifer Yuen-Man. “Exploring the Role of CCR6/CCL20 Axis in B Cell Migration into the CNS during EAE.” 2016. Web. 29 Oct 2020.

Vancouver:

Yam JY. Exploring the Role of CCR6/CCL20 Axis in B Cell Migration into the CNS during EAE. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/92618.

Council of Science Editors:

Yam JY. Exploring the Role of CCR6/CCL20 Axis in B Cell Migration into the CNS during EAE. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/92618


University of Toronto

8. Cheng, Lee. Relevance of Neutrophils and Neutrophil Extracellular Traps in Bronchiolitis Obliterans Syndrome of Patients Receiving Stem Cell Therapy.

Degree: 2015, University of Toronto

Bronchiolitis Obliterans Syndrome (BOS) is a lung complication that occurs in children undergoing hematopoietic stem cell transplantation (HSCT) and is characterized by inflammation and airway… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Cheng, L. (2015). Relevance of Neutrophils and Neutrophil Extracellular Traps in Bronchiolitis Obliterans Syndrome of Patients Receiving Stem Cell Therapy. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/80272

Chicago Manual of Style (16th Edition):

Cheng, Lee. “Relevance of Neutrophils and Neutrophil Extracellular Traps in Bronchiolitis Obliterans Syndrome of Patients Receiving Stem Cell Therapy.” 2015. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/80272.

MLA Handbook (7th Edition):

Cheng, Lee. “Relevance of Neutrophils and Neutrophil Extracellular Traps in Bronchiolitis Obliterans Syndrome of Patients Receiving Stem Cell Therapy.” 2015. Web. 29 Oct 2020.

Vancouver:

Cheng L. Relevance of Neutrophils and Neutrophil Extracellular Traps in Bronchiolitis Obliterans Syndrome of Patients Receiving Stem Cell Therapy. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/80272.

Council of Science Editors:

Cheng L. Relevance of Neutrophils and Neutrophil Extracellular Traps in Bronchiolitis Obliterans Syndrome of Patients Receiving Stem Cell Therapy. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/80272


University of Toronto

9. Ensan, Sherine. The Origin and Maintenance of Resident Aortic Macrophages.

Degree: 2015, University of Toronto

Macrophages maintain tissues homeostasis, while also contributing to numerous pathological processes, making them attractive targets for therapeutic intervention. Therapeutic design however, requires detailed understanding of… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Ensan, S. (2015). The Origin and Maintenance of Resident Aortic Macrophages. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/80273

Chicago Manual of Style (16th Edition):

Ensan, Sherine. “The Origin and Maintenance of Resident Aortic Macrophages.” 2015. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/80273.

MLA Handbook (7th Edition):

Ensan, Sherine. “The Origin and Maintenance of Resident Aortic Macrophages.” 2015. Web. 29 Oct 2020.

Vancouver:

Ensan S. The Origin and Maintenance of Resident Aortic Macrophages. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/80273.

Council of Science Editors:

Ensan S. The Origin and Maintenance of Resident Aortic Macrophages. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/80273


University of Toronto

10. Achita, Paulina. Expansion and Characterization of Human Double Negative Regulatory T Cells.

Degree: 2018, University of Toronto

A subset of αβ-T cell receptor (TCR) positive, NK lineage marker negative, CD4−CD8− double negative regulatory T cells (DN Tregs) comprise only ~1% of peripheral… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Achita, P. (2018). Expansion and Characterization of Human Double Negative Regulatory T Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/82875

Chicago Manual of Style (16th Edition):

Achita, Paulina. “Expansion and Characterization of Human Double Negative Regulatory T Cells.” 2018. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/82875.

MLA Handbook (7th Edition):

Achita, Paulina. “Expansion and Characterization of Human Double Negative Regulatory T Cells.” 2018. Web. 29 Oct 2020.

Vancouver:

Achita P. Expansion and Characterization of Human Double Negative Regulatory T Cells. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/82875.

Council of Science Editors:

Achita P. Expansion and Characterization of Human Double Negative Regulatory T Cells. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/82875


University of Toronto

11. Pikor, Natalia. Elucidating Disease Modifying Roles of Radio-resistant, CNS Resident Cells in a Rodent Model of Multiple Sclerosis.

Degree: PhD, 2014, University of Toronto

Multiple sclerosis (MS) is an inflammatory disease of the central nervous system that can manifest as relapsing-remitting MS or progressive MS. Autoreactive T cells play… (more)

Subjects/Keywords: 0982

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APA (6th Edition):

Pikor, N. (2014). Elucidating Disease Modifying Roles of Radio-resistant, CNS Resident Cells in a Rodent Model of Multiple Sclerosis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/74788

Chicago Manual of Style (16th Edition):

Pikor, Natalia. “Elucidating Disease Modifying Roles of Radio-resistant, CNS Resident Cells in a Rodent Model of Multiple Sclerosis.” 2014. Doctoral Dissertation, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/74788.

MLA Handbook (7th Edition):

Pikor, Natalia. “Elucidating Disease Modifying Roles of Radio-resistant, CNS Resident Cells in a Rodent Model of Multiple Sclerosis.” 2014. Web. 29 Oct 2020.

Vancouver:

Pikor N. Elucidating Disease Modifying Roles of Radio-resistant, CNS Resident Cells in a Rodent Model of Multiple Sclerosis. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/74788.

Council of Science Editors:

Pikor N. Elucidating Disease Modifying Roles of Radio-resistant, CNS Resident Cells in a Rodent Model of Multiple Sclerosis. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/74788

12. Moemeni, Behrouz. Unique and Interdependent Roles of Lck and Fyn in TcR Signalling.

Degree: 2014, University of Toronto

It is not known whether or how the functions of Lck and Fyn are coordinated during TcR-medicated T cell activation. Our laboratory has previously demonstrated… (more)

Subjects/Keywords: Immunology; 0982

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APA (6th Edition):

Moemeni, B. (2014). Unique and Interdependent Roles of Lck and Fyn in TcR Signalling. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68995

Chicago Manual of Style (16th Edition):

Moemeni, Behrouz. “Unique and Interdependent Roles of Lck and Fyn in TcR Signalling.” 2014. Doctoral Dissertation, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/68995.

MLA Handbook (7th Edition):

Moemeni, Behrouz. “Unique and Interdependent Roles of Lck and Fyn in TcR Signalling.” 2014. Web. 29 Oct 2020.

Vancouver:

Moemeni B. Unique and Interdependent Roles of Lck and Fyn in TcR Signalling. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/68995.

Council of Science Editors:

Moemeni B. Unique and Interdependent Roles of Lck and Fyn in TcR Signalling. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68995


University of Toronto

13. Gregory, Allison. Structural and Functional Characteristics of a Soluble Form of Endoglin in the Context of Preeclampsia.

Degree: 2011, University of Toronto

Endoglin is an auxiliary receptor for ligands of TGF-β receptor superfamily, present in endothelial cells and the placental syncytiotrophoblast. The expression of placental membrane endoglin… (more)

Subjects/Keywords: preeclampsia; endoglin; 0982

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APA (6th Edition):

Gregory, A. (2011). Structural and Functional Characteristics of a Soluble Form of Endoglin in the Context of Preeclampsia. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30615

Chicago Manual of Style (16th Edition):

Gregory, Allison. “Structural and Functional Characteristics of a Soluble Form of Endoglin in the Context of Preeclampsia.” 2011. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/30615.

MLA Handbook (7th Edition):

Gregory, Allison. “Structural and Functional Characteristics of a Soluble Form of Endoglin in the Context of Preeclampsia.” 2011. Web. 29 Oct 2020.

Vancouver:

Gregory A. Structural and Functional Characteristics of a Soluble Form of Endoglin in the Context of Preeclampsia. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/30615.

Council of Science Editors:

Gregory A. Structural and Functional Characteristics of a Soluble Form of Endoglin in the Context of Preeclampsia. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30615


University of Toronto

14. Mikhailova, Anastassia. Characterization of a Novel Dendritic Cell Population.

Degree: 2012, University of Toronto

Conventional DC (cDC) arise from circulating immediate precursors (pre-cDC), and are currently thought to be terminally differentiated. Here we show that cDC are capable of… (more)

Subjects/Keywords: dendritic cell; 0982

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APA (6th Edition):

Mikhailova, A. (2012). Characterization of a Novel Dendritic Cell Population. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33452

Chicago Manual of Style (16th Edition):

Mikhailova, Anastassia. “Characterization of a Novel Dendritic Cell Population.” 2012. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/33452.

MLA Handbook (7th Edition):

Mikhailova, Anastassia. “Characterization of a Novel Dendritic Cell Population.” 2012. Web. 29 Oct 2020.

Vancouver:

Mikhailova A. Characterization of a Novel Dendritic Cell Population. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/33452.

Council of Science Editors:

Mikhailova A. Characterization of a Novel Dendritic Cell Population. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33452


University of Toronto

15. Shyu, Wendy Huei-Ping. Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation.

Degree: 2013, University of Toronto

Therapies that promote tolerance will improve outcomes in solid organ transplantation by eliminating the need for long-term immunosuppression. This thesis investigates two possible tolerance induction… (more)

Subjects/Keywords: Transplantation; Tolerance; 0982

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APA (6th Edition):

Shyu, W. H. (2013). Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42931

Chicago Manual of Style (16th Edition):

Shyu, Wendy Huei-Ping. “Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation.” 2013. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/42931.

MLA Handbook (7th Edition):

Shyu, Wendy Huei-Ping. “Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation.” 2013. Web. 29 Oct 2020.

Vancouver:

Shyu WH. Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/42931.

Council of Science Editors:

Shyu WH. Induction of Tolerance: Mechanisms and Implications for Clinical Transplantation. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42931


University of Toronto

16. Yi, Tae Joon. The Impact of Herpes Therapy on Genital and Systemic immunology.

Degree: 2013, University of Toronto

HIV infects more than 34 million people globally. Herpes simplex virus type 2 (HSV-2) has been associated with a 3-fold increase in the rate of… (more)

Subjects/Keywords: HIV; HSV; 0982

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APA (6th Edition):

Yi, T. J. (2013). The Impact of Herpes Therapy on Genital and Systemic immunology. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/75242

Chicago Manual of Style (16th Edition):

Yi, Tae Joon. “The Impact of Herpes Therapy on Genital and Systemic immunology.” 2013. Doctoral Dissertation, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/75242.

MLA Handbook (7th Edition):

Yi, Tae Joon. “The Impact of Herpes Therapy on Genital and Systemic immunology.” 2013. Web. 29 Oct 2020.

Vancouver:

Yi TJ. The Impact of Herpes Therapy on Genital and Systemic immunology. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/75242.

Council of Science Editors:

Yi TJ. The Impact of Herpes Therapy on Genital and Systemic immunology. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/75242


University of Toronto

17. Minty, Gillian Eleanor Summersgill. The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice.

Degree: 2013, University of Toronto

The New Zealand Black (NZB) mouse chromosome 13 (c13) is linked to development of autoimmunity. B6 mice containing a portion of NZBc13 (B6.NZBc13 (c13)) develop… (more)

Subjects/Keywords: Autoimmunity; mouse model; SLE; 0982

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APA (6th Edition):

Minty, G. E. S. (2013). The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43245

Chicago Manual of Style (16th Edition):

Minty, Gillian Eleanor Summersgill. “The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice.” 2013. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/43245.

MLA Handbook (7th Edition):

Minty, Gillian Eleanor Summersgill. “The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice.” 2013. Web. 29 Oct 2020.

Vancouver:

Minty GES. The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/43245.

Council of Science Editors:

Minty GES. The Role of TLR3 in the Development of Lupus-like Autoimmunity in B6.NZBc13 Mice. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43245


University of Toronto

18. Lifeso, Kimberley. Creation of a Retroviral RNAi Knockdown System to Investigate Gene Variants in SLE.

Degree: 2013, University of Toronto

Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by the production of autoantibodies against self-antigens. SLE has a complex multifactorial genetic basis. Genome wide… (more)

Subjects/Keywords: Immunology; Systemic Lupus Erythematosus; 0982

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APA (6th Edition):

Lifeso, K. (2013). Creation of a Retroviral RNAi Knockdown System to Investigate Gene Variants in SLE. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43083

Chicago Manual of Style (16th Edition):

Lifeso, Kimberley. “Creation of a Retroviral RNAi Knockdown System to Investigate Gene Variants in SLE.” 2013. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/43083.

MLA Handbook (7th Edition):

Lifeso, Kimberley. “Creation of a Retroviral RNAi Knockdown System to Investigate Gene Variants in SLE.” 2013. Web. 29 Oct 2020.

Vancouver:

Lifeso K. Creation of a Retroviral RNAi Knockdown System to Investigate Gene Variants in SLE. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/43083.

Council of Science Editors:

Lifeso K. Creation of a Retroviral RNAi Knockdown System to Investigate Gene Variants in SLE. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43083


University of Toronto

19. Kim, Nam Yun. Characterization of the Immune Basis for Reduced IFN-α in Serologically Active Clinically Quiescent SLE Patients.

Degree: 2015, University of Toronto

Serologically active clinically quiescent (SACQ) patients with systemic lupus erythematosus (SLE) are clinically quiescent despite the presence of autoantibodies. SACQ patients differ from serologically active… (more)

Subjects/Keywords: Interferon; SACQ; SLE; 0982

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APA (6th Edition):

Kim, N. Y. (2015). Characterization of the Immune Basis for Reduced IFN-α in Serologically Active Clinically Quiescent SLE Patients. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70417

Chicago Manual of Style (16th Edition):

Kim, Nam Yun. “Characterization of the Immune Basis for Reduced IFN-α in Serologically Active Clinically Quiescent SLE Patients.” 2015. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/70417.

MLA Handbook (7th Edition):

Kim, Nam Yun. “Characterization of the Immune Basis for Reduced IFN-α in Serologically Active Clinically Quiescent SLE Patients.” 2015. Web. 29 Oct 2020.

Vancouver:

Kim NY. Characterization of the Immune Basis for Reduced IFN-α in Serologically Active Clinically Quiescent SLE Patients. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/70417.

Council of Science Editors:

Kim NY. Characterization of the Immune Basis for Reduced IFN-α in Serologically Active Clinically Quiescent SLE Patients. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/70417


University of Toronto

20. Farr, Christina. Calpain and Calpastatin in a Mouse Model of Acute Myeloid Leukemia.

Degree: 2011, University of Toronto

I have studied the calpain system in acute myeloid leukemia using the 32D and 32Dkit cell lines. Specifically, I characterized the calpain system in the… (more)

Subjects/Keywords: calpain; acute myeloid leukemia; 0982

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APA (6th Edition):

Farr, C. (2011). Calpain and Calpastatin in a Mouse Model of Acute Myeloid Leukemia. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/30589

Chicago Manual of Style (16th Edition):

Farr, Christina. “Calpain and Calpastatin in a Mouse Model of Acute Myeloid Leukemia.” 2011. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/30589.

MLA Handbook (7th Edition):

Farr, Christina. “Calpain and Calpastatin in a Mouse Model of Acute Myeloid Leukemia.” 2011. Web. 29 Oct 2020.

Vancouver:

Farr C. Calpain and Calpastatin in a Mouse Model of Acute Myeloid Leukemia. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/30589.

Council of Science Editors:

Farr C. Calpain and Calpastatin in a Mouse Model of Acute Myeloid Leukemia. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/30589


University of Toronto

21. Khattar, Ramzi. Targeted Deletion of Fibrinogen-like Protein 2 (FGL2) ENHANCES Immunity in a Murine Model of Acute Viral Hepatitis Caused by Lymphocytic Choriomeningitis Virus (LCMV).

Degree: 2011, University of Toronto

Viral hepatitis infection represents a significant epidemiological and economic burden on society. Following infection, some patients mount a blunted immune response to the virus, which… (more)

Subjects/Keywords: LCMV; HCV pathogenesis; 0982

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APA (6th Edition):

Khattar, R. (2011). Targeted Deletion of Fibrinogen-like Protein 2 (FGL2) ENHANCES Immunity in a Murine Model of Acute Viral Hepatitis Caused by Lymphocytic Choriomeningitis Virus (LCMV). (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31278

Chicago Manual of Style (16th Edition):

Khattar, Ramzi. “Targeted Deletion of Fibrinogen-like Protein 2 (FGL2) ENHANCES Immunity in a Murine Model of Acute Viral Hepatitis Caused by Lymphocytic Choriomeningitis Virus (LCMV).” 2011. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/31278.

MLA Handbook (7th Edition):

Khattar, Ramzi. “Targeted Deletion of Fibrinogen-like Protein 2 (FGL2) ENHANCES Immunity in a Murine Model of Acute Viral Hepatitis Caused by Lymphocytic Choriomeningitis Virus (LCMV).” 2011. Web. 29 Oct 2020.

Vancouver:

Khattar R. Targeted Deletion of Fibrinogen-like Protein 2 (FGL2) ENHANCES Immunity in a Murine Model of Acute Viral Hepatitis Caused by Lymphocytic Choriomeningitis Virus (LCMV). [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/31278.

Council of Science Editors:

Khattar R. Targeted Deletion of Fibrinogen-like Protein 2 (FGL2) ENHANCES Immunity in a Murine Model of Acute Viral Hepatitis Caused by Lymphocytic Choriomeningitis Virus (LCMV). [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31278


University of Toronto

22. Liang, Lisa. Costimulation-mediated Rescue of Superantigen-activated T cells in an Animal Model of Kawasaki Disease.

Degree: 2012, University of Toronto

Lactobacillus casei cell wall extract (LCWE)- induced coronary arteritis in mice models Kawasaki disease (KD). LCWE injections consist of T-cell dependent factors that expand superantigen… (more)

Subjects/Keywords: kawasaki disease; superantigens; 0982

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APA (6th Edition):

Liang, L. (2012). Costimulation-mediated Rescue of Superantigen-activated T cells in an Animal Model of Kawasaki Disease. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/32598

Chicago Manual of Style (16th Edition):

Liang, Lisa. “Costimulation-mediated Rescue of Superantigen-activated T cells in an Animal Model of Kawasaki Disease.” 2012. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/32598.

MLA Handbook (7th Edition):

Liang, Lisa. “Costimulation-mediated Rescue of Superantigen-activated T cells in an Animal Model of Kawasaki Disease.” 2012. Web. 29 Oct 2020.

Vancouver:

Liang L. Costimulation-mediated Rescue of Superantigen-activated T cells in an Animal Model of Kawasaki Disease. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/32598.

Council of Science Editors:

Liang L. Costimulation-mediated Rescue of Superantigen-activated T cells in an Animal Model of Kawasaki Disease. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/32598


University of Toronto

23. Farrokhi, Kaveh. Fibrinogen Like Protein 2 (FGL2): A Novel Regulator of Macrophage M1 Polarization.

Degree: 2018, University of Toronto

Fibrinogen-like protein 2 (FGL2) is a potent immunosuppressive molecule. The effects of FGL2 on macrophages, however, has not been studied. Peritoneal cell accumulation in fgl2-/-,… (more)

Subjects/Keywords: FGL2; Immunology; Macrophage; Polarization; 0982

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APA (6th Edition):

Farrokhi, K. (2018). Fibrinogen Like Protein 2 (FGL2): A Novel Regulator of Macrophage M1 Polarization. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/89550

Chicago Manual of Style (16th Edition):

Farrokhi, Kaveh. “Fibrinogen Like Protein 2 (FGL2): A Novel Regulator of Macrophage M1 Polarization.” 2018. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/89550.

MLA Handbook (7th Edition):

Farrokhi, Kaveh. “Fibrinogen Like Protein 2 (FGL2): A Novel Regulator of Macrophage M1 Polarization.” 2018. Web. 29 Oct 2020.

Vancouver:

Farrokhi K. Fibrinogen Like Protein 2 (FGL2): A Novel Regulator of Macrophage M1 Polarization. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/89550.

Council of Science Editors:

Farrokhi K. Fibrinogen Like Protein 2 (FGL2): A Novel Regulator of Macrophage M1 Polarization. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89550


University of Toronto

24. Lo, Calvin Chun Chung. Characterizing Plasmacytoid Dendritic Cell Activation in the Context of HIV Stimulation.

Degree: 2010, University of Toronto

Plasmacytoid dendritic cells (pDCs) are important in innate and adaptive immune responses against viral infections, producing remarkable levels of type I interferon as well as… (more)

Subjects/Keywords: HIV; pDC; Interferon; Cytokine; 0982

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APA (6th Edition):

Lo, C. C. C. (2010). Characterizing Plasmacytoid Dendritic Cell Activation in the Context of HIV Stimulation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25772

Chicago Manual of Style (16th Edition):

Lo, Calvin Chun Chung. “Characterizing Plasmacytoid Dendritic Cell Activation in the Context of HIV Stimulation.” 2010. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/25772.

MLA Handbook (7th Edition):

Lo, Calvin Chun Chung. “Characterizing Plasmacytoid Dendritic Cell Activation in the Context of HIV Stimulation.” 2010. Web. 29 Oct 2020.

Vancouver:

Lo CCC. Characterizing Plasmacytoid Dendritic Cell Activation in the Context of HIV Stimulation. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/25772.

Council of Science Editors:

Lo CCC. Characterizing Plasmacytoid Dendritic Cell Activation in the Context of HIV Stimulation. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25772


University of Toronto

25. Tai, Kelly. The Expression and Function of CCL5 in Early Atherosclerosis.

Degree: 2017, University of Toronto

Atherosclerosis is a chronic cardiovascular disease initiated by the accumulation of lipid-loaded macrophages within the artery wall. Chemokines can have several potential functions in atherosclerosis.… (more)

Subjects/Keywords: atherosclerosis; CCL5; mice; RANTES; 0982

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APA (6th Edition):

Tai, K. (2017). The Expression and Function of CCL5 in Early Atherosclerosis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79197

Chicago Manual of Style (16th Edition):

Tai, Kelly. “The Expression and Function of CCL5 in Early Atherosclerosis.” 2017. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/79197.

MLA Handbook (7th Edition):

Tai, Kelly. “The Expression and Function of CCL5 in Early Atherosclerosis.” 2017. Web. 29 Oct 2020.

Vancouver:

Tai K. The Expression and Function of CCL5 in Early Atherosclerosis. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/79197.

Council of Science Editors:

Tai K. The Expression and Function of CCL5 in Early Atherosclerosis. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79197


University of Toronto

26. Ling, Alexanda Ka-Shing. The Role of BLNK in Avian B-cell Development.

Degree: 2013, University of Toronto

BLNK is an adaptor protein that functions in B-cell receptor signalling, and is vitally necessary at signalling checkpoints of mammalian B-cell development. However, its importance… (more)

Subjects/Keywords: B-cell development; BLNK; 0982

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APA (6th Edition):

Ling, A. K. (2013). The Role of BLNK in Avian B-cell Development. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/43087

Chicago Manual of Style (16th Edition):

Ling, Alexanda Ka-Shing. “The Role of BLNK in Avian B-cell Development.” 2013. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/43087.

MLA Handbook (7th Edition):

Ling, Alexanda Ka-Shing. “The Role of BLNK in Avian B-cell Development.” 2013. Web. 29 Oct 2020.

Vancouver:

Ling AK. The Role of BLNK in Avian B-cell Development. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/43087.

Council of Science Editors:

Ling AK. The Role of BLNK in Avian B-cell Development. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/43087


University of Toronto

27. Daniella, Perri. The Role of Intravenous Immunoglobulin Anti-A and Anti-B in Complement Activation and Red Blood Cell Phagocytosis.

Degree: 2009, University of Toronto

Intravenous immunoglobulin is a human blood derived product that is used to treat immunodeficiencies and autoimmune disorders. An adverse side effect of IVIg therapy is… (more)

Subjects/Keywords: Immunohematology; 0982

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APA (6th Edition):

Daniella, P. (2009). The Role of Intravenous Immunoglobulin Anti-A and Anti-B in Complement Activation and Red Blood Cell Phagocytosis. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/18976

Chicago Manual of Style (16th Edition):

Daniella, Perri. “The Role of Intravenous Immunoglobulin Anti-A and Anti-B in Complement Activation and Red Blood Cell Phagocytosis.” 2009. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/18976.

MLA Handbook (7th Edition):

Daniella, Perri. “The Role of Intravenous Immunoglobulin Anti-A and Anti-B in Complement Activation and Red Blood Cell Phagocytosis.” 2009. Web. 29 Oct 2020.

Vancouver:

Daniella P. The Role of Intravenous Immunoglobulin Anti-A and Anti-B in Complement Activation and Red Blood Cell Phagocytosis. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/18976.

Council of Science Editors:

Daniella P. The Role of Intravenous Immunoglobulin Anti-A and Anti-B in Complement Activation and Red Blood Cell Phagocytosis. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/18976


University of Toronto

28. Kei, Chan Pak. The Role of FKBP5 in Influenza Virus Infection.

Degree: 2010, University of Toronto

FK506 binding protein 5 (FKBP5) is a peptidyl propyl cis-trans isomerase that has been shown to interact with cellular immune pathways such as calcineurin and… (more)

Subjects/Keywords: FKBP5; Influenza; Glucocorticoid; 0982

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APA (6th Edition):

Kei, C. P. (2010). The Role of FKBP5 in Influenza Virus Infection. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24547

Chicago Manual of Style (16th Edition):

Kei, Chan Pak. “The Role of FKBP5 in Influenza Virus Infection.” 2010. Masters Thesis, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/24547.

MLA Handbook (7th Edition):

Kei, Chan Pak. “The Role of FKBP5 in Influenza Virus Infection.” 2010. Web. 29 Oct 2020.

Vancouver:

Kei CP. The Role of FKBP5 in Influenza Virus Infection. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/24547.

Council of Science Editors:

Kei CP. The Role of FKBP5 in Influenza Virus Infection. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24547


University of Toronto

29. Stanojcic, Mile. The Role of NLPR3 Inflammasome in Response to Thermal Injury and Sepsis.

Degree: PhD, 2017, University of Toronto

 Although the induction of acute-phase inflammation after burn injury is essential, if prolonged it can induce increased risk of infection and sepsis. The NLRP3 inflammasome… (more)

Subjects/Keywords: Burn; Inflammasome; Inflammation; Sepsis; 0982

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APA (6th Edition):

Stanojcic, M. (2017). The Role of NLPR3 Inflammasome in Response to Thermal Injury and Sepsis. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80947

Chicago Manual of Style (16th Edition):

Stanojcic, Mile. “The Role of NLPR3 Inflammasome in Response to Thermal Injury and Sepsis.” 2017. Doctoral Dissertation, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/80947.

MLA Handbook (7th Edition):

Stanojcic, Mile. “The Role of NLPR3 Inflammasome in Response to Thermal Injury and Sepsis.” 2017. Web. 29 Oct 2020.

Vancouver:

Stanojcic M. The Role of NLPR3 Inflammasome in Response to Thermal Injury and Sepsis. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/80947.

Council of Science Editors:

Stanojcic M. The Role of NLPR3 Inflammasome in Response to Thermal Injury and Sepsis. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/80947


University of Toronto

30. Johnson, Radia Marie. The Role And Molecular Mechanism of Flt3 Over-expression In A Murine Model Of Precursor-B Acute Lymphoblastic Leukemia.

Degree: 2013, University of Toronto

Precursor B-cell acute lymphoblastic leukemia (pre-B ALL) is thought to arise from a dysregulated developmental process that results in abnormal survival, proliferation and dissemination of… (more)

Subjects/Keywords: Leukemia; B-Cell; 0982

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APA (6th Edition):

Johnson, R. M. (2013). The Role And Molecular Mechanism of Flt3 Over-expression In A Murine Model Of Precursor-B Acute Lymphoblastic Leukemia. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68946

Chicago Manual of Style (16th Edition):

Johnson, Radia Marie. “The Role And Molecular Mechanism of Flt3 Over-expression In A Murine Model Of Precursor-B Acute Lymphoblastic Leukemia.” 2013. Doctoral Dissertation, University of Toronto. Accessed October 29, 2020. http://hdl.handle.net/1807/68946.

MLA Handbook (7th Edition):

Johnson, Radia Marie. “The Role And Molecular Mechanism of Flt3 Over-expression In A Murine Model Of Precursor-B Acute Lymphoblastic Leukemia.” 2013. Web. 29 Oct 2020.

Vancouver:

Johnson RM. The Role And Molecular Mechanism of Flt3 Over-expression In A Murine Model Of Precursor-B Acute Lymphoblastic Leukemia. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2020 Oct 29]. Available from: http://hdl.handle.net/1807/68946.

Council of Science Editors:

Johnson RM. The Role And Molecular Mechanism of Flt3 Over-expression In A Murine Model Of Precursor-B Acute Lymphoblastic Leukemia. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/68946

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