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You searched for +publisher:"University of Saskatchewan" +contributor:("Xiang, Jim"). Showing records 1 – 18 of 18 total matches.

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University of Saskatchewan

1. Zhang, Xueying. TRANSGENE IL-21-ENGINEERED ANTIGEN-SPECIFIC EXOSOME TARGETED T CELL-BASED VACCINE POTENTLY CONVERTS CTL EXHAUSTION IN CHRONIC INFECTION.

Degree: 2018, University of Saskatchewan

 CD8+ cytotoxic T lymphocytes (CTLs), the potent effector T cells, capable of directly destroying virus-infected cells, correlate with acute viral control and long-term non-progression in… (more)

Subjects/Keywords: IL-21; chronic infection; CTL exhaustion; exosome; T cell vaccine

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APA (6th Edition):

Zhang, X. (2018). TRANSGENE IL-21-ENGINEERED ANTIGEN-SPECIFIC EXOSOME TARGETED T CELL-BASED VACCINE POTENTLY CONVERTS CTL EXHAUSTION IN CHRONIC INFECTION. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/8603

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhang, Xueying. “TRANSGENE IL-21-ENGINEERED ANTIGEN-SPECIFIC EXOSOME TARGETED T CELL-BASED VACCINE POTENTLY CONVERTS CTL EXHAUSTION IN CHRONIC INFECTION.” 2018. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/8603.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhang, Xueying. “TRANSGENE IL-21-ENGINEERED ANTIGEN-SPECIFIC EXOSOME TARGETED T CELL-BASED VACCINE POTENTLY CONVERTS CTL EXHAUSTION IN CHRONIC INFECTION.” 2018. Web. 20 Oct 2019.

Vancouver:

Zhang X. TRANSGENE IL-21-ENGINEERED ANTIGEN-SPECIFIC EXOSOME TARGETED T CELL-BASED VACCINE POTENTLY CONVERTS CTL EXHAUSTION IN CHRONIC INFECTION. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/8603.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhang X. TRANSGENE IL-21-ENGINEERED ANTIGEN-SPECIFIC EXOSOME TARGETED T CELL-BASED VACCINE POTENTLY CONVERTS CTL EXHAUSTION IN CHRONIC INFECTION. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/8603

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

2. Hebbandi Nanjundappa, Roopa. HIV-1 Glycoprotein 120-Specific Exosome-Targeted CD8+ T Cell Vaccine.

Degree: 2011, University of Saskatchewan

 Immunosuppression is a hallmark of human immunodeficiency virus-1 (HIV-1) infection. Upon binding to cluster of differentiation (CD) 4 receptor via trimeric glycoprotein (Gp) 120, HIV-1… (more)

Subjects/Keywords: HIV-1 infection; T cell vaccine; glycoprotein-120; adenovirus; exosomes

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APA (6th Edition):

Hebbandi Nanjundappa, R. (2011). HIV-1 Glycoprotein 120-Specific Exosome-Targeted CD8+ T Cell Vaccine. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-12-275

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Hebbandi Nanjundappa, Roopa. “HIV-1 Glycoprotein 120-Specific Exosome-Targeted CD8+ T Cell Vaccine.” 2011. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2011-12-275.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Hebbandi Nanjundappa, Roopa. “HIV-1 Glycoprotein 120-Specific Exosome-Targeted CD8+ T Cell Vaccine.” 2011. Web. 20 Oct 2019.

Vancouver:

Hebbandi Nanjundappa R. HIV-1 Glycoprotein 120-Specific Exosome-Targeted CD8+ T Cell Vaccine. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2011-12-275.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Hebbandi Nanjundappa R. HIV-1 Glycoprotein 120-Specific Exosome-Targeted CD8+ T Cell Vaccine. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-12-275

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

3. Xiao, Shujun (Jennifer) 1991-. Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells.

Degree: 2018, University of Saskatchewan

 Breast cancer is the third most common cancer in Canada. Even though the morbidity and mortality rates have reduced in recent years because of early… (more)

Subjects/Keywords: Breast cancer; sphingosine-1-phosphate; S1P receptor 1; carboplatin

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APA (6th Edition):

Xiao, S. (. 1. (2018). Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/11253

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Xiao, Shujun (Jennifer) 1991-. “Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells.” 2018. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/11253.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Xiao, Shujun (Jennifer) 1991-. “Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells.” 2018. Web. 20 Oct 2019.

Vancouver:

Xiao S(1. Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/11253.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Xiao S(1. Antitumor effect of the combination of exogenous sphingosine-1-phosphate(S1P), S1P receptor 1(S1PR1) antibody and carboplatin against human breast cancer cells. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/11253

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

4. Jahan, Sheikh Tasnim 1984-. DESIGN AND DEVELOPMENT OF CD205 TARGETED PLGA NANOPARTICLES AND EVALUATION OF ANTIGEN SPECIFIC IMMUNE RESPONSES.

Degree: 2017, University of Saskatchewan

 Stimulation of a patient’s immune system to fight cancer is the underlying mechanism of immunotherapy. Cancer immunotherapy manipulates the dendritic cells (DCs) to identify the… (more)

Subjects/Keywords: PLGA Nanoparticle; Dendritic cells; Vaccine

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APA (6th Edition):

Jahan, S. T. 1. (2017). DESIGN AND DEVELOPMENT OF CD205 TARGETED PLGA NANOPARTICLES AND EVALUATION OF ANTIGEN SPECIFIC IMMUNE RESPONSES. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7881

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Jahan, Sheikh Tasnim 1984-. “DESIGN AND DEVELOPMENT OF CD205 TARGETED PLGA NANOPARTICLES AND EVALUATION OF ANTIGEN SPECIFIC IMMUNE RESPONSES.” 2017. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/7881.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Jahan, Sheikh Tasnim 1984-. “DESIGN AND DEVELOPMENT OF CD205 TARGETED PLGA NANOPARTICLES AND EVALUATION OF ANTIGEN SPECIFIC IMMUNE RESPONSES.” 2017. Web. 20 Oct 2019.

Vancouver:

Jahan ST1. DESIGN AND DEVELOPMENT OF CD205 TARGETED PLGA NANOPARTICLES AND EVALUATION OF ANTIGEN SPECIFIC IMMUNE RESPONSES. [Internet] [Thesis]. University of Saskatchewan; 2017. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/7881.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Jahan ST1. DESIGN AND DEVELOPMENT OF CD205 TARGETED PLGA NANOPARTICLES AND EVALUATION OF ANTIGEN SPECIFIC IMMUNE RESPONSES. [Thesis]. University of Saskatchewan; 2017. Available from: http://hdl.handle.net/10388/7881

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

5. Zhang, Bei. IL-6-engineered DC stimulate efficient antitumor immunity via enhanced and prolonged T cell cytotoxicity and survival.

Degree: 2009, University of Saskatchewan

 Dendritic cells (DCs) modified by some immunomodulatory genes can stimulate a strong antitumor immunity and improve the treatment of tumor cells on the condition that… (more)

Subjects/Keywords: antitumor; T cells; DC; IL-6

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APA (6th Edition):

Zhang, B. (2009). IL-6-engineered DC stimulate efficient antitumor immunity via enhanced and prolonged T cell cytotoxicity and survival. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-02262009-152419

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhang, Bei. “IL-6-engineered DC stimulate efficient antitumor immunity via enhanced and prolonged T cell cytotoxicity and survival.” 2009. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-02262009-152419.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhang, Bei. “IL-6-engineered DC stimulate efficient antitumor immunity via enhanced and prolonged T cell cytotoxicity and survival.” 2009. Web. 20 Oct 2019.

Vancouver:

Zhang B. IL-6-engineered DC stimulate efficient antitumor immunity via enhanced and prolonged T cell cytotoxicity and survival. [Internet] [Thesis]. University of Saskatchewan; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-02262009-152419.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhang B. IL-6-engineered DC stimulate efficient antitumor immunity via enhanced and prolonged T cell cytotoxicity and survival. [Thesis]. University of Saskatchewan; 2009. Available from: http://hdl.handle.net/10388/etd-02262009-152419

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

6. Mackenzie-Dyck, Sarah. Enhancing The Efficacy Of DNA Vaccines.

Degree: 2014, University of Saskatchewan

 Bovine herpesvirus-1 (BoHV-1) causes recurrent respiratory and genital infections in cattle; and predisposes them to lethal secondary bacterial infections. Vaccination is a primary strategy to… (more)

Subjects/Keywords: BoHV-1; DNA Vaccines; Dendritic Cells: Beta-Defensins

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APA (6th Edition):

Mackenzie-Dyck, S. (2014). Enhancing The Efficacy Of DNA Vaccines. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-07-1616

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Mackenzie-Dyck, Sarah. “Enhancing The Efficacy Of DNA Vaccines.” 2014. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2014-07-1616.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Mackenzie-Dyck, Sarah. “Enhancing The Efficacy Of DNA Vaccines.” 2014. Web. 20 Oct 2019.

Vancouver:

Mackenzie-Dyck S. Enhancing The Efficacy Of DNA Vaccines. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2014-07-1616.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Mackenzie-Dyck S. Enhancing The Efficacy Of DNA Vaccines. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-07-1616

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

7. Chen, Yuxiu. HER2/neu-specific Breast Cancer Vaccine.

Degree: 2013, University of Saskatchewan

 Breast cancer is the most common cancer among women. Of all breast cancers cases, approximately 30 percent have amplification of the self-antigen HER2/neu. Later studies… (more)

Subjects/Keywords: HER2/neu; Adenovirus; DC vaccine

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APA (6th Edition):

Chen, Y. (2013). HER2/neu-specific Breast Cancer Vaccine. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2013-01-876

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chen, Yuxiu. “HER2/neu-specific Breast Cancer Vaccine.” 2013. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2013-01-876.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chen, Yuxiu. “HER2/neu-specific Breast Cancer Vaccine.” 2013. Web. 20 Oct 2019.

Vancouver:

Chen Y. HER2/neu-specific Breast Cancer Vaccine. [Internet] [Thesis]. University of Saskatchewan; 2013. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2013-01-876.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chen Y. HER2/neu-specific Breast Cancer Vaccine. [Thesis]. University of Saskatchewan; 2013. Available from: http://hdl.handle.net/10388/ETD-2013-01-876

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

8. WANG, LU. Ex vivo imaging immune cell interactions in T cell vaccine-induced immunity and CD8+CD25+ T regulatory cell-mediated immune suppression.

Degree: 2013, University of Saskatchewan

 The ultimate goal of antitumor vaccines is to develop memory CD8+ cytotoxic T lymphocytes (CTLs), which are critical mediators of antitumor immunity. Previous work in… (more)

Subjects/Keywords: Exosome-based T-cell Vaccine; Antitumor Immunity; CD8+ Regulatory T Cells; Two-photon Microscopy

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APA (6th Edition):

WANG, L. (2013). Ex vivo imaging immune cell interactions in T cell vaccine-induced immunity and CD8+CD25+ T regulatory cell-mediated immune suppression. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2013-10-1254

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

WANG, LU. “Ex vivo imaging immune cell interactions in T cell vaccine-induced immunity and CD8+CD25+ T regulatory cell-mediated immune suppression.” 2013. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2013-10-1254.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

WANG, LU. “Ex vivo imaging immune cell interactions in T cell vaccine-induced immunity and CD8+CD25+ T regulatory cell-mediated immune suppression.” 2013. Web. 20 Oct 2019.

Vancouver:

WANG L. Ex vivo imaging immune cell interactions in T cell vaccine-induced immunity and CD8+CD25+ T regulatory cell-mediated immune suppression. [Internet] [Thesis]. University of Saskatchewan; 2013. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2013-10-1254.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

WANG L. Ex vivo imaging immune cell interactions in T cell vaccine-induced immunity and CD8+CD25+ T regulatory cell-mediated immune suppression. [Thesis]. University of Saskatchewan; 2013. Available from: http://hdl.handle.net/10388/ETD-2013-10-1254

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

9. Yang, Junbao. Genetic engineering of a fusion protein possessing anti-tumor Fv and tumor necrosis factor alpha.

Degree: 1999, University of Saskatchewan

 In order to target tumor necrosis factor alpha (TNF-α) specifically to tumor cells, we designed, constructed and expressed a recombinant fusion protein single-chain Fv/TNF-α (scFv/TNF-α)… (more)

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APA (6th Edition):

Yang, J. (1999). Genetic engineering of a fusion protein possessing anti-tumor Fv and tumor necrosis factor alpha. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-10212004-002517

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Yang, Junbao. “Genetic engineering of a fusion protein possessing anti-tumor Fv and tumor necrosis factor alpha.” 1999. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-10212004-002517.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Yang, Junbao. “Genetic engineering of a fusion protein possessing anti-tumor Fv and tumor necrosis factor alpha.” 1999. Web. 20 Oct 2019.

Vancouver:

Yang J. Genetic engineering of a fusion protein possessing anti-tumor Fv and tumor necrosis factor alpha. [Internet] [Thesis]. University of Saskatchewan; 1999. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-10212004-002517.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Yang J. Genetic engineering of a fusion protein possessing anti-tumor Fv and tumor necrosis factor alpha. [Thesis]. University of Saskatchewan; 1999. Available from: http://hdl.handle.net/10388/etd-10212004-002517

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

10. Ankathatti Munegowda, Manjunatha. Targeting Th (Th17 and Th2) suppressive and stimulatory effect on cytotoxic T cells.

Degree: 2012, University of Saskatchewan

 As the name indicates, T-helper cells are shown to help in primary and secondary cellular and humoral immune responses. They behave as conductors of immune… (more)

Subjects/Keywords: Th17; Tumor immunity; Autoimmunity; Th2 plasticity

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APA (6th Edition):

Ankathatti Munegowda, M. (2012). Targeting Th (Th17 and Th2) suppressive and stimulatory effect on cytotoxic T cells. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2012-04-512

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ankathatti Munegowda, Manjunatha. “Targeting Th (Th17 and Th2) suppressive and stimulatory effect on cytotoxic T cells.” 2012. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2012-04-512.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ankathatti Munegowda, Manjunatha. “Targeting Th (Th17 and Th2) suppressive and stimulatory effect on cytotoxic T cells.” 2012. Web. 20 Oct 2019.

Vancouver:

Ankathatti Munegowda M. Targeting Th (Th17 and Th2) suppressive and stimulatory effect on cytotoxic T cells. [Internet] [Thesis]. University of Saskatchewan; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2012-04-512.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Ankathatti Munegowda M. Targeting Th (Th17 and Th2) suppressive and stimulatory effect on cytotoxic T cells. [Thesis]. University of Saskatchewan; 2012. Available from: http://hdl.handle.net/10388/ETD-2012-04-512

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

11. Zhang, Rui. The Effect of Transcription Factor Zhangfei/CREBZF on Osteosarcoma Cells and the Mechanisms Responsible.

Degree: 2014, University of Saskatchewan

 Osteosarcoma (OS) is the most common primary malignant bone tumour in humans and dogs. Although medicine has made dramatic progress in treating osteosarcoma by surgery,… (more)

Subjects/Keywords: Zhangfei/CREBZF; osteosarcoma; cell growth; UPR; p53

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APA (6th Edition):

Zhang, R. (2014). The Effect of Transcription Factor Zhangfei/CREBZF on Osteosarcoma Cells and the Mechanisms Responsible. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-06-1557

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhang, Rui. “The Effect of Transcription Factor Zhangfei/CREBZF on Osteosarcoma Cells and the Mechanisms Responsible.” 2014. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2014-06-1557.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhang, Rui. “The Effect of Transcription Factor Zhangfei/CREBZF on Osteosarcoma Cells and the Mechanisms Responsible.” 2014. Web. 20 Oct 2019.

Vancouver:

Zhang R. The Effect of Transcription Factor Zhangfei/CREBZF on Osteosarcoma Cells and the Mechanisms Responsible. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2014-06-1557.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhang R. The Effect of Transcription Factor Zhangfei/CREBZF on Osteosarcoma Cells and the Mechanisms Responsible. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-06-1557

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

12. Sokke Umeshappa, Channakeshava. THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY.

Degree: 2012, University of Saskatchewan

 The goal of this body of research was to elucidate the mechanism by which CD4+ T cells provide help for CD8+ cytotoxic T lymphocyte (CTL)… (more)

Subjects/Keywords: Cognate CD4+ Th help; peptide-MHC complexes; IL-2, CD80 and CD40L signaling; CTL survival; memory development; apoptosis and cell survival pathway; anti-tumor immunity; CD8+ T precursor frequency; Adenoviral immunization

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APA (6th Edition):

Sokke Umeshappa, C. (2012). THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2012-04-424

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sokke Umeshappa, Channakeshava. “THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY.” 2012. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2012-04-424.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sokke Umeshappa, Channakeshava. “THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY.” 2012. Web. 20 Oct 2019.

Vancouver:

Sokke Umeshappa C. THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY. [Internet] [Thesis]. University of Saskatchewan; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2012-04-424.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sokke Umeshappa C. THE CRITICAL ROLE OF CD4+ TH CELLS IN CD8+ CTL RESPONSES AND ANTI-TUMOR IMMUNITY. [Thesis]. University of Saskatchewan; 2012. Available from: http://hdl.handle.net/10388/ETD-2012-04-424

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

13. Li, Chunyan. Comparison of the Abilities of IL-10- and Retinoic Acid- Differentiated Dendritic Cells to Induce Allergen Tolerance in a Mouse Model of Asthma.

Degree: 2014, University of Saskatchewan

 Dendritic cells (DCs) in different compartments can affect tolerance via distinct mechanisms. Thus, retinoid acid (RA) and integrins expressed by CD103+ dendritic cells in the… (more)

Subjects/Keywords: IL-10; Retinoic Acid; Dendritic Cells; Tolerance; Asthma

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APA (6th Edition):

Li, C. (2014). Comparison of the Abilities of IL-10- and Retinoic Acid- Differentiated Dendritic Cells to Induce Allergen Tolerance in a Mouse Model of Asthma. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2014-10-1804

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Li, Chunyan. “Comparison of the Abilities of IL-10- and Retinoic Acid- Differentiated Dendritic Cells to Induce Allergen Tolerance in a Mouse Model of Asthma.” 2014. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/ETD-2014-10-1804.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Li, Chunyan. “Comparison of the Abilities of IL-10- and Retinoic Acid- Differentiated Dendritic Cells to Induce Allergen Tolerance in a Mouse Model of Asthma.” 2014. Web. 20 Oct 2019.

Vancouver:

Li C. Comparison of the Abilities of IL-10- and Retinoic Acid- Differentiated Dendritic Cells to Induce Allergen Tolerance in a Mouse Model of Asthma. [Internet] [Thesis]. University of Saskatchewan; 2014. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/ETD-2014-10-1804.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Li C. Comparison of the Abilities of IL-10- and Retinoic Acid- Differentiated Dendritic Cells to Induce Allergen Tolerance in a Mouse Model of Asthma. [Thesis]. University of Saskatchewan; 2014. Available from: http://hdl.handle.net/10388/ETD-2014-10-1804

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

14. Scott, Stuart Alexander. Aberrant epigenetics in the molecular pathogenesis of human acute myeloid leukemia.

Degree: 2005, University of Saskatchewan

 Promoter hypermethylation mediated gene silencing is a frequent epigenetic finding in many cancers that affects genes known to have important roles in several aspects of… (more)

Subjects/Keywords: histone modification; p15INK4B; 5-Aza-2'-deoxycytidine; zebularine; cDNA microarray; metallothionein; promoter hypermethylation

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APA (6th Edition):

Scott, S. A. (2005). Aberrant epigenetics in the molecular pathogenesis of human acute myeloid leukemia. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-05242005-153230

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Scott, Stuart Alexander. “Aberrant epigenetics in the molecular pathogenesis of human acute myeloid leukemia.” 2005. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-05242005-153230.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Scott, Stuart Alexander. “Aberrant epigenetics in the molecular pathogenesis of human acute myeloid leukemia.” 2005. Web. 20 Oct 2019.

Vancouver:

Scott SA. Aberrant epigenetics in the molecular pathogenesis of human acute myeloid leukemia. [Internet] [Thesis]. University of Saskatchewan; 2005. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-05242005-153230.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Scott SA. Aberrant epigenetics in the molecular pathogenesis of human acute myeloid leukemia. [Thesis]. University of Saskatchewan; 2005. Available from: http://hdl.handle.net/10388/etd-05242005-153230

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

15. Sohn, Namseok. Release of Cardiac Biomarkers and Inflammatory Response during Cardiopulmonary Bypass: Comparison of Different Biocompatible Materials Used in Cardiopulmonary Bypass.

Degree: 2008, University of Saskatchewan

 Coronary Artery Bypass Grafting (CABG) is an effective and invasive cardiac surgery to salvage blocked coronary artery. Cardiopulmonary bypass (CPB) is usually applied to support… (more)

Subjects/Keywords: cardiac markers; cardiopulmonary bypass; biocompatible materials

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APA (6th Edition):

Sohn, N. (2008). Release of Cardiac Biomarkers and Inflammatory Response during Cardiopulmonary Bypass: Comparison of Different Biocompatible Materials Used in Cardiopulmonary Bypass. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-08202008-111304

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sohn, Namseok. “Release of Cardiac Biomarkers and Inflammatory Response during Cardiopulmonary Bypass: Comparison of Different Biocompatible Materials Used in Cardiopulmonary Bypass.” 2008. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-08202008-111304.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sohn, Namseok. “Release of Cardiac Biomarkers and Inflammatory Response during Cardiopulmonary Bypass: Comparison of Different Biocompatible Materials Used in Cardiopulmonary Bypass.” 2008. Web. 20 Oct 2019.

Vancouver:

Sohn N. Release of Cardiac Biomarkers and Inflammatory Response during Cardiopulmonary Bypass: Comparison of Different Biocompatible Materials Used in Cardiopulmonary Bypass. [Internet] [Thesis]. University of Saskatchewan; 2008. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-08202008-111304.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sohn N. Release of Cardiac Biomarkers and Inflammatory Response during Cardiopulmonary Bypass: Comparison of Different Biocompatible Materials Used in Cardiopulmonary Bypass. [Thesis]. University of Saskatchewan; 2008. Available from: http://hdl.handle.net/10388/etd-08202008-111304

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

16. Chan, Tim. Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70.

Degree: 2006, University of Saskatchewan

 Human Epidermal Growth Factor Receptor 2 (HER-2/neu) is a breast tumor antigen (Ag) commonly overexpressed in 30% of breast cancer cases. Both HER-2/neu-targeted DNA-based and… (more)

Subjects/Keywords: replication deficient adenovirus; cancer vaccine; breast cancer; dendritic cell; HER-2/neu; apoptosis; Heat Shock Protein 70

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APA (6th Edition):

Chan, T. (2006). Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-08232006-203717

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chan, Tim. “Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70.” 2006. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-08232006-203717.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chan, Tim. “Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70.” 2006. Web. 20 Oct 2019.

Vancouver:

Chan T. Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70. [Internet] [Thesis]. University of Saskatchewan; 2006. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-08232006-203717.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chan T. Dendritic cell based cancer vaccines using adenovirally mediated expression of the HER-2/neu gene and apoptotic tumor cells expressing heat shock protein 70. [Thesis]. University of Saskatchewan; 2006. Available from: http://hdl.handle.net/10388/etd-08232006-203717

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

17. Danabassis, Michael. The importance of the F4 receptor in post-weaned pigs In eliciting F4 specific immune responses in the intestine.

Degree: 2006, University of Saskatchewan

 In this Master’s dissertation, various doses of solubulized crude F4 fimbrial protein in conjunction with the adjuvants CpG ODN and porcine â-defensin 1 (pBD-1) were… (more)

Subjects/Keywords: Gut-loop model; crude F4

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APA (6th Edition):

Danabassis, M. (2006). The importance of the F4 receptor in post-weaned pigs In eliciting F4 specific immune responses in the intestine. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-05272006-110859

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Danabassis, Michael. “The importance of the F4 receptor in post-weaned pigs In eliciting F4 specific immune responses in the intestine.” 2006. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-05272006-110859.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Danabassis, Michael. “The importance of the F4 receptor in post-weaned pigs In eliciting F4 specific immune responses in the intestine.” 2006. Web. 20 Oct 2019.

Vancouver:

Danabassis M. The importance of the F4 receptor in post-weaned pigs In eliciting F4 specific immune responses in the intestine. [Internet] [Thesis]. University of Saskatchewan; 2006. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-05272006-110859.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Danabassis M. The importance of the F4 receptor in post-weaned pigs In eliciting F4 specific immune responses in the intestine. [Thesis]. University of Saskatchewan; 2006. Available from: http://hdl.handle.net/10388/etd-05272006-110859

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Saskatchewan

18. Sas, Sheena Emm. HER-2/neu-targeted immunoprevention of breast cancer.

Degree: 2007, University of Saskatchewan

 Improvements in the use of traditional breast cancer therapies have improved the overall survival of women with early stage disease. Remarkable advances in research have… (more)

Subjects/Keywords: cancer vaccine; dendritic cell; fiber modified adenovirus; HER-2/neu; breast cancer

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APA (6th Edition):

Sas, S. E. (2007). HER-2/neu-targeted immunoprevention of breast cancer. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-03262007-161505

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Sas, Sheena Emm. “HER-2/neu-targeted immunoprevention of breast cancer.” 2007. Thesis, University of Saskatchewan. Accessed October 20, 2019. http://hdl.handle.net/10388/etd-03262007-161505.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Sas, Sheena Emm. “HER-2/neu-targeted immunoprevention of breast cancer.” 2007. Web. 20 Oct 2019.

Vancouver:

Sas SE. HER-2/neu-targeted immunoprevention of breast cancer. [Internet] [Thesis]. University of Saskatchewan; 2007. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/10388/etd-03262007-161505.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Sas SE. HER-2/neu-targeted immunoprevention of breast cancer. [Thesis]. University of Saskatchewan; 2007. Available from: http://hdl.handle.net/10388/etd-03262007-161505

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

.