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You searched for subject:(T cell exhaustion). Showing records 1 – 30 of 33 total matches.

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University of Manchester

1. Dookie, Rebecca. Dissecting the molecular mechanisms of CD4+ T cell exhaustion during malaria.

Degree: 2019, University of Manchester

Malaria is a global life-threatening disease responsible for 400,000 deaths each year. Chronic infection with Plasmodium species drives CD4+ T cell exhaustion, which is characterised… (more)

Subjects/Keywords: CD4+ T cells; Malaria; T cell exhaustion

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

APA (6th Edition):

Dookie, R. (2019). Dissecting the molecular mechanisms of CD4+ T cell exhaustion during malaria. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319548

Chicago Manual of Style (16th Edition):

Dookie, Rebecca. “Dissecting the molecular mechanisms of CD4+ T cell exhaustion during malaria.” 2019. Doctoral Dissertation, University of Manchester. Accessed April 16, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319548.

MLA Handbook (7th Edition):

Dookie, Rebecca. “Dissecting the molecular mechanisms of CD4+ T cell exhaustion during malaria.” 2019. Web. 16 Apr 2021.

Vancouver:

Dookie R. Dissecting the molecular mechanisms of CD4+ T cell exhaustion during malaria. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2021 Apr 16]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319548.

Council of Science Editors:

Dookie R. Dissecting the molecular mechanisms of CD4+ T cell exhaustion during malaria. [Doctoral Dissertation]. University of Manchester; 2019. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:319548


University of Texas – Austin

2. -6996-7733. Role of TCR affinity in function, proliferation, memory generation, and exhaustion during human viral infection.

Degree: PhD, Biomedical Engineering, 2019, University of Texas – Austin

 TCR affinity is a strong predictor of T cell function, proliferation, exhaustion, and generation of immune memory. 2D TCR affinity quantification is derived from direct… (more)

Subjects/Keywords: T cell; TCR affinity; T cell function; T cell exhaustion; Human viral infection; Cytomegalovirus

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APA (6th Edition):

-6996-7733. (2019). Role of TCR affinity in function, proliferation, memory generation, and exhaustion during human viral infection. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/12039

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

Chicago Manual of Style (16th Edition):

-6996-7733. “Role of TCR affinity in function, proliferation, memory generation, and exhaustion during human viral infection.” 2019. Doctoral Dissertation, University of Texas – Austin. Accessed April 16, 2021. http://dx.doi.org/10.26153/tsw/12039.

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

MLA Handbook (7th Edition):

-6996-7733. “Role of TCR affinity in function, proliferation, memory generation, and exhaustion during human viral infection.” 2019. Web. 16 Apr 2021.

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

Vancouver:

-6996-7733. Role of TCR affinity in function, proliferation, memory generation, and exhaustion during human viral infection. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2019. [cited 2021 Apr 16]. Available from: http://dx.doi.org/10.26153/tsw/12039.

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

Council of Science Editors:

-6996-7733. Role of TCR affinity in function, proliferation, memory generation, and exhaustion during human viral infection. [Doctoral Dissertation]. University of Texas – Austin; 2019. Available from: http://dx.doi.org/10.26153/tsw/12039

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


University of California – San Diego

3. Chen, Joyce. Defining the Role of Nr4a Transcription Factors in CD8+ T Cell Exhaustion Using a Murine CAR T Cell Tumor Model.

Degree: Biomedical Sciences, 2019, University of California – San Diego

 In cancer immunotherapy, T cells expressing chimeric antigen receptors (CAR T) targeting human CD19 (hCD19) antigen have exhibited impressive clinical efficacy against B cell leukemias… (more)

Subjects/Keywords: Immunology; CAR T cells; Nr4a; T cell exhaustion

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APA (6th Edition):

Chen, J. (2019). Defining the Role of Nr4a Transcription Factors in CD8+ T Cell Exhaustion Using a Murine CAR T Cell Tumor Model. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/5mj1t7tp

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, Joyce. “Defining the Role of Nr4a Transcription Factors in CD8+ T Cell Exhaustion Using a Murine CAR T Cell Tumor Model.” 2019. Thesis, University of California – San Diego. Accessed April 16, 2021. http://www.escholarship.org/uc/item/5mj1t7tp.

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

MLA Handbook (7th Edition):

Chen, Joyce. “Defining the Role of Nr4a Transcription Factors in CD8+ T Cell Exhaustion Using a Murine CAR T Cell Tumor Model.” 2019. Web. 16 Apr 2021.

Vancouver:

Chen J. Defining the Role of Nr4a Transcription Factors in CD8+ T Cell Exhaustion Using a Murine CAR T Cell Tumor Model. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2021 Apr 16]. Available from: http://www.escholarship.org/uc/item/5mj1t7tp.

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

Council of Science Editors:

Chen J. Defining the Role of Nr4a Transcription Factors in CD8+ T Cell Exhaustion Using a Murine CAR T Cell Tumor Model. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/5mj1t7tp

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


University of Iowa

4. Christiaansen, Allison Fae. T cell regulation of acute and chronic viral infection.

Degree: PhD, Microbiology, 2016, University of Iowa

  A balanced immune response is required to mediate clearance of a virus infection without immune-mediated disease. CD4 and CD8 T cells are capable of… (more)

Subjects/Keywords: Immune regulation; Infection; T cell exhaustion; T cells; Tregs; Microbiology

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APA (6th Edition):

Christiaansen, A. F. (2016). T cell regulation of acute and chronic viral infection. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/6076

Chicago Manual of Style (16th Edition):

Christiaansen, Allison Fae. “T cell regulation of acute and chronic viral infection.” 2016. Doctoral Dissertation, University of Iowa. Accessed April 16, 2021. https://ir.uiowa.edu/etd/6076.

MLA Handbook (7th Edition):

Christiaansen, Allison Fae. “T cell regulation of acute and chronic viral infection.” 2016. Web. 16 Apr 2021.

Vancouver:

Christiaansen AF. T cell regulation of acute and chronic viral infection. [Internet] [Doctoral dissertation]. University of Iowa; 2016. [cited 2021 Apr 16]. Available from: https://ir.uiowa.edu/etd/6076.

Council of Science Editors:

Christiaansen AF. T cell regulation of acute and chronic viral infection. [Doctoral Dissertation]. University of Iowa; 2016. Available from: https://ir.uiowa.edu/etd/6076


University of Cambridge

5. Pecchia-Bekkum, Annika Gabriel. Not-so-innocent bystanders? Investigating non-antigen specific CD8+ T cell activation in autoimmune prognosis.

Degree: PhD, 2019, University of Cambridge

 Clinical outcome in patients with the same diagnosis of immune disease varies substantially. Understanding the biology of prognosis could greatly improve treatment options for patients… (more)

Subjects/Keywords: CD8+ T cells; Autoimmune disease; T cell exhaustion; Bystander activation; Prognosis

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APA (6th Edition):

Pecchia-Bekkum, A. G. (2019). Not-so-innocent bystanders? Investigating non-antigen specific CD8+ T cell activation in autoimmune prognosis. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293250

Chicago Manual of Style (16th Edition):

Pecchia-Bekkum, Annika Gabriel. “Not-so-innocent bystanders? Investigating non-antigen specific CD8+ T cell activation in autoimmune prognosis.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 16, 2021. https://www.repository.cam.ac.uk/handle/1810/293250.

MLA Handbook (7th Edition):

Pecchia-Bekkum, Annika Gabriel. “Not-so-innocent bystanders? Investigating non-antigen specific CD8+ T cell activation in autoimmune prognosis.” 2019. Web. 16 Apr 2021.

Vancouver:

Pecchia-Bekkum AG. Not-so-innocent bystanders? Investigating non-antigen specific CD8+ T cell activation in autoimmune prognosis. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 16]. Available from: https://www.repository.cam.ac.uk/handle/1810/293250.

Council of Science Editors:

Pecchia-Bekkum AG. Not-so-innocent bystanders? Investigating non-antigen specific CD8+ T cell activation in autoimmune prognosis. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293250

6. Jacques, Miye K. Role of Tim3 in Mediating T Cell Exhaustion During Chronic Mycobacterium Tuberculosis Infection.

Degree: Immunology and Microbiology, Microbiology and Physiological Systems, 2017, U of Massachusetts : Med

  Mycobacterium tuberculosis infection is one of the leading causes of mortality worldwide. One third of the population is estimated to be infected, however only… (more)

Subjects/Keywords: Tuberculosis; T cell exhaustion; TIM3; Immunology of Infectious Disease

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APA (6th Edition):

Jacques, M. K. (2017). Role of Tim3 in Mediating T Cell Exhaustion During Chronic Mycobacterium Tuberculosis Infection. (Masters Thesis). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/912

Chicago Manual of Style (16th Edition):

Jacques, Miye K. “Role of Tim3 in Mediating T Cell Exhaustion During Chronic Mycobacterium Tuberculosis Infection.” 2017. Masters Thesis, U of Massachusetts : Med. Accessed April 16, 2021. http://escholarship.umassmed.edu/gsbs_diss/912.

MLA Handbook (7th Edition):

Jacques, Miye K. “Role of Tim3 in Mediating T Cell Exhaustion During Chronic Mycobacterium Tuberculosis Infection.” 2017. Web. 16 Apr 2021.

Vancouver:

Jacques MK. Role of Tim3 in Mediating T Cell Exhaustion During Chronic Mycobacterium Tuberculosis Infection. [Internet] [Masters thesis]. U of Massachusetts : Med; 2017. [cited 2021 Apr 16]. Available from: http://escholarship.umassmed.edu/gsbs_diss/912.

Council of Science Editors:

Jacques MK. Role of Tim3 in Mediating T Cell Exhaustion During Chronic Mycobacterium Tuberculosis Infection. [Masters Thesis]. U of Massachusetts : Med; 2017. Available from: http://escholarship.umassmed.edu/gsbs_diss/912


University of Saskatchewan

7. Wang, Rong. Novel HIV-1 Gag-specific Exosome-targeted CD8+ T cell-Based Therapeutic Vaccine Capable of Converting CTL Exhaustion in Chronic Infection.

Degree: 2015, University of Saskatchewan

 Human immunodeficiency virus type 1 (HIV-1) is the cause of acquired immune deficiency syndrome (AIDS). HIV-1 is a worldwide epidemic that currently affects over 35… (more)

Subjects/Keywords: HIV-1; exosome; T-cell vaccine; therapeutic; chronic infection; CTLs exhaustion.

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APA (6th Edition):

Wang, R. (2015). Novel HIV-1 Gag-specific Exosome-targeted CD8+ T cell-Based Therapeutic Vaccine Capable of Converting CTL Exhaustion in Chronic Infection. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/12614

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, Rong. “Novel HIV-1 Gag-specific Exosome-targeted CD8+ T cell-Based Therapeutic Vaccine Capable of Converting CTL Exhaustion in Chronic Infection.” 2015. Thesis, University of Saskatchewan. Accessed April 16, 2021. http://hdl.handle.net/10388/12614.

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

MLA Handbook (7th Edition):

Wang, Rong. “Novel HIV-1 Gag-specific Exosome-targeted CD8+ T cell-Based Therapeutic Vaccine Capable of Converting CTL Exhaustion in Chronic Infection.” 2015. Web. 16 Apr 2021.

Vancouver:

Wang R. Novel HIV-1 Gag-specific Exosome-targeted CD8+ T cell-Based Therapeutic Vaccine Capable of Converting CTL Exhaustion in Chronic Infection. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10388/12614.

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

Council of Science Editors:

Wang R. Novel HIV-1 Gag-specific Exosome-targeted CD8+ T cell-Based Therapeutic Vaccine Capable of Converting CTL Exhaustion in Chronic Infection. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/12614

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


University of Saskatchewan

8. 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 April 16, 2021. 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. 16 Apr 2021.

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 2021 Apr 16]. 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 Toronto

9. Clayton, Kiera Leigh. Elucidating Tim-3 Function and Regulation in Human CD8+ T cells.

Degree: PhD, 2015, University of Toronto

Chronic HIV infection results in a loss of HIV-specific CD8+ T cell effector function, termed "exhaustion", which contributes to loss of viral control and progression… (more)

Subjects/Keywords: HIV/AIDS; T cell exhaustion; Tim-3; 0982

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APA (6th Edition):

Clayton, K. L. (2015). Elucidating Tim-3 Function and Regulation in Human CD8+ T cells. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89023

Chicago Manual of Style (16th Edition):

Clayton, Kiera Leigh. “Elucidating Tim-3 Function and Regulation in Human CD8+ T cells.” 2015. Doctoral Dissertation, University of Toronto. Accessed April 16, 2021. http://hdl.handle.net/1807/89023.

MLA Handbook (7th Edition):

Clayton, Kiera Leigh. “Elucidating Tim-3 Function and Regulation in Human CD8+ T cells.” 2015. Web. 16 Apr 2021.

Vancouver:

Clayton KL. Elucidating Tim-3 Function and Regulation in Human CD8+ T cells. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1807/89023.

Council of Science Editors:

Clayton KL. Elucidating Tim-3 Function and Regulation in Human CD8+ T cells. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/89023


University of Melbourne

10. Daehling, Sabrina. Essential and complementary function of dendritic cell subsets during immunotherapy.

Degree: 2019, University of Melbourne

T lymphocytes are critical components of the adaptive immune system that protects us against a variety of infections. However, during chronic infections such as with… (more)

Subjects/Keywords: Checkpoint immunotherapy; CD8 T cell exhaustion; Dendritic cells; Chronic viral infection

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APA (6th Edition):

Daehling, S. (2019). Essential and complementary function of dendritic cell subsets during immunotherapy. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/234269

Chicago Manual of Style (16th Edition):

Daehling, Sabrina. “Essential and complementary function of dendritic cell subsets during immunotherapy.” 2019. Doctoral Dissertation, University of Melbourne. Accessed April 16, 2021. http://hdl.handle.net/11343/234269.

MLA Handbook (7th Edition):

Daehling, Sabrina. “Essential and complementary function of dendritic cell subsets during immunotherapy.” 2019. Web. 16 Apr 2021.

Vancouver:

Daehling S. Essential and complementary function of dendritic cell subsets during immunotherapy. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/11343/234269.

Council of Science Editors:

Daehling S. Essential and complementary function of dendritic cell subsets during immunotherapy. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/234269


University of Sydney

11. Suprunenko, Tamara. Significance of IRF9-dependent IFN-I signalling on immune responses during LCMV infection of mice .

Degree: 2020, University of Sydney

 Type I interferons (IFN-Is) are master regulators of the immune system. They are responsible for initiating the antiviral response but also have immunomodulatory effects on… (more)

Subjects/Keywords: LCMV; interferon; T cell; exhaustion; PD-L1; IFN-I

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APA (6th Edition):

Suprunenko, T. (2020). Significance of IRF9-dependent IFN-I signalling on immune responses during LCMV infection of mice . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/23391

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):

Suprunenko, Tamara. “Significance of IRF9-dependent IFN-I signalling on immune responses during LCMV infection of mice .” 2020. Thesis, University of Sydney. Accessed April 16, 2021. http://hdl.handle.net/2123/23391.

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

MLA Handbook (7th Edition):

Suprunenko, Tamara. “Significance of IRF9-dependent IFN-I signalling on immune responses during LCMV infection of mice .” 2020. Web. 16 Apr 2021.

Vancouver:

Suprunenko T. Significance of IRF9-dependent IFN-I signalling on immune responses during LCMV infection of mice . [Internet] [Thesis]. University of Sydney; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2123/23391.

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

Council of Science Editors:

Suprunenko T. Significance of IRF9-dependent IFN-I signalling on immune responses during LCMV infection of mice . [Thesis]. University of Sydney; 2020. Available from: http://hdl.handle.net/2123/23391

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


Duke University

12. Woroniecka, Karolina. T Cell Exhaustion in Glioblastoma .

Degree: 2020, Duke University

  Glioblastoma (GBM) is the most common primary malignant brain tumor. Despite standard of care treatment GBM remains universally lethal, demonstrating a significant need for… (more)

Subjects/Keywords: Oncology; Immunology; Neurosciences; Glioblastoma; Immune Checkpoint Blockade; T Cell Exhaustion

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APA (6th Edition):

Woroniecka, K. (2020). T Cell Exhaustion in Glioblastoma . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/20843

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):

Woroniecka, Karolina. “T Cell Exhaustion in Glioblastoma .” 2020. Thesis, Duke University. Accessed April 16, 2021. http://hdl.handle.net/10161/20843.

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

MLA Handbook (7th Edition):

Woroniecka, Karolina. “T Cell Exhaustion in Glioblastoma .” 2020. Web. 16 Apr 2021.

Vancouver:

Woroniecka K. T Cell Exhaustion in Glioblastoma . [Internet] [Thesis]. Duke University; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10161/20843.

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

Council of Science Editors:

Woroniecka K. T Cell Exhaustion in Glioblastoma . [Thesis]. Duke University; 2020. Available from: http://hdl.handle.net/10161/20843

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


University of California – Irvine

13. Jagadish, Bharath. Mathematical Modeling of T-cell Exhaustion and PD-1 Blockade in Chronic Infections.

Degree: Chemical and Biochemical Engineering, 2015, University of California – Irvine

 Immune responses to persistent viral infections often fail because of intense regulation of antigen-specific T-cells-a process referred to as T cell exhaustion, characterized by progressive… (more)

Subjects/Keywords: Immunology; Mathematics; Blockade; CD8+ T-cells; Inhibitory receptors; Mathematical modeling; T-cell exhaustion

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APA (6th Edition):

Jagadish, B. (2015). Mathematical Modeling of T-cell Exhaustion and PD-1 Blockade in Chronic Infections. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/86g562mt

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):

Jagadish, Bharath. “Mathematical Modeling of T-cell Exhaustion and PD-1 Blockade in Chronic Infections.” 2015. Thesis, University of California – Irvine. Accessed April 16, 2021. http://www.escholarship.org/uc/item/86g562mt.

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

MLA Handbook (7th Edition):

Jagadish, Bharath. “Mathematical Modeling of T-cell Exhaustion and PD-1 Blockade in Chronic Infections.” 2015. Web. 16 Apr 2021.

Vancouver:

Jagadish B. Mathematical Modeling of T-cell Exhaustion and PD-1 Blockade in Chronic Infections. [Internet] [Thesis]. University of California – Irvine; 2015. [cited 2021 Apr 16]. Available from: http://www.escholarship.org/uc/item/86g562mt.

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

Council of Science Editors:

Jagadish B. Mathematical Modeling of T-cell Exhaustion and PD-1 Blockade in Chronic Infections. [Thesis]. University of California – Irvine; 2015. Available from: http://www.escholarship.org/uc/item/86g562mt

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


Arizona State University

14. Krishna, Sri. T-Cell Immunogenicity and Dysfunction in Cancer and Viral Diseases.

Degree: Biological Design, 2017, Arizona State University

 CD8+ T-lymphocytes (CTLs) are central to the immunologic control of infections and are currently at the forefront of strategies that enhance immune based treatment of… (more)

Subjects/Keywords: Immunology; Oncology; Virology; Cancer Immunotherapy; CD8+ T-cell Epitopes; Head and Neck Cancer; HPV; Self/Non-self; T-cell Exhaustion

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APA (6th Edition):

Krishna, S. (2017). T-Cell Immunogenicity and Dysfunction in Cancer and Viral Diseases. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/46218

Chicago Manual of Style (16th Edition):

Krishna, Sri. “T-Cell Immunogenicity and Dysfunction in Cancer and Viral Diseases.” 2017. Doctoral Dissertation, Arizona State University. Accessed April 16, 2021. http://repository.asu.edu/items/46218.

MLA Handbook (7th Edition):

Krishna, Sri. “T-Cell Immunogenicity and Dysfunction in Cancer and Viral Diseases.” 2017. Web. 16 Apr 2021.

Vancouver:

Krishna S. T-Cell Immunogenicity and Dysfunction in Cancer and Viral Diseases. [Internet] [Doctoral dissertation]. Arizona State University; 2017. [cited 2021 Apr 16]. Available from: http://repository.asu.edu/items/46218.

Council of Science Editors:

Krishna S. T-Cell Immunogenicity and Dysfunction in Cancer and Viral Diseases. [Doctoral Dissertation]. Arizona State University; 2017. Available from: http://repository.asu.edu/items/46218


UCLA

15. Cunningham, Cameron Ray. Immunosuppression and Immune Dysfunction During Persistent Virus Infection.

Degree: Microbiology, Immunology, & Molecular Genetics, 2015, UCLA

 Persistent virus infections are a significant burden on global health with over 500 million people afflicted with human immunodeficiency virus (HIV), and hepatitis B and… (more)

Subjects/Keywords: Immunology; Dendritic Cells; Immunosuppression; Interferon; Persistent Virus Infection; T Cell Exhaustion; Thymus

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

APA (6th Edition):

Cunningham, C. R. (2015). Immunosuppression and Immune Dysfunction During Persistent Virus Infection. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/5td2s77b

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):

Cunningham, Cameron Ray. “Immunosuppression and Immune Dysfunction During Persistent Virus Infection.” 2015. Thesis, UCLA. Accessed April 16, 2021. http://www.escholarship.org/uc/item/5td2s77b.

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

MLA Handbook (7th Edition):

Cunningham, Cameron Ray. “Immunosuppression and Immune Dysfunction During Persistent Virus Infection.” 2015. Web. 16 Apr 2021.

Vancouver:

Cunningham CR. Immunosuppression and Immune Dysfunction During Persistent Virus Infection. [Internet] [Thesis]. UCLA; 2015. [cited 2021 Apr 16]. Available from: http://www.escholarship.org/uc/item/5td2s77b.

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

Council of Science Editors:

Cunningham CR. Immunosuppression and Immune Dysfunction During Persistent Virus Infection. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/5td2s77b

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


University of Plymouth

16. Ahmed, Asma. A study of immune responses during antiviral treatment for hepatitis C virus infection.

Degree: Thesis (M.D.), 2020, University of Plymouth

 Hepatitis C virus (HCV) is an RNA virus that primarily infects the liver, affecting 70 million people worldwide, according to new estimates (Polaris Observatory HCV… (more)

Subjects/Keywords: 616.3; Hepatitis C virus; HCV; antiviral treatment; immune response; Elispot; T cell exhaustion; innate immunity

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

APA (6th Edition):

Ahmed, A. (2020). A study of immune responses during antiviral treatment for hepatitis C virus infection. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/15774

Chicago Manual of Style (16th Edition):

Ahmed, Asma. “A study of immune responses during antiviral treatment for hepatitis C virus infection.” 2020. Doctoral Dissertation, University of Plymouth. Accessed April 16, 2021. http://hdl.handle.net/10026.1/15774.

MLA Handbook (7th Edition):

Ahmed, Asma. “A study of immune responses during antiviral treatment for hepatitis C virus infection.” 2020. Web. 16 Apr 2021.

Vancouver:

Ahmed A. A study of immune responses during antiviral treatment for hepatitis C virus infection. [Internet] [Doctoral dissertation]. University of Plymouth; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10026.1/15774.

Council of Science Editors:

Ahmed A. A study of immune responses during antiviral treatment for hepatitis C virus infection. [Doctoral Dissertation]. University of Plymouth; 2020. Available from: http://hdl.handle.net/10026.1/15774


Washington University in St. Louis

17. Raju, Saravanan. Signaling Mechanisms in Adaptive Immunity.

Degree: PhD, Biology & Biomedical Sciences (Immunology), 2020, Washington University in St. Louis

 The adaptive immune response consists of interplay between CD4 T cells, CD8 T cells, and B cells which function in control of pathogen in the… (more)

Subjects/Keywords: Checkpoint Blockade, PD-1, T cell Exhaustion, T Follicular Helper; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology

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APA (6th Edition):

Raju, S. (2020). Signaling Mechanisms in Adaptive Immunity. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/2234

Chicago Manual of Style (16th Edition):

Raju, Saravanan. “Signaling Mechanisms in Adaptive Immunity.” 2020. Doctoral Dissertation, Washington University in St. Louis. Accessed April 16, 2021. https://openscholarship.wustl.edu/art_sci_etds/2234.

MLA Handbook (7th Edition):

Raju, Saravanan. “Signaling Mechanisms in Adaptive Immunity.” 2020. Web. 16 Apr 2021.

Vancouver:

Raju S. Signaling Mechanisms in Adaptive Immunity. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2020. [cited 2021 Apr 16]. Available from: https://openscholarship.wustl.edu/art_sci_etds/2234.

Council of Science Editors:

Raju S. Signaling Mechanisms in Adaptive Immunity. [Doctoral Dissertation]. Washington University in St. Louis; 2020. Available from: https://openscholarship.wustl.edu/art_sci_etds/2234


University of Pennsylvania

18. Pombo, Carolina. Expression of Pd-1, Cd160 and 2b4 on Cd8 T Cells During HIV infection: Markers of Exhaustion?.

Degree: 2015, University of Pennsylvania

 HIV infection is typically associated with dysfunction of the immune system. Evidence indicates that CD8 T-cells are crucial in the fight against HIV, but with… (more)

Subjects/Keywords: CD8 T cells; HIV; Inhibitory Receptors; T cell Exhaustion; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology; Microbiology; Virology

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APA (6th Edition):

Pombo, C. (2015). Expression of Pd-1, Cd160 and 2b4 on Cd8 T Cells During HIV infection: Markers of Exhaustion?. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1951

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):

Pombo, Carolina. “Expression of Pd-1, Cd160 and 2b4 on Cd8 T Cells During HIV infection: Markers of Exhaustion?.” 2015. Thesis, University of Pennsylvania. Accessed April 16, 2021. https://repository.upenn.edu/edissertations/1951.

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

MLA Handbook (7th Edition):

Pombo, Carolina. “Expression of Pd-1, Cd160 and 2b4 on Cd8 T Cells During HIV infection: Markers of Exhaustion?.” 2015. Web. 16 Apr 2021.

Vancouver:

Pombo C. Expression of Pd-1, Cd160 and 2b4 on Cd8 T Cells During HIV infection: Markers of Exhaustion?. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2021 Apr 16]. Available from: https://repository.upenn.edu/edissertations/1951.

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

Council of Science Editors:

Pombo C. Expression of Pd-1, Cd160 and 2b4 on Cd8 T Cells During HIV infection: Markers of Exhaustion?. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/1951

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

19. Leclerc, Marine. Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux : Immuno-modulatory effects of neuropilin-1 on anti-tumor CD8 T cell functions.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Université Paris-Saclay (ComUE)

De récents progrès dans la compréhension de la régulation de l'interaction moléculaire entre les lymphocytes T CD8 (LT CD8) et les cellules tumorales ont donné… (more)

Subjects/Keywords: Neuropiline-1; Cancer; Épuisement; Lymphocyte T CD8; Immunothérapie; Neuropilin-1; Cancer; Exhaustion; CD8 T cell; Immunotherapy

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APA (6th Edition):

Leclerc, M. (2018). Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux : Immuno-modulatory effects of neuropilin-1 on anti-tumor CD8 T cell functions. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS458

Chicago Manual of Style (16th Edition):

Leclerc, Marine. “Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux : Immuno-modulatory effects of neuropilin-1 on anti-tumor CD8 T cell functions.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed April 16, 2021. http://www.theses.fr/2018SACLS458.

MLA Handbook (7th Edition):

Leclerc, Marine. “Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux : Immuno-modulatory effects of neuropilin-1 on anti-tumor CD8 T cell functions.” 2018. Web. 16 Apr 2021.

Vancouver:

Leclerc M. Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux : Immuno-modulatory effects of neuropilin-1 on anti-tumor CD8 T cell functions. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2018SACLS458.

Council of Science Editors:

Leclerc M. Rôle de la Neuropiline-1 dans les fonctions effectrices des lymphocytes T CD8 antitumoraux : Immuno-modulatory effects of neuropilin-1 on anti-tumor CD8 T cell functions. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS458


University of Michigan

20. Yu, Amy. Gut Microbiota Modulate CD8 T Cell Responses to Influence Colitis-Associated Tumorigenesis.

Degree: PhD, Immunology, 2020, University of Michigan

 The gut microbiome plays important physiological roles, including aiding in digestion of non-digestible starches and fibers, production of nutrients, protection against pathogens, as well as… (more)

Subjects/Keywords: gut microbiome; colon cancer; inflammation; CD8 T cells; T cell exhaustion; colitis; Microbiology and Immunology; Oncology and Hematology; Health Sciences; Science

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APA (6th Edition):

Yu, A. (2020). Gut Microbiota Modulate CD8 T Cell Responses to Influence Colitis-Associated Tumorigenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/162892

Chicago Manual of Style (16th Edition):

Yu, Amy. “Gut Microbiota Modulate CD8 T Cell Responses to Influence Colitis-Associated Tumorigenesis.” 2020. Doctoral Dissertation, University of Michigan. Accessed April 16, 2021. http://hdl.handle.net/2027.42/162892.

MLA Handbook (7th Edition):

Yu, Amy. “Gut Microbiota Modulate CD8 T Cell Responses to Influence Colitis-Associated Tumorigenesis.” 2020. Web. 16 Apr 2021.

Vancouver:

Yu A. Gut Microbiota Modulate CD8 T Cell Responses to Influence Colitis-Associated Tumorigenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/2027.42/162892.

Council of Science Editors:

Yu A. Gut Microbiota Modulate CD8 T Cell Responses to Influence Colitis-Associated Tumorigenesis. [Doctoral Dissertation]. University of Michigan; 2020. Available from: http://hdl.handle.net/2027.42/162892


Iowa State University

21. Esch, Kevin Jan. Mechanisms of immunity and pathology during canine leishmaniasis: Leading the way to prevention and treatment.

Degree: 2013, Iowa State University

 Visceral leishmaniasis (VL) caused by certain species of the genus Leishmania results in a significant disease burden worldwide. This is most pronounced in some of… (more)

Subjects/Keywords: canine; cytokine; leishmania; renal; T cell exhaustion; vaccine; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology; Pathology; Veterinary Medicine

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APA (6th Edition):

Esch, K. J. (2013). Mechanisms of immunity and pathology during canine leishmaniasis: Leading the way to prevention and treatment. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16084

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):

Esch, Kevin Jan. “Mechanisms of immunity and pathology during canine leishmaniasis: Leading the way to prevention and treatment.” 2013. Thesis, Iowa State University. Accessed April 16, 2021. https://lib.dr.iastate.edu/etd/16084.

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

MLA Handbook (7th Edition):

Esch, Kevin Jan. “Mechanisms of immunity and pathology during canine leishmaniasis: Leading the way to prevention and treatment.” 2013. Web. 16 Apr 2021.

Vancouver:

Esch KJ. Mechanisms of immunity and pathology during canine leishmaniasis: Leading the way to prevention and treatment. [Internet] [Thesis]. Iowa State University; 2013. [cited 2021 Apr 16]. Available from: https://lib.dr.iastate.edu/etd/16084.

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

Council of Science Editors:

Esch KJ. Mechanisms of immunity and pathology during canine leishmaniasis: Leading the way to prevention and treatment. [Thesis]. Iowa State University; 2013. Available from: https://lib.dr.iastate.edu/etd/16084

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

22. Frencher, James T. Role of Isoprenoid Biosynthesis in Listeria-based Tuberculosis Vaccine Efficacy.

Degree: 2015, University of Illinois – Chicago

 Tuberculosis is a leading infectious cause of death worldwide. Antibiotics are increasingly ineffective in treatment, and the only approved vaccine shows minimal protection against disease… (more)

Subjects/Keywords: Vaccine Listeria Tuberculosis Isoprenoid T Cell Exhaustion

…purified I result in activation and proliferation of Vγ2Vδ2 T cells. Vγ2Vδ2 T cell activation… …antigen presenting molecule. TCR of the Vγ2Vδ2 T cell is shown in blue, and unknown antigen… …12 3 Potency of Isoprenoid Biosynthesis pathways in Vγ2Vδ2 T cell induction. A)… …inducing Vγ2Vδ2 T cell activation and expansion due to production of high levels of IPP or… …lysates, and representative flow histograms of CD3+Vγ2+ T cell percentages (bottom)… 

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APA (6th Edition):

Frencher, J. T. (2015). Role of Isoprenoid Biosynthesis in Listeria-based Tuberculosis Vaccine Efficacy. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19481

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):

Frencher, James T. “Role of Isoprenoid Biosynthesis in Listeria-based Tuberculosis Vaccine Efficacy.” 2015. Thesis, University of Illinois – Chicago. Accessed April 16, 2021. http://hdl.handle.net/10027/19481.

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

MLA Handbook (7th Edition):

Frencher, James T. “Role of Isoprenoid Biosynthesis in Listeria-based Tuberculosis Vaccine Efficacy.” 2015. Web. 16 Apr 2021.

Vancouver:

Frencher JT. Role of Isoprenoid Biosynthesis in Listeria-based Tuberculosis Vaccine Efficacy. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10027/19481.

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

Council of Science Editors:

Frencher JT. Role of Isoprenoid Biosynthesis in Listeria-based Tuberculosis Vaccine Efficacy. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19481

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


University of Oxford

23. Gupta, Prakash K. Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection.

Degree: PhD, 2014, University of Oxford

 During the course of infection with chronic pathogens such as Hepatitis C virus (HCV), Hepatitis B virus (HBV) and HIV, virus-specific CD8<sup>+</sup> T cells differentiate… (more)

Subjects/Keywords: 616.3; Medical sciences; Gastroenterology; Immunology; Infectious diseases; Genetics (medical sciences); Genomics; T cell exhaustion; Hepatitis C

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APA (6th Edition):

Gupta, P. K. (2014). Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:f28b67d7-287d-4594-a2d1-161f35e9c5a2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655052

Chicago Manual of Style (16th Edition):

Gupta, Prakash K. “Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection.” 2014. Doctoral Dissertation, University of Oxford. Accessed April 16, 2021. http://ora.ox.ac.uk/objects/uuid:f28b67d7-287d-4594-a2d1-161f35e9c5a2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655052.

MLA Handbook (7th Edition):

Gupta, Prakash K. “Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection.” 2014. Web. 16 Apr 2021.

Vancouver:

Gupta PK. Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2021 Apr 16]. Available from: http://ora.ox.ac.uk/objects/uuid:f28b67d7-287d-4594-a2d1-161f35e9c5a2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655052.

Council of Science Editors:

Gupta PK. Use of genome wide expression profiles in analysis of T cell dysfunction in Hepatitis C virus infection. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:f28b67d7-287d-4594-a2d1-161f35e9c5a2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655052


Arizona State University

24. Lussier, Danielle Marie. Increasing T Cell Immunity to Metastatic Osteosarcoma via Modulation of Inhibitory T Cell Receptors.

Degree: Molecular and Cellular Biology, 2015, Arizona State University

 Osteosarcoma is the most common bone cancer in children and adolescents. Patients with metastatic osteosarcoma are typically refractory to treatment. Numerous lines of evidence suggest… (more)

Subjects/Keywords: Immunology; Molecular biology; Cellular biology; CTLA-4; Inhibitory Receptors; Metastatic Osteosarcoma; PD-1; PD-L1; T cell exhaustion

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APA (6th Edition):

Lussier, D. M. (2015). Increasing T Cell Immunity to Metastatic Osteosarcoma via Modulation of Inhibitory T Cell Receptors. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/29627

Chicago Manual of Style (16th Edition):

Lussier, Danielle Marie. “Increasing T Cell Immunity to Metastatic Osteosarcoma via Modulation of Inhibitory T Cell Receptors.” 2015. Doctoral Dissertation, Arizona State University. Accessed April 16, 2021. http://repository.asu.edu/items/29627.

MLA Handbook (7th Edition):

Lussier, Danielle Marie. “Increasing T Cell Immunity to Metastatic Osteosarcoma via Modulation of Inhibitory T Cell Receptors.” 2015. Web. 16 Apr 2021.

Vancouver:

Lussier DM. Increasing T Cell Immunity to Metastatic Osteosarcoma via Modulation of Inhibitory T Cell Receptors. [Internet] [Doctoral dissertation]. Arizona State University; 2015. [cited 2021 Apr 16]. Available from: http://repository.asu.edu/items/29627.

Council of Science Editors:

Lussier DM. Increasing T Cell Immunity to Metastatic Osteosarcoma via Modulation of Inhibitory T Cell Receptors. [Doctoral Dissertation]. Arizona State University; 2015. Available from: http://repository.asu.edu/items/29627


University of Pennsylvania

25. Zhang, Ying Zhang. Blocking Immunosuppressive Factors and Taking Advantage of the Nutrient Supply Within the Tumor Microenvironment: Pathways to Achieve Improved Cancer Immunotherapeutic Efficacy for Patients With Metastatic Melanoma.

Degree: 2016, University of Pennsylvania

 The incidence of melanoma is increasing. Immunotherapy commonly fails due to the immunosuppressive tumor microenvironment (TME). The aim of my dissertation is to develop strategies… (more)

Subjects/Keywords: Cancer Immunotherapy; Checkpoint inhibitor; Melanoma; Metabolism; T cell exhaustion; Vaccine; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology

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APA (6th Edition):

Zhang, Y. Z. (2016). Blocking Immunosuppressive Factors and Taking Advantage of the Nutrient Supply Within the Tumor Microenvironment: Pathways to Achieve Improved Cancer Immunotherapeutic Efficacy for Patients With Metastatic Melanoma. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2125

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, Ying Zhang. “Blocking Immunosuppressive Factors and Taking Advantage of the Nutrient Supply Within the Tumor Microenvironment: Pathways to Achieve Improved Cancer Immunotherapeutic Efficacy for Patients With Metastatic Melanoma.” 2016. Thesis, University of Pennsylvania. Accessed April 16, 2021. https://repository.upenn.edu/edissertations/2125.

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

MLA Handbook (7th Edition):

Zhang, Ying Zhang. “Blocking Immunosuppressive Factors and Taking Advantage of the Nutrient Supply Within the Tumor Microenvironment: Pathways to Achieve Improved Cancer Immunotherapeutic Efficacy for Patients With Metastatic Melanoma.” 2016. Web. 16 Apr 2021.

Vancouver:

Zhang YZ. Blocking Immunosuppressive Factors and Taking Advantage of the Nutrient Supply Within the Tumor Microenvironment: Pathways to Achieve Improved Cancer Immunotherapeutic Efficacy for Patients With Metastatic Melanoma. [Internet] [Thesis]. University of Pennsylvania; 2016. [cited 2021 Apr 16]. Available from: https://repository.upenn.edu/edissertations/2125.

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

Council of Science Editors:

Zhang YZ. Blocking Immunosuppressive Factors and Taking Advantage of the Nutrient Supply Within the Tumor Microenvironment: Pathways to Achieve Improved Cancer Immunotherapeutic Efficacy for Patients With Metastatic Melanoma. [Thesis]. University of Pennsylvania; 2016. Available from: https://repository.upenn.edu/edissertations/2125

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

26. Wolski, David. Integrative analysis of CD8 T-cell responses in the context of adaptive immunity to acute Hepatitis C virus infection : Analyse intégrative de la réponse T CD8+ spécifique du virus de l'hépatite C au cours de la phase aigüe de l'infection.

Degree: Docteur es, Immunologie, 2017, Université de Strasbourg

Le virus de l'hépatite C (VHC) établit généralement une infection chronique. Néanmoins, environ 20% des sujets vont résoudre spontanément l’infection. Il existe des preuves solides… (more)

Subjects/Keywords: Virus de l’hépatite C; Lymphocytes T CD8; Régulation Transcriptionnelle; Dysfonction des Lymphocytes T; Lymphocytes T CD4 auxiliaires; Hepatitis C virus; CD8 T cells; Transcriptional regulation; T cell exhaustion; CD4 help; 571.96; 572.8; 616.91

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APA (6th Edition):

Wolski, D. (2017). Integrative analysis of CD8 T-cell responses in the context of adaptive immunity to acute Hepatitis C virus infection : Analyse intégrative de la réponse T CD8+ spécifique du virus de l'hépatite C au cours de la phase aigüe de l'infection. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2017STRAJ018

Chicago Manual of Style (16th Edition):

Wolski, David. “Integrative analysis of CD8 T-cell responses in the context of adaptive immunity to acute Hepatitis C virus infection : Analyse intégrative de la réponse T CD8+ spécifique du virus de l'hépatite C au cours de la phase aigüe de l'infection.” 2017. Doctoral Dissertation, Université de Strasbourg. Accessed April 16, 2021. http://www.theses.fr/2017STRAJ018.

MLA Handbook (7th Edition):

Wolski, David. “Integrative analysis of CD8 T-cell responses in the context of adaptive immunity to acute Hepatitis C virus infection : Analyse intégrative de la réponse T CD8+ spécifique du virus de l'hépatite C au cours de la phase aigüe de l'infection.” 2017. Web. 16 Apr 2021.

Vancouver:

Wolski D. Integrative analysis of CD8 T-cell responses in the context of adaptive immunity to acute Hepatitis C virus infection : Analyse intégrative de la réponse T CD8+ spécifique du virus de l'hépatite C au cours de la phase aigüe de l'infection. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2017. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2017STRAJ018.

Council of Science Editors:

Wolski D. Integrative analysis of CD8 T-cell responses in the context of adaptive immunity to acute Hepatitis C virus infection : Analyse intégrative de la réponse T CD8+ spécifique du virus de l'hépatite C au cours de la phase aigüe de l'infection. [Doctoral Dissertation]. Université de Strasbourg; 2017. Available from: http://www.theses.fr/2017STRAJ018


University of Pennsylvania

27. Shin, Haina. Regulation of Cd8 T Cell Dysfunction During a Chronic Viral infection.

Degree: 2009, University of Pennsylvania

 After an acute infection or vaccination, antigen-specific CD8 T cells undergo memory differentiation once the pathogen has been completely cleared. Memory CD8 T cells acquire… (more)

Subjects/Keywords: chronic infection; CD8 T cell; memory; functional exhaustion; Immunology and Infectious Disease

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APA (6th Edition):

Shin, H. (2009). Regulation of Cd8 T Cell Dysfunction During a Chronic Viral infection. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/20

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):

Shin, Haina. “Regulation of Cd8 T Cell Dysfunction During a Chronic Viral infection.” 2009. Thesis, University of Pennsylvania. Accessed April 16, 2021. https://repository.upenn.edu/edissertations/20.

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

MLA Handbook (7th Edition):

Shin, Haina. “Regulation of Cd8 T Cell Dysfunction During a Chronic Viral infection.” 2009. Web. 16 Apr 2021.

Vancouver:

Shin H. Regulation of Cd8 T Cell Dysfunction During a Chronic Viral infection. [Internet] [Thesis]. University of Pennsylvania; 2009. [cited 2021 Apr 16]. Available from: https://repository.upenn.edu/edissertations/20.

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

Council of Science Editors:

Shin H. Regulation of Cd8 T Cell Dysfunction During a Chronic Viral infection. [Thesis]. University of Pennsylvania; 2009. Available from: https://repository.upenn.edu/edissertations/20

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

28. Weulersse, Marianne. L'absence de CD226 caractérise des LT CD8+ hyporépondeurs au TCR et aux fonctions antitumorales défectueuses : CD226 absence affects TCR responsiveness and restrains tumor infiltrating T lymphocytes functions.

Degree: Docteur es, Immunologie, 2019, Université Toulouse III – Paul Sabatier

Les lymphocytes cytotoxiques T CD8+ (LT CD8+) sont des cellules de l'immunité adaptative qui jouent un rôle majeur dans les réponses immunitaires antitumorales puisqu'ils reconnaissent… (more)

Subjects/Keywords: CD226 (DNAM-1); Lymphocytes T CD8+ cytotoxiques; Signalisation TCR; Costimulation; Echappement tumoral; Epuisement lymphocytaire; Immunothérapie; CD226 (DNAM-1); Cytotoxic CD8+ T lymphocytes; TCR signaling; Costimulation; Tumor immune escape; T cell exhaustion; Immunotherapy

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

APA (6th Edition):

Weulersse, M. (2019). L'absence de CD226 caractérise des LT CD8+ hyporépondeurs au TCR et aux fonctions antitumorales défectueuses : CD226 absence affects TCR responsiveness and restrains tumor infiltrating T lymphocytes functions. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2019TOU30174

Chicago Manual of Style (16th Edition):

Weulersse, Marianne. “L'absence de CD226 caractérise des LT CD8+ hyporépondeurs au TCR et aux fonctions antitumorales défectueuses : CD226 absence affects TCR responsiveness and restrains tumor infiltrating T lymphocytes functions.” 2019. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed April 16, 2021. http://www.theses.fr/2019TOU30174.

MLA Handbook (7th Edition):

Weulersse, Marianne. “L'absence de CD226 caractérise des LT CD8+ hyporépondeurs au TCR et aux fonctions antitumorales défectueuses : CD226 absence affects TCR responsiveness and restrains tumor infiltrating T lymphocytes functions.” 2019. Web. 16 Apr 2021.

Vancouver:

Weulersse M. L'absence de CD226 caractérise des LT CD8+ hyporépondeurs au TCR et aux fonctions antitumorales défectueuses : CD226 absence affects TCR responsiveness and restrains tumor infiltrating T lymphocytes functions. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2019. [cited 2021 Apr 16]. Available from: http://www.theses.fr/2019TOU30174.

Council of Science Editors:

Weulersse M. L'absence de CD226 caractérise des LT CD8+ hyporépondeurs au TCR et aux fonctions antitumorales défectueuses : CD226 absence affects TCR responsiveness and restrains tumor infiltrating T lymphocytes functions. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2019. Available from: http://www.theses.fr/2019TOU30174

29. Sen, Debattama R. Epigenetic Determinants of CD8+ T Cell Exhaustion.

Degree: PhD, 2019, Harvard University

T cell exhaustion describes an acquired dysfunction common in settings of chronic viral infection. Despite clinical efforts to rescue exhaustion, the fundamental mechanisms specifying this… (more)

Subjects/Keywords: Epigenetics; T cell exhaustion; Cancer immunology; immunology; CD8+ T cell; Immunotherapy

…myself. vii Table of Contents Chapter 1. Introduction Section I: T cell exhaustion Section… …State-specific epigenetic landscape defines CD8+ T cell exhaustion in chronic LCMV… …Introduction Results CD8+ T cell exhaustion is associated with extensive changes in accessible… …T cell exhaustion is conserved across chronic viral infections Cure of chronic infection… …dysfunction and coined the term “T cell exhaustion.” T cell exhaustion is now known to occur in… 

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APA (6th Edition):

Sen, D. R. (2019). Epigenetic Determinants of CD8+ T Cell Exhaustion. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029661

Chicago Manual of Style (16th Edition):

Sen, Debattama R. “Epigenetic Determinants of CD8+ T Cell Exhaustion.” 2019. Doctoral Dissertation, Harvard University. Accessed April 16, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029661.

MLA Handbook (7th Edition):

Sen, Debattama R. “Epigenetic Determinants of CD8+ T Cell Exhaustion.” 2019. Web. 16 Apr 2021.

Vancouver:

Sen DR. Epigenetic Determinants of CD8+ T Cell Exhaustion. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2021 Apr 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029661.

Council of Science Editors:

Sen DR. Epigenetic Determinants of CD8+ T Cell Exhaustion. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029661


Leiden University

30. Zwan, A. van der. The immune compartment at the maternal-fetal interface throughout human pregnancy.

Degree: 2020, Leiden University

 <table><tbody><tr><td> During pregnancy a unique situation arises in which the mother's immune system accepts the fetus, which carries both maternal and paternal genes, and does… (more)

Subjects/Keywords: Pregnancy; Immunology; Placenta; Trophoblasts; Decidua; Tolerance; T cell exhaustion; Regulatory T cells; Heterologous immunity; HLA-C

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

APA (6th Edition):

Zwan, A. v. d. (2020). The immune compartment at the maternal-fetal interface throughout human pregnancy. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/84689

Chicago Manual of Style (16th Edition):

Zwan, A van der. “The immune compartment at the maternal-fetal interface throughout human pregnancy.” 2020. Doctoral Dissertation, Leiden University. Accessed April 16, 2021. http://hdl.handle.net/1887/84689.

MLA Handbook (7th Edition):

Zwan, A van der. “The immune compartment at the maternal-fetal interface throughout human pregnancy.” 2020. Web. 16 Apr 2021.

Vancouver:

Zwan Avd. The immune compartment at the maternal-fetal interface throughout human pregnancy. [Internet] [Doctoral dissertation]. Leiden University; 2020. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1887/84689.

Council of Science Editors:

Zwan Avd. The immune compartment at the maternal-fetal interface throughout human pregnancy. [Doctoral Dissertation]. Leiden University; 2020. Available from: http://hdl.handle.net/1887/84689

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