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You searched for subject:(CD8 T cell). Showing records 1 – 30 of 222 total matches.

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1. Wilson, Douglas C. Interleukin-12: A Critical Regulator of Protective CD8+ T Cell Immunity During Toxoplasma gondii Infection.

Degree: PhD, Division of Biology and Medicine. Pathobiology, 2009, Brown University

 Immunity to Toxoplasma gondii infection is principally mediated by the activation of CD8+ T cells producing the protective cytokine IFN-?. To characterize primary CTL activation,… (more)

Subjects/Keywords: CD8+ T cell

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APA (6th Edition):

Wilson, D. C. (2009). Interleukin-12: A Critical Regulator of Protective CD8+ T Cell Immunity During Toxoplasma gondii Infection. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:75/

Chicago Manual of Style (16th Edition):

Wilson, Douglas C. “Interleukin-12: A Critical Regulator of Protective CD8+ T Cell Immunity During Toxoplasma gondii Infection.” 2009. Doctoral Dissertation, Brown University. Accessed May 08, 2021. https://repository.library.brown.edu/studio/item/bdr:75/.

MLA Handbook (7th Edition):

Wilson, Douglas C. “Interleukin-12: A Critical Regulator of Protective CD8+ T Cell Immunity During Toxoplasma gondii Infection.” 2009. Web. 08 May 2021.

Vancouver:

Wilson DC. Interleukin-12: A Critical Regulator of Protective CD8+ T Cell Immunity During Toxoplasma gondii Infection. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2021 May 08]. Available from: https://repository.library.brown.edu/studio/item/bdr:75/.

Council of Science Editors:

Wilson DC. Interleukin-12: A Critical Regulator of Protective CD8+ T Cell Immunity During Toxoplasma gondii Infection. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:75/


University of New South Wales

2. Villanueva, Jeanette Elizabeth. TRAF proteins and their role in T cell effector function and homeostasis.

Degree: Clinical School - St Vincent's Hospital, 2014, University of New South Wales

 TNF-receptor associated factor (TRAF) 2 integrates multiple TNF-family signaling pathways in T cells making it a unifying target for immunomodulation based on co-stimulation. This thesis… (more)

Subjects/Keywords: T cell; TRAF2; Transplantation; CD8 T cell; NKT cell; IL-15

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APA (6th Edition):

Villanueva, J. E. (2014). TRAF proteins and their role in T cell effector function and homeostasis. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53661 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12356/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Villanueva, Jeanette Elizabeth. “TRAF proteins and their role in T cell effector function and homeostasis.” 2014. Doctoral Dissertation, University of New South Wales. Accessed May 08, 2021. http://handle.unsw.edu.au/1959.4/53661 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12356/SOURCE02?view=true.

MLA Handbook (7th Edition):

Villanueva, Jeanette Elizabeth. “TRAF proteins and their role in T cell effector function and homeostasis.” 2014. Web. 08 May 2021.

Vancouver:

Villanueva JE. TRAF proteins and their role in T cell effector function and homeostasis. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2021 May 08]. Available from: http://handle.unsw.edu.au/1959.4/53661 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12356/SOURCE02?view=true.

Council of Science Editors:

Villanueva JE. TRAF proteins and their role in T cell effector function and homeostasis. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53661 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12356/SOURCE02?view=true


University of Rochester

3. Walling, Brandon L. Chemokine Insensitive CD8+ T cell Migration.

Degree: PhD, 2020, University of Rochester

 Our current understanding of T cell migration has focused on chemokine-mediated integrin activation, which dictates that chemokines provide critical directional signals to guide T cell(more)

Subjects/Keywords: CD8+ T cell; Migration; LFA-1.

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APA (6th Edition):

Walling, B. L. (2020). Chemokine Insensitive CD8+ T cell Migration. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/35514

Chicago Manual of Style (16th Edition):

Walling, Brandon L. “Chemokine Insensitive CD8+ T cell Migration.” 2020. Doctoral Dissertation, University of Rochester. Accessed May 08, 2021. http://hdl.handle.net/1802/35514.

MLA Handbook (7th Edition):

Walling, Brandon L. “Chemokine Insensitive CD8+ T cell Migration.” 2020. Web. 08 May 2021.

Vancouver:

Walling BL. Chemokine Insensitive CD8+ T cell Migration. [Internet] [Doctoral dissertation]. University of Rochester; 2020. [cited 2021 May 08]. Available from: http://hdl.handle.net/1802/35514.

Council of Science Editors:

Walling BL. Chemokine Insensitive CD8+ T cell Migration. [Doctoral Dissertation]. University of Rochester; 2020. Available from: http://hdl.handle.net/1802/35514


Penn State University

4. Vakil, Devashree S. Autocrine IL-2 Signaling And The Memory CD8+ T Cell Response.

Degree: 2012, Penn State University

 Generation of potent long-lived CD8 T cell immunological memory is the ultimate goal of all vaccines directed against intracellular pathogens and cancer. It has been… (more)

Subjects/Keywords: IL-2; Memory CD8 T Cell

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APA (6th Edition):

Vakil, D. S. (2012). Autocrine IL-2 Signaling And The Memory CD8+ T Cell Response. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15301

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):

Vakil, Devashree S. “Autocrine IL-2 Signaling And The Memory CD8+ T Cell Response.” 2012. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/15301.

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

MLA Handbook (7th Edition):

Vakil, Devashree S. “Autocrine IL-2 Signaling And The Memory CD8+ T Cell Response.” 2012. Web. 08 May 2021.

Vancouver:

Vakil DS. Autocrine IL-2 Signaling And The Memory CD8+ T Cell Response. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/15301.

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

Council of Science Editors:

Vakil DS. Autocrine IL-2 Signaling And The Memory CD8+ T Cell Response. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/15301

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


Victoria University of Wellington

5. Gibbins, John David. The Role of Langerin⁺ CD8α⁺ Dendritic Cells in Tumour Immunotherapy.

Degree: 2014, Victoria University of Wellington

 The immune system has the potential to selectively target and eliminate tumours cells. However, the induction of an immunosuppressive environment by factors released by tumours… (more)

Subjects/Keywords: Dendritic cells; Tumour immunotherapy; CD8 T cell

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APA (6th Edition):

Gibbins, J. D. (2014). The Role of Langerin⁺ CD8α⁺ Dendritic Cells in Tumour Immunotherapy. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/3646

Chicago Manual of Style (16th Edition):

Gibbins, John David. “The Role of Langerin⁺ CD8α⁺ Dendritic Cells in Tumour Immunotherapy.” 2014. Doctoral Dissertation, Victoria University of Wellington. Accessed May 08, 2021. http://hdl.handle.net/10063/3646.

MLA Handbook (7th Edition):

Gibbins, John David. “The Role of Langerin⁺ CD8α⁺ Dendritic Cells in Tumour Immunotherapy.” 2014. Web. 08 May 2021.

Vancouver:

Gibbins JD. The Role of Langerin⁺ CD8α⁺ Dendritic Cells in Tumour Immunotherapy. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/10063/3646.

Council of Science Editors:

Gibbins JD. The Role of Langerin⁺ CD8α⁺ Dendritic Cells in Tumour Immunotherapy. [Doctoral Dissertation]. Victoria University of Wellington; 2014. Available from: http://hdl.handle.net/10063/3646


University of Ottawa

6. Burke, Stephanie. Generalized Impairment of CD8+ T-cells in HCV Mono- and HIV-HCV Co-infection .

Degree: 2015, University of Ottawa

 Chronic hepatitis C virus (HCV) infection has global effects on the immune system. CD8+ T-cells, responsible for viral clearance and control, are dysfunctional for as… (more)

Subjects/Keywords: Hepatitis C Virus; CD8+ T cell; HIV

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APA (6th Edition):

Burke, S. (2015). Generalized Impairment of CD8+ T-cells in HCV Mono- and HIV-HCV Co-infection . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32770

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):

Burke, Stephanie. “Generalized Impairment of CD8+ T-cells in HCV Mono- and HIV-HCV Co-infection .” 2015. Thesis, University of Ottawa. Accessed May 08, 2021. http://hdl.handle.net/10393/32770.

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

MLA Handbook (7th Edition):

Burke, Stephanie. “Generalized Impairment of CD8+ T-cells in HCV Mono- and HIV-HCV Co-infection .” 2015. Web. 08 May 2021.

Vancouver:

Burke S. Generalized Impairment of CD8+ T-cells in HCV Mono- and HIV-HCV Co-infection . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2021 May 08]. Available from: http://hdl.handle.net/10393/32770.

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

Council of Science Editors:

Burke S. Generalized Impairment of CD8+ T-cells in HCV Mono- and HIV-HCV Co-infection . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32770

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


University of Melbourne

7. Valkenburg, Sophie Alessandra. Understanding mechanisms of influenza A virus escape from CD8+ T cells in mouse and human models of infection.

Degree: 2011, University of Melbourne

CD8+ T cells can provide cross-reactive immunity between different influenza strains and subtypes, when there is sufficient sequence or structural homology of the pMHC-I. Otherwise… (more)

Subjects/Keywords: influenza; immunology; CD8+ T cell; elderly; escape

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APA (6th Edition):

Valkenburg, S. A. (2011). Understanding mechanisms of influenza A virus escape from CD8+ T cells in mouse and human models of infection. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37002

Chicago Manual of Style (16th Edition):

Valkenburg, Sophie Alessandra. “Understanding mechanisms of influenza A virus escape from CD8+ T cells in mouse and human models of infection.” 2011. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/37002.

MLA Handbook (7th Edition):

Valkenburg, Sophie Alessandra. “Understanding mechanisms of influenza A virus escape from CD8+ T cells in mouse and human models of infection.” 2011. Web. 08 May 2021.

Vancouver:

Valkenburg SA. Understanding mechanisms of influenza A virus escape from CD8+ T cells in mouse and human models of infection. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/37002.

Council of Science Editors:

Valkenburg SA. Understanding mechanisms of influenza A virus escape from CD8+ T cells in mouse and human models of infection. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/37002


University of Arizona

8. Renkema, Kristin. Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age .

Degree: 2013, University of Arizona

 Infectious diseases remain amongst leading causes of death in people aged 65 years and older; therefore, much research is focused on determining the immune components… (more)

Subjects/Keywords: CD8⁺ T cell; Homeostasis; Immunobiology; Aging

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APA (6th Edition):

Renkema, K. (2013). Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/293484

Chicago Manual of Style (16th Edition):

Renkema, Kristin. “Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age .” 2013. Doctoral Dissertation, University of Arizona. Accessed May 08, 2021. http://hdl.handle.net/10150/293484.

MLA Handbook (7th Edition):

Renkema, Kristin. “Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age .” 2013. Web. 08 May 2021.

Vancouver:

Renkema K. Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2021 May 08]. Available from: http://hdl.handle.net/10150/293484.

Council of Science Editors:

Renkema K. Differential Maintenance, Function, and Transcriptional Profile of CD8⁺ T cells with Age . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/293484


Penn State University

9. Maru, Saumya Yogesh. Enhancing host control of polyomavirus infection.

Degree: 2017, Penn State University

 Polyomaviruses are small, double-stranded DNA viruses that infect a wide range of host species. Seroprevalence of anti-PyV antibodies in the human population is as high… (more)

Subjects/Keywords: polyomavirus; persistent infection; CD8 T cells; TRM cell; memory CD8 T cell; miRNA; viral miRNA

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APA (6th Edition):

Maru, S. Y. (2017). Enhancing host control of polyomavirus infection. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14338sym118

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):

Maru, Saumya Yogesh. “Enhancing host control of polyomavirus infection.” 2017. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/14338sym118.

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

MLA Handbook (7th Edition):

Maru, Saumya Yogesh. “Enhancing host control of polyomavirus infection.” 2017. Web. 08 May 2021.

Vancouver:

Maru SY. Enhancing host control of polyomavirus infection. [Internet] [Thesis]. Penn State University; 2017. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/14338sym118.

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

Council of Science Editors:

Maru SY. Enhancing host control of polyomavirus infection. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14338sym118

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


University of Minnesota

10. Lee, June-Yong. Immunologic function of Virtual Memory CD8+ T cells & Role of KLF2 in effector CD4+ T cell lineage commitment.

Degree: PhD, Molecular, Cellular, Developmental Biology and Genetics, 2014, University of Minnesota

 During my Ph.D. training, my research has been focused on two distinct topics: investigating the immunologic fuction of Virtual Memory CD8+ T cells; and elucidating… (more)

Subjects/Keywords: Follicular helper T cell; KLF2; Virtual memory CD8 T cell

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APA (6th Edition):

Lee, J. (2014). Immunologic function of Virtual Memory CD8+ T cells & Role of KLF2 in effector CD4+ T cell lineage commitment. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/177144

Chicago Manual of Style (16th Edition):

Lee, June-Yong. “Immunologic function of Virtual Memory CD8+ T cells & Role of KLF2 in effector CD4+ T cell lineage commitment.” 2014. Doctoral Dissertation, University of Minnesota. Accessed May 08, 2021. http://hdl.handle.net/11299/177144.

MLA Handbook (7th Edition):

Lee, June-Yong. “Immunologic function of Virtual Memory CD8+ T cells & Role of KLF2 in effector CD4+ T cell lineage commitment.” 2014. Web. 08 May 2021.

Vancouver:

Lee J. Immunologic function of Virtual Memory CD8+ T cells & Role of KLF2 in effector CD4+ T cell lineage commitment. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/11299/177144.

Council of Science Editors:

Lee J. Immunologic function of Virtual Memory CD8+ T cells & Role of KLF2 in effector CD4+ T cell lineage commitment. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/177144


University of Minnesota

11. Steinert, Elizabeth. Evaluating memory CD8 T cell quantity, distribution and migration.

Degree: PhD, Microbiology, Immunology and Cancer Biology, 2016, University of Minnesota

 Memory CD8 T cells protect against intracellular pathogens by scanning host cell surfaces, thus infection detection rates depend on memory cell number and distribution. Many… (more)

Subjects/Keywords: CD8 T cell; Male genital tract; Migration; Resident Memory; T cell

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APA (6th Edition):

Steinert, E. (2016). Evaluating memory CD8 T cell quantity, distribution and migration. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/201105

Chicago Manual of Style (16th Edition):

Steinert, Elizabeth. “Evaluating memory CD8 T cell quantity, distribution and migration.” 2016. Doctoral Dissertation, University of Minnesota. Accessed May 08, 2021. http://hdl.handle.net/11299/201105.

MLA Handbook (7th Edition):

Steinert, Elizabeth. “Evaluating memory CD8 T cell quantity, distribution and migration.” 2016. Web. 08 May 2021.

Vancouver:

Steinert E. Evaluating memory CD8 T cell quantity, distribution and migration. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2021 May 08]. Available from: http://hdl.handle.net/11299/201105.

Council of Science Editors:

Steinert E. Evaluating memory CD8 T cell quantity, distribution and migration. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/201105


University of Cincinnati

12. Kurtulus, Sema. Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells.

Degree: PhD, Medicine: Immunology, 2013, University of Cincinnati

 Naive T cells recruited to respond to an infection often undergo 15-20 rounds of cell division. After the infection is cleared, most of these T(more)

Subjects/Keywords: Immunology; CD8+ T cell; Bim; Bcl-2; effector T cell; memory T cell; apoptosis

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APA (6th Edition):

Kurtulus, S. (2013). Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026339

Chicago Manual of Style (16th Edition):

Kurtulus, Sema. “Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells.” 2013. Doctoral Dissertation, University of Cincinnati. Accessed May 08, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026339.

MLA Handbook (7th Edition):

Kurtulus, Sema. “Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells.” 2013. Web. 08 May 2021.

Vancouver:

Kurtulus S. Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2021 May 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026339.

Council of Science Editors:

Kurtulus S. Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells. [Doctoral Dissertation]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1368026339

13. Villani, Axel. Rôle des lymphocytes T CD8+ dans les hypersensibilités retardées cutanées médicamenteuses : Impact of CD8+ T cells in Cutaneous Adverse Drug Reactions : how to explain the severity associated with those reactions ?.

Degree: Docteur es, Biologie cellulaire, 2019, Lyon

La nécrolyse épidermique toxique (NET) est une réaction cutanée médicamenteuse (CADR - Cutaneous Adverse Drug Reaction) rare et sévère qui se caractérise par une nécrose… (more)

Subjects/Keywords: Lymphocyte T CD8+; Cytotoxicité; Nécrolyse épidermique toxique; CD8+ T cell; Cytotoxicity; Toxic epidermal necrolysis; 570

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APA (6th Edition):

Villani, A. (2019). Rôle des lymphocytes T CD8+ dans les hypersensibilités retardées cutanées médicamenteuses : Impact of CD8+ T cells in Cutaneous Adverse Drug Reactions : how to explain the severity associated with those reactions ?. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2019LYSE1143

Chicago Manual of Style (16th Edition):

Villani, Axel. “Rôle des lymphocytes T CD8+ dans les hypersensibilités retardées cutanées médicamenteuses : Impact of CD8+ T cells in Cutaneous Adverse Drug Reactions : how to explain the severity associated with those reactions ?.” 2019. Doctoral Dissertation, Lyon. Accessed May 08, 2021. http://www.theses.fr/2019LYSE1143.

MLA Handbook (7th Edition):

Villani, Axel. “Rôle des lymphocytes T CD8+ dans les hypersensibilités retardées cutanées médicamenteuses : Impact of CD8+ T cells in Cutaneous Adverse Drug Reactions : how to explain the severity associated with those reactions ?.” 2019. Web. 08 May 2021.

Vancouver:

Villani A. Rôle des lymphocytes T CD8+ dans les hypersensibilités retardées cutanées médicamenteuses : Impact of CD8+ T cells in Cutaneous Adverse Drug Reactions : how to explain the severity associated with those reactions ?. [Internet] [Doctoral dissertation]. Lyon; 2019. [cited 2021 May 08]. Available from: http://www.theses.fr/2019LYSE1143.

Council of Science Editors:

Villani A. Rôle des lymphocytes T CD8+ dans les hypersensibilités retardées cutanées médicamenteuses : Impact of CD8+ T cells in Cutaneous Adverse Drug Reactions : how to explain the severity associated with those reactions ?. [Doctoral Dissertation]. Lyon; 2019. Available from: http://www.theses.fr/2019LYSE1143


University of New South Wales

14. Jin, Dongbin. Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells.

Degree: Clinical School - St Vincent's Hospital, 2015, University of New South Wales

 Immunotherapy has emerged as a promising tool to treat diseases via enhancing or suppressing immune responses of T cells. For infectious diseases and cancer, inducing… (more)

Subjects/Keywords: Membrane vesicle; Immunotherapy; CD8 T cell; Antigen presenting cell; Dendritic cell

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APA (6th Edition):

Jin, D. (2015). Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Jin, Dongbin. “Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells.” 2015. Doctoral Dissertation, University of New South Wales. Accessed May 08, 2021. http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true.

MLA Handbook (7th Edition):

Jin, Dongbin. “Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells.” 2015. Web. 08 May 2021.

Vancouver:

Jin D. Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2021 May 08]. Available from: http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true.

Council of Science Editors:

Jin D. Stimulation of CD8 T cells with membrane vesicles prepared from antigen presenting cells. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/54605 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:35345/SOURCE02?view=true


University of Melbourne

15. CUKALAC, TANIA. Analysis of factors influencing CD8+ T cell responses after influenza A virus infection.

Degree: 2013, University of Melbourne

CD8+ T cell responses to pathogens are characterised by the clonal expansion of cells expressing T cell receptors (TCRs) of unique specificity for antigenic peptide… (more)

Subjects/Keywords: immunology; CD8+ T cell; T cell receptors; cellular immunity; cell mediated immunity; virus infection; T cell receptor repertoires; T cell immunodominance

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APA (6th Edition):

CUKALAC, T. (2013). Analysis of factors influencing CD8+ T cell responses after influenza A virus infection. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38114

Chicago Manual of Style (16th Edition):

CUKALAC, TANIA. “Analysis of factors influencing CD8+ T cell responses after influenza A virus infection.” 2013. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/38114.

MLA Handbook (7th Edition):

CUKALAC, TANIA. “Analysis of factors influencing CD8+ T cell responses after influenza A virus infection.” 2013. Web. 08 May 2021.

Vancouver:

CUKALAC T. Analysis of factors influencing CD8+ T cell responses after influenza A virus infection. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/38114.

Council of Science Editors:

CUKALAC T. Analysis of factors influencing CD8+ T cell responses after influenza A virus infection. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38114


University of Edinburgh

16. Li, Xiaoying. T cell receptor repertoires of immunodominant CD8 T cell responses to Theileria parva.

Degree: PhD, 2015, University of Edinburgh

 Previous research has provided evidence that CD8 T cells mediate immunity against infection with Theileria parva. However, the immunity induced by one parasite strain doesn‟t(more)

Subjects/Keywords: 616.07; T cell receptor; immunodominant; CD8 T cells; Theileria parva

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

APA (6th Edition):

Li, X. (2015). T cell receptor repertoires of immunodominant CD8 T cell responses to Theileria parva. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/19552

Chicago Manual of Style (16th Edition):

Li, Xiaoying. “T cell receptor repertoires of immunodominant CD8 T cell responses to Theileria parva.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed May 08, 2021. http://hdl.handle.net/1842/19552.

MLA Handbook (7th Edition):

Li, Xiaoying. “T cell receptor repertoires of immunodominant CD8 T cell responses to Theileria parva.” 2015. Web. 08 May 2021.

Vancouver:

Li X. T cell receptor repertoires of immunodominant CD8 T cell responses to Theileria parva. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2021 May 08]. Available from: http://hdl.handle.net/1842/19552.

Council of Science Editors:

Li X. T cell receptor repertoires of immunodominant CD8 T cell responses to Theileria parva. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/19552


University of Cambridge

17. 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/1810/293250https://www.repository.cam.ac.uk/bitstream/1810/293250/4/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/5/21ce4b72-0fef-458d-8e92-ee62aff41279.zip ; https://www.repository.cam.ac.uk/bitstream/1810/293250/7/AGPecchia-Bekkum_Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/8/AGPecchia-Bekkum_Thesis.pdf.jpg

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 May 08, 2021. https://www.repository.cam.ac.uk/handle/1810/293250https://www.repository.cam.ac.uk/bitstream/1810/293250/4/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/5/21ce4b72-0fef-458d-8e92-ee62aff41279.zip ; https://www.repository.cam.ac.uk/bitstream/1810/293250/7/AGPecchia-Bekkum_Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/8/AGPecchia-Bekkum_Thesis.pdf.jpg.

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. 08 May 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 May 08]. Available from: https://www.repository.cam.ac.uk/handle/1810/293250https://www.repository.cam.ac.uk/bitstream/1810/293250/4/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/5/21ce4b72-0fef-458d-8e92-ee62aff41279.zip ; https://www.repository.cam.ac.uk/bitstream/1810/293250/7/AGPecchia-Bekkum_Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/8/AGPecchia-Bekkum_Thesis.pdf.jpg.

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/1810/293250https://www.repository.cam.ac.uk/bitstream/1810/293250/4/license.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/5/21ce4b72-0fef-458d-8e92-ee62aff41279.zip ; https://www.repository.cam.ac.uk/bitstream/1810/293250/7/AGPecchia-Bekkum_Thesis.pdf.txt ; https://www.repository.cam.ac.uk/bitstream/1810/293250/8/AGPecchia-Bekkum_Thesis.pdf.jpg


Monash University

18. SNG, YI XIONG. The Role of MHCI Quality and Quantity in Determining CD8 T cell Development, Survival and Function.

Degree: Medicine, Nursing and Health Sciences, 2020, Monash University

 The major histocompatibility complex class I (MHCI) molecule is essential for the development, homeostatic maintenance and activation of CD8 T cells. While it is clear… (more)

Subjects/Keywords: Immunology; Cellular Immunology; CD8 T cell; T cell development; T cell maintenance; T cell activation; MHCI; Viral infection

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

APA (6th Edition):

SNG, Y. X. (2020). The Role of MHCI Quality and Quantity in Determining CD8 T cell Development, Survival and Function. (Thesis). Monash University. Retrieved from http://hdl.handle.net/10.26180/5e8baa6cbd5fb

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):

SNG, YI XIONG. “The Role of MHCI Quality and Quantity in Determining CD8 T cell Development, Survival and Function.” 2020. Thesis, Monash University. Accessed May 08, 2021. http://hdl.handle.net/10.26180/5e8baa6cbd5fb.

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

MLA Handbook (7th Edition):

SNG, YI XIONG. “The Role of MHCI Quality and Quantity in Determining CD8 T cell Development, Survival and Function.” 2020. Web. 08 May 2021.

Vancouver:

SNG YX. The Role of MHCI Quality and Quantity in Determining CD8 T cell Development, Survival and Function. [Internet] [Thesis]. Monash University; 2020. [cited 2021 May 08]. Available from: http://hdl.handle.net/10.26180/5e8baa6cbd5fb.

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

Council of Science Editors:

SNG YX. The Role of MHCI Quality and Quantity in Determining CD8 T cell Development, Survival and Function. [Thesis]. Monash University; 2020. Available from: http://hdl.handle.net/10.26180/5e8baa6cbd5fb

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


University of California – San Francisco

19. Mahne, Ashley. Dissecting immune regulation and dysregulation in autoimmune diabetes from the vantage point of the target tissue.

Degree: Biomedical Sciences, 2013, University of California – San Francisco

 Regulatory T cells (Tregs) are critical to the maintenance of immune homeostasis and the prevention of autoimmunity. In the NOD mouse model of autoimmune diabetes,… (more)

Subjects/Keywords: Immunology; CD8 T cell; dendritic cell; NOD mouse; regulatory T cell; type 1 diabetes

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

APA (6th Edition):

Mahne, A. (2013). Dissecting immune regulation and dysregulation in autoimmune diabetes from the vantage point of the target tissue. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/48n2c0n8

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):

Mahne, Ashley. “Dissecting immune regulation and dysregulation in autoimmune diabetes from the vantage point of the target tissue.” 2013. Thesis, University of California – San Francisco. Accessed May 08, 2021. http://www.escholarship.org/uc/item/48n2c0n8.

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

MLA Handbook (7th Edition):

Mahne, Ashley. “Dissecting immune regulation and dysregulation in autoimmune diabetes from the vantage point of the target tissue.” 2013. Web. 08 May 2021.

Vancouver:

Mahne A. Dissecting immune regulation and dysregulation in autoimmune diabetes from the vantage point of the target tissue. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2021 May 08]. Available from: http://www.escholarship.org/uc/item/48n2c0n8.

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

Council of Science Editors:

Mahne A. Dissecting immune regulation and dysregulation in autoimmune diabetes from the vantage point of the target tissue. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/48n2c0n8

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

20. Kaplon, Hélène. Rôle des lymphocytes B associés aux structures lymphoïdes tertiaires dans la réponse clinique des patients atteints d’un cancer pulmonaire : Role of tertiary lymphoid structure-associated B cells in the clinical response of lung cancer patients.

Degree: Docteur es, Immunologie, 2018, Sorbonne université

Le microenvironnement tumoral est un acteur majeur du contrôle immunitaire du développement tumoral. Ce contrôle commence à distance des cellules tumorales, dans le stroma tumoral,… (more)

Subjects/Keywords: Plasmocyte; IgA; IgG; Lymphocyte T CD8+; Structure lymphoïde tertiaire; Cancer du poumon; Plasma cell; CD8+ T cell; Lung; 616.0798; 614.5999

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APA (6th Edition):

Kaplon, H. (2018). Rôle des lymphocytes B associés aux structures lymphoïdes tertiaires dans la réponse clinique des patients atteints d’un cancer pulmonaire : Role of tertiary lymphoid structure-associated B cells in the clinical response of lung cancer patients. (Doctoral Dissertation). Sorbonne université. Retrieved from http://www.theses.fr/2018SORUS565

Chicago Manual of Style (16th Edition):

Kaplon, Hélène. “Rôle des lymphocytes B associés aux structures lymphoïdes tertiaires dans la réponse clinique des patients atteints d’un cancer pulmonaire : Role of tertiary lymphoid structure-associated B cells in the clinical response of lung cancer patients.” 2018. Doctoral Dissertation, Sorbonne université. Accessed May 08, 2021. http://www.theses.fr/2018SORUS565.

MLA Handbook (7th Edition):

Kaplon, Hélène. “Rôle des lymphocytes B associés aux structures lymphoïdes tertiaires dans la réponse clinique des patients atteints d’un cancer pulmonaire : Role of tertiary lymphoid structure-associated B cells in the clinical response of lung cancer patients.” 2018. Web. 08 May 2021.

Vancouver:

Kaplon H. Rôle des lymphocytes B associés aux structures lymphoïdes tertiaires dans la réponse clinique des patients atteints d’un cancer pulmonaire : Role of tertiary lymphoid structure-associated B cells in the clinical response of lung cancer patients. [Internet] [Doctoral dissertation]. Sorbonne université; 2018. [cited 2021 May 08]. Available from: http://www.theses.fr/2018SORUS565.

Council of Science Editors:

Kaplon H. Rôle des lymphocytes B associés aux structures lymphoïdes tertiaires dans la réponse clinique des patients atteints d’un cancer pulmonaire : Role of tertiary lymphoid structure-associated B cells in the clinical response of lung cancer patients. [Doctoral Dissertation]. Sorbonne université; 2018. Available from: http://www.theses.fr/2018SORUS565


University of California – San Diego

21. Phan, Anthony T. Hypoxia Inducible Factors: Redefining Metabolic Regulation of CD8 T cell Differentiation and Function.

Degree: Biology, 2016, University of California – San Diego

T cell responses are initiated by detection of cognate peptide presented by antigen presenting cells in secondary lymphoid tissues and result in migration of T(more)

Subjects/Keywords: Immunology; Cellular biology; differentiation; HIF; Hypoxia; memory CD8+ T cell; metabolism; T cell

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APA (6th Edition):

Phan, A. T. (2016). Hypoxia Inducible Factors: Redefining Metabolic Regulation of CD8 T cell Differentiation and Function. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/40w7v71j

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):

Phan, Anthony T. “Hypoxia Inducible Factors: Redefining Metabolic Regulation of CD8 T cell Differentiation and Function.” 2016. Thesis, University of California – San Diego. Accessed May 08, 2021. http://www.escholarship.org/uc/item/40w7v71j.

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

MLA Handbook (7th Edition):

Phan, Anthony T. “Hypoxia Inducible Factors: Redefining Metabolic Regulation of CD8 T cell Differentiation and Function.” 2016. Web. 08 May 2021.

Vancouver:

Phan AT. Hypoxia Inducible Factors: Redefining Metabolic Regulation of CD8 T cell Differentiation and Function. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2021 May 08]. Available from: http://www.escholarship.org/uc/item/40w7v71j.

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

Council of Science Editors:

Phan AT. Hypoxia Inducible Factors: Redefining Metabolic Regulation of CD8 T cell Differentiation and Function. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/40w7v71j

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


Penn State University

22. Ward-kavanagh, Lindsay Kate. The broad applicability of adoptive immunotherapy in cancer: optimization through host conditioning and target selection.

Degree: 2015, Penn State University

 Adoptive cell therapy (ACT) holds the potential to cure advanced cancer through selective elimination of tumor cells with cytotoxic T lymphocytes, yet this approach has… (more)

Subjects/Keywords: Immunotherapy; Cancer; Adoptive Cell Therapy; Radiation; Anti-CD40; Conditioning; SV40 T Antigen; CD8+ T cell

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APA (6th Edition):

Ward-kavanagh, L. K. (2015). The broad applicability of adoptive immunotherapy in cancer: optimization through host conditioning and target selection. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/26450

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):

Ward-kavanagh, Lindsay Kate. “The broad applicability of adoptive immunotherapy in cancer: optimization through host conditioning and target selection.” 2015. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/26450.

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

MLA Handbook (7th Edition):

Ward-kavanagh, Lindsay Kate. “The broad applicability of adoptive immunotherapy in cancer: optimization through host conditioning and target selection.” 2015. Web. 08 May 2021.

Vancouver:

Ward-kavanagh LK. The broad applicability of adoptive immunotherapy in cancer: optimization through host conditioning and target selection. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/26450.

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

Council of Science Editors:

Ward-kavanagh LK. The broad applicability of adoptive immunotherapy in cancer: optimization through host conditioning and target selection. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/26450

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


Harvard University

23. Osuna-Gutierrez, Christa Elyse. Characterization of the Mamu-A*01-Restricted CD8-Positive T Lymphocyte Immunodominance Hierarchy in Simian Immunodeficiency Virus-Infected Rhesus Monkeys.

Degree: PhD, Immunology, 2012, Harvard University

 (CD8+) cytotoxic T lymphocytes (CTLs) play a critical role in controlling human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) replication. The CTL responses that… (more)

Subjects/Keywords: CD8 T cell; differentiation; HIV; SIV; T cell receptor; vaccine; immunology; molecular biology; virology

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APA (6th Edition):

Osuna-Gutierrez, C. E. (2012). Characterization of the Mamu-A*01-Restricted CD8-Positive T Lymphocyte Immunodominance Hierarchy in Simian Immunodeficiency Virus-Infected Rhesus Monkeys. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817660

Chicago Manual of Style (16th Edition):

Osuna-Gutierrez, Christa Elyse. “Characterization of the Mamu-A*01-Restricted CD8-Positive T Lymphocyte Immunodominance Hierarchy in Simian Immunodeficiency Virus-Infected Rhesus Monkeys.” 2012. Doctoral Dissertation, Harvard University. Accessed May 08, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817660.

MLA Handbook (7th Edition):

Osuna-Gutierrez, Christa Elyse. “Characterization of the Mamu-A*01-Restricted CD8-Positive T Lymphocyte Immunodominance Hierarchy in Simian Immunodeficiency Virus-Infected Rhesus Monkeys.” 2012. Web. 08 May 2021.

Vancouver:

Osuna-Gutierrez CE. Characterization of the Mamu-A*01-Restricted CD8-Positive T Lymphocyte Immunodominance Hierarchy in Simian Immunodeficiency Virus-Infected Rhesus Monkeys. [Internet] [Doctoral dissertation]. Harvard University; 2012. [cited 2021 May 08]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817660.

Council of Science Editors:

Osuna-Gutierrez CE. Characterization of the Mamu-A*01-Restricted CD8-Positive T Lymphocyte Immunodominance Hierarchy in Simian Immunodeficiency Virus-Infected Rhesus Monkeys. [Doctoral Dissertation]. Harvard University; 2012. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:9817660


University of Melbourne

24. McQuilten, Hayley Ann. Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation.

Degree: 2017, University of Melbourne

 Immunological memory is a hallmark feature of the adaptive immune system, providing superior protection against re-infection with previously encountered pathogens. Memory in CD8+ T cells… (more)

Subjects/Keywords: CD8+ T cell; memory; CTL; epigenetics; RNA-seq; ChIP-seq; T cell help; TCR; CD28

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

APA (6th Edition):

McQuilten, H. A. (2017). Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/208759

Chicago Manual of Style (16th Edition):

McQuilten, Hayley Ann. “Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation.” 2017. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/208759.

MLA Handbook (7th Edition):

McQuilten, Hayley Ann. “Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation.” 2017. Web. 08 May 2021.

Vancouver:

McQuilten HA. Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/208759.

Council of Science Editors:

McQuilten HA. Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/208759


University of Ottawa

25. Aloufi, Nawaf. The role of sCD127 in IL-7-Mediated T Cell Homeostasis in Vivo.

Degree: MSc, Médecine / Medicine, 2020, University of Ottawa

 Interleukin-7 is an essential cytokine that plays a major role in the development and homeostatic maintenance of T-cells. The presence of soluble forms of various… (more)

Subjects/Keywords: IL-7; Soluble CD127; CD4+ T cells; CD8+ T cells; T cell proliferation; T cell reconstitution

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

APA (6th Edition):

Aloufi, N. (2020). The role of sCD127 in IL-7-Mediated T Cell Homeostasis in Vivo. (Masters Thesis). University of Ottawa. Retrieved from http://dx.doi.org/10.20381/ruor-25313

Chicago Manual of Style (16th Edition):

Aloufi, Nawaf. “The role of sCD127 in IL-7-Mediated T Cell Homeostasis in Vivo.” 2020. Masters Thesis, University of Ottawa. Accessed May 08, 2021. http://dx.doi.org/10.20381/ruor-25313.

MLA Handbook (7th Edition):

Aloufi, Nawaf. “The role of sCD127 in IL-7-Mediated T Cell Homeostasis in Vivo.” 2020. Web. 08 May 2021.

Vancouver:

Aloufi N. The role of sCD127 in IL-7-Mediated T Cell Homeostasis in Vivo. [Internet] [Masters thesis]. University of Ottawa; 2020. [cited 2021 May 08]. Available from: http://dx.doi.org/10.20381/ruor-25313.

Council of Science Editors:

Aloufi N. The role of sCD127 in IL-7-Mediated T Cell Homeostasis in Vivo. [Masters Thesis]. University of Ottawa; 2020. Available from: http://dx.doi.org/10.20381/ruor-25313


Johannes Gutenberg Universität Mainz

26. Singh, Vijay Kumar. Generation of FLT3-ITD-reactive T-cell populations from different sources.

Degree: 2013, Johannes Gutenberg Universität Mainz

 Approximately 25% of acute myeloid leukemias (AMLs) carry internal tandem duplications (ITD) of various lengths within the gene encoding the FMS-like tyrosine kinase receptor 3… (more)

Subjects/Keywords: FLT3-ITD; CD8 positiver T-Zell response; AML; FLT3-ITD; CD8 positive T-cell response; AML; Medical sciences Medicine

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APA (6th Edition):

Singh, V. K. (2013). Generation of FLT3-ITD-reactive T-cell populations from different sources. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2013/3416/

Chicago Manual of Style (16th Edition):

Singh, Vijay Kumar. “Generation of FLT3-ITD-reactive T-cell populations from different sources.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed May 08, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2013/3416/.

MLA Handbook (7th Edition):

Singh, Vijay Kumar. “Generation of FLT3-ITD-reactive T-cell populations from different sources.” 2013. Web. 08 May 2021.

Vancouver:

Singh VK. Generation of FLT3-ITD-reactive T-cell populations from different sources. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2021 May 08]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3416/.

Council of Science Editors:

Singh VK. Generation of FLT3-ITD-reactive T-cell populations from different sources. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2013/3416/

27. 김, 소민. Transcriptomes of CD27-CD28- and CD27+CD28+ CD8+ T subsets disclose differentially expressed novel genes and signaling pathways in Behçet's disease.

Degree: 2019, Ajou University

 BACKGROUND AND OBJECTIVES: Behçet’s disease (BD) is a chronic inflammatory disease characterized by recurrent mucocutaneous ulceration and other complications such as blindness and large vessel… (more)

Subjects/Keywords: Behçet's disease; transcriptome analysis; RNA sequencing; CD8+ T cell; immunosenescence; 베체트병; 전사체 분석; RNA 서열분석; CD8+ T 세포; 면역노화

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APA (6th Edition):

김, . (2019). Transcriptomes of CD27-CD28- and CD27+CD28+ CD8+ T subsets disclose differentially expressed novel genes and signaling pathways in Behçet's disease. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/17871 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000029178

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):

김, 소민. “Transcriptomes of CD27-CD28- and CD27+CD28+ CD8+ T subsets disclose differentially expressed novel genes and signaling pathways in Behçet's disease.” 2019. Thesis, Ajou University. Accessed May 08, 2021. http://repository.ajou.ac.kr/handle/201003/17871 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000029178.

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

MLA Handbook (7th Edition):

김, 소민. “Transcriptomes of CD27-CD28- and CD27+CD28+ CD8+ T subsets disclose differentially expressed novel genes and signaling pathways in Behçet's disease.” 2019. Web. 08 May 2021.

Vancouver:

김 . Transcriptomes of CD27-CD28- and CD27+CD28+ CD8+ T subsets disclose differentially expressed novel genes and signaling pathways in Behçet's disease. [Internet] [Thesis]. Ajou University; 2019. [cited 2021 May 08]. Available from: http://repository.ajou.ac.kr/handle/201003/17871 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000029178.

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

Council of Science Editors:

김 . Transcriptomes of CD27-CD28- and CD27+CD28+ CD8+ T subsets disclose differentially expressed novel genes and signaling pathways in Behçet's disease. [Thesis]. Ajou University; 2019. Available from: http://repository.ajou.ac.kr/handle/201003/17871 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000029178

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


University of Melbourne

28. Seah, Gek Kheng Shirley. Costimulatory requirements of helpindependent anti-influenza CTL.

Degree: 2012, University of Melbourne

 This thesis focused on the role of costimulatory molecules, CD28 and CD40L, on the induction and expansion of help-independent CD8+ T cell response during primary… (more)

Subjects/Keywords: costimulation; CD8 T cells; influenza virus; tetramers; immunology; help-independent CD8 T cell responses; influenza virus infection

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APA (6th Edition):

Seah, G. K. S. (2012). Costimulatory requirements of helpindependent anti-influenza CTL. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37327

Chicago Manual of Style (16th Edition):

Seah, Gek Kheng Shirley. “Costimulatory requirements of helpindependent anti-influenza CTL.” 2012. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/37327.

MLA Handbook (7th Edition):

Seah, Gek Kheng Shirley. “Costimulatory requirements of helpindependent anti-influenza CTL.” 2012. Web. 08 May 2021.

Vancouver:

Seah GKS. Costimulatory requirements of helpindependent anti-influenza CTL. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/37327.

Council of Science Editors:

Seah GKS. Costimulatory requirements of helpindependent anti-influenza CTL. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37327

29. Mastrodimou, Ioanna - Semeli. Μελέτη του ρεπερτορίου των γονιδίων της β΄αλυσίδας του υποδοχέα των CD8⁺ T-λεμφοκυττάρων σε ασθενείς με χρόνια ιδιοπαθή ουδετεροπενία.

Degree: 2018, University of Crete (UOC); Πανεπιστήμιο Κρήτης

Chronic idiopathic neutropenia (CIN) is an acquired disorder of granulopoiesis characterized by female predominance and mostly uncomplicated course. Crucial to CIN pathophysiology is the presence… (more)

Subjects/Keywords: Χρόνια ιδιοπαθής ουδετεροπενία; Τ κυτταρικός υποδοχέας; CD8+ Τ-λεμφοκύτταρα; Chronic idiopathic neutropenia; T cell receptor; CD8+ T cells

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

APA (6th Edition):

Mastrodimou, I. -. S. (2018). Μελέτη του ρεπερτορίου των γονιδίων της β΄αλυσίδας του υποδοχέα των CD8⁺ T-λεμφοκυττάρων σε ασθενείς με χρόνια ιδιοπαθή ουδετεροπενία. (Thesis). University of Crete (UOC); Πανεπιστήμιο Κρήτης. Retrieved from http://hdl.handle.net/10442/hedi/44710

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):

Mastrodimou, Ioanna - Semeli. “Μελέτη του ρεπερτορίου των γονιδίων της β΄αλυσίδας του υποδοχέα των CD8⁺ T-λεμφοκυττάρων σε ασθενείς με χρόνια ιδιοπαθή ουδετεροπενία.” 2018. Thesis, University of Crete (UOC); Πανεπιστήμιο Κρήτης. Accessed May 08, 2021. http://hdl.handle.net/10442/hedi/44710.

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

MLA Handbook (7th Edition):

Mastrodimou, Ioanna - Semeli. “Μελέτη του ρεπερτορίου των γονιδίων της β΄αλυσίδας του υποδοχέα των CD8⁺ T-λεμφοκυττάρων σε ασθενείς με χρόνια ιδιοπαθή ουδετεροπενία.” 2018. Web. 08 May 2021.

Vancouver:

Mastrodimou I-S. Μελέτη του ρεπερτορίου των γονιδίων της β΄αλυσίδας του υποδοχέα των CD8⁺ T-λεμφοκυττάρων σε ασθενείς με χρόνια ιδιοπαθή ουδετεροπενία. [Internet] [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2018. [cited 2021 May 08]. Available from: http://hdl.handle.net/10442/hedi/44710.

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

Council of Science Editors:

Mastrodimou I-S. Μελέτη του ρεπερτορίου των γονιδίων της β΄αλυσίδας του υποδοχέα των CD8⁺ T-λεμφοκυττάρων σε ασθενείς με χρόνια ιδιοπαθή ουδετεροπενία. [Thesis]. University of Crete (UOC); Πανεπιστήμιο Κρήτης; 2018. Available from: http://hdl.handle.net/10442/hedi/44710

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

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

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 May 08, 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. 08 May 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 May 08]. 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

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