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You searched for subject:(T cell). Showing records 1 – 30 of 1584 total matches.

[1] [2] [3] [4] [5] … [53]

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University of Minnesota

1. Kotov, Dmitri. The role of T cell receptor affinity in CD4+ T cell differentiation.

Degree: PhD, Microbiology, Immunology and Cancer Biology, 2019, University of Minnesota

 Naïve helper T cells become activated when their T cell receptor (TCR) recognizes a microbial peptide presented on MHCII (p:MHCII) by dendritic cells (DCs). During… (more)

Subjects/Keywords: CD4+ T cell; Dendritic Cell; Helper T cell; T cell receptor

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

APA (6th Edition):

Kotov, D. (2019). The role of T cell receptor affinity in CD4+ T cell differentiation. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/202415

Chicago Manual of Style (16th Edition):

Kotov, Dmitri. “The role of T cell receptor affinity in CD4+ T cell differentiation.” 2019. Doctoral Dissertation, University of Minnesota. Accessed October 17, 2019. http://hdl.handle.net/11299/202415.

MLA Handbook (7th Edition):

Kotov, Dmitri. “The role of T cell receptor affinity in CD4+ T cell differentiation.” 2019. Web. 17 Oct 2019.

Vancouver:

Kotov D. The role of T cell receptor affinity in CD4+ T cell differentiation. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11299/202415.

Council of Science Editors:

Kotov D. The role of T cell receptor affinity in CD4+ T cell differentiation. [Doctoral Dissertation]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/202415


University of California – San Diego

2. Shaw, Laura Ann. The role of Id proteins in T cell immunity.

Degree: Biomedical Sciences, 2016, University of California – San Diego

 Upon infection, naive T lymphocytes proliferate and differentiate into highly specialized cell types to combat the pathogen: CD4+ T cells into specialized helper subsets and… (more)

Subjects/Keywords: Immunology; T cell

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APA (6th Edition):

Shaw, L. A. (2016). The role of Id proteins in T cell immunity. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1d22p4pg

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):

Shaw, Laura Ann. “The role of Id proteins in T cell immunity.” 2016. Thesis, University of California – San Diego. Accessed October 17, 2019. http://www.escholarship.org/uc/item/1d22p4pg.

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

MLA Handbook (7th Edition):

Shaw, Laura Ann. “The role of Id proteins in T cell immunity.” 2016. Web. 17 Oct 2019.

Vancouver:

Shaw LA. The role of Id proteins in T cell immunity. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2019 Oct 17]. Available from: http://www.escholarship.org/uc/item/1d22p4pg.

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

Council of Science Editors:

Shaw LA. The role of Id proteins in T cell immunity. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/1d22p4pg

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

3. 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 October 17, 2019. 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. 17 Oct 2019.

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 2019 Oct 17]. 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/


California State Polytechnic University – Pomona

4. Tronti, Sharese. Lymphotactin Mediates Antiviral T cell Trafficking into the Central Nervous System During West Nile Encephalitis.

Degree: MS, Department of Biological Sciences, 2019, California State Polytechnic University – Pomona

 West Nile Virus (WNV), a neurotropic flavivirus, can cause neuroinvasive disease in humans. After peripheral infection, WNV is able to enter the central nervous system… (more)

Subjects/Keywords: T cell trafficking

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APA (6th Edition):

Tronti, S. (2019). Lymphotactin Mediates Antiviral T cell Trafficking into the Central Nervous System During West Nile Encephalitis. (Masters Thesis). California State Polytechnic University – Pomona. Retrieved from http://hdl.handle.net/10211.3/213387

Chicago Manual of Style (16th Edition):

Tronti, Sharese. “Lymphotactin Mediates Antiviral T cell Trafficking into the Central Nervous System During West Nile Encephalitis.” 2019. Masters Thesis, California State Polytechnic University – Pomona. Accessed October 17, 2019. http://hdl.handle.net/10211.3/213387.

MLA Handbook (7th Edition):

Tronti, Sharese. “Lymphotactin Mediates Antiviral T cell Trafficking into the Central Nervous System During West Nile Encephalitis.” 2019. Web. 17 Oct 2019.

Vancouver:

Tronti S. Lymphotactin Mediates Antiviral T cell Trafficking into the Central Nervous System During West Nile Encephalitis. [Internet] [Masters thesis]. California State Polytechnic University – Pomona; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10211.3/213387.

Council of Science Editors:

Tronti S. Lymphotactin Mediates Antiviral T cell Trafficking into the Central Nervous System During West Nile Encephalitis. [Masters Thesis]. California State Polytechnic University – Pomona; 2019. Available from: http://hdl.handle.net/10211.3/213387


University of Cambridge

5. Fairbairn, Camilla Jayne. Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL) : surplus to requirements or a protagonist in lymphomagenesis?.

Degree: PhD, 2018, University of Cambridge

 Anaplastic Large Cell Lymphoma (ALCL) is a peripheral T cell lymphoma divided into three distinct entities: ALCL, Anaplastic Lymphoma Kinase (ALK)+, ALCL ALK- and cutaneous… (more)

Subjects/Keywords: Analplastic Large Cell Lymphoma; T Cell; Lyphoma; T Cell Receptor; T Cell Signaling

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APA (6th Edition):

Fairbairn, C. J. (2018). Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL) : surplus to requirements or a protagonist in lymphomagenesis?. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273245 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744544

Chicago Manual of Style (16th Edition):

Fairbairn, Camilla Jayne. “Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL) : surplus to requirements or a protagonist in lymphomagenesis?.” 2018. Doctoral Dissertation, University of Cambridge. Accessed October 17, 2019. https://www.repository.cam.ac.uk/handle/1810/273245 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744544.

MLA Handbook (7th Edition):

Fairbairn, Camilla Jayne. “Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL) : surplus to requirements or a protagonist in lymphomagenesis?.” 2018. Web. 17 Oct 2019.

Vancouver:

Fairbairn CJ. Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL) : surplus to requirements or a protagonist in lymphomagenesis?. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Oct 17]. Available from: https://www.repository.cam.ac.uk/handle/1810/273245 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744544.

Council of Science Editors:

Fairbairn CJ. Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL) : surplus to requirements or a protagonist in lymphomagenesis?. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273245 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744544


University of Cambridge

6. Fairbairn, Camilla Jayne. Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL): Surplus to requirements or a protagonist in lymphomagenesis? .

Degree: 2018, University of Cambridge

 Anaplastic Large Cell Lymphoma (ALCL) is a peripheral T cell lymphoma divided into three distinct entities: ALCL, Anaplastic Lymphoma Kinase (ALK)+, ALCL ALK- and cutaneous… (more)

Subjects/Keywords: Analplastic Large Cell Lymphoma; T Cell; Lyphoma; T Cell Receptor; T Cell Signaling

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APA (6th Edition):

Fairbairn, C. J. (2018). Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL): Surplus to requirements or a protagonist in lymphomagenesis? . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273245

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):

Fairbairn, Camilla Jayne. “Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL): Surplus to requirements or a protagonist in lymphomagenesis? .” 2018. Thesis, University of Cambridge. Accessed October 17, 2019. https://www.repository.cam.ac.uk/handle/1810/273245.

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

MLA Handbook (7th Edition):

Fairbairn, Camilla Jayne. “Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL): Surplus to requirements or a protagonist in lymphomagenesis? .” 2018. Web. 17 Oct 2019.

Vancouver:

Fairbairn CJ. Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL): Surplus to requirements or a protagonist in lymphomagenesis? . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Oct 17]. Available from: https://www.repository.cam.ac.uk/handle/1810/273245.

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

Council of Science Editors:

Fairbairn CJ. Searching for the missing T Cell Receptor (TCR) in Anaplastic Large Cell Lymphoma (ALCL): Surplus to requirements or a protagonist in lymphomagenesis? . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273245

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


Penn State University

7. Stamer, Mindy Marie. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.

Degree: MS, Microbiology and Immunology, 2009, Penn State University

 Adoptive T cell therapy is commonly used for prophylactic and therapeutic treatment of cytomegalovirus (CMV) disease following HSC transplantation of CMV-seropositive recipients of CMV-seropositive donors.… (more)

Subjects/Keywords: T cells; adoptive T cell therapy; cytomegalovirus; T cell priming

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APA (6th Edition):

Stamer, M. M. (2009). PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10539

Chicago Manual of Style (16th Edition):

Stamer, Mindy Marie. “PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.” 2009. Masters Thesis, Penn State University. Accessed October 17, 2019. https://etda.libraries.psu.edu/catalog/10539.

MLA Handbook (7th Edition):

Stamer, Mindy Marie. “PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS.” 2009. Web. 17 Oct 2019.

Vancouver:

Stamer MM. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2019 Oct 17]. Available from: https://etda.libraries.psu.edu/catalog/10539.

Council of Science Editors:

Stamer MM. PRIMARY IN VITRO T CELL RESPONSES TO CYTOMEGALOVIRUS. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10539


Colorado State University

8. Hughes, Kelly. T zone lymphoma: cellular origin and function.

Degree: PhD, Microbiology, Immunology, and Pathology, 2019, Colorado State University

 ABSTRACT T ZONE LYMPHOMA: CELLULAR ORIGIN AND FUNCTION The lymphoid system is exceedingly complex with specialized subsets of lymphocytes involved in both the innate and… (more)

Subjects/Keywords: lymphoma; T zone lymphoma; T-cell; canine

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APA (6th Edition):

Hughes, K. (2019). T zone lymphoma: cellular origin and function. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/193135

Chicago Manual of Style (16th Edition):

Hughes, Kelly. “T zone lymphoma: cellular origin and function.” 2019. Doctoral Dissertation, Colorado State University. Accessed October 17, 2019. http://hdl.handle.net/10217/193135.

MLA Handbook (7th Edition):

Hughes, Kelly. “T zone lymphoma: cellular origin and function.” 2019. Web. 17 Oct 2019.

Vancouver:

Hughes K. T zone lymphoma: cellular origin and function. [Internet] [Doctoral dissertation]. Colorado State University; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10217/193135.

Council of Science Editors:

Hughes K. T zone lymphoma: cellular origin and function. [Doctoral Dissertation]. Colorado State University; 2019. Available from: http://hdl.handle.net/10217/193135


Queen Mary, University of London

9. Kishore, Madhav. The role of co-stimulatory receptors in the regulation of regulatory T cell migration.

Degree: PhD, 2016, Queen Mary, University of London

 Once an immune response is initiated, a combination of several mechanisms coordinates and directs the homing of T cells to their target tissue. Co-stimulatory receptors… (more)

Subjects/Keywords: Medicine; regulatory T cells; T cell migration

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APA (6th Edition):

Kishore, M. (2016). The role of co-stimulatory receptors in the regulation of regulatory T cell migration. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/12869 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775244

Chicago Manual of Style (16th Edition):

Kishore, Madhav. “The role of co-stimulatory receptors in the regulation of regulatory T cell migration.” 2016. Doctoral Dissertation, Queen Mary, University of London. Accessed October 17, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/12869 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775244.

MLA Handbook (7th Edition):

Kishore, Madhav. “The role of co-stimulatory receptors in the regulation of regulatory T cell migration.” 2016. Web. 17 Oct 2019.

Vancouver:

Kishore M. The role of co-stimulatory receptors in the regulation of regulatory T cell migration. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2016. [cited 2019 Oct 17]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12869 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775244.

Council of Science Editors:

Kishore M. The role of co-stimulatory receptors in the regulation of regulatory T cell migration. [Doctoral Dissertation]. Queen Mary, University of London; 2016. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/12869 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.775244


University of New South Wales

10. 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 October 17, 2019. 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. 17 Oct 2019.

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 2019 Oct 17]. 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


ETH Zürich

11. Borsa, Mariana. Impact of asymmetric cell division on T cell differentiation.

Degree: 2018, ETH Zürich

 Successful immune responses rely on diversity. Being equipped with highly variable T cell receptors (TCRs), which convey antigen specificity, CD8+ T cells exhibit an immense… (more)

Subjects/Keywords: T cell differentiation; T cell memory; asymmetric cell division

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APA (6th Edition):

Borsa, M. (2018). Impact of asymmetric cell division on T cell differentiation. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/283722

Chicago Manual of Style (16th Edition):

Borsa, Mariana. “Impact of asymmetric cell division on T cell differentiation.” 2018. Doctoral Dissertation, ETH Zürich. Accessed October 17, 2019. http://hdl.handle.net/20.500.11850/283722.

MLA Handbook (7th Edition):

Borsa, Mariana. “Impact of asymmetric cell division on T cell differentiation.” 2018. Web. 17 Oct 2019.

Vancouver:

Borsa M. Impact of asymmetric cell division on T cell differentiation. [Internet] [Doctoral dissertation]. ETH Zürich; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/20.500.11850/283722.

Council of Science Editors:

Borsa M. Impact of asymmetric cell division on T cell differentiation. [Doctoral Dissertation]. ETH Zürich; 2018. Available from: http://hdl.handle.net/20.500.11850/283722


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 October 17, 2019. 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. 17 Oct 2019.

Vancouver:

Kurtulus S. Mechanisms Regulating Survival of Effector and Memory CD8+ T Cells. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2019 Oct 17]. 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. Purushothaman, Divya. Regulation of activated T cell death; -.

Degree: Chemical and Biotechnology, 2014, SASTRA University

Abstract included

Reference p116-134, List of publications p114-115, List of abbreviations p135-137, Summary included

Advisors/Committee Members: Sarin, Apurva.

Subjects/Keywords: Immune System; T cell death

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APA (6th Edition):

Purushothaman, D. (2014). Regulation of activated T cell death; -. (Thesis). SASTRA University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/22846

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):

Purushothaman, Divya. “Regulation of activated T cell death; -.” 2014. Thesis, SASTRA University. Accessed October 17, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/22846.

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

MLA Handbook (7th Edition):

Purushothaman, Divya. “Regulation of activated T cell death; -.” 2014. Web. 17 Oct 2019.

Vancouver:

Purushothaman D. Regulation of activated T cell death; -. [Internet] [Thesis]. SASTRA University; 2014. [cited 2019 Oct 17]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/22846.

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

Council of Science Editors:

Purushothaman D. Regulation of activated T cell death; -. [Thesis]. SASTRA University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/22846

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


Texas A&M University

14. Seelye, Stacie Lynn. Genomic Organization of Zebrafish (Danio rerio) T Cell Receptor ?/? Locus and Analysis of Expressed Products.

Degree: 2016, Texas A&M University

 In testing the hypothesis that all jawed vertebrate classes employ immunoglobulin heavy chain V (IgHV) gene segments in their T cell receptor (TCR)? encoding loci,… (more)

Subjects/Keywords: T Cell Receptor ?/?; Danio rerio

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APA (6th Edition):

Seelye, S. L. (2016). Genomic Organization of Zebrafish (Danio rerio) T Cell Receptor ?/? Locus and Analysis of Expressed Products. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156980

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):

Seelye, Stacie Lynn. “Genomic Organization of Zebrafish (Danio rerio) T Cell Receptor ?/? Locus and Analysis of Expressed Products.” 2016. Thesis, Texas A&M University. Accessed October 17, 2019. http://hdl.handle.net/1969.1/156980.

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

MLA Handbook (7th Edition):

Seelye, Stacie Lynn. “Genomic Organization of Zebrafish (Danio rerio) T Cell Receptor ?/? Locus and Analysis of Expressed Products.” 2016. Web. 17 Oct 2019.

Vancouver:

Seelye SL. Genomic Organization of Zebrafish (Danio rerio) T Cell Receptor ?/? Locus and Analysis of Expressed Products. [Internet] [Thesis]. Texas A&M University; 2016. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1969.1/156980.

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

Council of Science Editors:

Seelye SL. Genomic Organization of Zebrafish (Danio rerio) T Cell Receptor ?/? Locus and Analysis of Expressed Products. [Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/156980

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


Addis Ababa University

15. Haile, Benti. Lost opportunities to complete CD4+ T cell testing among HIV positive patients attending selected health centers in Afar region Northeast Ethiopia, 2014.

Degree: 2014, Addis Ababa University

 Background: In resource limited settings CD4+ T cell count (CD4 testing) facility is not available in peripheral areas and often either patients need to travel… (more)

Subjects/Keywords: CD4+ T cell count; HIV

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APA (6th Edition):

Haile, B. (2014). Lost opportunities to complete CD4+ T cell testing among HIV positive patients attending selected health centers in Afar region Northeast Ethiopia, 2014. (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/5655

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):

Haile, Benti. “Lost opportunities to complete CD4+ T cell testing among HIV positive patients attending selected health centers in Afar region Northeast Ethiopia, 2014. ” 2014. Thesis, Addis Ababa University. Accessed October 17, 2019. http://etd.aau.edu.et/dspace/handle/123456789/5655.

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

MLA Handbook (7th Edition):

Haile, Benti. “Lost opportunities to complete CD4+ T cell testing among HIV positive patients attending selected health centers in Afar region Northeast Ethiopia, 2014. ” 2014. Web. 17 Oct 2019.

Vancouver:

Haile B. Lost opportunities to complete CD4+ T cell testing among HIV positive patients attending selected health centers in Afar region Northeast Ethiopia, 2014. [Internet] [Thesis]. Addis Ababa University; 2014. [cited 2019 Oct 17]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/5655.

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

Council of Science Editors:

Haile B. Lost opportunities to complete CD4+ T cell testing among HIV positive patients attending selected health centers in Afar region Northeast Ethiopia, 2014. [Thesis]. Addis Ababa University; 2014. Available from: http://etd.aau.edu.et/dspace/handle/123456789/5655

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


University of Western Australia

16. Burchell, Jennifer Theresa. The role of regulatory T cells and dendritic cells in allergen-induced airways hyperresponsiveness.

Degree: PhD, 2008, University of Western Australia

 [Truncated abstract] Airway hyperresponsiveness (AHR) is one of the primary features of allergic airways disease. Despite continuous allergen exposure atopic asthmatics do not develop progressively… (more)

Subjects/Keywords: Asthma; Regulatory T cell; Allergen

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APA (6th Edition):

Burchell, J. T. (2008). The role of regulatory T cells and dendritic cells in allergen-induced airways hyperresponsiveness. (Doctoral Dissertation). University of Western Australia. Retrieved from http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5727&local_base=GEN01-INS01

Chicago Manual of Style (16th Edition):

Burchell, Jennifer Theresa. “The role of regulatory T cells and dendritic cells in allergen-induced airways hyperresponsiveness.” 2008. Doctoral Dissertation, University of Western Australia. Accessed October 17, 2019. http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5727&local_base=GEN01-INS01.

MLA Handbook (7th Edition):

Burchell, Jennifer Theresa. “The role of regulatory T cells and dendritic cells in allergen-induced airways hyperresponsiveness.” 2008. Web. 17 Oct 2019.

Vancouver:

Burchell JT. The role of regulatory T cells and dendritic cells in allergen-induced airways hyperresponsiveness. [Internet] [Doctoral dissertation]. University of Western Australia; 2008. [cited 2019 Oct 17]. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5727&local_base=GEN01-INS01.

Council of Science Editors:

Burchell JT. The role of regulatory T cells and dendritic cells in allergen-induced airways hyperresponsiveness. [Doctoral Dissertation]. University of Western Australia; 2008. Available from: http://repository.uwa.edu.au:80/R/?func=dbin-jump-full&object_id=5727&local_base=GEN01-INS01


University of Saskatchewan

17. Rudulier, Christopher. CD4+ T cell interactions through CD28/B7 molecules affects their Th1/Th2 phenotype.

Degree: 2011, University of Saskatchewan

 The Th1/Th2 phenotype of the immune response generated against a pathogen or disease can have a profound impact upon the survival of the host. Thus,… (more)

Subjects/Keywords: CD4 T cell differentiation

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APA (6th Edition):

Rudulier, C. (2011). CD4+ T cell interactions through CD28/B7 molecules affects their Th1/Th2 phenotype. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2011-12-282

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):

Rudulier, Christopher. “CD4+ T cell interactions through CD28/B7 molecules affects their Th1/Th2 phenotype.” 2011. Thesis, University of Saskatchewan. Accessed October 17, 2019. http://hdl.handle.net/10388/ETD-2011-12-282.

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

MLA Handbook (7th Edition):

Rudulier, Christopher. “CD4+ T cell interactions through CD28/B7 molecules affects their Th1/Th2 phenotype.” 2011. Web. 17 Oct 2019.

Vancouver:

Rudulier C. CD4+ T cell interactions through CD28/B7 molecules affects their Th1/Th2 phenotype. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10388/ETD-2011-12-282.

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

Council of Science Editors:

Rudulier C. CD4+ T cell interactions through CD28/B7 molecules affects their Th1/Th2 phenotype. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/ETD-2011-12-282

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


University of Illinois – Chicago

18. Ryan Payseur, Bridgett K. Host T Cell Responses to Malaria, Acquired Immunodeficiency Virus, and Listeria Infections.

Degree: 2012, University of Illinois – Chicago

 Understanding of T cell responses during infections will be vital to rational vaccine design. Malaria and AIDS represent two leading causes of death from infectious… (more)

Subjects/Keywords: T cell; malaria; listeria; AIDS

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APA (6th Edition):

Ryan Payseur, B. K. (2012). Host T Cell Responses to Malaria, Acquired Immunodeficiency Virus, and Listeria Infections. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9078

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):

Ryan Payseur, Bridgett K. “Host T Cell Responses to Malaria, Acquired Immunodeficiency Virus, and Listeria Infections.” 2012. Thesis, University of Illinois – Chicago. Accessed October 17, 2019. http://hdl.handle.net/10027/9078.

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

MLA Handbook (7th Edition):

Ryan Payseur, Bridgett K. “Host T Cell Responses to Malaria, Acquired Immunodeficiency Virus, and Listeria Infections.” 2012. Web. 17 Oct 2019.

Vancouver:

Ryan Payseur BK. Host T Cell Responses to Malaria, Acquired Immunodeficiency Virus, and Listeria Infections. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10027/9078.

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

Council of Science Editors:

Ryan Payseur BK. Host T Cell Responses to Malaria, Acquired Immunodeficiency Virus, and Listeria Infections. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9078

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

19. Park, Christa. The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity .

Degree: 2017, California State University – San Marcos

 According to the Journal of the American Medical Association and the Centers for Disease Control and Prevention, one in six children and adolescents in the… (more)

Subjects/Keywords: T cell; Mice; Obesity

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APA (6th Edition):

Park, C. (2017). The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/194723

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):

Park, Christa. “The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity .” 2017. Thesis, California State University – San Marcos. Accessed October 17, 2019. http://hdl.handle.net/10211.3/194723.

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

MLA Handbook (7th Edition):

Park, Christa. “The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity .” 2017. Web. 17 Oct 2019.

Vancouver:

Park C. The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity . [Internet] [Thesis]. California State University – San Marcos; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10211.3/194723.

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

Council of Science Editors:

Park C. The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity . [Thesis]. California State University – San Marcos; 2017. Available from: http://hdl.handle.net/10211.3/194723

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


University of Manchester

20. Brignall, Ruth. The single-cell and gene expression analysis of T cell activation and signalling.

Degree: 2016, University of Manchester

 Our immune system must be able to rapidly fight against pathogens, but at the same time be tightly regulated to prevent harmful autoimmune and inflammatory… (more)

Subjects/Keywords: T cell; Signalling; NFAT

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APA (6th Edition):

Brignall, R. (2016). The single-cell and gene expression analysis of T cell activation and signalling. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305715

Chicago Manual of Style (16th Edition):

Brignall, Ruth. “The single-cell and gene expression analysis of T cell activation and signalling.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305715.

MLA Handbook (7th Edition):

Brignall, Ruth. “The single-cell and gene expression analysis of T cell activation and signalling.” 2016. Web. 17 Oct 2019.

Vancouver:

Brignall R. The single-cell and gene expression analysis of T cell activation and signalling. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305715.

Council of Science Editors:

Brignall R. The single-cell and gene expression analysis of T cell activation and signalling. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:305715


Montana Tech

21. Emmons, Tiffany. THE EFFECTS OF ESTROGEN IN ATRAZINE-MEDIATED FOXP3 INDUCTION AND INHIBITION OF CD4+ T EFFECTOR CELLS.

Degree: MS, 2014, Montana Tech

 Atrazine (ATR) is a chlorotriazine herbicide that is heavily used in agricultural areas. Atrazine was banned in Europe in 2006 but it is still used… (more)

Subjects/Keywords: regulatory T cell; immunotoxicity

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APA (6th Edition):

Emmons, T. (2014). THE EFFECTS OF ESTROGEN IN ATRAZINE-MEDIATED FOXP3 INDUCTION AND INHIBITION OF CD4+ T EFFECTOR CELLS. (Masters Thesis). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/4350

Chicago Manual of Style (16th Edition):

Emmons, Tiffany. “THE EFFECTS OF ESTROGEN IN ATRAZINE-MEDIATED FOXP3 INDUCTION AND INHIBITION OF CD4+ T EFFECTOR CELLS.” 2014. Masters Thesis, Montana Tech. Accessed October 17, 2019. https://scholarworks.umt.edu/etd/4350.

MLA Handbook (7th Edition):

Emmons, Tiffany. “THE EFFECTS OF ESTROGEN IN ATRAZINE-MEDIATED FOXP3 INDUCTION AND INHIBITION OF CD4+ T EFFECTOR CELLS.” 2014. Web. 17 Oct 2019.

Vancouver:

Emmons T. THE EFFECTS OF ESTROGEN IN ATRAZINE-MEDIATED FOXP3 INDUCTION AND INHIBITION OF CD4+ T EFFECTOR CELLS. [Internet] [Masters thesis]. Montana Tech; 2014. [cited 2019 Oct 17]. Available from: https://scholarworks.umt.edu/etd/4350.

Council of Science Editors:

Emmons T. THE EFFECTS OF ESTROGEN IN ATRAZINE-MEDIATED FOXP3 INDUCTION AND INHIBITION OF CD4+ T EFFECTOR CELLS. [Masters Thesis]. Montana Tech; 2014. Available from: https://scholarworks.umt.edu/etd/4350


McMaster University

22. Afsahi, Arya. Development of novel chimeric receptors for delivery of costimulation to tumor-reactive engineered T cells.

Degree: MSc, 2015, McMaster University

Introduction: Manipulation of the immune system to eliminate cancer, known as cancer immunotherapy, is an emerging field that has shown impressive clinical success and promise.… (more)

Subjects/Keywords: Immunology; T cell; Cancer; Immunotherapy

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APA (6th Edition):

Afsahi, A. (2015). Development of novel chimeric receptors for delivery of costimulation to tumor-reactive engineered T cells. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/18413

Chicago Manual of Style (16th Edition):

Afsahi, Arya. “Development of novel chimeric receptors for delivery of costimulation to tumor-reactive engineered T cells.” 2015. Masters Thesis, McMaster University. Accessed October 17, 2019. http://hdl.handle.net/11375/18413.

MLA Handbook (7th Edition):

Afsahi, Arya. “Development of novel chimeric receptors for delivery of costimulation to tumor-reactive engineered T cells.” 2015. Web. 17 Oct 2019.

Vancouver:

Afsahi A. Development of novel chimeric receptors for delivery of costimulation to tumor-reactive engineered T cells. [Internet] [Masters thesis]. McMaster University; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11375/18413.

Council of Science Editors:

Afsahi A. Development of novel chimeric receptors for delivery of costimulation to tumor-reactive engineered T cells. [Masters Thesis]. McMaster University; 2015. Available from: http://hdl.handle.net/11375/18413


University of Manchester

23. Brignall, Ruth. The single-cell and gene expression analysis of T cell activation and signalling.

Degree: PhD, 2016, University of Manchester

 Our immune system must be able to rapidly fight against pathogens, but at the same time be tightly regulated to prevent harmful autoimmune and inflammatory… (more)

Subjects/Keywords: 616.07; T cell; Signalling; NFAT

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APA (6th Edition):

Brignall, R. (2016). The single-cell and gene expression analysis of T cell activation and signalling. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-singlecell-and-gene-expression-analysis-of-t-cell-activation-and-signalling(d4f814bf-b4f7-4e23-8130-5ba4b9f38c13).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697799

Chicago Manual of Style (16th Edition):

Brignall, Ruth. “The single-cell and gene expression analysis of T cell activation and signalling.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 17, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-singlecell-and-gene-expression-analysis-of-t-cell-activation-and-signalling(d4f814bf-b4f7-4e23-8130-5ba4b9f38c13).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697799.

MLA Handbook (7th Edition):

Brignall, Ruth. “The single-cell and gene expression analysis of T cell activation and signalling.” 2016. Web. 17 Oct 2019.

Vancouver:

Brignall R. The single-cell and gene expression analysis of T cell activation and signalling. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-singlecell-and-gene-expression-analysis-of-t-cell-activation-and-signalling(d4f814bf-b4f7-4e23-8130-5ba4b9f38c13).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697799.

Council of Science Editors:

Brignall R. The single-cell and gene expression analysis of T cell activation and signalling. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-singlecell-and-gene-expression-analysis-of-t-cell-activation-and-signalling(d4f814bf-b4f7-4e23-8130-5ba4b9f38c13).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.697799


University of Illinois – Urbana-Champaign

24. Harris, Daniel Thomas. Engineering and characterizing human T cell receptors for cancer immunotherapies.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

 The T cell receptor (TCR) is an heterodimer that binds to a short peptide bound to a product of the major histocompatibility complex (MHC). The… (more)

Subjects/Keywords: Immunotherapy; T Cell Receptor

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APA (6th Edition):

Harris, D. T. (2016). Engineering and characterizing human T cell receptors for cancer immunotherapies. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95531

Chicago Manual of Style (16th Edition):

Harris, Daniel Thomas. “Engineering and characterizing human T cell receptors for cancer immunotherapies.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 17, 2019. http://hdl.handle.net/2142/95531.

MLA Handbook (7th Edition):

Harris, Daniel Thomas. “Engineering and characterizing human T cell receptors for cancer immunotherapies.” 2016. Web. 17 Oct 2019.

Vancouver:

Harris DT. Engineering and characterizing human T cell receptors for cancer immunotherapies. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2142/95531.

Council of Science Editors:

Harris DT. Engineering and characterizing human T cell receptors for cancer immunotherapies. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95531


University of Melbourne

25. Yang, Kun. Molecular control of CD8 liver resident memory T cell differentiation and function.

Degree: 2017, University of Melbourne

 Immune memory forms after clearance of antigens to support the build-up of a more efficient defence in which memory B cells and memory T cells… (more)

Subjects/Keywords: resident memory T cell; liver

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APA (6th Edition):

Yang, K. (2017). Molecular control of CD8 liver resident memory T cell differentiation and function. (Masters Thesis). University of Melbourne. Retrieved from http://hdl.handle.net/11343/196414

Chicago Manual of Style (16th Edition):

Yang, Kun. “Molecular control of CD8 liver resident memory T cell differentiation and function.” 2017. Masters Thesis, University of Melbourne. Accessed October 17, 2019. http://hdl.handle.net/11343/196414.

MLA Handbook (7th Edition):

Yang, Kun. “Molecular control of CD8 liver resident memory T cell differentiation and function.” 2017. Web. 17 Oct 2019.

Vancouver:

Yang K. Molecular control of CD8 liver resident memory T cell differentiation and function. [Internet] [Masters thesis]. University of Melbourne; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11343/196414.

Council of Science Editors:

Yang K. Molecular control of CD8 liver resident memory T cell differentiation and function. [Masters Thesis]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/196414


University of Melbourne

26. Pathiraja, Vimukthi A. P. Identification of β-cell antigens recognized by human islet-infiltrating T-cells in type 1 diabetes.

Degree: 2016, University of Melbourne

 Type 1 diabetes (T1D) is an autoimmune disease caused by the T-cell mediated destruction of the pancreatic insulin-producing beta cells. Currently the β-cell derived antigens… (more)

Subjects/Keywords: T-cell; islet-infiltration

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APA (6th Edition):

Pathiraja, V. A. P. (2016). Identification of β-cell antigens recognized by human islet-infiltrating T-cells in type 1 diabetes. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/119538

Chicago Manual of Style (16th Edition):

Pathiraja, Vimukthi A P. “Identification of β-cell antigens recognized by human islet-infiltrating T-cells in type 1 diabetes.” 2016. Doctoral Dissertation, University of Melbourne. Accessed October 17, 2019. http://hdl.handle.net/11343/119538.

MLA Handbook (7th Edition):

Pathiraja, Vimukthi A P. “Identification of β-cell antigens recognized by human islet-infiltrating T-cells in type 1 diabetes.” 2016. Web. 17 Oct 2019.

Vancouver:

Pathiraja VAP. Identification of β-cell antigens recognized by human islet-infiltrating T-cells in type 1 diabetes. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11343/119538.

Council of Science Editors:

Pathiraja VAP. Identification of β-cell antigens recognized by human islet-infiltrating T-cells in type 1 diabetes. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/119538


University of Manchester

27. Rich, Kevin Robert. The Role of Transforming Growth Factor-Beta in T-Cell Signalling.

Degree: 2016, University of Manchester

Transforming Growth Factor beta (TGFβ) is a pivotal cytokine in regulating our immune responses. TGFβ exerts many effects through T-cells, which are an important cell(more)

Subjects/Keywords: TGFb; T-cell; Smad

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APA (6th Edition):

Rich, K. R. (2016). The Role of Transforming Growth Factor-Beta in T-Cell Signalling. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301779

Chicago Manual of Style (16th Edition):

Rich, Kevin Robert. “The Role of Transforming Growth Factor-Beta in T-Cell Signalling.” 2016. Doctoral Dissertation, University of Manchester. Accessed October 17, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301779.

MLA Handbook (7th Edition):

Rich, Kevin Robert. “The Role of Transforming Growth Factor-Beta in T-Cell Signalling.” 2016. Web. 17 Oct 2019.

Vancouver:

Rich KR. The Role of Transforming Growth Factor-Beta in T-Cell Signalling. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2019 Oct 17]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301779.

Council of Science Editors:

Rich KR. The Role of Transforming Growth Factor-Beta in T-Cell Signalling. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:301779


Vanderbilt University

28. Conrad, Joseph Allen. Clonotypic Dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment.

Degree: PhD, Microbiology and Immunology, 2011, Vanderbilt University

 HIV-epitope-specific T cell responses are critical components of the natural immune response to HIV infection, but these cells often become dysfunctional in chronic infection. Structural… (more)

Subjects/Keywords: TCR; HIV; T cell; CTL

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APA (6th Edition):

Conrad, J. A. (2011). Clonotypic Dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-04292011-141143/ ;

Chicago Manual of Style (16th Edition):

Conrad, Joseph Allen. “Clonotypic Dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed October 17, 2019. http://etd.library.vanderbilt.edu/available/etd-04292011-141143/ ;.

MLA Handbook (7th Edition):

Conrad, Joseph Allen. “Clonotypic Dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment.” 2011. Web. 17 Oct 2019.

Vancouver:

Conrad JA. Clonotypic Dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2019 Oct 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-04292011-141143/ ;.

Council of Science Editors:

Conrad JA. Clonotypic Dominance within the HIV-epitope-specific T cell receptor repertoire correlates with phenotypic and functional impairment. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-04292011-141143/ ;


University of Rochester

29. Chapman, Lesley Maraina. MicroRNA-451 Regulates T Helper Cell Responses.

Degree: PhD, 2015, University of Rochester

 Background: Malaria parasite evasion of host defense mechanisms leads to uncontrolled parasite growth, anemia, morbidity, and often mortality. A number of studies have shown that… (more)

Subjects/Keywords: CD4 T Cell; Plasmodium; MYC

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

APA (6th Edition):

Chapman, L. M. (2015). MicroRNA-451 Regulates T Helper Cell Responses. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30109

Chicago Manual of Style (16th Edition):

Chapman, Lesley Maraina. “MicroRNA-451 Regulates T Helper Cell Responses.” 2015. Doctoral Dissertation, University of Rochester. Accessed October 17, 2019. http://hdl.handle.net/1802/30109.

MLA Handbook (7th Edition):

Chapman, Lesley Maraina. “MicroRNA-451 Regulates T Helper Cell Responses.” 2015. Web. 17 Oct 2019.

Vancouver:

Chapman LM. MicroRNA-451 Regulates T Helper Cell Responses. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1802/30109.

Council of Science Editors:

Chapman LM. MicroRNA-451 Regulates T Helper Cell Responses. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30109

30. Helou, Ynes. Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics.

Degree: PhD, Molecular Pharmacology, Physiology, and Biotechnology, 2015, Brown University

 Activation of T cells via the T cell receptor (TCR) is a crucial event in the adaptive immune response, and is mediated by a delicate… (more)

Subjects/Keywords: T cell receptor signaling

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

APA (6th Edition):

Helou, Y. (2015). Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419500/

Chicago Manual of Style (16th Edition):

Helou, Ynes. “Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics.” 2015. Doctoral Dissertation, Brown University. Accessed October 17, 2019. https://repository.library.brown.edu/studio/item/bdr:419500/.

MLA Handbook (7th Edition):

Helou, Ynes. “Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics.” 2015. Web. 17 Oct 2019.

Vancouver:

Helou Y. Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2019 Oct 17]. Available from: https://repository.library.brown.edu/studio/item/bdr:419500/.

Council of Science Editors:

Helou Y. Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419500/

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