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You searched for subject:(T cell receptor TCR ). Showing records 1 – 30 of 43226 total matches.

[1] [2] [3] [4] [5] … [1441]

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Australian National University

1. Singh, Mandeep. An investigation into autoimmune pathogenesis by tracking and profiling T cell clones .

Degree: 2017, Australian National University

 Multiple immune tolerance checkpoints ensure that T cells carrying self-reactive T cell receptors (TCRs) are either purged during development or inactivated in the periphery. How… (more)

Subjects/Keywords: Autoimmunity; T cell tolerance; T cell receptor; TCR deep sequencing

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APA (6th Edition):

Singh, M. (2017). An investigation into autoimmune pathogenesis by tracking and profiling T cell clones . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/132693

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):

Singh, Mandeep. “An investigation into autoimmune pathogenesis by tracking and profiling T cell clones .” 2017. Thesis, Australian National University. Accessed October 28, 2020. http://hdl.handle.net/1885/132693.

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

MLA Handbook (7th Edition):

Singh, Mandeep. “An investigation into autoimmune pathogenesis by tracking and profiling T cell clones .” 2017. Web. 28 Oct 2020.

Vancouver:

Singh M. An investigation into autoimmune pathogenesis by tracking and profiling T cell clones . [Internet] [Thesis]. Australian National University; 2017. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1885/132693.

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

Council of Science Editors:

Singh M. An investigation into autoimmune pathogenesis by tracking and profiling T cell clones . [Thesis]. Australian National University; 2017. Available from: http://hdl.handle.net/1885/132693

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


University of New South Wales

2. Cornely, Rhea. The role of Annexin A6 in T cell activation.

Degree: Centre for Vascular Research, 2013, University of New South Wales

 The activation of T cells by an antigen presenting cell is one of the essential first steps for an effective immune response. Activation of the… (more)

Subjects/Keywords: IL-2 receptor; T cell activation; TCR; Membrane lipids

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APA (6th Edition):

Cornely, R. (2013). The role of Annexin A6 in T cell activation. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53646 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12341/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Cornely, Rhea. “The role of Annexin A6 in T cell activation.” 2013. Doctoral Dissertation, University of New South Wales. Accessed October 28, 2020. http://handle.unsw.edu.au/1959.4/53646 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12341/SOURCE02?view=true.

MLA Handbook (7th Edition):

Cornely, Rhea. “The role of Annexin A6 in T cell activation.” 2013. Web. 28 Oct 2020.

Vancouver:

Cornely R. The role of Annexin A6 in T cell activation. [Internet] [Doctoral dissertation]. University of New South Wales; 2013. [cited 2020 Oct 28]. Available from: http://handle.unsw.edu.au/1959.4/53646 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12341/SOURCE02?view=true.

Council of Science Editors:

Cornely R. The role of Annexin A6 in T cell activation. [Doctoral Dissertation]. University of New South Wales; 2013. Available from: http://handle.unsw.edu.au/1959.4/53646 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12341/SOURCE02?view=true


University of California – Berkeley

3. Fay, Nicole Cheung. Spatiotemporal receptor dynamics during early T cell signaling.

Degree: Molecular & Cell Biology, 2014, University of California – Berkeley

 A given T cell receptor (TCR) can robustly discern a pathogen-derived agonist peptide amidst a myriad of background peptides, all bound to major histocompatibility complexes… (more)

Subjects/Keywords: Molecular biology; Immunology; Biophysics; antigen recognition; CD28; CD80; costimulation; T cell; T cell receptor (TCR)

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APA (6th Edition):

Fay, N. C. (2014). Spatiotemporal receptor dynamics during early T cell signaling. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/6pk117x3

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):

Fay, Nicole Cheung. “Spatiotemporal receptor dynamics during early T cell signaling.” 2014. Thesis, University of California – Berkeley. Accessed October 28, 2020. http://www.escholarship.org/uc/item/6pk117x3.

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

MLA Handbook (7th Edition):

Fay, Nicole Cheung. “Spatiotemporal receptor dynamics during early T cell signaling.” 2014. Web. 28 Oct 2020.

Vancouver:

Fay NC. Spatiotemporal receptor dynamics during early T cell signaling. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2020 Oct 28]. Available from: http://www.escholarship.org/uc/item/6pk117x3.

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

Council of Science Editors:

Fay NC. Spatiotemporal receptor dynamics during early T cell signaling. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/6pk117x3

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


University of Cambridge

4. Smid, Andrei Iosif. Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment.

Degree: PhD, 2019, University of Cambridge

T-cell development is a complex multi-step process, driving the maturation of hematopoietic stem cells into fully functional mature T-cells that play a major role in… (more)

Subjects/Keywords: T-cell; T-cell development; Pre-T-cell receptor; Trafficking; TCR signalling; γδ-TCR; OP9-DL1 co-culture; hematopoietic stem cells; BioID2

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APA (6th Edition):

Smid, A. I. (2019). Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/297674

Chicago Manual of Style (16th Edition):

Smid, Andrei Iosif. “Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 28, 2020. https://www.repository.cam.ac.uk/handle/1810/297674.

MLA Handbook (7th Edition):

Smid, Andrei Iosif. “Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment.” 2019. Web. 28 Oct 2020.

Vancouver:

Smid AI. Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 28]. Available from: https://www.repository.cam.ac.uk/handle/1810/297674.

Council of Science Editors:

Smid AI. Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/297674


Vanderbilt University

5. 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://hdl.handle.net/1803/12236

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 28, 2020. http://hdl.handle.net/1803/12236.

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. 28 Oct 2020.

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 2020 Oct 28]. Available from: http://hdl.handle.net/1803/12236.

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://hdl.handle.net/1803/12236


Brigham Young University

6. Freitas, Claudia Mercedes. Regulation of Immune Cell Activation and Functionby the nBMPp2 Protein andthe CD5 Co-Receptor.

Degree: PhD, 2019, Brigham Young University

 According to the centers for disease control and prevention (CDC) and the world healthorganization (WHO), heart disease and immune related diseases such as diabetes and… (more)

Subjects/Keywords: nBMP2; bone morphogenetic protein; CD5; co-receptor; calcium (Ca2+); metabolism; behavior; TCR; T cell receptor; microbiome; macrophage; T helper cells

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

APA (6th Edition):

Freitas, C. M. (2019). Regulation of Immune Cell Activation and Functionby the nBMPp2 Protein andthe CD5 Co-Receptor. (Doctoral Dissertation). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9257&context=etd

Chicago Manual of Style (16th Edition):

Freitas, Claudia Mercedes. “Regulation of Immune Cell Activation and Functionby the nBMPp2 Protein andthe CD5 Co-Receptor.” 2019. Doctoral Dissertation, Brigham Young University. Accessed October 28, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9257&context=etd.

MLA Handbook (7th Edition):

Freitas, Claudia Mercedes. “Regulation of Immune Cell Activation and Functionby the nBMPp2 Protein andthe CD5 Co-Receptor.” 2019. Web. 28 Oct 2020.

Vancouver:

Freitas CM. Regulation of Immune Cell Activation and Functionby the nBMPp2 Protein andthe CD5 Co-Receptor. [Internet] [Doctoral dissertation]. Brigham Young University; 2019. [cited 2020 Oct 28]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9257&context=etd.

Council of Science Editors:

Freitas CM. Regulation of Immune Cell Activation and Functionby the nBMPp2 Protein andthe CD5 Co-Receptor. [Doctoral Dissertation]. Brigham Young University; 2019. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=9257&context=etd

7. Ellestad, Kristofor K. Mechanisms underlying lymphopenia-driven autoimmunity in the setting of co-inhibitory molecule deficiency.

Degree: PhD, Department of Medical Microbiology and Immunology, 2016, University of Alberta

T lymphocytes (T cells) are powerful directors and effectors of immunity. The system of pseudo-random rearrangements of the T cell receptor (TCR) loci that underlie… (more)

Subjects/Keywords: Autoimmunity; Tolerance; Co-stimulation; Co-inhibition; Lymphopenia; T cell receptor; TCR; PD-1

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APA (6th Edition):

Ellestad, K. K. (2016). Mechanisms underlying lymphopenia-driven autoimmunity in the setting of co-inhibitory molecule deficiency. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/ckk91fk70f

Chicago Manual of Style (16th Edition):

Ellestad, Kristofor K. “Mechanisms underlying lymphopenia-driven autoimmunity in the setting of co-inhibitory molecule deficiency.” 2016. Doctoral Dissertation, University of Alberta. Accessed October 28, 2020. https://era.library.ualberta.ca/files/ckk91fk70f.

MLA Handbook (7th Edition):

Ellestad, Kristofor K. “Mechanisms underlying lymphopenia-driven autoimmunity in the setting of co-inhibitory molecule deficiency.” 2016. Web. 28 Oct 2020.

Vancouver:

Ellestad KK. Mechanisms underlying lymphopenia-driven autoimmunity in the setting of co-inhibitory molecule deficiency. [Internet] [Doctoral dissertation]. University of Alberta; 2016. [cited 2020 Oct 28]. Available from: https://era.library.ualberta.ca/files/ckk91fk70f.

Council of Science Editors:

Ellestad KK. Mechanisms underlying lymphopenia-driven autoimmunity in the setting of co-inhibitory molecule deficiency. [Doctoral Dissertation]. University of Alberta; 2016. Available from: https://era.library.ualberta.ca/files/ckk91fk70f


Georgia Tech

8. Hong, Jin Sung. Study of 2D kinetics and force regulation in T cell recognition.

Degree: PhD, Mechanical Engineering, 2014, Georgia Tech

T cell activation and thymic selection are thought to be determined by the binding propensity (avidity or affinity) of the T cell receptor (TCR) to… (more)

Subjects/Keywords: T cell recognition; T cell activation; Thymic selection; TCR-pMHC interaction; Co-receptor cooperativity; 2D kinetics; Catch bond

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APA (6th Edition):

Hong, J. S. (2014). Study of 2D kinetics and force regulation in T cell recognition. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53430

Chicago Manual of Style (16th Edition):

Hong, Jin Sung. “Study of 2D kinetics and force regulation in T cell recognition.” 2014. Doctoral Dissertation, Georgia Tech. Accessed October 28, 2020. http://hdl.handle.net/1853/53430.

MLA Handbook (7th Edition):

Hong, Jin Sung. “Study of 2D kinetics and force regulation in T cell recognition.” 2014. Web. 28 Oct 2020.

Vancouver:

Hong JS. Study of 2D kinetics and force regulation in T cell recognition. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/1853/53430.

Council of Science Editors:

Hong JS. Study of 2D kinetics and force regulation in T cell recognition. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53430


University of Texas – Austin

9. -7757-895X. Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis.

Degree: PhD, Biomedical Engineering, 2020, University of Texas – Austin

 Multiple sclerosis (MS) is a debilitating neurodegenerative autoimmune disorder caused by autoreactive T cells that recognize and initiate immune attack of the myelin sheath that… (more)

Subjects/Keywords: T cell receptor; TCR; Multiple sclerosis; MS; Protein engineering; T cell engineering; T regulatory cells; Cellular therapeutics; Autoimmunity; Yeast display; T cell activation

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APA (6th Edition):

-7757-895X. (2020). Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/9439

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

Chicago Manual of Style (16th Edition):

-7757-895X. “Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis.” 2020. Doctoral Dissertation, University of Texas – Austin. Accessed October 28, 2020. http://dx.doi.org/10.26153/tsw/9439.

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

MLA Handbook (7th Edition):

-7757-895X. “Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis.” 2020. Web. 28 Oct 2020.

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

Vancouver:

-7757-895X. Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2020. [cited 2020 Oct 28]. Available from: http://dx.doi.org/10.26153/tsw/9439.

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

Council of Science Editors:

-7757-895X. Engineering human autoimmune T cell receptors towards the development of a cellular therapy for multiple sclerosis. [Doctoral Dissertation]. University of Texas – Austin; 2020. Available from: http://dx.doi.org/10.26153/tsw/9439

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


University of New South Wales

10. Williamson, David. The role of LAT clusters in early immune cell signalling.

Degree: Centre for Vascular Research, 2010, University of New South Wales

T cell activation is an essential part of the immune response and requires segregation of signalling proteins into specialised membrane domains to transmit and sustain… (more)

Subjects/Keywords: T-cell receptor (TCR); signalling; LAT clusters; triggering

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APA (6th Edition):

Williamson, D. (2010). The role of LAT clusters in early immune cell signalling. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Williamson, David. “The role of LAT clusters in early immune cell signalling.” 2010. Doctoral Dissertation, University of New South Wales. Accessed October 28, 2020. http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true.

MLA Handbook (7th Edition):

Williamson, David. “The role of LAT clusters in early immune cell signalling.” 2010. Web. 28 Oct 2020.

Vancouver:

Williamson D. The role of LAT clusters in early immune cell signalling. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2020 Oct 28]. Available from: http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true.

Council of Science Editors:

Williamson D. The role of LAT clusters in early immune cell signalling. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/51514 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10201/SOURCE02?view=true


University of Pennsylvania

11. Delong, Jonathan Howard. Role Of Il-27 And Tcr Stimulation In Inhibitory Receptor Expression.

Degree: 2018, University of Pennsylvania

 The adaptive immune response is necessary for control of pathogen burden in a wide range of infections. However, in the absence of active regulatory mechanisms,… (more)

Subjects/Keywords: IL-27; Immunopathology; Inhibitory receptor; T cell; TCR; Toxoplasma gondii; Allergy and Immunology; Immunology and Infectious Disease; Medical Immunology

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APA (6th Edition):

Delong, J. H. (2018). Role Of Il-27 And Tcr Stimulation In Inhibitory Receptor Expression. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/3105

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):

Delong, Jonathan Howard. “Role Of Il-27 And Tcr Stimulation In Inhibitory Receptor Expression.” 2018. Thesis, University of Pennsylvania. Accessed October 28, 2020. https://repository.upenn.edu/edissertations/3105.

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

MLA Handbook (7th Edition):

Delong, Jonathan Howard. “Role Of Il-27 And Tcr Stimulation In Inhibitory Receptor Expression.” 2018. Web. 28 Oct 2020.

Vancouver:

Delong JH. Role Of Il-27 And Tcr Stimulation In Inhibitory Receptor Expression. [Internet] [Thesis]. University of Pennsylvania; 2018. [cited 2020 Oct 28]. Available from: https://repository.upenn.edu/edissertations/3105.

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

Council of Science Editors:

Delong JH. Role Of Il-27 And Tcr Stimulation In Inhibitory Receptor Expression. [Thesis]. University of Pennsylvania; 2018. Available from: https://repository.upenn.edu/edissertations/3105

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


University of Melbourne

12. QUIÑONES PARRA, SERGIO MANUEL. Understanding influenza CD8+ T cell immune escape from pre-existing immunity and T cell receptor cross-strain recognition.

Degree: 2015, University of Melbourne

 Protective immunity against influenza virus infections relies heavily in neutralising antibodies (nAbs) and CD8+ T lymphocytes (CTLs). Current nAbs-based influenza vaccines are greatly undermined by… (more)

Subjects/Keywords: CD8 T cells; cytotoxic T cells; CTLs; CTL cell escape; T cell receptor; TCR; cross-reactivity; antigenic peptide; epitope; H7N9; H2N2; CD8+ tissue resident memory; TRM

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APA (6th Edition):

QUIÑONES PARRA, S. M. (2015). Understanding influenza CD8+ T cell immune escape from pre-existing immunity and T cell receptor cross-strain recognition. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/59641

Chicago Manual of Style (16th Edition):

QUIÑONES PARRA, SERGIO MANUEL. “Understanding influenza CD8+ T cell immune escape from pre-existing immunity and T cell receptor cross-strain recognition.” 2015. Doctoral Dissertation, University of Melbourne. Accessed October 28, 2020. http://hdl.handle.net/11343/59641.

MLA Handbook (7th Edition):

QUIÑONES PARRA, SERGIO MANUEL. “Understanding influenza CD8+ T cell immune escape from pre-existing immunity and T cell receptor cross-strain recognition.” 2015. Web. 28 Oct 2020.

Vancouver:

QUIÑONES PARRA SM. Understanding influenza CD8+ T cell immune escape from pre-existing immunity and T cell receptor cross-strain recognition. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/11343/59641.

Council of Science Editors:

QUIÑONES PARRA SM. Understanding influenza CD8+ T cell immune escape from pre-existing immunity and T cell receptor cross-strain recognition. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/59641


University of Arizona

13. Bronnimann, Heather. Functional Analysis of Interactions within the TCR-CD3-pMHC-CD4 Macro-complex .

Degree: 2016, University of Arizona

 CD4⁺ T cells are a critical component of the adaptive immune compartment. Each T cell expresses a clonotypic T cell receptor (TCR) that must discriminate… (more)

Subjects/Keywords: pMHC; restriction; T cell; TCR; Immunobiology; CD4

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APA (6th Edition):

Bronnimann, H. (2016). Functional Analysis of Interactions within the TCR-CD3-pMHC-CD4 Macro-complex . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/612427

Chicago Manual of Style (16th Edition):

Bronnimann, Heather. “Functional Analysis of Interactions within the TCR-CD3-pMHC-CD4 Macro-complex .” 2016. Doctoral Dissertation, University of Arizona. Accessed October 28, 2020. http://hdl.handle.net/10150/612427.

MLA Handbook (7th Edition):

Bronnimann, Heather. “Functional Analysis of Interactions within the TCR-CD3-pMHC-CD4 Macro-complex .” 2016. Web. 28 Oct 2020.

Vancouver:

Bronnimann H. Functional Analysis of Interactions within the TCR-CD3-pMHC-CD4 Macro-complex . [Internet] [Doctoral dissertation]. University of Arizona; 2016. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/10150/612427.

Council of Science Editors:

Bronnimann H. Functional Analysis of Interactions within the TCR-CD3-pMHC-CD4 Macro-complex . [Doctoral Dissertation]. University of Arizona; 2016. Available from: http://hdl.handle.net/10150/612427

14. Carras, Sylvain. Rôles de la stimulation chronique du TCR et de la reprogrammation cellulaire dans les lymphomes T périphériques : Roles of chronic TCR stimulation and cell reprogramming in peripheral T-cell lymphomas.

Degree: Docteur es, Immunologie et Cancérologie, 2018, Lyon

Les lymphomes T périphériques (ou PTCL) sont des lymphomes malins non Hodgkiniens ayant pour cellules d’origine des lymphocytes T (LT) ou Natural Killer matures. Ces… (more)

Subjects/Keywords: Lymphomes T périphériques; TCR; Reprogrammation cellulaire; Peripheral T-cell lymphomas; TCR; Cell reprogramming; 570

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APA (6th Edition):

Carras, S. (2018). Rôles de la stimulation chronique du TCR et de la reprogrammation cellulaire dans les lymphomes T périphériques : Roles of chronic TCR stimulation and cell reprogramming in peripheral T-cell lymphomas. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSE1322

Chicago Manual of Style (16th Edition):

Carras, Sylvain. “Rôles de la stimulation chronique du TCR et de la reprogrammation cellulaire dans les lymphomes T périphériques : Roles of chronic TCR stimulation and cell reprogramming in peripheral T-cell lymphomas.” 2018. Doctoral Dissertation, Lyon. Accessed October 28, 2020. http://www.theses.fr/2018LYSE1322.

MLA Handbook (7th Edition):

Carras, Sylvain. “Rôles de la stimulation chronique du TCR et de la reprogrammation cellulaire dans les lymphomes T périphériques : Roles of chronic TCR stimulation and cell reprogramming in peripheral T-cell lymphomas.” 2018. Web. 28 Oct 2020.

Vancouver:

Carras S. Rôles de la stimulation chronique du TCR et de la reprogrammation cellulaire dans les lymphomes T périphériques : Roles of chronic TCR stimulation and cell reprogramming in peripheral T-cell lymphomas. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2018LYSE1322.

Council of Science Editors:

Carras S. Rôles de la stimulation chronique du TCR et de la reprogrammation cellulaire dans les lymphomes T périphériques : Roles of chronic TCR stimulation and cell reprogramming in peripheral T-cell lymphomas. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSE1322

15. Chouaki-Benmansour, Nassima. Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate.

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

L'activation des lymphocytes T est un événement fondamental de la réponse immunitaire adaptative. Elle est déclenchée par la transduction du signal médiée par le complexe… (more)

Subjects/Keywords: Tcr; Cd3; Pip2; Cellule T; Activation; Tcr; Cd3; Pip2; T Cell; Activation; 571

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

APA (6th Edition):

Chouaki-Benmansour, N. (2014). Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4052

Chicago Manual of Style (16th Edition):

Chouaki-Benmansour, Nassima. “Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed October 28, 2020. http://www.theses.fr/2014AIXM4052.

MLA Handbook (7th Edition):

Chouaki-Benmansour, Nassima. “Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate.” 2014. Web. 28 Oct 2020.

Vancouver:

Chouaki-Benmansour N. Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2014AIXM4052.

Council of Science Editors:

Chouaki-Benmansour N. Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4052

16. Correia de Almeida Fontaine Costa, A.I. Features that shape CD8+ T-cell responses to viruses.

Degree: 2014, Universiteit Utrecht

 CD8+ T cells, via their specific T-cell receptor (TCR), target infected cells when recognizing pathogen-derived peptides (epitopes) bound to class I major histocompatibility complex molecules… (more)

Subjects/Keywords: Geneeskunde; Human leukocyte antigen (HLA); immunodominance; epitope diversity; binding affinity; conservation; promiscuity; CD8+ T cells; T-cell receptor (TCR) repertoire/diversity; virus

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APA (6th Edition):

Correia de Almeida Fontaine Costa, A. I. (2014). Features that shape CD8+ T-cell responses to viruses. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/301929

Chicago Manual of Style (16th Edition):

Correia de Almeida Fontaine Costa, A I. “Features that shape CD8+ T-cell responses to viruses.” 2014. Doctoral Dissertation, Universiteit Utrecht. Accessed October 28, 2020. http://dspace.library.uu.nl:8080/handle/1874/301929.

MLA Handbook (7th Edition):

Correia de Almeida Fontaine Costa, A I. “Features that shape CD8+ T-cell responses to viruses.” 2014. Web. 28 Oct 2020.

Vancouver:

Correia de Almeida Fontaine Costa AI. Features that shape CD8+ T-cell responses to viruses. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2014. [cited 2020 Oct 28]. Available from: http://dspace.library.uu.nl:8080/handle/1874/301929.

Council of Science Editors:

Correia de Almeida Fontaine Costa AI. Features that shape CD8+ T-cell responses to viruses. [Doctoral Dissertation]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/301929


University of Melbourne

17. Johnson, Darryl Neil. Investigation of antigen-specific CD4+ T cell immune repertoire and the relationship between TCR affinity and effector function.

Degree: 2014, University of Melbourne

T cells recognise peptide antigens displayed in complex with MHC molecules via a T cell receptor (TCR). The antigen-specific responses of both CD8+ and CD4+… (more)

Subjects/Keywords: Immunology; CD4+ T cells; TCR affinity; TCR repertoire diversity; T cell antigen recognition; T cell function

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APA (6th Edition):

Johnson, D. N. (2014). Investigation of antigen-specific CD4+ T cell immune repertoire and the relationship between TCR affinity and effector function. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/42082

Chicago Manual of Style (16th Edition):

Johnson, Darryl Neil. “Investigation of antigen-specific CD4+ T cell immune repertoire and the relationship between TCR affinity and effector function.” 2014. Doctoral Dissertation, University of Melbourne. Accessed October 28, 2020. http://hdl.handle.net/11343/42082.

MLA Handbook (7th Edition):

Johnson, Darryl Neil. “Investigation of antigen-specific CD4+ T cell immune repertoire and the relationship between TCR affinity and effector function.” 2014. Web. 28 Oct 2020.

Vancouver:

Johnson DN. Investigation of antigen-specific CD4+ T cell immune repertoire and the relationship between TCR affinity and effector function. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/11343/42082.

Council of Science Editors:

Johnson DN. Investigation of antigen-specific CD4+ T cell immune repertoire and the relationship between TCR affinity and effector function. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/42082

18. Sawicka, Anna. Aspects biophysiques de l'activation des cellules T : Biophysical aspects of T cell activation.

Degree: Docteur es, Interdisciplinaire, 2018, Sorbonne Paris Cité

 Les cellules T jouent différents rôles dans la réponse immunitaire adaptative : elles stimulent les cellules B à produire les anticorps ; elles sécrètent les… (more)

Subjects/Keywords: Lymphocytes T; Mesure de forces en biologie; Mécanotransduction; TCR signalling; Transduction de signal de récepteurs; Biologie cellulaire; Biophysique; Synapse immunologique; T-Cells; T lymphocytes; Force measurement in biology; Mechanotransduction; T-Cell receptor signalling; T cell biology; Adaptive immunity; Biophysics; Immune synapse; 616.079

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APA (6th Edition):

Sawicka, A. (2018). Aspects biophysiques de l'activation des cellules T : Biophysical aspects of T cell activation. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCB079

Chicago Manual of Style (16th Edition):

Sawicka, Anna. “Aspects biophysiques de l'activation des cellules T : Biophysical aspects of T cell activation.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 28, 2020. http://www.theses.fr/2018USPCB079.

MLA Handbook (7th Edition):

Sawicka, Anna. “Aspects biophysiques de l'activation des cellules T : Biophysical aspects of T cell activation.” 2018. Web. 28 Oct 2020.

Vancouver:

Sawicka A. Aspects biophysiques de l'activation des cellules T : Biophysical aspects of T cell activation. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2018USPCB079.

Council of Science Editors:

Sawicka A. Aspects biophysiques de l'activation des cellules T : Biophysical aspects of T cell activation. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCB079


University of Illinois – Urbana-Champaign

19. Soto, Carolina. Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma.

Degree: PhD, 0323, 2013, University of Illinois – Urbana-Champaign

 Over the past few decades, our knowledge of tumor immunology and the role antitumor immune responses play in tumor recognition and eradication has greatly increased… (more)

Subjects/Keywords: Cancer Immunotherapy; Tumor Targeting; T cell receptors (TCR); T cell; Melanoma; Adoptive Cell Therapy; Glioma

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APA (6th Edition):

Soto, C. (2013). Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42476

Chicago Manual of Style (16th Edition):

Soto, Carolina. “Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 28, 2020. http://hdl.handle.net/2142/42476.

MLA Handbook (7th Edition):

Soto, Carolina. “Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma.” 2013. Web. 28 Oct 2020.

Vancouver:

Soto C. Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/2142/42476.

Council of Science Editors:

Soto C. Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42476

20. Hauck, Fabian. Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK.

Degree: Docteur es, Immunologie, 2013, Université Paris Descartes – Paris V

Les lymphocytes T sont caractérisés par l’expression d’un récepteur à l’antigène des cellules T (TCR), soit le preTCR, soit le γδ TCR et le αβ… (more)

Subjects/Keywords: PID; SCID; CID; TCR; T cell; Lck; Zap-70; Itk; PID; SCID; CID; TCR; T cell; Lck; Zap-70; Itk; 616.079

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APA (6th Edition):

Hauck, F. (2013). Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05T031

Chicago Manual of Style (16th Edition):

Hauck, Fabian. “Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 28, 2020. http://www.theses.fr/2013PA05T031.

MLA Handbook (7th Edition):

Hauck, Fabian. “Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK.” 2013. Web. 28 Oct 2020.

Vancouver:

Hauck F. Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2013PA05T031.

Council of Science Editors:

Hauck F. Primary T cell immunodeficiencies associated with disturbed proximal T cell receptor signalling caused by human autosomal recessive LCK, ZAP-70 and ITK-mutations : Immunodéficiences primaires des cellules T associées avec une signalisation proximale du récepteur à l’antigène des cellules T perturbée et causées par des mutations autosomiques récessives humaines de LCK, ZAP-70 et ITK. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05T031


University of Minnesota

21. 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 (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 28, 2020. 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. 28 Oct 2020.

Vancouver:

Kotov D. The role of T cell receptor affinity in CD4+ T cell differentiation. [Internet] [Doctoral dissertation]. University of Minnesota; 2019. [cited 2020 Oct 28]. 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

22. 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 (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 28, 2020. 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. 28 Oct 2020.

Vancouver:

Helou Y. Dissection of T cell receptor-mediated signaling pathways using quantitative phosphoproteomics. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2020 Oct 28]. 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/


University of Illinois – Urbana-Champaign

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

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 28, 2020. 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. 28 Oct 2020.

Vancouver:

Harris DT. Engineering and characterizing human T cell receptors for cancer immunotherapies. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2020 Oct 28]. 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

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 (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 October 28, 2020. 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. 28 Oct 2020.

Vancouver:

McQuilten HA. Transcriptional and epigenetic signatures of memory CD8+ T cell differentiation. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2020 Oct 28]. 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

25. Xia, Fan. Décryptage des mécanismes de signalisation précoce de la costimulation dans l' activation des lymphocytes T naifs : Deciphering the mechanisms of TCR and CD28 early signaling pathway cooperation required for naïve T cell activation.

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

L'objectif de notre travail est de comprendre la contribution relative des voies de signalisation précoces du TCR et de CD28 dans l'activation des lymphocytes T(more)

Subjects/Keywords: Tcr; Cd28; Costimulation; La mobilisation des ions calcique; Lymphocytes T naïfs; Tcr; Cd28; Costimulation; Calcium mobilization; Naïve T cell; 571

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

APA (6th Edition):

Xia, F. (2014). Décryptage des mécanismes de signalisation précoce de la costimulation dans l' activation des lymphocytes T naifs : Deciphering the mechanisms of TCR and CD28 early signaling pathway cooperation required for naïve T cell activation. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4064

Chicago Manual of Style (16th Edition):

Xia, Fan. “Décryptage des mécanismes de signalisation précoce de la costimulation dans l' activation des lymphocytes T naifs : Deciphering the mechanisms of TCR and CD28 early signaling pathway cooperation required for naïve T cell activation.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed October 28, 2020. http://www.theses.fr/2014AIXM4064.

MLA Handbook (7th Edition):

Xia, Fan. “Décryptage des mécanismes de signalisation précoce de la costimulation dans l' activation des lymphocytes T naifs : Deciphering the mechanisms of TCR and CD28 early signaling pathway cooperation required for naïve T cell activation.” 2014. Web. 28 Oct 2020.

Vancouver:

Xia F. Décryptage des mécanismes de signalisation précoce de la costimulation dans l' activation des lymphocytes T naifs : Deciphering the mechanisms of TCR and CD28 early signaling pathway cooperation required for naïve T cell activation. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2020 Oct 28]. Available from: http://www.theses.fr/2014AIXM4064.

Council of Science Editors:

Xia F. Décryptage des mécanismes de signalisation précoce de la costimulation dans l' activation des lymphocytes T naifs : Deciphering the mechanisms of TCR and CD28 early signaling pathway cooperation required for naïve T cell activation. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4064


University of Melbourne

26. Reantragoon, Rangsima. The molecular basis of MR1 and MAIT TCR interaction.

Degree: 2014, University of Melbourne

 MAIT (Mucosal-associated invariant T) cells comprise a subpopulation of T cells that has been conserved in mammalian evolution. One of the unique characteristics of MAIT… (more)

Subjects/Keywords: MAIT cells; MAIT TCR; MR1; T-cell recognition; molecular mechanism

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APA (6th Edition):

Reantragoon, R. (2014). The molecular basis of MR1 and MAIT TCR interaction. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/42168

Chicago Manual of Style (16th Edition):

Reantragoon, Rangsima. “The molecular basis of MR1 and MAIT TCR interaction.” 2014. Doctoral Dissertation, University of Melbourne. Accessed October 28, 2020. http://hdl.handle.net/11343/42168.

MLA Handbook (7th Edition):

Reantragoon, Rangsima. “The molecular basis of MR1 and MAIT TCR interaction.” 2014. Web. 28 Oct 2020.

Vancouver:

Reantragoon R. The molecular basis of MR1 and MAIT TCR interaction. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2020 Oct 28]. Available from: http://hdl.handle.net/11343/42168.

Council of Science Editors:

Reantragoon R. The molecular basis of MR1 and MAIT TCR interaction. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/42168


Texas Medical Center

27. ALPERT, amir. THE CHARACTERIZATION OF T-CELL MANUFACTURING FOR ADOPTIVE T-CELL THERAPIES.

Degree: PhD, 2019, Texas Medical Center

  Adoptive T-cell therapy using genetically modified T cells has emerged as a potential therapeutic option for several malignancies. Central to the production of the… (more)

Subjects/Keywords: T cell; CD28; TCR; Adoptive; Cell Therapy; ACT; Biotechnology; Immunology and Infectious Disease

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APA (6th Edition):

ALPERT, a. (2019). THE CHARACTERIZATION OF T-CELL MANUFACTURING FOR ADOPTIVE T-CELL THERAPIES. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/946

Chicago Manual of Style (16th Edition):

ALPERT, amir. “THE CHARACTERIZATION OF T-CELL MANUFACTURING FOR ADOPTIVE T-CELL THERAPIES.” 2019. Doctoral Dissertation, Texas Medical Center. Accessed October 28, 2020. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/946.

MLA Handbook (7th Edition):

ALPERT, amir. “THE CHARACTERIZATION OF T-CELL MANUFACTURING FOR ADOPTIVE T-CELL THERAPIES.” 2019. Web. 28 Oct 2020.

Vancouver:

ALPERT a. THE CHARACTERIZATION OF T-CELL MANUFACTURING FOR ADOPTIVE T-CELL THERAPIES. [Internet] [Doctoral dissertation]. Texas Medical Center; 2019. [cited 2020 Oct 28]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/946.

Council of Science Editors:

ALPERT a. THE CHARACTERIZATION OF T-CELL MANUFACTURING FOR ADOPTIVE T-CELL THERAPIES. [Doctoral Dissertation]. Texas Medical Center; 2019. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/946

28. Correia de Almeida Fontaine Costa, A.I. Features that shape CD8+ T-cell responses to viruses.

Degree: 2014, University Utrecht

 CD8+ T cells, via their specific T-cell receptor (TCR), target infected cells when recognizing pathogen-derived peptides (epitopes) bound to class I major histocompatibility complex molecules… (more)

Subjects/Keywords: Human leukocyte antigen (HLA); immunodominance; epitope diversity; binding affinity; conservation; promiscuity; CD8+ T cells; T-cell receptor (TCR) repertoire/diversity; virus

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APA (6th Edition):

Correia de Almeida Fontaine Costa, A. I. (2014). Features that shape CD8+ T-cell responses to viruses. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; http://dspace.library.uu.nl/handle/1874/301929

Chicago Manual of Style (16th Edition):

Correia de Almeida Fontaine Costa, A I. “Features that shape CD8+ T-cell responses to viruses.” 2014. Doctoral Dissertation, University Utrecht. Accessed October 28, 2020. http://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; http://dspace.library.uu.nl/handle/1874/301929.

MLA Handbook (7th Edition):

Correia de Almeida Fontaine Costa, A I. “Features that shape CD8+ T-cell responses to viruses.” 2014. Web. 28 Oct 2020.

Vancouver:

Correia de Almeida Fontaine Costa AI. Features that shape CD8+ T-cell responses to viruses. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2020 Oct 28]. Available from: http://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; http://dspace.library.uu.nl/handle/1874/301929.

Council of Science Editors:

Correia de Almeida Fontaine Costa AI. Features that shape CD8+ T-cell responses to viruses. [Doctoral Dissertation]. University Utrecht; 2014. Available from: http://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; http://dspace.library.uu.nl/handle/1874/301929

29. Correia de Almeida Fontaine Costa, A.I. Features that shape CD8+ T-cell responses to viruses.

Degree: 2014, University Utrecht

 CD8+ T cells, via their specific T-cell receptor (TCR), target infected cells when recognizing pathogen-derived peptides (epitopes) bound to class I major histocompatibility complex molecules… (more)

Subjects/Keywords: Human leukocyte antigen (HLA); immunodominance; epitope diversity; binding affinity; conservation; promiscuity; CD8+ T cells; T-cell receptor (TCR) repertoire/diversity; virus

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

APA (6th Edition):

Correia de Almeida Fontaine Costa, A. I. (2014). Features that shape CD8+ T-cell responses to viruses. (Doctoral Dissertation). University Utrecht. Retrieved from https://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; https://dspace.library.uu.nl/handle/1874/301929

Chicago Manual of Style (16th Edition):

Correia de Almeida Fontaine Costa, A I. “Features that shape CD8+ T-cell responses to viruses.” 2014. Doctoral Dissertation, University Utrecht. Accessed October 28, 2020. https://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; https://dspace.library.uu.nl/handle/1874/301929.

MLA Handbook (7th Edition):

Correia de Almeida Fontaine Costa, A I. “Features that shape CD8+ T-cell responses to viruses.” 2014. Web. 28 Oct 2020.

Vancouver:

Correia de Almeida Fontaine Costa AI. Features that shape CD8+ T-cell responses to viruses. [Internet] [Doctoral dissertation]. University Utrecht; 2014. [cited 2020 Oct 28]. Available from: https://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; https://dspace.library.uu.nl/handle/1874/301929.

Council of Science Editors:

Correia de Almeida Fontaine Costa AI. Features that shape CD8+ T-cell responses to viruses. [Doctoral Dissertation]. University Utrecht; 2014. Available from: https://dspace.library.uu.nl/handle/1874/301929 ; URN:NBN:NL:UI:10-1874-301929 ; urn:isbn:867-90-393-6211-2 ; URN:NBN:NL:UI:10-1874-301929 ; https://dspace.library.uu.nl/handle/1874/301929

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

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

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 28, 2020. https://www.repository.cam.ac.uk/handle/1810/273245.

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. 28 Oct 2020.

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 2020 Oct 28]. Available from: https://www.repository.cam.ac.uk/handle/1810/273245.

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

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