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You searched for subject:(TCR). Showing records 1 – 30 of 187 total matches.

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1. JI, QINQIN. QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS TO UNRAVELT CELL SIGNALING PATHWAYS.

Degree: PhD, Chemistry, 2015, Brown University

 The activation of T-lymphocytes through antigen-mediated T-cell receptor (TCR) clustering is vital in the regulation of the adaptive-immune response and must be properly regulated to… (more)

Subjects/Keywords: TCR signaling

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APA (6th Edition):

JI, Q. (2015). QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS TO UNRAVELT CELL SIGNALING PATHWAYS. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419406/

Chicago Manual of Style (16th Edition):

JI, QINQIN. “QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS TO UNRAVELT CELL SIGNALING PATHWAYS.” 2015. Doctoral Dissertation, Brown University. Accessed October 24, 2020. https://repository.library.brown.edu/studio/item/bdr:419406/.

MLA Handbook (7th Edition):

JI, QINQIN. “QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS TO UNRAVELT CELL SIGNALING PATHWAYS.” 2015. Web. 24 Oct 2020.

Vancouver:

JI Q. QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS TO UNRAVELT CELL SIGNALING PATHWAYS. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2020 Oct 24]. Available from: https://repository.library.brown.edu/studio/item/bdr:419406/.

Council of Science Editors:

JI Q. QUANTITATIVE PHOSPHOPROTEOMIC ANALYSIS TO UNRAVELT CELL SIGNALING PATHWAYS. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419406/


Universitat de Valencia

2. García Ballesteros, Carlos. Apoptosis linfocitaria según receptor TCR- αβ y TCR- γδ en sujetos sanos .

Degree: 2015, Universitat de Valencia

 Durante décadas, los LTγδ han generado cierto desconcierto debido a su preponderancia en los tejidos periféricos sobre la sangre periférica y a la presencia de… (more)

Subjects/Keywords: Apoptosis Linfocito TCR- αβ Linfocito TCR- γδ

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APA (6th Edition):

García Ballesteros, C. (2015). Apoptosis linfocitaria según receptor TCR- αβ y TCR- γδ en sujetos sanos . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/50557

Chicago Manual of Style (16th Edition):

García Ballesteros, Carlos. “Apoptosis linfocitaria según receptor TCR- αβ y TCR- γδ en sujetos sanos .” 2015. Doctoral Dissertation, Universitat de Valencia. Accessed October 24, 2020. http://hdl.handle.net/10550/50557.

MLA Handbook (7th Edition):

García Ballesteros, Carlos. “Apoptosis linfocitaria según receptor TCR- αβ y TCR- γδ en sujetos sanos .” 2015. Web. 24 Oct 2020.

Vancouver:

García Ballesteros C. Apoptosis linfocitaria según receptor TCR- αβ y TCR- γδ en sujetos sanos . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2015. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10550/50557.

Council of Science Editors:

García Ballesteros C. Apoptosis linfocitaria según receptor TCR- αβ y TCR- γδ en sujetos sanos . [Doctoral Dissertation]. Universitat de Valencia; 2015. Available from: http://hdl.handle.net/10550/50557


University of Debrecen

3. Józsa, Márta. Társadalmi célú reklámok kreativitássablonjainak hatásvizsgálata és a hatásosság prediktor változói .

Degree: DE – TEK – Bölcsészettudományi Kar, 2013, University of Debrecen

Jelen kutatás a TCR kreativitássablonok hatásmechanizmusa közötti különbségeket tárta fel, részletesen kitérve a prediktor változókra is. A vizsgálat eredményei jól használhatók gyakorlati célokra is, de elsődlegesen elméleti megközelítésűek. Advisors/Committee Members: Balázs, Katalin (advisor).

Subjects/Keywords: reklámpszichológia; TCR; kreativitássablon

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APA (6th Edition):

Józsa, M. (2013). Társadalmi célú reklámok kreativitássablonjainak hatásvizsgálata és a hatásosság prediktor változói . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/167829

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):

Józsa, Márta. “Társadalmi célú reklámok kreativitássablonjainak hatásvizsgálata és a hatásosság prediktor változói .” 2013. Thesis, University of Debrecen. Accessed October 24, 2020. http://hdl.handle.net/2437/167829.

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

MLA Handbook (7th Edition):

Józsa, Márta. “Társadalmi célú reklámok kreativitássablonjainak hatásvizsgálata és a hatásosság prediktor változói .” 2013. Web. 24 Oct 2020.

Vancouver:

Józsa M. Társadalmi célú reklámok kreativitássablonjainak hatásvizsgálata és a hatásosság prediktor változói . [Internet] [Thesis]. University of Debrecen; 2013. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/2437/167829.

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

Council of Science Editors:

Józsa M. Társadalmi célú reklámok kreativitássablonjainak hatásvizsgálata és a hatásosság prediktor változói . [Thesis]. University of Debrecen; 2013. Available from: http://hdl.handle.net/2437/167829

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


University of Limerick

4. Downey, Fergus. A study into the electrical trim of silicon chromium thin film resistors.

Degree: 2014, University of Limerick

peer-reviewed

Silicon Chromium (SiCr) Thin Film Resistors (TFRs) have been developed and integrated into CMOS ICs for over twenty years. Current state of the art… (more)

Subjects/Keywords: silicon chromium; TCR

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APA (6th Edition):

Downey, F. (2014). A study into the electrical trim of silicon chromium thin film resistors. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/8100

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):

Downey, Fergus. “A study into the electrical trim of silicon chromium thin film resistors.” 2014. Thesis, University of Limerick. Accessed October 24, 2020. http://hdl.handle.net/10344/8100.

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

MLA Handbook (7th Edition):

Downey, Fergus. “A study into the electrical trim of silicon chromium thin film resistors.” 2014. Web. 24 Oct 2020.

Vancouver:

Downey F. A study into the electrical trim of silicon chromium thin film resistors. [Internet] [Thesis]. University of Limerick; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/10344/8100.

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

Council of Science Editors:

Downey F. A study into the electrical trim of silicon chromium thin film resistors. [Thesis]. University of Limerick; 2014. Available from: http://hdl.handle.net/10344/8100

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


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 24, 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. 24 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 24]. 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

6. Mukhopadhyay, Madhura. DNA vaccination amplifiers HLA-DR cross-restricted public TCR clonotypes shared with HIV controllers : La vaccination ADN amplifie des TCR publics à large restriction HLA-DR partages avec les contrôleurs du VIH.

Degree: Docteur es, Sciences de la vie et de la santé. Immunologie, 2017, Sorbonne Paris Cité

 Les contrôleurs du VIH (HICs) sont de rares patients qui contrôlent spontanément la réplication du VIH en absence de thérapie antirétrovirale. Ces patients sont caractérisés… (more)

Subjects/Keywords: Contrôleurs du VIH; TCR clonotype publique; HIV controllers; Public TCR clonotypes

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APA (6th Edition):

Mukhopadhyay, M. (2017). DNA vaccination amplifiers HLA-DR cross-restricted public TCR clonotypes shared with HIV controllers : La vaccination ADN amplifie des TCR publics à large restriction HLA-DR partages avec les contrôleurs du VIH. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC210

Chicago Manual of Style (16th Edition):

Mukhopadhyay, Madhura. “DNA vaccination amplifiers HLA-DR cross-restricted public TCR clonotypes shared with HIV controllers : La vaccination ADN amplifie des TCR publics à large restriction HLA-DR partages avec les contrôleurs du VIH.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 24, 2020. http://www.theses.fr/2017USPCC210.

MLA Handbook (7th Edition):

Mukhopadhyay, Madhura. “DNA vaccination amplifiers HLA-DR cross-restricted public TCR clonotypes shared with HIV controllers : La vaccination ADN amplifie des TCR publics à large restriction HLA-DR partages avec les contrôleurs du VIH.” 2017. Web. 24 Oct 2020.

Vancouver:

Mukhopadhyay M. DNA vaccination amplifiers HLA-DR cross-restricted public TCR clonotypes shared with HIV controllers : La vaccination ADN amplifie des TCR publics à large restriction HLA-DR partages avec les contrôleurs du VIH. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2017USPCC210.

Council of Science Editors:

Mukhopadhyay M. DNA vaccination amplifiers HLA-DR cross-restricted public TCR clonotypes shared with HIV controllers : La vaccination ADN amplifie des TCR publics à large restriction HLA-DR partages avec les contrôleurs du VIH. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC210

7. Hazgui, Hana. Modélisation de la dynamique des réseaux biologiques : applications en génétique et immunologie : Modeling the dynamics ofbiological networks : applications in genetics and immunology.

Degree: Docteur es, Modèles, méthodes et algorithmes en biologie, santé et environnement, 2015, Université Grenoble Alpes (ComUE); Université de Sfax. Faculté des sciences

Dans cette thèse, nous nous intéressons à la modélisation statistique de données biologiques, et plus particulièrement à l'étude de l'information génétique et protéique.Dans un premier… (more)

Subjects/Keywords: Gène; Recombinaison; Modélisation; Tcr; Réseau; Genome; Modelling; Recombinations; Tcr; Network; 570

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APA (6th Edition):

Hazgui, H. (2015). Modélisation de la dynamique des réseaux biologiques : applications en génétique et immunologie : Modeling the dynamics ofbiological networks : applications in genetics and immunology. (Doctoral Dissertation). Université Grenoble Alpes (ComUE); Université de Sfax. Faculté des sciences. Retrieved from http://www.theses.fr/2015GREAS040

Chicago Manual of Style (16th Edition):

Hazgui, Hana. “Modélisation de la dynamique des réseaux biologiques : applications en génétique et immunologie : Modeling the dynamics ofbiological networks : applications in genetics and immunology.” 2015. Doctoral Dissertation, Université Grenoble Alpes (ComUE); Université de Sfax. Faculté des sciences. Accessed October 24, 2020. http://www.theses.fr/2015GREAS040.

MLA Handbook (7th Edition):

Hazgui, Hana. “Modélisation de la dynamique des réseaux biologiques : applications en génétique et immunologie : Modeling the dynamics ofbiological networks : applications in genetics and immunology.” 2015. Web. 24 Oct 2020.

Vancouver:

Hazgui H. Modélisation de la dynamique des réseaux biologiques : applications en génétique et immunologie : Modeling the dynamics ofbiological networks : applications in genetics and immunology. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); Université de Sfax. Faculté des sciences; 2015. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2015GREAS040.

Council of Science Editors:

Hazgui H. Modélisation de la dynamique des réseaux biologiques : applications en génétique et immunologie : Modeling the dynamics ofbiological networks : applications in genetics and immunology. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); Université de Sfax. Faculté des sciences; 2015. Available from: http://www.theses.fr/2015GREAS040


University of Notre Dame

8. Kurt Henry Piepenbrink. Understanding the Energetic Basis for T-cell Receptor Recognition</h1>.

Degree: Chemistry and Biochemistry, 2011, University of Notre Dame

  T-cell receptors (TCRs) are clonotypic, heterodimeric receptors on the surface of T-cells which possess Complementarity Determining Region (CDR) loops similar to immunoglobulins. Their function… (more)

Subjects/Keywords: Double Mutant Cycle; TCR; SPR; MHC

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APA (6th Edition):

Piepenbrink, K. H. (2011). Understanding the Energetic Basis for T-cell Receptor Recognition</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/pr76f190d5t

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):

Piepenbrink, Kurt Henry. “Understanding the Energetic Basis for T-cell Receptor Recognition</h1>.” 2011. Thesis, University of Notre Dame. Accessed October 24, 2020. https://curate.nd.edu/show/pr76f190d5t.

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

MLA Handbook (7th Edition):

Piepenbrink, Kurt Henry. “Understanding the Energetic Basis for T-cell Receptor Recognition</h1>.” 2011. Web. 24 Oct 2020.

Vancouver:

Piepenbrink KH. Understanding the Energetic Basis for T-cell Receptor Recognition</h1>. [Internet] [Thesis]. University of Notre Dame; 2011. [cited 2020 Oct 24]. Available from: https://curate.nd.edu/show/pr76f190d5t.

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

Council of Science Editors:

Piepenbrink KH. Understanding the Energetic Basis for T-cell Receptor Recognition</h1>. [Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/pr76f190d5t

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


University of Minnesota

9. Holzapfel, Keli Lee. The role of antigen receptor signaling in activation and development of invariant Natural Killer T cells.

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

 CD1d-reactive invariant Natural Killer T cells (iNKT) are a T cell subset that have characteristics of both innate immune cells and adaptive immune cells. As… (more)

Subjects/Keywords: Infection; iNKT cells; Nur77gfp; OP9-DL1; TCR

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APA (6th Edition):

Holzapfel, K. L. (2014). The role of antigen receptor signaling in activation and development of invariant Natural Killer T cells. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/163756

Chicago Manual of Style (16th Edition):

Holzapfel, Keli Lee. “The role of antigen receptor signaling in activation and development of invariant Natural Killer T cells.” 2014. Doctoral Dissertation, University of Minnesota. Accessed October 24, 2020. http://hdl.handle.net/11299/163756.

MLA Handbook (7th Edition):

Holzapfel, Keli Lee. “The role of antigen receptor signaling in activation and development of invariant Natural Killer T cells.” 2014. Web. 24 Oct 2020.

Vancouver:

Holzapfel KL. The role of antigen receptor signaling in activation and development of invariant Natural Killer T cells. [Internet] [Doctoral dissertation]. University of Minnesota; 2014. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/11299/163756.

Council of Science Editors:

Holzapfel KL. The role of antigen receptor signaling in activation and development of invariant Natural Killer T cells. [Doctoral Dissertation]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/163756


University of Melbourne

10. Sant, Sneha Ashok. Tracking human CD8+ and γδ T cell receptor repertoire dynamics to understand the impact on immune responses towards influenza viruses.

Degree: 2018, University of Melbourne

 Seasonal IAV epidemics cause severe morbidity and mortality, resulting in up to 250,000 -600,000 deaths worldwide annually, especially in the young, elderly, immunocompromised, pregnant and… (more)

Subjects/Keywords: influenza; human; TCR repertoire; immunodominance; T cells

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APA (6th Edition):

Sant, S. A. (2018). Tracking human CD8+ and γδ T cell receptor repertoire dynamics to understand the impact on immune responses towards influenza viruses. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/217238

Chicago Manual of Style (16th Edition):

Sant, Sneha Ashok. “Tracking human CD8+ and γδ T cell receptor repertoire dynamics to understand the impact on immune responses towards influenza viruses.” 2018. Doctoral Dissertation, University of Melbourne. Accessed October 24, 2020. http://hdl.handle.net/11343/217238.

MLA Handbook (7th Edition):

Sant, Sneha Ashok. “Tracking human CD8+ and γδ T cell receptor repertoire dynamics to understand the impact on immune responses towards influenza viruses.” 2018. Web. 24 Oct 2020.

Vancouver:

Sant SA. Tracking human CD8+ and γδ T cell receptor repertoire dynamics to understand the impact on immune responses towards influenza viruses. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/11343/217238.

Council of Science Editors:

Sant SA. Tracking human CD8+ and γδ T cell receptor repertoire dynamics to understand the impact on immune responses towards influenza viruses. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/217238


University of Arizona

11. 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 24, 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. 24 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 24]. 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


University of Kansas

12. Zhang, Elizabeth Yan. THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY.

Degree: PhD, Microbiology, Molecular Genetics & Immunology, 2011, University of Kansas

 CD8+ T cells are the branch of the adaptive immune system responsible for recognizing and killing tumor cells or cells infected with intracellular pathogens, such… (more)

Subjects/Keywords: Immunology; Cd8+ t cells; Gads; Tcr signaling

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APA (6th Edition):

Zhang, E. Y. (2011). THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9710

Chicago Manual of Style (16th Edition):

Zhang, Elizabeth Yan. “THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY.” 2011. Doctoral Dissertation, University of Kansas. Accessed October 24, 2020. http://hdl.handle.net/1808/9710.

MLA Handbook (7th Edition):

Zhang, Elizabeth Yan. “THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY.” 2011. Web. 24 Oct 2020.

Vancouver:

Zhang EY. THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1808/9710.

Council of Science Editors:

Zhang EY. THE ROLE OF ADAPTOR PROTEIN GADS IN CD8+ T CELL-MEDIATED IMMUNITY. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9710


University of Bath

13. Crean, Rory. Utilising molecular dynamics simulations to understand and engineer T-cell receptors.

Degree: PhD, 2020, University of Bath

 Approximately 90% of all therapeutic targets in the human proteome operate solely inside the cell, making them unavailable for recognition by antibodies which instead bind… (more)

Subjects/Keywords: TCR; pHLA; Molecular dynamics; affinity; free energy

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APA (6th Edition):

Crean, R. (2020). Utilising molecular dynamics simulations to understand and engineer T-cell receptors. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/utilising-molecular-dynamics-simulations-to-understand-and-engineer-tcell-receptors(d8c626a7-9b6e-4e6f-8f2c-716b48d14b49).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805664

Chicago Manual of Style (16th Edition):

Crean, Rory. “Utilising molecular dynamics simulations to understand and engineer T-cell receptors.” 2020. Doctoral Dissertation, University of Bath. Accessed October 24, 2020. https://researchportal.bath.ac.uk/en/studentthesis/utilising-molecular-dynamics-simulations-to-understand-and-engineer-tcell-receptors(d8c626a7-9b6e-4e6f-8f2c-716b48d14b49).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805664.

MLA Handbook (7th Edition):

Crean, Rory. “Utilising molecular dynamics simulations to understand and engineer T-cell receptors.” 2020. Web. 24 Oct 2020.

Vancouver:

Crean R. Utilising molecular dynamics simulations to understand and engineer T-cell receptors. [Internet] [Doctoral dissertation]. University of Bath; 2020. [cited 2020 Oct 24]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/utilising-molecular-dynamics-simulations-to-understand-and-engineer-tcell-receptors(d8c626a7-9b6e-4e6f-8f2c-716b48d14b49).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805664.

Council of Science Editors:

Crean R. Utilising molecular dynamics simulations to understand and engineer T-cell receptors. [Doctoral Dissertation]. University of Bath; 2020. Available from: https://researchportal.bath.ac.uk/en/studentthesis/utilising-molecular-dynamics-simulations-to-understand-and-engineer-tcell-receptors(d8c626a7-9b6e-4e6f-8f2c-716b48d14b49).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805664

14. Nassereddine, Aya. Surface patterning strategies to dissect T-Cell adhesion and actin organisation : Stratégies de surfaces pour décortiquer l’aire d’adhésion et l’organisation d’actine des cellules T.

Degree: Docteur es, Biophysique, 2019, Aix Marseille Université

Pour une réponse immunitaire efficace, une interaction optimale entre les cellules T et les cellules présentatrices d'antigène (APC) est nécessaire. Elle se présente sous la… (more)

Subjects/Keywords: Motifs; Cellule T; Actine; Tcr; Tirf; Storm; Pattern; T cells; Actin; Tcr; Tirf; Microscopy; 530

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APA (6th Edition):

Nassereddine, A. (2019). Surface patterning strategies to dissect T-Cell adhesion and actin organisation : Stratégies de surfaces pour décortiquer l’aire d’adhésion et l’organisation d’actine des cellules T. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2019AIXM0458

Chicago Manual of Style (16th Edition):

Nassereddine, Aya. “Surface patterning strategies to dissect T-Cell adhesion and actin organisation : Stratégies de surfaces pour décortiquer l’aire d’adhésion et l’organisation d’actine des cellules T.” 2019. Doctoral Dissertation, Aix Marseille Université. Accessed October 24, 2020. http://www.theses.fr/2019AIXM0458.

MLA Handbook (7th Edition):

Nassereddine, Aya. “Surface patterning strategies to dissect T-Cell adhesion and actin organisation : Stratégies de surfaces pour décortiquer l’aire d’adhésion et l’organisation d’actine des cellules T.” 2019. Web. 24 Oct 2020.

Vancouver:

Nassereddine A. Surface patterning strategies to dissect T-Cell adhesion and actin organisation : Stratégies de surfaces pour décortiquer l’aire d’adhésion et l’organisation d’actine des cellules T. [Internet] [Doctoral dissertation]. Aix Marseille Université 2019. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2019AIXM0458.

Council of Science Editors:

Nassereddine A. Surface patterning strategies to dissect T-Cell adhesion and actin organisation : Stratégies de surfaces pour décortiquer l’aire d’adhésion et l’organisation d’actine des cellules T. [Doctoral Dissertation]. Aix Marseille Université 2019. Available from: http://www.theses.fr/2019AIXM0458

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 (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 24, 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. 24 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 24]. 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. 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 24, 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. 24 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 24]. 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


Université Paris-Sud – Paris XI

17. Poalas, Konstantinos. Ubiquitinylation and deubiquitinylation in the regulation of the transcription factor NF-kB activation : Ubiquitinylation et déubiquitinylation dans la régulation de l’activation du facteur de transcription NF-kB.

Degree: Docteur es, Biochimie, Biologie Cellulaire et Moléculaire, 2013, Université Paris-Sud – Paris XI

L’activation de la signalisation NF-κB par de nombreux immunorécepteurs met en jeu un large signalosome. Afin de propager cette signalisation en réponse à différents stimuli,… (more)

Subjects/Keywords: NF-kB; TCR; Ubiquitinylation; Déubiquitinylation; USP34; MTDH; NF-kB; TCR; Ubiquitinylation; Deubiquitinylation; USP34; MTDH

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APA (6th Edition):

Poalas, K. (2013). Ubiquitinylation and deubiquitinylation in the regulation of the transcription factor NF-kB activation : Ubiquitinylation et déubiquitinylation dans la régulation de l’activation du facteur de transcription NF-kB. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2013PA11T058

Chicago Manual of Style (16th Edition):

Poalas, Konstantinos. “Ubiquitinylation and deubiquitinylation in the regulation of the transcription factor NF-kB activation : Ubiquitinylation et déubiquitinylation dans la régulation de l’activation du facteur de transcription NF-kB.” 2013. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed October 24, 2020. http://www.theses.fr/2013PA11T058.

MLA Handbook (7th Edition):

Poalas, Konstantinos. “Ubiquitinylation and deubiquitinylation in the regulation of the transcription factor NF-kB activation : Ubiquitinylation et déubiquitinylation dans la régulation de l’activation du facteur de transcription NF-kB.” 2013. Web. 24 Oct 2020.

Vancouver:

Poalas K. Ubiquitinylation and deubiquitinylation in the regulation of the transcription factor NF-kB activation : Ubiquitinylation et déubiquitinylation dans la régulation de l’activation du facteur de transcription NF-kB. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2013. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2013PA11T058.

Council of Science Editors:

Poalas K. Ubiquitinylation and deubiquitinylation in the regulation of the transcription factor NF-kB activation : Ubiquitinylation et déubiquitinylation dans la régulation de l’activation du facteur de transcription NF-kB. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2013. Available from: http://www.theses.fr/2013PA11T058


University of Cambridge

18. Luff, Daisy Helen. Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling.

Degree: PhD, 2019, University of Cambridge

 Phosphoinositide 3-kinases (PI3Ks) are activated in immune cells downstream of the antigen recognition receptors, the signals from which are crucial for the development, differentiation and… (more)

Subjects/Keywords: PI3K; TCR Signalling; Proteomics; CRISPR/Cas9; T Cells; p110δ; TCR; Interactomics; Lymphocyte Signalling; AviTag

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APA (6th Edition):

Luff, D. H. (2019). Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291052

Chicago Manual of Style (16th Edition):

Luff, Daisy Helen. “Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 24, 2020. https://www.repository.cam.ac.uk/handle/1810/291052.

MLA Handbook (7th Edition):

Luff, Daisy Helen. “Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling.” 2019. Web. 24 Oct 2020.

Vancouver:

Luff DH. Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Oct 24]. Available from: https://www.repository.cam.ac.uk/handle/1810/291052.

Council of Science Editors:

Luff DH. Elucidating the molecular mechanisms of p110δ activation in T cell antigen receptor signalling. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291052

19. 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 (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 24, 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. 24 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 24]. 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


Université de Lorraine

20. Fonte, Coralie. Effets de différents modèles de stress sur le développement lymphocytaire : Effects of different stress models on lymphocyte development.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université de Lorraine

Les vols spatiaux sont source de nombreux stress conduisant à un affaiblissement du système immunitaire. L’efficacité de ce système repose notamment sur la diversité des… (more)

Subjects/Keywords: Répertoires de BCR et TCR; Lymphopoïèse; Stress; Vols spatiaux; Vieillissement; BCR and TCR repertoires; Lymphopoiesis; Stress; Spaceflight; Ageing; 616.079

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APA (6th Edition):

Fonte, C. (2018). Effets de différents modèles de stress sur le développement lymphocytaire : Effects of different stress models on lymphocyte development. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2018LORR0185

Chicago Manual of Style (16th Edition):

Fonte, Coralie. “Effets de différents modèles de stress sur le développement lymphocytaire : Effects of different stress models on lymphocyte development.” 2018. Doctoral Dissertation, Université de Lorraine. Accessed October 24, 2020. http://www.theses.fr/2018LORR0185.

MLA Handbook (7th Edition):

Fonte, Coralie. “Effets de différents modèles de stress sur le développement lymphocytaire : Effects of different stress models on lymphocyte development.” 2018. Web. 24 Oct 2020.

Vancouver:

Fonte C. Effets de différents modèles de stress sur le développement lymphocytaire : Effects of different stress models on lymphocyte development. [Internet] [Doctoral dissertation]. Université de Lorraine; 2018. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2018LORR0185.

Council of Science Editors:

Fonte C. Effets de différents modèles de stress sur le développement lymphocytaire : Effects of different stress models on lymphocyte development. [Doctoral Dissertation]. Université de Lorraine; 2018. Available from: http://www.theses.fr/2018LORR0185


Université de Sherbrooke

21. Gagnon, Julien. Les effets synergiques des cytokines pro-inflammatoires et des cytokines impliquées dans l’homéostasie sur les réponses des lymphocytes T CD8 aux antigènes: Increased antigen responsiveness of CD8 T cells after cytokine primings.

Degree: 2016, Université de Sherbrooke

 Abstract : Homeostasis of naive and memory CD8[superscript +] T lymphocytes is dependent on two cytokines IL-7 and IL-15, respectively. During an immune response to… (more)

Subjects/Keywords: IL-7; IL-15; IL-6; IL-21; TCR avidité; CD5; CD8+ T lymphocytes; TCR avidity

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APA (6th Edition):

Gagnon, J. (2016). Les effets synergiques des cytokines pro-inflammatoires et des cytokines impliquées dans l’homéostasie sur les réponses des lymphocytes T CD8 aux antigènes: Increased antigen responsiveness of CD8 T cells after cytokine primings. (Doctoral Dissertation). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/8777

Chicago Manual of Style (16th Edition):

Gagnon, Julien. “Les effets synergiques des cytokines pro-inflammatoires et des cytokines impliquées dans l’homéostasie sur les réponses des lymphocytes T CD8 aux antigènes: Increased antigen responsiveness of CD8 T cells after cytokine primings.” 2016. Doctoral Dissertation, Université de Sherbrooke. Accessed October 24, 2020. http://hdl.handle.net/11143/8777.

MLA Handbook (7th Edition):

Gagnon, Julien. “Les effets synergiques des cytokines pro-inflammatoires et des cytokines impliquées dans l’homéostasie sur les réponses des lymphocytes T CD8 aux antigènes: Increased antigen responsiveness of CD8 T cells after cytokine primings.” 2016. Web. 24 Oct 2020.

Vancouver:

Gagnon J. Les effets synergiques des cytokines pro-inflammatoires et des cytokines impliquées dans l’homéostasie sur les réponses des lymphocytes T CD8 aux antigènes: Increased antigen responsiveness of CD8 T cells after cytokine primings. [Internet] [Doctoral dissertation]. Université de Sherbrooke; 2016. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/11143/8777.

Council of Science Editors:

Gagnon J. Les effets synergiques des cytokines pro-inflammatoires et des cytokines impliquées dans l’homéostasie sur les réponses des lymphocytes T CD8 aux antigènes: Increased antigen responsiveness of CD8 T cells after cytokine primings. [Doctoral Dissertation]. Université de Sherbrooke; 2016. Available from: http://hdl.handle.net/11143/8777


University of Melbourne

22. 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 24, 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. 24 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 24]. 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


University of Melbourne

23. dos Santos Sá e Almeida, Catarina Filipa. Antigen recognition by Type 2 NKT cells and other unconventional T cells.

Degree: 2015, University of Melbourne

 Natural Killer T (NKT) cells are T lymphocytes specialized in the recognition of lipid antigens presented by the cell-surface molecule CD1d, via their T cell… (more)

Subjects/Keywords: Type 2 NKT; CD1d; TCR; antigen recognition; antigen specificity; diversity; MHC-independen TCR specificityt; R-phycoerythrin

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APA (6th Edition):

dos Santos Sá e Almeida, C. F. (2015). Antigen recognition by Type 2 NKT cells and other unconventional T cells. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/56631

Chicago Manual of Style (16th Edition):

dos Santos Sá e Almeida, Catarina Filipa. “Antigen recognition by Type 2 NKT cells and other unconventional T cells.” 2015. Doctoral Dissertation, University of Melbourne. Accessed October 24, 2020. http://hdl.handle.net/11343/56631.

MLA Handbook (7th Edition):

dos Santos Sá e Almeida, Catarina Filipa. “Antigen recognition by Type 2 NKT cells and other unconventional T cells.” 2015. Web. 24 Oct 2020.

Vancouver:

dos Santos Sá e Almeida CF. Antigen recognition by Type 2 NKT cells and other unconventional T cells. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/11343/56631.

Council of Science Editors:

dos Santos Sá e Almeida CF. Antigen recognition by Type 2 NKT cells and other unconventional T cells. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/56631

24. 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 24, 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. 24 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 24]. 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


Universiteit Utrecht

25. Gründer, E.C. It's all in the mix : γδTCR meets αβT-cell for therapy.

Degree: 2016, Universiteit Utrecht

 Cancer – the “Emperor of all Maladies” is one of the most threatening diseases of our times. In one way or the other nearly everyone… (more)

Subjects/Keywords: adoptive cell transfer; TCR-gene therapy; γδT-cells

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APA (6th Edition):

Gründer, E. C. (2016). It's all in the mix : γδTCR meets αβT-cell for therapy. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/328110

Chicago Manual of Style (16th Edition):

Gründer, E C. “It's all in the mix : γδTCR meets αβT-cell for therapy.” 2016. Doctoral Dissertation, Universiteit Utrecht. Accessed October 24, 2020. http://dspace.library.uu.nl:8080/handle/1874/328110.

MLA Handbook (7th Edition):

Gründer, E C. “It's all in the mix : γδTCR meets αβT-cell for therapy.” 2016. Web. 24 Oct 2020.

Vancouver:

Gründer EC. It's all in the mix : γδTCR meets αβT-cell for therapy. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2020 Oct 24]. Available from: http://dspace.library.uu.nl:8080/handle/1874/328110.

Council of Science Editors:

Gründer EC. It's all in the mix : γδTCR meets αβT-cell for therapy. [Doctoral Dissertation]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/328110


University of Rochester

26. Huang, Yu-Hui (1979 - ). Regulatory T Cell Control of CD4 T Cell Signaling.

Degree: PhD, 2012, University of Rochester

 Nature Regulatory T cells (nTregs) have functions that inhibit the activation of T and B lymphocytes and innate cells. Their suppressive function is critical in… (more)

Subjects/Keywords: Regulatory T Cells; TCR Signaling; NFKB; NFAT; AP-1

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

APA (6th Edition):

Huang, Y. (. -. ). (2012). Regulatory T Cell Control of CD4 T Cell Signaling. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/25534

Chicago Manual of Style (16th Edition):

Huang, Yu-Hui (1979 - ). “Regulatory T Cell Control of CD4 T Cell Signaling.” 2012. Doctoral Dissertation, University of Rochester. Accessed October 24, 2020. http://hdl.handle.net/1802/25534.

MLA Handbook (7th Edition):

Huang, Yu-Hui (1979 - ). “Regulatory T Cell Control of CD4 T Cell Signaling.” 2012. Web. 24 Oct 2020.

Vancouver:

Huang Y(-). Regulatory T Cell Control of CD4 T Cell Signaling. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2020 Oct 24]. Available from: http://hdl.handle.net/1802/25534.

Council of Science Editors:

Huang Y(-). Regulatory T Cell Control of CD4 T Cell Signaling. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/25534


Penn State University

27. BASANTANI, Hitesh Arjun. Thin Film Materials and Devices for Resistive Temperature Sensing Applications.

Degree: 2014, Penn State University

 Thin films of vanadium oxide (VOx) and hydrogenated amorphous silicon (a-Si:H) are the two dominant material systems used in resistive infrared radiation detectors (microbolometers) for… (more)

Subjects/Keywords: Microbolometer; High TCR; 1/f Noise; Infrared Imaging; Hydrogenated Germanium

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

APA (6th Edition):

BASANTANI, H. A. (2014). Thin Film Materials and Devices for Resistive Temperature Sensing Applications. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/23039

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):

BASANTANI, Hitesh Arjun. “Thin Film Materials and Devices for Resistive Temperature Sensing Applications.” 2014. Thesis, Penn State University. Accessed October 24, 2020. https://submit-etda.libraries.psu.edu/catalog/23039.

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

MLA Handbook (7th Edition):

BASANTANI, Hitesh Arjun. “Thin Film Materials and Devices for Resistive Temperature Sensing Applications.” 2014. Web. 24 Oct 2020.

Vancouver:

BASANTANI HA. Thin Film Materials and Devices for Resistive Temperature Sensing Applications. [Internet] [Thesis]. Penn State University; 2014. [cited 2020 Oct 24]. Available from: https://submit-etda.libraries.psu.edu/catalog/23039.

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

Council of Science Editors:

BASANTANI HA. Thin Film Materials and Devices for Resistive Temperature Sensing Applications. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/23039

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


North Carolina State University

28. Orcutt, Timothy Michael. Dissecting the Epigenetic Regulation of V-beta Recombination.

Degree: MS, Microbiology, 2007, North Carolina State University

 V(D)J recombination in developing lymphocytes is essential for producing a diverse repertoire of antigen receptors (TCR and Ig). During recombination, the proteins encoded by the… (more)

Subjects/Keywords: V(D)J; TCR; recombination

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

APA (6th Edition):

Orcutt, T. M. (2007). Dissecting the Epigenetic Regulation of V-beta Recombination. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/485

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):

Orcutt, Timothy Michael. “Dissecting the Epigenetic Regulation of V-beta Recombination.” 2007. Thesis, North Carolina State University. Accessed October 24, 2020. http://www.lib.ncsu.edu/resolver/1840.16/485.

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

MLA Handbook (7th Edition):

Orcutt, Timothy Michael. “Dissecting the Epigenetic Regulation of V-beta Recombination.” 2007. Web. 24 Oct 2020.

Vancouver:

Orcutt TM. Dissecting the Epigenetic Regulation of V-beta Recombination. [Internet] [Thesis]. North Carolina State University; 2007. [cited 2020 Oct 24]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/485.

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

Council of Science Editors:

Orcutt TM. Dissecting the Epigenetic Regulation of V-beta Recombination. [Thesis]. North Carolina State University; 2007. Available from: http://www.lib.ncsu.edu/resolver/1840.16/485

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

29. Salles, Audrey. Influence de l'organisation latérale de la membrane sur l'activation lymphocytaire T : Influence of the lateral membrane organization on T cell activation.

Degree: Docteur es, Immunologie, 2010, Aix-Marseille 2

Les rafts lipidiques sont des nanodomaines membranaires enrichis en cholestérol et en sphingolipides impliqués dans la régulation de la signalisation médiée par le TCR. Néanmoins… (more)

Subjects/Keywords: Raft nanodomaines; T lymphocytes; Tcr; Signaling; Calcium; Tracking; Membran

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

APA (6th Edition):

Salles, A. (2010). Influence de l'organisation latérale de la membrane sur l'activation lymphocytaire T : Influence of the lateral membrane organization on T cell activation. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX22137

Chicago Manual of Style (16th Edition):

Salles, Audrey. “Influence de l'organisation latérale de la membrane sur l'activation lymphocytaire T : Influence of the lateral membrane organization on T cell activation.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed October 24, 2020. http://www.theses.fr/2010AIX22137.

MLA Handbook (7th Edition):

Salles, Audrey. “Influence de l'organisation latérale de la membrane sur l'activation lymphocytaire T : Influence of the lateral membrane organization on T cell activation.” 2010. Web. 24 Oct 2020.

Vancouver:

Salles A. Influence de l'organisation latérale de la membrane sur l'activation lymphocytaire T : Influence of the lateral membrane organization on T cell activation. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2020 Oct 24]. Available from: http://www.theses.fr/2010AIX22137.

Council of Science Editors:

Salles A. Influence de l'organisation latérale de la membrane sur l'activation lymphocytaire T : Influence of the lateral membrane organization on T cell activation. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX22137


University of Debrecen

30. Ábel, Nikolett. A TCR meghatározó szerepe a társadalmi felelősségvállalásban .

Degree: DE – Bölcsészettudományi Kar, University of Debrecen

TCR reklámok elemzése, illetve hogy hogyan hatnak eszközeik a cégek, szervezetek és magánemberek felelős gondolkodására. A reklámok által felelősebben fogunk gondolkodni a Világunkról? Visszahat-e a… (more)

Subjects/Keywords: TCR; reklám; kommunikáció; marketing

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

APA (6th Edition):

Ábel, N. (n.d.). A TCR meghatározó szerepe a társadalmi felelősségvállalásban . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/208982

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Ábel, Nikolett. “A TCR meghatározó szerepe a társadalmi felelősségvállalásban .” Thesis, University of Debrecen. Accessed October 24, 2020. http://hdl.handle.net/2437/208982.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Ábel, Nikolett. “A TCR meghatározó szerepe a társadalmi felelősségvállalásban .” Web. 24 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Ábel N. A TCR meghatározó szerepe a társadalmi felelősségvállalásban . [Internet] [Thesis]. University of Debrecen; [cited 2020 Oct 24]. Available from: http://hdl.handle.net/2437/208982.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Ábel N. A TCR meghatározó szerepe a társadalmi felelősségvállalásban . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/208982

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

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