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You searched for subject:(CD4 T cells). Showing records 1 – 30 of 201 total matches.

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Montana Tech

1. Osborne, Douglas Grant. Biological effects of trogocytosis on CD4+ T lymphocytes.

Degree: PhD, 2013, Montana Tech

  Antigen recognition by CD4+ T cells leads to large-scale spatial and temporal molecular redistributions, forming the immunological synapse. We have previously shown that upon… (more)

Subjects/Keywords: T cells; trogocytosis; CD4; imaging

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APA (6th Edition):

Osborne, D. G. (2013). Biological effects of trogocytosis on CD4+ T lymphocytes. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/100

Chicago Manual of Style (16th Edition):

Osborne, Douglas Grant. “Biological effects of trogocytosis on CD4+ T lymphocytes.” 2013. Doctoral Dissertation, Montana Tech. Accessed November 12, 2019. https://scholarworks.umt.edu/etd/100.

MLA Handbook (7th Edition):

Osborne, Douglas Grant. “Biological effects of trogocytosis on CD4+ T lymphocytes.” 2013. Web. 12 Nov 2019.

Vancouver:

Osborne DG. Biological effects of trogocytosis on CD4+ T lymphocytes. [Internet] [Doctoral dissertation]. Montana Tech; 2013. [cited 2019 Nov 12]. Available from: https://scholarworks.umt.edu/etd/100.

Council of Science Editors:

Osborne DG. Biological effects of trogocytosis on CD4+ T lymphocytes. [Doctoral Dissertation]. Montana Tech; 2013. Available from: https://scholarworks.umt.edu/etd/100


Université de Montréal

2. Lemieux, William. Mécanismes d'action des cellules stromales mésenchymateuses dans le traitement de la réaction du greffon contre l'hôte .

Degree: 2016, Université de Montréal

 La maladie du greffon contre l’hôte (GvHD) est un effet secondaire sérieux de la transplantation de cellules souches hématopoïétiques (HSCT). Cette maladie entraine une haute… (more)

Subjects/Keywords: MSC; GvHD; Cellules T CD4+; HSCT; IDO1; CRISPR; CD4+ T cells

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APA (6th Edition):

Lemieux, W. (2016). Mécanismes d'action des cellules stromales mésenchymateuses dans le traitement de la réaction du greffon contre l'hôte . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13887

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):

Lemieux, William. “Mécanismes d'action des cellules stromales mésenchymateuses dans le traitement de la réaction du greffon contre l'hôte .” 2016. Thesis, Université de Montréal. Accessed November 12, 2019. http://hdl.handle.net/1866/13887.

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

MLA Handbook (7th Edition):

Lemieux, William. “Mécanismes d'action des cellules stromales mésenchymateuses dans le traitement de la réaction du greffon contre l'hôte .” 2016. Web. 12 Nov 2019.

Vancouver:

Lemieux W. Mécanismes d'action des cellules stromales mésenchymateuses dans le traitement de la réaction du greffon contre l'hôte . [Internet] [Thesis]. Université de Montréal; 2016. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1866/13887.

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

Council of Science Editors:

Lemieux W. Mécanismes d'action des cellules stromales mésenchymateuses dans le traitement de la réaction du greffon contre l'hôte . [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/13887

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

3. Doe, Henrietta Terko. Expression of PD-1/LAG-3 and cytokine production by CD4+T cells during infection with Plasmodiumparasites : マラリア原虫感染におけるCD4+T細胞のPD-1/LAG-3発現とサイトカイン産生の解析.

Degree: 博士(医学), 2016, Nagasaki University / 長崎大学

CD4+ T cells play critical roles in protection against the blood-stage of malaria infection, but their uncontrolled activation can be harmful to the host. We… (more)

Subjects/Keywords: malaria; CD4+ T cells; inhibitory receptor; cytokines

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APA (6th Edition):

Doe, H. T. (2016). Expression of PD-1/LAG-3 and cytokine production by CD4+T cells during infection with Plasmodiumparasites : マラリア原虫感染におけるCD4+T細胞のPD-1/LAG-3発現とサイトカイン産生の解析. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/37062

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):

Doe, Henrietta Terko. “Expression of PD-1/LAG-3 and cytokine production by CD4+T cells during infection with Plasmodiumparasites : マラリア原虫感染におけるCD4+T細胞のPD-1/LAG-3発現とサイトカイン産生の解析.” 2016. Thesis, Nagasaki University / 長崎大学. Accessed November 12, 2019. http://hdl.handle.net/10069/37062.

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

MLA Handbook (7th Edition):

Doe, Henrietta Terko. “Expression of PD-1/LAG-3 and cytokine production by CD4+T cells during infection with Plasmodiumparasites : マラリア原虫感染におけるCD4+T細胞のPD-1/LAG-3発現とサイトカイン産生の解析.” 2016. Web. 12 Nov 2019.

Vancouver:

Doe HT. Expression of PD-1/LAG-3 and cytokine production by CD4+T cells during infection with Plasmodiumparasites : マラリア原虫感染におけるCD4+T細胞のPD-1/LAG-3発現とサイトカイン産生の解析. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2016. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10069/37062.

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

Council of Science Editors:

Doe HT. Expression of PD-1/LAG-3 and cytokine production by CD4+T cells during infection with Plasmodiumparasites : マラリア原虫感染におけるCD4+T細胞のPD-1/LAG-3発現とサイトカイン産生の解析. [Thesis]. Nagasaki University / 長崎大学; 2016. Available from: http://hdl.handle.net/10069/37062

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


University of Washington

4. Moguche, Albanus O. Maintenance and function of antigen-specific CD4 T cells within the lung during tuberculosis.

Degree: PhD, 2014, University of Washington

 Tuberculosis (TB) is a chronic pulmonary disease caused by the intracellular bacterium Mycobacterium tuberculosis (Mtb). Even though CD4 T cells are critical for containing Mtb,… (more)

Subjects/Keywords: CD4 T cells; Immunology; Tuberculosis; Immunology; immunology

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

APA (6th Edition):

Moguche, A. O. (2014). Maintenance and function of antigen-specific CD4 T cells within the lung during tuberculosis. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/26105

Chicago Manual of Style (16th Edition):

Moguche, Albanus O. “Maintenance and function of antigen-specific CD4 T cells within the lung during tuberculosis.” 2014. Doctoral Dissertation, University of Washington. Accessed November 12, 2019. http://hdl.handle.net/1773/26105.

MLA Handbook (7th Edition):

Moguche, Albanus O. “Maintenance and function of antigen-specific CD4 T cells within the lung during tuberculosis.” 2014. Web. 12 Nov 2019.

Vancouver:

Moguche AO. Maintenance and function of antigen-specific CD4 T cells within the lung during tuberculosis. [Internet] [Doctoral dissertation]. University of Washington; 2014. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1773/26105.

Council of Science Editors:

Moguche AO. Maintenance and function of antigen-specific CD4 T cells within the lung during tuberculosis. [Doctoral Dissertation]. University of Washington; 2014. Available from: http://hdl.handle.net/1773/26105


Virginia Tech

5. Carbo Barrios, Adria. Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity.

Degree: PhD, Animal and Poultry Sciences, 2014, Virginia Tech

CD4+ T cells mediate and orchestrate a tremendous panoply of lymphoid cell subsets in the human immune system. CD4+ T cells are able to differentiate… (more)

Subjects/Keywords: Immunology; CD4+ T cells; computational modeling

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APA (6th Edition):

Carbo Barrios, A. (2014). Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/64833

Chicago Manual of Style (16th Edition):

Carbo Barrios, Adria. “Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity.” 2014. Doctoral Dissertation, Virginia Tech. Accessed November 12, 2019. http://hdl.handle.net/10919/64833.

MLA Handbook (7th Edition):

Carbo Barrios, Adria. “Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity.” 2014. Web. 12 Nov 2019.

Vancouver:

Carbo Barrios A. Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity. [Internet] [Doctoral dissertation]. Virginia Tech; 2014. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10919/64833.

Council of Science Editors:

Carbo Barrios A. Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity. [Doctoral Dissertation]. Virginia Tech; 2014. Available from: http://hdl.handle.net/10919/64833


Virginia Tech

6. Mazzei, Joseph Cayetano. Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: Importance of peroxisome proliferator-activated receptor γ expression.

Degree: MS, Human Nutrition, Foods, and Exercise, 2012, Virginia Tech

 Sphingolipid metabolites play a role in the initiation and perpetuation of inflammatory responses. Since intestinal inflammation is a driving force in the development of colon… (more)

Subjects/Keywords: Sphingomyelin; Inflammation; CD4+ T cells; Colon Cancer

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APA (6th Edition):

Mazzei, J. C. (2012). Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: Importance of peroxisome proliferator-activated receptor γ expression. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/43766

Chicago Manual of Style (16th Edition):

Mazzei, Joseph Cayetano. “Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: Importance of peroxisome proliferator-activated receptor γ expression.” 2012. Masters Thesis, Virginia Tech. Accessed November 12, 2019. http://hdl.handle.net/10919/43766.

MLA Handbook (7th Edition):

Mazzei, Joseph Cayetano. “Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: Importance of peroxisome proliferator-activated receptor γ expression.” 2012. Web. 12 Nov 2019.

Vancouver:

Mazzei JC. Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: Importance of peroxisome proliferator-activated receptor γ expression. [Internet] [Masters thesis]. Virginia Tech; 2012. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10919/43766.

Council of Science Editors:

Mazzei JC. Suppression of intestinal inflammation and inflammation-driven colon cancer in mice by dietary sphingomyelin: Importance of peroxisome proliferator-activated receptor γ expression. [Masters Thesis]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/43766


Virginia Tech

7. Hong, Tian. A framework for understanding heterogeneous differentiation of CD4⁺ T cells.

Degree: PhD, Genetics, Bioinformatics, and Computational Biology, 2013, Virginia Tech

CD4+ T cells are a group of lymphocytes that play critical roles in the immune system. By releasing cytokines, CD4+ T cells regulate other immune… (more)

Subjects/Keywords: CD4+ T cells; mathematical model; cell differentiation

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APA (6th Edition):

Hong, T. (2013). A framework for understanding heterogeneous differentiation of CD4⁺ T cells. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/51228

Chicago Manual of Style (16th Edition):

Hong, Tian. “A framework for understanding heterogeneous differentiation of CD4⁺ T cells.” 2013. Doctoral Dissertation, Virginia Tech. Accessed November 12, 2019. http://hdl.handle.net/10919/51228.

MLA Handbook (7th Edition):

Hong, Tian. “A framework for understanding heterogeneous differentiation of CD4⁺ T cells.” 2013. Web. 12 Nov 2019.

Vancouver:

Hong T. A framework for understanding heterogeneous differentiation of CD4⁺ T cells. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10919/51228.

Council of Science Editors:

Hong T. A framework for understanding heterogeneous differentiation of CD4⁺ T cells. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/51228


University of Rochester

8. Sant, Andrea J. The Influence of CD4 T Cell Specificity on Differentiation of the Repertoire and Shaping the Adaptive Immune Response to Influenza Infection.

Degree: PhD, 2016, University of Rochester

 We have sought to understand the role that epitope specificity in the CD4 T cell repertoire has on the functional outcome of both the CD4(more)

Subjects/Keywords: Influenza; CD4 T cells; Vaccination; Follicular helper T cells

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APA (6th Edition):

Sant, A. J. (2016). The Influence of CD4 T Cell Specificity on Differentiation of the Repertoire and Shaping the Adaptive Immune Response to Influenza Infection. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/31385

Chicago Manual of Style (16th Edition):

Sant, Andrea J. “The Influence of CD4 T Cell Specificity on Differentiation of the Repertoire and Shaping the Adaptive Immune Response to Influenza Infection.” 2016. Doctoral Dissertation, University of Rochester. Accessed November 12, 2019. http://hdl.handle.net/1802/31385.

MLA Handbook (7th Edition):

Sant, Andrea J. “The Influence of CD4 T Cell Specificity on Differentiation of the Repertoire and Shaping the Adaptive Immune Response to Influenza Infection.” 2016. Web. 12 Nov 2019.

Vancouver:

Sant AJ. The Influence of CD4 T Cell Specificity on Differentiation of the Repertoire and Shaping the Adaptive Immune Response to Influenza Infection. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1802/31385.

Council of Science Editors:

Sant AJ. The Influence of CD4 T Cell Specificity on Differentiation of the Repertoire and Shaping the Adaptive Immune Response to Influenza Infection. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/31385


University of Saskatchewan

9. Arendse, Germaine V 1966-. Characterization of the Immune Response to Alloantigens: An in vitro Model System for Cognate Regulation of CD4 T cell Differentiation by CD8 T cells.

Degree: 2018, University of Saskatchewan

 ABSTRACT It is accepted that CD4 T cells are required for the activation of naïve CD8 T cells. In this study, we have investigated the… (more)

Subjects/Keywords: CD8 T cells; CD4 T cells; cytokines; Th1; Th2

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APA (6th Edition):

Arendse, G. V. 1. (2018). Characterization of the Immune Response to Alloantigens: An in vitro Model System for Cognate Regulation of CD4 T cell Differentiation by CD8 T cells. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/9239

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):

Arendse, Germaine V 1966-. “Characterization of the Immune Response to Alloantigens: An in vitro Model System for Cognate Regulation of CD4 T cell Differentiation by CD8 T cells.” 2018. Thesis, University of Saskatchewan. Accessed November 12, 2019. http://hdl.handle.net/10388/9239.

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

MLA Handbook (7th Edition):

Arendse, Germaine V 1966-. “Characterization of the Immune Response to Alloantigens: An in vitro Model System for Cognate Regulation of CD4 T cell Differentiation by CD8 T cells.” 2018. Web. 12 Nov 2019.

Vancouver:

Arendse GV1. Characterization of the Immune Response to Alloantigens: An in vitro Model System for Cognate Regulation of CD4 T cell Differentiation by CD8 T cells. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10388/9239.

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

Council of Science Editors:

Arendse GV1. Characterization of the Immune Response to Alloantigens: An in vitro Model System for Cognate Regulation of CD4 T cell Differentiation by CD8 T cells. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/9239

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


Loyola University Chicago

10. Chandrasekaran, Uma. Phospholipase D Signaling in T Cells.

Degree: PhD, Microbiology and Immunology, 2010, Loyola University Chicago

  Antigen stimulation of T lymphocytes induces the activation of phospholipase D (PLD) signaling. Phospholipase D (PLD) is a phosphodiesterase that catalyzes the conversion of… (more)

Subjects/Keywords: CD4 T CELLS; EFFECTOR T CELLS; PLD SIGNALING; REGULATORY T CELLS; Immunology and Infectious Disease

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APA (6th Edition):

Chandrasekaran, U. (2010). Phospholipase D Signaling in T Cells. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/162

Chicago Manual of Style (16th Edition):

Chandrasekaran, Uma. “Phospholipase D Signaling in T Cells.” 2010. Doctoral Dissertation, Loyola University Chicago. Accessed November 12, 2019. https://ecommons.luc.edu/luc_diss/162.

MLA Handbook (7th Edition):

Chandrasekaran, Uma. “Phospholipase D Signaling in T Cells.” 2010. Web. 12 Nov 2019.

Vancouver:

Chandrasekaran U. Phospholipase D Signaling in T Cells. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2010. [cited 2019 Nov 12]. Available from: https://ecommons.luc.edu/luc_diss/162.

Council of Science Editors:

Chandrasekaran U. Phospholipase D Signaling in T Cells. [Doctoral Dissertation]. Loyola University Chicago; 2010. Available from: https://ecommons.luc.edu/luc_diss/162

11. Sounidaki, Maria. Μελέτη της ανοσοτροποποιητικής δράσης του διχλωροξικού σε καλλιέργειες ανθρώπινων CD4+ T λεμφοκυττάρων.

Degree: 2019, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας

Today, kidney transplantation is considered to be the most widespread treatment for end-stage renal failure. However, the development of novel, more effective and safer immunosuppressants… (more)

Subjects/Keywords: Διχλωροξικό οξύ; Μεταμόσχευση νεφρού; CD4+ T κύτταρα; Γλυκόλυση; Dichloroacetate; Kidney transplantation; CD4+ T cells; Glycolysis

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APA (6th Edition):

Sounidaki, M. (2019). Μελέτη της ανοσοτροποποιητικής δράσης του διχλωροξικού σε καλλιέργειες ανθρώπινων CD4+ T λεμφοκυττάρων. (Thesis). University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Retrieved from http://hdl.handle.net/10442/hedi/46010

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):

Sounidaki, Maria. “Μελέτη της ανοσοτροποποιητικής δράσης του διχλωροξικού σε καλλιέργειες ανθρώπινων CD4+ T λεμφοκυττάρων.” 2019. Thesis, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Accessed November 12, 2019. http://hdl.handle.net/10442/hedi/46010.

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

MLA Handbook (7th Edition):

Sounidaki, Maria. “Μελέτη της ανοσοτροποποιητικής δράσης του διχλωροξικού σε καλλιέργειες ανθρώπινων CD4+ T λεμφοκυττάρων.” 2019. Web. 12 Nov 2019.

Vancouver:

Sounidaki M. Μελέτη της ανοσοτροποποιητικής δράσης του διχλωροξικού σε καλλιέργειες ανθρώπινων CD4+ T λεμφοκυττάρων. [Internet] [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2019. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10442/hedi/46010.

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

Council of Science Editors:

Sounidaki M. Μελέτη της ανοσοτροποποιητικής δράσης του διχλωροξικού σε καλλιέργειες ανθρώπινων CD4+ T λεμφοκυττάρων. [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2019. Available from: http://hdl.handle.net/10442/hedi/46010

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


Université Paris-Sud – Paris XI

12. Jaafoura, Salma. Mémoire lymphocytaire T et persistance virale : T Memory lymphocyte and viral persistence.

Degree: Docteur es, Immunologie, 2014, Université Paris-Sud – Paris XI

Au cours d’une réponse immunitaire primaire, les lymphocytes T CD8 mémoires émergent à partir d'un environnement de forte activation immunitaire. Les cellules régulatrices T CD4(more)

Subjects/Keywords: Aide T CD4; Lymphocytes T CD8 mémoires; Lymphocyte T CD4; Réservoir latent; Sous populations mémoires CD4; TSCM; Taux de décroissance; VIH; CD4 help; Memory CD8 T cells; CD4 T cells; Latent reservoir; HIV; Memory CD4 T cells; TSCM; Decay rates

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APA (6th Edition):

Jaafoura, S. (2014). Mémoire lymphocytaire T et persistance virale : T Memory lymphocyte and viral persistence. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2014PA114847

Chicago Manual of Style (16th Edition):

Jaafoura, Salma. “Mémoire lymphocytaire T et persistance virale : T Memory lymphocyte and viral persistence.” 2014. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed November 12, 2019. http://www.theses.fr/2014PA114847.

MLA Handbook (7th Edition):

Jaafoura, Salma. “Mémoire lymphocytaire T et persistance virale : T Memory lymphocyte and viral persistence.” 2014. Web. 12 Nov 2019.

Vancouver:

Jaafoura S. Mémoire lymphocytaire T et persistance virale : T Memory lymphocyte and viral persistence. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2014. [cited 2019 Nov 12]. Available from: http://www.theses.fr/2014PA114847.

Council of Science Editors:

Jaafoura S. Mémoire lymphocytaire T et persistance virale : T Memory lymphocyte and viral persistence. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2014. Available from: http://www.theses.fr/2014PA114847


Universitat Pompeu Fabra

13. Alberdi Ibarzabal, Maria, 1986-. Regulation of T cell fates by the transcription factor NFAT5 in different microenvironments.

Degree: Departament de Ciències Experimentals i de la Salut, 2015, Universitat Pompeu Fabra

 Les cèl·lules T CD4+ poden adoptar programes funcionals diferents com a resposta a canvis en l’entorn com ara la disponibilitat de citocines, contactes entre cèl·lules… (more)

Subjects/Keywords: CD4+T cells; NFAT5; T cell differentiation; Cèl·lules T CD4; Colitis; Diferenciació de cèl·lules T; Estrès osmòtic; Osmotic stress; 576

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APA (6th Edition):

Alberdi Ibarzabal, Maria, 1. (2015). Regulation of T cell fates by the transcription factor NFAT5 in different microenvironments. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/481990

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):

Alberdi Ibarzabal, Maria, 1986-. “Regulation of T cell fates by the transcription factor NFAT5 in different microenvironments.” 2015. Thesis, Universitat Pompeu Fabra. Accessed November 12, 2019. http://hdl.handle.net/10803/481990.

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

MLA Handbook (7th Edition):

Alberdi Ibarzabal, Maria, 1986-. “Regulation of T cell fates by the transcription factor NFAT5 in different microenvironments.” 2015. Web. 12 Nov 2019.

Vancouver:

Alberdi Ibarzabal, Maria 1. Regulation of T cell fates by the transcription factor NFAT5 in different microenvironments. [Internet] [Thesis]. Universitat Pompeu Fabra; 2015. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10803/481990.

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

Council of Science Editors:

Alberdi Ibarzabal, Maria 1. Regulation of T cell fates by the transcription factor NFAT5 in different microenvironments. [Thesis]. Universitat Pompeu Fabra; 2015. Available from: http://hdl.handle.net/10803/481990

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


University of Cincinnati

14. Aksoylar, Halil I. A Critical Role for Gimap5 in CD4+ T Cell Homeostasis and Maintenance of Peripheral Immune Tolerance.

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

T cell lymphopenia is a condition which arises from defects in T cell development and/or peripheral homeostatic mechanisms. Importantly, lymphopenia is often associated with T(more)

Subjects/Keywords: Immunology; Giamp5; Lymphopenia; CD4 T cells; T cell homeostasis; Colitis; Autoimmunity

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

APA (6th Edition):

Aksoylar, H. I. (2013). A Critical Role for Gimap5 in CD4+ T Cell Homeostasis and Maintenance of Peripheral Immune Tolerance. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367937122

Chicago Manual of Style (16th Edition):

Aksoylar, Halil I. “A Critical Role for Gimap5 in CD4+ T Cell Homeostasis and Maintenance of Peripheral Immune Tolerance.” 2013. Doctoral Dissertation, University of Cincinnati. Accessed November 12, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367937122.

MLA Handbook (7th Edition):

Aksoylar, Halil I. “A Critical Role for Gimap5 in CD4+ T Cell Homeostasis and Maintenance of Peripheral Immune Tolerance.” 2013. Web. 12 Nov 2019.

Vancouver:

Aksoylar HI. A Critical Role for Gimap5 in CD4+ T Cell Homeostasis and Maintenance of Peripheral Immune Tolerance. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2019 Nov 12]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367937122.

Council of Science Editors:

Aksoylar HI. A Critical Role for Gimap5 in CD4+ T Cell Homeostasis and Maintenance of Peripheral Immune Tolerance. [Doctoral Dissertation]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1367937122


Université de Montréal

15. Gauthier, Simon-David. Impact de la maladie du greffon contre l’hôte sur la reconstitution immunitaire suite à une greffe de moelle osseuse allogénique .

Degree: 2012, Université de Montréal

 La transplantation allogénique de cellules souches hématopoïétiques est une technique très efficace pour traiter différents cancers du sang. Malheureusement la réaction du greffon contre l’hôte… (more)

Subjects/Keywords: GVHD; GVHD; reconstitution immunitaire; immune reconstitution; lymphocyte T CD4+; CD4+ T cells; cellule dendritique; dendritic cells; prolifération homéostatique; homeostatic proliferation

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APA (6th Edition):

Gauthier, S. (2012). Impact de la maladie du greffon contre l’hôte sur la reconstitution immunitaire suite à une greffe de moelle osseuse allogénique . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/6208

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):

Gauthier, Simon-David. “Impact de la maladie du greffon contre l’hôte sur la reconstitution immunitaire suite à une greffe de moelle osseuse allogénique .” 2012. Thesis, Université de Montréal. Accessed November 12, 2019. http://hdl.handle.net/1866/6208.

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

MLA Handbook (7th Edition):

Gauthier, Simon-David. “Impact de la maladie du greffon contre l’hôte sur la reconstitution immunitaire suite à une greffe de moelle osseuse allogénique .” 2012. Web. 12 Nov 2019.

Vancouver:

Gauthier S. Impact de la maladie du greffon contre l’hôte sur la reconstitution immunitaire suite à une greffe de moelle osseuse allogénique . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1866/6208.

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

Council of Science Editors:

Gauthier S. Impact de la maladie du greffon contre l’hôte sur la reconstitution immunitaire suite à une greffe de moelle osseuse allogénique . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/6208

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

16. Boucoiran, Agathe. Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases.

Degree: Docteur es, Immunologie et microbiologie, 2016, Côte d'Azur

Les maladies inflammatoires chroniques sont associées à un maintien de la réponse immunitaire et notamment la présence de cellules T CD4+ mémoires. Les maladies inflammatoires… (more)

Subjects/Keywords: Inflammation; Ostéoimmunologie; Ostéoclastes; Cellules CD4+ mémoires; Inflammation; Osteoimmunology; Osteoclasts; CD4+ memory T cells

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APA (6th Edition):

Boucoiran, A. (2016). Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases. (Doctoral Dissertation). Côte d'Azur. Retrieved from http://www.theses.fr/2016AZUR4064

Chicago Manual of Style (16th Edition):

Boucoiran, Agathe. “Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases.” 2016. Doctoral Dissertation, Côte d'Azur. Accessed November 12, 2019. http://www.theses.fr/2016AZUR4064.

MLA Handbook (7th Edition):

Boucoiran, Agathe. “Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases.” 2016. Web. 12 Nov 2019.

Vancouver:

Boucoiran A. Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases. [Internet] [Doctoral dissertation]. Côte d'Azur; 2016. [cited 2019 Nov 12]. Available from: http://www.theses.fr/2016AZUR4064.

Council of Science Editors:

Boucoiran A. Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases. [Doctoral Dissertation]. Côte d'Azur; 2016. Available from: http://www.theses.fr/2016AZUR4064

17. Michieletto, Michael. Rôles des facteurs de transcription Foxo3 et Eomes dans la différenciation et les fonctions des lymphocytes T CD4 : Roles of Foxo3 and Eomes in CD4 T cell differentiation and functions.

Degree: Docteur es, Immunologie, 2018, Université Toulouse III – Paul Sabatier

Les Lymphocytes T CD4 (LT CD4) sont des cellules du système immunitaire adaptatif extrêmement plastiques qui, en fonction des signaux présents dans le microenvironnement cellulaire,… (more)

Subjects/Keywords: CD4; Lymphocyte; Facteur de transcription; Auto-immunité; CD4; T cells; Transcription factor; Autoimmunity

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APA (6th Edition):

Michieletto, M. (2018). Rôles des facteurs de transcription Foxo3 et Eomes dans la différenciation et les fonctions des lymphocytes T CD4 : Roles of Foxo3 and Eomes in CD4 T cell differentiation and functions. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2018TOU30224

Chicago Manual of Style (16th Edition):

Michieletto, Michael. “Rôles des facteurs de transcription Foxo3 et Eomes dans la différenciation et les fonctions des lymphocytes T CD4 : Roles of Foxo3 and Eomes in CD4 T cell differentiation and functions.” 2018. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed November 12, 2019. http://www.theses.fr/2018TOU30224.

MLA Handbook (7th Edition):

Michieletto, Michael. “Rôles des facteurs de transcription Foxo3 et Eomes dans la différenciation et les fonctions des lymphocytes T CD4 : Roles of Foxo3 and Eomes in CD4 T cell differentiation and functions.” 2018. Web. 12 Nov 2019.

Vancouver:

Michieletto M. Rôles des facteurs de transcription Foxo3 et Eomes dans la différenciation et les fonctions des lymphocytes T CD4 : Roles of Foxo3 and Eomes in CD4 T cell differentiation and functions. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2018. [cited 2019 Nov 12]. Available from: http://www.theses.fr/2018TOU30224.

Council of Science Editors:

Michieletto M. Rôles des facteurs de transcription Foxo3 et Eomes dans la différenciation et les fonctions des lymphocytes T CD4 : Roles of Foxo3 and Eomes in CD4 T cell differentiation and functions. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2018. Available from: http://www.theses.fr/2018TOU30224

18. Aguilera-Sandoval, Christian Raul. The Dynamic Interplay between HIV-1 and T cells.

Degree: Microbiology, Immunology, & Molecular Genetics, 2016, UCLA

 Although it is well-documented that T cells are crucial in the pathogenesis of human immunodeficiency virus type 1 (HIV-1) yet the dynamic interplay between HIV-1… (more)

Subjects/Keywords: Immunology; Microbiology; Genetics; CD4 T cells; CD8 T cells; CTL Escape; HIV; immunotherapy; TCR repertoire

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APA (6th Edition):

Aguilera-Sandoval, C. R. (2016). The Dynamic Interplay between HIV-1 and T cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/60w2g35c

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):

Aguilera-Sandoval, Christian Raul. “The Dynamic Interplay between HIV-1 and T cells.” 2016. Thesis, UCLA. Accessed November 12, 2019. http://www.escholarship.org/uc/item/60w2g35c.

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

MLA Handbook (7th Edition):

Aguilera-Sandoval, Christian Raul. “The Dynamic Interplay between HIV-1 and T cells.” 2016. Web. 12 Nov 2019.

Vancouver:

Aguilera-Sandoval CR. The Dynamic Interplay between HIV-1 and T cells. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Nov 12]. Available from: http://www.escholarship.org/uc/item/60w2g35c.

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

Council of Science Editors:

Aguilera-Sandoval CR. The Dynamic Interplay between HIV-1 and T cells. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/60w2g35c

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


University of Washington

19. Soerens, Andrew Glenn. Regulatory T cell contributions to mucosal antiviral immunity.

Degree: PhD, 2016, University of Washington

 Regulatory T cells (Tregs) prevent autoimmunity and limit immunopathology using a variety of suppressive mechanisms, yet their roles during an immune response against pathogens remains… (more)

Subjects/Keywords: CD4 T cells; Herpes Simplex virus; HSV-2; Regulatory T Cells; Tregs; Immunology; pathobiology

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APA (6th Edition):

Soerens, A. G. (2016). Regulatory T cell contributions to mucosal antiviral immunity. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/35290

Chicago Manual of Style (16th Edition):

Soerens, Andrew Glenn. “Regulatory T cell contributions to mucosal antiviral immunity.” 2016. Doctoral Dissertation, University of Washington. Accessed November 12, 2019. http://hdl.handle.net/1773/35290.

MLA Handbook (7th Edition):

Soerens, Andrew Glenn. “Regulatory T cell contributions to mucosal antiviral immunity.” 2016. Web. 12 Nov 2019.

Vancouver:

Soerens AG. Regulatory T cell contributions to mucosal antiviral immunity. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1773/35290.

Council of Science Editors:

Soerens AG. Regulatory T cell contributions to mucosal antiviral immunity. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35290


University of Melbourne

20. Collins, Nicholas. Memory CD4 T cells in skin at steady-state and following infection.

Degree: 2015, University of Melbourne

 Peripheral tissues such as the skin, gut and lungs are exposed to the environment, making efficient immunosurveillance of these organs critical. This in part relies… (more)

Subjects/Keywords: immunology; memory T cells; CD4 T cells; skin biology, virology: HSV-1

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APA (6th Edition):

Collins, N. (2015). Memory CD4 T cells in skin at steady-state and following infection. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/90881

Chicago Manual of Style (16th Edition):

Collins, Nicholas. “Memory CD4 T cells in skin at steady-state and following infection.” 2015. Doctoral Dissertation, University of Melbourne. Accessed November 12, 2019. http://hdl.handle.net/11343/90881.

MLA Handbook (7th Edition):

Collins, Nicholas. “Memory CD4 T cells in skin at steady-state and following infection.” 2015. Web. 12 Nov 2019.

Vancouver:

Collins N. Memory CD4 T cells in skin at steady-state and following infection. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/11343/90881.

Council of Science Editors:

Collins N. Memory CD4 T cells in skin at steady-state and following infection. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/90881


University of New Mexico

21. Brunsing, Ryan. Induction of interleukin-10 within the T(H)17 effector population using the GPER agonist G-1.

Degree: Biomedical Sciences Graduate Program, 2013, University of New Mexico

 A critical mechanism in immune homeostasis is the ability to stop an ongoing inflammatory response once the inciting agent has been destroyed or neutralized. Failure… (more)

Subjects/Keywords: GPER; G-1; CD4+ T cells; interleukin-10; T(H)17 cells

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APA (6th Edition):

Brunsing, R. (2013). Induction of interleukin-10 within the T(H)17 effector population using the GPER agonist G-1. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/115

Chicago Manual of Style (16th Edition):

Brunsing, Ryan. “Induction of interleukin-10 within the T(H)17 effector population using the GPER agonist G-1.” 2013. Doctoral Dissertation, University of New Mexico. Accessed November 12, 2019. https://digitalrepository.unm.edu/biom_etds/115.

MLA Handbook (7th Edition):

Brunsing, Ryan. “Induction of interleukin-10 within the T(H)17 effector population using the GPER agonist G-1.” 2013. Web. 12 Nov 2019.

Vancouver:

Brunsing R. Induction of interleukin-10 within the T(H)17 effector population using the GPER agonist G-1. [Internet] [Doctoral dissertation]. University of New Mexico; 2013. [cited 2019 Nov 12]. Available from: https://digitalrepository.unm.edu/biom_etds/115.

Council of Science Editors:

Brunsing R. Induction of interleukin-10 within the T(H)17 effector population using the GPER agonist G-1. [Doctoral Dissertation]. University of New Mexico; 2013. Available from: https://digitalrepository.unm.edu/biom_etds/115

22. Faleiro, Rebecca Jacinto. Development of immunotherapies and vaccines against visceral leishmaiasis.

Degree: 2016, Queensland University of Technology

 Visceral leishmaniasis (VL) is a chronic parasitic disease prevalent in tropical and sub- tropical countries. This study focused on the development of immune-based therapy with… (more)

Subjects/Keywords: CD4+ T cells; Leishmania; Visceral leishmaniasis; Immunetherapy; Vaccines

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

APA (6th Edition):

Faleiro, R. J. (2016). Development of immunotherapies and vaccines against visceral leishmaiasis. (Thesis). Queensland University of Technology. Retrieved from http://eprints.qut.edu.au/92285/

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):

Faleiro, Rebecca Jacinto. “Development of immunotherapies and vaccines against visceral leishmaiasis.” 2016. Thesis, Queensland University of Technology. Accessed November 12, 2019. http://eprints.qut.edu.au/92285/.

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

MLA Handbook (7th Edition):

Faleiro, Rebecca Jacinto. “Development of immunotherapies and vaccines against visceral leishmaiasis.” 2016. Web. 12 Nov 2019.

Vancouver:

Faleiro RJ. Development of immunotherapies and vaccines against visceral leishmaiasis. [Internet] [Thesis]. Queensland University of Technology; 2016. [cited 2019 Nov 12]. Available from: http://eprints.qut.edu.au/92285/.

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

Council of Science Editors:

Faleiro RJ. Development of immunotherapies and vaccines against visceral leishmaiasis. [Thesis]. Queensland University of Technology; 2016. Available from: http://eprints.qut.edu.au/92285/

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


University of Otago

23. Ancelet, Lindsay Rae. The protective CD4⁺ memory T cell response to tuberculosis .

Degree: 2013, University of Otago

 Infection with Mycobacterium tuberculosis (Mtb), the pathogen responsible for tuberculosis (TB), results in 1.4 million deaths annually. The escalating rate of active TB, due to… (more)

Subjects/Keywords: BCG; memory; vaccination; immunity; tuberculosis; CD4+ T cells

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APA (6th Edition):

Ancelet, L. R. (2013). The protective CD4⁺ memory T cell response to tuberculosis . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/3922

Chicago Manual of Style (16th Edition):

Ancelet, Lindsay Rae. “The protective CD4⁺ memory T cell response to tuberculosis .” 2013. Doctoral Dissertation, University of Otago. Accessed November 12, 2019. http://hdl.handle.net/10523/3922.

MLA Handbook (7th Edition):

Ancelet, Lindsay Rae. “The protective CD4⁺ memory T cell response to tuberculosis .” 2013. Web. 12 Nov 2019.

Vancouver:

Ancelet LR. The protective CD4⁺ memory T cell response to tuberculosis . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/10523/3922.

Council of Science Editors:

Ancelet LR. The protective CD4⁺ memory T cell response to tuberculosis . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/3922


Georgia State University

24. Ko, Eunju. Immune mechanisms of influenza vaccine adjuvants and respiratory syncytial viral vaccines.

Degree: PhD, Biology, 2016, Georgia State University

  Adjuvants have been used for enhancing vaccine-specific immune responses, but the mechanisms of adjuvants and the roles of CD4 in adjuvant effects have been… (more)

Subjects/Keywords: Vaccine adjuvants; CD4+ T cells; Influenza virus; Respiratory syncytial virus

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APA (6th Edition):

Ko, E. (2016). Immune mechanisms of influenza vaccine adjuvants and respiratory syncytial viral vaccines. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/178

Chicago Manual of Style (16th Edition):

Ko, Eunju. “Immune mechanisms of influenza vaccine adjuvants and respiratory syncytial viral vaccines.” 2016. Doctoral Dissertation, Georgia State University. Accessed November 12, 2019. https://scholarworks.gsu.edu/biology_diss/178.

MLA Handbook (7th Edition):

Ko, Eunju. “Immune mechanisms of influenza vaccine adjuvants and respiratory syncytial viral vaccines.” 2016. Web. 12 Nov 2019.

Vancouver:

Ko E. Immune mechanisms of influenza vaccine adjuvants and respiratory syncytial viral vaccines. [Internet] [Doctoral dissertation]. Georgia State University; 2016. [cited 2019 Nov 12]. Available from: https://scholarworks.gsu.edu/biology_diss/178.

Council of Science Editors:

Ko E. Immune mechanisms of influenza vaccine adjuvants and respiratory syncytial viral vaccines. [Doctoral Dissertation]. Georgia State University; 2016. Available from: https://scholarworks.gsu.edu/biology_diss/178


University of Manchester

25. Zancanaro Krauss, Maria. CD4+ T cell metabolism during Trichuris muris infection.

Degree: 2018, University of Manchester

Trichuris trichiura is a gastrointestinal dwelling nematode that infects almost 500 million people worldwide. T. muris occurs naturally in mice and is very closely related… (more)

Subjects/Keywords: CD4+ T cells; immunometabolism; immunology; Trichuris muris; whipworm

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APA (6th Edition):

Zancanaro Krauss, M. (2018). CD4+ T cell metabolism during Trichuris muris infection. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314700

Chicago Manual of Style (16th Edition):

Zancanaro Krauss, Maria. “CD4+ T cell metabolism during Trichuris muris infection.” 2018. Doctoral Dissertation, University of Manchester. Accessed November 12, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314700.

MLA Handbook (7th Edition):

Zancanaro Krauss, Maria. “CD4+ T cell metabolism during Trichuris muris infection.” 2018. Web. 12 Nov 2019.

Vancouver:

Zancanaro Krauss M. CD4+ T cell metabolism during Trichuris muris infection. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Nov 12]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314700.

Council of Science Editors:

Zancanaro Krauss M. CD4+ T cell metabolism during Trichuris muris infection. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:314700


University of Manchester

26. Zancanaro Krauss, Maria Eduarda. CD4+ T cell metabolism during Trichuris muris infection.

Degree: PhD, 2018, University of Manchester

 Trichuris trichiura is a gastrointestinal dwelling nematode that infects almost 500 million people worldwide. T. muris occurs naturally in mice and is very closely related… (more)

Subjects/Keywords: Trichuris muris; whipworm; immunometabolism; CD4+ T cells; immunology

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APA (6th Edition):

Zancanaro Krauss, M. E. (2018). CD4+ T cell metabolism during Trichuris muris infection. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/cd4-t-cell-metabolism-during-trichuris-muris-infection(24eb0cc7-db70-46ea-ba49-e4fe3d5a5d03).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748068

Chicago Manual of Style (16th Edition):

Zancanaro Krauss, Maria Eduarda. “CD4+ T cell metabolism during Trichuris muris infection.” 2018. Doctoral Dissertation, University of Manchester. Accessed November 12, 2019. https://www.research.manchester.ac.uk/portal/en/theses/cd4-t-cell-metabolism-during-trichuris-muris-infection(24eb0cc7-db70-46ea-ba49-e4fe3d5a5d03).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748068.

MLA Handbook (7th Edition):

Zancanaro Krauss, Maria Eduarda. “CD4+ T cell metabolism during Trichuris muris infection.” 2018. Web. 12 Nov 2019.

Vancouver:

Zancanaro Krauss ME. CD4+ T cell metabolism during Trichuris muris infection. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2019 Nov 12]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/cd4-t-cell-metabolism-during-trichuris-muris-infection(24eb0cc7-db70-46ea-ba49-e4fe3d5a5d03).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748068.

Council of Science Editors:

Zancanaro Krauss ME. CD4+ T cell metabolism during Trichuris muris infection. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/cd4-t-cell-metabolism-during-trichuris-muris-infection(24eb0cc7-db70-46ea-ba49-e4fe3d5a5d03).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748068


University of Oxford

27. Baxter, Amy Elizabeth. HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis.

Degree: PhD, 2013, University of Oxford

 Within the paradigm of HIV-1 infection, macrophages play a crucial role as long-lived viral reservoirs. However, cell-free virus infection is inefficient and is unlikely to… (more)

Subjects/Keywords: 616.97; Infectious diseases; Viruses; macrophages; CD4 T cells; immune activation; phagocytosis

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APA (6th Edition):

Baxter, A. E. (2013). HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:1df105a3-1f0d-4159-8e01-3fdb231a0c42 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618453

Chicago Manual of Style (16th Edition):

Baxter, Amy Elizabeth. “HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis.” 2013. Doctoral Dissertation, University of Oxford. Accessed November 12, 2019. http://ora.ox.ac.uk/objects/uuid:1df105a3-1f0d-4159-8e01-3fdb231a0c42 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618453.

MLA Handbook (7th Edition):

Baxter, Amy Elizabeth. “HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis.” 2013. Web. 12 Nov 2019.

Vancouver:

Baxter AE. HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2019 Nov 12]. Available from: http://ora.ox.ac.uk/objects/uuid:1df105a3-1f0d-4159-8e01-3fdb231a0c42 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618453.

Council of Science Editors:

Baxter AE. HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:1df105a3-1f0d-4159-8e01-3fdb231a0c42 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.618453


University of Minnesota

28. Huddleston, Stephen James MD. Graft antigen-specific CD4+ T cells require CD154 expression to clonally expand and differentiate to the TH1 phenotype and initiate mTOR dependant intimal hyperplasia in cardiac allografts.

Degree: PhD, Surgery: Advisors: Marc K, 2009, University of Minnesota

 A defined model system was used to address the role of minor histocompatibility antigen-specific CD4+ T cells in cardiac allograft vasculoopathy (CAV). The coronary arteries… (more)

Subjects/Keywords: Cardiac Allograft; CD4+ T Cells; Intimal Hyperplasia; Vasculoopathy; Surgery

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

APA (6th Edition):

Huddleston, S. J. M. (2009). Graft antigen-specific CD4+ T cells require CD154 expression to clonally expand and differentiate to the TH1 phenotype and initiate mTOR dependant intimal hyperplasia in cardiac allografts. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/55013

Chicago Manual of Style (16th Edition):

Huddleston, Stephen James MD. “Graft antigen-specific CD4+ T cells require CD154 expression to clonally expand and differentiate to the TH1 phenotype and initiate mTOR dependant intimal hyperplasia in cardiac allografts.” 2009. Doctoral Dissertation, University of Minnesota. Accessed November 12, 2019. http://purl.umn.edu/55013.

MLA Handbook (7th Edition):

Huddleston, Stephen James MD. “Graft antigen-specific CD4+ T cells require CD154 expression to clonally expand and differentiate to the TH1 phenotype and initiate mTOR dependant intimal hyperplasia in cardiac allografts.” 2009. Web. 12 Nov 2019.

Vancouver:

Huddleston SJM. Graft antigen-specific CD4+ T cells require CD154 expression to clonally expand and differentiate to the TH1 phenotype and initiate mTOR dependant intimal hyperplasia in cardiac allografts. [Internet] [Doctoral dissertation]. University of Minnesota; 2009. [cited 2019 Nov 12]. Available from: http://purl.umn.edu/55013.

Council of Science Editors:

Huddleston SJM. Graft antigen-specific CD4+ T cells require CD154 expression to clonally expand and differentiate to the TH1 phenotype and initiate mTOR dependant intimal hyperplasia in cardiac allografts. [Doctoral Dissertation]. University of Minnesota; 2009. Available from: http://purl.umn.edu/55013


University of Newcastle

29. Graves, Moira Cecilia. Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis.

Degree: PhD, 2015, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Multiple sclerosis (MS) is proposed to be a T cell mediated immune disease of the central nervous system… (more)

Subjects/Keywords: multiple sclerosis; epigenetics; DNA methylation; CD4⁺ T cells

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

APA (6th Edition):

Graves, M. C. (2015). Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1310313

Chicago Manual of Style (16th Edition):

Graves, Moira Cecilia. “Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis.” 2015. Doctoral Dissertation, University of Newcastle. Accessed November 12, 2019. http://hdl.handle.net/1959.13/1310313.

MLA Handbook (7th Edition):

Graves, Moira Cecilia. “Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis.” 2015. Web. 12 Nov 2019.

Vancouver:

Graves MC. Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis. [Internet] [Doctoral dissertation]. University of Newcastle; 2015. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1959.13/1310313.

Council of Science Editors:

Graves MC. Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis. [Doctoral Dissertation]. University of Newcastle; 2015. Available from: http://hdl.handle.net/1959.13/1310313


University of Manitoba

30. Stalker, Andrew. Understanding the rapid expression of lymphocyte activation gene 3 (LAG-3) on healthy human T cells.

Degree: Medical Microbiology, 2015, University of Manitoba

 LAG-3 is an immune inhibitory marker. These immune inhibitory markers function to reduce the capability of immune cells to elicit a proper immune response and… (more)

Subjects/Keywords: LAG-3; Immunology; T cells; CD4; CD3; HIV

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

APA (6th Edition):

Stalker, A. (2015). Understanding the rapid expression of lymphocyte activation gene 3 (LAG-3) on healthy human T cells. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30708

Chicago Manual of Style (16th Edition):

Stalker, Andrew. “Understanding the rapid expression of lymphocyte activation gene 3 (LAG-3) on healthy human T cells.” 2015. Masters Thesis, University of Manitoba. Accessed November 12, 2019. http://hdl.handle.net/1993/30708.

MLA Handbook (7th Edition):

Stalker, Andrew. “Understanding the rapid expression of lymphocyte activation gene 3 (LAG-3) on healthy human T cells.” 2015. Web. 12 Nov 2019.

Vancouver:

Stalker A. Understanding the rapid expression of lymphocyte activation gene 3 (LAG-3) on healthy human T cells. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2019 Nov 12]. Available from: http://hdl.handle.net/1993/30708.

Council of Science Editors:

Stalker A. Understanding the rapid expression of lymphocyte activation gene 3 (LAG-3) on healthy human T cells. [Masters Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/30708

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