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You searched for subject:(CD4 T cells). Showing records 1 – 30 of 232 total matches.

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Tulane University

1. Moss, Daniel. Antigen Stability Influences Processing Efficiency and Immunogenicity of Pseudomonas Exotoxin Domain III and Ovalbumin.

Degree: 2020, Tulane University

[email protected]

Effective adaptive immune responses depend on the presentation to CD4+ T cells antigen peptides bound to major histocompatibility complex class II proteins. The structure… (more)

Subjects/Keywords: CD4+ T cells Antigen Processing

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APA (6th Edition):

Moss, D. (2020). Antigen Stability Influences Processing Efficiency and Immunogenicity of Pseudomonas Exotoxin Domain III and Ovalbumin. (Thesis). Tulane University. Retrieved from https://digitallibrary.tulane.edu/islandora/object/tulane:120437

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):

Moss, Daniel. “Antigen Stability Influences Processing Efficiency and Immunogenicity of Pseudomonas Exotoxin Domain III and Ovalbumin.” 2020. Thesis, Tulane University. Accessed September 30, 2020. https://digitallibrary.tulane.edu/islandora/object/tulane:120437.

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

MLA Handbook (7th Edition):

Moss, Daniel. “Antigen Stability Influences Processing Efficiency and Immunogenicity of Pseudomonas Exotoxin Domain III and Ovalbumin.” 2020. Web. 30 Sep 2020.

Vancouver:

Moss D. Antigen Stability Influences Processing Efficiency and Immunogenicity of Pseudomonas Exotoxin Domain III and Ovalbumin. [Internet] [Thesis]. Tulane University; 2020. [cited 2020 Sep 30]. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:120437.

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

Council of Science Editors:

Moss D. Antigen Stability Influences Processing Efficiency and Immunogenicity of Pseudomonas Exotoxin Domain III and Ovalbumin. [Thesis]. Tulane University; 2020. Available from: https://digitallibrary.tulane.edu/islandora/object/tulane:120437

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


University of Montana

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

Degree: PhD, 2013, University of Montana

  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). University of Montana. 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, University of Montana. Accessed September 30, 2020. https://scholarworks.umt.edu/etd/100.

MLA Handbook (7th Edition):

Osborne, Douglas Grant. “Biological effects of trogocytosis on CD4+ T lymphocytes.” 2013. Web. 30 Sep 2020.

Vancouver:

Osborne DG. Biological effects of trogocytosis on CD4+ T lymphocytes. [Internet] [Doctoral dissertation]. University of Montana; 2013. [cited 2020 Sep 30]. Available from: https://scholarworks.umt.edu/etd/100.

Council of Science Editors:

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

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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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


Virginia Tech

4. 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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Carbo Barrios A. Transdisciplinary Strategies to Study the Mechanisms of CD4+ T cell Differentiation and Heterogeneity. [Internet] [Doctoral dissertation]. Virginia Tech; 2014. [cited 2020 Sep 30]. 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

5. 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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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

6. 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 September 30, 2020. http://hdl.handle.net/10919/51228.

MLA Handbook (7th Edition):

Hong, Tian. “A framework for understanding heterogeneous differentiation of CD4⁺ T cells.” 2013. Web. 30 Sep 2020.

Vancouver:

Hong T. A framework for understanding heterogeneous differentiation of CD4⁺ T cells. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2020 Sep 30]. 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 Washington

7. 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 (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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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


University of KwaZulu-Natal

8. Laher, Faatima. Characterizing the role of CD4+ T cell immunoregulatory networks in peripheral blood and lymphoid tissue during HIV-1 clade C infection.

Degree: 2018, University of KwaZulu-Natal

 HIV eradication efforts have been unsuccessful due to virus persistence in cellular and tissue reservoirs. Recent evidence suggests that germinal centers (GCs) within lymph nodes… (more)

Subjects/Keywords: CD4⁺ T cell; CD4-Positive T-Lymphocytes immunology.; Immunology.; T cells.; HIV-1C.

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APA (6th Edition):

Laher, F. (2018). Characterizing the role of CD4+ T cell immunoregulatory networks in peripheral blood and lymphoid tissue during HIV-1 clade C infection. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/17525

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):

Laher, Faatima. “Characterizing the role of CD4+ T cell immunoregulatory networks in peripheral blood and lymphoid tissue during HIV-1 clade C infection.” 2018. Thesis, University of KwaZulu-Natal. Accessed September 30, 2020. https://researchspace.ukzn.ac.za/handle/10413/17525.

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

MLA Handbook (7th Edition):

Laher, Faatima. “Characterizing the role of CD4+ T cell immunoregulatory networks in peripheral blood and lymphoid tissue during HIV-1 clade C infection.” 2018. Web. 30 Sep 2020.

Vancouver:

Laher F. Characterizing the role of CD4+ T cell immunoregulatory networks in peripheral blood and lymphoid tissue during HIV-1 clade C infection. [Internet] [Thesis]. University of KwaZulu-Natal; 2018. [cited 2020 Sep 30]. Available from: https://researchspace.ukzn.ac.za/handle/10413/17525.

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

Council of Science Editors:

Laher F. Characterizing the role of CD4+ T cell immunoregulatory networks in peripheral blood and lymphoid tissue during HIV-1 clade C infection. [Thesis]. University of KwaZulu-Natal; 2018. Available from: https://researchspace.ukzn.ac.za/handle/10413/17525

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


University of Rochester

9. 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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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

10. 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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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

11. 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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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


University of Cincinnati

12. 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 (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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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

13. Binet, Bénédicte. Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1 : Epigenetic regulation of CD4 T cell programmation by SETDB1.

Degree: Docteur es, Immunologie, 2017, Université Toulouse III – Paul Sabatier

Chez les mammifères, les lymphocytes T CD4 sont essentiels à la défense de l’organisme contre des infections par des pathogènes ou le développement de tumeurs.… (more)

Subjects/Keywords: SETDB1; Lymphocytes T CD4; Épigénétique; Différenciation; T helper; Rétrovirus endogènes; CD4 T cells; Epigenetic; Differentiation; T helper; Endogenous retroviruses

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APA (6th Edition):

Binet, B. (2017). Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1 : Epigenetic regulation of CD4 T cell programmation by SETDB1. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2017TOU30217

Chicago Manual of Style (16th Edition):

Binet, Bénédicte. “Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1 : Epigenetic regulation of CD4 T cell programmation by SETDB1.” 2017. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed September 30, 2020. http://www.theses.fr/2017TOU30217.

MLA Handbook (7th Edition):

Binet, Bénédicte. “Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1 : Epigenetic regulation of CD4 T cell programmation by SETDB1.” 2017. Web. 30 Sep 2020.

Vancouver:

Binet B. Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1 : Epigenetic regulation of CD4 T cell programmation by SETDB1. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2017. [cited 2020 Sep 30]. Available from: http://www.theses.fr/2017TOU30217.

Council of Science Editors:

Binet B. Régulation épigénétique de la programmation des lymphocytes T CD4 par SETDB1 : Epigenetic regulation of CD4 T cell programmation by SETDB1. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2017. Available from: http://www.theses.fr/2017TOU30217


Universitat Pompeu Fabra

14. 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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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

15. 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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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

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, Université Côte d'Azur (ComUE)

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

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). Université Côte d'Azur (ComUE). 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, Université Côte d'Azur (ComUE). Accessed September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Boucoiran A. Étude des interactions ostéoimmunologiques dans les maladies inflammatoires chroniques de l’intestin : Osteoimmunological interaction in inflammatory bowel diseases. [Internet] [Doctoral dissertation]. Université Côte d'Azur (ComUE); 2016. [cited 2020 Sep 30]. 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]. Université Côte d'Azur (ComUE); 2016. Available from: http://www.theses.fr/2016AZUR4064

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

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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Aguilera-Sandoval CR. The Dynamic Interplay between HIV-1 and T cells. [Internet] [Thesis]. UCLA; 2016. [cited 2020 Sep 30]. 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

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

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 September 30, 2020. http://hdl.handle.net/1773/35290.

MLA Handbook (7th Edition):

Soerens, Andrew Glenn. “Regulatory T cell contributions to mucosal antiviral immunity.” 2016. Web. 30 Sep 2020.

Vancouver:

Soerens AG. Regulatory T cell contributions to mucosal antiviral immunity. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Sep 30]. 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 New Mexico

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

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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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


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

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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Collins N. Memory CD4 T cells in skin at steady-state and following infection. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2020 Sep 30]. 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 Melbourne

21. Wang, Minyu. Investigating the immune landscape in gastric cancer.

Degree: 2019, University of Melbourne

 This thesis investigates the relationship between the immunological microenvironment and clinical outcomes of patients diagnosed with gastric cancer (GC). I conducted a comprehensive study integrating… (more)

Subjects/Keywords: Gastric cancer; Immune response; Tumour microenvironment; CD8+ T cells; CD4+FOXP3+ T cells; Prognosis

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APA (6th Edition):

Wang, M. (2019). Investigating the immune landscape in gastric cancer. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/233656

Chicago Manual of Style (16th Edition):

Wang, Minyu. “Investigating the immune landscape in gastric cancer.” 2019. Doctoral Dissertation, University of Melbourne. Accessed September 30, 2020. http://hdl.handle.net/11343/233656.

MLA Handbook (7th Edition):

Wang, Minyu. “Investigating the immune landscape in gastric cancer.” 2019. Web. 30 Sep 2020.

Vancouver:

Wang M. Investigating the immune landscape in gastric cancer. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/11343/233656.

Council of Science Editors:

Wang M. Investigating the immune landscape in gastric cancer. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/233656


University of Georgia

22. Hohos, Natalie Marie. Epigenetics of obesity.

Degree: 2017, University of Georgia

 Obesity is a complex disease involving interactions between genetics and the environment. Epigenetic modifications are able to integrate changes in the environment (i.e. diet) into… (more)

Subjects/Keywords: DNA methylation; obesity; weight loss; leukocytes; CD4+ T cells; CD8+ T cells; adiposity; VAT

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APA (6th Edition):

Hohos, N. M. (2017). Epigenetics of obesity. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/36762

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):

Hohos, Natalie Marie. “Epigenetics of obesity.” 2017. Thesis, University of Georgia. Accessed September 30, 2020. http://hdl.handle.net/10724/36762.

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

MLA Handbook (7th Edition):

Hohos, Natalie Marie. “Epigenetics of obesity.” 2017. Web. 30 Sep 2020.

Vancouver:

Hohos NM. Epigenetics of obesity. [Internet] [Thesis]. University of Georgia; 2017. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/10724/36762.

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

Council of Science Editors:

Hohos NM. Epigenetics of obesity. [Thesis]. University of Georgia; 2017. Available from: http://hdl.handle.net/10724/36762

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

23. Mattiuz, Raphaël. Rôle des cellules dendritiques conventionnelles de type 1 dans l'immunosurveillance des cancers : Role of type 1 conventional dendritic cells in cancer immunosurveillance.

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

Nous avons généré les souris Xcr1-DTA, Karma et Xcr1-hDTR pour éliminer les cellules dendritiques conventionnelles de type 1 (cDC1) de manière constitutive ou conditionnelle, et… (more)

Subjects/Keywords: Cellules Dendritiques; Cdc1; Immunosurveillance des cancers; Lymphocytes T CD8+; Lymphocytes T CD4+; Interférons; Dendritic Cells; Cdc1; Cancer Immunosurveillance; CD8+ T cells; CD4+ T cells; Interferons; 571

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

APA (6th Edition):

Mattiuz, R. (2019). Rôle des cellules dendritiques conventionnelles de type 1 dans l'immunosurveillance des cancers : Role of type 1 conventional dendritic cells in cancer immunosurveillance. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2019AIXM0437

Chicago Manual of Style (16th Edition):

Mattiuz, Raphaël. “Rôle des cellules dendritiques conventionnelles de type 1 dans l'immunosurveillance des cancers : Role of type 1 conventional dendritic cells in cancer immunosurveillance.” 2019. Doctoral Dissertation, Aix Marseille Université. Accessed September 30, 2020. http://www.theses.fr/2019AIXM0437.

MLA Handbook (7th Edition):

Mattiuz, Raphaël. “Rôle des cellules dendritiques conventionnelles de type 1 dans l'immunosurveillance des cancers : Role of type 1 conventional dendritic cells in cancer immunosurveillance.” 2019. Web. 30 Sep 2020.

Vancouver:

Mattiuz R. Rôle des cellules dendritiques conventionnelles de type 1 dans l'immunosurveillance des cancers : Role of type 1 conventional dendritic cells in cancer immunosurveillance. [Internet] [Doctoral dissertation]. Aix Marseille Université 2019. [cited 2020 Sep 30]. Available from: http://www.theses.fr/2019AIXM0437.

Council of Science Editors:

Mattiuz R. Rôle des cellules dendritiques conventionnelles de type 1 dans l'immunosurveillance des cancers : Role of type 1 conventional dendritic cells in cancer immunosurveillance. [Doctoral Dissertation]. Aix Marseille Université 2019. Available from: http://www.theses.fr/2019AIXM0437


University of Manchester

24. 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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Zancanaro Krauss M. CD4+ T cell metabolism during Trichuris muris infection. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Sep 30]. 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 Newcastle

25. 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 (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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Graves MC. Epigenetic variations and psychosocial parameters in relapsing-remitting multiple sclerosis. [Internet] [Doctoral dissertation]. University of Newcastle; 2015. [cited 2020 Sep 30]. 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

26. 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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Faleiro RJ. Development of immunotherapies and vaccines against visceral leishmaiasis. [Internet] [Thesis]. Queensland University of Technology; 2016. [cited 2020 Sep 30]. 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

27. 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 September 30, 2020. http://hdl.handle.net/10523/3922.

MLA Handbook (7th Edition):

Ancelet, Lindsay Rae. “The protective CD4⁺ memory T cell response to tuberculosis .” 2013. Web. 30 Sep 2020.

Vancouver:

Ancelet LR. The protective CD4⁺ memory T cell response to tuberculosis . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2020 Sep 30]. 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


University of Manitoba

28. 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 (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 September 30, 2020. 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. 30 Sep 2020.

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 2020 Sep 30]. 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


University of Oxford

29. 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 September 30, 2020. 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. 30 Sep 2020.

Vancouver:

Baxter AE. HIV-1 transmission between T cells and macrophages : consequences for viral pathogenesis. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Sep 30]. 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 Melbourne

30. REECE, JEANETTE CAROLINE. Immune escape from Simian immunodeficiency virus (SIV): implications for vaccination and tracking latent virus.

Degree: 2013, University of Melbourne

 Background: Despite the urgency, a safe and effective human immunodeficiency virus (HIV) vaccine does not exist. Virus-specific cytotoxic T lymphocytes (CTLs) are important in modulating… (more)

Subjects/Keywords: SIV; latent virus; resting CD4+ T cells; vaccination; pigtail macaques

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

APA (6th Edition):

REECE, J. C. (2013). Immune escape from Simian immunodeficiency virus (SIV): implications for vaccination and tracking latent virus. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38585

Chicago Manual of Style (16th Edition):

REECE, JEANETTE CAROLINE. “Immune escape from Simian immunodeficiency virus (SIV): implications for vaccination and tracking latent virus.” 2013. Doctoral Dissertation, University of Melbourne. Accessed September 30, 2020. http://hdl.handle.net/11343/38585.

MLA Handbook (7th Edition):

REECE, JEANETTE CAROLINE. “Immune escape from Simian immunodeficiency virus (SIV): implications for vaccination and tracking latent virus.” 2013. Web. 30 Sep 2020.

Vancouver:

REECE JC. Immune escape from Simian immunodeficiency virus (SIV): implications for vaccination and tracking latent virus. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/11343/38585.

Council of Science Editors:

REECE JC. Immune escape from Simian immunodeficiency virus (SIV): implications for vaccination and tracking latent virus. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38585

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