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You searched for subject:(Cross presentation). Showing records 1 – 30 of 54 total matches.

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Queens University

1. Kim, Julia. The Influence of 1,25-Dihydroxyvitamin D3 on the Cross-Priming of Lymphocytic Choriomeningitis Virus Nucleoprotein .

Degree: Microbiology and Immunology, 2011, Queens University

 Biologically active 1,25-dihydroxyvitamin D3 (1,25-(OH)2D3) binds the vitamin D receptor (VDR) to exert its effect on target cells. VDR expression is found in a number… (more)

Subjects/Keywords: 1,25-Dihydroxyvitamin D3 ; Lymphocytic Choriomeningitis Virus Nucleoprotein ; Cross presentation ; 1,25-(OH)2D3 ; Cross priming

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APA (6th Edition):

Kim, J. (2011). The Influence of 1,25-Dihydroxyvitamin D3 on the Cross-Priming of Lymphocytic Choriomeningitis Virus Nucleoprotein . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6701

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):

Kim, Julia. “The Influence of 1,25-Dihydroxyvitamin D3 on the Cross-Priming of Lymphocytic Choriomeningitis Virus Nucleoprotein .” 2011. Thesis, Queens University. Accessed May 08, 2021. http://hdl.handle.net/1974/6701.

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

MLA Handbook (7th Edition):

Kim, Julia. “The Influence of 1,25-Dihydroxyvitamin D3 on the Cross-Priming of Lymphocytic Choriomeningitis Virus Nucleoprotein .” 2011. Web. 08 May 2021.

Vancouver:

Kim J. The Influence of 1,25-Dihydroxyvitamin D3 on the Cross-Priming of Lymphocytic Choriomeningitis Virus Nucleoprotein . [Internet] [Thesis]. Queens University; 2011. [cited 2021 May 08]. Available from: http://hdl.handle.net/1974/6701.

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

Council of Science Editors:

Kim J. The Influence of 1,25-Dihydroxyvitamin D3 on the Cross-Priming of Lymphocytic Choriomeningitis Virus Nucleoprotein . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6701

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


University of Sydney

2. Yuan, Ming. Who will be nice and who will be nasty?: a cross-cultural investigation of children’s moral trait inferences .

Degree: 2014, University of Sydney

 In this thesis, four studies were conducted to examine how children aged 4 to 8 years and adults from China and Australia made moral trait… (more)

Subjects/Keywords: Trait inference; Moral reasoning; Self-presentation; Impression management; Cross-cultural

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APA (6th Edition):

Yuan, M. (2014). Who will be nice and who will be nasty?: a cross-cultural investigation of children’s moral trait inferences . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/12734

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):

Yuan, Ming. “Who will be nice and who will be nasty?: a cross-cultural investigation of children’s moral trait inferences .” 2014. Thesis, University of Sydney. Accessed May 08, 2021. http://hdl.handle.net/2123/12734.

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

MLA Handbook (7th Edition):

Yuan, Ming. “Who will be nice and who will be nasty?: a cross-cultural investigation of children’s moral trait inferences .” 2014. Web. 08 May 2021.

Vancouver:

Yuan M. Who will be nice and who will be nasty?: a cross-cultural investigation of children’s moral trait inferences . [Internet] [Thesis]. University of Sydney; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/2123/12734.

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

Council of Science Editors:

Yuan M. Who will be nice and who will be nasty?: a cross-cultural investigation of children’s moral trait inferences . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/12734

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


University of Melbourne

3. OVEISSI, SARA. Cross‐priming of TCD8+ specific for cell‐associated antigens.

Degree: 2014, University of Melbourne

 TCD8+ of the adaptive immune system play critical roles in the host defence against viruses and other pathogens through elimination of infected host cells. After… (more)

Subjects/Keywords: cross-presentation; dendritic cells; microinjection transgenesis; allogeneic response; alternative reading frame

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APA (6th Edition):

OVEISSI, S. (2014). Cross‐priming of TCD8+ specific for cell‐associated antigens. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/44081

Chicago Manual of Style (16th Edition):

OVEISSI, SARA. “Cross‐priming of TCD8+ specific for cell‐associated antigens.” 2014. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/44081.

MLA Handbook (7th Edition):

OVEISSI, SARA. “Cross‐priming of TCD8+ specific for cell‐associated antigens.” 2014. Web. 08 May 2021.

Vancouver:

OVEISSI S. Cross‐priming of TCD8+ specific for cell‐associated antigens. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/44081.

Council of Science Editors:

OVEISSI S. Cross‐priming of TCD8+ specific for cell‐associated antigens. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/44081


Leiden University

4. Pawlak, J.B. Bioorthogonal Antigens.

Degree: 2017, Leiden University

  <table width="100%"> <tbody><tr> <td> The aim of this thesis is to explore the use of Bioorthogonal Antigens to study the cross-presentation pathway. Bioorthogonal Antigens… (more)

Subjects/Keywords: Antigen Cross Presentation; Click Chemistry

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APA (6th Edition):

Pawlak, J. B. (2017). Bioorthogonal Antigens. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/55262

Chicago Manual of Style (16th Edition):

Pawlak, J B. “Bioorthogonal Antigens.” 2017. Doctoral Dissertation, Leiden University. Accessed May 08, 2021. http://hdl.handle.net/1887/55262.

MLA Handbook (7th Edition):

Pawlak, J B. “Bioorthogonal Antigens.” 2017. Web. 08 May 2021.

Vancouver:

Pawlak JB. Bioorthogonal Antigens. [Internet] [Doctoral dissertation]. Leiden University; 2017. [cited 2021 May 08]. Available from: http://hdl.handle.net/1887/55262.

Council of Science Editors:

Pawlak JB. Bioorthogonal Antigens. [Doctoral Dissertation]. Leiden University; 2017. Available from: http://hdl.handle.net/1887/55262


Universiteit Utrecht

5. Compeer, E.B. Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity.

Degree: 2015, Universiteit Utrecht

 We, humans, are exposed daily to millions of potential pathogens, through contact, inhalation, or ingestion. Our ability to avoid infection depends on our immune system,… (more)

Subjects/Keywords: Antigen cross-presentation; tubulation; endosomes; MICAL-L1; Fcɣ-receptors; Common Variable Immunodeficiency; BLK

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APA (6th Edition):

Compeer, E. B. (2015). Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/312537

Chicago Manual of Style (16th Edition):

Compeer, E B. “Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed May 08, 2021. http://dspace.library.uu.nl:8080/handle/1874/312537.

MLA Handbook (7th Edition):

Compeer, E B. “Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity.” 2015. Web. 08 May 2021.

Vancouver:

Compeer EB. Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 May 08]. Available from: http://dspace.library.uu.nl:8080/handle/1874/312537.

Council of Science Editors:

Compeer EB. Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/312537


Texas Medical Center

6. Carmona, Selena. Characterizing the source of neutrophil elastase and proteinase 3 cross-presentation in B-cell acute lymphoblastic leukemia.

Degree: MS, 2017, Texas Medical Center

  Discovery of tumor-associated antigens is an important step in designing effective antigen-targeting immunotherapies. PR1 is a nonameric human leukocyte antigen (HLA)-A2 restricted leukemia-associated antigen… (more)

Subjects/Keywords: cross-presentation; neutrophil elastase; proteinase 3; 8F4; PR1; acute lymphoblastic leukemia; Medicine and Health Sciences

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APA (6th Edition):

Carmona, S. (2017). Characterizing the source of neutrophil elastase and proteinase 3 cross-presentation in B-cell acute lymphoblastic leukemia. (Thesis). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/751

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):

Carmona, Selena. “Characterizing the source of neutrophil elastase and proteinase 3 cross-presentation in B-cell acute lymphoblastic leukemia.” 2017. Thesis, Texas Medical Center. Accessed May 08, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/751.

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

MLA Handbook (7th Edition):

Carmona, Selena. “Characterizing the source of neutrophil elastase and proteinase 3 cross-presentation in B-cell acute lymphoblastic leukemia.” 2017. Web. 08 May 2021.

Vancouver:

Carmona S. Characterizing the source of neutrophil elastase and proteinase 3 cross-presentation in B-cell acute lymphoblastic leukemia. [Internet] [Thesis]. Texas Medical Center; 2017. [cited 2021 May 08]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/751.

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

Council of Science Editors:

Carmona S. Characterizing the source of neutrophil elastase and proteinase 3 cross-presentation in B-cell acute lymphoblastic leukemia. [Thesis]. Texas Medical Center; 2017. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/751

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


University of Adelaide

7. Trahair, Hugh Francis Llewellyn. Suicide genes in a novel vaccination strategy for hepatitis C.

Degree: 2012, University of Adelaide

 Hepatitis C virus (HCV) is a blood transmitted virus which causes persistent infection of the liver greatly resulting in cirrhosis and hepatocellular carcinoma. Current treatment… (more)

Subjects/Keywords: suicide genes; DNA vaccine; HCV; hepatitis C; cross presentation; CMI T-cells; necrosis

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APA (6th Edition):

Trahair, H. F. L. (2012). Suicide genes in a novel vaccination strategy for hepatitis C. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/96472

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):

Trahair, Hugh Francis Llewellyn. “Suicide genes in a novel vaccination strategy for hepatitis C.” 2012. Thesis, University of Adelaide. Accessed May 08, 2021. http://hdl.handle.net/2440/96472.

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

MLA Handbook (7th Edition):

Trahair, Hugh Francis Llewellyn. “Suicide genes in a novel vaccination strategy for hepatitis C.” 2012. Web. 08 May 2021.

Vancouver:

Trahair HFL. Suicide genes in a novel vaccination strategy for hepatitis C. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2021 May 08]. Available from: http://hdl.handle.net/2440/96472.

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

Council of Science Editors:

Trahair HFL. Suicide genes in a novel vaccination strategy for hepatitis C. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/96472

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


Freie Universität Berlin

8. Güttler, Steffen. Functional characterization of XCR1-positive dendritic cells in mouse and man.

Degree: 2012, Freie Universität Berlin

 The background for this study was the observation of selective expression of the chemokine receptor XCR1 on CD8+ Dendritic cells (DCs) of the murine spleen.… (more)

Subjects/Keywords: antigen; cross-presentation; Dendritic cell; XCR1; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Güttler, S. (2012). Functional characterization of XCR1-positive dendritic cells in mouse and man. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/11231

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):

Güttler, Steffen. “Functional characterization of XCR1-positive dendritic cells in mouse and man.” 2012. Thesis, Freie Universität Berlin. Accessed May 08, 2021. https://refubium.fu-berlin.de/handle/fub188/11231.

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

MLA Handbook (7th Edition):

Güttler, Steffen. “Functional characterization of XCR1-positive dendritic cells in mouse and man.” 2012. Web. 08 May 2021.

Vancouver:

Güttler S. Functional characterization of XCR1-positive dendritic cells in mouse and man. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2021 May 08]. Available from: https://refubium.fu-berlin.de/handle/fub188/11231.

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

Council of Science Editors:

Güttler S. Functional characterization of XCR1-positive dendritic cells in mouse and man. [Thesis]. Freie Universität Berlin; 2012. Available from: https://refubium.fu-berlin.de/handle/fub188/11231

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


University of Toronto

9. Anczurowski, Mark. Molecular Mechanisms of Cross-Presentation on HLA-DP84Gly.

Degree: PhD, 2019, University of Toronto

The human leukocyte antigens (HLA) genes are well-established in connecting the innate and adaptive arms of immunity. In humans, three subclasses of antigen-presenting HLA molecules… (more)

Subjects/Keywords: CLIP; Cross-presentation; HLA class II; HLA-DP; Invariant chain; MHC class II; 0982

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APA (6th Edition):

Anczurowski, M. (2019). Molecular Mechanisms of Cross-Presentation on HLA-DP84Gly. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/100344

Chicago Manual of Style (16th Edition):

Anczurowski, Mark. “Molecular Mechanisms of Cross-Presentation on HLA-DP84Gly.” 2019. Doctoral Dissertation, University of Toronto. Accessed May 08, 2021. http://hdl.handle.net/1807/100344.

MLA Handbook (7th Edition):

Anczurowski, Mark. “Molecular Mechanisms of Cross-Presentation on HLA-DP84Gly.” 2019. Web. 08 May 2021.

Vancouver:

Anczurowski M. Molecular Mechanisms of Cross-Presentation on HLA-DP84Gly. [Internet] [Doctoral dissertation]. University of Toronto; 2019. [cited 2021 May 08]. Available from: http://hdl.handle.net/1807/100344.

Council of Science Editors:

Anczurowski M. Molecular Mechanisms of Cross-Presentation on HLA-DP84Gly. [Doctoral Dissertation]. University of Toronto; 2019. Available from: http://hdl.handle.net/1807/100344

10. CHUA RONG YUAN, RAY. SORTING NEXIN 3 REGULATES PHAGOCYTOSIS AND CROSS-PRESENTATION IN DENDRITIC CELLS.

Degree: 2012, National University of Singapore

Subjects/Keywords: SNX-3; Phagocytosis; Cross-presentation; DC

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APA (6th Edition):

CHUA RONG YUAN, R. (2012). SORTING NEXIN 3 REGULATES PHAGOCYTOSIS AND CROSS-PRESENTATION IN DENDRITIC CELLS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/35584

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):

CHUA RONG YUAN, RAY. “SORTING NEXIN 3 REGULATES PHAGOCYTOSIS AND CROSS-PRESENTATION IN DENDRITIC CELLS.” 2012. Thesis, National University of Singapore. Accessed May 08, 2021. http://scholarbank.nus.edu.sg/handle/10635/35584.

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

MLA Handbook (7th Edition):

CHUA RONG YUAN, RAY. “SORTING NEXIN 3 REGULATES PHAGOCYTOSIS AND CROSS-PRESENTATION IN DENDRITIC CELLS.” 2012. Web. 08 May 2021.

Vancouver:

CHUA RONG YUAN R. SORTING NEXIN 3 REGULATES PHAGOCYTOSIS AND CROSS-PRESENTATION IN DENDRITIC CELLS. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2021 May 08]. Available from: http://scholarbank.nus.edu.sg/handle/10635/35584.

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

Council of Science Editors:

CHUA RONG YUAN R. SORTING NEXIN 3 REGULATES PHAGOCYTOSIS AND CROSS-PRESENTATION IN DENDRITIC CELLS. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/35584

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


Penn State University

11. Vigliotti, Beth Anne. CD8+ T CELL RESPONSES TO SIMIAN VIRUS 40 LARGE T ANTIGEN MINIMAL EPITOPES EXPRESSED BY NON-PROFESSIONAL ANTIGEN PRESENTING CELLS .

Degree: 2009, Penn State University

 In this study we describe a straightforward model that allows for the study of direct-presentation of antigen on transformed non-professional antigen presenting cells (non-pAPCs) in… (more)

Subjects/Keywords: CD8+ T cell; immunology; cross-presentation; direct-presentation; SV40; large T antigen; minigenes

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APA (6th Edition):

Vigliotti, B. A. (2009). CD8+ T CELL RESPONSES TO SIMIAN VIRUS 40 LARGE T ANTIGEN MINIMAL EPITOPES EXPRESSED BY NON-PROFESSIONAL ANTIGEN PRESENTING CELLS . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/9477

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):

Vigliotti, Beth Anne. “CD8+ T CELL RESPONSES TO SIMIAN VIRUS 40 LARGE T ANTIGEN MINIMAL EPITOPES EXPRESSED BY NON-PROFESSIONAL ANTIGEN PRESENTING CELLS .” 2009. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/9477.

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

MLA Handbook (7th Edition):

Vigliotti, Beth Anne. “CD8+ T CELL RESPONSES TO SIMIAN VIRUS 40 LARGE T ANTIGEN MINIMAL EPITOPES EXPRESSED BY NON-PROFESSIONAL ANTIGEN PRESENTING CELLS .” 2009. Web. 08 May 2021.

Vancouver:

Vigliotti BA. CD8+ T CELL RESPONSES TO SIMIAN VIRUS 40 LARGE T ANTIGEN MINIMAL EPITOPES EXPRESSED BY NON-PROFESSIONAL ANTIGEN PRESENTING CELLS . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/9477.

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

Council of Science Editors:

Vigliotti BA. CD8+ T CELL RESPONSES TO SIMIAN VIRUS 40 LARGE T ANTIGEN MINIMAL EPITOPES EXPRESSED BY NON-PROFESSIONAL ANTIGEN PRESENTING CELLS . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/9477

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

12. Choi, Aaron. IL-32-Derived Dendritic Cells Cross-Present Defined Mycobacterium leprae Antigens to CD8+ T cells.

Degree: Microbiology, Immunology, & Molecular Genetics, 2018, UCLA

 Leprosy is a human disease caused by the intracellular pathogen Mycobacterium leprae. By investigating leprosy, we discovered a novel pathway involving NOD2-mediated induction of interleukin-32… (more)

Subjects/Keywords: Immunology; antigen presentation; CD8; Cross-presentation; IL-32; Leprosy; NOD2

…polymorphisms were discovered to be associated with susceptibility to leprosy13. CROSS-PRESENTATION… …exogenous source13. There are two main pathways that have been suggested for cross-presentation… …the CD8+ T cell clones. Understanding cross-presentation will provide new information about… …endocytic pathway. Insights gained from cross-presentation and activation of CD8+ T cells may… …cross-presentation and a list of genes involved in both pathways that are upregulated in IL-32… 

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APA (6th Edition):

Choi, A. (2018). IL-32-Derived Dendritic Cells Cross-Present Defined Mycobacterium leprae Antigens to CD8+ T cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/8mg9460b

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):

Choi, Aaron. “IL-32-Derived Dendritic Cells Cross-Present Defined Mycobacterium leprae Antigens to CD8+ T cells.” 2018. Thesis, UCLA. Accessed May 08, 2021. http://www.escholarship.org/uc/item/8mg9460b.

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

MLA Handbook (7th Edition):

Choi, Aaron. “IL-32-Derived Dendritic Cells Cross-Present Defined Mycobacterium leprae Antigens to CD8+ T cells.” 2018. Web. 08 May 2021.

Vancouver:

Choi A. IL-32-Derived Dendritic Cells Cross-Present Defined Mycobacterium leprae Antigens to CD8+ T cells. [Internet] [Thesis]. UCLA; 2018. [cited 2021 May 08]. Available from: http://www.escholarship.org/uc/item/8mg9460b.

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

Council of Science Editors:

Choi A. IL-32-Derived Dendritic Cells Cross-Present Defined Mycobacterium leprae Antigens to CD8+ T cells. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/8mg9460b

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


Vrije Universiteit Amsterdam

13. Backer, R.A. Function and homeostasis of murine splenic dendritic cell subsets .

Degree: 2009, Vrije Universiteit Amsterdam

Subjects/Keywords: dendritic cell subsets; antigen-presentation; cross-presentation; antigen-transfer; SIRPalpha

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APA (6th Edition):

Backer, R. A. (2009). Function and homeostasis of murine splenic dendritic cell subsets . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/28773

Chicago Manual of Style (16th Edition):

Backer, R A. “Function and homeostasis of murine splenic dendritic cell subsets .” 2009. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed May 08, 2021. http://hdl.handle.net/1871/28773.

MLA Handbook (7th Edition):

Backer, R A. “Function and homeostasis of murine splenic dendritic cell subsets .” 2009. Web. 08 May 2021.

Vancouver:

Backer RA. Function and homeostasis of murine splenic dendritic cell subsets . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2009. [cited 2021 May 08]. Available from: http://hdl.handle.net/1871/28773.

Council of Science Editors:

Backer RA. Function and homeostasis of murine splenic dendritic cell subsets . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2009. Available from: http://hdl.handle.net/1871/28773


Penn State University

14. Watson, Alan Michael. PEPTIDE-MHC-STABILITY DETERMINES THE SIZE OF THE CD8+ T CELL RESPONSE TOWARD AN IMMUNORECESSIVE TUMOR ANTIGEN DETERMINANT .

Degree: 2011, Penn State University

 CD8+ T cells recognize peptide-determinants bound to major histocompatibility complex class-I (MHC-I) molecules on the surface of antigen presenting cells. Differences in the number of… (more)

Subjects/Keywords: Antigen Presentation; Cross-Priming; Peptide MHC Stability; Peptide; T cell; SV40 T Antigen; Tumor; Cancer; Mouse

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APA (6th Edition):

Watson, A. M. (2011). PEPTIDE-MHC-STABILITY DETERMINES THE SIZE OF THE CD8+ T CELL RESPONSE TOWARD AN IMMUNORECESSIVE TUMOR ANTIGEN DETERMINANT . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/11971

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):

Watson, Alan Michael. “PEPTIDE-MHC-STABILITY DETERMINES THE SIZE OF THE CD8+ T CELL RESPONSE TOWARD AN IMMUNORECESSIVE TUMOR ANTIGEN DETERMINANT .” 2011. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/11971.

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

MLA Handbook (7th Edition):

Watson, Alan Michael. “PEPTIDE-MHC-STABILITY DETERMINES THE SIZE OF THE CD8+ T CELL RESPONSE TOWARD AN IMMUNORECESSIVE TUMOR ANTIGEN DETERMINANT .” 2011. Web. 08 May 2021.

Vancouver:

Watson AM. PEPTIDE-MHC-STABILITY DETERMINES THE SIZE OF THE CD8+ T CELL RESPONSE TOWARD AN IMMUNORECESSIVE TUMOR ANTIGEN DETERMINANT . [Internet] [Thesis]. Penn State University; 2011. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/11971.

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

Council of Science Editors:

Watson AM. PEPTIDE-MHC-STABILITY DETERMINES THE SIZE OF THE CD8+ T CELL RESPONSE TOWARD AN IMMUNORECESSIVE TUMOR ANTIGEN DETERMINANT . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/11971

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


Texas Medical Center

15. Perakis, Alexander A. Cross-presentation Is A Source of Tumor Antigens For Multiple Myeloma Immunotherapy.

Degree: PhD, 2019, Texas Medical Center

Cross-presentation is an essential bridge between the innate and adaptive arms of the immune system where antigen presenting cells (APCs) prime cytotoxic T cell… (more)

Subjects/Keywords: multiple myeloma; immunotherapy; cross-presentation; antibody; Biology; Cancer Biology; Immunology and Infectious Disease; Medicine and Health Sciences

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

APA (6th Edition):

Perakis, A. A. (2019). Cross-presentation Is A Source of Tumor Antigens For Multiple Myeloma Immunotherapy. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/949

Chicago Manual of Style (16th Edition):

Perakis, Alexander A. “Cross-presentation Is A Source of Tumor Antigens For Multiple Myeloma Immunotherapy.” 2019. Doctoral Dissertation, Texas Medical Center. Accessed May 08, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/949.

MLA Handbook (7th Edition):

Perakis, Alexander A. “Cross-presentation Is A Source of Tumor Antigens For Multiple Myeloma Immunotherapy.” 2019. Web. 08 May 2021.

Vancouver:

Perakis AA. Cross-presentation Is A Source of Tumor Antigens For Multiple Myeloma Immunotherapy. [Internet] [Doctoral dissertation]. Texas Medical Center; 2019. [cited 2021 May 08]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/949.

Council of Science Editors:

Perakis AA. Cross-presentation Is A Source of Tumor Antigens For Multiple Myeloma Immunotherapy. [Doctoral Dissertation]. Texas Medical Center; 2019. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/949


Universidade Nova

16. Oliveira, Mariana Miguel Sabino. Cross-presentation by WASp deficient B cells and dendritic cells.

Degree: 2016, Universidade Nova

 The immune system comprises of different cell types whose role is to protect us against pathogens. This thesis investigates a very important mechanism for our… (more)

Subjects/Keywords: Cross-presentation; B cells; Dendritic cells; Acidification; ROS production; Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química

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APA (6th Edition):

Oliveira, M. M. S. (2016). Cross-presentation by WASp deficient B cells and dendritic cells. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/17047

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):

Oliveira, Mariana Miguel Sabino. “Cross-presentation by WASp deficient B cells and dendritic cells.” 2016. Thesis, Universidade Nova. Accessed May 08, 2021. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/17047.

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

MLA Handbook (7th Edition):

Oliveira, Mariana Miguel Sabino. “Cross-presentation by WASp deficient B cells and dendritic cells.” 2016. Web. 08 May 2021.

Vancouver:

Oliveira MMS. Cross-presentation by WASp deficient B cells and dendritic cells. [Internet] [Thesis]. Universidade Nova; 2016. [cited 2021 May 08]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/17047.

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

Council of Science Editors:

Oliveira MMS. Cross-presentation by WASp deficient B cells and dendritic cells. [Thesis]. Universidade Nova; 2016. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/17047

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


University of Melbourne

17. Lee, Chin Nien. Functional studies of dendritic cells in type 1 diabetes: non-obese diabetic (NOD) mouse model.

Degree: 2012, University of Melbourne

 Dendritic cells (DC) are highly efficient antigen presenting cells and are important in regulating immune defense and tolerance. Both conventional DC (cDC) and plasmacytoid DC… (more)

Subjects/Keywords: dendritic cells; DC; DCs; type 1 diabetes; T1D; non-obese diabetic; NOD; cross-presentation; CD8+ cDC; cDC; pDC; plasmacytoid DC

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

APA (6th Edition):

Lee, C. N. (2012). Functional studies of dendritic cells in type 1 diabetes: non-obese diabetic (NOD) mouse model. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37473

Chicago Manual of Style (16th Edition):

Lee, Chin Nien. “Functional studies of dendritic cells in type 1 diabetes: non-obese diabetic (NOD) mouse model.” 2012. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/37473.

MLA Handbook (7th Edition):

Lee, Chin Nien. “Functional studies of dendritic cells in type 1 diabetes: non-obese diabetic (NOD) mouse model.” 2012. Web. 08 May 2021.

Vancouver:

Lee CN. Functional studies of dendritic cells in type 1 diabetes: non-obese diabetic (NOD) mouse model. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/37473.

Council of Science Editors:

Lee CN. Functional studies of dendritic cells in type 1 diabetes: non-obese diabetic (NOD) mouse model. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37473


Queens University

18. Dunbar, Erin. An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo .

Degree: Microbiology and Immunology, 2007, Queens University

 During viral infections, CD8+ T cells only respond to a select few epitopes derived from the respective foreign pathogen. These epitopes can be organized into… (more)

Subjects/Keywords: LCMV ; Cross priming ; Antigen Presentation ; Cytotoxic T cells

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APA (6th Edition):

Dunbar, E. (2007). An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/439

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):

Dunbar, Erin. “An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo .” 2007. Thesis, Queens University. Accessed May 08, 2021. http://hdl.handle.net/1974/439.

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

MLA Handbook (7th Edition):

Dunbar, Erin. “An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo .” 2007. Web. 08 May 2021.

Vancouver:

Dunbar E. An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo . [Internet] [Thesis]. Queens University; 2007. [cited 2021 May 08]. Available from: http://hdl.handle.net/1974/439.

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

Council of Science Editors:

Dunbar E. An evaluation of the efficiency of lymphocytic choriomeningitis virus - nucleoprotein cross priming in vivo . [Thesis]. Queens University; 2007. Available from: http://hdl.handle.net/1974/439

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

19. Pham, Dinh-Chuong. Anti-Nucleic Acid Antibody-Mediated Cross Presentation of An Antigen and Its CD8+ T Cell Activation.

Degree: 2013, Ajou University

Cross-presentation is important for initiating cytotoxic T lymphocyte (CTL) responses against tumors. Delivery of exogenous antigens to the cross-presentation pathway in dendritic cells using a… (more)

Subjects/Keywords: Cross-presentation; Anti-nucleic acid antibody; Cell-penetrating antibody; OVA peptide; Internalization; 항 핵산 항체; 교차항원제시; T 세포 활성

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APA (6th Edition):

Pham, D. (2013). Anti-Nucleic Acid Antibody-Mediated Cross Presentation of An Antigen and Its CD8+ T Cell Activation. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/8582 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000013450

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):

Pham, Dinh-Chuong. “Anti-Nucleic Acid Antibody-Mediated Cross Presentation of An Antigen and Its CD8+ T Cell Activation.” 2013. Thesis, Ajou University. Accessed May 08, 2021. http://repository.ajou.ac.kr/handle/201003/8582 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000013450.

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

MLA Handbook (7th Edition):

Pham, Dinh-Chuong. “Anti-Nucleic Acid Antibody-Mediated Cross Presentation of An Antigen and Its CD8+ T Cell Activation.” 2013. Web. 08 May 2021.

Vancouver:

Pham D. Anti-Nucleic Acid Antibody-Mediated Cross Presentation of An Antigen and Its CD8+ T Cell Activation. [Internet] [Thesis]. Ajou University; 2013. [cited 2021 May 08]. Available from: http://repository.ajou.ac.kr/handle/201003/8582 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000013450.

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

Council of Science Editors:

Pham D. Anti-Nucleic Acid Antibody-Mediated Cross Presentation of An Antigen and Its CD8+ T Cell Activation. [Thesis]. Ajou University; 2013. Available from: http://repository.ajou.ac.kr/handle/201003/8582 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000013450

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

20. Tang-Huau, Tsing-Lee. Les cellules dendritiques inflammatoires humaines utilisent une voie non-cytosolique pour la présentation croisée : Human inflammatory dendritic cells use a non-cytosolic pathway for cross-presentation.

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

La présentation d'antigènes exogènes sur les molécules du CMH de classe I, appelée cross- présentation, est essentielle pour l'induction des réponses T CD8 cytotoxiques. La… (more)

Subjects/Keywords: Cellules dendritiques humaines; Cross-présentation; Mo-DC; Lymphocytes T CD8 cytotoxiques; Voie vacuolaire; Human dendritic cells; Cross-presentation; Mo-DC; Cytotoxic CD8 T cells; Vacuolar pathway; 616.079

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APA (6th Edition):

Tang-Huau, T. (2018). Les cellules dendritiques inflammatoires humaines utilisent une voie non-cytosolique pour la présentation croisée : Human inflammatory dendritic cells use a non-cytosolic pathway for cross-presentation. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2018USPCB001

Chicago Manual of Style (16th Edition):

Tang-Huau, Tsing-Lee. “Les cellules dendritiques inflammatoires humaines utilisent une voie non-cytosolique pour la présentation croisée : Human inflammatory dendritic cells use a non-cytosolic pathway for cross-presentation.” 2018. Doctoral Dissertation, Sorbonne Paris Cité. Accessed May 08, 2021. http://www.theses.fr/2018USPCB001.

MLA Handbook (7th Edition):

Tang-Huau, Tsing-Lee. “Les cellules dendritiques inflammatoires humaines utilisent une voie non-cytosolique pour la présentation croisée : Human inflammatory dendritic cells use a non-cytosolic pathway for cross-presentation.” 2018. Web. 08 May 2021.

Vancouver:

Tang-Huau T. Les cellules dendritiques inflammatoires humaines utilisent une voie non-cytosolique pour la présentation croisée : Human inflammatory dendritic cells use a non-cytosolic pathway for cross-presentation. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2018. [cited 2021 May 08]. Available from: http://www.theses.fr/2018USPCB001.

Council of Science Editors:

Tang-Huau T. Les cellules dendritiques inflammatoires humaines utilisent une voie non-cytosolique pour la présentation croisée : Human inflammatory dendritic cells use a non-cytosolic pathway for cross-presentation. [Doctoral Dissertation]. Sorbonne Paris Cité; 2018. Available from: http://www.theses.fr/2018USPCB001


University of Melbourne

21. Wei, Quanzhou (Joe). Mechanisms of Influenza A virus enhanced cross-priming.

Degree: 2010, University of Melbourne

Cross-presentation of cell-associated antigens enacts an important role in regulating CD8+ T cell response to tumour cells. Dendritic cells (DCs) can capture and process exogenous… (more)

Subjects/Keywords: immunology; cross-priming; Influenza A virus; cross-presentation; dendritic cells; CD8+ T cells

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

APA (6th Edition):

Wei, Q. (. (2010). Mechanisms of Influenza A virus enhanced cross-priming. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/35473

Chicago Manual of Style (16th Edition):

Wei, Quanzhou (Joe). “Mechanisms of Influenza A virus enhanced cross-priming.” 2010. Doctoral Dissertation, University of Melbourne. Accessed May 08, 2021. http://hdl.handle.net/11343/35473.

MLA Handbook (7th Edition):

Wei, Quanzhou (Joe). “Mechanisms of Influenza A virus enhanced cross-priming.” 2010. Web. 08 May 2021.

Vancouver:

Wei Q(. Mechanisms of Influenza A virus enhanced cross-priming. [Internet] [Doctoral dissertation]. University of Melbourne; 2010. [cited 2021 May 08]. Available from: http://hdl.handle.net/11343/35473.

Council of Science Editors:

Wei Q(. Mechanisms of Influenza A virus enhanced cross-priming. [Doctoral Dissertation]. University of Melbourne; 2010. Available from: http://hdl.handle.net/11343/35473

22. Rosalia, Rodney Alexander. Particulate based vaccines for cancer immunotherapy.

Degree: 2014, Department of Immunohematology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University

 In this thesis we describe our studies aimed at optimizing the efficacy of synthetic long peptide (SLP) vaccines via the encapsulation in Poly-(lactic-co-glycolic acid) (PLGA)particles.… (more)

Subjects/Keywords: Dendritic cells; SLP; PLGA; Cross-presentation; CTL; Dendritic cells; SLP; PLGA; Cross-presentation; CTL

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APA (6th Edition):

Rosalia, R. A. (2014). Particulate based vaccines for cancer immunotherapy. (Doctoral Dissertation). Department of Immunohematology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Retrieved from http://hdl.handle.net/1887/28971

Chicago Manual of Style (16th Edition):

Rosalia, Rodney Alexander. “Particulate based vaccines for cancer immunotherapy.” 2014. Doctoral Dissertation, Department of Immunohematology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University. Accessed May 08, 2021. http://hdl.handle.net/1887/28971.

MLA Handbook (7th Edition):

Rosalia, Rodney Alexander. “Particulate based vaccines for cancer immunotherapy.” 2014. Web. 08 May 2021.

Vancouver:

Rosalia RA. Particulate based vaccines for cancer immunotherapy. [Internet] [Doctoral dissertation]. Department of Immunohematology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/1887/28971.

Council of Science Editors:

Rosalia RA. Particulate based vaccines for cancer immunotherapy. [Doctoral Dissertation]. Department of Immunohematology, Faculty of Medicine / Leiden University Medical Center (LUMC), Leiden University; 2014. Available from: http://hdl.handle.net/1887/28971


Duke University

23. Bowers, Edith Villette. Receptor-Mediated Antigen Delivery by Α2-Macroglobulin: Effect on Cytotoxic T Lymphocyte Immunity and Implications for Vaccine Development .

Degree: 2009, Duke University

  The receptor-recognized form of α2-macroglobulin (α2M*) targets antigens (Ag) to professional Ag-presenting cells (APCs) for rapid internalization, processing, and presentation. When employed as an… (more)

Subjects/Keywords: Health Sciences, Pathology; Health Sciences, Immunology; antigen presentation; cross; presentation; cytotoxic T cells; dendritic cells; vaccination

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APA (6th Edition):

Bowers, E. V. (2009). Receptor-Mediated Antigen Delivery by Α2-Macroglobulin: Effect on Cytotoxic T Lymphocyte Immunity and Implications for Vaccine Development . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/1319

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):

Bowers, Edith Villette. “Receptor-Mediated Antigen Delivery by Α2-Macroglobulin: Effect on Cytotoxic T Lymphocyte Immunity and Implications for Vaccine Development .” 2009. Thesis, Duke University. Accessed May 08, 2021. http://hdl.handle.net/10161/1319.

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

MLA Handbook (7th Edition):

Bowers, Edith Villette. “Receptor-Mediated Antigen Delivery by Α2-Macroglobulin: Effect on Cytotoxic T Lymphocyte Immunity and Implications for Vaccine Development .” 2009. Web. 08 May 2021.

Vancouver:

Bowers EV. Receptor-Mediated Antigen Delivery by Α2-Macroglobulin: Effect on Cytotoxic T Lymphocyte Immunity and Implications for Vaccine Development . [Internet] [Thesis]. Duke University; 2009. [cited 2021 May 08]. Available from: http://hdl.handle.net/10161/1319.

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

Council of Science Editors:

Bowers EV. Receptor-Mediated Antigen Delivery by Α2-Macroglobulin: Effect on Cytotoxic T Lymphocyte Immunity and Implications for Vaccine Development . [Thesis]. Duke University; 2009. Available from: http://hdl.handle.net/10161/1319

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


University of Texas – Austin

24. -8146-3047. In vitro and in vivo characterization of Fc-receptor expression and function on various immune cell subsets.

Degree: PhD, Chemical engineering, 2018, University of Texas – Austin

 Over the years, the standard care in cancer treatment has changed from surgery, chemotherapy, and/or radiotherapy alone to include the promising field of immunotherapy. Cancer… (more)

Subjects/Keywords: Immunotherapy; T cells; FcgRs; FcRs; Fc receptors; Cancer immunotherapy; ICs; Immune complexes; T cell subsets; Cross presentation; FcgRI; FcgRIIb; FcgRIIIa; ADCP; CDCP; ADCC; Antigen presentation; T cell proliferation; T cell cytotoxicity; IgG ICs; IgG immune complexes

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APA (6th Edition):

-8146-3047. (2018). In vitro and in vivo characterization of Fc-receptor expression and function on various immune cell subsets. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://dx.doi.org/10.26153/tsw/7525

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

Chicago Manual of Style (16th Edition):

-8146-3047. “In vitro and in vivo characterization of Fc-receptor expression and function on various immune cell subsets.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed May 08, 2021. http://dx.doi.org/10.26153/tsw/7525.

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

MLA Handbook (7th Edition):

-8146-3047. “In vitro and in vivo characterization of Fc-receptor expression and function on various immune cell subsets.” 2018. Web. 08 May 2021.

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

Vancouver:

-8146-3047. In vitro and in vivo characterization of Fc-receptor expression and function on various immune cell subsets. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2021 May 08]. Available from: http://dx.doi.org/10.26153/tsw/7525.

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

Council of Science Editors:

-8146-3047. In vitro and in vivo characterization of Fc-receptor expression and function on various immune cell subsets. [Doctoral Dissertation]. University of Texas – Austin; 2018. Available from: http://dx.doi.org/10.26153/tsw/7525

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


Leiden University

25. Neijssen, J.J. The fate of intracellular peptides and MHC class I antigen presentation.

Degree: 2008, Leiden University

 Intracellular proteins are degraded by the proteasome. The resulting protein fragments can be regarded as waste, but it is clear that peptides play an important… (more)

Subjects/Keywords: Antigen presentation; Antigen Processing; Cross-Presentation; HLA-B27; MHC Class I; Peptidase; Peptides; TPPII

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

APA (6th Edition):

Neijssen, J. J. (2008). The fate of intracellular peptides and MHC class I antigen presentation. (Doctoral Dissertation). Leiden University. Retrieved from http://hdl.handle.net/1887/12591

Chicago Manual of Style (16th Edition):

Neijssen, J J. “The fate of intracellular peptides and MHC class I antigen presentation.” 2008. Doctoral Dissertation, Leiden University. Accessed May 08, 2021. http://hdl.handle.net/1887/12591.

MLA Handbook (7th Edition):

Neijssen, J J. “The fate of intracellular peptides and MHC class I antigen presentation.” 2008. Web. 08 May 2021.

Vancouver:

Neijssen JJ. The fate of intracellular peptides and MHC class I antigen presentation. [Internet] [Doctoral dissertation]. Leiden University; 2008. [cited 2021 May 08]. Available from: http://hdl.handle.net/1887/12591.

Council of Science Editors:

Neijssen JJ. The fate of intracellular peptides and MHC class I antigen presentation. [Doctoral Dissertation]. Leiden University; 2008. Available from: http://hdl.handle.net/1887/12591

26. Kourjian, Georgio. Effect of HIV antiretroviral drugs on antigen processing and epitope presentation by MHC-I to cytotoxic T cells : Effet des antirétroviraux sur la voie d’apprêtement des antigènes et la présentation directe ainsi que croisée des épitopes par les CMH-I.

Degree: Docteur es, Immunologie, 2015, Université de Strasbourg

L’apprêtement antigénique par les protéases intracellulaires et la présentation des épitopes sont essentiels pour la reconnaissance des cellules infectées par les lymphocytes CD8+. Ici nous… (more)

Subjects/Keywords: Apprêtement antigénique; Présentation croisée; Lymphocytes CD8 + VIH; NOX2; Inhibiteurs de la protéase de la VIH; Présentation des épitopes; Antigen processing; Epitope presentation; Cross-presentation; HIV CTL; NOX2; HIV protease inhibitors; 571.96; 579.2; 616.91

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APA (6th Edition):

Kourjian, G. (2015). Effect of HIV antiretroviral drugs on antigen processing and epitope presentation by MHC-I to cytotoxic T cells : Effet des antirétroviraux sur la voie d’apprêtement des antigènes et la présentation directe ainsi que croisée des épitopes par les CMH-I. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2015STRAJ027

Chicago Manual of Style (16th Edition):

Kourjian, Georgio. “Effect of HIV antiretroviral drugs on antigen processing and epitope presentation by MHC-I to cytotoxic T cells : Effet des antirétroviraux sur la voie d’apprêtement des antigènes et la présentation directe ainsi que croisée des épitopes par les CMH-I.” 2015. Doctoral Dissertation, Université de Strasbourg. Accessed May 08, 2021. http://www.theses.fr/2015STRAJ027.

MLA Handbook (7th Edition):

Kourjian, Georgio. “Effect of HIV antiretroviral drugs on antigen processing and epitope presentation by MHC-I to cytotoxic T cells : Effet des antirétroviraux sur la voie d’apprêtement des antigènes et la présentation directe ainsi que croisée des épitopes par les CMH-I.” 2015. Web. 08 May 2021.

Vancouver:

Kourjian G. Effect of HIV antiretroviral drugs on antigen processing and epitope presentation by MHC-I to cytotoxic T cells : Effet des antirétroviraux sur la voie d’apprêtement des antigènes et la présentation directe ainsi que croisée des épitopes par les CMH-I. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2015. [cited 2021 May 08]. Available from: http://www.theses.fr/2015STRAJ027.

Council of Science Editors:

Kourjian G. Effect of HIV antiretroviral drugs on antigen processing and epitope presentation by MHC-I to cytotoxic T cells : Effet des antirétroviraux sur la voie d’apprêtement des antigènes et la présentation directe ainsi que croisée des épitopes par les CMH-I. [Doctoral Dissertation]. Université de Strasbourg; 2015. Available from: http://www.theses.fr/2015STRAJ027


Penn State University

27. Tewalt , Eric Franklin. Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo .

Degree: 2009, Penn State University

 CD8+ T cells (TCD8+) are activated by peptide-MHC (pMHC) Class I complexes presented on the surface of professional antigen presenting cells (pAPC). Antigenic pMHC-I can… (more)

Subjects/Keywords: Scavenger Receptor; Cross-presentation; Vaccinia Virus; T cells; gp96; Dendritic Cell

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

APA (6th Edition):

Tewalt , E. F. (2009). Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8980

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):

Tewalt , Eric Franklin. “Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo .” 2009. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/8980.

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

MLA Handbook (7th Edition):

Tewalt , Eric Franklin. “Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo .” 2009. Web. 08 May 2021.

Vancouver:

Tewalt EF. Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/8980.

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

Council of Science Editors:

Tewalt EF. Antigen Processing and Presentation: Contributions of the Cross-Presentation Pathway in Eliciting CD8+ T cell Responses In Vivo . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/8980

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


Penn State University

28. Donohue, Keri B. TOWARD DESIGNING A MORE EFFECTIVE VACCINE: MECHANISMS OF PRIMING T CELLS IN VIVO .

Degree: 2009, Penn State University

 The infectious diseases that currently pose the greatest threat to humans, AIDS, tuberculosis and malaria, are likely to require a vaccine strategy designed to elicit… (more)

Subjects/Keywords: antigen presentation; T cell activation; cross-priming; antigen processing; vaccine vector

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

APA (6th Edition):

Donohue, K. B. (2009). TOWARD DESIGNING A MORE EFFECTIVE VACCINE: MECHANISMS OF PRIMING T CELLS IN VIVO . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/10284

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):

Donohue, Keri B. “TOWARD DESIGNING A MORE EFFECTIVE VACCINE: MECHANISMS OF PRIMING T CELLS IN VIVO .” 2009. Thesis, Penn State University. Accessed May 08, 2021. https://submit-etda.libraries.psu.edu/catalog/10284.

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

MLA Handbook (7th Edition):

Donohue, Keri B. “TOWARD DESIGNING A MORE EFFECTIVE VACCINE: MECHANISMS OF PRIMING T CELLS IN VIVO .” 2009. Web. 08 May 2021.

Vancouver:

Donohue KB. TOWARD DESIGNING A MORE EFFECTIVE VACCINE: MECHANISMS OF PRIMING T CELLS IN VIVO . [Internet] [Thesis]. Penn State University; 2009. [cited 2021 May 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/10284.

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

Council of Science Editors:

Donohue KB. TOWARD DESIGNING A MORE EFFECTIVE VACCINE: MECHANISMS OF PRIMING T CELLS IN VIVO . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/10284

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


Texas Medical Center

29. Mittendorf, Elizabeth A. Cellular Uptake of Neutrohpil Elastase Links Inflammation to Adaptive Immunity.

Degree: PhD, 2012, Texas Medical Center

  Many tumors arise from sites of inflammation providing evidence that innate immunity is a critical component in the development and progression of cancer. Neutrophils… (more)

Subjects/Keywords: neutrophils; neutrophil elastase; innate immunity; adaptive immunity; breast cancer; cyclin E; cross presentation; inflammation; immunotherapy; Immunology and Infectious Disease; Medicine and Health Sciences

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

APA (6th Edition):

Mittendorf, E. A. (2012). Cellular Uptake of Neutrohpil Elastase Links Inflammation to Adaptive Immunity. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/303

Chicago Manual of Style (16th Edition):

Mittendorf, Elizabeth A. “Cellular Uptake of Neutrohpil Elastase Links Inflammation to Adaptive Immunity.” 2012. Doctoral Dissertation, Texas Medical Center. Accessed May 08, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/303.

MLA Handbook (7th Edition):

Mittendorf, Elizabeth A. “Cellular Uptake of Neutrohpil Elastase Links Inflammation to Adaptive Immunity.” 2012. Web. 08 May 2021.

Vancouver:

Mittendorf EA. Cellular Uptake of Neutrohpil Elastase Links Inflammation to Adaptive Immunity. [Internet] [Doctoral dissertation]. Texas Medical Center; 2012. [cited 2021 May 08]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/303.

Council of Science Editors:

Mittendorf EA. Cellular Uptake of Neutrohpil Elastase Links Inflammation to Adaptive Immunity. [Doctoral Dissertation]. Texas Medical Center; 2012. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/303

30. Compeer, E.B. Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity.

Degree: 2015, University Utrecht

 We, humans, are exposed daily to millions of potential pathogens, through contact, inhalation, or ingestion. Our ability to avoid infection depends on our immune system,… (more)

Subjects/Keywords: Antigen cross-presentation; tubulation; endosomes; MICAL-L1; Fcɣ-receptors; Common Variable Immunodeficiency; BLK

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

APA (6th Edition):

Compeer, E. B. (2015). Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/312537 ; URN:NBN:NL:UI:10-1874-312537 ; urn:isbn:978-94-6295-183-9 ; URN:NBN:NL:UI:10-1874-312537 ; http://dspace.library.uu.nl/handle/1874/312537

Chicago Manual of Style (16th Edition):

Compeer, E B. “Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity.” 2015. Doctoral Dissertation, University Utrecht. Accessed May 08, 2021. http://dspace.library.uu.nl/handle/1874/312537 ; URN:NBN:NL:UI:10-1874-312537 ; urn:isbn:978-94-6295-183-9 ; URN:NBN:NL:UI:10-1874-312537 ; http://dspace.library.uu.nl/handle/1874/312537.

MLA Handbook (7th Edition):

Compeer, E B. “Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity.” 2015. Web. 08 May 2021.

Vancouver:

Compeer EB. Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity. [Internet] [Doctoral dissertation]. University Utrecht; 2015. [cited 2021 May 08]. Available from: http://dspace.library.uu.nl/handle/1874/312537 ; URN:NBN:NL:UI:10-1874-312537 ; urn:isbn:978-94-6295-183-9 ; URN:NBN:NL:UI:10-1874-312537 ; http://dspace.library.uu.nl/handle/1874/312537.

Council of Science Editors:

Compeer EB. Cell-biological mechanisms regulating antigen presentation : Signaling towards adaptive immunity. [Doctoral Dissertation]. University Utrecht; 2015. Available from: http://dspace.library.uu.nl/handle/1874/312537 ; URN:NBN:NL:UI:10-1874-312537 ; urn:isbn:978-94-6295-183-9 ; URN:NBN:NL:UI:10-1874-312537 ; http://dspace.library.uu.nl/handle/1874/312537

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