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You searched for +publisher:"University of North Carolina" +contributor:("Tisch, Roland"). Showing records 1 – 12 of 12 total matches.

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University of North Carolina

1. Scott, Eric. Immune Cells and Type I Interferon in Systemic Lupus Erythematosus Patient Urine and Kidney Immunopathology.

Degree: Microbiology and Immunology, 2015, University of North Carolina

 Murine models have demonstrated that systemic lupus erythematosus (SLE) results in kidney damage due to antibody mediated tissue destruction. Studies of peripheral blood immune subsets… (more)

Subjects/Keywords: Immunology; School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Scott, E. (2015). Immune Cells and Type I Interferon in Systemic Lupus Erythematosus Patient Urine and Kidney Immunopathology. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c3470669-53a7-40db-a40a-ad4e934d9b66

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):

Scott, Eric. “Immune Cells and Type I Interferon in Systemic Lupus Erythematosus Patient Urine and Kidney Immunopathology.” 2015. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:c3470669-53a7-40db-a40a-ad4e934d9b66.

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

MLA Handbook (7th Edition):

Scott, Eric. “Immune Cells and Type I Interferon in Systemic Lupus Erythematosus Patient Urine and Kidney Immunopathology.” 2015. Web. 31 Oct 2020.

Vancouver:

Scott E. Immune Cells and Type I Interferon in Systemic Lupus Erythematosus Patient Urine and Kidney Immunopathology. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:c3470669-53a7-40db-a40a-ad4e934d9b66.

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

Council of Science Editors:

Scott E. Immune Cells and Type I Interferon in Systemic Lupus Erythematosus Patient Urine and Kidney Immunopathology. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:c3470669-53a7-40db-a40a-ad4e934d9b66

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


University of North Carolina

2. Hong, Lee. CD30-REDIRECTED CHIMERIC ANTIGEN RECEPTOR T CELLS TARGET EMBRYONAL CARCINOMA VIA ANTIGEN-DEPENDENT AND FAS/FASL INTERACTIONS.

Degree: Microbiology and Immunology, 2018, University of North Carolina

 Embryonal carcinomas (ECs) and mixed testicular germ cell tumors (TGCTs) containing EC express CD30 and are the most aggressive TGCT subtypes. Chimeric antigen receptor T… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Hong, L. (2018). CD30-REDIRECTED CHIMERIC ANTIGEN RECEPTOR T CELLS TARGET EMBRYONAL CARCINOMA VIA ANTIGEN-DEPENDENT AND FAS/FASL INTERACTIONS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:519f1372-1638-487e-b82e-0681308db3e0

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):

Hong, Lee. “CD30-REDIRECTED CHIMERIC ANTIGEN RECEPTOR T CELLS TARGET EMBRYONAL CARCINOMA VIA ANTIGEN-DEPENDENT AND FAS/FASL INTERACTIONS.” 2018. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:519f1372-1638-487e-b82e-0681308db3e0.

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

MLA Handbook (7th Edition):

Hong, Lee. “CD30-REDIRECTED CHIMERIC ANTIGEN RECEPTOR T CELLS TARGET EMBRYONAL CARCINOMA VIA ANTIGEN-DEPENDENT AND FAS/FASL INTERACTIONS.” 2018. Web. 31 Oct 2020.

Vancouver:

Hong L. CD30-REDIRECTED CHIMERIC ANTIGEN RECEPTOR T CELLS TARGET EMBRYONAL CARCINOMA VIA ANTIGEN-DEPENDENT AND FAS/FASL INTERACTIONS. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:519f1372-1638-487e-b82e-0681308db3e0.

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

Council of Science Editors:

Hong L. CD30-REDIRECTED CHIMERIC ANTIGEN RECEPTOR T CELLS TARGET EMBRYONAL CARCINOMA VIA ANTIGEN-DEPENDENT AND FAS/FASL INTERACTIONS. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:519f1372-1638-487e-b82e-0681308db3e0

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


University of North Carolina

3. Allard Trout, Denise. Schwann cells promote spontaneous autoimmune peripheral polyneuropathy.

Degree: Microbiology and Immunology, 2018, University of North Carolina

 Chronic inflammatory demyelinating polyneuropathy (CIDP) and Guillain-Barré syndrome (GBS) are autoimmune demyelinating diseases of the peripheral nervous system (PNS). During CIDP and GBS, the immune… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Allard Trout, D. (2018). Schwann cells promote spontaneous autoimmune peripheral polyneuropathy. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d1ecd067-6919-437e-87d7-c588a8e81d6b

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):

Allard Trout, Denise. “Schwann cells promote spontaneous autoimmune peripheral polyneuropathy.” 2018. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:d1ecd067-6919-437e-87d7-c588a8e81d6b.

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

MLA Handbook (7th Edition):

Allard Trout, Denise. “Schwann cells promote spontaneous autoimmune peripheral polyneuropathy.” 2018. Web. 31 Oct 2020.

Vancouver:

Allard Trout D. Schwann cells promote spontaneous autoimmune peripheral polyneuropathy. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:d1ecd067-6919-437e-87d7-c588a8e81d6b.

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

Council of Science Editors:

Allard Trout D. Schwann cells promote spontaneous autoimmune peripheral polyneuropathy. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:d1ecd067-6919-437e-87d7-c588a8e81d6b

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


University of North Carolina

4. Johnson, Mark Christopher. Interleukin-2 based therapy for the treatment of Type I Diabetes.

Degree: Microbiology and Immunology, 2013, University of North Carolina

 Type I diabetes (T1D) is an autoimmune disease characterized by the destruction of the insulin producing beta cells. Although multiple cell types contribute, the main… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Johnson, M. C. (2013). Interleukin-2 based therapy for the treatment of Type I Diabetes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5bb0c80c-961e-43dc-ab4d-e723cf67f3e6

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):

Johnson, Mark Christopher. “Interleukin-2 based therapy for the treatment of Type I Diabetes.” 2013. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:5bb0c80c-961e-43dc-ab4d-e723cf67f3e6.

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

MLA Handbook (7th Edition):

Johnson, Mark Christopher. “Interleukin-2 based therapy for the treatment of Type I Diabetes.” 2013. Web. 31 Oct 2020.

Vancouver:

Johnson MC. Interleukin-2 based therapy for the treatment of Type I Diabetes. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:5bb0c80c-961e-43dc-ab4d-e723cf67f3e6.

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

Council of Science Editors:

Johnson MC. Interleukin-2 based therapy for the treatment of Type I Diabetes. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:5bb0c80c-961e-43dc-ab4d-e723cf67f3e6

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


University of North Carolina

5. Garland, Alaina L. Immunotherapy and T Cell Receptor Analysis in Recurrent Type 1 Diabetes.

Degree: Microbiology and Immunology, 2012, University of North Carolina

 Type 1 Diabetes (T1D) is a chronic autoimmune disease characterized by the T cell-mediated destruction of insulin-producing β cells in the islets of Langerhans. For… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Garland, A. L. (2012). Immunotherapy and T Cell Receptor Analysis in Recurrent Type 1 Diabetes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e4f5bb7f-5ea9-4560-bae0-a9e9c3e68184

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):

Garland, Alaina L. “Immunotherapy and T Cell Receptor Analysis in Recurrent Type 1 Diabetes.” 2012. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:e4f5bb7f-5ea9-4560-bae0-a9e9c3e68184.

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

MLA Handbook (7th Edition):

Garland, Alaina L. “Immunotherapy and T Cell Receptor Analysis in Recurrent Type 1 Diabetes.” 2012. Web. 31 Oct 2020.

Vancouver:

Garland AL. Immunotherapy and T Cell Receptor Analysis in Recurrent Type 1 Diabetes. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:e4f5bb7f-5ea9-4560-bae0-a9e9c3e68184.

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

Council of Science Editors:

Garland AL. Immunotherapy and T Cell Receptor Analysis in Recurrent Type 1 Diabetes. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:e4f5bb7f-5ea9-4560-bae0-a9e9c3e68184

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


University of North Carolina

6. Morillon, Yves. THYMIC DEVELOPMENT OF AUTOREACTIVE T CELLS IN NOD MICE, AND THE ALTERED TRAFFICKING OF T CELLS FOLLOWING ANTIBODY MEDIATED CROSSLINKING OF THE CD4 CORECEPTOR.

Degree: Microbiology and Immunology, 2014, University of North Carolina

 Two key processes in driving type 1 diabetes are the development and trafficking of β cell-specific T cells into the pancreas. The first part of… (more)

Subjects/Keywords: Immunology; School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Morillon, Y. (2014). THYMIC DEVELOPMENT OF AUTOREACTIVE T CELLS IN NOD MICE, AND THE ALTERED TRAFFICKING OF T CELLS FOLLOWING ANTIBODY MEDIATED CROSSLINKING OF THE CD4 CORECEPTOR. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6779d3c5-3461-4486-aef2-33ac9de0cd3c

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):

Morillon, Yves. “THYMIC DEVELOPMENT OF AUTOREACTIVE T CELLS IN NOD MICE, AND THE ALTERED TRAFFICKING OF T CELLS FOLLOWING ANTIBODY MEDIATED CROSSLINKING OF THE CD4 CORECEPTOR.” 2014. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:6779d3c5-3461-4486-aef2-33ac9de0cd3c.

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

MLA Handbook (7th Edition):

Morillon, Yves. “THYMIC DEVELOPMENT OF AUTOREACTIVE T CELLS IN NOD MICE, AND THE ALTERED TRAFFICKING OF T CELLS FOLLOWING ANTIBODY MEDIATED CROSSLINKING OF THE CD4 CORECEPTOR.” 2014. Web. 31 Oct 2020.

Vancouver:

Morillon Y. THYMIC DEVELOPMENT OF AUTOREACTIVE T CELLS IN NOD MICE, AND THE ALTERED TRAFFICKING OF T CELLS FOLLOWING ANTIBODY MEDIATED CROSSLINKING OF THE CD4 CORECEPTOR. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:6779d3c5-3461-4486-aef2-33ac9de0cd3c.

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

Council of Science Editors:

Morillon Y. THYMIC DEVELOPMENT OF AUTOREACTIVE T CELLS IN NOD MICE, AND THE ALTERED TRAFFICKING OF T CELLS FOLLOWING ANTIBODY MEDIATED CROSSLINKING OF THE CD4 CORECEPTOR. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:6779d3c5-3461-4486-aef2-33ac9de0cd3c

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


University of North Carolina

7. Manzoor, Fatima. Tissue-specific cytokine-based immunotherapy to treat type 1 diabetes.

Degree: Microbiology and Immunology, 2016, University of North Carolina

 Type 1 diabetes (T1D) is characterized by the T cell-mediated destruction of the insulin-producing β cells. Progressive loss of β cell mass results in the… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Manzoor, F. (2016). Tissue-specific cytokine-based immunotherapy to treat type 1 diabetes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3d21e01f-87c6-48ae-bbe7-f677faa3f639

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):

Manzoor, Fatima. “Tissue-specific cytokine-based immunotherapy to treat type 1 diabetes.” 2016. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:3d21e01f-87c6-48ae-bbe7-f677faa3f639.

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

MLA Handbook (7th Edition):

Manzoor, Fatima. “Tissue-specific cytokine-based immunotherapy to treat type 1 diabetes.” 2016. Web. 31 Oct 2020.

Vancouver:

Manzoor F. Tissue-specific cytokine-based immunotherapy to treat type 1 diabetes. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:3d21e01f-87c6-48ae-bbe7-f677faa3f639.

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

Council of Science Editors:

Manzoor F. Tissue-specific cytokine-based immunotherapy to treat type 1 diabetes. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:3d21e01f-87c6-48ae-bbe7-f677faa3f639

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


University of North Carolina

8. Nguyen, Khue. Effect of Heparin on the Immunobiology of Interleukin-12.

Degree: Microbiology and Immunology, 2018, University of North Carolina

 IL-12 is a potent pro-inflammatory cytokine that plays a central role in cellular immunity. Recently, we have shown that IL-12 is a specific heparin-binding protein.… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Nguyen, K. (2018). Effect of Heparin on the Immunobiology of Interleukin-12. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:44502cdb-4717-4c9c-a143-b0e64eeb17f4

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):

Nguyen, Khue. “Effect of Heparin on the Immunobiology of Interleukin-12.” 2018. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:44502cdb-4717-4c9c-a143-b0e64eeb17f4.

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

MLA Handbook (7th Edition):

Nguyen, Khue. “Effect of Heparin on the Immunobiology of Interleukin-12.” 2018. Web. 31 Oct 2020.

Vancouver:

Nguyen K. Effect of Heparin on the Immunobiology of Interleukin-12. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:44502cdb-4717-4c9c-a143-b0e64eeb17f4.

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

Council of Science Editors:

Nguyen K. Effect of Heparin on the Immunobiology of Interleukin-12. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:44502cdb-4717-4c9c-a143-b0e64eeb17f4

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


University of North Carolina

9. Spidale, Nicholas. Factors regulating thymic dendritic cell homeostasis and function.

Degree: Microbiology and Immunology, 2014, University of North Carolina

 The immune system must balance the generation of a diverse T cell repertoire responsive to various pathogens versus the prevention of tissue destruction by self-antigen-specific… (more)

Subjects/Keywords: Immunology; School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Spidale, N. (2014). Factors regulating thymic dendritic cell homeostasis and function. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:821c13c1-ff67-4848-a3c3-e506874313c9

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):

Spidale, Nicholas. “Factors regulating thymic dendritic cell homeostasis and function.” 2014. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:821c13c1-ff67-4848-a3c3-e506874313c9.

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

MLA Handbook (7th Edition):

Spidale, Nicholas. “Factors regulating thymic dendritic cell homeostasis and function.” 2014. Web. 31 Oct 2020.

Vancouver:

Spidale N. Factors regulating thymic dendritic cell homeostasis and function. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:821c13c1-ff67-4848-a3c3-e506874313c9.

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

Council of Science Editors:

Spidale N. Factors regulating thymic dendritic cell homeostasis and function. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:821c13c1-ff67-4848-a3c3-e506874313c9

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


University of North Carolina

10. Li, Li. Characterization and Modulation of Autoreactive CD4+ T cells in Type 1 Diabetes.

Degree: Microbiology and Immunology, 2007, University of North Carolina

 Type 1 diabetes (T1D) is an autoimmune disease mediated by pathogenic β cell-specific T cells. The soluble (s) IAg7- immunoglobulin (Ig) dimers covalently linked to… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Li, L. (2007). Characterization and Modulation of Autoreactive CD4+ T cells in Type 1 Diabetes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:64c483fd-2eb8-4468-b747-40ef99fab223

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):

Li, Li. “Characterization and Modulation of Autoreactive CD4+ T cells in Type 1 Diabetes.” 2007. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:64c483fd-2eb8-4468-b747-40ef99fab223.

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

MLA Handbook (7th Edition):

Li, Li. “Characterization and Modulation of Autoreactive CD4+ T cells in Type 1 Diabetes.” 2007. Web. 31 Oct 2020.

Vancouver:

Li L. Characterization and Modulation of Autoreactive CD4+ T cells in Type 1 Diabetes. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:64c483fd-2eb8-4468-b747-40ef99fab223.

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

Council of Science Editors:

Li L. Characterization and Modulation of Autoreactive CD4+ T cells in Type 1 Diabetes. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:64c483fd-2eb8-4468-b747-40ef99fab223

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


University of North Carolina

11. Goudy, Kevin Scott. Characterization and Immunomodulation of Regulatory T cells in Type 1 Diabetes.

Degree: Microbiology and Immunology, 2008, University of North Carolina

 Type 1 diabetes mellitus (T1D) is a chronic autoimmune disorder characterized by the complete destruction of the insulin-producing pancreatic β cells. The result of β… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Goudy, K. S. (2008). Characterization and Immunomodulation of Regulatory T cells in Type 1 Diabetes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3c4cfbcc-6b92-4756-a0af-b2b595516891

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):

Goudy, Kevin Scott. “Characterization and Immunomodulation of Regulatory T cells in Type 1 Diabetes.” 2008. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:3c4cfbcc-6b92-4756-a0af-b2b595516891.

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

MLA Handbook (7th Edition):

Goudy, Kevin Scott. “Characterization and Immunomodulation of Regulatory T cells in Type 1 Diabetes.” 2008. Web. 31 Oct 2020.

Vancouver:

Goudy KS. Characterization and Immunomodulation of Regulatory T cells in Type 1 Diabetes. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:3c4cfbcc-6b92-4756-a0af-b2b595516891.

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

Council of Science Editors:

Goudy KS. Characterization and Immunomodulation of Regulatory T cells in Type 1 Diabetes. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:3c4cfbcc-6b92-4756-a0af-b2b595516891

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


University of North Carolina

12. Wallet, Mark A. MerTK mediates immune homeostasis: effects upon dendritic cell function and Type 1 diabetes.

Degree: Microbiology and Immunology, 2006, University of North Carolina

 The receptor tyrosine kinase Mer (MerTK) is expressed by dendritic cells (DC) in mice. The heretofore undefined role of MerTK in DC was investigated in… (more)

Subjects/Keywords: School of Medicine; Department of Microbiology and Immunology

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APA (6th Edition):

Wallet, M. A. (2006). MerTK mediates immune homeostasis: effects upon dendritic cell function and Type 1 diabetes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4b5f3a16-7287-461e-86d9-e3e1f614d78f

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):

Wallet, Mark A. “MerTK mediates immune homeostasis: effects upon dendritic cell function and Type 1 diabetes.” 2006. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:4b5f3a16-7287-461e-86d9-e3e1f614d78f.

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

MLA Handbook (7th Edition):

Wallet, Mark A. “MerTK mediates immune homeostasis: effects upon dendritic cell function and Type 1 diabetes.” 2006. Web. 31 Oct 2020.

Vancouver:

Wallet MA. MerTK mediates immune homeostasis: effects upon dendritic cell function and Type 1 diabetes. [Internet] [Thesis]. University of North Carolina; 2006. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:4b5f3a16-7287-461e-86d9-e3e1f614d78f.

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

Council of Science Editors:

Wallet MA. MerTK mediates immune homeostasis: effects upon dendritic cell function and Type 1 diabetes. [Thesis]. University of North Carolina; 2006. Available from: https://cdr.lib.unc.edu/record/uuid:4b5f3a16-7287-461e-86d9-e3e1f614d78f

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

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