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You searched for +publisher:"University of North Carolina" +contributor:("Wan, Yisong"). Showing records 1 – 10 of 10 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. Erdogan, Ozgun. PROTEOMIC DISSECTION OF LPS-INDUCIBLE PHF8-DEPENDENT SECRETOME REVEALS NOVEL ROLES OF PHF8 IN TLR4-INDUCED ACUTE INFLAMMATION AND ACTIVATION OF ADAPTIVE IMMUNITY.

Degree: Biochemistry and Biophysics, 2016, University of North Carolina

 This dissertation examines the role of PHF8 in the regulation of LPS-induced inflammatory response in macrophages and activation of adaptive immunity. I extend prior work… (more)

Subjects/Keywords: School of Medicine; Department of Biochemistry and Biophysics

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APA (6th Edition):

Erdogan, O. (2016). PROTEOMIC DISSECTION OF LPS-INDUCIBLE PHF8-DEPENDENT SECRETOME REVEALS NOVEL ROLES OF PHF8 IN TLR4-INDUCED ACUTE INFLAMMATION AND ACTIVATION OF ADAPTIVE IMMUNITY. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:bd306eb9-e94b-4923-9e21-15adafd7b04e

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):

Erdogan, Ozgun. “PROTEOMIC DISSECTION OF LPS-INDUCIBLE PHF8-DEPENDENT SECRETOME REVEALS NOVEL ROLES OF PHF8 IN TLR4-INDUCED ACUTE INFLAMMATION AND ACTIVATION OF ADAPTIVE IMMUNITY.” 2016. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:bd306eb9-e94b-4923-9e21-15adafd7b04e.

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

MLA Handbook (7th Edition):

Erdogan, Ozgun. “PROTEOMIC DISSECTION OF LPS-INDUCIBLE PHF8-DEPENDENT SECRETOME REVEALS NOVEL ROLES OF PHF8 IN TLR4-INDUCED ACUTE INFLAMMATION AND ACTIVATION OF ADAPTIVE IMMUNITY.” 2016. Web. 31 Oct 2020.

Vancouver:

Erdogan O. PROTEOMIC DISSECTION OF LPS-INDUCIBLE PHF8-DEPENDENT SECRETOME REVEALS NOVEL ROLES OF PHF8 IN TLR4-INDUCED ACUTE INFLAMMATION AND ACTIVATION OF ADAPTIVE IMMUNITY. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:bd306eb9-e94b-4923-9e21-15adafd7b04e.

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

Council of Science Editors:

Erdogan O. PROTEOMIC DISSECTION OF LPS-INDUCIBLE PHF8-DEPENDENT SECRETOME REVEALS NOVEL ROLES OF PHF8 IN TLR4-INDUCED ACUTE INFLAMMATION AND ACTIVATION OF ADAPTIVE IMMUNITY. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:bd306eb9-e94b-4923-9e21-15adafd7b04e

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


University of North Carolina

3. Dant, Trisha. Examining Factors Critical to T Cell Suppression and Migration During Acute Graft-Versus-Host Disease.

Degree: Microbiology and Immunology, 2017, University of North Carolina

 Allogeneic stem cell transplant (allo-SCT) is a curative therapy for malignant and non-malignant diseases. Unfortunately, acute Graft-versus-Host Disease (aGvHD) is a complication of allo-SCT, and… (more)

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

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APA (6th Edition):

Dant, T. (2017). Examining Factors Critical to T Cell Suppression and Migration During Acute Graft-Versus-Host Disease. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:60e87d06-bfe3-43b7-9d31-40ca2895bdb9

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):

Dant, Trisha. “Examining Factors Critical to T Cell Suppression and Migration During Acute Graft-Versus-Host Disease.” 2017. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:60e87d06-bfe3-43b7-9d31-40ca2895bdb9.

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

MLA Handbook (7th Edition):

Dant, Trisha. “Examining Factors Critical to T Cell Suppression and Migration During Acute Graft-Versus-Host Disease.” 2017. Web. 31 Oct 2020.

Vancouver:

Dant T. Examining Factors Critical to T Cell Suppression and Migration During Acute Graft-Versus-Host Disease. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:60e87d06-bfe3-43b7-9d31-40ca2895bdb9.

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

Council of Science Editors:

Dant T. Examining Factors Critical to T Cell Suppression and Migration During Acute Graft-Versus-Host Disease. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:60e87d06-bfe3-43b7-9d31-40ca2895bdb9

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


University of North Carolina

4. HWANG, BIN-JIN. The hemidesmosomal protein BP180 (collagen XVII) in skin cancer and inflammation.

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

 BP180, also known as collagen XVII, is a transmembrane glycoprotein located in the hemidesmosome of basal keratinocytes, and functions as a key cell-matrix adhesion molecule.… (more)

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

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APA (6th Edition):

HWANG, B. (2018). The hemidesmosomal protein BP180 (collagen XVII) in skin cancer and inflammation. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4d7fa3fb-910e-49c4-a6fb-32a7c4836eca

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):

HWANG, BIN-JIN. “The hemidesmosomal protein BP180 (collagen XVII) in skin cancer and inflammation.” 2018. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:4d7fa3fb-910e-49c4-a6fb-32a7c4836eca.

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

MLA Handbook (7th Edition):

HWANG, BIN-JIN. “The hemidesmosomal protein BP180 (collagen XVII) in skin cancer and inflammation.” 2018. Web. 31 Oct 2020.

Vancouver:

HWANG B. The hemidesmosomal protein BP180 (collagen XVII) in skin cancer and inflammation. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:4d7fa3fb-910e-49c4-a6fb-32a7c4836eca.

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

Council of Science Editors:

HWANG B. The hemidesmosomal protein BP180 (collagen XVII) in skin cancer and inflammation. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:4d7fa3fb-910e-49c4-a6fb-32a7c4836eca

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


University of North Carolina

5. 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

6. dela Pena, Myra Grace. CD4+ T Cells in Infant Immunity.

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

 Age and immune maturation are interdependent and dynamic processes. The infant immune system undergoes many developmental changes after birth, and compared to adults, cellular and… (more)

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

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APA (6th Edition):

dela Pena, M. G. (2014). CD4+ T Cells in Infant Immunity. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:30129e46-30b0-4cdb-a2ec-a03f7d8d7155

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):

dela Pena, Myra Grace. “CD4+ T Cells in Infant Immunity.” 2014. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:30129e46-30b0-4cdb-a2ec-a03f7d8d7155.

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

MLA Handbook (7th Edition):

dela Pena, Myra Grace. “CD4+ T Cells in Infant Immunity.” 2014. Web. 31 Oct 2020.

Vancouver:

dela Pena MG. CD4+ T Cells in Infant Immunity. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:30129e46-30b0-4cdb-a2ec-a03f7d8d7155.

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

Council of Science Editors:

dela Pena MG. CD4+ T Cells in Infant Immunity. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:30129e46-30b0-4cdb-a2ec-a03f7d8d7155

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


University of North Carolina

7. 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

8. Taylor, Nicholas. Balancing Pro- and Anti-Inflammatory Signals for Effective Immunotherapy in the Post- Hematopoietic Stem Cell Transplant and Solid Tumor Settings.

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

 The immune system maintains a balance of activating and suppressive signals in order to promote homeostasis. However, diseases may arise when errant signals on either… (more)

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

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APA (6th Edition):

Taylor, N. (2014). Balancing Pro- and Anti-Inflammatory Signals for Effective Immunotherapy in the Post- Hematopoietic Stem Cell Transplant and Solid Tumor Settings. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6b69a57c-cbb8-4bdd-b5c7-835e92475e2f

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):

Taylor, Nicholas. “Balancing Pro- and Anti-Inflammatory Signals for Effective Immunotherapy in the Post- Hematopoietic Stem Cell Transplant and Solid Tumor Settings.” 2014. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:6b69a57c-cbb8-4bdd-b5c7-835e92475e2f.

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

MLA Handbook (7th Edition):

Taylor, Nicholas. “Balancing Pro- and Anti-Inflammatory Signals for Effective Immunotherapy in the Post- Hematopoietic Stem Cell Transplant and Solid Tumor Settings.” 2014. Web. 31 Oct 2020.

Vancouver:

Taylor N. Balancing Pro- and Anti-Inflammatory Signals for Effective Immunotherapy in the Post- Hematopoietic Stem Cell Transplant and Solid Tumor Settings. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:6b69a57c-cbb8-4bdd-b5c7-835e92475e2f.

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

Council of Science Editors:

Taylor N. Balancing Pro- and Anti-Inflammatory Signals for Effective Immunotherapy in the Post- Hematopoietic Stem Cell Transplant and Solid Tumor Settings. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:6b69a57c-cbb8-4bdd-b5c7-835e92475e2f

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


University of North Carolina

9. Mackey, Lantz. The Role of α(1,3)-Fucosylated Glycans in Homeostatic Immunity, Granulopoiesis, and Mucosal Injury.

Degree: Pathology and Laboratory Medicine, 2014, University of North Carolina

 The mechanisms that control granulopoiesis are poorly understood. Mice deficient in α(1,3)-fucosyltransferases (FUT) 4 and 7 (Fut-/-) lack selectin ligand activity and selectin-dependent leukocyte trafficking,… (more)

Subjects/Keywords: Pathology; Immunology; Molecular biology; School of Medicine; Department of Pathology and Laboratory Medicine

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APA (6th Edition):

Mackey, L. (2014). The Role of α(1,3)-Fucosylated Glycans in Homeostatic Immunity, Granulopoiesis, and Mucosal Injury. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:532275af-f63a-4934-97d0-2ee6c141ded0

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):

Mackey, Lantz. “The Role of α(1,3)-Fucosylated Glycans in Homeostatic Immunity, Granulopoiesis, and Mucosal Injury.” 2014. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:532275af-f63a-4934-97d0-2ee6c141ded0.

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

MLA Handbook (7th Edition):

Mackey, Lantz. “The Role of α(1,3)-Fucosylated Glycans in Homeostatic Immunity, Granulopoiesis, and Mucosal Injury.” 2014. Web. 31 Oct 2020.

Vancouver:

Mackey L. The Role of α(1,3)-Fucosylated Glycans in Homeostatic Immunity, Granulopoiesis, and Mucosal Injury. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:532275af-f63a-4934-97d0-2ee6c141ded0.

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

Council of Science Editors:

Mackey L. The Role of α(1,3)-Fucosylated Glycans in Homeostatic Immunity, Granulopoiesis, and Mucosal Injury. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:532275af-f63a-4934-97d0-2ee6c141ded0

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


University of North Carolina

10. Honeycutt, Jenna. Investigation of the Role of Myeloid and T Cells in Human Immunodeficiency Virus (HIV) Infection and Persistence in Vivo.

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

 Human immunodeficiency virus (HIV) infection is the causative agent of AIDS and readily infects CD4+ T cells. I have characterized a humanized T cell only… (more)

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

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APA (6th Edition):

Honeycutt, J. (2015). Investigation of the Role of Myeloid and T Cells in Human Immunodeficiency Virus (HIV) Infection and Persistence in Vivo. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:fc84b1db-7d13-44fc-96bf-168092a071df

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):

Honeycutt, Jenna. “Investigation of the Role of Myeloid and T Cells in Human Immunodeficiency Virus (HIV) Infection and Persistence in Vivo.” 2015. Thesis, University of North Carolina. Accessed October 31, 2020. https://cdr.lib.unc.edu/record/uuid:fc84b1db-7d13-44fc-96bf-168092a071df.

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

MLA Handbook (7th Edition):

Honeycutt, Jenna. “Investigation of the Role of Myeloid and T Cells in Human Immunodeficiency Virus (HIV) Infection and Persistence in Vivo.” 2015. Web. 31 Oct 2020.

Vancouver:

Honeycutt J. Investigation of the Role of Myeloid and T Cells in Human Immunodeficiency Virus (HIV) Infection and Persistence in Vivo. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Oct 31]. Available from: https://cdr.lib.unc.edu/record/uuid:fc84b1db-7d13-44fc-96bf-168092a071df.

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

Council of Science Editors:

Honeycutt J. Investigation of the Role of Myeloid and T Cells in Human Immunodeficiency Virus (HIV) Infection and Persistence in Vivo. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:fc84b1db-7d13-44fc-96bf-168092a071df

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

.