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You searched for +publisher:"University of North Carolina" +contributor:("Collins, Edward"). Showing records 1 – 7 of 7 total matches.

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University of North Carolina

1. Miller, Keith Russell. Use of T Cell Receptor-like Antibody Fragments for Imaging and Immunotherapy.

Degree: Biochemistry and Biophysics, 2013, University of North Carolina

 The cellular proteome, in both healthy and diseased cells, is presented on the cell membrane surface as peptides bound to the major histocompatibility complex (pMHC).… (more)

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

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

APA (6th Edition):

Miller, K. R. (2013). Use of T Cell Receptor-like Antibody Fragments for Imaging and Immunotherapy. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b9915fc6-932f-4955-b779-5086c453dcb2

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):

Miller, Keith Russell. “Use of T Cell Receptor-like Antibody Fragments for Imaging and Immunotherapy.” 2013. Thesis, University of North Carolina. Accessed January 18, 2021. https://cdr.lib.unc.edu/record/uuid:b9915fc6-932f-4955-b779-5086c453dcb2.

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

MLA Handbook (7th Edition):

Miller, Keith Russell. “Use of T Cell Receptor-like Antibody Fragments for Imaging and Immunotherapy.” 2013. Web. 18 Jan 2021.

Vancouver:

Miller KR. Use of T Cell Receptor-like Antibody Fragments for Imaging and Immunotherapy. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2021 Jan 18]. Available from: https://cdr.lib.unc.edu/record/uuid:b9915fc6-932f-4955-b779-5086c453dcb2.

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

Council of Science Editors:

Miller KR. Use of T Cell Receptor-like Antibody Fragments for Imaging and Immunotherapy. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:b9915fc6-932f-4955-b779-5086c453dcb2

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


University of North Carolina

2. Thompson, Peter. The structural and functional consequences of the interaction of the vinculin tail domain with F-actin and PIP2.

Degree: Biochemistry and Biophysics, 2015, University of North Carolina

 Vinculin is an essential, highly-conserved eukaryotic scaffolding protein. It localizes to focal adhesions and adherens juctions, where it assists in physically linking the actin cytoskeleton… (more)

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

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APA (6th Edition):

Thompson, P. (2015). The structural and functional consequences of the interaction of the vinculin tail domain with F-actin and PIP2. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:f8dcee81-c727-40cc-94ad-8d3a7736d4a1

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):

Thompson, Peter. “The structural and functional consequences of the interaction of the vinculin tail domain with F-actin and PIP2.” 2015. Thesis, University of North Carolina. Accessed January 18, 2021. https://cdr.lib.unc.edu/record/uuid:f8dcee81-c727-40cc-94ad-8d3a7736d4a1.

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

MLA Handbook (7th Edition):

Thompson, Peter. “The structural and functional consequences of the interaction of the vinculin tail domain with F-actin and PIP2.” 2015. Web. 18 Jan 2021.

Vancouver:

Thompson P. The structural and functional consequences of the interaction of the vinculin tail domain with F-actin and PIP2. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2021 Jan 18]. Available from: https://cdr.lib.unc.edu/record/uuid:f8dcee81-c727-40cc-94ad-8d3a7736d4a1.

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

Council of Science Editors:

Thompson P. The structural and functional consequences of the interaction of the vinculin tail domain with F-actin and PIP2. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:f8dcee81-c727-40cc-94ad-8d3a7736d4a1

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


University of North Carolina

3. Jacobs, Tim. De Novo Proteins Designed From Evolutionary Principles.

Degree: 2015, University of North Carolina

 Protein engineering has rapidly developed into a powerful method for the optimization, alteration, and creation of protein functions. Current protein engineering methods fall into the… (more)

Subjects/Keywords: Biochemistry; Bioinformatics; School of Medicine; Curriculum in Bioinformatics and Computational Biology

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APA (6th Edition):

Jacobs, T. (2015). De Novo Proteins Designed From Evolutionary Principles. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e5c99a71-24d2-46bc-bbfe-4ff6c8607fa5

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):

Jacobs, Tim. “De Novo Proteins Designed From Evolutionary Principles.” 2015. Thesis, University of North Carolina. Accessed January 18, 2021. https://cdr.lib.unc.edu/record/uuid:e5c99a71-24d2-46bc-bbfe-4ff6c8607fa5.

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

MLA Handbook (7th Edition):

Jacobs, Tim. “De Novo Proteins Designed From Evolutionary Principles.” 2015. Web. 18 Jan 2021.

Vancouver:

Jacobs T. De Novo Proteins Designed From Evolutionary Principles. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2021 Jan 18]. Available from: https://cdr.lib.unc.edu/record/uuid:e5c99a71-24d2-46bc-bbfe-4ff6c8607fa5.

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

Council of Science Editors:

Jacobs T. De Novo Proteins Designed From Evolutionary Principles. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:e5c99a71-24d2-46bc-bbfe-4ff6c8607fa5

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


University of North Carolina

4. Page, Stephani. Analysis of Receiver Domain Dephosphorylation Kinetics.

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

 Plants and microorganisms use two-component signal transduction systems (TCSs) to mediate responses to stimuli. Canonical TCSs consist of a sensory component, the sensor kinase (SK),… (more)

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

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APA (6th Edition):

Page, S. (2016). Analysis of Receiver Domain Dephosphorylation Kinetics. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c10f28e9-b05d-4513-a60f-56e3289c2734

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):

Page, Stephani. “Analysis of Receiver Domain Dephosphorylation Kinetics.” 2016. Thesis, University of North Carolina. Accessed January 18, 2021. https://cdr.lib.unc.edu/record/uuid:c10f28e9-b05d-4513-a60f-56e3289c2734.

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

MLA Handbook (7th Edition):

Page, Stephani. “Analysis of Receiver Domain Dephosphorylation Kinetics.” 2016. Web. 18 Jan 2021.

Vancouver:

Page S. Analysis of Receiver Domain Dephosphorylation Kinetics. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2021 Jan 18]. Available from: https://cdr.lib.unc.edu/record/uuid:c10f28e9-b05d-4513-a60f-56e3289c2734.

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

Council of Science Editors:

Page S. Analysis of Receiver Domain Dephosphorylation Kinetics. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:c10f28e9-b05d-4513-a60f-56e3289c2734

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


University of North Carolina

5. 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 January 18, 2021. 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. 18 Jan 2021.

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 2021 Jan 18]. 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

6. 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 January 18, 2021. 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. 18 Jan 2021.

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 2021 Jan 18]. 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


University of North Carolina

7. Miller, Peter Jason. The mechanisms of pMHC recognition by the AHIII T cell receptor.

Degree: Biochemistry and Biophysics, 2008, University of North Carolina

 Cytotoxic T lymphocytes (CTL), or CD8+ T cells, are responsible for clearing infected or diseased cells from the body. Diseased cells label themselves through presentation… (more)

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

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

APA (6th Edition):

Miller, P. J. (2008). The mechanisms of pMHC recognition by the AHIII T cell receptor. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:f9789689-f2c1-4693-8933-e327e04b31d7

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):

Miller, Peter Jason. “The mechanisms of pMHC recognition by the AHIII T cell receptor.” 2008. Thesis, University of North Carolina. Accessed January 18, 2021. https://cdr.lib.unc.edu/record/uuid:f9789689-f2c1-4693-8933-e327e04b31d7.

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

MLA Handbook (7th Edition):

Miller, Peter Jason. “The mechanisms of pMHC recognition by the AHIII T cell receptor.” 2008. Web. 18 Jan 2021.

Vancouver:

Miller PJ. The mechanisms of pMHC recognition by the AHIII T cell receptor. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2021 Jan 18]. Available from: https://cdr.lib.unc.edu/record/uuid:f9789689-f2c1-4693-8933-e327e04b31d7.

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

Council of Science Editors:

Miller PJ. The mechanisms of pMHC recognition by the AHIII T cell receptor. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:f9789689-f2c1-4693-8933-e327e04b31d7

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

.