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You searched for +publisher:"University of North Carolina" +contributor:("Major, Ben"). Showing records 1 – 6 of 6 total matches.

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University of North Carolina

1. Grabon, Agnieszka. Atomistic and Cellular Analysis of Start Phosphatidylinositol Transfer Proteins in the Context of the Phospholipid Extraction Mechanism and Phosphoinositide Signaling in the Parasite Toxoplasma.

Degree: Cell Biology and Physiology, 2016, University of North Carolina

 Phosphatidylinositol transfer proteins (PITPs) are essential regulators of the interface between phosphoinositide (PIP) signaling and membrane trafficking in eukaryotic cells. Genetic derangement of PITPs in… (more)

Subjects/Keywords: School of Medicine; Department of Cell Biology and Physiology

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

APA (6th Edition):

Grabon, A. (2016). Atomistic and Cellular Analysis of Start Phosphatidylinositol Transfer Proteins in the Context of the Phospholipid Extraction Mechanism and Phosphoinositide Signaling in the Parasite Toxoplasma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:686007f0-702c-405a-9545-7dafd11bd8fa

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):

Grabon, Agnieszka. “Atomistic and Cellular Analysis of Start Phosphatidylinositol Transfer Proteins in the Context of the Phospholipid Extraction Mechanism and Phosphoinositide Signaling in the Parasite Toxoplasma.” 2016. Thesis, University of North Carolina. Accessed October 28, 2020. https://cdr.lib.unc.edu/record/uuid:686007f0-702c-405a-9545-7dafd11bd8fa.

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

MLA Handbook (7th Edition):

Grabon, Agnieszka. “Atomistic and Cellular Analysis of Start Phosphatidylinositol Transfer Proteins in the Context of the Phospholipid Extraction Mechanism and Phosphoinositide Signaling in the Parasite Toxoplasma.” 2016. Web. 28 Oct 2020.

Vancouver:

Grabon A. Atomistic and Cellular Analysis of Start Phosphatidylinositol Transfer Proteins in the Context of the Phospholipid Extraction Mechanism and Phosphoinositide Signaling in the Parasite Toxoplasma. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Oct 28]. Available from: https://cdr.lib.unc.edu/record/uuid:686007f0-702c-405a-9545-7dafd11bd8fa.

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

Council of Science Editors:

Grabon A. Atomistic and Cellular Analysis of Start Phosphatidylinositol Transfer Proteins in the Context of the Phospholipid Extraction Mechanism and Phosphoinositide Signaling in the Parasite Toxoplasma. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:686007f0-702c-405a-9545-7dafd11bd8fa

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


University of North Carolina

2. Holk, Alicia. Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer.

Degree: 2016, University of North Carolina

 Cells are subjected to a range of DNA damaging agents from intrinsic, environmental, and therapeutic sources. The ability to cope with DNA damage is essential… (more)

Subjects/Keywords: School of Medicine; Curriculum in Genetics and Molecular Biology

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APA (6th Edition):

Holk, A. (2016). Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659

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):

Holk, Alicia. “Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer.” 2016. Thesis, University of North Carolina. Accessed October 28, 2020. https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659.

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

MLA Handbook (7th Edition):

Holk, Alicia. “Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer.” 2016. Web. 28 Oct 2020.

Vancouver:

Holk A. Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Oct 28]. Available from: https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659.

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

Council of Science Editors:

Holk A. Investigating novel mechanisms of Translesion Synthesis (TLS) regulation in cancer. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:44421fcc-2ffd-4fa1-8288-80a18d51f659

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


University of North Carolina

3. Hsia, Hung-Ching. ROLES AND REGULATION OF STAT3 IN INNATE IMMUNITY.

Degree: Cell Biology and Physiology, 2017, University of North Carolina

 Innate immunity is the first line of host defense to microbial infections. The rapid induction of the innate immune response is achieved through recognition of… (more)

Subjects/Keywords: School of Medicine; Department of Cell Biology and Physiology

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

APA (6th Edition):

Hsia, H. (2017). ROLES AND REGULATION OF STAT3 IN INNATE IMMUNITY. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:757e9627-ce60-4c50-9567-df37da02c123

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):

Hsia, Hung-Ching. “ROLES AND REGULATION OF STAT3 IN INNATE IMMUNITY.” 2017. Thesis, University of North Carolina. Accessed October 28, 2020. https://cdr.lib.unc.edu/record/uuid:757e9627-ce60-4c50-9567-df37da02c123.

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

MLA Handbook (7th Edition):

Hsia, Hung-Ching. “ROLES AND REGULATION OF STAT3 IN INNATE IMMUNITY.” 2017. Web. 28 Oct 2020.

Vancouver:

Hsia H. ROLES AND REGULATION OF STAT3 IN INNATE IMMUNITY. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Oct 28]. Available from: https://cdr.lib.unc.edu/record/uuid:757e9627-ce60-4c50-9567-df37da02c123.

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

Council of Science Editors:

Hsia H. ROLES AND REGULATION OF STAT3 IN INNATE IMMUNITY. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:757e9627-ce60-4c50-9567-df37da02c123

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


University of North Carolina

4. Lessey-Morillon, Elizabeth. The RhoA Guanine Nucleotide Exchange Factor, LARG, Mediates ICAM-1-Dependent Mechanotransduction In Endothelial Cells To Stimulate Transendothelial Migration.

Degree: Cell Biology and Physiology, 2014, University of North Carolina

 RhoA-mediated cytoskeletal rearrangements in endothelial cells (ECs) play an active role in leukocyte transendothelial cell migration (TEM), a normal physiological process in which leukocytes cross… (more)

Subjects/Keywords: Cytology; School of Medicine; Department of Cell Biology and Physiology

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APA (6th Edition):

Lessey-Morillon, E. (2014). The RhoA Guanine Nucleotide Exchange Factor, LARG, Mediates ICAM-1-Dependent Mechanotransduction In Endothelial Cells To Stimulate Transendothelial Migration. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e0425b15-91e2-46a9-aead-d82aee48dc8b

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):

Lessey-Morillon, Elizabeth. “The RhoA Guanine Nucleotide Exchange Factor, LARG, Mediates ICAM-1-Dependent Mechanotransduction In Endothelial Cells To Stimulate Transendothelial Migration.” 2014. Thesis, University of North Carolina. Accessed October 28, 2020. https://cdr.lib.unc.edu/record/uuid:e0425b15-91e2-46a9-aead-d82aee48dc8b.

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

MLA Handbook (7th Edition):

Lessey-Morillon, Elizabeth. “The RhoA Guanine Nucleotide Exchange Factor, LARG, Mediates ICAM-1-Dependent Mechanotransduction In Endothelial Cells To Stimulate Transendothelial Migration.” 2014. Web. 28 Oct 2020.

Vancouver:

Lessey-Morillon E. The RhoA Guanine Nucleotide Exchange Factor, LARG, Mediates ICAM-1-Dependent Mechanotransduction In Endothelial Cells To Stimulate Transendothelial Migration. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Oct 28]. Available from: https://cdr.lib.unc.edu/record/uuid:e0425b15-91e2-46a9-aead-d82aee48dc8b.

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

Council of Science Editors:

Lessey-Morillon E. The RhoA Guanine Nucleotide Exchange Factor, LARG, Mediates ICAM-1-Dependent Mechanotransduction In Endothelial Cells To Stimulate Transendothelial Migration. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:e0425b15-91e2-46a9-aead-d82aee48dc8b

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


University of North Carolina

5. Orgel, Kelly. Advances in Treatments and Animal Models of Peanut Allergy.

Degree: Cell Biology and Physiology, 2018, University of North Carolina

 Food allergies are a growing health concern affecting approximately 6-8% of the US population. In particular, peanut allergy has an estimated prevalence of greater than… (more)

Subjects/Keywords: School of Medicine; Department of Cell Biology and Physiology

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

APA (6th Edition):

Orgel, K. (2018). Advances in Treatments and Animal Models of Peanut Allergy. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d7fad2d6-7f70-4e8a-9a06-f50aa2902145

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):

Orgel, Kelly. “Advances in Treatments and Animal Models of Peanut Allergy.” 2018. Thesis, University of North Carolina. Accessed October 28, 2020. https://cdr.lib.unc.edu/record/uuid:d7fad2d6-7f70-4e8a-9a06-f50aa2902145.

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

MLA Handbook (7th Edition):

Orgel, Kelly. “Advances in Treatments and Animal Models of Peanut Allergy.” 2018. Web. 28 Oct 2020.

Vancouver:

Orgel K. Advances in Treatments and Animal Models of Peanut Allergy. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Oct 28]. Available from: https://cdr.lib.unc.edu/record/uuid:d7fad2d6-7f70-4e8a-9a06-f50aa2902145.

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

Council of Science Editors:

Orgel K. Advances in Treatments and Animal Models of Peanut Allergy. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:d7fad2d6-7f70-4e8a-9a06-f50aa2902145

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


University of North Carolina

6. Trogden, Kathryn. TOG Proteins are spatially regulated by Rac-GSK3β to control interphase microtubule dynamics.

Degree: Biology, 2015, University of North Carolina

 Within a cell, the ends of individual microtubules switch between three different phases: growth, shrinkage and pause without affecting the total mass of microtubule polymer.… (more)

Subjects/Keywords: Cytology; College of Arts and Sciences; Department of Biology

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

APA (6th Edition):

Trogden, K. (2015). TOG Proteins are spatially regulated by Rac-GSK3β to control interphase microtubule dynamics. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e7f154cb-e2de-418b-a81d-6446323d1fcb

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):

Trogden, Kathryn. “TOG Proteins are spatially regulated by Rac-GSK3β to control interphase microtubule dynamics.” 2015. Thesis, University of North Carolina. Accessed October 28, 2020. https://cdr.lib.unc.edu/record/uuid:e7f154cb-e2de-418b-a81d-6446323d1fcb.

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

MLA Handbook (7th Edition):

Trogden, Kathryn. “TOG Proteins are spatially regulated by Rac-GSK3β to control interphase microtubule dynamics.” 2015. Web. 28 Oct 2020.

Vancouver:

Trogden K. TOG Proteins are spatially regulated by Rac-GSK3β to control interphase microtubule dynamics. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Oct 28]. Available from: https://cdr.lib.unc.edu/record/uuid:e7f154cb-e2de-418b-a81d-6446323d1fcb.

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

Council of Science Editors:

Trogden K. TOG Proteins are spatially regulated by Rac-GSK3β to control interphase microtubule dynamics. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:e7f154cb-e2de-418b-a81d-6446323d1fcb

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

.