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You searched for subject:(Department of Pharmacology). Showing records 1 – 30 of 226 total matches.

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University of North Carolina

1. Warischalk, Jayme. UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMES.

Degree: Pharmacology, 2015, University of North Carolina

 Recombinant adeno-associated virus (rAAV) has become increasingly employed as a gene delivery vector in clinical trials. Despite several notable instances of success using rAAV-based gene… (more)

Subjects/Keywords: Pharmacology; School of Medicine; Department of Pharmacology

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

APA (6th Edition):

Warischalk, J. (2015). UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMES. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:2c8190bc-d735-4ce4-b087-51f0f652a92c

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):

Warischalk, Jayme. “UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMES.” 2015. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:2c8190bc-d735-4ce4-b087-51f0f652a92c.

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

MLA Handbook (7th Edition):

Warischalk, Jayme. “UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMES.” 2015. Web. 27 Sep 2020.

Vancouver:

Warischalk J. UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMES. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:2c8190bc-d735-4ce4-b087-51f0f652a92c.

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

Council of Science Editors:

Warischalk J. UNCOVERING STRUCTURAL COMPONENTS OF THE ADENO-ASSOCIATED VIRAL CAPSID THAT CAN BE MODIFIED TO IMPROVE CLINICAL GENE THERAPY OUTCOMES. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:2c8190bc-d735-4ce4-b087-51f0f652a92c

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


University of North Carolina

2. Gentry, Leanna. Targeting the Ras-Ral effector pathway for cancer treatment.

Degree: Pharmacology, 2015, University of North Carolina

 The RAS oncogene is the most frequently mutated gene in human cancers, and this activated Ras oncoprotein has been shown to be required for both… (more)

Subjects/Keywords: Pharmacology; School of Medicine; Department of Pharmacology

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APA (6th Edition):

Gentry, L. (2015). Targeting the Ras-Ral effector pathway for cancer treatment. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:c75ba6bc-3f00-4527-8f20-029bf699aad2

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):

Gentry, Leanna. “Targeting the Ras-Ral effector pathway for cancer treatment.” 2015. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:c75ba6bc-3f00-4527-8f20-029bf699aad2.

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

MLA Handbook (7th Edition):

Gentry, Leanna. “Targeting the Ras-Ral effector pathway for cancer treatment.” 2015. Web. 27 Sep 2020.

Vancouver:

Gentry L. Targeting the Ras-Ral effector pathway for cancer treatment. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:c75ba6bc-3f00-4527-8f20-029bf699aad2.

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

Council of Science Editors:

Gentry L. Targeting the Ras-Ral effector pathway for cancer treatment. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:c75ba6bc-3f00-4527-8f20-029bf699aad2

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


University of North Carolina

3. Eldridge, Meagan. Identifying biomarkers of response to modified FOLFIRINOX regimens using patient derived xenograft mouse models of pancreatic ductal adenocarcinoma.

Degree: Pharmacology, 2014, University of North Carolina

 Pancreatic ductal adenocarcinoma (PDAC) is a lethal disease with limited effective therapies. FOLFIRINOX is a chemotherapeutic regimen for patients with metastatic disease that provides an… (more)

Subjects/Keywords: Pharmacology; School of Medicine; Department of Pharmacology

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

APA (6th Edition):

Eldridge, M. (2014). Identifying biomarkers of response to modified FOLFIRINOX regimens using patient derived xenograft mouse models of pancreatic ductal adenocarcinoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:53f3ee63-f386-49e8-b5d3-a2569507dc6e

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):

Eldridge, Meagan. “Identifying biomarkers of response to modified FOLFIRINOX regimens using patient derived xenograft mouse models of pancreatic ductal adenocarcinoma.” 2014. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:53f3ee63-f386-49e8-b5d3-a2569507dc6e.

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

MLA Handbook (7th Edition):

Eldridge, Meagan. “Identifying biomarkers of response to modified FOLFIRINOX regimens using patient derived xenograft mouse models of pancreatic ductal adenocarcinoma.” 2014. Web. 27 Sep 2020.

Vancouver:

Eldridge M. Identifying biomarkers of response to modified FOLFIRINOX regimens using patient derived xenograft mouse models of pancreatic ductal adenocarcinoma. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:53f3ee63-f386-49e8-b5d3-a2569507dc6e.

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

Council of Science Editors:

Eldridge M. Identifying biomarkers of response to modified FOLFIRINOX regimens using patient derived xenograft mouse models of pancreatic ductal adenocarcinoma. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:53f3ee63-f386-49e8-b5d3-a2569507dc6e

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


University of North Carolina

4. Stratford, Jeran. Aberrant Gene Expression: Diagnostic Markers and Therapeutic Targets for Pancreatic Cancer.

Degree: Pharmacology, 2014, University of North Carolina

 Pancreatic ductal adenocarcinoma (PDAC) is an aggressive cancer and the fourth leading cause of cancer-related death in the United States. The overall median survival for… (more)

Subjects/Keywords: Pharmacology; School of Medicine; Department of Pharmacology

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APA (6th Edition):

Stratford, J. (2014). Aberrant Gene Expression: Diagnostic Markers and Therapeutic Targets for Pancreatic Cancer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:84f3613f-5709-4ae6-8407-999e9eb3a6eb

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):

Stratford, Jeran. “Aberrant Gene Expression: Diagnostic Markers and Therapeutic Targets for Pancreatic Cancer.” 2014. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:84f3613f-5709-4ae6-8407-999e9eb3a6eb.

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

MLA Handbook (7th Edition):

Stratford, Jeran. “Aberrant Gene Expression: Diagnostic Markers and Therapeutic Targets for Pancreatic Cancer.” 2014. Web. 27 Sep 2020.

Vancouver:

Stratford J. Aberrant Gene Expression: Diagnostic Markers and Therapeutic Targets for Pancreatic Cancer. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:84f3613f-5709-4ae6-8407-999e9eb3a6eb.

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

Council of Science Editors:

Stratford J. Aberrant Gene Expression: Diagnostic Markers and Therapeutic Targets for Pancreatic Cancer. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:84f3613f-5709-4ae6-8407-999e9eb3a6eb

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


University of North Carolina

5. White, Kate. Identification of Biased Kappa Opioid Receptor Ligands For In Vivo Probing of Specific Signal Transduction Pathways.

Degree: Pharmacology, 2014, University of North Carolina

 The κ opioid receptor (KOR)-dynorphin system has been implicated in the control of affect, cognition, motivation, and is thought to be dysregulated in mood and… (more)

Subjects/Keywords: Pharmacology; School of Medicine; Department of Pharmacology

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APA (6th Edition):

White, K. (2014). Identification of Biased Kappa Opioid Receptor Ligands For In Vivo Probing of Specific Signal Transduction Pathways. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:f1c03647-248b-4104-8356-1632c5c538b7

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):

White, Kate. “Identification of Biased Kappa Opioid Receptor Ligands For In Vivo Probing of Specific Signal Transduction Pathways.” 2014. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:f1c03647-248b-4104-8356-1632c5c538b7.

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

MLA Handbook (7th Edition):

White, Kate. “Identification of Biased Kappa Opioid Receptor Ligands For In Vivo Probing of Specific Signal Transduction Pathways.” 2014. Web. 27 Sep 2020.

Vancouver:

White K. Identification of Biased Kappa Opioid Receptor Ligands For In Vivo Probing of Specific Signal Transduction Pathways. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:f1c03647-248b-4104-8356-1632c5c538b7.

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

Council of Science Editors:

White K. Identification of Biased Kappa Opioid Receptor Ligands For In Vivo Probing of Specific Signal Transduction Pathways. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:f1c03647-248b-4104-8356-1632c5c538b7

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


University of North Carolina

6. Zand, Tanya Parisaw. Ras signaling through the RalGEF-Ral pathway in C. elegans.

Degree: Pharmacology, 2010, University of North Carolina

 The classical Ras effector pathway involves activation of the Raf-MEK-ERK mitogen-activated protein kinase cascade. Recent studies show that a second Ras effector cascade, Ral guanine… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Zand, T. P. (2010). Ras signaling through the RalGEF-Ral pathway in C. elegans. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:752d8586-c911-4e85-8cec-3671c6564a4d

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):

Zand, Tanya Parisaw. “Ras signaling through the RalGEF-Ral pathway in C. elegans.” 2010. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:752d8586-c911-4e85-8cec-3671c6564a4d.

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

MLA Handbook (7th Edition):

Zand, Tanya Parisaw. “Ras signaling through the RalGEF-Ral pathway in C. elegans.” 2010. Web. 27 Sep 2020.

Vancouver:

Zand TP. Ras signaling through the RalGEF-Ral pathway in C. elegans. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:752d8586-c911-4e85-8cec-3671c6564a4d.

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

Council of Science Editors:

Zand TP. Ras signaling through the RalGEF-Ral pathway in C. elegans. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:752d8586-c911-4e85-8cec-3671c6564a4d

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


University of North Carolina

7. Ricks, Tiffany K. Signal regulation of protease-activated receptor-2 and structural determinants of Gαq-dependent activation and deactivation of phospholipase C-β.

Degree: Pharmacology, 2010, University of North Carolina

 Cells respond to changes in their environment by relaying information from extracellular cues to intracellular compartments, and receptors play an important role in the transmission… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Ricks, T. K. (2010). Signal regulation of protease-activated receptor-2 and structural determinants of Gαq-dependent activation and deactivation of phospholipase C-β. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:df095959-028b-4e36-a6bd-f67dbd401a26

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):

Ricks, Tiffany K. “Signal regulation of protease-activated receptor-2 and structural determinants of Gαq-dependent activation and deactivation of phospholipase C-β.” 2010. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:df095959-028b-4e36-a6bd-f67dbd401a26.

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

MLA Handbook (7th Edition):

Ricks, Tiffany K. “Signal regulation of protease-activated receptor-2 and structural determinants of Gαq-dependent activation and deactivation of phospholipase C-β.” 2010. Web. 27 Sep 2020.

Vancouver:

Ricks TK. Signal regulation of protease-activated receptor-2 and structural determinants of Gαq-dependent activation and deactivation of phospholipase C-β. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:df095959-028b-4e36-a6bd-f67dbd401a26.

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

Council of Science Editors:

Ricks TK. Signal regulation of protease-activated receptor-2 and structural determinants of Gαq-dependent activation and deactivation of phospholipase C-β. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:df095959-028b-4e36-a6bd-f67dbd401a26

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


University of North Carolina

8. Hand, Randal Alan. The regulation of cortical development by Neurogenin2.

Degree: Pharmacology, 2010, University of North Carolina

 The mammalian nervous system consists of complex neuronal networks formed by extremely diverse sub-groups of neurons located throughout the body. Neurons of the cerebral cortex… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Hand, R. A. (2010). The regulation of cortical development by Neurogenin2. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:0fba9190-b71d-4cf5-9919-85b2ebee0fdb

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):

Hand, Randal Alan. “The regulation of cortical development by Neurogenin2.” 2010. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:0fba9190-b71d-4cf5-9919-85b2ebee0fdb.

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

MLA Handbook (7th Edition):

Hand, Randal Alan. “The regulation of cortical development by Neurogenin2.” 2010. Web. 27 Sep 2020.

Vancouver:

Hand RA. The regulation of cortical development by Neurogenin2. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:0fba9190-b71d-4cf5-9919-85b2ebee0fdb.

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

Council of Science Editors:

Hand RA. The regulation of cortical development by Neurogenin2. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:0fba9190-b71d-4cf5-9919-85b2ebee0fdb

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


University of North Carolina

9. Culmer, Tyechia L. CB1 Receptor Activity Modulates Responses in the Forced Swim Test and Open Field Test Paradigms.

Degree: Pharmacology, 2010, University of North Carolina

 Cannabinoid type I (CB1) receptor activation in the forced swim test (FST) and on locomotor activity (LMA) was examined by manipulating the endogenous agonist anandamide… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Culmer, T. L. (2010). CB1 Receptor Activity Modulates Responses in the Forced Swim Test and Open Field Test Paradigms. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:071aaf2a-5d89-41b5-ac8a-6f11bea39e4c

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):

Culmer, Tyechia L. “CB1 Receptor Activity Modulates Responses in the Forced Swim Test and Open Field Test Paradigms.” 2010. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:071aaf2a-5d89-41b5-ac8a-6f11bea39e4c.

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

MLA Handbook (7th Edition):

Culmer, Tyechia L. “CB1 Receptor Activity Modulates Responses in the Forced Swim Test and Open Field Test Paradigms.” 2010. Web. 27 Sep 2020.

Vancouver:

Culmer TL. CB1 Receptor Activity Modulates Responses in the Forced Swim Test and Open Field Test Paradigms. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:071aaf2a-5d89-41b5-ac8a-6f11bea39e4c.

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

Council of Science Editors:

Culmer TL. CB1 Receptor Activity Modulates Responses in the Forced Swim Test and Open Field Test Paradigms. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:071aaf2a-5d89-41b5-ac8a-6f11bea39e4c

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


University of North Carolina

10. McMullen, Allison B. Cellular, Histological and Behavioral Changes in the Pathogenesis of Hydrocephalus in the Ro1 Mouse Model.

Degree: Pharmacology, 2011, University of North Carolina

 Hydrocephalus is a highly prevalent neurological disorder characterized by elevated levels of cerebrospinal fluid (CSF) in the brain and subsequent enlargement of the lateral ventricles.… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

McMullen, A. B. (2011). Cellular, Histological and Behavioral Changes in the Pathogenesis of Hydrocephalus in the Ro1 Mouse Model. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:79730dbd-c913-4972-bbd9-0378ba2f39aa

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):

McMullen, Allison B. “Cellular, Histological and Behavioral Changes in the Pathogenesis of Hydrocephalus in the Ro1 Mouse Model.” 2011. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:79730dbd-c913-4972-bbd9-0378ba2f39aa.

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

MLA Handbook (7th Edition):

McMullen, Allison B. “Cellular, Histological and Behavioral Changes in the Pathogenesis of Hydrocephalus in the Ro1 Mouse Model.” 2011. Web. 27 Sep 2020.

Vancouver:

McMullen AB. Cellular, Histological and Behavioral Changes in the Pathogenesis of Hydrocephalus in the Ro1 Mouse Model. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:79730dbd-c913-4972-bbd9-0378ba2f39aa.

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

Council of Science Editors:

McMullen AB. Cellular, Histological and Behavioral Changes in the Pathogenesis of Hydrocephalus in the Ro1 Mouse Model. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:79730dbd-c913-4972-bbd9-0378ba2f39aa

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


University of North Carolina

11. Cappell, Steven D. Systematic analysis of essential genes reveals new regulators of G protein signaling.

Degree: Pharmacology, 2011, University of North Carolina

 Heterotrimeric G proteins are molecular switches that respond to a wide range of stimuli including light, neurotransmitters, small molecules and peptides. Due to their role… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Cappell, S. D. (2011). Systematic analysis of essential genes reveals new regulators of G protein signaling. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:246a6aed-44b1-47bf-a985-22a9c85cdbff

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):

Cappell, Steven D. “Systematic analysis of essential genes reveals new regulators of G protein signaling.” 2011. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:246a6aed-44b1-47bf-a985-22a9c85cdbff.

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

MLA Handbook (7th Edition):

Cappell, Steven D. “Systematic analysis of essential genes reveals new regulators of G protein signaling.” 2011. Web. 27 Sep 2020.

Vancouver:

Cappell SD. Systematic analysis of essential genes reveals new regulators of G protein signaling. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:246a6aed-44b1-47bf-a985-22a9c85cdbff.

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

Council of Science Editors:

Cappell SD. Systematic analysis of essential genes reveals new regulators of G protein signaling. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:246a6aed-44b1-47bf-a985-22a9c85cdbff

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


University of North Carolina

12. Bauman, John A. Modification of Bcl-x and Mcl-1 pre-mRNA splicing using splice-switching oligonucleotides.

Degree: Pharmacology, 2011, University of North Carolina

 Over 90% of multi-exon pre-mRNA transcripts undergo alternative splicing and up to one-half of disease-causing mutations affect splicing. Thus, alternative splicing has emerged as an… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Bauman, J. A. (2011). Modification of Bcl-x and Mcl-1 pre-mRNA splicing using splice-switching oligonucleotides. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3e988a9e-762c-4981-aa11-d892a9de95db

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):

Bauman, John A. “Modification of Bcl-x and Mcl-1 pre-mRNA splicing using splice-switching oligonucleotides.” 2011. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:3e988a9e-762c-4981-aa11-d892a9de95db.

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

MLA Handbook (7th Edition):

Bauman, John A. “Modification of Bcl-x and Mcl-1 pre-mRNA splicing using splice-switching oligonucleotides.” 2011. Web. 27 Sep 2020.

Vancouver:

Bauman JA. Modification of Bcl-x and Mcl-1 pre-mRNA splicing using splice-switching oligonucleotides. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:3e988a9e-762c-4981-aa11-d892a9de95db.

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

Council of Science Editors:

Bauman JA. Modification of Bcl-x and Mcl-1 pre-mRNA splicing using splice-switching oligonucleotides. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:3e988a9e-762c-4981-aa11-d892a9de95db

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


University of North Carolina

13. Phillips, Ryan Matthew. Development of a Novel Assay of Protein Tyrosine Phosphatase Activity in Single Cells Using Capillary Electrophoresis.

Degree: Pharmacology, 2013, University of North Carolina

 The inhalation of diesel exhaust particles has been linked to human diseases including airway inflammation, arrhythmias, heart attack, stroke, hypertension, and cancer. In vitro studies… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Phillips, R. M. (2013). Development of a Novel Assay of Protein Tyrosine Phosphatase Activity in Single Cells Using Capillary Electrophoresis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:8527a12d-7346-46d7-94b4-929cadc638fe

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):

Phillips, Ryan Matthew. “Development of a Novel Assay of Protein Tyrosine Phosphatase Activity in Single Cells Using Capillary Electrophoresis.” 2013. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:8527a12d-7346-46d7-94b4-929cadc638fe.

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

MLA Handbook (7th Edition):

Phillips, Ryan Matthew. “Development of a Novel Assay of Protein Tyrosine Phosphatase Activity in Single Cells Using Capillary Electrophoresis.” 2013. Web. 27 Sep 2020.

Vancouver:

Phillips RM. Development of a Novel Assay of Protein Tyrosine Phosphatase Activity in Single Cells Using Capillary Electrophoresis. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:8527a12d-7346-46d7-94b4-929cadc638fe.

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

Council of Science Editors:

Phillips RM. Development of a Novel Assay of Protein Tyrosine Phosphatase Activity in Single Cells Using Capillary Electrophoresis. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:8527a12d-7346-46d7-94b4-929cadc638fe

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


University of North Carolina

14. Dominguez, Daniel I. TRANSCRIPTOME DYNAMICS DURING THE MAMMALIAN CELL CYCLE.

Degree: Pharmacology, 2014, University of North Carolina

 In recent years, technologies capable of simultaneously deciphering the nucleotide sequence and expression level of most RNAs in the cell have challenged the simplistic view… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Dominguez, D. I. (2014). TRANSCRIPTOME DYNAMICS DURING THE MAMMALIAN CELL CYCLE. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:40ce8119-243d-4275-8c7f-ad575de3415f

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):

Dominguez, Daniel I. “TRANSCRIPTOME DYNAMICS DURING THE MAMMALIAN CELL CYCLE.” 2014. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:40ce8119-243d-4275-8c7f-ad575de3415f.

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

MLA Handbook (7th Edition):

Dominguez, Daniel I. “TRANSCRIPTOME DYNAMICS DURING THE MAMMALIAN CELL CYCLE.” 2014. Web. 27 Sep 2020.

Vancouver:

Dominguez DI. TRANSCRIPTOME DYNAMICS DURING THE MAMMALIAN CELL CYCLE. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:40ce8119-243d-4275-8c7f-ad575de3415f.

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

Council of Science Editors:

Dominguez DI. TRANSCRIPTOME DYNAMICS DURING THE MAMMALIAN CELL CYCLE. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:40ce8119-243d-4275-8c7f-ad575de3415f

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


University of North Carolina

15. English, Justin Gregory. Decoding the Yeast Stress Adaptation Circuit.

Degree: Pharmacology, 2014, University of North Carolina

 Cells must adapt to survive. To mount an appropriate adaptive response the cell must relay information from its surroundings to its adaptive machinery. This process,… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

English, J. G. (2014). Decoding the Yeast Stress Adaptation Circuit. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:84864611-1cdc-4881-a15c-2c5ca5b7a074

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):

English, Justin Gregory. “Decoding the Yeast Stress Adaptation Circuit.” 2014. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:84864611-1cdc-4881-a15c-2c5ca5b7a074.

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

MLA Handbook (7th Edition):

English, Justin Gregory. “Decoding the Yeast Stress Adaptation Circuit.” 2014. Web. 27 Sep 2020.

Vancouver:

English JG. Decoding the Yeast Stress Adaptation Circuit. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:84864611-1cdc-4881-a15c-2c5ca5b7a074.

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

Council of Science Editors:

English JG. Decoding the Yeast Stress Adaptation Circuit. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:84864611-1cdc-4881-a15c-2c5ca5b7a074

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


University of North Carolina

16. Huff, Lauren Parker. Impact of subcellular localization on oncogenic functions of the RhoGEF Ect2 and on its Rho GTPase targets.

Degree: Pharmacology, 2013, University of North Carolina

 Rho GTPases are molecular switches that canonically signal from the plasma membrane or endomembranes to control a wide variety of cellular processes. Their activation is… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Huff, L. P. (2013). Impact of subcellular localization on oncogenic functions of the RhoGEF Ect2 and on its Rho GTPase targets. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:d1e3a7f2-7613-4807-be51-d515341b9729

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):

Huff, Lauren Parker. “Impact of subcellular localization on oncogenic functions of the RhoGEF Ect2 and on its Rho GTPase targets.” 2013. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:d1e3a7f2-7613-4807-be51-d515341b9729.

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

MLA Handbook (7th Edition):

Huff, Lauren Parker. “Impact of subcellular localization on oncogenic functions of the RhoGEF Ect2 and on its Rho GTPase targets.” 2013. Web. 27 Sep 2020.

Vancouver:

Huff LP. Impact of subcellular localization on oncogenic functions of the RhoGEF Ect2 and on its Rho GTPase targets. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:d1e3a7f2-7613-4807-be51-d515341b9729.

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

Council of Science Editors:

Huff LP. Impact of subcellular localization on oncogenic functions of the RhoGEF Ect2 and on its Rho GTPase targets. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:d1e3a7f2-7613-4807-be51-d515341b9729

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


University of North Carolina

17. Richardson, Bryan Timothy. Defining the Molecular Mechanisms of the Cerebral Cavernous Malformation Proteins.

Degree: Pharmacology, 2013, University of North Carolina

 Cerebral cavernous malformations (CCM) are the second most common class of cerebrovascular brain malformations affecting .1-.5% of the population. The disease is manifested in endothelial… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Richardson, B. T. (2013). Defining the Molecular Mechanisms of the Cerebral Cavernous Malformation Proteins. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:6478fcfa-19a8-41df-9bea-f7ca335f9d7c

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):

Richardson, Bryan Timothy. “Defining the Molecular Mechanisms of the Cerebral Cavernous Malformation Proteins.” 2013. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:6478fcfa-19a8-41df-9bea-f7ca335f9d7c.

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

MLA Handbook (7th Edition):

Richardson, Bryan Timothy. “Defining the Molecular Mechanisms of the Cerebral Cavernous Malformation Proteins.” 2013. Web. 27 Sep 2020.

Vancouver:

Richardson BT. Defining the Molecular Mechanisms of the Cerebral Cavernous Malformation Proteins. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:6478fcfa-19a8-41df-9bea-f7ca335f9d7c.

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

Council of Science Editors:

Richardson BT. Defining the Molecular Mechanisms of the Cerebral Cavernous Malformation Proteins. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:6478fcfa-19a8-41df-9bea-f7ca335f9d7c

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


University of North Carolina

18. Whittle, Martin C. Targeting the Triple-Negative Breast Cancer Kinome with Chemical Proteomics.

Degree: Pharmacology, 2013, University of North Carolina

 Kinases are members of a large dynamic and cooperative signaling network, which senses inhibition of key nodal kinases and induces compensatory responses that offset pharmacological… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Whittle, M. C. (2013). Targeting the Triple-Negative Breast Cancer Kinome with Chemical Proteomics. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:9ae50bab-4c5d-47ec-a991-f6785a6e367b

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):

Whittle, Martin C. “Targeting the Triple-Negative Breast Cancer Kinome with Chemical Proteomics.” 2013. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:9ae50bab-4c5d-47ec-a991-f6785a6e367b.

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

MLA Handbook (7th Edition):

Whittle, Martin C. “Targeting the Triple-Negative Breast Cancer Kinome with Chemical Proteomics.” 2013. Web. 27 Sep 2020.

Vancouver:

Whittle MC. Targeting the Triple-Negative Breast Cancer Kinome with Chemical Proteomics. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:9ae50bab-4c5d-47ec-a991-f6785a6e367b.

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

Council of Science Editors:

Whittle MC. Targeting the Triple-Negative Breast Cancer Kinome with Chemical Proteomics. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:9ae50bab-4c5d-47ec-a991-f6785a6e367b

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


University of North Carolina

19. Zimmerman, Eric. MOLECULAR ADAPTATION TO ANTI-CANCER CHEMOTHERAPY IN LEUKEMIA.

Degree: Pharmacology, 2011, University of North Carolina

 Drug resistance to anti-cancer chemotherapy is a significant barrier to the treatment of leukemia patients. Many times, resistance results from molecular adaptation to drug exposure,… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Zimmerman, E. (2011). MOLECULAR ADAPTATION TO ANTI-CANCER CHEMOTHERAPY IN LEUKEMIA. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:ff100956-ccba-4659-b349-99bda9a325d6

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):

Zimmerman, Eric. “MOLECULAR ADAPTATION TO ANTI-CANCER CHEMOTHERAPY IN LEUKEMIA.” 2011. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:ff100956-ccba-4659-b349-99bda9a325d6.

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

MLA Handbook (7th Edition):

Zimmerman, Eric. “MOLECULAR ADAPTATION TO ANTI-CANCER CHEMOTHERAPY IN LEUKEMIA.” 2011. Web. 27 Sep 2020.

Vancouver:

Zimmerman E. MOLECULAR ADAPTATION TO ANTI-CANCER CHEMOTHERAPY IN LEUKEMIA. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:ff100956-ccba-4659-b349-99bda9a325d6.

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

Council of Science Editors:

Zimmerman E. MOLECULAR ADAPTATION TO ANTI-CANCER CHEMOTHERAPY IN LEUKEMIA. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:ff100956-ccba-4659-b349-99bda9a325d6

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


University of North Carolina

20. Rogan, Sarah. Remote Control of Neuronal Signaling in vivo.

Degree: Pharmacology, 2011, University of North Carolina

 A significant challenge for neuroscientists is to determine how both electrical and chemical signals affect the activity of cells and circuits and how the nervous… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Rogan, S. (2011). Remote Control of Neuronal Signaling in vivo. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:0172af27-f131-4573-b8f3-1523d34c3b79

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):

Rogan, Sarah. “Remote Control of Neuronal Signaling in vivo.” 2011. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:0172af27-f131-4573-b8f3-1523d34c3b79.

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

MLA Handbook (7th Edition):

Rogan, Sarah. “Remote Control of Neuronal Signaling in vivo.” 2011. Web. 27 Sep 2020.

Vancouver:

Rogan S. Remote Control of Neuronal Signaling in vivo. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:0172af27-f131-4573-b8f3-1523d34c3b79.

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

Council of Science Editors:

Rogan S. Remote Control of Neuronal Signaling in vivo. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:0172af27-f131-4573-b8f3-1523d34c3b79

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


University of North Carolina

21. Alan, Jamie. TYROSINE KINASE MODULATION OF TRAFFICKING AND BIOLOGICAL FUNCTIONS OF THE ATYPICAL RHO GTPASE, WRCH-1.

Degree: Pharmacology, 2010, University of North Carolina

 Wrch-1 is an atypical Rho family small GTPase with roles in oncogenic transformation, epithelial cell morphogenesis, osteoclastogenesis, and migration. We have shown previously that Wrch-1… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Alan, J. (2010). TYROSINE KINASE MODULATION OF TRAFFICKING AND BIOLOGICAL FUNCTIONS OF THE ATYPICAL RHO GTPASE, WRCH-1. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:afbc9ce5-f21d-4707-8744-357971e1eb3b

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):

Alan, Jamie. “TYROSINE KINASE MODULATION OF TRAFFICKING AND BIOLOGICAL FUNCTIONS OF THE ATYPICAL RHO GTPASE, WRCH-1.” 2010. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:afbc9ce5-f21d-4707-8744-357971e1eb3b.

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

MLA Handbook (7th Edition):

Alan, Jamie. “TYROSINE KINASE MODULATION OF TRAFFICKING AND BIOLOGICAL FUNCTIONS OF THE ATYPICAL RHO GTPASE, WRCH-1.” 2010. Web. 27 Sep 2020.

Vancouver:

Alan J. TYROSINE KINASE MODULATION OF TRAFFICKING AND BIOLOGICAL FUNCTIONS OF THE ATYPICAL RHO GTPASE, WRCH-1. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:afbc9ce5-f21d-4707-8744-357971e1eb3b.

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

Council of Science Editors:

Alan J. TYROSINE KINASE MODULATION OF TRAFFICKING AND BIOLOGICAL FUNCTIONS OF THE ATYPICAL RHO GTPASE, WRCH-1. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:afbc9ce5-f21d-4707-8744-357971e1eb3b

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


University of North Carolina

22. Blatt, Tasha. Role of the P2Y1 receptor in platelet activation.

Degree: Pharmacology, 2016, University of North Carolina

 Understanding and manipulating thrombosis and blood hemostasis is critical for the effective treatment of patients at risk for heart attack and stroke. ADP is an… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Blatt, T. (2016). Role of the P2Y1 receptor in platelet activation. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:44ab11e3-9091-4cfa-820f-93f471aaed92

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):

Blatt, Tasha. “Role of the P2Y1 receptor in platelet activation.” 2016. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:44ab11e3-9091-4cfa-820f-93f471aaed92.

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

MLA Handbook (7th Edition):

Blatt, Tasha. “Role of the P2Y1 receptor in platelet activation.” 2016. Web. 27 Sep 2020.

Vancouver:

Blatt T. Role of the P2Y1 receptor in platelet activation. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:44ab11e3-9091-4cfa-820f-93f471aaed92.

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

Council of Science Editors:

Blatt T. Role of the P2Y1 receptor in platelet activation. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:44ab11e3-9091-4cfa-820f-93f471aaed92

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


University of North Carolina

23. Schools, Zachary. Engineering and biophysical analysis of alpha adrenergic receptor crystallography constructs.

Degree: Pharmacology, 2016, University of North Carolina

 G protein-coupled receptors (GPCRs) are ubiquitously expressed membrane-spanning proteins that control all of human physiology. GPCRs are structurally complex and their mechanism of activation and… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Schools, Z. (2016). Engineering and biophysical analysis of alpha adrenergic receptor crystallography constructs. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5cc29081-8f96-4443-8ee6-f1f839f9a631

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):

Schools, Zachary. “Engineering and biophysical analysis of alpha adrenergic receptor crystallography constructs.” 2016. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:5cc29081-8f96-4443-8ee6-f1f839f9a631.

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

MLA Handbook (7th Edition):

Schools, Zachary. “Engineering and biophysical analysis of alpha adrenergic receptor crystallography constructs.” 2016. Web. 27 Sep 2020.

Vancouver:

Schools Z. Engineering and biophysical analysis of alpha adrenergic receptor crystallography constructs. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:5cc29081-8f96-4443-8ee6-f1f839f9a631.

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

Council of Science Editors:

Schools Z. Engineering and biophysical analysis of alpha adrenergic receptor crystallography constructs. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:5cc29081-8f96-4443-8ee6-f1f839f9a631

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


University of North Carolina

24. Ezekwe, Ejiofofr. Cellular Mechanisms of Staphylococcus aureus α-hemolysinmediated Activation of the NLRP3 Inflammasome.

Degree: Pharmacology, 2016, University of North Carolina

 Background: Staphylococcus aureus toxin, α-hemolysin, is secreted as a soluble monomer that forms a heptameric pore in the membranes of a range of host cell… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Ezekwe, E. (2016). Cellular Mechanisms of Staphylococcus aureus α-hemolysinmediated Activation of the NLRP3 Inflammasome. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b2765954-f2a2-473f-8501-6a8bd05a8935

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):

Ezekwe, Ejiofofr. “Cellular Mechanisms of Staphylococcus aureus α-hemolysinmediated Activation of the NLRP3 Inflammasome.” 2016. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:b2765954-f2a2-473f-8501-6a8bd05a8935.

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

MLA Handbook (7th Edition):

Ezekwe, Ejiofofr. “Cellular Mechanisms of Staphylococcus aureus α-hemolysinmediated Activation of the NLRP3 Inflammasome.” 2016. Web. 27 Sep 2020.

Vancouver:

Ezekwe E. Cellular Mechanisms of Staphylococcus aureus α-hemolysinmediated Activation of the NLRP3 Inflammasome. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:b2765954-f2a2-473f-8501-6a8bd05a8935.

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

Council of Science Editors:

Ezekwe E. Cellular Mechanisms of Staphylococcus aureus α-hemolysinmediated Activation of the NLRP3 Inflammasome. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:b2765954-f2a2-473f-8501-6a8bd05a8935

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


University of North Carolina

25. Constance, Brian. The role of tau in Alzheimer’s Disease: Effects of Lys-280 and Lys-281 acetylation on tau function and structure.

Degree: Pharmacology, 2016, University of North Carolina

 The tau protein is implicated in Alzheimer’s disease (AD), and it is a prominent feature of AD pathology. In AD, tau's normal ability to stabilize… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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

APA (6th Edition):

Constance, B. (2016). The role of tau in Alzheimer’s Disease: Effects of Lys-280 and Lys-281 acetylation on tau function and structure. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:80bdebaf-4ea9-45e7-8bd1-4e1e43c5c11a

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):

Constance, Brian. “The role of tau in Alzheimer’s Disease: Effects of Lys-280 and Lys-281 acetylation on tau function and structure.” 2016. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:80bdebaf-4ea9-45e7-8bd1-4e1e43c5c11a.

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

MLA Handbook (7th Edition):

Constance, Brian. “The role of tau in Alzheimer’s Disease: Effects of Lys-280 and Lys-281 acetylation on tau function and structure.” 2016. Web. 27 Sep 2020.

Vancouver:

Constance B. The role of tau in Alzheimer’s Disease: Effects of Lys-280 and Lys-281 acetylation on tau function and structure. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:80bdebaf-4ea9-45e7-8bd1-4e1e43c5c11a.

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

Council of Science Editors:

Constance B. The role of tau in Alzheimer’s Disease: Effects of Lys-280 and Lys-281 acetylation on tau function and structure. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:80bdebaf-4ea9-45e7-8bd1-4e1e43c5c11a

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


University of North Carolina

26. Zhou, Bingying. RAS signaling and therapeutic resistance in melanoma.

Degree: Pharmacology, 2016, University of North Carolina

 Increasing appreciation of the complexity of RAS signaling in cancer has led to a renewed wave of RAS research. I have focused on two key… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Zhou, B. (2016). RAS signaling and therapeutic resistance in melanoma. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:26347cfa-34a3-4849-b350-f66b6a70334a

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):

Zhou, Bingying. “RAS signaling and therapeutic resistance in melanoma.” 2016. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:26347cfa-34a3-4849-b350-f66b6a70334a.

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

MLA Handbook (7th Edition):

Zhou, Bingying. “RAS signaling and therapeutic resistance in melanoma.” 2016. Web. 27 Sep 2020.

Vancouver:

Zhou B. RAS signaling and therapeutic resistance in melanoma. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:26347cfa-34a3-4849-b350-f66b6a70334a.

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

Council of Science Editors:

Zhou B. RAS signaling and therapeutic resistance in melanoma. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:26347cfa-34a3-4849-b350-f66b6a70334a

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


University of North Carolina

27. Walter, Thomas. Ethanol and Microglia: From Molecules to Behavior.

Degree: Pharmacology, 2017, University of North Carolina

 Alcohol use disorders (AUDs) are prevalent mental health conditions involving problematic alcohol use despite negative consequences. Available treatments for AUDs are often unhelpful, prompting a… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Walter, T. (2017). Ethanol and Microglia: From Molecules to Behavior. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e4a31f62-4b30-4145-a953-9ff09b65a500

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):

Walter, Thomas. “Ethanol and Microglia: From Molecules to Behavior.” 2017. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:e4a31f62-4b30-4145-a953-9ff09b65a500.

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

MLA Handbook (7th Edition):

Walter, Thomas. “Ethanol and Microglia: From Molecules to Behavior.” 2017. Web. 27 Sep 2020.

Vancouver:

Walter T. Ethanol and Microglia: From Molecules to Behavior. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:e4a31f62-4b30-4145-a953-9ff09b65a500.

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

Council of Science Editors:

Walter T. Ethanol and Microglia: From Molecules to Behavior. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:e4a31f62-4b30-4145-a953-9ff09b65a500

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


University of North Carolina

28. Okumu, Denis. Lyn regulates drug resistance mechanisms in chronic myelogenous leukemia (CML).

Degree: Pharmacology, 2018, University of North Carolina

 Acquired resistance to anti-cancer therapy presents a critical challenge to effective clinical management of chronic myelogenous leukemia (CML). Drug-resistant CML cells devise diverse molecular adaptations… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Okumu, D. (2018). Lyn regulates drug resistance mechanisms in chronic myelogenous leukemia (CML). (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:070f858a-ab62-46b2-bec6-bf6e771fc340

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):

Okumu, Denis. “Lyn regulates drug resistance mechanisms in chronic myelogenous leukemia (CML).” 2018. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:070f858a-ab62-46b2-bec6-bf6e771fc340.

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

MLA Handbook (7th Edition):

Okumu, Denis. “Lyn regulates drug resistance mechanisms in chronic myelogenous leukemia (CML).” 2018. Web. 27 Sep 2020.

Vancouver:

Okumu D. Lyn regulates drug resistance mechanisms in chronic myelogenous leukemia (CML). [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:070f858a-ab62-46b2-bec6-bf6e771fc340.

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

Council of Science Editors:

Okumu D. Lyn regulates drug resistance mechanisms in chronic myelogenous leukemia (CML). [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:070f858a-ab62-46b2-bec6-bf6e771fc340

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


University of North Carolina

29. Mills, Christine. Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation.

Degree: Pharmacology, 2018, University of North Carolina

 Cell cycle is a tightly regulated process; however, it is mis-regulated in many cancers, leading to increased proliferation. Our lab is interested in better understanding… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Mills, C. (2018). Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4ee84949-170b-485b-b110-7e036074c852

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):

Mills, Christine. “Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation.” 2018. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:4ee84949-170b-485b-b110-7e036074c852.

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

MLA Handbook (7th Edition):

Mills, Christine. “Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation.” 2018. Web. 27 Sep 2020.

Vancouver:

Mills C. Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation. [Internet] [Thesis]. University of North Carolina; 2018. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:4ee84949-170b-485b-b110-7e036074c852.

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

Council of Science Editors:

Mills C. Ubiquitin and Ubiquitin-Like Proteins in Cell Cycle Regulation. [Thesis]. University of North Carolina; 2018. Available from: https://cdr.lib.unc.edu/record/uuid:4ee84949-170b-485b-b110-7e036074c852

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


University of North Carolina

30. Goldsmith, Jason Rosenbaum. Mechanisms of mu opioid receptor mediated protection from multiple models of acute injury.

Degree: Pharmacology, 2012, University of North Carolina

 Numerous intestinal pathologies involve breakdown of the intestinal barrier, including Inflammatory Bowel Diseases and ischemia/reperfusion injury. Damage to the intestinal barrier leads to immune system… (more)

Subjects/Keywords: School of Medicine; Department of Pharmacology

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APA (6th Edition):

Goldsmith, J. R. (2012). Mechanisms of mu opioid receptor mediated protection from multiple models of acute injury. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:37219baa-61f7-4ea6-8e19-7f3e0e9e7e92

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):

Goldsmith, Jason Rosenbaum. “Mechanisms of mu opioid receptor mediated protection from multiple models of acute injury.” 2012. Thesis, University of North Carolina. Accessed September 27, 2020. https://cdr.lib.unc.edu/record/uuid:37219baa-61f7-4ea6-8e19-7f3e0e9e7e92.

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

MLA Handbook (7th Edition):

Goldsmith, Jason Rosenbaum. “Mechanisms of mu opioid receptor mediated protection from multiple models of acute injury.” 2012. Web. 27 Sep 2020.

Vancouver:

Goldsmith JR. Mechanisms of mu opioid receptor mediated protection from multiple models of acute injury. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Sep 27]. Available from: https://cdr.lib.unc.edu/record/uuid:37219baa-61f7-4ea6-8e19-7f3e0e9e7e92.

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

Council of Science Editors:

Goldsmith JR. Mechanisms of mu opioid receptor mediated protection from multiple models of acute injury. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:37219baa-61f7-4ea6-8e19-7f3e0e9e7e92

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

[1] [2] [3] [4] [5] [6] [7] [8]

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