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You searched for +publisher:"University of North Carolina" +contributor:("Campbell, Sharon"). Showing records 1 – 11 of 11 total matches.

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University of North Carolina

1. Cable, Jennifer L. Investigation of phosphorylation and ligand binding of the focal adhesion targeting domain of focal adhesion kinase.

Degree: Biochemistry and Biophysics, 2011, University of North Carolina

 Focal adhesion kinase (FAK) is a nonreceptor tyrosine kinase that localizes to focal adhesions upon integrin activation. FAK plays a key role in cell migration,… (more)

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

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APA (6th Edition):

Cable, J. L. (2011). Investigation of phosphorylation and ligand binding of the focal adhesion targeting domain of focal adhesion kinase. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:032ef76c-a5c3-490e-824c-b9972a1f201e

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):

Cable, Jennifer L. “Investigation of phosphorylation and ligand binding of the focal adhesion targeting domain of focal adhesion kinase.” 2011. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:032ef76c-a5c3-490e-824c-b9972a1f201e.

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

MLA Handbook (7th Edition):

Cable, Jennifer L. “Investigation of phosphorylation and ligand binding of the focal adhesion targeting domain of focal adhesion kinase.” 2011. Web. 25 Nov 2020.

Vancouver:

Cable JL. Investigation of phosphorylation and ligand binding of the focal adhesion targeting domain of focal adhesion kinase. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:032ef76c-a5c3-490e-824c-b9972a1f201e.

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

Council of Science Editors:

Cable JL. Investigation of phosphorylation and ligand binding of the focal adhesion targeting domain of focal adhesion kinase. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:032ef76c-a5c3-490e-824c-b9972a1f201e

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


University of North Carolina

2. Hobbs, Guy Aaron. REGULATION OF RAS AND RHO GTPASES BY POST-TRANSLATIONAL MODIFICATION: CYSTEINE OXIDATION AND UBIQUITINATION.

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

 Ras superfamily GTPases cycle between active GTP-bound and inactive GDP-bound forms to regulate a multitude of cellular processes, including cell growth, differentiation, and apoptosis. The… (more)

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

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APA (6th Edition):

Hobbs, G. A. (2013). REGULATION OF RAS AND RHO GTPASES BY POST-TRANSLATIONAL MODIFICATION: CYSTEINE OXIDATION AND UBIQUITINATION. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:929a176a-46f9-4eb3-98a7-2beaf5501986

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):

Hobbs, Guy Aaron. “REGULATION OF RAS AND RHO GTPASES BY POST-TRANSLATIONAL MODIFICATION: CYSTEINE OXIDATION AND UBIQUITINATION.” 2013. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:929a176a-46f9-4eb3-98a7-2beaf5501986.

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

MLA Handbook (7th Edition):

Hobbs, Guy Aaron. “REGULATION OF RAS AND RHO GTPASES BY POST-TRANSLATIONAL MODIFICATION: CYSTEINE OXIDATION AND UBIQUITINATION.” 2013. Web. 25 Nov 2020.

Vancouver:

Hobbs GA. REGULATION OF RAS AND RHO GTPASES BY POST-TRANSLATIONAL MODIFICATION: CYSTEINE OXIDATION AND UBIQUITINATION. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:929a176a-46f9-4eb3-98a7-2beaf5501986.

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

Council of Science Editors:

Hobbs GA. REGULATION OF RAS AND RHO GTPASES BY POST-TRANSLATIONAL MODIFICATION: CYSTEINE OXIDATION AND UBIQUITINATION. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:929a176a-46f9-4eb3-98a7-2beaf5501986

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


University of North Carolina

3. Mitchell, Lauren Elizabeth. Redox Regulation of Rac1.

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

 Rac1 is a ubiquitous 21 kD guanine nucleotide binding protein that is a member of a large superfamily of GTPases, which plays a central role… (more)

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

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APA (6th Edition):

Mitchell, L. E. (2013). Redox Regulation of Rac1. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4ceed587-4e49-4763-b162-f7b89cca7397

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):

Mitchell, Lauren Elizabeth. “Redox Regulation of Rac1.” 2013. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:4ceed587-4e49-4763-b162-f7b89cca7397.

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

MLA Handbook (7th Edition):

Mitchell, Lauren Elizabeth. “Redox Regulation of Rac1.” 2013. Web. 25 Nov 2020.

Vancouver:

Mitchell LE. Redox Regulation of Rac1. [Internet] [Thesis]. University of North Carolina; 2013. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:4ceed587-4e49-4763-b162-f7b89cca7397.

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

Council of Science Editors:

Mitchell LE. Redox Regulation of Rac1. [Thesis]. University of North Carolina; 2013. Available from: https://cdr.lib.unc.edu/record/uuid:4ceed587-4e49-4763-b162-f7b89cca7397

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


University of North Carolina

4. 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 November 25, 2020. 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. 25 Nov 2020.

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 2020 Nov 25]. 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

5. Black, Justin. Exploration of the role of CIB1 in cell survival and tumor growth.

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

 CIB1 is an intracellular protein with diverse functions in cancer cell biology. Here I explore two important functions of CIB1: 1) The role of CIB1… (more)

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

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APA (6th Edition):

Black, J. (2015). Exploration of the role of CIB1 in cell survival and tumor growth. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b58ffcb6-4707-43a6-b86e-4644085f46e1

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):

Black, Justin. “Exploration of the role of CIB1 in cell survival and tumor growth.” 2015. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:b58ffcb6-4707-43a6-b86e-4644085f46e1.

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

MLA Handbook (7th Edition):

Black, Justin. “Exploration of the role of CIB1 in cell survival and tumor growth.” 2015. Web. 25 Nov 2020.

Vancouver:

Black J. Exploration of the role of CIB1 in cell survival and tumor growth. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:b58ffcb6-4707-43a6-b86e-4644085f46e1.

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

Council of Science Editors:

Black J. Exploration of the role of CIB1 in cell survival and tumor growth. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:b58ffcb6-4707-43a6-b86e-4644085f46e1

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


University of North Carolina

6. Jacak, Ronald. Explicit Consideration of Solubility and Interaction Specificity in Computational Protein Design.

Degree: Biochemistry and Biophysics, 2011, University of North Carolina

 Most successes to date in computational protein design have relied on optimizing sequences to fit well for a single structure. Multistate design represents a new… (more)

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

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APA (6th Edition):

Jacak, R. (2011). Explicit Consideration of Solubility and Interaction Specificity in Computational Protein Design. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:eee31c27-82d0-4e6b-bb39-6456860e0255

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):

Jacak, Ronald. “Explicit Consideration of Solubility and Interaction Specificity in Computational Protein Design.” 2011. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:eee31c27-82d0-4e6b-bb39-6456860e0255.

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

MLA Handbook (7th Edition):

Jacak, Ronald. “Explicit Consideration of Solubility and Interaction Specificity in Computational Protein Design.” 2011. Web. 25 Nov 2020.

Vancouver:

Jacak R. Explicit Consideration of Solubility and Interaction Specificity in Computational Protein Design. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:eee31c27-82d0-4e6b-bb39-6456860e0255.

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

Council of Science Editors:

Jacak R. Explicit Consideration of Solubility and Interaction Specificity in Computational Protein Design. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:eee31c27-82d0-4e6b-bb39-6456860e0255

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


University of North Carolina

7. Chandrasekaran, Srinivas Niranj. Parameter optimization on the convergence surface of PATH simulations.

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

 Computational treatments of protein conformational changes tend to focus on the trajectories themselves, despite the fact that it is the transition state structures that contain… (more)

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

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APA (6th Edition):

Chandrasekaran, S. N. (2016). Parameter optimization on the convergence surface of PATH simulations. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:a3c79ded-6255-40ca-8f2d-5da0e7dadb9c

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):

Chandrasekaran, Srinivas Niranj. “Parameter optimization on the convergence surface of PATH simulations.” 2016. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:a3c79ded-6255-40ca-8f2d-5da0e7dadb9c.

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

MLA Handbook (7th Edition):

Chandrasekaran, Srinivas Niranj. “Parameter optimization on the convergence surface of PATH simulations.” 2016. Web. 25 Nov 2020.

Vancouver:

Chandrasekaran SN. Parameter optimization on the convergence surface of PATH simulations. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:a3c79ded-6255-40ca-8f2d-5da0e7dadb9c.

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

Council of Science Editors:

Chandrasekaran SN. Parameter optimization on the convergence surface of PATH simulations. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:a3c79ded-6255-40ca-8f2d-5da0e7dadb9c

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


University of North Carolina

8. Case, Lindsay. SPATIOTEMPORAL COORDINATION OF THE ACTIN CYTOSKELETON AND INTEGRIN ADHESION.

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

 Integrin-based adhesions mediate critical interactions between the cell and its external environment. Integrins assemble into macromolecular "focal adhesions" (FAs) that contain hundreds of proteins and… (more)

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

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APA (6th Edition):

Case, L. (2014). SPATIOTEMPORAL COORDINATION OF THE ACTIN CYTOSKELETON AND INTEGRIN ADHESION. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:7cda075f-4cd5-4f13-b243-6ce9d9cd0d48

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):

Case, Lindsay. “SPATIOTEMPORAL COORDINATION OF THE ACTIN CYTOSKELETON AND INTEGRIN ADHESION.” 2014. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:7cda075f-4cd5-4f13-b243-6ce9d9cd0d48.

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

MLA Handbook (7th Edition):

Case, Lindsay. “SPATIOTEMPORAL COORDINATION OF THE ACTIN CYTOSKELETON AND INTEGRIN ADHESION.” 2014. Web. 25 Nov 2020.

Vancouver:

Case L. SPATIOTEMPORAL COORDINATION OF THE ACTIN CYTOSKELETON AND INTEGRIN ADHESION. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:7cda075f-4cd5-4f13-b243-6ce9d9cd0d48.

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

Council of Science Editors:

Case L. SPATIOTEMPORAL COORDINATION OF THE ACTIN CYTOSKELETON AND INTEGRIN ADHESION. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:7cda075f-4cd5-4f13-b243-6ce9d9cd0d48

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


University of North Carolina

9. Monteith, William. Residue Level Quantification of Protein Stability in Living Cells.

Degree: Chemistry, 2014, University of North Carolina

 The intracellular milieu differs from the dilute conditions in which most biophysical and biochemical studies are performed. This difference has led both experimentalists and theoreticians… (more)

Subjects/Keywords: Chemistry; Biochemistry; Biophysics; College of Arts and Sciences; Department of Chemistry

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APA (6th Edition):

Monteith, W. (2014). Residue Level Quantification of Protein Stability in Living Cells. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:2015b666-3d6f-4fce-98c8-d7f182ea4426

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):

Monteith, William. “Residue Level Quantification of Protein Stability in Living Cells.” 2014. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:2015b666-3d6f-4fce-98c8-d7f182ea4426.

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

MLA Handbook (7th Edition):

Monteith, William. “Residue Level Quantification of Protein Stability in Living Cells.” 2014. Web. 25 Nov 2020.

Vancouver:

Monteith W. Residue Level Quantification of Protein Stability in Living Cells. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:2015b666-3d6f-4fce-98c8-d7f182ea4426.

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

Council of Science Editors:

Monteith W. Residue Level Quantification of Protein Stability in Living Cells. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:2015b666-3d6f-4fce-98c8-d7f182ea4426

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


University of North Carolina

10. 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 November 25, 2020. 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. 25 Nov 2020.

Vancouver:

Page S. Analysis of Receiver Domain Dephosphorylation Kinetics. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Nov 25]. 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

11. Palmer, Sean Matthew. The role of pH, self-association, and lipid binding in vinculin tail structure and function.

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

 Vinculin is a highly conserved cytoskeletal protein that localized to sites of cell adhesion and is involved in linking the actin cytoskeleton to the cell… (more)

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

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APA (6th Edition):

Palmer, S. M. (2008). The role of pH, self-association, and lipid binding in vinculin tail structure and function. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:be197747-2c6f-43e8-bc1b-3355c7276f12

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):

Palmer, Sean Matthew. “The role of pH, self-association, and lipid binding in vinculin tail structure and function.” 2008. Thesis, University of North Carolina. Accessed November 25, 2020. https://cdr.lib.unc.edu/record/uuid:be197747-2c6f-43e8-bc1b-3355c7276f12.

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

MLA Handbook (7th Edition):

Palmer, Sean Matthew. “The role of pH, self-association, and lipid binding in vinculin tail structure and function.” 2008. Web. 25 Nov 2020.

Vancouver:

Palmer SM. The role of pH, self-association, and lipid binding in vinculin tail structure and function. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Nov 25]. Available from: https://cdr.lib.unc.edu/record/uuid:be197747-2c6f-43e8-bc1b-3355c7276f12.

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

Council of Science Editors:

Palmer SM. The role of pH, self-association, and lipid binding in vinculin tail structure and function. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:be197747-2c6f-43e8-bc1b-3355c7276f12

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

.