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You searched for +publisher:"University of North Carolina" +contributor:("Redinbo, Matthew R."). Showing records 1 – 27 of 27 total matches.

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University of North Carolina

1. Cheng, Yuan. Structural and functional studies of E. coli conjugative relaxase-helicase TraI and Arabidopsis thaliana protein arginine methyltransferase 10 (PRMT10).

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

 TraI, a bifunctional enzyme containing relaxase and helicase activities, initiates and drives the conjugative transfer of the E. coli F plasmid. In this work, we… (more)

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

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APA (6th Edition):

Cheng, Y. (2011). Structural and functional studies of E. coli conjugative relaxase-helicase TraI and Arabidopsis thaliana protein arginine methyltransferase 10 (PRMT10). (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:e736da73-7be1-4ff7-9376-c3c07dde3fe0

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):

Cheng, Yuan. “Structural and functional studies of E. coli conjugative relaxase-helicase TraI and Arabidopsis thaliana protein arginine methyltransferase 10 (PRMT10).” 2011. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:e736da73-7be1-4ff7-9376-c3c07dde3fe0.

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

MLA Handbook (7th Edition):

Cheng, Yuan. “Structural and functional studies of E. coli conjugative relaxase-helicase TraI and Arabidopsis thaliana protein arginine methyltransferase 10 (PRMT10).” 2011. Web. 03 Dec 2020.

Vancouver:

Cheng Y. Structural and functional studies of E. coli conjugative relaxase-helicase TraI and Arabidopsis thaliana protein arginine methyltransferase 10 (PRMT10). [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:e736da73-7be1-4ff7-9376-c3c07dde3fe0.

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

Council of Science Editors:

Cheng Y. Structural and functional studies of E. coli conjugative relaxase-helicase TraI and Arabidopsis thaliana protein arginine methyltransferase 10 (PRMT10). [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:e736da73-7be1-4ff7-9376-c3c07dde3fe0

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


University of North Carolina

2. Roberts, Adam Berkley. SELECTIVE MODULATION OF THE MICROBIOME: EFFORTS TOWARD A NEW PARADIGM IN HUMAN THERAPEUTICS.

Degree: Biochemistry and Biophysics, 2014, University of North Carolina

 Drug-induced toxicity, side effects of certain therapeutics, is often more toxic than the original disease and limits the potential for dose intensification. The dose-limiting side… (more)

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

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APA (6th Edition):

Roberts, A. B. (2014). SELECTIVE MODULATION OF THE MICROBIOME: EFFORTS TOWARD A NEW PARADIGM IN HUMAN THERAPEUTICS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:fb59f90b-fa6a-47ea-b02b-c4115ac41d6d

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):

Roberts, Adam Berkley. “SELECTIVE MODULATION OF THE MICROBIOME: EFFORTS TOWARD A NEW PARADIGM IN HUMAN THERAPEUTICS.” 2014. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:fb59f90b-fa6a-47ea-b02b-c4115ac41d6d.

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

MLA Handbook (7th Edition):

Roberts, Adam Berkley. “SELECTIVE MODULATION OF THE MICROBIOME: EFFORTS TOWARD A NEW PARADIGM IN HUMAN THERAPEUTICS.” 2014. Web. 03 Dec 2020.

Vancouver:

Roberts AB. SELECTIVE MODULATION OF THE MICROBIOME: EFFORTS TOWARD A NEW PARADIGM IN HUMAN THERAPEUTICS. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:fb59f90b-fa6a-47ea-b02b-c4115ac41d6d.

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

Council of Science Editors:

Roberts AB. SELECTIVE MODULATION OF THE MICROBIOME: EFFORTS TOWARD A NEW PARADIGM IN HUMAN THERAPEUTICS. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:fb59f90b-fa6a-47ea-b02b-c4115ac41d6d

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


University of North Carolina

3. Edwards, Jonathan S. Structure and Function of the NES Relaxase and C-terminal Domains Required for Vancomycin Resistance Transfer.

Degree: Biochemistry and Biophysics, 2012, University of North Carolina

 Antibiotic resistance has become a large burden in the healthcare setting due to increasing rates of mortality and increased healthcare costs due to extended treatment.… (more)

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

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APA (6th Edition):

Edwards, J. S. (2012). Structure and Function of the NES Relaxase and C-terminal Domains Required for Vancomycin Resistance Transfer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:ad52b7e2-50f6-48e2-b355-a515fca08298

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):

Edwards, Jonathan S. “Structure and Function of the NES Relaxase and C-terminal Domains Required for Vancomycin Resistance Transfer.” 2012. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:ad52b7e2-50f6-48e2-b355-a515fca08298.

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

MLA Handbook (7th Edition):

Edwards, Jonathan S. “Structure and Function of the NES Relaxase and C-terminal Domains Required for Vancomycin Resistance Transfer.” 2012. Web. 03 Dec 2020.

Vancouver:

Edwards JS. Structure and Function of the NES Relaxase and C-terminal Domains Required for Vancomycin Resistance Transfer. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:ad52b7e2-50f6-48e2-b355-a515fca08298.

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

Council of Science Editors:

Edwards JS. Structure and Function of the NES Relaxase and C-terminal Domains Required for Vancomycin Resistance Transfer. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:ad52b7e2-50f6-48e2-b355-a515fca08298

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


University of North Carolina

4. Hemmert, Andrew C. Novel protein-based solutions for organophosphorus nerve agent detection and elimination.

Degree: Biochemistry and Biophysics, 2010, University of North Carolina

 Organophosphorus (OP) nerve agents are some of the deadliest chemicals ever synthesized by man. These toxins, which include sarin, soman, cyclosarin, tabun, and VX, inhibit… (more)

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

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APA (6th Edition):

Hemmert, A. C. (2010). Novel protein-based solutions for organophosphorus nerve agent detection and elimination. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:54e5267b-95db-43de-8671-5ad7eb38ab34

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):

Hemmert, Andrew C. “Novel protein-based solutions for organophosphorus nerve agent detection and elimination.” 2010. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:54e5267b-95db-43de-8671-5ad7eb38ab34.

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

MLA Handbook (7th Edition):

Hemmert, Andrew C. “Novel protein-based solutions for organophosphorus nerve agent detection and elimination.” 2010. Web. 03 Dec 2020.

Vancouver:

Hemmert AC. Novel protein-based solutions for organophosphorus nerve agent detection and elimination. [Internet] [Thesis]. University of North Carolina; 2010. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:54e5267b-95db-43de-8671-5ad7eb38ab34.

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

Council of Science Editors:

Hemmert AC. Novel protein-based solutions for organophosphorus nerve agent detection and elimination. [Thesis]. University of North Carolina; 2010. Available from: https://cdr.lib.unc.edu/record/uuid:54e5267b-95db-43de-8671-5ad7eb38ab34

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


University of North Carolina

5. Frazier, Monica L. The Yersinia pestis autotransporter YapG contains a fast folding [beta]-helix domain.

Degree: Biochemistry and Biophysics, 2012, University of North Carolina

 Autotransporter proteins are the most widely secreted protein family in gram-negative bacteria; their passenger domains are predicted to be [beta]-helical in 97% of cases. The… (more)

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

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APA (6th Edition):

Frazier, M. L. (2012). The Yersinia pestis autotransporter YapG contains a fast folding [beta]-helix domain. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:706e3f9a-0a33-4e6d-bef3-c245ecaff549

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):

Frazier, Monica L. “The Yersinia pestis autotransporter YapG contains a fast folding [beta]-helix domain.” 2012. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:706e3f9a-0a33-4e6d-bef3-c245ecaff549.

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

MLA Handbook (7th Edition):

Frazier, Monica L. “The Yersinia pestis autotransporter YapG contains a fast folding [beta]-helix domain.” 2012. Web. 03 Dec 2020.

Vancouver:

Frazier ML. The Yersinia pestis autotransporter YapG contains a fast folding [beta]-helix domain. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:706e3f9a-0a33-4e6d-bef3-c245ecaff549.

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

Council of Science Editors:

Frazier ML. The Yersinia pestis autotransporter YapG contains a fast folding [beta]-helix domain. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:706e3f9a-0a33-4e6d-bef3-c245ecaff549

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


University of North Carolina

6. Nash, Rebekah Potts. The Structure of the Plasmid pCU1 TraI Relaxase and the Role of the pCU1 TraI Relaxase-Helicase during Conjugative Plasmid Transfer.

Degree: Chemistry, 2011, University of North Carolina

 Bacteria disseminate genetic material to neighboring cells using conjugative plasmid transfer (CPT). During CPT, a donor bacterium transfers one strand of a double-stranded DNA plasmid… (more)

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

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APA (6th Edition):

Nash, R. P. (2011). The Structure of the Plasmid pCU1 TraI Relaxase and the Role of the pCU1 TraI Relaxase-Helicase during Conjugative Plasmid Transfer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b3587d7e-b0a3-48c0-a4ab-6d8f54e04d59

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):

Nash, Rebekah Potts. “The Structure of the Plasmid pCU1 TraI Relaxase and the Role of the pCU1 TraI Relaxase-Helicase during Conjugative Plasmid Transfer.” 2011. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:b3587d7e-b0a3-48c0-a4ab-6d8f54e04d59.

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

MLA Handbook (7th Edition):

Nash, Rebekah Potts. “The Structure of the Plasmid pCU1 TraI Relaxase and the Role of the pCU1 TraI Relaxase-Helicase during Conjugative Plasmid Transfer.” 2011. Web. 03 Dec 2020.

Vancouver:

Nash RP. The Structure of the Plasmid pCU1 TraI Relaxase and the Role of the pCU1 TraI Relaxase-Helicase during Conjugative Plasmid Transfer. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:b3587d7e-b0a3-48c0-a4ab-6d8f54e04d59.

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

Council of Science Editors:

Nash RP. The Structure of the Plasmid pCU1 TraI Relaxase and the Role of the pCU1 TraI Relaxase-Helicase during Conjugative Plasmid Transfer. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:b3587d7e-b0a3-48c0-a4ab-6d8f54e04d59

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


University of North Carolina

7. Johnson, Michael D. L. The effect of calcium binding on adhesion and pilus biogenesis in the PilC family of proteins.

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

 Pseudomonas aeruginosa is an opportunistic pathogen prevalent in people on immunosuppressants, recent open wounds, or cystic fibrosis patients. P. aeruginosa attaches to the host cell… (more)

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

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APA (6th Edition):

Johnson, M. D. L. (2011). The effect of calcium binding on adhesion and pilus biogenesis in the PilC family of proteins. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:477521a5-b326-48ce-9192-3234ffd2cb9b

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):

Johnson, Michael D L. “The effect of calcium binding on adhesion and pilus biogenesis in the PilC family of proteins.” 2011. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:477521a5-b326-48ce-9192-3234ffd2cb9b.

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

MLA Handbook (7th Edition):

Johnson, Michael D L. “The effect of calcium binding on adhesion and pilus biogenesis in the PilC family of proteins.” 2011. Web. 03 Dec 2020.

Vancouver:

Johnson MDL. The effect of calcium binding on adhesion and pilus biogenesis in the PilC family of proteins. [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:477521a5-b326-48ce-9192-3234ffd2cb9b.

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

Council of Science Editors:

Johnson MDL. The effect of calcium binding on adhesion and pilus biogenesis in the PilC family of proteins. [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:477521a5-b326-48ce-9192-3234ffd2cb9b

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


University of North Carolina

8. Lomino, Joseph V. Triggered folding of a mycobacterium tuberculosis adhesin, heparin binding hemagglutinin adhesin (HBHA).

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

 The heparin-binding hemagglutinin (HBHA) is a surface adhesin on human pathogen Mycobacterium tuberculosis. Previously, it has been shown that HBHA exists as a dimer in… (more)

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

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APA (6th Edition):

Lomino, J. V. (2011). Triggered folding of a mycobacterium tuberculosis adhesin, heparin binding hemagglutinin adhesin (HBHA). (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:31d10309-2cfe-43fd-98a7-e1827a455e1a

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):

Lomino, Joseph V. “Triggered folding of a mycobacterium tuberculosis adhesin, heparin binding hemagglutinin adhesin (HBHA).” 2011. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:31d10309-2cfe-43fd-98a7-e1827a455e1a.

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

MLA Handbook (7th Edition):

Lomino, Joseph V. “Triggered folding of a mycobacterium tuberculosis adhesin, heparin binding hemagglutinin adhesin (HBHA).” 2011. Web. 03 Dec 2020.

Vancouver:

Lomino JV. Triggered folding of a mycobacterium tuberculosis adhesin, heparin binding hemagglutinin adhesin (HBHA). [Internet] [Thesis]. University of North Carolina; 2011. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:31d10309-2cfe-43fd-98a7-e1827a455e1a.

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

Council of Science Editors:

Lomino JV. Triggered folding of a mycobacterium tuberculosis adhesin, heparin binding hemagglutinin adhesin (HBHA). [Thesis]. University of North Carolina; 2011. Available from: https://cdr.lib.unc.edu/record/uuid:31d10309-2cfe-43fd-98a7-e1827a455e1a

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


University of North Carolina

9. Bradford, Kira. Structure-Function Studies of the Initiation Response of Human Mismatch Repair Proteins to DNA Containing a Mismatch.

Degree: Chemistry, 2015, University of North Carolina

 DNA mismatch repair (MMR) is the post-replicative process that recognizes and repairs misincorporated bases that occur during replication. Deficiencies in MMR are linked to greater… (more)

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

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APA (6th Edition):

Bradford, K. (2015). Structure-Function Studies of the Initiation Response of Human Mismatch Repair Proteins to DNA Containing a Mismatch. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:88069a25-82a7-4202-b068-7f42dea7368a

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):

Bradford, Kira. “Structure-Function Studies of the Initiation Response of Human Mismatch Repair Proteins to DNA Containing a Mismatch.” 2015. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:88069a25-82a7-4202-b068-7f42dea7368a.

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

MLA Handbook (7th Edition):

Bradford, Kira. “Structure-Function Studies of the Initiation Response of Human Mismatch Repair Proteins to DNA Containing a Mismatch.” 2015. Web. 03 Dec 2020.

Vancouver:

Bradford K. Structure-Function Studies of the Initiation Response of Human Mismatch Repair Proteins to DNA Containing a Mismatch. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:88069a25-82a7-4202-b068-7f42dea7368a.

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

Council of Science Editors:

Bradford K. Structure-Function Studies of the Initiation Response of Human Mismatch Repair Proteins to DNA Containing a Mismatch. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:88069a25-82a7-4202-b068-7f42dea7368a

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


University of North Carolina

10. Garrett, Christopher. Characterization of a Key Mycobacterium tuberculosis Lipase, LipY.

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

 The causative agent of tuberculosis, Mycobacterium tuberculosis is estimated to be present in roughly a third of the world’s population. One of the hallmarks of… (more)

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

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APA (6th Edition):

Garrett, C. (2015). Characterization of a Key Mycobacterium tuberculosis Lipase, LipY. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:80107563-6511-4298-9a76-7185a0292ea6

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):

Garrett, Christopher. “Characterization of a Key Mycobacterium tuberculosis Lipase, LipY.” 2015. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:80107563-6511-4298-9a76-7185a0292ea6.

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

MLA Handbook (7th Edition):

Garrett, Christopher. “Characterization of a Key Mycobacterium tuberculosis Lipase, LipY.” 2015. Web. 03 Dec 2020.

Vancouver:

Garrett C. Characterization of a Key Mycobacterium tuberculosis Lipase, LipY. [Internet] [Thesis]. University of North Carolina; 2015. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:80107563-6511-4298-9a76-7185a0292ea6.

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

Council of Science Editors:

Garrett C. Characterization of a Key Mycobacterium tuberculosis Lipase, LipY. [Thesis]. University of North Carolina; 2015. Available from: https://cdr.lib.unc.edu/record/uuid:80107563-6511-4298-9a76-7185a0292ea6

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


University of North Carolina

11. Cohen, Rachel. Quinary structure alters protein folding landscapes.

Degree: Chemistry, 2017, University of North Carolina

 Most knowledge of protein chemistry is derived from experiments performed in dilute, buffered solutions. Although such experiments provide essential information, proteins function in the crowded… (more)

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

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APA (6th Edition):

Cohen, R. (2017). Quinary structure alters protein folding landscapes. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:7b21bc35-13d7-417c-856d-683de8dd6205

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):

Cohen, Rachel. “Quinary structure alters protein folding landscapes.” 2017. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:7b21bc35-13d7-417c-856d-683de8dd6205.

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

MLA Handbook (7th Edition):

Cohen, Rachel. “Quinary structure alters protein folding landscapes.” 2017. Web. 03 Dec 2020.

Vancouver:

Cohen R. Quinary structure alters protein folding landscapes. [Internet] [Thesis]. University of North Carolina; 2017. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:7b21bc35-13d7-417c-856d-683de8dd6205.

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

Council of Science Editors:

Cohen R. Quinary structure alters protein folding landscapes. [Thesis]. University of North Carolina; 2017. Available from: https://cdr.lib.unc.edu/record/uuid:7b21bc35-13d7-417c-856d-683de8dd6205

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


University of North Carolina

12. Das, Alakananda. The Crescerin protein family uses arrayed TOG domains to regulate microtubules in cilia.

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

 The eukaryotic primary cilium is a solitary, antenna-like projection from the surface of a cell, critical for sensing the extracellular environment. Many mammalian cell types… (more)

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

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APA (6th Edition):

Das, A. (2016). The Crescerin protein family uses arrayed TOG domains to regulate microtubules in cilia. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:9df60130-436e-487a-ad28-a1de3395450a

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):

Das, Alakananda. “The Crescerin protein family uses arrayed TOG domains to regulate microtubules in cilia.” 2016. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:9df60130-436e-487a-ad28-a1de3395450a.

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

MLA Handbook (7th Edition):

Das, Alakananda. “The Crescerin protein family uses arrayed TOG domains to regulate microtubules in cilia.” 2016. Web. 03 Dec 2020.

Vancouver:

Das A. The Crescerin protein family uses arrayed TOG domains to regulate microtubules in cilia. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:9df60130-436e-487a-ad28-a1de3395450a.

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

Council of Science Editors:

Das A. The Crescerin protein family uses arrayed TOG domains to regulate microtubules in cilia. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:9df60130-436e-487a-ad28-a1de3395450a

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


University of North Carolina

13. Gauer, Jacob. SINGLE-MOLECULE FLUORESCENCE STUDIES OF DNA BENDING DURING PROKARYOTIC MISMATCH REPAIR INITIATION.

Degree: Chemistry, 2016, University of North Carolina

 DNA mismatch repair (MMR) is a process that is responsible for repairing base-base mismatches and insertion/deletion loop errors incorporated during DNA replication. In humans, deficiencies… (more)

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

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APA (6th Edition):

Gauer, J. (2016). SINGLE-MOLECULE FLUORESCENCE STUDIES OF DNA BENDING DURING PROKARYOTIC MISMATCH REPAIR INITIATION. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:62d39d9a-c72e-4658-98f1-c1457a8275c8

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):

Gauer, Jacob. “SINGLE-MOLECULE FLUORESCENCE STUDIES OF DNA BENDING DURING PROKARYOTIC MISMATCH REPAIR INITIATION.” 2016. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:62d39d9a-c72e-4658-98f1-c1457a8275c8.

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

MLA Handbook (7th Edition):

Gauer, Jacob. “SINGLE-MOLECULE FLUORESCENCE STUDIES OF DNA BENDING DURING PROKARYOTIC MISMATCH REPAIR INITIATION.” 2016. Web. 03 Dec 2020.

Vancouver:

Gauer J. SINGLE-MOLECULE FLUORESCENCE STUDIES OF DNA BENDING DURING PROKARYOTIC MISMATCH REPAIR INITIATION. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:62d39d9a-c72e-4658-98f1-c1457a8275c8.

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

Council of Science Editors:

Gauer J. SINGLE-MOLECULE FLUORESCENCE STUDIES OF DNA BENDING DURING PROKARYOTIC MISMATCH REPAIR INITIATION. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:62d39d9a-c72e-4658-98f1-c1457a8275c8

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


University of North Carolina

14. Wallace, Bret David. Alleviating Cancer Drug Toxicity Through Targeted Inhibition of a Bacterial Enzyme and Exploring the Structural and Functional Properties of the Xenobiotic Nuclear Receptor PXR.

Degree: Chemistry, 2012, University of North Carolina

 Although symbiotic GI bacteria are essential to human health, in some cases these organisms contribute to undesirable side effects during the treatment of disease. For… (more)

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

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APA (6th Edition):

Wallace, B. D. (2012). Alleviating Cancer Drug Toxicity Through Targeted Inhibition of a Bacterial Enzyme and Exploring the Structural and Functional Properties of the Xenobiotic Nuclear Receptor PXR. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:308a7d17-44e5-497d-9613-5de5fc03cd78

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):

Wallace, Bret David. “Alleviating Cancer Drug Toxicity Through Targeted Inhibition of a Bacterial Enzyme and Exploring the Structural and Functional Properties of the Xenobiotic Nuclear Receptor PXR.” 2012. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:308a7d17-44e5-497d-9613-5de5fc03cd78.

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

MLA Handbook (7th Edition):

Wallace, Bret David. “Alleviating Cancer Drug Toxicity Through Targeted Inhibition of a Bacterial Enzyme and Exploring the Structural and Functional Properties of the Xenobiotic Nuclear Receptor PXR.” 2012. Web. 03 Dec 2020.

Vancouver:

Wallace BD. Alleviating Cancer Drug Toxicity Through Targeted Inhibition of a Bacterial Enzyme and Exploring the Structural and Functional Properties of the Xenobiotic Nuclear Receptor PXR. [Internet] [Thesis]. University of North Carolina; 2012. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:308a7d17-44e5-497d-9613-5de5fc03cd78.

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

Council of Science Editors:

Wallace BD. Alleviating Cancer Drug Toxicity Through Targeted Inhibition of a Bacterial Enzyme and Exploring the Structural and Functional Properties of the Xenobiotic Nuclear Receptor PXR. [Thesis]. University of North Carolina; 2012. Available from: https://cdr.lib.unc.edu/record/uuid:308a7d17-44e5-497d-9613-5de5fc03cd78

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


University of North Carolina

15. Godinho, Justin. Packing and Characterization of Capillary Columns for Ultrahigh Pressure Liquid Chromatography.

Degree: Chemistry, 2016, University of North Carolina

 Improving the performance of the column remains paramount to the continued growth of ultrahigh pressure liquid chromatography. Realization of the theoretical benefits associated with sub-2… (more)

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

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APA (6th Edition):

Godinho, J. (2016). Packing and Characterization of Capillary Columns for Ultrahigh Pressure Liquid Chromatography. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:3428b71b-d940-44c1-91ad-e7735f0677fd

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):

Godinho, Justin. “Packing and Characterization of Capillary Columns for Ultrahigh Pressure Liquid Chromatography.” 2016. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:3428b71b-d940-44c1-91ad-e7735f0677fd.

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

MLA Handbook (7th Edition):

Godinho, Justin. “Packing and Characterization of Capillary Columns for Ultrahigh Pressure Liquid Chromatography.” 2016. Web. 03 Dec 2020.

Vancouver:

Godinho J. Packing and Characterization of Capillary Columns for Ultrahigh Pressure Liquid Chromatography. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:3428b71b-d940-44c1-91ad-e7735f0677fd.

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

Council of Science Editors:

Godinho J. Packing and Characterization of Capillary Columns for Ultrahigh Pressure Liquid Chromatography. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:3428b71b-d940-44c1-91ad-e7735f0677fd

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


University of North Carolina

16. Pollet, Rebecca. STRUCTURE AND FUNCTION STUDIES OF MICROBIAL CONJUGATIVE DNA TRANSFER & GI DRUG REACTIVATION PROCESSES.

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

 Antimicrobial resistance in Staphylococcus aureus presents an increasing threat to human health. This resistance is often encoded on mobile plasmids, such as pSK41; however, the… (more)

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

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APA (6th Edition):

Pollet, R. (2016). STRUCTURE AND FUNCTION STUDIES OF MICROBIAL CONJUGATIVE DNA TRANSFER & GI DRUG REACTIVATION PROCESSES. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:911890b6-9734-41d1-9e1b-b4eaf15ff4d9

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):

Pollet, Rebecca. “STRUCTURE AND FUNCTION STUDIES OF MICROBIAL CONJUGATIVE DNA TRANSFER & GI DRUG REACTIVATION PROCESSES.” 2016. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:911890b6-9734-41d1-9e1b-b4eaf15ff4d9.

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

MLA Handbook (7th Edition):

Pollet, Rebecca. “STRUCTURE AND FUNCTION STUDIES OF MICROBIAL CONJUGATIVE DNA TRANSFER & GI DRUG REACTIVATION PROCESSES.” 2016. Web. 03 Dec 2020.

Vancouver:

Pollet R. STRUCTURE AND FUNCTION STUDIES OF MICROBIAL CONJUGATIVE DNA TRANSFER & GI DRUG REACTIVATION PROCESSES. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:911890b6-9734-41d1-9e1b-b4eaf15ff4d9.

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

Council of Science Editors:

Pollet R. STRUCTURE AND FUNCTION STUDIES OF MICROBIAL CONJUGATIVE DNA TRANSFER & GI DRUG REACTIVATION PROCESSES. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:911890b6-9734-41d1-9e1b-b4eaf15ff4d9

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


University of North Carolina

17. Huang, Julianne. SHORT PALATE LUNG AND NASAL EPITHELIUM 1 AND AIRWAY DISEASE.

Degree: Chemistry, 2016, University of North Carolina

 Airway disease such as asthma and infection is the cause substantial morbidity and mortality in the world today. Although modern medicine has developed many drugs… (more)

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

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APA (6th Edition):

Huang, J. (2016). SHORT PALATE LUNG AND NASAL EPITHELIUM 1 AND AIRWAY DISEASE. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:890b4002-9b2d-495d-8d67-1e05e0c9d183

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):

Huang, Julianne. “SHORT PALATE LUNG AND NASAL EPITHELIUM 1 AND AIRWAY DISEASE.” 2016. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:890b4002-9b2d-495d-8d67-1e05e0c9d183.

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

MLA Handbook (7th Edition):

Huang, Julianne. “SHORT PALATE LUNG AND NASAL EPITHELIUM 1 AND AIRWAY DISEASE.” 2016. Web. 03 Dec 2020.

Vancouver:

Huang J. SHORT PALATE LUNG AND NASAL EPITHELIUM 1 AND AIRWAY DISEASE. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:890b4002-9b2d-495d-8d67-1e05e0c9d183.

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

Council of Science Editors:

Huang J. SHORT PALATE LUNG AND NASAL EPITHELIUM 1 AND AIRWAY DISEASE. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:890b4002-9b2d-495d-8d67-1e05e0c9d183

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


University of North Carolina

18. Houston, Kaiulani. Development of Protease-Resistant β-Hairpin Peptides for the Detection of Enzymatic Activity in Cancer Cells.

Degree: Chemistry, 2014, University of North Carolina

 Multiple myeloma (MM) is an incurable malignancy of the antibody-producing plasma cells in the bone marrow and is characterized by the targeted degradation of antitumor… (more)

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

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APA (6th Edition):

Houston, K. (2014). Development of Protease-Resistant β-Hairpin Peptides for the Detection of Enzymatic Activity in Cancer Cells. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b3a7e356-cb33-45bb-8157-5e2a53bcde82

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):

Houston, Kaiulani. “Development of Protease-Resistant β-Hairpin Peptides for the Detection of Enzymatic Activity in Cancer Cells.” 2014. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:b3a7e356-cb33-45bb-8157-5e2a53bcde82.

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

MLA Handbook (7th Edition):

Houston, Kaiulani. “Development of Protease-Resistant β-Hairpin Peptides for the Detection of Enzymatic Activity in Cancer Cells.” 2014. Web. 03 Dec 2020.

Vancouver:

Houston K. Development of Protease-Resistant β-Hairpin Peptides for the Detection of Enzymatic Activity in Cancer Cells. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:b3a7e356-cb33-45bb-8157-5e2a53bcde82.

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

Council of Science Editors:

Houston K. Development of Protease-Resistant β-Hairpin Peptides for the Detection of Enzymatic Activity in Cancer Cells. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:b3a7e356-cb33-45bb-8157-5e2a53bcde82

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


University of North Carolina

19. Slevin, Lauren K. A Structural Study of Conserved Centriole Duplication Machinery.

Degree: Biology, 2014, University of North Carolina

 Centrioles are microtubule-based cylindrical structures that act within organelles responsible for nucleating polarized microtubule networks. Centrioles have an inherent nine-fold radial symmetry with species-dependent dimensions.… (more)

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

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APA (6th Edition):

Slevin, L. K. (2014). A Structural Study of Conserved Centriole Duplication Machinery. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:b50097c1-8ea0-424c-a054-1226e022b7ec

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):

Slevin, Lauren K. “A Structural Study of Conserved Centriole Duplication Machinery.” 2014. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:b50097c1-8ea0-424c-a054-1226e022b7ec.

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

MLA Handbook (7th Edition):

Slevin, Lauren K. “A Structural Study of Conserved Centriole Duplication Machinery.” 2014. Web. 03 Dec 2020.

Vancouver:

Slevin LK. A Structural Study of Conserved Centriole Duplication Machinery. [Internet] [Thesis]. University of North Carolina; 2014. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:b50097c1-8ea0-424c-a054-1226e022b7ec.

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

Council of Science Editors:

Slevin LK. A Structural Study of Conserved Centriole Duplication Machinery. [Thesis]. University of North Carolina; 2014. Available from: https://cdr.lib.unc.edu/record/uuid:b50097c1-8ea0-424c-a054-1226e022b7ec

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


University of North Carolina

20. Plevock Haase, Karen. REGULATION AND FUNCTION OF CENTROSOME ASSOCIATED PROTEINS.

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

 Centrosomes are the main microtubule organizing center in cells, composed of a pair of centrioles surrounded by pericentriolar material (PCM). Centrosomes are a highly organized… (more)

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

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APA (6th Edition):

Plevock Haase, K. (2016). REGULATION AND FUNCTION OF CENTROSOME ASSOCIATED PROTEINS. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:61c538ce-3b37-4ab2-8faf-08064aed4875

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):

Plevock Haase, Karen. “REGULATION AND FUNCTION OF CENTROSOME ASSOCIATED PROTEINS.” 2016. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:61c538ce-3b37-4ab2-8faf-08064aed4875.

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

MLA Handbook (7th Edition):

Plevock Haase, Karen. “REGULATION AND FUNCTION OF CENTROSOME ASSOCIATED PROTEINS.” 2016. Web. 03 Dec 2020.

Vancouver:

Plevock Haase K. REGULATION AND FUNCTION OF CENTROSOME ASSOCIATED PROTEINS. [Internet] [Thesis]. University of North Carolina; 2016. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:61c538ce-3b37-4ab2-8faf-08064aed4875.

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

Council of Science Editors:

Plevock Haase K. REGULATION AND FUNCTION OF CENTROSOME ASSOCIATED PROTEINS. [Thesis]. University of North Carolina; 2016. Available from: https://cdr.lib.unc.edu/record/uuid:61c538ce-3b37-4ab2-8faf-08064aed4875

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


University of North Carolina

21. Carnahan, Virginia Elaine. Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties.

Degree: Biochemistry and Biophysics, 2007, University of North Carolina

 Pregnane X Receptor is a ligand-activated transcription factor critical in protecting tissues from xenobiotics and endobiotics. PXR is shown to interact with GRIP- 1 and… (more)

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

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APA (6th Edition):

Carnahan, V. E. (2007). Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:547992b6-5fe8-43ed-83e2-c75594d17d5a

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):

Carnahan, Virginia Elaine. “Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties.” 2007. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:547992b6-5fe8-43ed-83e2-c75594d17d5a.

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

MLA Handbook (7th Edition):

Carnahan, Virginia Elaine. “Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties.” 2007. Web. 03 Dec 2020.

Vancouver:

Carnahan VE. Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:547992b6-5fe8-43ed-83e2-c75594d17d5a.

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

Council of Science Editors:

Carnahan VE. Characterizing the Pregnane X Receptor’s Interactions and Biophysical Properties. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:547992b6-5fe8-43ed-83e2-c75594d17d5a

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


University of North Carolina

22. Kennedy, Sarah A. Structural and molecular dynamics simulation studies support Symplekin's protein scaffolding role and a novel fold in the TraI relaxase-helicase C-terminus is essential for conjugative DNA transfer.

Degree: Chemistry, 2009, University of North Carolina

 The majority of eukaryotic pre-mRNAs are processed by 3'-end cleavage and polyadenylation, although in metazoa the replication-dependant histone mRNAs are subject only to 3'-end cleavage… (more)

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

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APA (6th Edition):

Kennedy, S. A. (2009). Structural and molecular dynamics simulation studies support Symplekin's protein scaffolding role and a novel fold in the TraI relaxase-helicase C-terminus is essential for conjugative DNA transfer. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:ec9a87fd-1c6b-4fdd-9722-e941166ed76c

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):

Kennedy, Sarah A. “Structural and molecular dynamics simulation studies support Symplekin's protein scaffolding role and a novel fold in the TraI relaxase-helicase C-terminus is essential for conjugative DNA transfer.” 2009. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:ec9a87fd-1c6b-4fdd-9722-e941166ed76c.

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

MLA Handbook (7th Edition):

Kennedy, Sarah A. “Structural and molecular dynamics simulation studies support Symplekin's protein scaffolding role and a novel fold in the TraI relaxase-helicase C-terminus is essential for conjugative DNA transfer.” 2009. Web. 03 Dec 2020.

Vancouver:

Kennedy SA. Structural and molecular dynamics simulation studies support Symplekin's protein scaffolding role and a novel fold in the TraI relaxase-helicase C-terminus is essential for conjugative DNA transfer. [Internet] [Thesis]. University of North Carolina; 2009. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:ec9a87fd-1c6b-4fdd-9722-e941166ed76c.

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

Council of Science Editors:

Kennedy SA. Structural and molecular dynamics simulation studies support Symplekin's protein scaffolding role and a novel fold in the TraI relaxase-helicase C-terminus is essential for conjugative DNA transfer. [Thesis]. University of North Carolina; 2009. Available from: https://cdr.lib.unc.edu/record/uuid:ec9a87fd-1c6b-4fdd-9722-e941166ed76c

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


University of North Carolina

23. Orans, Jillian. Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis.

Degree: Chemistry, 2007, University of North Carolina

 Pseudomonas aeruginosa is an opportunistic pathogen that is of particular concern to people afflicted with Cystic Fibrosis (CF). Patients with this disease have significantly decreased… (more)

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

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

APA (6th Edition):

Orans, J. (2007). Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:5bda9c80-8453-4026-b6cb-1b0235f59e23

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):

Orans, Jillian. “Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis.” 2007. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:5bda9c80-8453-4026-b6cb-1b0235f59e23.

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

MLA Handbook (7th Edition):

Orans, Jillian. “Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis.” 2007. Web. 03 Dec 2020.

Vancouver:

Orans J. Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:5bda9c80-8453-4026-b6cb-1b0235f59e23.

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

Council of Science Editors:

Orans J. Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:5bda9c80-8453-4026-b6cb-1b0235f59e23

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


University of North Carolina

24. Teotico, Denise Maria Gamboa. Static and dynamic insights into the function of the human nuclear xenobiotic receptor PXR.

Degree: Chemistry, 2007, University of North Carolina

 The nuclear xenobiotic receptor PXR is a highly promiscuous protein that binds to a spectrum of structurally distinct endogenous compounds and clinical drugs and regulates… (more)

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

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APA (6th Edition):

Teotico, D. M. G. (2007). Static and dynamic insights into the function of the human nuclear xenobiotic receptor PXR. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:4f1d5c1e-0b61-49dc-830a-5a9361cb4fde

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):

Teotico, Denise Maria Gamboa. “Static and dynamic insights into the function of the human nuclear xenobiotic receptor PXR.” 2007. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:4f1d5c1e-0b61-49dc-830a-5a9361cb4fde.

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

MLA Handbook (7th Edition):

Teotico, Denise Maria Gamboa. “Static and dynamic insights into the function of the human nuclear xenobiotic receptor PXR.” 2007. Web. 03 Dec 2020.

Vancouver:

Teotico DMG. Static and dynamic insights into the function of the human nuclear xenobiotic receptor PXR. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:4f1d5c1e-0b61-49dc-830a-5a9361cb4fde.

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

Council of Science Editors:

Teotico DMG. Static and dynamic insights into the function of the human nuclear xenobiotic receptor PXR. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:4f1d5c1e-0b61-49dc-830a-5a9361cb4fde

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


University of North Carolina

25. Fleming, Christopher Daniel. Structural insights into xenobiotic and organophosphate binding by human carboxylesterase 1 and efforts made towards the characterization of the androgen receptor modulator MAGE-11.

Degree: Biochemistry and Biophysics, 2007, University of North Carolina

 The processing and elimination of harmful exogenous compounds is important for the successful survival of an organism in its environment. Several proteins classified as drug… (more)

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

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

APA (6th Edition):

Fleming, C. D. (2007). Structural insights into xenobiotic and organophosphate binding by human carboxylesterase 1 and efforts made towards the characterization of the androgen receptor modulator MAGE-11. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:946ac20c-fdd7-461b-9111-1789a9786512

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):

Fleming, Christopher Daniel. “Structural insights into xenobiotic and organophosphate binding by human carboxylesterase 1 and efforts made towards the characterization of the androgen receptor modulator MAGE-11.” 2007. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:946ac20c-fdd7-461b-9111-1789a9786512.

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

MLA Handbook (7th Edition):

Fleming, Christopher Daniel. “Structural insights into xenobiotic and organophosphate binding by human carboxylesterase 1 and efforts made towards the characterization of the androgen receptor modulator MAGE-11.” 2007. Web. 03 Dec 2020.

Vancouver:

Fleming CD. Structural insights into xenobiotic and organophosphate binding by human carboxylesterase 1 and efforts made towards the characterization of the androgen receptor modulator MAGE-11. [Internet] [Thesis]. University of North Carolina; 2007. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:946ac20c-fdd7-461b-9111-1789a9786512.

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

Council of Science Editors:

Fleming CD. Structural insights into xenobiotic and organophosphate binding by human carboxylesterase 1 and efforts made towards the characterization of the androgen receptor modulator MAGE-11. [Thesis]. University of North Carolina; 2007. Available from: https://cdr.lib.unc.edu/record/uuid:946ac20c-fdd7-461b-9111-1789a9786512

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


University of North Carolina

26. Lujan, Scott. Bacterial Conjugation and its Inhibition: The Hows and Whys of Conjugation and What Can be Done to Control It.

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

 Conjugation is the primary vehicle for the horizontal transfer virulence factor genes, such as antibiotic resistance, within and between bacterial strains. In certain epicenters, such… (more)

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

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APA (6th Edition):

Lujan, S. (2008). Bacterial Conjugation and its Inhibition: The Hows and Whys of Conjugation and What Can be Done to Control It. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:479d9a87-b137-4371-b5de-c871ab80e258

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):

Lujan, Scott. “Bacterial Conjugation and its Inhibition: The Hows and Whys of Conjugation and What Can be Done to Control It.” 2008. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:479d9a87-b137-4371-b5de-c871ab80e258.

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

MLA Handbook (7th Edition):

Lujan, Scott. “Bacterial Conjugation and its Inhibition: The Hows and Whys of Conjugation and What Can be Done to Control It.” 2008. Web. 03 Dec 2020.

Vancouver:

Lujan S. Bacterial Conjugation and its Inhibition: The Hows and Whys of Conjugation and What Can be Done to Control It. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:479d9a87-b137-4371-b5de-c871ab80e258.

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

Council of Science Editors:

Lujan S. Bacterial Conjugation and its Inhibition: The Hows and Whys of Conjugation and What Can be Done to Control It. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:479d9a87-b137-4371-b5de-c871ab80e258

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


University of North Carolina

27. Holley, Cynthia. The Dock Family of Atypical Guanine Nucleotide Exchange Factors: Regulation by ELMO1 and RhoG.

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

 The Dock family of proteins regulates diverse biological processes including cell migration, phagocytosis and neuronal polarization. These proteins contain a unique type of guanine nucleotide… (more)

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

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

APA (6th Edition):

Holley, C. (2008). The Dock Family of Atypical Guanine Nucleotide Exchange Factors: Regulation by ELMO1 and RhoG. (Thesis). University of North Carolina. Retrieved from https://cdr.lib.unc.edu/record/uuid:a8456c8c-9459-4655-8d3d-0ce7a1274282

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):

Holley, Cynthia. “The Dock Family of Atypical Guanine Nucleotide Exchange Factors: Regulation by ELMO1 and RhoG.” 2008. Thesis, University of North Carolina. Accessed December 03, 2020. https://cdr.lib.unc.edu/record/uuid:a8456c8c-9459-4655-8d3d-0ce7a1274282.

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

MLA Handbook (7th Edition):

Holley, Cynthia. “The Dock Family of Atypical Guanine Nucleotide Exchange Factors: Regulation by ELMO1 and RhoG.” 2008. Web. 03 Dec 2020.

Vancouver:

Holley C. The Dock Family of Atypical Guanine Nucleotide Exchange Factors: Regulation by ELMO1 and RhoG. [Internet] [Thesis]. University of North Carolina; 2008. [cited 2020 Dec 03]. Available from: https://cdr.lib.unc.edu/record/uuid:a8456c8c-9459-4655-8d3d-0ce7a1274282.

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

Council of Science Editors:

Holley C. The Dock Family of Atypical Guanine Nucleotide Exchange Factors: Regulation by ELMO1 and RhoG. [Thesis]. University of North Carolina; 2008. Available from: https://cdr.lib.unc.edu/record/uuid:a8456c8c-9459-4655-8d3d-0ce7a1274282

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

.