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You searched for +publisher:"Vanderbilt University" +contributor:("Craig L. Duvall"). Showing records 1 – 26 of 26 total matches.

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Vanderbilt University

1. Evans, Brian Connor. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.

Degree: MS, Biomedical Engineering, 2013, Vanderbilt University

 Peptide-based therapeutics have significant potential for use in a variety of clinical applications ranging from cancer therapy to promotion of cardiovascular health. However, the efficacy… (more)

Subjects/Keywords: intracellular; polyplex; Drug delivery; peptide

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APA (6th Edition):

Evans, B. C. (2013). Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11302

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):

Evans, Brian Connor. “Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.” 2013. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11302.

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

MLA Handbook (7th Edition):

Evans, Brian Connor. “Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior.” 2013. Web. 26 Nov 2020.

Vancouver:

Evans BC. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. [Internet] [Thesis]. Vanderbilt University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11302.

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

Council of Science Editors:

Evans BC. Enhanced intracellular peptide delivery with pH-responsive, endosomolytic nano-polyplexes to modulate vascular smooth muscle cell behavior. [Thesis]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/11302

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


Vanderbilt University

2. Crowder, Spencer William. Modular Design of Stent Polymers Regulates Human Coronary Artery Cell Type-Specific Oxidative Response and Phenotype.

Degree: MS, Biomedical Engineering, 2011, Vanderbilt University

 Polymer properties can be altered by copolymerizing subunits with specific physicochemical characteristics. Vascular stent materials require biocompatibility, mechanical strength, and prevention of restenosis. Here we… (more)

Subjects/Keywords: coronary stent; Copolymerization; biomaterials; oxidative stress

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APA (6th Edition):

Crowder, S. W. (2011). Modular Design of Stent Polymers Regulates Human Coronary Artery Cell Type-Specific Oxidative Response and Phenotype. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11996

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):

Crowder, Spencer William. “Modular Design of Stent Polymers Regulates Human Coronary Artery Cell Type-Specific Oxidative Response and Phenotype.” 2011. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11996.

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

MLA Handbook (7th Edition):

Crowder, Spencer William. “Modular Design of Stent Polymers Regulates Human Coronary Artery Cell Type-Specific Oxidative Response and Phenotype.” 2011. Web. 26 Nov 2020.

Vancouver:

Crowder SW. Modular Design of Stent Polymers Regulates Human Coronary Artery Cell Type-Specific Oxidative Response and Phenotype. [Internet] [Thesis]. Vanderbilt University; 2011. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11996.

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

Council of Science Editors:

Crowder SW. Modular Design of Stent Polymers Regulates Human Coronary Artery Cell Type-Specific Oxidative Response and Phenotype. [Thesis]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/11996

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


Vanderbilt University

3. Poole, Kristin Marie. Quantitative optical imaging of vascular structure and function in a model of peripheral arterial disease.

Degree: MS, Biomedical Engineering, 2012, Vanderbilt University

 Peripheral arterial disease (PAD) leads to an increased risk of myocardial infarction and stroke, increased mortality, and reduced quality of life. The mouse hind limb… (more)

Subjects/Keywords: hyperspectral imaging; optical coherence tomography

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APA (6th Edition):

Poole, K. M. (2012). Quantitative optical imaging of vascular structure and function in a model of peripheral arterial disease. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13329

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):

Poole, Kristin Marie. “Quantitative optical imaging of vascular structure and function in a model of peripheral arterial disease.” 2012. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/13329.

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

MLA Handbook (7th Edition):

Poole, Kristin Marie. “Quantitative optical imaging of vascular structure and function in a model of peripheral arterial disease.” 2012. Web. 26 Nov 2020.

Vancouver:

Poole KM. Quantitative optical imaging of vascular structure and function in a model of peripheral arterial disease. [Internet] [Thesis]. Vanderbilt University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/13329.

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

Council of Science Editors:

Poole KM. Quantitative optical imaging of vascular structure and function in a model of peripheral arterial disease. [Thesis]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/13329

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


Vanderbilt University

4. Miteva, Martina. Optimizing PEG Molecular Weight and Molar Composition for Enhanced In Vivo Pharmacokinetics of a Mixed Micellar siRNA Carrier.

Degree: MS, Biomedical Engineering, 2013, Vanderbilt University

 RNA interference (RNAi) by small interfering RNA (siRNA) possesses great promise as a therapeutic for pathologies whose etiology is related to gene overexpression. However, due… (more)

Subjects/Keywords: PEG; pharmacokinetics; siRNA; cationic micelles; in vivo

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APA (6th Edition):

Miteva, M. (2013). Optimizing PEG Molecular Weight and Molar Composition for Enhanced In Vivo Pharmacokinetics of a Mixed Micellar siRNA Carrier. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15044

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):

Miteva, Martina. “Optimizing PEG Molecular Weight and Molar Composition for Enhanced In Vivo Pharmacokinetics of a Mixed Micellar siRNA Carrier.” 2013. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15044.

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

MLA Handbook (7th Edition):

Miteva, Martina. “Optimizing PEG Molecular Weight and Molar Composition for Enhanced In Vivo Pharmacokinetics of a Mixed Micellar siRNA Carrier.” 2013. Web. 26 Nov 2020.

Vancouver:

Miteva M. Optimizing PEG Molecular Weight and Molar Composition for Enhanced In Vivo Pharmacokinetics of a Mixed Micellar siRNA Carrier. [Internet] [Thesis]. Vanderbilt University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15044.

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

Council of Science Editors:

Miteva M. Optimizing PEG Molecular Weight and Molar Composition for Enhanced In Vivo Pharmacokinetics of a Mixed Micellar siRNA Carrier. [Thesis]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/15044

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


Vanderbilt University

5. McCormack, Devin Rei. <i>In vivo</i> Hyperspectral Imaging of Microvessel Response to Trastuzumab Treatment in Breast Cancer Xenografts.

Degree: MS, Biomedical Engineering, 2014, Vanderbilt University

 HER2-amplified (HER2+) breast cancers are treated with the anti-HER2 monoclonal antibody trastuzumab. Although trastuzumab reduces production of the angiogenic factor VEGF in HER2+ tumors, the… (more)

Subjects/Keywords: Optical Imaging; Image Processing; Vascular Imaging; Automated Image Quantification

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APA (6th Edition):

McCormack, D. R. (2014). <i>In vivo</i> Hyperspectral Imaging of Microvessel Response to Trastuzumab Treatment in Breast Cancer Xenografts. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12593

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):

McCormack, Devin Rei. “<i>In vivo</i> Hyperspectral Imaging of Microvessel Response to Trastuzumab Treatment in Breast Cancer Xenografts.” 2014. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/12593.

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

MLA Handbook (7th Edition):

McCormack, Devin Rei. “<i>In vivo</i> Hyperspectral Imaging of Microvessel Response to Trastuzumab Treatment in Breast Cancer Xenografts.” 2014. Web. 26 Nov 2020.

Vancouver:

McCormack DR. <i>In vivo</i> Hyperspectral Imaging of Microvessel Response to Trastuzumab Treatment in Breast Cancer Xenografts. [Internet] [Thesis]. Vanderbilt University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/12593.

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

Council of Science Editors:

McCormack DR. <i>In vivo</i> Hyperspectral Imaging of Microvessel Response to Trastuzumab Treatment in Breast Cancer Xenografts. [Thesis]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/12593

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


Vanderbilt University

6. Werfel, Thomas Anthony. Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation.

Degree: MS, Biomedical Engineering, 2015, Vanderbilt University

 A combinatorial library of ternary polyplexes was herein investigated to optimize formulations for siRNA delivery. The compositions tested build from our previous finding that balancing… (more)

Subjects/Keywords: Polyplexes; pH-responsive; intravenous delivery; siRNA

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APA (6th Edition):

Werfel, T. A. (2015). Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10946

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):

Werfel, Thomas Anthony. “Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation.” 2015. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/10946.

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

MLA Handbook (7th Edition):

Werfel, Thomas Anthony. “Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation.” 2015. Web. 26 Nov 2020.

Vancouver:

Werfel TA. Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation. [Internet] [Thesis]. Vanderbilt University; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/10946.

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

Council of Science Editors:

Werfel TA. Combinatorial Library of Ternary Polyplexes Enables Identification of Improved siRNA Nanocarriers for Rapid In Vivo Translation. [Thesis]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/10946

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


Vanderbilt University

7. Martin, John Robert. Synthesis of a Porous, Biocompatible Tissue Engineering Scaffold Selectively Degraded by Cell-Generated Reactive Oxygen Species.

Degree: MS, Biomedical Engineering, 2013, Vanderbilt University

 Biodegradable tissue engineering scaffolds are commonly fabricated from poly(lactide-co-glycolide) (PLGA) or similar polyesters that degrade by hydrolysis. PLGA hydrolysis generates acidic byproducts that trigger an… (more)

Subjects/Keywords: polyurethane; oxidation; biodegradation; macrophage; wound healing; scaffold

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APA (6th Edition):

Martin, J. R. (2013). Synthesis of a Porous, Biocompatible Tissue Engineering Scaffold Selectively Degraded by Cell-Generated Reactive Oxygen Species. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14799

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):

Martin, John Robert. “Synthesis of a Porous, Biocompatible Tissue Engineering Scaffold Selectively Degraded by Cell-Generated Reactive Oxygen Species.” 2013. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/14799.

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

MLA Handbook (7th Edition):

Martin, John Robert. “Synthesis of a Porous, Biocompatible Tissue Engineering Scaffold Selectively Degraded by Cell-Generated Reactive Oxygen Species.” 2013. Web. 26 Nov 2020.

Vancouver:

Martin JR. Synthesis of a Porous, Biocompatible Tissue Engineering Scaffold Selectively Degraded by Cell-Generated Reactive Oxygen Species. [Internet] [Thesis]. Vanderbilt University; 2013. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/14799.

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

Council of Science Editors:

Martin JR. Synthesis of a Porous, Biocompatible Tissue Engineering Scaffold Selectively Degraded by Cell-Generated Reactive Oxygen Species. [Thesis]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14799

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


Vanderbilt University

8. Joshi, Rucha Vinay. Smart Microspheres for Stimuli Responsive Drug Delivery, W/O/W double emulsion method, O/W single emulsion method.

Degree: MS, Biomedical Engineering, 2011, Vanderbilt University

 Tunable and sustained drug delivery platforms have great unmet potential to be used for more optimal treatment of human disease. Such delivery devices avoid bolus… (more)

Subjects/Keywords: LCST; ROS; temperature; pH; microspheres; stimuli responsive polymers; cumulative release; characterization of microspheres; PPS

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APA (6th Edition):

Joshi, R. V. (2011). Smart Microspheres for Stimuli Responsive Drug Delivery, W/O/W double emulsion method, O/W single emulsion method. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15231

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):

Joshi, Rucha Vinay. “Smart Microspheres for Stimuli Responsive Drug Delivery, W/O/W double emulsion method, O/W single emulsion method.” 2011. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15231.

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

MLA Handbook (7th Edition):

Joshi, Rucha Vinay. “Smart Microspheres for Stimuli Responsive Drug Delivery, W/O/W double emulsion method, O/W single emulsion method.” 2011. Web. 26 Nov 2020.

Vancouver:

Joshi RV. Smart Microspheres for Stimuli Responsive Drug Delivery, W/O/W double emulsion method, O/W single emulsion method. [Internet] [Thesis]. Vanderbilt University; 2011. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15231.

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

Council of Science Editors:

Joshi RV. Smart Microspheres for Stimuli Responsive Drug Delivery, W/O/W double emulsion method, O/W single emulsion method. [Thesis]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/15231

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


Vanderbilt University

9. Jackson, Meredith Allyn. Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery.

Degree: MS, Biomedical Engineering, 2016, Vanderbilt University

 Although siRNA-based therapeutics hold great promise for systemic cancer treatment, polyplex nanocarrier systems face many intravenous challenges that limit their pharmacokinetic potential and therefore reduce… (more)

Subjects/Keywords: siRNA; pharmacokinetics; zwitterionic materials; polyplexes; drug delivery

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APA (6th Edition):

Jackson, M. A. (2016). Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14579

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):

Jackson, Meredith Allyn. “Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery.” 2016. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/14579.

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

MLA Handbook (7th Edition):

Jackson, Meredith Allyn. “Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery.” 2016. Web. 26 Nov 2020.

Vancouver:

Jackson MA. Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery. [Internet] [Thesis]. Vanderbilt University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/14579.

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

Council of Science Editors:

Jackson MA. Exploring Zwitterionic Coronas as Alternatives to Traditional PEG Architectures for Improved siRNA Polyplex Pharmacokinetics and Tumor Delivery. [Thesis]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/14579

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


Vanderbilt University

10. Gibson, Lauren Elizabeth. Development of Sensitive Biomolecule Detection Strategies for Low-Resource Settings.

Degree: PhD, Chemistry, 2017, Vanderbilt University

 In low-resource areas of the world, accurate diagnosis of disease is especially challenging, as resources are limited and environmental conditions uncontrolled. Consequently, reliable low-resource diagnostics… (more)

Subjects/Keywords: plasmodium lactate dehydrogenase; aptamers; creatinine; dried blood spots

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APA (6th Edition):

Gibson, L. E. (2017). Development of Sensitive Biomolecule Detection Strategies for Low-Resource Settings. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12054

Chicago Manual of Style (16th Edition):

Gibson, Lauren Elizabeth. “Development of Sensitive Biomolecule Detection Strategies for Low-Resource Settings.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/12054.

MLA Handbook (7th Edition):

Gibson, Lauren Elizabeth. “Development of Sensitive Biomolecule Detection Strategies for Low-Resource Settings.” 2017. Web. 26 Nov 2020.

Vancouver:

Gibson LE. Development of Sensitive Biomolecule Detection Strategies for Low-Resource Settings. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/12054.

Council of Science Editors:

Gibson LE. Development of Sensitive Biomolecule Detection Strategies for Low-Resource Settings. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/12054


Vanderbilt University

11. Evans, Brian Connor. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.

Degree: PhD, Biomedical Engineering, 2015, Vanderbilt University

 Peptide-based therapeutics hold significant therapeutic potential for use in a variety of clinical applications ranging from cancer to cardiovascular disease. However, the potential of peptide-based… (more)

Subjects/Keywords: intimal hyperplasia; peptide; drug delivery; endosomal escape; polyplex; nanoparticle

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APA (6th Edition):

Evans, B. C. (2015). Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10864

Chicago Manual of Style (16th Edition):

Evans, Brian Connor. “Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/10864.

MLA Handbook (7th Edition):

Evans, Brian Connor. “Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules.” 2015. Web. 26 Nov 2020.

Vancouver:

Evans BC. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/10864.

Council of Science Editors:

Evans BC. Development of pH-responsive nano-polyplexes for intracellular delivery of therapeutic biomacromolecules. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/10864


Vanderbilt University

12. Martin, John Robert. Poly(thioketal) Polymers and Their Use in the Formation of Hydrophobic and Hydrophilic Cell-Degradable Tissue Engineering Materials.

Degree: PhD, Biomedical Engineering, 2016, Vanderbilt University

 The fields of regenerative medicine and tissue engineering are founded on the usage of bulk-scale, biodegradable material implants that help direct the repair of damaged… (more)

Subjects/Keywords: wound healing; reactive oxygen species; regenerative medicine

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APA (6th Edition):

Martin, J. R. (2016). Poly(thioketal) Polymers and Their Use in the Formation of Hydrophobic and Hydrophilic Cell-Degradable Tissue Engineering Materials. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15222

Chicago Manual of Style (16th Edition):

Martin, John Robert. “Poly(thioketal) Polymers and Their Use in the Formation of Hydrophobic and Hydrophilic Cell-Degradable Tissue Engineering Materials.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15222.

MLA Handbook (7th Edition):

Martin, John Robert. “Poly(thioketal) Polymers and Their Use in the Formation of Hydrophobic and Hydrophilic Cell-Degradable Tissue Engineering Materials.” 2016. Web. 26 Nov 2020.

Vancouver:

Martin JR. Poly(thioketal) Polymers and Their Use in the Formation of Hydrophobic and Hydrophilic Cell-Degradable Tissue Engineering Materials. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15222.

Council of Science Editors:

Martin JR. Poly(thioketal) Polymers and Their Use in the Formation of Hydrophobic and Hydrophilic Cell-Degradable Tissue Engineering Materials. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/15222


Vanderbilt University

13. Zachman, Angela Laurie. Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease.

Degree: PhD, Biomedical Engineering, 2014, Vanderbilt University

 Peripheral artery disease (PAD) is characterized by platelet activation and aggregation on arterial walls, resulting in vessel occlusion and ischemia. To treat PAD, it is… (more)

Subjects/Keywords: inflammation; injectable polymer; atherosclerosis; peripheral artery disease; peptide; angiogenesis

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APA (6th Edition):

Zachman, A. L. (2014). Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11870

Chicago Manual of Style (16th Edition):

Zachman, Angela Laurie. “Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11870.

MLA Handbook (7th Edition):

Zachman, Angela Laurie. “Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease.” 2014. Web. 26 Nov 2020.

Vancouver:

Zachman AL. Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11870.

Council of Science Editors:

Zachman AL. Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/11870


Vanderbilt University

14. Sewell-Loftin, Mary Kathryn. Mechanoregulation of endocardial to mesenchymal transformation and subsequent remodeling during heart valve development.

Degree: PhD, Biomedical Engineering, 2014, Vanderbilt University

 Nearly 300,000 heart valve (HV) replacement surgeries are performed annually, including both pediatric patients with valvular defects and elderly patients suffering from degenerative or calcific… (more)

Subjects/Keywords: hyodrgels; hyaluronic acid; atomic force microscopy; heart valves; biomechanics; epithelial to mesenchymal transformation

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APA (6th Edition):

Sewell-Loftin, M. K. (2014). Mechanoregulation of endocardial to mesenchymal transformation and subsequent remodeling during heart valve development. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10940

Chicago Manual of Style (16th Edition):

Sewell-Loftin, Mary Kathryn. “Mechanoregulation of endocardial to mesenchymal transformation and subsequent remodeling during heart valve development.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/10940.

MLA Handbook (7th Edition):

Sewell-Loftin, Mary Kathryn. “Mechanoregulation of endocardial to mesenchymal transformation and subsequent remodeling during heart valve development.” 2014. Web. 26 Nov 2020.

Vancouver:

Sewell-Loftin MK. Mechanoregulation of endocardial to mesenchymal transformation and subsequent remodeling during heart valve development. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/10940.

Council of Science Editors:

Sewell-Loftin MK. Mechanoregulation of endocardial to mesenchymal transformation and subsequent remodeling during heart valve development. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/10940


Vanderbilt University

15. Ortega, Ryan Adam. Immunomodulation of Tumor Associated Macrophages by Targeted, siRNA-Delivering Nanoparticles.

Degree: PhD, Biomedical Engineering, 2014, Vanderbilt University

 Tumor associated macrophages (TAMs) play an important role in establishing a pro-tumor environment in many tumor types. Produce low levels of inflammatory cytokines which creates… (more)

Subjects/Keywords: polymeric nanoparticles; macrophage targeting; immunoengineering; cancer immunology; RNAi

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APA (6th Edition):

Ortega, R. A. (2014). Immunomodulation of Tumor Associated Macrophages by Targeted, siRNA-Delivering Nanoparticles. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14749

Chicago Manual of Style (16th Edition):

Ortega, Ryan Adam. “Immunomodulation of Tumor Associated Macrophages by Targeted, siRNA-Delivering Nanoparticles.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/14749.

MLA Handbook (7th Edition):

Ortega, Ryan Adam. “Immunomodulation of Tumor Associated Macrophages by Targeted, siRNA-Delivering Nanoparticles.” 2014. Web. 26 Nov 2020.

Vancouver:

Ortega RA. Immunomodulation of Tumor Associated Macrophages by Targeted, siRNA-Delivering Nanoparticles. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/14749.

Council of Science Editors:

Ortega RA. Immunomodulation of Tumor Associated Macrophages by Targeted, siRNA-Delivering Nanoparticles. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14749


Vanderbilt University

16. Yu, Shann Claybourne Say. Biofunctional Materials for the Modulation of Macrophage Phenotype and Polarization.

Degree: PhD, Biomedical Engineering, 2012, Vanderbilt University

 Macrophages have been proposed as a potential therapeutic target because of their central role in the progression of a number of debilitating diseases, such as… (more)

Subjects/Keywords: mannose; biomaterials; cancer immunotherapy; macrophages; nanoparticles; PEG

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APA (6th Edition):

Yu, S. C. S. (2012). Biofunctional Materials for the Modulation of Macrophage Phenotype and Polarization. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14520

Chicago Manual of Style (16th Edition):

Yu, Shann Claybourne Say. “Biofunctional Materials for the Modulation of Macrophage Phenotype and Polarization.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/14520.

MLA Handbook (7th Edition):

Yu, Shann Claybourne Say. “Biofunctional Materials for the Modulation of Macrophage Phenotype and Polarization.” 2012. Web. 26 Nov 2020.

Vancouver:

Yu SCS. Biofunctional Materials for the Modulation of Macrophage Phenotype and Polarization. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/14520.

Council of Science Editors:

Yu SCS. Biofunctional Materials for the Modulation of Macrophage Phenotype and Polarization. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/14520


Vanderbilt University

17. Hocking, Kyle Mitchell. Uncoupling force and calcium flux to develop novel therapeutics for subarachnoid hemorrhage-induced vasospasm.

Degree: PhD, Biomedical Engineering, 2014, Vanderbilt University

 Subarachnoid hemorrhage (SAH) affects approximately 30,000 people each year and accounts for 1-7% of all strokes. Spontaneous SAH occurs due to the rupture of a… (more)

Subjects/Keywords: actin; vasp; myosin; vascular; calcium

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APA (6th Edition):

Hocking, K. M. (2014). Uncoupling force and calcium flux to develop novel therapeutics for subarachnoid hemorrhage-induced vasospasm. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13544

Chicago Manual of Style (16th Edition):

Hocking, Kyle Mitchell. “Uncoupling force and calcium flux to develop novel therapeutics for subarachnoid hemorrhage-induced vasospasm.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/13544.

MLA Handbook (7th Edition):

Hocking, Kyle Mitchell. “Uncoupling force and calcium flux to develop novel therapeutics for subarachnoid hemorrhage-induced vasospasm.” 2014. Web. 26 Nov 2020.

Vancouver:

Hocking KM. Uncoupling force and calcium flux to develop novel therapeutics for subarachnoid hemorrhage-induced vasospasm. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/13544.

Council of Science Editors:

Hocking KM. Uncoupling force and calcium flux to develop novel therapeutics for subarachnoid hemorrhage-induced vasospasm. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/13544


Vanderbilt University

18. Werfel, Thomas Anthony. Strategies to ‘Hydrophobize’ Systemic siRNA Vectors and Selectively Inhibit mTORC2 in Breast Tumors Through RNA Interference.

Degree: PhD, Biomedical Engineering, 2017, Vanderbilt University

 In theory, siRNAs can inhibit every known cancer-causing gene through sequence-specific RNA interference. However, almost twenty years after the discovery of RNA interference, the use… (more)

Subjects/Keywords: Rictor; mTOR; Breast Cancer; Polymer Nanoparticles; Pharmacokinetics; siRNA; RNA Interference

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APA (6th Edition):

Werfel, T. A. (2017). Strategies to ‘Hydrophobize’ Systemic siRNA Vectors and Selectively Inhibit mTORC2 in Breast Tumors Through RNA Interference. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10848

Chicago Manual of Style (16th Edition):

Werfel, Thomas Anthony. “Strategies to ‘Hydrophobize’ Systemic siRNA Vectors and Selectively Inhibit mTORC2 in Breast Tumors Through RNA Interference.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/10848.

MLA Handbook (7th Edition):

Werfel, Thomas Anthony. “Strategies to ‘Hydrophobize’ Systemic siRNA Vectors and Selectively Inhibit mTORC2 in Breast Tumors Through RNA Interference.” 2017. Web. 26 Nov 2020.

Vancouver:

Werfel TA. Strategies to ‘Hydrophobize’ Systemic siRNA Vectors and Selectively Inhibit mTORC2 in Breast Tumors Through RNA Interference. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/10848.

Council of Science Editors:

Werfel TA. Strategies to ‘Hydrophobize’ Systemic siRNA Vectors and Selectively Inhibit mTORC2 in Breast Tumors Through RNA Interference. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/10848


Vanderbilt University

19. Bowler, Meghan Allardyce. Mechanobiology of cadherin-11 in calcific aortic valve disease.

Degree: PhD, Biomedical Engineering, 2018, Vanderbilt University

 Calcific aortic valve disease affects a quarter of those over 65 in the US alone. The only treatment is aortic valve replacement, but this intervention… (more)

Subjects/Keywords: calcification; myofibroblast; interstitial cell; heart valve; cadherin-11; mechanobiology

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APA (6th Edition):

Bowler, M. A. (2018). Mechanobiology of cadherin-11 in calcific aortic valve disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15400

Chicago Manual of Style (16th Edition):

Bowler, Meghan Allardyce. “Mechanobiology of cadherin-11 in calcific aortic valve disease.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15400.

MLA Handbook (7th Edition):

Bowler, Meghan Allardyce. “Mechanobiology of cadherin-11 in calcific aortic valve disease.” 2018. Web. 26 Nov 2020.

Vancouver:

Bowler MA. Mechanobiology of cadherin-11 in calcific aortic valve disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15400.

Council of Science Editors:

Bowler MA. Mechanobiology of cadherin-11 in calcific aortic valve disease. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/15400


Vanderbilt University

20. Kilchrist, Kameron V. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.

Degree: PhD, Biomedical Engineering, 2019, Vanderbilt University

 Since the FDA approved the first recombinant protein 37 years ago, drug developers have harnessed biologics to treat human disease. Despite tremendous progress in extracellular… (more)

Subjects/Keywords: intracellular drug delivery; drug delivery; endosome disruption; assay development

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APA (6th Edition):

Kilchrist, K. V. (2019). New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15474

Chicago Manual of Style (16th Edition):

Kilchrist, Kameron V. “New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15474.

MLA Handbook (7th Edition):

Kilchrist, Kameron V. “New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery.” 2019. Web. 26 Nov 2020.

Vancouver:

Kilchrist KV. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15474.

Council of Science Editors:

Kilchrist KV. New Technologies for Mechanism Elucidation and High Throughput Screening of Endosome Disruption by Carriers Designed for Intracellular Biologic Drug Delivery. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/15474


Vanderbilt University

21. McGough, Madison Ashli Pauline. In Vivo Remodeling of Settable, Cell-Degradable, and Application-Specific Poly(thioketal urethane) Tissue Engineering Composite Bone Grafts with Bone-Like Strength.

Degree: PhD, Biomedical Engineering, 2018, Vanderbilt University

 Bone grafts are scaffold constructs required for the treatment of bone diseases and fracture when a defect is above a critical size to heal naturally.… (more)

Subjects/Keywords: poly(thioketal urethane); tissue engineering; bone graft

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APA (6th Edition):

McGough, M. A. P. (2018). In Vivo Remodeling of Settable, Cell-Degradable, and Application-Specific Poly(thioketal urethane) Tissue Engineering Composite Bone Grafts with Bone-Like Strength. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15510

Chicago Manual of Style (16th Edition):

McGough, Madison Ashli Pauline. “In Vivo Remodeling of Settable, Cell-Degradable, and Application-Specific Poly(thioketal urethane) Tissue Engineering Composite Bone Grafts with Bone-Like Strength.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15510.

MLA Handbook (7th Edition):

McGough, Madison Ashli Pauline. “In Vivo Remodeling of Settable, Cell-Degradable, and Application-Specific Poly(thioketal urethane) Tissue Engineering Composite Bone Grafts with Bone-Like Strength.” 2018. Web. 26 Nov 2020.

Vancouver:

McGough MAP. In Vivo Remodeling of Settable, Cell-Degradable, and Application-Specific Poly(thioketal urethane) Tissue Engineering Composite Bone Grafts with Bone-Like Strength. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15510.

Council of Science Editors:

McGough MAP. In Vivo Remodeling of Settable, Cell-Degradable, and Application-Specific Poly(thioketal urethane) Tissue Engineering Composite Bone Grafts with Bone-Like Strength. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/15510


Vanderbilt University

22. Boyer, Richard Brandon. Neurotrophic Factor Eluting Nerve Allografts for Peripheral Nerve Repair.

Degree: PhD, Biomedical Engineering, 2015, Vanderbilt University

 This dissertation is a compilation of two studies on the topic of reconstruction of traumatic peripheral nerve injuries. In the first study, I evaluate the… (more)

Subjects/Keywords: Nerve regeneration; neurotrophic factors; nerve growth factor; nerve repair; peripheral nerve; neurography; diffusion tensor imagin

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APA (6th Edition):

Boyer, R. B. (2015). Neurotrophic Factor Eluting Nerve Allografts for Peripheral Nerve Repair. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11945

Chicago Manual of Style (16th Edition):

Boyer, Richard Brandon. “Neurotrophic Factor Eluting Nerve Allografts for Peripheral Nerve Repair.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11945.

MLA Handbook (7th Edition):

Boyer, Richard Brandon. “Neurotrophic Factor Eluting Nerve Allografts for Peripheral Nerve Repair.” 2015. Web. 26 Nov 2020.

Vancouver:

Boyer RB. Neurotrophic Factor Eluting Nerve Allografts for Peripheral Nerve Repair. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11945.

Council of Science Editors:

Boyer RB. Neurotrophic Factor Eluting Nerve Allografts for Peripheral Nerve Repair. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/11945


Vanderbilt University

23. Travis, Adam Ryan. Governing the Biological Interactions of Monolayer Protected Gold Nanoparticles by Controlling the Composition and Spatial Structure of the Thiolate Shell.

Degree: PhD, Chemistry, 2017, Vanderbilt University

 The field of nanomedicine capitalizes on the unique chemical and physical properties of nanoscale materials. Tuning parameters such as the shape, size, and elemental composition… (more)

Subjects/Keywords: radioenhancement; janus gold nanoparticle; biomimetic vaccine; microformulator

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APA (6th Edition):

Travis, A. R. (2017). Governing the Biological Interactions of Monolayer Protected Gold Nanoparticles by Controlling the Composition and Spatial Structure of the Thiolate Shell. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/15486

Chicago Manual of Style (16th Edition):

Travis, Adam Ryan. “Governing the Biological Interactions of Monolayer Protected Gold Nanoparticles by Controlling the Composition and Spatial Structure of the Thiolate Shell.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/15486.

MLA Handbook (7th Edition):

Travis, Adam Ryan. “Governing the Biological Interactions of Monolayer Protected Gold Nanoparticles by Controlling the Composition and Spatial Structure of the Thiolate Shell.” 2017. Web. 26 Nov 2020.

Vancouver:

Travis AR. Governing the Biological Interactions of Monolayer Protected Gold Nanoparticles by Controlling the Composition and Spatial Structure of the Thiolate Shell. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/15486.

Council of Science Editors:

Travis AR. Governing the Biological Interactions of Monolayer Protected Gold Nanoparticles by Controlling the Composition and Spatial Structure of the Thiolate Shell. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/15486


Vanderbilt University

24. Nelson, Christopher Edward. Tunable Delivery of siRNA from a Biodegradable Scaffold for Regenerative Medicine.

Degree: PhD, Biomedical Engineering, 2014, Vanderbilt University

 Clinical translation of RNA interference has been impeded by the lack of safe and effective technologies for cytoplasmic delivery to target cells. Regenerative medicine is… (more)

Subjects/Keywords: endosomolytic nanoparticles; gene knockdown; controlled release; reversible addition-fragmentation chain transfer (RAFT) polymeriza; injectable scaffolds

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APA (6th Edition):

Nelson, C. E. (2014). Tunable Delivery of siRNA from a Biodegradable Scaffold for Regenerative Medicine. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11228

Chicago Manual of Style (16th Edition):

Nelson, Christopher Edward. “Tunable Delivery of siRNA from a Biodegradable Scaffold for Regenerative Medicine.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11228.

MLA Handbook (7th Edition):

Nelson, Christopher Edward. “Tunable Delivery of siRNA from a Biodegradable Scaffold for Regenerative Medicine.” 2014. Web. 26 Nov 2020.

Vancouver:

Nelson CE. Tunable Delivery of siRNA from a Biodegradable Scaffold for Regenerative Medicine. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11228.

Council of Science Editors:

Nelson CE. Tunable Delivery of siRNA from a Biodegradable Scaffold for Regenerative Medicine. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/11228


Vanderbilt University

25. Li, Jun. Novel TSPO ligands to facilitate rapid tracer discovery and as precision imaging diagnostics of cancer.

Degree: PhD, Interdisciplinary Materials Science, 2016, Vanderbilt University

 Translocator protein (TSPO) represents an attractive target for molecular imaging and therapy due to its prevalence and critical roles played in oncology and other pathologies.… (more)

Subjects/Keywords: TSPO; molecular imaging; precision medicine; tracer discovery; cancer

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APA (6th Edition):

Li, J. (2016). Novel TSPO ligands to facilitate rapid tracer discovery and as precision imaging diagnostics of cancer. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/12747

Chicago Manual of Style (16th Edition):

Li, Jun. “Novel TSPO ligands to facilitate rapid tracer discovery and as precision imaging diagnostics of cancer.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/12747.

MLA Handbook (7th Edition):

Li, Jun. “Novel TSPO ligands to facilitate rapid tracer discovery and as precision imaging diagnostics of cancer.” 2016. Web. 26 Nov 2020.

Vancouver:

Li J. Novel TSPO ligands to facilitate rapid tracer discovery and as precision imaging diagnostics of cancer. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/12747.

Council of Science Editors:

Li J. Novel TSPO ligands to facilitate rapid tracer discovery and as precision imaging diagnostics of cancer. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/12747


Vanderbilt University

26. Beavers, Kelsey Ross. Engineering Porous Silicon Nanoparticles for Delivery of Peptide Nucleic Acid Therapeutics.

Degree: PhD, Interdisciplinary Materials Science, 2017, Vanderbilt University

 Researchers discovered the existence of non-coding RNA while unraveling the secrets of the human genome. Non-coding RNA molecules are never translated into proteins, yet they… (more)

Subjects/Keywords: drug delivery; porous silicon; nanoparticle; miRNA; peptide nucleic acid; anti-miRNA

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APA (6th Edition):

Beavers, K. R. (2017). Engineering Porous Silicon Nanoparticles for Delivery of Peptide Nucleic Acid Therapeutics. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11253

Chicago Manual of Style (16th Edition):

Beavers, Kelsey Ross. “Engineering Porous Silicon Nanoparticles for Delivery of Peptide Nucleic Acid Therapeutics.” 2017. Doctoral Dissertation, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11253.

MLA Handbook (7th Edition):

Beavers, Kelsey Ross. “Engineering Porous Silicon Nanoparticles for Delivery of Peptide Nucleic Acid Therapeutics.” 2017. Web. 26 Nov 2020.

Vancouver:

Beavers KR. Engineering Porous Silicon Nanoparticles for Delivery of Peptide Nucleic Acid Therapeutics. [Internet] [Doctoral dissertation]. Vanderbilt University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11253.

Council of Science Editors:

Beavers KR. Engineering Porous Silicon Nanoparticles for Delivery of Peptide Nucleic Acid Therapeutics. [Doctoral Dissertation]. Vanderbilt University; 2017. Available from: http://hdl.handle.net/1803/11253

.