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You searched for +publisher:"Georgia Tech" +contributor:("Champion, Julie"). Showing records 1 – 30 of 35 total matches.

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Georgia Tech

1. Murray, Kathryn Elizabeth. Fabrication and characterization of multifunctional particles with spatially segregated proteins.

Degree: MS, Biomedical Engineering (Joint GT/Emory Department), 2017, Georgia Tech

 Multifunctional particles have been of great interest in a variety of fields including electronics, biology, chemistry, and medicine due to their ability to have multiple… (more)

Subjects/Keywords: Multifunctional particles; E-beam evaporation; Cerberus particles; Janus particles; Fabrication

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APA (6th Edition):

Murray, K. E. (2017). Fabrication and characterization of multifunctional particles with spatially segregated proteins. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59213

Chicago Manual of Style (16th Edition):

Murray, Kathryn Elizabeth. “Fabrication and characterization of multifunctional particles with spatially segregated proteins.” 2017. Masters Thesis, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/59213.

MLA Handbook (7th Edition):

Murray, Kathryn Elizabeth. “Fabrication and characterization of multifunctional particles with spatially segregated proteins.” 2017. Web. 20 Apr 2019.

Vancouver:

Murray KE. Fabrication and characterization of multifunctional particles with spatially segregated proteins. [Internet] [Masters thesis]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/59213.

Council of Science Editors:

Murray KE. Fabrication and characterization of multifunctional particles with spatially segregated proteins. [Masters Thesis]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59213


Georgia Tech

2. Arya, Jaya. Formulation and clinical translation of microneedles for vaccination in developing countries.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 Most vaccines are currently administered by healthcare personnel using a needle and syringe, which poses significant hurdles especially in developing countries. We propose dissolving microneedle… (more)

Subjects/Keywords: Microneedle patch; Transdermal drug delivery; Intradermal skin vaccination; Veterinary vaccination of dogs; Human study

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APA (6th Edition):

Arya, J. (2016). Formulation and clinical translation of microneedles for vaccination in developing countries. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58577

Chicago Manual of Style (16th Edition):

Arya, Jaya. “Formulation and clinical translation of microneedles for vaccination in developing countries.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58577.

MLA Handbook (7th Edition):

Arya, Jaya. “Formulation and clinical translation of microneedles for vaccination in developing countries.” 2016. Web. 20 Apr 2019.

Vancouver:

Arya J. Formulation and clinical translation of microneedles for vaccination in developing countries. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58577.

Council of Science Editors:

Arya J. Formulation and clinical translation of microneedles for vaccination in developing countries. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58577


Georgia Tech

3. Park, Won Min. Self-assembly of protein-based suprastructures.

Degree: PhD, Chemical and Biomolecular Engineering, 2015, Georgia Tech

 Strategies for self-assembly of protein-based suprastructures were developed. Recombinant protein building blocks were designed, produced, and self-assembled into various suprastructures, which include spheres, vesicles, nanosheets… (more)

Subjects/Keywords: Protein; Self-assembly

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APA (6th Edition):

Park, W. M. (2015). Self-assembly of protein-based suprastructures. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58135

Chicago Manual of Style (16th Edition):

Park, Won Min. “Self-assembly of protein-based suprastructures.” 2015. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58135.

MLA Handbook (7th Edition):

Park, Won Min. “Self-assembly of protein-based suprastructures.” 2015. Web. 20 Apr 2019.

Vancouver:

Park WM. Self-assembly of protein-based suprastructures. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58135.

Council of Science Editors:

Park WM. Self-assembly of protein-based suprastructures. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/58135


Georgia Tech

4. Peterson, Vincent. Progress towards the development of G-protein coupled receptor based logic gates.

Degree: MS, Chemistry and Biochemistry, 2016, Georgia Tech

 The yeast Saccharomyces cerevisiae along with the bacterium Escherichia coli have been popular model organisms for the creation or modification of chemical producing or chemical… (more)

Subjects/Keywords: Synthetic biology; GPCRs; Yeast; Cell signaling; Biosensors

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APA (6th Edition):

Peterson, V. (2016). Progress towards the development of G-protein coupled receptor based logic gates. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58141

Chicago Manual of Style (16th Edition):

Peterson, Vincent. “Progress towards the development of G-protein coupled receptor based logic gates.” 2016. Masters Thesis, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58141.

MLA Handbook (7th Edition):

Peterson, Vincent. “Progress towards the development of G-protein coupled receptor based logic gates.” 2016. Web. 20 Apr 2019.

Vancouver:

Peterson V. Progress towards the development of G-protein coupled receptor based logic gates. [Internet] [Masters thesis]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58141.

Council of Science Editors:

Peterson V. Progress towards the development of G-protein coupled receptor based logic gates. [Masters Thesis]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58141


Georgia Tech

5. Rathan, Swetha. Aortic valve mechanobiology- role of altered hemodynamics in mediating aortic valve inflammation and calcification.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 Calcific aortic valve (AV) disease is a strong risk factor for cardiovascular related deaths and is a significant source of mortality worldwide, with the number… (more)

Subjects/Keywords: Aortic valve; Hemodynamics; Mechanobiology; MicroRNA; Calcification

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APA (6th Edition):

Rathan, S. (2016). Aortic valve mechanobiology- role of altered hemodynamics in mediating aortic valve inflammation and calcification. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58144

Chicago Manual of Style (16th Edition):

Rathan, Swetha. “Aortic valve mechanobiology- role of altered hemodynamics in mediating aortic valve inflammation and calcification.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58144.

MLA Handbook (7th Edition):

Rathan, Swetha. “Aortic valve mechanobiology- role of altered hemodynamics in mediating aortic valve inflammation and calcification.” 2016. Web. 20 Apr 2019.

Vancouver:

Rathan S. Aortic valve mechanobiology- role of altered hemodynamics in mediating aortic valve inflammation and calcification. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58144.

Council of Science Editors:

Rathan S. Aortic valve mechanobiology- role of altered hemodynamics in mediating aortic valve inflammation and calcification. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58144


Georgia Tech

6. Mistilis, Matthew Joseph. Thermostabilization of influenza vaccine in microneedle patches.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 Vaccine delivery to the skin via microneedles confers several advantages over the traditional hypodermic needle and syringe. This work focuses on developing microneedles as a… (more)

Subjects/Keywords: Vaccine delivery; Vaccine stability; Microneedles; Drug delivery; Formulations; Dermal delivery

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APA (6th Edition):

Mistilis, M. J. (2016). Thermostabilization of influenza vaccine in microneedle patches. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58153

Chicago Manual of Style (16th Edition):

Mistilis, Matthew Joseph. “Thermostabilization of influenza vaccine in microneedle patches.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58153.

MLA Handbook (7th Edition):

Mistilis, Matthew Joseph. “Thermostabilization of influenza vaccine in microneedle patches.” 2016. Web. 20 Apr 2019.

Vancouver:

Mistilis MJ. Thermostabilization of influenza vaccine in microneedle patches. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58153.

Council of Science Editors:

Mistilis MJ. Thermostabilization of influenza vaccine in microneedle patches. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58153


Georgia Tech

7. Pacheco, Patricia Marie. Fc coated micro/nanoparticles for humoral immune system modulation.

Degree: PhD, Mechanical Engineering, 2014, Georgia Tech

 The body’s humoral immune response plays a larger role in the body’s defenses beyond screening for invading pathogens. Modulation of this response is also vital… (more)

Subjects/Keywords: Fc; Macrophages; Complement system; Micro- and nanoparticles; Biomaterials; Immunoengineering; Tuberculosis

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APA (6th Edition):

Pacheco, P. M. (2014). Fc coated micro/nanoparticles for humoral immune system modulation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54300

Chicago Manual of Style (16th Edition):

Pacheco, Patricia Marie. “Fc coated micro/nanoparticles for humoral immune system modulation.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/54300.

MLA Handbook (7th Edition):

Pacheco, Patricia Marie. “Fc coated micro/nanoparticles for humoral immune system modulation.” 2014. Web. 20 Apr 2019.

Vancouver:

Pacheco PM. Fc coated micro/nanoparticles for humoral immune system modulation. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/54300.

Council of Science Editors:

Pacheco PM. Fc coated micro/nanoparticles for humoral immune system modulation. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54300


Georgia Tech

8. Liu, Wenying. Electrospun nanofibers for regenerative medicine.

Degree: PhD, Chemical and Biomolecular Engineering, 2014, Georgia Tech

 Electrospun nanofibers represent a class of versatile scaffolds for tissue engineering applications owing to their ability to mimic the nanoscale features of the native extracellular… (more)

Subjects/Keywords: Electrospinning; Nanofibers

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APA (6th Edition):

Liu, W. (2014). Electrospun nanofibers for regenerative medicine. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54305

Chicago Manual of Style (16th Edition):

Liu, Wenying. “Electrospun nanofibers for regenerative medicine.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/54305.

MLA Handbook (7th Edition):

Liu, Wenying. “Electrospun nanofibers for regenerative medicine.” 2014. Web. 20 Apr 2019.

Vancouver:

Liu W. Electrospun nanofibers for regenerative medicine. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/54305.

Council of Science Editors:

Liu W. Electrospun nanofibers for regenerative medicine. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54305


Georgia Tech

9. Padmore, Trudy J. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 Peptide drugs are highly specific and efficacious; interest in them remains high despite the challenges of rapid clearance and degradation. To overcome these limitations peptide… (more)

Subjects/Keywords: GLP-1; Controlled release; Affinity-based release; Protein microspheres; Fiber length; Length models

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APA (6th Edition):

Padmore, T. J. (2016). Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56336

Chicago Manual of Style (16th Edition):

Padmore, Trudy J. “Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/56336.

MLA Handbook (7th Edition):

Padmore, Trudy J. “Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.” 2016. Web. 20 Apr 2019.

Vancouver:

Padmore TJ. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/56336.

Council of Science Editors:

Padmore TJ. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/56336


Georgia Tech

10. Kim, Yoo C. Targeted drug delivery within the eye.

Degree: PhD, Chemical and Biomolecular Engineering, 2013, Georgia Tech

 This work introduces novel approaches to enhance targeting of pharmacotherapies to cornea, ciliary body, choroid, and posterior segment of the eye using microneedles as a… (more)

Subjects/Keywords: Drug delivery; Eye

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APA (6th Edition):

Kim, Y. C. (2013). Targeted drug delivery within the eye. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52971

Chicago Manual of Style (16th Edition):

Kim, Yoo C. “Targeted drug delivery within the eye.” 2013. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/52971.

MLA Handbook (7th Edition):

Kim, Yoo C. “Targeted drug delivery within the eye.” 2013. Web. 20 Apr 2019.

Vancouver:

Kim YC. Targeted drug delivery within the eye. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/52971.

Council of Science Editors:

Kim YC. Targeted drug delivery within the eye. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52971


Georgia Tech

11. Gray, Warren Dale. Development of therapeutic systems to treat the infarcted heart.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

 Cardiovascular disease is the leading cause of morbidity and mortality in developed nations, and heart disease is predicted to remain the leading killer for the… (more)

Subjects/Keywords: Myocardial infarction; Cardiac protection; Cardiac regeneration; Angiogenesis; Therapeutic system; Nanoparticle; Dendrimer; Exosome; Hypoxia; N-acetylglucosamine

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APA (6th Edition):

Gray, W. D. (2014). Development of therapeutic systems to treat the infarcted heart. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53429

Chicago Manual of Style (16th Edition):

Gray, Warren Dale. “Development of therapeutic systems to treat the infarcted heart.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/53429.

MLA Handbook (7th Edition):

Gray, Warren Dale. “Development of therapeutic systems to treat the infarcted heart.” 2014. Web. 20 Apr 2019.

Vancouver:

Gray WD. Development of therapeutic systems to treat the infarcted heart. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/53429.

Council of Science Editors:

Gray WD. Development of therapeutic systems to treat the infarcted heart. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53429


Georgia Tech

12. Tiernan, Aubrey Rose. Development of a pancreatic substitute based on genetically engineered intestinal endocrine cells.

Degree: PhD, Chemical and Biomolecular Engineering, 2014, Georgia Tech

 Cell-based insulin therapies can potentially improve glycemic regulation in insulin dependent diabetes patients and thus help reduce secondary complications. The long-term goal of our work… (more)

Subjects/Keywords: Diabetes; Bioluminescence; Intestinal L cells; Pancreatic substitute; Cell encapsulation

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APA (6th Edition):

Tiernan, A. R. (2014). Development of a pancreatic substitute based on genetically engineered intestinal endocrine cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53987

Chicago Manual of Style (16th Edition):

Tiernan, Aubrey Rose. “Development of a pancreatic substitute based on genetically engineered intestinal endocrine cells.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/53987.

MLA Handbook (7th Edition):

Tiernan, Aubrey Rose. “Development of a pancreatic substitute based on genetically engineered intestinal endocrine cells.” 2014. Web. 20 Apr 2019.

Vancouver:

Tiernan AR. Development of a pancreatic substitute based on genetically engineered intestinal endocrine cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/53987.

Council of Science Editors:

Tiernan AR. Development of a pancreatic substitute based on genetically engineered intestinal endocrine cells. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53987


Georgia Tech

13. Sengupta, Aritra. Intracellular drug delivery using laser activated carbon nanoparticles.

Degree: PhD, Chemical and Biomolecular Engineering, 2014, Georgia Tech

 We demonstrate intracellular delivery of various molecules by inducing controlled and reversible cell damage through pulsed laser irradiation of carbon black (CB) nanoparticles. We then… (more)

Subjects/Keywords: Laser; Nanosecond; Carbon black; Intracellular; Drug delivery; Photoacoustics; Pluronics; Poloxamer; siRNA; EGFR; In-vivo; In-vitro

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APA (6th Edition):

Sengupta, A. (2014). Intracellular drug delivery using laser activated carbon nanoparticles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53996

Chicago Manual of Style (16th Edition):

Sengupta, Aritra. “Intracellular drug delivery using laser activated carbon nanoparticles.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/53996.

MLA Handbook (7th Edition):

Sengupta, Aritra. “Intracellular drug delivery using laser activated carbon nanoparticles.” 2014. Web. 20 Apr 2019.

Vancouver:

Sengupta A. Intracellular drug delivery using laser activated carbon nanoparticles. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/53996.

Council of Science Editors:

Sengupta A. Intracellular drug delivery using laser activated carbon nanoparticles. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53996


Georgia Tech

14. Duncanson, Stephanie. Improving the bioartificial pancreas: Investigation of the effects of pro-survival and insulinotropic factor delivery and the development of PEGylated alginate microcapsules to support the function and survival of encapsulated islets and beta cells.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2014, Georgia Tech

 The development of a bioartificial pancreas (BAP) has the potential to substantially improve the treatment of insulin-dependent diabetes. Composed of insulin-secreting cells encapsulated in a… (more)

Subjects/Keywords: Bioartificial pancreas; Diabetes; Alginate microcapsule; Islet; Beta-cell; CXCL12; SDF-1; GLP-1; PEG; Hypoxia; Exendin-4

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APA (6th Edition):

Duncanson, S. (2014). Improving the bioartificial pancreas: Investigation of the effects of pro-survival and insulinotropic factor delivery and the development of PEGylated alginate microcapsules to support the function and survival of encapsulated islets and beta cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54015

Chicago Manual of Style (16th Edition):

Duncanson, Stephanie. “Improving the bioartificial pancreas: Investigation of the effects of pro-survival and insulinotropic factor delivery and the development of PEGylated alginate microcapsules to support the function and survival of encapsulated islets and beta cells.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/54015.

MLA Handbook (7th Edition):

Duncanson, Stephanie. “Improving the bioartificial pancreas: Investigation of the effects of pro-survival and insulinotropic factor delivery and the development of PEGylated alginate microcapsules to support the function and survival of encapsulated islets and beta cells.” 2014. Web. 20 Apr 2019.

Vancouver:

Duncanson S. Improving the bioartificial pancreas: Investigation of the effects of pro-survival and insulinotropic factor delivery and the development of PEGylated alginate microcapsules to support the function and survival of encapsulated islets and beta cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/54015.

Council of Science Editors:

Duncanson S. Improving the bioartificial pancreas: Investigation of the effects of pro-survival and insulinotropic factor delivery and the development of PEGylated alginate microcapsules to support the function and survival of encapsulated islets and beta cells. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54015


Georgia Tech

15. Herrera Estrada, Lina Paola. Production and Engineering of Therapeutic Protein Nanoparticles.

Degree: PhD, Chemical and Biomolecular Engineering, 2014, Georgia Tech

 Protein nanoparticles were proposed as therapeutic protein or enzyme delivery vehicles. The production of protein-enzyme nanoparticles via desolvation and self-assembly was investigated and optimized. First,… (more)

Subjects/Keywords: Nanoparticles; Enzymes; Bacterial Protein Effectors; Desolvation; Self-assembly; IBD; Breast Cancer; YopJ; AvrA

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APA (6th Edition):

Herrera Estrada, L. P. (2014). Production and Engineering of Therapeutic Protein Nanoparticles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56153

Chicago Manual of Style (16th Edition):

Herrera Estrada, Lina Paola. “Production and Engineering of Therapeutic Protein Nanoparticles.” 2014. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/56153.

MLA Handbook (7th Edition):

Herrera Estrada, Lina Paola. “Production and Engineering of Therapeutic Protein Nanoparticles.” 2014. Web. 20 Apr 2019.

Vancouver:

Herrera Estrada LP. Production and Engineering of Therapeutic Protein Nanoparticles. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/56153.

Council of Science Editors:

Herrera Estrada LP. Production and Engineering of Therapeutic Protein Nanoparticles. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/56153


Georgia Tech

16. Au, Samantha Kaling. Development of amine dehydrogenases toward production of chiral amines.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 One in four of the top 200 selling pharmaceutical drugs contain a chiral amine. Chiral amines often require difficult synthesis through traditional heterogeneous catalysts. As… (more)

Subjects/Keywords: Chiral amines; Dehydrogenases; Biocatalysts

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APA (6th Edition):

Au, S. K. (2016). Development of amine dehydrogenases toward production of chiral amines. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58172

Chicago Manual of Style (16th Edition):

Au, Samantha Kaling. “Development of amine dehydrogenases toward production of chiral amines.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58172.

MLA Handbook (7th Edition):

Au, Samantha Kaling. “Development of amine dehydrogenases toward production of chiral amines.” 2016. Web. 20 Apr 2019.

Vancouver:

Au SK. Development of amine dehydrogenases toward production of chiral amines. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58172.

Council of Science Editors:

Au SK. Development of amine dehydrogenases toward production of chiral amines. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58172


Georgia Tech

17. Tsao, Joanna. Role of surface roughness for colloidal interactions in aqueous media.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 The stability of colloidal dispersions is important for many industrial applications, but there are often discrepancies between theoretical descriptions and experimental observations of surface roughness… (more)

Subjects/Keywords: Surface roughness; Total internal reflection microscopy; Electrostatic repulsion; Van der Waals attraction; Depletion interactions

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APA (6th Edition):

Tsao, J. (2016). Role of surface roughness for colloidal interactions in aqueous media. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59136

Chicago Manual of Style (16th Edition):

Tsao, Joanna. “Role of surface roughness for colloidal interactions in aqueous media.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/59136.

MLA Handbook (7th Edition):

Tsao, Joanna. “Role of surface roughness for colloidal interactions in aqueous media.” 2016. Web. 20 Apr 2019.

Vancouver:

Tsao J. Role of surface roughness for colloidal interactions in aqueous media. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/59136.

Council of Science Editors:

Tsao J. Role of surface roughness for colloidal interactions in aqueous media. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59136


Georgia Tech

18. Srinivasan, Sangeetha. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2016, Georgia Tech

 Pivotal discoveries in the field of immunology over the last five decades have changed the way new therapies are designed for applications as varied as… (more)

Subjects/Keywords: Biomaterial; Immunotherapy; Dendritic cells; Microparticles; Scaffold; Controlled release; Drug delivery; Autoimmune

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APA (6th Edition):

Srinivasan, S. (2016). Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59153

Chicago Manual of Style (16th Edition):

Srinivasan, Sangeetha. “Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/59153.

MLA Handbook (7th Edition):

Srinivasan, Sangeetha. “Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.” 2016. Web. 20 Apr 2019.

Vancouver:

Srinivasan S. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/59153.

Council of Science Editors:

Srinivasan S. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59153


Georgia Tech

19. Chang, Timothy Z. Protein nanoparticle vaccines.

Degree: PhD, Chemical and Biomolecular Engineering, 2017, Georgia Tech

 Highly conserved pathogen proteins are essential for broadly cross-protective vaccines, but tend to be poorly immunogenic. Protein nanoparticle vaccines made from conserved influenza matrix protein… (more)

Subjects/Keywords: Nanoparticle; Vaccine; Immunoengineering

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APA (6th Edition):

Chang, T. Z. (2017). Protein nanoparticle vaccines. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59778

Chicago Manual of Style (16th Edition):

Chang, Timothy Z. “Protein nanoparticle vaccines.” 2017. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/59778.

MLA Handbook (7th Edition):

Chang, Timothy Z. “Protein nanoparticle vaccines.” 2017. Web. 20 Apr 2019.

Vancouver:

Chang TZ. Protein nanoparticle vaccines. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/59778.

Council of Science Editors:

Chang TZ. Protein nanoparticle vaccines. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59778


Georgia Tech

20. Casas, Maria Elena. Analysis of lipid storage in C. elegans enabled by image processing and microfluidics.

Degree: PhD, Chemical and Biomolecular Engineering, 2017, Georgia Tech

 While the genetic origin of obesity has yet to be fully understood, the risk of this serious health issue has been linked to fat and… (more)

Subjects/Keywords: C. elegans; Microfluidics; Lipid droplets; Image processing; Granulometry; Metabolism; Diet; Genetic screen; Atlastin

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APA (6th Edition):

Casas, M. E. (2017). Analysis of lipid storage in C. elegans enabled by image processing and microfluidics. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59803

Chicago Manual of Style (16th Edition):

Casas, Maria Elena. “Analysis of lipid storage in C. elegans enabled by image processing and microfluidics.” 2017. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/59803.

MLA Handbook (7th Edition):

Casas, Maria Elena. “Analysis of lipid storage in C. elegans enabled by image processing and microfluidics.” 2017. Web. 20 Apr 2019.

Vancouver:

Casas ME. Analysis of lipid storage in C. elegans enabled by image processing and microfluidics. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/59803.

Council of Science Editors:

Casas ME. Analysis of lipid storage in C. elegans enabled by image processing and microfluidics. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59803


Georgia Tech

21. Tuet, Wing-Yin. Cellular and acellular assays for measuring oxidative stress induced by ambient and laboratory-generated aerosol.

Degree: PhD, Chemical and Biomolecular Engineering, 2018, Georgia Tech

 Exposure to atmospheric particulate matter (PM) is a leading global health risk with various proposed mechanisms of action, including the induction of oxidative stress through… (more)

Subjects/Keywords: Particulate matter; Oxidative stress

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APA (6th Edition):

Tuet, W. (2018). Cellular and acellular assays for measuring oxidative stress induced by ambient and laboratory-generated aerosol. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59870

Chicago Manual of Style (16th Edition):

Tuet, Wing-Yin. “Cellular and acellular assays for measuring oxidative stress induced by ambient and laboratory-generated aerosol.” 2018. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/59870.

MLA Handbook (7th Edition):

Tuet, Wing-Yin. “Cellular and acellular assays for measuring oxidative stress induced by ambient and laboratory-generated aerosol.” 2018. Web. 20 Apr 2019.

Vancouver:

Tuet W. Cellular and acellular assays for measuring oxidative stress induced by ambient and laboratory-generated aerosol. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/59870.

Council of Science Editors:

Tuet W. Cellular and acellular assays for measuring oxidative stress induced by ambient and laboratory-generated aerosol. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/59870


Georgia Tech

22. Joyce, Jessica Cheng. Development of microneedle patches for measles-rubella vaccination and extended delivery vaccination.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2017, Georgia Tech

 Despite cheap and effective vaccines, nearly 1.5 million children die each year from vaccine preventable diseases. The World Health Organization has called for novel vaccine… (more)

Subjects/Keywords: Microneedle patch; Vaccine; Drug delivery; Immune response; Skin vaccination; Measles; Rubella; Polio; Stability; Formulation; Antibody

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APA (6th Edition):

Joyce, J. C. (2017). Development of microneedle patches for measles-rubella vaccination and extended delivery vaccination. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60658

Chicago Manual of Style (16th Edition):

Joyce, Jessica Cheng. “Development of microneedle patches for measles-rubella vaccination and extended delivery vaccination.” 2017. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/60658.

MLA Handbook (7th Edition):

Joyce, Jessica Cheng. “Development of microneedle patches for measles-rubella vaccination and extended delivery vaccination.” 2017. Web. 20 Apr 2019.

Vancouver:

Joyce JC. Development of microneedle patches for measles-rubella vaccination and extended delivery vaccination. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/60658.

Council of Science Editors:

Joyce JC. Development of microneedle patches for measles-rubella vaccination and extended delivery vaccination. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60658


Georgia Tech

23. Watstein, Daniel Marcus. Engineering a whole-cell zinc biosensor.

Degree: PhD, Chemical and Biomolecular Engineering, 2017, Georgia Tech

 Malnutrition is a significant healthcare concern across the globe. Though normally evocative of images of starvation or hunger, malnutrition also encompasses deficiencies of critical micronutrients… (more)

Subjects/Keywords: Synthetic biology; Biosensor; Whole cell biosensor; Metabolic engineering; Zinc

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APA (6th Edition):

Watstein, D. M. (2017). Engineering a whole-cell zinc biosensor. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60665

Chicago Manual of Style (16th Edition):

Watstein, Daniel Marcus. “Engineering a whole-cell zinc biosensor.” 2017. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/60665.

MLA Handbook (7th Edition):

Watstein, Daniel Marcus. “Engineering a whole-cell zinc biosensor.” 2017. Web. 20 Apr 2019.

Vancouver:

Watstein DM. Engineering a whole-cell zinc biosensor. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/60665.

Council of Science Editors:

Watstein DM. Engineering a whole-cell zinc biosensor. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60665

24. Roberts, Evan Kellett. Solid state NMR structural evaluation of the SAF-p1/p2a co-assembling peptide nanofiber system.

Degree: MS, Chemical and Biomolecular Engineering, 2017, Georgia Tech

 This work presents a structural investigation of two variants of SAF (Self-Assembling Fiber) binary peptides designed by Prof. Derek N. Woolfson and coworkers. SAF refers… (more)

Subjects/Keywords: Peptide co-assembly; Supramolecular structure; Structural dynamics; Solid state NMR; Coiled-coil designer peptides

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APA (6th Edition):

Roberts, E. K. (2017). Solid state NMR structural evaluation of the SAF-p1/p2a co-assembling peptide nanofiber system. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58744

Chicago Manual of Style (16th Edition):

Roberts, Evan Kellett. “Solid state NMR structural evaluation of the SAF-p1/p2a co-assembling peptide nanofiber system.” 2017. Masters Thesis, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58744.

MLA Handbook (7th Edition):

Roberts, Evan Kellett. “Solid state NMR structural evaluation of the SAF-p1/p2a co-assembling peptide nanofiber system.” 2017. Web. 20 Apr 2019.

Vancouver:

Roberts EK. Solid state NMR structural evaluation of the SAF-p1/p2a co-assembling peptide nanofiber system. [Internet] [Masters thesis]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58744.

Council of Science Editors:

Roberts EK. Solid state NMR structural evaluation of the SAF-p1/p2a co-assembling peptide nanofiber system. [Masters Thesis]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58744


Georgia Tech

25. Smith, McKenzie L. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 A systems-level understanding of metabolism will have far-reaching benefits from medicine to ecology to industry, as it will facilitate the comprehensive profiling and prediction of… (more)

Subjects/Keywords: Allostery; Metabolomics; Systems biology

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APA (6th Edition):

Smith, M. L. (2016). Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56353

Chicago Manual of Style (16th Edition):

Smith, McKenzie L. “Systematic investigation of protein-metabolite regulatory interactions: methodologies and context.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/56353.

MLA Handbook (7th Edition):

Smith, McKenzie L. “Systematic investigation of protein-metabolite regulatory interactions: methodologies and context.” 2016. Web. 20 Apr 2019.

Vancouver:

Smith ML. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/56353.

Council of Science Editors:

Smith ML. Systematic investigation of protein-metabolite regulatory interactions: methodologies and context. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/56353

26. Levario, Thomas James. Microfluidics and imaging techniques for high-throughput studies of early embryonic development.

Degree: PhD, Chemical and Biomolecular Engineering, 2016, Georgia Tech

 Understanding how developmental systems achieve robustness is a key goal of developmental biology. The fruit fly Drosophila melanogaster is a model of development and developmental… (more)

Subjects/Keywords: Microfluidics; Developmental biology

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APA (6th Edition):

Levario, T. J. (2016). Microfluidics and imaging techniques for high-throughput studies of early embryonic development. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58573

Chicago Manual of Style (16th Edition):

Levario, Thomas James. “Microfluidics and imaging techniques for high-throughput studies of early embryonic development.” 2016. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58573.

MLA Handbook (7th Edition):

Levario, Thomas James. “Microfluidics and imaging techniques for high-throughput studies of early embryonic development.” 2016. Web. 20 Apr 2019.

Vancouver:

Levario TJ. Microfluidics and imaging techniques for high-throughput studies of early embryonic development. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58573.

Council of Science Editors:

Levario TJ. Microfluidics and imaging techniques for high-throughput studies of early embryonic development. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58573

27. Hsieh, Ming-Chien. Kinetic and structural evolution of functional peptide assembling networks.

Degree: PhD, Chemical and Biomolecular Engineering, 2017, Georgia Tech

 The peptide assembly mechanism is important for the development of both functional biomaterials and clinical therapies. Although the assembly structures and assembling pathways have been… (more)

Subjects/Keywords: Peptide assembly; Kinetics; Catalysis; System chemistry

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APA (6th Edition):

Hsieh, M. (2017). Kinetic and structural evolution of functional peptide assembling networks. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58708

Chicago Manual of Style (16th Edition):

Hsieh, Ming-Chien. “Kinetic and structural evolution of functional peptide assembling networks.” 2017. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/58708.

MLA Handbook (7th Edition):

Hsieh, Ming-Chien. “Kinetic and structural evolution of functional peptide assembling networks.” 2017. Web. 20 Apr 2019.

Vancouver:

Hsieh M. Kinetic and structural evolution of functional peptide assembling networks. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/58708.

Council of Science Editors:

Hsieh M. Kinetic and structural evolution of functional peptide assembling networks. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58708

28. Arnold, Lindsay G. Engineering thermo-responsive affinity ligands for glycoprotein purification by affinity precipitation.

Degree: PhD, Chemical and Biomolecular Engineering, 2015, Georgia Tech

 Effective methods for isolation and purification of glycoproteins are of increasing significance to the rapidly growing biopharmaceutical and diagnostic industry. Glycoproteins represent the majority of… (more)

Subjects/Keywords: Lectin fusions; ELP fusions; Affinity precipitation; Glycoprotein purification

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APA (6th Edition):

Arnold, L. G. (2015). Engineering thermo-responsive affinity ligands for glycoprotein purification by affinity precipitation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53493

Chicago Manual of Style (16th Edition):

Arnold, Lindsay G. “Engineering thermo-responsive affinity ligands for glycoprotein purification by affinity precipitation.” 2015. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/53493.

MLA Handbook (7th Edition):

Arnold, Lindsay G. “Engineering thermo-responsive affinity ligands for glycoprotein purification by affinity precipitation.” 2015. Web. 20 Apr 2019.

Vancouver:

Arnold LG. Engineering thermo-responsive affinity ligands for glycoprotein purification by affinity precipitation. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/53493.

Council of Science Editors:

Arnold LG. Engineering thermo-responsive affinity ligands for glycoprotein purification by affinity precipitation. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53493

29. McClendon, Shara Demetria. Molecular design, construction, and characterization of a xylanosome: a protein nanostructure for biomass utilization.

Degree: PhD, Chemical Engineering, 2011, Georgia Tech

 Lignocellulosic biomass is an abundant renewable resource targeted for biofuel production. Cellulose and hemicellulose from biomass both contain fermentable sugars and other moieties that can… (more)

Subjects/Keywords: Cellulosomes; Cohesin-dockerin interaction; Xylan hydroysis; Consolidated bioprocessing; Ferulic acid esterase; Cellulose Chemistry; Cellulose; Cellulose Biodegradation; Biomass; Renewable energy sources; Renewable natural resources

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APA (6th Edition):

McClendon, S. D. (2011). Molecular design, construction, and characterization of a xylanosome: a protein nanostructure for biomass utilization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/43610

Chicago Manual of Style (16th Edition):

McClendon, Shara Demetria. “Molecular design, construction, and characterization of a xylanosome: a protein nanostructure for biomass utilization.” 2011. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/43610.

MLA Handbook (7th Edition):

McClendon, Shara Demetria. “Molecular design, construction, and characterization of a xylanosome: a protein nanostructure for biomass utilization.” 2011. Web. 20 Apr 2019.

Vancouver:

McClendon SD. Molecular design, construction, and characterization of a xylanosome: a protein nanostructure for biomass utilization. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/43610.

Council of Science Editors:

McClendon SD. Molecular design, construction, and characterization of a xylanosome: a protein nanostructure for biomass utilization. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/43610

30. Shekaran, Asha. Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing.

Degree: PhD, Biomedical Engineering, 2013, Georgia Tech

 Healing large bone defects remains a clinical challenge. While autografts are the gold standard treatment for large bone defects, they are limited by availability and… (more)

Subjects/Keywords: Orthopaedic biomaterials; Regenerative medicine; Integrins; Bone regeneration; Integrins; Colloids; Biomimetic materials; Biocolloids; Bone-grafting

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APA (6th Edition):

Shekaran, A. (2013). Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51720

Chicago Manual of Style (16th Edition):

Shekaran, Asha. “Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing.” 2013. Doctoral Dissertation, Georgia Tech. Accessed April 20, 2019. http://hdl.handle.net/1853/51720.

MLA Handbook (7th Edition):

Shekaran, Asha. “Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing.” 2013. Web. 20 Apr 2019.

Vancouver:

Shekaran A. Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1853/51720.

Council of Science Editors:

Shekaran A. Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/51720

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