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You searched for +publisher:"Georgia Tech" +contributor:("Niren Murthy"). Showing records 1 – 20 of 20 total matches.

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Georgia Tech

1. Agarwal, Abhiruchi. Nanocarrier mediated therapies for the gliomas of the brain.

Degree: PhD, Bioengineering, 2011, Georgia Tech

 Existing methods of treating glioma are not effective for eradicating the disease. Therefore, new and innovative methods of treatment alone or in combination with existing… (more)

Subjects/Keywords: Thermosensitive; Gold nanorods; Liposomes; Nanocarrier; Tumor distribution; In vivo fluorescence imaging; Bioavailability; Drug delivery; Doxorubicin; Active targeting; Gliomas; Liposomes; Drug delivery systems; Tumor markers

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APA (6th Edition):

Agarwal, A. (2011). Nanocarrier mediated therapies for the gliomas of the brain. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/39468

Chicago Manual of Style (16th Edition):

Agarwal, Abhiruchi. “Nanocarrier mediated therapies for the gliomas of the brain.” 2011. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/39468.

MLA Handbook (7th Edition):

Agarwal, Abhiruchi. “Nanocarrier mediated therapies for the gliomas of the brain.” 2011. Web. 23 Oct 2020.

Vancouver:

Agarwal A. Nanocarrier mediated therapies for the gliomas of the brain. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/39468.

Council of Science Editors:

Agarwal A. Nanocarrier mediated therapies for the gliomas of the brain. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/39468

2. Wilson, David Scott. Rational design and synthesis of drug delivery platforms for treating diseases associated with intestinal inflammation.

Degree: PhD, Bioengineering, 2011, Georgia Tech

 Over 500 million people worldwide suffer from disease associated with intestinal inflammation, including gastric cancer, inflammatory bowel disease, h. pylori infections, and numerous viral and… (more)

Subjects/Keywords: Inflammatory bowel disease; Reactive oxygen species; Polymer; Biomaterial; Nanoparticle; Inflammation; Cancer; SiRNA; Drug delivery; Nanoparticles; Intestines Diseases; Small interfering RNA

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APA (6th Edition):

Wilson, D. S. (2011). Rational design and synthesis of drug delivery platforms for treating diseases associated with intestinal inflammation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/45803

Chicago Manual of Style (16th Edition):

Wilson, David Scott. “Rational design and synthesis of drug delivery platforms for treating diseases associated with intestinal inflammation.” 2011. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/45803.

MLA Handbook (7th Edition):

Wilson, David Scott. “Rational design and synthesis of drug delivery platforms for treating diseases associated with intestinal inflammation.” 2011. Web. 23 Oct 2020.

Vancouver:

Wilson DS. Rational design and synthesis of drug delivery platforms for treating diseases associated with intestinal inflammation. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/45803.

Council of Science Editors:

Wilson DS. Rational design and synthesis of drug delivery platforms for treating diseases associated with intestinal inflammation. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/45803

3. Heffernan, Michael John. Biodegradable polymeric delivery systems for protein subunit vaccines.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 The prevention and treatment of cancer and infectious diseases requires vaccines that can mediate cytotoxic T lymphocyte-based immunity. A promising strategy is protein subunit vaccines… (more)

Subjects/Keywords: Vaccine delivery; Drug delivery; Microencapsulation; Nanospheres; Microspheres; Nanoparticles; Polyacetal; PH-responsive; TLR ligands; Poly(I)-poly(C); Acid-degradable; Vaccines; Polymeric drug delivery systems; Biodegradable plastics

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APA (6th Edition):

Heffernan, M. J. (2008). Biodegradable polymeric delivery systems for protein subunit vaccines. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/24787

Chicago Manual of Style (16th Edition):

Heffernan, Michael John. “Biodegradable polymeric delivery systems for protein subunit vaccines.” 2008. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/24787.

MLA Handbook (7th Edition):

Heffernan, Michael John. “Biodegradable polymeric delivery systems for protein subunit vaccines.” 2008. Web. 23 Oct 2020.

Vancouver:

Heffernan MJ. Biodegradable polymeric delivery systems for protein subunit vaccines. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/24787.

Council of Science Editors:

Heffernan MJ. Biodegradable polymeric delivery systems for protein subunit vaccines. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/24787

4. Choi, Sungmoon. Fluorescent noble metal nanodots for biological applications.

Degree: PhD, Chemistry and Biochemistry, 2010, Georgia Tech

 Commercial organic dyes are widely used for cellular staining due to their small size, high brightness, and chemical functionality. However, their blinking and photobleaching are… (more)

Subjects/Keywords: DNA; Nanodots; Drug delivery; Cellular staining; Fluorophores; Silver; Drug delivery systems; Biomedical materials Imaging compatibility; Diagnostic imaging

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APA (6th Edition):

Choi, S. (2010). Fluorescent noble metal nanodots for biological applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37195

Chicago Manual of Style (16th Edition):

Choi, Sungmoon. “Fluorescent noble metal nanodots for biological applications.” 2010. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/37195.

MLA Handbook (7th Edition):

Choi, Sungmoon. “Fluorescent noble metal nanodots for biological applications.” 2010. Web. 23 Oct 2020.

Vancouver:

Choi S. Fluorescent noble metal nanodots for biological applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/37195.

Council of Science Editors:

Choi S. Fluorescent noble metal nanodots for biological applications. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/37195

5. Hermann, Christopher Douglas. Hydrogel therapy for re-synostosis based on the developmental and regenerative changes of murine cranial sutures.

Degree: PhD, Biomedical Engineering, 2012, Georgia Tech

 Craniosynostosis is the premature fusion of one or more cranial sutures in the developing skull. If left untreated, craniosynostosis can result in developmental delays, blindness,… (more)

Subjects/Keywords: Craniosynostosis; Hydrogel; Re-synostosis; Image segmentation; Micro-CT; Cranial sutures; Skull Diseases; Craniosynostoses; Skull Abnormalities

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APA (6th Edition):

Hermann, C. D. (2012). Hydrogel therapy for re-synostosis based on the developmental and regenerative changes of murine cranial sutures. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/44763

Chicago Manual of Style (16th Edition):

Hermann, Christopher Douglas. “Hydrogel therapy for re-synostosis based on the developmental and regenerative changes of murine cranial sutures.” 2012. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/44763.

MLA Handbook (7th Edition):

Hermann, Christopher Douglas. “Hydrogel therapy for re-synostosis based on the developmental and regenerative changes of murine cranial sutures.” 2012. Web. 23 Oct 2020.

Vancouver:

Hermann CD. Hydrogel therapy for re-synostosis based on the developmental and regenerative changes of murine cranial sutures. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/44763.

Council of Science Editors:

Hermann CD. Hydrogel therapy for re-synostosis based on the developmental and regenerative changes of murine cranial sutures. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/44763

6. Carpenedo, Richard L. Microsphere-mediated control of embryoid body microenvironments.

Degree: PhD, Biomedical Engineering, 2010, Georgia Tech

 Embryonic stem cells (ESCs) hold great promise for treatment of degenerative disorders such as Parkinson's and Alzheimer's disease, diabetes, and cardiovascular disease. The ability of… (more)

Subjects/Keywords: Microsphere; Retinoic acid; Embryoid body; Embryonic stem cell; Stem cells; Tretinoin; Degeneration (Pathology); Regenerative medicine

…Spain. While work has made up a significant portion of my time at Georgia Tech and in Atlanta… …thank you for all his support. Many friends from my first few years at Georgia Tech have… 

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APA (6th Edition):

Carpenedo, R. L. (2010). Microsphere-mediated control of embryoid body microenvironments. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/33948

Chicago Manual of Style (16th Edition):

Carpenedo, Richard L. “Microsphere-mediated control of embryoid body microenvironments.” 2010. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/33948.

MLA Handbook (7th Edition):

Carpenedo, Richard L. “Microsphere-mediated control of embryoid body microenvironments.” 2010. Web. 23 Oct 2020.

Vancouver:

Carpenedo RL. Microsphere-mediated control of embryoid body microenvironments. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/33948.

Council of Science Editors:

Carpenedo RL. Microsphere-mediated control of embryoid body microenvironments. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/33948


Georgia Tech

7. Kao, Chen-Yu. Developing a Minimally Invasive Sustained Release System for Glioma Therapy.

Degree: MS, Biomedical Engineering, 2007, Georgia Tech

 Malignant brain tumor is one of the most lethal forms of cancers. In the United States alone, approximately 20,500 new cases of primary malignant brain… (more)

Subjects/Keywords: BBB; Hydrogel; Local sustained delivery; PLGA; Doxorubicin; Gliomas; Intracranial tumors; Blood-brain barrier; Controlled release technology; Doxorubicin

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APA (6th Edition):

Kao, C. (2007). Developing a Minimally Invasive Sustained Release System for Glioma Therapy. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/19757

Chicago Manual of Style (16th Edition):

Kao, Chen-Yu. “Developing a Minimally Invasive Sustained Release System for Glioma Therapy.” 2007. Masters Thesis, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/19757.

MLA Handbook (7th Edition):

Kao, Chen-Yu. “Developing a Minimally Invasive Sustained Release System for Glioma Therapy.” 2007. Web. 23 Oct 2020.

Vancouver:

Kao C. Developing a Minimally Invasive Sustained Release System for Glioma Therapy. [Internet] [Masters thesis]. Georgia Tech; 2007. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/19757.

Council of Science Editors:

Kao C. Developing a Minimally Invasive Sustained Release System for Glioma Therapy. [Masters Thesis]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/19757


Georgia Tech

8. Shankar, Sucharita P. Glycoprotein-mediated interactions of dendritic cells with surfaces of defined chemistries.

Degree: PhD, Biomedical Engineering, 2007, Georgia Tech

 Implanted combination devices comprising both biological as well as biomaterial components may trigger non-specific inflammatory responses against the biomaterial component as well as specific immune… (more)

Subjects/Keywords: Biomaterial; Dendritic cells; Self-assembled monolayers; Glycoprotein; Dendritic cells; Biomedical materials; Immunological adjuvants

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APA (6th Edition):

Shankar, S. P. (2007). Glycoprotein-mediated interactions of dendritic cells with surfaces of defined chemistries. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29790

Chicago Manual of Style (16th Edition):

Shankar, Sucharita P. “Glycoprotein-mediated interactions of dendritic cells with surfaces of defined chemistries.” 2007. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/29790.

MLA Handbook (7th Edition):

Shankar, Sucharita P. “Glycoprotein-mediated interactions of dendritic cells with surfaces of defined chemistries.” 2007. Web. 23 Oct 2020.

Vancouver:

Shankar SP. Glycoprotein-mediated interactions of dendritic cells with surfaces of defined chemistries. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/29790.

Council of Science Editors:

Shankar SP. Glycoprotein-mediated interactions of dendritic cells with surfaces of defined chemistries. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/29790


Georgia Tech

9. Landazuri, Natalia. Effects of flocculation on retrovirus processing, delivery and transduction.

Degree: PhD, Biomedical Engineering, 2005, Georgia Tech

 The efficiency of retrovirus-mediated gene transfer can be dramatically enhanced by inducing flocculation of viruses. Addition of oppositely charged polymers to virus stocks resulted in… (more)

Subjects/Keywords: Flocculation; Polymers; Lentivirus; Retrovirus; Gene therapy; Gene transfer

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APA (6th Edition):

Landazuri, N. (2005). Effects of flocculation on retrovirus processing, delivery and transduction. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/6884

Chicago Manual of Style (16th Edition):

Landazuri, Natalia. “Effects of flocculation on retrovirus processing, delivery and transduction.” 2005. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/6884.

MLA Handbook (7th Edition):

Landazuri, Natalia. “Effects of flocculation on retrovirus processing, delivery and transduction.” 2005. Web. 23 Oct 2020.

Vancouver:

Landazuri N. Effects of flocculation on retrovirus processing, delivery and transduction. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/6884.

Council of Science Editors:

Landazuri N. Effects of flocculation on retrovirus processing, delivery and transduction. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/6884


Georgia Tech

10. Smith, Andrew Michael. Engineering semiconductor nanocrystals for molecular, cellular, and in vivo imaging.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 Biomedicine has recently exploited many nanotechnology platforms for the detection and treatment of disease as well as for the fundamental study of cellular biology. A… (more)

Subjects/Keywords: Polymer; Ligand; CdSe; Amphiphilic; Multidentate; Epitaxy; HgTe; CdTe; Endocytosis; Phagocytosis; Protein A; Solid state physics; Coordinating; Tumor; Nonspecific; Semiconductor nanocrystals; Quantum dots; Macromolecules

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APA (6th Edition):

Smith, A. M. (2008). Engineering semiconductor nanocrystals for molecular, cellular, and in vivo imaging. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37124

Chicago Manual of Style (16th Edition):

Smith, Andrew Michael. “Engineering semiconductor nanocrystals for molecular, cellular, and in vivo imaging.” 2008. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/37124.

MLA Handbook (7th Edition):

Smith, Andrew Michael. “Engineering semiconductor nanocrystals for molecular, cellular, and in vivo imaging.” 2008. Web. 23 Oct 2020.

Vancouver:

Smith AM. Engineering semiconductor nanocrystals for molecular, cellular, and in vivo imaging. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/37124.

Council of Science Editors:

Smith AM. Engineering semiconductor nanocrystals for molecular, cellular, and in vivo imaging. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/37124


Georgia Tech

11. Andrews, Samantha Nacole. Microdermabrasion for transdermal drug delivery.

Degree: PhD, Biomedical Engineering, 2010, Georgia Tech

 The skin serves as a semi-permeable barrier that protects the body from pathogens and water loss. The stratum corneum, the upper 10-15 µm layer of… (more)

Subjects/Keywords: Microdermabrasion; Transdermal drug delivery; Skin; Transdermal medication

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APA (6th Edition):

Andrews, S. N. (2010). Microdermabrasion for transdermal drug delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37150

Chicago Manual of Style (16th Edition):

Andrews, Samantha Nacole. “Microdermabrasion for transdermal drug delivery.” 2010. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/37150.

MLA Handbook (7th Edition):

Andrews, Samantha Nacole. “Microdermabrasion for transdermal drug delivery.” 2010. Web. 23 Oct 2020.

Vancouver:

Andrews SN. Microdermabrasion for transdermal drug delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/37150.

Council of Science Editors:

Andrews SN. Microdermabrasion for transdermal drug delivery. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/37150


Georgia Tech

12. Kao, Chen-Yu. Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles.

Degree: PhD, Biomedical Engineering, 2009, Georgia Tech

 Amyotrophic lateral sclerosis (ALS) is a devastating disease. Currently, there is no cure for this disease, and effective treatment strategies are greatly needed. Calpain activation… (more)

Subjects/Keywords: Microparticle; Polyketal; Sustained release; Amyotrophic lateral sclerosis; Intrapinal cord injection; Drug delivery; Hydrophobic; Calpain inhibitors; Calpain; Polymeric drug delivery systems; Polymers in medicine; Biomedical materials

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APA (6th Edition):

Kao, C. (2009). Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37304

Chicago Manual of Style (16th Edition):

Kao, Chen-Yu. “Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles.” 2009. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/37304.

MLA Handbook (7th Edition):

Kao, Chen-Yu. “Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles.” 2009. Web. 23 Oct 2020.

Vancouver:

Kao C. Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/37304.

Council of Science Editors:

Kao C. Local and sustained delivery of hydrophobic drugs to the spinal cord with polyketal microparticles. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/37304


Georgia Tech

13. Gotz, Marion Gabriele. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.

Degree: PhD, Chemistry and Biochemistry, 2004, Georgia Tech

 Cysteine proteases are a class of proteolytic enzymes, which are involved in a series of metabolic and catabolic processes, such as protein turnover, digestion, blood… (more)

Subjects/Keywords: Allyl sulfone; Aza-peptide; Biosynthesis; Cysteine protease; Cysteine proteinases; Irreversible inhibitors; Protease inhibitors; Sulphones; Vinyl sulfone

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APA (6th Edition):

Gotz, M. G. (2004). Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/8072

Chicago Manual of Style (16th Edition):

Gotz, Marion Gabriele. “Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.” 2004. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/8072.

MLA Handbook (7th Edition):

Gotz, Marion Gabriele. “Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases.” 2004. Web. 23 Oct 2020.

Vancouver:

Gotz MG. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/8072.

Council of Science Editors:

Gotz MG. Design, synthesis, and evaluation of irreversible peptidyl inhibitors for clan CA and clan CD cysteine proteases. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/8072


Georgia Tech

14. Singh, Neetu. Synthetic routes to new core/shell nanogels:design and application in biomaterials.

Degree: PhD, Chemistry and Biochemistry, 2008, Georgia Tech

 A very interesting class of nanoparticles extensively used for bio-applications is that of hydrogel particles, also called nanogels. There is an increasing interest in the… (more)

Subjects/Keywords: Nanogels; Microgels; Synthesis; Bioconjugation; Nanostructured materials; Biomedical materials; Colloids

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APA (6th Edition):

Singh, N. (2008). Synthetic routes to new core/shell nanogels:design and application in biomaterials. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/28261

Chicago Manual of Style (16th Edition):

Singh, Neetu. “Synthetic routes to new core/shell nanogels:design and application in biomaterials.” 2008. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/28261.

MLA Handbook (7th Edition):

Singh, Neetu. “Synthetic routes to new core/shell nanogels:design and application in biomaterials.” 2008. Web. 23 Oct 2020.

Vancouver:

Singh N. Synthetic routes to new core/shell nanogels:design and application in biomaterials. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/28261.

Council of Science Editors:

Singh N. Synthetic routes to new core/shell nanogels:design and application in biomaterials. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/28261


Georgia Tech

15. Lee, Hyun-Jung. Delivery of thermostabilized chondroitinase ABC enhances axonal sprouting and functional recovery after spinal cord injury.

Degree: PhD, Biomedical Engineering, 2009, Georgia Tech

 Chondroitin sulfate proteoglycans (CSPGs) are one major class of axon growth inhibitors that are upregulated and accumulated around the lesion site after spinal cord injury… (more)

Subjects/Keywords: Lipid microtube; Hydrogel; Regeneration; Chondroitin sulfate proteoglycan; Spinal cord injury; Chondroitinase ABC; Chondroitin sulfates; Protein engineering; Spinal cord Wounds and injuries; Spinal cord Regeneration

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APA (6th Edition):

Lee, H. (2009). Delivery of thermostabilized chondroitinase ABC enhances axonal sprouting and functional recovery after spinal cord injury. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31734

Chicago Manual of Style (16th Edition):

Lee, Hyun-Jung. “Delivery of thermostabilized chondroitinase ABC enhances axonal sprouting and functional recovery after spinal cord injury.” 2009. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/31734.

MLA Handbook (7th Edition):

Lee, Hyun-Jung. “Delivery of thermostabilized chondroitinase ABC enhances axonal sprouting and functional recovery after spinal cord injury.” 2009. Web. 23 Oct 2020.

Vancouver:

Lee H. Delivery of thermostabilized chondroitinase ABC enhances axonal sprouting and functional recovery after spinal cord injury. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/31734.

Council of Science Editors:

Lee H. Delivery of thermostabilized chondroitinase ABC enhances axonal sprouting and functional recovery after spinal cord injury. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/31734


Georgia Tech

16. Foster, Michael Scott. Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation.

Degree: PhD, Chemistry and Biochemistry, 2008, Georgia Tech

 Novel, rationally-designed acrylate analogs of various known dipeptide substrates were found to be mechanism-based inactivators of the enzyme peptidylglycine alpha-amidating monooxygenase (PAM, EC 1.14.17.3). This… (more)

Subjects/Keywords: Molecular modeling; Stereochemistry; Molecules Models; Peptides; Chemical structure; Peptide hormones; Neuropeptides

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APA (6th Edition):

Foster, M. S. (2008). Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31816

Chicago Manual of Style (16th Edition):

Foster, Michael Scott. “Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation.” 2008. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/31816.

MLA Handbook (7th Edition):

Foster, Michael Scott. “Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation.” 2008. Web. 23 Oct 2020.

Vancouver:

Foster MS. Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/31816.

Council of Science Editors:

Foster MS. Design, synthesis, kinetic analysis, molecular modeling, and pharmacological evaluation of novel inhibitors of peptide amidation. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/31816


Georgia Tech

17. Nitin, Nitin. Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells.

Degree: PhD, Biomedical Engineering, 2005, Georgia Tech

 Detection, imaging and quantification of gene expression in living cells can provide essential information on basic biological issues and disease processes. To establish this technology,… (more)

Subjects/Keywords: Magnetic nanoparticles; RNA; MRI; Optical; Molecular beacons; Molecular imaging; RNA Detection; Nanoparticles Magnetic properties; Molecular spectroscopy; Molecular probes; Magnetic resonance imaging; Diagnostic imaging

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APA (6th Edition):

Nitin, N. (2005). Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/7458

Chicago Manual of Style (16th Edition):

Nitin, Nitin. “Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells.” 2005. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/7458.

MLA Handbook (7th Edition):

Nitin, Nitin. “Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells.” 2005. Web. 23 Oct 2020.

Vancouver:

Nitin N. Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2005. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/7458.

Council of Science Editors:

Nitin N. Optical and MR Molecular Imaging Probes and Peptide-based Cellular Delivery for RNA Detection in Living Cells. [Doctoral Dissertation]. Georgia Tech; 2005. Available from: http://hdl.handle.net/1853/7458


Georgia Tech

18. South, Antoinette Bonhivert. Assembly and dynamic behavior of microgel thin films and their application to biointerfacees.

Degree: PhD, Chemistry and Biochemistry, 2010, Georgia Tech

 Hydrogels, which are polymeric cross-linked networks that swell in aqueous environments, are versatile materials that can contain a variety of chemical functionalities, mechanical properties, and… (more)

Subjects/Keywords: Biomaterials; Film assembly; Colloids; Thin films; Biomedical materials; Colloids in medicine; Centrifugation

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APA (6th Edition):

South, A. B. (2010). Assembly and dynamic behavior of microgel thin films and their application to biointerfacees. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/34686

Chicago Manual of Style (16th Edition):

South, Antoinette Bonhivert. “Assembly and dynamic behavior of microgel thin films and their application to biointerfacees.” 2010. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/34686.

MLA Handbook (7th Edition):

South, Antoinette Bonhivert. “Assembly and dynamic behavior of microgel thin films and their application to biointerfacees.” 2010. Web. 23 Oct 2020.

Vancouver:

South AB. Assembly and dynamic behavior of microgel thin films and their application to biointerfacees. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/34686.

Council of Science Editors:

South AB. Assembly and dynamic behavior of microgel thin films and their application to biointerfacees. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/34686


Georgia Tech

19. McNeeley, Kathleen Margaret. Modulating liposomal stealth properties to evade RES and target tumors.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 Liposomal nanocarriers offer much promise in chemotherapeutic drug delivery because they may be specifically targeted to tumors thereby shielding healthy organs from toxic side effects… (more)

Subjects/Keywords: Liposomes; Glioma; Targeting; Chemotherapy; Folate; Transferrin; OX26; APN; Stealth; Drug delivery; Tumor markers; Gliomas; Liposomes; Drug delivery systems

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

APA (6th Edition):

McNeeley, K. M. (2008). Modulating liposomal stealth properties to evade RES and target tumors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26650

Chicago Manual of Style (16th Edition):

McNeeley, Kathleen Margaret. “Modulating liposomal stealth properties to evade RES and target tumors.” 2008. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/26650.

MLA Handbook (7th Edition):

McNeeley, Kathleen Margaret. “Modulating liposomal stealth properties to evade RES and target tumors.” 2008. Web. 23 Oct 2020.

Vancouver:

McNeeley KM. Modulating liposomal stealth properties to evade RES and target tumors. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/26650.

Council of Science Editors:

McNeeley KM. Modulating liposomal stealth properties to evade RES and target tumors. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/26650


Georgia Tech

20. Gill, Harvinder Singh. Coated microneedles and microdermabrasion for transdermal delivery.

Degree: PhD, Bioengineering, 2007, Georgia Tech

 The major hurdle in the development of transdermal route as a versatile drug delivery method is the formidable transport barrier provided by the stratum corneum.… (more)

Subjects/Keywords: Microneedle coatings; Protein delivery; Protein coatings; Hepatitis C virus; Dip coating; Removal of stratum corneum; Microdermabrasion; DNA delivery; Vaccine delivery; Coating formulation; Microfabricated microneedles; Pocketed microneedles; Stainless steel microneedles; Transdermal medication; Drug delivery devices; Skin absorption; Dermabrasion

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

APA (6th Edition):

Gill, H. S. (2007). Coated microneedles and microdermabrasion for transdermal delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/24711

Chicago Manual of Style (16th Edition):

Gill, Harvinder Singh. “Coated microneedles and microdermabrasion for transdermal delivery.” 2007. Doctoral Dissertation, Georgia Tech. Accessed October 23, 2020. http://hdl.handle.net/1853/24711.

MLA Handbook (7th Edition):

Gill, Harvinder Singh. “Coated microneedles and microdermabrasion for transdermal delivery.” 2007. Web. 23 Oct 2020.

Vancouver:

Gill HS. Coated microneedles and microdermabrasion for transdermal delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2020 Oct 23]. Available from: http://hdl.handle.net/1853/24711.

Council of Science Editors:

Gill HS. Coated microneedles and microdermabrasion for transdermal delivery. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/24711

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