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You searched for +publisher:"Georgia Tech" +contributor:("Platt, Manu O."). Showing records 1 – 24 of 24 total matches.

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1. Park, Keon-Young. Predicting patient-to-patient variability in proteolytic activity and breast cancer progression.

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

 About one in eight women in the United States will develop breast cancer over the course of her lifetime. Moreover, patient-to-patient variability in disease progression… (more)

Subjects/Keywords: Breast cancer; Macrophages; Kinases; Cathepsin; Protease; Personalized medicine; Predictive medicine

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APA (6th Edition):

Park, K. (2014). Predicting patient-to-patient variability in proteolytic activity and breast cancer progression. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53479

Chicago Manual of Style (16th Edition):

Park, Keon-Young. “Predicting patient-to-patient variability in proteolytic activity and breast cancer progression.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/53479.

MLA Handbook (7th Edition):

Park, Keon-Young. “Predicting patient-to-patient variability in proteolytic activity and breast cancer progression.” 2014. Web. 11 May 2021.

Vancouver:

Park K. Predicting patient-to-patient variability in proteolytic activity and breast cancer progression. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/53479.

Council of Science Editors:

Park K. Predicting patient-to-patient variability in proteolytic activity and breast cancer progression. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53479

2. Parks, Akia Nichelle. Temporal cathepsin and matrix metalloproteinase activity in tendon extracellular matrix damage.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2018, Georgia Tech

 Tendinopathy, or tendon overuse, is one of the most common musculoskeletal disorders affecting athletes, laborers, and aging adults. If left untreated, overuse injury can progress… (more)

Subjects/Keywords: Tendinopathy; Cathepsin; Matrix metalloproteinase; Extracellular matrix; Type I collagen; Overuse injury; Supraspinatus tendon; Cartilage; Zymography; Micro-computed tomography; Cathepsin cannibalism

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APA (6th Edition):

Parks, A. N. (2018). Temporal cathepsin and matrix metalloproteinase activity in tendon extracellular matrix damage. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60737

Chicago Manual of Style (16th Edition):

Parks, Akia Nichelle. “Temporal cathepsin and matrix metalloproteinase activity in tendon extracellular matrix damage.” 2018. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/60737.

MLA Handbook (7th Edition):

Parks, Akia Nichelle. “Temporal cathepsin and matrix metalloproteinase activity in tendon extracellular matrix damage.” 2018. Web. 11 May 2021.

Vancouver:

Parks AN. Temporal cathepsin and matrix metalloproteinase activity in tendon extracellular matrix damage. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/60737.

Council of Science Editors:

Parks AN. Temporal cathepsin and matrix metalloproteinase activity in tendon extracellular matrix damage. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/60737

3. Rosen, Tania. Polyvalent vaccines and therapeutics against viral pathogens.

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

 Viral infections caused by HIV or influenza viruses have killed millions of people worldwide. Currently available drugs against such viruses do combat the infections to… (more)

Subjects/Keywords: Polyvalency; Linker; Hemagglutinin; Influenza; HIV; CCR5

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APA (6th Edition):

Rosen, T. (2017). Polyvalent vaccines and therapeutics against viral pathogens. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58755

Chicago Manual of Style (16th Edition):

Rosen, Tania. “Polyvalent vaccines and therapeutics against viral pathogens.” 2017. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/58755.

MLA Handbook (7th Edition):

Rosen, Tania. “Polyvalent vaccines and therapeutics against viral pathogens.” 2017. Web. 11 May 2021.

Vancouver:

Rosen T. Polyvalent vaccines and therapeutics against viral pathogens. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/58755.

Council of Science Editors:

Rosen T. Polyvalent vaccines and therapeutics against viral pathogens. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/58755


Georgia Tech

4. Kinney, Melissa. Biophysical and biochemical control of three-dimensional embryonic stem cell differentiation and morphogenesis.

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

 Stem cell differentiation is regulated by the complex interplay of multiple parameters, including adhesive intercellular interactions, cytoskeletal and extracellular matrix remodeling, and gradients of agonists… (more)

Subjects/Keywords: BMP-4; Embryonic stem cells; Differentiation; Morphogenesis; Spheroid; Embryoid body; Regenerative medicine; Tissue engineering; Transport; Biomechanics

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APA (6th Edition):

Kinney, M. (2014). Biophysical and biochemical control of three-dimensional embryonic stem cell differentiation and morphogenesis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53465

Chicago Manual of Style (16th Edition):

Kinney, Melissa. “Biophysical and biochemical control of three-dimensional embryonic stem cell differentiation and morphogenesis.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/53465.

MLA Handbook (7th Edition):

Kinney, Melissa. “Biophysical and biochemical control of three-dimensional embryonic stem cell differentiation and morphogenesis.” 2014. Web. 11 May 2021.

Vancouver:

Kinney M. Biophysical and biochemical control of three-dimensional embryonic stem cell differentiation and morphogenesis. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/53465.

Council of Science Editors:

Kinney M. Biophysical and biochemical control of three-dimensional embryonic stem cell differentiation and morphogenesis. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53465


Georgia Tech

5. Dwivedi, Gaurav. Computational modeling of the IL-4 pathway to understand principles of systemic redox regulation in cell signaling.

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

 Elevated levels of reactive oxygen species (ROS) cause or aggravate a variety of pathological conditions such as cardiovascular disease, cancer and rheumatoid arthritis. Despite known… (more)

Subjects/Keywords: Redox regulation; IL-4 signaling; Systems biology; Computational modeling

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APA (6th Edition):

Dwivedi, G. (2014). Computational modeling of the IL-4 pathway to understand principles of systemic redox regulation in cell signaling. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53467

Chicago Manual of Style (16th Edition):

Dwivedi, Gaurav. “Computational modeling of the IL-4 pathway to understand principles of systemic redox regulation in cell signaling.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/53467.

MLA Handbook (7th Edition):

Dwivedi, Gaurav. “Computational modeling of the IL-4 pathway to understand principles of systemic redox regulation in cell signaling.” 2014. Web. 11 May 2021.

Vancouver:

Dwivedi G. Computational modeling of the IL-4 pathway to understand principles of systemic redox regulation in cell signaling. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/53467.

Council of Science Editors:

Dwivedi G. Computational modeling of the IL-4 pathway to understand principles of systemic redox regulation in cell signaling. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53467


Georgia Tech

6. French, Kristin Marie. Microenvironmental stimulation of cardiac progenitor cells.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2015, Georgia Tech

 Heart failure, predominately caused by myocardial infarction (MI), is the leading cause of death in the United States. Currently the only treatment for heart failure… (more)

Subjects/Keywords: Cardiac progenitor cells; Decellularized extracellular matrix; Microenvironment; Myocardial infarction; Cyclic strain

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APA (6th Edition):

French, K. M. (2015). Microenvironmental stimulation of cardiac progenitor cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53867

Chicago Manual of Style (16th Edition):

French, Kristin Marie. “Microenvironmental stimulation of cardiac progenitor cells.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/53867.

MLA Handbook (7th Edition):

French, Kristin Marie. “Microenvironmental stimulation of cardiac progenitor cells.” 2015. Web. 11 May 2021.

Vancouver:

French KM. Microenvironmental stimulation of cardiac progenitor cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/53867.

Council of Science Editors:

French KM. Microenvironmental stimulation of cardiac progenitor cells. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53867


Georgia Tech

7. Lin, Yanni. Design and optimization of engineered nucleases for genome editing applications.

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

 Genome editing mediated by engineered nucleases, including Transcription Activator-Like Effector Nucleases (TALENs) and Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR) / CRISPR-associated (Cas) systems, holds… (more)

Subjects/Keywords: Genome engineering; Genome editing; TALENs; CRISPRs

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APA (6th Edition):

Lin, Y. (2014). Design and optimization of engineered nucleases for genome editing applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54249

Chicago Manual of Style (16th Edition):

Lin, Yanni. “Design and optimization of engineered nucleases for genome editing applications.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/54249.

MLA Handbook (7th Edition):

Lin, Yanni. “Design and optimization of engineered nucleases for genome editing applications.” 2014. Web. 11 May 2021.

Vancouver:

Lin Y. Design and optimization of engineered nucleases for genome editing applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/54249.

Council of Science Editors:

Lin Y. Design and optimization of engineered nucleases for genome editing applications. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54249


Georgia Tech

8. Awojoodu, Anthony O. Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation.

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

 Sickle cell disease is a hereditary blood disorder caused by a point mutation in the gene encoding hemoglobin. This mutation causes hemoglobin molecules to polymerize… (more)

Subjects/Keywords: Sickle cell disease; Inflammation; Sphingolipid; Microparticles

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APA (6th Edition):

Awojoodu, A. O. (2014). Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54286

Chicago Manual of Style (16th Edition):

Awojoodu, Anthony O. “Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/54286.

MLA Handbook (7th Edition):

Awojoodu, Anthony O. “Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation.” 2014. Web. 11 May 2021.

Vancouver:

Awojoodu AO. Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/54286.

Council of Science Editors:

Awojoodu AO. Sphingolipid dysregulation in erythrocytes during sickle cell disease contributes to pro-inflammatory microparticle generation and subsequent inflammatory cell activation. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54286


Georgia Tech

9. Keegan, Philip Michael. Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease.

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

 Sickle cell disease is a genetic disorder that affects 100,000 Americans and millions more worldwide. Although the sickle mutation affects one protein, which is only… (more)

Subjects/Keywords: Sickle cell disease; Arterial remodeling; Cathepsins; Stroke; Hemodynamics; Shear stress

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APA (6th Edition):

Keegan, P. M. (2014). Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54289

Chicago Manual of Style (16th Edition):

Keegan, Philip Michael. “Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/54289.

MLA Handbook (7th Edition):

Keegan, Philip Michael. “Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease.” 2014. Web. 11 May 2021.

Vancouver:

Keegan PM. Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/54289.

Council of Science Editors:

Keegan PM. Shear stress, hemodynamics, and proteolytic mechanisms underlying large artery remodeling in sickle cell disease. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54289


Georgia Tech

10. Mejias, Joscelyn Claraluz. Nano-in-Micro Multi-Stage Particles for Pulmonary Drug Delivery.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2019, Georgia Tech

 Pulmonary drug delivery is a non-invasive method for targeted delivery of therapeutics for the treatment of respiratory diseases such as asthma, idiopathic pulmonary fibrosis, or… (more)

Subjects/Keywords: Nano-in-Microgel; Lung delivery; Nanoparticle; Microparticle; Microphysiologic Lung-on-a-Chip

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APA (6th Edition):

Mejias, J. C. (2019). Nano-in-Micro Multi-Stage Particles for Pulmonary Drug Delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/63512

Chicago Manual of Style (16th Edition):

Mejias, Joscelyn Claraluz. “Nano-in-Micro Multi-Stage Particles for Pulmonary Drug Delivery.” 2019. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/63512.

MLA Handbook (7th Edition):

Mejias, Joscelyn Claraluz. “Nano-in-Micro Multi-Stage Particles for Pulmonary Drug Delivery.” 2019. Web. 11 May 2021.

Vancouver:

Mejias JC. Nano-in-Micro Multi-Stage Particles for Pulmonary Drug Delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/63512.

Council of Science Editors:

Mejias JC. Nano-in-Micro Multi-Stage Particles for Pulmonary Drug Delivery. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/63512


Georgia Tech

11. Trevino, Elda Alicia. Development of a controlled-release platform for investigation of proteases following rotator cuff tear.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2020, Georgia Tech

 Surgical reattachment of torn rotator cuff tendons has a high rate of re-tear (failure) and the procedure does not reverse joint tissue degeneration present at… (more)

Subjects/Keywords: Rotator cuff; Protease

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APA (6th Edition):

Trevino, E. A. (2020). Development of a controlled-release platform for investigation of proteases following rotator cuff tear. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/63629

Chicago Manual of Style (16th Edition):

Trevino, Elda Alicia. “Development of a controlled-release platform for investigation of proteases following rotator cuff tear.” 2020. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/63629.

MLA Handbook (7th Edition):

Trevino, Elda Alicia. “Development of a controlled-release platform for investigation of proteases following rotator cuff tear.” 2020. Web. 11 May 2021.

Vancouver:

Trevino EA. Development of a controlled-release platform for investigation of proteases following rotator cuff tear. [Internet] [Doctoral dissertation]. Georgia Tech; 2020. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/63629.

Council of Science Editors:

Trevino EA. Development of a controlled-release platform for investigation of proteases following rotator cuff tear. [Doctoral Dissertation]. Georgia Tech; 2020. Available from: http://hdl.handle.net/1853/63629

12. Nsiah, Barbara Akua. Fluid shear stress modulation of embryonic stem cell differentiation.

Degree: PhD, Mechanical Engineering, 2012, Georgia Tech

 Vascularization of tissue-engineered substitutes is imperative for successful implantation into sites of injury. Strategies to promote vascularization within tissue-engineered constructs have focused on incorporating endothelial… (more)

Subjects/Keywords: Vasculogenesis; Morphogenesis; Differentiation; Fluid shear; Stem cells; Tissue engineering; Regenerative medicine; Cell differentiation; Endothelial cells

Georgia Tech. This program has provided me with numerous mentors such as Dr. Gary May, Dr… …Rob have been constant supports while at Georgia Tech. My parents would call to check up on… 

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APA (6th Edition):

Nsiah, B. A. (2012). Fluid shear stress modulation of embryonic stem cell differentiation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/47552

Chicago Manual of Style (16th Edition):

Nsiah, Barbara Akua. “Fluid shear stress modulation of embryonic stem cell differentiation.” 2012. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/47552.

MLA Handbook (7th Edition):

Nsiah, Barbara Akua. “Fluid shear stress modulation of embryonic stem cell differentiation.” 2012. Web. 11 May 2021.

Vancouver:

Nsiah BA. Fluid shear stress modulation of embryonic stem cell differentiation. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/47552.

Council of Science Editors:

Nsiah BA. Fluid shear stress modulation of embryonic stem cell differentiation. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/47552

13. Parker, Ivana Kennedy. The role of HIV-1 tat and antiretrovirals in cathepsin mediated arterial remodeling.

Degree: PhD, Mechanical Engineering, 2015, Georgia Tech

 Major advances in highly active antiretroviral therapies (ARVs) have extended the lives of people living with HIV, but there still remains an increased risk of… (more)

Subjects/Keywords: HIV; Cardiovascular disease; Arterial remodeling; Cathepsins; antiretroviral therapy; Shear stress; Endothelial cell; Tat

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APA (6th Edition):

Parker, I. K. (2015). The role of HIV-1 tat and antiretrovirals in cathepsin mediated arterial remodeling. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53574

Chicago Manual of Style (16th Edition):

Parker, Ivana Kennedy. “The role of HIV-1 tat and antiretrovirals in cathepsin mediated arterial remodeling.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/53574.

MLA Handbook (7th Edition):

Parker, Ivana Kennedy. “The role of HIV-1 tat and antiretrovirals in cathepsin mediated arterial remodeling.” 2015. Web. 11 May 2021.

Vancouver:

Parker IK. The role of HIV-1 tat and antiretrovirals in cathepsin mediated arterial remodeling. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/53574.

Council of Science Editors:

Parker IK. The role of HIV-1 tat and antiretrovirals in cathepsin mediated arterial remodeling. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53574

14. Boopathy, Archana Vidya. Engineering stem cell responses using oxidative stress and notch ligand containing hydrogels.

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

 Heart failure is the leading cause of death worldwide. In 2013, the American Heart Association estimated that one American will die of cardiovascular disease every… (more)

Subjects/Keywords: Adult stem cells; Notch; Hydrogel; Oxidative stress; Myocardial infarction; Colloids in medicine; Biocolloids; Myocardium Regeneration; Mesenchymal stem cells; Oxidative stress; Notch genes

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APA (6th Edition):

Boopathy, A. V. (2014). Engineering stem cell responses using oxidative stress and notch ligand containing hydrogels. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51837

Chicago Manual of Style (16th Edition):

Boopathy, Archana Vidya. “Engineering stem cell responses using oxidative stress and notch ligand containing hydrogels.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/51837.

MLA Handbook (7th Edition):

Boopathy, Archana Vidya. “Engineering stem cell responses using oxidative stress and notch ligand containing hydrogels.” 2014. Web. 11 May 2021.

Vancouver:

Boopathy AV. Engineering stem cell responses using oxidative stress and notch ligand containing hydrogels. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/51837.

Council of Science Editors:

Boopathy AV. Engineering stem cell responses using oxidative stress and notch ligand containing hydrogels. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/51837

15. Seto, Song P. The development of heparin-based materials for tissue engineering applications to treat rotator cuff tendon injuries.

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

 Surgical repair of torn rotator cuff tendons have a high rate of failure and does not address the underlying pathophysiology. Tissue engineering strategies, employing the… (more)

Subjects/Keywords: Rotator cuff; Heparin-containing hydrogels; Tendon overuse; Growth factor bioactivity; Supraspinatus tendon; Coculture of mesenchymal stem cells; Tissue engineering; Shoulder joint Rotator cuff; Tendons Wounds and injuries Healing; Heparin; Biomedical materials

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APA (6th Edition):

Seto, S. P. (2014). The development of heparin-based materials for tissue engineering applications to treat rotator cuff tendon injuries. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51898

Chicago Manual of Style (16th Edition):

Seto, Song P. “The development of heparin-based materials for tissue engineering applications to treat rotator cuff tendon injuries.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/51898.

MLA Handbook (7th Edition):

Seto, Song P. “The development of heparin-based materials for tissue engineering applications to treat rotator cuff tendon injuries.” 2014. Web. 11 May 2021.

Vancouver:

Seto SP. The development of heparin-based materials for tissue engineering applications to treat rotator cuff tendon injuries. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/51898.

Council of Science Editors:

Seto SP. The development of heparin-based materials for tissue engineering applications to treat rotator cuff tendon injuries. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/51898

16. Li, Melissa. Microfluidic system for thrombosis under multiple shear rates and platelet therapies.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2013, Georgia Tech

 Thrombosis is the pathological formation of platelet aggregates that cause stroke and heart attackemdash the leading causes of death in developed nations. Determining effective dosages… (more)

Subjects/Keywords: Microfluidics; Thrombosis; Shear; Platelets; Platelet therapy; Aspirin; Eptifibatide; Dose

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APA (6th Edition):

Li, M. (2013). Microfluidic system for thrombosis under multiple shear rates and platelet therapies. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52154

Chicago Manual of Style (16th Edition):

Li, Melissa. “Microfluidic system for thrombosis under multiple shear rates and platelet therapies.” 2013. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/52154.

MLA Handbook (7th Edition):

Li, Melissa. “Microfluidic system for thrombosis under multiple shear rates and platelet therapies.” 2013. Web. 11 May 2021.

Vancouver:

Li M. Microfluidic system for thrombosis under multiple shear rates and platelet therapies. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/52154.

Council of Science Editors:

Li M. Microfluidic system for thrombosis under multiple shear rates and platelet therapies. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52154

17. White, Douglas. Analyzing multicellular interactions: A hybrid computational and biological pattern recognition approach.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2015, Georgia Tech

 Pluripotent embryonic stem cells (ESCs) can differentiate into all somatic cell types, making them a useful platform for studying a variety of cellular phenomenon. Furthermore,… (more)

Subjects/Keywords: Computational modeling; Machine learning; Embryonic stem cells; Image informatics; Spatial patterns; 3D cellular aggregates

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APA (6th Edition):

White, D. (2015). Analyzing multicellular interactions: A hybrid computational and biological pattern recognition approach. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54876

Chicago Manual of Style (16th Edition):

White, Douglas. “Analyzing multicellular interactions: A hybrid computational and biological pattern recognition approach.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/54876.

MLA Handbook (7th Edition):

White, Douglas. “Analyzing multicellular interactions: A hybrid computational and biological pattern recognition approach.” 2015. Web. 11 May 2021.

Vancouver:

White D. Analyzing multicellular interactions: A hybrid computational and biological pattern recognition approach. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/54876.

Council of Science Editors:

White D. Analyzing multicellular interactions: A hybrid computational and biological pattern recognition approach. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54876

18. Raykin, Julia. A theoretical and experimental model to predict biaxial failure of tissue engineered blood vessels.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2013, Georgia Tech

 The development of small diameter tissue engineered blood vessels (TEBVs) with low thrombogenicity, low immunogenicity, suitable mechanical properties, and a capacity to remodel to their… (more)

Subjects/Keywords: Tissue engineering; Vascular grafts; Blood vessel; Vessel failure; Volumetric growth; Damage mechanics; Biomedical engineering; Biomedical materials; Blood vessel prosthesis; Blood-vessels

…all of the friends that I have made during graduate career at Georgia Tech. It would be… …Karan were the first friends I made at Georgia Tech. I really appreciate their open-mindedness… 

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APA (6th Edition):

Raykin, J. (2013). A theoretical and experimental model to predict biaxial failure of tissue engineered blood vessels. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/50211

Chicago Manual of Style (16th Edition):

Raykin, Julia. “A theoretical and experimental model to predict biaxial failure of tissue engineered blood vessels.” 2013. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/50211.

MLA Handbook (7th Edition):

Raykin, Julia. “A theoretical and experimental model to predict biaxial failure of tissue engineered blood vessels.” 2013. Web. 11 May 2021.

Vancouver:

Raykin J. A theoretical and experimental model to predict biaxial failure of tissue engineered blood vessels. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/50211.

Council of Science Editors:

Raykin J. A theoretical and experimental model to predict biaxial failure of tissue engineered blood vessels. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/50211

19. Ferrall-Fairbanks, Meghan C. Effects of cathepsin proteolytic network dynamics on extracellular matrix degradation in biological machines and invasive disease.

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

 Proteases are enzymes that degrade proteins and play a major role in cellular homeostasis. When proteins are aged, defective, or just extracellular proteins taken up… (more)

Subjects/Keywords: Cathepsin; Extracellular matrix; Proteolytic network; Biological machines; Computational modeling; Tissue remodeling

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APA (6th Edition):

Ferrall-Fairbanks, M. C. (2017). Effects of cathepsin proteolytic network dynamics on extracellular matrix degradation in biological machines and invasive disease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60657

Chicago Manual of Style (16th Edition):

Ferrall-Fairbanks, Meghan C. “Effects of cathepsin proteolytic network dynamics on extracellular matrix degradation in biological machines and invasive disease.” 2017. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/60657.

MLA Handbook (7th Edition):

Ferrall-Fairbanks, Meghan C. “Effects of cathepsin proteolytic network dynamics on extracellular matrix degradation in biological machines and invasive disease.” 2017. Web. 11 May 2021.

Vancouver:

Ferrall-Fairbanks MC. Effects of cathepsin proteolytic network dynamics on extracellular matrix degradation in biological machines and invasive disease. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/60657.

Council of Science Editors:

Ferrall-Fairbanks MC. Effects of cathepsin proteolytic network dynamics on extracellular matrix degradation in biological machines and invasive disease. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60657

20. Caulk, Alexander Wilson. Biomechanics and modeling methods for quantifying mechanically-mediated disease progression in neglected populations.

Degree: PhD, Mechanical Engineering, 2015, Georgia Tech

 It is well known that biological tissue grows and remodels in response to changes in mechanical loading. Arteries and lymphatic vessels share many similar mechanical… (more)

Subjects/Keywords: Biomechanics; HIV; HAART; lymphedema; growth and remodeling; constitutive modeling

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APA (6th Edition):

Caulk, A. W. (2015). Biomechanics and modeling methods for quantifying mechanically-mediated disease progression in neglected populations. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55490

Chicago Manual of Style (16th Edition):

Caulk, Alexander Wilson. “Biomechanics and modeling methods for quantifying mechanically-mediated disease progression in neglected populations.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/55490.

MLA Handbook (7th Edition):

Caulk, Alexander Wilson. “Biomechanics and modeling methods for quantifying mechanically-mediated disease progression in neglected populations.” 2015. Web. 11 May 2021.

Vancouver:

Caulk AW. Biomechanics and modeling methods for quantifying mechanically-mediated disease progression in neglected populations. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/55490.

Council of Science Editors:

Caulk AW. Biomechanics and modeling methods for quantifying mechanically-mediated disease progression in neglected populations. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/55490

21. Rivera, Christian Poblete. The role of geometry in the hemodynamics associated with stroke development in sickle cell anemia.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2019, Georgia Tech

 Sickle cell anemia (SCA) is a genetic blood disorder which affects over 4 million people globally. Though SCA is caused by a single point mutation… (more)

Subjects/Keywords: Sickle cell; Computational fluid dynamics; Stroke; Cardiovascular disease; Cerebral arteries

…creating the joint BME Graduate Program between Georgia Tech, Emory, and Peking University. Not… 

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APA (6th Edition):

Rivera, C. P. (2019). The role of geometry in the hemodynamics associated with stroke development in sickle cell anemia. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61275

Chicago Manual of Style (16th Edition):

Rivera, Christian Poblete. “The role of geometry in the hemodynamics associated with stroke development in sickle cell anemia.” 2019. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/61275.

MLA Handbook (7th Edition):

Rivera, Christian Poblete. “The role of geometry in the hemodynamics associated with stroke development in sickle cell anemia.” 2019. Web. 11 May 2021.

Vancouver:

Rivera CP. The role of geometry in the hemodynamics associated with stroke development in sickle cell anemia. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/61275.

Council of Science Editors:

Rivera CP. The role of geometry in the hemodynamics associated with stroke development in sickle cell anemia. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/61275

22. Shockey, William Andrew. Proteolytic network dynamics in breast cancer and tumor associated macrophages.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2019, Georgia Tech

 Breast cancer metastasis is a complex process, promoted by a variety of cell types including cancerous mammary epithelial cells and stromal cells such as tumor… (more)

Subjects/Keywords: Breast cancer; Metastasis; Cathepsin; Protease; Systems biology; Ordinary differential equations; Zymography

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APA (6th Edition):

Shockey, W. A. (2019). Proteolytic network dynamics in breast cancer and tumor associated macrophages. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61276

Chicago Manual of Style (16th Edition):

Shockey, William Andrew. “Proteolytic network dynamics in breast cancer and tumor associated macrophages.” 2019. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/61276.

MLA Handbook (7th Edition):

Shockey, William Andrew. “Proteolytic network dynamics in breast cancer and tumor associated macrophages.” 2019. Web. 11 May 2021.

Vancouver:

Shockey WA. Proteolytic network dynamics in breast cancer and tumor associated macrophages. [Internet] [Doctoral dissertation]. Georgia Tech; 2019. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/61276.

Council of Science Editors:

Shockey WA. Proteolytic network dynamics in breast cancer and tumor associated macrophages. [Doctoral Dissertation]. Georgia Tech; 2019. Available from: http://hdl.handle.net/1853/61276


Georgia Tech

23. Wang, Jason Lee. Skeletal development and bone healing in HIV-1 transgenic animal models.

Degree: PhD, Mechanical Engineering, 2018, Georgia Tech

 HIV and AIDS have drastically compromised the quality of life and lifespan for millions of people worldwide. The increasing effectiveness of and access to antiretroviral… (more)

Subjects/Keywords: HIV; Transgenic rodent models; Bone microarchitecture; Bone biomechanics; Bone healing

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APA (6th Edition):

Wang, J. L. (2018). Skeletal development and bone healing in HIV-1 transgenic animal models. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/62245

Chicago Manual of Style (16th Edition):

Wang, Jason Lee. “Skeletal development and bone healing in HIV-1 transgenic animal models.” 2018. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/62245.

MLA Handbook (7th Edition):

Wang, Jason Lee. “Skeletal development and bone healing in HIV-1 transgenic animal models.” 2018. Web. 11 May 2021.

Vancouver:

Wang JL. Skeletal development and bone healing in HIV-1 transgenic animal models. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/62245.

Council of Science Editors:

Wang JL. Skeletal development and bone healing in HIV-1 transgenic animal models. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/62245


Georgia Tech

24. Douglas, Simone A. Cathepsin-mediated fibrin(ogen)olysis in engineered microvascular networks and chronic coagulation in sickle cell disease.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2020, Georgia Tech

 Cysteine cathepsins are powerful proteases involved in tissue destructive disease progression, including angiogenesis and pathogenic vascular remodeling. However, some of their functions and mechanisms in… (more)

Subjects/Keywords: Cathepsin; Fibrinolysis; Matrix remodeling; Biomaterials; Coagulation; Sickle cell anemia

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APA (6th Edition):

Douglas, S. A. (2020). Cathepsin-mediated fibrin(ogen)olysis in engineered microvascular networks and chronic coagulation in sickle cell disease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/63609

Chicago Manual of Style (16th Edition):

Douglas, Simone A. “Cathepsin-mediated fibrin(ogen)olysis in engineered microvascular networks and chronic coagulation in sickle cell disease.” 2020. Doctoral Dissertation, Georgia Tech. Accessed May 11, 2021. http://hdl.handle.net/1853/63609.

MLA Handbook (7th Edition):

Douglas, Simone A. “Cathepsin-mediated fibrin(ogen)olysis in engineered microvascular networks and chronic coagulation in sickle cell disease.” 2020. Web. 11 May 2021.

Vancouver:

Douglas SA. Cathepsin-mediated fibrin(ogen)olysis in engineered microvascular networks and chronic coagulation in sickle cell disease. [Internet] [Doctoral dissertation]. Georgia Tech; 2020. [cited 2021 May 11]. Available from: http://hdl.handle.net/1853/63609.

Council of Science Editors:

Douglas SA. Cathepsin-mediated fibrin(ogen)olysis in engineered microvascular networks and chronic coagulation in sickle cell disease. [Doctoral Dissertation]. Georgia Tech; 2020. Available from: http://hdl.handle.net/1853/63609

.