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You searched for +publisher:"Georgia Tech" +contributor:("Botchwey, Edward A."). Showing records 1 – 15 of 15 total matches.

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Georgia Tech

1. Mokarram-Dorri, Nassir. Modulating immune response inside biomaterial-based nerve conduits to stimulate endogenous peripheral nerve regeneration.

Degree: PhD, Materials Science and Engineering, 2015, Georgia Tech

 Injuries to the peripheral nervous system (PNS) are major and common source of disability, impairing the ability to move muscles and/or feel normal sensations, or… (more)

Subjects/Keywords: Nerve repair; Immunomodulation; Macrophage

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APA (6th Edition):

Mokarram-Dorri, N. (2015). Modulating immune response inside biomaterial-based nerve conduits to stimulate endogenous peripheral nerve regeneration. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54860

Chicago Manual of Style (16th Edition):

Mokarram-Dorri, Nassir. “Modulating immune response inside biomaterial-based nerve conduits to stimulate endogenous peripheral nerve regeneration.” 2015. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/54860.

MLA Handbook (7th Edition):

Mokarram-Dorri, Nassir. “Modulating immune response inside biomaterial-based nerve conduits to stimulate endogenous peripheral nerve regeneration.” 2015. Web. 16 Sep 2019.

Vancouver:

Mokarram-Dorri N. Modulating immune response inside biomaterial-based nerve conduits to stimulate endogenous peripheral nerve regeneration. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/54860.

Council of Science Editors:

Mokarram-Dorri N. Modulating immune response inside biomaterial-based nerve conduits to stimulate endogenous peripheral nerve regeneration. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54860


Georgia Tech

2. 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 September 16, 2019. 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. 16 Sep 2019.

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 2019 Sep 16]. 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

3. Wilson, Jenna L. Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors.

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

 The results of initial stem cell transplantation studies indicate that many of the observed functional improvements are due to transient paracrine actions of the transplanted… (more)

Subjects/Keywords: Stem cells; Bioprocessing; Bioreactor; Pluripotent stem cells; Microencapsulation; Ex vivo expansion

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APA (6th Edition):

Wilson, J. L. (2015). Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56201

Chicago Manual of Style (16th Edition):

Wilson, Jenna L. “Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors.” 2015. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/56201.

MLA Handbook (7th Edition):

Wilson, Jenna L. “Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors.” 2015. Web. 16 Sep 2019.

Vancouver:

Wilson JL. Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/56201.

Council of Science Editors:

Wilson JL. Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/56201


Georgia Tech

4. Rohner, Nathan A. Role of vascular remodeling in the accumulation, clearance, and biodistribution of biomolecular factors in melanoma.

Degree: PhD, Mechanical Engineering, 2017, Georgia Tech

 Local inflammation within the tumor microenvironment is implicated in the systemic effects of disease progression, such as immune suppression and metastasis. Soluble factors (SF) produced… (more)

Subjects/Keywords: Cancer; Bioavailability; Drug delivery; Vascular remodeling; Lymphatics; Melanoma

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APA (6th Edition):

Rohner, N. A. (2017). Role of vascular remodeling in the accumulation, clearance, and biodistribution of biomolecular factors in melanoma. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60122

Chicago Manual of Style (16th Edition):

Rohner, Nathan A. “Role of vascular remodeling in the accumulation, clearance, and biodistribution of biomolecular factors in melanoma.” 2017. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/60122.

MLA Handbook (7th Edition):

Rohner, Nathan A. “Role of vascular remodeling in the accumulation, clearance, and biodistribution of biomolecular factors in melanoma.” 2017. Web. 16 Sep 2019.

Vancouver:

Rohner NA. Role of vascular remodeling in the accumulation, clearance, and biodistribution of biomolecular factors in melanoma. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/60122.

Council of Science Editors:

Rohner NA. Role of vascular remodeling in the accumulation, clearance, and biodistribution of biomolecular factors in melanoma. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60122


Georgia Tech

5. 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 September 16, 2019. http://hdl.handle.net/1853/59153.

MLA Handbook (7th Edition):

Srinivasan, Sangeetha. “Conditioning dendritic cell responses using engineered biomaterials for immunotherapy.” 2016. Web. 16 Sep 2019.

Vancouver:

Srinivasan S. Conditioning dendritic cell responses using engineered biomaterials for immunotherapy. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Sep 16]. 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

6. Olingy, Claire Eliza. Engineered materials for spatiotemporal regulation of monocyte and macrophage recruitment.

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

 Significant advances have been made in the development of materials that better mimic native tissues through incorporation of biofunctionality, transplantation of exogenous cells, and recapitulation… (more)

Subjects/Keywords: Biomaterials; Inflammation; Innate immunity; Vascularization; Tissue repair

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APA (6th Edition):

Olingy, C. E. (2017). Engineered materials for spatiotemporal regulation of monocyte and macrophage recruitment. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60134

Chicago Manual of Style (16th Edition):

Olingy, Claire Eliza. “Engineered materials for spatiotemporal regulation of monocyte and macrophage recruitment.” 2017. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/60134.

MLA Handbook (7th Edition):

Olingy, Claire Eliza. “Engineered materials for spatiotemporal regulation of monocyte and macrophage recruitment.” 2017. Web. 16 Sep 2019.

Vancouver:

Olingy CE. Engineered materials for spatiotemporal regulation of monocyte and macrophage recruitment. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/60134.

Council of Science Editors:

Olingy CE. Engineered materials for spatiotemporal regulation of monocyte and macrophage recruitment. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60134


Georgia Tech

7. Goldman, Stephen M. Development and validation of a microfluidic hydrogel platform for osteochondral tissue engineering.

Degree: PhD, Mechanical Engineering, 2014, Georgia Tech

 Due to the inability of intra-articular injuries to adequately self-heal, current therapies are largely focused on palliative care and restoration of joint function rather than… (more)

Subjects/Keywords: Osteochondral tissue engineering; Microfluidic hydrogels

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APA (6th Edition):

Goldman, S. M. (2014). Development and validation of a microfluidic hydrogel platform for osteochondral tissue engineering. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54295

Chicago Manual of Style (16th Edition):

Goldman, Stephen M. “Development and validation of a microfluidic hydrogel platform for osteochondral tissue engineering.” 2014. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/54295.

MLA Handbook (7th Edition):

Goldman, Stephen M. “Development and validation of a microfluidic hydrogel platform for osteochondral tissue engineering.” 2014. Web. 16 Sep 2019.

Vancouver:

Goldman SM. Development and validation of a microfluidic hydrogel platform for osteochondral tissue engineering. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/54295.

Council of Science Editors:

Goldman SM. Development and validation of a microfluidic hydrogel platform for osteochondral tissue engineering. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54295


Georgia Tech

8. Chen, Po Wei. Characterization of sphingolipid-based stress responses in the yeast Saccharomyces cerevisiae through reverse engineering.

Degree: PhD, Mechanical Engineering, 2015, Georgia Tech

 Sphingolipids regulate numerous cell functions through the activation of specific signaling cascades. Although sphingolipids have been investigated for several decades, a detailed mechanistic and systemic… (more)

Subjects/Keywords: Sphingolipid; ceramide; heat stress; hydroxyurea stress; piecewise optimization approach

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APA (6th Edition):

Chen, P. W. (2015). Characterization of sphingolipid-based stress responses in the yeast Saccharomyces cerevisiae through reverse engineering. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55534

Chicago Manual of Style (16th Edition):

Chen, Po Wei. “Characterization of sphingolipid-based stress responses in the yeast Saccharomyces cerevisiae through reverse engineering.” 2015. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/55534.

MLA Handbook (7th Edition):

Chen, Po Wei. “Characterization of sphingolipid-based stress responses in the yeast Saccharomyces cerevisiae through reverse engineering.” 2015. Web. 16 Sep 2019.

Vancouver:

Chen PW. Characterization of sphingolipid-based stress responses in the yeast Saccharomyces cerevisiae through reverse engineering. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/55534.

Council of Science Editors:

Chen PW. Characterization of sphingolipid-based stress responses in the yeast Saccharomyces cerevisiae through reverse engineering. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/55534


Georgia Tech

9. Lei, Jennifer. The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications.

Degree: PhD, Mechanical Engineering, 2016, Georgia Tech

 Mesenchymal stem cells are multipotent cells that have the ability to differentiate down multiple lineages as well as secrete trophic and anti-inflammatory factors. These qualities… (more)

Subjects/Keywords: Heparin; Mesenchymal stem cells

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APA (6th Edition):

Lei, J. (2016). The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54949

Chicago Manual of Style (16th Edition):

Lei, Jennifer. “The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications.” 2016. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/54949.

MLA Handbook (7th Edition):

Lei, Jennifer. “The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications.” 2016. Web. 16 Sep 2019.

Vancouver:

Lei J. The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/54949.

Council of Science Editors:

Lei J. The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/54949


Georgia Tech

10. Martinez, Mario Daniel. Targeted drug delivery for the treatment and diagnosis of cardiovascular disease.

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

 Cardiovascular disease has accounted for more deaths than any other major cause of death in the United States every year since 1900, with the exception… (more)

Subjects/Keywords: Peripheral artery disease; Hoechst; VEGF; Myocariditis; Imaging; Peptide; Phage display; Molecular imaging

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APA (6th Edition):

Martinez, M. D. (2017). Targeted drug delivery for the treatment and diagnosis of cardiovascular disease. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59201

Chicago Manual of Style (16th Edition):

Martinez, Mario Daniel. “Targeted drug delivery for the treatment and diagnosis of cardiovascular disease.” 2017. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/59201.

MLA Handbook (7th Edition):

Martinez, Mario Daniel. “Targeted drug delivery for the treatment and diagnosis of cardiovascular disease.” 2017. Web. 16 Sep 2019.

Vancouver:

Martinez MD. Targeted drug delivery for the treatment and diagnosis of cardiovascular disease. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/59201.

Council of Science Editors:

Martinez MD. Targeted drug delivery for the treatment and diagnosis of cardiovascular disease. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/59201


Georgia Tech

11. Hettiaratchi, Marian Hirushika. Heparin microparticle-mediated delivery of BMP-2 and pluripotent stem cell morphogens for bone repair.

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

 The delivery of bone morphogenetic protein-2 (BMP-2) offers a promising means of stimulating endogenous repair mechanisms to heal severe bone injuries. However, clinical application of… (more)

Subjects/Keywords: Heparin microparticles; Bone morphogenetic protein-2; Embryonic stem cells; Bone repair

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APA (6th Edition):

Hettiaratchi, M. H. (2016). Heparin microparticle-mediated delivery of BMP-2 and pluripotent stem cell morphogens for bone repair. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59144

Chicago Manual of Style (16th Edition):

Hettiaratchi, Marian Hirushika. “Heparin microparticle-mediated delivery of BMP-2 and pluripotent stem cell morphogens for bone repair.” 2016. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/59144.

MLA Handbook (7th Edition):

Hettiaratchi, Marian Hirushika. “Heparin microparticle-mediated delivery of BMP-2 and pluripotent stem cell morphogens for bone repair.” 2016. Web. 16 Sep 2019.

Vancouver:

Hettiaratchi MH. Heparin microparticle-mediated delivery of BMP-2 and pluripotent stem cell morphogens for bone repair. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/59144.

Council of Science Editors:

Hettiaratchi MH. Heparin microparticle-mediated delivery of BMP-2 and pluripotent stem cell morphogens for bone repair. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59144


Georgia Tech

12. Johnson, Christopher T. Lysostaphin-delivering hydrogels to treat orthopaedic device infections.

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

 Orthopaedic hardware infections are a significant clinical problem with current therapies limited to surgical debridement and systemic antibiotic regimens. Lysostaphin is a bacteriolytic enzyme with… (more)

Subjects/Keywords: Orthopaedic implant infection; Biomaterials associated infection; Lysostaphin; Hydrogel; Bone repair; Drug delivery

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APA (6th Edition):

Johnson, C. T. (2018). Lysostaphin-delivering hydrogels to treat orthopaedic device infections. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61143

Chicago Manual of Style (16th Edition):

Johnson, Christopher T. “Lysostaphin-delivering hydrogels to treat orthopaedic device infections.” 2018. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/61143.

MLA Handbook (7th Edition):

Johnson, Christopher T. “Lysostaphin-delivering hydrogels to treat orthopaedic device infections.” 2018. Web. 16 Sep 2019.

Vancouver:

Johnson CT. Lysostaphin-delivering hydrogels to treat orthopaedic device infections. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/61143.

Council of Science Editors:

Johnson CT. Lysostaphin-delivering hydrogels to treat orthopaedic device infections. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/61143


Georgia Tech

13. 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

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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 September 16, 2019. 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. 16 Sep 2019.

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 2019 Sep 16]. 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

14. Ghosh, Deepraj. Soluble factor mediated manipulation of mesenchymal stem cell mechanics for improved function of cell-based therapeutics.

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

 Mesenchymal stem cells (MSCs) are bone marrow derived multipotent cells with the ability to self-renew and differentiate into multiple connective cell lineages. In vivo, MSCs… (more)

Subjects/Keywords: Cell mechanics; Wound healing; Mesenchymal stem cells; Transforming growth factor-β1 (TGF-β1); Platelet derived growth factor (PDGF)

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APA (6th Edition):

Ghosh, D. (2014). Soluble factor mediated manipulation of mesenchymal stem cell mechanics for improved function of cell-based therapeutics. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54032

Chicago Manual of Style (16th Edition):

Ghosh, Deepraj. “Soluble factor mediated manipulation of mesenchymal stem cell mechanics for improved function of cell-based therapeutics.” 2014. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/54032.

MLA Handbook (7th Edition):

Ghosh, Deepraj. “Soluble factor mediated manipulation of mesenchymal stem cell mechanics for improved function of cell-based therapeutics.” 2014. Web. 16 Sep 2019.

Vancouver:

Ghosh D. Soluble factor mediated manipulation of mesenchymal stem cell mechanics for improved function of cell-based therapeutics. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/54032.

Council of Science Editors:

Ghosh D. Soluble factor mediated manipulation of mesenchymal stem cell mechanics for improved function of cell-based therapeutics. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54032

15. Zhang, Yu. Inverse opal scaffolds and photoacoustic microscopy for regenerative medicine.

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

 This research centers on the fabrication, characterization, and engineering of inverse opal scaffolds, a novel class of three-dimensional (3D) porous scaffolds made of biocompatible and… (more)

Subjects/Keywords: Tissue engineering; Regenerative medicine; Inverse opal scaffolds; Uniform; Poly(D,L-lactic-co-glycolic acid) (PLGA); Photoacoustic microscopy; Biomedical Imaging; Regeneration (Biology); Tissue scaffolds; Imaging systems in medicine; Biopolymers

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APA (6th Edition):

Zhang, Y. (2013). Inverse opal scaffolds and photoacoustic microscopy for regenerative medicine. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/50231

Chicago Manual of Style (16th Edition):

Zhang, Yu. “Inverse opal scaffolds and photoacoustic microscopy for regenerative medicine.” 2013. Doctoral Dissertation, Georgia Tech. Accessed September 16, 2019. http://hdl.handle.net/1853/50231.

MLA Handbook (7th Edition):

Zhang, Yu. “Inverse opal scaffolds and photoacoustic microscopy for regenerative medicine.” 2013. Web. 16 Sep 2019.

Vancouver:

Zhang Y. Inverse opal scaffolds and photoacoustic microscopy for regenerative medicine. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2019 Sep 16]. Available from: http://hdl.handle.net/1853/50231.

Council of Science Editors:

Zhang Y. Inverse opal scaffolds and photoacoustic microscopy for regenerative medicine. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/50231

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