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You searched for +publisher:"Georgia Tech" +contributor:("McDevitt, Todd"). Showing records 1 – 30 of 44 total matches.

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1. Sullivan, Denise D. Incorporation of bio-inspired microparticles within embryonnic stem cell aggregates for directed differentiation.

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

 Embryonic stem cells (ESCs) are a unique cell population that can differentiate into all three embryonic germ layers (endoderm, mesoderm, and ectoderm), rendering them an… (more)

Subjects/Keywords: Embryonic stem cells; Microparticles; Embryoid bodies; Heparin; Stem cell differentiation

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APA (6th Edition):

Sullivan, D. D. (2015). Incorporation of bio-inspired microparticles within embryonnic stem cell aggregates for directed differentiation. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54909

Chicago Manual of Style (16th Edition):

Sullivan, Denise D. “Incorporation of bio-inspired microparticles within embryonnic stem cell aggregates for directed differentiation.” 2015. Masters Thesis, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/54909.

MLA Handbook (7th Edition):

Sullivan, Denise D. “Incorporation of bio-inspired microparticles within embryonnic stem cell aggregates for directed differentiation.” 2015. Web. 09 May 2021.

Vancouver:

Sullivan DD. Incorporation of bio-inspired microparticles within embryonnic stem cell aggregates for directed differentiation. [Internet] [Masters thesis]. Georgia Tech; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/54909.

Council of Science Editors:

Sullivan DD. Incorporation of bio-inspired microparticles within embryonnic stem cell aggregates for directed differentiation. [Masters Thesis]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54909


Georgia Tech

2. Goude, Melissa Chou. Chondroitin sulfate microparticles modulate TGF-B1-induced chondrogenesis in human mesenchymal stem cell spheroids.

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

 Due to the limited intrinsic healing ability of mature cartilage tissue, stem cell therapies offer the potential to restore cartilage lost due to trauma or… (more)

Subjects/Keywords: Mesenchymal stem cells; Chondrogenic differentiation; Microparticles; Glycosaminoglycan; Cartilage tissue engineering

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APA (6th Edition):

Goude, M. C. (2014). Chondroitin sulfate microparticles modulate TGF-B1-induced chondrogenesis in human mesenchymal stem cell spheroids. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53469

Chicago Manual of Style (16th Edition):

Goude, Melissa Chou. “Chondroitin sulfate microparticles modulate TGF-B1-induced chondrogenesis in human mesenchymal stem cell spheroids.” 2014. Masters Thesis, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/53469.

MLA Handbook (7th Edition):

Goude, Melissa Chou. “Chondroitin sulfate microparticles modulate TGF-B1-induced chondrogenesis in human mesenchymal stem cell spheroids.” 2014. Web. 09 May 2021.

Vancouver:

Goude MC. Chondroitin sulfate microparticles modulate TGF-B1-induced chondrogenesis in human mesenchymal stem cell spheroids. [Internet] [Masters thesis]. Georgia Tech; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/53469.

Council of Science Editors:

Goude MC. Chondroitin sulfate microparticles modulate TGF-B1-induced chondrogenesis in human mesenchymal stem cell spheroids. [Masters Thesis]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53469


Georgia Tech

3. Lassahn, Katy Ann. Delivery of prolyl hydroxylase inhibitors to MSC spheroids for enhanced angiogenic factor secretion.

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

 Mesenchymal stromal cells (MSCs) are of clinical interest due to their ability to differentiate towards musculoskeletal lineages, modulate inflammatory responses, and promote new blood vessel… (more)

Subjects/Keywords: Mesenchymal stem cells; Hypoxia; Angiogenesis

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APA (6th Edition):

Lassahn, K. A. (2015). Delivery of prolyl hydroxylase inhibitors to MSC spheroids for enhanced angiogenic factor secretion. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55552

Chicago Manual of Style (16th Edition):

Lassahn, Katy Ann. “Delivery of prolyl hydroxylase inhibitors to MSC spheroids for enhanced angiogenic factor secretion.” 2015. Masters Thesis, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/55552.

MLA Handbook (7th Edition):

Lassahn, Katy Ann. “Delivery of prolyl hydroxylase inhibitors to MSC spheroids for enhanced angiogenic factor secretion.” 2015. Web. 09 May 2021.

Vancouver:

Lassahn KA. Delivery of prolyl hydroxylase inhibitors to MSC spheroids for enhanced angiogenic factor secretion. [Internet] [Masters thesis]. Georgia Tech; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/55552.

Council of Science Editors:

Lassahn KA. Delivery of prolyl hydroxylase inhibitors to MSC spheroids for enhanced angiogenic factor secretion. [Masters Thesis]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/55552


Georgia Tech

4. Rinker, Torri Elise. Heparin and PEG-based hydrogels to modulate and interrogate dynamic cell behavior.

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

 Hydrogel-based biomaterials are often used for biomolecule delivery or encapsulation of cells for tissue engineering and regenerative medicine applications. However, utilizing hydrogels in dynamic cell… (more)

Subjects/Keywords: Biomaterials; Mesenchymal stem cells; Poly-(ethlyene gycol); Heparin; Hydrogel; Chondrogenesis; Hyperglycemia; Core-shell microparticles; Microparticles; Three-dimensional cell culture; Co-culture; Principal component analysis

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APA (6th Edition):

Rinker, T. E. (2016). Heparin and PEG-based hydrogels to modulate and interrogate dynamic cell behavior. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56283

Chicago Manual of Style (16th Edition):

Rinker, Torri Elise. “Heparin and PEG-based hydrogels to modulate and interrogate dynamic cell behavior.” 2016. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/56283.

MLA Handbook (7th Edition):

Rinker, Torri Elise. “Heparin and PEG-based hydrogels to modulate and interrogate dynamic cell behavior.” 2016. Web. 09 May 2021.

Vancouver:

Rinker TE. Heparin and PEG-based hydrogels to modulate and interrogate dynamic cell behavior. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/56283.

Council of Science Editors:

Rinker TE. Heparin and PEG-based hydrogels to modulate and interrogate dynamic cell behavior. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/56283


Georgia Tech

5. Dysart, Marilyn Markowski. Remodeling of the pulmonary microenvironment controls transforming growth factor-beta activation and alveolar type II epithelial to mesenchymal transition.

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

 Pulmonary fibrosis is a potentially deadly pathology characterized by excessive deposition of extracellular matrix (ECM), increased tissue stiffness, and loss of tissue structure and function.… (more)

Subjects/Keywords: Alveolar epithelial cell; Transforming growth factor-beta; Epithelial to mesenchymal transition; Particulate matter; Reactive oxygen species

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APA (6th Edition):

Dysart, M. M. (2014). Remodeling of the pulmonary microenvironment controls transforming growth factor-beta activation and alveolar type II epithelial to mesenchymal transition. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53421

Chicago Manual of Style (16th Edition):

Dysart, Marilyn Markowski. “Remodeling of the pulmonary microenvironment controls transforming growth factor-beta activation and alveolar type II epithelial to mesenchymal transition.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/53421.

MLA Handbook (7th Edition):

Dysart, Marilyn Markowski. “Remodeling of the pulmonary microenvironment controls transforming growth factor-beta activation and alveolar type II epithelial to mesenchymal transition.” 2014. Web. 09 May 2021.

Vancouver:

Dysart MM. Remodeling of the pulmonary microenvironment controls transforming growth factor-beta activation and alveolar type II epithelial to mesenchymal transition. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/53421.

Council of Science Editors:

Dysart MM. Remodeling of the pulmonary microenvironment controls transforming growth factor-beta activation and alveolar type II epithelial to mesenchymal transition. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53421


Georgia Tech

6. 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 09, 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. 09 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 09]. 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

7. Gaulding, Jeffrey Clinton. Hydrogel nanoparticles and assemblies for bioapplications.

Degree: PhD, Chemistry and Biochemistry, 2013, Georgia Tech

 Hydrogels are cross-linked networks of highly hydrophilic polymer chains. When reduced to colloidal dimensions, particles of this sort are termed “microgels�? and both discrete particles… (more)

Subjects/Keywords: Hydrogel; Microgel; Biomaterials

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APA (6th Edition):

Gaulding, J. C. (2013). Hydrogel nanoparticles and assemblies for bioapplications. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52155

Chicago Manual of Style (16th Edition):

Gaulding, Jeffrey Clinton. “Hydrogel nanoparticles and assemblies for bioapplications.” 2013. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/52155.

MLA Handbook (7th Edition):

Gaulding, Jeffrey Clinton. “Hydrogel nanoparticles and assemblies for bioapplications.” 2013. Web. 09 May 2021.

Vancouver:

Gaulding JC. Hydrogel nanoparticles and assemblies for bioapplications. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/52155.

Council of Science Editors:

Gaulding JC. Hydrogel nanoparticles and assemblies for bioapplications. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52155


Georgia Tech

8. Bongiorno, Thomas. Cellular stiffness as a sorting-compatible indicator of stem cell potency.

Degree: PhD, Mechanical Engineering, 2016, Georgia Tech

 Due to their characteristic properties of self-renewal and differentiation, stem cells hold the capacity to serve as phenotype-specific cell factories for various regenerative medicine and… (more)

Subjects/Keywords: Cell mechanics; Stem cell; Atomic force microscopy; Microfluidics

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APA (6th Edition):

Bongiorno, T. (2016). Cellular stiffness as a sorting-compatible indicator of stem cell potency. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59150

Chicago Manual of Style (16th Edition):

Bongiorno, Thomas. “Cellular stiffness as a sorting-compatible indicator of stem cell potency.” 2016. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/59150.

MLA Handbook (7th Edition):

Bongiorno, Thomas. “Cellular stiffness as a sorting-compatible indicator of stem cell potency.” 2016. Web. 09 May 2021.

Vancouver:

Bongiorno T. Cellular stiffness as a sorting-compatible indicator of stem cell potency. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/59150.

Council of Science Editors:

Bongiorno T. Cellular stiffness as a sorting-compatible indicator of stem cell potency. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59150


Georgia Tech

9. Burnsed, Olivia A. Engineering an improved cartilage repair strategy combining cells and ECM-derived materials.

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

 Osteoarthritis (OA) is the leading cause of disability in the US. The avascularity, low cellularity, and slow proliferation of chondrocytes as well as joint inflammation… (more)

Subjects/Keywords: ECM; Cartilage tissue engineering; Chondrocyte expansion; MSC; Microparticle; Decellularization; Osteoarthritis; Inflammation; Immunomodulation

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APA (6th Edition):

Burnsed, O. A. (2017). Engineering an improved cartilage repair strategy combining cells and ECM-derived materials. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/60710

Chicago Manual of Style (16th Edition):

Burnsed, Olivia A. “Engineering an improved cartilage repair strategy combining cells and ECM-derived materials.” 2017. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/60710.

MLA Handbook (7th Edition):

Burnsed, Olivia A. “Engineering an improved cartilage repair strategy combining cells and ECM-derived materials.” 2017. Web. 09 May 2021.

Vancouver:

Burnsed OA. Engineering an improved cartilage repair strategy combining cells and ECM-derived materials. [Internet] [Doctoral dissertation]. Georgia Tech; 2017. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/60710.

Council of Science Editors:

Burnsed OA. Engineering an improved cartilage repair strategy combining cells and ECM-derived materials. [Doctoral Dissertation]. Georgia Tech; 2017. Available from: http://hdl.handle.net/1853/60710

10. Jackson-Holmes, Emily Louise. Microfluidics-based tools for culture and multi-functional assessments of three-dimensional pluripotent stem cell derived tissues.

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

 Due to their capacity for self-renew and differentiation, pluripotent stem cells (PSCs) are used as a cell source in applications including tissue engineering, regenerative medicine,… (more)

Subjects/Keywords: Microfluidics; Stem cell; Organoid

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APA (6th Edition):

Jackson-Holmes, E. L. (2018). Microfluidics-based tools for culture and multi-functional assessments of three-dimensional pluripotent stem cell derived tissues. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/61633

Chicago Manual of Style (16th Edition):

Jackson-Holmes, Emily Louise. “Microfluidics-based tools for culture and multi-functional assessments of three-dimensional pluripotent stem cell derived tissues.” 2018. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/61633.

MLA Handbook (7th Edition):

Jackson-Holmes, Emily Louise. “Microfluidics-based tools for culture and multi-functional assessments of three-dimensional pluripotent stem cell derived tissues.” 2018. Web. 09 May 2021.

Vancouver:

Jackson-Holmes EL. Microfluidics-based tools for culture and multi-functional assessments of three-dimensional pluripotent stem cell derived tissues. [Internet] [Doctoral dissertation]. Georgia Tech; 2018. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/61633.

Council of Science Editors:

Jackson-Holmes EL. Microfluidics-based tools for culture and multi-functional assessments of three-dimensional pluripotent stem cell derived tissues. [Doctoral Dissertation]. Georgia Tech; 2018. Available from: http://hdl.handle.net/1853/61633


Georgia Tech

11. Nguyen, Anh H. Proteolytically degradable microparticles for engineering the extracellular microenvironment of pluripotent stem cell aggregates.

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

 During embryo development, extracellular matrix (ECM) remodeling by matrix metalloproteinases (MMPs) and promotes downstream cell specifications. Pluripotent stem cell (PSC) aggregates can recapitulate various aspects… (more)

Subjects/Keywords: Gelatin methacrylate; Microparticles; Pluripotent; Stem cells; Differentiation

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APA (6th Edition):

Nguyen, A. H. (2014). Proteolytically degradable microparticles for engineering the extracellular microenvironment of pluripotent stem cell aggregates. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54845

Chicago Manual of Style (16th Edition):

Nguyen, Anh H. “Proteolytically degradable microparticles for engineering the extracellular microenvironment of pluripotent stem cell aggregates.” 2014. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/54845.

MLA Handbook (7th Edition):

Nguyen, Anh H. “Proteolytically degradable microparticles for engineering the extracellular microenvironment of pluripotent stem cell aggregates.” 2014. Web. 09 May 2021.

Vancouver:

Nguyen AH. Proteolytically degradable microparticles for engineering the extracellular microenvironment of pluripotent stem cell aggregates. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/54845.

Council of Science Editors:

Nguyen AH. Proteolytically degradable microparticles for engineering the extracellular microenvironment of pluripotent stem cell aggregates. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/54845


Georgia Tech

12. Allen, Ashley. Modulation of stem cell delivery strategy by platelet lysate utilization and cell aggregation for enhanced bone regeneration.

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

 Challenges to control delivered cell behavior, including viability and differentiation, remain a significant barrier to the translation of cell-based bone tissue engineering strategies. Our research… (more)

Subjects/Keywords: Mesenchymal stem cells; Bioluminescent imaging; Bone regeneration; Human platelet lysate; Cell Aggregation

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APA (6th Edition):

Allen, A. (2015). Modulation of stem cell delivery strategy by platelet lysate utilization and cell aggregation for enhanced bone regeneration. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/55519

Chicago Manual of Style (16th Edition):

Allen, Ashley. “Modulation of stem cell delivery strategy by platelet lysate utilization and cell aggregation for enhanced bone regeneration.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/55519.

MLA Handbook (7th Edition):

Allen, Ashley. “Modulation of stem cell delivery strategy by platelet lysate utilization and cell aggregation for enhanced bone regeneration.” 2015. Web. 09 May 2021.

Vancouver:

Allen A. Modulation of stem cell delivery strategy by platelet lysate utilization and cell aggregation for enhanced bone regeneration. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/55519.

Council of Science Editors:

Allen A. Modulation of stem cell delivery strategy by platelet lysate utilization and cell aggregation for enhanced bone regeneration. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/55519


Georgia Tech

13. 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 May 09, 2021. 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. 09 May 2021.

Vancouver:

Wilson JL. Engineering a Platform to Harness Pluripotent Stem Cell-Derived Paracrine Factors. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 09]. 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

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Padmore, Trudy J. “Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.” 2016. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/56336.

MLA Handbook (7th Edition):

Padmore, Trudy J. “Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages.” 2016. Web. 09 May 2021.

Vancouver:

Padmore TJ. Controlled release of GLP-1 from affinity-based protein microspheres and quantitative analysis of the role of fiber length on phagocytosis and inflammatory response by macrophages. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/56336.

Council of Science Editors:

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

15. Leslie, Shirae. The controlled release of rat adipose-derived stem cells from alginate microbeads for bone regeneration.

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

 Cell-based therapies have potential for tissue regeneration but poor delivery methods lead to low viability or dispersal of cells from target sites, limiting clinical utility.… (more)

Subjects/Keywords: Cell encapsulation; Alginate degradation; Hydrogel; Stem cells; Bone regeneration; Fractures Treatment; Cellular therapy

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APA (6th Edition):

Leslie, S. (2013). The controlled release of rat adipose-derived stem cells from alginate microbeads for bone regeneration. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/48946

Chicago Manual of Style (16th Edition):

Leslie, Shirae. “The controlled release of rat adipose-derived stem cells from alginate microbeads for bone regeneration.” 2013. Masters Thesis, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/48946.

MLA Handbook (7th Edition):

Leslie, Shirae. “The controlled release of rat adipose-derived stem cells from alginate microbeads for bone regeneration.” 2013. Web. 09 May 2021.

Vancouver:

Leslie S. The controlled release of rat adipose-derived stem cells from alginate microbeads for bone regeneration. [Internet] [Masters thesis]. Georgia Tech; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/48946.

Council of Science Editors:

Leslie S. The controlled release of rat adipose-derived stem cells from alginate microbeads for bone regeneration. [Masters Thesis]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/48946

16. Deutsch, Eric R. The use of stem cell synthesized extracellular matrix for bone repair.

Degree: MS, Mechanical Engineering, 2009, Georgia Tech

 Stem cell synthesized extracellular matrix (ECM) may serve as a replacement for current bone grafting techniques. The overall goal of this thesis is to quantify… (more)

Subjects/Keywords: Bone; Tissue engineering; Stem cells; Extracellular matrix; Mesenchymal stem cells; Amniotic fluid stem cells; Extracellular matrix; Stem cells; Bone-grafting; Tissue engineering

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APA (6th Edition):

Deutsch, E. R. (2009). The use of stem cell synthesized extracellular matrix for bone repair. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31784

Chicago Manual of Style (16th Edition):

Deutsch, Eric R. “The use of stem cell synthesized extracellular matrix for bone repair.” 2009. Masters Thesis, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/31784.

MLA Handbook (7th Edition):

Deutsch, Eric R. “The use of stem cell synthesized extracellular matrix for bone repair.” 2009. Web. 09 May 2021.

Vancouver:

Deutsch ER. The use of stem cell synthesized extracellular matrix for bone repair. [Internet] [Masters thesis]. Georgia Tech; 2009. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/31784.

Council of Science Editors:

Deutsch ER. The use of stem cell synthesized extracellular matrix for bone repair. [Masters Thesis]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/31784


Georgia Tech

17. Zimmermann, Joshua A. Engineering mesenchymal stromal cell constructs to enhance immunomodulation.

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

 Mesenchymal stem/stromal cells (MSCs) are potent modulators of inflammatory and immune responses due to their ability to secrete soluble paracrine factors that regulate both innate… (more)

Subjects/Keywords: Mesenchymal stem cells; Mesenchymal stromal cells; Immunomodulation; Biomaterials

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APA (6th Edition):

Zimmermann, J. A. (2016). Engineering mesenchymal stromal cell constructs to enhance immunomodulation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58590

Chicago Manual of Style (16th Edition):

Zimmermann, Joshua A. “Engineering mesenchymal stromal cell constructs to enhance immunomodulation.” 2016. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/58590.

MLA Handbook (7th Edition):

Zimmermann, Joshua A. “Engineering mesenchymal stromal cell constructs to enhance immunomodulation.” 2016. Web. 09 May 2021.

Vancouver:

Zimmermann JA. Engineering mesenchymal stromal cell constructs to enhance immunomodulation. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/58590.

Council of Science Editors:

Zimmermann JA. Engineering mesenchymal stromal cell constructs to enhance immunomodulation. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58590


Georgia Tech

18. Sutha, Ken. Osteoinductive material derived from differentiating embryonic stem cells.

Degree: PhD, Biomedical Engineering, 2012, Georgia Tech

 The loss of regenerative capacity of bone, from fetal to adult to aged animals, has been attributed not only to a decline in the function… (more)

Subjects/Keywords: Regenerative medicine; Regenerative therapy; Bone therapy; Embryonic stem cells; Embryonic stem cells; Bone regeneration

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APA (6th Edition):

Sutha, K. (2012). Osteoinductive material derived from differentiating embryonic stem cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/51722

Chicago Manual of Style (16th Edition):

Sutha, Ken. “Osteoinductive material derived from differentiating embryonic stem cells.” 2012. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/51722.

MLA Handbook (7th Edition):

Sutha, Ken. “Osteoinductive material derived from differentiating embryonic stem cells.” 2012. Web. 09 May 2021.

Vancouver:

Sutha K. Osteoinductive material derived from differentiating embryonic stem cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/51722.

Council of Science Editors:

Sutha K. Osteoinductive material derived from differentiating embryonic stem cells. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/51722


Georgia Tech

19. 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 May 09, 2021. 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. 09 May 2021.

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 2021 May 09]. 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

20. 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 May 09, 2021. 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. 09 May 2021.

Vancouver:

Lei J. The development of glycosaminoglycan coatings for mesenchymal stem cell-based culture applications. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 May 09]. 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

21. Bloomquist, Ryan F. Developmental plasticity of stem cells in teeth and taste bud renewal.

Degree: PhD, Biology, 2015, Georgia Tech

 Science and medicine have progressed in unfathomable ways over the past century. Paradoxically, as our result of our advancements in medicine we live in a… (more)

Subjects/Keywords: Dental regeneration; Lake Malawi cichlids; Odontogenesis

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APA (6th Edition):

Bloomquist, R. F. (2015). Developmental plasticity of stem cells in teeth and taste bud renewal. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53565

Chicago Manual of Style (16th Edition):

Bloomquist, Ryan F. “Developmental plasticity of stem cells in teeth and taste bud renewal.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/53565.

MLA Handbook (7th Edition):

Bloomquist, Ryan F. “Developmental plasticity of stem cells in teeth and taste bud renewal.” 2015. Web. 09 May 2021.

Vancouver:

Bloomquist RF. Developmental plasticity of stem cells in teeth and taste bud renewal. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/53565.

Council of Science Editors:

Bloomquist RF. Developmental plasticity of stem cells in teeth and taste bud renewal. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/53565

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

Degree: PhD, Biomedical Engineering, 2013, Georgia Tech

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Shekaran, Asha. “Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing.” 2013. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/51720.

MLA Handbook (7th Edition):

Shekaran, Asha. “Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing.” 2013. Web. 09 May 2021.

Vancouver:

Shekaran A. Beta 1 integrins in bone formation during development and engineering integrin-specific hydrogels for enhanced bone healing. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/51720.

Council of Science Editors:

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

23. Park, Jaehyung. Biomaterials for tissue engineering for rheumatoid arthritis based on controlling dendritic cell phenotype.

Degree: PhD, Biomedical Engineering, 2009, Georgia Tech

 The host response toward biomaterial component of tissue-engineered devices has been extensively investigated. The objective of this research was to understand the response of dendritic… (more)

Subjects/Keywords: Immune response; Phenotype; Inflammatory; Tissue engineering; Adaptive immunity; Host response; Dendritic cell; Rheumatoid arthritis; Biomaterial; Tissue engineering; Biomedical materials; Dendritic cells; Immune response; Rheumatoid arthritis

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APA (6th Edition):

Park, J. (2009). Biomaterials for tissue engineering for rheumatoid arthritis based on controlling dendritic cell phenotype. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/42174

Chicago Manual of Style (16th Edition):

Park, Jaehyung. “Biomaterials for tissue engineering for rheumatoid arthritis based on controlling dendritic cell phenotype.” 2009. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/42174.

MLA Handbook (7th Edition):

Park, Jaehyung. “Biomaterials for tissue engineering for rheumatoid arthritis based on controlling dendritic cell phenotype.” 2009. Web. 09 May 2021.

Vancouver:

Park J. Biomaterials for tissue engineering for rheumatoid arthritis based on controlling dendritic cell phenotype. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/42174.

Council of Science Editors:

Park J. Biomaterials for tissue engineering for rheumatoid arthritis based on controlling dendritic cell phenotype. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/42174

24. Sargent, Carolyn Yeago. Effects of hydrodynamic culture on embryonic stem cell differentiation: cardiogenic modulation.

Degree: PhD, Biomedical Engineering, 2010, Georgia Tech

 Stem and progenitor cells are an attractive cell source for the treatment of degenerative diseases due to their potential to differentiate into multiple cell types… (more)

Subjects/Keywords: Embryonic stem cells; Embryoid body; Hydrodynamic; Bioprocessing; Differentiation; Cardiomyocyte; Heart cells; Degeneration (Pathology); Hydrodynamics; Embryonic stem cells Research

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APA (6th Edition):

Sargent, C. Y. (2010). Effects of hydrodynamic culture on embryonic stem cell differentiation: cardiogenic modulation. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/34710

Chicago Manual of Style (16th Edition):

Sargent, Carolyn Yeago. “Effects of hydrodynamic culture on embryonic stem cell differentiation: cardiogenic modulation.” 2010. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/34710.

MLA Handbook (7th Edition):

Sargent, Carolyn Yeago. “Effects of hydrodynamic culture on embryonic stem cell differentiation: cardiogenic modulation.” 2010. Web. 09 May 2021.

Vancouver:

Sargent CY. Effects of hydrodynamic culture on embryonic stem cell differentiation: cardiogenic modulation. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/34710.

Council of Science Editors:

Sargent CY. Effects of hydrodynamic culture on embryonic stem cell differentiation: cardiogenic modulation. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/34710

25. Tison, Christopher Kirby. Programmable, isothermal disassembly of DNA-linked colloidal particles.

Degree: PhD, Materials Science and Engineering, 2009, Georgia Tech

 Colloidal particles serve as useful building blocks for materials applications ranging from controlled band-gap materials to rationally designed drug delivery systems. Thus, developing approaches to… (more)

Subjects/Keywords: Drug delivery; Isothermal redispersion; Programmed assembly; DNA-mediated assembly; Colloid; Colloids; Polymeric drug delivery systems; Self-organizing systems; DNA

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APA (6th Edition):

Tison, C. K. (2009). Programmable, isothermal disassembly of DNA-linked colloidal particles. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/28189

Chicago Manual of Style (16th Edition):

Tison, Christopher Kirby. “Programmable, isothermal disassembly of DNA-linked colloidal particles.” 2009. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/28189.

MLA Handbook (7th Edition):

Tison, Christopher Kirby. “Programmable, isothermal disassembly of DNA-linked colloidal particles.” 2009. Web. 09 May 2021.

Vancouver:

Tison CK. Programmable, isothermal disassembly of DNA-linked colloidal particles. [Internet] [Doctoral dissertation]. Georgia Tech; 2009. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/28189.

Council of Science Editors:

Tison CK. Programmable, isothermal disassembly of DNA-linked colloidal particles. [Doctoral Dissertation]. Georgia Tech; 2009. Available from: http://hdl.handle.net/1853/28189

26. Crapo, Peter Maughan. Development of a tissue engineering strategy to create highly compliant blood vessels.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 Compliance mismatch is a significant hurdle to long-term patency in small-diameter arterial bypass grafts. Vascular tissue engineering has the potential to produce compliant, non-thrombogenic small-diameter… (more)

Subjects/Keywords: Tissue engineering; Small-diameter artery; Compliance; Elastin; Blood vessel; Poly(glycerol sebacate); PGS; Tissue engineering; Blood-vessels; Blood vessel prosthesis; Vascular grafts

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APA (6th Edition):

Crapo, P. M. (2008). Development of a tissue engineering strategy to create highly compliant blood vessels. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/28245

Chicago Manual of Style (16th Edition):

Crapo, Peter Maughan. “Development of a tissue engineering strategy to create highly compliant blood vessels.” 2008. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/28245.

MLA Handbook (7th Edition):

Crapo, Peter Maughan. “Development of a tissue engineering strategy to create highly compliant blood vessels.” 2008. Web. 09 May 2021.

Vancouver:

Crapo PM. Development of a tissue engineering strategy to create highly compliant blood vessels. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/28245.

Council of Science Editors:

Crapo PM. Development of a tissue engineering strategy to create highly compliant blood vessels. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/28245

27. Chen, Jiaxuan. The role of Pdia3 in vitamin D signaling in osteoblasts.

Degree: PhD, Biomedical Engineering, 2012, Georgia Tech

 1a,25-Dihydroxyvitamin D3 (1a,25(OH)2D3) is a major functional metabolic form of vitamin D. 1a,25(OH)2D3 has drawn increasing attention due to its functions in addition to maintaining… (more)

Subjects/Keywords: Rapid response; Osteoblasts; Vitamin D; VDR; Pdia3; Cholecalciferol; Cell receptors; Steroid hormones

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APA (6th Edition):

Chen, J. (2012). The role of Pdia3 in vitamin D signaling in osteoblasts. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/50147

Chicago Manual of Style (16th Edition):

Chen, Jiaxuan. “The role of Pdia3 in vitamin D signaling in osteoblasts.” 2012. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/50147.

MLA Handbook (7th Edition):

Chen, Jiaxuan. “The role of Pdia3 in vitamin D signaling in osteoblasts.” 2012. Web. 09 May 2021.

Vancouver:

Chen J. The role of Pdia3 in vitamin D signaling in osteoblasts. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/50147.

Council of Science Editors:

Chen J. The role of Pdia3 in vitamin D signaling in osteoblasts. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/50147

28. Clark, Amy Yee lae. Integrin specificity as a novel strategy for enhancing transplanted stem cell survival and tissue repair in vivo.

Degree: PhD, Mechanical Engineering, 2016, Georgia Tech

 Despite the promising clinical results for the use of human mesenchymal stem cells (hMSC) in musculoskeletal defect treatment, inadequate control of cell survival, engraftment and… (more)

Subjects/Keywords: Integrin; Hydrogel; Mesenchymal stem cells; Bone repair; Immunomodulation

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APA (6th Edition):

Clark, A. Y. l. (2016). Integrin specificity as a novel strategy for enhancing transplanted stem cell survival and tissue repair in vivo. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/58178

Chicago Manual of Style (16th Edition):

Clark, Amy Yee lae. “Integrin specificity as a novel strategy for enhancing transplanted stem cell survival and tissue repair in vivo.” 2016. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/58178.

MLA Handbook (7th Edition):

Clark, Amy Yee lae. “Integrin specificity as a novel strategy for enhancing transplanted stem cell survival and tissue repair in vivo.” 2016. Web. 09 May 2021.

Vancouver:

Clark AYl. Integrin specificity as a novel strategy for enhancing transplanted stem cell survival and tissue repair in vivo. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/58178.

Council of Science Editors:

Clark AYl. Integrin specificity as a novel strategy for enhancing transplanted stem cell survival and tissue repair in vivo. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/58178

29. Lim, Jeremy James. The development of glycosaminoglycan-based materials to promote chondrogenic differentiation of mesenchymal stem cells.

Degree: PhD, Biomedical Engineering, 2012, Georgia Tech

 Tissue engineering strategies represent exciting potential therapies to repair cartilage injuries; however, difficulty regenerating the complex extracellular matrix (ECM) organization of native cartilage remains a… (more)

Subjects/Keywords: Tissue engineering; Cartilage; Mesenchymal stem cell; Extracellular matrix; Glycosaminoglycan; Chondroitin sulfate; Mesenchymal stem cells Differentiation; Cell differentiation; Glycosaminoglycans; Chondroitin sulfates; Stem cells

…Andrés and Erin viii have been my most loyal friends at Georgia Tech. They treated me like… 

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APA (6th Edition):

Lim, J. J. (2012). The development of glycosaminoglycan-based materials to promote chondrogenic differentiation of mesenchymal stem cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/44849

Chicago Manual of Style (16th Edition):

Lim, Jeremy James. “The development of glycosaminoglycan-based materials to promote chondrogenic differentiation of mesenchymal stem cells.” 2012. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/44849.

MLA Handbook (7th Edition):

Lim, Jeremy James. “The development of glycosaminoglycan-based materials to promote chondrogenic differentiation of mesenchymal stem cells.” 2012. Web. 09 May 2021.

Vancouver:

Lim JJ. The development of glycosaminoglycan-based materials to promote chondrogenic differentiation of mesenchymal stem cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/44849.

Council of Science Editors:

Lim JJ. The development of glycosaminoglycan-based materials to promote chondrogenic differentiation of mesenchymal stem cells. [Doctoral Dissertation]. Georgia Tech; 2012. Available from: http://hdl.handle.net/1853/44849

30. 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 09, 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. 09 May 2021.

Vancouver:

Nsiah BA. Fluid shear stress modulation of embryonic stem cell differentiation. [Internet] [Doctoral dissertation]. Georgia Tech; 2012. [cited 2021 May 09]. 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

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