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You searched for +publisher:"Georgia Tech" +contributor:("Yadong Wang"). Showing records 1 – 4 of 4 total matches.

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1. Lee, Jinhyun. Development of an anisotropic swelling hydrogel for tissue expansion: control over the degree, rate and direction of hydrogel swelling.

Degree: PhD, Polymer, Textile and Fiber Engineering, 2008, Georgia Tech

 Hydrogels are polymeric materials with chemically, physically or topologically crosslinked networks which have a capacity to absorb and retain water. They have been frequently used… (more)

Subjects/Keywords: Anisotropic swelling; Hydrogel; Swelling; Tissue expansion; Swelling rate; Degree of swelling; Swelling direction; Colloids Absorption and adsorption; Tissue engineering

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APA (6th Edition):

Lee, J. (2008). Development of an anisotropic swelling hydrogel for tissue expansion: control over the degree, rate and direction of hydrogel swelling. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31693

Chicago Manual of Style (16th Edition):

Lee, Jinhyun. “Development of an anisotropic swelling hydrogel for tissue expansion: control over the degree, rate and direction of hydrogel swelling.” 2008. Doctoral Dissertation, Georgia Tech. Accessed November 25, 2020. http://hdl.handle.net/1853/31693.

MLA Handbook (7th Edition):

Lee, Jinhyun. “Development of an anisotropic swelling hydrogel for tissue expansion: control over the degree, rate and direction of hydrogel swelling.” 2008. Web. 25 Nov 2020.

Vancouver:

Lee J. Development of an anisotropic swelling hydrogel for tissue expansion: control over the degree, rate and direction of hydrogel swelling. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1853/31693.

Council of Science Editors:

Lee J. Development of an anisotropic swelling hydrogel for tissue expansion: control over the degree, rate and direction of hydrogel swelling. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/31693

2. Rincón-Rosenbaum, Charlene. Development of poly(3-octylthiophene) thin films for regulating osteoblast growth.

Degree: PhD, Chemical Engineering, 2008, Georgia Tech

 The overall objective of this work was to assess the suitability of poly(3-octylthiophene) (P3OT) to sustain MC3T3-E1 osteoblast attachment and growth. The central hypothesis was… (more)

Subjects/Keywords: Cell proliferation; Cell attachment; Poly(3-octylthiophene); Conducting polymers; MC3T3-E1 osteoblasts; Thiophenes; Thin films; Conducting polymers; Biomedical materials

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APA (6th Edition):

Rincón-Rosenbaum, C. (2008). Development of poly(3-octylthiophene) thin films for regulating osteoblast growth. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/26493

Chicago Manual of Style (16th Edition):

Rincón-Rosenbaum, Charlene. “Development of poly(3-octylthiophene) thin films for regulating osteoblast growth.” 2008. Doctoral Dissertation, Georgia Tech. Accessed November 25, 2020. http://hdl.handle.net/1853/26493.

MLA Handbook (7th Edition):

Rincón-Rosenbaum, Charlene. “Development of poly(3-octylthiophene) thin films for regulating osteoblast growth.” 2008. Web. 25 Nov 2020.

Vancouver:

Rincón-Rosenbaum C. Development of poly(3-octylthiophene) thin films for regulating osteoblast growth. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1853/26493.

Council of Science Editors:

Rincón-Rosenbaum C. Development of poly(3-octylthiophene) thin films for regulating osteoblast growth. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/26493


Georgia Tech

3. Sallach, Rory Elizabeth. Recombinant elastin-mimetic protein polymers as design elements for an arterial substitute.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 Recombinant synthesis of elastin-mimetic proteins has been employed for several decades, however, long-term biocompatibility and biostability of such proteins was not fully defined. We present… (more)

Subjects/Keywords: Mechanical testing; Protein experession; Biostability; Biocompatibility; Genetic engineering; Recombinant elastin; Crosslinking (Polymerization); Recombinant proteins; Polytef; Vascular grafts; Blood vessel prosthesis

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

APA (6th Edition):

Sallach, R. E. (2008). Recombinant elastin-mimetic protein polymers as design elements for an arterial substitute. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29614

Chicago Manual of Style (16th Edition):

Sallach, Rory Elizabeth. “Recombinant elastin-mimetic protein polymers as design elements for an arterial substitute.” 2008. Doctoral Dissertation, Georgia Tech. Accessed November 25, 2020. http://hdl.handle.net/1853/29614.

MLA Handbook (7th Edition):

Sallach, Rory Elizabeth. “Recombinant elastin-mimetic protein polymers as design elements for an arterial substitute.” 2008. Web. 25 Nov 2020.

Vancouver:

Sallach RE. Recombinant elastin-mimetic protein polymers as design elements for an arterial substitute. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1853/29614.

Council of Science Editors:

Sallach RE. Recombinant elastin-mimetic protein polymers as design elements for an arterial substitute. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/29614


Georgia Tech

4. Glaus, Charles R. M. Development and analysis of radiolabeled magnetic nanoparticles for positron emission tomography and magnetic resonance imaging.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 Nanoparticles possess unique characteristics that make them well suited for molecular imaging. Particles can be synthesized in a systematic fashion with tight control over diameter… (more)

Subjects/Keywords: Cancer; Nanotechnology; Nuclear; Integrin; Tumor; Molecular imaging; Diagnostic imaging; Tomography, Emission; Nanoparticles; Positrons Emission; Imaging systems; Radiolabeling

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

APA (6th Edition):

Glaus, C. R. M. (2008). Development and analysis of radiolabeled magnetic nanoparticles for positron emission tomography and magnetic resonance imaging. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/31692

Chicago Manual of Style (16th Edition):

Glaus, Charles R M. “Development and analysis of radiolabeled magnetic nanoparticles for positron emission tomography and magnetic resonance imaging.” 2008. Doctoral Dissertation, Georgia Tech. Accessed November 25, 2020. http://hdl.handle.net/1853/31692.

MLA Handbook (7th Edition):

Glaus, Charles R M. “Development and analysis of radiolabeled magnetic nanoparticles for positron emission tomography and magnetic resonance imaging.” 2008. Web. 25 Nov 2020.

Vancouver:

Glaus CRM. Development and analysis of radiolabeled magnetic nanoparticles for positron emission tomography and magnetic resonance imaging. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1853/31692.

Council of Science Editors:

Glaus CRM. Development and analysis of radiolabeled magnetic nanoparticles for positron emission tomography and magnetic resonance imaging. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/31692

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