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Dept: Biomedical Engineering

You searched for subject:(Angiogenesis). Showing records 1 – 29 of 29 total matches.

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University of Texas – Austin

1. -9024-5383. Glypican-1 proteoliposomes enhance growth factor activity for therapeutic angiogenesis.

Degree: Biomedical Engineering, 2018, University of Texas – Austin

 Peripheral arterial disease affects more than 27 million patients in the United States. PAD can lead to peripheral limb ischemia and result in non-healing foot… (more)

Subjects/Keywords: Glypican-1; FGF-2; VEGF; Ischemia; Angiogenesis; Growth factor

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APA (6th Edition):

-9024-5383. (2018). Glypican-1 proteoliposomes enhance growth factor activity for therapeutic angiogenesis. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68372

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

-9024-5383. “Glypican-1 proteoliposomes enhance growth factor activity for therapeutic angiogenesis.” 2018. Thesis, University of Texas – Austin. Accessed August 17, 2019. http://hdl.handle.net/2152/68372.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

-9024-5383. “Glypican-1 proteoliposomes enhance growth factor activity for therapeutic angiogenesis.” 2018. Web. 17 Aug 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-9024-5383. Glypican-1 proteoliposomes enhance growth factor activity for therapeutic angiogenesis. [Internet] [Thesis]. University of Texas – Austin; 2018. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/2152/68372.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

-9024-5383. Glypican-1 proteoliposomes enhance growth factor activity for therapeutic angiogenesis. [Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68372

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

2. Wiet, Matthew G. Mast Cell-Intervertebral Disc Cell Interactions Regulate Inflammation, Catabolism, and Angiogenesis in Discogenic Back Pain.

Degree: MS, Biomedical Engineering, 2017, The Ohio State University

 Low back pain is a widespread debilitating disorder of significant socio-economic importance and intervertebral disc (IVD) degeneration has been implicated in its pathogenesis. Despite its… (more)

Subjects/Keywords: Biomedical Engineering; intervertebral disc; low back pain; immune cell; mast cell; catabolism; angiogenesis; inflammation

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APA (6th Edition):

Wiet, M. G. (2017). Mast Cell-Intervertebral Disc Cell Interactions Regulate Inflammation, Catabolism, and Angiogenesis in Discogenic Back Pain. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1492637455128773

Chicago Manual of Style (16th Edition):

Wiet, Matthew G. “Mast Cell-Intervertebral Disc Cell Interactions Regulate Inflammation, Catabolism, and Angiogenesis in Discogenic Back Pain.” 2017. Masters Thesis, The Ohio State University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1492637455128773.

MLA Handbook (7th Edition):

Wiet, Matthew G. “Mast Cell-Intervertebral Disc Cell Interactions Regulate Inflammation, Catabolism, and Angiogenesis in Discogenic Back Pain.” 2017. Web. 17 Aug 2019.

Vancouver:

Wiet MG. Mast Cell-Intervertebral Disc Cell Interactions Regulate Inflammation, Catabolism, and Angiogenesis in Discogenic Back Pain. [Internet] [Masters thesis]. The Ohio State University; 2017. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1492637455128773.

Council of Science Editors:

Wiet MG. Mast Cell-Intervertebral Disc Cell Interactions Regulate Inflammation, Catabolism, and Angiogenesis in Discogenic Back Pain. [Masters Thesis]. The Ohio State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1492637455128773

3. Singh, Rahul K. The Role of Endothelial Mechanosensing in Capillary Development and Organization.

Degree: PhD, Biomedical Engineering, 2015, University of Michigan

 Ischemic injury is a leading cause of morbidity and mortality with the most common causes being heart attack, stroke, and peripheral artery disease. Therapies attempt… (more)

Subjects/Keywords: Angiogenesis; PEG Hydrogel; Mechanotransduction; Endothelial Cell; Capillary Morphogenesis; Biomaterials; Biomedical Engineering; Engineering

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APA (6th Edition):

Singh, R. K. (2015). The Role of Endothelial Mechanosensing in Capillary Development and Organization. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/111562

Chicago Manual of Style (16th Edition):

Singh, Rahul K. “The Role of Endothelial Mechanosensing in Capillary Development and Organization.” 2015. Doctoral Dissertation, University of Michigan. Accessed August 17, 2019. http://hdl.handle.net/2027.42/111562.

MLA Handbook (7th Edition):

Singh, Rahul K. “The Role of Endothelial Mechanosensing in Capillary Development and Organization.” 2015. Web. 17 Aug 2019.

Vancouver:

Singh RK. The Role of Endothelial Mechanosensing in Capillary Development and Organization. [Internet] [Doctoral dissertation]. University of Michigan; 2015. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/2027.42/111562.

Council of Science Editors:

Singh RK. The Role of Endothelial Mechanosensing in Capillary Development and Organization. [Doctoral Dissertation]. University of Michigan; 2015. Available from: http://hdl.handle.net/2027.42/111562

4. Goette, Matthew John. Absolute Quantitation for MR Molecular Imaging of Angiogenesis.

Degree: PhD, Biomedical Engineering, 2014, Washington University in St. Louis

  Medical imaging is undergoing a transition from an art that is used to make static images of human physiology into a scientific tool that… (more)

Subjects/Keywords: Angiogenesis; Fluorine (19F) MRI; Magnetic Resonance Imaging; Molecular Imaging

…Figure 1.2 Gd-bearing nanoparticles targeted to angiogenesis provide T1-weighted signal to… …patchy areas of high angiogenesis. On the week 1 image, the signal enhancement has clearly… …statin-treated animals showed a constant level of angiogenesis in the aortic wall. Animals… …treated with targeted fumagillin nanoparticles at 0 and 4 weeks showed decreased angiogenesis… …angiogenesis (*p < 0.05). [Figure reprinted with permission from Winter et al.]… 

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APA (6th Edition):

Goette, M. J. (2014). Absolute Quantitation for MR Molecular Imaging of Angiogenesis. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/1304

Chicago Manual of Style (16th Edition):

Goette, Matthew John. “Absolute Quantitation for MR Molecular Imaging of Angiogenesis.” 2014. Doctoral Dissertation, Washington University in St. Louis. Accessed August 17, 2019. https://openscholarship.wustl.edu/etd/1304.

MLA Handbook (7th Edition):

Goette, Matthew John. “Absolute Quantitation for MR Molecular Imaging of Angiogenesis.” 2014. Web. 17 Aug 2019.

Vancouver:

Goette MJ. Absolute Quantitation for MR Molecular Imaging of Angiogenesis. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2014. [cited 2019 Aug 17]. Available from: https://openscholarship.wustl.edu/etd/1304.

Council of Science Editors:

Goette MJ. Absolute Quantitation for MR Molecular Imaging of Angiogenesis. [Doctoral Dissertation]. Washington University in St. Louis; 2014. Available from: https://openscholarship.wustl.edu/etd/1304


University of Texas – Austin

5. Das, Subhamoy. Syndesomes for enhanced wound healing and therapeutic angiogenesis in a diabetic diseased state.

Degree: Biomedical Engineering, 2014, University of Texas – Austin

 Peripheral vascular disease (PVD) affects more than 202 million people globally and about 20% of the population above 65 years of age in the United… (more)

Subjects/Keywords: Angiogenesis; Wound healing

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APA (6th Edition):

Das, S. (2014). Syndesomes for enhanced wound healing and therapeutic angiogenesis in a diabetic diseased state. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/44095

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Das, Subhamoy. “Syndesomes for enhanced wound healing and therapeutic angiogenesis in a diabetic diseased state.” 2014. Thesis, University of Texas – Austin. Accessed August 17, 2019. http://hdl.handle.net/2152/44095.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Das, Subhamoy. “Syndesomes for enhanced wound healing and therapeutic angiogenesis in a diabetic diseased state.” 2014. Web. 17 Aug 2019.

Vancouver:

Das S. Syndesomes for enhanced wound healing and therapeutic angiogenesis in a diabetic diseased state. [Internet] [Thesis]. University of Texas – Austin; 2014. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/2152/44095.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Das S. Syndesomes for enhanced wound healing and therapeutic angiogenesis in a diabetic diseased state. [Thesis]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/44095

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Vanderbilt University

6. Zachman, Angela Laurie. Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease.

Degree: PhD, Biomedical Engineering, 2014, Vanderbilt University

 Peripheral artery disease (PAD) is characterized by platelet activation and aggregation on arterial walls, resulting in vessel occlusion and ischemia. To treat PAD, it is… (more)

Subjects/Keywords: inflammation; injectable polymer; atherosclerosis; peripheral artery disease; peptide; angiogenesis

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APA (6th Edition):

Zachman, A. L. (2014). Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03312014-183105/ ;

Chicago Manual of Style (16th Edition):

Zachman, Angela Laurie. “Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed August 17, 2019. http://etd.library.vanderbilt.edu//available/etd-03312014-183105/ ;.

MLA Handbook (7th Edition):

Zachman, Angela Laurie. “Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease.” 2014. Web. 17 Aug 2019.

Vancouver:

Zachman AL. Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2019 Aug 17]. Available from: http://etd.library.vanderbilt.edu//available/etd-03312014-183105/ ;.

Council of Science Editors:

Zachman AL. Peptide-functionalized Polymers Regulating Angiogenesis and Inflammation in Peripheral Artery Disease. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu//available/etd-03312014-183105/ ;


Case Western Reserve University

7. Rivera, Edgardo. Affinity-Based Drug Delivery Devices and its Applications in the Modulation of Cellular Processes.

Degree: PhD, Biomedical Engineering, 2014, Case Western Reserve University

 Alteration of cell behavior is at the core of pathological diseases and design of drug delivery systems. Among those behaviors are cell morphogenesis, engraftment and… (more)

Subjects/Keywords: Biomedical Engineering; drug delivery; affinity delivery; local release; CCL7; heparin; mesenchymal stem cells; urinary incontinence; glioblastoma; angiogenesis; SPR; transgene; cyclodextrin

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APA (6th Edition):

Rivera, E. (2014). Affinity-Based Drug Delivery Devices and its Applications in the Modulation of Cellular Processes. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1417792663

Chicago Manual of Style (16th Edition):

Rivera, Edgardo. “Affinity-Based Drug Delivery Devices and its Applications in the Modulation of Cellular Processes.” 2014. Doctoral Dissertation, Case Western Reserve University. Accessed August 17, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1417792663.

MLA Handbook (7th Edition):

Rivera, Edgardo. “Affinity-Based Drug Delivery Devices and its Applications in the Modulation of Cellular Processes.” 2014. Web. 17 Aug 2019.

Vancouver:

Rivera E. Affinity-Based Drug Delivery Devices and its Applications in the Modulation of Cellular Processes. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2014. [cited 2019 Aug 17]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1417792663.

Council of Science Editors:

Rivera E. Affinity-Based Drug Delivery Devices and its Applications in the Modulation of Cellular Processes. [Doctoral Dissertation]. Case Western Reserve University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1417792663


University of California – Irvine

8. Tian, Lei. Creation of Thick Prevascularized Implantable Tissues.

Degree: Biomedical Engineering, 2014, University of California – Irvine

 Engineered thick tissues require rapid blood perfusion upon implantation for survival. We have previously described a method to prevascularize (in vitro development of a vascular… (more)

Subjects/Keywords: Biomedical engineering; anastomosis; angiogenesis; endothelial; prericyte; prevascularization; vessel

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APA (6th Edition):

Tian, L. (2014). Creation of Thick Prevascularized Implantable Tissues. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/20s98036

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tian, Lei. “Creation of Thick Prevascularized Implantable Tissues.” 2014. Thesis, University of California – Irvine. Accessed August 17, 2019. http://www.escholarship.org/uc/item/20s98036.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tian, Lei. “Creation of Thick Prevascularized Implantable Tissues.” 2014. Web. 17 Aug 2019.

Vancouver:

Tian L. Creation of Thick Prevascularized Implantable Tissues. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2019 Aug 17]. Available from: http://www.escholarship.org/uc/item/20s98036.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tian L. Creation of Thick Prevascularized Implantable Tissues. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/20s98036

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Florida

9. Tonello, Sarah. Development of a Heterogeneous Pro-Angiogenic Protein Mixture Encapsulation System.

Degree: MS, Biomedical Engineering, 2014, University of Florida

Subjects/Keywords: Alginates; Angiogenesis; Cell growth; Cells; Controlled release; Encapsulation; Endothelial cells; In vitro fertilization; Placenta; Tissue engineering; angiogenesis

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APA (6th Edition):

Tonello, S. (2014). Development of a Heterogeneous Pro-Angiogenic Protein Mixture Encapsulation System. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0047192

Chicago Manual of Style (16th Edition):

Tonello, Sarah. “Development of a Heterogeneous Pro-Angiogenic Protein Mixture Encapsulation System.” 2014. Masters Thesis, University of Florida. Accessed August 17, 2019. http://ufdc.ufl.edu/UFE0047192.

MLA Handbook (7th Edition):

Tonello, Sarah. “Development of a Heterogeneous Pro-Angiogenic Protein Mixture Encapsulation System.” 2014. Web. 17 Aug 2019.

Vancouver:

Tonello S. Development of a Heterogeneous Pro-Angiogenic Protein Mixture Encapsulation System. [Internet] [Masters thesis]. University of Florida; 2014. [cited 2019 Aug 17]. Available from: http://ufdc.ufl.edu/UFE0047192.

Council of Science Editors:

Tonello S. Development of a Heterogeneous Pro-Angiogenic Protein Mixture Encapsulation System. [Masters Thesis]. University of Florida; 2014. Available from: http://ufdc.ufl.edu/UFE0047192


Vanderbilt University

10. Lee, Sue Hyun. In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells.

Degree: MS, Biomedical Engineering, 2013, Vanderbilt University

 Gelatin is a hydrolyzed and denatured form of collagen, which comprises the majority of extracellular matrix. Despite its numerous advantages for tissue engineering, its use… (more)

Subjects/Keywords: tissue engineering; Angiogenesis; Gelatin; hydrogels; Mesenchymal Stem Cells

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APA (6th Edition):

Lee, S. H. (2013). In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ ;

Chicago Manual of Style (16th Edition):

Lee, Sue Hyun. “In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells.” 2013. Masters Thesis, Vanderbilt University. Accessed August 17, 2019. http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ ;.

MLA Handbook (7th Edition):

Lee, Sue Hyun. “In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells.” 2013. Web. 17 Aug 2019.

Vancouver:

Lee SH. In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells. [Internet] [Masters thesis]. Vanderbilt University; 2013. [cited 2019 Aug 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ ;.

Council of Science Editors:

Lee SH. In Situ Crosslinkable Gelatin Hydrogels For Vasculogenic Delivery of Mesenchymal Stem Cells. [Masters Thesis]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-12062013-152551/ ;


Virginia Tech

11. Buchanan, Cara F. Shear Stress-Mediated Tumor-Endothelial Cross Talk Regulates the Angiogenic Potential of Breast Tumors In Vitro.

Degree: PhD, Biomedical Engineering, 2013, Virginia Tech

 The structural and functional abnormalities of the tumor vasculature generate regions of elevated interstitial fluid pressure and aberrant flow shear stress within the tumor microenvironment.… (more)

Subjects/Keywords: Tissue Engineering; Cancer Biology; Microfluidics; Angiogenesis

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APA (6th Edition):

Buchanan, C. F. (2013). Shear Stress-Mediated Tumor-Endothelial Cross Talk Regulates the Angiogenic Potential of Breast Tumors In Vitro. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/50604

Chicago Manual of Style (16th Edition):

Buchanan, Cara F. “Shear Stress-Mediated Tumor-Endothelial Cross Talk Regulates the Angiogenic Potential of Breast Tumors In Vitro.” 2013. Doctoral Dissertation, Virginia Tech. Accessed August 17, 2019. http://hdl.handle.net/10919/50604.

MLA Handbook (7th Edition):

Buchanan, Cara F. “Shear Stress-Mediated Tumor-Endothelial Cross Talk Regulates the Angiogenic Potential of Breast Tumors In Vitro.” 2013. Web. 17 Aug 2019.

Vancouver:

Buchanan CF. Shear Stress-Mediated Tumor-Endothelial Cross Talk Regulates the Angiogenic Potential of Breast Tumors In Vitro. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/10919/50604.

Council of Science Editors:

Buchanan CF. Shear Stress-Mediated Tumor-Endothelial Cross Talk Regulates the Angiogenic Potential of Breast Tumors In Vitro. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/50604


Virginia Tech

12. Szot, Christopher Sang. A three-dimensional in vitro tumor model representative of the in vivo tumor microenvironment.

Degree: PhD, Biomedical Engineering, 2013, Virginia Tech

 The inability to accurately reproduce the complexities of the in vivo tumor microenvironment with reductionist-based two-dimensional in vitro cell culture models has been a notable… (more)

Subjects/Keywords: tissue engineering; co-culture; collagen I hydrogel; cancer; angiogenesis

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APA (6th Edition):

Szot, C. S. (2013). A three-dimensional in vitro tumor model representative of the in vivo tumor microenvironment. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/49597

Chicago Manual of Style (16th Edition):

Szot, Christopher Sang. “A three-dimensional in vitro tumor model representative of the in vivo tumor microenvironment.” 2013. Doctoral Dissertation, Virginia Tech. Accessed August 17, 2019. http://hdl.handle.net/10919/49597.

MLA Handbook (7th Edition):

Szot, Christopher Sang. “A three-dimensional in vitro tumor model representative of the in vivo tumor microenvironment.” 2013. Web. 17 Aug 2019.

Vancouver:

Szot CS. A three-dimensional in vitro tumor model representative of the in vivo tumor microenvironment. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/10919/49597.

Council of Science Editors:

Szot CS. A three-dimensional in vitro tumor model representative of the in vivo tumor microenvironment. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/49597


University of Florida

13. Cambiaghi, Alice. Development of a 3-D in Vitro Angiogenesis Assay Using Gelatin Microparticles for Controlled Release of Placental Extract.

Degree: MS, Biomedical Engineering, 2013, University of Florida

Subjects/Keywords: Angiogenesis; Blood vessels; Cells; Collagens; Endothelial cells; Gelatins; In vitro fertilization; Inoculation; Placenta; Tissue engineering; angiogenesis; microparticles; placentalextract

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APA (6th Edition):

Cambiaghi, A. (2013). Development of a 3-D in Vitro Angiogenesis Assay Using Gelatin Microparticles for Controlled Release of Placental Extract. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045972

Chicago Manual of Style (16th Edition):

Cambiaghi, Alice. “Development of a 3-D in Vitro Angiogenesis Assay Using Gelatin Microparticles for Controlled Release of Placental Extract.” 2013. Masters Thesis, University of Florida. Accessed August 17, 2019. http://ufdc.ufl.edu/UFE0045972.

MLA Handbook (7th Edition):

Cambiaghi, Alice. “Development of a 3-D in Vitro Angiogenesis Assay Using Gelatin Microparticles for Controlled Release of Placental Extract.” 2013. Web. 17 Aug 2019.

Vancouver:

Cambiaghi A. Development of a 3-D in Vitro Angiogenesis Assay Using Gelatin Microparticles for Controlled Release of Placental Extract. [Internet] [Masters thesis]. University of Florida; 2013. [cited 2019 Aug 17]. Available from: http://ufdc.ufl.edu/UFE0045972.

Council of Science Editors:

Cambiaghi A. Development of a 3-D in Vitro Angiogenesis Assay Using Gelatin Microparticles for Controlled Release of Placental Extract. [Masters Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045972


University of Florida

14. Moore, Marc C. Modulation of Nutrient Deficiencies Occurring in Engineered Ex Vivo Tissue Scaffolds.

Degree: PhD, Biomedical Engineering, 2013, University of Florida

Subjects/Keywords: Angiogenesis; Cell growth; Cells; Cultured cells; Endothelial cells; Nutrients; Oxygen; Placenta; Scaffolds; Tissue engineering; delivery; engineering; graft; human; mass; nutrient; scaffold; tissue; transfer; umbilical; vascular; vein

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APA (6th Edition):

Moore, M. C. (2013). Modulation of Nutrient Deficiencies Occurring in Engineered Ex Vivo Tissue Scaffolds. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0045157

Chicago Manual of Style (16th Edition):

Moore, Marc C. “Modulation of Nutrient Deficiencies Occurring in Engineered Ex Vivo Tissue Scaffolds.” 2013. Doctoral Dissertation, University of Florida. Accessed August 17, 2019. http://ufdc.ufl.edu/UFE0045157.

MLA Handbook (7th Edition):

Moore, Marc C. “Modulation of Nutrient Deficiencies Occurring in Engineered Ex Vivo Tissue Scaffolds.” 2013. Web. 17 Aug 2019.

Vancouver:

Moore MC. Modulation of Nutrient Deficiencies Occurring in Engineered Ex Vivo Tissue Scaffolds. [Internet] [Doctoral dissertation]. University of Florida; 2013. [cited 2019 Aug 17]. Available from: http://ufdc.ufl.edu/UFE0045157.

Council of Science Editors:

Moore MC. Modulation of Nutrient Deficiencies Occurring in Engineered Ex Vivo Tissue Scaffolds. [Doctoral Dissertation]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/UFE0045157

15. Ceccarelli, Jacob. Understanding the Effects of Cyclic Strain on Angiogenesis.

Degree: PhD, Biomedical Engineering, 2013, University of Michigan

 The size of engineered tissues is currently limited by oxygen diffusion. Vascularization of these constructs could alleviate this problem if the cues that control blood… (more)

Subjects/Keywords: Angiogenesis; Mechanobiology; Extracellular Matrix; Polydimethylsiloxane; Fibrin; Traction Forces; Biomedical Engineering; Engineering

…68 Figure 3-1. Effects of cyclic strain on angiogenesis… …72 Figure 3-2. Effects of a change in strain regimen on angiogenesis. .......... 74 Figure… …3-3. Confocal reflectance images of the fibrin matrix at days 2-5 of the angiogenesis… …responsible for directional angiogenesis in response to strain. xii Chapter 1 Introduction 1.1… …have met with less success. 1.2 Angiogenesis and Vascularization of Engineered Tissues There… 

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APA (6th Edition):

Ceccarelli, J. (2013). Understanding the Effects of Cyclic Strain on Angiogenesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102453

Chicago Manual of Style (16th Edition):

Ceccarelli, Jacob. “Understanding the Effects of Cyclic Strain on Angiogenesis.” 2013. Doctoral Dissertation, University of Michigan. Accessed August 17, 2019. http://hdl.handle.net/2027.42/102453.

MLA Handbook (7th Edition):

Ceccarelli, Jacob. “Understanding the Effects of Cyclic Strain on Angiogenesis.” 2013. Web. 17 Aug 2019.

Vancouver:

Ceccarelli J. Understanding the Effects of Cyclic Strain on Angiogenesis. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/2027.42/102453.

Council of Science Editors:

Ceccarelli J. Understanding the Effects of Cyclic Strain on Angiogenesis. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102453


Vanderbilt University

16. Irvin, Michael Warren. Angiogenic outgrowth from a perfused vascular explant: design and implementation of a perfused vascular explant bioreactor.

Degree: MS, Biomedical Engineering, 2012, Vanderbilt University

 This project is concerned with in vitro assays of angiogenesis and how mechanical stimuli are controllably incorporated into them. The vascular explant assay is considered… (more)

Subjects/Keywords: perfusion; organ explant cultures; assay; mechanical stimuli; bioreactor; angiogenesis

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APA (6th Edition):

Irvin, M. W. (2012). Angiogenic outgrowth from a perfused vascular explant: design and implementation of a perfused vascular explant bioreactor. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-01172012-172925/ ;

Chicago Manual of Style (16th Edition):

Irvin, Michael Warren. “Angiogenic outgrowth from a perfused vascular explant: design and implementation of a perfused vascular explant bioreactor.” 2012. Masters Thesis, Vanderbilt University. Accessed August 17, 2019. http://etd.library.vanderbilt.edu//available/etd-01172012-172925/ ;.

MLA Handbook (7th Edition):

Irvin, Michael Warren. “Angiogenic outgrowth from a perfused vascular explant: design and implementation of a perfused vascular explant bioreactor.” 2012. Web. 17 Aug 2019.

Vancouver:

Irvin MW. Angiogenic outgrowth from a perfused vascular explant: design and implementation of a perfused vascular explant bioreactor. [Internet] [Masters thesis]. Vanderbilt University; 2012. [cited 2019 Aug 17]. Available from: http://etd.library.vanderbilt.edu//available/etd-01172012-172925/ ;.

Council of Science Editors:

Irvin MW. Angiogenic outgrowth from a perfused vascular explant: design and implementation of a perfused vascular explant bioreactor. [Masters Thesis]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu//available/etd-01172012-172925/ ;


Virginia Commonwealth University

17. Garg, Koyal. REGENERATION OF ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS: A PHENOMENON ASSOCIATED WITH VASCULAR GRAFT PROPERTIES AND MACROPHAGE PHENOTYPES (M1/M2).

Degree: PhD, Biomedical Engineering, 2012, Virginia Commonwealth University

  Macrophages (MФ) and mast cells are important cell types in the context of tissue remodeling and regeneration. Mast cells participate in the early stages… (more)

Subjects/Keywords: Macrophages; electrospinning; angiogenesis; mast cells; Biomedical Engineering and Bioengineering; Engineering

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APA (6th Edition):

Garg, K. (2012). REGENERATION OF ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS: A PHENOMENON ASSOCIATED WITH VASCULAR GRAFT PROPERTIES AND MACROPHAGE PHENOTYPES (M1/M2). (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/404

Chicago Manual of Style (16th Edition):

Garg, Koyal. “REGENERATION OF ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS: A PHENOMENON ASSOCIATED WITH VASCULAR GRAFT PROPERTIES AND MACROPHAGE PHENOTYPES (M1/M2).” 2012. Doctoral Dissertation, Virginia Commonwealth University. Accessed August 17, 2019. https://scholarscompass.vcu.edu/etd/404.

MLA Handbook (7th Edition):

Garg, Koyal. “REGENERATION OF ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS: A PHENOMENON ASSOCIATED WITH VASCULAR GRAFT PROPERTIES AND MACROPHAGE PHENOTYPES (M1/M2).” 2012. Web. 17 Aug 2019.

Vancouver:

Garg K. REGENERATION OF ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS: A PHENOMENON ASSOCIATED WITH VASCULAR GRAFT PROPERTIES AND MACROPHAGE PHENOTYPES (M1/M2). [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2012. [cited 2019 Aug 17]. Available from: https://scholarscompass.vcu.edu/etd/404.

Council of Science Editors:

Garg K. REGENERATION OF ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS: A PHENOMENON ASSOCIATED WITH VASCULAR GRAFT PROPERTIES AND MACROPHAGE PHENOTYPES (M1/M2). [Doctoral Dissertation]. Virginia Commonwealth University; 2012. Available from: https://scholarscompass.vcu.edu/etd/404

18. Grainger, Stephanie Jo. Engineering Functional Capillary Networks.

Degree: PhD, Biomedical Engineering, 2012, University of Michigan

 A major translational challenge in the fields of therapeutic angiogenesis and tissue engineering is the ability to form functional networks of blood vessels. Cell-based strategies… (more)

Subjects/Keywords: Angiogenesis; Stem Cells; Capillary Morphogenesis; Biomedical Engineering; Engineering

…challenge in the fields of therapeutic angiogenesis and tissue engineering is the ability to form… …angiogenesis, is a complex process that is difficult to control.(7) Several pro-angiogenic… …angiogenesis via the plasminogen activator-plasmin axis. Based on these cues from previous work, the… …peripheral ischemic diseases could also benefit from therapeutic angiogenesis or treatment with… …angiogenesis. If the matrix is incomplete or lacking one or more key components, the resulting 10… 

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APA (6th Edition):

Grainger, S. J. (2012). Engineering Functional Capillary Networks. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/91412

Chicago Manual of Style (16th Edition):

Grainger, Stephanie Jo. “Engineering Functional Capillary Networks.” 2012. Doctoral Dissertation, University of Michigan. Accessed August 17, 2019. http://hdl.handle.net/2027.42/91412.

MLA Handbook (7th Edition):

Grainger, Stephanie Jo. “Engineering Functional Capillary Networks.” 2012. Web. 17 Aug 2019.

Vancouver:

Grainger SJ. Engineering Functional Capillary Networks. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/2027.42/91412.

Council of Science Editors:

Grainger SJ. Engineering Functional Capillary Networks. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/91412

19. Ngangan, Alyssa V. Bioactive factors secreted by differentiating embryonic stem cells.

Degree: PhD, Biomedical Engineering, 2011, Georgia Tech

 Current therapeutic strategies to stimulate endogenous angiogenic processes within injured tissue areas are typically based on introducing exogenous pro-angiogenic molecules or cell populations. Stem cell… (more)

Subjects/Keywords: Angiogenesis; Extracellular matrix; Growth factors; Embryonic stem cells; Stem cells; Stem cells Research; Embryonic stem cells Research; Neovascularization

…stem cells 9 Angiogenesis 10 Models to study angiogenesis 10 Angiogenic therapies and… …growth factors 13 Angiogenesis and the ECM 14 Acellular Matrices 15 Methods for… …ANGIOGENESIS 116 Introduction 116 Methods 118 Cell culture 118 Acellularization of EBs 120… …Vascular endothelial growth factor xviii SUMMARY Angiogenesis is the biological process… …transiently induce endogenous angiogenesis of tissues undergoing regeneration. Early differentiating… 

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APA (6th Edition):

Ngangan, A. V. (2011). Bioactive factors secreted by differentiating embryonic stem cells. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/44913

Chicago Manual of Style (16th Edition):

Ngangan, Alyssa V. “Bioactive factors secreted by differentiating embryonic stem cells.” 2011. Doctoral Dissertation, Georgia Tech. Accessed August 17, 2019. http://hdl.handle.net/1853/44913.

MLA Handbook (7th Edition):

Ngangan, Alyssa V. “Bioactive factors secreted by differentiating embryonic stem cells.” 2011. Web. 17 Aug 2019.

Vancouver:

Ngangan AV. Bioactive factors secreted by differentiating embryonic stem cells. [Internet] [Doctoral dissertation]. Georgia Tech; 2011. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1853/44913.

Council of Science Editors:

Ngangan AV. Bioactive factors secreted by differentiating embryonic stem cells. [Doctoral Dissertation]. Georgia Tech; 2011. Available from: http://hdl.handle.net/1853/44913


Vanderbilt University

20. Zachman, Angela Laurie. Parsing Inflammatory Cues in Angiogenesis using Bioactive Hydrogels.

Degree: MS, Biomedical Engineering, 2011, Vanderbilt University

 Both angiogenesis and inflammation are inescapable in vivo responses to any type of biomaterials implanted for regeneration. Continuous progress has been made in biomaterial design… (more)

Subjects/Keywords: scaffold; hydrogel; inflammation; angiogenesis

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APA (6th Edition):

Zachman, A. L. (2011). Parsing Inflammatory Cues in Angiogenesis using Bioactive Hydrogels. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-04042011-140317/ ;

Chicago Manual of Style (16th Edition):

Zachman, Angela Laurie. “Parsing Inflammatory Cues in Angiogenesis using Bioactive Hydrogels.” 2011. Masters Thesis, Vanderbilt University. Accessed August 17, 2019. http://etd.library.vanderbilt.edu/available/etd-04042011-140317/ ;.

MLA Handbook (7th Edition):

Zachman, Angela Laurie. “Parsing Inflammatory Cues in Angiogenesis using Bioactive Hydrogels.” 2011. Web. 17 Aug 2019.

Vancouver:

Zachman AL. Parsing Inflammatory Cues in Angiogenesis using Bioactive Hydrogels. [Internet] [Masters thesis]. Vanderbilt University; 2011. [cited 2019 Aug 17]. Available from: http://etd.library.vanderbilt.edu/available/etd-04042011-140317/ ;.

Council of Science Editors:

Zachman AL. Parsing Inflammatory Cues in Angiogenesis using Bioactive Hydrogels. [Masters Thesis]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-04042011-140317/ ;

21. Robinson, Scott Thomas. Determining the role of endothelial progenitor cells in post-natal neovascularization.

Degree: PhD, Biomedical Engineering, 2010, Georgia Tech

 Endothelial Progenitor Cells (EPCs) were first identified from human blood samples as a population of circulating mononuclear cells capable of displaying a mature endothelial cell… (more)

Subjects/Keywords: Endothelial progenitor cell; Neovascularization; EPC; Angiogenesis; Blood-vessels Growth

…vessel growth was the result of two distinct processes: angiogenesis and arteriogenesis… …Angiogenesis consists of the generation of new blood vessels from the existing endothelial cells… …that VEGFinduced angiogenesis is often a consequence of tissue ischemia (6)… …experienced by endothelial cells as a result in increase in flow. B) Angiogenesis is the… …angiogenesis, wound healing, and hind limb ischemia (12), establishing the bone marrow… 

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APA (6th Edition):

Robinson, S. T. (2010). Determining the role of endothelial progenitor cells in post-natal neovascularization. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/37178

Chicago Manual of Style (16th Edition):

Robinson, Scott Thomas. “Determining the role of endothelial progenitor cells in post-natal neovascularization.” 2010. Doctoral Dissertation, Georgia Tech. Accessed August 17, 2019. http://hdl.handle.net/1853/37178.

MLA Handbook (7th Edition):

Robinson, Scott Thomas. “Determining the role of endothelial progenitor cells in post-natal neovascularization.” 2010. Web. 17 Aug 2019.

Vancouver:

Robinson ST. Determining the role of endothelial progenitor cells in post-natal neovascularization. [Internet] [Doctoral dissertation]. Georgia Tech; 2010. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1853/37178.

Council of Science Editors:

Robinson ST. Determining the role of endothelial progenitor cells in post-natal neovascularization. [Doctoral Dissertation]. Georgia Tech; 2010. Available from: http://hdl.handle.net/1853/37178


Virginia Tech

22. Lee, Won Hee. Molecular mechanisms of radiation-induced brain injury.

Degree: PhD, Biomedical Engineering, 2010, Virginia Tech

 Radiation therapy has been most commonly used modality in the treatment of brain tumors. About 200,000 patients with brain tumors are treated with either partial… (more)

Subjects/Keywords: angiogenesis; aging; brain inflammation; extracellular matrix; Whole brain irradiation

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APA (6th Edition):

Lee, W. H. (2010). Molecular mechanisms of radiation-induced brain injury. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77254

Chicago Manual of Style (16th Edition):

Lee, Won Hee. “Molecular mechanisms of radiation-induced brain injury.” 2010. Doctoral Dissertation, Virginia Tech. Accessed August 17, 2019. http://hdl.handle.net/10919/77254.

MLA Handbook (7th Edition):

Lee, Won Hee. “Molecular mechanisms of radiation-induced brain injury.” 2010. Web. 17 Aug 2019.

Vancouver:

Lee WH. Molecular mechanisms of radiation-induced brain injury. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/10919/77254.

Council of Science Editors:

Lee WH. Molecular mechanisms of radiation-induced brain injury. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/77254


University of Florida

23. Wankhede, Mamta. Spectral Imaging Based in Vivo Model System for Characterization of Tumor Microvessel Response to Vascular Targeting Agents.

Degree: PhD, Biomedical Engineering, 2010, University of Florida

 SPECTRAL IMAGING BASED MODEL IN VIVO SYSTEM FOR CHARACTERIZATION OF TUMOR MICROVESSEL RESPONSE TO VASCULAR TARGETING AGENTS Functional vasculature is vital for tumor growth, proliferation,… (more)

Subjects/Keywords: Angiogenesis; Blood vessels; Cancer; Cardiovascular system; Hemoglobins; Imaging; Microvessels; Tissue oxygenation; Tumors; Venules; 4t1, antiangiogenic, avastin, caki1, chamber, characterization, dorsal, hbsat, hemoglobin, imaging, microvasculature, oxi4503, oxygenation, saturation, skinflap, spectral, targeting, therapeutics, tumor, vasculature, vda, vta, window

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APA (6th Edition):

Wankhede, M. (2010). Spectral Imaging Based in Vivo Model System for Characterization of Tumor Microvessel Response to Vascular Targeting Agents. (Doctoral Dissertation). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042528

Chicago Manual of Style (16th Edition):

Wankhede, Mamta. “Spectral Imaging Based in Vivo Model System for Characterization of Tumor Microvessel Response to Vascular Targeting Agents.” 2010. Doctoral Dissertation, University of Florida. Accessed August 17, 2019. http://ufdc.ufl.edu/UFE0042528.

MLA Handbook (7th Edition):

Wankhede, Mamta. “Spectral Imaging Based in Vivo Model System for Characterization of Tumor Microvessel Response to Vascular Targeting Agents.” 2010. Web. 17 Aug 2019.

Vancouver:

Wankhede M. Spectral Imaging Based in Vivo Model System for Characterization of Tumor Microvessel Response to Vascular Targeting Agents. [Internet] [Doctoral dissertation]. University of Florida; 2010. [cited 2019 Aug 17]. Available from: http://ufdc.ufl.edu/UFE0042528.

Council of Science Editors:

Wankhede M. Spectral Imaging Based in Vivo Model System for Characterization of Tumor Microvessel Response to Vascular Targeting Agents. [Doctoral Dissertation]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042528


Washington University in St. Louis

24. McKenzie, Jennifer. Investigations into the Ulnar Response to Mechanical Stimuli Activating Lamellar and Woven Bone Formation.

Degree: PhD, Biomedical Engineering, 2009, Washington University in St. Louis

 Woven and lamellar bone formation can be stimulated using mechanical loading. Woven bone forms rapidly in response to damaging loading in a disorganized manner with… (more)

Subjects/Keywords: Biomechanics; Engineering, Biomedical; angiogenesis, gene expression, lamellar bone, microarray, ulna loading, woven bone

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APA (6th Edition):

McKenzie, J. (2009). Investigations into the Ulnar Response to Mechanical Stimuli Activating Lamellar and Woven Bone Formation. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/417

Chicago Manual of Style (16th Edition):

McKenzie, Jennifer. “Investigations into the Ulnar Response to Mechanical Stimuli Activating Lamellar and Woven Bone Formation.” 2009. Doctoral Dissertation, Washington University in St. Louis. Accessed August 17, 2019. https://openscholarship.wustl.edu/etd/417.

MLA Handbook (7th Edition):

McKenzie, Jennifer. “Investigations into the Ulnar Response to Mechanical Stimuli Activating Lamellar and Woven Bone Formation.” 2009. Web. 17 Aug 2019.

Vancouver:

McKenzie J. Investigations into the Ulnar Response to Mechanical Stimuli Activating Lamellar and Woven Bone Formation. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2009. [cited 2019 Aug 17]. Available from: https://openscholarship.wustl.edu/etd/417.

Council of Science Editors:

McKenzie J. Investigations into the Ulnar Response to Mechanical Stimuli Activating Lamellar and Woven Bone Formation. [Doctoral Dissertation]. Washington University in St. Louis; 2009. Available from: https://openscholarship.wustl.edu/etd/417


Virginia Commonwealth University

25. Garg, Koyal. ANGIOGENIC POTENTIAL OF HUMAN MACROPHAGES ON ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS.

Degree: MS, Biomedical Engineering, 2008, Virginia Commonwealth University

 The aim of this study was to investigate macrophage interactions with electrospun scaffolds and quantify the expression of vital angiogenic growth factors in vitro. This… (more)

Subjects/Keywords: Angiogenesis; electrospinning; macrophages; biomaterials; Biomedical Engineering and Bioengineering; Engineering

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APA (6th Edition):

Garg, K. (2008). ANGIOGENIC POTENTIAL OF HUMAN MACROPHAGES ON ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1652

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Garg, Koyal. “ANGIOGENIC POTENTIAL OF HUMAN MACROPHAGES ON ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS.” 2008. Thesis, Virginia Commonwealth University. Accessed August 17, 2019. https://scholarscompass.vcu.edu/etd/1652.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Garg, Koyal. “ANGIOGENIC POTENTIAL OF HUMAN MACROPHAGES ON ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS.” 2008. Web. 17 Aug 2019.

Vancouver:

Garg K. ANGIOGENIC POTENTIAL OF HUMAN MACROPHAGES ON ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS. [Internet] [Thesis]. Virginia Commonwealth University; 2008. [cited 2019 Aug 17]. Available from: https://scholarscompass.vcu.edu/etd/1652.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Garg K. ANGIOGENIC POTENTIAL OF HUMAN MACROPHAGES ON ELECTROSPUN BIORESORBABLE VASCULAR GRAFTS. [Thesis]. Virginia Commonwealth University; 2008. Available from: https://scholarscompass.vcu.edu/etd/1652

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Georgia Tech

26. Tressel, Sarah Lynne. Role of shear stress in angiopoietin-2-dependent neovascularization: implications in occlusive vascular disease and atherosclerosis.

Degree: PhD, Biomedical Engineering, 2008, Georgia Tech

 Neovascularization, or the formation of blood vessels, is important in both normal physiological processes as well as pathophysiological processes. The main players in neovascularization, endothelial… (more)

Subjects/Keywords: Hindlimb ischemia; Endothelial cells; Arteriogenesis; Shear stress; Angiopoietin-2; Angiogenesis; Vascular endothelium; Blood-vessels Growth; Shear flow; Neovascularization

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APA (6th Edition):

Tressel, S. L. (2008). Role of shear stress in angiopoietin-2-dependent neovascularization: implications in occlusive vascular disease and atherosclerosis. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/22646

Chicago Manual of Style (16th Edition):

Tressel, Sarah Lynne. “Role of shear stress in angiopoietin-2-dependent neovascularization: implications in occlusive vascular disease and atherosclerosis.” 2008. Doctoral Dissertation, Georgia Tech. Accessed August 17, 2019. http://hdl.handle.net/1853/22646.

MLA Handbook (7th Edition):

Tressel, Sarah Lynne. “Role of shear stress in angiopoietin-2-dependent neovascularization: implications in occlusive vascular disease and atherosclerosis.” 2008. Web. 17 Aug 2019.

Vancouver:

Tressel SL. Role of shear stress in angiopoietin-2-dependent neovascularization: implications in occlusive vascular disease and atherosclerosis. [Internet] [Doctoral dissertation]. Georgia Tech; 2008. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1853/22646.

Council of Science Editors:

Tressel SL. Role of shear stress in angiopoietin-2-dependent neovascularization: implications in occlusive vascular disease and atherosclerosis. [Doctoral Dissertation]. Georgia Tech; 2008. Available from: http://hdl.handle.net/1853/22646


University of Florida

27. Wankhede, Mamta. Spectral Imaging of Tumor Microvascular Oxygenation Changes after Administration of Vascular Disrupting Agent OXi4503.

Degree: MS, Biomedical Engineering, 2008, University of Florida

 Vascular disrupting agent-induced alterations in tumor and normal tissue vasculature are essential parameters for the assessment of drug-efficacy and its effect on combinatorial cancer therapies.… (more)

Subjects/Keywords: Angiogenesis; Cancer; Carcinoma; Cardiovascular system; Cell lines; Hemoglobins; Imaging; Perfusion; Tissue oxygenation; Tumors; chamber, disrupting, hemoglobin, hyperspectral, model, oxi4503, saturation, spectral, targeting, tumor, vasculature, vessel, window

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APA (6th Edition):

Wankhede, M. (2008). Spectral Imaging of Tumor Microvascular Oxygenation Changes after Administration of Vascular Disrupting Agent OXi4503. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0022689

Chicago Manual of Style (16th Edition):

Wankhede, Mamta. “Spectral Imaging of Tumor Microvascular Oxygenation Changes after Administration of Vascular Disrupting Agent OXi4503.” 2008. Masters Thesis, University of Florida. Accessed August 17, 2019. http://ufdc.ufl.edu/UFE0022689.

MLA Handbook (7th Edition):

Wankhede, Mamta. “Spectral Imaging of Tumor Microvascular Oxygenation Changes after Administration of Vascular Disrupting Agent OXi4503.” 2008. Web. 17 Aug 2019.

Vancouver:

Wankhede M. Spectral Imaging of Tumor Microvascular Oxygenation Changes after Administration of Vascular Disrupting Agent OXi4503. [Internet] [Masters thesis]. University of Florida; 2008. [cited 2019 Aug 17]. Available from: http://ufdc.ufl.edu/UFE0022689.

Council of Science Editors:

Wankhede M. Spectral Imaging of Tumor Microvascular Oxygenation Changes after Administration of Vascular Disrupting Agent OXi4503. [Masters Thesis]. University of Florida; 2008. Available from: http://ufdc.ufl.edu/UFE0022689


Georgia Tech

28. Duvall, Craig Lewis. The Role of Osteopontin in Postnatal Vascular Growth: Functional Effects in Ischemic Limb Collateral Vessel Formation and Long Bone Fracture Healing.

Degree: PhD, Biomedical Engineering, 2007, Georgia Tech

 Postnatal vascular growth is a complex process involving multiple cells types whose functionality is orchestrated by a variety of soluble extracellular growth factors, mechanical stimuli,… (more)

Subjects/Keywords: Angiogenesis; Arteriogenesis; Postnatal vascular growth; Osteopontin; Microcomputed tomography; Fracture healing; Bone; Biomechanics; Extracellular matrix; Vascular imaging

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APA (6th Edition):

Duvall, C. L. (2007). The Role of Osteopontin in Postnatal Vascular Growth: Functional Effects in Ischemic Limb Collateral Vessel Formation and Long Bone Fracture Healing. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/14567

Chicago Manual of Style (16th Edition):

Duvall, Craig Lewis. “The Role of Osteopontin in Postnatal Vascular Growth: Functional Effects in Ischemic Limb Collateral Vessel Formation and Long Bone Fracture Healing.” 2007. Doctoral Dissertation, Georgia Tech. Accessed August 17, 2019. http://hdl.handle.net/1853/14567.

MLA Handbook (7th Edition):

Duvall, Craig Lewis. “The Role of Osteopontin in Postnatal Vascular Growth: Functional Effects in Ischemic Limb Collateral Vessel Formation and Long Bone Fracture Healing.” 2007. Web. 17 Aug 2019.

Vancouver:

Duvall CL. The Role of Osteopontin in Postnatal Vascular Growth: Functional Effects in Ischemic Limb Collateral Vessel Formation and Long Bone Fracture Healing. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1853/14567.

Council of Science Editors:

Duvall CL. The Role of Osteopontin in Postnatal Vascular Growth: Functional Effects in Ischemic Limb Collateral Vessel Formation and Long Bone Fracture Healing. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/14567


Georgia Tech

29. Sung, Hak-Joon. Matrix Metalloproteinase 9 (MMP-9) and Biodegradable Polymers in the Engineering of a Vascular Construct.

Degree: PhD, Biomedical Engineering, 2004, Georgia Tech

 The role of matrix metalloproteinase (MMP)-9 and processing conditions of biodegradable polymer scaffolds has been investigated to optimize engineering vascular constructs. For a small diameter… (more)

Subjects/Keywords: Combinatorial biosurface chip; Biomaterials; Tissue engineering; Vascular construct; Biodegradable polymers; MMP-9; Angiogenesis; Vascular grafts Materials; Tissue engineering; Neovascularization; Metalloproteinases

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APA (6th Edition):

Sung, H. (2004). Matrix Metalloproteinase 9 (MMP-9) and Biodegradable Polymers in the Engineering of a Vascular Construct. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/5106

Chicago Manual of Style (16th Edition):

Sung, Hak-Joon. “Matrix Metalloproteinase 9 (MMP-9) and Biodegradable Polymers in the Engineering of a Vascular Construct.” 2004. Doctoral Dissertation, Georgia Tech. Accessed August 17, 2019. http://hdl.handle.net/1853/5106.

MLA Handbook (7th Edition):

Sung, Hak-Joon. “Matrix Metalloproteinase 9 (MMP-9) and Biodegradable Polymers in the Engineering of a Vascular Construct.” 2004. Web. 17 Aug 2019.

Vancouver:

Sung H. Matrix Metalloproteinase 9 (MMP-9) and Biodegradable Polymers in the Engineering of a Vascular Construct. [Internet] [Doctoral dissertation]. Georgia Tech; 2004. [cited 2019 Aug 17]. Available from: http://hdl.handle.net/1853/5106.

Council of Science Editors:

Sung H. Matrix Metalloproteinase 9 (MMP-9) and Biodegradable Polymers in the Engineering of a Vascular Construct. [Doctoral Dissertation]. Georgia Tech; 2004. Available from: http://hdl.handle.net/1853/5106

.