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You searched for subject:(Chondrogenesis). Showing records 1 – 30 of 104 total matches.

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California State University – East Bay

1. Rath, Madhusikta. The Role of DNA Demethylation During Chondrogenesis.

Degree: 2013, California State University – East Bay

This thesis aims to study the role of 5-hydroxymethylation during chondrocyte differentiation. Understanding the mechanisms of the DNA demethylation machinery via this process during chondrogenesis will lead to a variety of possibilities for targeted therapeutic approaches. Advisors/Committee Members: Curr, Dr. Kenneth (advisor), Bhutani, Dr. Nidhi (primaryAdvisor).

Subjects/Keywords: Chondrogenesis

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APA (6th Edition):

Rath, M. (2013). The Role of DNA Demethylation During Chondrogenesis. (Thesis). California State University – East Bay. Retrieved from http://hdl.handle.net/10211.5/70

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):

Rath, Madhusikta. “The Role of DNA Demethylation During Chondrogenesis.” 2013. Thesis, California State University – East Bay. Accessed July 19, 2019. http://hdl.handle.net/10211.5/70.

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

MLA Handbook (7th Edition):

Rath, Madhusikta. “The Role of DNA Demethylation During Chondrogenesis.” 2013. Web. 19 Jul 2019.

Vancouver:

Rath M. The Role of DNA Demethylation During Chondrogenesis. [Internet] [Thesis]. California State University – East Bay; 2013. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10211.5/70.

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

Council of Science Editors:

Rath M. The Role of DNA Demethylation During Chondrogenesis. [Thesis]. California State University – East Bay; 2013. Available from: http://hdl.handle.net/10211.5/70

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


University of Hong Kong

2. Tam, Wai-kit. Role of hypoxia inducible factor-alpha (HIF-α) genes inchondrogenesis.

Degree: PhD, 2012, University of Hong Kong

Cartilage is an essential skeletal connective tissue in vertebrates. It comprises extracellular matrix components, especially for collagens and proteoglycans. Once the cartilage is damaged, it… (more)

Subjects/Keywords: Chondrogenesis.; Anoxemia.

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APA (6th Edition):

Tam, W. (2012). Role of hypoxia inducible factor-alpha (HIF-α) genes inchondrogenesis. (Doctoral Dissertation). University of Hong Kong. Retrieved from Tam, W. [譚偉傑]. (2012). Role of hypoxia inducible factor-alpha (HIF-α) genes in chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784977 ; http://dx.doi.org/10.5353/th_b4784977 ; http://hdl.handle.net/10722/174535

Chicago Manual of Style (16th Edition):

Tam, Wai-kit. “Role of hypoxia inducible factor-alpha (HIF-α) genes inchondrogenesis.” 2012. Doctoral Dissertation, University of Hong Kong. Accessed July 19, 2019. Tam, W. [譚偉傑]. (2012). Role of hypoxia inducible factor-alpha (HIF-α) genes in chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784977 ; http://dx.doi.org/10.5353/th_b4784977 ; http://hdl.handle.net/10722/174535.

MLA Handbook (7th Edition):

Tam, Wai-kit. “Role of hypoxia inducible factor-alpha (HIF-α) genes inchondrogenesis.” 2012. Web. 19 Jul 2019.

Vancouver:

Tam W. Role of hypoxia inducible factor-alpha (HIF-α) genes inchondrogenesis. [Internet] [Doctoral dissertation]. University of Hong Kong; 2012. [cited 2019 Jul 19]. Available from: Tam, W. [譚偉傑]. (2012). Role of hypoxia inducible factor-alpha (HIF-α) genes in chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784977 ; http://dx.doi.org/10.5353/th_b4784977 ; http://hdl.handle.net/10722/174535.

Council of Science Editors:

Tam W. Role of hypoxia inducible factor-alpha (HIF-α) genes inchondrogenesis. [Doctoral Dissertation]. University of Hong Kong; 2012. Available from: Tam, W. [譚偉傑]. (2012). Role of hypoxia inducible factor-alpha (HIF-α) genes in chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4784977 ; http://dx.doi.org/10.5353/th_b4784977 ; http://hdl.handle.net/10722/174535


East Carolina University

3. Iyengar, Sheelah. Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid.

Degree: 2012, East Carolina University

 The chondroitin sulfate antigens d1C4 and TC2 have been hypothesized to play a role in cartilage differentiation in the limb and early morphogenesis of the… (more)

Subjects/Keywords: Biology; Chondrogenesis; Chondroitin sulfates; Proteoglycans

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APA (6th Edition):

Iyengar, S. (2012). Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4088

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):

Iyengar, Sheelah. “Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid.” 2012. Thesis, East Carolina University. Accessed July 19, 2019. http://hdl.handle.net/10342/4088.

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

MLA Handbook (7th Edition):

Iyengar, Sheelah. “Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid.” 2012. Web. 19 Jul 2019.

Vancouver:

Iyengar S. Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid. [Internet] [Thesis]. East Carolina University; 2012. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10342/4088.

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

Council of Science Editors:

Iyengar S. Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid. [Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4088

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


University of British Columbia

4. Karamboulas, Konstantina. Delineating the molecular mechanisms regulating chondrogenesis .

Degree: 2008, University of British Columbia

 Sox9, (SRY-type HMG box), has been shown to play a critical role throughout chondrogenesis. Haploinsufficiency of Sox9 in humans leads to a skeletal malformation syndrome… (more)

Subjects/Keywords: Chondrogenesis; Limb

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APA (6th Edition):

Karamboulas, K. (2008). Delineating the molecular mechanisms regulating chondrogenesis . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/811

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):

Karamboulas, Konstantina. “Delineating the molecular mechanisms regulating chondrogenesis .” 2008. Thesis, University of British Columbia. Accessed July 19, 2019. http://hdl.handle.net/2429/811.

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

MLA Handbook (7th Edition):

Karamboulas, Konstantina. “Delineating the molecular mechanisms regulating chondrogenesis .” 2008. Web. 19 Jul 2019.

Vancouver:

Karamboulas K. Delineating the molecular mechanisms regulating chondrogenesis . [Internet] [Thesis]. University of British Columbia; 2008. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2429/811.

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

Council of Science Editors:

Karamboulas K. Delineating the molecular mechanisms regulating chondrogenesis . [Thesis]. University of British Columbia; 2008. Available from: http://hdl.handle.net/2429/811

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


Drexel University

5. Chernets, Natalie. Enhancement of Skeletal Cell Differentiation by Microsecond Pulsed Dielectric Barrier Discharge.

Degree: 2014, Drexel University

 Plasma medicine, specifically non-thermal plasma (NT-plasma) technology, has clinical potential in medicine and biology, which has yet to be realized. Current concepts being tested range… (more)

Subjects/Keywords: Electrical engineering; Chondrogenesis; Dielectric devices

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APA (6th Edition):

Chernets, N. (2014). Enhancement of Skeletal Cell Differentiation by Microsecond Pulsed Dielectric Barrier Discharge. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7047

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):

Chernets, Natalie. “Enhancement of Skeletal Cell Differentiation by Microsecond Pulsed Dielectric Barrier Discharge.” 2014. Thesis, Drexel University. Accessed July 19, 2019. http://hdl.handle.net/1860/idea:7047.

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

MLA Handbook (7th Edition):

Chernets, Natalie. “Enhancement of Skeletal Cell Differentiation by Microsecond Pulsed Dielectric Barrier Discharge.” 2014. Web. 19 Jul 2019.

Vancouver:

Chernets N. Enhancement of Skeletal Cell Differentiation by Microsecond Pulsed Dielectric Barrier Discharge. [Internet] [Thesis]. Drexel University; 2014. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1860/idea:7047.

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

Council of Science Editors:

Chernets N. Enhancement of Skeletal Cell Differentiation by Microsecond Pulsed Dielectric Barrier Discharge. [Thesis]. Drexel University; 2014. Available from: http://hdl.handle.net/1860/idea:7047

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


Michigan State University

6. Oppermann, Dean Alan. P(dl)A/PGA/FE and P(dl)A/PGA/SmCo₅ composites for use as a delivery mechanism for magnetically directed chondrogenesis.

Degree: PhD, Department of Materials Science and Mechanics, 2000, Michigan State University

Subjects/Keywords: Chondrogenesis; Magnets

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APA (6th Edition):

Oppermann, D. A. (2000). P(dl)A/PGA/FE and P(dl)A/PGA/SmCo₅ composites for use as a delivery mechanism for magnetically directed chondrogenesis. (Doctoral Dissertation). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:30293

Chicago Manual of Style (16th Edition):

Oppermann, Dean Alan. “P(dl)A/PGA/FE and P(dl)A/PGA/SmCo₅ composites for use as a delivery mechanism for magnetically directed chondrogenesis.” 2000. Doctoral Dissertation, Michigan State University. Accessed July 19, 2019. http://etd.lib.msu.edu/islandora/object/etd:30293.

MLA Handbook (7th Edition):

Oppermann, Dean Alan. “P(dl)A/PGA/FE and P(dl)A/PGA/SmCo₅ composites for use as a delivery mechanism for magnetically directed chondrogenesis.” 2000. Web. 19 Jul 2019.

Vancouver:

Oppermann DA. P(dl)A/PGA/FE and P(dl)A/PGA/SmCo₅ composites for use as a delivery mechanism for magnetically directed chondrogenesis. [Internet] [Doctoral dissertation]. Michigan State University; 2000. [cited 2019 Jul 19]. Available from: http://etd.lib.msu.edu/islandora/object/etd:30293.

Council of Science Editors:

Oppermann DA. P(dl)A/PGA/FE and P(dl)A/PGA/SmCo₅ composites for use as a delivery mechanism for magnetically directed chondrogenesis. [Doctoral Dissertation]. Michigan State University; 2000. Available from: http://etd.lib.msu.edu/islandora/object/etd:30293


East Carolina University

7. Iyengar, Sheelah. Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid.

Degree: 2012, East Carolina University

 The chondroitin sulfate antigens d1C4 and TC2 have been hypothesized to play a role in cartilage differentiation in the limb and early morphogenesis of the… (more)

Subjects/Keywords: Chondrogenesis; Chondroitin sulfates; Proteoglycans

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APA (6th Edition):

Iyengar, S. (2012). Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid. (Masters Thesis). East Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14568

Chicago Manual of Style (16th Edition):

Iyengar, Sheelah. “Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid.” 2012. Masters Thesis, East Carolina University. Accessed July 19, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14568.

MLA Handbook (7th Edition):

Iyengar, Sheelah. “Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid.” 2012. Web. 19 Jul 2019.

Vancouver:

Iyengar S. Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2019 Jul 19]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14568.

Council of Science Editors:

Iyengar S. Spatio-Temporal Expression of Chondroitin Sulfate Antigens in Early Chick Pituitary and Thyroid. [Masters Thesis]. East Carolina University; 2012. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=14568


East Carolina University

8. Nagchowdhuri, Partha Sarathi. Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development.

Degree: 2012, East Carolina University

 The different mechanisms involved in vertebrate synovial joint development are actively being uncovered. A variety of studies have thus far discovered the involvement of several large molecules… (more)

Subjects/Keywords: Proteoglycans; Joints; Chondrogenesis; Embryology

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APA (6th Edition):

Nagchowdhuri, P. S. (2012). Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development. (Masters Thesis). East Carolina University. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13923

Chicago Manual of Style (16th Edition):

Nagchowdhuri, Partha Sarathi. “Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development.” 2012. Masters Thesis, East Carolina University. Accessed July 19, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13923.

MLA Handbook (7th Edition):

Nagchowdhuri, Partha Sarathi. “Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development.” 2012. Web. 19 Jul 2019.

Vancouver:

Nagchowdhuri PS. Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development. [Internet] [Masters thesis]. East Carolina University; 2012. [cited 2019 Jul 19]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13923.

Council of Science Editors:

Nagchowdhuri PS. Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development. [Masters Thesis]. East Carolina University; 2012. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=13923


University of Rochester

9. Kung, Ming Hsien; Zuscik, Michael J. Investigating the Molecular Mechanisms of Cigarette Smoke Inhibition of Fracture Healing.

Degree: PhD, 2012, University of Rochester

 There is strong clinical evidence of a link between smoking and impaired fracture healing. Despite much effort, the molecular mechanisms underlying these effects remain poorly… (more)

Subjects/Keywords: Fracture; Smoking; Cigarette; Chondrogenesis; AhR

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APA (6th Edition):

Kung, Ming Hsien; Zuscik, M. J. (2012). Investigating the Molecular Mechanisms of Cigarette Smoke Inhibition of Fracture Healing. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/19823

Chicago Manual of Style (16th Edition):

Kung, Ming Hsien; Zuscik, Michael J. “Investigating the Molecular Mechanisms of Cigarette Smoke Inhibition of Fracture Healing.” 2012. Doctoral Dissertation, University of Rochester. Accessed July 19, 2019. http://hdl.handle.net/1802/19823.

MLA Handbook (7th Edition):

Kung, Ming Hsien; Zuscik, Michael J. “Investigating the Molecular Mechanisms of Cigarette Smoke Inhibition of Fracture Healing.” 2012. Web. 19 Jul 2019.

Vancouver:

Kung, Ming Hsien; Zuscik MJ. Investigating the Molecular Mechanisms of Cigarette Smoke Inhibition of Fracture Healing. [Internet] [Doctoral dissertation]. University of Rochester; 2012. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1802/19823.

Council of Science Editors:

Kung, Ming Hsien; Zuscik MJ. Investigating the Molecular Mechanisms of Cigarette Smoke Inhibition of Fracture Healing. [Doctoral Dissertation]. University of Rochester; 2012. Available from: http://hdl.handle.net/1802/19823


University of Alberta

10. Yu, Hana. Enhancing chondrogenesis of mesenchymal stromal cells through anti-Thy1 strategies.

Degree: MS, Department of Surgery, 2014, University of Alberta

 The intricate arrangement and composition of articular cartilage confer the structure its unique material and mechanical properties. Degeneration of articular cartilage, especially osteoarthritis, imposes great… (more)

Subjects/Keywords: chondrogenesis; CD90; Thy-1; mesenchymal stem cells

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APA (6th Edition):

Yu, H. (2014). Enhancing chondrogenesis of mesenchymal stromal cells through anti-Thy1 strategies. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/wm117n98w

Chicago Manual of Style (16th Edition):

Yu, Hana. “Enhancing chondrogenesis of mesenchymal stromal cells through anti-Thy1 strategies.” 2014. Masters Thesis, University of Alberta. Accessed July 19, 2019. https://era.library.ualberta.ca/files/wm117n98w.

MLA Handbook (7th Edition):

Yu, Hana. “Enhancing chondrogenesis of mesenchymal stromal cells through anti-Thy1 strategies.” 2014. Web. 19 Jul 2019.

Vancouver:

Yu H. Enhancing chondrogenesis of mesenchymal stromal cells through anti-Thy1 strategies. [Internet] [Masters thesis]. University of Alberta; 2014. [cited 2019 Jul 19]. Available from: https://era.library.ualberta.ca/files/wm117n98w.

Council of Science Editors:

Yu H. Enhancing chondrogenesis of mesenchymal stromal cells through anti-Thy1 strategies. [Masters Thesis]. University of Alberta; 2014. Available from: https://era.library.ualberta.ca/files/wm117n98w


University of Hong Kong

11. Chan, Chun-leung, Sherwin. Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis.

Degree: M. Phil., 2010, University of Hong Kong

published_or_final_version

Biochemistry

Master

Master of Philosophy

Subjects/Keywords: Chondrogenesis.; Homeobox genes.

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APA (6th Edition):

Chan, Chun-leung, S. (2010). Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. (Masters Thesis). University of Hong Kong. Retrieved from Chan, C. S. [陳俊良]. (2010). Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4451553 ; http://dx.doi.org/10.5353/th_b4451553 ; http://hdl.handle.net/10722/128630

Chicago Manual of Style (16th Edition):

Chan, Chun-leung, Sherwin. “Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis.” 2010. Masters Thesis, University of Hong Kong. Accessed July 19, 2019. Chan, C. S. [陳俊良]. (2010). Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4451553 ; http://dx.doi.org/10.5353/th_b4451553 ; http://hdl.handle.net/10722/128630.

MLA Handbook (7th Edition):

Chan, Chun-leung, Sherwin. “Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis.” 2010. Web. 19 Jul 2019.

Vancouver:

Chan, Chun-leung S. Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. [Internet] [Masters thesis]. University of Hong Kong; 2010. [cited 2019 Jul 19]. Available from: Chan, C. S. [陳俊良]. (2010). Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4451553 ; http://dx.doi.org/10.5353/th_b4451553 ; http://hdl.handle.net/10722/128630.

Council of Science Editors:

Chan, Chun-leung S. Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. [Masters Thesis]. University of Hong Kong; 2010. Available from: Chan, C. S. [陳俊良]. (2010). Expression profiling and epigenetic regulation of Hox genes in cellular models of chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4451553 ; http://dx.doi.org/10.5353/th_b4451553 ; http://hdl.handle.net/10722/128630


Boston University

12. Burke, Elaine. The effects of age or sex on chondrogenesis of human MSCs.

Degree: MS, Medical Sciences, 2017, Boston University

 INTRODUCTION: Stem cells have become promising treatments for osteoarthritis due to the cells’ ability to regenerate cartilage and availability from bone marrow. Various studies have… (more)

Subjects/Keywords: Cellular biology; MSC; TGF; Age; Chondrogenesis; Differentiation

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APA (6th Edition):

Burke, E. (2017). The effects of age or sex on chondrogenesis of human MSCs. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/23744

Chicago Manual of Style (16th Edition):

Burke, Elaine. “The effects of age or sex on chondrogenesis of human MSCs.” 2017. Masters Thesis, Boston University. Accessed July 19, 2019. http://hdl.handle.net/2144/23744.

MLA Handbook (7th Edition):

Burke, Elaine. “The effects of age or sex on chondrogenesis of human MSCs.” 2017. Web. 19 Jul 2019.

Vancouver:

Burke E. The effects of age or sex on chondrogenesis of human MSCs. [Internet] [Masters thesis]. Boston University; 2017. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2144/23744.

Council of Science Editors:

Burke E. The effects of age or sex on chondrogenesis of human MSCs. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/23744


Columbia University

13. Li, Ang. Regulation of Chondrogenesis in Human Mesenchymal Stem Cells by Cartilage Extracellular Matrix and Therapeutic Applications.

Degree: 2018, Columbia University

 Cartilage has limited intrinsic healing potential upon injury, due to the low cell density and the lack of blood supply. Degenerative disease of the cartilage,… (more)

Subjects/Keywords: Biomedical engineering; Chondrogenesis; Cartilage; Extracellular matrix

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APA (6th Edition):

Li, A. (2018). Regulation of Chondrogenesis in Human Mesenchymal Stem Cells by Cartilage Extracellular Matrix and Therapeutic Applications. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8VH74XC

Chicago Manual of Style (16th Edition):

Li, Ang. “Regulation of Chondrogenesis in Human Mesenchymal Stem Cells by Cartilage Extracellular Matrix and Therapeutic Applications.” 2018. Doctoral Dissertation, Columbia University. Accessed July 19, 2019. https://doi.org/10.7916/D8VH74XC.

MLA Handbook (7th Edition):

Li, Ang. “Regulation of Chondrogenesis in Human Mesenchymal Stem Cells by Cartilage Extracellular Matrix and Therapeutic Applications.” 2018. Web. 19 Jul 2019.

Vancouver:

Li A. Regulation of Chondrogenesis in Human Mesenchymal Stem Cells by Cartilage Extracellular Matrix and Therapeutic Applications. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Jul 19]. Available from: https://doi.org/10.7916/D8VH74XC.

Council of Science Editors:

Li A. Regulation of Chondrogenesis in Human Mesenchymal Stem Cells by Cartilage Extracellular Matrix and Therapeutic Applications. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8VH74XC


Duke University

14. Adkar, Shaunak. Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling .

Degree: 2019, Duke University

  The differentiation of human induced pluripotent stem cells (hiPSCs) to prescribed cell fates enables the engineering of patient-specific tissue types, such as hyaline cartilage,… (more)

Subjects/Keywords: Cellular biology; Genetics; chondrogenesis; CRISPR; iPSC

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APA (6th Edition):

Adkar, S. (2019). Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/18649

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):

Adkar, Shaunak. “Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling .” 2019. Thesis, Duke University. Accessed July 19, 2019. http://hdl.handle.net/10161/18649.

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

MLA Handbook (7th Edition):

Adkar, Shaunak. “Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling .” 2019. Web. 19 Jul 2019.

Vancouver:

Adkar S. Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling . [Internet] [Thesis]. Duke University; 2019. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10161/18649.

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

Council of Science Editors:

Adkar S. Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/18649

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


University of Florida

15. Slota, Leslie. Deep conservation of the genetic program for cartilage development: the mechanism of invertebrate cartilage.

Degree: 2013, University of Florida

 Cartilage has been proposed to be a defining character of vertebrates, however this tissue type has evolved independently in a number of invertebrate lineages, including… (more)

Subjects/Keywords: Arthropods; Cartilage; Cephalopods; Chondrogenesis; Collagens; Extracellular matrix; Horseshoe crabs; Invertebrates; Vertebrates; Worms; Cartilage; Chondrogenesis; Collagen; Invertebrates

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APA (6th Edition):

Slota, L. (2013). Deep conservation of the genetic program for cartilage development: the mechanism of invertebrate cartilage. (Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/AA00059570

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):

Slota, Leslie. “Deep conservation of the genetic program for cartilage development: the mechanism of invertebrate cartilage.” 2013. Thesis, University of Florida. Accessed July 19, 2019. http://ufdc.ufl.edu/AA00059570.

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

MLA Handbook (7th Edition):

Slota, Leslie. “Deep conservation of the genetic program for cartilage development: the mechanism of invertebrate cartilage.” 2013. Web. 19 Jul 2019.

Vancouver:

Slota L. Deep conservation of the genetic program for cartilage development: the mechanism of invertebrate cartilage. [Internet] [Thesis]. University of Florida; 2013. [cited 2019 Jul 19]. Available from: http://ufdc.ufl.edu/AA00059570.

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

Council of Science Editors:

Slota L. Deep conservation of the genetic program for cartilage development: the mechanism of invertebrate cartilage. [Thesis]. University of Florida; 2013. Available from: http://ufdc.ufl.edu/AA00059570

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

16. SHEA, CLAIRE ANN. A mechanistic basis for the mechanical regulation of skeletal development.

Degree: School of Natural Sciences. Discipline of Zoology, 2018, Trinity College Dublin

 Movement is essential to embryonic skeletal development. In humans, Foetal Akinesia Deformation Syndrome results when inhibited movement causes joint contractures and weakened bones susceptible to… (more)

Subjects/Keywords: skeletal development; mechanoregulation; mechanosensitive; embryonic skeletogenesis; movement; chondrogenesis; osteogenesis; tissue differentiation

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APA (6th Edition):

SHEA, C. A. (2018). A mechanistic basis for the mechanical regulation of skeletal development. (Thesis). Trinity College Dublin. Retrieved from http://hdl.handle.net/2262/82837

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):

SHEA, CLAIRE ANN. “A mechanistic basis for the mechanical regulation of skeletal development.” 2018. Thesis, Trinity College Dublin. Accessed July 19, 2019. http://hdl.handle.net/2262/82837.

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

MLA Handbook (7th Edition):

SHEA, CLAIRE ANN. “A mechanistic basis for the mechanical regulation of skeletal development.” 2018. Web. 19 Jul 2019.

Vancouver:

SHEA CA. A mechanistic basis for the mechanical regulation of skeletal development. [Internet] [Thesis]. Trinity College Dublin; 2018. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2262/82837.

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

Council of Science Editors:

SHEA CA. A mechanistic basis for the mechanical regulation of skeletal development. [Thesis]. Trinity College Dublin; 2018. Available from: http://hdl.handle.net/2262/82837

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


Texas A&M University

17. MacIver, Melissa. Optimizing Chondrogenesis of Canine Mesenchymal Stem Cells for Future Use in Treatment of Osteochondral Defects.

Degree: 2017, Texas A&M University

 Osteochondrosis and traumatic osteochondral defects are debilitating disorders affecting articular cartilage of millions of human and veterinary species. As articular cartilage is highly specialized and… (more)

Subjects/Keywords: Canine; mesenchymal stem cells; chondrogenesis; 3D scaffold; type I collagen

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APA (6th Edition):

MacIver, M. (2017). Optimizing Chondrogenesis of Canine Mesenchymal Stem Cells for Future Use in Treatment of Osteochondral Defects. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161652

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):

MacIver, Melissa. “Optimizing Chondrogenesis of Canine Mesenchymal Stem Cells for Future Use in Treatment of Osteochondral Defects.” 2017. Thesis, Texas A&M University. Accessed July 19, 2019. http://hdl.handle.net/1969.1/161652.

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

MLA Handbook (7th Edition):

MacIver, Melissa. “Optimizing Chondrogenesis of Canine Mesenchymal Stem Cells for Future Use in Treatment of Osteochondral Defects.” 2017. Web. 19 Jul 2019.

Vancouver:

MacIver M. Optimizing Chondrogenesis of Canine Mesenchymal Stem Cells for Future Use in Treatment of Osteochondral Defects. [Internet] [Thesis]. Texas A&M University; 2017. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1969.1/161652.

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

Council of Science Editors:

MacIver M. Optimizing Chondrogenesis of Canine Mesenchymal Stem Cells for Future Use in Treatment of Osteochondral Defects. [Thesis]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/161652

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


Univerzitet u Beogradu

18. Francuski, Jelena V. Ex vivo karakteristike mezenhimalnih matičnih ćelija izolovanih iz sinovijalne tečnosti kolenog zgloba pasa različite starosti.

Degree: Fakultet veterinarske medicine, 2016, Univerzitet u Beogradu

veterinarska medicina - matične ćelije / veterinary medicine - stem cells

Cilj ovog rada je bio da se utvrdi: da li ćelije izolovane iz sinovijalne… (more)

Subjects/Keywords: cartilage; chondrogenesis; dog; mesenchymal stem cells; synovial fluid

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APA (6th Edition):

Francuski, J. V. (2016). Ex vivo karakteristike mezenhimalnih matičnih ćelija izolovanih iz sinovijalne tečnosti kolenog zgloba pasa različite starosti. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11312/bdef:Content/get

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):

Francuski, Jelena V. “Ex vivo karakteristike mezenhimalnih matičnih ćelija izolovanih iz sinovijalne tečnosti kolenog zgloba pasa različite starosti.” 2016. Thesis, Univerzitet u Beogradu. Accessed July 19, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:11312/bdef:Content/get.

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

MLA Handbook (7th Edition):

Francuski, Jelena V. “Ex vivo karakteristike mezenhimalnih matičnih ćelija izolovanih iz sinovijalne tečnosti kolenog zgloba pasa različite starosti.” 2016. Web. 19 Jul 2019.

Vancouver:

Francuski JV. Ex vivo karakteristike mezenhimalnih matičnih ćelija izolovanih iz sinovijalne tečnosti kolenog zgloba pasa različite starosti. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Jul 19]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11312/bdef:Content/get.

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

Council of Science Editors:

Francuski JV. Ex vivo karakteristike mezenhimalnih matičnih ćelija izolovanih iz sinovijalne tečnosti kolenog zgloba pasa različite starosti. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11312/bdef:Content/get

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


East Carolina University

19. Nagchowdhuri, Partha Sarathi. Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development.

Degree: 2012, East Carolina University

 The different mechanisms involved in vertebrate synovial joint development are actively  being uncovered. A variety of studies have thus far discovered the involvement of several large  molecules… (more)

Subjects/Keywords: Biology, Molecular; Molecular biology; Proteoglycans; Joints; Chondrogenesis; Embryology

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APA (6th Edition):

Nagchowdhuri, P. S. (2012). Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development. (Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4090

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):

Nagchowdhuri, Partha Sarathi. “Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development.” 2012. Thesis, East Carolina University. Accessed July 19, 2019. http://hdl.handle.net/10342/4090.

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

MLA Handbook (7th Edition):

Nagchowdhuri, Partha Sarathi. “Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development.” 2012. Web. 19 Jul 2019.

Vancouver:

Nagchowdhuri PS. Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development. [Internet] [Thesis]. East Carolina University; 2012. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10342/4090.

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

Council of Science Editors:

Nagchowdhuri PS. Consequences of Reduced Versican Expression in Embryonic Chick Synovial Joint Development. [Thesis]. East Carolina University; 2012. Available from: http://hdl.handle.net/10342/4090

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


University of Hong Kong

20. 梁靜雯.; Leung, Ching-man. Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis.

Degree: M. Phil., 2002, University of Hong Kong

published_or_final_version

Biochemistry

Master

Master of Philosophy

Subjects/Keywords: Chondrogenesis.; Cartilage cells - Genetics.; Exostosis.

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APA (6th Edition):

梁靜雯.; Leung, C. (2002). Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. (Masters Thesis). University of Hong Kong. Retrieved from Leung, C. [梁靜雯]. (2002). Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122756 ; http://dx.doi.org/10.5353/th_b3122756 ; http://hdl.handle.net/10722/39459

Chicago Manual of Style (16th Edition):

梁靜雯.; Leung, Ching-man. “Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis.” 2002. Masters Thesis, University of Hong Kong. Accessed July 19, 2019. Leung, C. [梁靜雯]. (2002). Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122756 ; http://dx.doi.org/10.5353/th_b3122756 ; http://hdl.handle.net/10722/39459.

MLA Handbook (7th Edition):

梁靜雯.; Leung, Ching-man. “Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis.” 2002. Web. 19 Jul 2019.

Vancouver:

梁靜雯.; Leung C. Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. [Internet] [Masters thesis]. University of Hong Kong; 2002. [cited 2019 Jul 19]. Available from: Leung, C. [梁靜雯]. (2002). Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122756 ; http://dx.doi.org/10.5353/th_b3122756 ; http://hdl.handle.net/10722/39459.

Council of Science Editors:

梁靜雯.; Leung C. Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. [Masters Thesis]. University of Hong Kong; 2002. Available from: Leung, C. [梁靜雯]. (2002). Effects of Ext1 and Ext2 mutations in a chondrocyte cell line on heparan sulfate synthesis and in vitro chondrogenesis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122756 ; http://dx.doi.org/10.5353/th_b3122756 ; http://hdl.handle.net/10722/39459


University of Otago

21. Milazzo, Christopher. Sheep Fat Bingo: A comparison of subcutaneous adipose-derived mesenchymal stem cells with infrapatellar adipose-derived mesenchymal stem cells with regard to their chondrogenic ability in a sheep model of osteochondral defect repair.

Degree: 2011, University of Otago

 Articular cartilage is an avascular, aneural, alymphatic tissue that has a very low capability for intrinsic repair. Injuries to the tissue often lead to progressive… (more)

Subjects/Keywords: adipose-derived mesenchymal stem cell; cartilage repair; tissue engineering; chondrogenesis

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APA (6th Edition):

Milazzo, C. (2011). Sheep Fat Bingo: A comparison of subcutaneous adipose-derived mesenchymal stem cells with infrapatellar adipose-derived mesenchymal stem cells with regard to their chondrogenic ability in a sheep model of osteochondral defect repair. (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/1817

Chicago Manual of Style (16th Edition):

Milazzo, Christopher. “Sheep Fat Bingo: A comparison of subcutaneous adipose-derived mesenchymal stem cells with infrapatellar adipose-derived mesenchymal stem cells with regard to their chondrogenic ability in a sheep model of osteochondral defect repair. ” 2011. Doctoral Dissertation, University of Otago. Accessed July 19, 2019. http://hdl.handle.net/10523/1817.

MLA Handbook (7th Edition):

Milazzo, Christopher. “Sheep Fat Bingo: A comparison of subcutaneous adipose-derived mesenchymal stem cells with infrapatellar adipose-derived mesenchymal stem cells with regard to their chondrogenic ability in a sheep model of osteochondral defect repair. ” 2011. Web. 19 Jul 2019.

Vancouver:

Milazzo C. Sheep Fat Bingo: A comparison of subcutaneous adipose-derived mesenchymal stem cells with infrapatellar adipose-derived mesenchymal stem cells with regard to their chondrogenic ability in a sheep model of osteochondral defect repair. [Internet] [Doctoral dissertation]. University of Otago; 2011. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10523/1817.

Council of Science Editors:

Milazzo C. Sheep Fat Bingo: A comparison of subcutaneous adipose-derived mesenchymal stem cells with infrapatellar adipose-derived mesenchymal stem cells with regard to their chondrogenic ability in a sheep model of osteochondral defect repair. [Doctoral Dissertation]. University of Otago; 2011. Available from: http://hdl.handle.net/10523/1817


University of Melbourne

22. Ye, Kenneth. Osteochondral repair using structured biological scaffold and stem cell technologies.

Degree: 2015, University of Melbourne

 Introduction: Articular cartilage damage can result in pain and loss of function for many patients. The traditional management of moderate to severe defects has been… (more)

Subjects/Keywords: cartilage; arthritis; biomaterials; tissue engineering; stem cells; chondrogenesis; repair; regeneration

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APA (6th Edition):

Ye, K. (2015). Osteochondral repair using structured biological scaffold and stem cell technologies. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/55574

Chicago Manual of Style (16th Edition):

Ye, Kenneth. “Osteochondral repair using structured biological scaffold and stem cell technologies.” 2015. Doctoral Dissertation, University of Melbourne. Accessed July 19, 2019. http://hdl.handle.net/11343/55574.

MLA Handbook (7th Edition):

Ye, Kenneth. “Osteochondral repair using structured biological scaffold and stem cell technologies.” 2015. Web. 19 Jul 2019.

Vancouver:

Ye K. Osteochondral repair using structured biological scaffold and stem cell technologies. [Internet] [Doctoral dissertation]. University of Melbourne; 2015. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/11343/55574.

Council of Science Editors:

Ye K. Osteochondral repair using structured biological scaffold and stem cell technologies. [Doctoral Dissertation]. University of Melbourne; 2015. Available from: http://hdl.handle.net/11343/55574


University of Miami

23. Deitzer, Melissa Anne. Fibrin Gels: A Potential Biomaterial for the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells.

Degree: MS, Biomedical Engineering (Engineering), 2006, University of Miami

 The purpose of this study was to develop a fibrin gel system capable of serving as a three dimensional scaffold for the chondrogenesis of rabbit… (more)

Subjects/Keywords: Bone Marrow; Fibrin Gels; Chondrogenesis

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APA (6th Edition):

Deitzer, M. A. (2006). Fibrin Gels: A Potential Biomaterial for the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells. (Thesis). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_theses/105

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):

Deitzer, Melissa Anne. “Fibrin Gels: A Potential Biomaterial for the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells.” 2006. Thesis, University of Miami. Accessed July 19, 2019. https://scholarlyrepository.miami.edu/oa_theses/105.

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

MLA Handbook (7th Edition):

Deitzer, Melissa Anne. “Fibrin Gels: A Potential Biomaterial for the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells.” 2006. Web. 19 Jul 2019.

Vancouver:

Deitzer MA. Fibrin Gels: A Potential Biomaterial for the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells. [Internet] [Thesis]. University of Miami; 2006. [cited 2019 Jul 19]. Available from: https://scholarlyrepository.miami.edu/oa_theses/105.

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

Council of Science Editors:

Deitzer MA. Fibrin Gels: A Potential Biomaterial for the Chondrogenesis of Bone Marrow Mesenchymal Stem Cells. [Thesis]. University of Miami; 2006. Available from: https://scholarlyrepository.miami.edu/oa_theses/105

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


Wright State University

24. Zohora, Fatema Tuj. Effect of Dimensionality on In Vitro Growth Environment and Mesenchymal Stem Cell Function.

Degree: MSBME, Biomedical Engineering, 2018, Wright State University

 The use of the standard two dimensional (2D) cell culture has laid down the fundamentals of molecular and cell biology. However, recent advances in cell-based… (more)

Subjects/Keywords: Biomedical Engineering; Mesenchymal stem cells; culture dimension; adipogenesis; osteogenesis; chondrogenesis

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APA (6th Edition):

Zohora, F. T. (2018). Effect of Dimensionality on In Vitro Growth Environment and Mesenchymal Stem Cell Function. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1535328622898468

Chicago Manual of Style (16th Edition):

Zohora, Fatema Tuj. “Effect of Dimensionality on In Vitro Growth Environment and Mesenchymal Stem Cell Function.” 2018. Masters Thesis, Wright State University. Accessed July 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1535328622898468.

MLA Handbook (7th Edition):

Zohora, Fatema Tuj. “Effect of Dimensionality on In Vitro Growth Environment and Mesenchymal Stem Cell Function.” 2018. Web. 19 Jul 2019.

Vancouver:

Zohora FT. Effect of Dimensionality on In Vitro Growth Environment and Mesenchymal Stem Cell Function. [Internet] [Masters thesis]. Wright State University; 2018. [cited 2019 Jul 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1535328622898468.

Council of Science Editors:

Zohora FT. Effect of Dimensionality on In Vitro Growth Environment and Mesenchymal Stem Cell Function. [Masters Thesis]. Wright State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1535328622898468


University of Texas – Austin

25. -1021-0306. Mechanisms directing chondrocyte specification in the developing limb.

Degree: Cellular and Molecular Biology, 2018, University of Texas – Austin

 During limb development, skeletal elements originate from highly proliferative mesodermal progenitor cells that differentiate into chondrocytes. While this process must be tightly regulated to ensure… (more)

Subjects/Keywords: BMP; Prmt5; Limb development; Polydactyly; Chondrogenesis; Chondroprogenitor; Gremlin; Sox9

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APA (6th Edition):

-1021-0306. (2018). Mechanisms directing chondrocyte specification in the developing limb. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68374

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):

-1021-0306. “Mechanisms directing chondrocyte specification in the developing limb.” 2018. Thesis, University of Texas – Austin. Accessed July 19, 2019. http://hdl.handle.net/2152/68374.

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):

-1021-0306. “Mechanisms directing chondrocyte specification in the developing limb.” 2018. Web. 19 Jul 2019.

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

Vancouver:

-1021-0306. Mechanisms directing chondrocyte specification in the developing limb. [Internet] [Thesis]. University of Texas – Austin; 2018. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/2152/68374.

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:

-1021-0306. Mechanisms directing chondrocyte specification in the developing limb. [Thesis]. University of Texas – Austin; 2018. Available from: http://hdl.handle.net/2152/68374

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


University of Kansas

26. Bhamidipati, Manjari. Osteogenic and Chondrogenic Differentiation of rBMSCs on Microsphere-Based Scaffolds Sintered Using Subcritical CO2.

Degree: MS, Bioengineering, 2011, University of Kansas

 Large bone defects remain a major clinical orthopedic challenge. It has been predicted that osteoarthritis will affect over 100 million adults in the United States… (more)

Subjects/Keywords: Biomedical engineering; Chondrogenesis; Microspheres; Osteogenesis; Sintering; Sub-critical co2

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APA (6th Edition):

Bhamidipati, M. (2011). Osteogenic and Chondrogenic Differentiation of rBMSCs on Microsphere-Based Scaffolds Sintered Using Subcritical CO2. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/9738

Chicago Manual of Style (16th Edition):

Bhamidipati, Manjari. “Osteogenic and Chondrogenic Differentiation of rBMSCs on Microsphere-Based Scaffolds Sintered Using Subcritical CO2.” 2011. Masters Thesis, University of Kansas. Accessed July 19, 2019. http://hdl.handle.net/1808/9738.

MLA Handbook (7th Edition):

Bhamidipati, Manjari. “Osteogenic and Chondrogenic Differentiation of rBMSCs on Microsphere-Based Scaffolds Sintered Using Subcritical CO2.” 2011. Web. 19 Jul 2019.

Vancouver:

Bhamidipati M. Osteogenic and Chondrogenic Differentiation of rBMSCs on Microsphere-Based Scaffolds Sintered Using Subcritical CO2. [Internet] [Masters thesis]. University of Kansas; 2011. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/1808/9738.

Council of Science Editors:

Bhamidipati M. Osteogenic and Chondrogenic Differentiation of rBMSCs on Microsphere-Based Scaffolds Sintered Using Subcritical CO2. [Masters Thesis]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9738


Columbia University

27. Khanarian, Nora. Scaffold Design and Optimization for Osteochondral Interface Tissue Engineering.

Degree: 2012, Columbia University

 A thin layer of calcified cartilage at the native cartilage-to-bone junction facilitates integration between deep zone articular cartilage and subchondral bone, while maintaining the integrity… (more)

Subjects/Keywords: Biomedical engineering; Tissue engineering; Biomimetics; Chondrogenesis; Tissue scaffolds

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

APA (6th Edition):

Khanarian, N. (2012). Scaffold Design and Optimization for Osteochondral Interface Tissue Engineering. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8TH908N

Chicago Manual of Style (16th Edition):

Khanarian, Nora. “Scaffold Design and Optimization for Osteochondral Interface Tissue Engineering.” 2012. Doctoral Dissertation, Columbia University. Accessed July 19, 2019. https://doi.org/10.7916/D8TH908N.

MLA Handbook (7th Edition):

Khanarian, Nora. “Scaffold Design and Optimization for Osteochondral Interface Tissue Engineering.” 2012. Web. 19 Jul 2019.

Vancouver:

Khanarian N. Scaffold Design and Optimization for Osteochondral Interface Tissue Engineering. [Internet] [Doctoral dissertation]. Columbia University; 2012. [cited 2019 Jul 19]. Available from: https://doi.org/10.7916/D8TH908N.

Council of Science Editors:

Khanarian N. Scaffold Design and Optimization for Osteochondral Interface Tissue Engineering. [Doctoral Dissertation]. Columbia University; 2012. Available from: https://doi.org/10.7916/D8TH908N


Columbia University

28. Cigan, Alexander Drake. Nutrient Channels to Aid the Growth of Articular Surface-Sized Engineered Cartilage Constructs.

Degree: 2016, Columbia University

 Osteoarthritis is a joint disease associated with the irreversible breakdown of articular cartilage in joints, causing pain, impaired mobility, and reduced quality of life in… (more)

Subjects/Keywords: Cartilage; Tissue engineering; Chondrogenesis; Cartilage cells; Osteoarthritis; Biomedical engineering

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

APA (6th Edition):

Cigan, A. D. (2016). Nutrient Channels to Aid the Growth of Articular Surface-Sized Engineered Cartilage Constructs. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8B8583F

Chicago Manual of Style (16th Edition):

Cigan, Alexander Drake. “Nutrient Channels to Aid the Growth of Articular Surface-Sized Engineered Cartilage Constructs.” 2016. Doctoral Dissertation, Columbia University. Accessed July 19, 2019. https://doi.org/10.7916/D8B8583F.

MLA Handbook (7th Edition):

Cigan, Alexander Drake. “Nutrient Channels to Aid the Growth of Articular Surface-Sized Engineered Cartilage Constructs.” 2016. Web. 19 Jul 2019.

Vancouver:

Cigan AD. Nutrient Channels to Aid the Growth of Articular Surface-Sized Engineered Cartilage Constructs. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2019 Jul 19]. Available from: https://doi.org/10.7916/D8B8583F.

Council of Science Editors:

Cigan AD. Nutrient Channels to Aid the Growth of Articular Surface-Sized Engineered Cartilage Constructs. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8B8583F

29. ZHANG TIANTING. Dynamic Mechanical Stimulation for Mesenchymal Stem Cell Chondrogenesis in An Elastomeric Scaffold.

Degree: 2014, National University of Singapore

Subjects/Keywords: Chondrogenesis; compression; shearing; pathways

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APA (6th Edition):

TIANTING, Z. (2014). Dynamic Mechanical Stimulation for Mesenchymal Stem Cell Chondrogenesis in An Elastomeric Scaffold. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/119515

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):

TIANTING, ZHANG. “Dynamic Mechanical Stimulation for Mesenchymal Stem Cell Chondrogenesis in An Elastomeric Scaffold.” 2014. Thesis, National University of Singapore. Accessed July 19, 2019. http://scholarbank.nus.edu.sg/handle/10635/119515.

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

MLA Handbook (7th Edition):

TIANTING, ZHANG. “Dynamic Mechanical Stimulation for Mesenchymal Stem Cell Chondrogenesis in An Elastomeric Scaffold.” 2014. Web. 19 Jul 2019.

Vancouver:

TIANTING Z. Dynamic Mechanical Stimulation for Mesenchymal Stem Cell Chondrogenesis in An Elastomeric Scaffold. [Internet] [Thesis]. National University of Singapore; 2014. [cited 2019 Jul 19]. Available from: http://scholarbank.nus.edu.sg/handle/10635/119515.

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

Council of Science Editors:

TIANTING Z. Dynamic Mechanical Stimulation for Mesenchymal Stem Cell Chondrogenesis in An Elastomeric Scaffold. [Thesis]. National University of Singapore; 2014. Available from: http://scholarbank.nus.edu.sg/handle/10635/119515

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


Colorado State University

30. Tangtrongsup, Suwimol. Effects of dexamethasone and oxidative environment on chondrogenesis of bone marrow-derived mesenchymal stem cells.

Degree: PhD, Clinical Sciences, 2017, Colorado State University

 Bone marrow-derived mesenchymal stem cell (MSCs) have received extensive consideration for applications to musculoskeletal tissue engineering based on their ability to differentiate into multiple skeletal… (more)

Subjects/Keywords: Chondrogenesis; Extracellular Matrix; Reactive oxygen species; Dexamethasone; Antioxidant; Mesenchymal stem cell

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

APA (6th Edition):

Tangtrongsup, S. (2017). Effects of dexamethasone and oxidative environment on chondrogenesis of bone marrow-derived mesenchymal stem cells. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/183903

Chicago Manual of Style (16th Edition):

Tangtrongsup, Suwimol. “Effects of dexamethasone and oxidative environment on chondrogenesis of bone marrow-derived mesenchymal stem cells.” 2017. Doctoral Dissertation, Colorado State University. Accessed July 19, 2019. http://hdl.handle.net/10217/183903.

MLA Handbook (7th Edition):

Tangtrongsup, Suwimol. “Effects of dexamethasone and oxidative environment on chondrogenesis of bone marrow-derived mesenchymal stem cells.” 2017. Web. 19 Jul 2019.

Vancouver:

Tangtrongsup S. Effects of dexamethasone and oxidative environment on chondrogenesis of bone marrow-derived mesenchymal stem cells. [Internet] [Doctoral dissertation]. Colorado State University; 2017. [cited 2019 Jul 19]. Available from: http://hdl.handle.net/10217/183903.

Council of Science Editors:

Tangtrongsup S. Effects of dexamethasone and oxidative environment on chondrogenesis of bone marrow-derived mesenchymal stem cells. [Doctoral Dissertation]. Colorado State University; 2017. Available from: http://hdl.handle.net/10217/183903

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