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You searched for subject:(OSTEOBLAST DIFFERENTIATION). Showing records 1 – 30 of 51 total matches.

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University of New South Wales

1. Twine, Natalie. Systems analysis of human mesenchymal stem cells during differentiation into osteoblasts.

Degree: Biotechnology & Biomolecular Sciences, 2015, University of New South Wales

 To better understand human Mesenchymal Stem Cells (hMSCs) ex vivo and their use in therapy, we have studied the molecular phenotype of telomerised hMSC (hMSC-TERT)… (more)

Subjects/Keywords: Systems biology; Transcriptomics; Osteoblast differentiation

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APA (6th Edition):

Twine, N. (2015). Systems analysis of human mesenchymal stem cells during differentiation into osteoblasts. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56859 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:41773/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Twine, Natalie. “Systems analysis of human mesenchymal stem cells during differentiation into osteoblasts.” 2015. Doctoral Dissertation, University of New South Wales. Accessed September 18, 2020. http://handle.unsw.edu.au/1959.4/56859 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:41773/SOURCE02?view=true.

MLA Handbook (7th Edition):

Twine, Natalie. “Systems analysis of human mesenchymal stem cells during differentiation into osteoblasts.” 2015. Web. 18 Sep 2020.

Vancouver:

Twine N. Systems analysis of human mesenchymal stem cells during differentiation into osteoblasts. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2020 Sep 18]. Available from: http://handle.unsw.edu.au/1959.4/56859 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:41773/SOURCE02?view=true.

Council of Science Editors:

Twine N. Systems analysis of human mesenchymal stem cells during differentiation into osteoblasts. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/56859 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:41773/SOURCE02?view=true


University of Toronto

2. Fiorino, Cara Erica. Examining Novel Factors that Influence Contact-dependent Osteoblast and Osteoclast Differentiation.

Degree: PhD, 2016, University of Toronto

 A dynamic equilibrium between bone destruction by osteoclasts and bone formation by osteoblasts is responsible for the maintenance of bone integrity, mineral homeostasis and protection… (more)

Subjects/Keywords: differentiation; EB1; E-cadherin; osteoblast; osteoclast; 0379

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APA (6th Edition):

Fiorino, C. E. (2016). Examining Novel Factors that Influence Contact-dependent Osteoblast and Osteoclast Differentiation. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/76405

Chicago Manual of Style (16th Edition):

Fiorino, Cara Erica. “Examining Novel Factors that Influence Contact-dependent Osteoblast and Osteoclast Differentiation.” 2016. Doctoral Dissertation, University of Toronto. Accessed September 18, 2020. http://hdl.handle.net/1807/76405.

MLA Handbook (7th Edition):

Fiorino, Cara Erica. “Examining Novel Factors that Influence Contact-dependent Osteoblast and Osteoclast Differentiation.” 2016. Web. 18 Sep 2020.

Vancouver:

Fiorino CE. Examining Novel Factors that Influence Contact-dependent Osteoblast and Osteoclast Differentiation. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/1807/76405.

Council of Science Editors:

Fiorino CE. Examining Novel Factors that Influence Contact-dependent Osteoblast and Osteoclast Differentiation. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/76405


University of Southern California

3. Yu, Jiali. Preosteoblast-specific RUNX2 promotes RANKL membrane association: antagonism by sex steroids through a non-genomic mechanism.

Degree: MS, Biochemistry and Molecular Biology, 2015, University of Southern California

 Molecular mechanisms underlying the bone‐sparing effects of sex steroid hormones are not fully understood. We show that RUNX2, a master regulator of osteoblast differentiation and… (more)

Subjects/Keywords: RUNX2; RANKL; sex steroids; osteoblast differentiation

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APA (6th Edition):

Yu, J. (2015). Preosteoblast-specific RUNX2 promotes RANKL membrane association: antagonism by sex steroids through a non-genomic mechanism. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/571674/rec/5188

Chicago Manual of Style (16th Edition):

Yu, Jiali. “Preosteoblast-specific RUNX2 promotes RANKL membrane association: antagonism by sex steroids through a non-genomic mechanism.” 2015. Masters Thesis, University of Southern California. Accessed September 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/571674/rec/5188.

MLA Handbook (7th Edition):

Yu, Jiali. “Preosteoblast-specific RUNX2 promotes RANKL membrane association: antagonism by sex steroids through a non-genomic mechanism.” 2015. Web. 18 Sep 2020.

Vancouver:

Yu J. Preosteoblast-specific RUNX2 promotes RANKL membrane association: antagonism by sex steroids through a non-genomic mechanism. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Sep 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/571674/rec/5188.

Council of Science Editors:

Yu J. Preosteoblast-specific RUNX2 promotes RANKL membrane association: antagonism by sex steroids through a non-genomic mechanism. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/571674/rec/5188


Georgia Tech

4. Cheng, Alice. Multi-scale structural design of titanium implants for improved osseointegration.

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

 Osseointegration success of bone-interfacing implants is reduced for many compromised patients, necessitating improved implant design. Though material and mechanical properties of titanium make it attractive… (more)

Subjects/Keywords: biomaterials; osseointegration, osteoblast differentiation; titanium; additive manufacturing

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APA (6th Edition):

Cheng, A. (2016). Multi-scale structural design of titanium implants for improved osseointegration. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56287

Chicago Manual of Style (16th Edition):

Cheng, Alice. “Multi-scale structural design of titanium implants for improved osseointegration.” 2016. Doctoral Dissertation, Georgia Tech. Accessed September 18, 2020. http://hdl.handle.net/1853/56287.

MLA Handbook (7th Edition):

Cheng, Alice. “Multi-scale structural design of titanium implants for improved osseointegration.” 2016. Web. 18 Sep 2020.

Vancouver:

Cheng A. Multi-scale structural design of titanium implants for improved osseointegration. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/1853/56287.

Council of Science Editors:

Cheng A. Multi-scale structural design of titanium implants for improved osseointegration. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/56287


IUPUI

5. Pauly, Katherine L. The effects of electromagnetic wave stimulation (EMS) on osteoblast differentiation and activity.

Degree: 2020, IUPUI

Indiana University School of Dentistry

Introduction: The goal of nonsurgical root canal therapy is to reduce the bacterial load within an infected root canal system,… (more)

Subjects/Keywords: electromagnetic wave stimulation; electromagnetic; osteoblast; osteoblast differentiation; osteoblast activity; Alkaline Phosphatase; Cell Differentiation; Cell Proliferation; Electromagnetic Radiation; Osteoblasts; Regenerative Endodontics

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APA (6th Edition):

Pauly, K. L. (2020). The effects of electromagnetic wave stimulation (EMS) on osteoblast differentiation and activity. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/23185

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):

Pauly, Katherine L. “The effects of electromagnetic wave stimulation (EMS) on osteoblast differentiation and activity.” 2020. Thesis, IUPUI. Accessed September 18, 2020. http://hdl.handle.net/1805/23185.

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

MLA Handbook (7th Edition):

Pauly, Katherine L. “The effects of electromagnetic wave stimulation (EMS) on osteoblast differentiation and activity.” 2020. Web. 18 Sep 2020.

Vancouver:

Pauly KL. The effects of electromagnetic wave stimulation (EMS) on osteoblast differentiation and activity. [Internet] [Thesis]. IUPUI; 2020. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/1805/23185.

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

Council of Science Editors:

Pauly KL. The effects of electromagnetic wave stimulation (EMS) on osteoblast differentiation and activity. [Thesis]. IUPUI; 2020. Available from: http://hdl.handle.net/1805/23185

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


University of Toronto

6. Gupta, Shaan. MicroRNA-17 Targets JAK1 and STAT3 to Inhibit Osteoblast Differentiation.

Degree: 2014, University of Toronto

MicroRNA-17 (miR-17) was hypothesized to target janus kinase 1 (JAK1) and signal transducer and activator of transcription 3 (STAT3) to inhibit osteogenesis in pre-osteoblast cells.… (more)

Subjects/Keywords: bone formation; JAK-STAT; microRNA; Osteoblast Differentiation; Osteogenesis; osteoporosis; 0307

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APA (6th Edition):

Gupta, S. (2014). MicroRNA-17 Targets JAK1 and STAT3 to Inhibit Osteoblast Differentiation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67894

Chicago Manual of Style (16th Edition):

Gupta, Shaan. “MicroRNA-17 Targets JAK1 and STAT3 to Inhibit Osteoblast Differentiation.” 2014. Masters Thesis, University of Toronto. Accessed September 18, 2020. http://hdl.handle.net/1807/67894.

MLA Handbook (7th Edition):

Gupta, Shaan. “MicroRNA-17 Targets JAK1 and STAT3 to Inhibit Osteoblast Differentiation.” 2014. Web. 18 Sep 2020.

Vancouver:

Gupta S. MicroRNA-17 Targets JAK1 and STAT3 to Inhibit Osteoblast Differentiation. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/1807/67894.

Council of Science Editors:

Gupta S. MicroRNA-17 Targets JAK1 and STAT3 to Inhibit Osteoblast Differentiation. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67894


University of Connecticut

7. Ackell, Elizabeth R. Optimization of culture conditions for equine bone marrow mesenchymal stem cells and their differentiation into osteoblasts.

Degree: MS, Animal Science, 2011, University of Connecticut

  The horse industry is a multibillion dollar industry where the health of the animals is of great focus for horse owners.  Bone fractures are… (more)

Subjects/Keywords: equine bone marrow mesenchymal stem cells; osteoblast differentiation; transctription factors

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APA (6th Edition):

Ackell, E. R. (2011). Optimization of culture conditions for equine bone marrow mesenchymal stem cells and their differentiation into osteoblasts. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/119

Chicago Manual of Style (16th Edition):

Ackell, Elizabeth R. “Optimization of culture conditions for equine bone marrow mesenchymal stem cells and their differentiation into osteoblasts.” 2011. Masters Thesis, University of Connecticut. Accessed September 18, 2020. https://opencommons.uconn.edu/gs_theses/119.

MLA Handbook (7th Edition):

Ackell, Elizabeth R. “Optimization of culture conditions for equine bone marrow mesenchymal stem cells and their differentiation into osteoblasts.” 2011. Web. 18 Sep 2020.

Vancouver:

Ackell ER. Optimization of culture conditions for equine bone marrow mesenchymal stem cells and their differentiation into osteoblasts. [Internet] [Masters thesis]. University of Connecticut; 2011. [cited 2020 Sep 18]. Available from: https://opencommons.uconn.edu/gs_theses/119.

Council of Science Editors:

Ackell ER. Optimization of culture conditions for equine bone marrow mesenchymal stem cells and their differentiation into osteoblasts. [Masters Thesis]. University of Connecticut; 2011. Available from: https://opencommons.uconn.edu/gs_theses/119


University of Illinois – Chicago

8. Eapen, Asha S. DMP1 Activates Osteolytic Cycle in a Tumor Environment.

Degree: 2012, University of Illinois – Chicago

 Bone metastasis is one of the skeletal malignancies that could be caused by breast cancer. Dentin matrix protein 1 (DMP1) is an acidic noncollagenous protein… (more)

Subjects/Keywords: DMP1; Osteoblast; Osteoclast; Differentiation; Breast cancer; Bone; Mineralization; Signaling pathways; Osteolysis

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APA (6th Edition):

Eapen, A. S. (2012). DMP1 Activates Osteolytic Cycle in a Tumor Environment. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9101

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):

Eapen, Asha S. “DMP1 Activates Osteolytic Cycle in a Tumor Environment.” 2012. Thesis, University of Illinois – Chicago. Accessed September 18, 2020. http://hdl.handle.net/10027/9101.

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

MLA Handbook (7th Edition):

Eapen, Asha S. “DMP1 Activates Osteolytic Cycle in a Tumor Environment.” 2012. Web. 18 Sep 2020.

Vancouver:

Eapen AS. DMP1 Activates Osteolytic Cycle in a Tumor Environment. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/10027/9101.

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

Council of Science Editors:

Eapen AS. DMP1 Activates Osteolytic Cycle in a Tumor Environment. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9101

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

9. Juignet, Laura. Effets de la macro-architecture du substrat sur l'activité et la différenciation des ostéoblastes : Impact of substrate macro-architecture on osteoblast activity and differentiation.

Degree: Docteur es, Sciences de la vie et de la santé, 2016, Lyon

 In vivo, les cellules osseuses évoluent dans un microenvironnement complexe, tridimensionnel et interagissent avec celui-ci à de nombreuses échelles, depuis le nanomètre (tropocollagène) jusqu’à des… (more)

Subjects/Keywords: Macrotopographie; Différenciation ostéoblastique; Matrice extracellulaire; Hydroxyapatite; Macroarchitecture; Macrotopography; Osteoblast differentiation; Extracellular matrix; Hydroxyapatite; Macroarchitecture

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APA (6th Edition):

Juignet, L. (2016). Effets de la macro-architecture du substrat sur l'activité et la différenciation des ostéoblastes : Impact of substrate macro-architecture on osteoblast activity and differentiation. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSES060

Chicago Manual of Style (16th Edition):

Juignet, Laura. “Effets de la macro-architecture du substrat sur l'activité et la différenciation des ostéoblastes : Impact of substrate macro-architecture on osteoblast activity and differentiation.” 2016. Doctoral Dissertation, Lyon. Accessed September 18, 2020. http://www.theses.fr/2016LYSES060.

MLA Handbook (7th Edition):

Juignet, Laura. “Effets de la macro-architecture du substrat sur l'activité et la différenciation des ostéoblastes : Impact of substrate macro-architecture on osteoblast activity and differentiation.” 2016. Web. 18 Sep 2020.

Vancouver:

Juignet L. Effets de la macro-architecture du substrat sur l'activité et la différenciation des ostéoblastes : Impact of substrate macro-architecture on osteoblast activity and differentiation. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2020 Sep 18]. Available from: http://www.theses.fr/2016LYSES060.

Council of Science Editors:

Juignet L. Effets de la macro-architecture du substrat sur l'activité et la différenciation des ostéoblastes : Impact of substrate macro-architecture on osteoblast activity and differentiation. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSES060

10. 吉澤, 祐. Early gene and protein expression associated with osteoblast differentiation in response to fish collagen peptides powder : フィッシュコラーゲンを骨芽細胞に加えた際の、骨芽細胞の分化に対する影響を遺伝子、タンパク発現において検討を行った.

Degree: 博士(歯学), 2013, Nagasaki University / 長崎大学

 This study was designed to investigate the biological effects of fish collagen peptide (FCP) on human osteoblasts. Human osteoblasts were treated with 0.1% FCP, which… (more)

Subjects/Keywords: Alkaline phosphatase activity; Fish collagen peptide; Osteoblast differentiation; Real-time PCR; Western blot analysis

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APA (6th Edition):

吉澤, . (2013). Early gene and protein expression associated with osteoblast differentiation in response to fish collagen peptides powder : フィッシュコラーゲンを骨芽細胞に加えた際の、骨芽細胞の分化に対する影響を遺伝子、タンパク発現において検討を行った. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/35254

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):

吉澤, 祐. “Early gene and protein expression associated with osteoblast differentiation in response to fish collagen peptides powder : フィッシュコラーゲンを骨芽細胞に加えた際の、骨芽細胞の分化に対する影響を遺伝子、タンパク発現において検討を行った.” 2013. Thesis, Nagasaki University / 長崎大学. Accessed September 18, 2020. http://hdl.handle.net/10069/35254.

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

MLA Handbook (7th Edition):

吉澤, 祐. “Early gene and protein expression associated with osteoblast differentiation in response to fish collagen peptides powder : フィッシュコラーゲンを骨芽細胞に加えた際の、骨芽細胞の分化に対する影響を遺伝子、タンパク発現において検討を行った.” 2013. Web. 18 Sep 2020.

Vancouver:

吉澤 . Early gene and protein expression associated with osteoblast differentiation in response to fish collagen peptides powder : フィッシュコラーゲンを骨芽細胞に加えた際の、骨芽細胞の分化に対する影響を遺伝子、タンパク発現において検討を行った. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2013. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/10069/35254.

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

Council of Science Editors:

吉澤 . Early gene and protein expression associated with osteoblast differentiation in response to fish collagen peptides powder : フィッシュコラーゲンを骨芽細胞に加えた際の、骨芽細胞の分化に対する影響を遺伝子、タンパク発現において検討を行った. [Thesis]. Nagasaki University / 長崎大学; 2013. Available from: http://hdl.handle.net/10069/35254

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


Queensland University of Technology

11. Manitzky, Louise J. Mathematical modelling of intramembranous bone formation during fracture healing.

Degree: 2014, Queensland University of Technology

 During fracture healing, many complex and cryptic interactions occur between cells and bio-chemical molecules to bring about repair of damaged bone. In this thesis two… (more)

Subjects/Keywords: Fracture Healing; Intramembranous Bone Formation; Mathematical Modelling; Mineralisation; Osteoblast differentiation; Turing Patterns

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APA (6th Edition):

Manitzky, L. J. (2014). Mathematical modelling of intramembranous bone formation during fracture healing. (Thesis). Queensland University of Technology. Retrieved from https://eprints.qut.edu.au/78983/

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):

Manitzky, Louise J. “Mathematical modelling of intramembranous bone formation during fracture healing.” 2014. Thesis, Queensland University of Technology. Accessed September 18, 2020. https://eprints.qut.edu.au/78983/.

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

MLA Handbook (7th Edition):

Manitzky, Louise J. “Mathematical modelling of intramembranous bone formation during fracture healing.” 2014. Web. 18 Sep 2020.

Vancouver:

Manitzky LJ. Mathematical modelling of intramembranous bone formation during fracture healing. [Internet] [Thesis]. Queensland University of Technology; 2014. [cited 2020 Sep 18]. Available from: https://eprints.qut.edu.au/78983/.

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

Council of Science Editors:

Manitzky LJ. Mathematical modelling of intramembranous bone formation during fracture healing. [Thesis]. Queensland University of Technology; 2014. Available from: https://eprints.qut.edu.au/78983/

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


National University of Ireland – Galway

12. Mc Garrigle, Myles. The role of matrix properties and extrinsic loading in osteoblast-osteocyte differentiation in tissue engineered scaffolds .

Degree: 2018, National University of Ireland – Galway

 Bone tissue engineering is a promising field with the potential to generate tissue substitutes, by taking advantage of mesenchymal stem cells ability to grow and… (more)

Subjects/Keywords: Bone tissue engineering; Osteoblast-osteocyte differentiation; Compression perfusion bioreactor; Biomedical engineering; Engineering and Informatics

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APA (6th Edition):

Mc Garrigle, M. (2018). The role of matrix properties and extrinsic loading in osteoblast-osteocyte differentiation in tissue engineered scaffolds . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/7128

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):

Mc Garrigle, Myles. “The role of matrix properties and extrinsic loading in osteoblast-osteocyte differentiation in tissue engineered scaffolds .” 2018. Thesis, National University of Ireland – Galway. Accessed September 18, 2020. http://hdl.handle.net/10379/7128.

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

MLA Handbook (7th Edition):

Mc Garrigle, Myles. “The role of matrix properties and extrinsic loading in osteoblast-osteocyte differentiation in tissue engineered scaffolds .” 2018. Web. 18 Sep 2020.

Vancouver:

Mc Garrigle M. The role of matrix properties and extrinsic loading in osteoblast-osteocyte differentiation in tissue engineered scaffolds . [Internet] [Thesis]. National University of Ireland – Galway; 2018. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/10379/7128.

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

Council of Science Editors:

Mc Garrigle M. The role of matrix properties and extrinsic loading in osteoblast-osteocyte differentiation in tissue engineered scaffolds . [Thesis]. National University of Ireland – Galway; 2018. Available from: http://hdl.handle.net/10379/7128

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


Boise State University

13. Shefa, Neda. Effects of Bone Morphogenetic Protein-2 and Parathyroid Hormone-Related Peptide on Collagen XI During Skeletal Development.

Degree: 2015, Boise State University

 Long bones develop via endochondral ossification, a process in which cartilage precedes bone. During endochondral ossification prechondrogenic cells undergo proliferation and apoptose as cells of… (more)

Subjects/Keywords: Collagen XI; BMP-2; osteoblast differentiation; PTHrP; endochondral ossification; bone collar; Cell and Developmental Biology

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APA (6th Edition):

Shefa, N. (2015). Effects of Bone Morphogenetic Protein-2 and Parathyroid Hormone-Related Peptide on Collagen XI During Skeletal Development. (Thesis). Boise State University. Retrieved from https://scholarworks.boisestate.edu/td/1056

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):

Shefa, Neda. “Effects of Bone Morphogenetic Protein-2 and Parathyroid Hormone-Related Peptide on Collagen XI During Skeletal Development.” 2015. Thesis, Boise State University. Accessed September 18, 2020. https://scholarworks.boisestate.edu/td/1056.

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

MLA Handbook (7th Edition):

Shefa, Neda. “Effects of Bone Morphogenetic Protein-2 and Parathyroid Hormone-Related Peptide on Collagen XI During Skeletal Development.” 2015. Web. 18 Sep 2020.

Vancouver:

Shefa N. Effects of Bone Morphogenetic Protein-2 and Parathyroid Hormone-Related Peptide on Collagen XI During Skeletal Development. [Internet] [Thesis]. Boise State University; 2015. [cited 2020 Sep 18]. Available from: https://scholarworks.boisestate.edu/td/1056.

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

Council of Science Editors:

Shefa N. Effects of Bone Morphogenetic Protein-2 and Parathyroid Hormone-Related Peptide on Collagen XI During Skeletal Development. [Thesis]. Boise State University; 2015. Available from: https://scholarworks.boisestate.edu/td/1056

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

14. Silva, Diana. Le rôle du système nerveux sensoriel dans l'orchestration de la formation osseuse, le remodelage et la régénération tissulaire : The role of sensory nervous system in the regulation of bone formation, remodeling, and repair.

Degree: Docteur es, Biologie cellulaire et physiopathologie, 2017, Bordeaux

Les progrès dans la compréhension de la biologie osseuse ont permis d’identifier le rôle du système nerveux sensoriel dans la formation osseuse, le remodelage et… (more)

Subjects/Keywords: Neurones sensoriels; Cellules mésenchymateuses; Différenciation des ostéoblastes; DRG neurons; Mesenchymal stem cells; Osteoblast differentiation

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

APA (6th Edition):

Silva, D. (2017). Le rôle du système nerveux sensoriel dans l'orchestration de la formation osseuse, le remodelage et la régénération tissulaire : The role of sensory nervous system in the regulation of bone formation, remodeling, and repair. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2017BORD0919

Chicago Manual of Style (16th Edition):

Silva, Diana. “Le rôle du système nerveux sensoriel dans l'orchestration de la formation osseuse, le remodelage et la régénération tissulaire : The role of sensory nervous system in the regulation of bone formation, remodeling, and repair.” 2017. Doctoral Dissertation, Bordeaux. Accessed September 18, 2020. http://www.theses.fr/2017BORD0919.

MLA Handbook (7th Edition):

Silva, Diana. “Le rôle du système nerveux sensoriel dans l'orchestration de la formation osseuse, le remodelage et la régénération tissulaire : The role of sensory nervous system in the regulation of bone formation, remodeling, and repair.” 2017. Web. 18 Sep 2020.

Vancouver:

Silva D. Le rôle du système nerveux sensoriel dans l'orchestration de la formation osseuse, le remodelage et la régénération tissulaire : The role of sensory nervous system in the regulation of bone formation, remodeling, and repair. [Internet] [Doctoral dissertation]. Bordeaux; 2017. [cited 2020 Sep 18]. Available from: http://www.theses.fr/2017BORD0919.

Council of Science Editors:

Silva D. Le rôle du système nerveux sensoriel dans l'orchestration de la formation osseuse, le remodelage et la régénération tissulaire : The role of sensory nervous system in the regulation of bone formation, remodeling, and repair. [Doctoral Dissertation]. Bordeaux; 2017. Available from: http://www.theses.fr/2017BORD0919

15. Abuna, Rodrigo Paolo Flores. Análise do potencial osteogênico e adipogênico de células-tronco mesenquimais derivadas de medula óssea e de tecido adiposo.

Degree: Mestrado, Biologia Oral, 2014, University of São Paulo

Células-tronco mesenquimais derivadas de medula óssea (CTMs-MO) e de tecido adiposo (CTMs-TA) são uma ferramenta atrativa para a reparação do tecido ósseo baseada na terapia… (more)

Subjects/Keywords: adipócitos; adipocyte; adipose tissue; bone marrow; células-tronco mesenquimais; diferenciação; differentiation; medula óssea; mesenchymal stem cells; osteoblast; osteoblastos; tecido adiposo

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APA (6th Edition):

Abuna, R. P. F. (2014). Análise do potencial osteogênico e adipogênico de células-tronco mesenquimais derivadas de medula óssea e de tecido adiposo. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/58/58137/tde-03022015-110025/ ;

Chicago Manual of Style (16th Edition):

Abuna, Rodrigo Paolo Flores. “Análise do potencial osteogênico e adipogênico de células-tronco mesenquimais derivadas de medula óssea e de tecido adiposo.” 2014. Masters Thesis, University of São Paulo. Accessed September 18, 2020. http://www.teses.usp.br/teses/disponiveis/58/58137/tde-03022015-110025/ ;.

MLA Handbook (7th Edition):

Abuna, Rodrigo Paolo Flores. “Análise do potencial osteogênico e adipogênico de células-tronco mesenquimais derivadas de medula óssea e de tecido adiposo.” 2014. Web. 18 Sep 2020.

Vancouver:

Abuna RPF. Análise do potencial osteogênico e adipogênico de células-tronco mesenquimais derivadas de medula óssea e de tecido adiposo. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2020 Sep 18]. Available from: http://www.teses.usp.br/teses/disponiveis/58/58137/tde-03022015-110025/ ;.

Council of Science Editors:

Abuna RPF. Análise do potencial osteogênico e adipogênico de células-tronco mesenquimais derivadas de medula óssea e de tecido adiposo. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/58/58137/tde-03022015-110025/ ;


Temple University

16. Singh, Maneet. TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS.

Degree: PhD, 2011, Temple University

Cell Biology

Osteoactivin (OA) is a glycoprotein required for the differentiation of osteoblasts. In osteoblasts, Bone Morphogenetic Protein-2 (BMP-2) activated Smad1 signaling enhances OA expression.… (more)

Subjects/Keywords: Cellular Biology; Molecular Biology; Biology; HOMEDOMAIN PROTEIN; OSTEOACTIVIN; OSTEOBLAST DIFFERENTIATION; RUNX2; SMAD1 AND SMAD4; TRANSCRIPTIONAL REGULATION

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APA (6th Edition):

Singh, M. (2011). TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,135232

Chicago Manual of Style (16th Edition):

Singh, Maneet. “TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS.” 2011. Doctoral Dissertation, Temple University. Accessed September 18, 2020. http://digital.library.temple.edu/u?/p245801coll10,135232.

MLA Handbook (7th Edition):

Singh, Maneet. “TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS.” 2011. Web. 18 Sep 2020.

Vancouver:

Singh M. TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2020 Sep 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,135232.

Council of Science Editors:

Singh M. TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS. [Doctoral Dissertation]. Temple University; 2011. Available from: http://digital.library.temple.edu/u?/p245801coll10,135232


University of Michigan

17. Bennett, Christina Noel. Regulation of adipocyte and osteoblast differentiation by Wnt signaling.

Degree: PhD, Cellular biology, 2005, University of Michigan

 Wnts comprise a family of secreted signaling proteins that regulate diverse developmental processes. In this dissertation I explore the role of Wnt signaling in adipocyte… (more)

Subjects/Keywords: Adipocyte; Bone; Differentiation; Fat; Osteoblast; Regulation; Signaling; Wnt

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APA (6th Edition):

Bennett, C. N. (2005). Regulation of adipocyte and osteoblast differentiation by Wnt signaling. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/125020

Chicago Manual of Style (16th Edition):

Bennett, Christina Noel. “Regulation of adipocyte and osteoblast differentiation by Wnt signaling.” 2005. Doctoral Dissertation, University of Michigan. Accessed September 18, 2020. http://hdl.handle.net/2027.42/125020.

MLA Handbook (7th Edition):

Bennett, Christina Noel. “Regulation of adipocyte and osteoblast differentiation by Wnt signaling.” 2005. Web. 18 Sep 2020.

Vancouver:

Bennett CN. Regulation of adipocyte and osteoblast differentiation by Wnt signaling. [Internet] [Doctoral dissertation]. University of Michigan; 2005. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/2027.42/125020.

Council of Science Editors:

Bennett CN. Regulation of adipocyte and osteoblast differentiation by Wnt signaling. [Doctoral Dissertation]. University of Michigan; 2005. Available from: http://hdl.handle.net/2027.42/125020


Freie Universität Berlin

18. Grünhagen, Johannes. Non coding RNAs in bone development.

Degree: 2015, Freie Universität Berlin

 Introduction: MiRNAs are noncoding RNAs that represent a powerful modulator of signal transduction. In bone cell biology many microRNA-studies focused on single miRNA-target interactions or… (more)

Subjects/Keywords: miRNAs; miR-195; miR-497; miR-15 family; bmp-signaling; osteoblast differentiation; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Grünhagen, J. (2015). Non coding RNAs in bone development. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12345

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):

Grünhagen, Johannes. “Non coding RNAs in bone development.” 2015. Thesis, Freie Universität Berlin. Accessed September 18, 2020. https://refubium.fu-berlin.de/handle/fub188/12345.

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

MLA Handbook (7th Edition):

Grünhagen, Johannes. “Non coding RNAs in bone development.” 2015. Web. 18 Sep 2020.

Vancouver:

Grünhagen J. Non coding RNAs in bone development. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2020 Sep 18]. Available from: https://refubium.fu-berlin.de/handle/fub188/12345.

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

Council of Science Editors:

Grünhagen J. Non coding RNAs in bone development. [Thesis]. Freie Universität Berlin; 2015. Available from: https://refubium.fu-berlin.de/handle/fub188/12345

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


University of Gothenburg / Göteborgs Universitet

19. Jönsson, Sofia. Aspects on long-term treatment with tyrosine kinase inhibitors in Chronic myeloid leukemia.

Degree: 2011, University of Gothenburg / Göteborgs Universitet

 Chronic myeloid leukemia (CML) is caused by the tyrosine kinase activity of the oncoprotein BCR-ABL. The introduction of tyrosine kinase inhibitors (TKIs) targeting BCR-ABL has… (more)

Subjects/Keywords: Chronic myeloid leukemia; tyrosine kinase inhibitor; imatinib; molecular response; adherence; mesechymal stem cells; osteoblast differentiation; dasatinib

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APA (6th Edition):

Jönsson, S. (2011). Aspects on long-term treatment with tyrosine kinase inhibitors in Chronic myeloid leukemia. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/26270

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):

Jönsson, Sofia. “Aspects on long-term treatment with tyrosine kinase inhibitors in Chronic myeloid leukemia.” 2011. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed September 18, 2020. http://hdl.handle.net/2077/26270.

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

MLA Handbook (7th Edition):

Jönsson, Sofia. “Aspects on long-term treatment with tyrosine kinase inhibitors in Chronic myeloid leukemia.” 2011. Web. 18 Sep 2020.

Vancouver:

Jönsson S. Aspects on long-term treatment with tyrosine kinase inhibitors in Chronic myeloid leukemia. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/2077/26270.

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

Council of Science Editors:

Jönsson S. Aspects on long-term treatment with tyrosine kinase inhibitors in Chronic myeloid leukemia. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2011. Available from: http://hdl.handle.net/2077/26270

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


University of Melbourne

20. Hosseini Far, Hani. Using human induced pluripotent stem cells to reveal the molecular pathology involved in osteogenesis imperfecta resulting from two type I collagen C-propeptide mutations.

Degree: 2019, University of Melbourne

 While the genes underlying the genetic brittle bone disease, osteogenesis imperfecta (OI), are well established, the precise pathological mechanisms are unclear. Recent studies have suggested… (more)

Subjects/Keywords: skeletal dysplasia; osteogenesis imperfecta; type I collagen mutations; ER stress; human induced pluripotent stem cells; osteoblast differentiation; human disease model

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APA (6th Edition):

Hosseini Far, H. (2019). Using human induced pluripotent stem cells to reveal the molecular pathology involved in osteogenesis imperfecta resulting from two type I collagen C-propeptide mutations. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/230722

Chicago Manual of Style (16th Edition):

Hosseini Far, Hani. “Using human induced pluripotent stem cells to reveal the molecular pathology involved in osteogenesis imperfecta resulting from two type I collagen C-propeptide mutations.” 2019. Doctoral Dissertation, University of Melbourne. Accessed September 18, 2020. http://hdl.handle.net/11343/230722.

MLA Handbook (7th Edition):

Hosseini Far, Hani. “Using human induced pluripotent stem cells to reveal the molecular pathology involved in osteogenesis imperfecta resulting from two type I collagen C-propeptide mutations.” 2019. Web. 18 Sep 2020.

Vancouver:

Hosseini Far H. Using human induced pluripotent stem cells to reveal the molecular pathology involved in osteogenesis imperfecta resulting from two type I collagen C-propeptide mutations. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/11343/230722.

Council of Science Editors:

Hosseini Far H. Using human induced pluripotent stem cells to reveal the molecular pathology involved in osteogenesis imperfecta resulting from two type I collagen C-propeptide mutations. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/230722


University of Southern California

21. Pregizer, Steven. Runx2 interactions with the osteoblast genome.

Degree: PhD, Biochemistry & Molecular Biology, 2008, University of Southern California

 Runx2 is a master transcription factor in osteoblasts, yet its mechanism is poorly understood. In particular, there is a paucity of information about its target… (more)

Subjects/Keywords: Runx2; osteoblast differentiation; transcriptional regulation; location analysis

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APA (6th Edition):

Pregizer, S. (2008). Runx2 interactions with the osteoblast genome. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5668

Chicago Manual of Style (16th Edition):

Pregizer, Steven. “Runx2 interactions with the osteoblast genome.” 2008. Doctoral Dissertation, University of Southern California. Accessed September 18, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5668.

MLA Handbook (7th Edition):

Pregizer, Steven. “Runx2 interactions with the osteoblast genome.” 2008. Web. 18 Sep 2020.

Vancouver:

Pregizer S. Runx2 interactions with the osteoblast genome. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Sep 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5668.

Council of Science Editors:

Pregizer S. Runx2 interactions with the osteoblast genome. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/86806/rec/5668


Georgia Tech

22. Zhao, Ge. Interaction of surface energy and microarchitecture in determining cell and tissue response to biomaterials.

Degree: PhD, Biomedical Engineering, 2007, Georgia Tech

 Biomaterials are widely used in medical practice to help maintain, improve or restore diseased tissues or organs. The successful integration of biomaterials with host tissue… (more)

Subjects/Keywords: Titanium; Surface structure; Osteoblast differentiation; Biomedical materials; Biological interfaces

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APA (6th Edition):

Zhao, G. (2007). Interaction of surface energy and microarchitecture in determining cell and tissue response to biomaterials. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/24656

Chicago Manual of Style (16th Edition):

Zhao, Ge. “Interaction of surface energy and microarchitecture in determining cell and tissue response to biomaterials.” 2007. Doctoral Dissertation, Georgia Tech. Accessed September 18, 2020. http://hdl.handle.net/1853/24656.

MLA Handbook (7th Edition):

Zhao, Ge. “Interaction of surface energy and microarchitecture in determining cell and tissue response to biomaterials.” 2007. Web. 18 Sep 2020.

Vancouver:

Zhao G. Interaction of surface energy and microarchitecture in determining cell and tissue response to biomaterials. [Internet] [Doctoral dissertation]. Georgia Tech; 2007. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/1853/24656.

Council of Science Editors:

Zhao G. Interaction of surface energy and microarchitecture in determining cell and tissue response to biomaterials. [Doctoral Dissertation]. Georgia Tech; 2007. Available from: http://hdl.handle.net/1853/24656

23. Okuzu, Yaichiro. Strontium and magnesium ions released from bioactive titanium metal promote early bone bonding in a rabbit implant model .

Degree: 2018, Kyoto University

Subjects/Keywords: Strontium ion; Magnesium ion; Bioactive titanium metal; Osteoblast differentiation

Page 1 Page 2

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APA (6th Edition):

Okuzu, Y. (2018). Strontium and magnesium ions released from bioactive titanium metal promote early bone bonding in a rabbit implant model . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/232122

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):

Okuzu, Yaichiro. “Strontium and magnesium ions released from bioactive titanium metal promote early bone bonding in a rabbit implant model .” 2018. Thesis, Kyoto University. Accessed September 18, 2020. http://hdl.handle.net/2433/232122.

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

MLA Handbook (7th Edition):

Okuzu, Yaichiro. “Strontium and magnesium ions released from bioactive titanium metal promote early bone bonding in a rabbit implant model .” 2018. Web. 18 Sep 2020.

Vancouver:

Okuzu Y. Strontium and magnesium ions released from bioactive titanium metal promote early bone bonding in a rabbit implant model . [Internet] [Thesis]. Kyoto University; 2018. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/2433/232122.

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

Council of Science Editors:

Okuzu Y. Strontium and magnesium ions released from bioactive titanium metal promote early bone bonding in a rabbit implant model . [Thesis]. Kyoto University; 2018. Available from: http://hdl.handle.net/2433/232122

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


Virginia Tech

24. Popp, Jenni Rebecca. Bioactive Poly(Lactic-co-Glycolic Acid)-Calcium Phosphate Scaffolds for Bone Tissue Regeneration.

Degree: PhD, Biomedical Engineering, 2009, Virginia Tech

 Bone is currently the second most transplanted tissue, second only to blood. However, significant hurdles including graft supply and implant failure continue to plague researchers… (more)

Subjects/Keywords: Amorphous Calcium Phosphate; Hydroxyapatite; Zinc; Microspheres; Osteoblast Differentiation

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APA (6th Edition):

Popp, J. R. (2009). Bioactive Poly(Lactic-co-Glycolic Acid)-Calcium Phosphate Scaffolds for Bone Tissue Regeneration. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/37558

Chicago Manual of Style (16th Edition):

Popp, Jenni Rebecca. “Bioactive Poly(Lactic-co-Glycolic Acid)-Calcium Phosphate Scaffolds for Bone Tissue Regeneration.” 2009. Doctoral Dissertation, Virginia Tech. Accessed September 18, 2020. http://hdl.handle.net/10919/37558.

MLA Handbook (7th Edition):

Popp, Jenni Rebecca. “Bioactive Poly(Lactic-co-Glycolic Acid)-Calcium Phosphate Scaffolds for Bone Tissue Regeneration.” 2009. Web. 18 Sep 2020.

Vancouver:

Popp JR. Bioactive Poly(Lactic-co-Glycolic Acid)-Calcium Phosphate Scaffolds for Bone Tissue Regeneration. [Internet] [Doctoral dissertation]. Virginia Tech; 2009. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/10919/37558.

Council of Science Editors:

Popp JR. Bioactive Poly(Lactic-co-Glycolic Acid)-Calcium Phosphate Scaffolds for Bone Tissue Regeneration. [Doctoral Dissertation]. Virginia Tech; 2009. Available from: http://hdl.handle.net/10919/37558

25. Valenzuela, Juan Carlos Bustos. Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos.

Degree: PhD, Bioquímica, 2008, University of São Paulo

As BMPs (Bone Morphogenetic Proteins) são membros da superfamília de proteínas TGF-β (Transforming Growth Factor β ), regulam o crescimento e diferenciação de vários tipos… (more)

Subjects/Keywords: BMPs; BMPs; Bone repair; Cellular differentiation; Diferenciação celular; Diferenciação osteoblástica; Expressão de proteínas recombinantes; Osteoblast differentiation; Osteoblastos; Osteoblasts; Recombinant protein expression; Reparo ósseo

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APA (6th Edition):

Valenzuela, J. C. B. (2008). Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-31072009-140027/ ;

Chicago Manual of Style (16th Edition):

Valenzuela, Juan Carlos Bustos. “Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos.” 2008. Doctoral Dissertation, University of São Paulo. Accessed September 18, 2020. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-31072009-140027/ ;.

MLA Handbook (7th Edition):

Valenzuela, Juan Carlos Bustos. “Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos.” 2008. Web. 18 Sep 2020.

Vancouver:

Valenzuela JCB. Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos. [Internet] [Doctoral dissertation]. University of São Paulo; 2008. [cited 2020 Sep 18]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-31072009-140027/ ;.

Council of Science Editors:

Valenzuela JCB. Análise dos genes diferencialmente expressos durante a osteodiferenciação induzida por proteínas morfogenéticas de osso (BMP2 e BMP7) em células C2C12 e super-expressão de rhBMP2 e rhBMP7 em células de mamíferos. [Doctoral Dissertation]. University of São Paulo; 2008. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-31072009-140027/ ;


Loma Linda University

26. Moran, Colleen M. Effects of Neurotrophic Factors on Osteoblast Growth and Differentiation.

Degree: PhD, Basic Sciences, 2011, Loma Linda University

  Recent evidence suggests that bone metabolism may be influenced by the innervation of skeletal tissues. Innervation of skeletal tissues might directly influence bone volume… (more)

Subjects/Keywords: Anatomy; Medicine and Health Sciences; Musculoskeletal System; Tissues; Osteoblasts; Cell Differentiation; Nerve Growth Factors; Neuropeptides; Receptors - Neurokinin-1; Interleukins; Growth Inhibitors; Bone Morphogenetic Proteins; Calcification - Physiologic;

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APA (6th Edition):

Moran, C. M. (2011). Effects of Neurotrophic Factors on Osteoblast Growth and Differentiation. (Doctoral Dissertation). Loma Linda University. Retrieved from https://scholarsrepository.llu.edu/etd/306

Chicago Manual of Style (16th Edition):

Moran, Colleen M. “Effects of Neurotrophic Factors on Osteoblast Growth and Differentiation.” 2011. Doctoral Dissertation, Loma Linda University. Accessed September 18, 2020. https://scholarsrepository.llu.edu/etd/306.

MLA Handbook (7th Edition):

Moran, Colleen M. “Effects of Neurotrophic Factors on Osteoblast Growth and Differentiation.” 2011. Web. 18 Sep 2020.

Vancouver:

Moran CM. Effects of Neurotrophic Factors on Osteoblast Growth and Differentiation. [Internet] [Doctoral dissertation]. Loma Linda University; 2011. [cited 2020 Sep 18]. Available from: https://scholarsrepository.llu.edu/etd/306.

Council of Science Editors:

Moran CM. Effects of Neurotrophic Factors on Osteoblast Growth and Differentiation. [Doctoral Dissertation]. Loma Linda University; 2011. Available from: https://scholarsrepository.llu.edu/etd/306

27. Paula, Leonardo Barcelos de. Análise proteômica das diversas fases de diferenciação osteoblástica de células-tronco mesenquimais de medula óssea.

Degree: Mestrado, Biologia Celular e Molecular, 2010, University of São Paulo

 O crescimento, desenvolvimento e manutenção do tecido ósseo são processos altamente regulados. Diversas proteínas como hormônios, fatores de crescimento e citocinas estão envolvidas nestes processos… (more)

Subjects/Keywords: . Shotgun proteomics and iTRAQ; Células-tronco mesenquimal; Diferenciação osteoblástica; Mesenchymal stem cells; Osteoblast differentiation; Process of bone regeneration.; Processo de regeneração óssea.; Shotgun proteomics e iTRAQ

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APA (6th Edition):

Paula, L. B. d. (2010). Análise proteômica das diversas fases de diferenciação osteoblástica de células-tronco mesenquimais de medula óssea. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17136/tde-26012011-101120/ ;

Chicago Manual of Style (16th Edition):

Paula, Leonardo Barcelos de. “Análise proteômica das diversas fases de diferenciação osteoblástica de células-tronco mesenquimais de medula óssea.” 2010. Masters Thesis, University of São Paulo. Accessed September 18, 2020. http://www.teses.usp.br/teses/disponiveis/17/17136/tde-26012011-101120/ ;.

MLA Handbook (7th Edition):

Paula, Leonardo Barcelos de. “Análise proteômica das diversas fases de diferenciação osteoblástica de células-tronco mesenquimais de medula óssea.” 2010. Web. 18 Sep 2020.

Vancouver:

Paula LBd. Análise proteômica das diversas fases de diferenciação osteoblástica de células-tronco mesenquimais de medula óssea. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Sep 18]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17136/tde-26012011-101120/ ;.

Council of Science Editors:

Paula LBd. Análise proteômica das diversas fases de diferenciação osteoblástica de células-tronco mesenquimais de medula óssea. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/17/17136/tde-26012011-101120/ ;

28. Alves, Olivia Cherubin. Análise da diferenciação osteoblástica in vitro sobre superfícies de materiais vítreos e vitrocerâmicos bioativos.

Degree: Mestrado, Biologia Oral, 2012, University of São Paulo

Materiais vítreos e vitrocerâmicos bioativos podem ser usados particulados ou como scaffolds em diferentes tratamentos de defeitos ósseos. Tratamentos térmicos que possibilitam o desenvolvimento de… (more)

Subjects/Keywords: bioactive glass; bioactive glass-ceramic; cell culture; cell differentiation; cultura de células; diferenciação celular; expressão gênica; gene expression; osteoblast; osteoblastos; vidros bioativos; vitrocerâmicas bioativas

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

APA (6th Edition):

Alves, O. C. (2012). Análise da diferenciação osteoblástica in vitro sobre superfícies de materiais vítreos e vitrocerâmicos bioativos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/58/58137/tde-18092012-155747/ ;

Chicago Manual of Style (16th Edition):

Alves, Olivia Cherubin. “Análise da diferenciação osteoblástica in vitro sobre superfícies de materiais vítreos e vitrocerâmicos bioativos.” 2012. Masters Thesis, University of São Paulo. Accessed September 18, 2020. http://www.teses.usp.br/teses/disponiveis/58/58137/tde-18092012-155747/ ;.

MLA Handbook (7th Edition):

Alves, Olivia Cherubin. “Análise da diferenciação osteoblástica in vitro sobre superfícies de materiais vítreos e vitrocerâmicos bioativos.” 2012. Web. 18 Sep 2020.

Vancouver:

Alves OC. Análise da diferenciação osteoblástica in vitro sobre superfícies de materiais vítreos e vitrocerâmicos bioativos. [Internet] [Masters thesis]. University of São Paulo; 2012. [cited 2020 Sep 18]. Available from: http://www.teses.usp.br/teses/disponiveis/58/58137/tde-18092012-155747/ ;.

Council of Science Editors:

Alves OC. Análise da diferenciação osteoblástica in vitro sobre superfícies de materiais vítreos e vitrocerâmicos bioativos. [Masters Thesis]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/58/58137/tde-18092012-155747/ ;

29. Raucci, Larissa Moreira Spinola de Castro. Osteogênese in vitro sobre vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®): efeitos do condicionamento de superfície e dos produtos de dissolução iônica.

Degree: Mestrado, Biologia Oral, 2009, University of São Paulo

O objetivo deste estudo foi avaliar o efeito do condicionamento de superfície de uma vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®) e de seus produtos… (more)

Subjects/Keywords: bioactive glass-ceramic; cell culture; cell differentiation; cultura de células; diferenciação celular; dissolução iônica; ionic dissolution products; osteoblast; osteogênese; osteogenesis; surface conditioning; tratamento de superfície; vitrocerâmica bioativa

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

APA (6th Edition):

Raucci, L. M. S. d. C. (2009). Osteogênese in vitro sobre vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®): efeitos do condicionamento de superfície e dos produtos de dissolução iônica. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/58/58137/tde-26032010-164221/ ;

Chicago Manual of Style (16th Edition):

Raucci, Larissa Moreira Spinola de Castro. “Osteogênese in vitro sobre vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®): efeitos do condicionamento de superfície e dos produtos de dissolução iônica.” 2009. Masters Thesis, University of São Paulo. Accessed September 18, 2020. http://www.teses.usp.br/teses/disponiveis/58/58137/tde-26032010-164221/ ;.

MLA Handbook (7th Edition):

Raucci, Larissa Moreira Spinola de Castro. “Osteogênese in vitro sobre vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®): efeitos do condicionamento de superfície e dos produtos de dissolução iônica.” 2009. Web. 18 Sep 2020.

Vancouver:

Raucci LMSdC. Osteogênese in vitro sobre vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®): efeitos do condicionamento de superfície e dos produtos de dissolução iônica. [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2020 Sep 18]. Available from: http://www.teses.usp.br/teses/disponiveis/58/58137/tde-26032010-164221/ ;.

Council of Science Editors:

Raucci LMSdC. Osteogênese in vitro sobre vitrocerâmica 100% cristalina e altamente bioativa (Biosilicato®): efeitos do condicionamento de superfície e dos produtos de dissolução iônica. [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/58/58137/tde-26032010-164221/ ;


University of Michigan

30. Phimphilai, Mattabhorn. Cooperative interactions between bone morphogenetic proteins and the RUNX2 transcription factor in osteoblast differentiation.

Degree: PhD, Pure Sciences, 2006, University of Michigan

 Bone morphogenetic proteins (BMPs) are potent osteogenic factors that stimulate osteoblast differentiation and bone formation. BMPs are known to induce expression of RUNX2/CBFA1 and DLX5… (more)

Subjects/Keywords: Bone Morphogenetic Proteins; Cooperative; Differentiation; Interactions; Osteoblast; Runx2; Transcription Factor

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

APA (6th Edition):

Phimphilai, M. (2006). Cooperative interactions between bone morphogenetic proteins and the RUNX2 transcription factor in osteoblast differentiation. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/125736

Chicago Manual of Style (16th Edition):

Phimphilai, Mattabhorn. “Cooperative interactions between bone morphogenetic proteins and the RUNX2 transcription factor in osteoblast differentiation.” 2006. Doctoral Dissertation, University of Michigan. Accessed September 18, 2020. http://hdl.handle.net/2027.42/125736.

MLA Handbook (7th Edition):

Phimphilai, Mattabhorn. “Cooperative interactions between bone morphogenetic proteins and the RUNX2 transcription factor in osteoblast differentiation.” 2006. Web. 18 Sep 2020.

Vancouver:

Phimphilai M. Cooperative interactions between bone morphogenetic proteins and the RUNX2 transcription factor in osteoblast differentiation. [Internet] [Doctoral dissertation]. University of Michigan; 2006. [cited 2020 Sep 18]. Available from: http://hdl.handle.net/2027.42/125736.

Council of Science Editors:

Phimphilai M. Cooperative interactions between bone morphogenetic proteins and the RUNX2 transcription factor in osteoblast differentiation. [Doctoral Dissertation]. University of Michigan; 2006. Available from: http://hdl.handle.net/2027.42/125736

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