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You searched for subject:(RUNX2). Showing records 1 – 30 of 50 total matches.

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Universidad de Chile

1. Vega Villa, Óscar Andrés. RUNX2 promueve la progresión tumor en osteosarcoma.

Degree: 2011, Universidad de Chile

 El Osteosarcoma (OS) es el tumor sólido maligno más frecuente en la infancia y la adolescencia, corresponde al 20% de todos los tumores óseos y… (more)

Subjects/Keywords: Osteosarcoma; Proteína Runx2

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APA (6th Edition):

Vega Villa, O. A. (2011). RUNX2 promueve la progresión tumor en osteosarcoma. (Thesis). Universidad de Chile. Retrieved from http://repositorio.uchile.cl/handle/2250/170931

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):

Vega Villa, Óscar Andrés. “RUNX2 promueve la progresión tumor en osteosarcoma.” 2011. Thesis, Universidad de Chile. Accessed September 24, 2020. http://repositorio.uchile.cl/handle/2250/170931.

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

MLA Handbook (7th Edition):

Vega Villa, Óscar Andrés. “RUNX2 promueve la progresión tumor en osteosarcoma.” 2011. Web. 24 Sep 2020.

Vancouver:

Vega Villa OA. RUNX2 promueve la progresión tumor en osteosarcoma. [Internet] [Thesis]. Universidad de Chile; 2011. [cited 2020 Sep 24]. Available from: http://repositorio.uchile.cl/handle/2250/170931.

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

Council of Science Editors:

Vega Villa OA. RUNX2 promueve la progresión tumor en osteosarcoma. [Thesis]. Universidad de Chile; 2011. Available from: http://repositorio.uchile.cl/handle/2250/170931

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


University of Manchester

2. Ayub, Rahna. The Role of the Runx2/CBFβ complex in Breast Cancer.

Degree: 2014, University of Manchester

 Breast cancers frequently metastasise to the skeleton where they cause osteolytic bone destruction. Effective treatment of bone metastasis remains a considerable clinical challenge. In the… (more)

Subjects/Keywords: Breast Cancer; Runx2; CBF beta

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APA (6th Edition):

Ayub, R. (2014). The Role of the Runx2/CBFβ complex in Breast Cancer. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:218330

Chicago Manual of Style (16th Edition):

Ayub, Rahna. “The Role of the Runx2/CBFβ complex in Breast Cancer.” 2014. Doctoral Dissertation, University of Manchester. Accessed September 24, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:218330.

MLA Handbook (7th Edition):

Ayub, Rahna. “The Role of the Runx2/CBFβ complex in Breast Cancer.” 2014. Web. 24 Sep 2020.

Vancouver:

Ayub R. The Role of the Runx2/CBFβ complex in Breast Cancer. [Internet] [Doctoral dissertation]. University of Manchester; 2014. [cited 2020 Sep 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:218330.

Council of Science Editors:

Ayub R. The Role of the Runx2/CBFβ complex in Breast Cancer. [Doctoral Dissertation]. University of Manchester; 2014. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:218330


University of Rochester

3. Shen, Run; Chen, Di (1955 - ). Regulation of Runx2 protein stability in chondrocyte development.

Degree: PhD, 2009, University of Rochester

 During endochondral bone formation, cartilages provide the template for vascular invasion, which brings in osteoblasts to deposit bone matrix on the debris of apoptotic chondrocytes.… (more)

Subjects/Keywords: Ubiquitin; Runx2; Chondrocyte; PTHrP; Cartilage

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APA (6th Edition):

Shen, Run; Chen, D. (. -. ). (2009). Regulation of Runx2 protein stability in chondrocyte development. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/6536

Chicago Manual of Style (16th Edition):

Shen, Run; Chen, Di (1955 - ). “Regulation of Runx2 protein stability in chondrocyte development.” 2009. Doctoral Dissertation, University of Rochester. Accessed September 24, 2020. http://hdl.handle.net/1802/6536.

MLA Handbook (7th Edition):

Shen, Run; Chen, Di (1955 - ). “Regulation of Runx2 protein stability in chondrocyte development.” 2009. Web. 24 Sep 2020.

Vancouver:

Shen, Run; Chen D(-). Regulation of Runx2 protein stability in chondrocyte development. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/1802/6536.

Council of Science Editors:

Shen, Run; Chen D(-). Regulation of Runx2 protein stability in chondrocyte development. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/6536


University of Manchester

4. Lopez Camacho, Cesar. A new role for Filamin A as a regulator of Runx2 function.

Degree: 2011, University of Manchester

 AbstractThe University of Manchester, Cesar Lopez Camacho PhD in Molecular BiologyThesis title: A new role for Filamin A as a regulator of Runx2 functionJanuary 2011Filamin… (more)

Subjects/Keywords: Filamin A; Runx2; osteoblastic differentiation; nucleolus

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APA (6th Edition):

Lopez Camacho, C. (2011). A new role for Filamin A as a regulator of Runx2 function. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:120116

Chicago Manual of Style (16th Edition):

Lopez Camacho, Cesar. “A new role for Filamin A as a regulator of Runx2 function.” 2011. Doctoral Dissertation, University of Manchester. Accessed September 24, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:120116.

MLA Handbook (7th Edition):

Lopez Camacho, Cesar. “A new role for Filamin A as a regulator of Runx2 function.” 2011. Web. 24 Sep 2020.

Vancouver:

Lopez Camacho C. A new role for Filamin A as a regulator of Runx2 function. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Sep 24]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:120116.

Council of Science Editors:

Lopez Camacho C. A new role for Filamin A as a regulator of Runx2 function. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:120116


University of Vermont

5. Ojemann, Alexandra. Understanding the Role of Runx2 in a Breast Cancer Progression Cell Model.

Degree: MS, Biochemistry, 2017, University of Vermont

Runx2 is a transcription factor required for bone formation and osteoblastic differentiation during normal development and is implicated in metastatic disease during breast cancer… (more)

Subjects/Keywords: Breast; Cancer; MCF10AT1; MCF10CA1a; Progression; Runx2; Biochemistry

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APA (6th Edition):

Ojemann, A. (2017). Understanding the Role of Runx2 in a Breast Cancer Progression Cell Model. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/741

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):

Ojemann, Alexandra. “Understanding the Role of Runx2 in a Breast Cancer Progression Cell Model.” 2017. Thesis, University of Vermont. Accessed September 24, 2020. https://scholarworks.uvm.edu/graddis/741.

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

MLA Handbook (7th Edition):

Ojemann, Alexandra. “Understanding the Role of Runx2 in a Breast Cancer Progression Cell Model.” 2017. Web. 24 Sep 2020.

Vancouver:

Ojemann A. Understanding the Role of Runx2 in a Breast Cancer Progression Cell Model. [Internet] [Thesis]. University of Vermont; 2017. [cited 2020 Sep 24]. Available from: https://scholarworks.uvm.edu/graddis/741.

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

Council of Science Editors:

Ojemann A. Understanding the Role of Runx2 in a Breast Cancer Progression Cell Model. [Thesis]. University of Vermont; 2017. Available from: https://scholarworks.uvm.edu/graddis/741

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


University of Manchester

6. Lopez Camacho, Cesar. A new role for Filamin A as a regulator of Runx2 function.

Degree: PhD, 2011, University of Manchester

 Filamin A is a well-characterised cytoskeletal protein which regulates cell shape and migration by cross-linking with actin. Filamin A mutations cause a number of human… (more)

Subjects/Keywords: 612; Filamin A, Runx2, osteoblastic differentiation, nucleolus

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APA (6th Edition):

Lopez Camacho, C. (2011). A new role for Filamin A as a regulator of Runx2 function. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-new-role-for-filamin-a-as-a-regulator-of-runx2-function(88321064-5c82-4f2b-a755-911ed3b42b2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538413

Chicago Manual of Style (16th Edition):

Lopez Camacho, Cesar. “A new role for Filamin A as a regulator of Runx2 function.” 2011. Doctoral Dissertation, University of Manchester. Accessed September 24, 2020. https://www.research.manchester.ac.uk/portal/en/theses/a-new-role-for-filamin-a-as-a-regulator-of-runx2-function(88321064-5c82-4f2b-a755-911ed3b42b2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538413.

MLA Handbook (7th Edition):

Lopez Camacho, Cesar. “A new role for Filamin A as a regulator of Runx2 function.” 2011. Web. 24 Sep 2020.

Vancouver:

Lopez Camacho C. A new role for Filamin A as a regulator of Runx2 function. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Sep 24]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-new-role-for-filamin-a-as-a-regulator-of-runx2-function(88321064-5c82-4f2b-a755-911ed3b42b2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538413.

Council of Science Editors:

Lopez Camacho C. A new role for Filamin A as a regulator of Runx2 function. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-new-role-for-filamin-a-as-a-regulator-of-runx2-function(88321064-5c82-4f2b-a755-911ed3b42b2e).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538413


University of Melbourne

7. BEST, SARAH. Roles of the transcription factors Runx2, Id4 and Snai2 in mammary gland development.

Degree: 2014, University of Melbourne

 Transcription factors govern the development and maintenance of many tissues, including the mammary gland. Over recent years, several transcription factors have been found to have… (more)

Subjects/Keywords: transcription factors; mammary development; Runx2; Id4; Snai2

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APA (6th Edition):

BEST, S. (2014). Roles of the transcription factors Runx2, Id4 and Snai2 in mammary gland development. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/42991

Chicago Manual of Style (16th Edition):

BEST, SARAH. “Roles of the transcription factors Runx2, Id4 and Snai2 in mammary gland development.” 2014. Doctoral Dissertation, University of Melbourne. Accessed September 24, 2020. http://hdl.handle.net/11343/42991.

MLA Handbook (7th Edition):

BEST, SARAH. “Roles of the transcription factors Runx2, Id4 and Snai2 in mammary gland development.” 2014. Web. 24 Sep 2020.

Vancouver:

BEST S. Roles of the transcription factors Runx2, Id4 and Snai2 in mammary gland development. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/11343/42991.

Council of Science Editors:

BEST S. Roles of the transcription factors Runx2, Id4 and Snai2 in mammary gland development. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/42991


University of Southern California

8. 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 24, 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. 24 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 24]. 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


University of Southern California

9. Champagne, Eri Morimoto. Glucocorticoids and Runx2 synergistically stimulate Wif1 and compromise pre-osteoblats in vitro.

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

 For over six decades, glucocorticoids (GCs) have been used to treat inflammatory diseases such as rheumatoid arthritis, but their long‐term use causes severe side effects,… (more)

Subjects/Keywords: Wif1; glucocorticoids; Runx2; osteoporosis; mesenchymal stem cells

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APA (6th Edition):

Champagne, E. M. (2015). Glucocorticoids and Runx2 synergistically stimulate Wif1 and compromise pre-osteoblats in vitro. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595782/rec/3074

Chicago Manual of Style (16th Edition):

Champagne, Eri Morimoto. “Glucocorticoids and Runx2 synergistically stimulate Wif1 and compromise pre-osteoblats in vitro.” 2015. Masters Thesis, University of Southern California. Accessed September 24, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595782/rec/3074.

MLA Handbook (7th Edition):

Champagne, Eri Morimoto. “Glucocorticoids and Runx2 synergistically stimulate Wif1 and compromise pre-osteoblats in vitro.” 2015. Web. 24 Sep 2020.

Vancouver:

Champagne EM. Glucocorticoids and Runx2 synergistically stimulate Wif1 and compromise pre-osteoblats in vitro. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Sep 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595782/rec/3074.

Council of Science Editors:

Champagne EM. Glucocorticoids and Runx2 synergistically stimulate Wif1 and compromise pre-osteoblats in vitro. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/595782/rec/3074


University of Southern California

10. Xiong, Jian. RUNX2 stimulates osteoblast-driven osteoclastogenesis by RANKL presentation.

Degree: MS, Biochemistry and Molecular Biology, 2013, University of Southern California

 In mammalian bodies, bones are continuously remodeled via two processes: bone formation and bone resorption. RUNX2, used to be recognized as activator of osteoblast differentiation… (more)

Subjects/Keywords: RUNX2; RANKL; osteoclastogenesis; mouse primary osteoblasts

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APA (6th Edition):

Xiong, J. (2013). RUNX2 stimulates osteoblast-driven osteoclastogenesis by RANKL presentation. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/316502/rec/5669

Chicago Manual of Style (16th Edition):

Xiong, Jian. “RUNX2 stimulates osteoblast-driven osteoclastogenesis by RANKL presentation.” 2013. Masters Thesis, University of Southern California. Accessed September 24, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/316502/rec/5669.

MLA Handbook (7th Edition):

Xiong, Jian. “RUNX2 stimulates osteoblast-driven osteoclastogenesis by RANKL presentation.” 2013. Web. 24 Sep 2020.

Vancouver:

Xiong J. RUNX2 stimulates osteoblast-driven osteoclastogenesis by RANKL presentation. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2020 Sep 24]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/316502/rec/5669.

Council of Science Editors:

Xiong J. RUNX2 stimulates osteoblast-driven osteoclastogenesis by RANKL presentation. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/316502/rec/5669


Queens University

11. Martin, Jeff. Role of Amplification of Chromosome 6P12-P21 in Human Osteosarcoma .

Degree: Pathology and Molecular Medicine, 2015, Queens University

 Osteosarcoma is an aggressive bone malignancy with neither reliable prognostic or predictive biomarkers nor drugs for targeted therapy. It is the most common malignant tumour… (more)

Subjects/Keywords: Osteosarcoma ; Cytogenetics ; Fluorescence In Situ Hybridisation ; RUNX2

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APA (6th Edition):

Martin, J. (2015). Role of Amplification of Chromosome 6P12-P21 in Human Osteosarcoma . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13891

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):

Martin, Jeff. “Role of Amplification of Chromosome 6P12-P21 in Human Osteosarcoma .” 2015. Thesis, Queens University. Accessed September 24, 2020. http://hdl.handle.net/1974/13891.

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

MLA Handbook (7th Edition):

Martin, Jeff. “Role of Amplification of Chromosome 6P12-P21 in Human Osteosarcoma .” 2015. Web. 24 Sep 2020.

Vancouver:

Martin J. Role of Amplification of Chromosome 6P12-P21 in Human Osteosarcoma . [Internet] [Thesis]. Queens University; 2015. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/1974/13891.

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

Council of Science Editors:

Martin J. Role of Amplification of Chromosome 6P12-P21 in Human Osteosarcoma . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13891

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


Temple University

12. Hendesi, Honey. CONNECTIVE TISSUE GROWTH FACTOR (CTGF/CCN2) REGULATES OSTEOBLAST CYTOSKELETAL REORGANIZATION AND MOTILITY AND ENHANCES DIFFERENTIATION VIA BINDING TO INTEGRIN RECEPTORS AND ACTIVATION OF DOWNSTREAM SIGNALINGS.

Degree: PhD, 2014, Temple University

Cell Biology

Connective Tissue Growth Factor (CTGF) is a matricellular protein that has been shown to mediate cell adhesion, and as a consequence, it regulates… (more)

Subjects/Keywords: Cellular biology;

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APA (6th Edition):

Hendesi, H. (2014). CONNECTIVE TISSUE GROWTH FACTOR (CTGF/CCN2) REGULATES OSTEOBLAST CYTOSKELETAL REORGANIZATION AND MOTILITY AND ENHANCES DIFFERENTIATION VIA BINDING TO INTEGRIN RECEPTORS AND ACTIVATION OF DOWNSTREAM SIGNALINGS. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,263674

Chicago Manual of Style (16th Edition):

Hendesi, Honey. “CONNECTIVE TISSUE GROWTH FACTOR (CTGF/CCN2) REGULATES OSTEOBLAST CYTOSKELETAL REORGANIZATION AND MOTILITY AND ENHANCES DIFFERENTIATION VIA BINDING TO INTEGRIN RECEPTORS AND ACTIVATION OF DOWNSTREAM SIGNALINGS.” 2014. Doctoral Dissertation, Temple University. Accessed September 24, 2020. http://digital.library.temple.edu/u?/p245801coll10,263674.

MLA Handbook (7th Edition):

Hendesi, Honey. “CONNECTIVE TISSUE GROWTH FACTOR (CTGF/CCN2) REGULATES OSTEOBLAST CYTOSKELETAL REORGANIZATION AND MOTILITY AND ENHANCES DIFFERENTIATION VIA BINDING TO INTEGRIN RECEPTORS AND ACTIVATION OF DOWNSTREAM SIGNALINGS.” 2014. Web. 24 Sep 2020.

Vancouver:

Hendesi H. CONNECTIVE TISSUE GROWTH FACTOR (CTGF/CCN2) REGULATES OSTEOBLAST CYTOSKELETAL REORGANIZATION AND MOTILITY AND ENHANCES DIFFERENTIATION VIA BINDING TO INTEGRIN RECEPTORS AND ACTIVATION OF DOWNSTREAM SIGNALINGS. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2020 Sep 24]. Available from: http://digital.library.temple.edu/u?/p245801coll10,263674.

Council of Science Editors:

Hendesi H. CONNECTIVE TISSUE GROWTH FACTOR (CTGF/CCN2) REGULATES OSTEOBLAST CYTOSKELETAL REORGANIZATION AND MOTILITY AND ENHANCES DIFFERENTIATION VIA BINDING TO INTEGRIN RECEPTORS AND ACTIVATION OF DOWNSTREAM SIGNALINGS. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,263674


Penn State University

13. Radford, Thomas. Differentiation of mesenchymal stem cells to tendon-like progenitor cells via growth factor stimulation.

Degree: 2020, Penn State University

 There are an estimated 130 million health care encounters pertaining to musculoskeletal injury in the United States each year, with an economic burden of nearly… (more)

Subjects/Keywords: GDF7; mesenchymal stem cells; tenocyte differentiation; scleraxis; runx2

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APA (6th Edition):

Radford, T. (2020). Differentiation of mesenchymal stem cells to tendon-like progenitor cells via growth factor stimulation. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/17681tir14

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):

Radford, Thomas. “Differentiation of mesenchymal stem cells to tendon-like progenitor cells via growth factor stimulation.” 2020. Thesis, Penn State University. Accessed September 24, 2020. https://submit-etda.libraries.psu.edu/catalog/17681tir14.

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

MLA Handbook (7th Edition):

Radford, Thomas. “Differentiation of mesenchymal stem cells to tendon-like progenitor cells via growth factor stimulation.” 2020. Web. 24 Sep 2020.

Vancouver:

Radford T. Differentiation of mesenchymal stem cells to tendon-like progenitor cells via growth factor stimulation. [Internet] [Thesis]. Penn State University; 2020. [cited 2020 Sep 24]. Available from: https://submit-etda.libraries.psu.edu/catalog/17681tir14.

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

Council of Science Editors:

Radford T. Differentiation of mesenchymal stem cells to tendon-like progenitor cells via growth factor stimulation. [Thesis]. Penn State University; 2020. Available from: https://submit-etda.libraries.psu.edu/catalog/17681tir14

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


University of Pennsylvania

14. Weber, Christopher. Multiple Conserved Enhancers of the Osteoblast Master Transcription Factor, Runx2, Integrate Diverse Signaling Pathways to Direct Expression to Developing Bone.

Degree: 2013, University of Pennsylvania

 The vertebrate skeleton forms via two distinct modes of ossification, membranous and endochondral. Osteoblasts are also heterogeneous in embryonic origin; bone formed by either mode… (more)

Subjects/Keywords: BMP; FGF; osteoblast; RUNX2; WNT; zebrafish; Genetics; Molecular Biology

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APA (6th Edition):

Weber, C. (2013). Multiple Conserved Enhancers of the Osteoblast Master Transcription Factor, Runx2, Integrate Diverse Signaling Pathways to Direct Expression to Developing Bone. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/941

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):

Weber, Christopher. “Multiple Conserved Enhancers of the Osteoblast Master Transcription Factor, Runx2, Integrate Diverse Signaling Pathways to Direct Expression to Developing Bone.” 2013. Thesis, University of Pennsylvania. Accessed September 24, 2020. https://repository.upenn.edu/edissertations/941.

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

MLA Handbook (7th Edition):

Weber, Christopher. “Multiple Conserved Enhancers of the Osteoblast Master Transcription Factor, Runx2, Integrate Diverse Signaling Pathways to Direct Expression to Developing Bone.” 2013. Web. 24 Sep 2020.

Vancouver:

Weber C. Multiple Conserved Enhancers of the Osteoblast Master Transcription Factor, Runx2, Integrate Diverse Signaling Pathways to Direct Expression to Developing Bone. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2020 Sep 24]. Available from: https://repository.upenn.edu/edissertations/941.

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

Council of Science Editors:

Weber C. Multiple Conserved Enhancers of the Osteoblast Master Transcription Factor, Runx2, Integrate Diverse Signaling Pathways to Direct Expression to Developing Bone. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/941

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

15. 梅林, 真由美. Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation : BMP4/Runx2遺伝子活性化基質によるラット頭蓋骨骨増生の試み.

Degree: 博士(歯学), 2015, Nagasaki University / 長崎大学

 To date, therapeutic method for in vivo gene delivery has not been established on bone engineering though its potential usefulness has been suggested. For clinical… (more)

Subjects/Keywords: atelocollagen; bmp4; bone regeneration; gene-activated matrix; in vivo; runx2

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APA (6th Edition):

梅林, . (2015). Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation : BMP4/Runx2遺伝子活性化基質によるラット頭蓋骨骨増生の試み. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/36080

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):

梅林, 真由美. “Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation : BMP4/Runx2遺伝子活性化基質によるラット頭蓋骨骨増生の試み.” 2015. Thesis, Nagasaki University / 長崎大学. Accessed September 24, 2020. http://hdl.handle.net/10069/36080.

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

MLA Handbook (7th Edition):

梅林, 真由美. “Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation : BMP4/Runx2遺伝子活性化基質によるラット頭蓋骨骨増生の試み.” 2015. Web. 24 Sep 2020.

Vancouver:

梅林 . Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation : BMP4/Runx2遺伝子活性化基質によるラット頭蓋骨骨増生の試み. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2015. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/10069/36080.

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

Council of Science Editors:

梅林 . Gene-Activated Matrix Comprised of Atelocollagen and Plasmid DNA Encoding BMP4 or Runx2 Promotes Rat Cranial Bone Augmentation : BMP4/Runx2遺伝子活性化基質によるラット頭蓋骨骨増生の試み. [Thesis]. Nagasaki University / 長崎大学; 2015. Available from: http://hdl.handle.net/10069/36080

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


University of Connecticut

16. Kim, Yung Kyun, DDS. Osteogenesis During Early Healing Around Titanium and Titanium Zirconium Implants: Immunohistochemistry and mRNA Expression of Bone Markers in Miniature Pigs.

Degree: Master of Dental Science, Dental Science, 2011, University of Connecticut

  Background: To better understand the effect of implant surface modification on bone, more information is needed on the early stages of bone healing around… (more)

Subjects/Keywords: immunohistochemistry; RT-PCR; implant; Roxolid; osteogenesis; histomorphometry; osteocalcin; osteopontin; osterix; Runx2

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APA (6th Edition):

Kim, Yung Kyun, D. (2011). Osteogenesis During Early Healing Around Titanium and Titanium Zirconium Implants: Immunohistochemistry and mRNA Expression of Bone Markers in Miniature Pigs. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/176

Chicago Manual of Style (16th Edition):

Kim, Yung Kyun, DDS. “Osteogenesis During Early Healing Around Titanium and Titanium Zirconium Implants: Immunohistochemistry and mRNA Expression of Bone Markers in Miniature Pigs.” 2011. Masters Thesis, University of Connecticut. Accessed September 24, 2020. https://opencommons.uconn.edu/gs_theses/176.

MLA Handbook (7th Edition):

Kim, Yung Kyun, DDS. “Osteogenesis During Early Healing Around Titanium and Titanium Zirconium Implants: Immunohistochemistry and mRNA Expression of Bone Markers in Miniature Pigs.” 2011. Web. 24 Sep 2020.

Vancouver:

Kim, Yung Kyun D. Osteogenesis During Early Healing Around Titanium and Titanium Zirconium Implants: Immunohistochemistry and mRNA Expression of Bone Markers in Miniature Pigs. [Internet] [Masters thesis]. University of Connecticut; 2011. [cited 2020 Sep 24]. Available from: https://opencommons.uconn.edu/gs_theses/176.

Council of Science Editors:

Kim, Yung Kyun D. Osteogenesis During Early Healing Around Titanium and Titanium Zirconium Implants: Immunohistochemistry and mRNA Expression of Bone Markers in Miniature Pigs. [Masters Thesis]. University of Connecticut; 2011. Available from: https://opencommons.uconn.edu/gs_theses/176


University of Vermont

17. Taber, Thomas Howland. Thyroid Hormone Receptor SS (trß) Regulation Of Runt-Related Transcription Factor 2 (runx2) In Thyroid Tumorigenesis: Determination Of The Trß Nuclear Protein Complexes That Associate With The Runx2 Gene.

Degree: MS, Pharmacology, 2017, University of Vermont

  Thyroid Tumorigenesis is typically a well understood process, with well delineated oncogenic factors. Follicular and papillary thyroid cancers are typically survivable, with 5-year survival… (more)

Subjects/Keywords: Cancer; RUNX2; SWI/SNF; THRB; Thyroid; Thyroid Cancer; Cell Biology; Oncology

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APA (6th Edition):

Taber, T. H. (2017). Thyroid Hormone Receptor SS (trß) Regulation Of Runt-Related Transcription Factor 2 (runx2) In Thyroid Tumorigenesis: Determination Of The Trß Nuclear Protein Complexes That Associate With The Runx2 Gene. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/820

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):

Taber, Thomas Howland. “Thyroid Hormone Receptor SS (trß) Regulation Of Runt-Related Transcription Factor 2 (runx2) In Thyroid Tumorigenesis: Determination Of The Trß Nuclear Protein Complexes That Associate With The Runx2 Gene.” 2017. Thesis, University of Vermont. Accessed September 24, 2020. https://scholarworks.uvm.edu/graddis/820.

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

MLA Handbook (7th Edition):

Taber, Thomas Howland. “Thyroid Hormone Receptor SS (trß) Regulation Of Runt-Related Transcription Factor 2 (runx2) In Thyroid Tumorigenesis: Determination Of The Trß Nuclear Protein Complexes That Associate With The Runx2 Gene.” 2017. Web. 24 Sep 2020.

Vancouver:

Taber TH. Thyroid Hormone Receptor SS (trß) Regulation Of Runt-Related Transcription Factor 2 (runx2) In Thyroid Tumorigenesis: Determination Of The Trß Nuclear Protein Complexes That Associate With The Runx2 Gene. [Internet] [Thesis]. University of Vermont; 2017. [cited 2020 Sep 24]. Available from: https://scholarworks.uvm.edu/graddis/820.

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

Council of Science Editors:

Taber TH. Thyroid Hormone Receptor SS (trß) Regulation Of Runt-Related Transcription Factor 2 (runx2) In Thyroid Tumorigenesis: Determination Of The Trß Nuclear Protein Complexes That Associate With The Runx2 Gene. [Thesis]. University of Vermont; 2017. Available from: https://scholarworks.uvm.edu/graddis/820

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


University of Adelaide

18. Stewart, Trudy Ann. Expression of runt related transcription factor 2 and vascular endothelial growth factor in the pulp, periodontal ligament and alveolar bone: an immunohistochemical study using a rat ankylotic model.

Degree: 2013, University of Adelaide

 The current study investigated the expression Runx2 and VEGF in the pulp, periodontal ligament and alveolar bone following hypothermal insult. Methods and Materials: Materials from… (more)

Subjects/Keywords: Runx2; VEGF; rat; ankylotic; PDL; pulp; alveolar bone; immunohistochemical

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APA (6th Edition):

Stewart, T. A. (2013). Expression of runt related transcription factor 2 and vascular endothelial growth factor in the pulp, periodontal ligament and alveolar bone: an immunohistochemical study using a rat ankylotic model. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/82553

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):

Stewart, Trudy Ann. “Expression of runt related transcription factor 2 and vascular endothelial growth factor in the pulp, periodontal ligament and alveolar bone: an immunohistochemical study using a rat ankylotic model.” 2013. Thesis, University of Adelaide. Accessed September 24, 2020. http://hdl.handle.net/2440/82553.

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

MLA Handbook (7th Edition):

Stewart, Trudy Ann. “Expression of runt related transcription factor 2 and vascular endothelial growth factor in the pulp, periodontal ligament and alveolar bone: an immunohistochemical study using a rat ankylotic model.” 2013. Web. 24 Sep 2020.

Vancouver:

Stewart TA. Expression of runt related transcription factor 2 and vascular endothelial growth factor in the pulp, periodontal ligament and alveolar bone: an immunohistochemical study using a rat ankylotic model. [Internet] [Thesis]. University of Adelaide; 2013. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/2440/82553.

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

Council of Science Editors:

Stewart TA. Expression of runt related transcription factor 2 and vascular endothelial growth factor in the pulp, periodontal ligament and alveolar bone: an immunohistochemical study using a rat ankylotic model. [Thesis]. University of Adelaide; 2013. Available from: http://hdl.handle.net/2440/82553

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


Univerzitet u Beogradu

19. Živković-Sandić, Marija. Uticaj mutacija RUNX2 i WNT10A gena na broj i veličinu zuba.

Degree: Stomatološki fakultet, 2017, Univerzitet u Beogradu

stomatologija - ortopedija vilica

Hipodoncija-urodjeni nedostatak zuba, predstavlja jednu od najĉešćih razvojnih anomalija kod ljudi, i moţe biti nesindromska i sindromska. Do razvoja hipodoncije moţe… (more)

Subjects/Keywords: odontogenesis; genes; RUNX2; WNT10A; hypodontia; oligodontia; tooth size

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APA (6th Edition):

Živković-Sandić, M. (2017). Uticaj mutacija RUNX2 i WNT10A gena na broj i veličinu zuba. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:14872/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):

Živković-Sandić, Marija. “Uticaj mutacija RUNX2 i WNT10A gena na broj i veličinu zuba.” 2017. Thesis, Univerzitet u Beogradu. Accessed September 24, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:14872/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):

Živković-Sandić, Marija. “Uticaj mutacija RUNX2 i WNT10A gena na broj i veličinu zuba.” 2017. Web. 24 Sep 2020.

Vancouver:

Živković-Sandić M. Uticaj mutacija RUNX2 i WNT10A gena na broj i veličinu zuba. [Internet] [Thesis]. Univerzitet u Beogradu; 2017. [cited 2020 Sep 24]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:14872/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:

Živković-Sandić M. Uticaj mutacija RUNX2 i WNT10A gena na broj i veličinu zuba. [Thesis]. Univerzitet u Beogradu; 2017. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:14872/bdef:Content/get

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


University of Washington

20. Chen, Theodore. Runx2 and Vascular Calcification.

Degree: PhD, 2016, University of Washington

 Complications arising from vascular calcification, the inappropriate deposition of calcium phosphate crystals in the vasculature, have become more evident in recent years as human longevity… (more)

Subjects/Keywords: atherosclerosis; macrophage polarization; Runx2; Vascular calcification; Engineering; Biology; bioengineering

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APA (6th Edition):

Chen, T. (2016). Runx2 and Vascular Calcification. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/36495

Chicago Manual of Style (16th Edition):

Chen, Theodore. “Runx2 and Vascular Calcification.” 2016. Doctoral Dissertation, University of Washington. Accessed September 24, 2020. http://hdl.handle.net/1773/36495.

MLA Handbook (7th Edition):

Chen, Theodore. “Runx2 and Vascular Calcification.” 2016. Web. 24 Sep 2020.

Vancouver:

Chen T. Runx2 and Vascular Calcification. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/1773/36495.

Council of Science Editors:

Chen T. Runx2 and Vascular Calcification. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/36495


University of Toronto

21. Alvandi, Zahra. c-Src Controls Mouse Embryonic Osteogenic Differentiation Through Regulation of Stat1 Stability.

Degree: PhD, 2018, University of Toronto

The protein tyrosine kinase Src is expressed ubiquitously and is involved in differentiation. However, the role of Src in osteogenic differentiation is complex since it… (more)

Subjects/Keywords: Bone; Differentiation; Embryonic stem cells; Runx2; Src; Stat1; 0306

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APA (6th Edition):

Alvandi, Z. (2018). c-Src Controls Mouse Embryonic Osteogenic Differentiation Through Regulation of Stat1 Stability. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/95652

Chicago Manual of Style (16th Edition):

Alvandi, Zahra. “c-Src Controls Mouse Embryonic Osteogenic Differentiation Through Regulation of Stat1 Stability.” 2018. Doctoral Dissertation, University of Toronto. Accessed September 24, 2020. http://hdl.handle.net/1807/95652.

MLA Handbook (7th Edition):

Alvandi, Zahra. “c-Src Controls Mouse Embryonic Osteogenic Differentiation Through Regulation of Stat1 Stability.” 2018. Web. 24 Sep 2020.

Vancouver:

Alvandi Z. c-Src Controls Mouse Embryonic Osteogenic Differentiation Through Regulation of Stat1 Stability. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/1807/95652.

Council of Science Editors:

Alvandi Z. c-Src Controls Mouse Embryonic Osteogenic Differentiation Through Regulation of Stat1 Stability. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/95652

22. Olesin, Elizabeth A. Transcriptional Regulation of Effector and Memory Responses during Acute and Chronic Lymphocytic Choriomeningitis Virus (LCMV) Infection.

Degree: Immunology and Microbiology, Pathology, 2018, U of Massachusetts : Med

  Transcriptional regulation of CD8+ T cell differentiation during acute and chronic viral infections is an intricate web made up of many of transcription factors.… (more)

Subjects/Keywords: LCMV; Memory; Effector; CD8; T Cell; Runx2; IRF4; Viral Infection; Immunology of Infectious Disease

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APA (6th Edition):

Olesin, E. A. (2018). Transcriptional Regulation of Effector and Memory Responses during Acute and Chronic Lymphocytic Choriomeningitis Virus (LCMV) Infection. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/1000

Chicago Manual of Style (16th Edition):

Olesin, Elizabeth A. “Transcriptional Regulation of Effector and Memory Responses during Acute and Chronic Lymphocytic Choriomeningitis Virus (LCMV) Infection.” 2018. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 24, 2020. https://escholarship.umassmed.edu/gsbs_diss/1000.

MLA Handbook (7th Edition):

Olesin, Elizabeth A. “Transcriptional Regulation of Effector and Memory Responses during Acute and Chronic Lymphocytic Choriomeningitis Virus (LCMV) Infection.” 2018. Web. 24 Sep 2020.

Vancouver:

Olesin EA. Transcriptional Regulation of Effector and Memory Responses during Acute and Chronic Lymphocytic Choriomeningitis Virus (LCMV) Infection. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2018. [cited 2020 Sep 24]. Available from: https://escholarship.umassmed.edu/gsbs_diss/1000.

Council of Science Editors:

Olesin EA. Transcriptional Regulation of Effector and Memory Responses during Acute and Chronic Lymphocytic Choriomeningitis Virus (LCMV) Infection. [Doctoral Dissertation]. U of Massachusetts : Med; 2018. Available from: https://escholarship.umassmed.edu/gsbs_diss/1000

23. CHAN HSIAO YUN. ELUCIDATION OF THE GENE REGULATION NETWORK CONTROLLING EMBRYONIC SKELETAL DEVELOPMENT.

Degree: 2012, National University of Singapore

Subjects/Keywords: Runx2; Runx3; EGFP; Skeletal; Osteoblast; Chondrocyte

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APA (6th Edition):

YUN, C. H. (2012). ELUCIDATION OF THE GENE REGULATION NETWORK CONTROLLING EMBRYONIC SKELETAL DEVELOPMENT. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/47607

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):

YUN, CHAN HSIAO. “ELUCIDATION OF THE GENE REGULATION NETWORK CONTROLLING EMBRYONIC SKELETAL DEVELOPMENT.” 2012. Thesis, National University of Singapore. Accessed September 24, 2020. http://scholarbank.nus.edu.sg/handle/10635/47607.

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

MLA Handbook (7th Edition):

YUN, CHAN HSIAO. “ELUCIDATION OF THE GENE REGULATION NETWORK CONTROLLING EMBRYONIC SKELETAL DEVELOPMENT.” 2012. Web. 24 Sep 2020.

Vancouver:

YUN CH. ELUCIDATION OF THE GENE REGULATION NETWORK CONTROLLING EMBRYONIC SKELETAL DEVELOPMENT. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2020 Sep 24]. Available from: http://scholarbank.nus.edu.sg/handle/10635/47607.

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

Council of Science Editors:

YUN CH. ELUCIDATION OF THE GENE REGULATION NETWORK CONTROLLING EMBRYONIC SKELETAL DEVELOPMENT. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/47607

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


Freie Universität Berlin

24. Hein, Hendrikje. Functional analysis of transcription factors in chondrogenic and osteogenic differentiation using ChIP-seq.

Degree: 2013, Freie Universität Berlin

 Chromatin immunoprecipitation followed by next-generation-sequencing (ChIP- seq) of precipitated fragments has become an important tool to study transcription factor-DNA-interactions in a genome wide scale and… (more)

Subjects/Keywords: ChIP-seq; RUNX2; MSX2; gene regulatory networks; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Hein, H. (2013). Functional analysis of transcription factors in chondrogenic and osteogenic differentiation using ChIP-seq. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-6863

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):

Hein, Hendrikje. “Functional analysis of transcription factors in chondrogenic and osteogenic differentiation using ChIP-seq.” 2013. Thesis, Freie Universität Berlin. Accessed September 24, 2020. http://dx.doi.org/10.17169/refubium-6863.

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

MLA Handbook (7th Edition):

Hein, Hendrikje. “Functional analysis of transcription factors in chondrogenic and osteogenic differentiation using ChIP-seq.” 2013. Web. 24 Sep 2020.

Vancouver:

Hein H. Functional analysis of transcription factors in chondrogenic and osteogenic differentiation using ChIP-seq. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Sep 24]. Available from: http://dx.doi.org/10.17169/refubium-6863.

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

Council of Science Editors:

Hein H. Functional analysis of transcription factors in chondrogenic and osteogenic differentiation using ChIP-seq. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-6863

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


Mississippi State University

25. Pregonero Gamez, Carol Andrea. OSTEOGENIC REGULATORY MECHANISMS ACTIVATED BY PRESSURE IN AORTIC HEART VALVE.

Degree: PhD, Agricultural and Biological Engineering, 2009, Mississippi State University

  Calcific aortic valve disease (CAVD) is the most common cause of aortic valve failure and replacement in the elderly population, affecting 25% of the… (more)

Subjects/Keywords: OPN; RUNX2; Angiotensin II; ALP; Cyclic Pressure; Valvular Interstitial Cells; BMP-7; SMAD1

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APA (6th Edition):

Pregonero Gamez, C. A. (2009). OSTEOGENIC REGULATORY MECHANISMS ACTIVATED BY PRESSURE IN AORTIC HEART VALVE. (Doctoral Dissertation). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-11062009-160017/ ;

Chicago Manual of Style (16th Edition):

Pregonero Gamez, Carol Andrea. “OSTEOGENIC REGULATORY MECHANISMS ACTIVATED BY PRESSURE IN AORTIC HEART VALVE.” 2009. Doctoral Dissertation, Mississippi State University. Accessed September 24, 2020. http://sun.library.msstate.edu/ETD-db/theses/available/etd-11062009-160017/ ;.

MLA Handbook (7th Edition):

Pregonero Gamez, Carol Andrea. “OSTEOGENIC REGULATORY MECHANISMS ACTIVATED BY PRESSURE IN AORTIC HEART VALVE.” 2009. Web. 24 Sep 2020.

Vancouver:

Pregonero Gamez CA. OSTEOGENIC REGULATORY MECHANISMS ACTIVATED BY PRESSURE IN AORTIC HEART VALVE. [Internet] [Doctoral dissertation]. Mississippi State University; 2009. [cited 2020 Sep 24]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-11062009-160017/ ;.

Council of Science Editors:

Pregonero Gamez CA. OSTEOGENIC REGULATORY MECHANISMS ACTIVATED BY PRESSURE IN AORTIC HEART VALVE. [Doctoral Dissertation]. Mississippi State University; 2009. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-11062009-160017/ ;


University of Kansas

26. Wenger, Luke William. Ewsa-dependent regulation of Runx2 during zebrafish skeletogenesis.

Degree: MA, Molecular Biosciences, 2016, University of Kansas

 Ewing’s sarcoma is the second most common malignant bone cancer found in adolescents, and the genetic hallmark of this disease is the presence of the… (more)

Subjects/Keywords: Molecular biology; Developmental biology; Cellular biology; Axis; Chondrogenesis; Ewing sarcoma; EWS; Extracellular matrix; RUNX2

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APA (6th Edition):

Wenger, L. W. (2016). Ewsa-dependent regulation of Runx2 during zebrafish skeletogenesis. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21913

Chicago Manual of Style (16th Edition):

Wenger, Luke William. “Ewsa-dependent regulation of Runx2 during zebrafish skeletogenesis.” 2016. Masters Thesis, University of Kansas. Accessed September 24, 2020. http://hdl.handle.net/1808/21913.

MLA Handbook (7th Edition):

Wenger, Luke William. “Ewsa-dependent regulation of Runx2 during zebrafish skeletogenesis.” 2016. Web. 24 Sep 2020.

Vancouver:

Wenger LW. Ewsa-dependent regulation of Runx2 during zebrafish skeletogenesis. [Internet] [Masters thesis]. University of Kansas; 2016. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/1808/21913.

Council of Science Editors:

Wenger LW. Ewsa-dependent regulation of Runx2 during zebrafish skeletogenesis. [Masters Thesis]. University of Kansas; 2016. Available from: http://hdl.handle.net/1808/21913


Temple University

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

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 24, 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. 24 Sep 2020.

Vancouver:

Singh M. TRANSCRIPTIONAL REGULATION OF OSTEOACTIVIN EXPRESSION BY BMP-2 IN OSTEOBLASTS. [Internet] [Doctoral dissertation]. Temple University; 2011. [cited 2020 Sep 24]. 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

28. Παπαχρήστου, Νικόλαος. Μελέτη του ρόλου της απολιποπρωτεΐνης Ε (apoE) στην παθογένεια της οστεοπόρωσης σε πειραματικά μοντέλα ποντικιών.

Degree: 2015, University of Patras

 Σκοπός: Πρόσφατα δεδομένα, υποδεικνύουν ότι διαταραχή της ισορροπίας του λιπιδικού μεταβολισμού επηρεάζει τη λειτουργία των κυττάρων του οστού, με αποτέλεσμα την ανάπτυξη εκφυλιστικών και μεταβολικών… (more)

Subjects/Keywords: Οστεοπόρωση; Οστική ανακατασκευή; Απολιποπρωτεΐνη Ε; Οστεοβλάστες; Οστεοκλάστες; 616.716 071; Osteoporosis; Bone remodeling; Osteoblasts; Runx2; Osx; RANKL; RANK; OPG; Pparγ

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APA (6th Edition):

Παπαχρήστου, . (2015). Μελέτη του ρόλου της απολιποπρωτεΐνης Ε (apoE) στην παθογένεια της οστεοπόρωσης σε πειραματικά μοντέλα ποντικιών. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/8799

Chicago Manual of Style (16th Edition):

Παπαχρήστου, Νικόλαος. “Μελέτη του ρόλου της απολιποπρωτεΐνης Ε (apoE) στην παθογένεια της οστεοπόρωσης σε πειραματικά μοντέλα ποντικιών.” 2015. Masters Thesis, University of Patras. Accessed September 24, 2020. http://hdl.handle.net/10889/8799.

MLA Handbook (7th Edition):

Παπαχρήστου, Νικόλαος. “Μελέτη του ρόλου της απολιποπρωτεΐνης Ε (apoE) στην παθογένεια της οστεοπόρωσης σε πειραματικά μοντέλα ποντικιών.” 2015. Web. 24 Sep 2020.

Vancouver:

Παπαχρήστου . Μελέτη του ρόλου της απολιποπρωτεΐνης Ε (apoE) στην παθογένεια της οστεοπόρωσης σε πειραματικά μοντέλα ποντικιών. [Internet] [Masters thesis]. University of Patras; 2015. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/10889/8799.

Council of Science Editors:

Παπαχρήστου . Μελέτη του ρόλου της απολιποπρωτεΐνης Ε (apoE) στην παθογένεια της οστεοπόρωσης σε πειραματικά μοντέλα ποντικιών. [Masters Thesis]. University of Patras; 2015. Available from: http://hdl.handle.net/10889/8799

29. Kalyvioti, Eleni. Μελέτη του ρόλου των συστατικών του μεταβολικού μονοπατιού της HDL στην παθογένεια της οστεοπόρωσης και της οστεοαρθρίτιδας.

Degree: 2017, University of Patras; Πανεπιστήμιο Πατρών

 Introduction: Recent data suggest that lipid metabolism imbalances affect osteoblast function and therefore may result in the development of degenerative and metabolic diseases such as… (more)

Subjects/Keywords: Οστεοπόρωση; Λιποβλάστες; Οστεοαρθρίτιδα; Οστεοβλάστες; Οστεοκλάστες; Osteoporosis; HDL; Adipocytes; APOA1; PPARγs; CXCR4; ANXA2; CXCL12; RUNX2; Osteoarthritis; Osteoblasts; Osteoclasts

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

APA (6th Edition):

Kalyvioti, E. (2017). Μελέτη του ρόλου των συστατικών του μεταβολικού μονοπατιού της HDL στην παθογένεια της οστεοπόρωσης και της οστεοαρθρίτιδας. (Thesis). University of Patras; Πανεπιστήμιο Πατρών. Retrieved from http://hdl.handle.net/10442/hedi/42084

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):

Kalyvioti, Eleni. “Μελέτη του ρόλου των συστατικών του μεταβολικού μονοπατιού της HDL στην παθογένεια της οστεοπόρωσης και της οστεοαρθρίτιδας.” 2017. Thesis, University of Patras; Πανεπιστήμιο Πατρών. Accessed September 24, 2020. http://hdl.handle.net/10442/hedi/42084.

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

MLA Handbook (7th Edition):

Kalyvioti, Eleni. “Μελέτη του ρόλου των συστατικών του μεταβολικού μονοπατιού της HDL στην παθογένεια της οστεοπόρωσης και της οστεοαρθρίτιδας.” 2017. Web. 24 Sep 2020.

Vancouver:

Kalyvioti E. Μελέτη του ρόλου των συστατικών του μεταβολικού μονοπατιού της HDL στην παθογένεια της οστεοπόρωσης και της οστεοαρθρίτιδας. [Internet] [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2017. [cited 2020 Sep 24]. Available from: http://hdl.handle.net/10442/hedi/42084.

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

Council of Science Editors:

Kalyvioti E. Μελέτη του ρόλου των συστατικών του μεταβολικού μονοπατιού της HDL στην παθογένεια της οστεοπόρωσης και της οστεοαρθρίτιδας. [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2017. Available from: http://hdl.handle.net/10442/hedi/42084

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


Penn State University

30. Wei, Jianwen. PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY.

Degree: 2008, Penn State University

 PERK (eukaryotic translation initiation factor 2 alpha kinase 3) is an endoplasmic reticulum (ER) resident transmembrane protein. In response to alterations of ER homeostasis, PERK… (more)

Subjects/Keywords: PERK; osteoblast; Runx2; procollagen; proliferation; endoplasmic reticulum

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

APA (6th Edition):

Wei, J. (2008). PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/8441

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):

Wei, Jianwen. “PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY.” 2008. Thesis, Penn State University. Accessed September 24, 2020. https://submit-etda.libraries.psu.edu/catalog/8441.

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

MLA Handbook (7th Edition):

Wei, Jianwen. “PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY.” 2008. Web. 24 Sep 2020.

Vancouver:

Wei J. PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY. [Internet] [Thesis]. Penn State University; 2008. [cited 2020 Sep 24]. Available from: https://submit-etda.libraries.psu.edu/catalog/8441.

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

Council of Science Editors:

Wei J. PERK IS ESSENTIAL FOR NEONATAL SKELETAL DEVELOPMENT TO REGULATE OSTEOBLAST BIOLOGY. [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/8441

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

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