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You searched for subject:(Sox9). Showing records 1 – 30 of 58 total matches.

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Université Montpellier II

1. Farhat, Andalib. Implication de la voie Prostaglandine D synthase/PGD2/SOX9 dans l'ovaire normal et pathologique et régulation par la signalisation estrogénique : Implication of the Prostaglandin D synthase/PGD2/SOX9 pathway in the normal and pathological ovary and regulation by estrogenic signalling.

Degree: Docteur es, Biochimie et biologie moléculaire, 2010, Université Montpellier II

L'ovaire représente à la fois un organe cible et le principal organe producteur d'estrogènes et de progestérone qui maintiennent le développement des caractères sexuels féminins… (more)

Subjects/Keywords: Ovaire; Sox9; Pgd2; Ovary; Pgd2; Sox9

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APA (6th Edition):

Farhat, A. (2010). Implication de la voie Prostaglandine D synthase/PGD2/SOX9 dans l'ovaire normal et pathologique et régulation par la signalisation estrogénique : Implication of the Prostaglandin D synthase/PGD2/SOX9 pathway in the normal and pathological ovary and regulation by estrogenic signalling. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2010MON20206

Chicago Manual of Style (16th Edition):

Farhat, Andalib. “Implication de la voie Prostaglandine D synthase/PGD2/SOX9 dans l'ovaire normal et pathologique et régulation par la signalisation estrogénique : Implication of the Prostaglandin D synthase/PGD2/SOX9 pathway in the normal and pathological ovary and regulation by estrogenic signalling.” 2010. Doctoral Dissertation, Université Montpellier II. Accessed January 22, 2020. http://www.theses.fr/2010MON20206.

MLA Handbook (7th Edition):

Farhat, Andalib. “Implication de la voie Prostaglandine D synthase/PGD2/SOX9 dans l'ovaire normal et pathologique et régulation par la signalisation estrogénique : Implication of the Prostaglandin D synthase/PGD2/SOX9 pathway in the normal and pathological ovary and regulation by estrogenic signalling.” 2010. Web. 22 Jan 2020.

Vancouver:

Farhat A. Implication de la voie Prostaglandine D synthase/PGD2/SOX9 dans l'ovaire normal et pathologique et régulation par la signalisation estrogénique : Implication of the Prostaglandin D synthase/PGD2/SOX9 pathway in the normal and pathological ovary and regulation by estrogenic signalling. [Internet] [Doctoral dissertation]. Université Montpellier II; 2010. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2010MON20206.

Council of Science Editors:

Farhat A. Implication de la voie Prostaglandine D synthase/PGD2/SOX9 dans l'ovaire normal et pathologique et régulation par la signalisation estrogénique : Implication of the Prostaglandin D synthase/PGD2/SOX9 pathway in the normal and pathological ovary and regulation by estrogenic signalling. [Doctoral Dissertation]. Université Montpellier II; 2010. Available from: http://www.theses.fr/2010MON20206


University of Manchester

2. Roberts, Neil Alistair. The role of SOX9 during human pancreas development.

Degree: PhD, 2011, University of Manchester

 The work presented in this thesis is a study of human pancreas development. The principle goal of this work is to provide information that can… (more)

Subjects/Keywords: 611; SOX9; pancreas; development

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APA (6th Edition):

Roberts, N. A. (2011). The role of SOX9 during human pancreas development. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-sox9-during-human-pancreas-development(dab5d8da-4c02-4592-b05e-471984461dcc).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549036

Chicago Manual of Style (16th Edition):

Roberts, Neil Alistair. “The role of SOX9 during human pancreas development.” 2011. Doctoral Dissertation, University of Manchester. Accessed January 22, 2020. https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-sox9-during-human-pancreas-development(dab5d8da-4c02-4592-b05e-471984461dcc).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549036.

MLA Handbook (7th Edition):

Roberts, Neil Alistair. “The role of SOX9 during human pancreas development.” 2011. Web. 22 Jan 2020.

Vancouver:

Roberts NA. The role of SOX9 during human pancreas development. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Jan 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-sox9-during-human-pancreas-development(dab5d8da-4c02-4592-b05e-471984461dcc).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549036.

Council of Science Editors:

Roberts NA. The role of SOX9 during human pancreas development. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-sox9-during-human-pancreas-development(dab5d8da-4c02-4592-b05e-471984461dcc).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.549036

3. Soualhi, Salima. Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal : Roles of SOX9 on self-renewal and differentiation of the intestinal epithelium.

Degree: Docteur es, Biologie Santé, 2014, Université Montpellier I

Sox9 est un facteur de transcription exprimé au cours du développement de l'intestin et son expression est maintenue à l'âge adulte dans trois populations cellulaires… (more)

Subjects/Keywords: Sox9; Différenciation; Intestin; Prolifération; Sox9; Differentiation; Intestine; Proliferation; 616

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APA (6th Edition):

Soualhi, S. (2014). Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal : Roles of SOX9 on self-renewal and differentiation of the intestinal epithelium. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2014MON13519

Chicago Manual of Style (16th Edition):

Soualhi, Salima. “Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal : Roles of SOX9 on self-renewal and differentiation of the intestinal epithelium.” 2014. Doctoral Dissertation, Université Montpellier I. Accessed January 22, 2020. http://www.theses.fr/2014MON13519.

MLA Handbook (7th Edition):

Soualhi, Salima. “Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal : Roles of SOX9 on self-renewal and differentiation of the intestinal epithelium.” 2014. Web. 22 Jan 2020.

Vancouver:

Soualhi S. Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal : Roles of SOX9 on self-renewal and differentiation of the intestinal epithelium. [Internet] [Doctoral dissertation]. Université Montpellier I; 2014. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2014MON13519.

Council of Science Editors:

Soualhi S. Rôles de SOX9 dans l’auto-renouvellement et la différenciation de l’épithélium intestinal : Roles of SOX9 on self-renewal and differentiation of the intestinal epithelium. [Doctoral Dissertation]. Université Montpellier I; 2014. Available from: http://www.theses.fr/2014MON13519


University of Rochester

4. Sun, Wei. Studies of Astrocytes Using Gene Expression Analysis.

Degree: PhD, 2015, University of Rochester

 Although astrocytes are one of the major glial cell types in the brain, little is known about their roles in complex neural functions. Use of… (more)

Subjects/Keywords: Astrocytes; Metabotropic Glutamate Receptors; Transcriptome; SOX9

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APA (6th Edition):

Sun, W. (2015). Studies of Astrocytes Using Gene Expression Analysis. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30110

Chicago Manual of Style (16th Edition):

Sun, Wei. “Studies of Astrocytes Using Gene Expression Analysis.” 2015. Doctoral Dissertation, University of Rochester. Accessed January 22, 2020. http://hdl.handle.net/1802/30110.

MLA Handbook (7th Edition):

Sun, Wei. “Studies of Astrocytes Using Gene Expression Analysis.” 2015. Web. 22 Jan 2020.

Vancouver:

Sun W. Studies of Astrocytes Using Gene Expression Analysis. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1802/30110.

Council of Science Editors:

Sun W. Studies of Astrocytes Using Gene Expression Analysis. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/30110

5. 松島, 肇. Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma : 肝内胆管癌の発癌過程におけるSox9の発現とその臨床的意義.

Degree: 博士(医学), 2016, Nagasaki University / 長崎大学

 Background: Intrahepatic cholangiocarcinomas develop through a multi-step carcinogenesis. Precancerous lesions are defined as biliary intraepithelial neoplasia. Sex determining region Y-box9 (Sox9) is required for the… (more)

Subjects/Keywords: Biliary intraepithelial neoplasia; Intrahepatic cholangiocarcinoma; Sox9

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APA (6th Edition):

松島, . (2016). Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma : 肝内胆管癌の発癌過程におけるSox9の発現とその臨床的意義. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/36263

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):

松島, 肇. “Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma : 肝内胆管癌の発癌過程におけるSox9の発現とその臨床的意義.” 2016. Thesis, Nagasaki University / 長崎大学. Accessed January 22, 2020. http://hdl.handle.net/10069/36263.

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

MLA Handbook (7th Edition):

松島, 肇. “Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma : 肝内胆管癌の発癌過程におけるSox9の発現とその臨床的意義.” 2016. Web. 22 Jan 2020.

Vancouver:

松島 . Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma : 肝内胆管癌の発癌過程におけるSox9の発現とその臨床的意義. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2016. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10069/36263.

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

Council of Science Editors:

松島 . Sox9 expression in carcinogenesis and its clinical significance in intrahepatic cholangiocarcinoma : 肝内胆管癌の発癌過程におけるSox9の発現とその臨床的意義. [Thesis]. Nagasaki University / 長崎大学; 2016. Available from: http://hdl.handle.net/10069/36263

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


Brigham Young University

6. Grigorova, Fialka. Characterization of the Role Nuclear Bmp2 (nBmp2) Plays in Regulating Gene Expression.

Degree: MS, 2011, Brigham Young University

  The nBmp2 protein was first identified in a DNA affinity chromatography/mass spectrometry screen designed to detect proteins that interact with a cartilage-specific enhancer element… (more)

Subjects/Keywords: nBmp2; SOX9; Col11a1; Col2a1; Col9a1; Col27a1; Microbiology

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APA (6th Edition):

Grigorova, F. (2011). Characterization of the Role Nuclear Bmp2 (nBmp2) Plays in Regulating Gene Expression. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4195&context=etd

Chicago Manual of Style (16th Edition):

Grigorova, Fialka. “Characterization of the Role Nuclear Bmp2 (nBmp2) Plays in Regulating Gene Expression.” 2011. Masters Thesis, Brigham Young University. Accessed January 22, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4195&context=etd.

MLA Handbook (7th Edition):

Grigorova, Fialka. “Characterization of the Role Nuclear Bmp2 (nBmp2) Plays in Regulating Gene Expression.” 2011. Web. 22 Jan 2020.

Vancouver:

Grigorova F. Characterization of the Role Nuclear Bmp2 (nBmp2) Plays in Regulating Gene Expression. [Internet] [Masters thesis]. Brigham Young University; 2011. [cited 2020 Jan 22]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4195&context=etd.

Council of Science Editors:

Grigorova F. Characterization of the Role Nuclear Bmp2 (nBmp2) Plays in Regulating Gene Expression. [Masters Thesis]. Brigham Young University; 2011. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4195&context=etd

7. Rammah-Bouazza, Cyrine. Implication de SOX9 et de MiniSOX9 dans la tumorigenèse colorectale : SOX9 and MiniSOX9 in intestinal tumorigenesis.

Degree: Docteur es, Biologie Santé, 2012, Université Montpellier I

SOX9 est un facteur de transcription, appartenant à la famille des protéines à domaine HMG, et connu pour réguler la transcription grâce à la liaison… (more)

Subjects/Keywords: Minisox9; Sox9; Cancer; Activité oncogénique; Variant d'épissage; Minisox9; Sox9; Cancer; Oncogenic activity; Splice variant

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APA (6th Edition):

Rammah-Bouazza, C. (2012). Implication de SOX9 et de MiniSOX9 dans la tumorigenèse colorectale : SOX9 and MiniSOX9 in intestinal tumorigenesis. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2012MON1T020

Chicago Manual of Style (16th Edition):

Rammah-Bouazza, Cyrine. “Implication de SOX9 et de MiniSOX9 dans la tumorigenèse colorectale : SOX9 and MiniSOX9 in intestinal tumorigenesis.” 2012. Doctoral Dissertation, Université Montpellier I. Accessed January 22, 2020. http://www.theses.fr/2012MON1T020.

MLA Handbook (7th Edition):

Rammah-Bouazza, Cyrine. “Implication de SOX9 et de MiniSOX9 dans la tumorigenèse colorectale : SOX9 and MiniSOX9 in intestinal tumorigenesis.” 2012. Web. 22 Jan 2020.

Vancouver:

Rammah-Bouazza C. Implication de SOX9 et de MiniSOX9 dans la tumorigenèse colorectale : SOX9 and MiniSOX9 in intestinal tumorigenesis. [Internet] [Doctoral dissertation]. Université Montpellier I; 2012. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2012MON1T020.

Council of Science Editors:

Rammah-Bouazza C. Implication de SOX9 et de MiniSOX9 dans la tumorigenèse colorectale : SOX9 and MiniSOX9 in intestinal tumorigenesis. [Doctoral Dissertation]. Université Montpellier I; 2012. Available from: http://www.theses.fr/2012MON1T020

8. Hyon, Capucine. Etude des gènes impliqués dans le déterminisme gonadique chez l'homme : Genetic study of gonadal development in human.

Degree: Docteur es, Génétique Humaine, 2016, Université Pierre et Marie Curie – Paris VI

Les anomalies du développement sexuel recouvrent un spectre phénotypique large. Les hommes XX présentent dans la majorité des cas un développement testiculaire normal, lié à… (more)

Subjects/Keywords: Anomalie du développement sexuel; SOX9; Insuffisance ovarienne prématurée; CPEB1; CASP3; REVSEX; Disorders of sex development; SOX9; Disorders of gonadal development; 572.8

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APA (6th Edition):

Hyon, C. (2016). Etude des gènes impliqués dans le déterminisme gonadique chez l'homme : Genetic study of gonadal development in human. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066493

Chicago Manual of Style (16th Edition):

Hyon, Capucine. “Etude des gènes impliqués dans le déterminisme gonadique chez l'homme : Genetic study of gonadal development in human.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed January 22, 2020. http://www.theses.fr/2016PA066493.

MLA Handbook (7th Edition):

Hyon, Capucine. “Etude des gènes impliqués dans le déterminisme gonadique chez l'homme : Genetic study of gonadal development in human.” 2016. Web. 22 Jan 2020.

Vancouver:

Hyon C. Etude des gènes impliqués dans le déterminisme gonadique chez l'homme : Genetic study of gonadal development in human. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2016PA066493.

Council of Science Editors:

Hyon C. Etude des gènes impliqués dans le déterminisme gonadique chez l'homme : Genetic study of gonadal development in human. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066493


Université Montpellier II

9. Abdel-Samad, Rana. SOX9 et MiniSOX9 dans la tumorigenèse intestinale : SOX9 and MiniSOX9 in intestinal tumorigenesis.

Degree: Docteur es, Biologie cellulaire, 2010, Université Montpellier II

SOX9 est un facteur de transcription à domaine HMG. Il est impliqué dans de multiples processus biologiques au cours du développement et de la vie… (more)

Subjects/Keywords: Sox9; PKCalpha; MiniSOX9; Transcription; Cancer colorectal; Partenaires protéiques; Sox9; PKCalpha; MiniSOX9; Transcription; Colorectal cancer; Protein partners

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APA (6th Edition):

Abdel-Samad, R. (2010). SOX9 et MiniSOX9 dans la tumorigenèse intestinale : SOX9 and MiniSOX9 in intestinal tumorigenesis. (Doctoral Dissertation). Université Montpellier II. Retrieved from http://www.theses.fr/2010MON20068

Chicago Manual of Style (16th Edition):

Abdel-Samad, Rana. “SOX9 et MiniSOX9 dans la tumorigenèse intestinale : SOX9 and MiniSOX9 in intestinal tumorigenesis.” 2010. Doctoral Dissertation, Université Montpellier II. Accessed January 22, 2020. http://www.theses.fr/2010MON20068.

MLA Handbook (7th Edition):

Abdel-Samad, Rana. “SOX9 et MiniSOX9 dans la tumorigenèse intestinale : SOX9 and MiniSOX9 in intestinal tumorigenesis.” 2010. Web. 22 Jan 2020.

Vancouver:

Abdel-Samad R. SOX9 et MiniSOX9 dans la tumorigenèse intestinale : SOX9 and MiniSOX9 in intestinal tumorigenesis. [Internet] [Doctoral dissertation]. Université Montpellier II; 2010. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2010MON20068.

Council of Science Editors:

Abdel-Samad R. SOX9 et MiniSOX9 dans la tumorigenèse intestinale : SOX9 and MiniSOX9 in intestinal tumorigenesis. [Doctoral Dissertation]. Université Montpellier II; 2010. Available from: http://www.theses.fr/2010MON20068


University of Kansas

10. Merkes, Chris M. Ewing's Sarcoma EWS protein regulates skeletogenesis by modulation of SOX9.

Degree: MA, Molecular Biosciences, 2013, University of Kansas

 Ewing sarcoma is the second most common form of bone cancer in adolescents, characterized by the presence of an aberrant chimeric fusion gene EWS/FLI1. Wildtype… (more)

Subjects/Keywords: Developmental biology; Ewing's Sarcoma; ews; skeletal development; sox9; zebrafish

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APA (6th Edition):

Merkes, C. M. (2013). Ewing's Sarcoma EWS protein regulates skeletogenesis by modulation of SOX9. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/19610

Chicago Manual of Style (16th Edition):

Merkes, Chris M. “Ewing's Sarcoma EWS protein regulates skeletogenesis by modulation of SOX9.” 2013. Masters Thesis, University of Kansas. Accessed January 22, 2020. http://hdl.handle.net/1808/19610.

MLA Handbook (7th Edition):

Merkes, Chris M. “Ewing's Sarcoma EWS protein regulates skeletogenesis by modulation of SOX9.” 2013. Web. 22 Jan 2020.

Vancouver:

Merkes CM. Ewing's Sarcoma EWS protein regulates skeletogenesis by modulation of SOX9. [Internet] [Masters thesis]. University of Kansas; 2013. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/1808/19610.

Council of Science Editors:

Merkes CM. Ewing's Sarcoma EWS protein regulates skeletogenesis by modulation of SOX9. [Masters Thesis]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/19610

11. Roberts, Neil Alistair. THE ROLE OF SOX9 DURING HUMAN PANCREAS DEVELOPMENT.

Degree: 2011, University of Manchester

 The work presented in this thesis is a study of human pancreas development. Theprinciple goal of this work is to provide information that can be… (more)

Subjects/Keywords: SOX9; pancreas; development

…160 CHAPTER 5. DOWNSTREAM TARGETS OF SOX9 DURING PANCREAS DEVELOPMENT… …162 5.1.1. DOWNSTREAM TARGETS OF SOX9................................................ 162… …CO-EXPRESSION OF GATA4 AND SOX9 DURING HUMAN PANCREAS DEVELOPMENT… …165 5.2.2. IDENTIFICATION OF POTENTIAL SOX9/GATA4 TARGETS ....... 165 5.2.3. EXPRESSION… …165 5.2.4. DETERMINE DOWNSTREAM TARGETS SOX9 REGULATED BY SOX9 IN SOX9 KNOCKDOWN PANC1… 

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APA (6th Edition):

Roberts, N. A. (2011). THE ROLE OF SOX9 DURING HUMAN PANCREAS DEVELOPMENT. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:130870

Chicago Manual of Style (16th Edition):

Roberts, Neil Alistair. “THE ROLE OF SOX9 DURING HUMAN PANCREAS DEVELOPMENT.” 2011. Doctoral Dissertation, University of Manchester. Accessed January 22, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:130870.

MLA Handbook (7th Edition):

Roberts, Neil Alistair. “THE ROLE OF SOX9 DURING HUMAN PANCREAS DEVELOPMENT.” 2011. Web. 22 Jan 2020.

Vancouver:

Roberts NA. THE ROLE OF SOX9 DURING HUMAN PANCREAS DEVELOPMENT. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2020 Jan 22]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:130870.

Council of Science Editors:

Roberts NA. THE ROLE OF SOX9 DURING HUMAN PANCREAS DEVELOPMENT. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:130870


Brigham Young University

12. Genzer, Mary Ann. Characterization of the Role of SOX9 in Cartilage-Specific Gene Regulation.

Degree: MS, 2006, Brigham Young University

 Although advances have been made toward understanding the complex mechanisms that regulate the process of DNA transcription, the specific mechanisms of activation for many individual… (more)

Subjects/Keywords: SOX9; cartilage gene regulation; Microbiology

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APA (6th Edition):

Genzer, M. A. (2006). Characterization of the Role of SOX9 in Cartilage-Specific Gene Regulation. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1344&context=etd

Chicago Manual of Style (16th Edition):

Genzer, Mary Ann. “Characterization of the Role of SOX9 in Cartilage-Specific Gene Regulation.” 2006. Masters Thesis, Brigham Young University. Accessed January 22, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1344&context=etd.

MLA Handbook (7th Edition):

Genzer, Mary Ann. “Characterization of the Role of SOX9 in Cartilage-Specific Gene Regulation.” 2006. Web. 22 Jan 2020.

Vancouver:

Genzer MA. Characterization of the Role of SOX9 in Cartilage-Specific Gene Regulation. [Internet] [Masters thesis]. Brigham Young University; 2006. [cited 2020 Jan 22]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1344&context=etd.

Council of Science Editors:

Genzer MA. Characterization of the Role of SOX9 in Cartilage-Specific Gene Regulation. [Masters Thesis]. Brigham Young University; 2006. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=1344&context=etd


University of Miami

13. Peacock, Jacqueline D. The Role of Sox9 in Heart Valve Development and Disease.

Degree: PhD, Molecular and Cellular Pharmacology (Medicine), 2011, University of Miami

 Heart valve structures open and close during the cardiac cycle to provide unidirectional blood flow through the heart, critical for efficient cardiovascular function. Valve dysfunction… (more)

Subjects/Keywords: Sox9; transcription factor; heart valves; development; valve calcification

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APA (6th Edition):

Peacock, J. D. (2011). The Role of Sox9 in Heart Valve Development and Disease. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/543

Chicago Manual of Style (16th Edition):

Peacock, Jacqueline D. “The Role of Sox9 in Heart Valve Development and Disease.” 2011. Doctoral Dissertation, University of Miami. Accessed January 22, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/543.

MLA Handbook (7th Edition):

Peacock, Jacqueline D. “The Role of Sox9 in Heart Valve Development and Disease.” 2011. Web. 22 Jan 2020.

Vancouver:

Peacock JD. The Role of Sox9 in Heart Valve Development and Disease. [Internet] [Doctoral dissertation]. University of Miami; 2011. [cited 2020 Jan 22]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/543.

Council of Science Editors:

Peacock JD. The Role of Sox9 in Heart Valve Development and Disease. [Doctoral Dissertation]. University of Miami; 2011. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/543

14. Martin, Elise. Etude de la différenciation des progéniteurs musculaires lisses de l'uretère chez la souris : A study of the smooth muscle progenitors differentiation in the mouse ureter.

Degree: Docteur es, Biologie des eucaryotes, 2010, Aix-Marseille 2

Les malformations obstructives congénitales de l’uretère sont parmi les défauts les plus fréquents à la naissance chez l’Homme mais leur étiologie reste peu comprise au… (more)

Subjects/Keywords: Muscle lisse; Uretère; Morphogénèse; Tshz3; Sox9; Myocardin; Souris

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APA (6th Edition):

Martin, E. (2010). Etude de la différenciation des progéniteurs musculaires lisses de l'uretère chez la souris : A study of the smooth muscle progenitors differentiation in the mouse ureter. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX22074

Chicago Manual of Style (16th Edition):

Martin, Elise. “Etude de la différenciation des progéniteurs musculaires lisses de l'uretère chez la souris : A study of the smooth muscle progenitors differentiation in the mouse ureter.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed January 22, 2020. http://www.theses.fr/2010AIX22074.

MLA Handbook (7th Edition):

Martin, Elise. “Etude de la différenciation des progéniteurs musculaires lisses de l'uretère chez la souris : A study of the smooth muscle progenitors differentiation in the mouse ureter.” 2010. Web. 22 Jan 2020.

Vancouver:

Martin E. Etude de la différenciation des progéniteurs musculaires lisses de l'uretère chez la souris : A study of the smooth muscle progenitors differentiation in the mouse ureter. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2010AIX22074.

Council of Science Editors:

Martin E. Etude de la différenciation des progéniteurs musculaires lisses de l'uretère chez la souris : A study of the smooth muscle progenitors differentiation in the mouse ureter. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX22074


University of Texas – Austin

15. -1021-0306. Mechanisms directing chondrocyte specification in the developing limb.

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

-1021-0306. “Mechanisms directing chondrocyte specification in the developing limb.” 2018. Doctoral Dissertation, University of Texas – Austin. Accessed January 22, 2020. http://hdl.handle.net/2152/68374.

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

MLA Handbook (7th Edition):

-1021-0306. “Mechanisms directing chondrocyte specification in the developing limb.” 2018. Web. 22 Jan 2020.

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

Vancouver:

-1021-0306. Mechanisms directing chondrocyte specification in the developing limb. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2018. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2152/68374.

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

Council of Science Editors:

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

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


University of Gothenburg / Göteborgs Universitet

16. Shawn, Liang. Growth regulation in thyroid development.

Degree: 2018, University of Gothenburg / Göteborgs Universitet

 The fundamental aspects of developmental mechanisms that regulate embryonic and postnatal thyroid growth gaining the final size of the gland are still largely undetermined. In… (more)

Subjects/Keywords: Thyroid; growth regulation; branching morphogenesis; Fgf10; Sox9; Shh; Brafv600e

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APA (6th Edition):

Shawn, L. (2018). Growth regulation in thyroid development. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/56262

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):

Shawn, Liang. “Growth regulation in thyroid development.” 2018. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed January 22, 2020. http://hdl.handle.net/2077/56262.

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

MLA Handbook (7th Edition):

Shawn, Liang. “Growth regulation in thyroid development.” 2018. Web. 22 Jan 2020.

Vancouver:

Shawn L. Growth regulation in thyroid development. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2018. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2077/56262.

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

Council of Science Editors:

Shawn L. Growth regulation in thyroid development. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2018. Available from: http://hdl.handle.net/2077/56262

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


Université de Lorraine

17. Al-Asaad, Imane. Étude de marqueurs de différenciation testiculaire Sox9 et Amh lors d'un développement normal, d'une inversion sexuelle et d'un développement en absence de cellules germinales chez l'amphibien urodèle Pleurodeles waltl. Intérêt pour la physiologie comparée de la reproduction des vertébrés : Study of testis differentiation markers Sox9 and Amh during normal development, sex reversal, and development in the absence of germ cells in the newt Pleurodeles waltl. Interest in comparative physiology of reproduction.

Degree: Docteur es, Sciences de la vie et de la santé, 2013, Université de Lorraine

Dans le contexte de la physiologie comparée de la reproduction, les amphibiens sont peu étudiés. Le travail réalisé durant cette thèse visait à analyser des… (more)

Subjects/Keywords: Amphibien; Pleurodeles waltl; Différenciation gonadique; Cellules germinales; Sox9; AMH; Aromatase; Busulfan; Amphibian; Pleurodeles waltl; Gonadal differentiation; Germ cells; Sox9; AMH; Aromatase; Busulfan; 571.816; 571.882

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APA (6th Edition):

Al-Asaad, I. (2013). Étude de marqueurs de différenciation testiculaire Sox9 et Amh lors d'un développement normal, d'une inversion sexuelle et d'un développement en absence de cellules germinales chez l'amphibien urodèle Pleurodeles waltl. Intérêt pour la physiologie comparée de la reproduction des vertébrés : Study of testis differentiation markers Sox9 and Amh during normal development, sex reversal, and development in the absence of germ cells in the newt Pleurodeles waltl. Interest in comparative physiology of reproduction. (Doctoral Dissertation). Université de Lorraine. Retrieved from http://www.theses.fr/2013LORR0229

Chicago Manual of Style (16th Edition):

Al-Asaad, Imane. “Étude de marqueurs de différenciation testiculaire Sox9 et Amh lors d'un développement normal, d'une inversion sexuelle et d'un développement en absence de cellules germinales chez l'amphibien urodèle Pleurodeles waltl. Intérêt pour la physiologie comparée de la reproduction des vertébrés : Study of testis differentiation markers Sox9 and Amh during normal development, sex reversal, and development in the absence of germ cells in the newt Pleurodeles waltl. Interest in comparative physiology of reproduction.” 2013. Doctoral Dissertation, Université de Lorraine. Accessed January 22, 2020. http://www.theses.fr/2013LORR0229.

MLA Handbook (7th Edition):

Al-Asaad, Imane. “Étude de marqueurs de différenciation testiculaire Sox9 et Amh lors d'un développement normal, d'une inversion sexuelle et d'un développement en absence de cellules germinales chez l'amphibien urodèle Pleurodeles waltl. Intérêt pour la physiologie comparée de la reproduction des vertébrés : Study of testis differentiation markers Sox9 and Amh during normal development, sex reversal, and development in the absence of germ cells in the newt Pleurodeles waltl. Interest in comparative physiology of reproduction.” 2013. Web. 22 Jan 2020.

Vancouver:

Al-Asaad I. Étude de marqueurs de différenciation testiculaire Sox9 et Amh lors d'un développement normal, d'une inversion sexuelle et d'un développement en absence de cellules germinales chez l'amphibien urodèle Pleurodeles waltl. Intérêt pour la physiologie comparée de la reproduction des vertébrés : Study of testis differentiation markers Sox9 and Amh during normal development, sex reversal, and development in the absence of germ cells in the newt Pleurodeles waltl. Interest in comparative physiology of reproduction. [Internet] [Doctoral dissertation]. Université de Lorraine; 2013. [cited 2020 Jan 22]. Available from: http://www.theses.fr/2013LORR0229.

Council of Science Editors:

Al-Asaad I. Étude de marqueurs de différenciation testiculaire Sox9 et Amh lors d'un développement normal, d'une inversion sexuelle et d'un développement en absence de cellules germinales chez l'amphibien urodèle Pleurodeles waltl. Intérêt pour la physiologie comparée de la reproduction des vertébrés : Study of testis differentiation markers Sox9 and Amh during normal development, sex reversal, and development in the absence of germ cells in the newt Pleurodeles waltl. Interest in comparative physiology of reproduction. [Doctoral Dissertation]. Université de Lorraine; 2013. Available from: http://www.theses.fr/2013LORR0229


Texas Medical Center

18. Gonzalez, Gabriel. ROLE OF SOX9 IN UTERINE GLAND DEVELOPMENT AND DISEASE INITIATION.

Degree: PhD, 2012, Texas Medical Center

  The female reproductive tract (FRT) develops midway through embryogenesis, and consists of oviducts, uterine horns, cervix and upper part of the vagina. The uterine… (more)

Subjects/Keywords: SOX9; Uterine Gland Hyperplasia; Female Reproductive Tract Development; Medicine and Health Sciences

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APA (6th Edition):

Gonzalez, G. (2012). ROLE OF SOX9 IN UTERINE GLAND DEVELOPMENT AND DISEASE INITIATION. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/254

Chicago Manual of Style (16th Edition):

Gonzalez, Gabriel. “ROLE OF SOX9 IN UTERINE GLAND DEVELOPMENT AND DISEASE INITIATION.” 2012. Doctoral Dissertation, Texas Medical Center. Accessed January 22, 2020. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/254.

MLA Handbook (7th Edition):

Gonzalez, Gabriel. “ROLE OF SOX9 IN UTERINE GLAND DEVELOPMENT AND DISEASE INITIATION.” 2012. Web. 22 Jan 2020.

Vancouver:

Gonzalez G. ROLE OF SOX9 IN UTERINE GLAND DEVELOPMENT AND DISEASE INITIATION. [Internet] [Doctoral dissertation]. Texas Medical Center; 2012. [cited 2020 Jan 22]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/254.

Council of Science Editors:

Gonzalez G. ROLE OF SOX9 IN UTERINE GLAND DEVELOPMENT AND DISEASE INITIATION. [Doctoral Dissertation]. Texas Medical Center; 2012. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/254


Kyoto University / 京都大学

19. Sugimoto, Yuki. Scx[+]/Sox9[+] progenitors contribute to the establishment of the junction between cartilage and tendon/ligament : Scx[+]/Sox9[+]前駆細胞は軟骨と腱/靭帯の連結部の構築に寄与する.

Degree: 博士(医学), 2014, Kyoto University / 京都大学

新制・論文博士

乙第12802号

論医博第2074号

Subjects/Keywords: Sox9; Scx; Tenocytes; Ligamentocytes; Chondrocytes; Mouse

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APA (6th Edition):

Sugimoto, Y. (2014). Scx[+]/Sox9[+] progenitors contribute to the establishment of the junction between cartilage and tendon/ligament : Scx[+]/Sox9[+]前駆細胞は軟骨と腱/靭帯の連結部の構築に寄与する. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/185191 ; http://dx.doi.org/10.14989/doctor.r12802

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):

Sugimoto, Yuki. “Scx[+]/Sox9[+] progenitors contribute to the establishment of the junction between cartilage and tendon/ligament : Scx[+]/Sox9[+]前駆細胞は軟骨と腱/靭帯の連結部の構築に寄与する.” 2014. Thesis, Kyoto University / 京都大学. Accessed January 22, 2020. http://hdl.handle.net/2433/185191 ; http://dx.doi.org/10.14989/doctor.r12802.

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

MLA Handbook (7th Edition):

Sugimoto, Yuki. “Scx[+]/Sox9[+] progenitors contribute to the establishment of the junction between cartilage and tendon/ligament : Scx[+]/Sox9[+]前駆細胞は軟骨と腱/靭帯の連結部の構築に寄与する.” 2014. Web. 22 Jan 2020.

Vancouver:

Sugimoto Y. Scx[+]/Sox9[+] progenitors contribute to the establishment of the junction between cartilage and tendon/ligament : Scx[+]/Sox9[+]前駆細胞は軟骨と腱/靭帯の連結部の構築に寄与する. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2433/185191 ; http://dx.doi.org/10.14989/doctor.r12802.

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

Council of Science Editors:

Sugimoto Y. Scx[+]/Sox9[+] progenitors contribute to the establishment of the junction between cartilage and tendon/ligament : Scx[+]/Sox9[+]前駆細胞は軟骨と腱/靭帯の連結部の構築に寄与する. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/185191 ; http://dx.doi.org/10.14989/doctor.r12802

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

20. Hosokawa, Shinichi. Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice : Sox9発現量とHes1を介したNotch signalingによるマウス成体膵管細胞の可塑性制御.

Degree: 博士(医学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19224号

医博第4023号

Subjects/Keywords: Sox9; Notch; Hes1; duct cell plasticity

Page 1 Page 2

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APA (6th Edition):

Hosokawa, S. (2015). Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice : Sox9発現量とHes1を介したNotch signalingによるマウス成体膵管細胞の可塑性制御. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/200490 ; http://dx.doi.org/10.14989/doctor.k19224

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):

Hosokawa, Shinichi. “Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice : Sox9発現量とHes1を介したNotch signalingによるマウス成体膵管細胞の可塑性制御.” 2015. Thesis, Kyoto University / 京都大学. Accessed January 22, 2020. http://hdl.handle.net/2433/200490 ; http://dx.doi.org/10.14989/doctor.k19224.

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

MLA Handbook (7th Edition):

Hosokawa, Shinichi. “Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice : Sox9発現量とHes1を介したNotch signalingによるマウス成体膵管細胞の可塑性制御.” 2015. Web. 22 Jan 2020.

Vancouver:

Hosokawa S. Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice : Sox9発現量とHes1を介したNotch signalingによるマウス成体膵管細胞の可塑性制御. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2433/200490 ; http://dx.doi.org/10.14989/doctor.k19224.

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

Council of Science Editors:

Hosokawa S. Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice : Sox9発現量とHes1を介したNotch signalingによるマウス成体膵管細胞の可塑性制御. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/200490 ; http://dx.doi.org/10.14989/doctor.k19224

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


Université Catholique de Louvain

21. Grimont, Adrien. Roles of the transcription factors HNF6 and Sox9 in the initiation of metaplastic and neoplastic lesions of the pancreas.

Degree: 2013, Université Catholique de Louvain

Pancreatic ductal adenocarcinoma originates from acinar cells that undergo acinar-to-ductal metaplasia (ADM) and evolve to pancreatic intraepithelial neoplasia (PanIN), and eventually to invasive cancer. Ductal… (more)

Subjects/Keywords: Pancreatic ductal adenocarcinoma; Sox9; HNF6; EGFR; ErbB2; acinar-to-ductal metaplasia; pancreatic intraepithelial neoplasia

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APA (6th Edition):

Grimont, A. (2013). Roles of the transcription factors HNF6 and Sox9 in the initiation of metaplastic and neoplastic lesions of the pancreas. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/137159

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):

Grimont, Adrien. “Roles of the transcription factors HNF6 and Sox9 in the initiation of metaplastic and neoplastic lesions of the pancreas.” 2013. Thesis, Université Catholique de Louvain. Accessed January 22, 2020. http://hdl.handle.net/2078.1/137159.

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

MLA Handbook (7th Edition):

Grimont, Adrien. “Roles of the transcription factors HNF6 and Sox9 in the initiation of metaplastic and neoplastic lesions of the pancreas.” 2013. Web. 22 Jan 2020.

Vancouver:

Grimont A. Roles of the transcription factors HNF6 and Sox9 in the initiation of metaplastic and neoplastic lesions of the pancreas. [Internet] [Thesis]. Université Catholique de Louvain; 2013. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2078.1/137159.

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

Council of Science Editors:

Grimont A. Roles of the transcription factors HNF6 and Sox9 in the initiation of metaplastic and neoplastic lesions of the pancreas. [Thesis]. Université Catholique de Louvain; 2013. Available from: http://hdl.handle.net/2078.1/137159

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


University of Western Ontario

22. Bass, Bethany Robin Lenore. Investigation of Sox9 ablation on neuroplasticity and recovery after ischemic stroke.

Degree: 2014, University of Western Ontario

 Neuroplasticity is a key factor in post-stroke functional recovery. A chief inhibitor of post-stroke neuroplasticity is the expression of chondroitin sulfate proteoglycans (CSPGs). Recent research… (more)

Subjects/Keywords: stroke; Sox9; chondroitin sulfate proteoglcans; neuroplasticity; tract tracing; recovery; middle cerebral artery occlusion; Neurosciences

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APA (6th Edition):

Bass, B. R. L. (2014). Investigation of Sox9 ablation on neuroplasticity and recovery after ischemic stroke. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2338

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):

Bass, Bethany Robin Lenore. “Investigation of Sox9 ablation on neuroplasticity and recovery after ischemic stroke.” 2014. Thesis, University of Western Ontario. Accessed January 22, 2020. https://ir.lib.uwo.ca/etd/2338.

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

MLA Handbook (7th Edition):

Bass, Bethany Robin Lenore. “Investigation of Sox9 ablation on neuroplasticity and recovery after ischemic stroke.” 2014. Web. 22 Jan 2020.

Vancouver:

Bass BRL. Investigation of Sox9 ablation on neuroplasticity and recovery after ischemic stroke. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2020 Jan 22]. Available from: https://ir.lib.uwo.ca/etd/2338.

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

Council of Science Editors:

Bass BRL. Investigation of Sox9 ablation on neuroplasticity and recovery after ischemic stroke. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/2338

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


University of Western Ontario

23. McKillop, William M. Sox9 conditional knockdown reduces chondroitin sulphate proteoglycan expression, increases neuroplasticity, and improves motor function in a mouse model of spinal cord injury.

Degree: 2014, University of Western Ontario

 This thesis investigates the effect of Sox9 knockdown on anti-regenerative scar gene expression, neuroplasticity, and hind limb functional recovery following mouse spinal cord injury. We… (more)

Subjects/Keywords: spinal cord injury; sox9; chondroitin sulfate proteoglycans; neuroplasticity; reactive sprouting; Molecular and Cellular Neuroscience

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APA (6th Edition):

McKillop, W. M. (2014). Sox9 conditional knockdown reduces chondroitin sulphate proteoglycan expression, increases neuroplasticity, and improves motor function in a mouse model of spinal cord injury. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/2153

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):

McKillop, William M. “Sox9 conditional knockdown reduces chondroitin sulphate proteoglycan expression, increases neuroplasticity, and improves motor function in a mouse model of spinal cord injury.” 2014. Thesis, University of Western Ontario. Accessed January 22, 2020. https://ir.lib.uwo.ca/etd/2153.

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

MLA Handbook (7th Edition):

McKillop, William M. “Sox9 conditional knockdown reduces chondroitin sulphate proteoglycan expression, increases neuroplasticity, and improves motor function in a mouse model of spinal cord injury.” 2014. Web. 22 Jan 2020.

Vancouver:

McKillop WM. Sox9 conditional knockdown reduces chondroitin sulphate proteoglycan expression, increases neuroplasticity, and improves motor function in a mouse model of spinal cord injury. [Internet] [Thesis]. University of Western Ontario; 2014. [cited 2020 Jan 22]. Available from: https://ir.lib.uwo.ca/etd/2153.

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

Council of Science Editors:

McKillop WM. Sox9 conditional knockdown reduces chondroitin sulphate proteoglycan expression, increases neuroplasticity, and improves motor function in a mouse model of spinal cord injury. [Thesis]. University of Western Ontario; 2014. Available from: https://ir.lib.uwo.ca/etd/2153

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


Kyoto University

24. Hosokawa, Shinichi. Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice .

Degree: 2015, Kyoto University

Subjects/Keywords: Sox9; Notch; Hes1; duct cell plasticity

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

APA (6th Edition):

Hosokawa, S. (2015). Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/200490

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):

Hosokawa, Shinichi. “Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice .” 2015. Thesis, Kyoto University. Accessed January 22, 2020. http://hdl.handle.net/2433/200490.

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

MLA Handbook (7th Edition):

Hosokawa, Shinichi. “Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice .” 2015. Web. 22 Jan 2020.

Vancouver:

Hosokawa S. Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice . [Internet] [Thesis]. Kyoto University; 2015. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2433/200490.

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

Council of Science Editors:

Hosokawa S. Impact of Sox9 Dosage and Hes1-mediated Notch Signaling in Controlling the Plasticity of Adult Pancreatic Duct Cells in Mice . [Thesis]. Kyoto University; 2015. Available from: http://hdl.handle.net/2433/200490

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


University of Texas Southwestern Medical Center

25. Smith, Christopher Lacey. Regulation of Cardiac Fibroblast and Coronary Vascular Smooth Muscle Development by Platelet Derived Growth Factor Receptors.

Degree: 2013, University of Texas Southwestern Medical Center

 Coronary vascular smooth muscle cells (cVSMC) and cardiac fibroblasts are essential for coronary artery development and are important mediators of myocardial pathogenesis. These cells form… (more)

Subjects/Keywords: Epithelial-Mesenchymal Transition; Muscle, Smooth, Vascular; Platelet-Derived Growth Factor; SOX9 Transcription Factor

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APA (6th Edition):

Smith, C. L. (2013). Regulation of Cardiac Fibroblast and Coronary Vascular Smooth Muscle Development by Platelet Derived Growth Factor Receptors. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1707

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):

Smith, Christopher Lacey. “Regulation of Cardiac Fibroblast and Coronary Vascular Smooth Muscle Development by Platelet Derived Growth Factor Receptors.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed January 22, 2020. http://hdl.handle.net/2152.5/1707.

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

MLA Handbook (7th Edition):

Smith, Christopher Lacey. “Regulation of Cardiac Fibroblast and Coronary Vascular Smooth Muscle Development by Platelet Derived Growth Factor Receptors.” 2013. Web. 22 Jan 2020.

Vancouver:

Smith CL. Regulation of Cardiac Fibroblast and Coronary Vascular Smooth Muscle Development by Platelet Derived Growth Factor Receptors. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2152.5/1707.

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

Council of Science Editors:

Smith CL. Regulation of Cardiac Fibroblast and Coronary Vascular Smooth Muscle Development by Platelet Derived Growth Factor Receptors. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1707

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

26. Ramsook, Sarah Neeta. The SOX9 Dimerization Domain And Its Role in Cooperative DNA Binding.

Degree: MSc -MS, Biology, 2015, York University

 Nucleic acid binding proteins are key regulators in developmental processes and controlling the onset of diseases. Human SOX9 is a group E member of the… (more)

Subjects/Keywords: Biology; Molecular biology; Biochemistry; Science; Proteomics; Structural Biology; SOX9; DNA Binding; NMR

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APA (6th Edition):

Ramsook, S. N. (2015). The SOX9 Dimerization Domain And Its Role in Cooperative DNA Binding. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/30731

Chicago Manual of Style (16th Edition):

Ramsook, Sarah Neeta. “The SOX9 Dimerization Domain And Its Role in Cooperative DNA Binding.” 2015. Masters Thesis, York University. Accessed January 22, 2020. http://hdl.handle.net/10315/30731.

MLA Handbook (7th Edition):

Ramsook, Sarah Neeta. “The SOX9 Dimerization Domain And Its Role in Cooperative DNA Binding.” 2015. Web. 22 Jan 2020.

Vancouver:

Ramsook SN. The SOX9 Dimerization Domain And Its Role in Cooperative DNA Binding. [Internet] [Masters thesis]. York University; 2015. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/10315/30731.

Council of Science Editors:

Ramsook SN. The SOX9 Dimerization Domain And Its Role in Cooperative DNA Binding. [Masters Thesis]. York University; 2015. Available from: http://hdl.handle.net/10315/30731

27. Huk, Danielle. The Role of Sox9 in Heart Valve Maintenance and Disease.

Degree: PhD, Molecular and Cellular Pharmacology (Medicine), 2015, University of Miami

  Heart valve disease results in over 23,000 deaths annually in the United States, with calcific aortic valve disease (CAVD) being the most prevalent (Go… (more)

Subjects/Keywords: Heart Valve; Calcification; Sox9; CAVD

…4 1.3 Transcriptional role of Sox9 in skeletal development… …4 1.4 Sox9 protein shuttling in development and disease… …7 1.5 The role of Sox9 in heart valves… …24 Chapter 3. Identification of novel downstream targets of Sox9 .................... 26… …27 3.2.1 Identification of Sox9 binding to Spp1 by ChIP-on-chip analysis… 

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

APA (6th Edition):

Huk, D. (2015). The Role of Sox9 in Heart Valve Maintenance and Disease. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/1361

Chicago Manual of Style (16th Edition):

Huk, Danielle. “The Role of Sox9 in Heart Valve Maintenance and Disease.” 2015. Doctoral Dissertation, University of Miami. Accessed January 22, 2020. https://scholarlyrepository.miami.edu/oa_dissertations/1361.

MLA Handbook (7th Edition):

Huk, Danielle. “The Role of Sox9 in Heart Valve Maintenance and Disease.” 2015. Web. 22 Jan 2020.

Vancouver:

Huk D. The Role of Sox9 in Heart Valve Maintenance and Disease. [Internet] [Doctoral dissertation]. University of Miami; 2015. [cited 2020 Jan 22]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1361.

Council of Science Editors:

Huk D. The Role of Sox9 in Heart Valve Maintenance and Disease. [Doctoral Dissertation]. University of Miami; 2015. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1361


Kyoto University / 京都大学

28. Murao, Hiroki. Periosteal cells are a major source of soft callus in bone fracture : 骨折修復過程における軟性仮骨は主に骨膜細胞に由来する.

Degree: 博士(医学), 2014, Kyoto University / 京都大学

新制・課程博士

甲第18510号

医博第3930号

Subjects/Keywords: fracture healing; periosteal cells; soft callus; cell lineage; Sox9

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APA (6th Edition):

Murao, H. (2014). Periosteal cells are a major source of soft callus in bone fracture : 骨折修復過程における軟性仮骨は主に骨膜細胞に由来する. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/189667 ; http://dx.doi.org/10.14989/doctor.k18510

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):

Murao, Hiroki. “Periosteal cells are a major source of soft callus in bone fracture : 骨折修復過程における軟性仮骨は主に骨膜細胞に由来する.” 2014. Thesis, Kyoto University / 京都大学. Accessed January 22, 2020. http://hdl.handle.net/2433/189667 ; http://dx.doi.org/10.14989/doctor.k18510.

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

MLA Handbook (7th Edition):

Murao, Hiroki. “Periosteal cells are a major source of soft callus in bone fracture : 骨折修復過程における軟性仮骨は主に骨膜細胞に由来する.” 2014. Web. 22 Jan 2020.

Vancouver:

Murao H. Periosteal cells are a major source of soft callus in bone fracture : 骨折修復過程における軟性仮骨は主に骨膜細胞に由来する. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2433/189667 ; http://dx.doi.org/10.14989/doctor.k18510.

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

Council of Science Editors:

Murao H. Periosteal cells are a major source of soft callus in bone fracture : 骨折修復過程における軟性仮骨は主に骨膜細胞に由来する. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/189667 ; http://dx.doi.org/10.14989/doctor.k18510

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


Kyoto University / 京都大学

29. Nakano, Yasuhiro. Disappearance of centroacinar cells in the Notch ligand-deficient pancreas : Notch ligand欠失による膵腺房中心細胞の消失.

Degree: 博士(医科学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第19231号

医科博第63号

Subjects/Keywords: Pancreatic development; Notch signaling; Centroacinar cell; Acinar construction; Sox9

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APA (6th Edition):

Nakano, Y. (2015). Disappearance of centroacinar cells in the Notch ligand-deficient pancreas : Notch ligand欠失による膵腺房中心細胞の消失. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/200497 ; http://dx.doi.org/10.14989/doctor.k19231

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):

Nakano, Yasuhiro. “Disappearance of centroacinar cells in the Notch ligand-deficient pancreas : Notch ligand欠失による膵腺房中心細胞の消失.” 2015. Thesis, Kyoto University / 京都大学. Accessed January 22, 2020. http://hdl.handle.net/2433/200497 ; http://dx.doi.org/10.14989/doctor.k19231.

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

MLA Handbook (7th Edition):

Nakano, Yasuhiro. “Disappearance of centroacinar cells in the Notch ligand-deficient pancreas : Notch ligand欠失による膵腺房中心細胞の消失.” 2015. Web. 22 Jan 2020.

Vancouver:

Nakano Y. Disappearance of centroacinar cells in the Notch ligand-deficient pancreas : Notch ligand欠失による膵腺房中心細胞の消失. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2020 Jan 22]. Available from: http://hdl.handle.net/2433/200497 ; http://dx.doi.org/10.14989/doctor.k19231.

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

Council of Science Editors:

Nakano Y. Disappearance of centroacinar cells in the Notch ligand-deficient pancreas : Notch ligand欠失による膵腺房中心細胞の消失. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/200497 ; http://dx.doi.org/10.14989/doctor.k19231

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


Kent State University

30. Yagi, Rieko. Bcl-2 Regulates Chondrocyte Phenotype Through MEK-ERK1/2 Pathway; Relevance to Osteoarthritis and Cartilage Biology.

Degree: PhD, School of Biomedical Sciences, 2005, Kent State University

 Bcl-2 is an anti-apoptotic protein that has recently been shown to regulate other cellular functions. We previously reported the novel function of Bcl-2 that regulates… (more)

Subjects/Keywords: Chondrocytes; Osteoarthritis; Sox9; Bcl-2; MEK-ERK1/2

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APA (6th Edition):

Yagi, R. (2005). Bcl-2 Regulates Chondrocyte Phenotype Through MEK-ERK1/2 Pathway; Relevance to Osteoarthritis and Cartilage Biology. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1118329494

Chicago Manual of Style (16th Edition):

Yagi, Rieko. “Bcl-2 Regulates Chondrocyte Phenotype Through MEK-ERK1/2 Pathway; Relevance to Osteoarthritis and Cartilage Biology.” 2005. Doctoral Dissertation, Kent State University. Accessed January 22, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1118329494.

MLA Handbook (7th Edition):

Yagi, Rieko. “Bcl-2 Regulates Chondrocyte Phenotype Through MEK-ERK1/2 Pathway; Relevance to Osteoarthritis and Cartilage Biology.” 2005. Web. 22 Jan 2020.

Vancouver:

Yagi R. Bcl-2 Regulates Chondrocyte Phenotype Through MEK-ERK1/2 Pathway; Relevance to Osteoarthritis and Cartilage Biology. [Internet] [Doctoral dissertation]. Kent State University; 2005. [cited 2020 Jan 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1118329494.

Council of Science Editors:

Yagi R. Bcl-2 Regulates Chondrocyte Phenotype Through MEK-ERK1/2 Pathway; Relevance to Osteoarthritis and Cartilage Biology. [Doctoral Dissertation]. Kent State University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1118329494

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