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You searched for subject:( NANOG). Showing records 1 – 30 of 46 total matches.

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University of Edinburgh

1. Karwacki-Neisius, Violetta Anna. Dynamic control of Nanog expression in embryonic stem cells.

Degree: PhD, 2011, University of Edinburgh

 Embryonic stem cells are defined by two key characteristics; apparently symmetrical self-renewing cell division and the ability to differentiate into cells of all three germ… (more)

Subjects/Keywords: 616.02; Nanog; stem cells

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APA (6th Edition):

Karwacki-Neisius, V. A. (2011). Dynamic control of Nanog expression in embryonic stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9510

Chicago Manual of Style (16th Edition):

Karwacki-Neisius, Violetta Anna. “Dynamic control of Nanog expression in embryonic stem cells.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2020. http://hdl.handle.net/1842/9510.

MLA Handbook (7th Edition):

Karwacki-Neisius, Violetta Anna. “Dynamic control of Nanog expression in embryonic stem cells.” 2011. Web. 23 Jan 2020.

Vancouver:

Karwacki-Neisius VA. Dynamic control of Nanog expression in embryonic stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1842/9510.

Council of Science Editors:

Karwacki-Neisius VA. Dynamic control of Nanog expression in embryonic stem cells. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/9510


University of Edinburgh

2. Meek, Stephen Earl. Experimental approaches to establish rat embryonic stem cells.

Degree: PhD, 2011, University of Edinburgh

 The rat has been an established experimental animal model within many areas of biological investigation for over one hundred years due to its size, breeding… (more)

Subjects/Keywords: 571.6; ES cells; 2i; rat; Oct4; Nanog

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APA (6th Edition):

Meek, S. E. (2011). Experimental approaches to establish rat embryonic stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5040

Chicago Manual of Style (16th Edition):

Meek, Stephen Earl. “Experimental approaches to establish rat embryonic stem cells.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2020. http://hdl.handle.net/1842/5040.

MLA Handbook (7th Edition):

Meek, Stephen Earl. “Experimental approaches to establish rat embryonic stem cells.” 2011. Web. 23 Jan 2020.

Vancouver:

Meek SE. Experimental approaches to establish rat embryonic stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1842/5040.

Council of Science Editors:

Meek SE. Experimental approaches to establish rat embryonic stem cells. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5040


Penn State University

3. Siefring, Christopher Brian. GENERATION OF A NANOG PROMOTER DRIVEN SELECTIVE GENE LENTIVIRUS UNDER IN VITRO INDUCED PLURIPOTENT STEM CELL CONDITIONS.

Degree: MS, Anatomy, 2010, Penn State University

 Stem cell research is quickly rising as a new frontier in the field of regenerative medicine. Social stigmas and disfavor for embryonic stem cell research… (more)

Subjects/Keywords: induced pluripotent stem cells; NANOG; selection

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APA (6th Edition):

Siefring, C. B. (2010). GENERATION OF A NANOG PROMOTER DRIVEN SELECTIVE GENE LENTIVIRUS UNDER IN VITRO INDUCED PLURIPOTENT STEM CELL CONDITIONS. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11429

Chicago Manual of Style (16th Edition):

Siefring, Christopher Brian. “GENERATION OF A NANOG PROMOTER DRIVEN SELECTIVE GENE LENTIVIRUS UNDER IN VITRO INDUCED PLURIPOTENT STEM CELL CONDITIONS.” 2010. Masters Thesis, Penn State University. Accessed January 23, 2020. https://etda.libraries.psu.edu/catalog/11429.

MLA Handbook (7th Edition):

Siefring, Christopher Brian. “GENERATION OF A NANOG PROMOTER DRIVEN SELECTIVE GENE LENTIVIRUS UNDER IN VITRO INDUCED PLURIPOTENT STEM CELL CONDITIONS.” 2010. Web. 23 Jan 2020.

Vancouver:

Siefring CB. GENERATION OF A NANOG PROMOTER DRIVEN SELECTIVE GENE LENTIVIRUS UNDER IN VITRO INDUCED PLURIPOTENT STEM CELL CONDITIONS. [Internet] [Masters thesis]. Penn State University; 2010. [cited 2020 Jan 23]. Available from: https://etda.libraries.psu.edu/catalog/11429.

Council of Science Editors:

Siefring CB. GENERATION OF A NANOG PROMOTER DRIVEN SELECTIVE GENE LENTIVIRUS UNDER IN VITRO INDUCED PLURIPOTENT STEM CELL CONDITIONS. [Masters Thesis]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/11429


University of Illinois – Chicago

4. Kohler, Erin E. The Role of Nanog in Wnt Signaling-Mediated Endothelial Cell Dedifferentiation and Neovascularization.

Degree: 2014, University of Illinois – Chicago

 Cardiovascular disease is the leading cause of death worldwide, attributing to seven million deaths per year. Coronary artery bypass grafts (CABG) using the saphenous vein… (more)

Subjects/Keywords: Nanog; Dedifferentiation; BIO; Neovascularization; Endothelial Cells

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APA (6th Edition):

Kohler, E. E. (2014). The Role of Nanog in Wnt Signaling-Mediated Endothelial Cell Dedifferentiation and Neovascularization. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/11290

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):

Kohler, Erin E. “The Role of Nanog in Wnt Signaling-Mediated Endothelial Cell Dedifferentiation and Neovascularization.” 2014. Thesis, University of Illinois – Chicago. Accessed January 23, 2020. http://hdl.handle.net/10027/11290.

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

MLA Handbook (7th Edition):

Kohler, Erin E. “The Role of Nanog in Wnt Signaling-Mediated Endothelial Cell Dedifferentiation and Neovascularization.” 2014. Web. 23 Jan 2020.

Vancouver:

Kohler EE. The Role of Nanog in Wnt Signaling-Mediated Endothelial Cell Dedifferentiation and Neovascularization. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10027/11290.

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

Council of Science Editors:

Kohler EE. The Role of Nanog in Wnt Signaling-Mediated Endothelial Cell Dedifferentiation and Neovascularization. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/11290

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

5. Bessonnard, Sylvain. Régulations génétiques contrôlant l'engagement cellulaire au cours du développement murin : différenciation de l'épiblaste versus l'endoderme primitif : Hybridization capture coupled to next-generation sequencing to explore metagenomic samples.

Degree: Docteur es, Biologie du développement, 2012, Clermont-Ferrand 1

A 3.5 jours de développement (J3.5), l'embryon de souris est constitué d'un épithélium externe, le trophectoderme, et d'une masse cellulaire interne (MCI). La MCI est… (more)

Subjects/Keywords: Développement embryonnaire préimplantatoire; Nanog; Gata6; Bmi1; EPr

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APA (6th Edition):

Bessonnard, S. (2012). Régulations génétiques contrôlant l'engagement cellulaire au cours du développement murin : différenciation de l'épiblaste versus l'endoderme primitif : Hybridization capture coupled to next-generation sequencing to explore metagenomic samples. (Doctoral Dissertation). Clermont-Ferrand 1. Retrieved from http://www.theses.fr/2012CLF1MM06

Chicago Manual of Style (16th Edition):

Bessonnard, Sylvain. “Régulations génétiques contrôlant l'engagement cellulaire au cours du développement murin : différenciation de l'épiblaste versus l'endoderme primitif : Hybridization capture coupled to next-generation sequencing to explore metagenomic samples.” 2012. Doctoral Dissertation, Clermont-Ferrand 1. Accessed January 23, 2020. http://www.theses.fr/2012CLF1MM06.

MLA Handbook (7th Edition):

Bessonnard, Sylvain. “Régulations génétiques contrôlant l'engagement cellulaire au cours du développement murin : différenciation de l'épiblaste versus l'endoderme primitif : Hybridization capture coupled to next-generation sequencing to explore metagenomic samples.” 2012. Web. 23 Jan 2020.

Vancouver:

Bessonnard S. Régulations génétiques contrôlant l'engagement cellulaire au cours du développement murin : différenciation de l'épiblaste versus l'endoderme primitif : Hybridization capture coupled to next-generation sequencing to explore metagenomic samples. [Internet] [Doctoral dissertation]. Clermont-Ferrand 1; 2012. [cited 2020 Jan 23]. Available from: http://www.theses.fr/2012CLF1MM06.

Council of Science Editors:

Bessonnard S. Régulations génétiques contrôlant l'engagement cellulaire au cours du développement murin : différenciation de l'épiblaste versus l'endoderme primitif : Hybridization capture coupled to next-generation sequencing to explore metagenomic samples. [Doctoral Dissertation]. Clermont-Ferrand 1; 2012. Available from: http://www.theses.fr/2012CLF1MM06

6. Barros, Flavia Regina Oliveira de. Identificação de marcadores de pluripotência em células-tronco embrionárias e embriões suínos.

Degree: Mestrado, Reprodução Animal, 2009, University of São Paulo

 Células-tronco embrionárias (CTE) são importantes para estudos de desenvolvimento embrionário, diferenciação e manipulação genética. Além disso, essas células podem ser utilizadas na terapia celular e… (more)

Subjects/Keywords: Células-tronco embrionárias; Embryonic stem cells; FoxD3; FoxD3; Nanog; Nanog; Sox2; Sox2; Suínos; Swine

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APA (6th Edition):

Barros, F. R. O. d. (2009). Identificação de marcadores de pluripotência em células-tronco embrionárias e embriões suínos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10131/tde-10022009-130827/ ;

Chicago Manual of Style (16th Edition):

Barros, Flavia Regina Oliveira de. “Identificação de marcadores de pluripotência em células-tronco embrionárias e embriões suínos.” 2009. Masters Thesis, University of São Paulo. Accessed January 23, 2020. http://www.teses.usp.br/teses/disponiveis/10/10131/tde-10022009-130827/ ;.

MLA Handbook (7th Edition):

Barros, Flavia Regina Oliveira de. “Identificação de marcadores de pluripotência em células-tronco embrionárias e embriões suínos.” 2009. Web. 23 Jan 2020.

Vancouver:

Barros FROd. Identificação de marcadores de pluripotência em células-tronco embrionárias e embriões suínos. [Internet] [Masters thesis]. University of São Paulo; 2009. [cited 2020 Jan 23]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10131/tde-10022009-130827/ ;.

Council of Science Editors:

Barros FROd. Identificação de marcadores de pluripotência em células-tronco embrionárias e embriões suínos. [Masters Thesis]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/10/10131/tde-10022009-130827/ ;

7. Chauveau, Sabine. Etude des embryons doubles mutants Nanog-/- ; Gata6-/- durant la spécification de la masse cellulaire interne. Mise en évidence d'une nouvelle hétérogénéité. : Study of mutant double embryos Nanog - / -; Gata6 - / - during the specification of the internal cell mass. Highlighting a new heterogeneity.

Degree: Docteur es, Sciences de la vie et de la sante, 2016, Clermont-Ferrand 1

Lors de la formation du blastocyste, l'embryon de souris est constitué d'un épithélium externe, le trophectoderme (TE), et d'une masse cellulaire interne (MCI). L’épiblaste (EPI)… (more)

Subjects/Keywords: Développement pré-implantatoire; Sox2; Epiblaste; FGF4; Nanog; Pre-implantatory development; Sox2; Epiblast; FGF4; Nanog; 571.6

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APA (6th Edition):

Chauveau, S. (2016). Etude des embryons doubles mutants Nanog-/- ; Gata6-/- durant la spécification de la masse cellulaire interne. Mise en évidence d'une nouvelle hétérogénéité. : Study of mutant double embryos Nanog - / -; Gata6 - / - during the specification of the internal cell mass. Highlighting a new heterogeneity. (Doctoral Dissertation). Clermont-Ferrand 1. Retrieved from http://www.theses.fr/2016CLF1MM29

Chicago Manual of Style (16th Edition):

Chauveau, Sabine. “Etude des embryons doubles mutants Nanog-/- ; Gata6-/- durant la spécification de la masse cellulaire interne. Mise en évidence d'une nouvelle hétérogénéité. : Study of mutant double embryos Nanog - / -; Gata6 - / - during the specification of the internal cell mass. Highlighting a new heterogeneity.” 2016. Doctoral Dissertation, Clermont-Ferrand 1. Accessed January 23, 2020. http://www.theses.fr/2016CLF1MM29.

MLA Handbook (7th Edition):

Chauveau, Sabine. “Etude des embryons doubles mutants Nanog-/- ; Gata6-/- durant la spécification de la masse cellulaire interne. Mise en évidence d'une nouvelle hétérogénéité. : Study of mutant double embryos Nanog - / -; Gata6 - / - during the specification of the internal cell mass. Highlighting a new heterogeneity.” 2016. Web. 23 Jan 2020.

Vancouver:

Chauveau S. Etude des embryons doubles mutants Nanog-/- ; Gata6-/- durant la spécification de la masse cellulaire interne. Mise en évidence d'une nouvelle hétérogénéité. : Study of mutant double embryos Nanog - / -; Gata6 - / - during the specification of the internal cell mass. Highlighting a new heterogeneity. [Internet] [Doctoral dissertation]. Clermont-Ferrand 1; 2016. [cited 2020 Jan 23]. Available from: http://www.theses.fr/2016CLF1MM29.

Council of Science Editors:

Chauveau S. Etude des embryons doubles mutants Nanog-/- ; Gata6-/- durant la spécification de la masse cellulaire interne. Mise en évidence d'une nouvelle hétérogénéité. : Study of mutant double embryos Nanog - / -; Gata6 - / - during the specification of the internal cell mass. Highlighting a new heterogeneity. [Doctoral Dissertation]. Clermont-Ferrand 1; 2016. Available from: http://www.theses.fr/2016CLF1MM29


Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

8. Παπαμίχος, Σπύρος. Μελέτη μοριακών δεικτών βλαστικών κυττάρων στο γυναικολογικό καρκίνο.

Degree: 2013, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ)

 The cancer stem cell hypothesis provides an attractive cellular mechanism to account for thetherapeutic refractoriness and the heterogeneity of most solid tumors. Cancer stem-like cells,… (more)

Subjects/Keywords: Βλαστικά κύτταρα; Γυναικολογικός καρκίνος; Ισομορφές γονιδίου OCT4; Γονίδιο NANOG; Stem cells; Gynecologic cancer; OCT4 gene isoforms; NANOG gene

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APA (6th Edition):

Παπαμίχος, . . (2013). Μελέτη μοριακών δεικτών βλαστικών κυττάρων στο γυναικολογικό καρκίνο. (Thesis). Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Retrieved from http://hdl.handle.net/10442/hedi/38090

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):

Παπαμίχος, Σπύρος. “Μελέτη μοριακών δεικτών βλαστικών κυττάρων στο γυναικολογικό καρκίνο.” 2013. Thesis, Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ). Accessed January 23, 2020. http://hdl.handle.net/10442/hedi/38090.

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

MLA Handbook (7th Edition):

Παπαμίχος, Σπύρος. “Μελέτη μοριακών δεικτών βλαστικών κυττάρων στο γυναικολογικό καρκίνο.” 2013. Web. 23 Jan 2020.

Vancouver:

Παπαμίχος . Μελέτη μοριακών δεικτών βλαστικών κυττάρων στο γυναικολογικό καρκίνο. [Internet] [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2013. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10442/hedi/38090.

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

Council of Science Editors:

Παπαμίχος . Μελέτη μοριακών δεικτών βλαστικών κυττάρων στο γυναικολογικό καρκίνο. [Thesis]. Aristotle University Of Thessaloniki (AUTH); Αριστοτέλειο Πανεπιστήμιο Θεσσαλονίκης (ΑΠΘ); 2013. Available from: http://hdl.handle.net/10442/hedi/38090

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


Université Paris-Sud – Paris XI

9. Khan, Daulat Raheem. Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l’embryon bovin : Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo.

Degree: Docteur es, Reproduction - Développement, 2011, Université Paris-Sud – Paris XI

 Lors de la fécondation, le sperme et l'ovule s'unissent pour former un zygote totipotent. Initialement, le zygote est transcriptionnellement inactif. Au cours des premiers clivages… (more)

Subjects/Keywords: Embryon bovin; Mise en route du génome; OCT4; SOX2; NANOG; Clonage; Bovine embryo; Embryonic genome activation (EGA); OCT4; SOX2; NANOG; Cloning

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APA (6th Edition):

Khan, D. R. (2011). Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l’embryon bovin : Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA11T060

Chicago Manual of Style (16th Edition):

Khan, Daulat Raheem. “Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l’embryon bovin : Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed January 23, 2020. http://www.theses.fr/2011PA11T060.

MLA Handbook (7th Edition):

Khan, Daulat Raheem. “Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l’embryon bovin : Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo.” 2011. Web. 23 Jan 2020.

Vancouver:

Khan DR. Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l’embryon bovin : Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Jan 23]. Available from: http://www.theses.fr/2011PA11T060.

Council of Science Editors:

Khan DR. Reprogrammation embryonnaire et somatique au moment de la mise en route du génome dans l’embryon bovin : Embryonic and somatic reprogramming at the time of embryonic genome activation in the bovine embryo. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA11T060

10. Bonaventura, Gabriele. New analytical scenarios and new approaches in the embryonic genetic investigation of the macromolecular alterations responsible for the neurodegenerative diseases.

Degree: 2014, Università degli Studi di Catania

 Systematic, genome-wide interrogations have identified hundreds of genes, including several transcription factors, which have expression patterns tightly correlated with ES cell differentiation. OCT4, SOX2 and… (more)

Subjects/Keywords: Area 05 - Scienze biologiche; hESCs, Oct4, Sox2, Nanog, F.C.S., N&B.

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APA (6th Edition):

Bonaventura, G. (2014). New analytical scenarios and new approaches in the embryonic genetic investigation of the macromolecular alterations responsible for the neurodegenerative diseases. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/1534

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):

Bonaventura, Gabriele. “New analytical scenarios and new approaches in the embryonic genetic investigation of the macromolecular alterations responsible for the neurodegenerative diseases.” 2014. Thesis, Università degli Studi di Catania. Accessed January 23, 2020. http://hdl.handle.net/10761/1534.

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

MLA Handbook (7th Edition):

Bonaventura, Gabriele. “New analytical scenarios and new approaches in the embryonic genetic investigation of the macromolecular alterations responsible for the neurodegenerative diseases.” 2014. Web. 23 Jan 2020.

Vancouver:

Bonaventura G. New analytical scenarios and new approaches in the embryonic genetic investigation of the macromolecular alterations responsible for the neurodegenerative diseases. [Internet] [Thesis]. Università degli Studi di Catania; 2014. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10761/1534.

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

Council of Science Editors:

Bonaventura G. New analytical scenarios and new approaches in the embryonic genetic investigation of the macromolecular alterations responsible for the neurodegenerative diseases. [Thesis]. Università degli Studi di Catania; 2014. Available from: http://hdl.handle.net/10761/1534

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


University of Southern California

11. Uthaya Kumar, Dinesh Babu. Roles of epithelial-mesenchymal transition and niche in tumorigenesis of tumor-initiating cells.

Degree: MS, Molecular Microbiology and Immunology, 2015, University of Southern California

 Abstract Study – 1 (Chapter 2) ❧ BACKGROUND & AIMS: Alcohol and obesity cause steatohepatitis through activation of Toll‐like receptor‐4 (TLR4) signaling and enhance hepatitis… (more)

Subjects/Keywords: tumor-initiating stem-like cells; TLR4; NANOG; TWIST1; HCFD

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APA (6th Edition):

Uthaya Kumar, D. B. (2015). Roles of epithelial-mesenchymal transition and niche in tumorigenesis of tumor-initiating cells. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/447164/rec/5645

Chicago Manual of Style (16th Edition):

Uthaya Kumar, Dinesh Babu. “Roles of epithelial-mesenchymal transition and niche in tumorigenesis of tumor-initiating cells.” 2015. Masters Thesis, University of Southern California. Accessed January 23, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/447164/rec/5645.

MLA Handbook (7th Edition):

Uthaya Kumar, Dinesh Babu. “Roles of epithelial-mesenchymal transition and niche in tumorigenesis of tumor-initiating cells.” 2015. Web. 23 Jan 2020.

Vancouver:

Uthaya Kumar DB. Roles of epithelial-mesenchymal transition and niche in tumorigenesis of tumor-initiating cells. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Jan 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/447164/rec/5645.

Council of Science Editors:

Uthaya Kumar DB. Roles of epithelial-mesenchymal transition and niche in tumorigenesis of tumor-initiating cells. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/447164/rec/5645


University of Edinburgh

12. Festuccia, Nicola. Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development.

Degree: PhD, 2013, University of Edinburgh

 Embryonic stem (ES) cell pluripotency is sustained by a network of transcription factors centred on Oct4, Sox2 and Nanog. Whilst Oct4 and Sox2 expression is… (more)

Subjects/Keywords: 572; transcriptional profiling; embryonic stem; Nanog; Estrogen-related receptor b; Esrrb

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APA (6th Edition):

Festuccia, N. (2013). Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/12232

Chicago Manual of Style (16th Edition):

Festuccia, Nicola. “Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2020. http://hdl.handle.net/1842/12232.

MLA Handbook (7th Edition):

Festuccia, Nicola. “Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development.” 2013. Web. 23 Jan 2020.

Vancouver:

Festuccia N. Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1842/12232.

Council of Science Editors:

Festuccia N. Esrrb is a prominent target of Nanog that substitutes for Nanog function in ES cell self-renewal, reprogramming and germline development. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/12232


Universitat de Valencia

13. Serrano Tejero, Felipe. Transdiferenciación de fibroblastos a hepatocitos mediante reprogramación celular : papel de Gata4 en el bloqueo de la reprogramación de células somáticas .

Degree: 2013, Universitat de Valencia

 En esta tesis doctoral se muestra la conversión directa de fibroblastos embrionarios de ratón a células con morfología y fenotipo similares al hepatocito mediante la… (more)

Subjects/Keywords: pluripotencia; IPS; hepatocitos; conversion directa; nanog; iHep; reprogramación celular

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APA (6th Edition):

Serrano Tejero, F. (2013). Transdiferenciación de fibroblastos a hepatocitos mediante reprogramación celular : papel de Gata4 en el bloqueo de la reprogramación de células somáticas . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/26596

Chicago Manual of Style (16th Edition):

Serrano Tejero, Felipe. “Transdiferenciación de fibroblastos a hepatocitos mediante reprogramación celular : papel de Gata4 en el bloqueo de la reprogramación de células somáticas .” 2013. Doctoral Dissertation, Universitat de Valencia. Accessed January 23, 2020. http://hdl.handle.net/10550/26596.

MLA Handbook (7th Edition):

Serrano Tejero, Felipe. “Transdiferenciación de fibroblastos a hepatocitos mediante reprogramación celular : papel de Gata4 en el bloqueo de la reprogramación de células somáticas .” 2013. Web. 23 Jan 2020.

Vancouver:

Serrano Tejero F. Transdiferenciación de fibroblastos a hepatocitos mediante reprogramación celular : papel de Gata4 en el bloqueo de la reprogramación de células somáticas . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2013. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10550/26596.

Council of Science Editors:

Serrano Tejero F. Transdiferenciación de fibroblastos a hepatocitos mediante reprogramación celular : papel de Gata4 en el bloqueo de la reprogramación de células somáticas . [Doctoral Dissertation]. Universitat de Valencia; 2013. Available from: http://hdl.handle.net/10550/26596


University of Waikato

14. Chibnall, Alice Margaret. Doxycycline-inducible overexpression of NANOG in bovine fibroblasts and nuclear transfer embryos .

Degree: 2015, University of Waikato

 Naïve pluripotent embryonic stem cells (ES cells) have the ability to give rise to all cell types including functional gametes. These cells have been well… (more)

Subjects/Keywords: Embryonic stem cells; Pluripotency; Bovine; NANOG; Overexpression; Doxycyline-inducible

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APA (6th Edition):

Chibnall, A. M. (2015). Doxycycline-inducible overexpression of NANOG in bovine fibroblasts and nuclear transfer embryos . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/9494

Chicago Manual of Style (16th Edition):

Chibnall, Alice Margaret. “Doxycycline-inducible overexpression of NANOG in bovine fibroblasts and nuclear transfer embryos .” 2015. Masters Thesis, University of Waikato. Accessed January 23, 2020. http://hdl.handle.net/10289/9494.

MLA Handbook (7th Edition):

Chibnall, Alice Margaret. “Doxycycline-inducible overexpression of NANOG in bovine fibroblasts and nuclear transfer embryos .” 2015. Web. 23 Jan 2020.

Vancouver:

Chibnall AM. Doxycycline-inducible overexpression of NANOG in bovine fibroblasts and nuclear transfer embryos . [Internet] [Masters thesis]. University of Waikato; 2015. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10289/9494.

Council of Science Editors:

Chibnall AM. Doxycycline-inducible overexpression of NANOG in bovine fibroblasts and nuclear transfer embryos . [Masters Thesis]. University of Waikato; 2015. Available from: http://hdl.handle.net/10289/9494


University of Waikato

15. Wilson, Brooke Carol. MicroRNA-mediated silencing of bovine NANOG and MBD3 .

Degree: 2015, University of Waikato

 Embryonic stem cells (ESCs) are pluripotent due to their ability to differentiate into any cell type of the body, including functional gametes. These cells are… (more)

Subjects/Keywords: microRNA; bovine; embryonic stem cells; NANOG; MBD3; knockdown; RNA interference

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APA (6th Edition):

Wilson, B. C. (2015). MicroRNA-mediated silencing of bovine NANOG and MBD3 . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/9603

Chicago Manual of Style (16th Edition):

Wilson, Brooke Carol. “MicroRNA-mediated silencing of bovine NANOG and MBD3 .” 2015. Masters Thesis, University of Waikato. Accessed January 23, 2020. http://hdl.handle.net/10289/9603.

MLA Handbook (7th Edition):

Wilson, Brooke Carol. “MicroRNA-mediated silencing of bovine NANOG and MBD3 .” 2015. Web. 23 Jan 2020.

Vancouver:

Wilson BC. MicroRNA-mediated silencing of bovine NANOG and MBD3 . [Internet] [Masters thesis]. University of Waikato; 2015. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10289/9603.

Council of Science Editors:

Wilson BC. MicroRNA-mediated silencing of bovine NANOG and MBD3 . [Masters Thesis]. University of Waikato; 2015. Available from: http://hdl.handle.net/10289/9603


University of Edinburgh

16. Zhang, Jingchao. Functional analysis of the role of the Nanog tryptophan repeat in ES cells.

Degree: PhD, 2016, University of Edinburgh

Nanog is a transcription factor that plays a central part in the gene regulatory network that maintains and induces pluripotency of embryonic stem cells (ESCs).… (more)

Subjects/Keywords: 616.02; ES cells; Nanog; Otx2; tryptophan repeats; pluripotency

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APA (6th Edition):

Zhang, J. (2016). Functional analysis of the role of the Nanog tryptophan repeat in ES cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/15972

Chicago Manual of Style (16th Edition):

Zhang, Jingchao. “Functional analysis of the role of the Nanog tryptophan repeat in ES cells.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2020. http://hdl.handle.net/1842/15972.

MLA Handbook (7th Edition):

Zhang, Jingchao. “Functional analysis of the role of the Nanog tryptophan repeat in ES cells.” 2016. Web. 23 Jan 2020.

Vancouver:

Zhang J. Functional analysis of the role of the Nanog tryptophan repeat in ES cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1842/15972.

Council of Science Editors:

Zhang J. Functional analysis of the role of the Nanog tryptophan repeat in ES cells. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/15972


University of Edinburgh

17. Gagliardi, Alessia. Protein interactions underpinning pluripotency.

Degree: PhD, 2014, University of Edinburgh

 Embryonic stem (ES) cells are maintained in an undifferentiated state by a gene regulatory network centred on the triumvirate of transcription factors Nanog, Oct4 and… (more)

Subjects/Keywords: 572; embryonic stem cells; Nanog; Sox2; protein interaction; pluripotency

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APA (6th Edition):

Gagliardi, A. (2014). Protein interactions underpinning pluripotency. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/18004

Chicago Manual of Style (16th Edition):

Gagliardi, Alessia. “Protein interactions underpinning pluripotency.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2020. http://hdl.handle.net/1842/18004.

MLA Handbook (7th Edition):

Gagliardi, Alessia. “Protein interactions underpinning pluripotency.” 2014. Web. 23 Jan 2020.

Vancouver:

Gagliardi A. Protein interactions underpinning pluripotency. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1842/18004.

Council of Science Editors:

Gagliardi A. Protein interactions underpinning pluripotency. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/18004


University of Toronto

18. Schwartz, Michael Louis. Characterizing Changes in the Transcriptional Networks underlying Pluripotency in Mouse Embryonic Stem Cells upon the Induction of Differentiation.

Degree: 2012, University of Toronto

Mouse embryonic stem cells (mESCs) are pluripotent cells capable of differentiating into all three germ layers present in the adult mouse. In this thesis, I… (more)

Subjects/Keywords: Gene Expression; Pluripotency; Mouse Embryonic Stem Cells; Nanog; 0369

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APA (6th Edition):

Schwartz, M. L. (2012). Characterizing Changes in the Transcriptional Networks underlying Pluripotency in Mouse Embryonic Stem Cells upon the Induction of Differentiation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33522

Chicago Manual of Style (16th Edition):

Schwartz, Michael Louis. “Characterizing Changes in the Transcriptional Networks underlying Pluripotency in Mouse Embryonic Stem Cells upon the Induction of Differentiation.” 2012. Masters Thesis, University of Toronto. Accessed January 23, 2020. http://hdl.handle.net/1807/33522.

MLA Handbook (7th Edition):

Schwartz, Michael Louis. “Characterizing Changes in the Transcriptional Networks underlying Pluripotency in Mouse Embryonic Stem Cells upon the Induction of Differentiation.” 2012. Web. 23 Jan 2020.

Vancouver:

Schwartz ML. Characterizing Changes in the Transcriptional Networks underlying Pluripotency in Mouse Embryonic Stem Cells upon the Induction of Differentiation. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1807/33522.

Council of Science Editors:

Schwartz ML. Characterizing Changes in the Transcriptional Networks underlying Pluripotency in Mouse Embryonic Stem Cells upon the Induction of Differentiation. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33522


University of Illinois – Chicago

19. Baruah, Jugajyoti. Role of Endothelial Nanog in Homeostasis of Adult Tissue Microenvironment.

Degree: 2018, University of Illinois – Chicago

 Elevated level of expression of transcription factor (TF) Nanog regulates pluripotency of stem cells. However, the biological significance of low-level expression of Nanog remains unknown.… (more)

Subjects/Keywords: Cardiac Hypertrophy; Endothelial Cell Homeostasis; Nanog; Telomerase Reverse Transcriptase; Wnt-signaling.

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APA (6th Edition):

Baruah, J. (2018). Role of Endothelial Nanog in Homeostasis of Adult Tissue Microenvironment. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22635

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):

Baruah, Jugajyoti. “Role of Endothelial Nanog in Homeostasis of Adult Tissue Microenvironment.” 2018. Thesis, University of Illinois – Chicago. Accessed January 23, 2020. http://hdl.handle.net/10027/22635.

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

MLA Handbook (7th Edition):

Baruah, Jugajyoti. “Role of Endothelial Nanog in Homeostasis of Adult Tissue Microenvironment.” 2018. Web. 23 Jan 2020.

Vancouver:

Baruah J. Role of Endothelial Nanog in Homeostasis of Adult Tissue Microenvironment. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10027/22635.

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

Council of Science Editors:

Baruah J. Role of Endothelial Nanog in Homeostasis of Adult Tissue Microenvironment. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/22635

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


University of Toronto

20. Tang, Calvin Chun Man. Nanog Regulates Chromatin Organization in Mouse Stem Cells.

Degree: 2013, University of Toronto

Mouse embryonic stem cells (ESCs) are known to possess an “open” global chromatin architecture characterized by dispersed chromatin fibres throughout the nucleus. This is in… (more)

Subjects/Keywords: chromatin; nanog; electron spectroscopic imaging; stem cell; 0379

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APA (6th Edition):

Tang, C. C. M. (2013). Nanog Regulates Chromatin Organization in Mouse Stem Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42949

Chicago Manual of Style (16th Edition):

Tang, Calvin Chun Man. “Nanog Regulates Chromatin Organization in Mouse Stem Cells.” 2013. Masters Thesis, University of Toronto. Accessed January 23, 2020. http://hdl.handle.net/1807/42949.

MLA Handbook (7th Edition):

Tang, Calvin Chun Man. “Nanog Regulates Chromatin Organization in Mouse Stem Cells.” 2013. Web. 23 Jan 2020.

Vancouver:

Tang CCM. Nanog Regulates Chromatin Organization in Mouse Stem Cells. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1807/42949.

Council of Science Editors:

Tang CCM. Nanog Regulates Chromatin Organization in Mouse Stem Cells. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42949

21. Bassalert, Cécilia. Influence des voies de signalisation IGF et MAPK sur la spécification des lignages de l'embryon de souris préimplantatoire : Influence of signaling pathways IGF and MAPK on lineage specification in murine preimplantatory embryon.

Degree: Docteur es, Génétique et Physiologie, 2018, Clermont Auvergne

Au cours de la préimplantation, l'embryon de souris produit deux lignages cellulaires, le trophectoderme (TE), et la masse cellulaire interne (MCI) qui elle-même se différencie… (more)

Subjects/Keywords: Développement embryonnaire préimplantatoire; MAPK; ERK; DUSP4; ETV5; IGF; IGF1R; NANOG; GATA6; Epiblaste; Endoderme Primitif; Preimplantatory embryonic development; MAPK; ERK; DUSP4; ETV5; IGF; IGF1R; NANOG; GATA6; Epiblast; Primitive Endoderm

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APA (6th Edition):

Bassalert, C. (2018). Influence des voies de signalisation IGF et MAPK sur la spécification des lignages de l'embryon de souris préimplantatoire : Influence of signaling pathways IGF and MAPK on lineage specification in murine preimplantatory embryon. (Doctoral Dissertation). Clermont Auvergne. Retrieved from http://www.theses.fr/2018CLFAC029

Chicago Manual of Style (16th Edition):

Bassalert, Cécilia. “Influence des voies de signalisation IGF et MAPK sur la spécification des lignages de l'embryon de souris préimplantatoire : Influence of signaling pathways IGF and MAPK on lineage specification in murine preimplantatory embryon.” 2018. Doctoral Dissertation, Clermont Auvergne. Accessed January 23, 2020. http://www.theses.fr/2018CLFAC029.

MLA Handbook (7th Edition):

Bassalert, Cécilia. “Influence des voies de signalisation IGF et MAPK sur la spécification des lignages de l'embryon de souris préimplantatoire : Influence of signaling pathways IGF and MAPK on lineage specification in murine preimplantatory embryon.” 2018. Web. 23 Jan 2020.

Vancouver:

Bassalert C. Influence des voies de signalisation IGF et MAPK sur la spécification des lignages de l'embryon de souris préimplantatoire : Influence of signaling pathways IGF and MAPK on lineage specification in murine preimplantatory embryon. [Internet] [Doctoral dissertation]. Clermont Auvergne; 2018. [cited 2020 Jan 23]. Available from: http://www.theses.fr/2018CLFAC029.

Council of Science Editors:

Bassalert C. Influence des voies de signalisation IGF et MAPK sur la spécification des lignages de l'embryon de souris préimplantatoire : Influence of signaling pathways IGF and MAPK on lineage specification in murine preimplantatory embryon. [Doctoral Dissertation]. Clermont Auvergne; 2018. Available from: http://www.theses.fr/2018CLFAC029


Texas Medical Center

22. Badeaux, Mark D. UNDERSTANDING NANOG'S ROLE IN CANCER BIOLOGY.

Degree: PhD, 2011, Texas Medical Center

  Understanding Nanog’s Role in Cancer Biology Mark Daniel Badeaux Supervisory Professor Dean Tang, PhD The cancer stem cell model holds that tumor heterogeneity and… (more)

Subjects/Keywords: Nanog; transgenic mouse; miR-128a; ceRNA; stem cells; cancer stem cells; Medicine and Health Sciences

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APA (6th Edition):

Badeaux, M. D. (2011). UNDERSTANDING NANOG'S ROLE IN CANCER BIOLOGY. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/205

Chicago Manual of Style (16th Edition):

Badeaux, Mark D. “UNDERSTANDING NANOG'S ROLE IN CANCER BIOLOGY.” 2011. Doctoral Dissertation, Texas Medical Center. Accessed January 23, 2020. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/205.

MLA Handbook (7th Edition):

Badeaux, Mark D. “UNDERSTANDING NANOG'S ROLE IN CANCER BIOLOGY.” 2011. Web. 23 Jan 2020.

Vancouver:

Badeaux MD. UNDERSTANDING NANOG'S ROLE IN CANCER BIOLOGY. [Internet] [Doctoral dissertation]. Texas Medical Center; 2011. [cited 2020 Jan 23]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/205.

Council of Science Editors:

Badeaux MD. UNDERSTANDING NANOG'S ROLE IN CANCER BIOLOGY. [Doctoral Dissertation]. Texas Medical Center; 2011. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/205


NSYSU

23. Hsieh, I-chien. Association of Oct4, Sox2, and Nanog Expression with Development and Prognosis in Oral Tongue Squamous Cell Carcinoma and Buccal Mucosal Squamous Cell Carcinoma.

Degree: Master, Biological Sciences, 2013, NSYSU

 In Taiwan, oral cancer is the 4th leading cause of cancer death for males and the top common cancer in young adult males. The most… (more)

Subjects/Keywords: Nanog; Sox2; Oct4; Buccal mucosal SCC; Oral tongue SCC; Cancer stem cell; Tissue microarry

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APA (6th Edition):

Hsieh, I. (2013). Association of Oct4, Sox2, and Nanog Expression with Development and Prognosis in Oral Tongue Squamous Cell Carcinoma and Buccal Mucosal Squamous Cell Carcinoma. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0811113-155550

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):

Hsieh, I-chien. “Association of Oct4, Sox2, and Nanog Expression with Development and Prognosis in Oral Tongue Squamous Cell Carcinoma and Buccal Mucosal Squamous Cell Carcinoma.” 2013. Thesis, NSYSU. Accessed January 23, 2020. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0811113-155550.

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

MLA Handbook (7th Edition):

Hsieh, I-chien. “Association of Oct4, Sox2, and Nanog Expression with Development and Prognosis in Oral Tongue Squamous Cell Carcinoma and Buccal Mucosal Squamous Cell Carcinoma.” 2013. Web. 23 Jan 2020.

Vancouver:

Hsieh I. Association of Oct4, Sox2, and Nanog Expression with Development and Prognosis in Oral Tongue Squamous Cell Carcinoma and Buccal Mucosal Squamous Cell Carcinoma. [Internet] [Thesis]. NSYSU; 2013. [cited 2020 Jan 23]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0811113-155550.

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

Council of Science Editors:

Hsieh I. Association of Oct4, Sox2, and Nanog Expression with Development and Prognosis in Oral Tongue Squamous Cell Carcinoma and Buccal Mucosal Squamous Cell Carcinoma. [Thesis]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0811113-155550

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


Universitat Pompeu Fabra

24. Pedone, Elisa, 1985-. β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated reprogramming of somatic cells to pluripotency.

Degree: Departament de Ciències Experimentals i de la Salut, 2014, Universitat Pompeu Fabra

 Las células madre embrionarias de ratón (ES) derivadas de la masa celular interna del blastocisto, se pueden mantener en estado de pluripotencia, utilizando condiciones de… (more)

Subjects/Keywords: Embryonic stem cells; Fluctuations; β-catenin; Nanog; Reprogramming; Cèl·lules mare; Fluctuacions; Reprogramació; 576

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APA (6th Edition):

Pedone, Elisa, 1. (2014). β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated reprogramming of somatic cells to pluripotency. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/289619

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):

Pedone, Elisa, 1985-. “β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated reprogramming of somatic cells to pluripotency.” 2014. Thesis, Universitat Pompeu Fabra. Accessed January 23, 2020. http://hdl.handle.net/10803/289619.

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

MLA Handbook (7th Edition):

Pedone, Elisa, 1985-. “β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated reprogramming of somatic cells to pluripotency.” 2014. Web. 23 Jan 2020.

Vancouver:

Pedone, Elisa 1. β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated reprogramming of somatic cells to pluripotency. [Internet] [Thesis]. Universitat Pompeu Fabra; 2014. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/10803/289619.

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

Council of Science Editors:

Pedone, Elisa 1. β-catenin fluctuates in mouse ESCs and is essential for Nanog-mediated reprogramming of somatic cells to pluripotency. [Thesis]. Universitat Pompeu Fabra; 2014. Available from: http://hdl.handle.net/10803/289619

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


University of Edinburgh

25. Roy, Marcia Michelle. Post-translational regulation of Nanog and Nanog-interacting proteins in mouse embryonic stem cells.

Degree: PhD, 2012, University of Edinburgh

 Pluripotent embryonic stem cells (ESCs) possess an unlimited capacity for self-renewal. This property of ES cells is both defining and unique. Harnessing this potential of… (more)

Subjects/Keywords: 616.02; stem cells; LC-MS/MS; Nanog; small molecules; cell cycle; CRLs

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APA (6th Edition):

Roy, M. M. (2012). Post-translational regulation of Nanog and Nanog-interacting proteins in mouse embryonic stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8936

Chicago Manual of Style (16th Edition):

Roy, Marcia Michelle. “Post-translational regulation of Nanog and Nanog-interacting proteins in mouse embryonic stem cells.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed January 23, 2020. http://hdl.handle.net/1842/8936.

MLA Handbook (7th Edition):

Roy, Marcia Michelle. “Post-translational regulation of Nanog and Nanog-interacting proteins in mouse embryonic stem cells.” 2012. Web. 23 Jan 2020.

Vancouver:

Roy MM. Post-translational regulation of Nanog and Nanog-interacting proteins in mouse embryonic stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2020 Jan 23]. Available from: http://hdl.handle.net/1842/8936.

Council of Science Editors:

Roy MM. Post-translational regulation of Nanog and Nanog-interacting proteins in mouse embryonic stem cells. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/8936

26. CHEW JOON LIN. Identification of Oct4 and Sox2 targets in mouse embryonic stem cells.

Degree: 2008, National University of Singapore

Subjects/Keywords: Oct4; Sox2; Stat3; Nanog; ChIP; mESC

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APA (6th Edition):

LIN, C. J. (2008). Identification of Oct4 and Sox2 targets in mouse embryonic stem cells. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/28139

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):

LIN, CHEW JOON. “Identification of Oct4 and Sox2 targets in mouse embryonic stem cells.” 2008. Thesis, National University of Singapore. Accessed January 23, 2020. http://scholarbank.nus.edu.sg/handle/10635/28139.

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

MLA Handbook (7th Edition):

LIN, CHEW JOON. “Identification of Oct4 and Sox2 targets in mouse embryonic stem cells.” 2008. Web. 23 Jan 2020.

Vancouver:

LIN CJ. Identification of Oct4 and Sox2 targets in mouse embryonic stem cells. [Internet] [Thesis]. National University of Singapore; 2008. [cited 2020 Jan 23]. Available from: http://scholarbank.nus.edu.sg/handle/10635/28139.

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

Council of Science Editors:

LIN CJ. Identification of Oct4 and Sox2 targets in mouse embryonic stem cells. [Thesis]. National University of Singapore; 2008. Available from: http://scholarbank.nus.edu.sg/handle/10635/28139

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


Utah State University

27. Hall, Justin Scott. Regulation and Expression of Nanog, Oct4, and Sox2 in the Bovine Blastocyst following Somatic Cell Nuclear Transfer.

Degree: MS, Animal, Dairy, and Veterinary Sciences, 2013, Utah State University

  A live birth from a somatic cell nuclear transfer (SCNT) embryo represents a small percentage of donor cells that survived the reprogramming gauntlet. The… (more)

Subjects/Keywords: Blastocyst; Bovine; Nanog; Nuclear Transfer; Oct4; Sox2; Animal Sciences; Dairy Science; Life Sciences

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

APA (6th Edition):

Hall, J. S. (2013). Regulation and Expression of Nanog, Oct4, and Sox2 in the Bovine Blastocyst following Somatic Cell Nuclear Transfer. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/1713

Chicago Manual of Style (16th Edition):

Hall, Justin Scott. “Regulation and Expression of Nanog, Oct4, and Sox2 in the Bovine Blastocyst following Somatic Cell Nuclear Transfer.” 2013. Masters Thesis, Utah State University. Accessed January 23, 2020. https://digitalcommons.usu.edu/etd/1713.

MLA Handbook (7th Edition):

Hall, Justin Scott. “Regulation and Expression of Nanog, Oct4, and Sox2 in the Bovine Blastocyst following Somatic Cell Nuclear Transfer.” 2013. Web. 23 Jan 2020.

Vancouver:

Hall JS. Regulation and Expression of Nanog, Oct4, and Sox2 in the Bovine Blastocyst following Somatic Cell Nuclear Transfer. [Internet] [Masters thesis]. Utah State University; 2013. [cited 2020 Jan 23]. Available from: https://digitalcommons.usu.edu/etd/1713.

Council of Science Editors:

Hall JS. Regulation and Expression of Nanog, Oct4, and Sox2 in the Bovine Blastocyst following Somatic Cell Nuclear Transfer. [Masters Thesis]. Utah State University; 2013. Available from: https://digitalcommons.usu.edu/etd/1713


University of Southern California

28. Nakagawa, Chad Isamu. Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy.

Degree: MS, Molecular Microbiology and Immunology, 2015, University of Southern California

 Hepatocellular carcinoma (HCC) is the fifth most common type of cancer. The mortality rate continues to rise every year. Hepatitis B virus (HBV) is a… (more)

Subjects/Keywords: hepatocellular carcinoma; HCC; hepatitis B virus X protein; HBx; NANOG; YAP1; β -catenin; tumor initiating cells; TICs

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APA (6th Edition):

Nakagawa, C. I. (2015). Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615884/rec/3149

Chicago Manual of Style (16th Edition):

Nakagawa, Chad Isamu. “Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy.” 2015. Masters Thesis, University of Southern California. Accessed January 23, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615884/rec/3149.

MLA Handbook (7th Edition):

Nakagawa, Chad Isamu. “Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy.” 2015. Web. 23 Jan 2020.

Vancouver:

Nakagawa CI. Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Jan 23]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615884/rec/3149.

Council of Science Editors:

Nakagawa CI. Hepatitis B virus X protein regulation of β-catenin and NANOG and co-regulatory role with YAP1 in HCC malignancy. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/615884/rec/3149


University of California – Berkeley

29. Zhang, Yolanda Yue. Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival.

Degree: Bioengineering, 2011, University of California – Berkeley

 Here we present a microfluidic culture platform for enhancing single stem cell survival. Traditional plate culture is inadequate for large scale single cell studies because… (more)

Subjects/Keywords: Biomedical engineering; Cellular biology; cell survival; embryonic stem cell; induced pluripotent stem cell; long-term culture; microfluidics; Nanog

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APA (6th Edition):

Zhang, Y. Y. (2011). Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/40j4h0mn

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):

Zhang, Yolanda Yue. “Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival.” 2011. Thesis, University of California – Berkeley. Accessed January 23, 2020. http://www.escholarship.org/uc/item/40j4h0mn.

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

MLA Handbook (7th Edition):

Zhang, Yolanda Yue. “Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival.” 2011. Web. 23 Jan 2020.

Vancouver:

Zhang YY. Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Jan 23]. Available from: http://www.escholarship.org/uc/item/40j4h0mn.

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

Council of Science Editors:

Zhang YY. Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/40j4h0mn

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


Universidade de Lisboa

30. Aquino, Tomás de Campos. Physical modeling of cellular processes: stochastic gene regulation in embryonic stem cells.

Degree: 2011, Universidade de Lisboa

Tese de mestrado em Física (Física Estatística e Não Linear), apresentada à Universidade de Lisboa, através da Faculdade de Ciências, 2011

In the last few… (more)

Subjects/Keywords: Física de sistemas biológicos; Processos estocásticos; Regulação genética; Master equation; Nanog; Células estaminais embrionárias; Teses de mestrado - 2011

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

APA (6th Edition):

Aquino, T. d. C. (2011). Physical modeling of cellular processes: stochastic gene regulation in embryonic stem cells. (Thesis). Universidade de Lisboa. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/8520

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):

Aquino, Tomás de Campos. “Physical modeling of cellular processes: stochastic gene regulation in embryonic stem cells.” 2011. Thesis, Universidade de Lisboa. Accessed January 23, 2020. http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/8520.

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

MLA Handbook (7th Edition):

Aquino, Tomás de Campos. “Physical modeling of cellular processes: stochastic gene regulation in embryonic stem cells.” 2011. Web. 23 Jan 2020.

Vancouver:

Aquino TdC. Physical modeling of cellular processes: stochastic gene regulation in embryonic stem cells. [Internet] [Thesis]. Universidade de Lisboa; 2011. [cited 2020 Jan 23]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/8520.

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

Council of Science Editors:

Aquino TdC. Physical modeling of cellular processes: stochastic gene regulation in embryonic stem cells. [Thesis]. Universidade de Lisboa; 2011. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/8520

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

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