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You searched for subject:(pluripotency). Showing records 1 – 30 of 191 total matches.

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University of Otago

1. Rhodes, Jenny Marie. Linking cohesin-dependent transcription with cell pluripotency .

Degree: 2012, University of Otago

 Embryonic stem cells are pluripotent; they have the ability to form any cell type of the developing embryo. Due to their pluripotent nature there is… (more)

Subjects/Keywords: cohesin; transcription; pluripotency; c-Myc

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APA (6th Edition):

Rhodes, J. M. (2012). Linking cohesin-dependent transcription with cell pluripotency . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/2343

Chicago Manual of Style (16th Edition):

Rhodes, Jenny Marie. “Linking cohesin-dependent transcription with cell pluripotency .” 2012. Doctoral Dissertation, University of Otago. Accessed January 15, 2021. http://hdl.handle.net/10523/2343.

MLA Handbook (7th Edition):

Rhodes, Jenny Marie. “Linking cohesin-dependent transcription with cell pluripotency .” 2012. Web. 15 Jan 2021.

Vancouver:

Rhodes JM. Linking cohesin-dependent transcription with cell pluripotency . [Internet] [Doctoral dissertation]. University of Otago; 2012. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10523/2343.

Council of Science Editors:

Rhodes JM. Linking cohesin-dependent transcription with cell pluripotency . [Doctoral Dissertation]. University of Otago; 2012. Available from: http://hdl.handle.net/10523/2343


University of Cambridge

2. Hodgson, Andrew Christopher. Microfluidic Devices for the Investigation of Pluripotency in Embryonic Stem Cells.

Degree: PhD, 2017, University of Cambridge

 This thesis presents the development of microfluidic devices designed to facilitate research into mouse embryonic stem cells (ESCs). ESCs are a well-studied cell, largely due… (more)

Subjects/Keywords: Microfluidics; Embryonic Stem Cells; Pluripotency

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APA (6th Edition):

Hodgson, A. C. (2017). Microfluidic Devices for the Investigation of Pluripotency in Embryonic Stem Cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267893

Chicago Manual of Style (16th Edition):

Hodgson, Andrew Christopher. “Microfluidic Devices for the Investigation of Pluripotency in Embryonic Stem Cells.” 2017. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://www.repository.cam.ac.uk/handle/1810/267893.

MLA Handbook (7th Edition):

Hodgson, Andrew Christopher. “Microfluidic Devices for the Investigation of Pluripotency in Embryonic Stem Cells.” 2017. Web. 15 Jan 2021.

Vancouver:

Hodgson AC. Microfluidic Devices for the Investigation of Pluripotency in Embryonic Stem Cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2021 Jan 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/267893.

Council of Science Editors:

Hodgson AC. Microfluidic Devices for the Investigation of Pluripotency in Embryonic Stem Cells. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://www.repository.cam.ac.uk/handle/1810/267893


University of Cambridge

3. Stuart, Hannah Taylor. Studying the principles of cell identity transitions using naïve pluripotency induction as a model.

Degree: PhD, 2019, University of Cambridge

 In multicellular biology, an astounding array of cellular identities are specified from the same genome, by drawing on a finite pool of transcription factors and… (more)

Subjects/Keywords: pluripotency; cell identity; development

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APA (6th Edition):

Stuart, H. T. (2019). Studying the principles of cell identity transitions using naïve pluripotency induction as a model. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293137

Chicago Manual of Style (16th Edition):

Stuart, Hannah Taylor. “Studying the principles of cell identity transitions using naïve pluripotency induction as a model.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://www.repository.cam.ac.uk/handle/1810/293137.

MLA Handbook (7th Edition):

Stuart, Hannah Taylor. “Studying the principles of cell identity transitions using naïve pluripotency induction as a model.” 2019. Web. 15 Jan 2021.

Vancouver:

Stuart HT. Studying the principles of cell identity transitions using naïve pluripotency induction as a model. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 15]. Available from: https://www.repository.cam.ac.uk/handle/1810/293137.

Council of Science Editors:

Stuart HT. Studying the principles of cell identity transitions using naïve pluripotency induction as a model. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293137


University of Toronto

4. DeVeale, Brian. Lineage Specification of Pluripotent Populations in Murine Development.

Degree: 2013, University of Toronto

“The scientist, by the very nature of his commitment, creates more and more questions, never fewer. Indeed the measure of our intellectual maturity, one philosopher… (more)

Subjects/Keywords: Lineage specification; Pluripotency; Imprinting; 0369

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APA (6th Edition):

DeVeale, B. (2013). Lineage Specification of Pluripotent Populations in Murine Development. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/65504

Chicago Manual of Style (16th Edition):

DeVeale, Brian. “Lineage Specification of Pluripotent Populations in Murine Development.” 2013. Doctoral Dissertation, University of Toronto. Accessed January 15, 2021. http://hdl.handle.net/1807/65504.

MLA Handbook (7th Edition):

DeVeale, Brian. “Lineage Specification of Pluripotent Populations in Murine Development.” 2013. Web. 15 Jan 2021.

Vancouver:

DeVeale B. Lineage Specification of Pluripotent Populations in Murine Development. [Internet] [Doctoral dissertation]. University of Toronto; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1807/65504.

Council of Science Editors:

DeVeale B. Lineage Specification of Pluripotent Populations in Murine Development. [Doctoral Dissertation]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/65504


Louisiana State University

5. Jarazo, Javier Martin. Effect of tissue source on adult equine multipotent stromal cell pluripotency induction treatment with synthetic mRNA.

Degree: MS, Animal Sciences, 2014, Louisiana State University

 Autogenous and autologous adult multipotent stromal cells are applied to treat equine musculoskeletal injuries in clinical practice. However, options for autologous therapy in the equine… (more)

Subjects/Keywords: induction of pluripotency; regenerative therapy

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APA (6th Edition):

Jarazo, J. M. (2014). Effect of tissue source on adult equine multipotent stromal cell pluripotency induction treatment with synthetic mRNA. (Masters Thesis). Louisiana State University. Retrieved from etd-04042014-164139 ; https://digitalcommons.lsu.edu/gradschool_theses/2646

Chicago Manual of Style (16th Edition):

Jarazo, Javier Martin. “Effect of tissue source on adult equine multipotent stromal cell pluripotency induction treatment with synthetic mRNA.” 2014. Masters Thesis, Louisiana State University. Accessed January 15, 2021. etd-04042014-164139 ; https://digitalcommons.lsu.edu/gradschool_theses/2646.

MLA Handbook (7th Edition):

Jarazo, Javier Martin. “Effect of tissue source on adult equine multipotent stromal cell pluripotency induction treatment with synthetic mRNA.” 2014. Web. 15 Jan 2021.

Vancouver:

Jarazo JM. Effect of tissue source on adult equine multipotent stromal cell pluripotency induction treatment with synthetic mRNA. [Internet] [Masters thesis]. Louisiana State University; 2014. [cited 2021 Jan 15]. Available from: etd-04042014-164139 ; https://digitalcommons.lsu.edu/gradschool_theses/2646.

Council of Science Editors:

Jarazo JM. Effect of tissue source on adult equine multipotent stromal cell pluripotency induction treatment with synthetic mRNA. [Masters Thesis]. Louisiana State University; 2014. Available from: etd-04042014-164139 ; https://digitalcommons.lsu.edu/gradschool_theses/2646

6. Li, Meng. Genetic dissection of the exit of pluripotency in mouse embryonic stem cells by CRISPR-based screening.

Degree: PhD, 2018, University of Cambridge

 The ground state naive pluripotency is established in the epiblast of the blastocyst and can be captured by culturing mouse embryonic stem cells (mESCs) with… (more)

Subjects/Keywords: 571.8; Pluripotency; CRISPR; Genetic screen

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APA (6th Edition):

Li, M. (2018). Genetic dissection of the exit of pluripotency in mouse embryonic stem cells by CRISPR-based screening. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.24867 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744978

Chicago Manual of Style (16th Edition):

Li, Meng. “Genetic dissection of the exit of pluripotency in mouse embryonic stem cells by CRISPR-based screening.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.24867 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744978.

MLA Handbook (7th Edition):

Li, Meng. “Genetic dissection of the exit of pluripotency in mouse embryonic stem cells by CRISPR-based screening.” 2018. Web. 15 Jan 2021.

Vancouver:

Li M. Genetic dissection of the exit of pluripotency in mouse embryonic stem cells by CRISPR-based screening. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.24867 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744978.

Council of Science Editors:

Li M. Genetic dissection of the exit of pluripotency in mouse embryonic stem cells by CRISPR-based screening. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.24867 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744978


University of Cambridge

7. Stuart, Hannah Taylor. Studying the principles of cell identity transitions using naïve pluripotency induction as a model.

Degree: PhD, 2019, University of Cambridge

 In multicellular biology, an astounding array of cellular identities are specified from the same genome, by drawing on a finite pool of transcription factors and… (more)

Subjects/Keywords: pluripotency; cell identity; development

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

APA (6th Edition):

Stuart, H. T. (2019). Studying the principles of cell identity transitions using naïve pluripotency induction as a model. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.40286 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774838

Chicago Manual of Style (16th Edition):

Stuart, Hannah Taylor. “Studying the principles of cell identity transitions using naïve pluripotency induction as a model.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.40286 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774838.

MLA Handbook (7th Edition):

Stuart, Hannah Taylor. “Studying the principles of cell identity transitions using naïve pluripotency induction as a model.” 2019. Web. 15 Jan 2021.

Vancouver:

Stuart HT. Studying the principles of cell identity transitions using naïve pluripotency induction as a model. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.40286 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774838.

Council of Science Editors:

Stuart HT. Studying the principles of cell identity transitions using naïve pluripotency induction as a model. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.40286 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774838


University of Cambridge

8. Myers, Samuel Philip. Determining the signalling pathways that govern human naive pluripotency.

Degree: PhD, 2018, University of Cambridge

 Conventional or “primed” human embryonic stem cells (hESCs) rely on FGF and TGFβ signalling for self-renewal, and occupy a developmentally advanced state of pluripotency comparable… (more)

Subjects/Keywords: 612.6; Human; Naive; Pluripotency; Signalling

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APA (6th Edition):

Myers, S. P. (2018). Determining the signalling pathways that govern human naive pluripotency. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.24723 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744959

Chicago Manual of Style (16th Edition):

Myers, Samuel Philip. “Determining the signalling pathways that govern human naive pluripotency.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.24723 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744959.

MLA Handbook (7th Edition):

Myers, Samuel Philip. “Determining the signalling pathways that govern human naive pluripotency.” 2018. Web. 15 Jan 2021.

Vancouver:

Myers SP. Determining the signalling pathways that govern human naive pluripotency. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.24723 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744959.

Council of Science Editors:

Myers SP. Determining the signalling pathways that govern human naive pluripotency. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.24723 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744959

9. Bouwman, B.A.M. Contactomics : Exploring New Dimensions of 3D Genome Architecture.

Degree: 2016, Universiteit Utrecht

 3D genome folding is increasingly recognized as an instrumental regulator of gene expression. This thesis contains two literature reviews in which the current knowledge regarding… (more)

Subjects/Keywords: 3D genome; transcription regulation; pluripotency; stem cell

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APA (6th Edition):

Bouwman, B. A. M. (2016). Contactomics : Exploring New Dimensions of 3D Genome Architecture. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/335407

Chicago Manual of Style (16th Edition):

Bouwman, B A M. “Contactomics : Exploring New Dimensions of 3D Genome Architecture.” 2016. Doctoral Dissertation, Universiteit Utrecht. Accessed January 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/335407.

MLA Handbook (7th Edition):

Bouwman, B A M. “Contactomics : Exploring New Dimensions of 3D Genome Architecture.” 2016. Web. 15 Jan 2021.

Vancouver:

Bouwman BAM. Contactomics : Exploring New Dimensions of 3D Genome Architecture. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2016. [cited 2021 Jan 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/335407.

Council of Science Editors:

Bouwman BAM. Contactomics : Exploring New Dimensions of 3D Genome Architecture. [Doctoral Dissertation]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/335407


Vanderbilt University

10. Armour, Eric Andrew. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.

Degree: PhD, Cell and Developmental Biology, 2013, Vanderbilt University

 Tuberous Sclerosis Complex (TSC) is a multi-organ hamartomatous disease caused by loss of function mutations in either the TSC1 or TSC2 genes. Despite involvement of… (more)

Subjects/Keywords: TSC; pluripotency; Tuberous Sclerosis; cilia; cystogenesis; mTOR

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APA (6th Edition):

Armour, E. A. (2013). Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14546

Chicago Manual of Style (16th Edition):

Armour, Eric Andrew. “Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed January 15, 2021. http://hdl.handle.net/1803/14546.

MLA Handbook (7th Edition):

Armour, Eric Andrew. “Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex.” 2013. Web. 15 Jan 2021.

Vancouver:

Armour EA. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1803/14546.

Council of Science Editors:

Armour EA. Dysregulated mTOR signaling and tissue-specific phenotypes in Tuberous Sclerosis Complex. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://hdl.handle.net/1803/14546


University of Manitoba

11. Zahedi Amiri, Ali. Effects of influenza A virus infection on the pluripotency and proteome of induced pluripotent stem cells.

Degree: Medical Microbiology and Infectious Diseases, 2019, University of Manitoba

 Maternal influenza infection during pregnancy was reported multiple times as the possible cause of many defects and congenital anomalies. Apart from several cases of influenza-related… (more)

Subjects/Keywords: RNA virus; Influenza; Proteomics; SOMAScans; Pluripotency; Autophagy

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APA (6th Edition):

Zahedi Amiri, A. (2019). Effects of influenza A virus infection on the pluripotency and proteome of induced pluripotent stem cells. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/33916

Chicago Manual of Style (16th Edition):

Zahedi Amiri, Ali. “Effects of influenza A virus infection on the pluripotency and proteome of induced pluripotent stem cells.” 2019. Masters Thesis, University of Manitoba. Accessed January 15, 2021. http://hdl.handle.net/1993/33916.

MLA Handbook (7th Edition):

Zahedi Amiri, Ali. “Effects of influenza A virus infection on the pluripotency and proteome of induced pluripotent stem cells.” 2019. Web. 15 Jan 2021.

Vancouver:

Zahedi Amiri A. Effects of influenza A virus infection on the pluripotency and proteome of induced pluripotent stem cells. [Internet] [Masters thesis]. University of Manitoba; 2019. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/1993/33916.

Council of Science Editors:

Zahedi Amiri A. Effects of influenza A virus infection on the pluripotency and proteome of induced pluripotent stem cells. [Masters Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/33916


University of Manchester

12. Gaobotse, Goabaone. The Expression and Regulation of Genes Correlating with human Embryonic Stem Cell (hESC) Pluripotency and Self-Renewal.

Degree: 2015, University of Manchester

 Stem cell pluripotency and self-renewal are two important attributes of human embryonic stem cells which have led to enhanced interest in stem cell research. Understanding… (more)

Subjects/Keywords: human Embryonic Stem Cells; Pluripotency; Self-Renewal

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APA (6th Edition):

Gaobotse, G. (2015). The Expression and Regulation of Genes Correlating with human Embryonic Stem Cell (hESC) Pluripotency and Self-Renewal. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265054

Chicago Manual of Style (16th Edition):

Gaobotse, Goabaone. “The Expression and Regulation of Genes Correlating with human Embryonic Stem Cell (hESC) Pluripotency and Self-Renewal.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 15, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265054.

MLA Handbook (7th Edition):

Gaobotse, Goabaone. “The Expression and Regulation of Genes Correlating with human Embryonic Stem Cell (hESC) Pluripotency and Self-Renewal.” 2015. Web. 15 Jan 2021.

Vancouver:

Gaobotse G. The Expression and Regulation of Genes Correlating with human Embryonic Stem Cell (hESC) Pluripotency and Self-Renewal. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Jan 15]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265054.

Council of Science Editors:

Gaobotse G. The Expression and Regulation of Genes Correlating with human Embryonic Stem Cell (hESC) Pluripotency and Self-Renewal. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:265054


University of Adelaide

13. Lin, Ni-Hung. Reprogramming of human gingival and periodontal ligament fibroblasts to pluripotency with defined factors.

Degree: 2010, University of Adelaide

 Background: The use of periodontal stem cells with tissue engineering techniques constitutes an attractive strategy for regenerative periodontal therapy. However, technical difficulties of isolating a… (more)

Subjects/Keywords: reprogramming; gingival fibroblasts; periodental ligament fibroblasts; pluripotency

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APA (6th Edition):

Lin, N. (2010). Reprogramming of human gingival and periodontal ligament fibroblasts to pluripotency with defined factors. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/65628

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, Ni-Hung. “Reprogramming of human gingival and periodontal ligament fibroblasts to pluripotency with defined factors.” 2010. Thesis, University of Adelaide. Accessed January 15, 2021. http://hdl.handle.net/2440/65628.

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

MLA Handbook (7th Edition):

Lin, Ni-Hung. “Reprogramming of human gingival and periodontal ligament fibroblasts to pluripotency with defined factors.” 2010. Web. 15 Jan 2021.

Vancouver:

Lin N. Reprogramming of human gingival and periodontal ligament fibroblasts to pluripotency with defined factors. [Internet] [Thesis]. University of Adelaide; 2010. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2440/65628.

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

Council of Science Editors:

Lin N. Reprogramming of human gingival and periodontal ligament fibroblasts to pluripotency with defined factors. [Thesis]. University of Adelaide; 2010. Available from: http://hdl.handle.net/2440/65628

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


University of Adelaide

14. Campbell, Jared Michael. Culturing embryos from the cleavage to blastocyst stage: an opportunity to improve pluripotency and embryonic stem cell generation efficiency.

Degree: 2013, University of Adelaide

 Human embryos for embryonic stem cell (ESC) derivation have often been cryopreserved for 5-10 years prior to their donation for research purposes. Many of these… (more)

Subjects/Keywords: embryo culture; blastocyst; embryonic stem cell; pluripotency

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APA (6th Edition):

Campbell, J. M. (2013). Culturing embryos from the cleavage to blastocyst stage: an opportunity to improve pluripotency and embryonic stem cell generation efficiency. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/87310

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):

Campbell, Jared Michael. “Culturing embryos from the cleavage to blastocyst stage: an opportunity to improve pluripotency and embryonic stem cell generation efficiency.” 2013. Thesis, University of Adelaide. Accessed January 15, 2021. http://hdl.handle.net/2440/87310.

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

MLA Handbook (7th Edition):

Campbell, Jared Michael. “Culturing embryos from the cleavage to blastocyst stage: an opportunity to improve pluripotency and embryonic stem cell generation efficiency.” 2013. Web. 15 Jan 2021.

Vancouver:

Campbell JM. Culturing embryos from the cleavage to blastocyst stage: an opportunity to improve pluripotency and embryonic stem cell generation efficiency. [Internet] [Thesis]. University of Adelaide; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/2440/87310.

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

Council of Science Editors:

Campbell JM. Culturing embryos from the cleavage to blastocyst stage: an opportunity to improve pluripotency and embryonic stem cell generation efficiency. [Thesis]. University of Adelaide; 2013. Available from: http://hdl.handle.net/2440/87310

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


University of Ottawa

15. Cook, David. SNF2H-Mediated Chromatin Remodelling and Its Regulation of the Pluripotent State .

Degree: 2016, University of Ottawa

 In embryonic stem cells (ESCs), the SWI/SNF, CHD, and INO80 families of ATP-dependent chromatin remodellers have been implicated in maintaining pluripotency-associated gene expression, however the… (more)

Subjects/Keywords: Chromatin; Remodelling; Pluripotency; Epigenetics; Sequencing; Bioinformatics

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APA (6th Edition):

Cook, D. (2016). SNF2H-Mediated Chromatin Remodelling and Its Regulation of the Pluripotent State . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35097

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):

Cook, David. “SNF2H-Mediated Chromatin Remodelling and Its Regulation of the Pluripotent State .” 2016. Thesis, University of Ottawa. Accessed January 15, 2021. http://hdl.handle.net/10393/35097.

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

MLA Handbook (7th Edition):

Cook, David. “SNF2H-Mediated Chromatin Remodelling and Its Regulation of the Pluripotent State .” 2016. Web. 15 Jan 2021.

Vancouver:

Cook D. SNF2H-Mediated Chromatin Remodelling and Its Regulation of the Pluripotent State . [Internet] [Thesis]. University of Ottawa; 2016. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10393/35097.

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

Council of Science Editors:

Cook D. SNF2H-Mediated Chromatin Remodelling and Its Regulation of the Pluripotent State . [Thesis]. University of Ottawa; 2016. Available from: http://hdl.handle.net/10393/35097

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


University of Cambridge

16. Osnato, Anna. Transcriptional networks variations during cell cycle progression in human embryonic stem cells.

Degree: PhD, 2018, University of Cambridge

 Differentiation and cell cycle regulation in stem cell have a key function for embryonic development, organ homeostasis and tissue repair. Recent results have shown that… (more)

Subjects/Keywords: 616.02; stem cells; hESCs; cell cycle; pluripotency

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APA (6th Edition):

Osnato, A. (2018). Transcriptional networks variations during cell cycle progression in human embryonic stem cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.23560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744884

Chicago Manual of Style (16th Edition):

Osnato, Anna. “Transcriptional networks variations during cell cycle progression in human embryonic stem cells.” 2018. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.23560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744884.

MLA Handbook (7th Edition):

Osnato, Anna. “Transcriptional networks variations during cell cycle progression in human embryonic stem cells.” 2018. Web. 15 Jan 2021.

Vancouver:

Osnato A. Transcriptional networks variations during cell cycle progression in human embryonic stem cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.23560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744884.

Council of Science Editors:

Osnato A. Transcriptional networks variations during cell cycle progression in human embryonic stem cells. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://doi.org/10.17863/CAM.23560 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744884


University of Manchester

17. Gaobotse, Goabaone. The expression and regulation of genes correlating with human Embryonic Stem Cell (hESC) pluripotency and self-renewal.

Degree: PhD, 2015, University of Manchester

 Stem cell pluripotency and self-renewal are two important attributes of human embryonic stem cells which have led to enhanced interest in stem cell research. Understanding… (more)

Subjects/Keywords: Self-Renewal; human Embryonic Stem Cells; Pluripotency

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APA (6th Edition):

Gaobotse, G. (2015). The expression and regulation of genes correlating with human Embryonic Stem Cell (hESC) pluripotency and self-renewal. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-expression-and-regulation-of-genes-correlating-with-human-embryonic-stem-cell-hesc-pluripotency-and-selfrenewal(f1f4ba87-e741-4291-b60e-cc1ed9fc24c7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764390

Chicago Manual of Style (16th Edition):

Gaobotse, Goabaone. “The expression and regulation of genes correlating with human Embryonic Stem Cell (hESC) pluripotency and self-renewal.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 15, 2021. https://www.research.manchester.ac.uk/portal/en/theses/the-expression-and-regulation-of-genes-correlating-with-human-embryonic-stem-cell-hesc-pluripotency-and-selfrenewal(f1f4ba87-e741-4291-b60e-cc1ed9fc24c7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764390.

MLA Handbook (7th Edition):

Gaobotse, Goabaone. “The expression and regulation of genes correlating with human Embryonic Stem Cell (hESC) pluripotency and self-renewal.” 2015. Web. 15 Jan 2021.

Vancouver:

Gaobotse G. The expression and regulation of genes correlating with human Embryonic Stem Cell (hESC) pluripotency and self-renewal. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Jan 15]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-expression-and-regulation-of-genes-correlating-with-human-embryonic-stem-cell-hesc-pluripotency-and-selfrenewal(f1f4ba87-e741-4291-b60e-cc1ed9fc24c7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764390.

Council of Science Editors:

Gaobotse G. The expression and regulation of genes correlating with human Embryonic Stem Cell (hESC) pluripotency and self-renewal. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-expression-and-regulation-of-genes-correlating-with-human-embryonic-stem-cell-hesc-pluripotency-and-selfrenewal(f1f4ba87-e741-4291-b60e-cc1ed9fc24c7).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.764390


University of Southern California

18. Mah, In Kyoung. The role of Prkci in stem cell maintenance and cell polarity using a 3-D culture system.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2014, University of Southern California

 Atypical PKCs (aPKC) (Prkci and Prkcz) are key signaling components that have been demonstrated to control asymmetric cell division and apical‐basal polarity in all animals.… (more)

Subjects/Keywords: Prkci; pluripotency; multipotency; asymmetric cell division; Numb

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APA (6th Edition):

Mah, I. K. (2014). The role of Prkci in stem cell maintenance and cell polarity using a 3-D culture system. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381613/rec/7250

Chicago Manual of Style (16th Edition):

Mah, In Kyoung. “The role of Prkci in stem cell maintenance and cell polarity using a 3-D culture system.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 15, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381613/rec/7250.

MLA Handbook (7th Edition):

Mah, In Kyoung. “The role of Prkci in stem cell maintenance and cell polarity using a 3-D culture system.” 2014. Web. 15 Jan 2021.

Vancouver:

Mah IK. The role of Prkci in stem cell maintenance and cell polarity using a 3-D culture system. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Jan 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381613/rec/7250.

Council of Science Editors:

Mah IK. The role of Prkci in stem cell maintenance and cell polarity using a 3-D culture system. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/381613/rec/7250

19. Hodgson, Andrew Christopher. Microfluidic devices for the investigation of pluripotency in embryonic stem cells.

Degree: PhD, 2017, University of Cambridge

 This thesis presents the development of microfluidic devices designed to facilitate research into mouse embryonic stem cells (ESCs). ESCs are a well-studied cell, largely due… (more)

Subjects/Keywords: 532; Microfluidics; Embryonic Stem Cells; Pluripotency

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APA (6th Edition):

Hodgson, A. C. (2017). Microfluidic devices for the investigation of pluripotency in embryonic stem cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.13821 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725576

Chicago Manual of Style (16th Edition):

Hodgson, Andrew Christopher. “Microfluidic devices for the investigation of pluripotency in embryonic stem cells.” 2017. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.13821 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725576.

MLA Handbook (7th Edition):

Hodgson, Andrew Christopher. “Microfluidic devices for the investigation of pluripotency in embryonic stem cells.” 2017. Web. 15 Jan 2021.

Vancouver:

Hodgson AC. Microfluidic devices for the investigation of pluripotency in embryonic stem cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.13821 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725576.

Council of Science Editors:

Hodgson AC. Microfluidic devices for the investigation of pluripotency in embryonic stem cells. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://doi.org/10.17863/CAM.13821 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.725576


Virginia Tech

20. Uh, Kyung-Jun. Maintaining Proper Levels of DNA Methylation Marks Through the TET Family is Critical for Normal Embryo Development in Pigs.

Degree: PhD, Animal and Poultry Sciences, 2020, Virginia Tech

 Epigenetic modifications are heritable changes affecting the level of gene expression without changing the sequence of the genome. DNA methylation, one of the biggest epigenetic… (more)

Subjects/Keywords: DNA methylation; TET family; preimplantation embryo; pluripotency

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APA (6th Edition):

Uh, K. (2020). Maintaining Proper Levels of DNA Methylation Marks Through the TET Family is Critical for Normal Embryo Development in Pigs. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/99834

Chicago Manual of Style (16th Edition):

Uh, Kyung-Jun. “Maintaining Proper Levels of DNA Methylation Marks Through the TET Family is Critical for Normal Embryo Development in Pigs.” 2020. Doctoral Dissertation, Virginia Tech. Accessed January 15, 2021. http://hdl.handle.net/10919/99834.

MLA Handbook (7th Edition):

Uh, Kyung-Jun. “Maintaining Proper Levels of DNA Methylation Marks Through the TET Family is Critical for Normal Embryo Development in Pigs.” 2020. Web. 15 Jan 2021.

Vancouver:

Uh K. Maintaining Proper Levels of DNA Methylation Marks Through the TET Family is Critical for Normal Embryo Development in Pigs. [Internet] [Doctoral dissertation]. Virginia Tech; 2020. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10919/99834.

Council of Science Editors:

Uh K. Maintaining Proper Levels of DNA Methylation Marks Through the TET Family is Critical for Normal Embryo Development in Pigs. [Doctoral Dissertation]. Virginia Tech; 2020. Available from: http://hdl.handle.net/10919/99834


University of Georgia

21. Blackstone, Hope. Nanog modification and degradation in murine embryonic stem cells.

Degree: 2014, University of Georgia

 Embryonic stem cells are pluripotent progenitors for virtually all cell types in our body and contain limitless potential for therapeutic use and regenerative medicine. Murine… (more)

Subjects/Keywords: Embryonic Stem Cells; Nanog; Pluripotency; Self-renewal

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APA (6th Edition):

Blackstone, H. (2014). Nanog modification and degradation in murine embryonic stem cells. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/24831

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):

Blackstone, Hope. “Nanog modification and degradation in murine embryonic stem cells.” 2014. Thesis, University of Georgia. Accessed January 15, 2021. http://hdl.handle.net/10724/24831.

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

MLA Handbook (7th Edition):

Blackstone, Hope. “Nanog modification and degradation in murine embryonic stem cells.” 2014. Web. 15 Jan 2021.

Vancouver:

Blackstone H. Nanog modification and degradation in murine embryonic stem cells. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10724/24831.

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

Council of Science Editors:

Blackstone H. Nanog modification and degradation in murine embryonic stem cells. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/24831

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


King Abdullah University of Science and Technology

22. Fadaili, Yara. Biological and Biochemical Properties of Two KDM1A Associated Alternatively Spliced SWIRM Domains.

Degree: 2018, King Abdullah University of Science and Technology

 LSD1 is the first described histone demethylase which demethylates H3K4me1/2 (Shi et el., 2004), thus, causing transcriptional repression. Alternatively, LSD1 was demonstrated to have H3K9me1/2… (more)

Subjects/Keywords: Pluripotency; Splicing Variant; SWIRM domain; KDM1A

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APA (6th Edition):

Fadaili, Y. (2018). Biological and Biochemical Properties of Two KDM1A Associated Alternatively Spliced SWIRM Domains. (Thesis). King Abdullah University of Science and Technology. Retrieved from http://hdl.handle.net/10754/630229

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):

Fadaili, Yara. “Biological and Biochemical Properties of Two KDM1A Associated Alternatively Spliced SWIRM Domains.” 2018. Thesis, King Abdullah University of Science and Technology. Accessed January 15, 2021. http://hdl.handle.net/10754/630229.

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

MLA Handbook (7th Edition):

Fadaili, Yara. “Biological and Biochemical Properties of Two KDM1A Associated Alternatively Spliced SWIRM Domains.” 2018. Web. 15 Jan 2021.

Vancouver:

Fadaili Y. Biological and Biochemical Properties of Two KDM1A Associated Alternatively Spliced SWIRM Domains. [Internet] [Thesis]. King Abdullah University of Science and Technology; 2018. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10754/630229.

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

Council of Science Editors:

Fadaili Y. Biological and Biochemical Properties of Two KDM1A Associated Alternatively Spliced SWIRM Domains. [Thesis]. King Abdullah University of Science and Technology; 2018. Available from: http://hdl.handle.net/10754/630229

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


University of Cambridge

23. Collier, Amanda. Characterising the reprogramming dynamics between human pluripotent states.

Degree: PhD, 2019, University of Cambridge

 Human pluripotent stem cells (hPSCs) exist in multiple states of pluripotency, broadly categorised as naïve and primed states. These provide an important model to investigate… (more)

Subjects/Keywords: 616.02; Nai¨ve pluripotency; Human pluripotency; Primed Pluripotency; Epigenetics; X-chromosome; DNA methylation; Reprogramming; Gene regulatory networks; Cell-surface markers; Embryonic Stem Cells

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APA (6th Edition):

Collier, A. (2019). Characterising the reprogramming dynamics between human pluripotent states. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.35268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763881

Chicago Manual of Style (16th Edition):

Collier, Amanda. “Characterising the reprogramming dynamics between human pluripotent states.” 2019. Doctoral Dissertation, University of Cambridge. Accessed January 15, 2021. https://doi.org/10.17863/CAM.35268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763881.

MLA Handbook (7th Edition):

Collier, Amanda. “Characterising the reprogramming dynamics between human pluripotent states.” 2019. Web. 15 Jan 2021.

Vancouver:

Collier A. Characterising the reprogramming dynamics between human pluripotent states. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Jan 15]. Available from: https://doi.org/10.17863/CAM.35268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763881.

Council of Science Editors:

Collier A. Characterising the reprogramming dynamics between human pluripotent states. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.35268 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763881


University of Helsinki

24. Pörsti, Elina. CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells.

Degree: Medicinska fakulteten, 2018, University of Helsinki

 The capability to generate human induced pluripotent stem cells (iPSC) from somatic cells provides remarkable possibilities for regenerative medicine. However, prior to clinical applications the… (more)

Subjects/Keywords: CRISPRa; iPSC; reprogramming; pluripotency; neural stem cell; neurosphere; cerebral organoid; CRISPRa; iPSC; reprogramming; pluripotency; neural stem cell; neurosphere; cerebral organoid

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APA (6th Edition):

Pörsti, E. (2018). CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells. (Masters Thesis). University of Helsinki. Retrieved from http://hdl.handle.net/10138/236384

Chicago Manual of Style (16th Edition):

Pörsti, Elina. “CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells.” 2018. Masters Thesis, University of Helsinki. Accessed January 15, 2021. http://hdl.handle.net/10138/236384.

MLA Handbook (7th Edition):

Pörsti, Elina. “CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells.” 2018. Web. 15 Jan 2021.

Vancouver:

Pörsti E. CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10138/236384.

Council of Science Editors:

Pörsti E. CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells. [Masters Thesis]. University of Helsinki; 2018. Available from: http://hdl.handle.net/10138/236384


Universiteit Utrecht

25. Boer, A.S. de. iPS cell reprogramming.

Degree: 2009, Universiteit Utrecht

 Recently, pluripotent cells that are not derived from an embryo have been generated. These so called induced pluripotent stem cells (iPS cells) are pluripotent stem… (more)

Subjects/Keywords: Geneeskunde; embryonic stem cells, induced pluripotent stem cells, reprogramming, pluripotency, epigenetics

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APA (6th Edition):

Boer, A. S. d. (2009). iPS cell reprogramming. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/35214

Chicago Manual of Style (16th Edition):

Boer, A S de. “iPS cell reprogramming.” 2009. Masters Thesis, Universiteit Utrecht. Accessed January 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/35214.

MLA Handbook (7th Edition):

Boer, A S de. “iPS cell reprogramming.” 2009. Web. 15 Jan 2021.

Vancouver:

Boer ASd. iPS cell reprogramming. [Internet] [Masters thesis]. Universiteit Utrecht; 2009. [cited 2021 Jan 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/35214.

Council of Science Editors:

Boer ASd. iPS cell reprogramming. [Masters Thesis]. Universiteit Utrecht; 2009. Available from: http://dspace.library.uu.nl:8080/handle/1874/35214

26. Zhu, Y. Factors shaping the 3D genome.

Degree: 2015, Universiteit Utrecht

 The nuclear organization of chromosomes has been suggested to be associated with regulation of gene expression. In embryonic stem cells, chromosomes were shown to segment… (more)

Subjects/Keywords: genome structure; gene expression; trans-acting factors; pluripotency factors; histone H1

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APA (6th Edition):

Zhu, Y. (2015). Factors shaping the 3D genome. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/313502

Chicago Manual of Style (16th Edition):

Zhu, Y. “Factors shaping the 3D genome.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed January 15, 2021. http://dspace.library.uu.nl:8080/handle/1874/313502.

MLA Handbook (7th Edition):

Zhu, Y. “Factors shaping the 3D genome.” 2015. Web. 15 Jan 2021.

Vancouver:

Zhu Y. Factors shaping the 3D genome. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2021 Jan 15]. Available from: http://dspace.library.uu.nl:8080/handle/1874/313502.

Council of Science Editors:

Zhu Y. Factors shaping the 3D genome. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/313502

27. 杉本, 浩司. Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果.

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

 Retroviral transduction of four transcription factors (Oct4, Sox2, Klf4 and c-Myc) or three factors, excluding c-Myc, has been shown to initiate a reprogramming process that… (more)

Subjects/Keywords: Hypoxia; Hypoxia inducible factors; IPS cells; Pluripotency; Transcription factors

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APA (6th Edition):

杉本, . (2013). Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/35466

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):

杉本, 浩司. “Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果.” 2013. Thesis, Nagasaki University / 長崎大学. Accessed January 15, 2021. http://hdl.handle.net/10069/35466.

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

MLA Handbook (7th Edition):

杉本, 浩司. “Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果.” 2013. Web. 15 Jan 2021.

Vancouver:

杉本 . Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2013. [cited 2021 Jan 15]. Available from: http://hdl.handle.net/10069/35466.

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

Council of Science Editors:

杉本 . Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果. [Thesis]. Nagasaki University / 長崎大学; 2013. Available from: http://hdl.handle.net/10069/35466

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


University of California – Santa Cruz

28. Frum, Tristan. Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo.

Degree: Molecular Cell and Developmental Biology, 2014, University of California – Santa Cruz

 Pluripotent cells have the potential to create any cell type, and therefore represent a source of healthy cells by which to replace diseased cells in… (more)

Subjects/Keywords: Developmental biology; Cellular biology; Cdx2; embryo; Oct4; Pluripotency; preimplantation; Sox2

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APA (6th Edition):

Frum, T. (2014). Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/0k16d6b4

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):

Frum, Tristan. “Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo.” 2014. Thesis, University of California – Santa Cruz. Accessed January 15, 2021. http://www.escholarship.org/uc/item/0k16d6b4.

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

MLA Handbook (7th Edition):

Frum, Tristan. “Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo.” 2014. Web. 15 Jan 2021.

Vancouver:

Frum T. Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo. [Internet] [Thesis]. University of California – Santa Cruz; 2014. [cited 2021 Jan 15]. Available from: http://www.escholarship.org/uc/item/0k16d6b4.

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

Council of Science Editors:

Frum T. Regulation of cell fate by the stem cell factors Cdx2, Oct4 and Sox2 in the early mouse embryo. [Thesis]. University of California – Santa Cruz; 2014. Available from: http://www.escholarship.org/uc/item/0k16d6b4

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


University of Minnesota

29. Lee, Catherine Ann Alsager. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.

Degree: MS, Stem Cell Biology, 2013, University of Minnesota

University of Minnesota M.S. thesis. January 2013. Major: Stem Cell Biology. Advisor: Nobuaki Kikyo. 1 computer file (PDF); vii, 46 pages.

Long noncoding RNAs (lncRNAs)… (more)

Subjects/Keywords: ChIP; MyoD; Pluripotency; RNA-ChIP; RNA-seq; Trithorax-group

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APA (6th Edition):

Lee, C. A. A. (2013). Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/146424

Chicago Manual of Style (16th Edition):

Lee, Catherine Ann Alsager. “Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.” 2013. Masters Thesis, University of Minnesota. Accessed January 15, 2021. http://purl.umn.edu/146424.

MLA Handbook (7th Edition):

Lee, Catherine Ann Alsager. “Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells.” 2013. Web. 15 Jan 2021.

Vancouver:

Lee CAA. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2021 Jan 15]. Available from: http://purl.umn.edu/146424.

Council of Science Editors:

Lee CAA. Isolation and identification of De Novo long noncoding RNAs from mouse myoblasts and embryonic stem cells. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/146424

30. Malta, Tathiane Maistro. Estudo da ação do gene TCL1 na reprogramação de células-tronco de pluripotência induzida (iPS) humanas.

Degree: PhD, Biociências Aplicadas à Farmácia, 2013, University of São Paulo

Células somáticas podem ser reprogramadas para um estádio pluripotente (iPS) adquirindo propriedades semelhantes às células-tronco embrionárias (CTE). O interesse nas células pluripotentes reside em sua… (more)

Subjects/Keywords: Expressão gênica; Gene expression; iPS; iPS; Pluripotência; Pluripotency; TCL1; TCL1

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

APA (6th Edition):

Malta, T. M. (2013). Estudo da ação do gene TCL1 na reprogramação de células-tronco de pluripotência induzida (iPS) humanas. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60135/tde-06092013-092916/ ;

Chicago Manual of Style (16th Edition):

Malta, Tathiane Maistro. “Estudo da ação do gene TCL1 na reprogramação de células-tronco de pluripotência induzida (iPS) humanas.” 2013. Doctoral Dissertation, University of São Paulo. Accessed January 15, 2021. http://www.teses.usp.br/teses/disponiveis/60/60135/tde-06092013-092916/ ;.

MLA Handbook (7th Edition):

Malta, Tathiane Maistro. “Estudo da ação do gene TCL1 na reprogramação de células-tronco de pluripotência induzida (iPS) humanas.” 2013. Web. 15 Jan 2021.

Vancouver:

Malta TM. Estudo da ação do gene TCL1 na reprogramação de células-tronco de pluripotência induzida (iPS) humanas. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2021 Jan 15]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-06092013-092916/ ;.

Council of Science Editors:

Malta TM. Estudo da ação do gene TCL1 na reprogramação de células-tronco de pluripotência induzida (iPS) humanas. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/60/60135/tde-06092013-092916/ ;

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