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You searched for subject:( mouse embryonic feeder MEF ). Showing records 1 – 30 of 3487 total matches.

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Tampere University

1. Marttila, Suvi. Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view .

Degree: 2017, Tampere University

 Research background and aims. The aim of this study was to establish and characterise iPSC-lines generated with two different methods, as well as to differentiate… (more)

Subjects/Keywords: induced pluripotent stem cell (iPSC); mouse embryonic feeder (MEF); cardiomyocyte; cardiac differentiation; reprogramming efficiency; differentiation efficiency; episomal plasmid indusoitu pluripotentti kantasolu (iPS-solu); hiiren alkion fibroblasti (MEF); episomaalinen plasmidi; sydänlihassolu; sydänerilaistus; uudelleenohjelmointitehokkuus; erilaistustehokkuus

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APA (6th Edition):

Marttila, S. (2017). Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view . (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/101732

Chicago Manual of Style (16th Edition):

Marttila, Suvi. “Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view .” 2017. Masters Thesis, Tampere University. Accessed December 14, 2019. https://trepo.tuni.fi/handle/10024/101732.

MLA Handbook (7th Edition):

Marttila, Suvi. “Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view .” 2017. Web. 14 Dec 2019.

Vancouver:

Marttila S. Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view . [Internet] [Masters thesis]. Tampere University; 2017. [cited 2019 Dec 14]. Available from: https://trepo.tuni.fi/handle/10024/101732.

Council of Science Editors:

Marttila S. Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view . [Masters Thesis]. Tampere University; 2017. Available from: https://trepo.tuni.fi/handle/10024/101732

2. Dingle, Yu-Ting Liu. In Vitro Modeling of the Central Nervous System: Towards Optimized Cell-based Therapies.

Degree: PhD, Biomedical Engineering, 2015, Brown University

 Cell-based therapy is a promising treatment option for central nervous system (CNS) disease and injury, but therapy strategies require optimization to achieve clinical improvement. The… (more)

Subjects/Keywords: mouse embryonic stem cells

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APA (6th Edition):

Dingle, Y. L. (2015). In Vitro Modeling of the Central Nervous System: Towards Optimized Cell-based Therapies. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:419530/

Chicago Manual of Style (16th Edition):

Dingle, Yu-Ting Liu. “In Vitro Modeling of the Central Nervous System: Towards Optimized Cell-based Therapies.” 2015. Doctoral Dissertation, Brown University. Accessed December 14, 2019. https://repository.library.brown.edu/studio/item/bdr:419530/.

MLA Handbook (7th Edition):

Dingle, Yu-Ting Liu. “In Vitro Modeling of the Central Nervous System: Towards Optimized Cell-based Therapies.” 2015. Web. 14 Dec 2019.

Vancouver:

Dingle YL. In Vitro Modeling of the Central Nervous System: Towards Optimized Cell-based Therapies. [Internet] [Doctoral dissertation]. Brown University; 2015. [cited 2019 Dec 14]. Available from: https://repository.library.brown.edu/studio/item/bdr:419530/.

Council of Science Editors:

Dingle YL. In Vitro Modeling of the Central Nervous System: Towards Optimized Cell-based Therapies. [Doctoral Dissertation]. Brown University; 2015. Available from: https://repository.library.brown.edu/studio/item/bdr:419530/


University of Cambridge

3. Schacker, Maria Anna. Defining the transcriptional and epigenetic signature of mouse embryonic stem cells with compromised developmental potency.

Degree: PhD, 2019, University of Cambridge

Mouse embryonic stem (ES) cells have played a crucial role in studying developmental processes and gene function in vivo. They are extremely useful in the… (more)

Subjects/Keywords: Embryonic Stem Cells; Epigenetics; Transcriptomics; Embryonic Development; Mouse Embryonic Stem Cells

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APA (6th Edition):

Schacker, M. A. (2019). Defining the transcriptional and epigenetic signature of mouse embryonic stem cells with compromised developmental potency. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/287725 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763866

Chicago Manual of Style (16th Edition):

Schacker, Maria Anna. “Defining the transcriptional and epigenetic signature of mouse embryonic stem cells with compromised developmental potency.” 2019. Doctoral Dissertation, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/287725 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763866.

MLA Handbook (7th Edition):

Schacker, Maria Anna. “Defining the transcriptional and epigenetic signature of mouse embryonic stem cells with compromised developmental potency.” 2019. Web. 14 Dec 2019.

Vancouver:

Schacker MA. Defining the transcriptional and epigenetic signature of mouse embryonic stem cells with compromised developmental potency. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/287725 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763866.

Council of Science Editors:

Schacker MA. Defining the transcriptional and epigenetic signature of mouse embryonic stem cells with compromised developmental potency. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/287725 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763866


University of Illinois – Urbana-Champaign

4. Borduin, Russell J. Cyclic loading of fibronectin coated beads induces differentiation in mouse embryonic stem cells.

Degree: MS, 0133, 2010, University of Illinois – Urbana-Champaign

 The role of soluble factors in determining embryonic stem cell fate has been well studied. A growing body of research indicates mechanical cues are equally… (more)

Subjects/Keywords: Embryonic Stem Cells; embryonic stem cell (ESC); mouse embryonic stem cell (mESC); mouse; mechanotransduction; Magnetic Twisting Cytometry (MTC); cell mechanics; fibronectin

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APA (6th Edition):

Borduin, R. J. (2010). Cyclic loading of fibronectin coated beads induces differentiation in mouse embryonic stem cells. (Thesis). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/15993

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):

Borduin, Russell J. “Cyclic loading of fibronectin coated beads induces differentiation in mouse embryonic stem cells.” 2010. Thesis, University of Illinois – Urbana-Champaign. Accessed December 14, 2019. http://hdl.handle.net/2142/15993.

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

MLA Handbook (7th Edition):

Borduin, Russell J. “Cyclic loading of fibronectin coated beads induces differentiation in mouse embryonic stem cells.” 2010. Web. 14 Dec 2019.

Vancouver:

Borduin RJ. Cyclic loading of fibronectin coated beads induces differentiation in mouse embryonic stem cells. [Internet] [Thesis]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/2142/15993.

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

Council of Science Editors:

Borduin RJ. Cyclic loading of fibronectin coated beads induces differentiation in mouse embryonic stem cells. [Thesis]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/15993

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


University of Edinburgh

5. Rao, Chandrika. Uncovering novel regulators of neural fate commitment in embryonic stem cells.

Degree: PhD, 2019, University of Edinburgh

 How do pluripotent stem cells reliably select the neural lineage during differentiation? When embryonic stem (ES) cells are exposed to a homogeneous signalling environment, differentiation… (more)

Subjects/Keywords: pluripotent cells; mouse model; E2A; mouse embryonic stem cells; neural differentiation

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APA (6th Edition):

Rao, C. (2019). Uncovering novel regulators of neural fate commitment in embryonic stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/35977

Chicago Manual of Style (16th Edition):

Rao, Chandrika. “Uncovering novel regulators of neural fate commitment in embryonic stem cells.” 2019. Doctoral Dissertation, University of Edinburgh. Accessed December 14, 2019. http://hdl.handle.net/1842/35977.

MLA Handbook (7th Edition):

Rao, Chandrika. “Uncovering novel regulators of neural fate commitment in embryonic stem cells.” 2019. Web. 14 Dec 2019.

Vancouver:

Rao C. Uncovering novel regulators of neural fate commitment in embryonic stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2019. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1842/35977.

Council of Science Editors:

Rao C. Uncovering novel regulators of neural fate commitment in embryonic stem cells. [Doctoral Dissertation]. University of Edinburgh; 2019. Available from: http://hdl.handle.net/1842/35977


University of Cambridge

6. Sadiq, Barzan A. A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids.

Degree: PhD, 2018, University of Cambridge

 Class I PI3Ks are a family (α, β, δ and γ) of ubiquitous lipid kinases that can be activated by cell surface receptors to 3-phosphorylate… (more)

Subjects/Keywords: Class I PI3K; PI(45)P2; PI(34)P2; PI(345)P3; phosphoinositide 3-kinase; phosphoinositide 3-kinase signalling; mouse embryonic fibroblasts; MEF; Prostate cancer; prostate organoids; PI3K/Akt signalling pathway; PI3K/PKB signalling pathway; Tumour microenvironment; Lipidomics; Microscopy; Confocal; TIRF; Widefield; MS Lipidomics; A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids; Lipid signalling; Phospholipid signalling; pH and Tumour microenvironment; Acidic extracellular microenvironment and cancer; PI3K nuclear localisation; AviTag; Avi-Tag; Streptavidin; Biotinylation; PTEN-null; PTEN; PI3Ka; PI3Kß; PI3Kd; PI3K?; Imaris; Bitplane Imaris; Therapeutic interventions; Effects of pH on class I PI3K signalling

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APA (6th Edition):

Sadiq, B. A. (2018). A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373

Chicago Manual of Style (16th Edition):

Sadiq, Barzan A. “A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids.” 2018. Doctoral Dissertation, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373.

MLA Handbook (7th Edition):

Sadiq, Barzan A. “A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids.” 2018. Web. 14 Dec 2019.

Vancouver:

Sadiq BA. A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373.

Council of Science Editors:

Sadiq BA. A dissection of class I phosphoinositide 3-kinase signalling in mouse embryonic fibroblasts and prostate organoids. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/278056 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753373

7. FU XIN. Establishment of Autologous Culture Systems for Human Embryonic Stem Cells.

Degree: 2010, National University of Singapore

Subjects/Keywords: human embryonic stem cells; cell culture; autologous; feeder-free

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APA (6th Edition):

XIN, F. (2010). Establishment of Autologous Culture Systems for Human Embryonic Stem Cells. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/19161

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):

XIN, FU. “Establishment of Autologous Culture Systems for Human Embryonic Stem Cells.” 2010. Thesis, National University of Singapore. Accessed December 14, 2019. http://scholarbank.nus.edu.sg/handle/10635/19161.

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

MLA Handbook (7th Edition):

XIN, FU. “Establishment of Autologous Culture Systems for Human Embryonic Stem Cells.” 2010. Web. 14 Dec 2019.

Vancouver:

XIN F. Establishment of Autologous Culture Systems for Human Embryonic Stem Cells. [Internet] [Thesis]. National University of Singapore; 2010. [cited 2019 Dec 14]. Available from: http://scholarbank.nus.edu.sg/handle/10635/19161.

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

Council of Science Editors:

XIN F. Establishment of Autologous Culture Systems for Human Embryonic Stem Cells. [Thesis]. National University of Singapore; 2010. Available from: http://scholarbank.nus.edu.sg/handle/10635/19161

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


Tampere University

8. Hongisto, Heidi. Fibroblast feeder cells in human pluripotent stem cell culture and retinal differentiation - progress toward clinical cell therapy .

Degree: 2013, Tampere University

 Ihmisen alkion kantasoluista (hESC) ja geneettisesti pluripotenttiin tilaan uudelleen ohjelmoiduista indusoiduista kantasoluista (hiPSC) voidaan tuottaa rajattomasti erilaisia solutyyppejä kliinisiin kantasoluhoitoihin. Yksi lupaavimmista käyttökohteista on sokeutumiseen… (more)

Subjects/Keywords: ihmisen alkion kantasolu; fibroblastitukisolu; eläinkomponentiton; retinan pigmenttiepiteeli; human embryonic stem cell; fibroblast feeder cell; xeno-free; retinal pigment epithelial cell

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APA (6th Edition):

Hongisto, H. (2013). Fibroblast feeder cells in human pluripotent stem cell culture and retinal differentiation - progress toward clinical cell therapy . (Doctoral Dissertation). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/67950

Chicago Manual of Style (16th Edition):

Hongisto, Heidi. “Fibroblast feeder cells in human pluripotent stem cell culture and retinal differentiation - progress toward clinical cell therapy .” 2013. Doctoral Dissertation, Tampere University. Accessed December 14, 2019. https://trepo.tuni.fi/handle/10024/67950.

MLA Handbook (7th Edition):

Hongisto, Heidi. “Fibroblast feeder cells in human pluripotent stem cell culture and retinal differentiation - progress toward clinical cell therapy .” 2013. Web. 14 Dec 2019.

Vancouver:

Hongisto H. Fibroblast feeder cells in human pluripotent stem cell culture and retinal differentiation - progress toward clinical cell therapy . [Internet] [Doctoral dissertation]. Tampere University; 2013. [cited 2019 Dec 14]. Available from: https://trepo.tuni.fi/handle/10024/67950.

Council of Science Editors:

Hongisto H. Fibroblast feeder cells in human pluripotent stem cell culture and retinal differentiation - progress toward clinical cell therapy . [Doctoral Dissertation]. Tampere University; 2013. Available from: https://trepo.tuni.fi/handle/10024/67950


Universiteit Utrecht

9. Schulpen, S.H.W. The application of mouse and human embryonic stem cells with transcriptomics in alternative developmental toxicity tests : A bridge from model species to man.

Degree: 2015, Universiteit Utrecht

 During life humans are exposed to diverse hazardous compounds, which can have toxicological effects. Reproductive and developmental toxicology are research areas dedicated to the study… (more)

Subjects/Keywords: developmental toxicity testing; mouse and human embryonic stem cells; transcriptomics

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APA (6th Edition):

Schulpen, S. H. W. (2015). The application of mouse and human embryonic stem cells with transcriptomics in alternative developmental toxicity tests : A bridge from model species to man. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/315183

Chicago Manual of Style (16th Edition):

Schulpen, S H W. “The application of mouse and human embryonic stem cells with transcriptomics in alternative developmental toxicity tests : A bridge from model species to man.” 2015. Doctoral Dissertation, Universiteit Utrecht. Accessed December 14, 2019. http://dspace.library.uu.nl:8080/handle/1874/315183.

MLA Handbook (7th Edition):

Schulpen, S H W. “The application of mouse and human embryonic stem cells with transcriptomics in alternative developmental toxicity tests : A bridge from model species to man.” 2015. Web. 14 Dec 2019.

Vancouver:

Schulpen SHW. The application of mouse and human embryonic stem cells with transcriptomics in alternative developmental toxicity tests : A bridge from model species to man. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2015. [cited 2019 Dec 14]. Available from: http://dspace.library.uu.nl:8080/handle/1874/315183.

Council of Science Editors:

Schulpen SHW. The application of mouse and human embryonic stem cells with transcriptomics in alternative developmental toxicity tests : A bridge from model species to man. [Doctoral Dissertation]. Universiteit Utrecht; 2015. Available from: http://dspace.library.uu.nl:8080/handle/1874/315183


Penn State University

10. Tian, Xi. The role of zinc in ovarian function.

Degree: PhD, Animal Science, 2013, Penn State University

 The ovarian environment is a prime determinant of oocyte quality, which plays a key role in determining the success of fertilization, pregnancy maintenance, embryonic development… (more)

Subjects/Keywords: zinc; ovary; follicular development; oocyte; embryonic development; mouse

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APA (6th Edition):

Tian, X. (2013). The role of zinc in ovarian function. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/18744

Chicago Manual of Style (16th Edition):

Tian, Xi. “The role of zinc in ovarian function.” 2013. Doctoral Dissertation, Penn State University. Accessed December 14, 2019. https://etda.libraries.psu.edu/catalog/18744.

MLA Handbook (7th Edition):

Tian, Xi. “The role of zinc in ovarian function.” 2013. Web. 14 Dec 2019.

Vancouver:

Tian X. The role of zinc in ovarian function. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2019 Dec 14]. Available from: https://etda.libraries.psu.edu/catalog/18744.

Council of Science Editors:

Tian X. The role of zinc in ovarian function. [Doctoral Dissertation]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/18744


University of Washington

11. Snyder, Jessica M. Versican Expression During Embryonic Development in the Mouse.

Degree: 2014, University of Washington

 Versican is a chondroitin sulfate proteoglycan and a component of the extracellular matrix that has previously been shown to have an important role during the… (more)

Subjects/Keywords: Development; DPEAAE; Embryonic; Immunohistochemistry; Mouse; Versican; Developmental biology; Pathology; comparative medicine

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APA (6th Edition):

Snyder, J. M. (2014). Versican Expression During Embryonic Development in the Mouse. (Thesis). University of Washington. Retrieved from http://hdl.handle.net/1773/25457

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):

Snyder, Jessica M. “Versican Expression During Embryonic Development in the Mouse.” 2014. Thesis, University of Washington. Accessed December 14, 2019. http://hdl.handle.net/1773/25457.

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

MLA Handbook (7th Edition):

Snyder, Jessica M. “Versican Expression During Embryonic Development in the Mouse.” 2014. Web. 14 Dec 2019.

Vancouver:

Snyder JM. Versican Expression During Embryonic Development in the Mouse. [Internet] [Thesis]. University of Washington; 2014. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1773/25457.

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

Council of Science Editors:

Snyder JM. Versican Expression During Embryonic Development in the Mouse. [Thesis]. University of Washington; 2014. Available from: http://hdl.handle.net/1773/25457

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


University of Cambridge

12. Harrison, Sarah Ellys. Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro.

Degree: PhD, 2018, University of Cambridge

 Successful mammalian development to term requires that embryonic and extra-embryonic tissues communicate and grow in coordination, to form the body. After implanting into the uterus,… (more)

Subjects/Keywords: Stem cells; embryonic development; mouse embryo; mammalian development; developmental biology

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APA (6th Edition):

Harrison, S. E. (2018). Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/275424 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744789

Chicago Manual of Style (16th Edition):

Harrison, Sarah Ellys. “Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro.” 2018. Doctoral Dissertation, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/275424 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744789.

MLA Handbook (7th Edition):

Harrison, Sarah Ellys. “Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro.” 2018. Web. 14 Dec 2019.

Vancouver:

Harrison SE. Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/275424 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744789.

Council of Science Editors:

Harrison SE. Utilising embryonic and extra-embryonic stem cells to model early mammalian embryogenesis in vitro. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/275424 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744789

13. Hara, Kentaro. Mechanisms for embryonic gene activation in the 1-cell mouse embryos : マウス1細胞期胚における胚性遺伝子の発現制御機構.

Degree: 博士(生命科学), 2017, The University of Tokyo / 東京大学

Subjects/Keywords: embryonic activation; mouse embryos

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APA (6th Edition):

Hara, K. (2017). Mechanisms for embryonic gene activation in the 1-cell mouse embryos : マウス1細胞期胚における胚性遺伝子の発現制御機構. (Thesis). The University of Tokyo / 東京大学. Retrieved from http://hdl.handle.net/2261/121

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):

Hara, Kentaro. “Mechanisms for embryonic gene activation in the 1-cell mouse embryos : マウス1細胞期胚における胚性遺伝子の発現制御機構.” 2017. Thesis, The University of Tokyo / 東京大学. Accessed December 14, 2019. http://hdl.handle.net/2261/121.

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

MLA Handbook (7th Edition):

Hara, Kentaro. “Mechanisms for embryonic gene activation in the 1-cell mouse embryos : マウス1細胞期胚における胚性遺伝子の発現制御機構.” 2017. Web. 14 Dec 2019.

Vancouver:

Hara K. Mechanisms for embryonic gene activation in the 1-cell mouse embryos : マウス1細胞期胚における胚性遺伝子の発現制御機構. [Internet] [Thesis]. The University of Tokyo / 東京大学; 2017. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/2261/121.

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

Council of Science Editors:

Hara K. Mechanisms for embryonic gene activation in the 1-cell mouse embryos : マウス1細胞期胚における胚性遺伝子の発現制御機構. [Thesis]. The University of Tokyo / 東京大学; 2017. Available from: http://hdl.handle.net/2261/121

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


University of Cambridge

14. Wiese, Meike. Characterisation of HP1γ in mammalian cells .

Degree: 2018, University of Cambridge

 The degree of chromatin compaction plays a fundamental role in controlling the accessibility of DNA to the transcription machinery as well as other DNA-dependent biological… (more)

Subjects/Keywords: HP1γ; citrullination; mouse embryonic stem cells; breast cancer; zinc finger genes

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APA (6th Edition):

Wiese, M. (2018). Characterisation of HP1γ in mammalian cells . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/273362

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):

Wiese, Meike. “Characterisation of HP1γ in mammalian cells .” 2018. Thesis, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/273362.

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

MLA Handbook (7th Edition):

Wiese, Meike. “Characterisation of HP1γ in mammalian cells .” 2018. Web. 14 Dec 2019.

Vancouver:

Wiese M. Characterisation of HP1γ in mammalian cells . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/273362.

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

Council of Science Editors:

Wiese M. Characterisation of HP1γ in mammalian cells . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/273362

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


University of Toronto

15. 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 December 14, 2019. 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. 14 Dec 2019.

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 2019 Dec 14]. 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


Queens University

16. Cameron, Donald. Identification of TULP3 as a negative regulator of Hedgehog signalling in the mouse .

Degree: Biochemistry, 2015, Queens University

 The Hedgehog (Hh) family of secreted signalling factors play diverse roles in animal development. In mammals, the Hh ortholog Sonic hedgehog (Shh) is critical for… (more)

Subjects/Keywords: Hedgehog signalling; Embryonic development; Congenital malformations; Mouse genetics

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APA (6th Edition):

Cameron, D. (2015). Identification of TULP3 as a negative regulator of Hedgehog signalling in the mouse . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13461

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):

Cameron, Donald. “Identification of TULP3 as a negative regulator of Hedgehog signalling in the mouse .” 2015. Thesis, Queens University. Accessed December 14, 2019. http://hdl.handle.net/1974/13461.

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

MLA Handbook (7th Edition):

Cameron, Donald. “Identification of TULP3 as a negative regulator of Hedgehog signalling in the mouse .” 2015. Web. 14 Dec 2019.

Vancouver:

Cameron D. Identification of TULP3 as a negative regulator of Hedgehog signalling in the mouse . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1974/13461.

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

Council of Science Editors:

Cameron D. Identification of TULP3 as a negative regulator of Hedgehog signalling in the mouse . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13461

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


University of Cambridge

17. Bates, Lawrence E. Mechanisms of Oct4 in the entry to, maintenance of, and exit from pluripotency .

Degree: 2020, University of Cambridge

 Pluripotency is defined as the capacity to give rise to all cell types of the embryo proper. It arises in the early mammalian embryo but… (more)

Subjects/Keywords: naive pluripotency; mouse ESC; Oct4; Embryonic stem cell

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APA (6th Edition):

Bates, L. E. (2020). Mechanisms of Oct4 in the entry to, maintenance of, and exit from pluripotency . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/299006

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):

Bates, Lawrence E. “Mechanisms of Oct4 in the entry to, maintenance of, and exit from pluripotency .” 2020. Thesis, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/299006.

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

MLA Handbook (7th Edition):

Bates, Lawrence E. “Mechanisms of Oct4 in the entry to, maintenance of, and exit from pluripotency .” 2020. Web. 14 Dec 2019.

Vancouver:

Bates LE. Mechanisms of Oct4 in the entry to, maintenance of, and exit from pluripotency . [Internet] [Thesis]. University of Cambridge; 2020. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/299006.

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

Council of Science Editors:

Bates LE. Mechanisms of Oct4 in the entry to, maintenance of, and exit from pluripotency . [Thesis]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/299006

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


IUPUI

18. Taylor, Tammi M. MOUSE EMBRYONIC STEM CELLS EXPRESS FUNCTIONAL TOLL LIKE RECEPTOR 2.

Degree: 2010, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Embryonic stem cells (ESCs) are unique in that they have potential to give rise to every cell type of the… (more)

Subjects/Keywords: Bacterial Lipopolysaccharide, Pam3Cys, Mouse Embryonic Stem Cells, Toll Like Receptors; Embryonic stem cells  – Research; Cell receptors; Ligands (Biochemistry); Lipoproteins

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

APA (6th Edition):

Taylor, T. M. (2010). MOUSE EMBRYONIC STEM CELLS EXPRESS FUNCTIONAL TOLL LIKE RECEPTOR 2. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2123

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):

Taylor, Tammi M. “MOUSE EMBRYONIC STEM CELLS EXPRESS FUNCTIONAL TOLL LIKE RECEPTOR 2.” 2010. Thesis, IUPUI. Accessed December 14, 2019. http://hdl.handle.net/1805/2123.

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

MLA Handbook (7th Edition):

Taylor, Tammi M. “MOUSE EMBRYONIC STEM CELLS EXPRESS FUNCTIONAL TOLL LIKE RECEPTOR 2.” 2010. Web. 14 Dec 2019.

Vancouver:

Taylor TM. MOUSE EMBRYONIC STEM CELLS EXPRESS FUNCTIONAL TOLL LIKE RECEPTOR 2. [Internet] [Thesis]. IUPUI; 2010. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1805/2123.

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

Council of Science Editors:

Taylor TM. MOUSE EMBRYONIC STEM CELLS EXPRESS FUNCTIONAL TOLL LIKE RECEPTOR 2. [Thesis]. IUPUI; 2010. Available from: http://hdl.handle.net/1805/2123

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


Texas Medical Center

19. lee, moonsup. p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation.

Degree: PhD, 2014, Texas Medical Center

  The canonical-Wnt pathway and beta-catenin have been extensively studied to determine their contributions to stem cell biology, but less is known about p120-catenin in… (more)

Subjects/Keywords: p120-catenin; REST; CoREST; mouse embryonic stem cell; differentiation; pluripotency; Biochemistry; Cell Biology; Developmental Biology

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APA (6th Edition):

lee, m. (2014). p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/526

Chicago Manual of Style (16th Edition):

lee, moonsup. “p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed December 14, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/526.

MLA Handbook (7th Edition):

lee, moonsup. “p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation.” 2014. Web. 14 Dec 2019.

Vancouver:

lee m. p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2019 Dec 14]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/526.

Council of Science Editors:

lee m. p120-catenin regulates REST and CoREST, and modulates mouse embryonic stem cell differentiation. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/526


University of Ottawa

20. Zakariyah, Abeer. The Characterization of a Human Disease-Associated Mutation Nkx2.5 R142C Using In vitro and In vivo Models .

Degree: 2017, University of Ottawa

 Nkx2.5 is a cardiac transcription factor that plays a critical role in heart development. In humans, heterozygous mutations in the NKX2.5 gene result in congenital… (more)

Subjects/Keywords: Transcription factors; Congenital heart defects; mouse embryonic stem cells; cardiac muscle differentiation

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APA (6th Edition):

Zakariyah, A. (2017). The Characterization of a Human Disease-Associated Mutation Nkx2.5 R142C Using In vitro and In vivo Models . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/35817

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):

Zakariyah, Abeer. “The Characterization of a Human Disease-Associated Mutation Nkx2.5 R142C Using In vitro and In vivo Models .” 2017. Thesis, University of Ottawa. Accessed December 14, 2019. http://hdl.handle.net/10393/35817.

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

MLA Handbook (7th Edition):

Zakariyah, Abeer. “The Characterization of a Human Disease-Associated Mutation Nkx2.5 R142C Using In vitro and In vivo Models .” 2017. Web. 14 Dec 2019.

Vancouver:

Zakariyah A. The Characterization of a Human Disease-Associated Mutation Nkx2.5 R142C Using In vitro and In vivo Models . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/10393/35817.

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

Council of Science Editors:

Zakariyah A. The Characterization of a Human Disease-Associated Mutation Nkx2.5 R142C Using In vitro and In vivo Models . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/35817

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


University of Houston

21. Tennakoon, Jayantha 1969-. Impact of Dicer on the Embryonic Stem Cell Epigenome and Androgen Mediated AMPK-PGC-1α Signaling in Prostate Cancer.

Degree: Biology and Biochemistry, Department of, 2013, University of Houston

 What mechanisms govern a cellular phenotype is a fascinating question for which answers are yet being sought. The work presented in this dissertation is an… (more)

Subjects/Keywords: Dicer; mouse embryonic stem cells; epigenome; Androgen signaling; AMPK; PGC1a; prostate cancer; Biology

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APA (6th Edition):

Tennakoon, J. 1. (2013). Impact of Dicer on the Embryonic Stem Cell Epigenome and Androgen Mediated AMPK-PGC-1α Signaling in Prostate Cancer. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/1027

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):

Tennakoon, Jayantha 1969-. “Impact of Dicer on the Embryonic Stem Cell Epigenome and Androgen Mediated AMPK-PGC-1α Signaling in Prostate Cancer.” 2013. Thesis, University of Houston. Accessed December 14, 2019. http://hdl.handle.net/10657/1027.

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

MLA Handbook (7th Edition):

Tennakoon, Jayantha 1969-. “Impact of Dicer on the Embryonic Stem Cell Epigenome and Androgen Mediated AMPK-PGC-1α Signaling in Prostate Cancer.” 2013. Web. 14 Dec 2019.

Vancouver:

Tennakoon J1. Impact of Dicer on the Embryonic Stem Cell Epigenome and Androgen Mediated AMPK-PGC-1α Signaling in Prostate Cancer. [Internet] [Thesis]. University of Houston; 2013. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/10657/1027.

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

Council of Science Editors:

Tennakoon J1. Impact of Dicer on the Embryonic Stem Cell Epigenome and Androgen Mediated AMPK-PGC-1α Signaling in Prostate Cancer. [Thesis]. University of Houston; 2013. Available from: http://hdl.handle.net/10657/1027

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


Wayne State University

22. Slater, Jill A. Hyperosmotic Stress Enzyme Signaling Modulates Oct4, Nanog, And Rex1 Expression And Induces Prioritized Differentiation Of Murine Embryonic Stem Cells.

Degree: PhD, Physiology, 2012, Wayne State University

  HYPEROSMOTIC STRESS ENZYME SIGNALING MODULATES OCT4, NANOG, AND REX1 EXPRESSION AND INDUCES PRIORITIZED DIFFERENTIATION OF MURINE EMBRYONIC STEM CELLS by JILL SLATER MAY 2013… (more)

Subjects/Keywords: hyperosmotic stress; mouse embryonic stem cells; prioritized differentiation; Cell Biology; Developmental Biology

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APA (6th Edition):

Slater, J. A. (2012). Hyperosmotic Stress Enzyme Signaling Modulates Oct4, Nanog, And Rex1 Expression And Induces Prioritized Differentiation Of Murine Embryonic Stem Cells. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/700

Chicago Manual of Style (16th Edition):

Slater, Jill A. “Hyperosmotic Stress Enzyme Signaling Modulates Oct4, Nanog, And Rex1 Expression And Induces Prioritized Differentiation Of Murine Embryonic Stem Cells.” 2012. Doctoral Dissertation, Wayne State University. Accessed December 14, 2019. https://digitalcommons.wayne.edu/oa_dissertations/700.

MLA Handbook (7th Edition):

Slater, Jill A. “Hyperosmotic Stress Enzyme Signaling Modulates Oct4, Nanog, And Rex1 Expression And Induces Prioritized Differentiation Of Murine Embryonic Stem Cells.” 2012. Web. 14 Dec 2019.

Vancouver:

Slater JA. Hyperosmotic Stress Enzyme Signaling Modulates Oct4, Nanog, And Rex1 Expression And Induces Prioritized Differentiation Of Murine Embryonic Stem Cells. [Internet] [Doctoral dissertation]. Wayne State University; 2012. [cited 2019 Dec 14]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/700.

Council of Science Editors:

Slater JA. Hyperosmotic Stress Enzyme Signaling Modulates Oct4, Nanog, And Rex1 Expression And Induces Prioritized Differentiation Of Murine Embryonic Stem Cells. [Doctoral Dissertation]. Wayne State University; 2012. Available from: https://digitalcommons.wayne.edu/oa_dissertations/700


University of Toronto

23. Roy, Anna. CCCTC-binding Factor (Ctcf) is Required for Mouse Cardiovascular Development.

Degree: 2016, University of Toronto

Disruption of transcriptional programs controlling development of the cardiovascular system can cause congenital cardiovascular disease. These programs are tightly regulated by chromatin regulators that alter… (more)

Subjects/Keywords: Cardiovascular development; Chromatin regulators; CTCF; Long-range chromatin interactions; mouse embryonic development; 0307

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APA (6th Edition):

Roy, A. (2016). CCCTC-binding Factor (Ctcf) is Required for Mouse Cardiovascular Development. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72777

Chicago Manual of Style (16th Edition):

Roy, Anna. “CCCTC-binding Factor (Ctcf) is Required for Mouse Cardiovascular Development.” 2016. Masters Thesis, University of Toronto. Accessed December 14, 2019. http://hdl.handle.net/1807/72777.

MLA Handbook (7th Edition):

Roy, Anna. “CCCTC-binding Factor (Ctcf) is Required for Mouse Cardiovascular Development.” 2016. Web. 14 Dec 2019.

Vancouver:

Roy A. CCCTC-binding Factor (Ctcf) is Required for Mouse Cardiovascular Development. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1807/72777.

Council of Science Editors:

Roy A. CCCTC-binding Factor (Ctcf) is Required for Mouse Cardiovascular Development. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72777


University of Cambridge

24. Cao, Yang. Investigating mechanisms of genome folding by single-cell Hi-C .

Degree: 2019, University of Cambridge

 In recent years researchers have begun to reveal the hierarchy of mammalian DNA folding from the 10 nm fibre to the intact whole genome. One… (more)

Subjects/Keywords: genome structure; single-cell Hi-C; mouse embryonic stem cell; early differentiation

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APA (6th Edition):

Cao, Y. (2019). Investigating mechanisms of genome folding by single-cell Hi-C . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/294123

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):

Cao, Yang. “Investigating mechanisms of genome folding by single-cell Hi-C .” 2019. Thesis, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/294123.

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

MLA Handbook (7th Edition):

Cao, Yang. “Investigating mechanisms of genome folding by single-cell Hi-C .” 2019. Web. 14 Dec 2019.

Vancouver:

Cao Y. Investigating mechanisms of genome folding by single-cell Hi-C . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/294123.

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

Council of Science Editors:

Cao Y. Investigating mechanisms of genome folding by single-cell Hi-C . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/294123

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


Freie Universität Berlin

25. Kur, Esther. Die Rolle von LRP2 bei der Embryonalentwicklung von Zebrafisch und Maus.

Degree: 2012, Freie Universität Berlin

 LRP2 ist ein Mitglied der LDL-Rezeptorfamilie und wird in Wirbeltieren auf der apikalen Oberfläche zahlreicher Epithelien exprimiert. Im adulten Organismus ist LRP2 wichtig für die… (more)

Subjects/Keywords: Lrp2; embryonic development; zebrafish; mouse; forebrain; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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APA (6th Edition):

Kur, E. (2012). Die Rolle von LRP2 bei der Embryonalentwicklung von Zebrafisch und Maus. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-10989

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):

Kur, Esther. “Die Rolle von LRP2 bei der Embryonalentwicklung von Zebrafisch und Maus.” 2012. Thesis, Freie Universität Berlin. Accessed December 14, 2019. http://dx.doi.org/10.17169/refubium-10989.

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

MLA Handbook (7th Edition):

Kur, Esther. “Die Rolle von LRP2 bei der Embryonalentwicklung von Zebrafisch und Maus.” 2012. Web. 14 Dec 2019.

Vancouver:

Kur E. Die Rolle von LRP2 bei der Embryonalentwicklung von Zebrafisch und Maus. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2019 Dec 14]. Available from: http://dx.doi.org/10.17169/refubium-10989.

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

Council of Science Editors:

Kur E. Die Rolle von LRP2 bei der Embryonalentwicklung von Zebrafisch und Maus. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-10989

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


University of Cambridge

26. Edri, Shlomit. Date with destiny : genetic and epigenetic factors in cell fate decisions in populations of multipotent stem cells.

Degree: PhD, 2019, University of Cambridge

 The governance of cell fate decisions during development is a fundamental biological problem. An important aspect of this is how cells exit a multipotent state… (more)

Subjects/Keywords: Pluripotency; In vitro culture; Neural Mesodermal Progenitors; Epiblast Stem Cells; mouse Embryonic Stem Cells

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APA (6th Edition):

Edri, S. (2019). Date with destiny : genetic and epigenetic factors in cell fate decisions in populations of multipotent stem cells. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/288380 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763904

Chicago Manual of Style (16th Edition):

Edri, Shlomit. “Date with destiny : genetic and epigenetic factors in cell fate decisions in populations of multipotent stem cells.” 2019. Doctoral Dissertation, University of Cambridge. Accessed December 14, 2019. https://www.repository.cam.ac.uk/handle/1810/288380 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763904.

MLA Handbook (7th Edition):

Edri, Shlomit. “Date with destiny : genetic and epigenetic factors in cell fate decisions in populations of multipotent stem cells.” 2019. Web. 14 Dec 2019.

Vancouver:

Edri S. Date with destiny : genetic and epigenetic factors in cell fate decisions in populations of multipotent stem cells. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Dec 14]. Available from: https://www.repository.cam.ac.uk/handle/1810/288380 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763904.

Council of Science Editors:

Edri S. Date with destiny : genetic and epigenetic factors in cell fate decisions in populations of multipotent stem cells. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/288380 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763904


University of Sydney

27. Boumelhem, Badwi Bob. The in vitro differentiation of prostate epithelial cells and gonadal adipocytes from mouse embryonic stem cells .

Degree: 2017, University of Sydney

Mouse embryonic stem (ES) cells are pluripotent, undifferentiated cells that can differentiate into any cell of the three germ layers: the ectoderm, the mesoderm and… (more)

Subjects/Keywords: mouse embryonic stem cells; prostate; prostate differentiation; gonadal fat; flow cytometry; edoderm

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APA (6th Edition):

Boumelhem, B. B. (2017). The in vitro differentiation of prostate epithelial cells and gonadal adipocytes from mouse embryonic stem cells . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17991

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):

Boumelhem, Badwi Bob. “The in vitro differentiation of prostate epithelial cells and gonadal adipocytes from mouse embryonic stem cells .” 2017. Thesis, University of Sydney. Accessed December 14, 2019. http://hdl.handle.net/2123/17991.

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

MLA Handbook (7th Edition):

Boumelhem, Badwi Bob. “The in vitro differentiation of prostate epithelial cells and gonadal adipocytes from mouse embryonic stem cells .” 2017. Web. 14 Dec 2019.

Vancouver:

Boumelhem BB. The in vitro differentiation of prostate epithelial cells and gonadal adipocytes from mouse embryonic stem cells . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/2123/17991.

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

Council of Science Editors:

Boumelhem BB. The in vitro differentiation of prostate epithelial cells and gonadal adipocytes from mouse embryonic stem cells . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17991

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


University of Oxford

28. Stevens, Jonathan L. A novel role for Atmin as a transcription factor controlling ciliogenesis.

Degree: PhD, 2011, University of Oxford

 Cilia are cellular organelles involved in processing components of the hedgehog (hh) signalling pathway and determining left-right (L-R) axis formation in the embryo. An embryonic(more)

Subjects/Keywords: 571.861; Life Sciences; Genetics (life sciences); embryonic development; Atmin; mouse mutagenesis; cilia

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

APA (6th Edition):

Stevens, J. L. (2011). A novel role for Atmin as a transcription factor controlling ciliogenesis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:52de0cea-164d-4ca3-8ac1-0b2cda1ba4b2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542977

Chicago Manual of Style (16th Edition):

Stevens, Jonathan L. “A novel role for Atmin as a transcription factor controlling ciliogenesis.” 2011. Doctoral Dissertation, University of Oxford. Accessed December 14, 2019. http://ora.ox.ac.uk/objects/uuid:52de0cea-164d-4ca3-8ac1-0b2cda1ba4b2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542977.

MLA Handbook (7th Edition):

Stevens, Jonathan L. “A novel role for Atmin as a transcription factor controlling ciliogenesis.” 2011. Web. 14 Dec 2019.

Vancouver:

Stevens JL. A novel role for Atmin as a transcription factor controlling ciliogenesis. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Dec 14]. Available from: http://ora.ox.ac.uk/objects/uuid:52de0cea-164d-4ca3-8ac1-0b2cda1ba4b2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542977.

Council of Science Editors:

Stevens JL. A novel role for Atmin as a transcription factor controlling ciliogenesis. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:52de0cea-164d-4ca3-8ac1-0b2cda1ba4b2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.542977


Université de Montréal

29. Laflamme, Simon. La dérivation de cellules souches embryonnaires chez le cheval .

Degree: 2011, Université de Montréal

 Les cellules souches embryonnaires (ES) sont porteuses de grands espoirs en recherche biomédicale dans le but d’apporter un traitement définitif à l’ostéoarthrose. Parce que certaines… (more)

Subjects/Keywords: Cellules souches embryonnaires; Cellules nourricières; Blastocyste; Inhibiteurs de voies de signalisation; Pluripotence; Différenciation; Cheval; Embryonic stem cells; Feeder cell line; Blastocyst; Cell signalling inhibitors; pluripotency; Differentiation; Horse

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

APA (6th Edition):

Laflamme, S. (2011). La dérivation de cellules souches embryonnaires chez le cheval . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/5262

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):

Laflamme, Simon. “La dérivation de cellules souches embryonnaires chez le cheval .” 2011. Thesis, Université de Montréal. Accessed December 14, 2019. http://hdl.handle.net/1866/5262.

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

MLA Handbook (7th Edition):

Laflamme, Simon. “La dérivation de cellules souches embryonnaires chez le cheval .” 2011. Web. 14 Dec 2019.

Vancouver:

Laflamme S. La dérivation de cellules souches embryonnaires chez le cheval . [Internet] [Thesis]. Université de Montréal; 2011. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/1866/5262.

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

Council of Science Editors:

Laflamme S. La dérivation de cellules souches embryonnaires chez le cheval . [Thesis]. Université de Montréal; 2011. Available from: http://hdl.handle.net/1866/5262

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

30. Khadun, Shalinee. The support of undifferentiated human embryonic stem cell lines by different matrices .

Degree: 2014, University of Hertfordshire

 The future of human embryonic stem cell (hESC) research with regards to their applicability in a therapeutic setting, relies on the development and standardisation of… (more)

Subjects/Keywords: Human embryonic stem cell (hESC) culture; Stem cell comparative studies; Feeder matrices; In vitro differentiation studies; Chromosome stability; TissueFaxs image analysis; Stem cell characterisation; Standardisation; Stem cell banking

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

APA (6th Edition):

Khadun, S. (2014). The support of undifferentiated human embryonic stem cell lines by different matrices . (Thesis). University of Hertfordshire. Retrieved from http://hdl.handle.net/2299/14447

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):

Khadun, Shalinee. “The support of undifferentiated human embryonic stem cell lines by different matrices .” 2014. Thesis, University of Hertfordshire. Accessed December 14, 2019. http://hdl.handle.net/2299/14447.

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

MLA Handbook (7th Edition):

Khadun, Shalinee. “The support of undifferentiated human embryonic stem cell lines by different matrices .” 2014. Web. 14 Dec 2019.

Vancouver:

Khadun S. The support of undifferentiated human embryonic stem cell lines by different matrices . [Internet] [Thesis]. University of Hertfordshire; 2014. [cited 2019 Dec 14]. Available from: http://hdl.handle.net/2299/14447.

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

Council of Science Editors:

Khadun S. The support of undifferentiated human embryonic stem cell lines by different matrices . [Thesis]. University of Hertfordshire; 2014. Available from: http://hdl.handle.net/2299/14447

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

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