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You searched for subject:(pluripotent stem cell). Showing records 1 – 30 of 150 total matches.

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McMaster University

1. Hrenczuk, Amanda. The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells.

Degree: MSc, 2017, McMaster University

Pluripotent stem cells (PSCs) are unique in their capability to self-renew and differentiate into cell types of all three embryonic germ layers. Since their discovery,… (more)

Subjects/Keywords: Pluripotent Stem Cell; Biochemistry; Rex1/Zfp42

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APA (6th Edition):

Hrenczuk, A. (2017). The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/22339

Chicago Manual of Style (16th Edition):

Hrenczuk, Amanda. “The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells.” 2017. Masters Thesis, McMaster University. Accessed December 12, 2019. http://hdl.handle.net/11375/22339.

MLA Handbook (7th Edition):

Hrenczuk, Amanda. “The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells.” 2017. Web. 12 Dec 2019.

Vancouver:

Hrenczuk A. The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells. [Internet] [Masters thesis]. McMaster University; 2017. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11375/22339.

Council of Science Editors:

Hrenczuk A. The Role and Molecular Mechanisms of Rex1 in Pluripotent Stem Cells. [Masters Thesis]. McMaster University; 2017. Available from: http://hdl.handle.net/11375/22339


Harvard University

2. Vo, Linda T. Hematopoietic Cell Engineering From Human Pluripotent Stem Cells.

Degree: PhD, 2017, Harvard University

Hematopoietic stem cells (HSCs) reside at the apex of a complex cellular hierarchy that replenishes blood throughout life. Such extensive regenerative potential makes HSCs a… (more)

Subjects/Keywords: Hematopoiesis; cell engineering; human pluripotent stem cells

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APA (6th Edition):

Vo, L. T. (2017). Hematopoietic Cell Engineering From Human Pluripotent Stem Cells. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141484

Chicago Manual of Style (16th Edition):

Vo, Linda T. “Hematopoietic Cell Engineering From Human Pluripotent Stem Cells.” 2017. Doctoral Dissertation, Harvard University. Accessed December 12, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141484.

MLA Handbook (7th Edition):

Vo, Linda T. “Hematopoietic Cell Engineering From Human Pluripotent Stem Cells.” 2017. Web. 12 Dec 2019.

Vancouver:

Vo LT. Hematopoietic Cell Engineering From Human Pluripotent Stem Cells. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2019 Dec 12]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141484.

Council of Science Editors:

Vo LT. Hematopoietic Cell Engineering From Human Pluripotent Stem Cells. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:41141484


Queen Mary, University of London

3. Shephard, Matthew T. Targeted differentiation of pluripotent stem cells to hepatocytes.

Degree: PhD, 2018, Queen Mary, University of London

Pluripotent stem cells (PSCs) possess the ability to differentiate to virtually any cell type whilst retaining the capacity to self-renew. There is an unmet need… (more)

Subjects/Keywords: Pluripotent Stem Cells; hepatocytes; cell differentiation

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APA (6th Edition):

Shephard, M. T. (2018). Targeted differentiation of pluripotent stem cells to hepatocytes. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338

Chicago Manual of Style (16th Edition):

Shephard, Matthew T. “Targeted differentiation of pluripotent stem cells to hepatocytes.” 2018. Doctoral Dissertation, Queen Mary, University of London. Accessed December 12, 2019. http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338.

MLA Handbook (7th Edition):

Shephard, Matthew T. “Targeted differentiation of pluripotent stem cells to hepatocytes.” 2018. Web. 12 Dec 2019.

Vancouver:

Shephard MT. Targeted differentiation of pluripotent stem cells to hepatocytes. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2018. [cited 2019 Dec 12]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338.

Council of Science Editors:

Shephard MT. Targeted differentiation of pluripotent stem cells to hepatocytes. [Doctoral Dissertation]. Queen Mary, University of London; 2018. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/56077 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.786338


UCLA

4. Chin, Chee Jia. Forming the hematopoietic stem cell niche from pluripotent stem cells.

Degree: Cellular & Molecular Pathology, 2016, UCLA

 Hematopoietic stem cells (HSCs) are characterized by their ability to self-renew and contribute to multi-lineage differentiation, critical functions that ensure homeostatic production of all blood… (more)

Subjects/Keywords: Developmental biology; Hematopoiesis; hematopoietic stem cell niche; pericyte; pluripotent stem cells

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APA (6th Edition):

Chin, C. J. (2016). Forming the hematopoietic stem cell niche from pluripotent stem cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/5090j0jj

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):

Chin, Chee Jia. “Forming the hematopoietic stem cell niche from pluripotent stem cells.” 2016. Thesis, UCLA. Accessed December 12, 2019. http://www.escholarship.org/uc/item/5090j0jj.

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

MLA Handbook (7th Edition):

Chin, Chee Jia. “Forming the hematopoietic stem cell niche from pluripotent stem cells.” 2016. Web. 12 Dec 2019.

Vancouver:

Chin CJ. Forming the hematopoietic stem cell niche from pluripotent stem cells. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Dec 12]. Available from: http://www.escholarship.org/uc/item/5090j0jj.

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

Council of Science Editors:

Chin CJ. Forming the hematopoietic stem cell niche from pluripotent stem cells. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/5090j0jj

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


University of Melbourne

5. Motazedian, Ali. Lymphocyte differentiation from pluripotent stem cells.

Degree: 2017, University of Melbourne

 Human pluripotent stem cells (PSCs), including embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs), are cell types that can undergo unlimited self-renewal and,… (more)

Subjects/Keywords: pluripotent stem cells; iPS; ES; lymphocyte; T-cell; B-cell

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APA (6th Edition):

Motazedian, A. (2017). Lymphocyte differentiation from pluripotent stem cells. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/191658

Chicago Manual of Style (16th Edition):

Motazedian, Ali. “Lymphocyte differentiation from pluripotent stem cells.” 2017. Doctoral Dissertation, University of Melbourne. Accessed December 12, 2019. http://hdl.handle.net/11343/191658.

MLA Handbook (7th Edition):

Motazedian, Ali. “Lymphocyte differentiation from pluripotent stem cells.” 2017. Web. 12 Dec 2019.

Vancouver:

Motazedian A. Lymphocyte differentiation from pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11343/191658.

Council of Science Editors:

Motazedian A. Lymphocyte differentiation from pluripotent stem cells. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/191658


University of Manchester

6. Robertson, Abigail. Targeting the Hippo signalling pathway to enhance the protective effect of iPS cell derived cardiomyocytes.

Degree: PhD, 2017, University of Manchester

Cell based therapy using stem cell derived cardiomyocytes, has emerged as a potential therapeutic approach for cardiac diseases such as myocardial infarction and heart failure.… (more)

Subjects/Keywords: 612.1; Hippo pathway; Induced pluripotent stem cell; Cell therapy

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APA (6th Edition):

Robertson, A. (2017). Targeting the Hippo signalling pathway to enhance the protective effect of iPS cell derived cardiomyocytes. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/targeting-the-hippo-signalling-pathway-to-enhance-the-protective-effect-of-ips-cell-derived-cardiomyocytes(f80b12c7-5289-46f9-8829-28224f0c6270).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713586

Chicago Manual of Style (16th Edition):

Robertson, Abigail. “Targeting the Hippo signalling pathway to enhance the protective effect of iPS cell derived cardiomyocytes.” 2017. Doctoral Dissertation, University of Manchester. Accessed December 12, 2019. https://www.research.manchester.ac.uk/portal/en/theses/targeting-the-hippo-signalling-pathway-to-enhance-the-protective-effect-of-ips-cell-derived-cardiomyocytes(f80b12c7-5289-46f9-8829-28224f0c6270).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713586.

MLA Handbook (7th Edition):

Robertson, Abigail. “Targeting the Hippo signalling pathway to enhance the protective effect of iPS cell derived cardiomyocytes.” 2017. Web. 12 Dec 2019.

Vancouver:

Robertson A. Targeting the Hippo signalling pathway to enhance the protective effect of iPS cell derived cardiomyocytes. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Dec 12]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/targeting-the-hippo-signalling-pathway-to-enhance-the-protective-effect-of-ips-cell-derived-cardiomyocytes(f80b12c7-5289-46f9-8829-28224f0c6270).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713586.

Council of Science Editors:

Robertson A. Targeting the Hippo signalling pathway to enhance the protective effect of iPS cell derived cardiomyocytes. [Doctoral Dissertation]. University of Manchester; 2017. Available from: https://www.research.manchester.ac.uk/portal/en/theses/targeting-the-hippo-signalling-pathway-to-enhance-the-protective-effect-of-ips-cell-derived-cardiomyocytes(f80b12c7-5289-46f9-8829-28224f0c6270).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713586


University of California – Santa Cruz

7. Blij, Stephanie. Specification and regulation of mammalian extraembryonic and pluripotent embryonic lineages in vivo and in vitro.

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

 Pluripotency establishment and maintenance are critical for both the development of mammalian embryos and the production of pluripotent stem cells. Investigations into the molecular mechanisms… (more)

Subjects/Keywords: Biology; blastocyst; embryonic stem cell; induced pluripotent stem cell; maternal; pluripotency; sox2

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APA (6th Edition):

Blij, S. (2014). Specification and regulation of mammalian extraembryonic and pluripotent embryonic lineages in vivo and in vitro. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/9db2r8kw

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):

Blij, Stephanie. “Specification and regulation of mammalian extraembryonic and pluripotent embryonic lineages in vivo and in vitro.” 2014. Thesis, University of California – Santa Cruz. Accessed December 12, 2019. http://www.escholarship.org/uc/item/9db2r8kw.

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

MLA Handbook (7th Edition):

Blij, Stephanie. “Specification and regulation of mammalian extraembryonic and pluripotent embryonic lineages in vivo and in vitro.” 2014. Web. 12 Dec 2019.

Vancouver:

Blij S. Specification and regulation of mammalian extraembryonic and pluripotent embryonic lineages in vivo and in vitro. [Internet] [Thesis]. University of California – Santa Cruz; 2014. [cited 2019 Dec 12]. Available from: http://www.escholarship.org/uc/item/9db2r8kw.

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

Council of Science Editors:

Blij S. Specification and regulation of mammalian extraembryonic and pluripotent embryonic lineages in vivo and in vitro. [Thesis]. University of California – Santa Cruz; 2014. Available from: http://www.escholarship.org/uc/item/9db2r8kw

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


Tampere University

8. Harju, Venla. Neuronal differentiation, maturation and adhesion in vitro in 3D - effect of cell source and hydrogel scaffold.

Degree: 2018, Tampere University

 There is a great need for novel tissue engineering (TE) applications for central nervous system (CNS) defects, like spinal cord injury (SCI). One promising approach… (more)

Subjects/Keywords: tissue engineering; human embryonic stem cell; human pluripotent stem cell; neuron; hydrogel

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APA (6th Edition):

Harju, V. (2018). Neuronal differentiation, maturation and adhesion in vitro in 3D - effect of cell source and hydrogel scaffold. (Masters Thesis). Tampere University. Retrieved from https://trepo.tuni.fi/handle/10024/102723

Chicago Manual of Style (16th Edition):

Harju, Venla. “Neuronal differentiation, maturation and adhesion in vitro in 3D - effect of cell source and hydrogel scaffold.” 2018. Masters Thesis, Tampere University. Accessed December 12, 2019. https://trepo.tuni.fi/handle/10024/102723.

MLA Handbook (7th Edition):

Harju, Venla. “Neuronal differentiation, maturation and adhesion in vitro in 3D - effect of cell source and hydrogel scaffold.” 2018. Web. 12 Dec 2019.

Vancouver:

Harju V. Neuronal differentiation, maturation and adhesion in vitro in 3D - effect of cell source and hydrogel scaffold. [Internet] [Masters thesis]. Tampere University; 2018. [cited 2019 Dec 12]. Available from: https://trepo.tuni.fi/handle/10024/102723.

Council of Science Editors:

Harju V. Neuronal differentiation, maturation and adhesion in vitro in 3D - effect of cell source and hydrogel scaffold. [Masters Thesis]. Tampere University; 2018. Available from: https://trepo.tuni.fi/handle/10024/102723


Arizona State University

9. Raman, Sreedevi. Generation of a Human Induced Pluripotent Stem Cell Based Model of Progerin Induced Aging.

Degree: Bioengineering, 2017, Arizona State University

 An in vitro model of Alzheimer’s disease (AD) is required to study the poorly understood molecular mechanisms involved in the familial and sporadic forms of… (more)

Subjects/Keywords: Biomedical engineering; Aging; Alzheimer's disease; Disease modelling; Human pluripotent stem cell; Progerin; Stem cell engineering

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APA (6th Edition):

Raman, S. (2017). Generation of a Human Induced Pluripotent Stem Cell Based Model of Progerin Induced Aging. (Masters Thesis). Arizona State University. Retrieved from http://repository.asu.edu/items/44082

Chicago Manual of Style (16th Edition):

Raman, Sreedevi. “Generation of a Human Induced Pluripotent Stem Cell Based Model of Progerin Induced Aging.” 2017. Masters Thesis, Arizona State University. Accessed December 12, 2019. http://repository.asu.edu/items/44082.

MLA Handbook (7th Edition):

Raman, Sreedevi. “Generation of a Human Induced Pluripotent Stem Cell Based Model of Progerin Induced Aging.” 2017. Web. 12 Dec 2019.

Vancouver:

Raman S. Generation of a Human Induced Pluripotent Stem Cell Based Model of Progerin Induced Aging. [Internet] [Masters thesis]. Arizona State University; 2017. [cited 2019 Dec 12]. Available from: http://repository.asu.edu/items/44082.

Council of Science Editors:

Raman S. Generation of a Human Induced Pluripotent Stem Cell Based Model of Progerin Induced Aging. [Masters Thesis]. Arizona State University; 2017. Available from: http://repository.asu.edu/items/44082


University of Cambridge

10. Eldridge, Cara Bernadette. The effect of replication impediments on differentiation .

Degree: 2019, University of Cambridge

 In this thesis I set out to answer the question ‘is differentiation robust to replication impediments?’. Prior work in the group has focussed on the… (more)

Subjects/Keywords: differentiation; G-quadruplex; DNA damage response; induced pluripotent stem cell; stem cell; endoderm

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APA (6th Edition):

Eldridge, C. B. (2019). The effect of replication impediments on differentiation . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/295463

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):

Eldridge, Cara Bernadette. “The effect of replication impediments on differentiation .” 2019. Thesis, University of Cambridge. Accessed December 12, 2019. https://www.repository.cam.ac.uk/handle/1810/295463.

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

MLA Handbook (7th Edition):

Eldridge, Cara Bernadette. “The effect of replication impediments on differentiation .” 2019. Web. 12 Dec 2019.

Vancouver:

Eldridge CB. The effect of replication impediments on differentiation . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Dec 12]. Available from: https://www.repository.cam.ac.uk/handle/1810/295463.

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

Council of Science Editors:

Eldridge CB. The effect of replication impediments on differentiation . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/295463

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


Penn State University

11. Lin, Tzu. DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS.

Degree: 2017, Penn State University

 Owing to their ability to differentiate into all cell types in body, and therefore greatly impact the landscape of regenerative medicine and tissue engineering, the… (more)

Subjects/Keywords: Stem cell culture medium; LaSR; Xeno-free medium; Stem cell culture; Human induced pluripotent stem cells; Human embryonic stem cells

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APA (6th Edition):

Lin, T. (2017). DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS. (Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/13797txl5286

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, Tzu. “DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS.” 2017. Thesis, Penn State University. Accessed December 12, 2019. https://etda.libraries.psu.edu/catalog/13797txl5286.

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

MLA Handbook (7th Edition):

Lin, Tzu. “DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS.” 2017. Web. 12 Dec 2019.

Vancouver:

Lin T. DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS. [Internet] [Thesis]. Penn State University; 2017. [cited 2019 Dec 12]. Available from: https://etda.libraries.psu.edu/catalog/13797txl5286.

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

Council of Science Editors:

Lin T. DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS. [Thesis]. Penn State University; 2017. Available from: https://etda.libraries.psu.edu/catalog/13797txl5286

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


Kyoto University / 京都大学

12. Shimamoto, Ren. Generation and Characterization of Induced Pluripotent Stem Cells from Aid-deficient Mice : Aid欠損マウスからのiPS細胞誘導と性質評価.

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

Shimamoto R, Amano N, Ichisaka T, Watanabe A, Yamanaka S, et al. (2014) Generation and Characterization of Induced Pluripotent Stem Cells from Aid-Deficient Mice. PLoS ONE 9(4): e94735. doi:10.1371/journal.pone.0094735

新制・課程博士

甲第18515号

医科博第56号

Subjects/Keywords: Induced pluripotent stem cell; Reprogramming; DNA demethylation; Aid; epigenetics

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APA (6th Edition):

Shimamoto, R. (2014). Generation and Characterization of Induced Pluripotent Stem Cells from Aid-deficient Mice : Aid欠損マウスからのiPS細胞誘導と性質評価. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/189672 ; http://dx.doi.org/10.14989/doctor.k18515

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):

Shimamoto, Ren. “Generation and Characterization of Induced Pluripotent Stem Cells from Aid-deficient Mice : Aid欠損マウスからのiPS細胞誘導と性質評価.” 2014. Thesis, Kyoto University / 京都大学. Accessed December 12, 2019. http://hdl.handle.net/2433/189672 ; http://dx.doi.org/10.14989/doctor.k18515.

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

MLA Handbook (7th Edition):

Shimamoto, Ren. “Generation and Characterization of Induced Pluripotent Stem Cells from Aid-deficient Mice : Aid欠損マウスからのiPS細胞誘導と性質評価.” 2014. Web. 12 Dec 2019.

Vancouver:

Shimamoto R. Generation and Characterization of Induced Pluripotent Stem Cells from Aid-deficient Mice : Aid欠損マウスからのiPS細胞誘導と性質評価. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2433/189672 ; http://dx.doi.org/10.14989/doctor.k18515.

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

Council of Science Editors:

Shimamoto R. Generation and Characterization of Induced Pluripotent Stem Cells from Aid-deficient Mice : Aid欠損マウスからのiPS細胞誘導と性質評価. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/189672 ; http://dx.doi.org/10.14989/doctor.k18515

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


University of Cincinnati

13. Campbell, Ian. Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells.

Degree: MS, Medicine: Molecular and Developmental Biology, 2017, University of Cincinnati

 Human pluripotent stem cells (hPSCs) have the capacity for self-renewal and the ability to differentiate into any cell type providing an unlimited source of primary… (more)

Subjects/Keywords: Biomedical Research; iPSC; CRISPR; gene editing; Pluripotent stem cell; cas9

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APA (6th Edition):

Campbell, I. (2017). Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802720510926

Chicago Manual of Style (16th Edition):

Campbell, Ian. “Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells.” 2017. Masters Thesis, University of Cincinnati. Accessed December 12, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802720510926.

MLA Handbook (7th Edition):

Campbell, Ian. “Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells.” 2017. Web. 12 Dec 2019.

Vancouver:

Campbell I. Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells. [Internet] [Masters thesis]. University of Cincinnati; 2017. [cited 2019 Dec 12]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802720510926.

Council of Science Editors:

Campbell I. Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells. [Masters Thesis]. University of Cincinnati; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1504802720510926


McMaster University

14. Deng, Xiaoxiao (Daisy). FUNCTIONAL CHARACTERIZATION OF PUTATIVE MITOTIC BOOKMARKING FACTORS IN PLURIPOTENCY MAINTENANCE.

Degree: MSc, 2018, McMaster University

Pluripotent stem cells are a special population of stem cell with indefinitely self-renewal and unlimited differentiation capability, which makes them an attractive avenue for regenerative… (more)

Subjects/Keywords: Mitotic Bookmarking; Hdgf; Parp1; Psip1; Pluripotent Stem Cells; Cell Fate Regulation

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APA (6th Edition):

Deng, X. (. (2018). FUNCTIONAL CHARACTERIZATION OF PUTATIVE MITOTIC BOOKMARKING FACTORS IN PLURIPOTENCY MAINTENANCE. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/24291

Chicago Manual of Style (16th Edition):

Deng, Xiaoxiao (Daisy). “FUNCTIONAL CHARACTERIZATION OF PUTATIVE MITOTIC BOOKMARKING FACTORS IN PLURIPOTENCY MAINTENANCE.” 2018. Masters Thesis, McMaster University. Accessed December 12, 2019. http://hdl.handle.net/11375/24291.

MLA Handbook (7th Edition):

Deng, Xiaoxiao (Daisy). “FUNCTIONAL CHARACTERIZATION OF PUTATIVE MITOTIC BOOKMARKING FACTORS IN PLURIPOTENCY MAINTENANCE.” 2018. Web. 12 Dec 2019.

Vancouver:

Deng X(. FUNCTIONAL CHARACTERIZATION OF PUTATIVE MITOTIC BOOKMARKING FACTORS IN PLURIPOTENCY MAINTENANCE. [Internet] [Masters thesis]. McMaster University; 2018. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11375/24291.

Council of Science Editors:

Deng X(. FUNCTIONAL CHARACTERIZATION OF PUTATIVE MITOTIC BOOKMARKING FACTORS IN PLURIPOTENCY MAINTENANCE. [Masters Thesis]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/24291


University of Cincinnati

15. Trisno, Stephen L. Modeling esophageal development and disease in mice and in human pluripotent stem cell-derived organoids.

Degree: PhD, Medicine: Molecular and Developmental Biology, 2018, University of Cincinnati

 The esophagus is an organ of the gastrointestinal tract connecting the pharynx to the stomach. It consists of an epithelial layer, submucosa with glands, muscular… (more)

Subjects/Keywords: Developmental Biology; esophagus; organoid; pluripotent stem cell; foregut; sox2; disease modeling

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APA (6th Edition):

Trisno, S. L. (2018). Modeling esophageal development and disease in mice and in human pluripotent stem cell-derived organoids. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1539080161314324

Chicago Manual of Style (16th Edition):

Trisno, Stephen L. “Modeling esophageal development and disease in mice and in human pluripotent stem cell-derived organoids.” 2018. Doctoral Dissertation, University of Cincinnati. Accessed December 12, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1539080161314324.

MLA Handbook (7th Edition):

Trisno, Stephen L. “Modeling esophageal development and disease in mice and in human pluripotent stem cell-derived organoids.” 2018. Web. 12 Dec 2019.

Vancouver:

Trisno SL. Modeling esophageal development and disease in mice and in human pluripotent stem cell-derived organoids. [Internet] [Doctoral dissertation]. University of Cincinnati; 2018. [cited 2019 Dec 12]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1539080161314324.

Council of Science Editors:

Trisno SL. Modeling esophageal development and disease in mice and in human pluripotent stem cell-derived organoids. [Doctoral Dissertation]. University of Cincinnati; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1539080161314324


Kansas State University

16. Li, Quan. Synthetic hydrogel-based 3D culture system for maintenance of human induced pluripotent stem cell.

Degree: MS, Department of Grain Science and Industry, 2017, Kansas State University

 Human induced pluripotent stem cells (hiPSCs) are generated from human somatic cells using defined transcription factors. These cells possess characteristics very similar to that of… (more)

Subjects/Keywords: Human induced pluripotent stem cell; 3D culture; Hydrogel

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APA (6th Edition):

Li, Q. (2017). Synthetic hydrogel-based 3D culture system for maintenance of human induced pluripotent stem cell. (Masters Thesis). Kansas State University. Retrieved from http://hdl.handle.net/2097/36189

Chicago Manual of Style (16th Edition):

Li, Quan. “Synthetic hydrogel-based 3D culture system for maintenance of human induced pluripotent stem cell.” 2017. Masters Thesis, Kansas State University. Accessed December 12, 2019. http://hdl.handle.net/2097/36189.

MLA Handbook (7th Edition):

Li, Quan. “Synthetic hydrogel-based 3D culture system for maintenance of human induced pluripotent stem cell.” 2017. Web. 12 Dec 2019.

Vancouver:

Li Q. Synthetic hydrogel-based 3D culture system for maintenance of human induced pluripotent stem cell. [Internet] [Masters thesis]. Kansas State University; 2017. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2097/36189.

Council of Science Editors:

Li Q. Synthetic hydrogel-based 3D culture system for maintenance of human induced pluripotent stem cell. [Masters Thesis]. Kansas State University; 2017. Available from: http://hdl.handle.net/2097/36189


University of Toronto

17. Moghaddam, Bahar. Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions.

Degree: 2011, University of Toronto

Conjugation of the Human Immunodeficiency Virus Transactivator of Transcription (TAT) to active proteins allows transport into the intracellular environment. This feature can be harnessed to… (more)

Subjects/Keywords: Cell Penetrating Peptides; Induced pluripotent stem cells; Transcription Factor Delivery; 0541

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APA (6th Edition):

Moghaddam, B. (2011). Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31344

Chicago Manual of Style (16th Edition):

Moghaddam, Bahar. “Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions.” 2011. Masters Thesis, University of Toronto. Accessed December 12, 2019. http://hdl.handle.net/1807/31344.

MLA Handbook (7th Edition):

Moghaddam, Bahar. “Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions.” 2011. Web. 12 Dec 2019.

Vancouver:

Moghaddam B. Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/1807/31344.

Council of Science Editors:

Moghaddam B. Assessment of Cell Penetrating Peptides as a Vehicle for Delivering Transcription Factors for Stem Cell Reprogramming and Controlling Fate Decisions. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31344


University of Minnesota

18. Schaefer, Jeremy. Development of Bi-layer Engineered Cardiac Tissues Containing Cardiomyocytes and Microvessels.

Degree: PhD, Biomedical Engineering, 2016, University of Minnesota

 The prevalence of coronary heart disease and myocardial infarction coupled with the limited availability of donor hearts to replace damaged tissue leaves many patients with… (more)

Subjects/Keywords: induced pluripotent stem cell cardiomyocyte; microvessel; tissue engineering; vascularization

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APA (6th Edition):

Schaefer, J. (2016). Development of Bi-layer Engineered Cardiac Tissues Containing Cardiomyocytes and Microvessels. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182760

Chicago Manual of Style (16th Edition):

Schaefer, Jeremy. “Development of Bi-layer Engineered Cardiac Tissues Containing Cardiomyocytes and Microvessels.” 2016. Doctoral Dissertation, University of Minnesota. Accessed December 12, 2019. http://hdl.handle.net/11299/182760.

MLA Handbook (7th Edition):

Schaefer, Jeremy. “Development of Bi-layer Engineered Cardiac Tissues Containing Cardiomyocytes and Microvessels.” 2016. Web. 12 Dec 2019.

Vancouver:

Schaefer J. Development of Bi-layer Engineered Cardiac Tissues Containing Cardiomyocytes and Microvessels. [Internet] [Doctoral dissertation]. University of Minnesota; 2016. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11299/182760.

Council of Science Editors:

Schaefer J. Development of Bi-layer Engineered Cardiac Tissues Containing Cardiomyocytes and Microvessels. [Doctoral Dissertation]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/182760


Boston University

19. Rozelle, Sarah Sundstrom. Modeling of sickle cell anemia utilizing disease-specific induced pluripotent stem cells.

Degree: PhD, Molecular Medicine, 2014, Boston University

 Sickle cell anemia, caused by a point mutation that affects the HBB gene, is one of the most common human genetic disorders world-wide and has… (more)

Subjects/Keywords: Molecular biology; Erythropoiesis; Hematopoiesis; Induced pluripotent stem cells; Sickle cell disease

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APA (6th Edition):

Rozelle, S. S. (2014). Modeling of sickle cell anemia utilizing disease-specific induced pluripotent stem cells. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/14672

Chicago Manual of Style (16th Edition):

Rozelle, Sarah Sundstrom. “Modeling of sickle cell anemia utilizing disease-specific induced pluripotent stem cells.” 2014. Doctoral Dissertation, Boston University. Accessed December 12, 2019. http://hdl.handle.net/2144/14672.

MLA Handbook (7th Edition):

Rozelle, Sarah Sundstrom. “Modeling of sickle cell anemia utilizing disease-specific induced pluripotent stem cells.” 2014. Web. 12 Dec 2019.

Vancouver:

Rozelle SS. Modeling of sickle cell anemia utilizing disease-specific induced pluripotent stem cells. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2144/14672.

Council of Science Editors:

Rozelle SS. Modeling of sickle cell anemia utilizing disease-specific induced pluripotent stem cells. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14672


Queens University

20. Zhao, Yimu. The Characterization of Bovine Adipose-Derived Stem Cells in Conventional and Co-culture Environments for Tissue Engineering .

Degree: Chemical Engineering, 2011, Queens University

 Adipose-derived stem cells (ASCs) have been extensively investigated for their applicability in the field of tissue engineering due to their multi-lineage differentiation potential and the… (more)

Subjects/Keywords: Adipose-derived stem cell; co-culture; differentiation; pluripotent

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APA (6th Edition):

Zhao, Y. (2011). The Characterization of Bovine Adipose-Derived Stem Cells in Conventional and Co-culture Environments for Tissue Engineering . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/6335

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):

Zhao, Yimu. “The Characterization of Bovine Adipose-Derived Stem Cells in Conventional and Co-culture Environments for Tissue Engineering .” 2011. Thesis, Queens University. Accessed December 12, 2019. http://hdl.handle.net/1974/6335.

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

MLA Handbook (7th Edition):

Zhao, Yimu. “The Characterization of Bovine Adipose-Derived Stem Cells in Conventional and Co-culture Environments for Tissue Engineering .” 2011. Web. 12 Dec 2019.

Vancouver:

Zhao Y. The Characterization of Bovine Adipose-Derived Stem Cells in Conventional and Co-culture Environments for Tissue Engineering . [Internet] [Thesis]. Queens University; 2011. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/1974/6335.

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

Council of Science Editors:

Zhao Y. The Characterization of Bovine Adipose-Derived Stem Cells in Conventional and Co-culture Environments for Tissue Engineering . [Thesis]. Queens University; 2011. Available from: http://hdl.handle.net/1974/6335

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


UCLA

21. Awe, Jason Patrick. Investigating the Mechanisms of Reprogramming and Optimizing the Generation of Potentially Therapeutically Useful Induced Pluripotent Stem Cell Derivatives.

Degree: Molec & Med Pharmacology, 2014, UCLA

 Human induced pluripotent stem cells (hiPSCs), derived from easily obtainable skin cells, possess enormous opportunity for autologous cellular treatment therapies, gene correction, and disease modeling… (more)

Subjects/Keywords: Pharmacology; Clinical Grade; Human Induced Pluripotent Stem Cells; Immunogenicity; Reprogramming; Stem Cell

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APA (6th Edition):

Awe, J. P. (2014). Investigating the Mechanisms of Reprogramming and Optimizing the Generation of Potentially Therapeutically Useful Induced Pluripotent Stem Cell Derivatives. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/25v79301

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):

Awe, Jason Patrick. “Investigating the Mechanisms of Reprogramming and Optimizing the Generation of Potentially Therapeutically Useful Induced Pluripotent Stem Cell Derivatives.” 2014. Thesis, UCLA. Accessed December 12, 2019. http://www.escholarship.org/uc/item/25v79301.

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

MLA Handbook (7th Edition):

Awe, Jason Patrick. “Investigating the Mechanisms of Reprogramming and Optimizing the Generation of Potentially Therapeutically Useful Induced Pluripotent Stem Cell Derivatives.” 2014. Web. 12 Dec 2019.

Vancouver:

Awe JP. Investigating the Mechanisms of Reprogramming and Optimizing the Generation of Potentially Therapeutically Useful Induced Pluripotent Stem Cell Derivatives. [Internet] [Thesis]. UCLA; 2014. [cited 2019 Dec 12]. Available from: http://www.escholarship.org/uc/item/25v79301.

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

Council of Science Editors:

Awe JP. Investigating the Mechanisms of Reprogramming and Optimizing the Generation of Potentially Therapeutically Useful Induced Pluripotent Stem Cell Derivatives. [Thesis]. UCLA; 2014. Available from: http://www.escholarship.org/uc/item/25v79301

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


University of Pennsylvania

22. Outten, Joel Thomas. Development of a High Throughput Assay to Optimize Hematopoietic Differentiation of Human Pluripotent Stem Cells.

Degree: 2012, University of Pennsylvania

 Human embryonic stem cells (hESCs) offer the potential to develop in vitro protocols for the generation of any human somatic cell. In order for protocols… (more)

Subjects/Keywords: Differentiation; Embryonic stem cells; Hematopoiesis; High Throughput Screening; Megakaryocytes; Pluripotent stem cells; Biomedical; Cell Biology

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APA (6th Edition):

Outten, J. T. (2012). Development of a High Throughput Assay to Optimize Hematopoietic Differentiation of Human Pluripotent Stem Cells. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/559

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):

Outten, Joel Thomas. “Development of a High Throughput Assay to Optimize Hematopoietic Differentiation of Human Pluripotent Stem Cells.” 2012. Thesis, University of Pennsylvania. Accessed December 12, 2019. https://repository.upenn.edu/edissertations/559.

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

MLA Handbook (7th Edition):

Outten, Joel Thomas. “Development of a High Throughput Assay to Optimize Hematopoietic Differentiation of Human Pluripotent Stem Cells.” 2012. Web. 12 Dec 2019.

Vancouver:

Outten JT. Development of a High Throughput Assay to Optimize Hematopoietic Differentiation of Human Pluripotent Stem Cells. [Internet] [Thesis]. University of Pennsylvania; 2012. [cited 2019 Dec 12]. Available from: https://repository.upenn.edu/edissertations/559.

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

Council of Science Editors:

Outten JT. Development of a High Throughput Assay to Optimize Hematopoietic Differentiation of Human Pluripotent Stem Cells. [Thesis]. University of Pennsylvania; 2012. Available from: https://repository.upenn.edu/edissertations/559

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


Virginia Tech

23. Villafranca Locher, Maria Cristina. Fusion of bovine fibroblasts to mouse embryonic stem cells: a model to study nuclear reprogramming.

Degree: PhD, Biomedical and Veterinary Sciences, 2018, Virginia Tech

 The cells from the inner cell mass (ICM) of an early embryo have the potential to differentiate into all the different cell types present in… (more)

Subjects/Keywords: somatic cell nuclear reprogramming; pluripotency; induced pluripotent stem cells; cell fusion; Bos taurus; Mus musculus

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APA (6th Edition):

Villafranca Locher, M. C. (2018). Fusion of bovine fibroblasts to mouse embryonic stem cells: a model to study nuclear reprogramming. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/82864

Chicago Manual of Style (16th Edition):

Villafranca Locher, Maria Cristina. “Fusion of bovine fibroblasts to mouse embryonic stem cells: a model to study nuclear reprogramming.” 2018. Doctoral Dissertation, Virginia Tech. Accessed December 12, 2019. http://hdl.handle.net/10919/82864.

MLA Handbook (7th Edition):

Villafranca Locher, Maria Cristina. “Fusion of bovine fibroblasts to mouse embryonic stem cells: a model to study nuclear reprogramming.” 2018. Web. 12 Dec 2019.

Vancouver:

Villafranca Locher MC. Fusion of bovine fibroblasts to mouse embryonic stem cells: a model to study nuclear reprogramming. [Internet] [Doctoral dissertation]. Virginia Tech; 2018. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/10919/82864.

Council of Science Editors:

Villafranca Locher MC. Fusion of bovine fibroblasts to mouse embryonic stem cells: a model to study nuclear reprogramming. [Doctoral Dissertation]. Virginia Tech; 2018. Available from: http://hdl.handle.net/10919/82864


McMaster University

24. Mechael, Rami. Mechanism of Blood Maturation Induced by Hedgehog Inhibition in Pluripotent Sources.

Degree: MSc, 2013, McMaster University

The generation of hematopoietic progenitors from human pluripotent cell sources for use in personalized medicine is an attainable goal for the ease of clinical… (more)

Subjects/Keywords: human pluripotent stem cells; hematopoiesis; hedgehog signalling; epigenetics; Cell Biology; Cell Biology

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APA (6th Edition):

Mechael, R. (2013). Mechanism of Blood Maturation Induced by Hedgehog Inhibition in Pluripotent Sources. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13502

Chicago Manual of Style (16th Edition):

Mechael, Rami. “Mechanism of Blood Maturation Induced by Hedgehog Inhibition in Pluripotent Sources.” 2013. Masters Thesis, McMaster University. Accessed December 12, 2019. http://hdl.handle.net/11375/13502.

MLA Handbook (7th Edition):

Mechael, Rami. “Mechanism of Blood Maturation Induced by Hedgehog Inhibition in Pluripotent Sources.” 2013. Web. 12 Dec 2019.

Vancouver:

Mechael R. Mechanism of Blood Maturation Induced by Hedgehog Inhibition in Pluripotent Sources. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11375/13502.

Council of Science Editors:

Mechael R. Mechanism of Blood Maturation Induced by Hedgehog Inhibition in Pluripotent Sources. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13502


University of Minnesota

25. Ma, Chao. Derivation of lymphocytes from human induced pluripotent stem cells.

Degree: MS, Comparative and Molecular Biosciences, 2014, University of Minnesota

 Human pluripotent stem cells have the potential to produce essentially unlimited numbers of mature and functional blood lineage populations to study human hematopoiesis. Particularly, human… (more)

Subjects/Keywords: Disease model; Human; Lymphocyte; Natural killer cell; Pluripotent stem cell; Comparative and molecular biosciences

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APA (6th Edition):

Ma, C. (2014). Derivation of lymphocytes from human induced pluripotent stem cells. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/167296

Chicago Manual of Style (16th Edition):

Ma, Chao. “Derivation of lymphocytes from human induced pluripotent stem cells.” 2014. Masters Thesis, University of Minnesota. Accessed December 12, 2019. http://hdl.handle.net/11299/167296.

MLA Handbook (7th Edition):

Ma, Chao. “Derivation of lymphocytes from human induced pluripotent stem cells.” 2014. Web. 12 Dec 2019.

Vancouver:

Ma C. Derivation of lymphocytes from human induced pluripotent stem cells. [Internet] [Masters thesis]. University of Minnesota; 2014. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/11299/167296.

Council of Science Editors:

Ma C. Derivation of lymphocytes from human induced pluripotent stem cells. [Masters Thesis]. University of Minnesota; 2014. Available from: http://hdl.handle.net/11299/167296


University of California – Berkeley

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

Degree: Bioengineering, 2011, University of California – Berkeley

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Zhang, Yolanda Yue. “Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival.” 2011. Thesis, University of California – Berkeley. Accessed December 12, 2019. http://www.escholarship.org/uc/item/40j4h0mn.

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

MLA Handbook (7th Edition):

Zhang, Yolanda Yue. “Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival.” 2011. Web. 12 Dec 2019.

Vancouver:

Zhang YY. Enclosed Microfluidic Platform Realizing Enhanced Stem-cell Survival. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2019 Dec 12]. Available from: http://www.escholarship.org/uc/item/40j4h0mn.

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

Council of Science Editors:

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

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


Indian Institute of Science

27. Abbey, Deepti. Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells.

Degree: 2012, Indian Institute of Science

Pluripotent stem cells (PSCs) are specialized cells, which have remarkable ability to maintain in an undifferentiated state and are capable of undergoing differentiation to three… (more)

Subjects/Keywords: Molecular Regulation; Cardiac Differentiation; Cell Differentiation; Pluripotent Stem Cells; Embryonic Stem Cells; Embryonal Carcinoma Cells; Cardiomyocytes; Cardiomyocyte Differentiation; Mouse Pluripotent Stem Cells; Pluripotent Stem Cells (PSCs); Stem Cell Research; Embryonic Germ Cells; EC-cells; ES-cells; Molecular Biology

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APA (6th Edition):

Abbey, D. (2012). Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2455

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):

Abbey, Deepti. “Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells.” 2012. Thesis, Indian Institute of Science. Accessed December 12, 2019. http://hdl.handle.net/2005/2455.

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

MLA Handbook (7th Edition):

Abbey, Deepti. “Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells.” 2012. Web. 12 Dec 2019.

Vancouver:

Abbey D. Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells. [Internet] [Thesis]. Indian Institute of Science; 2012. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2005/2455.

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

Council of Science Editors:

Abbey D. Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells. [Thesis]. Indian Institute of Science; 2012. Available from: http://hdl.handle.net/2005/2455

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


University of Pennsylvania

28. Cedeno, Ryan James. Histone Variant Macroh2a In The Gut And Beyond: A Study Of Intestinal Fortitude.

Degree: 2017, University of Pennsylvania

 Epigenetic factors guide chromatin remodeling during cell state transitions and confer resistance to genotoxic stressors that could induce deleterious transformations. A particularly peculiar component of… (more)

Subjects/Keywords: Epigenetics; Histones; Histone variants; Induced pluripotent stem cells; Intestinal stem cells; Stem cells; Cell Biology; Developmental Biology; Molecular Biology

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APA (6th Edition):

Cedeno, R. J. (2017). Histone Variant Macroh2a In The Gut And Beyond: A Study Of Intestinal Fortitude. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2206

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):

Cedeno, Ryan James. “Histone Variant Macroh2a In The Gut And Beyond: A Study Of Intestinal Fortitude.” 2017. Thesis, University of Pennsylvania. Accessed December 12, 2019. https://repository.upenn.edu/edissertations/2206.

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

MLA Handbook (7th Edition):

Cedeno, Ryan James. “Histone Variant Macroh2a In The Gut And Beyond: A Study Of Intestinal Fortitude.” 2017. Web. 12 Dec 2019.

Vancouver:

Cedeno RJ. Histone Variant Macroh2a In The Gut And Beyond: A Study Of Intestinal Fortitude. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2019 Dec 12]. Available from: https://repository.upenn.edu/edissertations/2206.

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

Council of Science Editors:

Cedeno RJ. Histone Variant Macroh2a In The Gut And Beyond: A Study Of Intestinal Fortitude. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2206

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


University of Western Ontario

29. Ching, Jamie Emily. The Role of Pannexin 1 during Human Adipogenesis in vitro.

Degree: 2019, University of Western Ontario

 Obesity is the unhealthy accumulation of adipose tissue and affects 10% of the global population. A study reported the loss of mouse pannexin 1 (Panx1),… (more)

Subjects/Keywords: Pannexin 1; Mesenchymal Stem Cells; Adipocytes; Adipose Derived Stem Cells; Adipogenesis; Induced Pluripotent Stem Cells; Medical Cell Biology

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

APA (6th Edition):

Ching, J. E. (2019). The Role of Pannexin 1 during Human Adipogenesis in vitro. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6371

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):

Ching, Jamie Emily. “The Role of Pannexin 1 during Human Adipogenesis in vitro.” 2019. Thesis, University of Western Ontario. Accessed December 12, 2019. https://ir.lib.uwo.ca/etd/6371.

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

MLA Handbook (7th Edition):

Ching, Jamie Emily. “The Role of Pannexin 1 during Human Adipogenesis in vitro.” 2019. Web. 12 Dec 2019.

Vancouver:

Ching JE. The Role of Pannexin 1 during Human Adipogenesis in vitro. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2019 Dec 12]. Available from: https://ir.lib.uwo.ca/etd/6371.

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

Council of Science Editors:

Ching JE. The Role of Pannexin 1 during Human Adipogenesis in vitro. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6371

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


Freie Universität Berlin

30. Schinzel, Robert. Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten.

Degree: 2012, Freie Universität Berlin

 Humane pluripotente Stammzellen (hPSC) haben das Potential die biologische und medizinische Forschung zu revolutionieren. Zuvor müssen jedoch eine Reihe grundlegender Probleme gelöst werden. So sind… (more)

Subjects/Keywords: adipocytes; human embryonic stem cell; human induced pluripotent stem cells; differentiation; stem cells; programming; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie

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

APA (6th Edition):

Schinzel, R. (2012). Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/10315

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):

Schinzel, Robert. “Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten.” 2012. Thesis, Freie Universität Berlin. Accessed December 12, 2019. https://refubium.fu-berlin.de/handle/fub188/10315.

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

MLA Handbook (7th Edition):

Schinzel, Robert. “Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten.” 2012. Web. 12 Dec 2019.

Vancouver:

Schinzel R. Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2019 Dec 12]. Available from: https://refubium.fu-berlin.de/handle/fub188/10315.

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

Council of Science Editors:

Schinzel R. Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten. [Thesis]. Freie Universität Berlin; 2012. Available from: https://refubium.fu-berlin.de/handle/fub188/10315

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

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