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You searched for subject:(Human induced pluripotent stem iPS cells). Showing records 1 – 30 of 75365 total matches.

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NSYSU

1. Wang, Yin-Hsuan. The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells.

Degree: Master, Biological Sciences, 2017, NSYSU

 We previously described that PKA/GSKIP/GSK3β complex serves as a platform to anchor and phosphorylate Drp1 affecting mitochondria dynamics to provide neuroprotection. Recently, a known PKA/GSK3β… (more)

Subjects/Keywords: PKA; Tau; Alzheimer disease; Human induced pluripotent stem (iPS) cells; Aβ precursor protein (; GSK3β; GSKIP

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

APA (6th Edition):

Wang, Y. (2017). The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0404117-114837

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):

Wang, Yin-Hsuan. “The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells.” 2017. Thesis, NSYSU. Accessed April 11, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0404117-114837.

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

MLA Handbook (7th Edition):

Wang, Yin-Hsuan. “The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells.” 2017. Web. 11 Apr 2021.

Vancouver:

Wang Y. The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells. [Internet] [Thesis]. NSYSU; 2017. [cited 2021 Apr 11]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0404117-114837.

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

Council of Science Editors:

Wang Y. The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0404117-114837

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


Universiteit Utrecht

2. Hoeven, T. van den. Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming.

Degree: 2014, Universiteit Utrecht

 Induction of pluripotency is a process that reverses the phenotype of terminally differentiated cells. Somatic cells, induced by specific transcription factors, are reprogrammed to a… (more)

Subjects/Keywords: Stem Cells; Induced Pluripotent Stem Cells; iPS; pre-iPS; reprogramming; transcription factors

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APA (6th Edition):

Hoeven, T. v. d. (2014). Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/297927

Chicago Manual of Style (16th Edition):

Hoeven, T van den. “Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming.” 2014. Masters Thesis, Universiteit Utrecht. Accessed April 11, 2021. http://dspace.library.uu.nl:8080/handle/1874/297927.

MLA Handbook (7th Edition):

Hoeven, T van den. “Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming.” 2014. Web. 11 Apr 2021.

Vancouver:

Hoeven Tvd. Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2021 Apr 11]. Available from: http://dspace.library.uu.nl:8080/handle/1874/297927.

Council of Science Editors:

Hoeven Tvd. Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/297927


University of Edinburgh

3. Sartori, Chiara. Generation of ovine induced pluripotent stem cells.

Degree: PhD, 2012, University of Edinburgh

 Embryonic stem cells (ESCs) are pluripotent cells derived from the early embryo and are able to differentiate into cells belonging to the three germ layers.… (more)

Subjects/Keywords: 636.089; ovine iPS cells; induced pluripotent stem cells; iPSCs

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APA (6th Edition):

Sartori, C. (2012). Generation of ovine induced pluripotent stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/6491

Chicago Manual of Style (16th Edition):

Sartori, Chiara. “Generation of ovine induced pluripotent stem cells.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed April 11, 2021. http://hdl.handle.net/1842/6491.

MLA Handbook (7th Edition):

Sartori, Chiara. “Generation of ovine induced pluripotent stem cells.” 2012. Web. 11 Apr 2021.

Vancouver:

Sartori C. Generation of ovine induced pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1842/6491.

Council of Science Editors:

Sartori C. Generation of ovine induced pluripotent stem cells. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/6491


University of Southern California

4. Pomeroy, Jordan Elliott. Derivation and characterization of human embryonic stem (hES) cells and human induced pluripotent stem (hiPS) cells in clinical grade conditions.

Degree: PhD, Systems Biology and Disease, 2012, University of Southern California

 Future use of pluripotent cells for regenerative medicine will require the derivation and characterization of new cell lines in clinical grade conditions. Removing potential sources… (more)

Subjects/Keywords: embryonic; stem; induced; pluripotent; cells; clinical; human

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APA (6th Edition):

Pomeroy, J. E. (2012). Derivation and characterization of human embryonic stem (hES) cells and human induced pluripotent stem (hiPS) cells in clinical grade conditions. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/20555/rec/1847

Chicago Manual of Style (16th Edition):

Pomeroy, Jordan Elliott. “Derivation and characterization of human embryonic stem (hES) cells and human induced pluripotent stem (hiPS) cells in clinical grade conditions.” 2012. Doctoral Dissertation, University of Southern California. Accessed April 11, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/20555/rec/1847.

MLA Handbook (7th Edition):

Pomeroy, Jordan Elliott. “Derivation and characterization of human embryonic stem (hES) cells and human induced pluripotent stem (hiPS) cells in clinical grade conditions.” 2012. Web. 11 Apr 2021.

Vancouver:

Pomeroy JE. Derivation and characterization of human embryonic stem (hES) cells and human induced pluripotent stem (hiPS) cells in clinical grade conditions. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Apr 11]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/20555/rec/1847.

Council of Science Editors:

Pomeroy JE. Derivation and characterization of human embryonic stem (hES) cells and human induced pluripotent stem (hiPS) cells in clinical grade conditions. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/20555/rec/1847


University of Georgia

5. Avery, John Welch. Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells.

Degree: 2018, University of Georgia

Human pluripotent stem cells (hPSCs) are powerful tools to aid in the interrogation of the mechanisms of pathology of developmental disorders as well as modeling… (more)

Subjects/Keywords: Brown adipocytes; human pluripotent stem cells, induced pluripotent stem cells, neural crest cells, paraxial mesoderm

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APA (6th Edition):

Avery, J. W. (2018). Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/37263

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):

Avery, John Welch. “Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells.” 2018. Thesis, University of Georgia. Accessed April 11, 2021. http://hdl.handle.net/10724/37263.

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

MLA Handbook (7th Edition):

Avery, John Welch. “Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells.” 2018. Web. 11 Apr 2021.

Vancouver:

Avery JW. Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells. [Internet] [Thesis]. University of Georgia; 2018. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/10724/37263.

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

Council of Science Editors:

Avery JW. Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells. [Thesis]. University of Georgia; 2018. Available from: http://hdl.handle.net/10724/37263

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


University of Georgia

6. Avery, John Welch. Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells.

Degree: 2018, University of Georgia

Human pluripotent stem cells (hPSCs) are powerful tools to aid in the interrogation of the mechanisms of pathology of developmental disorders as well as modeling… (more)

Subjects/Keywords: Brown adipocytes; human pluripotent stem cells, induced pluripotent stem cells, neural crest cells, paraxial mesoderm

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APA (6th Edition):

Avery, J. W. (2018). Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/37106

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):

Avery, John Welch. “Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells.” 2018. Thesis, University of Georgia. Accessed April 11, 2021. http://hdl.handle.net/10724/37106.

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

MLA Handbook (7th Edition):

Avery, John Welch. “Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells.” 2018. Web. 11 Apr 2021.

Vancouver:

Avery JW. Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells. [Internet] [Thesis]. University of Georgia; 2018. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/10724/37106.

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

Council of Science Editors:

Avery JW. Modeling treacher collins syndrome and directed differentiation of brown adipocytes from human pluripotent stem cells. [Thesis]. University of Georgia; 2018. Available from: http://hdl.handle.net/10724/37106

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


University of Iowa

7. Manzar, Gohar Shahwar. Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells.

Degree: PhD, Biomedical Engineering, 2015, University of Iowa

  Type I diabetes (T1D) is caused by autoimmune destruction of pancreatic β-cells. Immediate consequences of T1D are severe weight loss, ketoacidosis and death unless… (more)

Subjects/Keywords: Diabetes; Induced Pluripotent Stem Cells; Insulin Producing Cells; iPS cells; Stem Cells; Tissue Engineering; Biomedical Engineering and Bioengineering

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APA (6th Edition):

Manzar, G. S. (2015). Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5808

Chicago Manual of Style (16th Edition):

Manzar, Gohar Shahwar. “Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells.” 2015. Doctoral Dissertation, University of Iowa. Accessed April 11, 2021. https://ir.uiowa.edu/etd/5808.

MLA Handbook (7th Edition):

Manzar, Gohar Shahwar. “Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells.” 2015. Web. 11 Apr 2021.

Vancouver:

Manzar GS. Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2021 Apr 11]. Available from: https://ir.uiowa.edu/etd/5808.

Council of Science Editors:

Manzar GS. Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/5808

8. Paredes, Maria Guadalupe. Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine.

Degree: Biomedical Engineering, 2018, Brown University

 Ischemic heart disease is the leading cause of death globally, which takes more than 17.7 million lives every year (WHO, 2018), yet current treatments and… (more)

Subjects/Keywords: induced pluripotent stem cells

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APA (6th Edition):

Paredes, M. G. (2018). Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine. (Thesis). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:792836/

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):

Paredes, Maria Guadalupe. “Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine.” 2018. Thesis, Brown University. Accessed April 11, 2021. https://repository.library.brown.edu/studio/item/bdr:792836/.

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

MLA Handbook (7th Edition):

Paredes, Maria Guadalupe. “Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine.” 2018. Web. 11 Apr 2021.

Vancouver:

Paredes MG. Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine. [Internet] [Thesis]. Brown University; 2018. [cited 2021 Apr 11]. Available from: https://repository.library.brown.edu/studio/item/bdr:792836/.

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

Council of Science Editors:

Paredes MG. Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine. [Thesis]. Brown University; 2018. Available from: https://repository.library.brown.edu/studio/item/bdr:792836/

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


University of Oxford

9. Khoja, Suhail. HSV-1 amplicon system for human artificial chromosome formation in human ES/iPS cells and pluripotency induction.

Degree: PhD, 2012, University of Oxford

 Development of safe and efficient approaches for gene delivery in human embryonic stem cells (hESc) and particularly in human induced pluripotent stem (hiPS) cells, which… (more)

Subjects/Keywords: 616.02774; Medical Sciences; Genetics; Stem cells; Human artificial chromosomes (HAC); Human embryonic stem cells (hESc); induced pluripotent stem cells (iPS); Herpes Simplex Virus (HSV)-1 amplicon system; gene delivery; gene therapy

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APA (6th Edition):

Khoja, S. (2012). HSV-1 amplicon system for human artificial chromosome formation in human ES/iPS cells and pluripotency induction. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:6b04170b-f2d9-4114-9511-05a1a98ccfec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561115

Chicago Manual of Style (16th Edition):

Khoja, Suhail. “HSV-1 amplicon system for human artificial chromosome formation in human ES/iPS cells and pluripotency induction.” 2012. Doctoral Dissertation, University of Oxford. Accessed April 11, 2021. http://ora.ox.ac.uk/objects/uuid:6b04170b-f2d9-4114-9511-05a1a98ccfec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561115.

MLA Handbook (7th Edition):

Khoja, Suhail. “HSV-1 amplicon system for human artificial chromosome formation in human ES/iPS cells and pluripotency induction.” 2012. Web. 11 Apr 2021.

Vancouver:

Khoja S. HSV-1 amplicon system for human artificial chromosome formation in human ES/iPS cells and pluripotency induction. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2021 Apr 11]. Available from: http://ora.ox.ac.uk/objects/uuid:6b04170b-f2d9-4114-9511-05a1a98ccfec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561115.

Council of Science Editors:

Khoja S. HSV-1 amplicon system for human artificial chromosome formation in human ES/iPS cells and pluripotency induction. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:6b04170b-f2d9-4114-9511-05a1a98ccfec ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.561115


Harvard University

10. McLaughlin, Heather Ward. Modeling sporadic Alzheimer's disease using induced pluripotent stem cells.

Degree: PhD, Biology: Medical Sciences, Division of, 2014, Harvard University

 Despite being the leading cause of neurodegeneration and dementia in the aging brain, the cause of Alzheimer's disease (AD) remains unknown in most patients. The… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Neurosciences; Alzheimer's disease; induced pluripotent stem cells; iPS cells; neural progenitors; neuronal differentiation

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APA (6th Edition):

McLaughlin, H. W. (2014). Modeling sporadic Alzheimer's disease using induced pluripotent stem cells. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13094355

Chicago Manual of Style (16th Edition):

McLaughlin, Heather Ward. “Modeling sporadic Alzheimer's disease using induced pluripotent stem cells.” 2014. Doctoral Dissertation, Harvard University. Accessed April 11, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13094355.

MLA Handbook (7th Edition):

McLaughlin, Heather Ward. “Modeling sporadic Alzheimer's disease using induced pluripotent stem cells.” 2014. Web. 11 Apr 2021.

Vancouver:

McLaughlin HW. Modeling sporadic Alzheimer's disease using induced pluripotent stem cells. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2021 Apr 11]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13094355.

Council of Science Editors:

McLaughlin HW. Modeling sporadic Alzheimer's disease using induced pluripotent stem cells. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13094355


University of Minnesota

11. Wendel, Jacqueline. Engineered Cardiac Tissues for Delivery of Cells to the Injured Myocardium.

Degree: PhD, Biomedical Engineering, 2015, University of Minnesota

 With the high incidence of heart failure in the developing world and the inherent risks and limited availability of donor hearts, cell-based solutions have become… (more)

Subjects/Keywords: Cardiac; Human Induced Pluripotent Stem Cells; Myocardial Infarction; Preclinical; Tissue Engineering

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APA (6th Edition):

Wendel, J. (2015). Engineered Cardiac Tissues for Delivery of Cells to the Injured Myocardium. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/175369

Chicago Manual of Style (16th Edition):

Wendel, Jacqueline. “Engineered Cardiac Tissues for Delivery of Cells to the Injured Myocardium.” 2015. Doctoral Dissertation, University of Minnesota. Accessed April 11, 2021. http://hdl.handle.net/11299/175369.

MLA Handbook (7th Edition):

Wendel, Jacqueline. “Engineered Cardiac Tissues for Delivery of Cells to the Injured Myocardium.” 2015. Web. 11 Apr 2021.

Vancouver:

Wendel J. Engineered Cardiac Tissues for Delivery of Cells to the Injured Myocardium. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/11299/175369.

Council of Science Editors:

Wendel J. Engineered Cardiac Tissues for Delivery of Cells to the Injured Myocardium. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/175369

12. Martins, Manuella. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.

Degree: 2013, Instituto Politécnico do Porto

A família de proteínas Shank é o principal conjunto de proteinas de suporte e está localizada na densidade pós-sináptica das sinapses excitatórias. Existem 3 genes… (more)

Subjects/Keywords: Shank3; Células estaminais pluripotente induzidas (iPS); Autism Spectrum Disorder (ASD); Phelan-McDermid Sindrome (PMS); mGluR5; Induced-pluripotent stem (iPS) cells; Cellule staminali pluripotente indotte (iPS)

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APA (6th Edition):

Martins, M. (2013). Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. (Thesis). Instituto Politécnico do Porto. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369

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):

Martins, Manuella. “Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.” 2013. Thesis, Instituto Politécnico do Porto. Accessed April 11, 2021. https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369.

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

MLA Handbook (7th Edition):

Martins, Manuella. “Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.” 2013. Web. 11 Apr 2021.

Vancouver:

Martins M. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. [Internet] [Thesis]. Instituto Politécnico do Porto; 2013. [cited 2021 Apr 11]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369.

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

Council of Science Editors:

Martins M. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. [Thesis]. Instituto Politécnico do Porto; 2013. Available from: https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369

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


Penn State University

13. Lin, Tzu Ting. 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. T. (2017). DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS. (Thesis). Penn State University. Retrieved from https://submit-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 Ting. “DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS.” 2017. Thesis, Penn State University. Accessed April 11, 2021. https://submit-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 Ting. “DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS.” 2017. Web. 11 Apr 2021.

Vancouver:

Lin TT. DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS. [Internet] [Thesis]. Penn State University; 2017. [cited 2021 Apr 11]. Available from: https://submit-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 TT. DEFINED AND XENO-FREE CULTURE FOR HUMAN PLURIPOTENT STEM CELLS. [Thesis]. Penn State University; 2017. Available from: https://submit-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


University of Georgia

14. Hayworth, Miranda Kristine. Multipotent mesothelial progenitors derived from human pluripotent stem cells function in development and tissue repair.

Degree: 2016, University of Georgia

 The mesothelium, which constitutes the outermost layer of the coelomic organs including the heart, lung, liver and gut, plays a critical role in the development,… (more)

Subjects/Keywords: Human embryonic stem cells, human induced pluripotent stem cells; mesothelium; pluripotency; differentiation; regeneration; mesenchymal stem cells

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APA (6th Edition):

Hayworth, M. K. (2016). Multipotent mesothelial progenitors derived from human pluripotent stem cells function in development and tissue repair. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/34226

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):

Hayworth, Miranda Kristine. “Multipotent mesothelial progenitors derived from human pluripotent stem cells function in development and tissue repair.” 2016. Thesis, University of Georgia. Accessed April 11, 2021. http://hdl.handle.net/10724/34226.

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

MLA Handbook (7th Edition):

Hayworth, Miranda Kristine. “Multipotent mesothelial progenitors derived from human pluripotent stem cells function in development and tissue repair.” 2016. Web. 11 Apr 2021.

Vancouver:

Hayworth MK. Multipotent mesothelial progenitors derived from human pluripotent stem cells function in development and tissue repair. [Internet] [Thesis]. University of Georgia; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/10724/34226.

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

Council of Science Editors:

Hayworth MK. Multipotent mesothelial progenitors derived from human pluripotent stem cells function in development and tissue repair. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/34226

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

15. Vinícius Bassaneze. Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT.

Degree: 2012, University of São Paulo

 Os vírus são eficazes na transferência de genes em células devido aos seus mecanismos especializados. No entanto, vírus como veículos de entrega de genes podem… (more)

Subjects/Keywords: Células iPS; Células-tronco pluripotentes induzidas; Genes TAT; Proteínas recombinantes de fusão; Reprogramação nuclear; TATkappa; Genes TAT; Induced pluripotent stem cells; IPS cells; Nuclear reprogramming; Recombinant fusion protein; TATkappa

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APA (6th Edition):

Bassaneze, V. (2012). Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5166/tde-11052012-093336/

Chicago Manual of Style (16th Edition):

Bassaneze, Vinícius. “Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT.” 2012. Doctoral Dissertation, University of São Paulo. Accessed April 11, 2021. http://www.teses.usp.br/teses/disponiveis/5/5166/tde-11052012-093336/.

MLA Handbook (7th Edition):

Bassaneze, Vinícius. “Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT.” 2012. Web. 11 Apr 2021.

Vancouver:

Bassaneze V. Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2021 Apr 11]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5166/tde-11052012-093336/.

Council of Science Editors:

Bassaneze V. Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT. [Doctoral Dissertation]. University of São Paulo; 2012. Available from: http://www.teses.usp.br/teses/disponiveis/5/5166/tde-11052012-093336/


UCLA

16. 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 April 11, 2021. 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. 11 Apr 2021.

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 2021 Apr 11]. 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


Freie Universität Berlin

17. 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 (6th Edition):

Schinzel, R. (2012). Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-14513

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 April 11, 2021. http://dx.doi.org/10.17169/refubium-14513.

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. 11 Apr 2021.

Vancouver:

Schinzel R. Die Kultur und Differenzierung von Humanen Embryonalen Stammzellen in Braune und Weisse Adipozyten. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2021 Apr 11]. Available from: http://dx.doi.org/10.17169/refubium-14513.

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: http://dx.doi.org/10.17169/refubium-14513

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

18. Duchartre, Yann. Biothérapies des porphyries érythropoïétiques : thérapie cellulaire, thérapie génique et approche pharmacologique : Biotherapies of erythropoietic porphyrias : cell therapy, gene therapy and pharmacological approach.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2012, Université de Bordeaux Segalen

Les porphyries érythropoïétiques (PE) : Porphyrie Erythropoïétique Congénitale -PEC- et Protoporphyrie Erythropoïétique -PPE- sont caractérisées par le déficit d’une des enzymes de la voie de… (more)

Subjects/Keywords: Porphyries érythropoïétiques; Thérapies cellulaire et génique; Cellules souches pluripotentes induites (iPS); Erythropoietic porphyrias; Cell and gene therapies; Induced pluripotent stem cells (iPS)

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APA (6th Edition):

Duchartre, Y. (2012). Biothérapies des porphyries érythropoïétiques : thérapie cellulaire, thérapie génique et approche pharmacologique : Biotherapies of erythropoietic porphyrias : cell therapy, gene therapy and pharmacological approach. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2012BOR21994

Chicago Manual of Style (16th Edition):

Duchartre, Yann. “Biothérapies des porphyries érythropoïétiques : thérapie cellulaire, thérapie génique et approche pharmacologique : Biotherapies of erythropoietic porphyrias : cell therapy, gene therapy and pharmacological approach.” 2012. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed April 11, 2021. http://www.theses.fr/2012BOR21994.

MLA Handbook (7th Edition):

Duchartre, Yann. “Biothérapies des porphyries érythropoïétiques : thérapie cellulaire, thérapie génique et approche pharmacologique : Biotherapies of erythropoietic porphyrias : cell therapy, gene therapy and pharmacological approach.” 2012. Web. 11 Apr 2021.

Vancouver:

Duchartre Y. Biothérapies des porphyries érythropoïétiques : thérapie cellulaire, thérapie génique et approche pharmacologique : Biotherapies of erythropoietic porphyrias : cell therapy, gene therapy and pharmacological approach. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2012. [cited 2021 Apr 11]. Available from: http://www.theses.fr/2012BOR21994.

Council of Science Editors:

Duchartre Y. Biothérapies des porphyries érythropoïétiques : thérapie cellulaire, thérapie génique et approche pharmacologique : Biotherapies of erythropoietic porphyrias : cell therapy, gene therapy and pharmacological approach. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2012. Available from: http://www.theses.fr/2012BOR21994

19. Cereso, Nicolas. Preuve de concept de thérapie génique d’une dystrophie rétinienne en l’absence de modèle animal de la pathologie : cas de la Choroïdérémie : Proof of concept of gene therapy of retinal dystrophy in the absence of animal model of the disease : case of Choroideremia.

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

Les dystrophies rétiniennes héréditaires (DRH) sont des maladies qui conduisent à une perte de la vision au cours de leur évolution. Les premiers essais cliniques… (more)

Subjects/Keywords: Cellules souches pluripotentes induites (iPS); Dystrophies rétiniennes; Thérapie génique; Choroïdérémie; Epithélium Pigmentaire Rétinien (EPR); Induced Pluripotent Stem cells (iPS); Retinal Dystrophies; Gene Therapy; Choroideremia; Retinal Pigment Epithelium (RPE)

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APA (6th Edition):

Cereso, N. (2014). Preuve de concept de thérapie génique d’une dystrophie rétinienne en l’absence de modèle animal de la pathologie : cas de la Choroïdérémie : Proof of concept of gene therapy of retinal dystrophy in the absence of animal model of the disease : case of Choroideremia. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2014MON1T019

Chicago Manual of Style (16th Edition):

Cereso, Nicolas. “Preuve de concept de thérapie génique d’une dystrophie rétinienne en l’absence de modèle animal de la pathologie : cas de la Choroïdérémie : Proof of concept of gene therapy of retinal dystrophy in the absence of animal model of the disease : case of Choroideremia.” 2014. Doctoral Dissertation, Université Montpellier I. Accessed April 11, 2021. http://www.theses.fr/2014MON1T019.

MLA Handbook (7th Edition):

Cereso, Nicolas. “Preuve de concept de thérapie génique d’une dystrophie rétinienne en l’absence de modèle animal de la pathologie : cas de la Choroïdérémie : Proof of concept of gene therapy of retinal dystrophy in the absence of animal model of the disease : case of Choroideremia.” 2014. Web. 11 Apr 2021.

Vancouver:

Cereso N. Preuve de concept de thérapie génique d’une dystrophie rétinienne en l’absence de modèle animal de la pathologie : cas de la Choroïdérémie : Proof of concept of gene therapy of retinal dystrophy in the absence of animal model of the disease : case of Choroideremia. [Internet] [Doctoral dissertation]. Université Montpellier I; 2014. [cited 2021 Apr 11]. Available from: http://www.theses.fr/2014MON1T019.

Council of Science Editors:

Cereso N. Preuve de concept de thérapie génique d’une dystrophie rétinienne en l’absence de modèle animal de la pathologie : cas de la Choroïdérémie : Proof of concept of gene therapy of retinal dystrophy in the absence of animal model of the disease : case of Choroideremia. [Doctoral Dissertation]. Université Montpellier I; 2014. Available from: http://www.theses.fr/2014MON1T019

20. Fabiana Fernandes Bressan. Geração de células pluripotentes através da indução gênica e transferência de núcleo: modelo bovino de aquisição de pluripotência.

Degree: 2013, University of São Paulo

 Estratégias como a transferência nuclear e a reprogramação induzida vêm sendo empregadas com o objetivo de induzir células somáticas a um estado pluripotente similar ao… (more)

Subjects/Keywords: Bovino; Células pluripotentes induzidas (iPS); Pluripotência; Reprogramação celular; Transferência de núcleo; Bovine; Cellular reprogramming; Induced pluripotent stem cells (iPS); Nuclear transfers; Pluripotency

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APA (6th Edition):

Bressan, F. F. (2013). Geração de células pluripotentes através da indução gênica e transferência de núcleo: modelo bovino de aquisição de pluripotência. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/74/74131/tde-04072013-151314/

Chicago Manual of Style (16th Edition):

Bressan, Fabiana Fernandes. “Geração de células pluripotentes através da indução gênica e transferência de núcleo: modelo bovino de aquisição de pluripotência.” 2013. Doctoral Dissertation, University of São Paulo. Accessed April 11, 2021. http://www.teses.usp.br/teses/disponiveis/74/74131/tde-04072013-151314/.

MLA Handbook (7th Edition):

Bressan, Fabiana Fernandes. “Geração de células pluripotentes através da indução gênica e transferência de núcleo: modelo bovino de aquisição de pluripotência.” 2013. Web. 11 Apr 2021.

Vancouver:

Bressan FF. Geração de células pluripotentes através da indução gênica e transferência de núcleo: modelo bovino de aquisição de pluripotência. [Internet] [Doctoral dissertation]. University of São Paulo; 2013. [cited 2021 Apr 11]. Available from: http://www.teses.usp.br/teses/disponiveis/74/74131/tde-04072013-151314/.

Council of Science Editors:

Bressan FF. Geração de células pluripotentes através da indução gênica e transferência de núcleo: modelo bovino de aquisição de pluripotência. [Doctoral Dissertation]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/74/74131/tde-04072013-151314/


Universiteit Utrecht

21. Kolijn, K. The origin and future of hematopoietic stem cells.

Degree: 2012, Universiteit Utrecht

 Hematopoietic stem cell (HSCs) therapy in the form of bone marrow transplantations has been used successfully in the clinic for over 40 years and continues… (more)

Subjects/Keywords: Hematopoietic stem cells; embryonic stem cells; induced pluripotent stem cells; ontogeny

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APA (6th Edition):

Kolijn, K. (2012). The origin and future of hematopoietic stem cells. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/238606

Chicago Manual of Style (16th Edition):

Kolijn, K. “The origin and future of hematopoietic stem cells.” 2012. Masters Thesis, Universiteit Utrecht. Accessed April 11, 2021. http://dspace.library.uu.nl:8080/handle/1874/238606.

MLA Handbook (7th Edition):

Kolijn, K. “The origin and future of hematopoietic stem cells.” 2012. Web. 11 Apr 2021.

Vancouver:

Kolijn K. The origin and future of hematopoietic stem cells. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2021 Apr 11]. Available from: http://dspace.library.uu.nl:8080/handle/1874/238606.

Council of Science Editors:

Kolijn K. The origin and future of hematopoietic stem cells. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/238606


Louisiana State University

22. Addison, Meredith Kathleen. Lentiviral transduction of epigenetically modified bovine adult stem cells.

Degree: MS, Animal Sciences, 2012, Louisiana State University

 Bovine adipose-derived stem cells (ADS), a form of adult stem cells, are somatic cells that have similar characteristics of embryonic stem (ES) cells. Bovine ADS… (more)

Subjects/Keywords: bovine adult stem cells; induced pluripotent stem cells; stem cells

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APA (6th Edition):

Addison, M. K. (2012). Lentiviral transduction of epigenetically modified bovine adult stem cells. (Masters Thesis). Louisiana State University. Retrieved from etd-07162012-103728 ; https://digitalcommons.lsu.edu/gradschool_theses/4024

Chicago Manual of Style (16th Edition):

Addison, Meredith Kathleen. “Lentiviral transduction of epigenetically modified bovine adult stem cells.” 2012. Masters Thesis, Louisiana State University. Accessed April 11, 2021. etd-07162012-103728 ; https://digitalcommons.lsu.edu/gradschool_theses/4024.

MLA Handbook (7th Edition):

Addison, Meredith Kathleen. “Lentiviral transduction of epigenetically modified bovine adult stem cells.” 2012. Web. 11 Apr 2021.

Vancouver:

Addison MK. Lentiviral transduction of epigenetically modified bovine adult stem cells. [Internet] [Masters thesis]. Louisiana State University; 2012. [cited 2021 Apr 11]. Available from: etd-07162012-103728 ; https://digitalcommons.lsu.edu/gradschool_theses/4024.

Council of Science Editors:

Addison MK. Lentiviral transduction of epigenetically modified bovine adult stem cells. [Masters Thesis]. Louisiana State University; 2012. Available from: etd-07162012-103728 ; https://digitalcommons.lsu.edu/gradschool_theses/4024


University of Melbourne

23. Viventi, Serena. Characterization of dorsal root ganglia sensory neurons from human pluripotent stem cells and their application for developing therapies to treat Friedreich Ataxia.

Degree: 2019, University of Melbourne

 Sensory neurons of the dorsal root ganglia (DRG) are the primary responders to stimuli inducing feelings of touch, pain, temperature, vibration, pressure and muscle tension.… (more)

Subjects/Keywords: sensory neurons; human embryonic stem cells; induced pluripotent stem cells; Friedreich Ataxia; Dorsal Root Ganglia; stem cell therapy; gene-delivery; nanoparticles

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APA (6th Edition):

Viventi, S. (2019). Characterization of dorsal root ganglia sensory neurons from human pluripotent stem cells and their application for developing therapies to treat Friedreich Ataxia. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/227456

Chicago Manual of Style (16th Edition):

Viventi, Serena. “Characterization of dorsal root ganglia sensory neurons from human pluripotent stem cells and their application for developing therapies to treat Friedreich Ataxia.” 2019. Doctoral Dissertation, University of Melbourne. Accessed April 11, 2021. http://hdl.handle.net/11343/227456.

MLA Handbook (7th Edition):

Viventi, Serena. “Characterization of dorsal root ganglia sensory neurons from human pluripotent stem cells and their application for developing therapies to treat Friedreich Ataxia.” 2019. Web. 11 Apr 2021.

Vancouver:

Viventi S. Characterization of dorsal root ganglia sensory neurons from human pluripotent stem cells and their application for developing therapies to treat Friedreich Ataxia. [Internet] [Doctoral dissertation]. University of Melbourne; 2019. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/11343/227456.

Council of Science Editors:

Viventi S. Characterization of dorsal root ganglia sensory neurons from human pluripotent stem cells and their application for developing therapies to treat Friedreich Ataxia. [Doctoral Dissertation]. University of Melbourne; 2019. Available from: http://hdl.handle.net/11343/227456


Universiteit Utrecht

24. Wever, I. From fibroblast to neuron: The use of stem cells for Parkinson's disease.

Degree: 2012, Universiteit Utrecht

 One of the characterizations of Parkinson’s disease (PD) is the motor symptoms caused by the loss of the dopaminergic neurons of the substantia nigra pars… (more)

Subjects/Keywords: Parkinson's disease; Pluripotent Stem cells; Embryonic Stem cells; induced Pluripotent Stem cells; Neural development

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APA (6th Edition):

Wever, I. (2012). From fibroblast to neuron: The use of stem cells for Parkinson's disease. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/258934

Chicago Manual of Style (16th Edition):

Wever, I. “From fibroblast to neuron: The use of stem cells for Parkinson's disease.” 2012. Masters Thesis, Universiteit Utrecht. Accessed April 11, 2021. http://dspace.library.uu.nl:8080/handle/1874/258934.

MLA Handbook (7th Edition):

Wever, I. “From fibroblast to neuron: The use of stem cells for Parkinson's disease.” 2012. Web. 11 Apr 2021.

Vancouver:

Wever I. From fibroblast to neuron: The use of stem cells for Parkinson's disease. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2021 Apr 11]. Available from: http://dspace.library.uu.nl:8080/handle/1874/258934.

Council of Science Editors:

Wever I. From fibroblast to neuron: The use of stem cells for Parkinson's disease. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/258934


California State University – Sacramento

25. Roenspie, Sean P. An isogenic case-control study in which clonal cell lines are generated from a fibroblast population derived from an individual with a complex mosaic distribution of FMR1 alleles.

Degree: MA, Biological Science (Stem Cell, 2011, California State University – Sacramento

 Fragile X-associated tremor/ataxia syndrome (FXTAS) is an adult onset neurodegenerative disorder affecting carriers of premutation expansions (55-200 CGG repeats) of the fragile X mental retardation… (more)

Subjects/Keywords: FXTAS; Neurodegenerative diseases; Induced pluripotent stem cells

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APA (6th Edition):

Roenspie, S. P. (2011). An isogenic case-control study in which clonal cell lines are generated from a fibroblast population derived from an individual with a complex mosaic distribution of FMR1 alleles. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.9/1093

Chicago Manual of Style (16th Edition):

Roenspie, Sean P. “An isogenic case-control study in which clonal cell lines are generated from a fibroblast population derived from an individual with a complex mosaic distribution of FMR1 alleles.” 2011. Masters Thesis, California State University – Sacramento. Accessed April 11, 2021. http://hdl.handle.net/10211.9/1093.

MLA Handbook (7th Edition):

Roenspie, Sean P. “An isogenic case-control study in which clonal cell lines are generated from a fibroblast population derived from an individual with a complex mosaic distribution of FMR1 alleles.” 2011. Web. 11 Apr 2021.

Vancouver:

Roenspie SP. An isogenic case-control study in which clonal cell lines are generated from a fibroblast population derived from an individual with a complex mosaic distribution of FMR1 alleles. [Internet] [Masters thesis]. California State University – Sacramento; 2011. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/10211.9/1093.

Council of Science Editors:

Roenspie SP. An isogenic case-control study in which clonal cell lines are generated from a fibroblast population derived from an individual with a complex mosaic distribution of FMR1 alleles. [Masters Thesis]. California State University – Sacramento; 2011. Available from: http://hdl.handle.net/10211.9/1093


University of California – Irvine

26. Abud, Edsel Misael. Generation of Human Microglia from Induced Pluripotent Stem Cells to Study Innate Immunity in Neurological Diseases.

Degree: Biological Sciences, 2017, University of California – Irvine

 Microglia play an important role in developmental and homeostatic brain function. They profoundly influence the development and progression of neurological disorders, including Alzheimer’s disease (AD).… (more)

Subjects/Keywords: Neurosciences; Immunology; alzheimer's disease; disease modeling; human-mouse transplantation; induced pluripotent stem cells; microglia

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APA (6th Edition):

Abud, E. M. (2017). Generation of Human Microglia from Induced Pluripotent Stem Cells to Study Innate Immunity in Neurological Diseases. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/12b1q5fv

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):

Abud, Edsel Misael. “Generation of Human Microglia from Induced Pluripotent Stem Cells to Study Innate Immunity in Neurological Diseases.” 2017. Thesis, University of California – Irvine. Accessed April 11, 2021. http://www.escholarship.org/uc/item/12b1q5fv.

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

MLA Handbook (7th Edition):

Abud, Edsel Misael. “Generation of Human Microglia from Induced Pluripotent Stem Cells to Study Innate Immunity in Neurological Diseases.” 2017. Web. 11 Apr 2021.

Vancouver:

Abud EM. Generation of Human Microglia from Induced Pluripotent Stem Cells to Study Innate Immunity in Neurological Diseases. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2021 Apr 11]. Available from: http://www.escholarship.org/uc/item/12b1q5fv.

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

Council of Science Editors:

Abud EM. Generation of Human Microglia from Induced Pluripotent Stem Cells to Study Innate Immunity in Neurological Diseases. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/12b1q5fv

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


Vanderbilt University

27. Kumar, Kevin Krishan. Investigation of Neuronal Manganese Regulation in Physiology and Disease Using High Throughput Screening, Induced Pluripotent Stem Cells, and Chemical Biology Approaches.

Degree: PhD, Neuroscience, 2014, Vanderbilt University

 Manganese (Mn) is both an essential biological cofactor and neurotoxicant. Disruption of Mn biology in the basal ganglia has been implicated in the pathogenesis of… (more)

Subjects/Keywords: High Throughput Screening; Manganese; Neurodegenerative diseases; Human Induced Pluripotent Stem Cells; Metabolomics

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

APA (6th Edition):

Kumar, K. K. (2014). Investigation of Neuronal Manganese Regulation in Physiology and Disease Using High Throughput Screening, Induced Pluripotent Stem Cells, and Chemical Biology Approaches. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14021

Chicago Manual of Style (16th Edition):

Kumar, Kevin Krishan. “Investigation of Neuronal Manganese Regulation in Physiology and Disease Using High Throughput Screening, Induced Pluripotent Stem Cells, and Chemical Biology Approaches.” 2014. Doctoral Dissertation, Vanderbilt University. Accessed April 11, 2021. http://hdl.handle.net/1803/14021.

MLA Handbook (7th Edition):

Kumar, Kevin Krishan. “Investigation of Neuronal Manganese Regulation in Physiology and Disease Using High Throughput Screening, Induced Pluripotent Stem Cells, and Chemical Biology Approaches.” 2014. Web. 11 Apr 2021.

Vancouver:

Kumar KK. Investigation of Neuronal Manganese Regulation in Physiology and Disease Using High Throughput Screening, Induced Pluripotent Stem Cells, and Chemical Biology Approaches. [Internet] [Doctoral dissertation]. Vanderbilt University; 2014. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1803/14021.

Council of Science Editors:

Kumar KK. Investigation of Neuronal Manganese Regulation in Physiology and Disease Using High Throughput Screening, Induced Pluripotent Stem Cells, and Chemical Biology Approaches. [Doctoral Dissertation]. Vanderbilt University; 2014. Available from: http://hdl.handle.net/1803/14021


University of Edinburgh

28. Zhao, Chen. Investigation of the cell- and non-cell autonomous impact of the C9orf72 mutation on human induced pluripotent stem cell-derived astrocytes.

Degree: PhD, 2016, University of Edinburgh

 Amyotrophic lateral sclerosis (ALS) is a late onset neurodegenerative disorder characterised by selective loss of upper and lower motor neurons (MNs). Recently, the GGGGCC (G4C2)… (more)

Subjects/Keywords: 616.8; ALS; amyotrophic lateral sclerosis; astrocytes; human induced pluripotent stem cells; iPSCs

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

APA (6th Edition):

Zhao, C. (2016). Investigation of the cell- and non-cell autonomous impact of the C9orf72 mutation on human induced pluripotent stem cell-derived astrocytes. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25903

Chicago Manual of Style (16th Edition):

Zhao, Chen. “Investigation of the cell- and non-cell autonomous impact of the C9orf72 mutation on human induced pluripotent stem cell-derived astrocytes.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed April 11, 2021. http://hdl.handle.net/1842/25903.

MLA Handbook (7th Edition):

Zhao, Chen. “Investigation of the cell- and non-cell autonomous impact of the C9orf72 mutation on human induced pluripotent stem cell-derived astrocytes.” 2016. Web. 11 Apr 2021.

Vancouver:

Zhao C. Investigation of the cell- and non-cell autonomous impact of the C9orf72 mutation on human induced pluripotent stem cell-derived astrocytes. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2021 Apr 11]. Available from: http://hdl.handle.net/1842/25903.

Council of Science Editors:

Zhao C. Investigation of the cell- and non-cell autonomous impact of the C9orf72 mutation on human induced pluripotent stem cell-derived astrocytes. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25903


University of New South Wales

29. Fonoudi, Hananeh. Human Induced Pluripotent Stem Cells as a Model of Complex Cardiac Disorders.

Degree: Victor Chang Cardiac Research Institute, 2018, University of New South Wales

 Hypoplastic left heart (HLH) is a genetically complex disease, characterized by hypoplasia of the left side of the heart. Although it is one of the… (more)

Subjects/Keywords: Cardiomyocytes; Human induced pluripotent stem cells; Hypoplastic left heart; Congenital heart defect

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

APA (6th Edition):

Fonoudi, H. (2018). Human Induced Pluripotent Stem Cells as a Model of Complex Cardiac Disorders. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/60401 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:52016/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Fonoudi, Hananeh. “Human Induced Pluripotent Stem Cells as a Model of Complex Cardiac Disorders.” 2018. Doctoral Dissertation, University of New South Wales. Accessed April 11, 2021. http://handle.unsw.edu.au/1959.4/60401 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:52016/SOURCE02?view=true.

MLA Handbook (7th Edition):

Fonoudi, Hananeh. “Human Induced Pluripotent Stem Cells as a Model of Complex Cardiac Disorders.” 2018. Web. 11 Apr 2021.

Vancouver:

Fonoudi H. Human Induced Pluripotent Stem Cells as a Model of Complex Cardiac Disorders. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2021 Apr 11]. Available from: http://handle.unsw.edu.au/1959.4/60401 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:52016/SOURCE02?view=true.

Council of Science Editors:

Fonoudi H. Human Induced Pluripotent Stem Cells as a Model of Complex Cardiac Disorders. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/60401 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:52016/SOURCE02?view=true


Freie Universität Berlin

30. Metzler, Eric. Generierung von hiPSCs und Redifferenzierung in induzierte myogene Zellen - abhängig vom Ursprungszelltyp?.

Degree: 2020, Freie Universität Berlin

 Muskeldystrophien sind eine heterogene Gruppe von erblichen Muskelerkrankungen, die durch progressive Muskeldegeneration charakterisiert sind. Zellersatztherapien zielen darauf ab die geschädigten Muskelzellen zu ersetzten und den… (more)

Subjects/Keywords: Myogenic differentiation; human induced Pluripotent Stem Cells (hiPSCs); Epigenetic memory; Reprogramming; ddc:572

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

APA (6th Edition):

Metzler, E. (2020). Generierung von hiPSCs und Redifferenzierung in induzierte myogene Zellen - abhängig vom Ursprungszelltyp?. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-27214

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):

Metzler, Eric. “Generierung von hiPSCs und Redifferenzierung in induzierte myogene Zellen - abhängig vom Ursprungszelltyp?.” 2020. Thesis, Freie Universität Berlin. Accessed April 11, 2021. http://dx.doi.org/10.17169/refubium-27214.

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

MLA Handbook (7th Edition):

Metzler, Eric. “Generierung von hiPSCs und Redifferenzierung in induzierte myogene Zellen - abhängig vom Ursprungszelltyp?.” 2020. Web. 11 Apr 2021.

Vancouver:

Metzler E. Generierung von hiPSCs und Redifferenzierung in induzierte myogene Zellen - abhängig vom Ursprungszelltyp?. [Internet] [Thesis]. Freie Universität Berlin; 2020. [cited 2021 Apr 11]. Available from: http://dx.doi.org/10.17169/refubium-27214.

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

Council of Science Editors:

Metzler E. Generierung von hiPSCs und Redifferenzierung in induzierte myogene Zellen - abhängig vom Ursprungszelltyp?. [Thesis]. Freie Universität Berlin; 2020. Available from: http://dx.doi.org/10.17169/refubium-27214

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

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