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You searched for subject:(iPSC). Showing records 1 – 30 of 115 total matches.

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California State University – Sacramento

1. Fury, Brian Patrick. Therapeutic potential for the inhibition of HIV from CD34+ hematopoietic stem cell derived induced pluripotent stem cells expressing three anti-HIV genes.

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

 Human immunodeficiency virus continues to persist in millions of people worldwide. While antiretroviral drug therapies have improved life for many, a cure remains elusive. Long-term… (more)

Subjects/Keywords: iPSC; CCR5

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APA (6th Edition):

Fury, B. P. (2011). Therapeutic potential for the inhibition of HIV from CD34+ hematopoietic stem cell derived induced pluripotent stem cells expressing three anti-HIV genes. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.9/1314

Chicago Manual of Style (16th Edition):

Fury, Brian Patrick. “Therapeutic potential for the inhibition of HIV from CD34+ hematopoietic stem cell derived induced pluripotent stem cells expressing three anti-HIV genes.” 2011. Masters Thesis, California State University – Sacramento. Accessed July 13, 2020. http://hdl.handle.net/10211.9/1314.

MLA Handbook (7th Edition):

Fury, Brian Patrick. “Therapeutic potential for the inhibition of HIV from CD34+ hematopoietic stem cell derived induced pluripotent stem cells expressing three anti-HIV genes.” 2011. Web. 13 Jul 2020.

Vancouver:

Fury BP. Therapeutic potential for the inhibition of HIV from CD34+ hematopoietic stem cell derived induced pluripotent stem cells expressing three anti-HIV genes. [Internet] [Masters thesis]. California State University – Sacramento; 2011. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10211.9/1314.

Council of Science Editors:

Fury BP. Therapeutic potential for the inhibition of HIV from CD34+ hematopoietic stem cell derived induced pluripotent stem cells expressing three anti-HIV genes. [Masters Thesis]. California State University – Sacramento; 2011. Available from: http://hdl.handle.net/10211.9/1314

2. Telliam, Gladys. Leucémie myéloïde chronique : modélisation de l'hématopoïèse leucémique par les cellules souches pluripotentes induites : CML modelisation from induced pluripotent stem cell derived from CML patient.

Degree: Docteur es, Immunologie, 2016, Université Paris-Saclay (ComUE)

La leucémie myéloïde chronique (LMC) est un syndrome myéloprolifératif clonal initié par l’activité tyrosine kinase de l’oncoprotéine de fusion BCR-ABL dans une cellule souche hématopoïétique… (more)

Subjects/Keywords: Lmc; Ipsc; Modélisation; Cml; Ipsc; Modelisation

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APA (6th Edition):

Telliam, G. (2016). Leucémie myéloïde chronique : modélisation de l'hématopoïèse leucémique par les cellules souches pluripotentes induites : CML modelisation from induced pluripotent stem cell derived from CML patient. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2016SACLS273

Chicago Manual of Style (16th Edition):

Telliam, Gladys. “Leucémie myéloïde chronique : modélisation de l'hématopoïèse leucémique par les cellules souches pluripotentes induites : CML modelisation from induced pluripotent stem cell derived from CML patient.” 2016. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed July 13, 2020. http://www.theses.fr/2016SACLS273.

MLA Handbook (7th Edition):

Telliam, Gladys. “Leucémie myéloïde chronique : modélisation de l'hématopoïèse leucémique par les cellules souches pluripotentes induites : CML modelisation from induced pluripotent stem cell derived from CML patient.” 2016. Web. 13 Jul 2020.

Vancouver:

Telliam G. Leucémie myéloïde chronique : modélisation de l'hématopoïèse leucémique par les cellules souches pluripotentes induites : CML modelisation from induced pluripotent stem cell derived from CML patient. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2016. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2016SACLS273.

Council of Science Editors:

Telliam G. Leucémie myéloïde chronique : modélisation de l'hématopoïèse leucémique par les cellules souches pluripotentes induites : CML modelisation from induced pluripotent stem cell derived from CML patient. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2016. Available from: http://www.theses.fr/2016SACLS273

3. Belbachir, Nadjet. Mécanismes physiopathologies du syndrome de Brugada : caractérisation d'un nouveau gène morbide Rad GTPase : Physiopathological mechanisms of Brugada syndrome.

Degree: Docteur es, Physiologie cardiovasculaire, 2017, Nantes

Le syndrome de Brugada est un trouble du rythme cardiaque héréditaire qui mène à l’apparition de fibrillations ventriculaires et à la mort subite cardiaque. Seulement… (more)

Subjects/Keywords: IPSC; Rad GTpase

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APA (6th Edition):

Belbachir, N. (2017). Mécanismes physiopathologies du syndrome de Brugada : caractérisation d'un nouveau gène morbide Rad GTPase : Physiopathological mechanisms of Brugada syndrome. (Doctoral Dissertation). Nantes. Retrieved from http://www.theses.fr/2017NANT1015

Chicago Manual of Style (16th Edition):

Belbachir, Nadjet. “Mécanismes physiopathologies du syndrome de Brugada : caractérisation d'un nouveau gène morbide Rad GTPase : Physiopathological mechanisms of Brugada syndrome.” 2017. Doctoral Dissertation, Nantes. Accessed July 13, 2020. http://www.theses.fr/2017NANT1015.

MLA Handbook (7th Edition):

Belbachir, Nadjet. “Mécanismes physiopathologies du syndrome de Brugada : caractérisation d'un nouveau gène morbide Rad GTPase : Physiopathological mechanisms of Brugada syndrome.” 2017. Web. 13 Jul 2020.

Vancouver:

Belbachir N. Mécanismes physiopathologies du syndrome de Brugada : caractérisation d'un nouveau gène morbide Rad GTPase : Physiopathological mechanisms of Brugada syndrome. [Internet] [Doctoral dissertation]. Nantes; 2017. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2017NANT1015.

Council of Science Editors:

Belbachir N. Mécanismes physiopathologies du syndrome de Brugada : caractérisation d'un nouveau gène morbide Rad GTPase : Physiopathological mechanisms of Brugada syndrome. [Doctoral Dissertation]. Nantes; 2017. Available from: http://www.theses.fr/2017NANT1015


University of Cambridge

4. Ostick, Janine Louise. Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons.

Degree: PhD, 2019, University of Cambridge

 Microtubule-associated protein tau (MAPT) is a neuronal protein which promotes microtubule assembly and stabilisation. The MAPT gene is alternatively spliced to give six tau isoforms:… (more)

Subjects/Keywords: tau; mapt; ipsc

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APA (6th Edition):

Ostick, J. L. (2019). Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/295215

Chicago Manual of Style (16th Edition):

Ostick, Janine Louise. “Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons.” 2019. Doctoral Dissertation, University of Cambridge. Accessed July 13, 2020. https://www.repository.cam.ac.uk/handle/1810/295215.

MLA Handbook (7th Edition):

Ostick, Janine Louise. “Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons.” 2019. Web. 13 Jul 2020.

Vancouver:

Ostick JL. Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jul 13]. Available from: https://www.repository.cam.ac.uk/handle/1810/295215.

Council of Science Editors:

Ostick JL. Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/295215


University of Cambridge

5. Ostick, Janine Louise. Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons.

Degree: PhD, 2019, University of Cambridge

 Microtubule-associated protein tau (MAPT) is a neuronal protein which promotes microtubule assembly and stabilisation. The MAPT gene is alternatively spliced to give six tau isoforms:… (more)

Subjects/Keywords: tau; mapt; ipsc

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APA (6th Edition):

Ostick, J. L. (2019). Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/295215 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782987

Chicago Manual of Style (16th Edition):

Ostick, Janine Louise. “Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons.” 2019. Doctoral Dissertation, University of Cambridge. Accessed July 13, 2020. https://www.repository.cam.ac.uk/handle/1810/295215 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782987.

MLA Handbook (7th Edition):

Ostick, Janine Louise. “Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons.” 2019. Web. 13 Jul 2020.

Vancouver:

Ostick JL. Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jul 13]. Available from: https://www.repository.cam.ac.uk/handle/1810/295215 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782987.

Council of Science Editors:

Ostick JL. Investigating the effects of tau mutations in induced pluripotent stem cell-derived neurons. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/295215 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782987


University of Minnesota

6. Subramaniam, Sandhya. Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells.

Degree: 2013, University of Minnesota

University of Minnesota M.S. thesis. January 2013. Major: Stem cell biology. Advisors:Ann Parr James Dutton. 1 computer file (PDF); iv, 36 pages.

The similarity between… (more)

Subjects/Keywords: Differentiation; iPSC; Oligodendrocyte; OPC

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APA (6th Edition):

Subramaniam, S. (2013). Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/146515

Chicago Manual of Style (16th Edition):

Subramaniam, Sandhya. “Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells.” 2013. Masters Thesis, University of Minnesota. Accessed July 13, 2020. http://purl.umn.edu/146515.

MLA Handbook (7th Edition):

Subramaniam, Sandhya. “Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells.” 2013. Web. 13 Jul 2020.

Vancouver:

Subramaniam S. Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2020 Jul 13]. Available from: http://purl.umn.edu/146515.

Council of Science Editors:

Subramaniam S. Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/146515


University of Minnesota

7. Subramaniam, Sandhya. Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells.

Degree: MS, Stem cell biology, 2013, University of Minnesota

 The similarity between induced Pluripotent Stem Cells (iPSCs) and Embryonic Stem (ES) cells motivated the use of the Keirstead protocol in the differentiation of iPSCs… (more)

Subjects/Keywords: Differentiation; iPSC; Oligodendrocyte; OPC

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APA (6th Edition):

Subramaniam, S. (2013). Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells. (Masters Thesis). University of Minnesota. Retrieved from http://purl.umn.edu/146515

Chicago Manual of Style (16th Edition):

Subramaniam, Sandhya. “Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells.” 2013. Masters Thesis, University of Minnesota. Accessed July 13, 2020. http://purl.umn.edu/146515.

MLA Handbook (7th Edition):

Subramaniam, Sandhya. “Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells.” 2013. Web. 13 Jul 2020.

Vancouver:

Subramaniam S. Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells. [Internet] [Masters thesis]. University of Minnesota; 2013. [cited 2020 Jul 13]. Available from: http://purl.umn.edu/146515.

Council of Science Editors:

Subramaniam S. Differentiation of human induced pluripotent stem cells to oligodendrocyte progenitor cells. [Masters Thesis]. University of Minnesota; 2013. Available from: http://purl.umn.edu/146515

8. Creyssels, Sophie. Comprendre les mécanismes cellulaires déficients dans la MPS VII par l'utilisation de neurones humains dérivés d'iPSC. : To understand neuronal dysfunction in MPS VII using human iPSC-derived cells.

Degree: Docteur es, Biologie Santé, 2015, Montpellier

Les processus moléculaires mis en jeu lors de maladies de surcharge lysosomale (MSL) et qui conduisent à des dysfonctions neuronales sont peu connus. Afin de… (more)

Subjects/Keywords: Ipsc; Mps VII; Neurones; Ipsc; Mps vii; Neurons

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APA (6th Edition):

Creyssels, S. (2015). Comprendre les mécanismes cellulaires déficients dans la MPS VII par l'utilisation de neurones humains dérivés d'iPSC. : To understand neuronal dysfunction in MPS VII using human iPSC-derived cells. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2015MONTT009

Chicago Manual of Style (16th Edition):

Creyssels, Sophie. “Comprendre les mécanismes cellulaires déficients dans la MPS VII par l'utilisation de neurones humains dérivés d'iPSC. : To understand neuronal dysfunction in MPS VII using human iPSC-derived cells.” 2015. Doctoral Dissertation, Montpellier. Accessed July 13, 2020. http://www.theses.fr/2015MONTT009.

MLA Handbook (7th Edition):

Creyssels, Sophie. “Comprendre les mécanismes cellulaires déficients dans la MPS VII par l'utilisation de neurones humains dérivés d'iPSC. : To understand neuronal dysfunction in MPS VII using human iPSC-derived cells.” 2015. Web. 13 Jul 2020.

Vancouver:

Creyssels S. Comprendre les mécanismes cellulaires déficients dans la MPS VII par l'utilisation de neurones humains dérivés d'iPSC. : To understand neuronal dysfunction in MPS VII using human iPSC-derived cells. [Internet] [Doctoral dissertation]. Montpellier; 2015. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2015MONTT009.

Council of Science Editors:

Creyssels S. Comprendre les mécanismes cellulaires déficients dans la MPS VII par l'utilisation de neurones humains dérivés d'iPSC. : To understand neuronal dysfunction in MPS VII using human iPSC-derived cells. [Doctoral Dissertation]. Montpellier; 2015. Available from: http://www.theses.fr/2015MONTT009

9. Ruillier, Valentin. Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan : Pluripotent stem cells as a model for drug discovery using high throughput screening in Lesch-Nyhan disease.

Degree: Docteur es, Immunologie, 2019, Université Paris-Saclay (ComUE)

Les mutations affectant la fonction d'enzymes impliquées dans le cycle des purines sont responsables d'une multitude de syndromes pédiatriques, caractérisés par des atteintes neurologiques et… (more)

Subjects/Keywords: Cellules souches pluripotentes; Ipsc; Hgprt; Pluripotent stem cells; Ipsc; Hgprt

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APA (6th Edition):

Ruillier, V. (2019). Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan : Pluripotent stem cells as a model for drug discovery using high throughput screening in Lesch-Nyhan disease. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLE011

Chicago Manual of Style (16th Edition):

Ruillier, Valentin. “Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan : Pluripotent stem cells as a model for drug discovery using high throughput screening in Lesch-Nyhan disease.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed July 13, 2020. http://www.theses.fr/2019SACLE011.

MLA Handbook (7th Edition):

Ruillier, Valentin. “Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan : Pluripotent stem cells as a model for drug discovery using high throughput screening in Lesch-Nyhan disease.” 2019. Web. 13 Jul 2020.

Vancouver:

Ruillier V. Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan : Pluripotent stem cells as a model for drug discovery using high throughput screening in Lesch-Nyhan disease. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2019SACLE011.

Council of Science Editors:

Ruillier V. Utilisation des cellules souches pluripotentes pour le criblage à haut débit de molécules thérapeutiques dans la maladie de Lesch-Nyhan : Pluripotent stem cells as a model for drug discovery using high throughput screening in Lesch-Nyhan disease. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLE011


University of California – San Diego

10. Su, Fei. Developing cell based reporters for the investigation of human pluripotent stem cell derived Müller Glia.

Degree: Biology, 2018, University of California – San Diego

 Retinal neuron degenerations of an eye can result in permanent photoreceptor or retinal ganglion cell loss which leads to permanent blindness. One potential approach to… (more)

Subjects/Keywords: Biology; iPSC; Müller Glia; retina; stem cell

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APA (6th Edition):

Su, F. (2018). Developing cell based reporters for the investigation of human pluripotent stem cell derived Müller Glia. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/6dc633dr

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):

Su, Fei. “Developing cell based reporters for the investigation of human pluripotent stem cell derived Müller Glia.” 2018. Thesis, University of California – San Diego. Accessed July 13, 2020. http://www.escholarship.org/uc/item/6dc633dr.

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

MLA Handbook (7th Edition):

Su, Fei. “Developing cell based reporters for the investigation of human pluripotent stem cell derived Müller Glia.” 2018. Web. 13 Jul 2020.

Vancouver:

Su F. Developing cell based reporters for the investigation of human pluripotent stem cell derived Müller Glia. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Jul 13]. Available from: http://www.escholarship.org/uc/item/6dc633dr.

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

Council of Science Editors:

Su F. Developing cell based reporters for the investigation of human pluripotent stem cell derived Müller Glia. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/6dc633dr

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


University of Cambridge

11. McNamara, Madeline Elizabeth Odile. Development of Novel Therapies for Marfan Syndrome using a Human iPSC-disease model.

Degree: PhD, 2019, University of Cambridge

 Marfan syndrome (MFS) is a connective tissue disorder caused by mutations in fibrillin-1, a matrix component encoded by the gene FBN1, with pleiotropic manifestations including… (more)

Subjects/Keywords: iPSC; marfan syndrome; aortic disease; drug-screen

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APA (6th Edition):

McNamara, M. E. O. (2019). Development of Novel Therapies for Marfan Syndrome using a Human iPSC-disease model. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290862

Chicago Manual of Style (16th Edition):

McNamara, Madeline Elizabeth Odile. “Development of Novel Therapies for Marfan Syndrome using a Human iPSC-disease model.” 2019. Doctoral Dissertation, University of Cambridge. Accessed July 13, 2020. https://www.repository.cam.ac.uk/handle/1810/290862.

MLA Handbook (7th Edition):

McNamara, Madeline Elizabeth Odile. “Development of Novel Therapies for Marfan Syndrome using a Human iPSC-disease model.” 2019. Web. 13 Jul 2020.

Vancouver:

McNamara MEO. Development of Novel Therapies for Marfan Syndrome using a Human iPSC-disease model. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Jul 13]. Available from: https://www.repository.cam.ac.uk/handle/1810/290862.

Council of Science Editors:

McNamara MEO. Development of Novel Therapies for Marfan Syndrome using a Human iPSC-disease model. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290862


University of Toronto

12. Brimble, Nicole Fabris Elise. Investigating the Function of GTF2I and its Contribution to the Williams-Beuren Syndrome Neurological Profile.

Degree: 2014, University of Toronto

Williams-Beuren Syndrome (WBS) is a genetic neurodevelopmental disorder caused by the deletion of 25 protein-coding genes at chromosome 7q11.23. It is associated with a highly… (more)

Subjects/Keywords: 7q11.23; GTF2I; iPSC; neurogenesis; WBS; Williams; 0369

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APA (6th Edition):

Brimble, N. F. E. (2014). Investigating the Function of GTF2I and its Contribution to the Williams-Beuren Syndrome Neurological Profile. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/67620

Chicago Manual of Style (16th Edition):

Brimble, Nicole Fabris Elise. “Investigating the Function of GTF2I and its Contribution to the Williams-Beuren Syndrome Neurological Profile.” 2014. Masters Thesis, University of Toronto. Accessed July 13, 2020. http://hdl.handle.net/1807/67620.

MLA Handbook (7th Edition):

Brimble, Nicole Fabris Elise. “Investigating the Function of GTF2I and its Contribution to the Williams-Beuren Syndrome Neurological Profile.” 2014. Web. 13 Jul 2020.

Vancouver:

Brimble NFE. Investigating the Function of GTF2I and its Contribution to the Williams-Beuren Syndrome Neurological Profile. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/1807/67620.

Council of Science Editors:

Brimble NFE. Investigating the Function of GTF2I and its Contribution to the Williams-Beuren Syndrome Neurological Profile. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/67620


University of Oklahoma

13. Zhou, Ningyun. BACTERIOPHAGE-BASED BIOMATERIALS FOR MANIPULATING DERIVATION AND DIFFERENTIATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS.

Degree: PhD, 2020, University of Oklahoma

 Induced pluripotent stem cells (iPSCs), which are derived from somatic cells, can differentiate into any cell type. They are promising tools in medical applications including… (more)

Subjects/Keywords: Biomaterials; Cell reprogramming; Stem cell differentiation; iPSC

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APA (6th Edition):

Zhou, N. (2020). BACTERIOPHAGE-BASED BIOMATERIALS FOR MANIPULATING DERIVATION AND DIFFERENTIATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/324169

Chicago Manual of Style (16th Edition):

Zhou, Ningyun. “BACTERIOPHAGE-BASED BIOMATERIALS FOR MANIPULATING DERIVATION AND DIFFERENTIATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS.” 2020. Doctoral Dissertation, University of Oklahoma. Accessed July 13, 2020. http://hdl.handle.net/11244/324169.

MLA Handbook (7th Edition):

Zhou, Ningyun. “BACTERIOPHAGE-BASED BIOMATERIALS FOR MANIPULATING DERIVATION AND DIFFERENTIATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS.” 2020. Web. 13 Jul 2020.

Vancouver:

Zhou N. BACTERIOPHAGE-BASED BIOMATERIALS FOR MANIPULATING DERIVATION AND DIFFERENTIATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS. [Internet] [Doctoral dissertation]. University of Oklahoma; 2020. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/11244/324169.

Council of Science Editors:

Zhou N. BACTERIOPHAGE-BASED BIOMATERIALS FOR MANIPULATING DERIVATION AND DIFFERENTIATION OF HUMAN INDUCED PLURIPOTENT STEM CELLS. [Doctoral Dissertation]. University of Oklahoma; 2020. Available from: http://hdl.handle.net/11244/324169


University of Edinburgh

14. Megaw, Roland David. The role of RPGR in actin regulation in the rod photoreceptor.

Degree: PhD, 2015, University of Edinburgh

 Introduction Retinitis Pigmentosa affects 1 in 3000 people in the UK, causing photoreceptor degeneration and premature blindness. Mutations in the X-linked RPGR gene cause 20%… (more)

Subjects/Keywords: 617.7; Retinitis Pigmentosa; iPSC; photoreceptor; RPGR

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APA (6th Edition):

Megaw, R. D. (2015). The role of RPGR in actin regulation in the rod photoreceptor. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17884

Chicago Manual of Style (16th Edition):

Megaw, Roland David. “The role of RPGR in actin regulation in the rod photoreceptor.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed July 13, 2020. http://hdl.handle.net/1842/17884.

MLA Handbook (7th Edition):

Megaw, Roland David. “The role of RPGR in actin regulation in the rod photoreceptor.” 2015. Web. 13 Jul 2020.

Vancouver:

Megaw RD. The role of RPGR in actin regulation in the rod photoreceptor. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/1842/17884.

Council of Science Editors:

Megaw RD. The role of RPGR in actin regulation in the rod photoreceptor. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/17884

15. Evans, Amanda Lisabeth. The development of tissue explant and embryonic stem cell derived models to investigate the molecular and cellular mechanisms that coordinate vertebrate haematopoiesis and angiogenesis.

Degree: PhD, 2013, Anglia Ruskin University

 Understanding the processes that control the formation of blood (haematopoiesis), and blood vessels (vasculogenesis and angiogenesis) in vivo has huge clinical importance. The complex three-dimensional… (more)

Subjects/Keywords: 612.4; VEGF; haemangioblast; Brachyury; ESC; iPSC

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APA (6th Edition):

Evans, A. L. (2013). The development of tissue explant and embryonic stem cell derived models to investigate the molecular and cellular mechanisms that coordinate vertebrate haematopoiesis and angiogenesis. (Doctoral Dissertation). Anglia Ruskin University. Retrieved from http://arro.anglia.ac.uk/314732/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600154

Chicago Manual of Style (16th Edition):

Evans, Amanda Lisabeth. “The development of tissue explant and embryonic stem cell derived models to investigate the molecular and cellular mechanisms that coordinate vertebrate haematopoiesis and angiogenesis.” 2013. Doctoral Dissertation, Anglia Ruskin University. Accessed July 13, 2020. http://arro.anglia.ac.uk/314732/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600154.

MLA Handbook (7th Edition):

Evans, Amanda Lisabeth. “The development of tissue explant and embryonic stem cell derived models to investigate the molecular and cellular mechanisms that coordinate vertebrate haematopoiesis and angiogenesis.” 2013. Web. 13 Jul 2020.

Vancouver:

Evans AL. The development of tissue explant and embryonic stem cell derived models to investigate the molecular and cellular mechanisms that coordinate vertebrate haematopoiesis and angiogenesis. [Internet] [Doctoral dissertation]. Anglia Ruskin University; 2013. [cited 2020 Jul 13]. Available from: http://arro.anglia.ac.uk/314732/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600154.

Council of Science Editors:

Evans AL. The development of tissue explant and embryonic stem cell derived models to investigate the molecular and cellular mechanisms that coordinate vertebrate haematopoiesis and angiogenesis. [Doctoral Dissertation]. Anglia Ruskin University; 2013. Available from: http://arro.anglia.ac.uk/314732/ ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600154


Duke University

16. Adkar, Shaunak. Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling .

Degree: 2019, Duke University

  The differentiation of human induced pluripotent stem cells (hiPSCs) to prescribed cell fates enables the engineering of patient-specific tissue types, such as hyaline cartilage,… (more)

Subjects/Keywords: Cellular biology; Genetics; chondrogenesis; CRISPR; iPSC

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

APA (6th Edition):

Adkar, S. (2019). Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/18649

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):

Adkar, Shaunak. “Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling .” 2019. Thesis, Duke University. Accessed July 13, 2020. http://hdl.handle.net/10161/18649.

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

MLA Handbook (7th Edition):

Adkar, Shaunak. “Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling .” 2019. Web. 13 Jul 2020.

Vancouver:

Adkar S. Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling . [Internet] [Thesis]. Duke University; 2019. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10161/18649.

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

Council of Science Editors:

Adkar S. Development of a High-Throughput Human iPSC Chondrogenesis Platform and Applications for Arthritis Disease Modeling . [Thesis]. Duke University; 2019. Available from: http://hdl.handle.net/10161/18649

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

17. Jeziorowska, Dorota. Analyse des voies de régulation de la cardiogenèse et de la différenciation cardiomyocytaire : Analysis of the cardiogenenis pathways and the cardiac differentiation.

Degree: Docteur es, Physiologie et Physiopathologie, 2016, Université Pierre et Marie Curie – Paris VI

L'objectif général de ce travail de doctorat a été centré sur l'utilisation des cellules pluripotentes induites humaines dans la modélisation et l'évaluation thérapeutique des pathologies… (more)

Subjects/Keywords: IPSC; Différenciation; Cardiomyocytes; Modélisation; Edition du génome; CRISPRa; IPSC; Differentiation; Cardiomyocytes; 612.17

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APA (6th Edition):

Jeziorowska, D. (2016). Analyse des voies de régulation de la cardiogenèse et de la différenciation cardiomyocytaire : Analysis of the cardiogenenis pathways and the cardiac differentiation. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2016PA066631

Chicago Manual of Style (16th Edition):

Jeziorowska, Dorota. “Analyse des voies de régulation de la cardiogenèse et de la différenciation cardiomyocytaire : Analysis of the cardiogenenis pathways and the cardiac differentiation.” 2016. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed July 13, 2020. http://www.theses.fr/2016PA066631.

MLA Handbook (7th Edition):

Jeziorowska, Dorota. “Analyse des voies de régulation de la cardiogenèse et de la différenciation cardiomyocytaire : Analysis of the cardiogenenis pathways and the cardiac differentiation.” 2016. Web. 13 Jul 2020.

Vancouver:

Jeziorowska D. Analyse des voies de régulation de la cardiogenèse et de la différenciation cardiomyocytaire : Analysis of the cardiogenenis pathways and the cardiac differentiation. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2016PA066631.

Council of Science Editors:

Jeziorowska D. Analyse des voies de régulation de la cardiogenèse et de la différenciation cardiomyocytaire : Analysis of the cardiogenenis pathways and the cardiac differentiation. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2016. Available from: http://www.theses.fr/2016PA066631

18. Jung, Laura. Optimisation de protocoles de reprogrammation de cellules somatiques humaines en cellules souches à pluripotence induite (hiPSC) : Optimization of reprogramming protocols of human somatic cells into induced pluripotent stem cells (hiPSC).

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2013, Université de Strasbourg

En 2006 et 2007, les équipes de Yamanaka et Thomson réalisent la reprogrammation de cellules somatiques murines et humaines en cellules souches pluripotentes à partir… (more)

Subjects/Keywords: Cellules souches pluripotente induite; Reprogrammation; IPSC; Induced Pluripotent Stem Cells; Reprogramming; IPSC; 572.8

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

APA (6th Edition):

Jung, L. (2013). Optimisation de protocoles de reprogrammation de cellules somatiques humaines en cellules souches à pluripotence induite (hiPSC) : Optimization of reprogramming protocols of human somatic cells into induced pluripotent stem cells (hiPSC). (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2013STRAJ066

Chicago Manual of Style (16th Edition):

Jung, Laura. “Optimisation de protocoles de reprogrammation de cellules somatiques humaines en cellules souches à pluripotence induite (hiPSC) : Optimization of reprogramming protocols of human somatic cells into induced pluripotent stem cells (hiPSC).” 2013. Doctoral Dissertation, Université de Strasbourg. Accessed July 13, 2020. http://www.theses.fr/2013STRAJ066.

MLA Handbook (7th Edition):

Jung, Laura. “Optimisation de protocoles de reprogrammation de cellules somatiques humaines en cellules souches à pluripotence induite (hiPSC) : Optimization of reprogramming protocols of human somatic cells into induced pluripotent stem cells (hiPSC).” 2013. Web. 13 Jul 2020.

Vancouver:

Jung L. Optimisation de protocoles de reprogrammation de cellules somatiques humaines en cellules souches à pluripotence induite (hiPSC) : Optimization of reprogramming protocols of human somatic cells into induced pluripotent stem cells (hiPSC). [Internet] [Doctoral dissertation]. Université de Strasbourg; 2013. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2013STRAJ066.

Council of Science Editors:

Jung L. Optimisation de protocoles de reprogrammation de cellules somatiques humaines en cellules souches à pluripotence induite (hiPSC) : Optimization of reprogramming protocols of human somatic cells into induced pluripotent stem cells (hiPSC). [Doctoral Dissertation]. Université de Strasbourg; 2013. Available from: http://www.theses.fr/2013STRAJ066

19. Secardin, Lise. Modélisation des néoplasmes myéloprolifératifs grâce aux cellules souches induites à la pluripotence (IPSC) : Modeling of myeloproliferative neoplasms thanks to an induced pluripotent stem cell model (IPSC).

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie. Hématologie et oncologie, 2016, Sorbonne Paris Cité

Les néoplasmes myéloprolifératifs (NMP) sont hémopathies malignes aboutissant à la surproduction d'une ou plusieurs lignées myéloïdes. Elles sont dues à l'acquisition de mutations sur l'axe… (more)

Subjects/Keywords: Néoplasmes myéloprolifératifs; JAK/STAT; TET2; IPSC; Myeloproliferative neoplasms; JAK/STAT; TET2; IPSC

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APA (6th Edition):

Secardin, L. (2016). Modélisation des néoplasmes myéloprolifératifs grâce aux cellules souches induites à la pluripotence (IPSC) : Modeling of myeloproliferative neoplasms thanks to an induced pluripotent stem cell model (IPSC). (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCC313

Chicago Manual of Style (16th Edition):

Secardin, Lise. “Modélisation des néoplasmes myéloprolifératifs grâce aux cellules souches induites à la pluripotence (IPSC) : Modeling of myeloproliferative neoplasms thanks to an induced pluripotent stem cell model (IPSC).” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed July 13, 2020. http://www.theses.fr/2016USPCC313.

MLA Handbook (7th Edition):

Secardin, Lise. “Modélisation des néoplasmes myéloprolifératifs grâce aux cellules souches induites à la pluripotence (IPSC) : Modeling of myeloproliferative neoplasms thanks to an induced pluripotent stem cell model (IPSC).” 2016. Web. 13 Jul 2020.

Vancouver:

Secardin L. Modélisation des néoplasmes myéloprolifératifs grâce aux cellules souches induites à la pluripotence (IPSC) : Modeling of myeloproliferative neoplasms thanks to an induced pluripotent stem cell model (IPSC). [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2016USPCC313.

Council of Science Editors:

Secardin L. Modélisation des néoplasmes myéloprolifératifs grâce aux cellules souches induites à la pluripotence (IPSC) : Modeling of myeloproliferative neoplasms thanks to an induced pluripotent stem cell model (IPSC). [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCC313

20. Mitne Neto, Miguel. Análise in vitro da esclerose lateral amiotrófica tipo 8 e estudo genético da paraplegia espástica 4.

Degree: PhD, Biologia (Genética), 2011, University of São Paulo

As doenças do neurônio motor (DNM) apresentam grande variabilidade clínica e genética. A Esclerose Lateral Amiotrófica (ELA) é a forma mais comum de DNM de… (more)

Subjects/Keywords: Amyotrophic lateral sclerosis; Esclerose lateral amiotrófica; Genética humana; Human genetics; iPSC; iPSC; Motor neuro; Neurônio motor; Paraplegia espástica; Spastic paraplegia

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APA (6th Edition):

Mitne Neto, M. (2011). Análise in vitro da esclerose lateral amiotrófica tipo 8 e estudo genético da paraplegia espástica 4. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24052011-112414/ ;

Chicago Manual of Style (16th Edition):

Mitne Neto, Miguel. “Análise in vitro da esclerose lateral amiotrófica tipo 8 e estudo genético da paraplegia espástica 4.” 2011. Doctoral Dissertation, University of São Paulo. Accessed July 13, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24052011-112414/ ;.

MLA Handbook (7th Edition):

Mitne Neto, Miguel. “Análise in vitro da esclerose lateral amiotrófica tipo 8 e estudo genético da paraplegia espástica 4.” 2011. Web. 13 Jul 2020.

Vancouver:

Mitne Neto M. Análise in vitro da esclerose lateral amiotrófica tipo 8 e estudo genético da paraplegia espástica 4. [Internet] [Doctoral dissertation]. University of São Paulo; 2011. [cited 2020 Jul 13]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24052011-112414/ ;.

Council of Science Editors:

Mitne Neto M. Análise in vitro da esclerose lateral amiotrófica tipo 8 e estudo genético da paraplegia espástica 4. [Doctoral Dissertation]. University of São Paulo; 2011. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-24052011-112414/ ;

21. Charaf, Lucie. Utilisation de la stratégie iPSC pour la modélisation et l'étude des mécaniques de résistance des cellules souches cancéreuses : exemple de la leucémie myéloïde chronique : Use of iPSC for modelling and study cancer stem cells mechanisms in chronic myeloid leukemia.

Degree: Docteur es, Génétique, 2016, Bordeaux

La technologie iPSC (induced pluripotent stem cells) permet l’obtention d’une source cellulaire illimitée pour la modélisation et la thérapie de maladies génétiques, la médecine régénérative,… (more)

Subjects/Keywords: IPSC; Cellule souche cancéreuse; Leucémie myéloïde chronique; Inhibiteurs de tyrosine kinases; IPSC; Cancer stem cell; Chronic myeloid leukemia; Tyrosine kinase inhibitors

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APA (6th Edition):

Charaf, L. (2016). Utilisation de la stratégie iPSC pour la modélisation et l'étude des mécaniques de résistance des cellules souches cancéreuses : exemple de la leucémie myéloïde chronique : Use of iPSC for modelling and study cancer stem cells mechanisms in chronic myeloid leukemia. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0230

Chicago Manual of Style (16th Edition):

Charaf, Lucie. “Utilisation de la stratégie iPSC pour la modélisation et l'étude des mécaniques de résistance des cellules souches cancéreuses : exemple de la leucémie myéloïde chronique : Use of iPSC for modelling and study cancer stem cells mechanisms in chronic myeloid leukemia.” 2016. Doctoral Dissertation, Bordeaux. Accessed July 13, 2020. http://www.theses.fr/2016BORD0230.

MLA Handbook (7th Edition):

Charaf, Lucie. “Utilisation de la stratégie iPSC pour la modélisation et l'étude des mécaniques de résistance des cellules souches cancéreuses : exemple de la leucémie myéloïde chronique : Use of iPSC for modelling and study cancer stem cells mechanisms in chronic myeloid leukemia.” 2016. Web. 13 Jul 2020.

Vancouver:

Charaf L. Utilisation de la stratégie iPSC pour la modélisation et l'étude des mécaniques de résistance des cellules souches cancéreuses : exemple de la leucémie myéloïde chronique : Use of iPSC for modelling and study cancer stem cells mechanisms in chronic myeloid leukemia. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2016BORD0230.

Council of Science Editors:

Charaf L. Utilisation de la stratégie iPSC pour la modélisation et l'étude des mécaniques de résistance des cellules souches cancéreuses : exemple de la leucémie myéloïde chronique : Use of iPSC for modelling and study cancer stem cells mechanisms in chronic myeloid leukemia. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0230


University of Helsinki

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

Degree: Medicinska fakulteten, 2018, University of Helsinki

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Pörsti, Elina. “CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells.” 2018. Masters Thesis, University of Helsinki. Accessed July 13, 2020. http://hdl.handle.net/10138/236384.

MLA Handbook (7th Edition):

Pörsti, Elina. “CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells.” 2018. Web. 13 Jul 2020.

Vancouver:

Pörsti E. CRISPR activator-mediated reprogramming of human neuroectodermal stem cells to iPS cells. [Internet] [Masters thesis]. University of Helsinki; 2018. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/10138/236384.

Council of Science Editors:

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

23. Alkobtawi, Mansour. Genome-wide identification of Pax3 transcriptional targets during normal and pathological neural crest development : Identification à large échelle des gènes contrôlés par le facteur de transcription Pax3, durant le développement normal et pathologique de la crête neurale.

Degree: Docteur es, Sciences de la vie et de la santé, 2019, Université Paris-Saclay (ComUE)

La crête neurale est une population de cellules migratoires multipotentes qui se délaminent du tube neural et se différencient en plusieurs types cellulaires. Des altérations… (more)

Subjects/Keywords: Crête neurale; Syndrome de waardenburg; Pax3; Fh13; Xenopus laevis; IPSC; Neural crest; Waardenburg syndrom; Pax3; Fh13; Xenopus laevis; IPSC

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APA (6th Edition):

Alkobtawi, M. (2019). Genome-wide identification of Pax3 transcriptional targets during normal and pathological neural crest development : Identification à large échelle des gènes contrôlés par le facteur de transcription Pax3, durant le développement normal et pathologique de la crête neurale. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS385

Chicago Manual of Style (16th Edition):

Alkobtawi, Mansour. “Genome-wide identification of Pax3 transcriptional targets during normal and pathological neural crest development : Identification à large échelle des gènes contrôlés par le facteur de transcription Pax3, durant le développement normal et pathologique de la crête neurale.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed July 13, 2020. http://www.theses.fr/2019SACLS385.

MLA Handbook (7th Edition):

Alkobtawi, Mansour. “Genome-wide identification of Pax3 transcriptional targets during normal and pathological neural crest development : Identification à large échelle des gènes contrôlés par le facteur de transcription Pax3, durant le développement normal et pathologique de la crête neurale.” 2019. Web. 13 Jul 2020.

Vancouver:

Alkobtawi M. Genome-wide identification of Pax3 transcriptional targets during normal and pathological neural crest development : Identification à large échelle des gènes contrôlés par le facteur de transcription Pax3, durant le développement normal et pathologique de la crête neurale. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Jul 13]. Available from: http://www.theses.fr/2019SACLS385.

Council of Science Editors:

Alkobtawi M. Genome-wide identification of Pax3 transcriptional targets during normal and pathological neural crest development : Identification à large échelle des gènes contrôlés par le facteur de transcription Pax3, durant le développement normal et pathologique de la crête neurale. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS385

24. 柏木, 隆宏. Accelerated generation of human induced pluripotent stem cells from human oral mucosa using episomal plasmid vectors and maternal transcription factor Glis1 : エピソーマルプラスミドベクターと母性転写因子Glis1を用いたヒト口腔粘膜からのヒト人工多能性幹細胞樹立の加速化.

Degree: 博士(歯学), 2016, Osaka Dental University / 大阪歯科大学

Objective: Induced pluripotent stem cells (iPSCs) possess high pluripotency and differentiation potential and may constitute a possible source of autologous stem cells for clinical applications.… (more)

Subjects/Keywords: iPSC; integration-free plasmid vector; Glis1; human oral mucosal tissue

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APA (6th Edition):

柏木, . (2016). Accelerated generation of human induced pluripotent stem cells from human oral mucosa using episomal plasmid vectors and maternal transcription factor Glis1 : エピソーマルプラスミドベクターと母性転写因子Glis1を用いたヒト口腔粘膜からのヒト人工多能性幹細胞樹立の加速化. (Thesis). Osaka Dental University / 大阪歯科大学. Retrieved from http://id.nii.ac.jp/1392/00000097/

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):

柏木, 隆宏. “Accelerated generation of human induced pluripotent stem cells from human oral mucosa using episomal plasmid vectors and maternal transcription factor Glis1 : エピソーマルプラスミドベクターと母性転写因子Glis1を用いたヒト口腔粘膜からのヒト人工多能性幹細胞樹立の加速化.” 2016. Thesis, Osaka Dental University / 大阪歯科大学. Accessed July 13, 2020. http://id.nii.ac.jp/1392/00000097/.

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

MLA Handbook (7th Edition):

柏木, 隆宏. “Accelerated generation of human induced pluripotent stem cells from human oral mucosa using episomal plasmid vectors and maternal transcription factor Glis1 : エピソーマルプラスミドベクターと母性転写因子Glis1を用いたヒト口腔粘膜からのヒト人工多能性幹細胞樹立の加速化.” 2016. Web. 13 Jul 2020.

Vancouver:

柏木 . Accelerated generation of human induced pluripotent stem cells from human oral mucosa using episomal plasmid vectors and maternal transcription factor Glis1 : エピソーマルプラスミドベクターと母性転写因子Glis1を用いたヒト口腔粘膜からのヒト人工多能性幹細胞樹立の加速化. [Internet] [Thesis]. Osaka Dental University / 大阪歯科大学; 2016. [cited 2020 Jul 13]. Available from: http://id.nii.ac.jp/1392/00000097/.

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

Council of Science Editors:

柏木 . Accelerated generation of human induced pluripotent stem cells from human oral mucosa using episomal plasmid vectors and maternal transcription factor Glis1 : エピソーマルプラスミドベクターと母性転写因子Glis1を用いたヒト口腔粘膜からのヒト人工多能性幹細胞樹立の加速化. [Thesis]. Osaka Dental University / 大阪歯科大学; 2016. Available from: http://id.nii.ac.jp/1392/00000097/

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


University of Cincinnati

25. 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 July 13, 2020. 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. 13 Jul 2020.

Vancouver:

Campbell I. Optimization of Methods for Generating Customized Gene-Edited Human Pluripotent Stem Cells. [Internet] [Masters thesis]. University of Cincinnati; 2017. [cited 2020 Jul 13]. 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


University of California – San Diego

26. Dang, Jason Wai Leung. MicroRNA-mediated regulation of stem cell fate decisions during reprogramming and viral infection.

Degree: Bioengineering, 2017, University of California – San Diego

 Zika virus (ZIKV) is an emerging arbovirus linked to an increased incidence of microcephaly. To study the potential link between ZIKV and microcephaly, stem cell-based… (more)

Subjects/Keywords: Biology; Microbiology; Biomedical engineering; iPSC; microRNA; organoid; stem cell; Zika

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APA (6th Edition):

Dang, J. W. L. (2017). MicroRNA-mediated regulation of stem cell fate decisions during reprogramming and viral infection. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/1n12k33t

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):

Dang, Jason Wai Leung. “MicroRNA-mediated regulation of stem cell fate decisions during reprogramming and viral infection.” 2017. Thesis, University of California – San Diego. Accessed July 13, 2020. http://www.escholarship.org/uc/item/1n12k33t.

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

MLA Handbook (7th Edition):

Dang, Jason Wai Leung. “MicroRNA-mediated regulation of stem cell fate decisions during reprogramming and viral infection.” 2017. Web. 13 Jul 2020.

Vancouver:

Dang JWL. MicroRNA-mediated regulation of stem cell fate decisions during reprogramming and viral infection. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2020 Jul 13]. Available from: http://www.escholarship.org/uc/item/1n12k33t.

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

Council of Science Editors:

Dang JWL. MicroRNA-mediated regulation of stem cell fate decisions during reprogramming and viral infection. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/1n12k33t

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

27. Ohashi, Minori. Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells.

Degree: Molecular Biology, 2017, UCLA

 Rett syndrome is a neurodevelopmental disorder that predominately affects females and is one of the most common causes of intellectual disability in females. The syndrome… (more)

Subjects/Keywords: Molecular biology; Neurosciences; disease modeling; iPSC; Rett syndrome; telomere

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APA (6th Edition):

Ohashi, M. (2017). Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/6658h6r9

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):

Ohashi, Minori. “Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells.” 2017. Thesis, UCLA. Accessed July 13, 2020. http://www.escholarship.org/uc/item/6658h6r9.

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

MLA Handbook (7th Edition):

Ohashi, Minori. “Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells.” 2017. Web. 13 Jul 2020.

Vancouver:

Ohashi M. Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells. [Internet] [Thesis]. UCLA; 2017. [cited 2020 Jul 13]. Available from: http://www.escholarship.org/uc/item/6658h6r9.

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

Council of Science Editors:

Ohashi M. Modeling Rett Syndrome with Human Induced Pluripotent Stem Cells. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/6658h6r9

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


University of California – Irvine

28. Xiao, Zhongwen. Patient-derived induced pluripotent stem cells for Alzheimer’s Disease Model and 3D culture of neurons on a Multi-Electrode Array.

Degree: Biomedical Engineering, 2017, University of California – Irvine

 Induced pluripotent stem cells (iPSC) have opened a new direction on study of Alzheimer’s Disease due to their pluripotency. Differentiation of iPSC to neurons has… (more)

Subjects/Keywords: Neurosciences; Biomedical engineering; 3D; Hippocampus; iPSC; Matrigel; rat; stem cells

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

APA (6th Edition):

Xiao, Z. (2017). Patient-derived induced pluripotent stem cells for Alzheimer’s Disease Model and 3D culture of neurons on a Multi-Electrode Array. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/67h2f0fv

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):

Xiao, Zhongwen. “Patient-derived induced pluripotent stem cells for Alzheimer’s Disease Model and 3D culture of neurons on a Multi-Electrode Array.” 2017. Thesis, University of California – Irvine. Accessed July 13, 2020. http://www.escholarship.org/uc/item/67h2f0fv.

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

MLA Handbook (7th Edition):

Xiao, Zhongwen. “Patient-derived induced pluripotent stem cells for Alzheimer’s Disease Model and 3D culture of neurons on a Multi-Electrode Array.” 2017. Web. 13 Jul 2020.

Vancouver:

Xiao Z. Patient-derived induced pluripotent stem cells for Alzheimer’s Disease Model and 3D culture of neurons on a Multi-Electrode Array. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2020 Jul 13]. Available from: http://www.escholarship.org/uc/item/67h2f0fv.

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

Council of Science Editors:

Xiao Z. Patient-derived induced pluripotent stem cells for Alzheimer’s Disease Model and 3D culture of neurons on a Multi-Electrode Array. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/67h2f0fv

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


Université de Montréal

29. Poirier, Mikhael. Effets de la reprogrammation sur le gène empreinté H19 chez les équins .

Degree: 2015, Université de Montréal

 Lors de la fécondation, le génome subit des transformations épigénétiques qui vont guider le développement et le phénotype de l’embryon. L'avènement des techniques de reprogrammation… (more)

Subjects/Keywords: Épigénétique; Reprogrammation; SCNT; iPSC; H19; Équin; ICR; Epigenetics; Reprogramming; Equine

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

APA (6th Edition):

Poirier, M. (2015). Effets de la reprogrammation sur le gène empreinté H19 chez les équins . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/12406

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):

Poirier, Mikhael. “Effets de la reprogrammation sur le gène empreinté H19 chez les équins .” 2015. Thesis, Université de Montréal. Accessed July 13, 2020. http://hdl.handle.net/1866/12406.

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

MLA Handbook (7th Edition):

Poirier, Mikhael. “Effets de la reprogrammation sur le gène empreinté H19 chez les équins .” 2015. Web. 13 Jul 2020.

Vancouver:

Poirier M. Effets de la reprogrammation sur le gène empreinté H19 chez les équins . [Internet] [Thesis]. Université de Montréal; 2015. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/1866/12406.

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

Council of Science Editors:

Poirier M. Effets de la reprogrammation sur le gène empreinté H19 chez les équins . [Thesis]. Université de Montréal; 2015. Available from: http://hdl.handle.net/1866/12406

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

30. Seo, Hideya. A β1-tubulin-based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production .

Degree: 2019, Kyoto University

Subjects/Keywords: megakaryocyte; platelet production; iPSC; screening

Page 1 Page 2

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

APA (6th Edition):

Seo, H. (2019). A β1-tubulin-based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/236615

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):

Seo, Hideya. “A β1-tubulin-based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production .” 2019. Thesis, Kyoto University. Accessed July 13, 2020. http://hdl.handle.net/2433/236615.

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

MLA Handbook (7th Edition):

Seo, Hideya. “A β1-tubulin-based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production .” 2019. Web. 13 Jul 2020.

Vancouver:

Seo H. A β1-tubulin-based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production . [Internet] [Thesis]. Kyoto University; 2019. [cited 2020 Jul 13]. Available from: http://hdl.handle.net/2433/236615.

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

Council of Science Editors:

Seo H. A β1-tubulin-based megakaryocyte maturation reporter system identifies novel drugs that promote platelet production . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/236615

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

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