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You searched for subject:(induced pluripotent stem cell iPSC ). Showing records 1 – 30 of 37506 total matches.

[1] [2] [3] [4] [5] … [1251]

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University of Toronto

1. Corso, Andrew John. Identifying Novel MicroRNA Enhancers of Somatic Cell Reprogramming.

Degree: 2013, University of Toronto

In addition to the well-characterized Induced Pluripotent Stem cells (iPSCs) that closely resemble Embryonic Stem cells (ESCs), a recent study has proven the existence of… (more)

Subjects/Keywords: Induced Pluripotent Stem Cell; MicroRNA; iPSC; Reprogramming; miRNA; miR-214; 0307; 0369; 0379

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

APA (6th Edition):

Corso, A. J. (2013). Identifying Novel MicroRNA Enhancers of Somatic Cell Reprogramming. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42760

Chicago Manual of Style (16th Edition):

Corso, Andrew John. “Identifying Novel MicroRNA Enhancers of Somatic Cell Reprogramming.” 2013. Masters Thesis, University of Toronto. Accessed December 12, 2019. http://hdl.handle.net/1807/42760.

MLA Handbook (7th Edition):

Corso, Andrew John. “Identifying Novel MicroRNA Enhancers of Somatic Cell Reprogramming.” 2013. Web. 12 Dec 2019.

Vancouver:

Corso AJ. Identifying Novel MicroRNA Enhancers of Somatic Cell Reprogramming. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/1807/42760.

Council of Science Editors:

Corso AJ. Identifying Novel MicroRNA Enhancers of Somatic Cell Reprogramming. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42760

2. 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 (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 December 12, 2019. 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. 12 Dec 2019.

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 2019 Dec 12]. 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


University of Edinburgh

3. Brightwell, Sara. Identifying novel regulators of reprogramming using RNA interference.

Degree: PhD, 2015, University of Edinburgh

 Since Yamanaka and Takahashi first described the isolation of induced pluripotent stem cells (iPSCs) in 2006, researchers have invested a vast amount of time and… (more)

Subjects/Keywords: 572.8; reprogramming; iPSC; induced pluripotent stem cells; shRNA

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APA (6th Edition):

Brightwell, S. (2015). Identifying novel regulators of reprogramming using RNA interference. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/16156

Chicago Manual of Style (16th Edition):

Brightwell, Sara. “Identifying novel regulators of reprogramming using RNA interference.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 12, 2019. http://hdl.handle.net/1842/16156.

MLA Handbook (7th Edition):

Brightwell, Sara. “Identifying novel regulators of reprogramming using RNA interference.” 2015. Web. 12 Dec 2019.

Vancouver:

Brightwell S. Identifying novel regulators of reprogramming using RNA interference. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/1842/16156.

Council of Science Editors:

Brightwell S. Identifying novel regulators of reprogramming using RNA interference. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/16156


University of Oxford

4. Zambon, Federico. Studying α-Synuclein pathology using iPSC-derived dopaminergic neurons.

Degree: PhD, 2017, University of Oxford

 Parkinson's disease (PD) is characterised by the loss of dopaminergic neurons in the Substantia Nigra pars compacta in the midbrain and the presence of intracellular… (more)

Subjects/Keywords: Parkinson's disease; Induced pluripotent stem cells; synuclein; iPSC; dopaminergic neurons

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APA (6th Edition):

Zambon, F. (2017). Studying α-Synuclein pathology using iPSC-derived dopaminergic neurons. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:2856dcf3-0f38-4a37-9242-8c685d1c2c3a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.735932

Chicago Manual of Style (16th Edition):

Zambon, Federico. “Studying α-Synuclein pathology using iPSC-derived dopaminergic neurons.” 2017. Doctoral Dissertation, University of Oxford. Accessed December 12, 2019. http://ora.ox.ac.uk/objects/uuid:2856dcf3-0f38-4a37-9242-8c685d1c2c3a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.735932.

MLA Handbook (7th Edition):

Zambon, Federico. “Studying α-Synuclein pathology using iPSC-derived dopaminergic neurons.” 2017. Web. 12 Dec 2019.

Vancouver:

Zambon F. Studying α-Synuclein pathology using iPSC-derived dopaminergic neurons. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2019 Dec 12]. Available from: http://ora.ox.ac.uk/objects/uuid:2856dcf3-0f38-4a37-9242-8c685d1c2c3a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.735932.

Council of Science Editors:

Zambon F. Studying α-Synuclein pathology using iPSC-derived dopaminergic neurons. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:2856dcf3-0f38-4a37-9242-8c685d1c2c3a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.735932


University of Cincinnati

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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

6. Greenberg, Brittany E. Reprogramming to Pluripotency Using Small Molecule Compounds.

Degree: MS, Biomedical Sciences, 2015, University of Tennessee Health Science Center

  The generation of induced pluripotent stem cells (iPSCs) through the use of small molecule compounds has evolved as a potential cellular reprogramming strategy. Individually,… (more)

Subjects/Keywords: cell reprogramming; cell signaling; epigenetic modification; induced pluripotent stem cell (iPSC); small molecule compound; Medical Molecular Biology; Medical Sciences; Medicine and Health Sciences

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APA (6th Edition):

Greenberg, B. E. (2015). Reprogramming to Pluripotency Using Small Molecule Compounds. (Thesis). University of Tennessee Health Science Center. Retrieved from https://dc.uthsc.edu/dissertations/97

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):

Greenberg, Brittany E. “Reprogramming to Pluripotency Using Small Molecule Compounds.” 2015. Thesis, University of Tennessee Health Science Center. Accessed December 12, 2019. https://dc.uthsc.edu/dissertations/97.

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

MLA Handbook (7th Edition):

Greenberg, Brittany E. “Reprogramming to Pluripotency Using Small Molecule Compounds.” 2015. Web. 12 Dec 2019.

Vancouver:

Greenberg BE. Reprogramming to Pluripotency Using Small Molecule Compounds. [Internet] [Thesis]. University of Tennessee Health Science Center; 2015. [cited 2019 Dec 12]. Available from: https://dc.uthsc.edu/dissertations/97.

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

Council of Science Editors:

Greenberg BE. Reprogramming to Pluripotency Using Small Molecule Compounds. [Thesis]. University of Tennessee Health Science Center; 2015. Available from: https://dc.uthsc.edu/dissertations/97

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


University of Michigan

7. Bezenah, Jonathan. Evaluating an Alternative Endothelial Cell Source to Vascularize Engineered Tissue Constructs.

Degree: PhD, Chemical Engineering, 2018, University of Michigan

 A major translational challenge in the fields of therapeutic angiogenesis and regenerative medicine is the need to create functional microvasculature. Cell-based strategies to promote neovascularization… (more)

Subjects/Keywords: induced pluripotent stem cell derived endothelial cells (iPSC-ECs); vascularization; human umbilical vein endothelial cells (HUVECs); tissue engineering; angiogenesis; Biomedical Engineering; Chemical Engineering; Engineering; Science

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APA (6th Edition):

Bezenah, J. (2018). Evaluating an Alternative Endothelial Cell Source to Vascularize Engineered Tissue Constructs. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/147627

Chicago Manual of Style (16th Edition):

Bezenah, Jonathan. “Evaluating an Alternative Endothelial Cell Source to Vascularize Engineered Tissue Constructs.” 2018. Doctoral Dissertation, University of Michigan. Accessed December 12, 2019. http://hdl.handle.net/2027.42/147627.

MLA Handbook (7th Edition):

Bezenah, Jonathan. “Evaluating an Alternative Endothelial Cell Source to Vascularize Engineered Tissue Constructs.” 2018. Web. 12 Dec 2019.

Vancouver:

Bezenah J. Evaluating an Alternative Endothelial Cell Source to Vascularize Engineered Tissue Constructs. [Internet] [Doctoral dissertation]. University of Michigan; 2018. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2027.42/147627.

Council of Science Editors:

Bezenah J. Evaluating an Alternative Endothelial Cell Source to Vascularize Engineered Tissue Constructs. [Doctoral Dissertation]. University of Michigan; 2018. Available from: http://hdl.handle.net/2027.42/147627


Université de Montréal

8. Eilers Smith, Olivia. Dérivation de cellules souches pluripotentes induites autologues à partir du clonage somatique équin .

Degree: 2014, Université de Montréal

 Le recours aux cellules souches pour améliorer la réparation et guérison des blessures et maladies musculosquelettiques chez le cheval est de plus en plus fréquent.… (more)

Subjects/Keywords: Pluripotent; Cellules souches; iPS; ESC; Reprogrammation; Cheval; Autologue; Stem cell; SCNT; Reprogramming; Horse; Autologous; iPSC

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APA (6th Edition):

Eilers Smith, O. (2014). Dérivation de cellules souches pluripotentes induites autologues à partir du clonage somatique équin . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11564

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):

Eilers Smith, Olivia. “Dérivation de cellules souches pluripotentes induites autologues à partir du clonage somatique équin .” 2014. Thesis, Université de Montréal. Accessed December 12, 2019. http://hdl.handle.net/1866/11564.

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

MLA Handbook (7th Edition):

Eilers Smith, Olivia. “Dérivation de cellules souches pluripotentes induites autologues à partir du clonage somatique équin .” 2014. Web. 12 Dec 2019.

Vancouver:

Eilers Smith O. Dérivation de cellules souches pluripotentes induites autologues à partir du clonage somatique équin . [Internet] [Thesis]. Université de Montréal; 2014. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/1866/11564.

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

Council of Science Editors:

Eilers Smith O. Dérivation de cellules souches pluripotentes induites autologues à partir du clonage somatique équin . [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/11564

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


University of Manchester

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

Degree: PhD, 2017, University of Manchester

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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

10. Denholtz, Matthew. Long-range chromatin contacts reveal a role for the pluripotency and Polycomb networks in genome organization.

Degree: Molecular Biology, 2013, UCLA

 The spatial organization of the genome is linked to its biological function. However, the relationship between specific gene regulatory networks that govern cell identity and… (more)

Subjects/Keywords: Molecular biology; Embryonic stem cell; Genome organization; Induced pluripotent stem cell (iPSC)

…in embryonic stem cells (ESCs, pluripotent cells derived from the inner cell mass of… …the pre-implantation blastocyst), induced pluripotent stem cells (iPSCs, ES-like… …Center of Regenerative Medicine and Stem Cell Research at UCLA, the California Institute for… …supported by the Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research at… …Edythe Broad Center of Regenerative Medicine and Stem Cell Research, Molecular Biology… 

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APA (6th Edition):

Denholtz, M. (2013). Long-range chromatin contacts reveal a role for the pluripotency and Polycomb networks in genome organization. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3vk1t1q0

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):

Denholtz, Matthew. “Long-range chromatin contacts reveal a role for the pluripotency and Polycomb networks in genome organization.” 2013. Thesis, UCLA. Accessed December 12, 2019. http://www.escholarship.org/uc/item/3vk1t1q0.

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

MLA Handbook (7th Edition):

Denholtz, Matthew. “Long-range chromatin contacts reveal a role for the pluripotency and Polycomb networks in genome organization.” 2013. Web. 12 Dec 2019.

Vancouver:

Denholtz M. Long-range chromatin contacts reveal a role for the pluripotency and Polycomb networks in genome organization. [Internet] [Thesis]. UCLA; 2013. [cited 2019 Dec 12]. Available from: http://www.escholarship.org/uc/item/3vk1t1q0.

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

Council of Science Editors:

Denholtz M. Long-range chromatin contacts reveal a role for the pluripotency and Polycomb networks in genome organization. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/3vk1t1q0

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

11. 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, Paris Saclay

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). Paris Saclay. 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, Paris Saclay. Accessed December 12, 2019. 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. 12 Dec 2019.

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]. Paris Saclay; 2019. [cited 2019 Dec 12]. 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]. Paris Saclay; 2019. Available from: http://www.theses.fr/2019SACLE011


University of California – Santa Cruz

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

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

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

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

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

MLA Handbook (7th Edition):

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

Vancouver:

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

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

Council of Science Editors:

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

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


University of Cambridge

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

Degree: 2019, University of Cambridge

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

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

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

MLA Handbook (7th Edition):

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

Vancouver:

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

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

Council of Science Editors:

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

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


Kyoto University / 京都大学

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

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

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

新制・課程博士

甲第18515号

医科博第56号

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

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

APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

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

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

MLA Handbook (7th Edition):

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

Vancouver:

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

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

Council of Science Editors:

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

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


Kansas State University

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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


University of Toronto

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

Degree: 2011, University of Toronto

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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


University of Minnesota

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

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

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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


Boston University

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

Degree: PhD, Molecular Medicine, 2014, Boston University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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

19. 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 December 12, 2019. 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. 12 Dec 2019.

Vancouver:

Paredes MG. Utilizing geometric cues for hiPSC-cardiomyocytes maturation on 2D patterned surfaces for regenerative medicine. [Internet] [Thesis]. Brown University; 2018. [cited 2019 Dec 12]. 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


Penn State University

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

Degree: 2017, Penn State University

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

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

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

MLA Handbook (7th Edition):

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

Vancouver:

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

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

Council of Science Editors:

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

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


UCLA

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

Degree: Molec & Med Pharmacology, 2014, UCLA

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

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

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

MLA Handbook (7th Edition):

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

Vancouver:

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

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

Council of Science Editors:

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

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


Kyoto University / 京都大学

22. Hino, Kyosuke. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva : 進行性骨化性線維異形成症における変異ACVR1の新たな機能.

Degree: 博士(医学), 2016, Kyoto University / 京都大学

新制・論文博士

乙第13031号

論医博第2113号

Subjects/Keywords: induced pluripotent stem cell (iPSC); fibrodysplasia ossificans progressiva (FOP); heterotopic ossification; bone morphogenetic protein (BMP); transforming growth factor (TGF)

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APA (6th Edition):

Hino, K. (2016). Neofunction of ACVR1 in fibrodysplasia ossificans progressiva : 進行性骨化性線維異形成症における変異ACVR1の新たな機能. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215941 ; http://dx.doi.org/10.14989/doctor.r13031

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):

Hino, Kyosuke. “Neofunction of ACVR1 in fibrodysplasia ossificans progressiva : 進行性骨化性線維異形成症における変異ACVR1の新たな機能.” 2016. Thesis, Kyoto University / 京都大学. Accessed December 12, 2019. http://hdl.handle.net/2433/215941 ; http://dx.doi.org/10.14989/doctor.r13031.

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

MLA Handbook (7th Edition):

Hino, Kyosuke. “Neofunction of ACVR1 in fibrodysplasia ossificans progressiva : 進行性骨化性線維異形成症における変異ACVR1の新たな機能.” 2016. Web. 12 Dec 2019.

Vancouver:

Hino K. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva : 進行性骨化性線維異形成症における変異ACVR1の新たな機能. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2433/215941 ; http://dx.doi.org/10.14989/doctor.r13031.

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

Council of Science Editors:

Hino K. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva : 進行性骨化性線維異形成症における変異ACVR1の新たな機能. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215941 ; http://dx.doi.org/10.14989/doctor.r13031

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


Kyoto University

23. Hino, Kyosuke. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva .

Degree: 2016, Kyoto University

Subjects/Keywords: induced pluripotent stem cell (iPSC); fibrodysplasia ossificans progressiva (FOP); heterotopic ossification; bone morphogenetic protein (BMP); transforming growth factor (TGF)

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APA (6th Edition):

Hino, K. (2016). Neofunction of ACVR1 in fibrodysplasia ossificans progressiva . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/215941

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):

Hino, Kyosuke. “Neofunction of ACVR1 in fibrodysplasia ossificans progressiva .” 2016. Thesis, Kyoto University. Accessed December 12, 2019. http://hdl.handle.net/2433/215941.

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

MLA Handbook (7th Edition):

Hino, Kyosuke. “Neofunction of ACVR1 in fibrodysplasia ossificans progressiva .” 2016. Web. 12 Dec 2019.

Vancouver:

Hino K. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva . [Internet] [Thesis]. Kyoto University; 2016. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/2433/215941.

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

Council of Science Editors:

Hino K. Neofunction of ACVR1 in fibrodysplasia ossificans progressiva . [Thesis]. Kyoto University; 2016. Available from: http://hdl.handle.net/2433/215941

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

24. Pérez, B. Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type.

Degree: 2018, Elsevier B.V.

Subjects/Keywords: Induced pluripotent stem cell (iPSC); Fibroblast; Methylmalonic acidemia; Nucleotide of exon; Sendai virus; Biología y Biomedicina / Biología

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APA (6th Edition):

Pérez, B. (2018). Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. (Thesis). Elsevier B.V. Retrieved from http://hdl.handle.net/10486/683380

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):

Pérez, B. “Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type.” 2018. Thesis, Elsevier B.V. Accessed December 12, 2019. http://hdl.handle.net/10486/683380.

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

MLA Handbook (7th Edition):

Pérez, B. “Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type.” 2018. Web. 12 Dec 2019.

Vancouver:

Pérez B. Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. [Internet] [Thesis]. Elsevier B.V.; 2018. [cited 2019 Dec 12]. Available from: http://hdl.handle.net/10486/683380.

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

Council of Science Editors:

Pérez B. Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. [Thesis]. Elsevier B.V.; 2018. Available from: http://hdl.handle.net/10486/683380

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


Tampere University

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

Degree: 2017, Tampere University

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Marttila, Suvi. “Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view .” 2017. Masters Thesis, Tampere University. Accessed December 12, 2019. https://trepo.tuni.fi/handle/10024/101732.

MLA Handbook (7th Edition):

Marttila, Suvi. “Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view .” 2017. Web. 12 Dec 2019.

Vancouver:

Marttila S. Establishment and characterisation of new human induced pluripotent stem cell lines and cardiomyocyte differentiation : a comparative view . [Internet] [Masters thesis]. Tampere University; 2017. [cited 2019 Dec 12]. Available from: https://trepo.tuni.fi/handle/10024/101732.

Council of Science Editors:

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


Virginia Tech

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

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

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

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

MLA Handbook (7th Edition):

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

Vancouver:

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

Council of Science Editors:

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


University of California – Berkeley

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

Degree: Bioengineering, 2011, University of California – Berkeley

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

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

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

MLA Handbook (7th Edition):

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

Vancouver:

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

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

Council of Science Editors:

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

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


Texas Medical Center

28. Bui, Jacquelin Hanh. Correction of Cystic Fibrosis-specific Induced Pluripotent Stem Cells.

Degree: PhD, 2013, Texas Medical Center

  Cystic Fibrosis (CF), affecting 1 in 3,500 live births in the US, is a disease caused by aberrant expression of the Cystic Fibrosis Transmemebrane… (more)

Subjects/Keywords: induced pluripotent stem cell; zinc finger nucleases; Cystic Fibrosis; Medicine and Health Sciences

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

APA (6th Edition):

Bui, J. H. (2013). Correction of Cystic Fibrosis-specific Induced Pluripotent Stem Cells. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/521

Chicago Manual of Style (16th Edition):

Bui, Jacquelin Hanh. “Correction of Cystic Fibrosis-specific Induced Pluripotent Stem Cells.” 2013. Doctoral Dissertation, Texas Medical Center. Accessed December 12, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/521.

MLA Handbook (7th Edition):

Bui, Jacquelin Hanh. “Correction of Cystic Fibrosis-specific Induced Pluripotent Stem Cells.” 2013. Web. 12 Dec 2019.

Vancouver:

Bui JH. Correction of Cystic Fibrosis-specific Induced Pluripotent Stem Cells. [Internet] [Doctoral dissertation]. Texas Medical Center; 2013. [cited 2019 Dec 12]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/521.

Council of Science Editors:

Bui JH. Correction of Cystic Fibrosis-specific Induced Pluripotent Stem Cells. [Doctoral Dissertation]. Texas Medical Center; 2013. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/521


NSYSU

29. Huang, Sheng-feng. Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients.

Degree: Master, Institute of Biomedical Sciences, 2012, NSYSU

 Breast cancer is the most common cancer in Taiwanese women and the invasive ductal carcinoma (IDC) is the most common type. Increasing evidence shows that… (more)

Subjects/Keywords: reprogramming factor; induce induced pluripotent stem cell; tissue microarray; Invasive ductal carcinoma

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

APA (6th Edition):

Huang, S. (2012). Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255

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):

Huang, Sheng-feng. “Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients.” 2012. Thesis, NSYSU. Accessed December 12, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255.

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

MLA Handbook (7th Edition):

Huang, Sheng-feng. “Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients.” 2012. Web. 12 Dec 2019.

Vancouver:

Huang S. Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients. [Internet] [Thesis]. NSYSU; 2012. [cited 2019 Dec 12]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255.

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

Council of Science Editors:

Huang S. Association of Oct4, Sox2, Nanog and Lin28 Protein Expression Levels with the Prognosis of Invasive Mammary Ductal Carcinoma Patients. [Thesis]. NSYSU; 2012. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0830112-143255

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


University of California – San Diego

30. Li, Zhe. Integrative genomic analysis of cell fate conversion.

Degree: Biology, 2014, University of California – San Diego

 Ectopic expression of reprogramming factors has been widely adopted to reprogram somatic nucleus into a pluripotent state to generate induced pluripotent stem cells (iPSCs). However,… (more)

Subjects/Keywords: Biology; epigenomic; genomic; induced pluripotent stem cells; somatic cell nuclear transfer; transcriptomic

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

APA (6th Edition):

Li, Z. (2014). Integrative genomic analysis of cell fate conversion. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/8zb078tv

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):

Li, Zhe. “Integrative genomic analysis of cell fate conversion.” 2014. Thesis, University of California – San Diego. Accessed December 12, 2019. http://www.escholarship.org/uc/item/8zb078tv.

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

MLA Handbook (7th Edition):

Li, Zhe. “Integrative genomic analysis of cell fate conversion.” 2014. Web. 12 Dec 2019.

Vancouver:

Li Z. Integrative genomic analysis of cell fate conversion. [Internet] [Thesis]. University of California – San Diego; 2014. [cited 2019 Dec 12]. Available from: http://www.escholarship.org/uc/item/8zb078tv.

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

Council of Science Editors:

Li Z. Integrative genomic analysis of cell fate conversion. [Thesis]. University of California – San Diego; 2014. Available from: http://www.escholarship.org/uc/item/8zb078tv

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

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