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You searched for subject:(iPS cells). Showing records 1 – 30 of 55 total matches.

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1. Rossi, Maurizio. The cell cycle genes regulation of IPS cells and the role of SWI/SNF chromatin remodelling enzymes during them differentiation.

Degree: 2012, Università degli Studi di Catania

Lo stato di cellula pluripotente può essere raggiunto con l espressione ectopica di alcuni fattori di trascrizione che possono riprogrammare le cellule somatiche. (Takahashi, K., e Yamanaka, S., 2006; Takahashi, K., e Yamanaka, S., 2007).

Subjects/Keywords: Area 05 - Scienze biologiche; iPS cell Cycle, iPS differentiation and induced pluripoten setm cells (iPS)

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APA (6th Edition):

Rossi, M. (2012). The cell cycle genes regulation of IPS cells and the role of SWI/SNF chromatin remodelling enzymes during them differentiation. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/922

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):

Rossi, Maurizio. “The cell cycle genes regulation of IPS cells and the role of SWI/SNF chromatin remodelling enzymes during them differentiation.” 2012. Thesis, Università degli Studi di Catania. Accessed December 08, 2019. http://hdl.handle.net/10761/922.

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

MLA Handbook (7th Edition):

Rossi, Maurizio. “The cell cycle genes regulation of IPS cells and the role of SWI/SNF chromatin remodelling enzymes during them differentiation.” 2012. Web. 08 Dec 2019.

Vancouver:

Rossi M. The cell cycle genes regulation of IPS cells and the role of SWI/SNF chromatin remodelling enzymes during them differentiation. [Internet] [Thesis]. Università degli Studi di Catania; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10761/922.

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

Council of Science Editors:

Rossi M. The cell cycle genes regulation of IPS cells and the role of SWI/SNF chromatin remodelling enzymes during them differentiation. [Thesis]. Università degli Studi di Catania; 2012. Available from: http://hdl.handle.net/10761/922

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


University of Edinburgh

2. Sendfeld, Franziska. Modelling Brugada Syndrome using induced pluripotent stem cells.

Degree: PhD, 2015, University of Edinburgh

 Objective: Brugada Syndrome is an autosomal dominant congenital heart disease that is responsible for 20% of sudden deaths of patients with structurally normal hearts. The… (more)

Subjects/Keywords: 616.1; iPS cells; model systems; cardiomyocytes

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APA (6th Edition):

Sendfeld, F. (2015). Modelling Brugada Syndrome using induced pluripotent stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/19557

Chicago Manual of Style (16th Edition):

Sendfeld, Franziska. “Modelling Brugada Syndrome using induced pluripotent stem cells.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/19557.

MLA Handbook (7th Edition):

Sendfeld, Franziska. “Modelling Brugada Syndrome using induced pluripotent stem cells.” 2015. Web. 08 Dec 2019.

Vancouver:

Sendfeld F. Modelling Brugada Syndrome using induced pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/19557.

Council of Science Editors:

Sendfeld F. Modelling Brugada Syndrome using induced pluripotent stem cells. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/19557


University of Toronto

3. DiLabio, Julia Alexandra Maria. Reprogramming Mouse Glioma Stem Cells with Defined Factors.

Degree: 2012, University of Toronto

This thesis shows that p53-deficient mouse glioma brain tumour stem cells (BTSCs), which fail to express pluripotency factors, can be reprogrammed with specific transcription factors… (more)

Subjects/Keywords: cancer; glioma; reprogramming; stem cells; iPS; 0307

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APA (6th Edition):

DiLabio, J. A. M. (2012). Reprogramming Mouse Glioma Stem Cells with Defined Factors. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42904

Chicago Manual of Style (16th Edition):

DiLabio, Julia Alexandra Maria. “Reprogramming Mouse Glioma Stem Cells with Defined Factors.” 2012. Masters Thesis, University of Toronto. Accessed December 08, 2019. http://hdl.handle.net/1807/42904.

MLA Handbook (7th Edition):

DiLabio, Julia Alexandra Maria. “Reprogramming Mouse Glioma Stem Cells with Defined Factors.” 2012. Web. 08 Dec 2019.

Vancouver:

DiLabio JAM. Reprogramming Mouse Glioma Stem Cells with Defined Factors. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1807/42904.

Council of Science Editors:

DiLabio JAM. Reprogramming Mouse Glioma Stem Cells with Defined Factors. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/42904


Universiteit Utrecht

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

Degree: 2014, Universiteit Utrecht

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Hoeven, T van den. “Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming.” 2014. Masters Thesis, Universiteit Utrecht. Accessed December 08, 2019. http://dspace.library.uu.nl:8080/handle/1874/297927.

MLA Handbook (7th Edition):

Hoeven, T van den. “Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming.” 2014. Web. 08 Dec 2019.

Vancouver:

Hoeven Tvd. Induced pluripotent stem cells: Induction of pluripotency and the molecular mechanism of partial reprogramming. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2019 Dec 08]. Available from: http://dspace.library.uu.nl:8080/handle/1874/297927.

Council of Science Editors:

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

5. Zomer, Helena Debiazi. Estabelecimento de cultura de células de pluripotência induzida a partir de células tronco derivadas do tecido adiposo de coelhos.

Degree: Mestrado, Anatomia dos Animais Domésticos e Silvestres, 2013, University of São Paulo

As células de pluripotência induzida (iPS) foram reportadas pela primeira vez em 2006 por Takahashi e Yamanaka e desde então vem sendo extensivamente estudadas. Por… (more)

Subjects/Keywords: ADSC; ADSC; células tronco mesenquimais; iPS; iPS; mensechymal stem cells; MSC; MSC

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APA (6th Edition):

Zomer, H. D. (2013). Estabelecimento de cultura de células de pluripotência induzida a partir de células tronco derivadas do tecido adiposo de coelhos. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/10/10132/tde-18072014-103412/ ;

Chicago Manual of Style (16th Edition):

Zomer, Helena Debiazi. “Estabelecimento de cultura de células de pluripotência induzida a partir de células tronco derivadas do tecido adiposo de coelhos.” 2013. Masters Thesis, University of São Paulo. Accessed December 08, 2019. http://www.teses.usp.br/teses/disponiveis/10/10132/tde-18072014-103412/ ;.

MLA Handbook (7th Edition):

Zomer, Helena Debiazi. “Estabelecimento de cultura de células de pluripotência induzida a partir de células tronco derivadas do tecido adiposo de coelhos.” 2013. Web. 08 Dec 2019.

Vancouver:

Zomer HD. Estabelecimento de cultura de células de pluripotência induzida a partir de células tronco derivadas do tecido adiposo de coelhos. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2019 Dec 08]. Available from: http://www.teses.usp.br/teses/disponiveis/10/10132/tde-18072014-103412/ ;.

Council of Science Editors:

Zomer HD. Estabelecimento de cultura de células de pluripotência induzida a partir de células tronco derivadas do tecido adiposo de coelhos. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/10/10132/tde-18072014-103412/ ;


University of Edinburgh

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

Degree: PhD, 2012, University of Edinburgh

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Sartori, Chiara. “Generation of ovine induced pluripotent stem cells.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/6491.

MLA Handbook (7th Edition):

Sartori, Chiara. “Generation of ovine induced pluripotent stem cells.” 2012. Web. 08 Dec 2019.

Vancouver:

Sartori C. Generation of ovine induced pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/6491.

Council of Science Editors:

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


University of California – San Francisco

7. White, Mark Philip. The Role of NOTCH1 Signaling in Aortic Valve Calcification.

Degree: Biomedical Sciences, 2012, University of California – San Francisco

 Calcification of the aortic valve is a common disease affecting many people, and requires invasive valve replacement surgery to prevent irreparable damage to the heart.… (more)

Subjects/Keywords: Molecular biology; Aortic Valve; Calcification; iPS Cells; Stem Cells

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APA (6th Edition):

White, M. P. (2012). The Role of NOTCH1 Signaling in Aortic Valve Calcification. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/87s318ww

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):

White, Mark Philip. “The Role of NOTCH1 Signaling in Aortic Valve Calcification.” 2012. Thesis, University of California – San Francisco. Accessed December 08, 2019. http://www.escholarship.org/uc/item/87s318ww.

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

MLA Handbook (7th Edition):

White, Mark Philip. “The Role of NOTCH1 Signaling in Aortic Valve Calcification.” 2012. Web. 08 Dec 2019.

Vancouver:

White MP. The Role of NOTCH1 Signaling in Aortic Valve Calcification. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/87s318ww.

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

Council of Science Editors:

White MP. The Role of NOTCH1 Signaling in Aortic Valve Calcification. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/87s318ww

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


University of Lund

8. Wood, James. Integration and function of new neurons generated from fibroblasts and adult neural stem cells in the pathological brain.

Degree: 2011, University of Lund

 In Papers One through Six we have investigated the function and integration of “new” neurons – new neurons born from neural stem cells in the… (more)

Subjects/Keywords: Neurologi; neurogenesis; neural stem cells; iNs; iPS cells; stroke; epilepsy; electrophysiology

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APA (6th Edition):

Wood, J. (2011). Integration and function of new neurons generated from fibroblasts and adult neural stem cells in the pathological brain. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/2206020 ; http://portal.research.lu.se/ws/files/3453178/2206040.pdf

Chicago Manual of Style (16th Edition):

Wood, James. “Integration and function of new neurons generated from fibroblasts and adult neural stem cells in the pathological brain.” 2011. Doctoral Dissertation, University of Lund. Accessed December 08, 2019. http://lup.lub.lu.se/record/2206020 ; http://portal.research.lu.se/ws/files/3453178/2206040.pdf.

MLA Handbook (7th Edition):

Wood, James. “Integration and function of new neurons generated from fibroblasts and adult neural stem cells in the pathological brain.” 2011. Web. 08 Dec 2019.

Vancouver:

Wood J. Integration and function of new neurons generated from fibroblasts and adult neural stem cells in the pathological brain. [Internet] [Doctoral dissertation]. University of Lund; 2011. [cited 2019 Dec 08]. Available from: http://lup.lub.lu.se/record/2206020 ; http://portal.research.lu.se/ws/files/3453178/2206040.pdf.

Council of Science Editors:

Wood J. Integration and function of new neurons generated from fibroblasts and adult neural stem cells in the pathological brain. [Doctoral Dissertation]. University of Lund; 2011. Available from: http://lup.lub.lu.se/record/2206020 ; http://portal.research.lu.se/ws/files/3453178/2206040.pdf


Kyoto University / 京都大学

9. Oshima, Nobu. Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors : 特定因子による大腸癌細胞への癌幹細胞特性の誘導.

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

Oshima N, Yamada Y, Nagayama S, Kawada K, Hasegawa S, et al. (2014) Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors. PLoS ONE 9(7): e101735. doi:10.1371/journal.pone.0101735

新制・課程博士

甲第18547号

医博第3940号

Subjects/Keywords: Cancer Stem Cells; Reprogramming; iPS cells; Colon Cancer; Serial transplantation; Dye-efflux; Stem cells

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APA (6th Edition):

Oshima, N. (2014). Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors : 特定因子による大腸癌細胞への癌幹細胞特性の誘導. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/192147 ; http://dx.doi.org/10.14989/doctor.k18547

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):

Oshima, Nobu. “Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors : 特定因子による大腸癌細胞への癌幹細胞特性の誘導.” 2014. Thesis, Kyoto University / 京都大学. Accessed December 08, 2019. http://hdl.handle.net/2433/192147 ; http://dx.doi.org/10.14989/doctor.k18547.

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

MLA Handbook (7th Edition):

Oshima, Nobu. “Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors : 特定因子による大腸癌細胞への癌幹細胞特性の誘導.” 2014. Web. 08 Dec 2019.

Vancouver:

Oshima N. Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors : 特定因子による大腸癌細胞への癌幹細胞特性の誘導. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2433/192147 ; http://dx.doi.org/10.14989/doctor.k18547.

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

Council of Science Editors:

Oshima N. Induction of Cancer Stem Cell Properties in Colon Cancer Cells by Defined Factors : 特定因子による大腸癌細胞への癌幹細胞特性の誘導. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/192147 ; http://dx.doi.org/10.14989/doctor.k18547

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

10. Nasu, Akira. Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin : 同一ドナー由来のiPS細胞の軟骨・骨分化傾向は、由来細胞よりもクローンにより左右される.

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

新制・課程博士

甲第18504号

医博第3924号

Subjects/Keywords: iPS cells; Cartilage; Bone; Differentiation

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APA (6th Edition):

Nasu, A. (2014). Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin : 同一ドナー由来のiPS細胞の軟骨・骨分化傾向は、由来細胞よりもクローンにより左右される. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/189661 ; http://dx.doi.org/10.14989/doctor.k18504

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):

Nasu, Akira. “Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin : 同一ドナー由来のiPS細胞の軟骨・骨分化傾向は、由来細胞よりもクローンにより左右される.” 2014. Thesis, Kyoto University / 京都大学. Accessed December 08, 2019. http://hdl.handle.net/2433/189661 ; http://dx.doi.org/10.14989/doctor.k18504.

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

MLA Handbook (7th Edition):

Nasu, Akira. “Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin : 同一ドナー由来のiPS細胞の軟骨・骨分化傾向は、由来細胞よりもクローンにより左右される.” 2014. Web. 08 Dec 2019.

Vancouver:

Nasu A. Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin : 同一ドナー由来のiPS細胞の軟骨・骨分化傾向は、由来細胞よりもクローンにより左右される. [Internet] [Thesis]. Kyoto University / 京都大学; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2433/189661 ; http://dx.doi.org/10.14989/doctor.k18504.

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

Council of Science Editors:

Nasu A. Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin : 同一ドナー由来のiPS細胞の軟骨・骨分化傾向は、由来細胞よりもクローンにより左右される. [Thesis]. Kyoto University / 京都大学; 2014. Available from: http://hdl.handle.net/2433/189661 ; http://dx.doi.org/10.14989/doctor.k18504

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

11. Kondo, Takayuki. Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness : アルツハイマー病患者由来iPS細胞を用いた細胞内Aβ関連ストレスと薬剤応答性の解明.

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

Final publication is available at http://www.cell.com/cell-stem-cell/abstract/S1934-5909(13)00012-X

新制・課程博士

甲第19622号

医博第4129号

Subjects/Keywords: Alzheimer's disease; iPS cells; Aβ oligomer; disease modeling; sporadic case

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APA (6th Edition):

Kondo, T. (2016). Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness : アルツハイマー病患者由来iPS細胞を用いた細胞内Aβ関連ストレスと薬剤応答性の解明. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/215448 ; http://dx.doi.org/10.14989/doctor.k19622

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):

Kondo, Takayuki. “Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness : アルツハイマー病患者由来iPS細胞を用いた細胞内Aβ関連ストレスと薬剤応答性の解明.” 2016. Thesis, Kyoto University / 京都大学. Accessed December 08, 2019. http://hdl.handle.net/2433/215448 ; http://dx.doi.org/10.14989/doctor.k19622.

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

MLA Handbook (7th Edition):

Kondo, Takayuki. “Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness : アルツハイマー病患者由来iPS細胞を用いた細胞内Aβ関連ストレスと薬剤応答性の解明.” 2016. Web. 08 Dec 2019.

Vancouver:

Kondo T. Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness : アルツハイマー病患者由来iPS細胞を用いた細胞内Aβ関連ストレスと薬剤応答性の解明. [Internet] [Thesis]. Kyoto University / 京都大学; 2016. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2433/215448 ; http://dx.doi.org/10.14989/doctor.k19622.

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

Council of Science Editors:

Kondo T. Modeling Alzheimer’s Disease with iPSCs Reveals Stress Phenotypes Associated with Intracellular Aβ and Differential Drug Responsiveness : アルツハイマー病患者由来iPS細胞を用いた細胞内Aβ関連ストレスと薬剤応答性の解明. [Thesis]. Kyoto University / 京都大学; 2016. Available from: http://hdl.handle.net/2433/215448 ; http://dx.doi.org/10.14989/doctor.k19622

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


Case Western Reserve University

12. Balow, Stephanie Ann. Investigation of CHD7 Function in Developmental Models of CHARGE Syndrome.

Degree: PhD, Genetics, 2014, Case Western Reserve University

 Epigenetic regulation of the genome is essential for regulating gene expression to ensure proper tissue differentiation and patterning during embryonic development. The importance of epigenetic… (more)

Subjects/Keywords: Genetics; CHD7; FBXL10; CHARGE syndrome; zebrafish; development; iPS cells

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APA (6th Edition):

Balow, S. A. (2014). Investigation of CHD7 Function in Developmental Models of CHARGE Syndrome. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1396625345

Chicago Manual of Style (16th Edition):

Balow, Stephanie Ann. “Investigation of CHD7 Function in Developmental Models of CHARGE Syndrome.” 2014. Doctoral Dissertation, Case Western Reserve University. Accessed December 08, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1396625345.

MLA Handbook (7th Edition):

Balow, Stephanie Ann. “Investigation of CHD7 Function in Developmental Models of CHARGE Syndrome.” 2014. Web. 08 Dec 2019.

Vancouver:

Balow SA. Investigation of CHD7 Function in Developmental Models of CHARGE Syndrome. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2014. [cited 2019 Dec 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1396625345.

Council of Science Editors:

Balow SA. Investigation of CHD7 Function in Developmental Models of CHARGE Syndrome. [Doctoral Dissertation]. Case Western Reserve University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1396625345

13. 杉本, 浩司. Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果.

Degree: 博士(歯学), 2013, Nagasaki University / 長崎大学

 Retroviral transduction of four transcription factors (Oct4, Sox2, Klf4 and c-Myc) or three factors, excluding c-Myc, has been shown to initiate a reprogramming process that… (more)

Subjects/Keywords: Hypoxia; Hypoxia inducible factors; IPS cells; Pluripotency; Transcription factors

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APA (6th Edition):

杉本, . (2013). Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果. (Thesis). Nagasaki University / 長崎大学. Retrieved from http://hdl.handle.net/10069/35466

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):

杉本, 浩司. “Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果.” 2013. Thesis, Nagasaki University / 長崎大学. Accessed December 08, 2019. http://hdl.handle.net/10069/35466.

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

MLA Handbook (7th Edition):

杉本, 浩司. “Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果.” 2013. Web. 08 Dec 2019.

Vancouver:

杉本 . Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果. [Internet] [Thesis]. Nagasaki University / 長崎大学; 2013. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/10069/35466.

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

Council of Science Editors:

杉本 . Effects of hypoxia on pluripotency in murine iPS cells : マウスiPS細胞の多能性に対する低酸素の効果. [Thesis]. Nagasaki University / 長崎大学; 2013. Available from: http://hdl.handle.net/10069/35466

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


Kyoto University

14. Nasu, Akira. Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin .

Degree: 2014, Kyoto University

Subjects/Keywords: iPS cells; Cartilage; Bone; Differentiation

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APA (6th Edition):

Nasu, A. (2014). Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/189661

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):

Nasu, Akira. “Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin .” 2014. Thesis, Kyoto University. Accessed December 08, 2019. http://hdl.handle.net/2433/189661.

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

MLA Handbook (7th Edition):

Nasu, Akira. “Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin .” 2014. Web. 08 Dec 2019.

Vancouver:

Nasu A. Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin . [Internet] [Thesis]. Kyoto University; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2433/189661.

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

Council of Science Editors:

Nasu A. Genetically Matched Human iPS Cells Reveal that Propensity for Cartilage and Bone Differentiation Differs with Clones, not Cell Type of Origin . [Thesis]. Kyoto University; 2014. Available from: http://hdl.handle.net/2433/189661

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


Boston University

15. Koch, Clarissa. Characterizing the effect of transthyretin amyloid on the heart.

Degree: PhD, Pathology, 2015, Boston University

 Transthyretin (TTR)-associated amyloidoses are diseases wherein wild-type or mutant TTR forms amyloid fibrils that infiltrate multiple organs. Wild-type TTR amyloidosis, ATTRwt, is a sporadic disease… (more)

Subjects/Keywords: Cellular biology; Amyloid; Doxycycline; Heart; iPS cells; Oligomer; Transthyretin

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APA (6th Edition):

Koch, C. (2015). Characterizing the effect of transthyretin amyloid on the heart. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16195

Chicago Manual of Style (16th Edition):

Koch, Clarissa. “Characterizing the effect of transthyretin amyloid on the heart.” 2015. Doctoral Dissertation, Boston University. Accessed December 08, 2019. http://hdl.handle.net/2144/16195.

MLA Handbook (7th Edition):

Koch, Clarissa. “Characterizing the effect of transthyretin amyloid on the heart.” 2015. Web. 08 Dec 2019.

Vancouver:

Koch C. Characterizing the effect of transthyretin amyloid on the heart. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2144/16195.

Council of Science Editors:

Koch C. Characterizing the effect of transthyretin amyloid on the heart. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16195


University of Melbourne

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

Degree: 2017, University of Melbourne

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Motazedian, Ali. “Lymphocyte differentiation from pluripotent stem cells.” 2017. Doctoral Dissertation, University of Melbourne. Accessed December 08, 2019. http://hdl.handle.net/11343/191658.

MLA Handbook (7th Edition):

Motazedian, Ali. “Lymphocyte differentiation from pluripotent stem cells.” 2017. Web. 08 Dec 2019.

Vancouver:

Motazedian A. Lymphocyte differentiation from pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/11343/191658.

Council of Science Editors:

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

17. MARIANNE SHEILA D/O SURIAKUMARAN. PHENOTYPIC AND MOLECULAR FEATURES UNDERLYING MOTOR NEURON DEGENERATION IN SBMA IDENTIFIED THROUGH THE USE OF PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS.

Degree: 2017, National University of Singapore

Subjects/Keywords: SBMA; iPS cells; motor neurons

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APA (6th Edition):

SURIAKUMARAN, M. S. D. (2017). PHENOTYPIC AND MOLECULAR FEATURES UNDERLYING MOTOR NEURON DEGENERATION IN SBMA IDENTIFIED THROUGH THE USE OF PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/138901

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):

SURIAKUMARAN, MARIANNE SHEILA D/O. “PHENOTYPIC AND MOLECULAR FEATURES UNDERLYING MOTOR NEURON DEGENERATION IN SBMA IDENTIFIED THROUGH THE USE OF PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS.” 2017. Thesis, National University of Singapore. Accessed December 08, 2019. http://scholarbank.nus.edu.sg/handle/10635/138901.

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

MLA Handbook (7th Edition):

SURIAKUMARAN, MARIANNE SHEILA D/O. “PHENOTYPIC AND MOLECULAR FEATURES UNDERLYING MOTOR NEURON DEGENERATION IN SBMA IDENTIFIED THROUGH THE USE OF PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS.” 2017. Web. 08 Dec 2019.

Vancouver:

SURIAKUMARAN MSD. PHENOTYPIC AND MOLECULAR FEATURES UNDERLYING MOTOR NEURON DEGENERATION IN SBMA IDENTIFIED THROUGH THE USE OF PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS. [Internet] [Thesis]. National University of Singapore; 2017. [cited 2019 Dec 08]. Available from: http://scholarbank.nus.edu.sg/handle/10635/138901.

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

Council of Science Editors:

SURIAKUMARAN MSD. PHENOTYPIC AND MOLECULAR FEATURES UNDERLYING MOTOR NEURON DEGENERATION IN SBMA IDENTIFIED THROUGH THE USE OF PATIENT-DERIVED INDUCED PLURIPOTENT STEM CELLS. [Thesis]. National University of Singapore; 2017. Available from: http://scholarbank.nus.edu.sg/handle/10635/138901

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

18. LEE XING WEI, ESTHER. USE OF IPS CELL-DERIVED NEURAL STEM CELLS AS A CELLULAR VEHICLE FOR GLIOMA AND BREAST CANCER THERAPY.

Degree: 2011, National University of Singapore

Subjects/Keywords: iPS cells; cancer therapy

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APA (6th Edition):

LEE XING WEI, E. (2011). USE OF IPS CELL-DERIVED NEURAL STEM CELLS AS A CELLULAR VEHICLE FOR GLIOMA AND BREAST CANCER THERAPY. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/145324

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):

LEE XING WEI, ESTHER. “USE OF IPS CELL-DERIVED NEURAL STEM CELLS AS A CELLULAR VEHICLE FOR GLIOMA AND BREAST CANCER THERAPY.” 2011. Thesis, National University of Singapore. Accessed December 08, 2019. http://scholarbank.nus.edu.sg/handle/10635/145324.

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

MLA Handbook (7th Edition):

LEE XING WEI, ESTHER. “USE OF IPS CELL-DERIVED NEURAL STEM CELLS AS A CELLULAR VEHICLE FOR GLIOMA AND BREAST CANCER THERAPY.” 2011. Web. 08 Dec 2019.

Vancouver:

LEE XING WEI E. USE OF IPS CELL-DERIVED NEURAL STEM CELLS AS A CELLULAR VEHICLE FOR GLIOMA AND BREAST CANCER THERAPY. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2019 Dec 08]. Available from: http://scholarbank.nus.edu.sg/handle/10635/145324.

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

Council of Science Editors:

LEE XING WEI E. USE OF IPS CELL-DERIVED NEURAL STEM CELLS AS A CELLULAR VEHICLE FOR GLIOMA AND BREAST CANCER THERAPY. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/145324

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


University of California – San Francisco

19. Judson, Robert Laird. MicroRNAs Promote Induced Pluripotency Through the Regulation of Cooperative Gene Networks.

Degree: Biomedical Sciences, 2012, University of California – San Francisco

 MicroRNAs (miRNAs) are a class of endogenous non-coding RNAs that post-transcriptionally co‐regulate networks of genes. The evolutionary history of miRNAs suggests they may play major… (more)

Subjects/Keywords: Cellular biology; Molecular biology; iPS; microRNA; Reprogramming; Stem Cells

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APA (6th Edition):

Judson, R. L. (2012). MicroRNAs Promote Induced Pluripotency Through the Regulation of Cooperative Gene Networks. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3595s812

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):

Judson, Robert Laird. “MicroRNAs Promote Induced Pluripotency Through the Regulation of Cooperative Gene Networks.” 2012. Thesis, University of California – San Francisco. Accessed December 08, 2019. http://www.escholarship.org/uc/item/3595s812.

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

MLA Handbook (7th Edition):

Judson, Robert Laird. “MicroRNAs Promote Induced Pluripotency Through the Regulation of Cooperative Gene Networks.” 2012. Web. 08 Dec 2019.

Vancouver:

Judson RL. MicroRNAs Promote Induced Pluripotency Through the Regulation of Cooperative Gene Networks. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/3595s812.

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

Council of Science Editors:

Judson RL. MicroRNAs Promote Induced Pluripotency Through the Regulation of Cooperative Gene Networks. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/3595s812

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


University of Sydney

20. Rabbolini, David John. Genotyping and experimental modelling of inherited thrombocytopenias .

Degree: 2017, University of Sydney

 Inherited thrombocytopenia’s (IT) are characterised by low platelet counts and bleeding tendencies in affected individuals. Diagnosis of IT is important to guide treatment, inform prognosis… (more)

Subjects/Keywords: platelets; thrombocytopenia; transcription factors; next generation dequencing; IPS cells

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APA (6th Edition):

Rabbolini, D. J. (2017). Genotyping and experimental modelling of inherited thrombocytopenias . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/18144

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):

Rabbolini, David John. “Genotyping and experimental modelling of inherited thrombocytopenias .” 2017. Thesis, University of Sydney. Accessed December 08, 2019. http://hdl.handle.net/2123/18144.

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

MLA Handbook (7th Edition):

Rabbolini, David John. “Genotyping and experimental modelling of inherited thrombocytopenias .” 2017. Web. 08 Dec 2019.

Vancouver:

Rabbolini DJ. Genotyping and experimental modelling of inherited thrombocytopenias . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2123/18144.

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

Council of Science Editors:

Rabbolini DJ. Genotyping and experimental modelling of inherited thrombocytopenias . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/18144

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

21. Pini, Jonathan. Modélisation du syndrome d'Andersen dans les cellules souches pluripotentes induites : implication du canal potassique Kir2.1 dans la morphogenèse osseuse : Modeling Andersen's syndrome using induced Pluripotent Stem cells : implication of Kir2.1 potassium channel in bone morphogenesis.

Degree: Docteur es, Sciences de la vie et de la santé, 2016, Nice

Le syndrome d’Andersen est une maladie rare et associée à la perte de fonction du canal potassique Kir2.1. Afin d’étudier sa physiopathologie, nous avons généré… (more)

Subjects/Keywords: Syndrome d'Andersen; Cellules iPS; Développement osseux; Ostéoblastes; Cellules mésenchymateuses; Kir2.1; Andersen's syndrome; IPS; Bone morphogenesis; Osteoblasts; Mesenchymal cells; Kir2.1

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APA (6th Edition):

Pini, J. (2016). Modélisation du syndrome d'Andersen dans les cellules souches pluripotentes induites : implication du canal potassique Kir2.1 dans la morphogenèse osseuse : Modeling Andersen's syndrome using induced Pluripotent Stem cells : implication of Kir2.1 potassium channel in bone morphogenesis. (Doctoral Dissertation). Nice. Retrieved from http://www.theses.fr/2016NICE4042

Chicago Manual of Style (16th Edition):

Pini, Jonathan. “Modélisation du syndrome d'Andersen dans les cellules souches pluripotentes induites : implication du canal potassique Kir2.1 dans la morphogenèse osseuse : Modeling Andersen's syndrome using induced Pluripotent Stem cells : implication of Kir2.1 potassium channel in bone morphogenesis.” 2016. Doctoral Dissertation, Nice. Accessed December 08, 2019. http://www.theses.fr/2016NICE4042.

MLA Handbook (7th Edition):

Pini, Jonathan. “Modélisation du syndrome d'Andersen dans les cellules souches pluripotentes induites : implication du canal potassique Kir2.1 dans la morphogenèse osseuse : Modeling Andersen's syndrome using induced Pluripotent Stem cells : implication of Kir2.1 potassium channel in bone morphogenesis.” 2016. Web. 08 Dec 2019.

Vancouver:

Pini J. Modélisation du syndrome d'Andersen dans les cellules souches pluripotentes induites : implication du canal potassique Kir2.1 dans la morphogenèse osseuse : Modeling Andersen's syndrome using induced Pluripotent Stem cells : implication of Kir2.1 potassium channel in bone morphogenesis. [Internet] [Doctoral dissertation]. Nice; 2016. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2016NICE4042.

Council of Science Editors:

Pini J. Modélisation du syndrome d'Andersen dans les cellules souches pluripotentes induites : implication du canal potassique Kir2.1 dans la morphogenèse osseuse : Modeling Andersen's syndrome using induced Pluripotent Stem cells : implication of Kir2.1 potassium channel in bone morphogenesis. [Doctoral Dissertation]. Nice; 2016. Available from: http://www.theses.fr/2016NICE4042


University of Edinburgh

22. Liu, Jing. Reprogramming peripheral blood mononuclear cells using an efficient feeder-free, non-integration method to generate iPS cells and the effect of immunophenotype and epigenetic state on HSPC fate.

Degree: PhD, 2014, University of Edinburgh

 Background and objectives: In 2006 Shinya Yamanaka successfully reprogrammed mouse fibroblasts back to an embryonic stem cell-like state (called induced pluripotent cells, iPS cells) using… (more)

Subjects/Keywords: 616.02; iPS cells; MNC; CD34+ cells; feeder-free; episomal vectors; efficient reprogramming

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APA (6th Edition):

Liu, J. (2014). Reprogramming peripheral blood mononuclear cells using an efficient feeder-free, non-integration method to generate iPS cells and the effect of immunophenotype and epigenetic state on HSPC fate. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/10031

Chicago Manual of Style (16th Edition):

Liu, Jing. “Reprogramming peripheral blood mononuclear cells using an efficient feeder-free, non-integration method to generate iPS cells and the effect of immunophenotype and epigenetic state on HSPC fate.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed December 08, 2019. http://hdl.handle.net/1842/10031.

MLA Handbook (7th Edition):

Liu, Jing. “Reprogramming peripheral blood mononuclear cells using an efficient feeder-free, non-integration method to generate iPS cells and the effect of immunophenotype and epigenetic state on HSPC fate.” 2014. Web. 08 Dec 2019.

Vancouver:

Liu J. Reprogramming peripheral blood mononuclear cells using an efficient feeder-free, non-integration method to generate iPS cells and the effect of immunophenotype and epigenetic state on HSPC fate. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/1842/10031.

Council of Science Editors:

Liu J. Reprogramming peripheral blood mononuclear cells using an efficient feeder-free, non-integration method to generate iPS cells and the effect of immunophenotype and epigenetic state on HSPC fate. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/10031


University of Cincinnati

23. Buccini, Stephanie M. Cardiogenic differentiation of induced pluripotent stem cells for regeneration of the ischemic heart.

Degree: PhD, Medicine: Systems Biology and Physiology, 2013, University of Cincinnati

 Ischemic heart disease is the number one cause of death worldwide. Excessive cardiomyocyte death occurs following myocardial infarction, thus triggering downstream signaling cascades that alter… (more)

Subjects/Keywords: Physiological Psychology; iPS cells; myocardial infarction; cardiomyocyte differentiation; angiogenesis; mesenchymal stem cells; cardiac regeneration

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APA (6th Edition):

Buccini, S. M. (2013). Cardiogenic differentiation of induced pluripotent stem cells for regeneration of the ischemic heart. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1382373160

Chicago Manual of Style (16th Edition):

Buccini, Stephanie M. “Cardiogenic differentiation of induced pluripotent stem cells for regeneration of the ischemic heart.” 2013. Doctoral Dissertation, University of Cincinnati. Accessed December 08, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1382373160.

MLA Handbook (7th Edition):

Buccini, Stephanie M. “Cardiogenic differentiation of induced pluripotent stem cells for regeneration of the ischemic heart.” 2013. Web. 08 Dec 2019.

Vancouver:

Buccini SM. Cardiogenic differentiation of induced pluripotent stem cells for regeneration of the ischemic heart. [Internet] [Doctoral dissertation]. University of Cincinnati; 2013. [cited 2019 Dec 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1382373160.

Council of Science Editors:

Buccini SM. Cardiogenic differentiation of induced pluripotent stem cells for regeneration of the ischemic heart. [Doctoral Dissertation]. University of Cincinnati; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1382373160

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

Degree: 2013, Instituto Politécnico do Porto

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Martins, Manuella. “Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.” 2013. Thesis, Instituto Politécnico do Porto. Accessed December 08, 2019. https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369.

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

MLA Handbook (7th Edition):

Martins, Manuella. “Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts.” 2013. Web. 08 Dec 2019.

Vancouver:

Martins M. Identification of neuronal alterations induced by Shank3 mutations using iPS cells from Phelan-McDermid Patients' Fibroblasts. [Internet] [Thesis]. Instituto Politécnico do Porto; 2013. [cited 2019 Dec 08]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:recipp.ipp.pt:10400.22/2369.

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

Council of Science Editors:

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

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


University of Iowa

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

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

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Manzar, Gohar Shahwar. “Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells.” 2015. Doctoral Dissertation, University of Iowa. Accessed December 08, 2019. https://ir.uiowa.edu/etd/5808.

MLA Handbook (7th Edition):

Manzar, Gohar Shahwar. “Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells.” 2015. Web. 08 Dec 2019.

Vancouver:

Manzar GS. Generation and function of glucose-responsive insulin producing cells derived from human induced pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2019 Dec 08]. Available from: https://ir.uiowa.edu/etd/5808.

Council of Science Editors:

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

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

Degree: PhD, Distúrbios Genéticos de Desenvolvimento e Metabolismo, 2012, University of São Paulo

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

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

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

APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Bassaneze, Vinícius. “Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT.” 2012. Doctoral Dissertation, University of São Paulo. Accessed December 08, 2019. http://www.teses.usp.br/teses/disponiveis/5/5166/tde-11052012-093336/ ;.

MLA Handbook (7th Edition):

Bassaneze, Vinícius. “Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT.” 2012. Web. 08 Dec 2019.

Vancouver:

Bassaneze V. Reprogramação de células mesenquimais de tecido adiposo em células-tronco pluripotentes por meio de proteína de fusão TAT. [Internet] [Doctoral dissertation]. University of São Paulo; 2012. [cited 2019 Dec 08]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5166/tde-11052012-093336/ ;.

Council of Science Editors:

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

27. Gatinois, Vincent. Pathologies des hélicases et vieillissement précoce : modèle d'étude par dérivation de cellules souches pluripotentes induites (iPS) : Pathologies of helicases and premature aging : study by derivation of induced pluripotent stem cells.

Degree: Docteur es, Biologie Santé, 2017, Montpellier

Les hélicases sont des enzymes ubiquitaires catalysant la séparation de l’ADN double-brin et impliquées dans la réplication, la réparation de l’ADN et dans le maintien… (more)

Subjects/Keywords: Ips; Cellules souches; Hélicase; Instabilité chromosomique; Télomère; Ipsc; Stem Cells; Helicase; Chromosome instability; Telomere

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

APA (6th Edition):

Gatinois, V. (2017). Pathologies des hélicases et vieillissement précoce : modèle d'étude par dérivation de cellules souches pluripotentes induites (iPS) : Pathologies of helicases and premature aging : study by derivation of induced pluripotent stem cells. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2017MONTT042

Chicago Manual of Style (16th Edition):

Gatinois, Vincent. “Pathologies des hélicases et vieillissement précoce : modèle d'étude par dérivation de cellules souches pluripotentes induites (iPS) : Pathologies of helicases and premature aging : study by derivation of induced pluripotent stem cells.” 2017. Doctoral Dissertation, Montpellier. Accessed December 08, 2019. http://www.theses.fr/2017MONTT042.

MLA Handbook (7th Edition):

Gatinois, Vincent. “Pathologies des hélicases et vieillissement précoce : modèle d'étude par dérivation de cellules souches pluripotentes induites (iPS) : Pathologies of helicases and premature aging : study by derivation of induced pluripotent stem cells.” 2017. Web. 08 Dec 2019.

Vancouver:

Gatinois V. Pathologies des hélicases et vieillissement précoce : modèle d'étude par dérivation de cellules souches pluripotentes induites (iPS) : Pathologies of helicases and premature aging : study by derivation of induced pluripotent stem cells. [Internet] [Doctoral dissertation]. Montpellier; 2017. [cited 2019 Dec 08]. Available from: http://www.theses.fr/2017MONTT042.

Council of Science Editors:

Gatinois V. Pathologies des hélicases et vieillissement précoce : modèle d'étude par dérivation de cellules souches pluripotentes induites (iPS) : Pathologies of helicases and premature aging : study by derivation of induced pluripotent stem cells. [Doctoral Dissertation]. Montpellier; 2017. Available from: http://www.theses.fr/2017MONTT042


NSYSU

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

Degree: Master, Biological Sciences, 2017, NSYSU

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Wang, Yin-Hsuan. “The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells.” 2017. Thesis, NSYSU. Accessed December 08, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0404117-114837.

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

MLA Handbook (7th Edition):

Wang, Yin-Hsuan. “The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells.” 2017. Web. 08 Dec 2019.

Vancouver:

Wang Y. The cAMP/PKA-mediated Tau S409 phosphorylation through GSKIP/GSK3 axis in SH-SY5Y and iPS cells. [Internet] [Thesis]. NSYSU; 2017. [cited 2019 Dec 08]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0404117-114837.

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

Council of Science Editors:

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

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


University of California – San Francisco

29. Perez-Bermejo, Juan Alfredo. Protein Interaction Analysis of a Genetic Engineered, Stem Cell-Derived Model of Cardiomyopathy.

Degree: Biological and Medical Informatics, 2017, University of California – San Francisco

 Genetic association studies have yielded a wealth of information on specific variants that lead to the development of disease, but our mechanistic understanding for most… (more)

Subjects/Keywords: Molecular biology; Cellular biology; Genetics; CRISPR; Genome Engineering; iPS cells; Network Biology; Protein Interactions; Proteomics

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APA (6th Edition):

Perez-Bermejo, J. A. (2017). Protein Interaction Analysis of a Genetic Engineered, Stem Cell-Derived Model of Cardiomyopathy. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/90v7w9rv

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):

Perez-Bermejo, Juan Alfredo. “Protein Interaction Analysis of a Genetic Engineered, Stem Cell-Derived Model of Cardiomyopathy.” 2017. Thesis, University of California – San Francisco. Accessed December 08, 2019. http://www.escholarship.org/uc/item/90v7w9rv.

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

MLA Handbook (7th Edition):

Perez-Bermejo, Juan Alfredo. “Protein Interaction Analysis of a Genetic Engineered, Stem Cell-Derived Model of Cardiomyopathy.” 2017. Web. 08 Dec 2019.

Vancouver:

Perez-Bermejo JA. Protein Interaction Analysis of a Genetic Engineered, Stem Cell-Derived Model of Cardiomyopathy. [Internet] [Thesis]. University of California – San Francisco; 2017. [cited 2019 Dec 08]. Available from: http://www.escholarship.org/uc/item/90v7w9rv.

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

Council of Science Editors:

Perez-Bermejo JA. Protein Interaction Analysis of a Genetic Engineered, Stem Cell-Derived Model of Cardiomyopathy. [Thesis]. University of California – San Francisco; 2017. Available from: http://www.escholarship.org/uc/item/90v7w9rv

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


Kyoto University

30. Chen, Xike. Integration Capacity of Human Induced Pluripotent Stem Cell-Derived Cartilage .

Degree: 2019, Kyoto University

Subjects/Keywords: iPS cells; cartilage; FGF; perichondrium; chondrocyte

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APA (6th Edition):

Chen, X. (2019). Integration Capacity of Human Induced Pluripotent Stem Cell-Derived Cartilage . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242390

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):

Chen, Xike. “Integration Capacity of Human Induced Pluripotent Stem Cell-Derived Cartilage .” 2019. Thesis, Kyoto University. Accessed December 08, 2019. http://hdl.handle.net/2433/242390.

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

MLA Handbook (7th Edition):

Chen, Xike. “Integration Capacity of Human Induced Pluripotent Stem Cell-Derived Cartilage .” 2019. Web. 08 Dec 2019.

Vancouver:

Chen X. Integration Capacity of Human Induced Pluripotent Stem Cell-Derived Cartilage . [Internet] [Thesis]. Kyoto University; 2019. [cited 2019 Dec 08]. Available from: http://hdl.handle.net/2433/242390.

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

Council of Science Editors:

Chen X. Integration Capacity of Human Induced Pluripotent Stem Cell-Derived Cartilage . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242390

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

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