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You searched for subject:(ES cells). Showing records 1 – 30 of 44 total matches.

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Kyoto University / 京都大学

1. Shiraishi, Atsushi. Generation of thalamic neurons from mouse embryonic stem cells : マウス胚性幹細胞からの視床神経の分化誘導.

Degree: 博士(医学), 2018, Kyoto University / 京都大学

新制・課程博士

甲第20790号

医博第4290号

Subjects/Keywords: mouse ES cells; thalamus; caudal forebrain; self-organization; SFEBq

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

APA (6th Edition):

Shiraishi, A. (2018). Generation of thalamic neurons from mouse embryonic stem cells : マウス胚性幹細胞からの視床神経の分化誘導. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/230993 ; http://dx.doi.org/10.14989/doctor.k20790

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):

Shiraishi, Atsushi. “Generation of thalamic neurons from mouse embryonic stem cells : マウス胚性幹細胞からの視床神経の分化誘導.” 2018. Thesis, Kyoto University / 京都大学. Accessed October 16, 2019. http://hdl.handle.net/2433/230993 ; http://dx.doi.org/10.14989/doctor.k20790.

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

MLA Handbook (7th Edition):

Shiraishi, Atsushi. “Generation of thalamic neurons from mouse embryonic stem cells : マウス胚性幹細胞からの視床神経の分化誘導.” 2018. Web. 16 Oct 2019.

Vancouver:

Shiraishi A. Generation of thalamic neurons from mouse embryonic stem cells : マウス胚性幹細胞からの視床神経の分化誘導. [Internet] [Thesis]. Kyoto University / 京都大学; 2018. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2433/230993 ; http://dx.doi.org/10.14989/doctor.k20790.

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

Council of Science Editors:

Shiraishi A. Generation of thalamic neurons from mouse embryonic stem cells : マウス胚性幹細胞からの視床神経の分化誘導. [Thesis]. Kyoto University / 京都大学; 2018. Available from: http://hdl.handle.net/2433/230993 ; http://dx.doi.org/10.14989/doctor.k20790

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


Kyoto University

2. Shiraishi, Atsushi. Generation of thalamic neurons from mouse embryonic stem cells .

Degree: 2018, Kyoto University

Subjects/Keywords: mouse ES cells; thalamus; caudal forebrain; self-organization; SFEBq

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APA (6th Edition):

Shiraishi, A. (2018). Generation of thalamic neurons from mouse embryonic stem cells . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/230993

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):

Shiraishi, Atsushi. “Generation of thalamic neurons from mouse embryonic stem cells .” 2018. Thesis, Kyoto University. Accessed October 16, 2019. http://hdl.handle.net/2433/230993.

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

MLA Handbook (7th Edition):

Shiraishi, Atsushi. “Generation of thalamic neurons from mouse embryonic stem cells .” 2018. Web. 16 Oct 2019.

Vancouver:

Shiraishi A. Generation of thalamic neurons from mouse embryonic stem cells . [Internet] [Thesis]. Kyoto University; 2018. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2433/230993.

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

Council of Science Editors:

Shiraishi A. Generation of thalamic neurons from mouse embryonic stem cells . [Thesis]. Kyoto University; 2018. Available from: http://hdl.handle.net/2433/230993

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


University of Lund

3. Miskinyte, Giedre. Generation of cortical neurons through reprogramming technology.

Degree: 2018, University of Lund

 The human cortex is affected by several debilitating acute and chronic neurodegenerative disorders such as stroke, traumatic brain injury, amyotrophic lateral sclerosis and Alzheimer’s disease,… (more)

Subjects/Keywords: Cortex; Reprogramming; human ES cells; transcription factor programming; cortical projection neurons; Human adult cortical slices

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APA (6th Edition):

Miskinyte, G. (2018). Generation of cortical neurons through reprogramming technology. (Doctoral Dissertation). University of Lund. Retrieved from http://lup.lub.lu.se/record/d960f763-7d64-44c6-9574-c623790a429d ; http://portal.research.lu.se/ws/files/54878264/Kvist_kappa_G5_hela_avh.pdf

Chicago Manual of Style (16th Edition):

Miskinyte, Giedre. “Generation of cortical neurons through reprogramming technology.” 2018. Doctoral Dissertation, University of Lund. Accessed October 16, 2019. http://lup.lub.lu.se/record/d960f763-7d64-44c6-9574-c623790a429d ; http://portal.research.lu.se/ws/files/54878264/Kvist_kappa_G5_hela_avh.pdf.

MLA Handbook (7th Edition):

Miskinyte, Giedre. “Generation of cortical neurons through reprogramming technology.” 2018. Web. 16 Oct 2019.

Vancouver:

Miskinyte G. Generation of cortical neurons through reprogramming technology. [Internet] [Doctoral dissertation]. University of Lund; 2018. [cited 2019 Oct 16]. Available from: http://lup.lub.lu.se/record/d960f763-7d64-44c6-9574-c623790a429d ; http://portal.research.lu.se/ws/files/54878264/Kvist_kappa_G5_hela_avh.pdf.

Council of Science Editors:

Miskinyte G. Generation of cortical neurons through reprogramming technology. [Doctoral Dissertation]. University of Lund; 2018. Available from: http://lup.lub.lu.se/record/d960f763-7d64-44c6-9574-c623790a429d ; http://portal.research.lu.se/ws/files/54878264/Kvist_kappa_G5_hela_avh.pdf


Texas Medical Center

4. Chen, Tsai-Yu; and#60;pand#62;https://orcid.org/0000-0001-6150-6361and#60;/pand#62. The functions of SETD5 and miR-221 in embryonic stem cell differentiation.

Degree: PhD, 2017, Texas Medical Center

  Embryonic stem cells (ESCs) are a widely used model system to study cellular differentiation because of their pluripotent characteristics, and ESC differentiation is an… (more)

Subjects/Keywords: ES cells; SETD5; miR-221; Retinoic acid; differentiation; HCF1; stemness; pluripotent factors; Medicine and Health Sciences; Molecular Biology; Other Cell and Developmental Biology

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APA (6th Edition):

Chen, T. a. o. (2017). The functions of SETD5 and miR-221 in embryonic stem cell differentiation. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/817

Chicago Manual of Style (16th Edition):

Chen, Tsai-Yu; and#60;pand#62;https://orcid org/0000-0001-6150-6361and#60;/pand#62. “The functions of SETD5 and miR-221 in embryonic stem cell differentiation.” 2017. Doctoral Dissertation, Texas Medical Center. Accessed October 16, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/817.

MLA Handbook (7th Edition):

Chen, Tsai-Yu; and#60;pand#62;https://orcid org/0000-0001-6150-6361and#60;/pand#62. “The functions of SETD5 and miR-221 in embryonic stem cell differentiation.” 2017. Web. 16 Oct 2019.

Vancouver:

Chen Tao. The functions of SETD5 and miR-221 in embryonic stem cell differentiation. [Internet] [Doctoral dissertation]. Texas Medical Center; 2017. [cited 2019 Oct 16]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/817.

Council of Science Editors:

Chen Tao. The functions of SETD5 and miR-221 in embryonic stem cell differentiation. [Doctoral Dissertation]. Texas Medical Center; 2017. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/817

5. LIU QIZHI. IDENTIFICATION AND DISRUPTION OF PROVIRAL HOST FACTORS IN MEDAKA HAPLOID EMBRYONIC STEM CELLS.

Degree: 2017, National University of Singapore

Subjects/Keywords: medaka haploid ES cells; Singapore grouper iridovirus; proviral host factors; retroviral mutagenesis; global gene disruption; CRISPR-Cas9

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APA (6th Edition):

QIZHI, L. (2017). IDENTIFICATION AND DISRUPTION OF PROVIRAL HOST FACTORS IN MEDAKA HAPLOID EMBRYONIC STEM CELLS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/139362

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):

QIZHI, LIU. “IDENTIFICATION AND DISRUPTION OF PROVIRAL HOST FACTORS IN MEDAKA HAPLOID EMBRYONIC STEM CELLS.” 2017. Thesis, National University of Singapore. Accessed October 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/139362.

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

MLA Handbook (7th Edition):

QIZHI, LIU. “IDENTIFICATION AND DISRUPTION OF PROVIRAL HOST FACTORS IN MEDAKA HAPLOID EMBRYONIC STEM CELLS.” 2017. Web. 16 Oct 2019.

Vancouver:

QIZHI L. IDENTIFICATION AND DISRUPTION OF PROVIRAL HOST FACTORS IN MEDAKA HAPLOID EMBRYONIC STEM CELLS. [Internet] [Thesis]. National University of Singapore; 2017. [cited 2019 Oct 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/139362.

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

Council of Science Editors:

QIZHI L. IDENTIFICATION AND DISRUPTION OF PROVIRAL HOST FACTORS IN MEDAKA HAPLOID EMBRYONIC STEM CELLS. [Thesis]. National University of Singapore; 2017. Available from: http://scholarbank.nus.edu.sg/handle/10635/139362

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

6. 三浦, 太一. 多能性幹細胞の未分化・分化を制御するシグナル調節因子の解析.

Degree: 博士(工学), 2017, Soka University / 創価大学

Subjects/Keywords: ES cells; Naïve state; Primed state; O-GlcNAc; reactive species; Wnt signal; FGF4 signal

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APA (6th Edition):

三浦, . (2017). 多能性幹細胞の未分化・分化を制御するシグナル調節因子の解析. (Thesis). Soka University / 創価大学. Retrieved from http://hdl.handle.net/10911/4965

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):

三浦, 太一. “多能性幹細胞の未分化・分化を制御するシグナル調節因子の解析.” 2017. Thesis, Soka University / 創価大学. Accessed October 16, 2019. http://hdl.handle.net/10911/4965.

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

MLA Handbook (7th Edition):

三浦, 太一. “多能性幹細胞の未分化・分化を制御するシグナル調節因子の解析.” 2017. Web. 16 Oct 2019.

Vancouver:

三浦 . 多能性幹細胞の未分化・分化を制御するシグナル調節因子の解析. [Internet] [Thesis]. Soka University / 創価大学; 2017. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/10911/4965.

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

Council of Science Editors:

三浦 . 多能性幹細胞の未分化・分化を制御するシグナル調節因子の解析. [Thesis]. Soka University / 創価大学; 2017. Available from: http://hdl.handle.net/10911/4965

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

7. TAN ZI YING. GENE REGULATION IN PLURIPOTENT STEM CELLS.

Degree: 2017, National University of Singapore

Subjects/Keywords: 2C-like ES cells; MERVL; transcription factor binding; DNA motif; gain of function screening

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APA (6th Edition):

YING, T. Z. (2017). GENE REGULATION IN PLURIPOTENT STEM CELLS. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/136319

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):

YING, TAN ZI. “GENE REGULATION IN PLURIPOTENT STEM CELLS.” 2017. Thesis, National University of Singapore. Accessed October 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/136319.

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

MLA Handbook (7th Edition):

YING, TAN ZI. “GENE REGULATION IN PLURIPOTENT STEM CELLS.” 2017. Web. 16 Oct 2019.

Vancouver:

YING TZ. GENE REGULATION IN PLURIPOTENT STEM CELLS. [Internet] [Thesis]. National University of Singapore; 2017. [cited 2019 Oct 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/136319.

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

Council of Science Editors:

YING TZ. GENE REGULATION IN PLURIPOTENT STEM CELLS. [Thesis]. National University of Singapore; 2017. Available from: http://scholarbank.nus.edu.sg/handle/10635/136319

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


University of Vienna

8. Abdeen, Dana. Identification of novel regulators of sprouting angiogenesis using haploid ES cells.

Degree: 2017, University of Vienna

Die Expansion, Remodellierung und Reifung von Blutgefäßen ist ein wichtiges physiologisches Ereignis, das die embryonalen Entwicklungsstadien erfüllt und an der Pathophysiologie der Erwachsenen wie Augenerkrankungen… (more)

Subjects/Keywords: 42.13 Molekularbiologie; Angiogenesis / Haploid ES cells / Hyposprouters / Hypersprouters; Angiogenesis / Haploid ES cells / Hyposprouters / Hypersprouters

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APA (6th Edition):

Abdeen, D. (2017). Identification of novel regulators of sprouting angiogenesis using haploid ES cells. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/50257/

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):

Abdeen, Dana. “Identification of novel regulators of sprouting angiogenesis using haploid ES cells.” 2017. Thesis, University of Vienna. Accessed October 16, 2019. http://othes.univie.ac.at/50257/.

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

MLA Handbook (7th Edition):

Abdeen, Dana. “Identification of novel regulators of sprouting angiogenesis using haploid ES cells.” 2017. Web. 16 Oct 2019.

Vancouver:

Abdeen D. Identification of novel regulators of sprouting angiogenesis using haploid ES cells. [Internet] [Thesis]. University of Vienna; 2017. [cited 2019 Oct 16]. Available from: http://othes.univie.ac.at/50257/.

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

Council of Science Editors:

Abdeen D. Identification of novel regulators of sprouting angiogenesis using haploid ES cells. [Thesis]. University of Vienna; 2017. Available from: http://othes.univie.ac.at/50257/

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


University of Melbourne

9. 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 October 16, 2019. http://hdl.handle.net/11343/191658.

MLA Handbook (7th Edition):

Motazedian, Ali. “Lymphocyte differentiation from pluripotent stem cells.” 2017. Web. 16 Oct 2019.

Vancouver:

Motazedian A. Lymphocyte differentiation from pluripotent stem cells. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2019 Oct 16]. 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


Univerzitet u Beogradu

10. Mitić, Ivana D., 1981-. Modulacija eksperimentalnog autoimunskog encefalomijelitisa primenom ekskretorno-sekretornih antigena parazita Trichinella spiralis.

Degree: Medicinski fakultet, 2016, Univerzitet u Beogradu

Medicina - Imunologija / Medicine - Immunology

Savremena istraživanja na eksperimentalnim modelima autoimunskih bolesti ukazuju da infekcija helmintom Trichinella spiralis (T. spiralis), inhibira nastanak ili… (more)

Subjects/Keywords: Trichinella spiralis; EAE; ES L1; immune response; dendritic cells; regulatory T lymphocytes

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APA (6th Edition):

Mitić, Ivana D., 1. (2016). Modulacija eksperimentalnog autoimunskog encefalomijelitisa primenom ekskretorno-sekretornih antigena parazita Trichinella spiralis. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:14182/bdef:Content/get

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):

Mitić, Ivana D., 1981-. “Modulacija eksperimentalnog autoimunskog encefalomijelitisa primenom ekskretorno-sekretornih antigena parazita Trichinella spiralis.” 2016. Thesis, Univerzitet u Beogradu. Accessed October 16, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:14182/bdef:Content/get.

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

MLA Handbook (7th Edition):

Mitić, Ivana D., 1981-. “Modulacija eksperimentalnog autoimunskog encefalomijelitisa primenom ekskretorno-sekretornih antigena parazita Trichinella spiralis.” 2016. Web. 16 Oct 2019.

Vancouver:

Mitić, Ivana D. 1. Modulacija eksperimentalnog autoimunskog encefalomijelitisa primenom ekskretorno-sekretornih antigena parazita Trichinella spiralis. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Oct 16]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:14182/bdef:Content/get.

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

Council of Science Editors:

Mitić, Ivana D. 1. Modulacija eksperimentalnog autoimunskog encefalomijelitisa primenom ekskretorno-sekretornih antigena parazita Trichinella spiralis. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:14182/bdef:Content/get

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


University of Toronto

11. Vexelshtein, Olga. DNA Methylation of Endothelial Cell-enriched Genes during in Vitro Mouse ES Cell Differentiation and the Role of TET Proteins.

Degree: 2016, University of Toronto

Endothelial cell (EC)-enriched genes are regulated by numerous mechanisms, but especially epigenetic mechanisms such as DNA methylation. The current work examines the importance of TET1… (more)

Subjects/Keywords: DNA methylation; Endothelial cells; ES cells; TET proteins; 0379

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APA (6th Edition):

Vexelshtein, O. (2016). DNA Methylation of Endothelial Cell-enriched Genes during in Vitro Mouse ES Cell Differentiation and the Role of TET Proteins. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72845

Chicago Manual of Style (16th Edition):

Vexelshtein, Olga. “DNA Methylation of Endothelial Cell-enriched Genes during in Vitro Mouse ES Cell Differentiation and the Role of TET Proteins.” 2016. Masters Thesis, University of Toronto. Accessed October 16, 2019. http://hdl.handle.net/1807/72845.

MLA Handbook (7th Edition):

Vexelshtein, Olga. “DNA Methylation of Endothelial Cell-enriched Genes during in Vitro Mouse ES Cell Differentiation and the Role of TET Proteins.” 2016. Web. 16 Oct 2019.

Vancouver:

Vexelshtein O. DNA Methylation of Endothelial Cell-enriched Genes during in Vitro Mouse ES Cell Differentiation and the Role of TET Proteins. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1807/72845.

Council of Science Editors:

Vexelshtein O. DNA Methylation of Endothelial Cell-enriched Genes during in Vitro Mouse ES Cell Differentiation and the Role of TET Proteins. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72845


Indian Institute of Science

12. Verma, Isha. Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage.

Degree: 2016, Indian Institute of Science

 Pluripotent stem cells (PSCs: ESCs and iPSCs) provide an excellent model system for studying neural development and function. These cells also serve as a reliable… (more)

Subjects/Keywords: Mouse Pluripotent Stem Cells; Neural Lineage; Neural Differentiation of PSCs; Neural Differentiation; ES-cells; Neural Cell; Genetics

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APA (6th Edition):

Verma, I. (2016). Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/2885 ; http://etd.ncsi.iisc.ernet.in/abstracts/3747/G27748-Abs.pdf

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):

Verma, Isha. “Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage.” 2016. Thesis, Indian Institute of Science. Accessed October 16, 2019. http://etd.iisc.ernet.in/handle/2005/2885 ; http://etd.ncsi.iisc.ernet.in/abstracts/3747/G27748-Abs.pdf.

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

MLA Handbook (7th Edition):

Verma, Isha. “Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage.” 2016. Web. 16 Oct 2019.

Vancouver:

Verma I. Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Oct 16]. Available from: http://etd.iisc.ernet.in/handle/2005/2885 ; http://etd.ncsi.iisc.ernet.in/abstracts/3747/G27748-Abs.pdf.

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

Council of Science Editors:

Verma I. Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage. [Thesis]. Indian Institute of Science; 2016. Available from: http://etd.iisc.ernet.in/handle/2005/2885 ; http://etd.ncsi.iisc.ernet.in/abstracts/3747/G27748-Abs.pdf

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


Indian Institute of Science

13. Verma, Isha. Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage.

Degree: 2016, Indian Institute of Science

 Pluripotent stem cells (PSCs: ESCs and iPSCs) provide an excellent model system for studying neural development and function. These cells also serve as a reliable… (more)

Subjects/Keywords: Mouse Pluripotent Stem Cells; Neural Lineage; Neural Differentiation of PSCs; Neural Differentiation; ES-cells; Neural Cell; Genetics

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

APA (6th Edition):

Verma, I. (2016). Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2885

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):

Verma, Isha. “Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage.” 2016. Thesis, Indian Institute of Science. Accessed October 16, 2019. http://hdl.handle.net/2005/2885.

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

MLA Handbook (7th Edition):

Verma, Isha. “Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage.” 2016. Web. 16 Oct 2019.

Vancouver:

Verma I. Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage. [Internet] [Thesis]. Indian Institute of Science; 2016. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2005/2885.

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

Council of Science Editors:

Verma I. Insights into Differentiation of Mouse Pluripotent Stem Cells to Neural Lineage. [Thesis]. Indian Institute of Science; 2016. Available from: http://hdl.handle.net/2005/2885

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


University of Edinburgh

14. Zhang, Jingchao. Functional analysis of the role of the Nanog tryptophan repeat in ES cells.

Degree: PhD, 2016, University of Edinburgh

 Nanog is a transcription factor that plays a central part in the gene regulatory network that maintains and induces pluripotency of embryonic stem cells (ESCs).… (more)

Subjects/Keywords: 616.02; ES cells; Nanog; Otx2; tryptophan repeats; pluripotency

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

APA (6th Edition):

Zhang, J. (2016). Functional analysis of the role of the Nanog tryptophan repeat in ES cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/15972

Chicago Manual of Style (16th Edition):

Zhang, Jingchao. “Functional analysis of the role of the Nanog tryptophan repeat in ES cells.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed October 16, 2019. http://hdl.handle.net/1842/15972.

MLA Handbook (7th Edition):

Zhang, Jingchao. “Functional analysis of the role of the Nanog tryptophan repeat in ES cells.” 2016. Web. 16 Oct 2019.

Vancouver:

Zhang J. Functional analysis of the role of the Nanog tryptophan repeat in ES cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1842/15972.

Council of Science Editors:

Zhang J. Functional analysis of the role of the Nanog tryptophan repeat in ES cells. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/15972

15. SLIM MZOUGHI. CHARACTERIZATION OF THE PR-DOMAIN PROTEIN PRDM15: ROLE IN DEVELOPMENT AND CANCER.

Degree: 2015, National University of Singapore

Subjects/Keywords: PRDM15; ES cells; development; Transcription; chromatin

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APA (6th Edition):

MZOUGHI, S. (2015). CHARACTERIZATION OF THE PR-DOMAIN PROTEIN PRDM15: ROLE IN DEVELOPMENT AND CANCER. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/121262

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):

MZOUGHI, SLIM. “CHARACTERIZATION OF THE PR-DOMAIN PROTEIN PRDM15: ROLE IN DEVELOPMENT AND CANCER.” 2015. Thesis, National University of Singapore. Accessed October 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/121262.

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

MLA Handbook (7th Edition):

MZOUGHI, SLIM. “CHARACTERIZATION OF THE PR-DOMAIN PROTEIN PRDM15: ROLE IN DEVELOPMENT AND CANCER.” 2015. Web. 16 Oct 2019.

Vancouver:

MZOUGHI S. CHARACTERIZATION OF THE PR-DOMAIN PROTEIN PRDM15: ROLE IN DEVELOPMENT AND CANCER. [Internet] [Thesis]. National University of Singapore; 2015. [cited 2019 Oct 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/121262.

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

Council of Science Editors:

MZOUGHI S. CHARACTERIZATION OF THE PR-DOMAIN PROTEIN PRDM15: ROLE IN DEVELOPMENT AND CANCER. [Thesis]. National University of Singapore; 2015. Available from: http://scholarbank.nus.edu.sg/handle/10635/121262

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


University of Edinburgh

16. Wachter, Elisabeth. Influence of CpG islands on chromatin structure.

Degree: PhD, 2014, University of Edinburgh

 CpG islands (CGIs) are short GC rich sequences with a high frequency of CpGs that are associated with the active chromatin mark H3K4me3. Most occur… (more)

Subjects/Keywords: 572.8; CpG islands; chromatin; polycomb; ES cells

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

APA (6th Edition):

Wachter, E. (2014). Influence of CpG islands on chromatin structure. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9369

Chicago Manual of Style (16th Edition):

Wachter, Elisabeth. “Influence of CpG islands on chromatin structure.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed October 16, 2019. http://hdl.handle.net/1842/9369.

MLA Handbook (7th Edition):

Wachter, Elisabeth. “Influence of CpG islands on chromatin structure.” 2014. Web. 16 Oct 2019.

Vancouver:

Wachter E. Influence of CpG islands on chromatin structure. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1842/9369.

Council of Science Editors:

Wachter E. Influence of CpG islands on chromatin structure. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/9369


Universiteit Utrecht

17. Bekhuis, L.M. Evaluation of Midbrain Dopaminergic Neuron Specification in Rat ES Cell Derived Neurons.

Degree: 2013, Universiteit Utrecht

 Parkinson's disease (PD) is a chronic, neurodegenerative disorder, which arises as a result of the progressive loss of midbrain dopaminergic (mDA) neurons in the substantia… (more)

Subjects/Keywords: Diergeneeskunde; Parkinson's disease; midbrain dopaminergic neurons; embryonic stem cells; rat ES cells; MEK/ERK; RT-PCR; midbrain development

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APA (6th Edition):

Bekhuis, L. M. (2013). Evaluation of Midbrain Dopaminergic Neuron Specification in Rat ES Cell Derived Neurons. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/281018

Chicago Manual of Style (16th Edition):

Bekhuis, L M. “Evaluation of Midbrain Dopaminergic Neuron Specification in Rat ES Cell Derived Neurons.” 2013. Masters Thesis, Universiteit Utrecht. Accessed October 16, 2019. http://dspace.library.uu.nl:8080/handle/1874/281018.

MLA Handbook (7th Edition):

Bekhuis, L M. “Evaluation of Midbrain Dopaminergic Neuron Specification in Rat ES Cell Derived Neurons.” 2013. Web. 16 Oct 2019.

Vancouver:

Bekhuis LM. Evaluation of Midbrain Dopaminergic Neuron Specification in Rat ES Cell Derived Neurons. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Oct 16]. Available from: http://dspace.library.uu.nl:8080/handle/1874/281018.

Council of Science Editors:

Bekhuis LM. Evaluation of Midbrain Dopaminergic Neuron Specification in Rat ES Cell Derived Neurons. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/281018


University of Rochester

18. Gabay, Meital. Ric-8 Proteins Are Molecular Chaperones Required For The Biogenesis G Protein Alpha Subunits.

Degree: PhD, 2013, University of Rochester

 Ric-8A (resistance to inhibitors of cholinesterase 8A) and Ric-8B are guanine nucleotide exchange factors that enhance different heterotrimeric G protein signaling pathways by unknown mechanisms.… (more)

Subjects/Keywords: Ric-8; G Proteins; ES Cells; Folding; Chaperon

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APA (6th Edition):

Gabay, M. (2013). Ric-8 Proteins Are Molecular Chaperones Required For The Biogenesis G Protein Alpha Subunits. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/26791

Chicago Manual of Style (16th Edition):

Gabay, Meital. “Ric-8 Proteins Are Molecular Chaperones Required For The Biogenesis G Protein Alpha Subunits.” 2013. Doctoral Dissertation, University of Rochester. Accessed October 16, 2019. http://hdl.handle.net/1802/26791.

MLA Handbook (7th Edition):

Gabay, Meital. “Ric-8 Proteins Are Molecular Chaperones Required For The Biogenesis G Protein Alpha Subunits.” 2013. Web. 16 Oct 2019.

Vancouver:

Gabay M. Ric-8 Proteins Are Molecular Chaperones Required For The Biogenesis G Protein Alpha Subunits. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1802/26791.

Council of Science Editors:

Gabay M. Ric-8 Proteins Are Molecular Chaperones Required For The Biogenesis G Protein Alpha Subunits. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/26791


University of Edinburgh

19. Jin, Xin. Towards differentiation of mouse embryonic stem cells to thymic epithelial progenitor cells.

Degree: PhD, 2013, University of Edinburgh

 The thymus is the major site for T-cell generation and thus is important for the adaptive immune system. Development of a properly selected, functional T-cell… (more)

Subjects/Keywords: 611; thymus; TEPC; thymic epithelial cells; embryonic stem cells; ES cells

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

APA (6th Edition):

Jin, X. (2013). Towards differentiation of mouse embryonic stem cells to thymic epithelial progenitor cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/12227

Chicago Manual of Style (16th Edition):

Jin, Xin. “Towards differentiation of mouse embryonic stem cells to thymic epithelial progenitor cells.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed October 16, 2019. http://hdl.handle.net/1842/12227.

MLA Handbook (7th Edition):

Jin, Xin. “Towards differentiation of mouse embryonic stem cells to thymic epithelial progenitor cells.” 2013. Web. 16 Oct 2019.

Vancouver:

Jin X. Towards differentiation of mouse embryonic stem cells to thymic epithelial progenitor cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1842/12227.

Council of Science Editors:

Jin X. Towards differentiation of mouse embryonic stem cells to thymic epithelial progenitor cells. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/12227

20. Osorno Hernandez, Carlos Rodrigo. Transcription factor heterogeneity in epiblast pluripotency.

Degree: PhD, 2013, University of Edinburgh

 Pluripotency is the ability of a cell to differentiate into derivatives of all three somatic lineages and germ cells. In vivo, pluripotent cells exist transiently… (more)

Subjects/Keywords: 571.6; pluripotency; ES cells

…38 2.1 Culture and manipulation of mouse ES cells… …39 2.1.1.4 Reagents for passaging of ES cells… …41 2.1.3 Long-term storage of mouse ES cells… …43 2.1.4 Thawing mouse ES cells… …43 2.1.5 Transfection of DNA into mouse ES cells… 

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APA (6th Edition):

Osorno Hernandez, C. R. (2013). Transcription factor heterogeneity in epiblast pluripotency. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8081

Chicago Manual of Style (16th Edition):

Osorno Hernandez, Carlos Rodrigo. “Transcription factor heterogeneity in epiblast pluripotency.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed October 16, 2019. http://hdl.handle.net/1842/8081.

MLA Handbook (7th Edition):

Osorno Hernandez, Carlos Rodrigo. “Transcription factor heterogeneity in epiblast pluripotency.” 2013. Web. 16 Oct 2019.

Vancouver:

Osorno Hernandez CR. Transcription factor heterogeneity in epiblast pluripotency. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1842/8081.

Council of Science Editors:

Osorno Hernandez CR. Transcription factor heterogeneity in epiblast pluripotency. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/8081


Indian Institute of Science

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

Degree: 2012, Indian Institute of Science

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

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

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APA (6th Edition):

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

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

Chicago Manual of Style (16th Edition):

Abbey, Deepti. “Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells.” 2012. Thesis, Indian Institute of Science. Accessed October 16, 2019. http://hdl.handle.net/2005/2455.

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

MLA Handbook (7th Edition):

Abbey, Deepti. “Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells.” 2012. Web. 16 Oct 2019.

Vancouver:

Abbey D. Insights Into Molecular Regulation Of Cardiomyocyte Differentiation Of Mouse Pluripotent Stem Cells. [Internet] [Thesis]. Indian Institute of Science; 2012. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2005/2455.

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

Council of Science Editors:

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

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


University of Michigan

22. Ramamurthy, Poornapriya. Mouse Embryonic Stem Cells Differentiated into Neuron-like Cells or Schwann Cell-like Cells for the Development of Strategies to Ameliorate Deafness.

Degree: PhD, Biomedical Engineering, 2012, University of Michigan

 Cochlear prostheses (CI) can restore hearing to patients with extensive sensorineural hearing loss (SNHL) by replacing lost or damaged cochlear mechanosensory hair cells (HC) with… (more)

Subjects/Keywords: ES Cells, Neuron-like Cell, Schwann -Like Cell, Microfluidics, Cochlear Implant, Regenration, Cell Therapy; Biomedical Engineering; Engineering

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APA (6th Edition):

Ramamurthy, P. (2012). Mouse Embryonic Stem Cells Differentiated into Neuron-like Cells or Schwann Cell-like Cells for the Development of Strategies to Ameliorate Deafness. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/94096

Chicago Manual of Style (16th Edition):

Ramamurthy, Poornapriya. “Mouse Embryonic Stem Cells Differentiated into Neuron-like Cells or Schwann Cell-like Cells for the Development of Strategies to Ameliorate Deafness.” 2012. Doctoral Dissertation, University of Michigan. Accessed October 16, 2019. http://hdl.handle.net/2027.42/94096.

MLA Handbook (7th Edition):

Ramamurthy, Poornapriya. “Mouse Embryonic Stem Cells Differentiated into Neuron-like Cells or Schwann Cell-like Cells for the Development of Strategies to Ameliorate Deafness.” 2012. Web. 16 Oct 2019.

Vancouver:

Ramamurthy P. Mouse Embryonic Stem Cells Differentiated into Neuron-like Cells or Schwann Cell-like Cells for the Development of Strategies to Ameliorate Deafness. [Internet] [Doctoral dissertation]. University of Michigan; 2012. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2027.42/94096.

Council of Science Editors:

Ramamurthy P. Mouse Embryonic Stem Cells Differentiated into Neuron-like Cells or Schwann Cell-like Cells for the Development of Strategies to Ameliorate Deafness. [Doctoral Dissertation]. University of Michigan; 2012. Available from: http://hdl.handle.net/2027.42/94096

23. VINOTH KUMAR S/O JAYASEELAN. ROLE OF HUMAN EMBRYONIC STEM CELLS AND DERIVED PROGENIES IN GENOTOXICITY TESTING.

Degree: 2011, National University of Singapore

Subjects/Keywords: ES cells; Toxicology testing; Genotoxicity Testing

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APA (6th Edition):

JAYASEELAN, V. K. S. (2011). ROLE OF HUMAN EMBRYONIC STEM CELLS AND DERIVED PROGENIES IN GENOTOXICITY TESTING. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/26141

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):

JAYASEELAN, VINOTH KUMAR S/O. “ROLE OF HUMAN EMBRYONIC STEM CELLS AND DERIVED PROGENIES IN GENOTOXICITY TESTING.” 2011. Thesis, National University of Singapore. Accessed October 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/26141.

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

MLA Handbook (7th Edition):

JAYASEELAN, VINOTH KUMAR S/O. “ROLE OF HUMAN EMBRYONIC STEM CELLS AND DERIVED PROGENIES IN GENOTOXICITY TESTING.” 2011. Web. 16 Oct 2019.

Vancouver:

JAYASEELAN VKS. ROLE OF HUMAN EMBRYONIC STEM CELLS AND DERIVED PROGENIES IN GENOTOXICITY TESTING. [Internet] [Thesis]. National University of Singapore; 2011. [cited 2019 Oct 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/26141.

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

Council of Science Editors:

JAYASEELAN VKS. ROLE OF HUMAN EMBRYONIC STEM CELLS AND DERIVED PROGENIES IN GENOTOXICITY TESTING. [Thesis]. National University of Singapore; 2011. Available from: http://scholarbank.nus.edu.sg/handle/10635/26141

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


Indian Institute of Science

24. Singh, Gurbind. Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation.

Degree: 2011, Indian Institute of Science

 Genesis of life begins with the fusion of female and male haploid gametes through a process of fertilization leading to the formation of a diploid… (more)

Subjects/Keywords: Experimental Research; Stem Cells; Transgenic Mice; Cardiomyocyte Differentiation; Embryonic Stem Cells; Enhanced Green Fluorescent Protein (EGFP); Fibroblast Growth Factor (FGF); Embryonic Stem Cell Line; ES-cells; Molecular Biology

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APA (6th Edition):

Singh, G. (2011). Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/2116

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):

Singh, Gurbind. “Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation.” 2011. Thesis, Indian Institute of Science. Accessed October 16, 2019. http://hdl.handle.net/2005/2116.

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

MLA Handbook (7th Edition):

Singh, Gurbind. “Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation.” 2011. Web. 16 Oct 2019.

Vancouver:

Singh G. Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/2005/2116.

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

Council of Science Editors:

Singh G. Studies On Embryonic Stem Cells From Enhanced Green Fluorescent Protein Transgenic Mice : Induction Of Cardiomyocyte Differentiation. [Thesis]. Indian Institute of Science; 2011. Available from: http://hdl.handle.net/2005/2116

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


University of Edinburgh

25. Meek, Stephen Earl. Experimental approaches to establish rat embryonic stem cells.

Degree: PhD, 2011, University of Edinburgh

 The rat has been an established experimental animal model within many areas of biological investigation for over one hundred years due to its size, breeding… (more)

Subjects/Keywords: 571.6; ES cells; 2i; rat; Oct4; Nanog

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APA (6th Edition):

Meek, S. E. (2011). Experimental approaches to establish rat embryonic stem cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5040

Chicago Manual of Style (16th Edition):

Meek, Stephen Earl. “Experimental approaches to establish rat embryonic stem cells.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed October 16, 2019. http://hdl.handle.net/1842/5040.

MLA Handbook (7th Edition):

Meek, Stephen Earl. “Experimental approaches to establish rat embryonic stem cells.” 2011. Web. 16 Oct 2019.

Vancouver:

Meek SE. Experimental approaches to establish rat embryonic stem cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1842/5040.

Council of Science Editors:

Meek SE. Experimental approaches to establish rat embryonic stem cells. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5040


University of Bath

26. Sanchez Ripoll, Yolanda. Glycogen Synthase Kinase 3 (GSK-3) involvement in regulation of mouse embryonic stem cell fate.

Degree: PhD, 2011, University of Bath

Subjects/Keywords: 616.02774; ES cells; GSK-3

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APA (6th Edition):

Sanchez Ripoll, Y. (2011). Glycogen Synthase Kinase 3 (GSK-3) involvement in regulation of mouse embryonic stem cell fate. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/glycogen-synthase-kinase-3-gsk3-involvement-in-regulation-of-mouse-embryonic-stem-cell-fate(55f41abe-2856-455a-a76f-fd91e5034eea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550616

Chicago Manual of Style (16th Edition):

Sanchez Ripoll, Yolanda. “Glycogen Synthase Kinase 3 (GSK-3) involvement in regulation of mouse embryonic stem cell fate.” 2011. Doctoral Dissertation, University of Bath. Accessed October 16, 2019. https://researchportal.bath.ac.uk/en/studentthesis/glycogen-synthase-kinase-3-gsk3-involvement-in-regulation-of-mouse-embryonic-stem-cell-fate(55f41abe-2856-455a-a76f-fd91e5034eea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550616.

MLA Handbook (7th Edition):

Sanchez Ripoll, Yolanda. “Glycogen Synthase Kinase 3 (GSK-3) involvement in regulation of mouse embryonic stem cell fate.” 2011. Web. 16 Oct 2019.

Vancouver:

Sanchez Ripoll Y. Glycogen Synthase Kinase 3 (GSK-3) involvement in regulation of mouse embryonic stem cell fate. [Internet] [Doctoral dissertation]. University of Bath; 2011. [cited 2019 Oct 16]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/glycogen-synthase-kinase-3-gsk3-involvement-in-regulation-of-mouse-embryonic-stem-cell-fate(55f41abe-2856-455a-a76f-fd91e5034eea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550616.

Council of Science Editors:

Sanchez Ripoll Y. Glycogen Synthase Kinase 3 (GSK-3) involvement in regulation of mouse embryonic stem cell fate. [Doctoral Dissertation]. University of Bath; 2011. Available from: https://researchportal.bath.ac.uk/en/studentthesis/glycogen-synthase-kinase-3-gsk3-involvement-in-regulation-of-mouse-embryonic-stem-cell-fate(55f41abe-2856-455a-a76f-fd91e5034eea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.550616

27. LAI ZHENYANG. Transcriptome Study of Human Embryonic Stem Cells and Knockdown Study of a Pluripotency Marker, LIN28.

Degree: 2010, National University of Singapore

Subjects/Keywords: human ES cells; pluripotency; LIN28; RNAi; post-transcriptional regulation

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APA (6th Edition):

ZHENYANG, L. (2010). Transcriptome Study of Human Embryonic Stem Cells and Knockdown Study of a Pluripotency Marker, LIN28. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/20462

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):

ZHENYANG, LAI. “Transcriptome Study of Human Embryonic Stem Cells and Knockdown Study of a Pluripotency Marker, LIN28.” 2010. Thesis, National University of Singapore. Accessed October 16, 2019. http://scholarbank.nus.edu.sg/handle/10635/20462.

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

MLA Handbook (7th Edition):

ZHENYANG, LAI. “Transcriptome Study of Human Embryonic Stem Cells and Knockdown Study of a Pluripotency Marker, LIN28.” 2010. Web. 16 Oct 2019.

Vancouver:

ZHENYANG L. Transcriptome Study of Human Embryonic Stem Cells and Knockdown Study of a Pluripotency Marker, LIN28. [Internet] [Thesis]. National University of Singapore; 2010. [cited 2019 Oct 16]. Available from: http://scholarbank.nus.edu.sg/handle/10635/20462.

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

Council of Science Editors:

ZHENYANG L. Transcriptome Study of Human Embryonic Stem Cells and Knockdown Study of a Pluripotency Marker, LIN28. [Thesis]. National University of Singapore; 2010. Available from: http://scholarbank.nus.edu.sg/handle/10635/20462

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


Case Western Reserve University

28. Schnetz, Michael Paul. Investigation of the Molecular Function of CHD7, the Protein Implicated in CHARGE Syndrome, Using Next-Generation Genomics.

Degree: PhD, Genetics, 2010, Case Western Reserve University

 Eukaryotes use chromatin to package large, complex genomes into the nucleus of their cells. As such, chromatin structure plays a key role in virtually all… (more)

Subjects/Keywords: Genetics; CHD7; CHARGE Syndrome; Chromatin Remodeling; mouse ES cells

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APA (6th Edition):

Schnetz, M. P. (2010). Investigation of the Molecular Function of CHD7, the Protein Implicated in CHARGE Syndrome, Using Next-Generation Genomics. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1275581022

Chicago Manual of Style (16th Edition):

Schnetz, Michael Paul. “Investigation of the Molecular Function of CHD7, the Protein Implicated in CHARGE Syndrome, Using Next-Generation Genomics.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed October 16, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1275581022.

MLA Handbook (7th Edition):

Schnetz, Michael Paul. “Investigation of the Molecular Function of CHD7, the Protein Implicated in CHARGE Syndrome, Using Next-Generation Genomics.” 2010. Web. 16 Oct 2019.

Vancouver:

Schnetz MP. Investigation of the Molecular Function of CHD7, the Protein Implicated in CHARGE Syndrome, Using Next-Generation Genomics. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Oct 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1275581022.

Council of Science Editors:

Schnetz MP. Investigation of the Molecular Function of CHD7, the Protein Implicated in CHARGE Syndrome, Using Next-Generation Genomics. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1275581022


University of Toronto

29. Norman, Andreea. Characterization of ES Cell-derived Cortical Radial Precursor Differentiation.

Degree: 2010, University of Toronto

Murine neural precursor cells have been a well studied model for neural cell fate determination and stem cell function both in vivo and in primary… (more)

Subjects/Keywords: cortical precursors; neural stem cells; mouse ES cells; corticogenesis; in vitro differentiation; retinoic acid; 0317

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APA (6th Edition):

Norman, A. (2010). Characterization of ES Cell-derived Cortical Radial Precursor Differentiation. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25879

Chicago Manual of Style (16th Edition):

Norman, Andreea. “Characterization of ES Cell-derived Cortical Radial Precursor Differentiation.” 2010. Masters Thesis, University of Toronto. Accessed October 16, 2019. http://hdl.handle.net/1807/25879.

MLA Handbook (7th Edition):

Norman, Andreea. “Characterization of ES Cell-derived Cortical Radial Precursor Differentiation.” 2010. Web. 16 Oct 2019.

Vancouver:

Norman A. Characterization of ES Cell-derived Cortical Radial Precursor Differentiation. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1807/25879.

Council of Science Editors:

Norman A. Characterization of ES Cell-derived Cortical Radial Precursor Differentiation. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25879


University of Edinburgh

30. Cowan, Gillian. Fetal germ cell differentiation and the impact of the somatic cells.

Degree: 2009, University of Edinburgh

 Specification of a germ cell lineage and appropriate maturation are essential for the transfer of genetic information from one generation to the next. Germ cells(more)

Subjects/Keywords: 612.6; germ cells; sertoli cells; ES cells; meiosis

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APA (6th Edition):

Cowan, G. (2009). Fetal germ cell differentiation and the impact of the somatic cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4164

Chicago Manual of Style (16th Edition):

Cowan, Gillian. “Fetal germ cell differentiation and the impact of the somatic cells.” 2009. Doctoral Dissertation, University of Edinburgh. Accessed October 16, 2019. http://hdl.handle.net/1842/4164.

MLA Handbook (7th Edition):

Cowan, Gillian. “Fetal germ cell differentiation and the impact of the somatic cells.” 2009. Web. 16 Oct 2019.

Vancouver:

Cowan G. Fetal germ cell differentiation and the impact of the somatic cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2009. [cited 2019 Oct 16]. Available from: http://hdl.handle.net/1842/4164.

Council of Science Editors:

Cowan G. Fetal germ cell differentiation and the impact of the somatic cells. [Doctoral Dissertation]. University of Edinburgh; 2009. Available from: http://hdl.handle.net/1842/4164

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