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You searched for subject:(Neural Stem Cells). Showing records 1 – 30 of 244 total matches.

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University of Manitoba

1. Iqbal, Mohamed Ariff. Role of thioredoxin system in regulation of neural stem cell proliferation and differentiation.

Degree: Physiology and Pathophysiology, 2016, University of Manitoba

Neural precursor cells (NPCs) have been a hot research topic because of their regenerative potentials. These cells maintain a remarkable capacity for continuous neurogenesis throughout… (more)

Subjects/Keywords: Neural stem cells

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APA (6th Edition):

Iqbal, M. A. (2016). Role of thioredoxin system in regulation of neural stem cell proliferation and differentiation. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31813

Chicago Manual of Style (16th Edition):

Iqbal, Mohamed Ariff. “Role of thioredoxin system in regulation of neural stem cell proliferation and differentiation.” 2016. Masters Thesis, University of Manitoba. Accessed November 22, 2017. http://hdl.handle.net/1993/31813.

MLA Handbook (7th Edition):

Iqbal, Mohamed Ariff. “Role of thioredoxin system in regulation of neural stem cell proliferation and differentiation.” 2016. Web. 22 Nov 2017.

Vancouver:

Iqbal MA. Role of thioredoxin system in regulation of neural stem cell proliferation and differentiation. [Internet] [Masters thesis]. University of Manitoba; 2016. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1993/31813.

Council of Science Editors:

Iqbal MA. Role of thioredoxin system in regulation of neural stem cell proliferation and differentiation. [Masters Thesis]. University of Manitoba; 2016. Available from: http://hdl.handle.net/1993/31813


University of Toronto

2. Reeve, Rachel Leeder. Primitive Neural Stem Cells in the Mouse Brain.

Degree: PhD, 2015, University of Toronto

Neural stem cells (NSCs) reside in the tissue lining the lateral ventricles of the adult mouse brain. At the top of the hierarchy are primitive… (more)

Subjects/Keywords: neural stem cells; 0306

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APA (6th Edition):

Reeve, R. L. (2015). Primitive Neural Stem Cells in the Mouse Brain. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/69414

Chicago Manual of Style (16th Edition):

Reeve, Rachel Leeder. “Primitive Neural Stem Cells in the Mouse Brain.” 2015. Doctoral Dissertation, University of Toronto. Accessed November 22, 2017. http://hdl.handle.net/1807/69414.

MLA Handbook (7th Edition):

Reeve, Rachel Leeder. “Primitive Neural Stem Cells in the Mouse Brain.” 2015. Web. 22 Nov 2017.

Vancouver:

Reeve RL. Primitive Neural Stem Cells in the Mouse Brain. [Internet] [Doctoral dissertation]. University of Toronto; 2015. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1807/69414.

Council of Science Editors:

Reeve RL. Primitive Neural Stem Cells in the Mouse Brain. [Doctoral Dissertation]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/69414


University of Hong Kong

3. Chan, Yan-ho. The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newbornand adult rats.

Degree: Master of Medical Sciences, 2012, University of Hong Kong

 Neural stem cells (NSCs) are defined as multipotent stem cells. They are able to self-renew and differentiate into mature cells, such as neurons, oligodendrocytes and… (more)

Subjects/Keywords: Neural stem cells.; Lead - Toxicology.

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APA (6th Edition):

Chan, Y. (2012). The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newbornand adult rats. (Masters Thesis). University of Hong Kong. Retrieved from Chan, Y. [陳恩浩]. (2012). The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newborn and adult rats. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833322 ; http://dx.doi.org/10.5353/th_b4833322

Chicago Manual of Style (16th Edition):

Chan, Yan-ho. “The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newbornand adult rats.” 2012. Masters Thesis, University of Hong Kong. Accessed November 22, 2017. Chan, Y. [陳恩浩]. (2012). The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newborn and adult rats. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833322 ; http://dx.doi.org/10.5353/th_b4833322.

MLA Handbook (7th Edition):

Chan, Yan-ho. “The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newbornand adult rats.” 2012. Web. 22 Nov 2017.

Vancouver:

Chan Y. The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newbornand adult rats. [Internet] [Masters thesis]. University of Hong Kong; 2012. [cited 2017 Nov 22]. Available from: Chan, Y. [陳恩浩]. (2012). The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newborn and adult rats. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833322 ; http://dx.doi.org/10.5353/th_b4833322.

Council of Science Editors:

Chan Y. The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newbornand adult rats. [Masters Thesis]. University of Hong Kong; 2012. Available from: Chan, Y. [陳恩浩]. (2012). The influences of lead ions on viability, proliferation and neuronal differentiation of hippocampal-derived neural stem cells of newborn and adult rats. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4833322 ; http://dx.doi.org/10.5353/th_b4833322


University of Hong Kong

4. Wong, Mei-ki. Expression of chondroitin sulfotransferases in neural progenitor cells : impacts on cell motility.

Degree: M. Phil., 2014, University of Hong Kong

The specific order by which functional neural circuits are established relies on the timely migration of newly specified neurons to target sites where they complete… (more)

Subjects/Keywords: Proteoglycan; Neural stem cells

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APA (6th Edition):

Wong, M. (2014). Expression of chondroitin sulfotransferases in neural progenitor cells : impacts on cell motility. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/223028

Chicago Manual of Style (16th Edition):

Wong, Mei-ki. “Expression of chondroitin sulfotransferases in neural progenitor cells : impacts on cell motility.” 2014. Masters Thesis, University of Hong Kong. Accessed November 22, 2017. http://hdl.handle.net/10722/223028.

MLA Handbook (7th Edition):

Wong, Mei-ki. “Expression of chondroitin sulfotransferases in neural progenitor cells : impacts on cell motility.” 2014. Web. 22 Nov 2017.

Vancouver:

Wong M. Expression of chondroitin sulfotransferases in neural progenitor cells : impacts on cell motility. [Internet] [Masters thesis]. University of Hong Kong; 2014. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10722/223028.

Council of Science Editors:

Wong M. Expression of chondroitin sulfotransferases in neural progenitor cells : impacts on cell motility. [Masters Thesis]. University of Hong Kong; 2014. Available from: http://hdl.handle.net/10722/223028


University of Hong Kong

5. Tse, Wing-sze. Understanding Friedreich's ataxia via a disease-specific cell model.

Degree: M. Phil., 2015, University of Hong Kong

Friedreich’s ataxia (FA) is a hereditary, neurodegenerative disorder with significant disability and morbidity. The disease is characterised by deficiency of a nuclear encoded small mitochondrial… (more)

Subjects/Keywords: Neural stem cells; Friedreich's ataxia

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APA (6th Edition):

Tse, W. (2015). Understanding Friedreich's ataxia via a disease-specific cell model. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/223052

Chicago Manual of Style (16th Edition):

Tse, Wing-sze. “Understanding Friedreich's ataxia via a disease-specific cell model.” 2015. Masters Thesis, University of Hong Kong. Accessed November 22, 2017. http://hdl.handle.net/10722/223052.

MLA Handbook (7th Edition):

Tse, Wing-sze. “Understanding Friedreich's ataxia via a disease-specific cell model.” 2015. Web. 22 Nov 2017.

Vancouver:

Tse W. Understanding Friedreich's ataxia via a disease-specific cell model. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10722/223052.

Council of Science Editors:

Tse W. Understanding Friedreich's ataxia via a disease-specific cell model. [Masters Thesis]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/223052


University of Hong Kong

6. Liu, Xuqing. Effects of activated microglia on the properties of neural stem cells in vitro.

Degree: PhD, 2011, University of Hong Kong

Neural stem cell (NSC) transplantation strategy offers great potential to treat spinal cord injury (SCI). NSCs may replace lost neurons or oligodendrocytes, and act as… (more)

Subjects/Keywords: Microglia.; Neural stem cells.

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APA (6th Edition):

Liu, X. (2011). Effects of activated microglia on the properties of neural stem cells in vitro. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/180810

Chicago Manual of Style (16th Edition):

Liu, Xuqing. “Effects of activated microglia on the properties of neural stem cells in vitro.” 2011. Doctoral Dissertation, University of Hong Kong. Accessed November 22, 2017. http://hdl.handle.net/10722/180810.

MLA Handbook (7th Edition):

Liu, Xuqing. “Effects of activated microglia on the properties of neural stem cells in vitro.” 2011. Web. 22 Nov 2017.

Vancouver:

Liu X. Effects of activated microglia on the properties of neural stem cells in vitro. [Internet] [Doctoral dissertation]. University of Hong Kong; 2011. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10722/180810.

Council of Science Editors:

Liu X. Effects of activated microglia on the properties of neural stem cells in vitro. [Doctoral Dissertation]. University of Hong Kong; 2011. Available from: http://hdl.handle.net/10722/180810


University of Hong Kong

7. Hui, Man-ning. Investigating the role of SOX9 in human neural stem cells.

Degree: M. Phil., 2013, University of Hong Kong

Neural stem cells (NSCs) exist in both embryonic and adult neural tissues and are characterized by their self-renewal capacity and multipotency that contribute to the… (more)

Subjects/Keywords: Transcription factors; Neural stem cells

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APA (6th Edition):

Hui, M. (2013). Investigating the role of SOX9 in human neural stem cells. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/193481

Chicago Manual of Style (16th Edition):

Hui, Man-ning. “Investigating the role of SOX9 in human neural stem cells.” 2013. Masters Thesis, University of Hong Kong. Accessed November 22, 2017. http://hdl.handle.net/10722/193481.

MLA Handbook (7th Edition):

Hui, Man-ning. “Investigating the role of SOX9 in human neural stem cells.” 2013. Web. 22 Nov 2017.

Vancouver:

Hui M. Investigating the role of SOX9 in human neural stem cells. [Internet] [Masters thesis]. University of Hong Kong; 2013. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10722/193481.

Council of Science Editors:

Hui M. Investigating the role of SOX9 in human neural stem cells. [Masters Thesis]. University of Hong Kong; 2013. Available from: http://hdl.handle.net/10722/193481


Rutgers University

8. Davila, Jorge, 1977-. MIR-9 targets OC2 in proliferating and differentiating neural stem cells.

Degree: PhD, Cell and Developmental Biology, 2011, Rutgers University

MicroRNAs are key regulators of biological processes. In this thesis we identify mir-9 as a critical regulator during NSC proliferation and neuronal differentiation. Interestingly the… (more)

Subjects/Keywords: RNA; Neural stem cells

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APA (6th Edition):

Davila, Jorge, 1. (2011). MIR-9 targets OC2 in proliferating and differentiating neural stem cells. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061184

Chicago Manual of Style (16th Edition):

Davila, Jorge, 1977-. “MIR-9 targets OC2 in proliferating and differentiating neural stem cells.” 2011. Doctoral Dissertation, Rutgers University. Accessed November 22, 2017. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061184.

MLA Handbook (7th Edition):

Davila, Jorge, 1977-. “MIR-9 targets OC2 in proliferating and differentiating neural stem cells.” 2011. Web. 22 Nov 2017.

Vancouver:

Davila, Jorge 1. MIR-9 targets OC2 in proliferating and differentiating neural stem cells. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2017 Nov 22]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061184.

Council of Science Editors:

Davila, Jorge 1. MIR-9 targets OC2 in proliferating and differentiating neural stem cells. [Doctoral Dissertation]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000061184


University of Toronto

9. Doherty, James Patrick. The Isolation and Identification of the Definitive Adult Neural Stem Cell Following Ablation of the Neurogenic GFAP Expressing Subependymal Cell.

Degree: 2009, University of Toronto

Neural stem cells (NSCs) in the adult forebrain are thought to comprise a subpopulation of cells that express glial fibrillary acidic protein (GFAP), termed B… (more)

Subjects/Keywords: Adult neural stem cells; Neuroscience; Neural stem cells; 0317

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APA (6th Edition):

Doherty, J. P. (2009). The Isolation and Identification of the Definitive Adult Neural Stem Cell Following Ablation of the Neurogenic GFAP Expressing Subependymal Cell. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/17427

Chicago Manual of Style (16th Edition):

Doherty, James Patrick. “The Isolation and Identification of the Definitive Adult Neural Stem Cell Following Ablation of the Neurogenic GFAP Expressing Subependymal Cell.” 2009. Masters Thesis, University of Toronto. Accessed November 22, 2017. http://hdl.handle.net/1807/17427.

MLA Handbook (7th Edition):

Doherty, James Patrick. “The Isolation and Identification of the Definitive Adult Neural Stem Cell Following Ablation of the Neurogenic GFAP Expressing Subependymal Cell.” 2009. Web. 22 Nov 2017.

Vancouver:

Doherty JP. The Isolation and Identification of the Definitive Adult Neural Stem Cell Following Ablation of the Neurogenic GFAP Expressing Subependymal Cell. [Internet] [Masters thesis]. University of Toronto; 2009. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1807/17427.

Council of Science Editors:

Doherty JP. The Isolation and Identification of the Definitive Adult Neural Stem Cell Following Ablation of the Neurogenic GFAP Expressing Subependymal Cell. [Masters Thesis]. University of Toronto; 2009. Available from: http://hdl.handle.net/1807/17427


Universiteit Utrecht

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

Degree: 2012, Universiteit Utrecht

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

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

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APA (6th Edition):

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

Chicago Manual of Style (16th Edition):

Wever, I. “From fibroblast to neuron: The use of stem cells for Parkinson's disease.” 2012. Masters Thesis, Universiteit Utrecht. Accessed November 22, 2017. http://dspace.library.uu.nl:8080/handle/1874/258934.

MLA Handbook (7th Edition):

Wever, I. “From fibroblast to neuron: The use of stem cells for Parkinson's disease.” 2012. Web. 22 Nov 2017.

Vancouver:

Wever I. From fibroblast to neuron: The use of stem cells for Parkinson's disease. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2017 Nov 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/258934.

Council of Science Editors:

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


University of Toronto

11. Brandon, Caroline. Wnt Signaling in Human Neural Stem Cells and Brain Tumour Stem Cells.

Degree: 2010, University of Toronto

We sought to determine whether activation of the Wnt signaling pathway altered the function of hNSCs in vitro. We took three approaches to activate Wnt… (more)

Subjects/Keywords: Wnt Signaling; Neural Stem Cells; Cancer Stem Cells; Brain Tumour; 0379

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APA (6th Edition):

Brandon, C. (2010). Wnt Signaling in Human Neural Stem Cells and Brain Tumour Stem Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25435

Chicago Manual of Style (16th Edition):

Brandon, Caroline. “Wnt Signaling in Human Neural Stem Cells and Brain Tumour Stem Cells.” 2010. Masters Thesis, University of Toronto. Accessed November 22, 2017. http://hdl.handle.net/1807/25435.

MLA Handbook (7th Edition):

Brandon, Caroline. “Wnt Signaling in Human Neural Stem Cells and Brain Tumour Stem Cells.” 2010. Web. 22 Nov 2017.

Vancouver:

Brandon C. Wnt Signaling in Human Neural Stem Cells and Brain Tumour Stem Cells. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1807/25435.

Council of Science Editors:

Brandon C. Wnt Signaling in Human Neural Stem Cells and Brain Tumour Stem Cells. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25435

12. 山添, 知宏. Potent tumor tropism of induced pluripotent stem cells and induced pluripotent stem cell-derived neural stem cells in the mouse intracerebral glioma model : iPS細胞およびiPS細胞由来神経幹細胞はマウス脳内グリオーマモデルにおいて腫瘍への活発な遊走能を有する.

Degree: 博士(医学), 2015, Hamamatsu University School of Medicine / 浜松医科大学

Abstract. Although neural and mesenchymal stem cells have been well-known to have a strong glioma tropism, this activity in induced pluripotent stem cells (iPSCs) has… (more)

Subjects/Keywords: induced pluripotent stem cells; neural stem cells; glioma; migration; gene therapy

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APA (6th Edition):

山添, . (2015). Potent tumor tropism of induced pluripotent stem cells and induced pluripotent stem cell-derived neural stem cells in the mouse intracerebral glioma model : iPS細胞およびiPS細胞由来神経幹細胞はマウス脳内グリオーマモデルにおいて腫瘍への活発な遊走能を有する. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/2879

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):

山添, 知宏. “Potent tumor tropism of induced pluripotent stem cells and induced pluripotent stem cell-derived neural stem cells in the mouse intracerebral glioma model : iPS細胞およびiPS細胞由来神経幹細胞はマウス脳内グリオーマモデルにおいて腫瘍への活発な遊走能を有する.” 2015. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed November 22, 2017. http://hdl.handle.net/10271/2879.

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

MLA Handbook (7th Edition):

山添, 知宏. “Potent tumor tropism of induced pluripotent stem cells and induced pluripotent stem cell-derived neural stem cells in the mouse intracerebral glioma model : iPS細胞およびiPS細胞由来神経幹細胞はマウス脳内グリオーマモデルにおいて腫瘍への活発な遊走能を有する.” 2015. Web. 22 Nov 2017.

Vancouver:

山添 . Potent tumor tropism of induced pluripotent stem cells and induced pluripotent stem cell-derived neural stem cells in the mouse intracerebral glioma model : iPS細胞およびiPS細胞由来神経幹細胞はマウス脳内グリオーマモデルにおいて腫瘍への活発な遊走能を有する. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2015. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10271/2879.

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

Council of Science Editors:

山添 . Potent tumor tropism of induced pluripotent stem cells and induced pluripotent stem cell-derived neural stem cells in the mouse intracerebral glioma model : iPS細胞およびiPS細胞由来神経幹細胞はマウス脳内グリオーマモデルにおいて腫瘍への活発な遊走能を有する. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2015. Available from: http://hdl.handle.net/10271/2879

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


University of Toronto

13. Sacco, Raffaele. Cockayne Syndrome B is Required for Neural Precursor Self-renewal and Neuritegenesis after DNA Damage.

Degree: 2010, University of Toronto

Neural precursor cells self-renew and differentiate throughout development and in response to neural injury in the adult brain. The DNA damage response in NPCs has… (more)

Subjects/Keywords: Neural Stem Cells; DNA damage; 0383

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APA (6th Edition):

Sacco, R. (2010). Cockayne Syndrome B is Required for Neural Precursor Self-renewal and Neuritegenesis after DNA Damage. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25785

Chicago Manual of Style (16th Edition):

Sacco, Raffaele. “Cockayne Syndrome B is Required for Neural Precursor Self-renewal and Neuritegenesis after DNA Damage.” 2010. Masters Thesis, University of Toronto. Accessed November 22, 2017. http://hdl.handle.net/1807/25785.

MLA Handbook (7th Edition):

Sacco, Raffaele. “Cockayne Syndrome B is Required for Neural Precursor Self-renewal and Neuritegenesis after DNA Damage.” 2010. Web. 22 Nov 2017.

Vancouver:

Sacco R. Cockayne Syndrome B is Required for Neural Precursor Self-renewal and Neuritegenesis after DNA Damage. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1807/25785.

Council of Science Editors:

Sacco R. Cockayne Syndrome B is Required for Neural Precursor Self-renewal and Neuritegenesis after DNA Damage. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25785


University of Debrecen

14. Alexander, Philip Martin Indrajit. Neural stem cell proliferation in the subventricular zone of the lateral ventricle and dentate gyrus of the hippocampus .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

The aim of this thesis is to outline the recent discoveries made in the field of neurogenesis and the potential drugs that may give rise to permanent reparative treatment methods in brain-injured patients. Advisors/Committee Members: Pórszász, Róbert (advisor), Department of Pharmacology & Pharmacotherapy (advisor).

Subjects/Keywords: Neural Stem Cells

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APA (6th Edition):

Alexander, P. M. I. (n.d.). Neural stem cell proliferation in the subventricular zone of the lateral ventricle and dentate gyrus of the hippocampus . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/195536

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Alexander, Philip Martin Indrajit. “Neural stem cell proliferation in the subventricular zone of the lateral ventricle and dentate gyrus of the hippocampus .” Thesis, University of Debrecen. Accessed November 22, 2017. http://hdl.handle.net/2437/195536.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Alexander, Philip Martin Indrajit. “Neural stem cell proliferation in the subventricular zone of the lateral ventricle and dentate gyrus of the hippocampus .” Web. 22 Nov 2017.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Alexander PMI. Neural stem cell proliferation in the subventricular zone of the lateral ventricle and dentate gyrus of the hippocampus . [Internet] [Thesis]. University of Debrecen; [cited 2017 Nov 22]. Available from: http://hdl.handle.net/2437/195536.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Alexander PMI. Neural stem cell proliferation in the subventricular zone of the lateral ventricle and dentate gyrus of the hippocampus . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/195536

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


California State University – Sacramento

15. Meyer, Nathaniel Paul. Analyzing histone H3.3 function in neural stem cells via H3F3a knockout.

Degree: MA, Biology (Stem Cell, 2015, California State University – Sacramento

 The histone variant protein H3.3 plays necessary roles in embryogenesis, spermatogenesis, and transcription.H3.3 is encoded for by two genes: H3F3A and H3F3B in humans and… (more)

Subjects/Keywords: H3f3a; H3.3; Neural stem cells; Histone proteins

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APA (6th Edition):

Meyer, N. P. (2015). Analyzing histone H3.3 function in neural stem cells via H3F3a knockout. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/139193

Chicago Manual of Style (16th Edition):

Meyer, Nathaniel Paul. “Analyzing histone H3.3 function in neural stem cells via H3F3a knockout.” 2015. Masters Thesis, California State University – Sacramento. Accessed November 22, 2017. http://hdl.handle.net/10211.3/139193.

MLA Handbook (7th Edition):

Meyer, Nathaniel Paul. “Analyzing histone H3.3 function in neural stem cells via H3F3a knockout.” 2015. Web. 22 Nov 2017.

Vancouver:

Meyer NP. Analyzing histone H3.3 function in neural stem cells via H3F3a knockout. [Internet] [Masters thesis]. California State University – Sacramento; 2015. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10211.3/139193.

Council of Science Editors:

Meyer NP. Analyzing histone H3.3 function in neural stem cells via H3F3a knockout. [Masters Thesis]. California State University – Sacramento; 2015. Available from: http://hdl.handle.net/10211.3/139193


University of Texas Southwestern Medical Center

16. Ure, Kerstin Maria. Transcriptional Regulation of Adult Neurogenesis by NRSF/REST and NeuroD1.

Degree: 2011, University of Texas Southwestern Medical Center

 Neurogenesis in the adult brain is a complex and lifelong process that is regulated by multiple pathways and is sensitive to many external stimuli. Two… (more)

Subjects/Keywords: Neurogenesis; Repressor Proteins; Neural Stem Cells

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APA (6th Edition):

Ure, K. M. (2011). Transcriptional Regulation of Adult Neurogenesis by NRSF/REST and NeuroD1. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/889

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):

Ure, Kerstin Maria. “Transcriptional Regulation of Adult Neurogenesis by NRSF/REST and NeuroD1.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed November 22, 2017. http://hdl.handle.net/2152.5/889.

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

MLA Handbook (7th Edition):

Ure, Kerstin Maria. “Transcriptional Regulation of Adult Neurogenesis by NRSF/REST and NeuroD1.” 2011. Web. 22 Nov 2017.

Vancouver:

Ure KM. Transcriptional Regulation of Adult Neurogenesis by NRSF/REST and NeuroD1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/2152.5/889.

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

Council of Science Editors:

Ure KM. Transcriptional Regulation of Adult Neurogenesis by NRSF/REST and NeuroD1. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/889

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


University of Texas Southwestern Medical Center

17. Llaguno, Sheila R. Alcantara. Neural Stem Cells in Brain Tumor Development.

Degree: 2009, University of Texas Southwestern Medical Center

 Malignant astrocytomas are highly invasive and incurable brain tumors. Mouse models that genetically resemble the human disease are valuable tools in understanding the pathogenesis of… (more)

Subjects/Keywords: Neural Stem Cells; Brain Neoplasms; Mice, Transgenic

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APA (6th Edition):

Llaguno, S. R. A. (2009). Neural Stem Cells in Brain Tumor Development. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/266

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):

Llaguno, Sheila R Alcantara. “Neural Stem Cells in Brain Tumor Development.” 2009. Thesis, University of Texas Southwestern Medical Center. Accessed November 22, 2017. http://hdl.handle.net/2152.5/266.

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

MLA Handbook (7th Edition):

Llaguno, Sheila R Alcantara. “Neural Stem Cells in Brain Tumor Development.” 2009. Web. 22 Nov 2017.

Vancouver:

Llaguno SRA. Neural Stem Cells in Brain Tumor Development. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2009. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/2152.5/266.

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

Council of Science Editors:

Llaguno SRA. Neural Stem Cells in Brain Tumor Development. [Thesis]. University of Texas Southwestern Medical Center; 2009. Available from: http://hdl.handle.net/2152.5/266

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


Universitat de Valencia

18. Kostic, Jelena. Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic effecys of ethanol .

Degree: 2012, Universitat de Valencia

 Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic… (more)

Subjects/Keywords: human embryonic stem cells; ethanol; neural development

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APA (6th Edition):

Kostic, J. (2012). Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic effecys of ethanol . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/25145

Chicago Manual of Style (16th Edition):

Kostic, Jelena. “Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic effecys of ethanol .” 2012. Doctoral Dissertation, Universitat de Valencia. Accessed November 22, 2017. http://hdl.handle.net/10550/25145.

MLA Handbook (7th Edition):

Kostic, Jelena. “Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic effecys of ethanol .” 2012. Web. 22 Nov 2017.

Vancouver:

Kostic J. Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic effecys of ethanol . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2012. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10550/25145.

Council of Science Editors:

Kostic J. Differentiation of human Embryonic Stem Cells (hESC) into neural progenitors as a tool to study both the pathways during early brain development and the neuroteratogenic effecys of ethanol . [Doctoral Dissertation]. Universitat de Valencia; 2012. Available from: http://hdl.handle.net/10550/25145


Vanderbilt University

19. Evans, Justin D. Dissecting Location-Specific Signaling Pathway Activity in the Neurogenic Niche.

Degree: MS, Cancer Biology, 2014, Vanderbilt University

 The adult mammalian brain hosts two regions of quiescent neural stem cells that continually generate new neurons throughout life. One of these regions, the subventricular… (more)

Subjects/Keywords: Indentity; Sonic Hedgehog; SVZ; Neural Stem Cells

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APA (6th Edition):

Evans, J. D. (2014). Dissecting Location-Specific Signaling Pathway Activity in the Neurogenic Niche. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03252014-155436/ ;

Chicago Manual of Style (16th Edition):

Evans, Justin D. “Dissecting Location-Specific Signaling Pathway Activity in the Neurogenic Niche.” 2014. Masters Thesis, Vanderbilt University. Accessed November 22, 2017. http://etd.library.vanderbilt.edu/available/etd-03252014-155436/ ;.

MLA Handbook (7th Edition):

Evans, Justin D. “Dissecting Location-Specific Signaling Pathway Activity in the Neurogenic Niche.” 2014. Web. 22 Nov 2017.

Vancouver:

Evans JD. Dissecting Location-Specific Signaling Pathway Activity in the Neurogenic Niche. [Internet] [Masters thesis]. Vanderbilt University; 2014. [cited 2017 Nov 22]. Available from: http://etd.library.vanderbilt.edu/available/etd-03252014-155436/ ;.

Council of Science Editors:

Evans JD. Dissecting Location-Specific Signaling Pathway Activity in the Neurogenic Niche. [Masters Thesis]. Vanderbilt University; 2014. Available from: http://etd.library.vanderbilt.edu/available/etd-03252014-155436/ ;


University of Canterbury

20. O'Leary, James Daniel. The role of the dentate gyrus and adult neurogenesis in hippocampal-basal ganglia associated behaviour.

Degree: 2012, University of Canterbury

 The ability of the brain to continually generate new neurons throughout life is one of the most intensely researched areas of modern neuroscience. While great… (more)

Subjects/Keywords: Stress; Learning; Memory; Neural Stem Cells

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APA (6th Edition):

O'Leary, J. D. (2012). The role of the dentate gyrus and adult neurogenesis in hippocampal-basal ganglia associated behaviour. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/7426

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):

O'Leary, James Daniel. “The role of the dentate gyrus and adult neurogenesis in hippocampal-basal ganglia associated behaviour.” 2012. Thesis, University of Canterbury. Accessed November 22, 2017. http://hdl.handle.net/10092/7426.

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

MLA Handbook (7th Edition):

O'Leary, James Daniel. “The role of the dentate gyrus and adult neurogenesis in hippocampal-basal ganglia associated behaviour.” 2012. Web. 22 Nov 2017.

Vancouver:

O'Leary JD. The role of the dentate gyrus and adult neurogenesis in hippocampal-basal ganglia associated behaviour. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/10092/7426.

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

Council of Science Editors:

O'Leary JD. The role of the dentate gyrus and adult neurogenesis in hippocampal-basal ganglia associated behaviour. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/7426

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


University of Toledo Health Science Campus

21. Ge, Shufan. Impact of Muscarinic Receptor Activation on Neural Stem Cell Differentiation.

Degree: MSP, College of Pharmacy, 2010, University of Toledo Health Science Campus

 Since neurogenesis was demonstrated in adult mammalian brain, the field ofneural stem cell (NSC) research has been in a state of rapid growth. However, it… (more)

Subjects/Keywords: Pharmacology; muscarinic receptors; neural stem cells; differentiation

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APA (6th Edition):

Ge, S. (2010). Impact of Muscarinic Receptor Activation on Neural Stem Cell Differentiation. (Masters Thesis). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1291827018

Chicago Manual of Style (16th Edition):

Ge, Shufan. “Impact of Muscarinic Receptor Activation on Neural Stem Cell Differentiation.” 2010. Masters Thesis, University of Toledo Health Science Campus. Accessed November 22, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=mco1291827018.

MLA Handbook (7th Edition):

Ge, Shufan. “Impact of Muscarinic Receptor Activation on Neural Stem Cell Differentiation.” 2010. Web. 22 Nov 2017.

Vancouver:

Ge S. Impact of Muscarinic Receptor Activation on Neural Stem Cell Differentiation. [Internet] [Masters thesis]. University of Toledo Health Science Campus; 2010. [cited 2017 Nov 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1291827018.

Council of Science Editors:

Ge S. Impact of Muscarinic Receptor Activation on Neural Stem Cell Differentiation. [Masters Thesis]. University of Toledo Health Science Campus; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1291827018


University of Manchester

22. Phillips, Nick. Modelling and analysis of oscillations in gene expression through neural development.

Degree: 2016, University of Manchester

The timing of differentiation underlies the development of any organ system. In neural development, the expression of the transcription factor Hes1 has been shown to… (more)

Subjects/Keywords: neural stem cells; stochasticity; gaussian process; differentiation

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APA (6th Edition):

Phillips, N. (2016). Modelling and analysis of oscillations in gene expression through neural development. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:299629

Chicago Manual of Style (16th Edition):

Phillips, Nick. “Modelling and analysis of oscillations in gene expression through neural development.” 2016. Doctoral Dissertation, University of Manchester. Accessed November 22, 2017. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:299629.

MLA Handbook (7th Edition):

Phillips, Nick. “Modelling and analysis of oscillations in gene expression through neural development.” 2016. Web. 22 Nov 2017.

Vancouver:

Phillips N. Modelling and analysis of oscillations in gene expression through neural development. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2017 Nov 22]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:299629.

Council of Science Editors:

Phillips N. Modelling and analysis of oscillations in gene expression through neural development. [Doctoral Dissertation]. University of Manchester; 2016. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:299629


University of Manchester

23. Phillips, Nick. Modelling and analysis of oscillations in gene expression through neural development.

Degree: PhD, 2016, University of Manchester

 The timing of differentiation underlies the development of any organ system. In neural development, the expression of the transcription factor Hes1 has been shown to… (more)

Subjects/Keywords: gaussian process; differentiation; neural stem cells; stochasticity

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APA (6th Edition):

Phillips, N. (2016). Modelling and analysis of oscillations in gene expression through neural development. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/modelling-and-analysis-of-oscillations-in-gene-expression-through-neural-development(099f8bee-c1ce-4ca2-951e-a1e3fb7321bd).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713558

Chicago Manual of Style (16th Edition):

Phillips, Nick. “Modelling and analysis of oscillations in gene expression through neural development.” 2016. Doctoral Dissertation, University of Manchester. Accessed November 22, 2017. https://www.research.manchester.ac.uk/portal/en/theses/modelling-and-analysis-of-oscillations-in-gene-expression-through-neural-development(099f8bee-c1ce-4ca2-951e-a1e3fb7321bd).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713558.

MLA Handbook (7th Edition):

Phillips, Nick. “Modelling and analysis of oscillations in gene expression through neural development.” 2016. Web. 22 Nov 2017.

Vancouver:

Phillips N. Modelling and analysis of oscillations in gene expression through neural development. [Internet] [Doctoral dissertation]. University of Manchester; 2016. [cited 2017 Nov 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modelling-and-analysis-of-oscillations-in-gene-expression-through-neural-development(099f8bee-c1ce-4ca2-951e-a1e3fb7321bd).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713558.

Council of Science Editors:

Phillips N. Modelling and analysis of oscillations in gene expression through neural development. [Doctoral Dissertation]. University of Manchester; 2016. Available from: https://www.research.manchester.ac.uk/portal/en/theses/modelling-and-analysis-of-oscillations-in-gene-expression-through-neural-development(099f8bee-c1ce-4ca2-951e-a1e3fb7321bd).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.713558


Drexel University

24. Marino, Michael. Comparison of NCD and CNN based mitotic classification of neural stem cells in phase contrast microscopy.

Degree: 2016, Drexel University

Automated mitosis detection is a major difficulty in segmentation and tracking algorithms. This thesis explores the implementation of an automated mitotic detection algorithm for phase-contrast… (more)

Subjects/Keywords: Electrical engineering; Neural stem cells; Cell cycle

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APA (6th Edition):

Marino, M. (2016). Comparison of NCD and CNN based mitotic classification of neural stem cells in phase contrast microscopy. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7127

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):

Marino, Michael. “Comparison of NCD and CNN based mitotic classification of neural stem cells in phase contrast microscopy.” 2016. Thesis, Drexel University. Accessed November 22, 2017. http://hdl.handle.net/1860/idea:7127.

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

MLA Handbook (7th Edition):

Marino, Michael. “Comparison of NCD and CNN based mitotic classification of neural stem cells in phase contrast microscopy.” 2016. Web. 22 Nov 2017.

Vancouver:

Marino M. Comparison of NCD and CNN based mitotic classification of neural stem cells in phase contrast microscopy. [Internet] [Thesis]. Drexel University; 2016. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1860/idea:7127.

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

Council of Science Editors:

Marino M. Comparison of NCD and CNN based mitotic classification of neural stem cells in phase contrast microscopy. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:7127

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


Universidade Nova

25. Gomes, Cátia Sofia Vicente. Cues for cancer stem cells origin.

Degree: 2012, Universidade Nova

Dissertação para obtenção do Grau de Mestre em Genética Molecular e Biomedicina

Neural stem/progenitor cells (NSPC) can differentiate into neurons and glial cells in the… (more)

Subjects/Keywords: Astrocytes; Neural progenitor cells; Neural stem cells; Glioma cells; Gliomagenesis; Tumour-related factors

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APA (6th Edition):

Gomes, C. S. V. (2012). Cues for cancer stem cells origin. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12439

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):

Gomes, Cátia Sofia Vicente. “Cues for cancer stem cells origin.” 2012. Thesis, Universidade Nova. Accessed November 22, 2017. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12439.

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

MLA Handbook (7th Edition):

Gomes, Cátia Sofia Vicente. “Cues for cancer stem cells origin.” 2012. Web. 22 Nov 2017.

Vancouver:

Gomes CSV. Cues for cancer stem cells origin. [Internet] [Thesis]. Universidade Nova; 2012. [cited 2017 Nov 22]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12439.

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

Council of Science Editors:

Gomes CSV. Cues for cancer stem cells origin. [Thesis]. Universidade Nova; 2012. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/12439

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


University of Toronto

26. Azimi, Ashkan. Examining the Fundamental Biology of Primitive Neural Stem Cells.

Degree: 2017, University of Toronto

Definitive (d) neural stem cells (dNSCs) are multipotent, self-renewing, neurally committed stem cells. More recently, a novel primitive (p)NSC was identified in the early postnatal… (more)

Subjects/Keywords: Developmental Biology; Neural Stem Cells; Pluripotency vs Multipotency; Primitive Neural Stem Cells; Stem Cell Biology; 0317

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APA (6th Edition):

Azimi, A. (2017). Examining the Fundamental Biology of Primitive Neural Stem Cells. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79303

Chicago Manual of Style (16th Edition):

Azimi, Ashkan. “Examining the Fundamental Biology of Primitive Neural Stem Cells.” 2017. Masters Thesis, University of Toronto. Accessed November 22, 2017. http://hdl.handle.net/1807/79303.

MLA Handbook (7th Edition):

Azimi, Ashkan. “Examining the Fundamental Biology of Primitive Neural Stem Cells.” 2017. Web. 22 Nov 2017.

Vancouver:

Azimi A. Examining the Fundamental Biology of Primitive Neural Stem Cells. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1807/79303.

Council of Science Editors:

Azimi A. Examining the Fundamental Biology of Primitive Neural Stem Cells. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79303


University of Southern California

27. Zhong, Jingyang. Neural fate regulated by extrinsic signaling and epigenetics.

Degree: PhD, Neuroscience, 2013, University of Southern California

 The mammalian central nervous system is the most complex organ among all the mammalian organs and we have just began understanding the highly orchestrated but… (more)

Subjects/Keywords: neural stem cells; neuron; oligodendrocyte; histone modification; neural development

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APA (6th Edition):

Zhong, J. (2013). Neural fate regulated by extrinsic signaling and epigenetics. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314961/rec/4343

Chicago Manual of Style (16th Edition):

Zhong, Jingyang. “Neural fate regulated by extrinsic signaling and epigenetics.” 2013. Doctoral Dissertation, University of Southern California. Accessed November 22, 2017. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314961/rec/4343.

MLA Handbook (7th Edition):

Zhong, Jingyang. “Neural fate regulated by extrinsic signaling and epigenetics.” 2013. Web. 22 Nov 2017.

Vancouver:

Zhong J. Neural fate regulated by extrinsic signaling and epigenetics. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2017 Nov 22]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314961/rec/4343.

Council of Science Editors:

Zhong J. Neural fate regulated by extrinsic signaling and epigenetics. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/314961/rec/4343


University of Lund

28. 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 November 22, 2017. 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. 22 Nov 2017.

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 2017 Nov 22]. 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


University of Toronto

29. Salewski, Ryan P. Definitive Neural Stem Cell Clonally Generated from Pluripotent Stem Cells Promote Recovery following Spinal Cord Injury.

Degree: PhD, 2014, University of Toronto

 Advancements in medical management for spinal cord injury (SCI) have resulted in greatly improved survival rates following this devastating event; although medical interventions to regenerate… (more)

Subjects/Keywords: Embryonic Stem Cells; Induced Pluripotent Stem Cell; Myelination; Neural Stem Cell; Spinal Cord Injury; 0317

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APA (6th Edition):

Salewski, R. P. (2014). Definitive Neural Stem Cell Clonally Generated from Pluripotent Stem Cells Promote Recovery following Spinal Cord Injury. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/68474

Chicago Manual of Style (16th Edition):

Salewski, Ryan P. “Definitive Neural Stem Cell Clonally Generated from Pluripotent Stem Cells Promote Recovery following Spinal Cord Injury.” 2014. Doctoral Dissertation, University of Toronto. Accessed November 22, 2017. http://hdl.handle.net/1807/68474.

MLA Handbook (7th Edition):

Salewski, Ryan P. “Definitive Neural Stem Cell Clonally Generated from Pluripotent Stem Cells Promote Recovery following Spinal Cord Injury.” 2014. Web. 22 Nov 2017.

Vancouver:

Salewski RP. Definitive Neural Stem Cell Clonally Generated from Pluripotent Stem Cells Promote Recovery following Spinal Cord Injury. [Internet] [Doctoral dissertation]. University of Toronto; 2014. [cited 2017 Nov 22]. Available from: http://hdl.handle.net/1807/68474.

Council of Science Editors:

Salewski RP. Definitive Neural Stem Cell Clonally Generated from Pluripotent Stem Cells Promote Recovery following Spinal Cord Injury. [Doctoral Dissertation]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/68474


University of Miami

30. Acosta Torres, Zenith. Characterization of a Connexin 43 Enriched Population of Stem Cells Derived from Human Exfoliated Deciduous Teeth.

Degree: MS, Biomedical Engineering (Engineering), 2013, University of Miami

 This research aims to characterize the neural crest (NC) remnant population in Human Exfoliated Deciduous Teeth (SHED). This study applies a recently identified technique that… (more)

Subjects/Keywords: Neural crest stem cells; Stem Cells Derived from Human Exfoliated Deciduous Teeth; Connexin 43; Pluripotency

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

APA (6th Edition):

Acosta Torres, Z. (2013). Characterization of a Connexin 43 Enriched Population of Stem Cells Derived from Human Exfoliated Deciduous Teeth. (Thesis). University of Miami. Retrieved from http://scholarlyrepository.miami.edu/oa_theses/452

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):

Acosta Torres, Zenith. “Characterization of a Connexin 43 Enriched Population of Stem Cells Derived from Human Exfoliated Deciduous Teeth.” 2013. Thesis, University of Miami. Accessed November 22, 2017. http://scholarlyrepository.miami.edu/oa_theses/452.

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

MLA Handbook (7th Edition):

Acosta Torres, Zenith. “Characterization of a Connexin 43 Enriched Population of Stem Cells Derived from Human Exfoliated Deciduous Teeth.” 2013. Web. 22 Nov 2017.

Vancouver:

Acosta Torres Z. Characterization of a Connexin 43 Enriched Population of Stem Cells Derived from Human Exfoliated Deciduous Teeth. [Internet] [Thesis]. University of Miami; 2013. [cited 2017 Nov 22]. Available from: http://scholarlyrepository.miami.edu/oa_theses/452.

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

Council of Science Editors:

Acosta Torres Z. Characterization of a Connexin 43 Enriched Population of Stem Cells Derived from Human Exfoliated Deciduous Teeth. [Thesis]. University of Miami; 2013. Available from: http://scholarlyrepository.miami.edu/oa_theses/452

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

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