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You searched for +publisher:"Rutgers University" +contributor:("Grumet, Martin"). Showing records 1 – 15 of 15 total matches.

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Rutgers University

1. Kabat, Maciej, 1995-. Alginate encapsulation of cells to provide a commercially viable delivery for cell therapy.

Degree: MS, Biomedical Engineering, 2018, Rutgers University

 A leading cause of disease and death for all age groups are syndromes characterized by widespread uncontrollable inflammation. Severe trauma induces pro-inflammatory responses, increasing the… (more)

Subjects/Keywords: Drug delivery systems; Cellular therapy

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APA (6th Edition):

Kabat, Maciej, 1. (2018). Alginate encapsulation of cells to provide a commercially viable delivery for cell therapy. (Masters Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/57625/

Chicago Manual of Style (16th Edition):

Kabat, Maciej, 1995-. “Alginate encapsulation of cells to provide a commercially viable delivery for cell therapy.” 2018. Masters Thesis, Rutgers University. Accessed March 05, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/57625/.

MLA Handbook (7th Edition):

Kabat, Maciej, 1995-. “Alginate encapsulation of cells to provide a commercially viable delivery for cell therapy.” 2018. Web. 05 Mar 2021.

Vancouver:

Kabat, Maciej 1. Alginate encapsulation of cells to provide a commercially viable delivery for cell therapy. [Internet] [Masters thesis]. Rutgers University; 2018. [cited 2021 Mar 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/57625/.

Council of Science Editors:

Kabat, Maciej 1. Alginate encapsulation of cells to provide a commercially viable delivery for cell therapy. [Masters Thesis]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/57625/


Rutgers University

2. Bennett, Neal, 1989-. Design of reprogrammed neuronal transplantation and nanobiomaterial-based microglial therapeutic technologies for management of Parkinson's disease.

Degree: PhD, Biomedical Engineering, 2016, Rutgers University

Parkinson's disease (PD) is a progressive neurodegenerative disorder marked by motor dysfunction, eventual cognitive impairment and dementia in advanced stages. These symptoms arise as a… (more)

Subjects/Keywords: Parkinson's disease – Treatment; Nanobiotechnology

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APA (6th Edition):

Bennett, Neal, 1. (2016). Design of reprogrammed neuronal transplantation and nanobiomaterial-based microglial therapeutic technologies for management of Parkinson's disease. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51233/

Chicago Manual of Style (16th Edition):

Bennett, Neal, 1989-. “Design of reprogrammed neuronal transplantation and nanobiomaterial-based microglial therapeutic technologies for management of Parkinson's disease.” 2016. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/51233/.

MLA Handbook (7th Edition):

Bennett, Neal, 1989-. “Design of reprogrammed neuronal transplantation and nanobiomaterial-based microglial therapeutic technologies for management of Parkinson's disease.” 2016. Web. 05 Mar 2021.

Vancouver:

Bennett, Neal 1. Design of reprogrammed neuronal transplantation and nanobiomaterial-based microglial therapeutic technologies for management of Parkinson's disease. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2021 Mar 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51233/.

Council of Science Editors:

Bennett, Neal 1. Design of reprogrammed neuronal transplantation and nanobiomaterial-based microglial therapeutic technologies for management of Parkinson's disease. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51233/


Rutgers University

3. Hsu, Shao-Yun, 1983-. The Fischer 344 spinal cord contusion model and effects of cyclosporin-A on the model.

Degree: PhD, Neuroscience, 2016, Rutgers University

The Multicenter Animal Spinal Cord Injury Study (MASCIS) standardized spinal cord injury (SCI) in Long-Evans hooded and Sprague-Dawley rats. In this thesis, we extended the… (more)

Subjects/Keywords: Cyclosporine; Spinal cord – Wounds and injuries

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APA (6th Edition):

Hsu, Shao-Yun, 1. (2016). The Fischer 344 spinal cord contusion model and effects of cyclosporin-A on the model. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/50009/

Chicago Manual of Style (16th Edition):

Hsu, Shao-Yun, 1983-. “The Fischer 344 spinal cord contusion model and effects of cyclosporin-A on the model.” 2016. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/50009/.

MLA Handbook (7th Edition):

Hsu, Shao-Yun, 1983-. “The Fischer 344 spinal cord contusion model and effects of cyclosporin-A on the model.” 2016. Web. 05 Mar 2021.

Vancouver:

Hsu, Shao-Yun 1. The Fischer 344 spinal cord contusion model and effects of cyclosporin-A on the model. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2021 Mar 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50009/.

Council of Science Editors:

Hsu, Shao-Yun 1. The Fischer 344 spinal cord contusion model and effects of cyclosporin-A on the model. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/50009/


Rutgers University

4. Li, Ying, 1987-. Gene regulation during central nervous system development and post-injury regeneration.

Degree: PhD, Biomedical Engineering, 2016, Rutgers University

Central nervous system (CNS) development and post-injury neurogenesis require accurate coordination of neural stem cell proliferation, progenitor cell differentiation, neuron, glia migration and maturation, and… (more)

Subjects/Keywords: Genetic regulation; Developmental neurobiology

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APA (6th Edition):

Li, Ying, 1. (2016). Gene regulation during central nervous system development and post-injury regeneration. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/49255/

Chicago Manual of Style (16th Edition):

Li, Ying, 1987-. “Gene regulation during central nervous system development and post-injury regeneration.” 2016. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/49255/.

MLA Handbook (7th Edition):

Li, Ying, 1987-. “Gene regulation during central nervous system development and post-injury regeneration.” 2016. Web. 05 Mar 2021.

Vancouver:

Li, Ying 1. Gene regulation during central nervous system development and post-injury regeneration. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2021 Mar 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49255/.

Council of Science Editors:

Li, Ying 1. Gene regulation during central nervous system development and post-injury regeneration. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/49255/

5. Tzatzalos, Evangeline, 1983-. A regulatory element for interneuron progenitors in the developing vertebrate central nervous system.

Degree: Biomedical Engineering, 2012, Rutgers University

Subjects/Keywords: Nerve tissue proteins; Nerve growth factor; Nervous system – Growth

…Neuroscience at Rutgers University. Heterozygous mutants reeler+/- were crossed with Notch1CR2-βGP… 

Page 1 Page 2 Page 3 Page 4 Page 5 Page 6 Page 7 Sample image

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APA (6th Edition):

Tzatzalos, Evangeline, 1. (2012). A regulatory element for interneuron progenitors in the developing vertebrate central nervous system. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065283

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):

Tzatzalos, Evangeline, 1983-. “A regulatory element for interneuron progenitors in the developing vertebrate central nervous system.” 2012. Thesis, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065283.

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

MLA Handbook (7th Edition):

Tzatzalos, Evangeline, 1983-. “A regulatory element for interneuron progenitors in the developing vertebrate central nervous system.” 2012. Web. 05 Mar 2021.

Vancouver:

Tzatzalos, Evangeline 1. A regulatory element for interneuron progenitors in the developing vertebrate central nervous system. [Internet] [Thesis]. Rutgers University; 2012. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065283.

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

Council of Science Editors:

Tzatzalos, Evangeline 1. A regulatory element for interneuron progenitors in the developing vertebrate central nervous system. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000065283

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

6. Barminko, Jeffrey Avi, 1985-. Encapsulated Mesenchymal stromal cells for spinal cord injury repair.

Degree: Biomedical Engineering, 2012, Rutgers University

Subjects/Keywords: Spinal cord – Wounds and injuries – Treatment; Mesenchymal stem cells – Transplantation

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APA (6th Edition):

Barminko, Jeffrey Avi, 1. (2012). Encapsulated Mesenchymal stromal cells for spinal cord injury repair. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066610

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):

Barminko, Jeffrey Avi, 1985-. “Encapsulated Mesenchymal stromal cells for spinal cord injury repair.” 2012. Thesis, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066610.

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

MLA Handbook (7th Edition):

Barminko, Jeffrey Avi, 1985-. “Encapsulated Mesenchymal stromal cells for spinal cord injury repair.” 2012. Web. 05 Mar 2021.

Vancouver:

Barminko, Jeffrey Avi 1. Encapsulated Mesenchymal stromal cells for spinal cord injury repair. [Internet] [Thesis]. Rutgers University; 2012. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066610.

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

Council of Science Editors:

Barminko, Jeffrey Avi 1. Encapsulated Mesenchymal stromal cells for spinal cord injury repair. [Thesis]. Rutgers University; 2012. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000066610

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


Rutgers University

7. 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 March 05, 2021. 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. 05 Mar 2021.

Vancouver:

Davila, Jorge 1. MIR-9 targets OC2 in proliferating and differentiating neural stem cells. [Internet] [Doctoral dissertation]. Rutgers University; 2011. [cited 2021 Mar 05]. 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


Rutgers University

8. Ricupero, Christopher L. Epigenetic regulation and transcription factor programming enhances neurogenesis in neural stem cells.

Degree: Neuroscience, 2011, Rutgers University

Subjects/Keywords: Developmental neurobiology; Epigenesis; Neural stem cells

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APA (6th Edition):

Ricupero, C. L. (2011). Epigenetic regulation and transcription factor programming enhances neurogenesis in neural stem cells. (Thesis). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063582

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):

Ricupero, Christopher L. “Epigenetic regulation and transcription factor programming enhances neurogenesis in neural stem cells.” 2011. Thesis, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063582.

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

MLA Handbook (7th Edition):

Ricupero, Christopher L. “Epigenetic regulation and transcription factor programming enhances neurogenesis in neural stem cells.” 2011. Web. 05 Mar 2021.

Vancouver:

Ricupero CL. Epigenetic regulation and transcription factor programming enhances neurogenesis in neural stem cells. [Internet] [Thesis]. Rutgers University; 2011. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063582.

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

Council of Science Editors:

Ricupero CL. Epigenetic regulation and transcription factor programming enhances neurogenesis in neural stem cells. [Thesis]. Rutgers University; 2011. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000063582

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


Rutgers University

9. Carlson, Aaron L., 1985-. Engineered synthetic microenvironments for human pluripotent stem cells: applications for neuronal regeneration.

Degree: Biomedical Engineering, 2013, Rutgers University

Subjects/Keywords: Stem cells – Research; Regenerative medicine; Nervous system – Regeneration

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APA (6th Edition):

Carlson, Aaron L., 1. (2013). Engineered synthetic microenvironments for human pluripotent stem cells: applications for neuronal regeneration. (Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/41738/

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):

Carlson, Aaron L., 1985-. “Engineered synthetic microenvironments for human pluripotent stem cells: applications for neuronal regeneration.” 2013. Thesis, Rutgers University. Accessed March 05, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/41738/.

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

MLA Handbook (7th Edition):

Carlson, Aaron L., 1985-. “Engineered synthetic microenvironments for human pluripotent stem cells: applications for neuronal regeneration.” 2013. Web. 05 Mar 2021.

Vancouver:

Carlson, Aaron L. 1. Engineered synthetic microenvironments for human pluripotent stem cells: applications for neuronal regeneration. [Internet] [Thesis]. Rutgers University; 2013. [cited 2021 Mar 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/41738/.

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

Council of Science Editors:

Carlson, Aaron L. 1. Engineered synthetic microenvironments for human pluripotent stem cells: applications for neuronal regeneration. [Thesis]. Rutgers University; 2013. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/41738/

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


Rutgers University

10. Cherry, Jocie Fatima, 1978-. Engineered presentation of neural cell adhesion molecules for directed neural and neural stem cell behaviors.

Degree: Biomedical Engineering, 2013, Rutgers University

Subjects/Keywords: Cytology – Research; Nervous system – Wounds and injuries; Regenerative medicine; Stem cells – Transplantation

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APA (6th Edition):

Cherry, Jocie Fatima, 1. (2013). Engineered presentation of neural cell adhesion molecules for directed neural and neural stem cell behaviors. (Thesis). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/41742/

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):

Cherry, Jocie Fatima, 1978-. “Engineered presentation of neural cell adhesion molecules for directed neural and neural stem cell behaviors.” 2013. Thesis, Rutgers University. Accessed March 05, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/41742/.

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

MLA Handbook (7th Edition):

Cherry, Jocie Fatima, 1978-. “Engineered presentation of neural cell adhesion molecules for directed neural and neural stem cell behaviors.” 2013. Web. 05 Mar 2021.

Vancouver:

Cherry, Jocie Fatima 1. Engineered presentation of neural cell adhesion molecules for directed neural and neural stem cell behaviors. [Internet] [Thesis]. Rutgers University; 2013. [cited 2021 Mar 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/41742/.

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

Council of Science Editors:

Cherry, Jocie Fatima 1. Engineered presentation of neural cell adhesion molecules for directed neural and neural stem cell behaviors. [Thesis]. Rutgers University; 2013. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/41742/

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


Rutgers University

11. Moore, Rebecca. Differentiation of human and murine embryonic stem cells: studies on the combined roles of adhesion molecules and growth factors.

Degree: PhD, Biomedical Engineering, 2008, Rutgers University

The field of stem cell bioengineering can potentially revolutionize cell-based therapies for functional replacement of complex systems like the liver and nervous system. Despite significant… (more)

Subjects/Keywords: Cell differentiation; Cell adhesion molecules; Cells – Growth

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APA (6th Edition):

Moore, R. (2008). Differentiation of human and murine embryonic stem cells: studies on the combined roles of adhesion molecules and growth factors. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17535

Chicago Manual of Style (16th Edition):

Moore, Rebecca. “Differentiation of human and murine embryonic stem cells: studies on the combined roles of adhesion molecules and growth factors.” 2008. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17535.

MLA Handbook (7th Edition):

Moore, Rebecca. “Differentiation of human and murine embryonic stem cells: studies on the combined roles of adhesion molecules and growth factors.” 2008. Web. 05 Mar 2021.

Vancouver:

Moore R. Differentiation of human and murine embryonic stem cells: studies on the combined roles of adhesion molecules and growth factors. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17535.

Council of Science Editors:

Moore R. Differentiation of human and murine embryonic stem cells: studies on the combined roles of adhesion molecules and growth factors. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17535


Rutgers University

12. Florek, Charles A., 1980-. A synthetic biomaterials approach to the prevention of postsurgical adhesions in neurosurgery.

Degree: PhD, Biomedical Engineering, 2010, Rutgers University

In the treatment of spinal stenosis and disc herniation, the lamina and ligamentum flavum are resected to access the spinal canal. When a fibrous scar… (more)

Subjects/Keywords: Nervous system – Surgery – Complications; Laminectomy; Electrospinning; Adhesives in surgery

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APA (6th Edition):

Florek, Charles A., 1. (2010). A synthetic biomaterials approach to the prevention of postsurgical adhesions in neurosurgery. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056345

Chicago Manual of Style (16th Edition):

Florek, Charles A., 1980-. “A synthetic biomaterials approach to the prevention of postsurgical adhesions in neurosurgery.” 2010. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056345.

MLA Handbook (7th Edition):

Florek, Charles A., 1980-. “A synthetic biomaterials approach to the prevention of postsurgical adhesions in neurosurgery.” 2010. Web. 05 Mar 2021.

Vancouver:

Florek, Charles A. 1. A synthetic biomaterials approach to the prevention of postsurgical adhesions in neurosurgery. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056345.

Council of Science Editors:

Florek, Charles A. 1. A synthetic biomaterials approach to the prevention of postsurgical adhesions in neurosurgery. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000056345


Rutgers University

13. Chang, Yu-Wen. Therapeutic potential of radial glial RG3.6 cells in rat spinal cord injury.

Degree: PhD, Neuroscience, 2007, Rutgers University

Spinal cord injury (SCI) triggers a cascade of pathophysiological changes that lead to secondary tissue damage after the mechanical insult. Early after SCI, cells are… (more)

Subjects/Keywords: Spinal cord – Wounds and injuries; Neuroglia

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APA (6th Edition):

Chang, Y. (2007). Therapeutic potential of radial glial RG3.6 cells in rat spinal cord injury. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.15795

Chicago Manual of Style (16th Edition):

Chang, Yu-Wen. “Therapeutic potential of radial glial RG3.6 cells in rat spinal cord injury.” 2007. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.15795.

MLA Handbook (7th Edition):

Chang, Yu-Wen. “Therapeutic potential of radial glial RG3.6 cells in rat spinal cord injury.” 2007. Web. 05 Mar 2021.

Vancouver:

Chang Y. Therapeutic potential of radial glial RG3.6 cells in rat spinal cord injury. [Internet] [Doctoral dissertation]. Rutgers University; 2007. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.15795.

Council of Science Editors:

Chang Y. Therapeutic potential of radial glial RG3.6 cells in rat spinal cord injury. [Doctoral Dissertation]. Rutgers University; 2007. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.15795


Rutgers University

14. Goff, Loyal Andrew. Brain-specific microRNAs induce neurogenesis through indirect regulation of Mef2C activity.

Degree: PhD, Cell and Developmental Biology, 2008, Rutgers University

MicroRNAs represent a group of functional non-coding RNAs (ncRNA) with a role in both translational repression and/or RNAi-mediated degradation of specific target mRNAs. Reports indicate… (more)

Subjects/Keywords: Non-coding RNA; Developmental neurobiology

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APA (6th Edition):

Goff, L. A. (2008). Brain-specific microRNAs induce neurogenesis through indirect regulation of Mef2C activity. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17318

Chicago Manual of Style (16th Edition):

Goff, Loyal Andrew. “Brain-specific microRNAs induce neurogenesis through indirect regulation of Mef2C activity.” 2008. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17318.

MLA Handbook (7th Edition):

Goff, Loyal Andrew. “Brain-specific microRNAs induce neurogenesis through indirect regulation of Mef2C activity.” 2008. Web. 05 Mar 2021.

Vancouver:

Goff LA. Brain-specific microRNAs induce neurogenesis through indirect regulation of Mef2C activity. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17318.

Council of Science Editors:

Goff LA. Brain-specific microRNAs induce neurogenesis through indirect regulation of Mef2C activity. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17318


Rutgers University

15. Qu, Zhao xia. Effects of erythropoietin and lithium on neural precursors and blood-derived cells.

Degree: PhD, Neuroscience, 2008, Rutgers University

Recent studies suggest that two hematopoietic drugs, erythropoietin (EPO) and lithium, can be used to treat various central nervous system (CNS) diseases, and that neural… (more)

Subjects/Keywords: Nervous system – Regeneration; Erythropoietin – Physiological effect; Lithium – Physiological effect

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APA (6th Edition):

Qu, Z. x. (2008). Effects of erythropoietin and lithium on neural precursors and blood-derived cells. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17546

Chicago Manual of Style (16th Edition):

Qu, Zhao xia. “Effects of erythropoietin and lithium on neural precursors and blood-derived cells.” 2008. Doctoral Dissertation, Rutgers University. Accessed March 05, 2021. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17546.

MLA Handbook (7th Edition):

Qu, Zhao xia. “Effects of erythropoietin and lithium on neural precursors and blood-derived cells.” 2008. Web. 05 Mar 2021.

Vancouver:

Qu Zx. Effects of erythropoietin and lithium on neural precursors and blood-derived cells. [Internet] [Doctoral dissertation]. Rutgers University; 2008. [cited 2021 Mar 05]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17546.

Council of Science Editors:

Qu Zx. Effects of erythropoietin and lithium on neural precursors and blood-derived cells. [Doctoral Dissertation]. Rutgers University; 2008. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.17546

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