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You searched for subject:(Central nervous system CNS ). Showing records 1 – 30 of 65567 total matches.

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University of Rochester

1. Herr, Megan. Antidepressant Use and Risk of Central Nervous System Metastasis.

Degree: PhD, 2016, University of Rochester

Central nervous system (CNS) metastasis is the spread of a primary cancer to the CNS and occurs in up to 25% of cancer patients. Antidepressant… (more)

Subjects/Keywords: Central nervous system metastasis; CNS metastasis; antidepressants; SSRIs; inflammation

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APA (6th Edition):

Herr, M. (2016). Antidepressant Use and Risk of Central Nervous System Metastasis. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30505

Chicago Manual of Style (16th Edition):

Herr, Megan. “Antidepressant Use and Risk of Central Nervous System Metastasis.” 2016. Doctoral Dissertation, University of Rochester. Accessed May 08, 2021. http://hdl.handle.net/1802/30505.

MLA Handbook (7th Edition):

Herr, Megan. “Antidepressant Use and Risk of Central Nervous System Metastasis.” 2016. Web. 08 May 2021.

Vancouver:

Herr M. Antidepressant Use and Risk of Central Nervous System Metastasis. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2021 May 08]. Available from: http://hdl.handle.net/1802/30505.

Council of Science Editors:

Herr M. Antidepressant Use and Risk of Central Nervous System Metastasis. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/30505


Vanderbilt University

2. Sutherland, Danica Marie. Functions of the viral attachment protein in reovirus neurovirulence.

Degree: PhD, Microbiology and Immunology, 2018, Vanderbilt University

 Viral encephalitis is a serious and life-threatening inflammation of the central nervous system (CNS). However, mechanisms of viral neuroinvasion and disease pathogenesis in the CNS(more)

Subjects/Keywords: hydrocephalus; encephalitis; CNS; brain; central nervous system; pathogenesis; virus

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APA (6th Edition):

Sutherland, D. M. (2018). Functions of the viral attachment protein in reovirus neurovirulence. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13968

Chicago Manual of Style (16th Edition):

Sutherland, Danica Marie. “Functions of the viral attachment protein in reovirus neurovirulence.” 2018. Doctoral Dissertation, Vanderbilt University. Accessed May 08, 2021. http://hdl.handle.net/1803/13968.

MLA Handbook (7th Edition):

Sutherland, Danica Marie. “Functions of the viral attachment protein in reovirus neurovirulence.” 2018. Web. 08 May 2021.

Vancouver:

Sutherland DM. Functions of the viral attachment protein in reovirus neurovirulence. [Internet] [Doctoral dissertation]. Vanderbilt University; 2018. [cited 2021 May 08]. Available from: http://hdl.handle.net/1803/13968.

Council of Science Editors:

Sutherland DM. Functions of the viral attachment protein in reovirus neurovirulence. [Doctoral Dissertation]. Vanderbilt University; 2018. Available from: http://hdl.handle.net/1803/13968


Monash University

3. RATCLIFFE, JULIAN CHARLES. Peptide hydrogels for the treatment of neurodegenerative diseases.

Degree: Engineering, 2018, Monash University

This thesis outlines the design of two new hydrogels which are capable of supporting the growth and survival of neural cells in the brain. The hydrogels were analysed as potential treatments for diseases such as Parkinson’s disease, with the aim of restoring brain function.

Subjects/Keywords: Central Nervous System; Biomaterials; Characterisation of Biological Macromolecules; Proteins and Peptides; Peptides; TEM; Cell Culture; CNS; Central Nervous System; Hydrogels; Macromolecules

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APA (6th Edition):

RATCLIFFE, J. C. (2018). Peptide hydrogels for the treatment of neurodegenerative diseases. (Thesis). Monash University. Retrieved from https://doi.org/10.26180/5b6e87b86cbc4

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):

RATCLIFFE, JULIAN CHARLES. “Peptide hydrogels for the treatment of neurodegenerative diseases.” 2018. Thesis, Monash University. Accessed May 08, 2021. https://doi.org/10.26180/5b6e87b86cbc4.

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

MLA Handbook (7th Edition):

RATCLIFFE, JULIAN CHARLES. “Peptide hydrogels for the treatment of neurodegenerative diseases.” 2018. Web. 08 May 2021.

Vancouver:

RATCLIFFE JC. Peptide hydrogels for the treatment of neurodegenerative diseases. [Internet] [Thesis]. Monash University; 2018. [cited 2021 May 08]. Available from: https://doi.org/10.26180/5b6e87b86cbc4.

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

Council of Science Editors:

RATCLIFFE JC. Peptide hydrogels for the treatment of neurodegenerative diseases. [Thesis]. Monash University; 2018. Available from: https://doi.org/10.26180/5b6e87b86cbc4

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


Humboldt State University

4. Servais, Benjamin. Regulating resistance exercise intensity using perceptual response and the ???anticipatory feedback??? model.

Degree: MS, Kinesiology, 2015, Humboldt State University

 PURPOSE: To assess how accurately trained subjects can predict exercise endpoint in resistance training. METHODS: 12 female (age 20.33 ?? 1.61 years; height 166.12 ??… (more)

Subjects/Keywords: Resistance training; Bench press; Failure; RPE; Exercise endpoint; CNS; Central nervous system; Anticipatory feedback

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APA (6th Edition):

Servais, B. (2015). Regulating resistance exercise intensity using perceptual response and the ???anticipatory feedback??? model. (Masters Thesis). Humboldt State University. Retrieved from http://hdl.handle.net/10211.3/143735

Chicago Manual of Style (16th Edition):

Servais, Benjamin. “Regulating resistance exercise intensity using perceptual response and the ???anticipatory feedback??? model.” 2015. Masters Thesis, Humboldt State University. Accessed May 08, 2021. http://hdl.handle.net/10211.3/143735.

MLA Handbook (7th Edition):

Servais, Benjamin. “Regulating resistance exercise intensity using perceptual response and the ???anticipatory feedback??? model.” 2015. Web. 08 May 2021.

Vancouver:

Servais B. Regulating resistance exercise intensity using perceptual response and the ???anticipatory feedback??? model. [Internet] [Masters thesis]. Humboldt State University; 2015. [cited 2021 May 08]. Available from: http://hdl.handle.net/10211.3/143735.

Council of Science Editors:

Servais B. Regulating resistance exercise intensity using perceptual response and the ???anticipatory feedback??? model. [Masters Thesis]. Humboldt State University; 2015. Available from: http://hdl.handle.net/10211.3/143735


Boston University

5. Burt, Daniel Robert. Optimization of viral transduction in the central nervous system.

Degree: MS, Medical Sciences, 2014, Boston University

 Genetically based Central Nervous System (CNS) disorders remain a largely unresolved issue in the world today. Our genome is the source of our greatest strengths… (more)

Subjects/Keywords: Biology; AAV; CNS; Adeno-associated virus; Central nervous system; Gene therapy; Transduction

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APA (6th Edition):

Burt, D. R. (2014). Optimization of viral transduction in the central nervous system. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/14650

Chicago Manual of Style (16th Edition):

Burt, Daniel Robert. “Optimization of viral transduction in the central nervous system.” 2014. Masters Thesis, Boston University. Accessed May 08, 2021. http://hdl.handle.net/2144/14650.

MLA Handbook (7th Edition):

Burt, Daniel Robert. “Optimization of viral transduction in the central nervous system.” 2014. Web. 08 May 2021.

Vancouver:

Burt DR. Optimization of viral transduction in the central nervous system. [Internet] [Masters thesis]. Boston University; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/2144/14650.

Council of Science Editors:

Burt DR. Optimization of viral transduction in the central nervous system. [Masters Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14650


University of New South Wales

6. Guest, Jade. Oxidative damage and inflammation in the central nervous system: influence of age and specific nutritional elements.

Degree: Medical Sciences, 2015, University of New South Wales

 The studies presented in this thesis were designed to quantitate and compare the influence of age and selected dietary elements on oxidative and inflammatory activity… (more)

Subjects/Keywords: Oxidative; Central nervous system; Nicotinamide adenine dinucleotide; Inflammation; Nutrition; NAD+; CNS; Aging; Brain

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APA (6th Edition):

Guest, J. (2015). Oxidative damage and inflammation in the central nervous system: influence of age and specific nutritional elements. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55558 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38051/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Guest, Jade. “Oxidative damage and inflammation in the central nervous system: influence of age and specific nutritional elements.” 2015. Doctoral Dissertation, University of New South Wales. Accessed May 08, 2021. http://handle.unsw.edu.au/1959.4/55558 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38051/SOURCE02?view=true.

MLA Handbook (7th Edition):

Guest, Jade. “Oxidative damage and inflammation in the central nervous system: influence of age and specific nutritional elements.” 2015. Web. 08 May 2021.

Vancouver:

Guest J. Oxidative damage and inflammation in the central nervous system: influence of age and specific nutritional elements. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2021 May 08]. Available from: http://handle.unsw.edu.au/1959.4/55558 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38051/SOURCE02?view=true.

Council of Science Editors:

Guest J. Oxidative damage and inflammation in the central nervous system: influence of age and specific nutritional elements. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/55558 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:38051/SOURCE02?view=true

7. Borin, Diego Becker. EFEITO ANTIOXIDANTE DE LIPOSSOMAS CONTENDO CREATINA NO PROCESSO DE ISQUEMIA/REPERFUSÃO CEREBRAL EM RATOS: DESENVOLVIMENTO, CARACTERIZAÇÃO E AVALIAÇÃO FARMACOLÓGICA.

Degree: 2013, Universidade Franciscana; Mestrado Acadêmico em Nanociências; UFN; BR; Biociências e Nanomateriais

Made available in DSpace on 2018-06-27T18:56:03Z (GMT). No. of bitstreams: 3 Diego Becker Borin.pdf: 1553948 bytes, checksum: b94d052c85f74f3bcc5e4cadbcb71e67 (MD5) Diego Becker Borin.pdf.txt: 134530 bytes, checksum:… (more)

Subjects/Keywords: lipossoma; creatina; barreira hematoencefálica (BHE); sistema nervoso central (SNC); liposome, creatine; blood-brain barrier (BBB); central nervous system (CNS); CNPQ::ENGENHARIAS

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APA (6th Edition):

Borin, D. B. (2013). EFEITO ANTIOXIDANTE DE LIPOSSOMAS CONTENDO CREATINA NO PROCESSO DE ISQUEMIA/REPERFUSÃO CEREBRAL EM RATOS: DESENVOLVIMENTO, CARACTERIZAÇÃO E AVALIAÇÃO FARMACOLÓGICA. (Masters Thesis). Universidade Franciscana; Mestrado Acadêmico em Nanociências; UFN; BR; Biociências e Nanomateriais. Retrieved from http://tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/206 ; http://www.tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/291

Chicago Manual of Style (16th Edition):

Borin, Diego Becker. “EFEITO ANTIOXIDANTE DE LIPOSSOMAS CONTENDO CREATINA NO PROCESSO DE ISQUEMIA/REPERFUSÃO CEREBRAL EM RATOS: DESENVOLVIMENTO, CARACTERIZAÇÃO E AVALIAÇÃO FARMACOLÓGICA.” 2013. Masters Thesis, Universidade Franciscana; Mestrado Acadêmico em Nanociências; UFN; BR; Biociências e Nanomateriais. Accessed May 08, 2021. http://tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/206 ; http://www.tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/291.

MLA Handbook (7th Edition):

Borin, Diego Becker. “EFEITO ANTIOXIDANTE DE LIPOSSOMAS CONTENDO CREATINA NO PROCESSO DE ISQUEMIA/REPERFUSÃO CEREBRAL EM RATOS: DESENVOLVIMENTO, CARACTERIZAÇÃO E AVALIAÇÃO FARMACOLÓGICA.” 2013. Web. 08 May 2021.

Vancouver:

Borin DB. EFEITO ANTIOXIDANTE DE LIPOSSOMAS CONTENDO CREATINA NO PROCESSO DE ISQUEMIA/REPERFUSÃO CEREBRAL EM RATOS: DESENVOLVIMENTO, CARACTERIZAÇÃO E AVALIAÇÃO FARMACOLÓGICA. [Internet] [Masters thesis]. Universidade Franciscana; Mestrado Acadêmico em Nanociências; UFN; BR; Biociências e Nanomateriais; 2013. [cited 2021 May 08]. Available from: http://tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/206 ; http://www.tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/291.

Council of Science Editors:

Borin DB. EFEITO ANTIOXIDANTE DE LIPOSSOMAS CONTENDO CREATINA NO PROCESSO DE ISQUEMIA/REPERFUSÃO CEREBRAL EM RATOS: DESENVOLVIMENTO, CARACTERIZAÇÃO E AVALIAÇÃO FARMACOLÓGICA. [Masters Thesis]. Universidade Franciscana; Mestrado Acadêmico em Nanociências; UFN; BR; Biociências e Nanomateriais; 2013. Available from: http://tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/206 ; http://www.tede.universidadefranciscana.edu.br:8080/handle/UFN-BDTD/291


University of KwaZulu-Natal

8. Ramruthan, Jenine. Genetic and functional diversity of central nervous system (CNS) derived Human Immunodeficiency Virus type 1 (HIV-1) tat from Tuberculous Meningitis (TBM) patients.

Degree: 2018, University of KwaZulu-Natal

 INTRODUCTION Human immunodeficiency virus type 1 (HIV-1) transactivator of transcription (tat) is a regulatory gene that encodes the transactivator of transcription Tat protein. The Tat… (more)

Subjects/Keywords: Central Nervous System (CNS).; Human Immunodeficiency Virus Type 1 (HIV-1).; Tuberculous Meningitis (TBM).; Transactivator of transcription (tat).

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APA (6th Edition):

Ramruthan, J. (2018). Genetic and functional diversity of central nervous system (CNS) derived Human Immunodeficiency Virus type 1 (HIV-1) tat from Tuberculous Meningitis (TBM) patients. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/18606

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):

Ramruthan, Jenine. “Genetic and functional diversity of central nervous system (CNS) derived Human Immunodeficiency Virus type 1 (HIV-1) tat from Tuberculous Meningitis (TBM) patients.” 2018. Thesis, University of KwaZulu-Natal. Accessed May 08, 2021. https://researchspace.ukzn.ac.za/handle/10413/18606.

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

MLA Handbook (7th Edition):

Ramruthan, Jenine. “Genetic and functional diversity of central nervous system (CNS) derived Human Immunodeficiency Virus type 1 (HIV-1) tat from Tuberculous Meningitis (TBM) patients.” 2018. Web. 08 May 2021.

Vancouver:

Ramruthan J. Genetic and functional diversity of central nervous system (CNS) derived Human Immunodeficiency Virus type 1 (HIV-1) tat from Tuberculous Meningitis (TBM) patients. [Internet] [Thesis]. University of KwaZulu-Natal; 2018. [cited 2021 May 08]. Available from: https://researchspace.ukzn.ac.za/handle/10413/18606.

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

Council of Science Editors:

Ramruthan J. Genetic and functional diversity of central nervous system (CNS) derived Human Immunodeficiency Virus type 1 (HIV-1) tat from Tuberculous Meningitis (TBM) patients. [Thesis]. University of KwaZulu-Natal; 2018. Available from: https://researchspace.ukzn.ac.za/handle/10413/18606

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


Freie Universität Berlin

9. Boato, Francesco. Hypothermie und das C3 Peptid unterstützen Neuriten Wachstum und Regeneration nach traumatischer ZNS Lesion.

Degree: 2010, Freie Universität Berlin

 Hypothermie ist ein etabliertes Verfahren zur Neuroprotektion nach perinataler Asphyxie, Schlaganfall und die hypotherme Therapie wird kontrovers diskutiert nach Schädel-Hirn Trauma. Wir konnten belegen, dass… (more)

Subjects/Keywords: central nervous system; CNS injury; regeneration; outgrowth; hypothermia; C3 protein; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Boato, F. (2010). Hypothermie und das C3 Peptid unterstützen Neuriten Wachstum und Regeneration nach traumatischer ZNS Lesion. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/11146

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):

Boato, Francesco. “Hypothermie und das C3 Peptid unterstützen Neuriten Wachstum und Regeneration nach traumatischer ZNS Lesion.” 2010. Thesis, Freie Universität Berlin. Accessed May 08, 2021. https://refubium.fu-berlin.de/handle/fub188/11146.

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

MLA Handbook (7th Edition):

Boato, Francesco. “Hypothermie und das C3 Peptid unterstützen Neuriten Wachstum und Regeneration nach traumatischer ZNS Lesion.” 2010. Web. 08 May 2021.

Vancouver:

Boato F. Hypothermie und das C3 Peptid unterstützen Neuriten Wachstum und Regeneration nach traumatischer ZNS Lesion. [Internet] [Thesis]. Freie Universität Berlin; 2010. [cited 2021 May 08]. Available from: https://refubium.fu-berlin.de/handle/fub188/11146.

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

Council of Science Editors:

Boato F. Hypothermie und das C3 Peptid unterstützen Neuriten Wachstum und Regeneration nach traumatischer ZNS Lesion. [Thesis]. Freie Universität Berlin; 2010. Available from: https://refubium.fu-berlin.de/handle/fub188/11146

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


University of Manitoba

10. Roberts, Lauren Emilienne. Localisation of equilibrative nucleoside transporter 3 (ENT3) in mouse brain.

Degree: Pharmacology and Therapeutics, 2015, University of Manitoba

 Adenosine is an essential purine nucleoside of particular importance within heart and brain. The widespread and diverse actions of adenosine, driven by activation of cell… (more)

Subjects/Keywords: Adenosine; Central nervous system (CNS); Equilibrative nucleoside transporter; Equilibrative nucleoside transporter 3; ENT3; Brain; Localisation; Transporters; ENT

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APA (6th Edition):

Roberts, L. E. (2015). Localisation of equilibrative nucleoside transporter 3 (ENT3) in mouse brain. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30193

Chicago Manual of Style (16th Edition):

Roberts, Lauren Emilienne. “Localisation of equilibrative nucleoside transporter 3 (ENT3) in mouse brain.” 2015. Masters Thesis, University of Manitoba. Accessed May 08, 2021. http://hdl.handle.net/1993/30193.

MLA Handbook (7th Edition):

Roberts, Lauren Emilienne. “Localisation of equilibrative nucleoside transporter 3 (ENT3) in mouse brain.” 2015. Web. 08 May 2021.

Vancouver:

Roberts LE. Localisation of equilibrative nucleoside transporter 3 (ENT3) in mouse brain. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2021 May 08]. Available from: http://hdl.handle.net/1993/30193.

Council of Science Editors:

Roberts LE. Localisation of equilibrative nucleoside transporter 3 (ENT3) in mouse brain. [Masters Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/30193


University of St. Andrews

11. Forbes, Lindsey H. Using human iPSC-derived neural progenitor cells to increase integrin expression in the CNS.

Degree: 2018, University of St. Andrews

 Repair of the adult mammalian spinal cord is prohibited by several extrinsic and intrinsic factors. As the CNS matures, growth-promoting proteins such as integrins are… (more)

Subjects/Keywords: Neuroregeneration; Stem cells; Integrin; Brain and spinal cord repair; Transplantation; CNS; QP370.F7; Central nervous system – Regeneration; Integrins

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APA (6th Edition):

Forbes, L. H. (2018). Using human iPSC-derived neural progenitor cells to increase integrin expression in the CNS. (Doctoral Dissertation). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/16567

Chicago Manual of Style (16th Edition):

Forbes, Lindsey H. “Using human iPSC-derived neural progenitor cells to increase integrin expression in the CNS.” 2018. Doctoral Dissertation, University of St. Andrews. Accessed May 08, 2021. http://hdl.handle.net/10023/16567.

MLA Handbook (7th Edition):

Forbes, Lindsey H. “Using human iPSC-derived neural progenitor cells to increase integrin expression in the CNS.” 2018. Web. 08 May 2021.

Vancouver:

Forbes LH. Using human iPSC-derived neural progenitor cells to increase integrin expression in the CNS. [Internet] [Doctoral dissertation]. University of St. Andrews; 2018. [cited 2021 May 08]. Available from: http://hdl.handle.net/10023/16567.

Council of Science Editors:

Forbes LH. Using human iPSC-derived neural progenitor cells to increase integrin expression in the CNS. [Doctoral Dissertation]. University of St. Andrews; 2018. Available from: http://hdl.handle.net/10023/16567


University of Georgia

12. Barber, Renee Marie. Etiopathogenesis studies of canine idiopathic meningoencephalomyelitis.

Degree: 2014, University of Georgia

 Numerous idiopathic inflammatory disorders of the canine central nervous system (CNS) have been described over the past several decades. These include specific histopathological entities such… (more)

Subjects/Keywords: Central nervous system; CNS; inflammation; Dog; Granulomatous meningoencephalomyelitis; GME; Necrotizing meningoencephalitis; NME; Meningoencephalomyelitis of unknown etiology; MUE

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APA (6th Edition):

Barber, R. M. (2014). Etiopathogenesis studies of canine idiopathic meningoencephalomyelitis. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/27663

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):

Barber, Renee Marie. “Etiopathogenesis studies of canine idiopathic meningoencephalomyelitis.” 2014. Thesis, University of Georgia. Accessed May 08, 2021. http://hdl.handle.net/10724/27663.

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

MLA Handbook (7th Edition):

Barber, Renee Marie. “Etiopathogenesis studies of canine idiopathic meningoencephalomyelitis.” 2014. Web. 08 May 2021.

Vancouver:

Barber RM. Etiopathogenesis studies of canine idiopathic meningoencephalomyelitis. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/10724/27663.

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

Council of Science Editors:

Barber RM. Etiopathogenesis studies of canine idiopathic meningoencephalomyelitis. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/27663

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


University of Missouri – Columbia

13. Thebeau, Christina N. Neuroprotective roles of the P2Y[subscript 2] nucleotide receptor.

Degree: 2014, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Alzheimer's disease (AD) is the most prevalent neurodegenerative disease. AD is an important disease to… (more)

Subjects/Keywords: Author supplied: inflammation, P2Y2, Alzheimer's Disease, neuroprotection, CNS, TgCRND8 mouse; Central nervous system; Inflammation; Alzheimer's disease

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APA (6th Edition):

Thebeau, C. N. (2014). Neuroprotective roles of the P2Y[subscript 2] nucleotide receptor. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/44374

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):

Thebeau, Christina N. “Neuroprotective roles of the P2Y[subscript 2] nucleotide receptor.” 2014. Thesis, University of Missouri – Columbia. Accessed May 08, 2021. https://doi.org/10.32469/10355/44374.

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

MLA Handbook (7th Edition):

Thebeau, Christina N. “Neuroprotective roles of the P2Y[subscript 2] nucleotide receptor.” 2014. Web. 08 May 2021.

Vancouver:

Thebeau CN. Neuroprotective roles of the P2Y[subscript 2] nucleotide receptor. [Internet] [Thesis]. University of Missouri – Columbia; 2014. [cited 2021 May 08]. Available from: https://doi.org/10.32469/10355/44374.

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

Council of Science Editors:

Thebeau CN. Neuroprotective roles of the P2Y[subscript 2] nucleotide receptor. [Thesis]. University of Missouri – Columbia; 2014. Available from: https://doi.org/10.32469/10355/44374

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


Purdue University

14. Bhattacharya, Chandrali S. MEASUREMENT OF STEREOSELECTIVE BUPROPION DISPOSITION IN RAT BRAIN TO SUPPORT TRANSLATIONAL PBPK/PD MODEL DEVELOPMENT AND APPLICATION.

Degree: Pharmacy Practice, 2020, Purdue University

 <b>Background:</b> Bupropion, an atypical antidepressant and smoking cessation aid, is associated with wide inter-subject variability in its efficacy and safety. Variability in response to bupropion… (more)

Subjects/Keywords: Central Nervous System; Clinical Pharmacology and Therapeutics; bupropion; cns; stereoselctive; population PK modeling; pbpk modleing; translational science

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APA (6th Edition):

Bhattacharya, C. S. (2020). MEASUREMENT OF STEREOSELECTIVE BUPROPION DISPOSITION IN RAT BRAIN TO SUPPORT TRANSLATIONAL PBPK/PD MODEL DEVELOPMENT AND APPLICATION. (Thesis). Purdue University. Retrieved from https://doi.org/10.25394/pgs.12611591.v1

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):

Bhattacharya, Chandrali S. “MEASUREMENT OF STEREOSELECTIVE BUPROPION DISPOSITION IN RAT BRAIN TO SUPPORT TRANSLATIONAL PBPK/PD MODEL DEVELOPMENT AND APPLICATION.” 2020. Thesis, Purdue University. Accessed May 08, 2021. https://doi.org/10.25394/pgs.12611591.v1.

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

MLA Handbook (7th Edition):

Bhattacharya, Chandrali S. “MEASUREMENT OF STEREOSELECTIVE BUPROPION DISPOSITION IN RAT BRAIN TO SUPPORT TRANSLATIONAL PBPK/PD MODEL DEVELOPMENT AND APPLICATION.” 2020. Web. 08 May 2021.

Vancouver:

Bhattacharya CS. MEASUREMENT OF STEREOSELECTIVE BUPROPION DISPOSITION IN RAT BRAIN TO SUPPORT TRANSLATIONAL PBPK/PD MODEL DEVELOPMENT AND APPLICATION. [Internet] [Thesis]. Purdue University; 2020. [cited 2021 May 08]. Available from: https://doi.org/10.25394/pgs.12611591.v1.

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

Council of Science Editors:

Bhattacharya CS. MEASUREMENT OF STEREOSELECTIVE BUPROPION DISPOSITION IN RAT BRAIN TO SUPPORT TRANSLATIONAL PBPK/PD MODEL DEVELOPMENT AND APPLICATION. [Thesis]. Purdue University; 2020. Available from: https://doi.org/10.25394/pgs.12611591.v1

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

15. Ramet, Lauriane. Caractérisation d'une mutation humaine du transporteur vésiculaire du glutamate de type 3 (VGLUT3) : VGLUT3-p.A211V dans le système nerveux central de souris : Characterization of a human mutation of vesicular glutamate transporter type three (VGLUT3) : VGLUT3-p.A211V in mouse central nervous system.

Degree: Docteur es, Neurosciences, 2015, Université Pierre et Marie Curie – Paris VI

Le glutamate est accumulé dans des vésicules synaptiques par des transporteurs vésiculaires du glutamate appelés VGLUT1-3. VGLUT1 et VGLUT2 sont utilisés par les neurones glutamatergiques… (more)

Subjects/Keywords: Transporteur vésiculaire du glutamate de type 3 (VGLUT3); Mutation ponctuelle; P.a211v; Système nerveux central; Synergie vésiculaire; STED; Vesicular glutamate transporter; Central Nervous System (CNS); Point mutation; 573.86

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APA (6th Edition):

Ramet, L. (2015). Caractérisation d'une mutation humaine du transporteur vésiculaire du glutamate de type 3 (VGLUT3) : VGLUT3-p.A211V dans le système nerveux central de souris : Characterization of a human mutation of vesicular glutamate transporter type three (VGLUT3) : VGLUT3-p.A211V in mouse central nervous system. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066700

Chicago Manual of Style (16th Edition):

Ramet, Lauriane. “Caractérisation d'une mutation humaine du transporteur vésiculaire du glutamate de type 3 (VGLUT3) : VGLUT3-p.A211V dans le système nerveux central de souris : Characterization of a human mutation of vesicular glutamate transporter type three (VGLUT3) : VGLUT3-p.A211V in mouse central nervous system.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed May 08, 2021. http://www.theses.fr/2015PA066700.

MLA Handbook (7th Edition):

Ramet, Lauriane. “Caractérisation d'une mutation humaine du transporteur vésiculaire du glutamate de type 3 (VGLUT3) : VGLUT3-p.A211V dans le système nerveux central de souris : Characterization of a human mutation of vesicular glutamate transporter type three (VGLUT3) : VGLUT3-p.A211V in mouse central nervous system.” 2015. Web. 08 May 2021.

Vancouver:

Ramet L. Caractérisation d'une mutation humaine du transporteur vésiculaire du glutamate de type 3 (VGLUT3) : VGLUT3-p.A211V dans le système nerveux central de souris : Characterization of a human mutation of vesicular glutamate transporter type three (VGLUT3) : VGLUT3-p.A211V in mouse central nervous system. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2021 May 08]. Available from: http://www.theses.fr/2015PA066700.

Council of Science Editors:

Ramet L. Caractérisation d'une mutation humaine du transporteur vésiculaire du glutamate de type 3 (VGLUT3) : VGLUT3-p.A211V dans le système nerveux central de souris : Characterization of a human mutation of vesicular glutamate transporter type three (VGLUT3) : VGLUT3-p.A211V in mouse central nervous system. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066700


University of the Western Cape

16. Kadernani, Yakub Esmail Y.E. Novel adamantane derivatives as multifunctional neuroprotective agents .

Degree: 2013, University of the Western Cape

 The pathology of neurodegenerative disorders involves multiple steps, and it is probably for this reason that targeting one particular step in a multi-step process has… (more)

Subjects/Keywords: Neurodegenerative disorders; Central nervous system

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APA (6th Edition):

Kadernani, Y. E. Y. E. (2013). Novel adamantane derivatives as multifunctional neuroprotective agents . (Thesis). University of the Western Cape. Retrieved from http://hdl.handle.net/11394/4256

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):

Kadernani, Yakub Esmail Y E. “Novel adamantane derivatives as multifunctional neuroprotective agents .” 2013. Thesis, University of the Western Cape. Accessed May 08, 2021. http://hdl.handle.net/11394/4256.

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

MLA Handbook (7th Edition):

Kadernani, Yakub Esmail Y E. “Novel adamantane derivatives as multifunctional neuroprotective agents .” 2013. Web. 08 May 2021.

Vancouver:

Kadernani YEYE. Novel adamantane derivatives as multifunctional neuroprotective agents . [Internet] [Thesis]. University of the Western Cape; 2013. [cited 2021 May 08]. Available from: http://hdl.handle.net/11394/4256.

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

Council of Science Editors:

Kadernani YEYE. Novel adamantane derivatives as multifunctional neuroprotective agents . [Thesis]. University of the Western Cape; 2013. Available from: http://hdl.handle.net/11394/4256

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


Montana State University

17. Waller, Hannah Rose. Analysis of the central nervous system in a mouse model of HSAN Type III.

Degree: MS, College of Letters & Science, 2013, Montana State University

 Familial Dysautonomia (FD), also called Riley Day Syndrome, is a Hereditary Sensory and Autonomic Neuropathy (HSAN Type III) that is characterized by dysfunction of the… (more)

Subjects/Keywords: Dysautonomia; Central nervous system

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APA (6th Edition):

Waller, H. R. (2013). Analysis of the central nervous system in a mouse model of HSAN Type III. (Masters Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/3026

Chicago Manual of Style (16th Edition):

Waller, Hannah Rose. “Analysis of the central nervous system in a mouse model of HSAN Type III.” 2013. Masters Thesis, Montana State University. Accessed May 08, 2021. https://scholarworks.montana.edu/xmlui/handle/1/3026.

MLA Handbook (7th Edition):

Waller, Hannah Rose. “Analysis of the central nervous system in a mouse model of HSAN Type III.” 2013. Web. 08 May 2021.

Vancouver:

Waller HR. Analysis of the central nervous system in a mouse model of HSAN Type III. [Internet] [Masters thesis]. Montana State University; 2013. [cited 2021 May 08]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/3026.

Council of Science Editors:

Waller HR. Analysis of the central nervous system in a mouse model of HSAN Type III. [Masters Thesis]. Montana State University; 2013. Available from: https://scholarworks.montana.edu/xmlui/handle/1/3026


University of Michigan

18. Davis, Tigwa H. Involvement of sodium channel beta1 subunits in neurite outgrowth and CNS development.

Degree: PhD, Pharmacology, 2006, University of Michigan

 Neuronal immunoglobulin superfamily cell adhesion molecules (IGSF CAMs) are important for cellular adhesion, cellular migration, myelination of central and peripheral axons, axonal pathfinding and neurite… (more)

Subjects/Keywords: Beta Subunits; Beta1; Central Nervous System; Cns; Development; Involvement; Neurite Outgrowth; Sodium Channel

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APA (6th Edition):

Davis, T. H. (2006). Involvement of sodium channel beta1 subunits in neurite outgrowth and CNS development. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/125640

Chicago Manual of Style (16th Edition):

Davis, Tigwa H. “Involvement of sodium channel beta1 subunits in neurite outgrowth and CNS development.” 2006. Doctoral Dissertation, University of Michigan. Accessed May 08, 2021. http://hdl.handle.net/2027.42/125640.

MLA Handbook (7th Edition):

Davis, Tigwa H. “Involvement of sodium channel beta1 subunits in neurite outgrowth and CNS development.” 2006. Web. 08 May 2021.

Vancouver:

Davis TH. Involvement of sodium channel beta1 subunits in neurite outgrowth and CNS development. [Internet] [Doctoral dissertation]. University of Michigan; 2006. [cited 2021 May 08]. Available from: http://hdl.handle.net/2027.42/125640.

Council of Science Editors:

Davis TH. Involvement of sodium channel beta1 subunits in neurite outgrowth and CNS development. [Doctoral Dissertation]. University of Michigan; 2006. Available from: http://hdl.handle.net/2027.42/125640


Lincoln University

19. Wilson, Michele. A study of C-type natriuretic peptide in cerebrospinal fluid and related tissues of sheep, and its regulation by dexamethasone.

Degree: 2017, Lincoln University

 C-type natriuretic peptide (CNP) has high abundance in cerebrospinal fluid (CSF) and central tissues, and has been implicated in the regulation of important processes in… (more)

Subjects/Keywords: C-type natriuretic peptide; CNP; NTproCNP; cerebrospinal fluid; CSF; sheep; central nervous system; CNS; dexamethasone; glucocorticoids; brain; pituitary; 070206 Animal Reproduction; 060803 Animal Developmental and Reproductive Biology

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APA (6th Edition):

Wilson, M. (2017). A study of C-type natriuretic peptide in cerebrospinal fluid and related tissues of sheep, and its regulation by dexamethasone. (Thesis). Lincoln University. Retrieved from http://hdl.handle.net/10182/8294

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):

Wilson, Michele. “A study of C-type natriuretic peptide in cerebrospinal fluid and related tissues of sheep, and its regulation by dexamethasone.” 2017. Thesis, Lincoln University. Accessed May 08, 2021. http://hdl.handle.net/10182/8294.

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

MLA Handbook (7th Edition):

Wilson, Michele. “A study of C-type natriuretic peptide in cerebrospinal fluid and related tissues of sheep, and its regulation by dexamethasone.” 2017. Web. 08 May 2021.

Vancouver:

Wilson M. A study of C-type natriuretic peptide in cerebrospinal fluid and related tissues of sheep, and its regulation by dexamethasone. [Internet] [Thesis]. Lincoln University; 2017. [cited 2021 May 08]. Available from: http://hdl.handle.net/10182/8294.

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

Council of Science Editors:

Wilson M. A study of C-type natriuretic peptide in cerebrospinal fluid and related tissues of sheep, and its regulation by dexamethasone. [Thesis]. Lincoln University; 2017. Available from: http://hdl.handle.net/10182/8294

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

20. Kaprelyan, Ara / Капрелян, Ара. Complex Study of Clinical Application of (18)F-FDG PET/CT in Patients with Central Nervous System Diseases /// Комплексно проучване на клиничното приложение на (18)F-FDG ПЕТ-КТ при болни със заболявания на централната нервна система.

Degree: 2016, Medical University of Varna

 [EN] Disorders of the central nervous system (CNS) are more than 8% of all diseases and are cause of 11.7% of mortality on a world… (more)

Subjects/Keywords: disorders of the central nervous system (CNS); multiple sclerosis; epilepsy; epileptic focus; dementia; Parkinson’s disease (PD); Alzheimer’s’ disease (AD); diagnosis; glucose metabolism; MRI; 18FFDG PET/CT; EEG; Неврология / Neurology

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APA (6th Edition):

Kaprelyan, Ara / Капрелян, . (2016). Complex Study of Clinical Application of (18)F-FDG PET/CT in Patients with Central Nervous System Diseases /// Комплексно проучване на клиничното приложение на (18)F-FDG ПЕТ-КТ при болни със заболявания на централната нервна система. (Thesis). Medical University of Varna. Retrieved from http://repository.mu-varna.bg/handle/nls/247

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):

Kaprelyan, Ara / Капрелян, Ара. “Complex Study of Clinical Application of (18)F-FDG PET/CT in Patients with Central Nervous System Diseases /// Комплексно проучване на клиничното приложение на (18)F-FDG ПЕТ-КТ при болни със заболявания на централната нервна система.” 2016. Thesis, Medical University of Varna. Accessed May 08, 2021. http://repository.mu-varna.bg/handle/nls/247.

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

MLA Handbook (7th Edition):

Kaprelyan, Ara / Капрелян, Ара. “Complex Study of Clinical Application of (18)F-FDG PET/CT in Patients with Central Nervous System Diseases /// Комплексно проучване на клиничното приложение на (18)F-FDG ПЕТ-КТ при болни със заболявания на централната нервна система.” 2016. Web. 08 May 2021.

Vancouver:

Kaprelyan, Ara / Капрелян . Complex Study of Clinical Application of (18)F-FDG PET/CT in Patients with Central Nervous System Diseases /// Комплексно проучване на клиничното приложение на (18)F-FDG ПЕТ-КТ при болни със заболявания на централната нервна система. [Internet] [Thesis]. Medical University of Varna; 2016. [cited 2021 May 08]. Available from: http://repository.mu-varna.bg/handle/nls/247.

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

Council of Science Editors:

Kaprelyan, Ara / Капрелян . Complex Study of Clinical Application of (18)F-FDG PET/CT in Patients with Central Nervous System Diseases /// Комплексно проучване на клиничното приложение на (18)F-FDG ПЕТ-КТ при болни със заболявания на централната нервна система. [Thesis]. Medical University of Varna; 2016. Available from: http://repository.mu-varna.bg/handle/nls/247

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


University of Sydney

21. Li, Wen. Investigation of Type I Interferon Signaling in the Cellular Response and Host Defense .

Degree: 2014, University of Sydney

 Type I interferons (IFN-I) mediate the antiviral host response through activation of interferon-stimulated gene factor 3 (ISGF3) complex consisting of STAT1, STAT2 and IRF9. However,… (more)

Subjects/Keywords: central nervous system (CNS); interferon regulator factor 7 (IRF7); lymphocytic choriomeningitis virus (LCMV); signal transducers and activators of transcription (STAT); type I interferons (IFN-I)

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APA (6th Edition):

Li, W. (2014). Investigation of Type I Interferon Signaling in the Cellular Response and Host Defense . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/10615

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

Chicago Manual of Style (16th Edition):

Li, Wen. “Investigation of Type I Interferon Signaling in the Cellular Response and Host Defense .” 2014. Thesis, University of Sydney. Accessed May 08, 2021. http://hdl.handle.net/2123/10615.

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

MLA Handbook (7th Edition):

Li, Wen. “Investigation of Type I Interferon Signaling in the Cellular Response and Host Defense .” 2014. Web. 08 May 2021.

Vancouver:

Li W. Investigation of Type I Interferon Signaling in the Cellular Response and Host Defense . [Internet] [Thesis]. University of Sydney; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/2123/10615.

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

Council of Science Editors:

Li W. Investigation of Type I Interferon Signaling in the Cellular Response and Host Defense . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/10615

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


University of Cincinnati

22. Lamvik, Kate K. Central Nervous System Associations in Neurofibromatosis Type 1.

Degree: MS, Allied Health Sciences : Genetic Counseling, 2007, University of Cincinnati

 Neurofibromatosis type 1 (NF1) frequently involves the central nervous system (CNS), but there is extreme variability in the expression of CNS complications, even within families… (more)

Subjects/Keywords: neurofibromatosis type 1 (NF1); optic pathway glioma (OPG); central nervous system (CNS)

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APA (6th Edition):

Lamvik, K. K. (2007). Central Nervous System Associations in Neurofibromatosis Type 1. (Masters Thesis). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179426618

Chicago Manual of Style (16th Edition):

Lamvik, Kate K. “Central Nervous System Associations in Neurofibromatosis Type 1.” 2007. Masters Thesis, University of Cincinnati. Accessed May 08, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179426618.

MLA Handbook (7th Edition):

Lamvik, Kate K. “Central Nervous System Associations in Neurofibromatosis Type 1.” 2007. Web. 08 May 2021.

Vancouver:

Lamvik KK. Central Nervous System Associations in Neurofibromatosis Type 1. [Internet] [Masters thesis]. University of Cincinnati; 2007. [cited 2021 May 08]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179426618.

Council of Science Editors:

Lamvik KK. Central Nervous System Associations in Neurofibromatosis Type 1. [Masters Thesis]. University of Cincinnati; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1179426618


Deakin University

23. Lloyd, Edward John. A common structural basis for central nervous system drug design.

Degree: 1986, Deakin University

 The main theme of this thesis is that there is a common structural basis for drugs acting on the central nervous system (CNS), and that… (more)

Subjects/Keywords: drugs; design; central nervous system; effect of drugs; structure-activity relationships; psychotropic drugs; CNS drugs; central nervous system

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APA (6th Edition):

Lloyd, E. J. (1986). A common structural basis for central nervous system drug design. (Thesis). Deakin University. Retrieved from http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050902.115505

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):

Lloyd, Edward John. “A common structural basis for central nervous system drug design.” 1986. Thesis, Deakin University. Accessed May 08, 2021. http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050902.115505.

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

MLA Handbook (7th Edition):

Lloyd, Edward John. “A common structural basis for central nervous system drug design.” 1986. Web. 08 May 2021.

Vancouver:

Lloyd EJ. A common structural basis for central nervous system drug design. [Internet] [Thesis]. Deakin University; 1986. [cited 2021 May 08]. Available from: http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050902.115505.

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

Council of Science Editors:

Lloyd EJ. A common structural basis for central nervous system drug design. [Thesis]. Deakin University; 1986. Available from: http://tux.lib.deakin.edu.au./adt-VDU/public/adt-VDU20050902.115505

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

24. Durnin, Leonie. Mechanisms of release, metabolism and action of purines in the enteric and central nervous systems.

Degree: 2013, University of Nevada – Reno

 It has been fifty years since the first descriptions of non-adrenergic non-cholinergic (NANC) neurotransmission were made in the gastrointestinal (GI) tract and more than forty… (more)

Subjects/Keywords: ATP; Central nervous system; Colon; Enteric nervous system; NAD; Purinergic neurotransmission

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APA (6th Edition):

Durnin, L. (2013). Mechanisms of release, metabolism and action of purines in the enteric and central nervous systems. (Thesis). University of Nevada – Reno. Retrieved from http://hdl.handle.net/11714/3121

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):

Durnin, Leonie. “Mechanisms of release, metabolism and action of purines in the enteric and central nervous systems.” 2013. Thesis, University of Nevada – Reno. Accessed May 08, 2021. http://hdl.handle.net/11714/3121.

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

MLA Handbook (7th Edition):

Durnin, Leonie. “Mechanisms of release, metabolism and action of purines in the enteric and central nervous systems.” 2013. Web. 08 May 2021.

Vancouver:

Durnin L. Mechanisms of release, metabolism and action of purines in the enteric and central nervous systems. [Internet] [Thesis]. University of Nevada – Reno; 2013. [cited 2021 May 08]. Available from: http://hdl.handle.net/11714/3121.

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

Council of Science Editors:

Durnin L. Mechanisms of release, metabolism and action of purines in the enteric and central nervous systems. [Thesis]. University of Nevada – Reno; 2013. Available from: http://hdl.handle.net/11714/3121

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


University of Utah

25. Weakly, James Neal. Analysis of presynaptic and postsynaptic actions of anesthetics on spinal monosynaptic transmission.

Degree: PhD, Pharmacology & Toxicology;, 1968, University of Utah

 The mechanism of the depression of central nervous functions produced by anesthetic agents has been of interest to physiologists, pharmacologist, and physicians for some time.… (more)

Subjects/Keywords: Central Nervous System

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APA (6th Edition):

Weakly, J. N. (1968). Analysis of presynaptic and postsynaptic actions of anesthetics on spinal monosynaptic transmission. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/514/rec/95

Chicago Manual of Style (16th Edition):

Weakly, James Neal. “Analysis of presynaptic and postsynaptic actions of anesthetics on spinal monosynaptic transmission.” 1968. Doctoral Dissertation, University of Utah. Accessed May 08, 2021. http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/514/rec/95.

MLA Handbook (7th Edition):

Weakly, James Neal. “Analysis of presynaptic and postsynaptic actions of anesthetics on spinal monosynaptic transmission.” 1968. Web. 08 May 2021.

Vancouver:

Weakly JN. Analysis of presynaptic and postsynaptic actions of anesthetics on spinal monosynaptic transmission. [Internet] [Doctoral dissertation]. University of Utah; 1968. [cited 2021 May 08]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/514/rec/95.

Council of Science Editors:

Weakly JN. Analysis of presynaptic and postsynaptic actions of anesthetics on spinal monosynaptic transmission. [Doctoral Dissertation]. University of Utah; 1968. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd2/id/514/rec/95


University of Alberta

26. Lagerquist, Olle. Neuromuscular electrical stimulation and the central nervous system.

Degree: PhD, Center for Neuroscience and the Faculty of Physical Education and Recreation, 2009, University of Alberta

 Neuromuscular electrical stimulation (NMES) is a common therapeutic tool for persons with movement disorders. The manner in which NMES generates muscular contractions has traditionally been… (more)

Subjects/Keywords: central nervous system; neuromuscular electrical stimulation

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APA (6th Edition):

Lagerquist, O. (2009). Neuromuscular electrical stimulation and the central nervous system. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1831ck60w

Chicago Manual of Style (16th Edition):

Lagerquist, Olle. “Neuromuscular electrical stimulation and the central nervous system.” 2009. Doctoral Dissertation, University of Alberta. Accessed May 08, 2021. https://era.library.ualberta.ca/files/1831ck60w.

MLA Handbook (7th Edition):

Lagerquist, Olle. “Neuromuscular electrical stimulation and the central nervous system.” 2009. Web. 08 May 2021.

Vancouver:

Lagerquist O. Neuromuscular electrical stimulation and the central nervous system. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2021 May 08]. Available from: https://era.library.ualberta.ca/files/1831ck60w.

Council of Science Editors:

Lagerquist O. Neuromuscular electrical stimulation and the central nervous system. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/1831ck60w


Universiteit Utrecht

27. Lam, J.C. Functional parameters for the development of the central nervous system of piglets.

Degree: 2016, Universiteit Utrecht

 Because of improved health care the survival rate of preterm infants and low birth weight infants is increased. These infants often have brain abnormalities resulting… (more)

Subjects/Keywords: central nervous system; piglets; test battery; development

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APA (6th Edition):

Lam, J. C. (2016). Functional parameters for the development of the central nervous system of piglets. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/330679

Chicago Manual of Style (16th Edition):

Lam, J C. “Functional parameters for the development of the central nervous system of piglets.” 2016. Masters Thesis, Universiteit Utrecht. Accessed May 08, 2021. http://dspace.library.uu.nl:8080/handle/1874/330679.

MLA Handbook (7th Edition):

Lam, J C. “Functional parameters for the development of the central nervous system of piglets.” 2016. Web. 08 May 2021.

Vancouver:

Lam JC. Functional parameters for the development of the central nervous system of piglets. [Internet] [Masters thesis]. Universiteit Utrecht; 2016. [cited 2021 May 08]. Available from: http://dspace.library.uu.nl:8080/handle/1874/330679.

Council of Science Editors:

Lam JC. Functional parameters for the development of the central nervous system of piglets. [Masters Thesis]. Universiteit Utrecht; 2016. Available from: http://dspace.library.uu.nl:8080/handle/1874/330679


Texas A&M University

28. Whitener, Amy Elizabeth. The Role of Wnt Signaling in Temporal Patterning and Cell Fate Specification of the Midbrain Hindbrain Domain.

Degree: PhD, Biology, 2017, Texas A&M University

 The Midbrain Hindbrain Domain (MHD) is a region of the central nervous system consisting of the midbrain, midbrain hindbrain boundary (MHB) and anterior hindbrain. The… (more)

Subjects/Keywords: Zebrafish; Central Nervous System; Embryonic Development

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APA (6th Edition):

Whitener, A. E. (2017). The Role of Wnt Signaling in Temporal Patterning and Cell Fate Specification of the Midbrain Hindbrain Domain. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161629

Chicago Manual of Style (16th Edition):

Whitener, Amy Elizabeth. “The Role of Wnt Signaling in Temporal Patterning and Cell Fate Specification of the Midbrain Hindbrain Domain.” 2017. Doctoral Dissertation, Texas A&M University. Accessed May 08, 2021. http://hdl.handle.net/1969.1/161629.

MLA Handbook (7th Edition):

Whitener, Amy Elizabeth. “The Role of Wnt Signaling in Temporal Patterning and Cell Fate Specification of the Midbrain Hindbrain Domain.” 2017. Web. 08 May 2021.

Vancouver:

Whitener AE. The Role of Wnt Signaling in Temporal Patterning and Cell Fate Specification of the Midbrain Hindbrain Domain. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2021 May 08]. Available from: http://hdl.handle.net/1969.1/161629.

Council of Science Editors:

Whitener AE. The Role of Wnt Signaling in Temporal Patterning and Cell Fate Specification of the Midbrain Hindbrain Domain. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/161629


University of Texas Southwestern Medical Center

29. Meredith, David Miles. Regulation and Function of PTF1a in the Developing Nervous System.

Degree: 2012, University of Texas Southwestern Medical Center

 Basic helix-loop-helix transcription factors serve many roles in development, including regulation of neurogenesis. Many of these factors are activated in naive neural progenitors and function… (more)

Subjects/Keywords: Central Nervous System; Transcription Factors; Neurogenesis

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APA (6th Edition):

Meredith, D. M. (2012). Regulation and Function of PTF1a in the Developing Nervous System. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1110

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):

Meredith, David Miles. “Regulation and Function of PTF1a in the Developing Nervous System.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed May 08, 2021. http://hdl.handle.net/2152.5/1110.

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

MLA Handbook (7th Edition):

Meredith, David Miles. “Regulation and Function of PTF1a in the Developing Nervous System.” 2012. Web. 08 May 2021.

Vancouver:

Meredith DM. Regulation and Function of PTF1a in the Developing Nervous System. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2021 May 08]. Available from: http://hdl.handle.net/2152.5/1110.

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

Council of Science Editors:

Meredith DM. Regulation and Function of PTF1a in the Developing Nervous System. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1110

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


University of Adelaide

30. Rogers, Nicholas Alan. Expression and functional analysis of SOX3 in murine neurogenesis.

Degree: 2014, University of Adelaide

 The Sox (SRY-related HMG box) family of proteins are transcription factors. There are, in total, 30 different genes in the Sox family. Each Sox protein… (more)

Subjects/Keywords: Sox3; neurogenesis; central nervous system; neural progenitor

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

APA (6th Edition):

Rogers, N. A. (2014). Expression and functional analysis of SOX3 in murine neurogenesis. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/92331

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):

Rogers, Nicholas Alan. “Expression and functional analysis of SOX3 in murine neurogenesis.” 2014. Thesis, University of Adelaide. Accessed May 08, 2021. http://hdl.handle.net/2440/92331.

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

MLA Handbook (7th Edition):

Rogers, Nicholas Alan. “Expression and functional analysis of SOX3 in murine neurogenesis.” 2014. Web. 08 May 2021.

Vancouver:

Rogers NA. Expression and functional analysis of SOX3 in murine neurogenesis. [Internet] [Thesis]. University of Adelaide; 2014. [cited 2021 May 08]. Available from: http://hdl.handle.net/2440/92331.

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

Council of Science Editors:

Rogers NA. Expression and functional analysis of SOX3 in murine neurogenesis. [Thesis]. University of Adelaide; 2014. Available from: http://hdl.handle.net/2440/92331

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

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