Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

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

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


University of Michigan

1. Hao, Yan. Regulation of Regenerative and Degenerative Responses to Axonal Injury.

Degree: PhD, Molecular, Cellular, and Developmental Biology, 2017, University of Michigan

 Axons allow neurons to communicate over long distances, however their long length makes them vulnerable to injury, since damage at any location leads to loss… (more)

Subjects/Keywords: axon regeneration; axon degeneration; Molecular, Cellular and Developmental Biology; Science

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hao, Y. (2017). Regulation of Regenerative and Degenerative Responses to Axonal Injury. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/137148

Chicago Manual of Style (16th Edition):

Hao, Yan. “Regulation of Regenerative and Degenerative Responses to Axonal Injury.” 2017. Doctoral Dissertation, University of Michigan. Accessed April 17, 2021. http://hdl.handle.net/2027.42/137148.

MLA Handbook (7th Edition):

Hao, Yan. “Regulation of Regenerative and Degenerative Responses to Axonal Injury.” 2017. Web. 17 Apr 2021.

Vancouver:

Hao Y. Regulation of Regenerative and Degenerative Responses to Axonal Injury. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2027.42/137148.

Council of Science Editors:

Hao Y. Regulation of Regenerative and Degenerative Responses to Axonal Injury. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/137148


Penn State University

2. Stone, Michelle Catherine. Microtubule Polarity and Drosophila Sensory Neuron Responses to Axon and Dendrite Injury.

Degree: 2014, Penn State University

 Microtubule polarity in axons and dendrites is essential for polarized transport and function of the neuron. It is also a key indicator of axonal or… (more)

Subjects/Keywords: Drosophila; axon; dendrite; injury; regeneration; microtubule polarity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Stone, M. C. (2014). Microtubule Polarity and Drosophila Sensory Neuron Responses to Axon and Dendrite Injury. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/23508

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):

Stone, Michelle Catherine. “Microtubule Polarity and Drosophila Sensory Neuron Responses to Axon and Dendrite Injury.” 2014. Thesis, Penn State University. Accessed April 17, 2021. https://submit-etda.libraries.psu.edu/catalog/23508.

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

MLA Handbook (7th Edition):

Stone, Michelle Catherine. “Microtubule Polarity and Drosophila Sensory Neuron Responses to Axon and Dendrite Injury.” 2014. Web. 17 Apr 2021.

Vancouver:

Stone MC. Microtubule Polarity and Drosophila Sensory Neuron Responses to Axon and Dendrite Injury. [Internet] [Thesis]. Penn State University; 2014. [cited 2021 Apr 17]. Available from: https://submit-etda.libraries.psu.edu/catalog/23508.

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

Council of Science Editors:

Stone MC. Microtubule Polarity and Drosophila Sensory Neuron Responses to Axon and Dendrite Injury. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/23508

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


University of Delaware

3. Phay, Monichan. Localization and local maturation of precursor microRNAs in axons of sensory neurons.

Degree: PhD, University of Delaware, Department of Biological Sciences, 2018, University of Delaware

 Subcellular localization of messenger RNAs (mRNAs) is a conserved mechanism that enables highly polarized cells such as adult mammalian neurons to exert spatial and temporal… (more)

Subjects/Keywords: Biological sciences; Axon; MicroRNA; Neuron; Regeneration

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Phay, M. (2018). Localization and local maturation of precursor microRNAs in axons of sensory neurons. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/24007

Chicago Manual of Style (16th Edition):

Phay, Monichan. “Localization and local maturation of precursor microRNAs in axons of sensory neurons.” 2018. Doctoral Dissertation, University of Delaware. Accessed April 17, 2021. http://udspace.udel.edu/handle/19716/24007.

MLA Handbook (7th Edition):

Phay, Monichan. “Localization and local maturation of precursor microRNAs in axons of sensory neurons.” 2018. Web. 17 Apr 2021.

Vancouver:

Phay M. Localization and local maturation of precursor microRNAs in axons of sensory neurons. [Internet] [Doctoral dissertation]. University of Delaware; 2018. [cited 2021 Apr 17]. Available from: http://udspace.udel.edu/handle/19716/24007.

Council of Science Editors:

Phay M. Localization and local maturation of precursor microRNAs in axons of sensory neurons. [Doctoral Dissertation]. University of Delaware; 2018. Available from: http://udspace.udel.edu/handle/19716/24007

4. 신, 혜영. Expression and regulation of genes associated with CNS regeneration and plasticity.

Degree: 2016, Ajou University

I. INTRODUCTION 1 A. Spinal cord injury pathophysiology 1 B. Factors for the failure of CNS axon regeneration 2 C. Conditioning injury (CI)-induced axon regeneration(more)

Subjects/Keywords: Axon regeneration; conditioning injury; RAGs; epigenetics

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

신, . (2016). Expression and regulation of genes associated with CNS regeneration and plasticity. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/13037 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021963

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):

신, 혜영. “Expression and regulation of genes associated with CNS regeneration and plasticity.” 2016. Thesis, Ajou University. Accessed April 17, 2021. http://repository.ajou.ac.kr/handle/201003/13037 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021963.

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

MLA Handbook (7th Edition):

신, 혜영. “Expression and regulation of genes associated with CNS regeneration and plasticity.” 2016. Web. 17 Apr 2021.

Vancouver:

신 . Expression and regulation of genes associated with CNS regeneration and plasticity. [Internet] [Thesis]. Ajou University; 2016. [cited 2021 Apr 17]. Available from: http://repository.ajou.ac.kr/handle/201003/13037 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021963.

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

Council of Science Editors:

신 . Expression and regulation of genes associated with CNS regeneration and plasticity. [Thesis]. Ajou University; 2016. Available from: http://repository.ajou.ac.kr/handle/201003/13037 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021963

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


University of Manitoba

5. Schartner, Emily. Mechanisms of Sirtuin-2 (SIRT2) enhancement of mitochondrial function and axon regeneration in control and diabetic adult sensory neurons.

Degree: Pharmacology and Therapeutics, 2016, University of Manitoba

 Rationale and hypothesis: Diabetic sensory neuropathy involves a distal dying-back of nerve fibers. Neuronal mitochondrial function is impaired in diabetes and Sirtuin 2 (SIRT2) is… (more)

Subjects/Keywords: SIRT2; Mitochondria; Diabetic Neuropathy; Axon regeneration

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Schartner, E. (2016). Mechanisms of Sirtuin-2 (SIRT2) enhancement of mitochondrial function and axon regeneration in control and diabetic adult sensory neurons. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/31829

Chicago Manual of Style (16th Edition):

Schartner, Emily. “Mechanisms of Sirtuin-2 (SIRT2) enhancement of mitochondrial function and axon regeneration in control and diabetic adult sensory neurons.” 2016. Masters Thesis, University of Manitoba. Accessed April 17, 2021. http://hdl.handle.net/1993/31829.

MLA Handbook (7th Edition):

Schartner, Emily. “Mechanisms of Sirtuin-2 (SIRT2) enhancement of mitochondrial function and axon regeneration in control and diabetic adult sensory neurons.” 2016. Web. 17 Apr 2021.

Vancouver:

Schartner E. Mechanisms of Sirtuin-2 (SIRT2) enhancement of mitochondrial function and axon regeneration in control and diabetic adult sensory neurons. [Internet] [Masters thesis]. University of Manitoba; 2016. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1993/31829.

Council of Science Editors:

Schartner E. Mechanisms of Sirtuin-2 (SIRT2) enhancement of mitochondrial function and axon regeneration in control and diabetic adult sensory neurons. [Masters Thesis]. University of Manitoba; 2016. Available from: http://hdl.handle.net/1993/31829


Harvard University

6. Norsworthy, Michael. Sox11 promotes neuronal regeneration or death: complexities from heterogeneity.

Degree: PhD, 2018, Harvard University

The objective of achieving central nervous system (CNS) restoration after disease or trauma has bedeviled researchers and practitioners for decades. Some of the more recent… (more)

Subjects/Keywords: RGC; regeneration; axon; Sox11; optic nerve

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Norsworthy, M. (2018). Sox11 promotes neuronal regeneration or death: complexities from heterogeneity. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42016096

Chicago Manual of Style (16th Edition):

Norsworthy, Michael. “Sox11 promotes neuronal regeneration or death: complexities from heterogeneity.” 2018. Doctoral Dissertation, Harvard University. Accessed April 17, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42016096.

MLA Handbook (7th Edition):

Norsworthy, Michael. “Sox11 promotes neuronal regeneration or death: complexities from heterogeneity.” 2018. Web. 17 Apr 2021.

Vancouver:

Norsworthy M. Sox11 promotes neuronal regeneration or death: complexities from heterogeneity. [Internet] [Doctoral dissertation]. Harvard University; 2018. [cited 2021 Apr 17]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42016096.

Council of Science Editors:

Norsworthy M. Sox11 promotes neuronal regeneration or death: complexities from heterogeneity. [Doctoral Dissertation]. Harvard University; 2018. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42016096


Washington University in St. Louis

7. Watt, Dana. Molecular Mechanisms of Axon Growth and Regeneration.

Degree: PhD, Biology & Biomedical Sciences (Neurosciences), 2015, Washington University in St. Louis

  Neurons are cells with unique and extremely polarized morphologies. The axon allows communication between the cell soma and the distantly located synaptic terminal and… (more)

Subjects/Keywords: axon; growth; JIP3; microtubule; Ran; regeneration

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Watt, D. (2015). Molecular Mechanisms of Axon Growth and Regeneration. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/690

Chicago Manual of Style (16th Edition):

Watt, Dana. “Molecular Mechanisms of Axon Growth and Regeneration.” 2015. Doctoral Dissertation, Washington University in St. Louis. Accessed April 17, 2021. https://openscholarship.wustl.edu/art_sci_etds/690.

MLA Handbook (7th Edition):

Watt, Dana. “Molecular Mechanisms of Axon Growth and Regeneration.” 2015. Web. 17 Apr 2021.

Vancouver:

Watt D. Molecular Mechanisms of Axon Growth and Regeneration. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2015. [cited 2021 Apr 17]. Available from: https://openscholarship.wustl.edu/art_sci_etds/690.

Council of Science Editors:

Watt D. Molecular Mechanisms of Axon Growth and Regeneration. [Doctoral Dissertation]. Washington University in St. Louis; 2015. Available from: https://openscholarship.wustl.edu/art_sci_etds/690


University of California – San Diego

8. Lim, Jung-Hwan Albert. Neural activity promotes long-distance, target-specific regeneration of adult retinal axons.

Degree: Biology, 2016, University of California – San Diego

 Axons in the mammalian central nervous system (CNS) fail to regenerate after injury. A major goal of neuroscience is to develop strategies to promote axon(more)

Subjects/Keywords: Neurosciences; Cellular biology; Axon regeneration; Circuit repair; CNS injury

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lim, J. A. (2016). Neural activity promotes long-distance, target-specific regeneration of adult retinal axons. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/3rm518kh

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):

Lim, Jung-Hwan Albert. “Neural activity promotes long-distance, target-specific regeneration of adult retinal axons.” 2016. Thesis, University of California – San Diego. Accessed April 17, 2021. http://www.escholarship.org/uc/item/3rm518kh.

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

MLA Handbook (7th Edition):

Lim, Jung-Hwan Albert. “Neural activity promotes long-distance, target-specific regeneration of adult retinal axons.” 2016. Web. 17 Apr 2021.

Vancouver:

Lim JA. Neural activity promotes long-distance, target-specific regeneration of adult retinal axons. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2021 Apr 17]. Available from: http://www.escholarship.org/uc/item/3rm518kh.

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

Council of Science Editors:

Lim JA. Neural activity promotes long-distance, target-specific regeneration of adult retinal axons. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/3rm518kh

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


Univerzitet u Beogradu

9. Anđelković, Slađana Z., 1967-. Povrede digitalnih nerava šake: epidemiološka analiza, hirurško lečenje i mogućnost spontanog oporavka.

Degree: Medicinski fakultet, 2017, Univerzitet u Beogradu

Medicina - Ortopedska hururgija sa traumatologijom / Medicine - Orthopaedic surgery and traumatology

Povrede nerava spadaju među najraznovrsnija stanja u hrirurgiji, a ishod je frustrirajući… (more)

Subjects/Keywords: hand injury; digital nerve; nerve repair; axon regeneration; sensory recovery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Anđelković, Slađana Z., 1. (2017). Povrede digitalnih nerava šake: epidemiološka analiza, hirurško lečenje i mogućnost spontanog oporavka. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:14229/bdef:Content/get

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

Chicago Manual of Style (16th Edition):

Anđelković, Slađana Z., 1967-. “Povrede digitalnih nerava šake: epidemiološka analiza, hirurško lečenje i mogućnost spontanog oporavka.” 2017. Thesis, Univerzitet u Beogradu. Accessed April 17, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:14229/bdef:Content/get.

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

MLA Handbook (7th Edition):

Anđelković, Slađana Z., 1967-. “Povrede digitalnih nerava šake: epidemiološka analiza, hirurško lečenje i mogućnost spontanog oporavka.” 2017. Web. 17 Apr 2021.

Vancouver:

Anđelković, Slađana Z. 1. Povrede digitalnih nerava šake: epidemiološka analiza, hirurško lečenje i mogućnost spontanog oporavka. [Internet] [Thesis]. Univerzitet u Beogradu; 2017. [cited 2021 Apr 17]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:14229/bdef:Content/get.

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

Council of Science Editors:

Anđelković, Slađana Z. 1. Povrede digitalnih nerava šake: epidemiološka analiza, hirurško lečenje i mogućnost spontanog oporavka. [Thesis]. Univerzitet u Beogradu; 2017. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:14229/bdef:Content/get

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


Washington University in St. Louis

10. Karney-Grobe, Scott. A high-content screen identifies HSP90 as a component of axon injury signaling.

Degree: PhD, Biology & Biomedical Sciences (Developmental, Regenerative, & Stem Cell Biology), 2018, Washington University in St. Louis

  Axons are unique compartments of neurons that extend tremendous distances throughout the body. Neurodegenerative or traumatic damage to axons destroys neuronal function and thus… (more)

Subjects/Keywords: axon regeneration, DLK, HSP90, injury signaling; Developmental Biology; Neuroscience and Neurobiology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Karney-Grobe, S. (2018). A high-content screen identifies HSP90 as a component of axon injury signaling. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/art_sci_etds/1630

Chicago Manual of Style (16th Edition):

Karney-Grobe, Scott. “A high-content screen identifies HSP90 as a component of axon injury signaling.” 2018. Doctoral Dissertation, Washington University in St. Louis. Accessed April 17, 2021. https://openscholarship.wustl.edu/art_sci_etds/1630.

MLA Handbook (7th Edition):

Karney-Grobe, Scott. “A high-content screen identifies HSP90 as a component of axon injury signaling.” 2018. Web. 17 Apr 2021.

Vancouver:

Karney-Grobe S. A high-content screen identifies HSP90 as a component of axon injury signaling. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2018. [cited 2021 Apr 17]. Available from: https://openscholarship.wustl.edu/art_sci_etds/1630.

Council of Science Editors:

Karney-Grobe S. A high-content screen identifies HSP90 as a component of axon injury signaling. [Doctoral Dissertation]. Washington University in St. Louis; 2018. Available from: https://openscholarship.wustl.edu/art_sci_etds/1630


Macquarie University

11. Gwee, Sze Ling Serene. Deciphering the role of Aurora kinase B in neurite outgrowth and axon regeneration.

Degree: 2017, Macquarie University

Theoretical thesis.

Bibliography: pages 295-348

Chapter 1 - Literature review  – Chapter 2 - Aurora kinase B regulates in vitro axonal outgrowth through a C-Raf/ERK-mediated… (more)

Subjects/Keywords: Protein kinases  – Research; Aurora kinase B; neurons; zebrafish; phosphoproteomics; axon regeneration

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gwee, S. L. S. (2017). Deciphering the role of Aurora kinase B in neurite outgrowth and axon regeneration. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/1280479

Chicago Manual of Style (16th Edition):

Gwee, Sze Ling Serene. “Deciphering the role of Aurora kinase B in neurite outgrowth and axon regeneration.” 2017. Doctoral Dissertation, Macquarie University. Accessed April 17, 2021. http://hdl.handle.net/1959.14/1280479.

MLA Handbook (7th Edition):

Gwee, Sze Ling Serene. “Deciphering the role of Aurora kinase B in neurite outgrowth and axon regeneration.” 2017. Web. 17 Apr 2021.

Vancouver:

Gwee SLS. Deciphering the role of Aurora kinase B in neurite outgrowth and axon regeneration. [Internet] [Doctoral dissertation]. Macquarie University; 2017. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1959.14/1280479.

Council of Science Editors:

Gwee SLS. Deciphering the role of Aurora kinase B in neurite outgrowth and axon regeneration. [Doctoral Dissertation]. Macquarie University; 2017. Available from: http://hdl.handle.net/1959.14/1280479


Drexel University

12. Kalinski, Ashley Lauren. Alterations in the Local Environment of Axons Converge on Intrinsic Pathways that Support Growth of Adult Neurons.

Degree: 2015, Drexel University

Neurons are a distinct population of cells that communicate information allowing us to think, move and respond to our environment. A typical neuron has a… (more)

Subjects/Keywords: Neurosciences; Axon; Messenger RNA; Histone deacetylase; Genetic translation; Regeneration (Biology)

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kalinski, A. L. (2015). Alterations in the Local Environment of Axons Converge on Intrinsic Pathways that Support Growth of Adult Neurons. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7474

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):

Kalinski, Ashley Lauren. “Alterations in the Local Environment of Axons Converge on Intrinsic Pathways that Support Growth of Adult Neurons.” 2015. Thesis, Drexel University. Accessed April 17, 2021. http://hdl.handle.net/1860/idea:7474.

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

MLA Handbook (7th Edition):

Kalinski, Ashley Lauren. “Alterations in the Local Environment of Axons Converge on Intrinsic Pathways that Support Growth of Adult Neurons.” 2015. Web. 17 Apr 2021.

Vancouver:

Kalinski AL. Alterations in the Local Environment of Axons Converge on Intrinsic Pathways that Support Growth of Adult Neurons. [Internet] [Thesis]. Drexel University; 2015. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1860/idea:7474.

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

Council of Science Editors:

Kalinski AL. Alterations in the Local Environment of Axons Converge on Intrinsic Pathways that Support Growth of Adult Neurons. [Thesis]. Drexel University; 2015. Available from: http://hdl.handle.net/1860/idea:7474

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


University of Michigan

13. Dickendesher, Travis L. Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury.

Degree: PhD, Neuroscience, 2013, University of Michigan

 Depending on location and severity, injury to the adult mammalian central nervous system (CNS) typically results in neurological deficits ranging from mild motor impairment to… (more)

Subjects/Keywords: Mammalian Central Nervous System Repair; Axon Regeneration; Novel Ligand-Receptor Interactions; Spinal Cord Injury; Axon Degeneration; Excitotoxicity; Neurosciences; Health Sciences; Science

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dickendesher, T. L. (2013). Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/102322

Chicago Manual of Style (16th Edition):

Dickendesher, Travis L. “Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury.” 2013. Doctoral Dissertation, University of Michigan. Accessed April 17, 2021. http://hdl.handle.net/2027.42/102322.

MLA Handbook (7th Edition):

Dickendesher, Travis L. “Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury.” 2013. Web. 17 Apr 2021.

Vancouver:

Dickendesher TL. Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2027.42/102322.

Council of Science Editors:

Dickendesher TL. Novel Mechanisms of Axonal Growth Inhibition Following Central Nervous System Injury. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/102322


University of Cambridge

14. Nieuwenhuis, Bart. Gene therapy for axon regeneration.

Degree: PhD, 2019, University of Cambridge

 Injury to the brain and spinal cord has devastating consequences because adult neurons in the central nervous system (CNS) do not regenerate. Traumatic CNS injuries… (more)

Subjects/Keywords: Axon regeneration; Integrins; CRISPR-Cas9; Axon initial segment; Phosphoinositide 3-kinases; Adeno-associated viral vectors; Corticospinal tract

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nieuwenhuis, B. (2019). Gene therapy for axon regeneration. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/293896

Chicago Manual of Style (16th Edition):

Nieuwenhuis, Bart. “Gene therapy for axon regeneration.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 17, 2021. https://www.repository.cam.ac.uk/handle/1810/293896.

MLA Handbook (7th Edition):

Nieuwenhuis, Bart. “Gene therapy for axon regeneration.” 2019. Web. 17 Apr 2021.

Vancouver:

Nieuwenhuis B. Gene therapy for axon regeneration. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 17]. Available from: https://www.repository.cam.ac.uk/handle/1810/293896.

Council of Science Editors:

Nieuwenhuis B. Gene therapy for axon regeneration. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/293896


University of Cambridge

15. Nieuwenhuis, Bart. Gene therapy for axon regeneration.

Degree: PhD, 2019, University of Cambridge

 Injury to the brain and spinal cord has devastating consequences because adult neurons in the central nervous system (CNS) do not regenerate. Traumatic CNS injuries… (more)

Subjects/Keywords: Axon regeneration; Integrins; CRISPR-Cas9; Axon initial segment; Phosphoinositide 3-kinases; Adeno-associated viral vectors; Corticospinal tract

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nieuwenhuis, B. (2019). Gene therapy for axon regeneration. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.41004 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782855

Chicago Manual of Style (16th Edition):

Nieuwenhuis, Bart. “Gene therapy for axon regeneration.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 17, 2021. https://doi.org/10.17863/CAM.41004 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782855.

MLA Handbook (7th Edition):

Nieuwenhuis, Bart. “Gene therapy for axon regeneration.” 2019. Web. 17 Apr 2021.

Vancouver:

Nieuwenhuis B. Gene therapy for axon regeneration. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 17]. Available from: https://doi.org/10.17863/CAM.41004 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782855.

Council of Science Editors:

Nieuwenhuis B. Gene therapy for axon regeneration. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.41004 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.782855


UCLA

16. Khankan, Rana R. Mechanisms of olfactory ensheathing cell-enhanced neurite outgrowth and axon regeneration after spinal cord injury.

Degree: Molec, Cell, & Integ Physiology, 2015, UCLA

 Olfactory ensheathing cells (OECs) provide a pro-regenerative environment for the axons of olfactory receptor neurons and therefore are a promising candidate for cell transplantation therapy… (more)

Subjects/Keywords: Physiology; Neurosciences; Axon regeneration; Immune modulation; Neurite outgrowth; Neuroprotection; Olfactory ensheathing cells; Spinal cord injury

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Khankan, R. R. (2015). Mechanisms of olfactory ensheathing cell-enhanced neurite outgrowth and axon regeneration after spinal cord injury. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1jp5r5ts

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):

Khankan, Rana R. “Mechanisms of olfactory ensheathing cell-enhanced neurite outgrowth and axon regeneration after spinal cord injury.” 2015. Thesis, UCLA. Accessed April 17, 2021. http://www.escholarship.org/uc/item/1jp5r5ts.

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

MLA Handbook (7th Edition):

Khankan, Rana R. “Mechanisms of olfactory ensheathing cell-enhanced neurite outgrowth and axon regeneration after spinal cord injury.” 2015. Web. 17 Apr 2021.

Vancouver:

Khankan RR. Mechanisms of olfactory ensheathing cell-enhanced neurite outgrowth and axon regeneration after spinal cord injury. [Internet] [Thesis]. UCLA; 2015. [cited 2021 Apr 17]. Available from: http://www.escholarship.org/uc/item/1jp5r5ts.

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

Council of Science Editors:

Khankan RR. Mechanisms of olfactory ensheathing cell-enhanced neurite outgrowth and axon regeneration after spinal cord injury. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/1jp5r5ts

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


UCLA

17. Thornton, Michael Andrew. Axonal regeneration is detected after olfactory ensheathing cell or fibroblast transplantation in Sprague-Dawley rats with completely transected spinal cords.

Degree: Physiological Science, 2016, UCLA

 Olfactory ensheathing cells (OECs) are unique glia that support axon outgrowth in the olfactory system and have shown some success as a cellular transplant therapy… (more)

Subjects/Keywords: Neurosciences; axon regeneration; cell transplantation; epidural stimulation; olfactory ensheathing cells; spinal cord injury; spinal interneurons

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thornton, M. A. (2016). Axonal regeneration is detected after olfactory ensheathing cell or fibroblast transplantation in Sprague-Dawley rats with completely transected spinal cords. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3sn673cj

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):

Thornton, Michael Andrew. “Axonal regeneration is detected after olfactory ensheathing cell or fibroblast transplantation in Sprague-Dawley rats with completely transected spinal cords.” 2016. Thesis, UCLA. Accessed April 17, 2021. http://www.escholarship.org/uc/item/3sn673cj.

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

MLA Handbook (7th Edition):

Thornton, Michael Andrew. “Axonal regeneration is detected after olfactory ensheathing cell or fibroblast transplantation in Sprague-Dawley rats with completely transected spinal cords.” 2016. Web. 17 Apr 2021.

Vancouver:

Thornton MA. Axonal regeneration is detected after olfactory ensheathing cell or fibroblast transplantation in Sprague-Dawley rats with completely transected spinal cords. [Internet] [Thesis]. UCLA; 2016. [cited 2021 Apr 17]. Available from: http://www.escholarship.org/uc/item/3sn673cj.

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

Council of Science Editors:

Thornton MA. Axonal regeneration is detected after olfactory ensheathing cell or fibroblast transplantation in Sprague-Dawley rats with completely transected spinal cords. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/3sn673cj

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


University of Tasmania

18. Landowski, LM. LRP receptors in a novel mechanism of axon pathfinding and peripheral nerve regeneration.

Degree: 2014, University of Tasmania

 Chemotactic axon guidance has an essential role in development and is important for re-innervation of target tissues after neuronal injury. The aim of the work… (more)

Subjects/Keywords: Nerve regeneration; therapeutics; low-density-lipoprotein-receptor-related protein (LRP) axon guidance; neuropathy; novel chemotactic

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Landowski, L. (2014). LRP receptors in a novel mechanism of axon pathfinding and peripheral nerve regeneration. (Thesis). University of Tasmania. Retrieved from https://eprints.utas.edu.au/22424/1/Whole-Landowski-thesis.pdf

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

Chicago Manual of Style (16th Edition):

Landowski, LM. “LRP receptors in a novel mechanism of axon pathfinding and peripheral nerve regeneration.” 2014. Thesis, University of Tasmania. Accessed April 17, 2021. https://eprints.utas.edu.au/22424/1/Whole-Landowski-thesis.pdf.

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

MLA Handbook (7th Edition):

Landowski, LM. “LRP receptors in a novel mechanism of axon pathfinding and peripheral nerve regeneration.” 2014. Web. 17 Apr 2021.

Vancouver:

Landowski L. LRP receptors in a novel mechanism of axon pathfinding and peripheral nerve regeneration. [Internet] [Thesis]. University of Tasmania; 2014. [cited 2021 Apr 17]. Available from: https://eprints.utas.edu.au/22424/1/Whole-Landowski-thesis.pdf.

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

Council of Science Editors:

Landowski L. LRP receptors in a novel mechanism of axon pathfinding and peripheral nerve regeneration. [Thesis]. University of Tasmania; 2014. Available from: https://eprints.utas.edu.au/22424/1/Whole-Landowski-thesis.pdf

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


Penn State University

19. Chen, Li. Investigation of the molecular basis underlying a multi-step model of axon injury responses.

Degree: 2015, Penn State University

 Neurons are susceptible to a range of genetic and environmental insults. The ability to survive and recover from these insults is critical to maintaining a… (more)

Subjects/Keywords: axon regeneration; neuroprotection; microtubules; gamma-tubulin; Nmnat; DLK; JNK; fos; caspases; mitochondria

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Chen, L. (2015). Investigation of the molecular basis underlying a multi-step model of axon injury responses. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/26347

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

Chicago Manual of Style (16th Edition):

Chen, Li. “Investigation of the molecular basis underlying a multi-step model of axon injury responses.” 2015. Thesis, Penn State University. Accessed April 17, 2021. https://submit-etda.libraries.psu.edu/catalog/26347.

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

MLA Handbook (7th Edition):

Chen, Li. “Investigation of the molecular basis underlying a multi-step model of axon injury responses.” 2015. Web. 17 Apr 2021.

Vancouver:

Chen L. Investigation of the molecular basis underlying a multi-step model of axon injury responses. [Internet] [Thesis]. Penn State University; 2015. [cited 2021 Apr 17]. Available from: https://submit-etda.libraries.psu.edu/catalog/26347.

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

Council of Science Editors:

Chen L. Investigation of the molecular basis underlying a multi-step model of axon injury responses. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/26347

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


Virginia Commonwealth University

20. Greer, John E. The characterization of the anterograde and retrograde consequences of traumatic axonal injury in a mouse model of diffuse brain injury.

Degree: PhD, Neuroscience, 2011, Virginia Commonwealth University

 Traumatic axonal injury (TAI) is a consistent feature of (TBI) and is responsible for much of its associated morbidity. TAI is now recognized to result… (more)

Subjects/Keywords: Traumatic brain injury; Axon regeneration; Diffuse axonal injury; Medical Sciences; Medicine and Health Sciences; Neurosciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Greer, J. E. (2011). The characterization of the anterograde and retrograde consequences of traumatic axonal injury in a mouse model of diffuse brain injury. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/NXSN-2E35 ; https://scholarscompass.vcu.edu/etd/407

Chicago Manual of Style (16th Edition):

Greer, John E. “The characterization of the anterograde and retrograde consequences of traumatic axonal injury in a mouse model of diffuse brain injury.” 2011. Doctoral Dissertation, Virginia Commonwealth University. Accessed April 17, 2021. https://doi.org/10.25772/NXSN-2E35 ; https://scholarscompass.vcu.edu/etd/407.

MLA Handbook (7th Edition):

Greer, John E. “The characterization of the anterograde and retrograde consequences of traumatic axonal injury in a mouse model of diffuse brain injury.” 2011. Web. 17 Apr 2021.

Vancouver:

Greer JE. The characterization of the anterograde and retrograde consequences of traumatic axonal injury in a mouse model of diffuse brain injury. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2011. [cited 2021 Apr 17]. Available from: https://doi.org/10.25772/NXSN-2E35 ; https://scholarscompass.vcu.edu/etd/407.

Council of Science Editors:

Greer JE. The characterization of the anterograde and retrograde consequences of traumatic axonal injury in a mouse model of diffuse brain injury. [Doctoral Dissertation]. Virginia Commonwealth University; 2011. Available from: https://doi.org/10.25772/NXSN-2E35 ; https://scholarscompass.vcu.edu/etd/407


University of Miami

21. Moore, Darcie L. Transcriptional Control of Axon Growth Ability.

Degree: PhD, Neuroscience (Medicine), 2010, University of Miami

  Mammalian central nervous system (CNS) neurons lose their ability to regenerate their axons after injury during development. For example, optic nerve injury studies in… (more)

Subjects/Keywords: Neuron; Intrinsic; KLF; Axon Growth; Transcription Factors; Retinal Ganglion Cell; Regeneration; CNS

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Moore, D. L. (2010). Transcriptional Control of Axon Growth Ability. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/639

Chicago Manual of Style (16th Edition):

Moore, Darcie L. “Transcriptional Control of Axon Growth Ability.” 2010. Doctoral Dissertation, University of Miami. Accessed April 17, 2021. https://scholarlyrepository.miami.edu/oa_dissertations/639.

MLA Handbook (7th Edition):

Moore, Darcie L. “Transcriptional Control of Axon Growth Ability.” 2010. Web. 17 Apr 2021.

Vancouver:

Moore DL. Transcriptional Control of Axon Growth Ability. [Internet] [Doctoral dissertation]. University of Miami; 2010. [cited 2021 Apr 17]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/639.

Council of Science Editors:

Moore DL. Transcriptional Control of Axon Growth Ability. [Doctoral Dissertation]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/639


University of Cambridge

22. Evans, Rachel Shane. The Effect of Manipulation of the Phosphoinositide 3-kinase Pathway on Axon Regeneration in vivo.

Degree: PhD, 2020, University of Cambridge

 Millions worldwide are visually impaired by optic nerve diseases, and glaucoma, the leading cause of irreversible blindness, is due to affect approximately 80 million people… (more)

Subjects/Keywords: axon regeneration; optic nerve crush; phosphoinositide 3-kinase pathway; retinal ganglion cell survival

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Evans, R. S. (2020). The Effect of Manipulation of the Phosphoinositide 3-kinase Pathway on Axon Regeneration in vivo. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/304797

Chicago Manual of Style (16th Edition):

Evans, Rachel Shane. “The Effect of Manipulation of the Phosphoinositide 3-kinase Pathway on Axon Regeneration in vivo.” 2020. Doctoral Dissertation, University of Cambridge. Accessed April 17, 2021. https://www.repository.cam.ac.uk/handle/1810/304797.

MLA Handbook (7th Edition):

Evans, Rachel Shane. “The Effect of Manipulation of the Phosphoinositide 3-kinase Pathway on Axon Regeneration in vivo.” 2020. Web. 17 Apr 2021.

Vancouver:

Evans RS. The Effect of Manipulation of the Phosphoinositide 3-kinase Pathway on Axon Regeneration in vivo. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 Apr 17]. Available from: https://www.repository.cam.ac.uk/handle/1810/304797.

Council of Science Editors:

Evans RS. The Effect of Manipulation of the Phosphoinositide 3-kinase Pathway on Axon Regeneration in vivo. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/304797

23. Wyatt, Cameron. Optic axon guidance during development and regeneration in the zebrafish.

Degree: PhD, 2011, University of Edinburgh

 Directed regeneration of axons in the CNS has potential for the treatment of CNS disorders and injuries. In contrast to mammals, following optic nerve lesion… (more)

Subjects/Keywords: 612.8; regeneration; development; axon guidance

…disability in humans, axon regeneration and its failure in mammals has been extensively studied… …axon regeneration RGCs with regenerating axons following axotomy present similar… …may undergo spontaneous axon regeneration following an optic nerve lesion, they do not… …1.3.5.6 Axon guidance in development and regeneration The ability of zebrafish RGC axons to… …mechanisms, are required for axon regeneration is currently one of the most 15 important… 

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wyatt, C. (2011). Optic axon guidance during development and regeneration in the zebrafish. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5947

Chicago Manual of Style (16th Edition):

Wyatt, Cameron. “Optic axon guidance during development and regeneration in the zebrafish.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed April 17, 2021. http://hdl.handle.net/1842/5947.

MLA Handbook (7th Edition):

Wyatt, Cameron. “Optic axon guidance during development and regeneration in the zebrafish.” 2011. Web. 17 Apr 2021.

Vancouver:

Wyatt C. Optic axon guidance during development and regeneration in the zebrafish. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1842/5947.

Council of Science Editors:

Wyatt C. Optic axon guidance during development and regeneration in the zebrafish. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5947


University of Maryland

24. Pathak, Gunja. STUDYING mRNA TRANSPORT AND REGULATION OF RETROGRADE INJURY SIGNALING ASSOCIATED AXONAL TRANSCRIPT LEVELS IN THE CONTEXT OF AXONAL REGENERATION.

Degree: Bioengineering, 2014, University of Maryland

 This dissertation focuses on a detailed mechanism of mRNA transport during development of hippocampal neurons, and regulation of retrograde injury signaling (RIS)-associated genes in the… (more)

Subjects/Keywords: Biomedical engineering; Biology; Axon Regeneration; CNS; mRNA Transport; Retrograde Injury Signaling; Whole explant culture System

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pathak, G. (2014). STUDYING mRNA TRANSPORT AND REGULATION OF RETROGRADE INJURY SIGNALING ASSOCIATED AXONAL TRANSCRIPT LEVELS IN THE CONTEXT OF AXONAL REGENERATION. (Thesis). University of Maryland. Retrieved from http://hdl.handle.net/1903/15227

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):

Pathak, Gunja. “STUDYING mRNA TRANSPORT AND REGULATION OF RETROGRADE INJURY SIGNALING ASSOCIATED AXONAL TRANSCRIPT LEVELS IN THE CONTEXT OF AXONAL REGENERATION.” 2014. Thesis, University of Maryland. Accessed April 17, 2021. http://hdl.handle.net/1903/15227.

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

MLA Handbook (7th Edition):

Pathak, Gunja. “STUDYING mRNA TRANSPORT AND REGULATION OF RETROGRADE INJURY SIGNALING ASSOCIATED AXONAL TRANSCRIPT LEVELS IN THE CONTEXT OF AXONAL REGENERATION.” 2014. Web. 17 Apr 2021.

Vancouver:

Pathak G. STUDYING mRNA TRANSPORT AND REGULATION OF RETROGRADE INJURY SIGNALING ASSOCIATED AXONAL TRANSCRIPT LEVELS IN THE CONTEXT OF AXONAL REGENERATION. [Internet] [Thesis]. University of Maryland; 2014. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1903/15227.

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

Council of Science Editors:

Pathak G. STUDYING mRNA TRANSPORT AND REGULATION OF RETROGRADE INJURY SIGNALING ASSOCIATED AXONAL TRANSCRIPT LEVELS IN THE CONTEXT OF AXONAL REGENERATION. [Thesis]. University of Maryland; 2014. Available from: http://hdl.handle.net/1903/15227

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


University of Texas – Austin

25. Nguyen, Hieu Trung 1980-. Controlling neural cell behavior with electric field stimulation across a conductive substrate.

Degree: PhD, Biomedical Engineering, 2012, University of Texas – Austin

 Electrical stimulation of tissues induces cell alignment, directed migration, extended processes, differentiation, and proliferation, but the mechanisms involved remain largely unknown. To reveal effects of… (more)

Subjects/Keywords: Nerve; Regeneration; Schwann cell; Neuron; Electric; Stimulation; Orientation; Alignment; Length; Axon; Collagen; Matrigel

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nguyen, H. T. 1. (2012). Controlling neural cell behavior with electric field stimulation across a conductive substrate. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/24731

Chicago Manual of Style (16th Edition):

Nguyen, Hieu Trung 1980-. “Controlling neural cell behavior with electric field stimulation across a conductive substrate.” 2012. Doctoral Dissertation, University of Texas – Austin. Accessed April 17, 2021. http://hdl.handle.net/2152/24731.

MLA Handbook (7th Edition):

Nguyen, Hieu Trung 1980-. “Controlling neural cell behavior with electric field stimulation across a conductive substrate.” 2012. Web. 17 Apr 2021.

Vancouver:

Nguyen HT1. Controlling neural cell behavior with electric field stimulation across a conductive substrate. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2012. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/2152/24731.

Council of Science Editors:

Nguyen HT1. Controlling neural cell behavior with electric field stimulation across a conductive substrate. [Doctoral Dissertation]. University of Texas – Austin; 2012. Available from: http://hdl.handle.net/2152/24731


University of Cambridge

26. Evans, Rachel Shane. The effect of manipulation of the phosphoinositide 3-kinase pathway on axon regeneration in vivo.

Degree: PhD, 2020, University of Cambridge

 Millions worldwide are visually impaired by optic nerve diseases, and glaucoma, the leading cause of irreversible blindness, is due to affect approximately 80 million people… (more)

Subjects/Keywords: 617.7; axon regeneration; optic nerve crush; phosphoinositide 3-kinase pathway; retinal ganglion cell survival

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Evans, R. S. (2020). The effect of manipulation of the phosphoinositide 3-kinase pathway on axon regeneration in vivo. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.51879 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805869

Chicago Manual of Style (16th Edition):

Evans, Rachel Shane. “The effect of manipulation of the phosphoinositide 3-kinase pathway on axon regeneration in vivo.” 2020. Doctoral Dissertation, University of Cambridge. Accessed April 17, 2021. https://doi.org/10.17863/CAM.51879 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805869.

MLA Handbook (7th Edition):

Evans, Rachel Shane. “The effect of manipulation of the phosphoinositide 3-kinase pathway on axon regeneration in vivo.” 2020. Web. 17 Apr 2021.

Vancouver:

Evans RS. The effect of manipulation of the phosphoinositide 3-kinase pathway on axon regeneration in vivo. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2021 Apr 17]. Available from: https://doi.org/10.17863/CAM.51879 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805869.

Council of Science Editors:

Evans RS. The effect of manipulation of the phosphoinositide 3-kinase pathway on axon regeneration in vivo. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://doi.org/10.17863/CAM.51879 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.805869


University of Plymouth

27. Carr, Lauren. The role of Slit/Robo signalling in peripheral nerve regeneration.

Degree: PhD, 2019, University of Plymouth

 The role of Slit/Robo signalling in peripheral nerve regeneration. Slit/Robo chemorepulsive signalling has been shown to play a role in axon pathfinding during the development… (more)

Subjects/Keywords: 616.8; Slit; Robo; Peripheral nerve regeneration; Schwann cells; in vivo; Macrophages; Slit3; Robo1; Axon regeneration; nerve injuries; conduit

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Carr, L. (2019). The role of Slit/Robo signalling in peripheral nerve regeneration. (Doctoral Dissertation). University of Plymouth. Retrieved from http://hdl.handle.net/10026.1/13433

Chicago Manual of Style (16th Edition):

Carr, Lauren. “The role of Slit/Robo signalling in peripheral nerve regeneration.” 2019. Doctoral Dissertation, University of Plymouth. Accessed April 17, 2021. http://hdl.handle.net/10026.1/13433.

MLA Handbook (7th Edition):

Carr, Lauren. “The role of Slit/Robo signalling in peripheral nerve regeneration.” 2019. Web. 17 Apr 2021.

Vancouver:

Carr L. The role of Slit/Robo signalling in peripheral nerve regeneration. [Internet] [Doctoral dissertation]. University of Plymouth; 2019. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/10026.1/13433.

Council of Science Editors:

Carr L. The role of Slit/Robo signalling in peripheral nerve regeneration. [Doctoral Dissertation]. University of Plymouth; 2019. Available from: http://hdl.handle.net/10026.1/13433


Penn State University

28. Rao, Kavitha S. EXPLORING MECHANISMS UNDERLYING AXON REGENERATION USING DROSOPHILA SENSORY NEURONS.

Degree: 2016, Penn State University

 Axons and dendrites form two morphologically and functionally distinct compartments of a polarized neuron, and thus require different sets of proteins and organelles. Microtubules are… (more)

Subjects/Keywords: neuron; injury; neuronal injury; axon regeneration; drosophila; zebrafish; axotomy; dendrite; microtubule; spastin; atlastin; hereditary spastic paraplegia

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rao, K. S. (2016). EXPLORING MECHANISMS UNDERLYING AXON REGENERATION USING DROSOPHILA SENSORY NEURONS. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/2514nk499

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):

Rao, Kavitha S. “EXPLORING MECHANISMS UNDERLYING AXON REGENERATION USING DROSOPHILA SENSORY NEURONS.” 2016. Thesis, Penn State University. Accessed April 17, 2021. https://submit-etda.libraries.psu.edu/catalog/2514nk499.

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

MLA Handbook (7th Edition):

Rao, Kavitha S. “EXPLORING MECHANISMS UNDERLYING AXON REGENERATION USING DROSOPHILA SENSORY NEURONS.” 2016. Web. 17 Apr 2021.

Vancouver:

Rao KS. EXPLORING MECHANISMS UNDERLYING AXON REGENERATION USING DROSOPHILA SENSORY NEURONS. [Internet] [Thesis]. Penn State University; 2016. [cited 2021 Apr 17]. Available from: https://submit-etda.libraries.psu.edu/catalog/2514nk499.

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

Council of Science Editors:

Rao KS. EXPLORING MECHANISMS UNDERLYING AXON REGENERATION USING DROSOPHILA SENSORY NEURONS. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/2514nk499

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


University of Manitoba

29. Aghanoori, MohamadReza. Mechanism of insulin/IGF-1 regulation of mitochondrial function and nerve repair in diabetic neuropathy.

Degree: Pharmacology and Therapeutics, 2019, University of Manitoba

 Background: There is impaired neurotrophic growth factor signaling, AMP-activated protein kinase (AMPK) activity and mitochondrial function in dorsal root ganglia (DRG) of animal models of… (more)

Subjects/Keywords: AMPK; axon regeneration; bioenergetics; diabetic neuropathy; dorsal root ganglia; endogenous IGF-1; IGF-1 therapy; insulin implant; mitochondrial function; neurite outgrowth

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Aghanoori, M. (2019). Mechanism of insulin/IGF-1 regulation of mitochondrial function and nerve repair in diabetic neuropathy. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/34177

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):

Aghanoori, MohamadReza. “Mechanism of insulin/IGF-1 regulation of mitochondrial function and nerve repair in diabetic neuropathy.” 2019. Thesis, University of Manitoba. Accessed April 17, 2021. http://hdl.handle.net/1993/34177.

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

MLA Handbook (7th Edition):

Aghanoori, MohamadReza. “Mechanism of insulin/IGF-1 regulation of mitochondrial function and nerve repair in diabetic neuropathy.” 2019. Web. 17 Apr 2021.

Vancouver:

Aghanoori M. Mechanism of insulin/IGF-1 regulation of mitochondrial function and nerve repair in diabetic neuropathy. [Internet] [Thesis]. University of Manitoba; 2019. [cited 2021 Apr 17]. Available from: http://hdl.handle.net/1993/34177.

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

Council of Science Editors:

Aghanoori M. Mechanism of insulin/IGF-1 regulation of mitochondrial function and nerve repair in diabetic neuropathy. [Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/34177

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


New Jersey Institute of Technology

30. Loverde, Joseph R. Deciphering the biology of axon stretch-growth.

Degree: MSin Biomedical Engineering - (M.S.), Biomedical Engineering, 2009, New Jersey Institute of Technology

  Traditional nerve regeneration strategies focus on growth cone-mediated growth, a form of nerve growth that occurs primarily during embryogenesis. Early axons continue to grow… (more)

Subjects/Keywords: Axon stretch growth; Nerve regeneration; Biomedical Engineering and Bioengineering

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Loverde, J. R. (2009). Deciphering the biology of axon stretch-growth. (Thesis). New Jersey Institute of Technology. Retrieved from https://digitalcommons.njit.edu/theses/297

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):

Loverde, Joseph R. “Deciphering the biology of axon stretch-growth.” 2009. Thesis, New Jersey Institute of Technology. Accessed April 17, 2021. https://digitalcommons.njit.edu/theses/297.

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

MLA Handbook (7th Edition):

Loverde, Joseph R. “Deciphering the biology of axon stretch-growth.” 2009. Web. 17 Apr 2021.

Vancouver:

Loverde JR. Deciphering the biology of axon stretch-growth. [Internet] [Thesis]. New Jersey Institute of Technology; 2009. [cited 2021 Apr 17]. Available from: https://digitalcommons.njit.edu/theses/297.

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

Council of Science Editors:

Loverde JR. Deciphering the biology of axon stretch-growth. [Thesis]. New Jersey Institute of Technology; 2009. Available from: https://digitalcommons.njit.edu/theses/297

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

[1] [2]

.