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You searched for subject:(integral membrane proteins Affymetrix GeneChip synaptic vesicle vesicle trafficking). Showing records 1 – 30 of 20455 total matches.

[1] [2] [3] [4] [5] … [682]

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Johannes Gutenberg Universität Mainz

1. Bai, Lin. Genetische und funktionelle Analyse von Vesikelmembranprotein-Mutanten in Maus und Caenorhabditis elegans.

Degree: 2008, Johannes Gutenberg Universität Mainz

 Tetraspan vesicle membrane proteins (TVPs) sind konservierte, ubiquitär vorkommende Membranproteine synaptischer Vesikel und zytoplasmatischer Transportvesikel. Bei Säugetieren lassen sie sich in die Physine, Gyrine und… (more)

Subjects/Keywords: Vesikelmembranproteine, Affymetrix GeneChip, synaptische Vesikel, Vesikel-Trafficking; integral membrane proteins, Affymetrix GeneChip, synaptic vesicle, vesicle trafficking; Life sciences

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APA (6th Edition):

Bai, L. (2008). Genetische und funktionelle Analyse von Vesikelmembranprotein-Mutanten in Maus und Caenorhabditis elegans. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2008/1605/

Chicago Manual of Style (16th Edition):

Bai, Lin. “Genetische und funktionelle Analyse von Vesikelmembranprotein-Mutanten in Maus und Caenorhabditis elegans.” 2008. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed July 11, 2020. http://ubm.opus.hbz-nrw.de/volltexte/2008/1605/.

MLA Handbook (7th Edition):

Bai, Lin. “Genetische und funktionelle Analyse von Vesikelmembranprotein-Mutanten in Maus und Caenorhabditis elegans.” 2008. Web. 11 Jul 2020.

Vancouver:

Bai L. Genetische und funktionelle Analyse von Vesikelmembranprotein-Mutanten in Maus und Caenorhabditis elegans. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2008. [cited 2020 Jul 11]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2008/1605/.

Council of Science Editors:

Bai L. Genetische und funktionelle Analyse von Vesikelmembranprotein-Mutanten in Maus und Caenorhabditis elegans. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2008. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2008/1605/


University of Oregon

2. Loftus, Andrew. Measurement of Membrane Rigidity and Its Modulation by the Vesicle Trafficking Protein Sar1.

Degree: PhD, Department of Chemistry and Biochemistry, 2014, University of Oregon

 Sculpting membranes into dynamic, curved shapes is central to intracellular cargo trafficking and other cellular functions. However, generation of membrane curvature during trafficking involves lipids… (more)

Subjects/Keywords: Membrane Rigidity; Sar1; Tether Pulling; Vesicle Fluctuations; Vesicle Trafficking

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APA (6th Edition):

Loftus, A. (2014). Measurement of Membrane Rigidity and Its Modulation by the Vesicle Trafficking Protein Sar1. (Doctoral Dissertation). University of Oregon. Retrieved from http://hdl.handle.net/1794/18311

Chicago Manual of Style (16th Edition):

Loftus, Andrew. “Measurement of Membrane Rigidity and Its Modulation by the Vesicle Trafficking Protein Sar1.” 2014. Doctoral Dissertation, University of Oregon. Accessed July 11, 2020. http://hdl.handle.net/1794/18311.

MLA Handbook (7th Edition):

Loftus, Andrew. “Measurement of Membrane Rigidity and Its Modulation by the Vesicle Trafficking Protein Sar1.” 2014. Web. 11 Jul 2020.

Vancouver:

Loftus A. Measurement of Membrane Rigidity and Its Modulation by the Vesicle Trafficking Protein Sar1. [Internet] [Doctoral dissertation]. University of Oregon; 2014. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1794/18311.

Council of Science Editors:

Loftus A. Measurement of Membrane Rigidity and Its Modulation by the Vesicle Trafficking Protein Sar1. [Doctoral Dissertation]. University of Oregon; 2014. Available from: http://hdl.handle.net/1794/18311


Cornell University

3. Singh, Pankaj. Continuum and Molecular Modeling of Synaptic Vesicle Docking and Fusion .

Degree: 2018, Cornell University

 Transmission of neural information starts by the fusion of a synaptic vesicle inside a neuron with the membrane of the neuron. This fusion process mainly… (more)

Subjects/Keywords: Coarse Grained Molecular Dynamics (CGMD); Continuum mechanics; Lipid bilayer membrane; SNARE proteins; Synaptic vesicle fusion; Mechanical engineering; Biomechanics; Hydrodynamics; Biophysics

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APA (6th Edition):

Singh, P. (2018). Continuum and Molecular Modeling of Synaptic Vesicle Docking and Fusion . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59773

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

Chicago Manual of Style (16th Edition):

Singh, Pankaj. “Continuum and Molecular Modeling of Synaptic Vesicle Docking and Fusion .” 2018. Thesis, Cornell University. Accessed July 11, 2020. http://hdl.handle.net/1813/59773.

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

MLA Handbook (7th Edition):

Singh, Pankaj. “Continuum and Molecular Modeling of Synaptic Vesicle Docking and Fusion .” 2018. Web. 11 Jul 2020.

Vancouver:

Singh P. Continuum and Molecular Modeling of Synaptic Vesicle Docking and Fusion . [Internet] [Thesis]. Cornell University; 2018. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1813/59773.

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

Council of Science Editors:

Singh P. Continuum and Molecular Modeling of Synaptic Vesicle Docking and Fusion . [Thesis]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59773

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


University of Edinburgh

4. Low, Darryl Weijun. Synaptic vesicle protein 2A-dependent function and dysfunction at the presynapse.

Degree: PhD, 2018, University of Edinburgh

 Neurotransmission is essential for neuronal communication. At the presynapse, synaptic vesicles (SVs) undergo exocytosis to release neurotransmitter in response to incoming action potentials, and endocytosis… (more)

Subjects/Keywords: SV2A; synaptotagmin; synaptic vesicle

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APA (6th Edition):

Low, D. W. (2018). Synaptic vesicle protein 2A-dependent function and dysfunction at the presynapse. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/31320

Chicago Manual of Style (16th Edition):

Low, Darryl Weijun. “Synaptic vesicle protein 2A-dependent function and dysfunction at the presynapse.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed July 11, 2020. http://hdl.handle.net/1842/31320.

MLA Handbook (7th Edition):

Low, Darryl Weijun. “Synaptic vesicle protein 2A-dependent function and dysfunction at the presynapse.” 2018. Web. 11 Jul 2020.

Vancouver:

Low DW. Synaptic vesicle protein 2A-dependent function and dysfunction at the presynapse. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1842/31320.

Council of Science Editors:

Low DW. Synaptic vesicle protein 2A-dependent function and dysfunction at the presynapse. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/31320


North Carolina State University

5. Choi, Ucheor B. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.

Degree: PhD, Physics, 2010, North Carolina State University

 Conformational information about proteins can often reveal the mechanisms of their biological functions. This thesis examines conformational aspects of the synaptic SNARE (soluble N-ethylmaleimide-sensitive factor… (more)

Subjects/Keywords: protein-protein interactions; synaptic vesicle; single molecule FRET; neurotransmitter release; membrane fusion

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APA (6th Edition):

Choi, U. B. (2010). Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/6220

Chicago Manual of Style (16th Edition):

Choi, Ucheor B. “Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.” 2010. Doctoral Dissertation, North Carolina State University. Accessed July 11, 2020. http://www.lib.ncsu.edu/resolver/1840.16/6220.

MLA Handbook (7th Edition):

Choi, Ucheor B. “Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies.” 2010. Web. 11 Jul 2020.

Vancouver:

Choi UB. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. [Internet] [Doctoral dissertation]. North Carolina State University; 2010. [cited 2020 Jul 11]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6220.

Council of Science Editors:

Choi UB. Single molecule fluorescence reveals dynamic structures of SNARE protein assemblies. [Doctoral Dissertation]. North Carolina State University; 2010. Available from: http://www.lib.ncsu.edu/resolver/1840.16/6220


University of Pennsylvania

6. Zhao, Yuting. The Role of the Exocyst in Membrane Deformation, Cell Migration and Exocytosis.

Degree: 2014, University of Pennsylvania

 Dynamic shape changes of the plasma membrane are fundamental to many processes ranging from morphogenesis and cell migration to phagocytosis and viral propagation. In this… (more)

Subjects/Keywords: Actin; Cell migration; Exocyst; Membrane curvature; SNARE complex; Vesicle trafficking; Cell Biology

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APA (6th Edition):

Zhao, Y. (2014). The Role of the Exocyst in Membrane Deformation, Cell Migration and Exocytosis. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1522

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):

Zhao, Yuting. “The Role of the Exocyst in Membrane Deformation, Cell Migration and Exocytosis.” 2014. Thesis, University of Pennsylvania. Accessed July 11, 2020. https://repository.upenn.edu/edissertations/1522.

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

MLA Handbook (7th Edition):

Zhao, Yuting. “The Role of the Exocyst in Membrane Deformation, Cell Migration and Exocytosis.” 2014. Web. 11 Jul 2020.

Vancouver:

Zhao Y. The Role of the Exocyst in Membrane Deformation, Cell Migration and Exocytosis. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2020 Jul 11]. Available from: https://repository.upenn.edu/edissertations/1522.

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

Council of Science Editors:

Zhao Y. The Role of the Exocyst in Membrane Deformation, Cell Migration and Exocytosis. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1522

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


University of Rochester

7. Zhu, Qiuyu. The Role of STXBP5, VAMP8, and SNAP23 in Endothelial Exocytosis.

Degree: PhD, 2015, University of Rochester

 Thromboembolic diseases are major causes of morbidity and mortality. Endothelial exocytosis plays a critical role in thrombosis. The exocytic machinery that regulates granule secretion from… (more)

Subjects/Keywords: Secretory Granules; Vesicle Trafficking; Regulated Secretion; Membrane Fusion; Haemostasis; von Willebrand Disease; Venous Thromboembolism

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APA (6th Edition):

Zhu, Q. (2015). The Role of STXBP5, VAMP8, and SNAP23 in Endothelial Exocytosis. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/29786

Chicago Manual of Style (16th Edition):

Zhu, Qiuyu. “The Role of STXBP5, VAMP8, and SNAP23 in Endothelial Exocytosis.” 2015. Doctoral Dissertation, University of Rochester. Accessed July 11, 2020. http://hdl.handle.net/1802/29786.

MLA Handbook (7th Edition):

Zhu, Qiuyu. “The Role of STXBP5, VAMP8, and SNAP23 in Endothelial Exocytosis.” 2015. Web. 11 Jul 2020.

Vancouver:

Zhu Q. The Role of STXBP5, VAMP8, and SNAP23 in Endothelial Exocytosis. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1802/29786.

Council of Science Editors:

Zhu Q. The Role of STXBP5, VAMP8, and SNAP23 in Endothelial Exocytosis. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/29786

8. Posey, Lisa Lipowski. AN ENHANCER OF A PRESYNAPTIC CALCIUM CHANNEL MUTANT REVEALS A ROLE FOR DROSOPHILA DISABLED IN SYNAPTIC TRANSMISSION.

Degree: MS, Genetics, 2008, Penn State University

Synaptic transmission is the basis for communication between neurons. At synapses, neurotransmitter-filled vesicles fuse to the presynaptic plasma membrane in response to a depolarizing action… (more)

Subjects/Keywords: temperature-sensitive mutant; Synaptic vesicle trafficking; Drosophila

…1.1.2 Core Proteins and the Molecular Mechanisms of Synaptic Vesicle Trafficking Exocytosis of… …proteins known to function in synaptic vesicle trafficking (Wang et al., 2008). Dap160… …respectively, for excitatory and inhibitory synapses. 1.1.1 The Synaptic Vesicle Trafficking Cycle… …Figure 1.2: The synaptic vesicle trafficking cycle. Modified from Südhof (2004)… …al., 1993b). The SNARE proteins involved in synaptic transmission are the vesicle… 

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APA (6th Edition):

Posey, L. L. (2008). AN ENHANCER OF A PRESYNAPTIC CALCIUM CHANNEL MUTANT REVEALS A ROLE FOR DROSOPHILA DISABLED IN SYNAPTIC TRANSMISSION. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8789

Chicago Manual of Style (16th Edition):

Posey, Lisa Lipowski. “AN ENHANCER OF A PRESYNAPTIC CALCIUM CHANNEL MUTANT REVEALS A ROLE FOR DROSOPHILA DISABLED IN SYNAPTIC TRANSMISSION.” 2008. Masters Thesis, Penn State University. Accessed July 11, 2020. https://etda.libraries.psu.edu/catalog/8789.

MLA Handbook (7th Edition):

Posey, Lisa Lipowski. “AN ENHANCER OF A PRESYNAPTIC CALCIUM CHANNEL MUTANT REVEALS A ROLE FOR DROSOPHILA DISABLED IN SYNAPTIC TRANSMISSION.” 2008. Web. 11 Jul 2020.

Vancouver:

Posey LL. AN ENHANCER OF A PRESYNAPTIC CALCIUM CHANNEL MUTANT REVEALS A ROLE FOR DROSOPHILA DISABLED IN SYNAPTIC TRANSMISSION. [Internet] [Masters thesis]. Penn State University; 2008. [cited 2020 Jul 11]. Available from: https://etda.libraries.psu.edu/catalog/8789.

Council of Science Editors:

Posey LL. AN ENHANCER OF A PRESYNAPTIC CALCIUM CHANNEL MUTANT REVEALS A ROLE FOR DROSOPHILA DISABLED IN SYNAPTIC TRANSMISSION. [Masters Thesis]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8789


University of Manchester

9. Vernon, Samuel William. Vesicular Loading and Synaptic Release at Central Cholinergic Synapses.

Degree: 2018, University of Manchester

 Neurotransmitter release from presynaptic terminals can be regulated by altering transmitter load per synaptic vesicle (SV) and/or through the probability of vesicle release. The vesicular… (more)

Subjects/Keywords: Acetylcholine; Drosophila; Insecticide Resistance; Synaptic Vesicle

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APA (6th Edition):

Vernon, S. W. (2018). Vesicular Loading and Synaptic Release at Central Cholinergic Synapses. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317546

Chicago Manual of Style (16th Edition):

Vernon, Samuel William. “Vesicular Loading and Synaptic Release at Central Cholinergic Synapses.” 2018. Doctoral Dissertation, University of Manchester. Accessed July 11, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317546.

MLA Handbook (7th Edition):

Vernon, Samuel William. “Vesicular Loading and Synaptic Release at Central Cholinergic Synapses.” 2018. Web. 11 Jul 2020.

Vancouver:

Vernon SW. Vesicular Loading and Synaptic Release at Central Cholinergic Synapses. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Jul 11]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317546.

Council of Science Editors:

Vernon SW. Vesicular Loading and Synaptic Release at Central Cholinergic Synapses. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317546


University of California – San Francisco

10. Foss, Sarah. Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1.

Degree: Cell Biology, 2012, University of California – San Francisco

 Three vesicular glutamate transporters (VGLUT1, -2, and -3) are found in the mammalian central nervous system. The transporters are expressed in different brain regions in… (more)

Subjects/Keywords: Neurosciences; Cellular biology; endocytosis; synaptic vesicle

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APA (6th Edition):

Foss, S. (2012). Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/66j3k3qw

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):

Foss, Sarah. “Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1.” 2012. Thesis, University of California – San Francisco. Accessed July 11, 2020. http://www.escholarship.org/uc/item/66j3k3qw.

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

MLA Handbook (7th Edition):

Foss, Sarah. “Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1.” 2012. Web. 11 Jul 2020.

Vancouver:

Foss S. Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2020 Jul 11]. Available from: http://www.escholarship.org/uc/item/66j3k3qw.

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

Council of Science Editors:

Foss S. Regulation of the synaptic trafficking of the vesicular glutamate transporter VGLUT1. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/66j3k3qw

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


Harvard University

11. Wang, Huaiying. Molecular Mechanisms for Active Zone Assembly at Vertebrate Synapses.

Degree: PhD, 2019, Harvard University

Neurons are unique for their ability to transmit a presynaptic signal to postsynaptic target cells on a sub-millisecond timescale. This rapid and precise exchange of… (more)

Subjects/Keywords: Synaptic transmission; Vesicle exocytosis; Presynaptic active zone

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APA (6th Edition):

Wang, H. (2019). Molecular Mechanisms for Active Zone Assembly at Vertebrate Synapses. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029509

Chicago Manual of Style (16th Edition):

Wang, Huaiying. “Molecular Mechanisms for Active Zone Assembly at Vertebrate Synapses.” 2019. Doctoral Dissertation, Harvard University. Accessed July 11, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029509.

MLA Handbook (7th Edition):

Wang, Huaiying. “Molecular Mechanisms for Active Zone Assembly at Vertebrate Synapses.” 2019. Web. 11 Jul 2020.

Vancouver:

Wang H. Molecular Mechanisms for Active Zone Assembly at Vertebrate Synapses. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2020 Jul 11]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029509.

Council of Science Editors:

Wang H. Molecular Mechanisms for Active Zone Assembly at Vertebrate Synapses. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029509


University of Manchester

12. Vernon, Samuel. Vesicular loading and synaptic release at central cholinergic synapses.

Degree: PhD, 2019, University of Manchester

 Neurotransmitter release from presynaptic terminals can be regulated by altering transmitter load per synaptic vesicle (SV) and/or through the probability of vesicle release. The vesicular… (more)

Subjects/Keywords: Synaptic Vesicle; Insecticide Resistance; Drosophila; Acetylcholine

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APA (6th Edition):

Vernon, S. (2019). Vesicular loading and synaptic release at central cholinergic synapses. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/vesicular-loading-and-synaptic-release-at-central-cholinergic-synapses(570e3205-911a-4333-b4c8-4acc98e36c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799366

Chicago Manual of Style (16th Edition):

Vernon, Samuel. “Vesicular loading and synaptic release at central cholinergic synapses.” 2019. Doctoral Dissertation, University of Manchester. Accessed July 11, 2020. https://www.research.manchester.ac.uk/portal/en/theses/vesicular-loading-and-synaptic-release-at-central-cholinergic-synapses(570e3205-911a-4333-b4c8-4acc98e36c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799366.

MLA Handbook (7th Edition):

Vernon, Samuel. “Vesicular loading and synaptic release at central cholinergic synapses.” 2019. Web. 11 Jul 2020.

Vancouver:

Vernon S. Vesicular loading and synaptic release at central cholinergic synapses. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Jul 11]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/vesicular-loading-and-synaptic-release-at-central-cholinergic-synapses(570e3205-911a-4333-b4c8-4acc98e36c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799366.

Council of Science Editors:

Vernon S. Vesicular loading and synaptic release at central cholinergic synapses. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/vesicular-loading-and-synaptic-release-at-central-cholinergic-synapses(570e3205-911a-4333-b4c8-4acc98e36c53).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799366


University of Victoria

13. Bilkey, Jessica. Modulation of Synaptic Vesicle Pools by Serotonin and the Spatial Organization of Vesicle Pools at the Crayfish Opener Neuromuscular Junction.

Degree: Department of Biology, 2015, University of Victoria

 The crayfish claw opener neuromuscular junction (NMJ) is a biological model for studying presynaptic neuromodulation by serotonin and synaptic vesicle recycling. Serotonin acts on crayfish… (more)

Subjects/Keywords: serotonin; Crayfish neuromuscular junction; synaptic vesicle pools

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APA (6th Edition):

Bilkey, J. (2015). Modulation of Synaptic Vesicle Pools by Serotonin and the Spatial Organization of Vesicle Pools at the Crayfish Opener Neuromuscular Junction. (Masters Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/6123

Chicago Manual of Style (16th Edition):

Bilkey, Jessica. “Modulation of Synaptic Vesicle Pools by Serotonin and the Spatial Organization of Vesicle Pools at the Crayfish Opener Neuromuscular Junction.” 2015. Masters Thesis, University of Victoria. Accessed July 11, 2020. http://hdl.handle.net/1828/6123.

MLA Handbook (7th Edition):

Bilkey, Jessica. “Modulation of Synaptic Vesicle Pools by Serotonin and the Spatial Organization of Vesicle Pools at the Crayfish Opener Neuromuscular Junction.” 2015. Web. 11 Jul 2020.

Vancouver:

Bilkey J. Modulation of Synaptic Vesicle Pools by Serotonin and the Spatial Organization of Vesicle Pools at the Crayfish Opener Neuromuscular Junction. [Internet] [Masters thesis]. University of Victoria; 2015. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1828/6123.

Council of Science Editors:

Bilkey J. Modulation of Synaptic Vesicle Pools by Serotonin and the Spatial Organization of Vesicle Pools at the Crayfish Opener Neuromuscular Junction. [Masters Thesis]. University of Victoria; 2015. Available from: http://hdl.handle.net/1828/6123


University of Edinburgh

14. Johnson, Alexander James. Role of Tyrosine Phosphorylation of Synaptophysin in the synaptic vesicle lifecycle.

Degree: PhD, 2012, University of Edinburgh

 Synaptophysin (Syp) is a major integral synaptic vesicle (SV) protein; there are 31 copies of Syp per vesicle, which totals up to 10% of the… (more)

Subjects/Keywords: 572; Tyrosine Phosphorylation; Synaptophysin; synaptic vesicle lifecycle

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APA (6th Edition):

Johnson, A. J. (2012). Role of Tyrosine Phosphorylation of Synaptophysin in the synaptic vesicle lifecycle. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9897

Chicago Manual of Style (16th Edition):

Johnson, Alexander James. “Role of Tyrosine Phosphorylation of Synaptophysin in the synaptic vesicle lifecycle.” 2012. Doctoral Dissertation, University of Edinburgh. Accessed July 11, 2020. http://hdl.handle.net/1842/9897.

MLA Handbook (7th Edition):

Johnson, Alexander James. “Role of Tyrosine Phosphorylation of Synaptophysin in the synaptic vesicle lifecycle.” 2012. Web. 11 Jul 2020.

Vancouver:

Johnson AJ. Role of Tyrosine Phosphorylation of Synaptophysin in the synaptic vesicle lifecycle. [Internet] [Doctoral dissertation]. University of Edinburgh; 2012. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1842/9897.

Council of Science Editors:

Johnson AJ. Role of Tyrosine Phosphorylation of Synaptophysin in the synaptic vesicle lifecycle. [Doctoral Dissertation]. University of Edinburgh; 2012. Available from: http://hdl.handle.net/1842/9897


University of Guelph

15. Conlon, Shannon. An Investigation of the Barrier Properties and pH Dependent Permeability of Scaffolded Vesicles .

Degree: 2015, University of Guelph

 Nutraceutical carriers rely on multiple features, including permeability and biocompatibility, in order to function properly. The scaffolded vesicle, which was recently proposed, has been able… (more)

Subjects/Keywords: vesicle; DMPC; membrane; drug delivery; scaffolded vesicle; cholesterol

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APA (6th Edition):

Conlon, S. (2015). An Investigation of the Barrier Properties and pH Dependent Permeability of Scaffolded Vesicles . (Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8665

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):

Conlon, Shannon. “An Investigation of the Barrier Properties and pH Dependent Permeability of Scaffolded Vesicles .” 2015. Thesis, University of Guelph. Accessed July 11, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8665.

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

MLA Handbook (7th Edition):

Conlon, Shannon. “An Investigation of the Barrier Properties and pH Dependent Permeability of Scaffolded Vesicles .” 2015. Web. 11 Jul 2020.

Vancouver:

Conlon S. An Investigation of the Barrier Properties and pH Dependent Permeability of Scaffolded Vesicles . [Internet] [Thesis]. University of Guelph; 2015. [cited 2020 Jul 11]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8665.

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

Council of Science Editors:

Conlon S. An Investigation of the Barrier Properties and pH Dependent Permeability of Scaffolded Vesicles . [Thesis]. University of Guelph; 2015. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/8665

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


University of Edinburgh

16. Bonnycastle, Katherine. Synaptic vesicle recycling in preclinical models of intellectual disability, autism spectrum disorder and epilepsy.

Degree: PhD, 2018, University of Edinburgh

 The development of the central nervous system is dysregulated in neurodevelopmental disorders such as intellectual disability, autism spectrum disorder, and epilepsy. These three disorders have… (more)

Subjects/Keywords: neurodevelopmental disorders; SYNGAP1 haploinsufficiency; synaptic vesicle recycling; clathrin-mediated endocytosis; CME; SV recycling dysfunction; membrane retrieval

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APA (6th Edition):

Bonnycastle, K. (2018). Synaptic vesicle recycling in preclinical models of intellectual disability, autism spectrum disorder and epilepsy. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/31344

Chicago Manual of Style (16th Edition):

Bonnycastle, Katherine. “Synaptic vesicle recycling in preclinical models of intellectual disability, autism spectrum disorder and epilepsy.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed July 11, 2020. http://hdl.handle.net/1842/31344.

MLA Handbook (7th Edition):

Bonnycastle, Katherine. “Synaptic vesicle recycling in preclinical models of intellectual disability, autism spectrum disorder and epilepsy.” 2018. Web. 11 Jul 2020.

Vancouver:

Bonnycastle K. Synaptic vesicle recycling in preclinical models of intellectual disability, autism spectrum disorder and epilepsy. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1842/31344.

Council of Science Editors:

Bonnycastle K. Synaptic vesicle recycling in preclinical models of intellectual disability, autism spectrum disorder and epilepsy. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/31344


Freie Universität Berlin

17. Rost, Benjamin. Präsynaptische Inhibition von Transmitterfreisetzung durch G-Protein gekoppelte Rezeptoren in der hippokampalen Formation.

Degree: 2012, Freie Universität Berlin

 Synaptische Informationsübertragung zwischen Neuronen wird durch präsynaptische, G-Protein gekoppelte Rezeptoren moduliert. Viele dieser Rezeptoren wirken inhibitorisch, da sie die Neurotransmitter Freisetzung verringern, und somit die… (more)

Subjects/Keywords: presynaptic inhibition; metabotropic receptor; synaptic vesicle fusion; SNARE proteins; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Rost, B. (2012). Präsynaptische Inhibition von Transmitterfreisetzung durch G-Protein gekoppelte Rezeptoren in der hippokampalen Formation. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-14448

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):

Rost, Benjamin. “Präsynaptische Inhibition von Transmitterfreisetzung durch G-Protein gekoppelte Rezeptoren in der hippokampalen Formation.” 2012. Thesis, Freie Universität Berlin. Accessed July 11, 2020. http://dx.doi.org/10.17169/refubium-14448.

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

MLA Handbook (7th Edition):

Rost, Benjamin. “Präsynaptische Inhibition von Transmitterfreisetzung durch G-Protein gekoppelte Rezeptoren in der hippokampalen Formation.” 2012. Web. 11 Jul 2020.

Vancouver:

Rost B. Präsynaptische Inhibition von Transmitterfreisetzung durch G-Protein gekoppelte Rezeptoren in der hippokampalen Formation. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Jul 11]. Available from: http://dx.doi.org/10.17169/refubium-14448.

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

Council of Science Editors:

Rost B. Präsynaptische Inhibition von Transmitterfreisetzung durch G-Protein gekoppelte Rezeptoren in der hippokampalen Formation. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-14448

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


Freie Universität Berlin

18. Jäpel, Maria. Das Gerüstprotein Intersektin 1 unterstützt verschiedene Schritte im Zyklus synaptischer Vesikel.

Degree: 2019, Freie Universität Berlin

 The multidomain scaffold protein intersectin 1 has been implicated in several cellular signaling pathways and processes. The best described function of intersectin 1 is its… (more)

Subjects/Keywords: neurotransmission; synaptic vesicle cycling; multidomain scaffold; SNARE proteins; 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie

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APA (6th Edition):

Jäpel, M. (2019). Das Gerüstprotein Intersektin 1 unterstützt verschiedene Schritte im Zyklus synaptischer Vesikel. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-2680

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):

Jäpel, Maria. “Das Gerüstprotein Intersektin 1 unterstützt verschiedene Schritte im Zyklus synaptischer Vesikel.” 2019. Thesis, Freie Universität Berlin. Accessed July 11, 2020. http://dx.doi.org/10.17169/refubium-2680.

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

MLA Handbook (7th Edition):

Jäpel, Maria. “Das Gerüstprotein Intersektin 1 unterstützt verschiedene Schritte im Zyklus synaptischer Vesikel.” 2019. Web. 11 Jul 2020.

Vancouver:

Jäpel M. Das Gerüstprotein Intersektin 1 unterstützt verschiedene Schritte im Zyklus synaptischer Vesikel. [Internet] [Thesis]. Freie Universität Berlin; 2019. [cited 2020 Jul 11]. Available from: http://dx.doi.org/10.17169/refubium-2680.

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

Council of Science Editors:

Jäpel M. Das Gerüstprotein Intersektin 1 unterstützt verschiedene Schritte im Zyklus synaptischer Vesikel. [Thesis]. Freie Universität Berlin; 2019. Available from: http://dx.doi.org/10.17169/refubium-2680

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


University of Utah

19. Gu, Mingyu. Synaptic vesicle recycling by clathrin-mediated endocytosis.

Degree: PhD, Biology, 2010, University of Utah

 Synapses are the places where neurons communicate with their targets. At chemical synapses, neurotransmitters are contained in synaptic vesicles and are released into the synaptic(more)

Subjects/Keywords: AP2; Endocytosis; Synapse; Clathrin-mediated; Synaptic vesicle recycling; Caenorhabditis elegans

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

APA (6th Edition):

Gu, M. (2010). Synaptic vesicle recycling by clathrin-mediated endocytosis. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/72/rec/2331

Chicago Manual of Style (16th Edition):

Gu, Mingyu. “Synaptic vesicle recycling by clathrin-mediated endocytosis.” 2010. Doctoral Dissertation, University of Utah. Accessed July 11, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/72/rec/2331.

MLA Handbook (7th Edition):

Gu, Mingyu. “Synaptic vesicle recycling by clathrin-mediated endocytosis.” 2010. Web. 11 Jul 2020.

Vancouver:

Gu M. Synaptic vesicle recycling by clathrin-mediated endocytosis. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2020 Jul 11]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/72/rec/2331.

Council of Science Editors:

Gu M. Synaptic vesicle recycling by clathrin-mediated endocytosis. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/72/rec/2331


Texas Medical Center

20. Hart, Anne. ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA.

Degree: PhD, 2011, Texas Medical Center

  Enhanced expression of the presynaptic protein synapsin has been correlated with certain forms of long-term plasticity and learning and memory. However, the regulation and… (more)

Subjects/Keywords: CREB; gene regulation; plasticity; synaptic vesicle protein; memory; Neuroscience and Neurobiology

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APA (6th Edition):

Hart, A. (2011). ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/148

Chicago Manual of Style (16th Edition):

Hart, Anne. “ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA.” 2011. Doctoral Dissertation, Texas Medical Center. Accessed July 11, 2020. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/148.

MLA Handbook (7th Edition):

Hart, Anne. “ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA.” 2011. Web. 11 Jul 2020.

Vancouver:

Hart A. ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA. [Internet] [Doctoral dissertation]. Texas Medical Center; 2011. [cited 2020 Jul 11]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/148.

Council of Science Editors:

Hart A. ROLE OF SYNAPSIN IN LONG-TERM SYNAPTIC FACILITATION IN APLYSIA. [Doctoral Dissertation]. Texas Medical Center; 2011. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/148


University of Toronto

21. Nath, Arup Ratan. On Cryoloading: A Novel Technique used for the Functional Analysis of CAV2.2 - Synaptic Vesicle Tethering.

Degree: 2015, University of Toronto

Temporal synchronization between quantal release and Ca2+ influx through single CaVs led to the prediction that SVs are attached by a molecular tether to channels.… (more)

Subjects/Keywords: Assay; Calcium channel; Cryoloading; Functional; Synaptic vesicle; Tether; 0317

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APA (6th Edition):

Nath, A. R. (2015). On Cryoloading: A Novel Technique used for the Functional Analysis of CAV2.2 - Synaptic Vesicle Tethering. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/88583

Chicago Manual of Style (16th Edition):

Nath, Arup Ratan. “On Cryoloading: A Novel Technique used for the Functional Analysis of CAV2.2 - Synaptic Vesicle Tethering.” 2015. Masters Thesis, University of Toronto. Accessed July 11, 2020. http://hdl.handle.net/1807/88583.

MLA Handbook (7th Edition):

Nath, Arup Ratan. “On Cryoloading: A Novel Technique used for the Functional Analysis of CAV2.2 - Synaptic Vesicle Tethering.” 2015. Web. 11 Jul 2020.

Vancouver:

Nath AR. On Cryoloading: A Novel Technique used for the Functional Analysis of CAV2.2 - Synaptic Vesicle Tethering. [Internet] [Masters thesis]. University of Toronto; 2015. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1807/88583.

Council of Science Editors:

Nath AR. On Cryoloading: A Novel Technique used for the Functional Analysis of CAV2.2 - Synaptic Vesicle Tethering. [Masters Thesis]. University of Toronto; 2015. Available from: http://hdl.handle.net/1807/88583


University of Washington

22. Zeigler, Maxwell Bertrand. Highly Sensitive Quantitative Microscopy for Cellular and Subcellular Analysis.

Degree: PhD, 2013, University of Washington

 The purpose of this research has been to implement optical methods to investigate subcellular biological function. The diffraction limit of light for conventional optical microscopy… (more)

Subjects/Keywords: anisotropy; fluorescence; microscopy; nanoparticle; polarization; synaptic vesicle; Chemistry; chemistry

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APA (6th Edition):

Zeigler, M. B. (2013). Highly Sensitive Quantitative Microscopy for Cellular and Subcellular Analysis. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/22861

Chicago Manual of Style (16th Edition):

Zeigler, Maxwell Bertrand. “Highly Sensitive Quantitative Microscopy for Cellular and Subcellular Analysis.” 2013. Doctoral Dissertation, University of Washington. Accessed July 11, 2020. http://hdl.handle.net/1773/22861.

MLA Handbook (7th Edition):

Zeigler, Maxwell Bertrand. “Highly Sensitive Quantitative Microscopy for Cellular and Subcellular Analysis.” 2013. Web. 11 Jul 2020.

Vancouver:

Zeigler MB. Highly Sensitive Quantitative Microscopy for Cellular and Subcellular Analysis. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1773/22861.

Council of Science Editors:

Zeigler MB. Highly Sensitive Quantitative Microscopy for Cellular and Subcellular Analysis. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/22861


University of Washington

23. Ciruelas, Kristine. Elucidating Levetiracetam action at the presynaptic terminal.

Degree: PhD, 2019, University of Washington

 Levetiracetam (KeppraTM, LEV) is the first of a growing class of anti-epileptic drugs that shows great promise in the treatment of multiple neurological disorders. LEV… (more)

Subjects/Keywords: Levetiracetam; Synaptic vesicle protein 2; Biochemistry; Molecular biology; Neurosciences; Pharmacology

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APA (6th Edition):

Ciruelas, K. (2019). Elucidating Levetiracetam action at the presynaptic terminal. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43732

Chicago Manual of Style (16th Edition):

Ciruelas, Kristine. “Elucidating Levetiracetam action at the presynaptic terminal.” 2019. Doctoral Dissertation, University of Washington. Accessed July 11, 2020. http://hdl.handle.net/1773/43732.

MLA Handbook (7th Edition):

Ciruelas, Kristine. “Elucidating Levetiracetam action at the presynaptic terminal.” 2019. Web. 11 Jul 2020.

Vancouver:

Ciruelas K. Elucidating Levetiracetam action at the presynaptic terminal. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1773/43732.

Council of Science Editors:

Ciruelas K. Elucidating Levetiracetam action at the presynaptic terminal. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43732


University of Toronto

24. Gardezi, Syeda Sabiha. Characterization of the Calcium Channel Scaffold and the Cav2.2-synaptic Vesicle Tether at the Presynaptic Nerve Terminal.

Degree: PhD, 2016, University of Toronto

Calcium ion influx through voltage-gated calcium channels (Cav) triggers synaptic vesicle (SV) fusion and neurotransmitter release at presynaptic nerve terminals. A single Cav can trigger… (more)

Subjects/Keywords: Cav2.2; Presynaptic nerve terminal; scaffold; Synaptic vesicle; tether; 0317

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

APA (6th Edition):

Gardezi, S. S. (2016). Characterization of the Calcium Channel Scaffold and the Cav2.2-synaptic Vesicle Tether at the Presynaptic Nerve Terminal. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89241

Chicago Manual of Style (16th Edition):

Gardezi, Syeda Sabiha. “Characterization of the Calcium Channel Scaffold and the Cav2.2-synaptic Vesicle Tether at the Presynaptic Nerve Terminal.” 2016. Doctoral Dissertation, University of Toronto. Accessed July 11, 2020. http://hdl.handle.net/1807/89241.

MLA Handbook (7th Edition):

Gardezi, Syeda Sabiha. “Characterization of the Calcium Channel Scaffold and the Cav2.2-synaptic Vesicle Tether at the Presynaptic Nerve Terminal.” 2016. Web. 11 Jul 2020.

Vancouver:

Gardezi SS. Characterization of the Calcium Channel Scaffold and the Cav2.2-synaptic Vesicle Tether at the Presynaptic Nerve Terminal. [Internet] [Doctoral dissertation]. University of Toronto; 2016. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1807/89241.

Council of Science Editors:

Gardezi SS. Characterization of the Calcium Channel Scaffold and the Cav2.2-synaptic Vesicle Tether at the Presynaptic Nerve Terminal. [Doctoral Dissertation]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/89241


University of Toronto

25. Chen, Robert. Ultrastructural Analysis of the Role of Voltage-Gated Calcium Channel Intracellular Domains in Synaptic Vesicle Tethering at Presynaptic Terminals.

Degree: PhD, 2017, University of Toronto

 Chemical synaptic transmission is the main basis by which neurons convey information. This transmission is mediated by the fusion of synaptic vesicles (SVs) and the… (more)

Subjects/Keywords: calcium channel; presynaptic; synaptic vesicle; tether; tethering; transmitter release; 0317

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APA (6th Edition):

Chen, R. (2017). Ultrastructural Analysis of the Role of Voltage-Gated Calcium Channel Intracellular Domains in Synaptic Vesicle Tethering at Presynaptic Terminals. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/80688

Chicago Manual of Style (16th Edition):

Chen, Robert. “Ultrastructural Analysis of the Role of Voltage-Gated Calcium Channel Intracellular Domains in Synaptic Vesicle Tethering at Presynaptic Terminals.” 2017. Doctoral Dissertation, University of Toronto. Accessed July 11, 2020. http://hdl.handle.net/1807/80688.

MLA Handbook (7th Edition):

Chen, Robert. “Ultrastructural Analysis of the Role of Voltage-Gated Calcium Channel Intracellular Domains in Synaptic Vesicle Tethering at Presynaptic Terminals.” 2017. Web. 11 Jul 2020.

Vancouver:

Chen R. Ultrastructural Analysis of the Role of Voltage-Gated Calcium Channel Intracellular Domains in Synaptic Vesicle Tethering at Presynaptic Terminals. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/1807/80688.

Council of Science Editors:

Chen R. Ultrastructural Analysis of the Role of Voltage-Gated Calcium Channel Intracellular Domains in Synaptic Vesicle Tethering at Presynaptic Terminals. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/80688


Montana Tech

26. Smith, Wesley Edward. Elucidation of the Specificity of Neuroactive Steroids and Related Compounds at the at the Vesicular Glutamate Transporter.

Degree: PhD, 2007, Montana Tech

 As the primary excitatory amino acid, glutamate is essential to proper functioning of the mammalian CNS. Proper regulation of the synaptic release of glutamate, potentially… (more)

Subjects/Keywords: glutamate; synaptic neurotransmission; synaptic vesicle; VLGUT

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APA (6th Edition):

Smith, W. E. (2007). Elucidation of the Specificity of Neuroactive Steroids and Related Compounds at the at the Vesicular Glutamate Transporter. (Doctoral Dissertation). Montana Tech. Retrieved from https://scholarworks.umt.edu/etd/370

Chicago Manual of Style (16th Edition):

Smith, Wesley Edward. “Elucidation of the Specificity of Neuroactive Steroids and Related Compounds at the at the Vesicular Glutamate Transporter.” 2007. Doctoral Dissertation, Montana Tech. Accessed July 11, 2020. https://scholarworks.umt.edu/etd/370.

MLA Handbook (7th Edition):

Smith, Wesley Edward. “Elucidation of the Specificity of Neuroactive Steroids and Related Compounds at the at the Vesicular Glutamate Transporter.” 2007. Web. 11 Jul 2020.

Vancouver:

Smith WE. Elucidation of the Specificity of Neuroactive Steroids and Related Compounds at the at the Vesicular Glutamate Transporter. [Internet] [Doctoral dissertation]. Montana Tech; 2007. [cited 2020 Jul 11]. Available from: https://scholarworks.umt.edu/etd/370.

Council of Science Editors:

Smith WE. Elucidation of the Specificity of Neuroactive Steroids and Related Compounds at the at the Vesicular Glutamate Transporter. [Doctoral Dissertation]. Montana Tech; 2007. Available from: https://scholarworks.umt.edu/etd/370


University of California – San Diego

27. Tran, Thuy TT. Cell Density Regulates the Golgi through Hippo, the STRIPAK Complex, and GOLPH3.

Degree: Biology, 2018, University of California – San Diego

 The Golgi is the main hub for the modification, sorting, and transporting of proteins to various intra- and extracellular destinations. Against conventional belief that most… (more)

Subjects/Keywords: Biology; GOLPH3; Hippo; phosphatidylinositol-4-phosphate; PP2A; STRIPAK; vesicle trafficking

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APA (6th Edition):

Tran, T. T. (2018). Cell Density Regulates the Golgi through Hippo, the STRIPAK Complex, and GOLPH3. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/624946kp

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):

Tran, Thuy TT. “Cell Density Regulates the Golgi through Hippo, the STRIPAK Complex, and GOLPH3.” 2018. Thesis, University of California – San Diego. Accessed July 11, 2020. http://www.escholarship.org/uc/item/624946kp.

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

MLA Handbook (7th Edition):

Tran, Thuy TT. “Cell Density Regulates the Golgi through Hippo, the STRIPAK Complex, and GOLPH3.” 2018. Web. 11 Jul 2020.

Vancouver:

Tran TT. Cell Density Regulates the Golgi through Hippo, the STRIPAK Complex, and GOLPH3. [Internet] [Thesis]. University of California – San Diego; 2018. [cited 2020 Jul 11]. Available from: http://www.escholarship.org/uc/item/624946kp.

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

Council of Science Editors:

Tran TT. Cell Density Regulates the Golgi through Hippo, the STRIPAK Complex, and GOLPH3. [Thesis]. University of California – San Diego; 2018. Available from: http://www.escholarship.org/uc/item/624946kp

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


University of California – San Francisco

28. Lee, Ching Fern Sue-Ann. Genetic and Cell Biological Dissection of Alpha-Synuclein Trafficking Defects in Yeast and Mammalian Cells.

Degree: Biomedical Sciences, 2010, University of California – San Francisco

 a-synuclein, a major player in idiopathic and familial forms of Parkinson's disease pathogenesis, is thought to impair vesicle trafficking as a toxic gain of function… (more)

Subjects/Keywords: Biology, Cell; Biology, Neuroscience; alpha-synuclein; Parkinson's disease; vesicle trafficking

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APA (6th Edition):

Lee, C. F. S. (2010). Genetic and Cell Biological Dissection of Alpha-Synuclein Trafficking Defects in Yeast and Mammalian Cells. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/2pk0t6p1

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):

Lee, Ching Fern Sue-Ann. “Genetic and Cell Biological Dissection of Alpha-Synuclein Trafficking Defects in Yeast and Mammalian Cells.” 2010. Thesis, University of California – San Francisco. Accessed July 11, 2020. http://www.escholarship.org/uc/item/2pk0t6p1.

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

MLA Handbook (7th Edition):

Lee, Ching Fern Sue-Ann. “Genetic and Cell Biological Dissection of Alpha-Synuclein Trafficking Defects in Yeast and Mammalian Cells.” 2010. Web. 11 Jul 2020.

Vancouver:

Lee CFS. Genetic and Cell Biological Dissection of Alpha-Synuclein Trafficking Defects in Yeast and Mammalian Cells. [Internet] [Thesis]. University of California – San Francisco; 2010. [cited 2020 Jul 11]. Available from: http://www.escholarship.org/uc/item/2pk0t6p1.

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

Council of Science Editors:

Lee CFS. Genetic and Cell Biological Dissection of Alpha-Synuclein Trafficking Defects in Yeast and Mammalian Cells. [Thesis]. University of California – San Francisco; 2010. Available from: http://www.escholarship.org/uc/item/2pk0t6p1

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

29. 高橋, 麻衣子. The localization of VAMP5 in skeletal and cardiac muscle : マウス骨格筋および心筋におけるVAMP5の発現と分布.

Degree: 博士(医学), 2015, Gunma University / 群馬大学

学位記番号:医博甲1522

Subjects/Keywords: VAMP5; SNARE; skeletal muscle; cardiac muscle; vesicle trafficking; membrane fusion

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

APA (6th Edition):

高橋, . (2015). The localization of VAMP5 in skeletal and cardiac muscle : マウス骨格筋および心筋におけるVAMP5の発現と分布. (Thesis). Gunma University / 群馬大学. Retrieved from http://hdl.handle.net/10087/9093

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):

高橋, 麻衣子. “The localization of VAMP5 in skeletal and cardiac muscle : マウス骨格筋および心筋におけるVAMP5の発現と分布.” 2015. Thesis, Gunma University / 群馬大学. Accessed July 11, 2020. http://hdl.handle.net/10087/9093.

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

MLA Handbook (7th Edition):

高橋, 麻衣子. “The localization of VAMP5 in skeletal and cardiac muscle : マウス骨格筋および心筋におけるVAMP5の発現と分布.” 2015. Web. 11 Jul 2020.

Vancouver:

高橋 . The localization of VAMP5 in skeletal and cardiac muscle : マウス骨格筋および心筋におけるVAMP5の発現と分布. [Internet] [Thesis]. Gunma University / 群馬大学; 2015. [cited 2020 Jul 11]. Available from: http://hdl.handle.net/10087/9093.

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

Council of Science Editors:

高橋 . The localization of VAMP5 in skeletal and cardiac muscle : マウス骨格筋および心筋におけるVAMP5の発現と分布. [Thesis]. Gunma University / 群馬大学; 2015. Available from: http://hdl.handle.net/10087/9093

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

30. Jiang, Hongyuan. Internal degrees of freedom in membranes and synchronization phenomena at low Reynolds number.

Degree: PhD, Division of Engineering. Mechanics of Solids, 2009, Brown University

 The cell membrane is not a simple assembly of lipids and proteins. There are many internal degrees of freedom in a membrane, such as the… (more)

Subjects/Keywords: vesicle shape

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

APA (6th Edition):

Jiang, H. (2009). Internal degrees of freedom in membranes and synchronization phenomena at low Reynolds number. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:184/

Chicago Manual of Style (16th Edition):

Jiang, Hongyuan. “Internal degrees of freedom in membranes and synchronization phenomena at low Reynolds number.” 2009. Doctoral Dissertation, Brown University. Accessed July 11, 2020. https://repository.library.brown.edu/studio/item/bdr:184/.

MLA Handbook (7th Edition):

Jiang, Hongyuan. “Internal degrees of freedom in membranes and synchronization phenomena at low Reynolds number.” 2009. Web. 11 Jul 2020.

Vancouver:

Jiang H. Internal degrees of freedom in membranes and synchronization phenomena at low Reynolds number. [Internet] [Doctoral dissertation]. Brown University; 2009. [cited 2020 Jul 11]. Available from: https://repository.library.brown.edu/studio/item/bdr:184/.

Council of Science Editors:

Jiang H. Internal degrees of freedom in membranes and synchronization phenomena at low Reynolds number. [Doctoral Dissertation]. Brown University; 2009. Available from: https://repository.library.brown.edu/studio/item/bdr:184/

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