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You searched for subject:(Dendritic Development). Showing records 1 – 18 of 18 total matches.

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Loyola University Chicago

1. Case, Alicia Marie. Effects of Neuronal Nogo-A on Properties of Excitatory Synapses of the Sensorimotor Cortex.

Degree: PhD, Neuroscience, 2011, Loyola University Chicago

  Recovery after central nervous system (CNS) injury has long been a challenge for clinical investigators. Blockade of the oligodendrocyte-associated inhibitor Nogo-A has shown great… (more)

Subjects/Keywords: AAV; dendritic spine; Development; Nogo-A; shRNA; synapse; Neuroscience and Neurobiology

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APA (6th Edition):

Case, A. M. (2011). Effects of Neuronal Nogo-A on Properties of Excitatory Synapses of the Sensorimotor Cortex. (Doctoral Dissertation). Loyola University Chicago. Retrieved from https://ecommons.luc.edu/luc_diss/192

Chicago Manual of Style (16th Edition):

Case, Alicia Marie. “Effects of Neuronal Nogo-A on Properties of Excitatory Synapses of the Sensorimotor Cortex.” 2011. Doctoral Dissertation, Loyola University Chicago. Accessed July 17, 2019. https://ecommons.luc.edu/luc_diss/192.

MLA Handbook (7th Edition):

Case, Alicia Marie. “Effects of Neuronal Nogo-A on Properties of Excitatory Synapses of the Sensorimotor Cortex.” 2011. Web. 17 Jul 2019.

Vancouver:

Case AM. Effects of Neuronal Nogo-A on Properties of Excitatory Synapses of the Sensorimotor Cortex. [Internet] [Doctoral dissertation]. Loyola University Chicago; 2011. [cited 2019 Jul 17]. Available from: https://ecommons.luc.edu/luc_diss/192.

Council of Science Editors:

Case AM. Effects of Neuronal Nogo-A on Properties of Excitatory Synapses of the Sensorimotor Cortex. [Doctoral Dissertation]. Loyola University Chicago; 2011. Available from: https://ecommons.luc.edu/luc_diss/192


University of Minnesota

2. Penrod-Martin, Rachel Dobrof. Morphological characterization of medium spiny neuron development in vitro.

Degree: PhD, Neuroscience, 2012, University of Minnesota

 Medium Spiny Neurons (MSNs) are the primary cell type of the striatum, a structure critically involved in motivation, memory, and movement. MSN structure and function… (more)

Subjects/Keywords: Cell culture; Dendritic spine; Development; Medium spiny neuron

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APA (6th Edition):

Penrod-Martin, R. D. (2012). Morphological characterization of medium spiny neuron development in vitro. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/151475

Chicago Manual of Style (16th Edition):

Penrod-Martin, Rachel Dobrof. “Morphological characterization of medium spiny neuron development in vitro.” 2012. Doctoral Dissertation, University of Minnesota. Accessed July 17, 2019. http://purl.umn.edu/151475.

MLA Handbook (7th Edition):

Penrod-Martin, Rachel Dobrof. “Morphological characterization of medium spiny neuron development in vitro.” 2012. Web. 17 Jul 2019.

Vancouver:

Penrod-Martin RD. Morphological characterization of medium spiny neuron development in vitro. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2019 Jul 17]. Available from: http://purl.umn.edu/151475.

Council of Science Editors:

Penrod-Martin RD. Morphological characterization of medium spiny neuron development in vitro. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/151475

3. Lee, Kevin Fu-Hsiang. Dynamics of Synapse Function during Postnatal Development and Homeostatic Plasticity in Central Neurons .

Degree: 2015, University of Ottawa

 The majority of fast excitatory neurotransmission in the brain occurs at glutamatergic synapses. The extensive dendritic arborisations of pyramidal neurons in the neocortex and hippocampus… (more)

Subjects/Keywords: Synapse; Dendritic spines; AMPA; NMDA; Electrophysiology; Two-photon; Calcium imaging; Glutamate uncaging; Neural circuit development; Dendritic spines

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APA (6th Edition):

Lee, K. F. (2015). Dynamics of Synapse Function during Postnatal Development and Homeostatic Plasticity in Central Neurons . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32449

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, Kevin Fu-Hsiang. “Dynamics of Synapse Function during Postnatal Development and Homeostatic Plasticity in Central Neurons .” 2015. Thesis, University of Ottawa. Accessed July 17, 2019. http://hdl.handle.net/10393/32449.

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

MLA Handbook (7th Edition):

Lee, Kevin Fu-Hsiang. “Dynamics of Synapse Function during Postnatal Development and Homeostatic Plasticity in Central Neurons .” 2015. Web. 17 Jul 2019.

Vancouver:

Lee KF. Dynamics of Synapse Function during Postnatal Development and Homeostatic Plasticity in Central Neurons . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/10393/32449.

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

Council of Science Editors:

Lee KF. Dynamics of Synapse Function during Postnatal Development and Homeostatic Plasticity in Central Neurons . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32449

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


University of Colorado

4. Hiester, Brian Gibson. Determining the role of Wnt signaling during BDNF-induced cortical neuron growth and dendritic spine formation.

Degree: PhD, 2012, University of Colorado

Dendritic spines are major sites of excitatory synaptic transmission and changes in their densities and morphologies have been linked to neurodevelopmental disorders and neurodegenerative… (more)

Subjects/Keywords: BDNF; Dendritic Spine; Neural Development; Neurotrophin; Synapse; Wnt; Cell Biology; Molecular Biology; Neuroscience and Neurobiology

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APA (6th Edition):

Hiester, B. G. (2012). Determining the role of Wnt signaling during BDNF-induced cortical neuron growth and dendritic spine formation. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/mcdb_gradetds/13

Chicago Manual of Style (16th Edition):

Hiester, Brian Gibson. “Determining the role of Wnt signaling during BDNF-induced cortical neuron growth and dendritic spine formation.” 2012. Doctoral Dissertation, University of Colorado. Accessed July 17, 2019. http://scholar.colorado.edu/mcdb_gradetds/13.

MLA Handbook (7th Edition):

Hiester, Brian Gibson. “Determining the role of Wnt signaling during BDNF-induced cortical neuron growth and dendritic spine formation.” 2012. Web. 17 Jul 2019.

Vancouver:

Hiester BG. Determining the role of Wnt signaling during BDNF-induced cortical neuron growth and dendritic spine formation. [Internet] [Doctoral dissertation]. University of Colorado; 2012. [cited 2019 Jul 17]. Available from: http://scholar.colorado.edu/mcdb_gradetds/13.

Council of Science Editors:

Hiester BG. Determining the role of Wnt signaling during BDNF-induced cortical neuron growth and dendritic spine formation. [Doctoral Dissertation]. University of Colorado; 2012. Available from: http://scholar.colorado.edu/mcdb_gradetds/13


University of Washington

5. Buechler, Matthew Bryan. Type I IFN, Toll-like Receptor Signaling and Myeloid Homeostasis.

Degree: PhD, 2014, University of Washington

 The roles of toll-like receptor and type I interferon signaling in modulating myeloid homeostasis are incompletely defined. Here, we investigate how these factors interact to… (more)

Subjects/Keywords: Emergency Myelopoiesis; Myeloid Development; Plasmacytoid Dendritic Cell; Toll-like Receptor; Type I IFN; Immunology; immunology

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APA (6th Edition):

Buechler, M. B. (2014). Type I IFN, Toll-like Receptor Signaling and Myeloid Homeostasis. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/26104

Chicago Manual of Style (16th Edition):

Buechler, Matthew Bryan. “Type I IFN, Toll-like Receptor Signaling and Myeloid Homeostasis.” 2014. Doctoral Dissertation, University of Washington. Accessed July 17, 2019. http://hdl.handle.net/1773/26104.

MLA Handbook (7th Edition):

Buechler, Matthew Bryan. “Type I IFN, Toll-like Receptor Signaling and Myeloid Homeostasis.” 2014. Web. 17 Jul 2019.

Vancouver:

Buechler MB. Type I IFN, Toll-like Receptor Signaling and Myeloid Homeostasis. [Internet] [Doctoral dissertation]. University of Washington; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1773/26104.

Council of Science Editors:

Buechler MB. Type I IFN, Toll-like Receptor Signaling and Myeloid Homeostasis. [Doctoral Dissertation]. University of Washington; 2014. Available from: http://hdl.handle.net/1773/26104


University of Oxford

6. Wefelmeyer, Winnie. Calcium and chloride dynamics in immature neurons and their role in dendritic growth.

Degree: PhD, 2010, University of Oxford

 Activity-dependent dendritic development is an important process in the maturation of neuronal circuits. The precise morphology of a neuron’s dendritic tree dictates which other cells… (more)

Subjects/Keywords: 612.8; Physiology and anatomy; Neuroscience; Medical Sciences; neuroscience; dendritic development; chloride; calcium; dendrites

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APA (6th Edition):

Wefelmeyer, W. (2010). Calcium and chloride dynamics in immature neurons and their role in dendritic growth. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:5b67b345-8469-4370-8e3f-68bef6a629e9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534177

Chicago Manual of Style (16th Edition):

Wefelmeyer, Winnie. “Calcium and chloride dynamics in immature neurons and their role in dendritic growth.” 2010. Doctoral Dissertation, University of Oxford. Accessed July 17, 2019. http://ora.ox.ac.uk/objects/uuid:5b67b345-8469-4370-8e3f-68bef6a629e9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534177.

MLA Handbook (7th Edition):

Wefelmeyer, Winnie. “Calcium and chloride dynamics in immature neurons and their role in dendritic growth.” 2010. Web. 17 Jul 2019.

Vancouver:

Wefelmeyer W. Calcium and chloride dynamics in immature neurons and their role in dendritic growth. [Internet] [Doctoral dissertation]. University of Oxford; 2010. [cited 2019 Jul 17]. Available from: http://ora.ox.ac.uk/objects/uuid:5b67b345-8469-4370-8e3f-68bef6a629e9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534177.

Council of Science Editors:

Wefelmeyer W. Calcium and chloride dynamics in immature neurons and their role in dendritic growth. [Doctoral Dissertation]. University of Oxford; 2010. Available from: http://ora.ox.ac.uk/objects/uuid:5b67b345-8469-4370-8e3f-68bef6a629e9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.534177


Vrije Universiteit Amsterdam

7. Beijer, M.R. Dendritic cells and macrophages in the spleen: Development, function, and collaboration .

Degree: 2014, Vrije Universiteit Amsterdam

Subjects/Keywords: Immunology; dendritic cell; macrophage; vitamin A; development

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APA (6th Edition):

Beijer, M. R. (2014). Dendritic cells and macrophages in the spleen: Development, function, and collaboration . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/53343

Chicago Manual of Style (16th Edition):

Beijer, M R. “Dendritic cells and macrophages in the spleen: Development, function, and collaboration .” 2014. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed July 17, 2019. http://hdl.handle.net/1871/53343.

MLA Handbook (7th Edition):

Beijer, M R. “Dendritic cells and macrophages in the spleen: Development, function, and collaboration .” 2014. Web. 17 Jul 2019.

Vancouver:

Beijer MR. Dendritic cells and macrophages in the spleen: Development, function, and collaboration . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1871/53343.

Council of Science Editors:

Beijer MR. Dendritic cells and macrophages in the spleen: Development, function, and collaboration . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2014. Available from: http://hdl.handle.net/1871/53343


University of Michigan

8. Wang, Xin. Molecular Mechanisms that Differentiate Dendritic and Axonal Growth.

Degree: PhD, Molecular, Cellular and Developmental Biology, 2014, University of Michigan

 The nervous system controls our perception, behavior, learning and memory. It consists of billions of cells called neurons. A neuron typically contains an information input… (more)

Subjects/Keywords: Dendritic Development; Axonal Development; Dual Leucine Zipper Kinase (DLK); Down Syndrome Cell Adhesion Molecule (Dscam); KrüPpel-like Transcription Factor Dar1; Synaptic Growth; Molecular, Cellular and Developmental Biology; Science

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APA (6th Edition):

Wang, X. (2014). Molecular Mechanisms that Differentiate Dendritic and Axonal Growth. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/107291

Chicago Manual of Style (16th Edition):

Wang, Xin. “Molecular Mechanisms that Differentiate Dendritic and Axonal Growth.” 2014. Doctoral Dissertation, University of Michigan. Accessed July 17, 2019. http://hdl.handle.net/2027.42/107291.

MLA Handbook (7th Edition):

Wang, Xin. “Molecular Mechanisms that Differentiate Dendritic and Axonal Growth.” 2014. Web. 17 Jul 2019.

Vancouver:

Wang X. Molecular Mechanisms that Differentiate Dendritic and Axonal Growth. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2027.42/107291.

Council of Science Editors:

Wang X. Molecular Mechanisms that Differentiate Dendritic and Axonal Growth. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/107291

9. Duarte, Joao Nuno Silva. Antigen-targeting strategies using single-domain antibody fragments.

Degree: 2017, University Utrecht

 Antibodies display high selectivity and affinity and have been the preferred platform for antigen targeting. Despite the development of antigen-delivery systems that enable T cell… (more)

Subjects/Keywords: Antibodies; VHH; sortase; antigen-targeting; vaccine development; dendritic cell; immunity

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APA (6th Edition):

Duarte, J. N. S. (2017). Antigen-targeting strategies using single-domain antibody fragments. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/348798 ; URN:NBN:NL:UI:10-1874-348798 ; URN:NBN:NL:UI:10-1874-348798 ; http://dspace.library.uu.nl/handle/1874/348798

Chicago Manual of Style (16th Edition):

Duarte, Joao Nuno Silva. “Antigen-targeting strategies using single-domain antibody fragments.” 2017. Doctoral Dissertation, University Utrecht. Accessed July 17, 2019. http://dspace.library.uu.nl/handle/1874/348798 ; URN:NBN:NL:UI:10-1874-348798 ; URN:NBN:NL:UI:10-1874-348798 ; http://dspace.library.uu.nl/handle/1874/348798.

MLA Handbook (7th Edition):

Duarte, Joao Nuno Silva. “Antigen-targeting strategies using single-domain antibody fragments.” 2017. Web. 17 Jul 2019.

Vancouver:

Duarte JNS. Antigen-targeting strategies using single-domain antibody fragments. [Internet] [Doctoral dissertation]. University Utrecht; 2017. [cited 2019 Jul 17]. Available from: http://dspace.library.uu.nl/handle/1874/348798 ; URN:NBN:NL:UI:10-1874-348798 ; URN:NBN:NL:UI:10-1874-348798 ; http://dspace.library.uu.nl/handle/1874/348798.

Council of Science Editors:

Duarte JNS. Antigen-targeting strategies using single-domain antibody fragments. [Doctoral Dissertation]. University Utrecht; 2017. Available from: http://dspace.library.uu.nl/handle/1874/348798 ; URN:NBN:NL:UI:10-1874-348798 ; URN:NBN:NL:UI:10-1874-348798 ; http://dspace.library.uu.nl/handle/1874/348798


University of Illinois – Urbana-Champaign

10. Aldridge, Georgina. When good synapses go bad: dendritic spine dysgenesis in a mouse model of Fragile X mental retardation.

Degree: PhD, 0323, 2012, University of Illinois – Urbana-Champaign

 Fragile X Syndrome (FXS) is the leading inherited cause of mental retardation, and the most common identified genetic cause of autism. Although many phenotypes have… (more)

Subjects/Keywords: Fragile X Syndrome; dendritic spines; development; 2-photon; multiphoton; lithium; Gene Therapy; viral vector; Fragile X Mental Retardation Protein (FMRP); synapse; mouse model

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APA (6th Edition):

Aldridge, G. (2012). When good synapses go bad: dendritic spine dysgenesis in a mouse model of Fragile X mental retardation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/29550

Chicago Manual of Style (16th Edition):

Aldridge, Georgina. “When good synapses go bad: dendritic spine dysgenesis in a mouse model of Fragile X mental retardation.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/29550.

MLA Handbook (7th Edition):

Aldridge, Georgina. “When good synapses go bad: dendritic spine dysgenesis in a mouse model of Fragile X mental retardation.” 2012. Web. 17 Jul 2019.

Vancouver:

Aldridge G. When good synapses go bad: dendritic spine dysgenesis in a mouse model of Fragile X mental retardation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/29550.

Council of Science Editors:

Aldridge G. When good synapses go bad: dendritic spine dysgenesis in a mouse model of Fragile X mental retardation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/29550

11. Vonhoff, Fernando Jaime. A Single Neuron Model to Study the Mechanisms and Functions of Dendritic Development.

Degree: PhD, Neuroscience, 2012, Arizona State University

 Dendrites are the structures of a neuron specialized to receive input signals and to provide the substrate for the formation of synaptic contacts with other… (more)

Subjects/Keywords: Neurosciences; Dendrite; Dendritic growth; Drosophila; Genetic model; Motoneuron; Neuronal development

…Bernhardt & Matus, 1984; Clark et al., 1997). Much less is known about dendritic development… …Dendritic Growth Studies on dendritic development have shown that dendritic architecture is… …specific genes regulate dendritic development. The nematode, Caenorhabditis elegans, the fruit… …into molecular mechanisms regulating dendritic development such as cytoskeletal dynamics… …dendritic shape development and then test the behavioral consequences from misregulation of MN5… 

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APA (6th Edition):

Vonhoff, F. J. (2012). A Single Neuron Model to Study the Mechanisms and Functions of Dendritic Development. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/14721

Chicago Manual of Style (16th Edition):

Vonhoff, Fernando Jaime. “A Single Neuron Model to Study the Mechanisms and Functions of Dendritic Development.” 2012. Doctoral Dissertation, Arizona State University. Accessed July 17, 2019. http://repository.asu.edu/items/14721.

MLA Handbook (7th Edition):

Vonhoff, Fernando Jaime. “A Single Neuron Model to Study the Mechanisms and Functions of Dendritic Development.” 2012. Web. 17 Jul 2019.

Vancouver:

Vonhoff FJ. A Single Neuron Model to Study the Mechanisms and Functions of Dendritic Development. [Internet] [Doctoral dissertation]. Arizona State University; 2012. [cited 2019 Jul 17]. Available from: http://repository.asu.edu/items/14721.

Council of Science Editors:

Vonhoff FJ. A Single Neuron Model to Study the Mechanisms and Functions of Dendritic Development. [Doctoral Dissertation]. Arizona State University; 2012. Available from: http://repository.asu.edu/items/14721

12. Sloniowski, Slawomir. Effects of Systemic Inflammation on Synaptogenesis in Developing Mouse Hippocampus.

Degree: Neuroscience, 2011, University of California – Riverside

 Synapses are specialized points of contact between neurons allowing for rapid transfer of signals in electrical or chemical form. Synaptic transmission and plasticity are integral… (more)

Subjects/Keywords: Neurosciences; Immunology; Developmental biology; dendritic spine; development; hippocampus; inflammation; synapse; TREM2

…44 Chapter 2 - Dendritic Spine and Synaptic Development in Healthy, Unmanipulated Wild… …reactive astrocytes ...…...52 Figure 2.1 Development of dendritic spines of hippocampal… …analysis of dendritic spine development ..….71 Figure 2.3 Quantitative… …morphometric analysis of dendritic spine development – distributions of spine measures …...…73… …2005). Dendritic spine formation During early rat hippocampal development, contribution… 

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APA (6th Edition):

Sloniowski, S. (2011). Effects of Systemic Inflammation on Synaptogenesis in Developing Mouse Hippocampus. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/29z9h1c3

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):

Sloniowski, Slawomir. “Effects of Systemic Inflammation on Synaptogenesis in Developing Mouse Hippocampus.” 2011. Thesis, University of California – Riverside. Accessed July 17, 2019. http://www.escholarship.org/uc/item/29z9h1c3.

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

MLA Handbook (7th Edition):

Sloniowski, Slawomir. “Effects of Systemic Inflammation on Synaptogenesis in Developing Mouse Hippocampus.” 2011. Web. 17 Jul 2019.

Vancouver:

Sloniowski S. Effects of Systemic Inflammation on Synaptogenesis in Developing Mouse Hippocampus. [Internet] [Thesis]. University of California – Riverside; 2011. [cited 2019 Jul 17]. Available from: http://www.escholarship.org/uc/item/29z9h1c3.

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

Council of Science Editors:

Sloniowski S. Effects of Systemic Inflammation on Synaptogenesis in Developing Mouse Hippocampus. [Thesis]. University of California – Riverside; 2011. Available from: http://www.escholarship.org/uc/item/29z9h1c3

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


McGill University

13. Haber, Michael. Investigating glial dynamics in the developing hippocampus.

Degree: PhD, Division of Neuroscience., 2008, McGill University

 Glial cells represent the most abundant cell population in the central nervous system (CNS), and yet, have historically been thought of as merely support cells… (more)

Subjects/Keywords: Hippocampus  – growth & development.; Hippocampus  – physiology.; Astrocytes  – physiology.; Oligodendroglia  – physiology.; Dendritic Spines  – physiology.; Axons  – physiology.; Cell Communication  – physiology.

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APA (6th Edition):

Haber, M. (2008). Investigating glial dynamics in the developing hippocampus. (Doctoral Dissertation). McGill University. Retrieved from http://digitool.library.mcgill.ca/thesisfile115681.pdf

Chicago Manual of Style (16th Edition):

Haber, Michael. “Investigating glial dynamics in the developing hippocampus.” 2008. Doctoral Dissertation, McGill University. Accessed July 17, 2019. http://digitool.library.mcgill.ca/thesisfile115681.pdf.

MLA Handbook (7th Edition):

Haber, Michael. “Investigating glial dynamics in the developing hippocampus.” 2008. Web. 17 Jul 2019.

Vancouver:

Haber M. Investigating glial dynamics in the developing hippocampus. [Internet] [Doctoral dissertation]. McGill University; 2008. [cited 2019 Jul 17]. Available from: http://digitool.library.mcgill.ca/thesisfile115681.pdf.

Council of Science Editors:

Haber M. Investigating glial dynamics in the developing hippocampus. [Doctoral Dissertation]. McGill University; 2008. Available from: http://digitool.library.mcgill.ca/thesisfile115681.pdf

14. Jarjour, Meryem. Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage : Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage.

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

Les Cellules Folliculaires Dendritiques (FDC) régulent l'homéostasie des lymphocytes B et sont indispensables à la mise en place des réponses immunes humorales. Les FDC s'organisent,… (more)

Subjects/Keywords: Cellules Folliculaires Dendritiques; Modèle murin; Traçage de la descendance cellulaire; Système multicolore in vivo; Developpement; Remodelage; Plasticité; Follicular Dendritic Cells; Mouse model; Fate mapping; Multicolor in vivo system; Development; Remodeling; Plasticity; 571

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APA (6th Edition):

Jarjour, M. (2014). Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage : Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4014

Chicago Manual of Style (16th Edition):

Jarjour, Meryem. “Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage : Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed July 17, 2019. http://www.theses.fr/2014AIXM4014.

MLA Handbook (7th Edition):

Jarjour, Meryem. “Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage : Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage.” 2014. Web. 17 Jul 2019.

Vancouver:

Jarjour M. Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage : Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2019 Jul 17]. Available from: http://www.theses.fr/2014AIXM4014.

Council of Science Editors:

Jarjour M. Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage : Plasticité des réseaux de cellules folliculaires dentritiques : Développement & remodelage. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4014


University of Melbourne

15. Naik, Shalin Hemant. Distinct precursors of the dendritic cell subtypes.

Degree: 2006, University of Melbourne

Dendritic cells (DC) are antigen-presenting cells that are critical for the initiation and regulation of the immune response. Several DC subtypes within mouse spleen have… (more)

Subjects/Keywords: dendritic cells; monocytes; subtypes; development; haematopoiesis; CD8+ DC; plasmacytoid DC; shortman; inflammation; GM-CSF; flt3 ligand; spleen

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APA (6th Edition):

Naik, S. H. (2006). Distinct precursors of the dendritic cell subtypes. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/39062

Chicago Manual of Style (16th Edition):

Naik, Shalin Hemant. “Distinct precursors of the dendritic cell subtypes.” 2006. Doctoral Dissertation, University of Melbourne. Accessed July 17, 2019. http://hdl.handle.net/11343/39062.

MLA Handbook (7th Edition):

Naik, Shalin Hemant. “Distinct precursors of the dendritic cell subtypes.” 2006. Web. 17 Jul 2019.

Vancouver:

Naik SH. Distinct precursors of the dendritic cell subtypes. [Internet] [Doctoral dissertation]. University of Melbourne; 2006. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/11343/39062.

Council of Science Editors:

Naik SH. Distinct precursors of the dendritic cell subtypes. [Doctoral Dissertation]. University of Melbourne; 2006. Available from: http://hdl.handle.net/11343/39062

16. Koss, Wendy. Development of the adolescent prefrontal cortex and basolateral amygdala and the effects of puberty and alcohol exposure.

Degree: PhD, 0338, 2013, University of Illinois – Urbana-Champaign

 Human structural magnetic resonance imaging (MRI) studies indicate that some neural regions such as the prefrontal cortex (PFC) and the amygdala continue to develop throughout… (more)

Subjects/Keywords: Development; Prefrontal Cortex; Adolescence; Basolateral Amygdala; Dendrites; Dendritic Spines; Alcohol; Puberty; Neuroanatomy

…consequences of late development and describesdendritic alterations that are occurring… …neural development during adolescence. Moreover, it has previously been found that the sex… …adult rats. 4 Adolescent Neural Development of the PFC and the Amygdala The PFC has been of… …underlying mechanisms of these changes may be reductionsin synapses or dendritic material, as well… …as well as early postnatal development inorder to establish proper neural connections… 

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

APA (6th Edition):

Koss, W. (2013). Development of the adolescent prefrontal cortex and basolateral amygdala and the effects of puberty and alcohol exposure. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45426

Chicago Manual of Style (16th Edition):

Koss, Wendy. “Development of the adolescent prefrontal cortex and basolateral amygdala and the effects of puberty and alcohol exposure.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed July 17, 2019. http://hdl.handle.net/2142/45426.

MLA Handbook (7th Edition):

Koss, Wendy. “Development of the adolescent prefrontal cortex and basolateral amygdala and the effects of puberty and alcohol exposure.” 2013. Web. 17 Jul 2019.

Vancouver:

Koss W. Development of the adolescent prefrontal cortex and basolateral amygdala and the effects of puberty and alcohol exposure. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/2142/45426.

Council of Science Editors:

Koss W. Development of the adolescent prefrontal cortex and basolateral amygdala and the effects of puberty and alcohol exposure. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45426

17. Paessens, L.C. Hematopoietic antigen presenting cells in the human thymic cortex: Evidence for a role in selection and removal of apoptotic thymocytes.

Degree: 2007, NARCIS

Subjects/Keywords: DC-SIGN; HLA-DM; ICAM-1; T-cell; T-cell development; TUNEL; VCAM-1; apoptosis; co-stimulation; co-stimulatory molecule; dendritic cell; hAPC; hematopoietic antigen presenting cell; macrophage; positive selection; removal of apoptotic cells; selection; thymocyte; thymus

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

APA (6th Edition):

Paessens, L. C. (2007). Hematopoietic antigen presenting cells in the human thymic cortex: Evidence for a role in selection and removal of apoptotic thymocytes. (Doctoral Dissertation). NARCIS. Retrieved from https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e ; urn:nbn:nl:ui:31-1871/13235 ; 38a368e5-cac8-4128-9948-f34655fcb85e ; 1871/13235 ; urn:nbn:nl:ui:31-1871/13235 ; https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e

Chicago Manual of Style (16th Edition):

Paessens, L C. “Hematopoietic antigen presenting cells in the human thymic cortex: Evidence for a role in selection and removal of apoptotic thymocytes.” 2007. Doctoral Dissertation, NARCIS. Accessed July 17, 2019. https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e ; urn:nbn:nl:ui:31-1871/13235 ; 38a368e5-cac8-4128-9948-f34655fcb85e ; 1871/13235 ; urn:nbn:nl:ui:31-1871/13235 ; https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e.

MLA Handbook (7th Edition):

Paessens, L C. “Hematopoietic antigen presenting cells in the human thymic cortex: Evidence for a role in selection and removal of apoptotic thymocytes.” 2007. Web. 17 Jul 2019.

Vancouver:

Paessens LC. Hematopoietic antigen presenting cells in the human thymic cortex: Evidence for a role in selection and removal of apoptotic thymocytes. [Internet] [Doctoral dissertation]. NARCIS; 2007. [cited 2019 Jul 17]. Available from: https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e ; urn:nbn:nl:ui:31-1871/13235 ; 38a368e5-cac8-4128-9948-f34655fcb85e ; 1871/13235 ; urn:nbn:nl:ui:31-1871/13235 ; https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e.

Council of Science Editors:

Paessens LC. Hematopoietic antigen presenting cells in the human thymic cortex: Evidence for a role in selection and removal of apoptotic thymocytes. [Doctoral Dissertation]. NARCIS; 2007. Available from: https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e ; urn:nbn:nl:ui:31-1871/13235 ; 38a368e5-cac8-4128-9948-f34655fcb85e ; 1871/13235 ; urn:nbn:nl:ui:31-1871/13235 ; https://research.vu.nl/en/publications/38a368e5-cac8-4128-9948-f34655fcb85e

18. Bergmann, Hannes. B cell and CD8- dendritic cell survival require CD74 proteolysis by the intramembrane endopeptidase SPPL2A .

Degree: 2016, Australian National University

 Unknown mechanisms that cause failures in B cell development can lead to humoral immunodeficiencies, autoimmune disorders or B cell malignancies. This thesis demonstrates that the… (more)

Subjects/Keywords: B cell development; dendritic cell development; SPPL2A; CD74; invariant chain; MHCII; Cathepsin S; antigen presentation; MIIC; endosome; intramembrane proteolysis; RIP; i-CLiPs; membrane protein degradation; storage disease; multilamellar bodies

…250 5.1 SPPL2A is needed for CD8- dendritic cell development........................ 251… …Mutation in Sppl2a causes defect in late B cell development”, Australasian Society for… …class II invariant chain cDC Conventional dendritic cells CFSE Carboxyfluorescein… …gene segment DAPI 4’,6-diamidino-2-phenylindole DC Dendritic cell DN Double negative… …buffer saline pDC plasmacytoid dendritic cells X PE Phytoerythrin PI… 

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

APA (6th Edition):

Bergmann, H. (2016). B cell and CD8- dendritic cell survival require CD74 proteolysis by the intramembrane endopeptidase SPPL2A . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/111074

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):

Bergmann, Hannes. “B cell and CD8- dendritic cell survival require CD74 proteolysis by the intramembrane endopeptidase SPPL2A .” 2016. Thesis, Australian National University. Accessed July 17, 2019. http://hdl.handle.net/1885/111074.

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

MLA Handbook (7th Edition):

Bergmann, Hannes. “B cell and CD8- dendritic cell survival require CD74 proteolysis by the intramembrane endopeptidase SPPL2A .” 2016. Web. 17 Jul 2019.

Vancouver:

Bergmann H. B cell and CD8- dendritic cell survival require CD74 proteolysis by the intramembrane endopeptidase SPPL2A . [Internet] [Thesis]. Australian National University; 2016. [cited 2019 Jul 17]. Available from: http://hdl.handle.net/1885/111074.

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

Council of Science Editors:

Bergmann H. B cell and CD8- dendritic cell survival require CD74 proteolysis by the intramembrane endopeptidase SPPL2A . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/111074

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

.