Auswahl der wissenschaftlichen Literatur zum Thema „Synaptic adhesion proteins“
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Zeitschriftenartikel zum Thema "Synaptic adhesion proteins"
Leshchyns’ka, Iryna, und Vladimir Sytnyk. „Synaptic Cell Adhesion Molecules in Alzheimer’s Disease“. Neural Plasticity 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/6427537.
Der volle Inhalt der QuelleZobel, K., S. E. Choi, R. Minakova, M. Gocyla und A. Offenhäusser. „N-Cadherin modified lipid bilayers promote neural network formation and circuitry“. Soft Matter 13, Nr. 44 (2017): 8096–107. http://dx.doi.org/10.1039/c7sm01214d.
Der volle Inhalt der QuelleHayano, Yasufumi, Yugo Ishino, Jung Ho Hyun, Carlos G. Orozco, André Steinecke, Elizabeth Potts, Yasuhiro Oisi et al. „IgSF11 homophilic adhesion proteins promote layer-specific synaptic assembly of the cortical interneuron subtype“. Science Advances 7, Nr. 29 (Juli 2021): eabf1600. http://dx.doi.org/10.1126/sciadv.abf1600.
Der volle Inhalt der QuelleBrose, N. „Neuroligin-family synaptic adhesion proteins in autism spectrum disorders“. European Neuropsychopharmacology 26 (Oktober 2016): S131. http://dx.doi.org/10.1016/s0924-977x(16)30913-0.
Der volle Inhalt der QuelleStewart, Luke T. „Cell adhesion proteins and the pathogenesis of autism spectrum disorders“. Journal of Neurophysiology 113, Nr. 5 (01.03.2015): 1283–86. http://dx.doi.org/10.1152/jn.00780.2013.
Der volle Inhalt der QuelleLee, Tet Woo, Vicky W. K. Tsang und Nigel P. Birch. „Synaptic plasticity-associated proteases and protease inhibitors in the brain linked to the processing of extracellular matrix and cell adhesion molecules“. Neuron Glia Biology 4, Nr. 3 (August 2008): 223–34. http://dx.doi.org/10.1017/s1740925x09990172.
Der volle Inhalt der QuelleUchida, N., Y. Honjo, K. R. Johnson, M. J. Wheelock und M. Takeichi. „The catenin/cadherin adhesion system is localized in synaptic junctions bordering transmitter release zones.“ Journal of Cell Biology 135, Nr. 3 (01.11.1996): 767–79. http://dx.doi.org/10.1083/jcb.135.3.767.
Der volle Inhalt der QuelleOlsen, Olav, Kimberly A. Moore, Masaki Fukata, Toshinari Kazuta, Jonathan C. Trinidad, Fred W. Kauer, Michel Streuli et al. „Neurotransmitter release regulated by a MALS–liprin-α presynaptic complex“. Journal of Cell Biology 170, Nr. 7 (26.09.2005): 1127–34. http://dx.doi.org/10.1083/jcb.200503011.
Der volle Inhalt der QuelleCostain, Willard J., Ingrid Rasquinha, Jagdeep K. Sandhu, Peter Rippstein, Bogdan Zurakowski, Jacqueline Slinn, John P. MacManus und Danica B. Stanimirovic. „Cerebral Ischemia Causes Dysregulation of Synaptic Adhesion in Mouse Synaptosomes“. Journal of Cerebral Blood Flow & Metabolism 28, Nr. 1 (16.05.2007): 99–110. http://dx.doi.org/10.1038/sj.jcbfm.9600510.
Der volle Inhalt der QuelleRibic, Adema, und Thomas Biederer. „Emerging Roles of Synapse Organizers in the Regulation of Critical Periods“. Neural Plasticity 2019 (03.09.2019): 1–9. http://dx.doi.org/10.1155/2019/1538137.
Der volle Inhalt der QuelleDissertationen zum Thema "Synaptic adhesion proteins"
Ashley, James A. „The Role of Cell Adhesion, the Cytoskeleton, and Membrane Trafficking during Synapse Outgrowth: A Dissertation“. eScholarship@UMMS, 2006. http://escholarship.umassmed.edu/gsbs_diss/302.
Der volle Inhalt der QuellePiette, Nathalie. „Micropatterning subcellulaire pour étudier la connectivité neuronale“. Electronic Thesis or Diss., Bordeaux, 2024. http://www.theses.fr/2024BORD0034.
Der volle Inhalt der QuelleMicropatterning was initially employed to replicate and understand the influence of the extracellular matrix on cells and some of their components. Over the past decade, subcellular printing has emerged, enabling the study of protein interactions and their role in signaling pathways as well as in the formation of synaptic, immunological, or neuronal pathways.The synaptic connection is mediated by synaptic adhesion proteins present on each side of the synapse. Due to the complexity of the synaptic environment and the lack of in vitro models to study synaptic connection in a biomimetic and controlled environment, the exact roles of these proteins in synaptogenesis remain uncertain. Subcellular protein printing presents a potential solution to address this gap. For this purpose, we have developed two biomimetic models based on protein printing: a first one using heterologous cells, providing insights into the interaction kinetics of protein pairs and linking them to their potential function. And a second one using primary neurons, allowing the formation of artificial synapses to study synaptic nano-organization during development.The protein printing system PRIMO, commercialized by Alvéole, which is co-funding this thesis, is underutilized by neuroscientists. Besides these biological objectives, the industrial aim of this thesis is to develop methodologies and proofs of concept to demonstrate the advantages and feasibility of the PRIMO technology in neuroscience.By coupling our first model, based on heterologous cells, with live-cell imaging techniques (sptPALM and FRAP), we differentiated interaction kinetics among various synaptic adhesion protein pairs and also for interactions with scaffold proteins. A labile interaction was observed for SynCAM1, known for its role in synaptic morphology. A strong and stable interaction was evident for Neuroligin1/Neurexine1β due to Neuroligin1's dimerization, which is essential for synaptic functionality.With the second model using primary hippocampal neurons, we demonstrated, in the presence of LRRTM2, the specific formation of artificial synapses. These hemi-synapses exhibited morphological and functional characteristics close to native synapses, including the presence of vesicles and spontaneous calcium activity. However, we were unable to form artificial postsynapses with Neurexine1β. Based on our observations and bibliographic analysis, we hypothesize that the postsynapse could be the initiating compartment for synaptogenesis.In conclusion, this study demonstrates: (1) that subcellular printing is an excellent model to study synaptic connectivity and adhesion from both a functional and organizational perspective. (2) That models of hemi-synapses using micropatterning are more specific than previous models. (3) That the PRIMO system opens numerous perspectives in neuroscience through its quantitative printing capabilities
FAVALORO, FLORES LIETTA. „Analysis of mutations in synaptic adhesion molecules involved in neurodevelopmental disorders: cell mechanisms of endoplasmic reticulum retention and unfolded protein response activation“. Doctoral thesis, 2016. http://hdl.handle.net/11573/875615.
Der volle Inhalt der QuelleBuchteile zum Thema "Synaptic adhesion proteins"
Rujescu, Dan, und Peter Riederer. „Non-Monoaminergig Transmitters, Glia Cell Markers, Cell Adhesion Molecules and Synaptic Proteins in Postmortem Brain Tissue“. In Neurobiological Foundation of Aberrant Behaviors, 387–94. Boston, MA: Springer US, 2002. http://dx.doi.org/10.1007/978-1-4757-3631-1_21.
Der volle Inhalt der QuelleBenarroch, Eduardo E. „Synaptic Transmission and Presynaptic Synaptopathies“. In Neuroscience for Clinicians, herausgegeben von Eduardo E. Benarroch, 259–75. Oxford University Press, 2021. http://dx.doi.org/10.1093/med/9780190948894.003.0015.
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