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Autor:
Josef Zamecnik, Anatoly Korotkov, Martha Feucht, Mark J. Luinenburg, Wim Van Hecke, Jeong H Lee, Caroline Mijnsbergen, Lieven Lagae, Till S. Zimmer, Wim G.M. Spliet, Floor E. Jansen, Katarzyna Kotulska, Jackelien van Scheppingen, Paolo Curatolo, Jasper J. Anink, Nam Suk Sim, Angelika Mühlebner, Pavel Krsek, Johannes A. Hainfellner, Sergiusz Jozwiak, Peter C. van Rijen, Erwin A. van Vliet, Diede W. M. Broekaart, David J. Kwiatkowski, Peter B. Crino, Anna Jansen, Eleonora Aronica, Anika Bongaarts, James D. Mills
Publikováno v:
Neuropathology and Applied Neurobiology
Neuropathology and Applied Neurobiology, 47, 796-811. Wiley-Blackwell
Neuropathology and Applied Neurobiology, 47(6), 796-811. Wiley-Blackwell
Neuropathology and applied neurobiology, 47(6), 796-811. Wiley-Blackwell
Neuropathology and Applied Neurobiology, 47, 796-811. Wiley-Blackwell
Neuropathology and Applied Neurobiology, 47(6), 796-811. Wiley-Blackwell
Neuropathology and applied neurobiology, 47(6), 796-811. Wiley-Blackwell
Aims Tuberous sclerosis complex (TSC) is a genetic disorder associated with dysregulation of the mechanistic target of rapamycin complex 1 (mTORC1) signalling pathway. Neurodevelopmental disorders, frequently present in TSC, are linked to cortical tu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eb0f7241374fa2ea6880a3964dbd171
https://dare.uva.nl/personal/pure/en/publications/microrna34a-activation-in-tuberous-sclerosis-complex-during-early-brain-development-may-lead-to-impaired-corticogenesis(54e41bc9-19fa-4850-90b0-8be834807835).html
https://dare.uva.nl/personal/pure/en/publications/microrna34a-activation-in-tuberous-sclerosis-complex-during-early-brain-development-may-lead-to-impaired-corticogenesis(54e41bc9-19fa-4850-90b0-8be834807835).html
Publikováno v:
Journal of neurochemistry 150(5), 535-565 (2019). doi:10.1111/jnc.14707
Alpha-synuclein (α-Syn) is a central player in Parkinson's disease (PD) and in a spectrum of neurodegenerative diseases collectively known as synucleinopathies. The protein was first associated with PD just over 20 years ago, when it was found to (i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::449364f3840dcc23bb9ebc5f313ab981
Autor:
Barbara Stiller, Eckhard Mandelkow, Eva Maria Mandelkow, Benjamin Caballero, Ana Maria Cuervo, Yves R. Juste, Inmaculada Tasset, Antonio Diaz, Yipeng Wang
Publikováno v:
Aging cell 17(1), e12692 (2017). doi:10.1111/acel.12692
Aging Cell
Aging Cell
Summary Loss of neuronal proteostasis, a common feature of the aging brain, is accelerated in neurodegenerative disorders, including different types of tauopathies. Aberrant turnover of tau, a microtubule‐stabilizing protein, contributes to its acc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b2b95a92cdc02add0f08c195e65bd176
Autor:
Paula Schiapparelli, Gabrielle T. Drummond, Montserrat Lara-Velazquez, Alfredo Quiñones-Hinojosa, Linda Chen, Anne E. Burke, Anna Christina Clements, Emily Lavell, Katrina Thaler, Vivian Capilla-Gonzalez, Liron Noiman, Hugo Guerrero-Cazares
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
Guerrero-Cazares, Hugo et al.
Human neural progenitor cell (NPC) migration within the subventricular zone (SVZ) of the lateral ganglionic eminence is an active process throughout early brain development. The migration of human NPCs from the SVZ
Human neural progenitor cell (NPC) migration within the subventricular zone (SVZ) of the lateral ganglionic eminence is an active process throughout early brain development. The migration of human NPCs from the SVZ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6539ef2ce4ecf8eb4c6b27fb8f140829
http://hdl.handle.net/10261/165429
http://hdl.handle.net/10261/165429
Autor:
Heinz Beck, Tony Kelly
Publikováno v:
Epilepsia 58(1), 160-171 (2016). doi:10.1111/epi.13605
SummaryObjective The maturation of adult-born granule cells and their functional integration into the network is thought to play a key role in the proper functioning of the dentate gyrus. In temporal lobe epilepsy, adult-born granule cells in the den
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e29345e46dd5193db4ac42c825c62880
https://pub.dzne.de/record/139031
https://pub.dzne.de/record/139031
Autor:
Judith Stegmüller, Matthis Synofzik
Publikováno v:
Journal of neurochemistry 139(2), 159-161 (2016). doi:10.1111/jnc.13775
This Editorial highlights a study by Huang and colleagues in the current issue of Journal of Neurochemistry. The authors introduce a novel ALS-FTD (amyotrophic lateral sclerosis-frontotemporal dementia) rat model to explore the role of the UBLQN2 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57729bc13c8172fafcfe6228fa9ddf53
https://pub.dzne.de/record/138833
https://pub.dzne.de/record/138833
Autor:
Gregor Rainer, Anne Catherine Clerc, Sarah Sonnay, Rolf Gruetter, Jordan Poirot, João M. N. Duarte, Nathalie Just
Astrocytes play an important role in glutamatergic neurotransmission, namely by clearing synaptic glutamate and converting it into glutamine that is transferred back to neurons. The rate of this glutamate–glutamine cycle (VNT) has been proposed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::757ddb7ec424b8e8a91d251025429c74
https://infoscience.epfl.ch/record/232388
https://infoscience.epfl.ch/record/232388
Autor:
Laurent Venance, Merie Nassar, Philippe Faure, Laura Vanopdenbosch, Olivier De Backer, Sébastien Valverde, Bérangère Detraux, Adeline Gazan, Serge N. Schiffmann, Giuseppe Cannazza, Michele Zoli, Alban de Kerchove d'Exaerde, David Gall, Stéphanie Monlezun, Lídia Cantacorps, Olga Valverde, Julian Cheron, Jean-François De Backer
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
EMBO reports, 19 (9
instname
EMBO reports, 19 (9
Melanoma antigen genes (Mage) were first described as tumour markers. However, some of Mage are also expressed in healthy cells where their functions remain poorly understood. Here, we describe an unexpected role for one of these genes, Maged1, in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f91ed8b64c30d9af176d3e92690e0f3e
http://hdl.handle.net/10230/37044
http://hdl.handle.net/10230/37044