Zobrazeno 1 - 10
of 12
pro vyhledávání: '"physiology [Nerve Tissue Proteins]"'
Publikováno v:
Cell Reports, Vol 29, Iss 12, Pp 3767-3774.e3 (2019)
Cell reports 29(12), 3767-3774.e3 (2019). doi:10.1016/j.celrep.2019.11.060
Cell reports 29(12), 3767-3774.e3 (2019). doi:10.1016/j.celrep.2019.11.060
Summary: At presynaptic terminals, neurotransmitters are released by synaptic vesicle exocytosis at the active zone. In order to maintain efficient neurotransmission and proper synaptic structure, sites of vesicle fusion must be cleared rapidly by en
Autor:
Kevin Thome, Carolina Urrutia-Ruiz, Stefanie Grabrucker, Carlo Sala, Günter Ehret, Johanna Schweizer, Andreas M. Grabrucker, Tobias M. Boeckers, Michael Schön, Rong Zhang, Juergen Bockmann, Bastian Hengerer, Jessica Pagano, Chiara Verpelli
Publikováno v:
The EMBO journal 40(5), e104267 (2021). doi:10.15252/embj.2019104267
The EMBO Journal
The EMBO Journal
Impairments in social relationships and awareness are features observed in autism spectrum disorders (ASDs). However, the underlying mechanisms remain poorly understood. Shank2 is a high���confidence ASD candidate gene and localizes primarily t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a338e9ab894eff16eec4c405d9ab335c
Autor:
Martin Balastik, Eran Perlson, Romana Weissova, Roy Maimon, Thomas Misgeld, Tomas Petrasek, Marie Kleisnerova, Radislav Sedlacek, Jakub Ziak, Barbora Pukajova, Monika S. Brill, Mengzhe Wang, Xunlei Zhou, Ales Stuchlik, Gonzalo Alvarez-Bolado, Petr Kasparek, Kateřina Jeřábková, Martina Janikova
Publikováno v:
EMBO reports 21(3), e48512 (2020). doi:10.15252/embr.201948512
EMBO Rep
EMBO Rep
Regulation of axon guidance and pruning of inappropriate synapses by class 3 semaphorins is key to development of neural circuits. Collapsin response mediator protein 2 (CRMP2) has been shown to regulate axon guidance by mediating Semaphorin 3A (Sema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a56216d97953369ea91f656705aad9e2
https://doi.org/10.1101/719617
https://doi.org/10.1101/719617
Autor:
Nigel J. Cairns, Merel O. Mol, Gregory D. Jenkins, Leonard Petrucelli, Nilufer Ertekin-Taner, Stuart Pickering-Brown, Carlos Cruchaga, Edward B. Lee, Jonathan D. Glass, John C. van Swieten, Jonathan D. Rohrer, Keith A. Josephs, Patrizia Rizzu, Johannes Prudlo, Edward D. Huey, Cristina T. Vicente, Shulan Tian, Claire Troakes, Ging-Yuek Robin Hsiung, Julie S. Snowden, Lawrence S. Honig, Jean Paul G. Vonsattel, Yan W. Asmann, Matthis Synofzik, Sigrun Roeber, Jeroen van Rooij, Ralph B. Perkerson, Eric M. Reiman, Charles L. White, Ethan G. Geier, Billie J. Matchett, Robert A. Rissman, Julia Keith, David J. Irwin, Manuela Neumann, Dieter Edbauer, M.-Marsel Mesulam, Jochen Herms, Vivianna M. Van Deerlin, Jordan Grafman, Melissa E. Murray, Oscar L. Lopez, Bernardino Ghetti, Rosa Rademakers, Bradley F. Boeve, Ekaterina Rogaeva, Sara Rollinson, Marla Gearing, Geoffrey L. Ahern, Zachary C. Fogarty, Peter Heutink, Yingxue Ren, Javier Simón-Sánchez, David G. Mann, Bryan K. Woodruff, Ryan J. Uitti, Martin R. Farlow, Lea T. Grinberg, Murray Grossman, Julia Kofler, Ian R. A. Mackenzie, Jennifer S. Yokoyama, Lorne Zinman, Matt Baker, John Q. Trojanowski, Zbigniew K. Wszolek, Cyril Pottier, Changiz Geula, Thomas Arzberger, Dennis W. Dickson, Joanna M. Biernacka, William W. Seeley, Caroline Graff, Olivier Piguet, John B.J. Kwok, Joseph E. Parisi, Safa Al-Sarraj, Harro Seelaar, Elizabeth Christopher, Ronald C. Petersen, Linn Öijerstedt, Anna Karydas, Salvatore Spina, Carlo Wilke, Marka van Blitterswijk, Simon Mead, Janine Diehl-Schmid, Bret M. Evers, David S. Knopman, Kevin F. Bieniek, John R. Hodges, Anthony Batzler, Mariely DeJesus-Hernandez, Elizabeth Finger, Thomas G. Beach, EunRan Suh, Maria Carmela Tartaglia, Sandra Weintraub, Shannon K. McDonnell, Bruce L. Miller, Glenda M. Halliday, Andy King, Eileen H. Bigio, Neill R. Graff-Radford, Richard J. Caselli
Publikováno v:
Acta Neuropathologica, 137(6), 879-899. Springer-Verlag
Acta Neuropathol
Acta neuropathologica 137(6), 879-899 (2019). doi:10.1007/s00401-019-01962-9
Acta neuropathologica
Acta Neuropathol
Acta neuropathologica 137(6), 879-899 (2019). doi:10.1007/s00401-019-01962-9
Acta neuropathologica
Frontotemporal lobar degeneration with neuronal inclusions of the TAR DNA-binding protein 43 (FTLD-TDP) represents the most common pathological subtype of FTLD. We established the international FTLD-TDP whole-genome sequencing consortium to thoroughl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1500c504ddc41a67b8cb5e111941d5d5
https://pure.eur.nl/en/publications/ec4efc7a-1a6b-4346-af9a-7b821d069c4d
https://pure.eur.nl/en/publications/ec4efc7a-1a6b-4346-af9a-7b821d069c4d
Autor:
Arne Buschler, Sarah A. Shoichet, Chae-Seok Lim, Stephanie Wegener, Denise Manahan-Vaughan, Bong-Kiun Kaang, Sukjae Joshua Kang, A. Vanessa Stempel, Dietmar Schmitz
Publikováno v:
eNeuro 5(3), ENEURO.0398-17.2018 (2018). doi:10.1523/ENEURO.0398-17.2018
eNeuro
eNeuro
Visual Abstract
Autism spectrum disorders (ASDs) are neurodevelopmental disorders with a strong genetic etiology. Since mutations in human SHANK genes have been found in patients with autism, genetic mouse models are used for a mechanistic under
Autism spectrum disorders (ASDs) are neurodevelopmental disorders with a strong genetic etiology. Since mutations in human SHANK genes have been found in patients with autism, genetic mouse models are used for a mechanistic under
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f2100f9d2faa3afd1ae792b20a199b1
https://pub.dzne.de/record/141133
https://pub.dzne.de/record/141133
Autor:
Eckart D. Gundelfinger, Wolfgang Tischmeyer, Sabrina Müller, Frank Angenstein, Eike Budinger, Anna Fejtova, Dirk Montag, Gürsel Çalışkan, Anil Annamneedi, Oliver Stork
Publikováno v:
Brain structure & function 223(7), 3423-3445 (2018). doi:10.1007/s00429-018-1692-3
Brain Structure & Function
Brain structure & function, 223(7):3423-3445
Brain Structure & Function
Brain structure & function, 223(7):3423-3445
Bassoon is a large scaffolding protein of the presynaptic active zone involved in the development of presynaptic terminals and in the regulation of neurotransmitter release at both excitatory and inhibitory brain synapses. Mice with constitutive abla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1783b1152bc05f81496da78ea2aee22c
Autor:
Lisa van Ninhuijs, Jean Jacques Martin, Jonathan Baets, Annette Schenck, Erik-Jan Kamsteeg, Bart P.C. van de Warrenburg, Tine Deconinck, Rebecca Schüle, Stephan Züchner, Ilse Eidhof, Peter De Jonghe
Publikováno v:
Brain
Brain, 141, 9, pp. 2592-2604
Brain, 141, 2592-2604
Brain 141(9), 2592-2604 (2018). doi:10.1093/brain/awy198
Brain, 141, 9, pp. 2592-2604
Brain, 141, 2592-2604
Brain 141(9), 2592-2604 (2018). doi:10.1093/brain/awy198
Eidhofet al. report a new subtype of autosomal recessive cerebellar ataxia caused by mutations inGDAP2, and show thatGdap2 knockdown inDrosophila recapitulates locomotor dysfunction and shortened lifespan. Susceptibility to cellular stress in theGdap
Autor:
Michele Curcio, Frank Bradke
Publikováno v:
Neuron 88(6), 1072-1074 (2015). doi:10.1016/j.neuron.2015.12.006
The microtubule cytoskeleton is a major determinant in neuronal polarity. In this issue of Neuron, van Beuningen et al. (2015) now report that TRIM46 forms parallel microtubule bundles in the proximal axon and reveal that it is crucial for the establ
Autor:
Elena Alvarez-Baron, Thoralf Opitz, Tobias Mittelstaedt, Susanne Schoch, Katrin Michel, Heinz Beck, Dirk Dietrich, Albert J. Becker, Frank Schmitz
Publikováno v:
The journal of neuroscience 33(2), 824-839 (2013). doi:10.1523/JNEUROSCI.2229-12.2013
The large isoforms of the Rab3 interacting molecule (RIM) family, RIM1α/β and RIM2α/β, have been shown to be centrally involved in mediating presynaptic active zone function. The RIM protein family contains two additional small isoforms, RIM3γ a
Publikováno v:
Neuroscience 250, 557-564 (2013). doi:10.1016/j.neuroscience.2013.06.060
Neuroscience
Neuroscience
Motor learning requires protein synthesis within the primary motor cortex (M1). Here, we show that the immediate early gene Arc/Arg3.1 is specifically induced in M1 by learning a motor skill. Arc mRNA was quantified using a fluorescent in situ hybrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3758e6bed48ef6228bf96a1c5a66f157
https://pub.dzne.de/record/137050
https://pub.dzne.de/record/137050