Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Juergen Bock"'
Autor:
Diedrich, Christian, Belyaev, Alexander, Blumenfeld, Rafi, Juergen Bock, Grimm, Stephan, Hermann, Jesko, Klausmann, Tobias, Köcher, Aljosha, Maurmaier, Matthias, Meixner, Kristof, Peschke, Jörn, Schleipen, Miriam, Siwara Schmitt, Schnebel, Boris, Stephan, Guido, Volkmann, Magnus, Wannagat, Andreas, Watson, Kym, Winter, Michael, Zimmermann, Patrick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa7952345f9b56dfe8fa802faa129eb8
Autor:
Diedrich, Christian, Belyaev, Alexander, Vialkowitsch, Jens, Usländer, Thomas, Deppe, Torben, Pethig, Florian, Juergen Bock, Reich, Johannes, Willner, Alexander, Nehls, Daniel, Schell, Otto, Vollmar, Friedrich, Neidig, Jörg, Lieske, Matthias, Schulz, Thomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b197a4113e0bff06709966a26deec02
Autor:
Ekaterina Atanasova, Andrea Pérez Arévalo, Ines Graf, Rong Zhang, Juergen Bockmann, Anne-Kathrin Lutz, Tobias M. Boeckers
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract Background Autism spectrum disorder (ASD) is mainly characterized by deficits in social interaction and communication and repetitive behaviors. Known causes of ASD are mutations of certain risk genes like the postsynaptic protein SHANK3 and
Externí odkaz:
https://doaj.org/article/508bd4040ef242d8bc937e9009dc09be
Autor:
Sarah Jesse, Hans‐Peter Müller, Michael Schoen, Harun Asoglu, Juergen Bockmann, Hans‐Juergen Huppertz, Volker Rasche, Albert C. Ludolph, Tobias M. Boeckers, Jan Kassubek
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 7, Iss 1, Pp 46-58 (2020)
Abstract Objective Heterozygous SHANK3 mutations or partial deletions of the long arm of chromosome 22, also known as Phelan–McDermid syndrome, result in a syndromic form of the autism spectrum as well as in global developmental delay, intellectual
Externí odkaz:
https://doaj.org/article/87eb5db2bd2045e083b594b2fcc12b32
Autor:
Michael Schoen, Harun Asoglu, Helen F. Bauer, Hans-Peter Müller, Alireza Abaei, Ann Katrin Sauer, Rong Zhang, Tian-jia Song, Juergen Bockmann, Jan Kassubek, Volker Rasche, Andreas M. Grabrucker, Tobias M. Boeckers
Publikováno v:
Frontiers in Neural Circuits, Vol 13 (2019)
Research efforts over the past decades have unraveled both genetic and environmental factors, which contribute to the development of autism spectrum disorders (ASD). It is, to date, largely unknown how different underlying causes result in a common p
Externí odkaz:
https://doaj.org/article/13d027f67c1f4822bf6240febe20bbc1
Autor:
Stefan Liebau, Julie Steinestel, Leonhard Linta, Alexander Kleger, Alexander Storch, Michael Schoen, Konrad Steinestel, Christian Proepper, Juergen Bockmann, Michael J Schmeisser, Tobias M Boeckers
Publikováno v:
PLoS ONE, Vol 6, Iss 3, p e18148 (2011)
BackgroundThe stabilization or regulated reorganization of the actin cytoskeleton is essential for cellular structure and function. Recently, we could show that the activation of the SK3-channel that represents the predominant SK-channel in neural st
Externí odkaz:
https://doaj.org/article/0e0ea8c5a24d4b38b35ba8be100c8676
Autor:
Christian Proepper, Konrad Steinestel, Michael J Schmeisser, Jutta Heinrich, Julie Steinestel, Juergen Bockmann, Stefan Liebau, Tobias M Boeckers
Publikováno v:
PLoS ONE, Vol 6, Iss 11, p e27045 (2011)
BACKGROUND: Abelson-interacting protein 1 (Abi-1) plays an important role for dendritic branching and synapse formation in the central nervous system. It is localized at the postsynaptic density (PSD) and rapidly translocates to the nucleus upon syna
Externí odkaz:
https://doaj.org/article/8f45e73726fe4835acf2ea593895ab9d