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Cells|February 5, 2020
Proteomic Analysis of Brain Region and Sex-Specific Synaptic Protein Expression in the Adult Mouse BrainUte Distler, Sven Schumann, Hans-Georg Kesseler, et al.
Frontiers in Synaptic Neuroscience|June 3, 2016
The Shank3 Interaction Partner ProSAPiP1 Regulates Postsynaptic SPAR Levels and the Maturation of Dendritic Spines in Hippocampal NeuronsDominik Reim, Tobias M Weis, Sonja Halbedl, et al.
Experimental Neurology|January 3, 2014
The PSD protein ProSAP2/Shank3 displays synapto-nuclear shuttling which is deregulated in a schizophrenia-associated mutationStefanie Grabrucker, Christian Proepper, Katharina Mangus, et al.
Frontiers in Molecular Neuroscience|March 7, 2017
Proteomic Analysis of Post-synaptic Density Fractions from Shank3 Mutant Mice Reveals Brain Region Specific Changes Relevant to Autism Spectrum DisorderDominik Reim, Ute Distler, Sonja Halbedl, et al.
Human Mutation|September 18, 2022
Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndromeErnestine Treimer, Tugba Kalayci, Sven Schumann, et al.
Neural Development|September 19, 2013
The Nedd4-binding protein 3 (N4BP3) is crucial for axonal and dendritic branching in developing neuronsMichael J Schmeisser, Susanne J Kühl, Michael Schoen, et al.
Frontiers in Cell and Developmental Biology|July 24, 2025
Itpka depletion implicates defects in anterior neural development of Xenopus laevisErnestine Saumweber, Marie-Christine Becker, Sophie Kunkel, et al.
Frontiers in Cellular Neuroscience|May 21, 2016
Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse HippocampusChristopher Heise, Jan C Schroeder, Michael Schoen, et al.
Deutsche Medizinische Wochenschrift (1946)|March 24, 1978
[Coronary angiographic findings in 308 patients with the clinical diagnosis of intramural myocardial infarction (author's transl)]H Roskamm, L Samek, T Cherchez, et al.
Molecular Autism|June 6, 2015
Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or IDDaniela M Cochoy, Alexander Kolevzon, Yuji Kajiwara, et al.
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