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Molecular Autism|August 1, 2023
Shank3 deletion in PV neurons is associated with abnormal behaviors and neuronal functions that are rescued by increasing GABAergic signalingJessica Pagano, Silvia Landi, Alessia Stefanoni, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 7, 2013
Shank3-Rich2 interaction regulates AMPA receptor recycling and synaptic long-term potentiationFabrice Raynaud, Andrea Janossy, Janine Dahl, et al.
Neurobiology of Disease|August 9, 2015
Stepwise acquirement of hallmark neuropathology in FUS-ALS iPSC models depends on mutation type and neuronal agingJulia Japtok, Xenia Lojewski, Marcel Naumann, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|July 22, 1999
Proline-rich synapse-associated protein-1/cortactin binding protein 1 (ProSAP1/CortBP1) is a PDZ-domain protein highly enriched in the postsynaptic densityT M Boeckers, M R Kreutz, C Winter, et al.
The Journal of Biological Chemistry|July 31, 2013
SHANK3 gene mutations associated with autism facilitate ligand binding to the Shank3 ankyrin repeat regionMarie Germaine Mameza, Elena Dvoretskova, Margarete Bamann, et al.
Neuroscience|February 28, 2001
Kainate-induced seizures alter protein composition and N-methyl-D-aspartate receptor function of rat forebrain postsynaptic densitiesU Wyneken, K H Smalla, J J Marengo, et al.
Frontiers in Molecular Neuroscience|July 5, 2018
Heterogeneity of Cell Surface Glutamate and GABA Receptor Expression in Shank and CNTN4 Autism Mouse ModelsChristopher Heise, Jonathan M Preuss, Jan C Schroeder, et al.
Molecular Psychiatry|January 7, 2015
Identification and functional characterization of rare SHANK2 variants in schizophreniaS Peykov, S Berkel, M Schoen, et al.
Molecular Psychiatry|January 6, 2021
Developmental impaired Akt signaling in the Shank1 and Shank3 double knock-out miceAdele Mossa, Jessica Pagano, Luisa Ponzoni, et al.
Molecular Psychiatry|March 16, 2025
Shank3 modulates Rpl3 expression and protein synthesis via mGlu5: implications for Phelan McDermid syndromeFederica Giona, Stefania Beretta, Antonio Zippo, et al.
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