Genetic influences of autism candidate genes on circuit wiring and olfactory decoding

por Hartig, Renée, Wolf, David, Schmeisser, Michael J., Kelsch, Wolfgang
Publicado no Cell Tissue Res (2021)

Abnormalities of synaptic mitochondria in autism spectrum disorder and related neurodevelopmental disorders

por Rojas-Charry, Liliana, Nardi, Leonardo, Methner, Axel, Schmeisser, Michael J.
Publicado no J Mol Med (Berl) (2020)

Synaptic Cross-talk between N-Methyl-d-aspartate Receptors and LAPSER1-β-Catenin at Excitatory Synapses

por Schmeisser, Michael J., Grabrucker, Andreas M., Bockmann, Juergen, Boeckers, Tobias M.
Publicado em 2009

Heterogeneous Nuclear Ribonucleoprotein K Interacts with Abi-1 at Postsynaptic Sites and Modulates Dendritic Spine Morphology

por Proepper, Christian, Steinestel, Konrad, Schmeisser, Michael J., Heinrich, Jutta, Steinestel, Julie, Bockmann, Juergen, Liebau, Stefan, Boeckers, Tobias M.
Publicado em 2011

The Shank3 Interaction Partner ProSAPiP1 Regulates Postsynaptic SPAR Levels and the Maturation of Dendritic Spines in Hippocampal Neurons

por Reim, Dominik, Weis, Tobias M., Halbedl, Sonja, Delling, Jan Philipp, Grabrucker, Andreas M., Boeckers, Tobias M., Schmeisser, Michael J.
Publicado no Front Synaptic Neurosci (2016)

Proteomic Analysis of Brain Region and Sex-Specific Synaptic Protein Expression in the Adult Mouse Brain

por Distler, Ute, Schumann, Sven, Kesseler, Hans-Georg, Pielot, Rainer, Smalla, Karl-Heinz, Sielaff, Malte, Schmeisser, Michael J, Tenzer, Stefan
Publicado no Cells (2020)

Proteomic Analysis of Post-synaptic Density Fractions from Shank3 Mutant Mice Reveals Brain Region Specific Changes Relevant to Autism Spectrum Disorder

por Reim, Dominik, Distler, Ute, Halbedl, Sonja, Verpelli, Chiara, Sala, Carlo, Bockmann, Juergen, Tenzer, Stefan, Boeckers, Tobias M., Schmeisser, Michael J.
Publicado no Front Mol Neurosci (2017)

The Nedd4-binding protein 3 (N4BP3) is crucial for axonal and dendritic branching in developing neurons

por Schmeisser, Michael J, Kühl, Susanne J, Schoen, Michael, Beth, Nathalie H, Weis, Tobias M, Grabrucker, Andreas M, Kühl, Michael, Boeckers, Tobias M
Publicado em 2013

Selective Localization of Shanks to VGLUT1-Positive Excitatory Synapses in the Mouse Hippocampus

por Heise, Christopher, Schroeder, Jan C., Schoen, Michael, Halbedl, Sonja, Reim, Dominik, Woelfle, Sarah, Kreutz, Michael R., Schmeisser, Michael J., Boeckers, Tobias M.
Publicado no Front Cell Neurosci (2016)

Phenotypic and functional analysis of SHANK3 stop mutations identified in individuals with ASD and/or ID

por Cochoy, Daniela M, Kolevzon, Alexander, Kajiwara, Yuji, Schoen, Michael, Pascual-Lucas, Maria, Lurie, Stacey, Buxbaum, Joseph D, Boeckers, Tobias M, Schmeisser, Michael J
Publicado no Mol Autism (2015)

An SK3 Channel/nWASP/Abi-1 Complex Is Involved in Early Neurogenesis

por Liebau, Stefan, Steinestel, Julie, Linta, Leonhard, Kleger, Alexander, Storch, Alexander, Schoen, Michael, Steinestel, Konrad, Proepper, Christian, Bockmann, Juergen, Schmeisser, Michael J., Boeckers, Tobias M.
Publicado em 2011

Super-Resolution Microscopy Reveals Presynaptic Localization of the ALS/FTD Related Protein FUS in Hippocampal Neurons

por Schoen, Michael, Reichel, Jochen M., Demestre, Maria, Putz, Stefan, Deshpande, Dhruva, Proepper, Christian, Liebau, Stefan, Schmeisser, Michael J., Ludolph, Albert C., Michaelis, Jens, Boeckers, Tobias M.
Publicado no Front Cell Neurosci (2016)

Hyperactivity and Hypermotivation Associated With Increased Striatal mGluR1 Signaling in a Shank2 Rat Model of Autism

por Modi, Meera E., Brooks, Julie M., Guilmette, Edward R., Beyna, Mercedes, Graf, Radka, Reim, Dominik, Schmeisser, Michael J., Boeckers, Tobias M., O’Donnell, Patricio, Buhl, Derek L.
Publicado no Front Mol Neurosci (2018)

Amyloid beta protein-induced zinc sequestration leads to synaptic loss via dysregulation of the ProSAP2/Shank3 scaffold

por Hof Patrick R, Andreasson Katrin I, Woodling Nathaniel S, Schoen Michael, Arons Magali, Udvardi Patrick T, Schmeisser Michael J, Grabrucker Andreas M, Buxbaum Joseph D, Garner Craig C, Boeckers Tobias M
Publicado em 2011-09-01

Amyloid beta protein-induced zinc sequestration leads to synaptic loss via dysregulation of the ProSAP2/Shank3 scaffold

por Grabrucker, Andreas M, Schmeisser, Michael J, Udvardi, Patrick T, Arons, Magali, Schoen, Michael, Woodling, Nathaniel S, Andreasson, Katrin I, Hof, Patrick R, Buxbaum, Joseph D, Garner, Craig C, Boeckers, Tobias M
Publicado em 2011

IκB Kinase/Nuclear Factor κB-Dependent Insulin-Like Growth Factor 2 (Igf2) Expression Regulates Synapse Formation and Spine Maturation via Igf2 Receptor Signaling

por Schmeisser, Michael J., Baumann, Bernd, Johannsen, Svenja, Vindedal, Gry F., Jensen, Vidar, Hvalby, Øivind C., Sprengel, Rolf, Seither, Jochen, Maqbool, Ayesha, Magnutzki, Alexander, Lattke, Michael, Oswald, Franz, Boeckers, Tobias M., Wirth, Thomas
Publicado no J Neurosci (2012)

Acitretin reverses early functional network degradation in a mouse model of familial Alzheimer’s disease

por Rosales Jubal, Eduardo, Schwalm, Miriam, dos Santos Guilherme, Malena, Schuck, Florian, Reinhardt, Sven, Tose, Amanda, Barger, Zeke, Roesler, Mona K., Ruffini, Nicolas, Wierczeiko, Anna, Schmeisser, Michael J., Schmitt, Ulrich, Endres, Kristina, Stroh, Albrecht
Publicado no Sci Rep (2021)

Early life adversity targets the transcriptional signature of hippocampal NG2+ glia and affects voltage gated sodium (Na(v)) channels properties

por Treccani, Giulia, Yigit, Hatice, Lingner, Thomas, Schleuβner, Vanessa, Mey, Franziska, van der Kooij, Michael A., Wennström, Malin, Herzog, David P., Linke, Matthias, Fricke, Markus, Schmeisser, Michael J., Wegener, Gregers, Mittmann, Thomas, Trotter, Jacqueline, Müller, Marianne B.
Publicado no Neurobiol Stress (2021)

Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice

por Peter, Saša, ten Brinke, Michiel M., Stedehouder, Jeffrey, Reinelt, Claudia M., Wu, Bin, Zhou, Haibo, Zhou, Kuikui, Boele, Henk-Jan, Kushner, Steven A., Lee, Min Goo, Schmeisser, Michael J., Boeckers, Tobias M., Schonewille, Martijn, Hoebeek, Freek E., De Zeeuw, Chris I.
Publicado no Nat Commun (2016)

Mutations in PRDM15 Are a Novel Cause of Galloway-Mowat Syndrome

por Mann, Nina, Mzoughi, Slim, Schneider, Ronen, Kühl, Susanne J., Schanze, Denny, Klämbt, Verena, Lovric, Svjetlana, Mao, Youying, Shi, Shasha, Tan, Weizhen, Kühl, Michael, Onuchic-Whitford, Ana C., Treimer, Ernestine, Kitzler, Thomas M., Kause, Franziska, Schumann, Sven, Nakayama, Makiko, Buerger, Florian, Shril, Shirlee, van der Ven, Amelie T., Majmundar, Amar J., Holton, Kristina Marie, Kolb, Amy, Braun, Daniela A., Rao, Jia, Jobst-Schwan, Tilman, Mildenberger, Eva, Lennert, Thomas, Kuechler, Alma, Wieczorek, Dagmar, Gross, Oliver, Ermisch-Omran, Beate, Werberger, Anja, Skalej, Martin, Janecke, Andreas R., Soliman, Neveen A., Mane, Shrikant M., Lifton, Richard P., Kadlec, Jan, Guccione, Ernesto, Schmeisser, Michael J., Zenker, Martin, Hildebrandt, Friedhelm
Publicado no J Am Soc Nephrol (2021)