Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Martin Lackinger"'
Autor:
Axel Krug, Markus Wöhr, Dominik Seffer, Henrike Rippberger, A. Özge Sungur, Bruno Dietsche, Frederike Stein, Sugirthan Sivalingam, Andreas J. Forstner, Stephanie H. Witt, Helene Dukal, Fabian Streit, Anna Maaser, Stefanie Heilmann-Heimbach, Till F. M. Andlauer, Stefan Herms, Per Hoffmann, Marcella Rietschel, Markus M. Nöthen, Martin Lackinger, Gerhard Schratt, Michael Koch, Rainer K. W. Schwarting, Tilo Kircher
Publikováno v:
Molecular Autism, Vol 11, Iss 1, Pp 1-19 (2020)
Abstract Advanced paternal age (APA) is a risk factor for several neurodevelopmental disorders, including autism and schizophrenia. The potential mechanisms conferring this risk are poorly understood. Here, we show that the personality traits schizot
Externí odkaz:
https://doaj.org/article/06f7773622724f6e8c4366eee4a1e2fc
Autor:
Pratibha Thakur, Martin Lackinger, Anastasia Diamantopoulou, Sneha Rao, Yijing Chen, Annie Ferng, Curt Mazur, Holly Kordasiewicz, Robert J. Shprintzen, Sander Markx, Bin Xu, Joseph A. Gogos
Up-regulation of Mirta22/Emc10 is a major transcriptional effect of the 22q11.2-associated microRNA dysregulation and underlies key cellular as well as behavioral deficits. EMC10 is a component of the ER membrane complex, which promotes membrane inse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7940b886dc609254baed996b61411e73
https://doi.org/10.1101/2022.03.01.482495
https://doi.org/10.1101/2022.03.01.482495
Autor:
Rainer K.W. Schwarting, Gerhard Schratt, Christoph Dieterich, Roberto Fiore, A. Özge Sungur, Tatjana Wüst, Markus Wöhr, Reetu Daswani, Michael Soutschek, Lea Stemmler, Martin Lackinger, Silvia Bicker
Publikováno v:
EMBO reports. 20(2)
Aberrant synaptic function is thought to underlie social deficits in neurodevelopmental disorders such as autism and schizophrenia. Although microRNAs have been shown to regulate synapse development and plasticity, their potential involvement in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09fcfe4c8c04503d948a996761b4686d
https://pubmed.ncbi.nlm.nih.gov/30674540
https://pubmed.ncbi.nlm.nih.gov/30674540
Autor:
Roberto Fiore, Simon Sumer, Tatjana Wüst, Rainer K.W. Schwarting, Franziska Metge, Dominik Seffer, Markus Wöhr, Ayla Aksoy-Aksel, Silvia Bicker, Jeremy Valluy, Christoph Dieterich, Gerhard Schratt, Martin Lackinger
Publikováno v:
Nature neuroscience. 18(5)
The E3 ubiquitin ligase Ube3a is an important regulator of activity-dependent synapse development and plasticity. Ube3a mutations cause Angelman syndrome and have been associated with autism spectrum disorders (ASD). However, the biological significa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2910d3c45d5e174e20965bca6c870313
https://pubmed.ncbi.nlm.nih.gov/25867122
https://pubmed.ncbi.nlm.nih.gov/25867122