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of 1 481
pro vyhledávání: '"Wöhr A"'
Autor:
Tania Aerts, Anneleen Boonen, Lieve Geenen, Anne Stulens, Luca Masin, Anna Pancho, Annick Francis, Elise Pepermans, Geert Baggerman, Frans Van Roy, Markus Wöhr, Eve Seuntjens
Publikováno v:
Open Biology, Vol 14, Iss 6 (2024)
Autism spectrum disorder (ASD) is a group of neurodevelopmental conditions associated with deficits in social interaction and communication, together with repetitive behaviours. The cell adhesion molecule protocadherin10 (PCDH10) is linked to ASD in
Externí odkaz:
https://doaj.org/article/ac7dafdace954edc990831b666085c59
Publikováno v:
In Neuroscience and Biobehavioral Reviews July 2024 162
Autor:
Julian Packheiser, Efe Soyman, Enrica Paradiso, Frédéric Michon, Eline Ramaaker, Neslihan Sahin, Sharmistha Muralidharan, Markus Wöhr, Valeria Gazzola, Christian Keysers
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-19 (2023)
Abstract Footshock self-experience enhances rodents’ reactions to the distress of others. Here, we tested one potential mechanism supporting this phenomenon, namely that animals auto-condition to their own pain squeaks during shock pre-exposure. In
Externí odkaz:
https://doaj.org/article/eeca2bd411c8417fad39c843a9284930
Publikováno v:
In Neuropharmacology 15 December 2023 241
Autor:
Brwa Ali Hussein, Linnea Kristenson, Silvia Pesce, Anne Wöhr, Yarong Tian, Alexander Hallner, Mats Brune, Kristoffer Hellstrand, Ka-Wei Tang, Elin Bernson, Fredrik B Thorén
Publikováno v:
Journal for ImmunoTherapy of Cancer, Vol 11, Iss 8 (2023)
Background The natural killer (NK) complex (NKC) harbors multiple genes such as KLRC1 (encoding NKG2A) and KLRK1 (encoding NKG2D) that are central to regulation of NK cell function. We aimed at determining to what extent NKC haplotypes impact on NK c
Externí odkaz:
https://doaj.org/article/b6c5fb919102458288b4d23545bab390
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 17 (2023)
BackgroundHealthy brain development depends on early social practices and experiences. The risk gene CACNA1C is implicated in numerous neuropsychiatric disorders, in which key characteristics include deficits in social functioning and communication.
Externí odkaz:
https://doaj.org/article/96b96acaaf6e43cd8c0c5f612a8553c6
Akademický článek
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Autor:
Valeria Petroni, Enejda Subashi, Marika Premoli, Markus Wöhr, Wim E. Crusio, Valerie Lemaire, Susanna Pietropaolo
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract Fragile X Syndrome (FXS) is the most common heritable form of mental retardation and monogenic cause of autism spectrum disorder (ASD). FXS is due to a mutation in the X-linked FMR1 gene and is characterized by motor, cognitive and social al
Externí odkaz:
https://doaj.org/article/9f5dab1e04fe4b39b655245abb5bb8bb
Autor:
Markus Wöhr, Wendy M. Fong, Justyna A. Janas, Moritz Mall, Christian Thome, Madhuri Vangipuram, Lingjun Meng, Thomas C. Südhof, Marius Wernig
Publikováno v:
Molecular Autism, Vol 13, Iss 1, Pp 1-28 (2022)
Abstract Background The zinc finger domain containing transcription factor Myt1l is tightly associated with neuronal identity and is the only transcription factor known that is both neuron-specific and expressed in all neuronal subtypes. We identifie
Externí odkaz:
https://doaj.org/article/b7ff67c9372c446f969eb6ed5f640478
Publikováno v:
Frontiers in Behavioral Neuroscience, Vol 17 (2023)
Vital early-life dyadic interaction in mice requires a pup to signal its needs adequately, and a dam to recognize and respond to the pup’s cues accurately and timely. Previous research might have missed important biological and/or environmental ele
Externí odkaz:
https://doaj.org/article/ecd2fb3396b94ec19df649178c1daf34