Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Andrea Pérez Arévalo"'
Autor:
Ekaterina Atanasova, Andrea Pérez Arévalo, Ines Graf, Rong Zhang, Juergen Bockmann, Anne-Kathrin Lutz, Tobias M. Boeckers
Publikováno v:
Molecular Autism, Vol 14, Iss 1, Pp 1-20 (2023)
Abstract Background Autism spectrum disorder (ASD) is mainly characterized by deficits in social interaction and communication and repetitive behaviors. Known causes of ASD are mutations of certain risk genes like the postsynaptic protein SHANK3 and
Externí odkaz:
https://doaj.org/article/508bd4040ef242d8bc937e9009dc09be
Publikováno v:
PLoS ONE, Vol 17, Iss 10 (2022)
Whole animal perfusion is a well-established method that has been used for the past decades in multiple research fields. Particularly, it has been very important for the study of the brain. The rapid and uniform fixation of tissue is essential for th
Externí odkaz:
https://doaj.org/article/c2348f1453be4f698e9af0311c7a73ad
Autor:
Anne-Kathrin Lutz, Andrea Pérez Arévalo, Valentin Ioannidis, Nadine Stirmlinger, Maria Demestre, Richard Delorme, Thomas Bourgeron, Tobias M. Boeckers
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 14 (2021)
SHANK2 (ProSAP1) is a postsynaptic scaffolding protein of excitatory synapses in the central nervous system and implicated in the development of autism spectrum disorders (ASD). Patients with mutations in SHANK2 show autism-like behaviors, developmen
Externí odkaz:
https://doaj.org/article/62de73e79ade401bb205c8be84ad16a1
Autor:
Andrea Pérez Arévalo
Whole animal perfusion is a well-established method that has been used for the past decades in multiple research fields. Particularly, it has been very important for the study of the brain. The rapid and uniform fixation of tissue is essential for th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::802ad4b9d9ff13530f450991e34bdd50
https://doi.org/10.17504/protocols.io.bp2l61ow5vqe/v1
https://doi.org/10.17504/protocols.io.bp2l61ow5vqe/v1
Autor:
Laura I, Sarasola, Claudia Llinas, Del Torrent, Andrea, Pérez-Arévalo, Josep, Argerich, Nil, Casajuana-Martín, Andy, Chevigné, Víctor, Fernández-Dueñas, Sergi, Ferré, Leonardo, Pardo, Francisco, Ciruela
Publikováno v:
Biomedicinepharmacotherapy = Biomedecinepharmacotherapie. 156
Adenosine modulates neurotransmission through inhibitory adenosine A
Autor:
Laura I. Sarasola, Claudia Llinas del Torrent, Andrea Pérez-Arévalo, Josep Argerich, Nil Casajuana-Martín, Andy Chevigné, Víctor Fernández-Dueñas, Sergi Ferré, Leonardo Pardo, Francisco Ciruela
Publikováno v:
Biomedicine & Pharmacotherapy. 156:113896
Adenosine modulates neurotransmission through inhibitory adenosine A1 receptors (A1Rs) and stimulatory A2A receptors (A2ARs). These G protein-coupled receptors are involved in motor function and related to neurodegenerative diseases such as Parkinson
Autor:
Víctor, Fernández-Dueñas, Andrea, Pérez-Arévalo, Xavier, Altafaj, Sergi, Ferré, Francisco, Ciruela
Publikováno v:
Frontiers in Neuroscience
Autor:
Ekaterina Atanasova, Andrea Pérez Arévalo, Ines Graf, Rong Zhang, Juergen Bockmann, Anne-Kathrin Lutz, Tobias M. Boeckers
Publikováno v:
Molecular autism 14(1), 1 (2023). doi:10.1186/s13229-022-00532-3
Background Autism spectrum disorder (ASD) is mainly characterized by deficits in social interaction and communication and repetitive behaviors. Known causes of ASD are mutations of certain risk genes like the postsynaptic protein SHANK3 and environme
Autor:
Mariagiovanna Malara, Anne-Kathrin Lutz, Berra Incearap, Helen Friedericke Bauer, Silvia Cursano, Katrin Volbracht, Joanna Janina Lerner, Rakshita Pandey, Jan Philipp Delling, Valentin Ioannidis, Andrea Pérez Arévalo, Jaime Eugenin von Bernhardi, Michael Schön, Jürgen Bockmann, Leda Dimou, Tobias M. Boeckers
Publikováno v:
Cellular and molecular life sciences 79(7), 371 (2022). doi:10.1007/s00018-022-04400-4
Mutations or deletions of the SHANK3 gene are causative for Phelan–McDermid syndrome (PMDS), a syndromic form of autism spectrum disorders (ASDs). We analyzed Shank3Δ11(−/−) mice and organoids from PMDS individuals to study effects on myelin.
Autor:
Víctor Fernández-Dueñas, Andrea Pérez-Arévalo, Xavier Altafaj, Sergi Ferré, Francisco Ciruela
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Frontiers in Neuroscience, Vol 11 (2017)
instname
Dipòsit Digital de la UB
Universidad de Barcelona
Frontiers in Neuroscience, Vol 11 (2017)
Parkinson's disease (PD) is a progressive, neurodegenerative disorder that affects ~1% of individuals over the age of 60, which turns to 5% in subjects up to 85 years (de Lau and Breteler, 2006). On the other hand, a form of PD, called early-onset PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1288f36f4d82b9d6bf50ee060726322f
http://hdl.handle.net/2445/148041
http://hdl.handle.net/2445/148041