Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Melanie, Ginger"'
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-16 (2023)
Abstract Excessive neural variability of sensory responses is a hallmark of atypical sensory processing in autistic individuals with cascading effects on other core autism symptoms but unknown neurobiological substrate. Here, by recording neocortical
Externí odkaz:
https://doaj.org/article/ea7cb2b5b3b045a195193f000535cd85
Autor:
Elisabetta Aloisi, Katy Le Corf, Julien Dupuis, Pei Zhang, Melanie Ginger, Virginie Labrousse, Michela Spatuzza, Matthias Georg Haberl, Lara Costa, Ryuichi Shigemoto, Anke Tappe-Theodor, Filippo Drago, Pier Vincenzo Piazza, Christophe Mulle, Laurent Groc, Lucia Ciranna, Maria Vincenza Catania, Andreas Frick
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-14 (2017)
Dysfunction of mGluR5 has been implicated in Fragile X syndrome. Here, using a single-molecule tracking technique, the authors found an increased lateral mobility of mGluR5 at the synaptic site in Fmr1 KO hippocampal neurons, leading to abnormal NMDA
Externí odkaz:
https://doaj.org/article/a5099cbf5e534deea4c2a121546338d3
Excessive trial-by-trial and inter-individual neural variability of sensory responses are hallmarks of atypical sensory processing in autistic individuals with cascading effects on other core autism symptoms. The neurobiological substrate of this exa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b5b624b69cdedd6ff5a95aa830f8d9c1
https://doi.org/10.21203/rs.3.rs-2572651/v1
https://doi.org/10.21203/rs.3.rs-2572651/v1
Autor:
Abdelmalik Moujahid, Andreas Frick, Guillaume Bony, Maria Carmen Medrano, Corentin Dechaud, Fabienne Martins, Enejda Subashi, Melanie Ginger, Elisabetta Aloisi, Susanna Pietropaolo, Xavier Leinekugel, Maria Isabel Carreno-Munoz
Publikováno v:
Neuropsychopharmacology. 43:492-502
In fragile X syndrome (FXS), sensory hypersensitivity and impaired habituation is thought to result in attention overload and various behavioral abnormalities in reaction to the excessive and remanent salience of environment features that would norma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91a7251d0c30b56119c594dfbde798a0
https://doi.org/10.1038/npp.2017.149
https://doi.org/10.1038/npp.2017.149
Autor:
Maurizio Memo, Susanna Pietropaolo, Marika Premoli, Andreas Frick, Julie Gaudissard, Melanie Ginger
Publikováno v:
Autism Research. 10:1584-1596
Fragile X syndrome (FXS) is a developmental disorder caused by a mutation in the X-linked FMR1 gene, coding for the FMRP protein which is largely involved in synaptic function. FXS patients present several behavioral abnormalities, including hyperact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f043295b3cb7485c2c74f19cecb7c5b1
https://doi.org/10.1002/aur.1814
https://doi.org/10.1002/aur.1814
Autor:
Han Bao, Mark F. Bear, Tamir Ben-Hur, Nissim Benvenisty, Elizabeth Berry-Kravis, Aditi Bhattacharya, Pietro Chiurazzi, Jeffrey Cohen, Lynda El-Hassar, Douglas W. Ethell, Andreas Frick, Christine M. Gall, Fabrizio Gasparini, Inbal Gazy, Melanie Ginger, Christina Gross, Jacalyn Guy, Randi Hagerman, Becky Hardiman, Charles Hoeffer, Jessica E. Hunter, Molly M. Huntsman, Aia E. Jønch, Sébastien Jacquemont, Peng Jin, Richard S. Jope, Leonard K. Kaczmarek, Peter Kind, R. Frank Kooy, Julie C. Lauterborn, Andrew Ligsay, Lothar Lindemann, Olivier J.J. Manzoni, Henry G.S. Martin, Montserrat Milà, David L. Nelson, Giovanni Neri, Daniela Neuhofer, Emily K. Osterweil, Jörg Richstein, Michael R. Santoro, Gaia Scerif, Sebastian S. Scharf, Stephanie L. Sherman, Harpreet Sidhu, Will Spooren, Laura J. Stoppel, Joshua Suhl, Elisabetta Tabolacci, Flora Tassone, Sally Till, Karen Usdin, Dan Vershkov, Stephen T. Warren, Rob Willemsen, Xiao-Nan Zhao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3e6c849b4f83ac11b71cbc2abf0a3bb
https://doi.org/10.1016/b978-0-12-804461-2.00026-3
https://doi.org/10.1016/b978-0-12-804461-2.00026-3
Autor:
Julie, Gaudissard, Melanie, Ginger, Marika, Premoli, Maurizio, Memo, Andreas, Frick, Susanna, Pietropaolo
Fragile X syndrome (FXS) is a developmental disorder caused by a mutation in the X-linked FMR1 gene, coding for the FMRP protein which is largely involved in synaptic function. FXS patients present several behavioral abnormalities, including hyperact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::4adb6b2e71a075a25982d9d8fb3bb65c
http://hdl.handle.net/11379/493597
http://hdl.handle.net/11379/493597
Defects in the function or expression level of voltage-gated ion channels are increasingly considered a crucial feature of many CNS disorders. In this chapter, we will summarize the current state of knowledge related to ion channel dysfunction in fra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d28ae48b322bbe91c33114cc0eaa4ce3
https://doi.org/10.1016/b978-0-12-804461-2.00016-0
https://doi.org/10.1016/b978-0-12-804461-2.00016-0
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 1538
Current large-scale approaches in neuroscience aim to unravel the complete connectivity map of specific neuronal circuits, or even the entire brain. This emerging research discipline has been termed connectomics. Recombinant glycoprotein-deleted rabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5398340fac874f2cf4e4c84e84c30179
https://pubmed.ncbi.nlm.nih.gov/27943199
https://pubmed.ncbi.nlm.nih.gov/27943199
Publikováno v:
Methods in Molecular Biology ISBN: 9781493966868
Current large-scale approaches in neuroscience aim to unravel the complete connectivity map of specific neuronal circuits, or even the entire brain. This emerging research discipline has been termed connectomics. Recombinant glycoprotein-deleted rabi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bc493640073e948d113f6c041776242
https://doi.org/10.1007/978-1-4939-6688-2_21
https://doi.org/10.1007/978-1-4939-6688-2_21