Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Paula Pousinha"'
Autor:
Marta Prieto, Alessandra Folci, Gwénola Poupon, Sara Schiavi, Valeria Buzzelli, Marie Pronot, Urielle François, Paula Pousinha, Norma Lattuada, Sophie Abelanet, Sara Castagnola, Magda Chafai, Anouar Khayachi, Carole Gwizdek, Frédéric Brau, Emmanuel Deval, Maura Francolini, Barbara Bardoni, Yann Humeau, Viviana Trezza, Stéphane Martin
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-15 (2021)
The R138Q mutation in the Fragile X Mental Retardation 1 (FMR1) gene has been associated with Fragile X syndrome (FXS). Here, the authors present a Fmr1 R138Q Knock-In mouse model and show that R138Q mutation results in impaired long-term potentiatio
Externí odkaz:
https://doaj.org/article/1f547051b6104cb2ae2a8dd5047148af
Autor:
Marie-Charlotte Allichon, Vanesa Ortiz, Paula Pousinha, Andry Andrianarivelo, Anna Petitbon, Nicolas Heck, Pierre Trifilieff, Jacques Barik, Peter Vanhoutte
Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 13 (2021)
Drug addiction is defined as a compulsive pattern of drug-seeking- and taking- behavior, with recurrent episodes of abstinence and relapse, and a loss of control despite negative consequences. Addictive drugs promote reinforcement by increasing dopam
Externí odkaz:
https://doaj.org/article/14e406d843c143d582144e687b4ea306
Autor:
Georgia-Ioanna Kartalou, Ana Rita Salgueiro-Pereira, Thomas Endres, Angelina Lesnikova, Plinio Casarotto, Paula Pousinha, Kevin Delanoe, Elke Edelmann, Eero Castrén, Kurt Gottmann, Hélène Marie, Volkmar Lessmann
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 23, p 8957 (2020)
Therapeutic approaches providing effective medication for Alzheimer’s disease (AD) patients after disease onset are urgently needed. Previous studies in AD mouse models suggested that physical exercise or changed lifestyle can delay AD-related syna
Externí odkaz:
https://doaj.org/article/0b66fe9c2ad341a78d6a37042b170cda
Autor:
Marta Prieto, Alessandra Folci, Gwénola Poupon, Sara Schiavi, Valeria Buzzelli, Marie Pronot, Urielle François, Paula Pousinha, Norma Lattuada, Sophie Abelanet, Sara Castagnola, Magda Chafai, Anouar Khayachi, Carole Gwizdek, Frédéric Brau, Emmanuel Deval, Maura Francolini, Barbara Bardoni, Yann Humeau, Viviana Trezza, Stéphane Martin
Fragile X syndrome (FXS) is the most frequent form of inherited intellectual disability and the best-described monogenic cause of autism. FXS is usually caused by a CGG-repeat expansion in the FMR1 gene leading to its silencing and the loss-of-expres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3a57bb38a2361ea05cd0dd2e888f113
https://hal.archives-ouvertes.fr/hal-03039153
https://hal.archives-ouvertes.fr/hal-03039153
Autor:
Marta Barrachina, Christophe Bernard, Theresa E. Bjorness, David Blum, Detlev Boison, Yijuang Chern, Francisco Ciruela, Elisabetta Coppi, Giovanni Cossu, Sofia Cristóvão-Ferreira, Ilaria Dettori, Raquel B. Dias, Maria R. Domenici, Víctor Fernández-Dueñas, Antonella Ferrante, Sergi Ferré, Michael Freissmuth, Irene Fusco, Jonathan D. Geiger, Robert W. Greene, Karl-Norbert Klotz, Chien-Yu Lin, Luísa V. Lopes, Alberto Martire, Alessia Melani, Alexandre de Mendonca, Micaela Morelli, Felicita Pedata, Annalisa Pinna, Traci Plumb, Patrizia Popoli, Paula Pousinha, Anna M. Pugliese, Joaquim A. Ribeiro, Ana M. Sebastião, Maria T. Tebano, Jadwiga Wardas, Stefania Zappettini
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d02d77238927366da529ce0a20387077
https://doi.org/10.1016/b978-0-12-803724-9.00021-1
https://doi.org/10.1016/b978-0-12-803724-9.00021-1