Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Fmr1-Δexon 8 rat"'
Autor:
Martina Parente, Claudia Tonini, Valeria Buzzelli, Emilia Carbone, Viviana Trezza, Valentina Pallottini
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 6; Pages: 3408
Fragile X Syndrome (FXS) is the most frequent form of inherited X-linked pathology, associated with an intellectual and developmental disability, and currently considered the first monogenic cause of autism spectrum disorder (ASD). Low levels of tota
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b17bde1d6f2c0e7210c2fd8cd1b62d03
https://hdl.handle.net/11590/401499
https://hdl.handle.net/11590/401499
Autor:
Schiavi, Sara1 (AUTHOR) sara.schiavi@uniroma3.it, Carbone, Emilia1 (AUTHOR), Melancia, Francesca1 (AUTHOR), Buzzelli, Valeria1 (AUTHOR), Manduca, Antonia1 (AUTHOR), Campolongo, Patrizia2,3 (AUTHOR), Pallottini, Valentina1 (AUTHOR), Trezza, Viviana1 (AUTHOR) viviana.trezza@uniroma3.it
Publikováno v:
Nutritional Neuroscience. May2022, Vol. 25 Issue 5, p898-911. 14p. 1 Diagram, 2 Charts, 5 Graphs.
Autor:
Parente, Martina1 (AUTHOR) martina.parente@uniroma3.it, Tonini, Claudia1 (AUTHOR) claudia.tonini@uniroma3.it, Buzzelli, Valeria1 (AUTHOR) valeria.buzzelli@uniroma3.it, Carbone, Emilia1 (AUTHOR) emilia.carbone@uniroma3.it, Trezza, Viviana1 (AUTHOR) viviana.trezza@uniroma3.it, Pallottini, Valentina1,2 (AUTHOR) valentina.pallottini@uniroma3.it
Publikováno v:
International Journal of Molecular Sciences. Mar2022, Vol. 23 Issue 6, p3408-3408. 14p.
Autor:
Buzzelli, Valeria1, Carbone, Emilia1, Manduca, Antonia1,2, Schiavi, Sara1, Feo, Alessandro1, Perederiy, Julia V.3, Ambert, Kyle H.3, Hausman, Marvin3, Trezza, Viviana1 viviana.trezza@uniroma3.it
Publikováno v:
Psychopharmacology. Jan2023, Vol. 240 Issue 1, p137-147. 11p. 4 Graphs.
Autor:
D'Elia, Annunziata1,2 (AUTHOR) annunziata.delia@ibbc.cnr.it, Schiavi, Sara2 (AUTHOR), Manduca, Antonia2,3 (AUTHOR), Rava, Alessandro2 (AUTHOR), Buzzelli, Valeria2 (AUTHOR), Ascone, Fabrizio2 (AUTHOR), Orsini, Tiziana1 (AUTHOR), Putti, Sabrina1 (AUTHOR), Soluri, Andrea1,4 (AUTHOR), Galli, Filippo5 (AUTHOR), Soluri, Alessandro1 (AUTHOR), Mattei, Maurizio6 (AUTHOR), Cicconi, Rosella6 (AUTHOR), Massari, Roberto1 (AUTHOR), Trezza, Viviana2 (AUTHOR) viviana.trezza@uniroma3.it
Publikováno v:
Scientific Reports. 12/29/2022, Vol. 12 Issue 1, p1-15. 15p.
Autor:
Manduca, Antonia1,2,3 (AUTHOR) antonia.manduca@uniroma1.it, Buzzelli, Valeria1,2 (AUTHOR), Rava, Alessandro2 (AUTHOR), Feo, Alessandro2 (AUTHOR), Carbone, Emilia2 (AUTHOR), Schiavi, Sara2 (AUTHOR), Peruzzi, Barbara4 (AUTHOR), D'Oria, Valentina5 (AUTHOR), Pezzullo, Marco6 (AUTHOR), Pasquadibisceglie, Andrea2 (AUTHOR), Polticelli, Fabio2 (AUTHOR), Micale, Vincenzo7 (AUTHOR), Kuchar, Martin8,9 (AUTHOR), Trezza, Viviana1,2,3 (AUTHOR) viviana.trezza@uniroma3.it
Publikováno v:
Pharmacological Research. May2024, Vol. 203, pN.PAG-N.PAG. 1p.
Autor:
Antonia Manduca, Valeria Buzzelli, Alessandro Rava, Alessandro Feo, Emilia Carbone, Sara Schiavi, Barbara Peruzzi, Valentina D’Oria, Marco Pezzullo, Andrea Pasquadibisceglie, Fabio Polticelli, Vincenzo Micale, Martin Kuchar, Viviana Trezza
Publikováno v:
Pharmacological Research, Vol 203, Iss , Pp 107176- (2024)
Cannabidiol (CBD), a non-psychotomimetic constituent of Cannabis sativa, has been recently approved for epileptic syndromes often associated with Autism spectrum disorder (ASD). However, the putative efficacy and mechanism of action of CBD in patient
Externí odkaz:
https://doaj.org/article/3f98b6a7fe6c49cfbcacdf110dfacd47
Autor:
Valentina Pallottini, Viviana Trezza, Sara Schiavi, Francesca Melancia, Emilia Carbone, Patrizia Campolongo, Antonia Manduca, Valeria Buzzelli
Publikováno v:
Nutritional Neuroscience. 25:898-911
Background and objective: Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder for which no treatments exist. Fragile X syndrome (FXS) is the most common form of inherited mental retardation and the most frequent monogenic cause of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91f0651e583252d7bea790d576ebf35b
https://doi.org/10.1080/1028415x.2020.1819107
https://doi.org/10.1080/1028415x.2020.1819107
Autor:
Golden, Carla E M, Breen, Michael S, Koro, Lacin, Sonar, Sankalp, Niblo, Kristi, Browne, Andrew, Burlant, Natalie, Marino, Daniele Di, Rubeis, Silvia De, Baxter, Mark G, Buxbaum, Joseph D, Harony-Nicolas, Hala
Publikováno v:
Cerebral Cortex; May2019, Vol. 29 Issue 5, p2228-2244, 17p
Autor:
Sara Schiavi, Emilia Carbone, Francesca Melancia, Alessandra di Masi, Marielle Jarjat, Fréderic Brau, Silvia Cardarelli, Mauro Giorgi, Barbara Bardoni, Viviana Trezza
Publikováno v:
Translational Psychiatry. 12
Pharmacological inhibition of phosphodiesterase 2A (PDE2A), which catalyzes the hydrolysis of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP), has recently been proposed as a novel therapeutic tool for Fragile X Syndro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe3687ddd2d617a3cad60553c047bb43
https://doi.org/10.1038/s41398-022-01885-2
https://doi.org/10.1038/s41398-022-01885-2