Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Mauro Mastrototaro"'
Autor:
Maria Grazia Mola, Grazia Paola Nicchia, Davide Basco, Maria Svelto, Francesco Pisani, Andrea Rossi, Antonio Frigeri, Cinzia Stigliano, Mauro Mastrototaro
Publikováno v:
Neuroscience. 168:903-914
Unlike other mammalian AQPs, multiple tetramers of AQP4 associate in the plasma membrane to form peculiar structures called Orthogonal Arrays of Particles (OAPs), that are observable by freeze-fracture electron microscopy (FFEM). However, FFEM cannot
Autor:
Andrea Rossi, Carla Tortorella, Francesco Pisani, Anna Lia, Maria Svelto, Grazia Paola Nicchia, Maria Trojano, Antonio Frigeri, Maddalena Ruggieri, Mauro Mastrototaro
Publikováno v:
Glia. 57:1363-1373
Neuromyelitis optica (NMO) is an inflammatory autoimmune demyelinating disease of the central nervous system (CNS) which in autoantibodies produced by patients with NMO (NMO-IgG) recognize a glial water channel protein, Aquaporin-4 (AQP4) expressed a
Autor:
Andrea Rossi, Maria Trojano, Maddalena Ruggieri, Antonio Frigeri, Mauro Mastrototaro, Grazia Paola Nicchia, Francesco Pisani, Maria Svelto, Carla Tortorella
Publikováno v:
The Journal of biological chemistry. 286(11)
Neuromyelitis optica (NMO) is an autoimmune demyelinating disease characterized by the presence of anti-aquaporin-4 (AQP4) antibodies in the patient sera. We recently reported that these autoantibodies are able to bind AQP4 when organized in the supr
Autor:
Maria Svelto, Angelo Sparaneo, Davide Basco, Mauro Mastrototaro, Antonio Frigeri, Grazia Paola Nicchia
Publikováno v:
Neuromuscular Disorders. 20:680
Autor:
Claudio Bruno, Michael P. Lisanti, Antonio Frigeri, Silvia Stringara, Stefania Assereto, Paolo Broda, Elisabetta Gazzerro, Grazia Paola Nicchia, Maria Svelto, Carlo Minetti, Mauro Mastrototaro, Vincenzo Nigro
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Aquaporin-4 (AQP4) is the major water channel expressed in fast-twitch skeletal muscle fibers. AQP4 is reduced in Duchenne and Becker Muscular Dystrophies, but not in caveolinopathies, thus suggesting an interaction with dystrophin or with members of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbe5330f7dc31ccb145df7efeb3c8575
http://www.scopus.com/inward/record.url?eid=2-s2.0-47749142452&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-47749142452&partnerID=MN8TOARS
Publikováno v:
Muscle & Nerve; May2007, Vol. 35 Issue 5, p625-631, 7p