Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Barbara Leva"'
Autor:
Angelisa Frasca, Eleonora Spiombi, Michela Palmieri, Elena Albizzati, Maria Maddalena Valente, Anna Bergo, Barbara Leva, Charlotte Kilstrup‐Nielsen, Federico Bianchi, Valerio Di Carlo, Ferdinando Di Cunto, Nicoletta Landsberger
Publikováno v:
EMBO Molecular Medicine, Vol 12, Iss 6, Pp n/a-n/a (2020)
Abstract Mutations in MECP2 cause several neurological disorders of which Rett syndrome (RTT) represents the best‐defined condition. Although mainly working as a transcriptional repressor, MeCP2 is a multifunctional protein revealing several activi
Externí odkaz:
https://doaj.org/article/b33103f72f62419ba99b856dddd50402
Autor:
Anna Gandaglia, Anna Bergo, Lara Pizzamiglio, Flavia Antonucci, Marco Cicerone, Michela Palmieri, Veronica Bianchi, Daniele Di Marino, Charlotte Kilstrup-Nielsen, Sara Carli, Francesco Bedogni, Ilda D'Annessa, Gilda Stefanelli, Elena Brivio, Patrizia D'Adamo, Nicoletta Landsberger, Angelisa Frasca, Barbara Leva, Chiara M Cattaneo
Publikováno v:
Molecular Neurobiology. 56:4838-4854
MeCP2 is a fundamental protein associated with several neurological disorders, including Rett syndrome. It is considered a multifunctional factor with a prominent role in regulating chromatin structure; however, a full comprehension of the consequenc
Autor:
Nicoletta Landsberger, Valerio Di Carlo, Ferdinando Di Cunto, Anna Bergo, Charlotte Kilstrup-Nielsen, Angelisa Frasca, Barbara Leva, Maria Maddalena Valente, Eleonora Spiombi, Michela Palmieri, Elena Albizzati, F. Bianchi
Publikováno v:
EMBO Molecular Medicine
EMBO Molecular Medicine, Vol 12, Iss 6, Pp n/a-n/a (2020)
EMBO Molecular Medicine, Vol 12, Iss 6, Pp n/a-n/a (2020)
Mutations in MECP2 cause several neurological disorders of which Rett syndrome (RTT) represents the best‐defined condition. Although mainly working as a transcriptional repressor, MeCP2 is a multifunctional protein revealing several activities, the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f10d5ff586bbe03d6f9ef9676251916
http://hdl.handle.net/11383/2113725
http://hdl.handle.net/11383/2113725
Autor:
Anna, Gandaglia, Elena, Brivio, Sara, Carli, Michela, Palmieri, Francesco, Bedogni, Gilda, Stefanelli, Anna, Bergo, Barbara, Leva, Chiara, Cattaneo, Lara, Pizzamiglio, Marco, Cicerone, Veronica, Bianchi, Charlotte, Kilstrup-Nielsen, Ilda, D'Annessa, Daniele, Di Marino, Patrizia, D'Adamo, Flavia, Antonucci, Angelisa, Frasca, Nicoletta, Landsberger
Publikováno v:
Molecular neurobiology. 56(7)
MeCP2 is a fundamental protein associated with several neurological disorders, including Rett syndrome. It is considered a multifunctional factor with a prominent role in regulating chromatin structure; however, a full comprehension of the consequenc
Publikováno v:
Frontiers in Medicine, Vol 7 (2021)
Pulmonary hypertension (PH) is recognized to be associated with a number of comorbid conditions. Based on these associations, PH is classified into 5 groups, considering common pathophysiologic drivers of disease, histopathologic features, clinical m
Externí odkaz:
https://doaj.org/article/95ef23065c69487eba0a0859f5417df9