Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Anna Bergo"'
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:
Isabella Barbiero, Davide Valente, Chetan Chandola, Fiorenza Magi, Anna Bergo, Laura Monteonofrio, Marco Tramarin, Maria Fazzari, Silvia Soddu, Nicoletta Landsberger, Cinzia Rinaldo, Charlotte Kilstrup-Nielsen
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Abstract The cyclin-dependent kinase-like 5 (CDKL5) gene has been associated with rare neurodevelopmental disorders characterized by the early onset of seizures and intellectual disability. The CDKL5 protein is widely expressed in most tissues and ce
Externí odkaz:
https://doaj.org/article/fbcbc72f52974687a41eb08fed046097
Autor:
Charlotte Kilstrup-Nielsen, Laura Rusconi, Paolo La Montanara, Dalila Ciceri, Anna Bergo, Francesco Bedogni, Nicoletta Landsberger
Publikováno v:
Neural Plasticity, Vol 2012 (2012)
In the last few years, the X-linked serine/threonine kinase cyclin-dependent kinase-like 5 (CDKL5) has been associated with early-onset epileptic encephalopathies characterized by the manifestation of intractable epilepsy within the first weeks of li
Externí odkaz:
https://doaj.org/article/53a5c07b60b2436aa84c4e742f6a6862
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:
Charlotte Kilstrup-Nielsen, Cinzia Rinaldo, Fiorenza Magi, Chetan Chandola, Nicoletta Landsberger, Maria Fazzari, Laura Monteonofrio, Isabella Barbiero, Silvia Soddu, Marco Tramarin, Anna Bergo, Davide Valente
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
Scientific Reports
Scientific Reports
The cyclin-dependent kinase-like 5 (CDKL5) gene has been associated with rare neurodevelopmental disorders characterized by the early onset of seizures and intellectual disability. The CDKL5 protein is widely expressed in most tissues and cells with
Autor:
Maria Lopez Chiloeches, Anna Bergonzini, Océane C. B. Martin, Nicole Bergstein, Saskia F. Erttmann, Kyaw Min Aung, Nelson O. Gekara, Javier F. Avila Cariño, Ioannis S. Pateras, Teresa Frisan
Publikováno v:
Frontiers in Immunology, Vol 14 (2024)
IntroductionTyphoid toxin-expressing Salmonella enterica causes DNA damage in the intestinal mucosa in vivo, activating the DNA damage response (DDR) in the absence of inflammation. To understand whether the tissue microenvironment constrains the inf
Externí odkaz:
https://doaj.org/article/0545a211a7184a09a1424f21bc292d35
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
Autor:
Marta Gai, Isabella Barbiero, Charlotte Kilstrup-Nielsen, Anna Bergo, Clementina Cobolli Gigli, Marta Strollo, Sarah Sertic, Nicoletta Landsberger, Ferdinando Di Cunto, Gilda Stefanelli
Publikováno v:
Journal of Biological Chemistry. 290:3223-3237
Mutations in MECP2 cause a broad spectrum of neuropsychiatric disorders of which Rett syndrome represents the best defined condition. Both neuronal and non-neuronal functions of the methyl-binding protein underlie the related pathologies. Nowadays Me
Autor:
Marta Gai, Anna Bergo, Nicoletta Landsberger, Anna Sapino, Jacqueline Bond, Selina Pasquero, Fiammetta Vernì, Laura Annaratone, Cristiana Vagnoni, Silvia Bonaccorsi, Ferdinando Di Cunto, Gaia Berto, Francesco Sgrò, Alessandra Maria Adelaide Chiotto, F. Bianchi, Wieland B. Huttner
Publikováno v:
Europe PubMed Central
Correct orientation of cell division is considered an important factor for the achievement of normal brain size, as mutations in genes that affect this process are among the leading causes of microcephaly. Abnormal spindle orientation is associated w