Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Maurizio Curcio"'
Autor:
Maria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, Alessandro Grottesi, Llenio Servettini, Luca Guglielmi, Lara Macchioni, Simona Saredi, Maurizio Curcio, Chiara De Nuccio, Sonia Hasan, Lanfranco Corazzi, Fabio Franciolini, Marina Mora, Luigi Catacuzzeno, Mauro Pessia
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0155516 (2016)
An autosomal dominant protein aggregate myopathy, characterized by high plasma creatine kinase and calsequestrin-1 (CASQ1) accumulation in skeletal muscle, has been recently associated with a missense mutation in CASQ1 gene. The mutation replaces an
Externí odkaz:
https://doaj.org/article/623e7a096e0b4a789396a7b416a2851c
Autor:
Marina Mora, Cinzia Bragato, Sara Gibertini, Simona Zanotti, Maurizio Curcio, Eleonora Canioni, Franco Salerno, Flavia Blasevich, Simona Saredi, Alessandra Ruggieri, Maria Barbara Pasanisi, Pia Bernasconi, Lorenzo Maggi, Renato Mantegazza, Francesca Andreetta
Publikováno v:
Open Journal of Bioresources, Vol 4, p 1 (2017)
The Biobank was established in 1986 as part of the routine diagnostic activity of the Division of Neuromuscular Diseases and Neuroimmunology, of the Carlo Besta Neurological Institute. It stores muscle tissue, cells and DNA from patients with neuromu
Externí odkaz:
https://doaj.org/article/a596ac99a75e4def9b92d996709ac1a3
Autor:
Sara Gibertini, Paolo Savadori, Ferdinando Cornelio, Barbara Pasanisi, Marina Mora, Maurizio Curcio, Simona Zanotti, Renato Mantegazza, Lucia Morandi
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1852:1451-1464
Excessive extracellular matrix deposition progressively replacing muscle fibres is the endpoint of most severe muscle diseases. Recent data indicate major involvement of microRNAs in regulating pro- and anti-fibrotic genes. To investigate the roles o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ce9ab005c9502d356ffd26c8843f2b0
https://doi.org/10.1016/j.bbadis.2015.04.013
https://doi.org/10.1016/j.bbadis.2015.04.013
Autor:
Eleonora Canioni, Cinzia Bragato, Maria Barbara Pasanisi, Simona Zanotti, Marina Mora, Sara Gibertini, Flavia Blasevich, Simona Saredi, Alessandra Ruggieri, Renato Mantegazza, Franco Salerno, Pia Bernasconi, Maurizio Curcio, Francesca Andreetta, Lorenzo Maggi
Publikováno v:
Open Journal of Bioresources, Vol 4, p 1 (2017)
Open Journal of Bioresources; Vol 4 (2017); 1
Open Journal of Bioresources; Vol 4 (2017); 1
The Biobank was established in 1986 as part of the routine diagnostic activity of the Division of Neuromuscular Diseases and Neuroimmunology, of the Carlo Besta Neurological Institute. It stores muscle tissue, cells and DNA from patients with neuromu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eef99422344e88e7cbc88a3055d607e
https://openbioresources.metajnl.com/articles/29
https://openbioresources.metajnl.com/articles/29
Autor:
Maria Cristina D'Adamo, Sergio Visentin, Lanfranco Corazzi, Fabio Franciolini, Luca Guglielmi, Maurizio Curcio, Simona Saredi, Mauro Pessia, Chiara De Nuccio, Alessandro Grottesi, Marina Mora, Lara Macchioni, Luigi Catacuzzeno, llenio Servettini, Luigi Sforna, Sonia Hasan
Publikováno v:
PLoS ONE
PLoS ONE, Vol 11, Iss 5, p e0155516 (2016)
PLoS ONE, Vol 11, Iss 5, p e0155516 (2016)
An autosomal dominant protein aggregate myopathy, characterized by high plasma creatine kinase and calsequestrin-1 (CASQ1) accumulation in skeletal muscle, has been recently associated with a missense mutation in CASQ1 gene. The mutation replaces an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed455a5c42409c8fa4abe816c9dde545
https://pubmed.ncbi.nlm.nih.gov/27196359
https://pubmed.ncbi.nlm.nih.gov/27196359
Autor:
Marina Mora, Paolo Savadori, Francesca Andreetta, Renato Mantegazza, Sara Gibertini, Franco Salerno, Simona Saredi, Simona Zanotti, Pia Bernasconi, Maurizio Curcio
The Sgcb-null mouse, with knocked-down β-sarcoglycan, develops severe muscular dystrophy as in type 2E human limb girdle muscular dystrophy. The mdx mouse, lacking dystrophin, is the most used model for Duchenne muscular dystrophy (DMD). Unlike DMD,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d3bc4545b0d4b5011673ef7daeee73
http://hdl.handle.net/10281/88347
http://hdl.handle.net/10281/88347
