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Author Pessina P |
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Article
Pessina P, Author ; Kharraz Y ; Jardí M ; Fukada S ; Serrano AL ; Perdiguero E ; Munoz-Canoves P | 2015Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Pessina P ; François S ; Azzoni E ; Brunelli S | 2008Muscular dystrophies are heterogeneous diseases characterized by a primary wasting of skeletal muscle. Replacement of diseased muscles with new healthy and functional muscle fibers has been for a long time a major therapeutic strategy for muscul[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; François S ; Deponti D ; Pessina P ; Azzoni E ; Maggioni M ; Clementi E ; Meneveri R ; Brunelli S | 2008Necdin is a transcriptional co-factor of the MAGE protein family and deletion of this gene in human is associated with Prader-Willi syndrome (PWS). Mice lacking Necdin display a variety of phenotypes mimicking some aspects of the PWS. Previous s[...]