Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Giada Mura"'
Autor:
Giuseppe Angelini, Emanuele Capra, Francesca Rossi, Giada Mura, Marielle Saclier, Valentina Taglietti, Gabriele Rovetta, Raffaele Epis, Giorgia Careccia, Chiara Bonfanti, Graziella Messina
Publikováno v:
iScience, Vol 27, Iss 1, Pp 108696- (2024)
Summary: Muscular dystrophies (MDs) are incurable genetic myopathies characterized by progressive degeneration of skeletal muscles. Dystrophic mice lacking the transcription factor Nfix display morphological and functional improvements of the disease
Externí odkaz:
https://doaj.org/article/ff37371dfe464b6aa3fa4a6f9534b14d
Autor:
Marielle Saclier, Giuseppe Angelini, Chiara Bonfanti, Giada Mura, Giulia Temponi, Graziella Messina
Publikováno v:
The Journal of pathology. 257(3)
Muscular dystrophies are genetic diseases characterized by chronic inflammation and fibrosis. Macrophages are immune cells that sustain muscle regeneration upon acute injury but seem deleterious in the context of chronic muscle injury such as in musc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2251ddff4d121f0e6ed2cbc95930854d
https://pubmed.ncbi.nlm.nih.gov/35297529
https://pubmed.ncbi.nlm.nih.gov/35297529
Publikováno v:
Experimental cell research. 410(2)
Muscular dystrophies (MDs) are heterogeneous diseases, characterized by primary wasting of skeletal muscle, which in severe cases, such as Duchenne Muscular Dystrophy (DMD), leads to wheelchair dependency, respiratory failure, and premature death. Re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb5adb85b80348353ab4035179a13ba3
https://pubmed.ncbi.nlm.nih.gov/34883113
https://pubmed.ncbi.nlm.nih.gov/34883113
Autor:
Chiara Bonfanti, Chiara Tonelli, Graziella Messina, Katia Petroni, Stefania Antonini, Giuseppe Angelini, Marco Sandri, Marielle Saclier, Federica Zanaglio, Marco Cassano, Valentina Taglietti, Giada Mura, Vanina Romanello
Publikováno v:
Cell Death and Disease, Vol 11, Iss 2, Pp 1-12 (2020)
Cell Death & Disease
Cell Death & Disease
Muscular Dystrophies are severe genetic diseases due to mutations in structural genes, characterized by progressive muscle wasting that compromises patients’ mobility and respiratory functions. Literature underlined oxidative stress and inflammatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce8ed36ba83a78e95feb65b2e00ee255
https://doi.org/10.1038/s41419-020-2332-4
https://doi.org/10.1038/s41419-020-2332-4
Autor:
Valentina, Taglietti, Giuseppe, Angelini, Giada, Mura, Chiara, Bonfanti, Enrico, Caruso, Stefania, Monteverde, Gilles, Le Carrou, Shahragim, Tajbakhsh, Frédéric, Relaix, Graziella, Messina
Publikováno v:
Development (Cambridge, England). 145(21)
The transcription factor Nfix belongs to the nuclear factor one family and has an essential role in prenatal skeletal muscle development, where it is a master regulator of the transition from embryonic to foetal myogenesis. Recently, Nfix was shown t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06d2c6e9075b0266432ed18d17d023a3
https://pubmed.ncbi.nlm.nih.gov/30266829
https://pubmed.ncbi.nlm.nih.gov/30266829
Autor:
Shahragim Tajbakhsh, Gilles Le Carrou, Stefania Monteverde, Frédéric Relaix, Giuseppe Angelini, Graziella Messina, Chiara Bonfanti, Enrico Caruso, Valentina Taglietti, Giada Mura
Publikováno v:
Development.
The transcription factor Nfix belongs to the nuclear factor one family and has an essential role in prenatal skeletal muscle development, where it is a master regulator of the transition from embryonic to foetal myogenesis. Recently, Nfix was shown t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd37363c514067d23a54fd7e3da8c824
https://doi.org/10.1242/dev.163956
https://doi.org/10.1242/dev.163956