Zobrazeno 1 - 5
of 5
pro vyhledávání: '"muscle fibrosi"'
Autor:
Nicola Carboni, Chiara Lanzuolo, Elisa Schena, Lucio Santoro, Tiziana Mongini, Elena Biagini, Lucia Morandi, Gisèle Bonne, Giovanna Lattanzi, Lorenzo Maggi, Patrizia Sabatelli, Giulia Ricci, Lucia Ruggiero, Cristina Cappelletti, Marta Columbaro, Luisa Politano, Antoine Muchir, Giuseppe Boriani, Camilla Evangelisti, Sabino Prencipe, Gabriele Siciliano, Elena Pegoraro, Pia Bernasconi, Paola Cavalcante, Liliana Vercelli, Carmelo Rodolico
Publikováno v:
Nucleus
Nucleus, Taylors and Francis, 2018, 9 (1), pp.337-349. ⟨10.1080/19491034.2018.1467722⟩
Nucleus, Taylors and Francis, 2018, 9 (1), pp.337-349. ⟨10.1080/19491034.2018.1467722⟩
International audience; Among rare diseases caused by mutations in LMNA gene, Emery-Dreifuss Muscular Dystrophy type 2 and Limb-Girdle muscular Dystrophy 1B are characterized by muscle weakness and wasting, joint contractures, cardiomyopathy with con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34680d56058eacc019f8c7663f233282
http://europepmc.org/articles/PMC5973167
http://europepmc.org/articles/PMC5973167
Autor:
Fiorentina Roviezzo, Antonio Lavecchia, Elena Morelli, Caterina Bernacchioni, Vincenzo Santagada, Ferdinando Fiorino, Elisa Perissutti, Alessandra Lo Bianco, Chiara Donati, Elisa Puliti, Beatrice Severino, Giuseppe Caliendo, Giuseppe Cirino, Angela Corvino, Ida Cerqua, Francesco Frecentese, Elisabetta Granato, Elisa Magli
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8861, p 8861 (2021)
Volume 22
Issue 16
International Journal of Molecular Sciences, Vol 22, Iss 8861, p 8861 (2021)
S1P is the final product of sphingolipid metabolism, which interacts with five widely expressed GPCRs (S1P1-5). Increasing numbers of studies have indicated the importance of S1P3 in various pathophysiological processes. Recently, we have identified
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a618ecd3649e24b07c5b6286f771c9
https://doi.org/10.3390/ijms22168861
https://doi.org/10.3390/ijms22168861
Publikováno v:
Cell and Tissue Research. 352:659-670
Severe muscle fibrosis is the endpoint of many chronic myopathies. Identification of factors that regulate fibrosis is important for understanding its pathogenesis and for developing anti-fibrotic treatments that prevent muscle destruction. We have d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12f848a299e6007c96b35c00a90f57d
https://doi.org/10.1007/s00441-013-1601-2
https://doi.org/10.1007/s00441-013-1601-2
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
Autor:
Rosa Anna Busiello, Marinella Pirozzi, Maria Sepe, Bruno Trimarco, Roberta Paolillo, Giuseppe Carotenuto, Gabriele G. Schiattarella, Marco Oliveti, Assunta Lombardi, Roman S. Polishchuk, Giovanni Esposito, Cinzia Perrino, Fabio Magliulo, Gianluigi Pironti, Fabio Cattaneo, Antonio Feliciello, Domenica Borzacchiello, Nicola Boccella, Marisa Avvedimento
Publikováno v:
PLoS ONE, Vol 11, Iss 5, p e0154076 (2016)
PLoS ONE
PLoS ONE
A-kinase anchoring proteins (AKAPs) transmit signals cues from seven-transmembrane receptors to specific sub-cellular locations. Mitochondrial AKAPs encoded by the Akap1 gene have been shown to modulate mitochondrial function and reactive oxygen spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5f57f456c85f7eec016ec9f0366d832
https://doi.org/10.1371/journal.pone.0154076
https://doi.org/10.1371/journal.pone.0154076