Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Martina Scano"'
Autor:
Francesco Dalla Barba, Michela Soardi, Leila Mouhib, Giovanni Risato, Eylem Emek Akyürek, Tyrone Lucon-Xiccato, Martina Scano, Alberto Benetollo, Roberta Sacchetto, Isabelle Richard, Francesco Argenton, Cristiano Bertolucci, Marcello Carotti, Dorianna Sandonà
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 16, p 12707 (2023)
Sarcoglycanopathies, also known as limb girdle muscular dystrophy 3-6, are rare muscular dystrophies characterized, although heterogeneous, by high disability, with patients often wheelchair-bound by late adolescence and frequently developing respira
Externí odkaz:
https://doaj.org/article/7c525ec0c945402a9196090eef95d5a7
Autor:
Dieter Blottner, Gabor Trautmann, Sandra Furlan, Guido Gambara, Katharina Block, Martina Gutsmann, Lian-Wen Sun, Paul F. Worley, Luisa Gorza, Martina Scano, Paola Lorenzon, Imre Vida, Pompeo Volpe, Michele Salanova
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 1, p 75 (2021)
The molecular mechanisms of skeletal muscle atrophy under extended periods of either disuse or microgravity are not yet fully understood. The transition of Homer isoforms may play a key role during neuromuscular junction (NMJ) imbalance/plasticity in
Externí odkaz:
https://doaj.org/article/fed4fe2771064e6894c12b6c3bbcde91
Autor:
Marcello Carotti, Martina Scano, Irene Fancello, Isabelle Richard, Giovanni Risato, Mona Bensalah, Michela Soardi, Dorianna Sandonà
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 5, p 1813 (2020)
Sarcoglycanopathies are rare limb girdle muscular dystrophies, still incurable, even though symptomatic treatments may slow down the disease progression. Most of the disease-causing defects are missense mutations leading to a folding defective protei
Externí odkaz:
https://doaj.org/article/1296b28e0b70450795dd8904e3328517
Autor:
Michela Bondì, Roberta Sacchetto, Marcello Carotti, Alberto Benetollo, Dorianna Sandonà, Bert Blaauw, Martina Scano, Eylem Emek Akyurek, Michela Soardi, Sandra Furlan, Paola Caccin, Leonardo Nogara, Francesco Dalla Barba
Limb-girdle muscular dystrophy R3 (LGMDR3) is caused by mutations in the SGCA gene coding for α-sarcoglycan (SG). Together with β- γ- and δ-SG, α-SG forms a tetramer embedded in the dystrophin associated protein complex crucial for protecting th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5db33b7e45a43a1f7e1b4fbfecbf0adb
http://hdl.handle.net/11577/3400586
http://hdl.handle.net/11577/3400586
Autor:
Salanova, Dieter Blottner, Gabor Trautmann, Sandra Furlan, Guido Gambara, Katharina Block, Martina Gutsmann, Lian-Wen Sun, Paul F. Worley, Luisa Gorza, Martina Scano, Paola Lorenzon, Imre Vida, Pompeo Volpe, Michele
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 1; Pages: 75
The molecular mechanisms of skeletal muscle atrophy under extended periods of either disuse or microgravity are not yet fully understood. The transition of Homer isoforms may play a key role during neuromuscular junction (NMJ) imbalance/plasticity in
Autor:
Dorianna Sandonà, Martina Scano, Isabelle Richard, Giovanni Risato, Marcello Carotti, Michela Soardi, Mona Bensalah, Irene Fancello
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, 2020, 21 (5), pp.1813. ⟨10.3390/ijms21051813⟩
International Journal of Molecular Sciences, MDPI, 2020, 21 (5), pp.1813. ⟨10.3390/ijms21051813⟩
Volume 21
Issue 5
International Journal of Molecular Sciences, Vol 21, Iss 5, p 1813 (2020)
International Journal of Molecular Sciences, 2020, 21 (5), pp.1813. ⟨10.3390/ijms21051813⟩
International Journal of Molecular Sciences, MDPI, 2020, 21 (5), pp.1813. ⟨10.3390/ijms21051813⟩
Volume 21
Issue 5
International Journal of Molecular Sciences, Vol 21, Iss 5, p 1813 (2020)
Sarcoglycanopathies are rare limb girdle muscular dystrophies, still incurable, even though symptomatic treatments may slow down the disease progression. Most of the disease-causing defects are missense mutations leading to a folding defective protei