Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ginevra Chioccioli Altadonna"'
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2023)
Despite improvements in treatment, lung cancer is still a major health problem worldwide. Among lung cancer subtypes, the most frequent is represented by adenocarcinoma (belonging to the Non-Small Cell Lung Cancer class) although the most challenging
Externí odkaz:
https://doaj.org/article/767f4d8955f54c4d8f86adb274e8c1c5
Autor:
Alberto Montalbano, Cesare Sala, Ginevra Chioccioli Altadonna, Andrea Becchetti, Annarosa Arcangeli
Publikováno v:
Heliyon, Vol 9, Iss 10, Pp e20112- (2023)
Pharmacological studies aimed at the development of newly synthesized drugs directed against ion channels (as well as genetic studies of ion channel mutations) involve the development and use of transfected cells. However, the identification of the b
Externí odkaz:
https://doaj.org/article/8755c13ce83541a580293f389aabe93b
Autor:
Ginevra Chioccioli Altadonna, Alberto Montalbano, Jessica Iorio, Andrea Becchetti, Annarosa Arcangeli, Claudia Duranti
Publikováno v:
Membranes, Vol 12, Iss 11, p 1162 (2022)
Ion channels are implicated in various diseases, including cancer, in which they modulate different aspects of cancer progression. In particular, potassium channels are often aberrantly expressed in cancers, a major example being provided by hERG1. T
Externí odkaz:
https://doaj.org/article/a6bae20526424c3b8684769e3e0b4094
Autor:
Lisa E.L. Romano, Wen Yih Aw, Kathryn M. Hixson, Tatiana V. Novoselova, Tammy M. Havener, Stefanie Howell, Bonnie Taylor-Blake, Charlotte L. Hall, Lei Xing, Josh Beri, Suran Nethisinghe, Laura Perna, Abubakar Hatimy, Ginevra Chioccioli Altadonna, Lee M. Graves, Laura E. Herring, Anthony J. Hickey, Konstantinos Thalassinos, J. Paul Chapple, Justin M. Wolter
Publikováno v:
Cell Reports. 41:111580
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is a childhood-onset cerebellar ataxia caused by mutations in SACS, which encodes the protein sacsin. Cellular ARSACS phenotypes include mitochondrial dysfunction, intermediate filame
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1efacf47940593ba8d8b563e29d0f497
https://doi.org/10.1016/j.celrep.2022.111580
https://doi.org/10.1016/j.celrep.2022.111580
Autor:
Anthony J. Hickey, Suran Nethisinghe, Abubakar Hatimy, Lei Xing, Charlotte L. Hall, Laura Perna, Wen Yih Aw, Stefanie D. Howell, Laura E. Herring, Tammy M. Havener, Josh Beri, Lee M. Graves, Ginevra Chioccioli Altadonna, Konstantinos Thalassinos, Justin M. Wolter, Kathryn M. Hixson, J. Paul Chapple, Lisa E.L. Romano, Tatiana V. Novoselova
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (ARSACS) is caused by mutations in SACS, which manifest as a childhood-onset cerebellar ataxia. Cellular ARSACS phenotypes include mitochondrial dysfunction, intermediate filament (IF) disorga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ddf55dbd3a1a1167cccb374e46fa9a4
https://doi.org/10.1101/2021.08.20.456807
https://doi.org/10.1101/2021.08.20.456807
