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of 195
pro vyhledávání: '"Galietta L"'
Novel tricyclic pyrrolo-quinolines as pharmacological correctors of the mutant CFTR chloride channel
Autor:
Renda M., Barreca M., Borrelli A., Spano' V., Montalbano A., Raimondi M. V., Bivacqua R., Musante I., Scudieri P., Guidone D., Buccirossi M., Genovese M., Venturini A., Bandiera T., Barraja P., Galietta L. J. V.
Publikováno v:
Scientific Reports. 13
F508del, the most frequent mutation in cystic fibrosis (CF), impairs the stability and folding of the CFTR chloride channel, thus resulting in intracellular retention and CFTR degradation. The F508del defect can be targeted with pharmacological corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56ad187e567b0fe97b88d1862050808e
https://doi.org/10.1038/s41598-023-34440-0
https://doi.org/10.1038/s41598-023-34440-0
Publikováno v:
In Journal of Cystic Fibrosis October 2023 22 Supplement 3:S157-S157
Autor:
Vega G., Guequen A., Johansson M. E. V., Arike L., Martinez-Abad B., Nystrom E. E. L., Scudieri P., Pedemonte N., Millar-Buchner P., Philp A. R., Galietta L. J., Hansson G. C., Flores C. A.
[This corrects the article DOI: 10.3389/fphys.2019.00694.].
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::554ac4d0bdc368a047d8f12700a2d62f
http://hdl.handle.net/11588/782412
http://hdl.handle.net/11588/782412
Autor:
Simonin J., Bille E., Crambert G., Noel S., Dreano E., Edwards A., Hatton A., Pranke I., Villeret B., Cottart C. -H., Vrel J. -P., Urbach V., Baatallah N., Hinzpeter A., Golec A., Touqui L., Nassif X., Galietta L. J. V., Planelles G., Sallenave J. -M., Edelman A., Sermet-Gaudelus I.
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::a23450137477cdb6b9397b8787da1d4f
http://hdl.handle.net/11588/782283
http://hdl.handle.net/11588/782283
Autor:
Tomati V., Caci E., Ferrera L., Pesce E., Sondo E., Cholon D. M., Quinney N. L., Boyles S. E., Armirotti A., Ravazzolo R., Galietta L. J. V., Gentzsch M., Pedemonte N.
The unit for the concentration of peptide in the proliferation study was incorrectly reported in the Results and Methods sections and the Figure 4 legend. The corrected sentences, with sections indicated, are below. Results Evaluation of Tα-1 sequen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::2a028541401ffec90510e9b30e7e468e
http://hdl.handle.net/11588/795518
http://hdl.handle.net/11588/795518
Autor:
Colombo, C., Alicandro, G., Bandera, A., Bouché, V., Biffi, A., Boraso, M., Cacchiarelli, D., Ciciriello, F., Cipolli, M., Gramegna, A., Itri, T., Lucidi, V., Medino, P., Rosazza, C., Galietta, L.
Publikováno v:
In Journal of Cystic Fibrosis October 2022 21 Supplement 2:S298-S298
Autor:
Jaboreck, M.-C., Merkert, S., von Schledorn, L., Zöllner, J., Cleve, N., Haase, A., Olmer, R., Martin, U., Galietta, L., Mall, M., Balázs, A.
Publikováno v:
In Journal of Cystic Fibrosis June 2022 21 Supplement 1:S65-S66
Autor:
CATENI, FRANCESCA, ZACCHIGNA, MARINA, Pedemonte N., Galietta L. J. V., Mazzei M. T., Fossa P., Giampieri M., Mazzei M.
The gating of the CFTR chloride channel is altered by a group of mutations that cause cystic fibrosis. This gating defect may be corrected by small molecules called potentiators. Some 1,4-dihydropyridine (DHP) derivatives, bearing a thiophen-2-yl and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6b5d3b292d27e725d061405ea5468f03
http://hdl.handle.net/11368/2297176
http://hdl.handle.net/11368/2297176
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Autor:
Galietta, L., Donaldson, S. H.
Our current understanding of the pathogenesis of cystic fibrosis (CF) lung disease stresses the importance of the physical and chemical properties of the airway surface liquid (ASL). In particular, the loss of cystic fibrosis transmembrane conductanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9edcb628393ffc39d04d82b03dfd1e99