Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mazzei M. T."'
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
Autor:
Paolo La Colla, M. Mazzei, Fabio Marongiu, Maurizio Fermeglia, Erika Nieddu, Marco Ferrone, Mauro Mazzei, Mariangela Miele, Cristina Ibba, Alessandro Balbi, Sabrina Pricl, Roberta Loddo
Publikováno v:
Bioorganic & Medicinal Chemistry. 16:2591-2605
Some Mannich bases of 7-hydroxycoumarin (2) and their simple derivatives (3 and 4) were prepared and tested against viruses containing single-stranded, positive-sense RNA genomes (ssRNA(+)). This study was directed toward Flaviviridae and, in particu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::865bd43a286f5b047cb6e9e251e22c72
https://doi.org/10.1016/j.bmc.2007.11.045
https://doi.org/10.1016/j.bmc.2007.11.045
Autor:
CATENI, FRANCESCA, ZACCHIGNA, MARINA, Mazzei, M., Mannino, S., Mazzei, M.t., Drioli, S., Pedemonte, N., Gallietta, L.
The search for drugs to treat cystic fibrosis (CF) has to take into account the large number of mutations affecting the gene and the variety of molecular mechanism through which these mutations cause the functional defect. For instance, deletion of p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2817c179548ffa7709730e58e216335c
http://hdl.handle.net/11368/2832274
http://hdl.handle.net/11368/2832274