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GM1 as Adjuvant of Innovative Therapies for Cystic Fibrosis Disease
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein is expressed at the apical plasma membrane (PM) of different epithelial cells. The most common mutation responsible for the onset of cystic fibrosis (CF), F508del, inhibits the biosynthesis and transport of the protein at PM, and als...
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| Pubblicato in: | Int J Mol Sci |
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| Autori principali: | , , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7350007/ https://ncbi.nlm.nih.gov/pubmed/32599772 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21124486 |
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