Cystic fibrosis: CFTR correctors to the rescue

Research output: Contribution to journalArticle (Academic Journal)peer-review

10 Citations (Scopus)

Abstract

Cystic fibrosis transmembrane conductance regulator (CFTR) correctors are small molecules that target the most common cause of cystic fibrosis: misfolded F508del-CFTR. Using differential scanning fluorimetry, Sampson et al. (2010) identify a CFTR corrector that interacts directly with the CFTR domain affected by the F508del mutation.
Translated title of the contributionCystic fibrosis: CFTR correctors to the rescue
Original languageEnglish
Pages (from-to)145 - 147
Number of pages3
JournalChemistry & Biology
Volume18
DOIs
Publication statusPublished - Feb 2011

Bibliographical note

Publisher: Elsevier Ltd
Other: Commentary

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