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TMEM16A in Cystic Fibrosis: Activating or Inhibiting?

The inflammatory airway disease cystic fibrosis (CF) is characterized by airway obstruction due to mucus hypersecretion, airway plugging, and bronchoconstriction. The cystic fibrosis transmembrane conductance regulator (CFTR) chloride channel is dysfunctional in CF, leading to defects in epithelial...

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書目詳細資料
發表在:Front Pharmacol
Main Authors: Kunzelmann, Karl, Ousingsawat, Jiraporn, Cabrita, Inês, Doušová, Tereza, Bähr, Andrea, Janda, Melanie, Schreiber, Rainer, Benedetto, Roberta
格式: Artigo
語言:Inglês
出版: Frontiers Media S.A. 2019
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6362895/
https://ncbi.nlm.nih.gov/pubmed/30761000
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2019.00003
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