BACKGROUND Increasing the activity of defective cystic fibrosis transmembrane conductance regulator (CFTR) protein is a potential treatment for cystic fibrosis.

背景提高有缺陷的囊性纤维化跨膜电导调节(CFTR)蛋白的活性是囊性纤维化的一种潜在治疗。

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Genistein, a naturally occurring isoflavone, augments in vitro epithelial anion transport via activation of the cystic fibrosis transmembrane conductance regulator chloride channel.

染料木素是一种天然的异黄酮，在体外通过活化膜纤维化跨膜转运调节氯离子通道增加上皮阴离子的转运。

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The idea is this: Kalydeco works by improving the function of the Cystic Fibrosis Transmembrane Regulator protein.

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Kalydeco works by correcting the protein that is defective in cystic fibrosis, called the cystic fibrosis transmembrane conductance regulator, which helps move salt ions across cells.

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