Fig. 2From: DMBT1 is upregulated in cystic fibrosis, affects ciliary motility, and is reduced by acetylcysteineExpression of Dmbt1 and interaction partners in a transgenic mouse model of cystic fibrosis-like lung disease. Dmbt1 and its binding partners surfactant protein A, surfactant protein D and Trefoil factor 2 were upregulated in the ENaC transgenic mouse model of cystic fibrosis-like lung disease (ENaC-tg mice) compared to wild-type control animals (wt mice) using qRT-PCR. ß-actin and Tfrc were used as housekeeping genes. Data were from 3 mice per groupBack to article page