Anthony J. Fischer

This study investigates how particle size affects mucociliary transport in normal and cystic fibrosis airways using a trachea-on-a-chip model.

This paper shows that in utero ivacaftor treatment rescues multiple organ defects in CFTR-G551D pigs, improving pancreatic, gallbladder, and vas deferens function.

This paper develops a PCD pig model with DNAI1 mutations and characterizes its respiratory and sinus disease features, showing similarities to human PCD.