Normalization of Sweat Chloride Concentration and Clinical Improvement With Ivacaftor in a Patient With Cystic Fibrosis With Mutation S549N

Por McGarry, Meghan E., Nielson, Dennis W.
Publicado no Chest (2013)

Airway surface liquid depth measured in ex vivo fragments of pig and human trachea: dependence on Na(+) and Cl(−) channel function

Por Song, Yuanlin, Namkung, Wan, Nielson, Dennis W., Lee, Jae-Woo, Finkbeiner, Walter E., Verkman, A. S.
Publicado em 2009

In Vivo and In Vitro Ivacaftor Response in Cystic Fibrosis Patients With Residual CFTR Function: N-of-1 Studies

Por McGarry, Meghan E., Illek, Beate, Ly, Ngoc P., Zlock, Lorna, Olshansky, Sabrina, Moreno, Courtney, Finkbeiner, Walter E., Nielson, Dennis W.
Publicado no Pediatr Pulmonol (2017)

Correctors and Potentiators Rescue Function of the Truncated W1282X-Cystic Fibrosis Transmembrane Regulator (CFTR) Translation Product

Por Haggie, Peter M., Phuan, Puay-Wah, Tan, Joseph-Anthony, Xu, Haijin, Avramescu, Radu G., Perdomo, Doranda, Zlock, Lorna, Nielson, Dennis W., Finkbeiner, Walter E., Lukacs, Gergely L., Verkman, Alan S.
Publicado no J Biol Chem (2017)