All Stories

  1. CFTR potentiators partially restore channel function to A561E‐CFTR, a cystic fibrosis mutant with a similar mechanism of dysfunction as F508del‐CFTR

    Article • British Journal of Pharmacology, September 2014, Wiley

    Dr David N Sheppard

  2. Revertant mutants modify, but do not rescue, the gating defect of the cystic fibrosis mutant G551D‐CFTR

    Article • The Journal of Physiology, March 2014, Wiley

    Dr David N Sheppard

  3. Loop diuretics are open-channel blockers of the cystic fibrosis transmembrane conductance regulator with distinct kinetics

    Article • British Journal of Pharmacology, December 2013, Wiley

    Dr David N Sheppard

  4. Acute inhibition of the cystic fibrosis transmembrane conductance regulator (CFTR) Cl- channel by thyroid hormones involves multiple mechanisms

    Article • AJP Cell Physiology, June 2013, American Physiological Society

    Dr David N Sheppard

  5. Impact of the cystic fibrosis mutation F508del-CFTR on renal cyst formation and growth

    Article • AJP Renal Physiology, August 2012, American Physiological Society

    Dr David N Sheppard