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The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways.
Mall M, Bleich M, Greger R, Schreiber R, Kunzelmann K. Mall M, et al. J Clin Invest. 1998 Jul 1;102(1):15-21. doi: 10.1172/JCI2729. J Clin Invest. 1998. PMID: 9649552 Free PMC article.
CFTR, a regulator of channels.
Kunzelmann K, Schreiber R. Kunzelmann K, et al. J Membr Biol. 1999 Mar 1;168(1):1-8. doi: 10.1007/s002329900492. J Membr Biol. 1999. PMID: 10051684 Review. No abstract available.
The first-nucleotide binding domain of the cystic-fibrosis transmembrane conductance regulator is important for inhibition of the epithelial Na+ channel.
Schreiber R, Hopf A, Mall M, Greger R, Kunzelmann K. Schreiber R, et al. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5310-5. doi: 10.1073/pnas.96.9.5310. Proc Natl Acad Sci U S A. 1999. PMID: 10220462 Free PMC article.
Molecular and functional characterization of the small Ca(2+)-regulated K+ channel (rSK4) of colonic crypts.
Warth R, Hamm K, Bleich M, Kunzelmann K, von Hahn T, Schreiber R, Ullrich E, Mengel M, Trautmann N, Kindle P, Schwab A, Greger R. Warth R, et al. Pflugers Arch. 1999 Sep;438(4):437-44. doi: 10.1007/s004249900059. Pflugers Arch. 1999. PMID: 10519135
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