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251 results
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Cystic fibrosis transmembrane conductance regulator inhibits epithelial Na+ channels carrying Liddle's syndrome mutations.
Hopf A, Schreiber R, Mall M, Greger R, Kunzelmann K. Hopf A, et al. Among authors: mall m. J Biol Chem. 1999 May 14;274(20):13894-9. doi: 10.1074/jbc.274.20.13894. J Biol Chem. 1999. PMID: 10318798
Mutations in the putative pore-forming domain of CFTR do not change anion selectivity of the cAMP activated Cl- conductance.
Hipper A, Mall M, Greger R, Kunzelmann K. Hipper A, et al. Among authors: mall m. FEBS Lett. 1995 Nov 6;374(3):312-6. doi: 10.1016/0014-5793(95)01132-x. FEBS Lett. 1995. PMID: 7589561
Wild type but not deltaF508 CFTR inhibits Na+ conductance when coexpressed in Xenopus oocytes.
Mall M, Hipper A, Greger R, Kunzelmann K. Mall M, et al. FEBS Lett. 1996 Feb 26;381(1-2):47-52. doi: 10.1016/0014-5793(96)00079-8. FEBS Lett. 1996. PMID: 8641437
cAMP stimulation of CFTR-expressing Xenopus oocytes activates a chromanol-inhibitable K+ conductance.
Mall M, Kunzelmann K, Hipper A, Busch AE, Greger R. Mall M, et al. Pflugers Arch. 1996 Jul;432(3):516-22. doi: 10.1007/s004240050164. Pflugers Arch. 1996. PMID: 8766012
Regulation of epithelial ion channels by the cystic fibrosis transmembrane conductance regulator.
Greger R, Mall M, Bleich M, Ecke D, Warth R, Riedemann N, Kunzelmann K. Greger R, et al. Among authors: mall m. J Mol Med (Berl). 1996 Sep;74(9):527-34. doi: 10.1007/BF00204979. J Mol Med (Berl). 1996. PMID: 8892058 Review.
The cystic fibrosis transmembrane conductance regulator attenuates the endogenous Ca2+ activated Cl- conductance of Xenopus oocytes.
Kunzelmann K, Mall M, Briel M, Hipper A, Nitschke R, Ricken S, Greger R. Kunzelmann K, et al. Among authors: mall m. Pflugers Arch. 1997 Dec;435(1):178-81. doi: 10.1007/s004240050498. Pflugers Arch. 1997. PMID: 9359918
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.
Cholinergic ion secretion in human colon requires coactivation by cAMP.
Mall M, Bleich M, Schürlein M, Kühr J, Seydewitz HH, Brandis M, Greger R, Kunzelmann K. Mall M, et al. Am J Physiol. 1998 Dec;275(6):G1274-81. doi: 10.1152/ajpgi.1998.275.6.G1274. Am J Physiol. 1998. PMID: 9843763
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. Among authors: mall m. 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.
CFTR-mediated inhibition of epithelial Na+ conductance in human colon is defective in cystic fibrosis.
Mall M, Bleich M, Kuehr J, Brandis M, Greger R, Kunzelmann K. Mall M, et al. Am J Physiol. 1999 Sep;277(3):G709-16. doi: 10.1152/ajpgi.1999.277.3.G709. Am J Physiol. 1999. PMID: 10484398
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