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Residual chloride secretion in intestinal tissue of ΔF508 homozygous twins and siblings with cystic fibrosis

Inez Bronsveld, Frauke Mekus, Jan Bijman, Manfred Ballmann, Joachim Greipel, J. Hundrieser, Dicky Halley, Ulrike Laabs, Roger Busche, Hugo R. de Jonge,

Gastroenterology · 2000 · 93 citations · 34 references

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34

The Metabolic Basis of Inherited Disease

Annals of Internal Medicine · 1990 · 4K citations

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Amiloride-sensitive epithelial Na+ channel is made of three homologous subunits

Cecilia M. Canessa, Laurent Schild, Gary Buell et al. · Nature · 1994 · 2K citations

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

Seng H. Cheng, Richard J. Gregory, John Marshall et al. · Cell · 1990 · 1.8K citations

, , +12

Purification and functional reconstitution of the cystic fibrosis transmembrane conductance regulator (CFTR)

Christine E. Bear, Canhui Li, Norbert Kartner et al. · Cell · 1992 · 946 citations

, , +14

Increased Bioelectric Potential Difference across Respiratory Epithelia in Cystic Fibrosis

Michael R. Knowles, John T. Gatzy, Richard C. Boucher · New England Journal of Medicine · 1981 · 582 citations

, , +17