Disulphonic stilbene block of cystic fibrosis transmembrane conductance regulator Cl- channels expressed in a mammalian cell line and its regulation by a critical pore residue.

Por Linsdell, P, Hanrahan, J W
Publicado em 1996

Molecular determinants of anion selectivity in the cystic fibrosis transmembrane conductance regulator chloride channel pore.

Por Linsdell, P, Evagelidis, A, Hanrahan, J W
Publicado em 2000

Single anion-selective channels in basolateral membrane of a mammalian tight epithelium.

Por Hanrahan, J W, Alles, W P, Lewis, S A
Publicado em 1985

The cystic fibrosis transmembrane conductance regulator chloride channel. Iodide block and permeation.

Por Tabcharani, J A, Chang, X B, Riordan, J R, Hanrahan, J W
Publicado em 1992

Phosphorylation of protein kinase C sites in NBD1 and the R domain control CFTR channel activation by PKA

Por Chappe, V, Hinkson, D A, Zhu, T, Chang, X-B, Riordan, J R, Hanrahan, J W
Publicado em 2003

Structural basis for specificity and potency of xanthine derivatives as activators of the CFTR chloride channel

Por Chappe, V, Mettey, Y, Vierfond, J M, Hanrahan, J W, Gola, M, Verrier, B, Becq, F
Publicado em 1998

Phosphatase inhibitors activate normal and defective CFTR chloride channels.

Por Becq, F, Jensen, T J, Chang, X B, Savoia, A, Rommens, J M, Tsui, L C, Buchwald, M, Riordan, J R, Hanrahan, J W
Publicado em 1994