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Lancet (London, England)|May 11, 1991
Diagnosis of genetic disease by primer-specified restriction map modification, with application to cystic fibrosis and retinitis pigmentosaE J Sorscher, Z HuangBiochemistry|August 10, 2000
R-domain interactions with distal regions of CFTR lead to phosphorylation and activationS A King, E J SorscherLancet (London, England)|February 13, 1982
Cystic fibrosis: a disorder of calcium-stimulated secretion and transepithelial sodium transport?E J Sorscher, J L BreslowJournal of Bioenergetics and Biomembranes|March 25, 1998
Purification, characterization, and expression of CFTR nucleotide-binding domainsJ P Clancy, Z Bebök, E J SorscherThe American Journal of Physiology|February 10, 1999
Adenosine and its nucleotides activate wild-type and R117H CFTR through an A2B receptor-coupled pathwayJ P Clancy, F E Ruiz, E J SorscherThe American Journal of Physiology|February 1, 1989
Immunocytochemical localization of Na+ channels in rat kidney medullaD Brown, E J Sorscher, D A Ausiello, et al.The Journal of Cell Biology|September 24, 1999
Characterization and dynamics of aggresome formation by a cytosolic GFP-chimeraR García-Mata, Z Bebök, E J Sorscher, et al.Proceedings of the National Academy of Sciences of the United States of America|March 1, 1992
Intrinsic anion channel activity of the recombinant first nucleotide binding fold domain of the cystic fibrosis transmembrane regulator proteinN Arispe, E Rojas, J Hartman, et al.The American Journal of Physiology|October 12, 1999
CFTR involvement in chloride, bicarbonate, and liquid secretion by airway submucosal glandsS T Ballard, L Trout, Z Bebök, et al.The Journal of Biological Chemistry|September 25, 1988
Phosphorylation of a single subunit of the epithelial Na+ channel protein following vasopressin treatment of A6 cellsS Sariban-Sohraby, E J Sorscher, B M Brenner, et al.Pageof 6