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The Journal of Pediatrics|March 20, 1998
Comparison of the clinical manifestations of cystic fibrosis in black and white patientsA Hamosh, S C FitzSimmons, M Macek, et al.
The Journal of Biological Chemistry|December 14, 1999
Correction of aberrant splicing of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by antisense oligonucleotidesK J Friedman, J Kole, J A Cohn, et al.
Science (New York, N.Y.)|September 9, 1983
Abnormal ion permeation through cystic fibrosis respiratory epitheliumM R Knowles, M J Stutts, A Spock, et al.
The Biochemical Journal|July 15, 1992
Bovine inositol monophosphatase. Modification, identification and mutagenesis of reactive cysteine residuesM R Knowles, N Gee, G McAllister, et al.
The Journal of Pediatrics|July 1, 1988
Electrical potential difference and ion transport across nasal epithelium of term neonates: correlation with mode of delivery, transient tachypnea of the newborn, and respiratory rateC W Gowen, E E Lawson, J Gingras, et al.
Gastroenterology|December 1, 2001
Cystic fibrosis gene mutations and pancreatitis risk: relation to epithelial ion transport and trypsin inhibitor gene mutationsP G Noone, Z Zhou, L M Silverman, et al.
FEBS Letters|November 9, 1992
Stable expression of human D3 dopamine receptors in GH4C1 pituitary cellsG R Seabrook, S Patel, R Marwood, et al.
Molecular Medicine (Cambridge, Mass.)|January 9, 2001
Basal nucleotide levels, release, and metabolism in normal and cystic fibrosis airwaysS H Donaldson, E R Lazarowski, M Picher, et al.
The Journal of Pharmacology and Experimental Therapeutics|January 1, 1994
Expression and pharmacological characterization of the human D3 dopamine receptorS B Freedman, S Patel, R Marwood, et al.
Chest|February 1, 1995
Pharmacologic treatment of abnormal ion transport in the airway epithelium in cystic fibrosisM R Knowles, K N Olivier, K W Hohneker, et al.
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