Author:
Puchelle Edith,Zahm Jean-Marie,de Bentzmann Sophie,Gaillard Dominique
Reference101 articles.
1. Engelhardt JF, Yankaskas JR, Emst SA, Yang Y, Marion CR, Boucher RC, Cohn JA, Wilson JM (1992) Submucosal glands are the predominant site of CFTR expression in the human bronchus. Nature Genet 2: 240–248.
2. Davis PB (1993) Pathophysiology of the lung disease in cystic fibrosis. In: Davis PB (ed.) Lung biology in health and disease. New York: Marcel Dekker, 193–218.
3. Boucher RC, Stutts MJ, Knowles MR, Cantley L, Gatzy JT (1986) Na’ transport in cystic fibrosis respiratory epithelial: Abnormal basal rate and response to adenylate cyclase activation. J Clin Invest 78: 1245–1252.
4. Boucher RC, Cotton CU, Gatzy JT, Knowles MR, Yankaskas JR (1988) Evidence for reduced C1- and increased Nam permeability in cystic fibrosis human primary cell cultures. JPhysiol; 405: 77–103.
5. Boucher RC (1994) Human airway ion transport: State of the Part. Part 1. Am JRespir Crit Care Med 150: 271–281.
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