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The DeltaF508 mutation results in loss of CFTR function and mature protein in native human colon.
Mall M, Kreda SM, Mengos A, Jensen TJ, Hirtz S, Seydewitz HH, Yankaskas J, Kunzelmann K, Riordan JR, Boucher RC. Mall M, et al. Gastroenterology. 2004 Jan;126(1):32-41. doi: 10.1053/j.gastro.2003.10.049. Gastroenterology. 2004. PMID: 14699484
Promoter of the canine tracheobronchial mucin gene.
Verma M, Murthy VV, Mathew S, Banerji D, Kurl RN, Olnes MJ, Yankaskas JR, Blass C, Davidson EA. Verma M, et al. Glycoconj J. 1996 Oct;13(5):797-807. doi: 10.1007/BF00702344. Glycoconj J. 1996. PMID: 8910007
Abnormal glutathione transport in cystic fibrosis airway epithelia.
Gao L, Kim KJ, Yankaskas JR, Forman HJ. Gao L, et al. Am J Physiol. 1999 Jul;277(1):L113-8. doi: 10.1152/ajplung.1999.277.1.L113. Am J Physiol. 1999. PMID: 10409237
Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.
Pier GB, Grout M, Zaidi TS, Olsen JC, Johnson LG, Yankaskas JR, Goldberg JB. Pier GB, et al. Science. 1996 Jan 5;271(5245):64-7. doi: 10.1126/science.271.5245.64. Science. 1996. PMID: 8539601 Free PMC article.
Coupled secretion of chloride and mucus in skin of Xenopus laevis: possible role for CFTR.
Engelhardt JF, Smith SS, Allen E, Yankaskas JR, Dawson DC, Wilson JM. Engelhardt JF, et al. Am J Physiol. 1994 Aug;267(2 Pt 1):C491-500. doi: 10.1152/ajpcell.1994.267.2.C491. Am J Physiol. 1994. PMID: 7521128
Expression of the cystic fibrosis gene in adult human lung.
Engelhardt JF, Zepeda M, Cohn JA, Yankaskas JR, Wilson JM. Engelhardt JF, et al. J Clin Invest. 1994 Feb;93(2):737-49. doi: 10.1172/JCI117028. J Clin Invest. 1994. PMID: 7509347 Free PMC article.
Correction of the apical membrane chloride permeability defect in polarized cystic fibrosis airway epithelia following retroviral-mediated gene transfer.
Olsen JC, Johnson LG, Stutts MJ, Sarkadi B, Yankaskas JR, Swanstrom R, Boucher RC. Olsen JC, et al. Hum Gene Ther. 1992 Jun;3(3):253-66. doi: 10.1089/hum.1992.3.3-253. Hum Gene Ther. 1992. PMID: 1379473
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