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Abnormal pro-gly-pro pathway and airway neutrophilia in pediatric cystic fibrosis.
Turnbull AR, Pyle CJ, Patel DF, Jackson PL, Hilliard TN, Regamey N, Tan HL, Brown S, Thursfield R, Short C, Mc Fie M, Alton EWFW, Gaggar A, Blalock JE, Lloyd CM, Bush A, Davies JC, Snelgrove RJ. Turnbull AR, et al. Among authors: davies jc. J Cyst Fibros. 2020 Jan;19(1):40-48. doi: 10.1016/j.jcf.2019.05.017. Epub 2019 Jun 5. J Cyst Fibros. 2020. PMID: 31176670 Free PMC article.
The clinical use of rhDNAse.
Davies J, Trindale M, Wallis C, Rosenthal M, Bush A. Davies J, et al. Pediatr Pulmonol Suppl. 1997;16:273-4. doi: 10.1002/ppul.19502308141. Pediatr Pulmonol Suppl. 1997. PMID: 9443309 Review. No abstract available.
Prospects for gene therapy for cystic fibrosis.
Davies JC, Geddes DM, Alton EW. Davies JC, et al. Mol Med Today. 1998 Jul;4(7):292-9. doi: 10.1016/s1357-4310(98)01265-9. Mol Med Today. 1998. PMID: 9743990 Review.
Cationic lipid-mediated CFTR gene transfer to the lungs and nose of patients with cystic fibrosis: a double-blind placebo-controlled trial.
Alton EW, Stern M, Farley R, Jaffe A, Chadwick SL, Phillips J, Davies J, Smith SN, Browning J, Davies MG, Hodson ME, Durham SR, Li D, Jeffery PK, Scallan M, Balfour R, Eastman SJ, Cheng SH, Smith AE, Meeker D, Geddes DM. Alton EW, et al. Lancet. 1999 Mar 20;353(9157):947-54. doi: 10.1016/s0140-6736(98)06532-5. Lancet. 1999. PMID: 10459902 Clinical Trial.
376 results