Taylor CJ - Search Results

1

Sodium channel blockers and uridine triphosphate: effects on nasal potential difference in cystic fibrosis mice.

Ghosal S, Taylor CJ, Colledge WH, Ratcliff R, Evans MJ. Ghosal S, et al. Among authors: taylor cj. Eur Respir J. 2000 Jan;15(1):146-50. doi: 10.1183/09031936.00.15114600. Eur Respir J. 2000. PMID: 10678637 Free article.

2

Evidence for cystic fibrosis transmembrane conductance regulator-dependent sodium reabsorption in kidney, using Cftr(tm2cam) mice.

Kibble JD, Neal AM, Colledge WH, Green R, Taylor CJ. Kibble JD, et al. Among authors: taylor cj. J Physiol. 2000 Jul 1;526 Pt 1(Pt 1):27-34. doi: 10.1111/j.1469-7793.2000.00027.x. J Physiol. 2000. PMID: 10878096 Free PMC article.

3

Acetylcholine induces cytosolic Ca2+ mobilization in isolated distal colonic crypts from normal and cystic fibrosis mice.

Klaren PH, Hardcastle J, Evans S, Colledge WH, Evans MJ, Taylor CJ, Hardcastle PT, White SJ. Klaren PH, et al. Among authors: taylor cj. J Pharm Pharmacol. 2001 Mar;53(3):371-7. doi: 10.1211/0022357011775424. J Pharm Pharmacol. 2001. PMID: 11291752

4

Effect of acute saline volume expansion in the anaesthetised DeltaF508 cystic fibrosis mouse.

Kibble JD, Neal A, Green R, Colledge WH, Taylor CJ. Kibble JD, et al. Among authors: taylor cj. Pflugers Arch. 2001;443 Suppl 1:S17-21. doi: 10.1007/s004240100638. Epub 2001 Jul 31. Pflugers Arch. 2001. PMID: 11845297

5

Modification of nasal membrane potential difference with inhaled amiloride and loperamide in the cystic fibrosis (CF) mouse.

Ghosal S, Taylor CJ, McGaw J. Ghosal S, et al. Among authors: taylor cj. Thorax. 1996 Dec;51(12):1229-32. doi: 10.1136/thx.51.12.1229. Thorax. 1996. PMID: 8994520 Free PMC article.

6

Head growth in cystic fibrosis following early diagnosis by neonatal screening.

Ghosal S, Taylor CJ, Pickering M, McGaw J. Ghosal S, et al. Among authors: taylor cj. Arch Dis Child. 1996 Sep;75(3):191-3. doi: 10.1136/adc.75.3.191. Arch Dis Child. 1996. PMID: 8976655 Free PMC article.

7

Disproportionate head growth retardation in cystic fibrosis.

Ghosal S, Taylor CJ, Pickering M, McGaw J, Beckles-Willson N, Wales JK. Ghosal S, et al. Among authors: taylor cj. Arch Dis Child. 1995 Feb;72(2):150-2. doi: 10.1136/adc.72.2.150. Arch Dis Child. 1995. PMID: 7702380 Free PMC article.

8

The use of dual-isotope imaging to compare the gastrointestinal transit of food and pancreatic enzyme pellets in cystic fibrosis patients.

Hillel PG, Tindale WB, Taylor CJ, Frier M, Senior S, Ghosal S. Hillel PG, et al. Among authors: taylor cj. Nucl Med Commun. 1998 Aug;19(8):761-9. doi: 10.1097/00006231-199808000-00006. Nucl Med Commun. 1998. PMID: 9751930

9

Gastric emptying and intestinal transit of pancreatic enzyme supplements in cystic fibrosis.

Taylor CJ, Hillel PG, Ghosal S, Frier M, Senior S, Tindale WB, Read N. Taylor CJ, et al. Arch Dis Child. 1999 Feb;80(2):149-52. doi: 10.1136/adc.80.2.149. Arch Dis Child. 1999. PMID: 10325730 Free PMC article.

10

Intravenous desensitization to ceftazidime in cystic fibrosis patients.

Ghosal S, Taylor CJ. Ghosal S, et al. Among authors: taylor cj. J Antimicrob Chemother. 1997 Apr;39(4):556-7. doi: 10.1093/jac/39.4.556. J Antimicrob Chemother. 1997. PMID: 9145836 Clinical Trial. No abstract available.

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