Welsh MJ - Search Results

1

CFTR is required for maximal transepithelial liquid transport in pig alveolar epithelia.

Li X, Comellas AP, Karp PH, Ernst SE, Moninger TO, Gansemer ND, Taft PJ, Pezzulo AA, Rector MV, Rossen N, Stoltz DA, McCray PB Jr, Welsh MJ, Zabner J. Li X, et al. Among authors: welsh mj. Am J Physiol Lung Cell Mol Physiol. 2012 Jul;303(2):L152-60. doi: 10.1152/ajplung.00116.2012. Epub 2012 May 25. Am J Physiol Lung Cell Mol Physiol. 2012. PMID: 22637155 Free PMC article.

2

Effect of ATP-sensitive K+ channel regulators on cystic fibrosis transmembrane conductance regulator chloride currents.

Sheppard DN, Welsh MJ. Sheppard DN, et al. Among authors: welsh mj. J Gen Physiol. 1992 Oct;100(4):573-91. doi: 10.1085/jgp.100.4.573. J Gen Physiol. 1992. PMID: 1281220 Free PMC article.

3

cAMP stimulates bicarbonate secretion across normal, but not cystic fibrosis airway epithelia.

Smith JJ, Welsh MJ. Smith JJ, et al. Among authors: welsh mj. J Clin Invest. 1992 Apr;89(4):1148-53. doi: 10.1172/JCI115696. J Clin Invest. 1992. PMID: 1313448 Free PMC article.

4

Chloride channels in the apical membrane of normal and cystic fibrosis airway and intestinal epithelia.

Anderson MP, Sheppard DN, Berger HA, Welsh MJ. Anderson MP, et al. Among authors: welsh mj. Am J Physiol. 1992 Jul;263(1 Pt 1):L1-14. doi: 10.1152/ajplung.1992.263.1.L1. Am J Physiol. 1992. PMID: 1322048 Review.

5

Localization of cystic fibrosis transmembrane conductance regulator in chloride secretory epithelia.

Denning GM, Ostedgaard LS, Cheng SH, Smith AE, Welsh MJ. Denning GM, et al. Among authors: welsh mj. J Clin Invest. 1992 Jan;89(1):339-49. doi: 10.1172/JCI115582. J Clin Invest. 1992. PMID: 1370301 Free PMC article.

6

Abnormal localization of cystic fibrosis transmembrane conductance regulator in primary cultures of cystic fibrosis airway epithelia.

Denning GM, Ostedgaard LS, Welsh MJ. Denning GM, et al. Among authors: welsh mj. J Cell Biol. 1992 Aug;118(3):551-9. doi: 10.1083/jcb.118.3.551. J Cell Biol. 1992. PMID: 1379244 Free PMC article.

7

Regulation by ATP and ADP of CFTR chloride channels that contain mutant nucleotide-binding domains.

Anderson MP, Welsh MJ. Anderson MP, et al. Among authors: welsh mj. Science. 1992 Sep 18;257(5077):1701-4. doi: 10.1126/science.1382316. Science. 1992. PMID: 1382316

8

Expression of cystic fibrosis transmembrane conductance regulator corrects defective chloride channel regulation in cystic fibrosis airway epithelial cells.

Rich DP, Anderson MP, Gregory RJ, Cheng SH, Paul S, Jefferson DM, McCann JD, Klinger KW, Smith AE, Welsh MJ. Rich DP, et al. Among authors: welsh mj. Nature. 1990 Sep 27;347(6291):358-63. doi: 10.1038/347358a0. Nature. 1990. PMID: 1699126

9

Generation of cAMP-activated chloride currents by expression of CFTR.

Anderson MP, Rich DP, Gregory RJ, Smith AE, Welsh MJ. Anderson MP, et al. Among authors: welsh mj. Science. 1991 Feb 8;251(4994):679-82. doi: 10.1126/science.1704151. Science. 1991. PMID: 1704151

10

Developing fetal alveolar epithelial cells secrete fluid in primary culture.

McCray PB Jr, Welsh MJ. McCray PB Jr, et al. Among authors: welsh mj. Am J Physiol. 1991 Jun;260(6 Pt 1):L494-500. doi: 10.1152/ajplung.1991.260.6.L494. Am J Physiol. 1991. PMID: 1711786

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