Welsh MJ - Search Results

1

The mammalian sodium channel BNC1 is required for normal touch sensation.

Price MP, Lewin GR, McIlwrath SL, Cheng C, Xie J, Heppenstall PA, Stucky CL, Mannsfeldt AG, Brennan TJ, Drummond HA, Qiao J, Benson CJ, Tarr DE, Hrstka RF, Yang B, Williamson RA, Welsh MJ. Price MP, et al. Among authors: welsh mj. Nature. 2000 Oct 26;407(6807):1007-11. doi: 10.1038/35039512. Nature. 2000. PMID: 11069180

2

Processing of mutant cystic fibrosis transmembrane conductance regulator is temperature-sensitive.

Denning GM, Anderson MP, Amara JF, Marshall J, Smith AE, Welsh MJ. Denning GM, et al. Among authors: welsh mj. Nature. 1992 Aug 27;358(6389):761-4. doi: 10.1038/358761a0. Nature. 1992. PMID: 1380673

3

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

4

Cyclic AMP-dependent protein kinase opens chloride channels in normal but not cystic fibrosis airway epithelium.

Li M, McCann JD, Liedtke CM, Nairn AC, Greengard P, Welsh MJ. Li M, et al. Among authors: welsh mj. Nature. 1988 Jan 28;331(6154):358-60. doi: 10.1038/331358a0. Nature. 1988. PMID: 2448645

5

Mutations in CFTR associated with mild-disease-form Cl- channels with altered pore properties.

Sheppard DN, Rich DP, Ostedgaard LS, Gregory RJ, Smith AE, Welsh MJ. Sheppard DN, et al. Among authors: welsh mj. Nature. 1993 Mar 11;362(6416):160-4. doi: 10.1038/362160a0. Nature. 1993. PMID: 7680769

6

Cloning and expression of the beta- and gamma-subunits of the human epithelial sodium channel.

McDonald FJ, Price MP, Snyder PM, Welsh MJ. McDonald FJ, et al. Among authors: welsh mj. Am J Physiol. 1995 May;268(5 Pt 1):C1157-63. doi: 10.1152/ajpcell.1995.268.5.C1157. Am J Physiol. 1995. PMID: 7762608

7

Mechanism by which Liddle's syndrome mutations increase activity of a human epithelial Na+ channel.

Snyder PM, Price MP, McDonald FJ, Adams CM, Volk KA, Zeiher BG, Stokes JB, Welsh MJ. Snyder PM, et al. Among authors: welsh mj. Cell. 1995 Dec 15;83(6):969-78. doi: 10.1016/0092-8674(95)90212-0. Cell. 1995. PMID: 8521520 Free article.

8

Cloning and expression of a novel human brain Na+ channel.

Price MP, Snyder PM, Welsh MJ. Price MP, et al. Among authors: welsh mj. J Biol Chem. 1996 Apr 5;271(14):7879-82. doi: 10.1074/jbc.271.14.7879. J Biol Chem. 1996. PMID: 8626462 Free article.

9

Function of Xenopus cystic fibrosis transmembrane conductance regulator (CFTR) Cl channels and use of human-Xenopus chimeras to investigate the pore properties of CFTR.

Price MP, Ishihara H, Sheppard DN, Welsh MJ. Price MP, et al. Among authors: welsh mj. J Biol Chem. 1996 Oct 11;271(41):25184-91. doi: 10.1074/jbc.271.41.25184. J Biol Chem. 1996. PMID: 8810276 Free article.

10

Stimulation of CFTR activity by its phosphorylated R domain.

Winter MC, Welsh MJ. Winter MC, et al. Among authors: welsh mj. Nature. 1997 Sep 18;389(6648):294-6. doi: 10.1038/38514. Nature. 1997. PMID: 9305845

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