Clancy JP - Search Results

1

Relationship between airway ion transport and a mild pulmonary disease mutation in CFTR.

Walker LC, Venglarik CJ, Aubin G, Weatherly MR, McCarty NA, Lesnick B, Ruiz F, Clancy JP, Sorscher EJ. Walker LC, et al. Among authors: clancy jp. Am J Respir Crit Care Med. 1997 May;155(5):1684-9. doi: 10.1164/ajrccm.155.5.9154877. Am J Respir Crit Care Med. 1997. PMID: 9154877

2

Restoration of W1282X CFTR activity by enhanced expression.

Rowe SM, Varga K, Rab A, Bebok Z, Byram K, Li Y, Sorscher EJ, Clancy JP. Rowe SM, et al. Among authors: clancy jp. Am J Respir Cell Mol Biol. 2007 Sep;37(3):347-56. doi: 10.1165/rcmb.2006-0176OC. Epub 2007 May 31. Am J Respir Cell Mol Biol. 2007. PMID: 17541014 Free PMC article.

3

Suppression of a CFTR premature stop mutation in a bronchial epithelial cell line.

Bedwell DM, Kaenjak A, Benos DJ, Bebok Z, Bubien JK, Hong J, Tousson A, Clancy JP, Sorscher EJ. Bedwell DM, et al. Among authors: clancy jp. Nat Med. 1997 Nov;3(11):1280-4. doi: 10.1038/nm1197-1280. Nat Med. 1997. PMID: 9359706

4

Purification, characterization, and expression of CFTR nucleotide-binding domains.

Clancy JP, Bebök Z, Sorscher EJ. Clancy JP, et al. J Bioenerg Biomembr. 1997 Oct;29(5):475-82. doi: 10.1023/a:1022487024031. J Bioenerg Biomembr. 1997. PMID: 9511932

5

Adenosine and its nucleotides activate wild-type and R117H CFTR through an A2B receptor-coupled pathway.

Clancy JP, Ruiz FE, Sorscher EJ. Clancy JP, et al. Am J Physiol. 1999 Feb;276(2):C361-9. doi: 10.1152/ajpcell.1999.276.2.C361. Am J Physiol. 1999. PMID: 9950763

6

Evidence that systemic gentamicin suppresses premature stop mutations in patients with cystic fibrosis.

Clancy JP, Bebök Z, Ruiz F, King C, Jones J, Walker L, Greer H, Hong J, Wing L, Macaluso M, Lyrene R, Sorscher EJ, Bedwell DM. Clancy JP, et al. Am J Respir Crit Care Med. 2001 Jun;163(7):1683-92. doi: 10.1164/ajrccm.163.7.2004001. Am J Respir Crit Care Med. 2001. PMID: 11401894

7

A(2) adenosine receptors regulate CFTR through PKA and PLA(2).

Cobb BR, Ruiz F, King CM, Fortenberry J, Greer H, Kovacs T, Sorscher EJ, Clancy JP. Cobb BR, et al. Among authors: clancy jp. Am J Physiol Lung Cell Mol Physiol. 2002 Jan;282(1):L12-25. doi: 10.1152/ajplung.2002.282.1.L12. Am J Physiol Lung Cell Mol Physiol. 2002. PMID: 11741811 Free article.

8

Adenosine receptors and phosphodiesterase inhibitors stimulate Cl- secretion in Calu-3 cells.

Cobb BR, Fan L, Kovacs TE, Sorscher EJ, Clancy JP. Cobb BR, et al. Among authors: clancy jp. Am J Respir Cell Mol Biol. 2003 Sep;29(3 Pt 1):410-8. doi: 10.1165/rcmb.2002-0247OC. Epub 2003 Apr 24. Am J Respir Cell Mol Biol. 2003. PMID: 12714375

9

Cystic fibrosis transmembrane conductance regulator (CFTR) nucleotide-binding domain 1 (NBD-1) and CFTR truncated within NBD-1 target to the epithelial plasma membrane and increase anion permeability.

Clancy JP, Hong JS, Bebök Z, King SA, Demolombe S, Bedwell DM, Sorscher EJ. Clancy JP, et al. Biochemistry. 1998 Oct 27;37(43):15222-30. doi: 10.1021/bi980436f. Biochemistry. 1998. PMID: 9790686

10

A clinical inflammatory syndrome attributable to aerosolized lipid-DNA administration in cystic fibrosis.

Ruiz FE, Clancy JP, Perricone MA, Bebok Z, Hong JS, Cheng SH, Meeker DP, Young KR, Schoumacher RA, Weatherly MR, Wing L, Morris JE, Sindel L, Rosenberg M, van Ginkel FW, McGhee JR, Kelly D, Lyrene RK, Sorscher EJ. Ruiz FE, et al. Among authors: clancy jp. Hum Gene Ther. 2001 May 1;12(7):751-61. doi: 10.1089/104303401750148667. Hum Gene Ther. 2001. PMID: 11339892 Clinical Trial.

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