Clancy JP - Search Results

1

Extracellular zinc and ATP restore chloride secretion across cystic fibrosis airway epithelia by triggering calcium entry.

Zsembery A, Fortenberry JA, Liang L, Bebok Z, Tucker TA, Boyce AT, Braunstein GM, Welty E, Bell PD, Sorscher EJ, Clancy JP, Schwiebert EM. Zsembery A, et al. Among authors: clancy jp. J Biol Chem. 2004 Mar 12;279(11):10720-9. doi: 10.1074/jbc.M313391200. Epub 2003 Dec 29. J Biol Chem. 2004. PMID: 14701827 Free article.

2

Activation of chloride secretion in cystic fibrosis cells and tissues by the substituted imidazole SRI 2931.

Jones JR, Schwiebert EM, DuVall MD, Venglarik CJ, Wen H, Kovacs T, Mazur M, Clancy JP, Braunstein G, Bates E, Greer H, Maddry JA, Sorscher EJ. Jones JR, et al. Among authors: clancy jp. Biochemistry. 2003 Nov 18;42(45):13241-9. doi: 10.1021/bi0340447. Biochemistry. 2003. PMID: 14609335

3

Mutations in the amino terminus of the cystic fibrosis transmembrane conductance regulator enhance endocytosis.

Jurkuvenaite A, Varga K, Nowotarski K, Kirk KL, Sorscher EJ, Li Y, Clancy JP, Bebok Z, Collawn JF. Jurkuvenaite A, et al. Among authors: clancy jp. J Biol Chem. 2006 Feb 10;281(6):3329-34. doi: 10.1074/jbc.M508131200. Epub 2005 Dec 8. J Biol Chem. 2006. PMID: 16339147 Free article.

4

Cystic fibrosis transmembrane conductance regulator facilitates ATP release by stimulating a separate ATP release channel for autocrine control of cell volume regulation.

Braunstein GM, Roman RM, Clancy JP, Kudlow BA, Taylor AL, Shylonsky VG, Jovov B, Peter K, Jilling T, Ismailov II, Benos DJ, Schwiebert LM, Fitz JG, Schwiebert EM. Braunstein GM, et al. Among authors: clancy jp. J Biol Chem. 2001 Mar 2;276(9):6621-30. doi: 10.1074/jbc.M005893200. Epub 2000 Nov 10. J Biol Chem. 2001. PMID: 11110786 Free article.

5

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

6

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.

7

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

8

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

9

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

10

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

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