Sorscher EJ - Search Results

1

Comparison of vectorial ion transport in primary murine airway and human sinonasal air-liquid interface cultures, models for studies of cystic fibrosis, and other airway diseases.

Zhang S, Fortenberry JA, Cohen NA, Sorscher EJ, Woodworth BA. Zhang S, et al. Among authors: sorscher ej. Am J Rhinol Allergy. 2009 Mar-Apr;23(2):149-52. doi: 10.2500/ajra.2009.23.3285. Am J Rhinol Allergy. 2009. PMID: 19401039

2

Antisense oligodeoxynucleotide to the cystic fibrosis gene inhibits anion transport in normal cultured sweat duct cells.

Sorscher EJ, Kirk KL, Weaver ML, Jilling T, Blalock JE, LeBoeuf RD. Sorscher EJ, et al. Proc Natl Acad Sci U S A. 1991 Sep 1;88(17):7759-62. doi: 10.1073/pnas.88.17.7759. Proc Natl Acad Sci U S A. 1991. PMID: 1715578 Free PMC article.

3

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: sorscher ej. 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

4

Activation of DeltaF508 CFTR in an epithelial monolayer.

Bebök Z, Venglarik CJ, Pánczél Z, Jilling T, Kirk KL, Sorscher EJ. Bebök Z, et al. Among authors: sorscher ej. Am J Physiol. 1998 Aug;275(2):C599-607. doi: 10.1152/ajpcell.1998.275.2.C599. Am J Physiol. 1998. PMID: 9688615

5

The mechanism underlying cystic fibrosis transmembrane conductance regulator transport from the endoplasmic reticulum to the proteasome includes Sec61beta and a cytosolic, deglycosylated intermediary.

Bebök Z, Mazzochi C, King SA, Hong JS, Sorscher EJ. Bebök Z, et al. Among authors: sorscher ej. J Biol Chem. 1998 Nov 6;273(45):29873-8. doi: 10.1074/jbc.273.45.29873. J Biol Chem. 1998. PMID: 9792704 Free article.

6

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. Among authors: sorscher ej. Am J Physiol. 1999 Feb;276(2):C361-9. doi: 10.1152/ajpcell.1999.276.2.C361. Am J Physiol. 1999. PMID: 9950763

7

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. Among authors: sorscher ej. 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

8

Chlorzoxazone or 1-EBIO increases Na(+) absorption across cystic fibrosis airway epithelial cells.

Gao L, Yankaskas JR, Fuller CM, Sorscher EJ, Matalon S, Forman HJ, Venglarik CJ. Gao L, et al. Among authors: sorscher ej. Am J Physiol Lung Cell Mol Physiol. 2001 Nov;281(5):L1123-9. doi: 10.1152/ajplung.2001.281.5.L1123. Am J Physiol Lung Cell Mol Physiol. 2001. PMID: 11597903 Free article.

9

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: sorscher ej. 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.

10

Reactive oxygen nitrogen species decrease cystic fibrosis transmembrane conductance regulator expression and cAMP-mediated Cl- secretion in airway epithelia.

Bebok Z, Varga K, Hicks JK, Venglarik CJ, Kovacs T, Chen L, Hardiman KM, Collawn JF, Sorscher EJ, Matalon S. Bebok Z, et al. Among authors: sorscher ej. J Biol Chem. 2002 Nov 8;277(45):43041-9. doi: 10.1074/jbc.M203154200. Epub 2002 Aug 22. J Biol Chem. 2002. PMID: 12194970 Free article.

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