Sorscher EJ - Search Results

1

Elevation of hepatic sulphotransferase activities in mice with resistance to cystic fibrosis.

Falany JL, Greer H, Kovacs T, Sorscher EJ, Falany CN. Falany JL, et al. Among authors: sorscher ej. Biochem J. 2002 May 15;364(Pt 1):115-20. doi: 10.1042/bj3640115. Biochem J. 2002. PMID: 11988083 Free PMC article.

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

Interaction between cystic fibrosis transmembrane conductance regulator and outwardly rectified chloride channels.

Jovov B, Ismailov II, Berdiev BK, Fuller CM, Sorscher EJ, Dedman JR, Kaetzel MA, Benos DJ. Jovov B, et al. Among authors: sorscher ej. J Biol Chem. 1995 Dec 8;270(49):29194-200. doi: 10.1074/jbc.270.49.29194. J Biol Chem. 1995. PMID: 7493947 Free article.

4

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.

5

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: sorscher ej. Hum Gene Ther. 2001 May 1;12(7):751-61. doi: 10.1089/104303401750148667. Hum Gene Ther. 2001. PMID: 11339892 Clinical Trial.

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. 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

7

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.

8

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.

9

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.

10

Aminoglycoside suppression of a premature stop mutation in a Cftr-/- mouse carrying a human CFTR-G542X transgene.

Du M, Jones JR, Lanier J, Keeling KM, Lindsey JR, Tousson A, Bebök Z, Whitsett JA, Dey CR, Colledge WH, Evans MJ, Sorscher EJ, Bedwell DM. Du M, et al. Among authors: sorscher ej. J Mol Med (Berl). 2002 Sep;80(9):595-604. doi: 10.1007/s00109-002-0363-1. Epub 2002 Jul 3. J Mol Med (Berl). 2002. PMID: 12226741

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