Sorscher EJ - Search Results

1

Comparison of cystic fibrosis transmembrane conductance regulator (CFTR) and ciliary beat frequency activation by the CFTR Modulators Genistein, VRT-532, and UCCF-152 in primary sinonasal epithelial cultures.

Conger BT, Zhang S, Skinner D, Hicks SB, Sorscher EJ, Rowe SM, Woodworth BA. Conger BT, et al. Among authors: sorscher ej. JAMA Otolaryngol Head Neck Surg. 2013 Aug 1;139(8):822-7. doi: 10.1001/jamaoto.2013.3917. JAMA Otolaryngol Head Neck Surg. 2013. PMID: 23949358 Free PMC article.

2

Regulation of plasma membrane recycling by CFTR.

Bradbury NA, Jilling T, Berta G, Sorscher EJ, Bridges RJ, Kirk KL. Bradbury NA, et al. Among authors: sorscher ej. Science. 1992 Apr 24;256(5056):530-2. doi: 10.1126/science.1373908. Science. 1992. PMID: 1373908

3

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.

4

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.

5

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

6

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: sorscher ej. Nat Med. 1997 Nov;3(11):1280-4. doi: 10.1038/nm1197-1280. Nat Med. 1997. PMID: 9359706

7

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

8

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. Among authors: sorscher ej. Biochemistry. 1998 Oct 27;37(43):15222-30. doi: 10.1021/bi980436f. Biochemistry. 1998. PMID: 9790686

9

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.

10

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

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