Sorscher E - Search Results

1

An Ancient CFTR Ortholog Informs Molecular Evolution in ABC Transporters.

Cui G, Hong J, Chung-Davidson YW, Infield D, Xu X, Li J, Simhaev L, Khazanov N, Stauffer B, Imhoff B, Cottrill K, Blalock JE, Li W, Senderowitz H, Sorscher E, McCarty NA, Gaggar A. Cui G, et al. Among authors: sorscher e. Dev Cell. 2019 Nov 18;51(4):421-430.e3. doi: 10.1016/j.devcel.2019.09.017. Epub 2019 Oct 31. Dev Cell. 2019. PMID: 31679858 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

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

5

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

6

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

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

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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