Surface Expression of the Cystic Fibrosis Transmembrane Conductance Regulator Mutant ΔF508 Is Markedly Upregulated by Combination Treatment with Sodium Butyrate and Low Temperature

By Heda G.D.   Marino C.R.  

Biochemical and Biophysical Research Communications, Vol. 271, Iss. 3, 2000-05 ,pp. : 659-664

Elsevier

Access to resources Recommend Favorite

Glycosylation of sputum mucins is altered in cystic fibrosis patients

By Schulz Benjamin L   Sloane Andrew J   Robinson Leanne J   Prasad Sindhu S   Lindner Robyn A   Robinson Michael   Bye Peter T   Nielson Dennis W   Harry Jenny L   Packer Nicolle H   Karlsson Niclas G  

Glycobiology, Vol. 17, Iss. 7, 2007-07 ,pp. : 698-712

Oxford University Press

Access to resources Recommend Favorite

Identification of molecular determinants that modulate trafficking of ∆F508 CFTR, the mutant ABC transporter associated with cystic fibrosis

By Tsigelny Igor   Hotchko Matthew   Yuan Jason   Keller Steven  

Cell Biochemistry and Biophysics, Vol. 42, Iss. 1, 2005-02 ,pp. : 41-53

Humana Press, Inc

Access to resources Recommend Favorite

Altered O-glycosylation and sulfation of airway mucins associated with cystic fibrosis

By Xia Baoyun  

Glycobiology, Vol. 15, Iss. 8, 2005-08 ,pp. : 747-775

Oxford University Press

Access to resources Recommend Favorite

Rethinking cystic fibrosis pathology: the critical role of abnormal reduced glutathione (GSH) transport caused by CFTR mutation

By Hudson V.M.  

Free Radical Biology and Medicine, Vol. 30, Iss. 12, 2001-06 ,pp. : 1440-1461

Elsevier

Access to resources Recommend Favorite