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6 in total

1. Characterization of wild-type and deltaF508 cystic fibrosis transmembrane regulator in human respiratory epithelia.

Authors: Silvia M Kreda; Marcus Mall; April Mengos; Lori Rochelle; James Yankaskas; John R Riordan; Richard C Boucher
Journal: Mol Biol Cell Date: 2005-02-16 Impact factor: 4.138

2. The CFTR-Associated Ligand Arrests the Trafficking of the Mutant ΔF508 CFTR Channel in the ER Contributing to Cystic Fibrosis.

Authors: Emily Bergbower; Clement Boinot; Inna Sabirzhanova; William Guggino; Liudmila Cebotaru
Journal: Cell Physiol Biochem Date: 2018-01-29

Review 3. Therapy through chaperones: sense or antisense? Cystic fibrosis as a model disease.

Authors: Margarida D Amaral
Journal: J Inherit Metab Dis Date: 2006 Apr-Jun Impact factor: 4.982

4. The cystic fibrosis transmembrane conductance regulator impedes proteolytic stimulation of the epithelial Na+ channel.

Authors: Martina Gentzsch; Hong Dang; Yan Dang; Agustin Garcia-Caballero; Hamsa Suchindran; Richard C Boucher; M Jackson Stutts
Journal: J Biol Chem Date: 2010-08-13 Impact factor: 5.157

5. Clinical and molecular characterization of S1118F-CFTR.

Authors: Himabindu Penmatsa; Carla A Frederick; Sunitha Nekkalapu; Veronica G Conoley; Weiqiang Zhang; Chunying Li; John Kappes; Dennis C Stokes; Anjaparavanda P Naren
Journal: Pediatr Pulmonol Date: 2009-10

6. Substitution of Yor1p NBD1 residues improves the thermal stability of Human Cystic Fibrosis Transmembrane Conductance Regulator.

Authors: B M Xavier; E Hildebrandt; F Jiang; H Ding; J C Kappes; I L Urbatsch
Journal: Protein Eng Des Sel Date: 2017-10-01 Impact factor: 1.650

6 in total