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Journal Article
Journal of Cystic Fibrosis, ISSN 1569-1993, 2011, Volume 10, Issue 2, pp. S86 - S102
Journal Article
Journal of Pediatrics, The, ISSN 0022-3476, 2016, Volume 181, pp. S33 - S44.e2
Journal Article
American Journal of Respiratory and Critical Care Medicine, ISSN 1073-449X, 06/2018, Volume 197, Issue 11, pp. 1433 - 1442
Journal Article
PEDIATRIC PULMONOLOGY, ISSN 8755-6863, 10/2016, Volume 51, pp. 127 - 128
Conference Proceeding
by Jung, A
Atemwegs- und Lungenkrankheiten, ISSN 0341-3055, 07/2017, Volume 43, Issue 7, pp. 310 - 320
Journal Article
JOURNAL OF CYSTIC FIBROSIS, ISSN 1569-1993, 09/2016, Volume 15, Issue 5, pp. 568 - 578
The potentiator VX-770 (ivacaftor/KALYDECO (TM)) targets defective gating of CFTR and has been approved for treatment of cystic fibrosis (CF) subjects carrying... 
IVACAFTOR | MECHANISM | Intestinal organoids | Genistein | Cystic fibrosis | Intestinal current measurements (ICM) | VX-770 | CL-CHANNELS | IN-VITRO | RESPIRATORY SYSTEM | VX-809 | Curcumin | CYSTIC-FIBROSIS | CELL-LINE
Journal Article
Molecular Genetics & Genomic Medicine, ISSN 2324-9269, 02/2019, Volume 7, Issue 2, pp. e00526 - n/a
The protein and functional phenotype of a complex CFTR allele of unknown clinical significance were characterized in native human tissue. 
intestinal current measurement | CFTR immunoblot | CFTR bioassay | complex allele | cystic fibrosis | GENETICS & HEREDITY | CYSTIC-FIBROSIS | CHLORIDE SECRETION | EXPRESSION | DELTA-F508 CFTR | Proteins | Phenotypes | Intestine | Bioassays | Alleles | Rectum | Measurement methods | Functional analysis | Mutation | Colon | Genotypes | Siblings | Index Medicus
Journal Article