×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Restoration of W1282X CFTR activity by enhanced expression.
17541014
2007
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
A mouse model for the delta F508 allele of cystic fibrosis.
7560099
1995
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation.
21083385
2010
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Development of novel aminoglycoside (NB54) with reduced toxicity and enhanced suppression of disease-causing premature stop mutations.
19309154
2009
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Proteasome-dependent pharmacological rescue of cystic fibrosis transmembrane conductance regulator revealed by mutation of glycine 622.
18230692
2008
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
BEFREE
Cystic Fibrosis of the Pancreas : The Role of CFTR Channel in the Regulation of Intracellular Ca<sup>2+</sup> Signaling and Mitochondrial Function in the Exocrine Pancreas.
30618777
2018
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Functional insertion of the SV40 large T oncogene in cystic fibrosis intestinal epithelium. Characterization of CFI-3 cells.
1718974
1991
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis.
16463024
2006
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
BEFREE
CFTR gene transfer to human cystic fibrosis pancreatic duct cells using a Sendai virus vector.
17654517
2008
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
No detectable improvements in cystic fibrosis transmembrane conductance regulator by nasal aminoglycosides in patients with cystic fibrosis with stop mutations.
17347447
2007
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Correction of CFTR malfunction and stimulation of Ca-activated Cl channels restore HCO3- secretion in cystic fibrosis bile ductular cells.
11786964
2002
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Rescue of CF airway epithelial cell function in vitro by a CFTR potentiator, VX-770.
19846789
2009
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
BEFREE
Expression of a wild-type CFTR maintains the integrity of the biosynthetic/secretory pathway in human cystic fibrosis pancreatic duct cells.
15956032
2005
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Cystic fibrosis in 65- and 67-year-old siblings. Clinical feature and nasal potential difference measurement in patients with genotypes F508del and 2789+5G-->A.
16763370
2006
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Evidence that systemic gentamicin suppresses premature stop mutations in patients with cystic fibrosis.
11401894
2001
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Nonsense-mediated mRNA decay affects nonsense transcript levels and governs response of cystic fibrosis patients to gentamicin.
17290305
2007
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Cystic fibrosis transmembrane regulator potentiators as promising cystic fibrosis therapies.
21303308
2011
×
Entrez Id:
1080
Gene Symbol:
CFTR
CFTR
0.330
Biomarker
disease
CTD_human
Probing conformational rescue induced by a chemical corrector of F508del-cystic fibrosis transmembrane conductance regulator (CFTR) mutant.
21602569
2011
×
Entrez Id:
6337
Gene Symbol:
SCNN1A
SCNN1A
0.300
Biomarker
disease
CTD_human
Increased airway epithelial Na+ absorption produces cystic fibrosis-like lung disease in mice.
15077107
2004
×
Entrez Id:
6338
Gene Symbol:
SCNN1B
SCNN1B
0.300
Biomarker
disease
CTD_human
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis.
16463024
2006
×
Entrez Id:
2212
Gene Symbol:
FCGR2A
FCGR2A
0.300
Biomarker
disease
CTD_human
TNFRSF1A
0.300
Biomarker
disease
CTD_human
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis.
16463024
2006
×
Entrez Id:
7040
Gene Symbol:
TGFB1
TGFB1
0.300
Biomarker
disease
CTD_human
×
Entrez Id:
6338
Gene Symbol:
SCNN1B
SCNN1B
0.300
Biomarker
disease
CTD_human
Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome.
16207733
2005
×
Entrez Id:
51164
Gene Symbol:
DCTN4
DCTN4
0.300
Biomarker
disease
CTD_human
Exome sequencing of extreme phenotypes identifies DCTN4 as a modifier of chronic Pseudomonas aeruginosa infection in cystic fibrosis.
22772370
2012