1 |
cystic fibrosis transmembrane conductance regulator
(5651 times)
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Biochemistry (807 times)
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CF (1933 times) ENaC (149 times) cAMP (133 times)
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1990 Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
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2 |
CF transmembrane conductance regulator
(694 times)
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Pulmonary Medicine (113 times)
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CF (677 times) WT (25 times) CFRD (16 times)
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1990 A frame-shift mutation in the cystic fibrosis gene.
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3 |
CF transmembrane regulator
(64 times)
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Pulmonary Medicine (17 times)
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CF (60 times) cAMP (3 times) LPS (3 times)
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1992 CFTR channels in immortalized human airway cells.
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4 |
cystic fibrosis
(33 times)
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Genetics, Medical (10 times)
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CF (4 times) CTRC (2 times) PAH (2 times)
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1991 MspI restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene.
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5 |
cystic fibrosis gene
(22 times)
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Genetics, Medical (7 times)
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CF (5 times) ABC (2 times) ICP (2 times)
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1990 Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport.
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6 |
cystic fibrosis gene product
(10 times)
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Physiology (4 times)
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cAMP (2 times) ATP (1 time) GCC (1 time)
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1991 Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.
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7 |
CF transmembrane conductance
(3 times)
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Pediatrics (1 time)
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CF (3 times) CFQ-R (1 time)
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2018 Subclinical Left Ventricular Dysfunction is Influenced by Genotype Severity in Patients with Cystic Fibrosis.
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8 |
cystic fibrosis transmembrane
(3 times)
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Molecular Biology (1 time)
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CF (2 times) CBAVD (1 time) ECG (1 time)
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2000 Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis.
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9 |
cystic-fibrosis protein
(2 times)
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General Surgery (1 time)
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---
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2001 [Pathogenetic concepts of chronic pancreatitis].
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10 |
caused by a defect in an anion channel protein
(1 time)
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Biosensing Techniques (1 time)
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CF (1 time)
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2019 New ISE-Based Apparatus for Na+, K+, Cl-, pH and Transepithelial Potential Difference Real-Time Simultaneous Measurements of Ion Transport across Epithelial Cells Monolayer⁻Advantages and Pitfalls.
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11 |
caused by defects in the transmembrane conductance regulatory
(1 time)
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Medicine (1 time)
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---
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2014 Rare large homozygous CFTR gene deletion in an Iranian patient with cystic fibrosis.
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12 |
caused by mutation of a transmembrane protein
(1 time)
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Biophysics (1 time)
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ASL (1 time)
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2009 A physiological phase separation in airway mucus.
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13 |
ceftriaxone
(1 time)
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Biochemistry (1 time)
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CEF (1 time) CFX (1 time)
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2005 Acidity constants of cefetamet, cefotaxime and ceftriaxone; the effect of the substituent at C3 position.
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14 |
CF gene proteins
(1 time)
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Biochemistry (1 time)
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CF (1 time)
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2006 Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the alpha-glucosidase inhibitor miglustat.
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15 |
CF gene-encoded transmembrane regulator
(1 time)
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Science (1 time)
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CF (1 time)
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1991 Defective acidification of intracellular organelles in cystic fibrosis.
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16 |
CFTR cells
(1 time)
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Physiology (1 time)
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CD (1 time) DPC (1 time) NRVM (1 time)
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1996 Role of the actin cytoskeleton in the regulation of the cystic fibrosis transmembrane conductance regulator.
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17 |
CFTR correctors
(1 time)
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Medicine (1 time)
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CF (1 time) PI (1 time)
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2013 Rescue of murine F508del CFTR activity in native intestine by low temperature and proteasome inhibitors.
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18 |
CFTR gene mutations
(1 time)
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Endocrine System Diseases (1 time)
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KS (1 time)
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2021 Stereological properties of seminiferous tubules in infertile men with chromosomal and genetic abnormalities.
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19 |
CFTR repleted
(1 time)
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Physiology (1 time)
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CF (1 time)
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1999 Abnormal glutathione transport in cystic fibrosis airway epithelia.
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20 |
CFTR-DeltaTRL
(1 time)
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Biochemistry (1 time)
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---
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2002 PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator.
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21 |
CFTR-Ub
(1 time)
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Biochemistry (1 time)
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CF (1 time) UCH-L1 (1 time) WT (1 time)
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2010 Ubiquitin C-terminal hydrolase-L1 protects cystic fibrosis transmembrane conductance regulator from early stages of proteasomal degradation.
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22 |
CFTR; glibenclamide, the standard inhibitor of I
(1 time)
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Pharmacology (1 time)
|
---
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1999 Potent inhibition of the CFTR chloride channel by suramin.
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23 |
chelerythrine, however, attenuated the PKA-mediated activation of I
(1 time)
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Physiology (1 time)
|
---
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2002 Dual regulation of cardiac Na+-K+ pumps and CFTR Cl- channels by protein kinases A and C.
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24 |
cochlear factor
(1 time)
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Otolaryngology (1 time)
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---
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2015 [Effects of intratympanic injection of dexamethasone on endolymphatic hydrops and changes in guinea pigs inner ear CFTR expression].
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25 |
Colonoscopic full-thickness resection
(1 time)
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Diagnostic Imaging (1 time)
|
---
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2009 Colonoscopic full-thickness resection of the colon in a porcine model as a prelude to endoscopic surgery of difficult colon polyps: a novel technique (with videos).
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26 |
conductance regulator factor
(1 time)
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Reproductive Medicine (1 time)
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CBAVD (1 time)
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2012 [Detection of the mutation of all the exons of the CFTR gene in Chinese men with congenital bilateral absence of the vas deferens].
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27 |
conventional flooded transplanted rice
(1 time)
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Environmental Health (1 time)
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AWD (1 time)
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2017 Water-saving technologies affect the grain characteristics and recovery of fine-grain rice cultivars in semi-arid environment.
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28 |
current significantly nor increased I
(1 time)
|
Physiology (1 time)
|
---
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2002 Dual regulation of cardiac Na+-K+ pumps and CFTR Cl- channels by protein kinases A and C.
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29 |
currents were distinct from those activated by forskolin
(1 time)
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Pharmacology (1 time)
|
sc (1 time)
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2001 Bradykinin regulation of salt transport across mouse inner medullary collecting duct epithelium involves activation of a Ca(2+)-dependent Cl(-) conductance.
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30 |
cystic fibrosis chloride channel
(1 time)
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Gastroenterology (1 time)
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CaCC (1 time)
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2013 Chloride channel inhibition by a red wine extract and a synthetic small molecule prevents rotaviral secretory diarrhoea in neonatal mice.
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31 |
cystic fibrosis conductance transmembrane regulator
(1 time)
|
Signal Transduction (1 time)
|
---
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2013 Coupled transport protein systems.
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32 |
cystic fibrosis gene encodes a chloride channel
(1 time)
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Physiology (1 time)
|
---
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2001 CFTR Chloride Channels: Binding Partners and Regulatory Networks.
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33 |
cystic fibrosis gene encodes a cyclic AMP-gated chloride channel
(1 time)
|
Science (1 time)
|
---
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1997 Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms.
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34 |
cystic fibrosis gene mutations
(1 time)
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Pulmonary Medicine (1 time)
|
---
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2013 Aquagenic keratoderma associated with a mutation of the cystic fibrosis gene.
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35 |
cystic fibrosis patient was found to express defective Cl channels
(1 time)
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Science (1 time)
|
Cl (1 time) EBV (1 time)
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1996 Characterization and relative abundance of maxi-chloride channels in Epstein-Barr virus (EBV) producer: B95-8 cells.
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36 |
cystic fibrosis regulator
(1 time)
|
Biochemistry (1 time)
|
ENaC (1 time)
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2002 Where have all the Na+ channels gone? In search of functional ENaC in exocrine pancreas.
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37 |
cystic fibrosis revealed the crucial role of chloride channel
(1 time)
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Gastroenterology (1 time)
|
---
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2000 Why should a clinician care about the molecular biology of transport?
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38 |
cystic fibrosis trans-regulator gene
(1 time)
|
|
---
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2017 The first case report of double homozygous of 2 different mutations in the CFTR gene in Saudi Arabia.
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39 |
DeltaF508-CF transmembrane conductance regulator
(1 time)
|
Physiology (1 time)
|
CF (1 time) DeltaF508 (1 time) DSG (1 time)
|
1998 Partial restoration of cAMP-stimulated CFTR chloride channel activity in DeltaF508 cells by deoxyspergualin.
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