| 1 |
cystic fibrosis transmembrane conductance regulator
(5200 times)
|
Biochemistry
(793 times)
|
CF (1706 times)
ENaC (139 times)
cAMP (129 times)
|
1990 Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
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| 2 |
CF transmembrane conductance regulator
(607 times)
|
Molecular Biology
(95 times)
|
CF (594 times)
WT (22 times)
ER (16 times)
|
1990 A frame-shift mutation in the cystic fibrosis gene.
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| 3 |
CF transmembrane regulator
(61 times)
|
Pulmonary Medicine
(16 times)
|
CF (58 times)
cAMP (3 times)
LPS (3 times)
|
1992 CFTR channels in immortalized human airway cells.
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| 4 |
cystic fibrosis
(32 times)
|
Genetics, Medical
(10 times)
|
CF (4 times)
CTRC (2 times)
PAH (2 times)
|
1991 MspI restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene.
|
| 5 |
cystic fibrosis gene
(22 times)
|
Genetics, Medical
(7 times)
|
CF (5 times)
ABC (2 times)
ICP (2 times)
|
1990 Structural model of ATP-binding proteins associated with cystic fibrosis, multidrug resistance and bacterial transport.
|
| 6 |
cystic fibrosis gene product
(10 times)
|
Physiology
(4 times)
|
cAMP (2 times)
ATP (1 time)
GCC (1 time)
|
1991 Expression of the cystic fibrosis gene in non-epithelial invertebrate cells produces a regulated anion conductance.
|
| 7 |
CF transmembrane conductance
(3 times)
|
Pulmonary Medicine
(1 time)
|
CF (3 times)
CFQ-R (1 time)
|
2018 Subclinical Left Ventricular Dysfunction is Influenced by Genotype Severity in Patients with Cystic Fibrosis.
|
| 8 |
cystic fibrosis transmembrane
(2 times)
|
Genetics, Medical
(1 time)
|
CF (2 times)
CBAVD (1 time)
ECG (1 time)
|
2000 Partial CFTR genotyping and characterisation of cystic fibrosis patients with myocardial fibrosis and necrosis.
|
| 9 |
cystic-fibrosis protein
(2 times)
|
General Surgery
(1 time)
|
---
|
2001 [Pathogenetic concepts of chronic pancreatitis].
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| 10 |
caused by a defect in an anion channel protein
(1 time)
|
Biosensing Techniques
(1 time)
|
CF (1 time)
|
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.
|
| 11 |
caused by defects in the transmembrane conductance regulatory
(1 time)
|
Medicine
(1 time)
|
---
|
2014 Rare large homozygous CFTR gene deletion in an Iranian patient with cystic fibrosis.
|
| 12 |
caused by mutation of a transmembrane protein
(1 time)
|
Biophysics
(1 time)
|
ASL (1 time)
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2009 A physiological phase separation in airway mucus.
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| 13 |
ceftriaxone
(1 time)
|
Biochemistry
(1 time)
|
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.
|
| 14 |
CF gene proteins
(1 time)
|
Biochemistry
(1 time)
|
CF (1 time)
|
2006 Rescue of functional delF508-CFTR channels in cystic fibrosis epithelial cells by the alpha-glucosidase inhibitor miglustat.
|
| 15 |
CF gene-encoded transmembrane regulator
(1 time)
|
Science
(1 time)
|
CF (1 time)
|
1991 Defective acidification of intracellular organelles in cystic fibrosis.
|
| 16 |
CFTR cells
(1 time)
|
Physiology
(1 time)
|
CD (1 time)
DPC (1 time)
NRVM (1 time)
|
1996 Role of the actin cytoskeleton in the regulation of the cystic fibrosis transmembrane conductance regulator.
|
| 17 |
CFTR correctors
(1 time)
|
Medicine
(1 time)
|
CF (1 time)
PI (1 time)
|
2013 Rescue of murine F508del CFTR activity in native intestine by low temperature and proteasome inhibitors.
|
| 18 |
CFTR repleted
(1 time)
|
Physiology
(1 time)
|
CF (1 time)
|
1999 Abnormal glutathione transport in cystic fibrosis airway epithelia.
|
| 19 |
CFTR-DeltaTRL
(1 time)
|
Biochemistry
(1 time)
|
---
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2002 PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator.
|
| 20 |
CFTR-Ub
(1 time)
|
Biochemistry
(1 time)
|
CF (1 time)
UCH-L1 (1 time)
WT (1 time)
|
2010 Ubiquitin C-terminal hydrolase-L1 protects cystic fibrosis transmembrane conductance regulator from early stages of proteasomal degradation.
|
| 21 |
CFTR; glibenclamide, the standard inhibitor of I
(1 time)
|
Pharmacology
(1 time)
|
---
|
1999 Potent inhibition of the CFTR chloride channel by suramin.
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| 22 |
chelerythrine, however, attenuated the PKA-mediated activation of I
(1 time)
|
Physiology
(1 time)
|
---
|
2002 Dual regulation of cardiac Na+-K+ pumps and CFTR Cl- channels by protein kinases A and C.
|
| 23 |
cochlear factor
(1 time)
|
Otolaryngology
(1 time)
|
---
|
2015 [Effects of intratympanic injection of dexamethasone on endolymphatic hydrops and changes in guinea pigs inner ear CFTR expression].
|
| 24 |
Colonoscopic full-thickness resection
(1 time)
|
Diagnostic Imaging
(1 time)
|
---
|
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).
|
| 25 |
conductance regulator factor
(1 time)
|
Reproductive Medicine
(1 time)
|
CBAVD (1 time)
|
2012 [Detection of the mutation of all the exons of the CFTR gene in Chinese men with congenital bilateral absence of the vas deferens].
|
| 26 |
conventional flooded transplanted rice
(1 time)
|
Environmental Health
(1 time)
|
AWD (1 time)
|
2017 Water-saving technologies affect the grain characteristics and recovery of fine-grain rice cultivars in semi-arid environment.
|
| 27 |
current significantly nor increased I
(1 time)
|
Physiology
(1 time)
|
---
|
2002 Dual regulation of cardiac Na+-K+ pumps and CFTR Cl- channels by protein kinases A and C.
|
| 28 |
currents were distinct from those activated by forskolin
(1 time)
|
Pharmacology
(1 time)
|
sc (1 time)
|
2001 Bradykinin regulation of salt transport across mouse inner medullary collecting duct epithelium involves activation of a Ca(2+)-dependent Cl(-) conductance.
|
| 29 |
cystic fibrosis chloride channel
(1 time)
|
Gastroenterology
(1 time)
|
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.
|
| 30 |
cystic fibrosis conductance transmembrane regulator
(1 time)
|
Signal Transduction
(1 time)
|
---
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2013 Coupled transport protein systems.
|
| 31 |
cystic fibrosis gene encodes a chloride channel
(1 time)
|
Physiology
(1 time)
|
---
|
2001 CFTR Chloride Channels: Binding Partners and Regulatory Networks.
|
| 32 |
cystic fibrosis gene encodes a cyclic AMP-gated chloride channel
(1 time)
|
Science
(1 time)
|
---
|
1997 Regulation of CFTR chloride channels by syntaxin and Munc18 isoforms.
|
| 33 |
cystic fibrosis gene mutations
(1 time)
|
Pulmonary Medicine
(1 time)
|
---
|
2013 Aquagenic keratoderma associated with a mutation of the cystic fibrosis gene.
|
| 34 |
cystic fibrosis patient was found to express defective Cl channels
(1 time)
|
Science
(1 time)
|
Cl (1 time)
EBV (1 time)
|
1996 Characterization and relative abundance of maxi-chloride channels in Epstein-Barr virus (EBV) producer: B95-8 cells.
|
| 35 |
cystic fibrosis regulator
(1 time)
|
Biochemistry
(1 time)
|
ENaC (1 time)
|
2002 Where have all the Na+ channels gone? In search of functional ENaC in exocrine pancreas.
|
| 36 |
cystic fibrosis revealed the crucial role of chloride channel
(1 time)
|
Gastroenterology
(1 time)
|
---
|
2000 Why should a clinician care about the molecular biology of transport?
|
| 37 |
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.
|
| 38 |
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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