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Abbreviation: CFTR
Appearance Frequency: 5259 time(s)
Long forms: 36

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Long Form No. Long Form Research Area Co-occurring Abbreviation PubMed/MEDLINE Info. (Year, Title)
cystic fibrosis transmembrane conductance regulator
(4614 times)
Biochemistry
(775 times)
CF (1394 times)
cAMP (124 times)
ENaC (121 times)
1990 Correction of the cystic fibrosis defect in vitro by retrovirus-mediated gene transfer.
CF transmembrane conductance regulator
(503 times)
Molecular Biology
(86 times)
CF (491 times)
WT (20 times)
ER (16 times)
1990 A frame-shift mutation in the cystic fibrosis gene.
CF transmembrane regulator
(47 times)
Pulmonary Medicine
(14 times)
CF (45 times)
LPS (3 times)
cAMP (2 times)
1992 CFTR channels in immortalized human airway cells.
cystic fibrosis
(31 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.
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.
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.
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.
cystic-fibrosis protein
(2 times)
Biochemistry
(1 time)
--- 2001 [Pathogenetic concepts of chronic pancreatitis].
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.
10  caused by mutation of a transmembrane protein
(1 time)
Biophysics
(1 time)
ASL (1 time)
2009 A physiological phase separation in airway mucus.
11  ceftriaxone
(1 time)
Biochemistry
(1 time)
CEF (1 time)
CFX (1 time)
2005 Acidity constants of cefetamet, cefotaxime and ceftriaxone; the effect of the substituent at C3 position.
12  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.
13  CF gene-encoded transmembrane regulator
(1 time)
Science
(1 time)
CF (1 time)
1991 Defective acidification of intracellular organelles in cystic fibrosis.
14  CF transmembrane conductance
(1 time)
Blood Circulation
(1 time)
CF (1 time)
2018 Subclinical Left Ventricular Dysfunction is Influenced by Genotype Severity in Patients with Cystic Fibrosis.
15  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.
16  CFTR correctors
(1 time)
Medicine
(1 time)
CF (1 time)
PI (1 time)
2012 Rescue of murine F508del CFTR activity in native intestine by low temperature and proteasome inhibitors.
17  CFTR repleted
(1 time)
Physiology
(1 time)
CF (1 time)
1999 Abnormal glutathione transport in cystic fibrosis airway epithelia.
18  CFTR-DeltaTRL
(1 time)
Biochemistry
(1 time)
--- 2002 PDZ domain interaction controls the endocytic recycling of the cystic fibrosis transmembrane conductance regulator.
19  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.
20  CFTR; glibenclamide, the standard inhibitor of I
(1 time)
Pharmacology
(1 time)
--- 1999 Potent inhibition of the CFTR chloride channel by suramin.
21  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.
22  cochlear factor
(1 time)
Otolaryngology
(1 time)
--- 2014 [Effects of intratympanic injection of dexamethasone on endolymphatic hydrops and changes in guinea pigs inner ear CFTR expression].
23  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).
24  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].
25  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.
26  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.
27  currents were distinct from those activated by forskolin
(1 time)
Pharmacology
(1 time)
sc (1 time)
2000 Bradykinin regulation of salt transport across mouse inner medullary collecting duct epithelium involves activation of a Ca(2+)-dependent Cl(-) conductance.
28  cystic fibrosis chloride channel
(1 time)
Gastroenterology
(1 time)
CaCC (1 time)
2014 Chloride channel inhibition by a red wine extract and a synthetic small molecule prevents rotaviral secretory diarrhoea in neonatal mice.
29  cystic fibrosis conductance transmembrane regulator
(1 time)
Signal Transduction
(1 time)
--- 2013 Coupled transport protein systems.
30  cystic fibrosis gene encodes a chloride channel
(1 time)
Physiology
(1 time)
--- 2000 CFTR Chloride Channels: Binding Partners and Regulatory Networks.
31  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.
32  cystic fibrosis gene mutations
(1 time)
Pulmonary Medicine
(1 time)
--- 2013 Aquagenic keratoderma associated with a mutation of the cystic fibrosis gene.
33  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.
34  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.
35  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?
36  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.