Published in Methods Mol Biol on January 01, 2011
CFTR, mucins, and mucus obstruction in cystic fibrosis. Cold Spring Harb Perspect Med (2012) 1.15
In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands. PLoS One (2013) 0.87
Glandular Proteome Identifies Antiprotease Cystatin C as a Critical Modulator of Airway Hydration and Clearance. Am J Respir Cell Mol Biol (2016) 0.77
Neural control of submucosal gland and apical membrane secretions in airways. Physiol Rep (2015) 0.75
Cutting edge: 1,25-dihydroxyvitamin D3 is a direct inducer of antimicrobial peptide gene expression. J Immunol (2004) 6.35
Disease phenotype of a ferret CFTR-knockout model of cystic fibrosis. J Clin Invest (2010) 2.45
Cystic fibrosis transmembrane conductance regulator function is suppressed in cigarette smokers. Am J Respir Crit Care Med (2006) 2.34
Identification of a NBD1-binding pharmacological chaperone that corrects the trafficking defect of F508del-CFTR. Chem Biol (2011) 1.92
Submucosal glands and airway defense. Proc Am Thorac Soc (2004) 1.76
Absent secretion to vasoactive intestinal peptide in cystic fibrosis airway glands. J Biol Chem (2002) 1.66
Impact of pressure load caused by right ventricular outflow tract obstruction on right ventricular volume overload in patients with repaired tetralogy of Fallot. J Thorac Cardiovasc Surg (2012) 1.62
Interleukin-1 beta and tumor necrosis factor-alpha induce MUC5AC overexpression through a mechanism involving ERK/p38 mitogen-activated protein kinases-MSK1-CREB activation in human airway epithelial cells. J Biol Chem (2003) 1.55
Novel role for pendrin in orchestrating bicarbonate secretion in cystic fibrosis transmembrane conductance regulator (CFTR)-expressing airway serous cells. J Biol Chem (2011) 1.55
BAP31 interacts with Sec61 translocons and promotes retrotranslocation of CFTRDeltaF508 via the derlin-1 complex. Cell (2008) 1.51
Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis. J Clin Invest (2007) 1.50
Hyposecretion, not hyperabsorption, is the basic defect of cystic fibrosis airway glands. J Biol Chem (2006) 1.43
Clinical characteristics and prognostic factors of primary pulmonary vein stenosis or atresia in children. Ann Thorac Surg (2012) 1.42
A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases. Hum Mol Genet (2003) 1.40
Correction of the Delta phe508 cystic fibrosis transmembrane conductance regulator trafficking defect by the bioavailable compound glafenine. Mol Pharmacol (2010) 1.36
Membrane lateral diffusion and capture of CFTR within transient confinement zones. Biophys J (2006) 1.36
Hemichorea-hemiballism in primary diabetic patients: MR correlation. J Comput Assist Tomogr (2002) 1.31
Regulation of the expression of the Na/Cl cotransporter by WNK4 and WNK1: evidence that accelerated dynamin-dependent endocytosis is not involved. Am J Physiol Renal Physiol (2006) 1.29
Mucus secretion from single submucosal glands of pig. Stimulation by carbachol and vasoactive intestinal peptide. J Biol Chem (2002) 1.29
Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers. J Physiol (2010) 1.27
WNK1 affects surface expression of the ROMK potassium channel independent of WNK4. J Am Soc Nephrol (2006) 1.27
Lack of CFTR in skeletal muscle predisposes to muscle wasting and diaphragm muscle pump failure in cystic fibrosis mice. PLoS Genet (2009) 1.26
Bacillus thuringiensis as a specific, safe, and effective tool for insect pest control. J Microbiol Biotechnol (2007) 1.25
Structural analog of sildenafil identified as a novel corrector of the F508del-CFTR trafficking defect. Mol Pharmacol (2007) 1.25
Correctors of protein trafficking defects identified by a novel high-throughput screening assay. Chembiochem (2007) 1.24
Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice. J Physiol (2007) 1.21
Natural selection shapes nucleotide polymorphism across the genome of the nematode Caenorhabditis briggsae. Genome Res (2010) 1.21
Hyposecretion of fluid from tracheal submucosal glands of CFTR-deficient pigs. J Clin Invest (2010) 1.20
Oxidant stress suppresses CFTR expression. Am J Physiol Cell Physiol (2005) 1.19
Acid and base secretion in the Calu-3 model of human serous cells. Am J Physiol Lung Cell Mol Physiol (2004) 1.17
Physiology of epithelial chloride and fluid secretion. Cold Spring Harb Perspect Med (2012) 1.16
Risk factors of developing new symptomatic vertebral compression fractures after percutaneous vertebroplasty in osteoporotic patients. Eur Spine J (2006) 1.14
Bicarbonate-dependent chloride transport drives fluid secretion by the human airway epithelial cell line Calu-3. J Physiol (2012) 1.14
Phosphorylation of CFTR by PKA promotes binding of the regulatory domain. EMBO J (2005) 1.14
ATP release from human airway epithelial cells studied using a capillary cell culture system. J Physiol (2002) 1.12
Substance P stimulates human airway submucosal gland secretion mainly via a CFTR-dependent process. J Clin Invest (2009) 1.11
Role of the cystic fibrosis transmembrane conductance channel in human airway smooth muscle. Am J Respir Cell Mol Biol (2008) 1.10
Transcatheter closure of atrial septal defect: does age matter? Korean Circ J (2011) 1.10
Probing graphene grain boundaries with optical microscopy. Nature (2012) 1.10
Proinflammatory cytokine secretion is suppressed by TMEM16A or CFTR channel activity in human cystic fibrosis bronchial epithelia. Mol Biol Cell (2012) 1.07
Trafficking of immature DeltaF508-CFTR to the plasma membrane and its detection by biotinylation. Biochem J (2009) 1.04
Investigating membrane protein dynamics in living cells. Biochem Cell Biol (2006) 1.04
Defective fluid secretion from submucosal glands of nasal turbinates from CFTR-/- and CFTR (ΔF508/ΔF508) pigs. PLoS One (2011) 1.02
The secret life of CFTR as a calcium-activated chloride channel. J Physiol (2013) 1.01
Stimulatory and inhibitory protein kinase C consensus sequences regulate the cystic fibrosis transmembrane conductance regulator. Proc Natl Acad Sci U S A (2003) 1.00
Compositional difference in middle ear effusion: mucous versus serous. Laryngoscope (2002) 0.98
Acinar origin of CFTR-dependent airway submucosal gland fluid secretion. Am J Physiol Lung Cell Mol Physiol (2006) 0.97
Mastoid and epitympanic obliteration in canal wall up mastoidectomy for prevention of retraction pocket. Otol Neurotol (2005) 0.97
Clinical outcome of transcatheter closure of patent ductus arteriosus in small children weighing 10 kg or less. Korean J Pediatr (2010) 0.97
Role of tyrosine phosphorylation in the muscarinic activation of the cystic fibrosis transmembrane conductance regulator (CFTR). J Biol Chem (2013) 0.96
Dissemination of metallo-β-lactamase-producing Pseudomonas aeruginosa of sequence type 235 in Asian countries. J Antimicrob Chemother (2013) 0.96
Idiopathic cardiomyopathies in Korean children. - 9-Year Korean Multicenter Study-. Circ J (2011) 0.96
Substance P stimulates CFTR-dependent fluid secretion by mouse tracheal submucosal glands. Pflugers Arch (2008) 0.96
A novel missense mutation in AE1 causing autosomal dominant distal renal tubular acidosis retains normal transport function but is mistargeted in polarized epithelial cells. J Biol Chem (2004) 0.94
Mutations of acetylcholinesterase1 contribute to prothiofos-resistance in Plutella xylostella (L.). Biochem Biophys Res Commun (2006) 0.94
Kawasaki disease and hyponatremia. Pediatr Nephrol (2006) 0.94
Application of impulse oscillometry for within-breath analysis in patients with chronic obstructive pulmonary disease: pilot study. BMJ Open (2011) 0.93
Basolateral chloride loading by the anion exchanger type 2: role in fluid secretion by the human airway epithelial cell line Calu-3. J Physiol (2012) 0.93
Enhanced Ca2+ entry due to Orai1 plasma membrane insertion increases IL-8 secretion by cystic fibrosis airways. FASEB J (2011) 0.92
The Autographa californica multiple nucleopolyhedrovirus ORF78 is essential for budded virus production and general occlusion body formation. J Virol (2013) 0.92
Transcatheter closure of perimembranous ventricular septal defect using Amplatzer ductal occluder. Catheter Cardiovasc Interv (2013) 0.92
Receptor-mediated gene delivery by folate-PEG-baculovirus in vitro. J Biotechnol (2007) 0.92
A rapid method for simultaneous screening of multi-gene mutations associated with hearing loss in the Korean population. PLoS One (2013) 0.91
Chronic epidural hematoma with rapid ossification. Childs Nerv Syst (2002) 0.91
CHD7 mutational analysis and clinical considerations for auditory rehabilitation in deaf patients with CHARGE syndrome. PLoS One (2011) 0.91
Interleukin-1beta upregulates Na+-K+-2Cl- cotransporter in human middle ear epithelia. J Cell Biochem (2007) 0.90
A "virtual gland" method for quantifying epithelial fluid secretion. Am J Physiol Lung Cell Mol Physiol (2004) 0.90
Mucus secretion from individual submucosal glands of the ferret trachea. Am J Physiol Lung Cell Mol Physiol (2010) 0.90
Prostaglandin E2 induces MUC8 gene expression via a mechanism involving ERK MAPK/RSK1/cAMP response element binding protein activation in human airway epithelial cells. J Biol Chem (2004) 0.90
Membrane-specific expression of functional purinergic receptors in normal human nasal epithelial cells. Am J Physiol Lung Cell Mol Physiol (2004) 0.90
Molecular and clinical characterization of the variable phenotype in Korean families with hearing loss associated with the mitochondrial A1555G mutation. PLoS One (2012) 0.89
Traumatic ventricular septal defect in a 4-year-old boy after blunt chest injury. Korean J Pediatr (2011) 0.88
Pou3f4 deficiency causes defects in otic fibrocytes and stria vascularis by different mechanisms. Biochem Biophys Res Commun (2010) 0.88
Local color vector binary patterns from multichannel face images for face recognition. IEEE Trans Image Process (2011) 0.88
The overexpression of acetylcholinesterase compensates for the reduced catalytic activity caused by resistance-conferring mutations in Tetranychus urticae. Insect Biochem Mol Biol (2011) 0.88
Developmental gene expression profiling along the tonotopic axis of the mouse cochlea. PLoS One (2012) 0.88
Mutation conferring apical-targeting motif on AE1 exchanger causes autosomal dominant distal RTA. J Am Soc Nephrol (2012) 0.88
An inwardly rectifying potassium channel in apical membrane of Calu-3 cells. J Biol Chem (2004) 0.87
Correlation of the aphicidal activity of Beauveria bassiana SFB-205 supernatant with enzymes. Fungal Biol (2009) 0.87
An improved baculovirus insecticide producing occlusion bodies that contain Bacillus thuringiensis insect toxin. J Invertebr Pathol (2003) 0.87
Genetic analysis of the CHD7 gene in Korean patients with CHARGE syndrome. Gene (2013) 0.87
In vivo readout of CFTR function: ratiometric measurement of CFTR-dependent secretion by individual, identifiable human sweat glands. PLoS One (2013) 0.87
Cystic fibrosis transmembrane conductance regulator is expressed in mucin granules from Calu-3 and primary human airway epithelial cells. Am J Respir Cell Mol Biol (2013) 0.87
Genomic sequence analysis of granulovirus isolated from the tobacco cutworm, Spodoptera litura. PLoS One (2011) 0.86
Activation of epithelial sodium channel in human middle ear epithelial cells by dexamethasone. Eur J Pharmacol (2008) 0.86