Published in Biochem Biophys Res Commun on June 28, 2002
Ion channels in microbes. Physiol Rev (2008) 1.33
Chloride homeostasis in Saccharomyces cerevisiae: high affinity influx, V-ATPase-dependent sequestration, and identification of a candidate Cl- sensor. J Gen Physiol (2008) 0.83
The functioning of mammalian ClC-2 chloride channel in Saccharomyces cerevisiae cells requires an increased level of Kha1p. Biochem J (2005) 0.79
The GEF1 proton-chloride exchanger affects tombusvirus replication via regulation of copper metabolism in yeast. J Virol (2012) 0.78
Outwardly rectifying anionic channel from the plasma membrane of the fungus Phycomyces blakesleeanus. Eukaryot Cell (2009) 0.75
A two-stage poly(ethylenimine)-mediated cytotoxicity: implications for gene transfer/therapy. Mol Ther (2005) 2.83
In vitro prediction of stop-codon suppression by intravenous gentamicin in patients with cystic fibrosis: a pilot study. BMC Med (2007) 1.82
Normal function of the cystic fibrosis conductance regulator protein can be associated with homozygous (Delta)F508 mutation. Pediatr Res (2002) 1.61
Association between Hsp90 and the ClC-2 chloride channel upregulates channel function. Am J Physiol Cell Physiol (2005) 1.56
NH3 is involved in the NH4+ transport induced by the functional expression of the human Rh C glycoprotein. J Biol Chem (2004) 1.51
Evaluation of MRP1-5 gene expression in cystic fibrosis patients homozygous for the delta F508 mutation. Pediatr Res (2003) 1.50
Distribution of ClC-2 chloride channel in rat and human epithelial tissues. Am J Physiol Cell Physiol (2002) 1.44
Hypoxia increases activity of the BK-channel in the inner mitochondrial membrane and reduces activity of the permeability transition pore. Cell Physiol Biochem (2008) 1.09
Antibodies for CFTR studies. J Cyst Fibros (2004) 1.06
Discovery of novel potent ΔF508-CFTR correctors that target the nucleotide binding domain. EMBO Mol Med (2013) 1.04
Rescue of DeltaF508-CFTR (cystic fibrosis transmembrane conductance regulator) by curcumin: involvement of the keratin 18 network. J Pharmacol Exp Ther (2006) 1.04
Chloride transport in nasal ciliated cells of cystic fibrosis heterozygotes. Am J Respir Crit Care Med (2005) 1.03
Neutrophil elastase degrades cystic fibrosis transmembrane conductance regulator via calpains and disables channel function in vitro and in vivo. Am J Respir Crit Care Med (2012) 1.03
Basic protocol for transepithelial nasal potential difference measurements. J Cyst Fibros (2004) 1.01
Opening of potassium channels modulates mitochondrial function in rat skeletal muscle. Biochim Biophys Acta (2002) 1.00
Cystic fibrosis enters the proteomics scene: new answers to old questions. Proteomics (2006) 1.00
Down-regulation of the anti-inflammatory protein annexin A1 in cystic fibrosis knock-out mice and patients. Mol Cell Proteomics (2005) 1.00
Biochemical methods to assess CFTR expression and membrane localization. J Cyst Fibros (2004) 1.00
Cystic fibrosis transmembrane regulator inhibitors CFTR(inh)-172 and GlyH-101 target mitochondrial functions, independently of chloride channel inhibition. J Pharmacol Exp Ther (2010) 0.99
Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells. Pflugers Arch (2005) 0.99
Peroxiredoxin 6 fails to limit phospholipid peroxidation in lung from Cftr-knockout mice subjected to oxidative challenge. PLoS One (2009) 0.97
Cell-specific posttranscriptional regulation of CFTR gene expression via influence of MAPK cascades on 3'UTR part of transcripts. Am J Physiol Cell Physiol (2005) 0.96
Blue native/SDS-PAGE analysis reveals reduced expression of the mClCA3 protein in cystic fibrosis knock-out mice. Mol Cell Proteomics (2005) 0.95
TGF-beta 1 downregulates CFTR expression and function in nasal polyps of non-CF patients. Am J Physiol Lung Cell Mol Physiol (2004) 0.94
Coronin-1 is associated with neutrophil survival and is cleaved during apoptosis: potential implication in neutrophils from cystic fibrosis patients. J Immunol (2009) 0.93
A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotype. Hum Genet (2005) 0.93
BK channel openers inhibit ROS production of isolated rat brain mitochondria. Exp Neurol (2008) 0.92
Lipid mapping of colonic mucosa by cluster TOF-SIMS imaging and multivariate analysis in cftr knockout mice. J Lipid Res (2010) 0.92
Calcium ions regulate K⁺ uptake into brain mitochondria: the evidence for a novel potassium channel. Int J Mol Sci (2009) 0.91
Lysenin-His, a sphingomyelin-recognizing toxin, requires tryptophan 20 for cation-selective channel assembly but not for membrane binding. Mol Membr Biol (2007) 0.91
A novel potassium channel in skeletal muscle mitochondria. Biochim Biophys Acta (2008) 0.91
Large-conductance K+ channel openers NS1619 and NS004 as inhibitors of mitochondrial function in glioma cells. Biochem Pharmacol (2003) 0.90
A novel lipidomic strategy reveals plasma phospholipid signatures associated with respiratory disease severity in cystic fibrosis patients. PLoS One (2009) 0.90
Plasma lipidomics reveals potential prognostic signatures within a cohort of cystic fibrosis patients. J Lipid Res (2011) 0.90
Global proteomic approach unmasks involvement of keratins 8 and 18 in the delivery of cystic fibrosis transmembrane conductance regulator (CFTR)/deltaF508-CFTR to the plasma membrane. Proteomics (2004) 0.90
Proteins interacting with Lin 1p, a putative link between chromosome segregation, mRNA splicing and DNA replication in Saccharomyces cerevisiae. Yeast (2002) 0.90
Measurement of halide efflux from cultured and primary airway epithelial cells using fluorescence indicators. J Cyst Fibros (2004) 0.89
Disruption of cytokeratin-8 interaction with F508del-CFTR corrects its functional defect. Hum Mol Genet (2011) 0.89
The testis anion transporter TAT1 (SLC26A8) physically and functionally interacts with the cystic fibrosis transmembrane conductance regulator channel: a potential role during sperm capacitation. Hum Mol Genet (2011) 0.89
Membrane cholesterol content modulates ClC-2 gating and sensitivity to oxidative stress. J Biol Chem (2006) 0.89
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport. Am J Respir Crit Care Med (2010) 0.88
Control of basal CFTR gene expression by bicarbonate-sensitive adenylyl cyclase in human pulmonary cells. Cell Physiol Biochem (2008) 0.88
Low and high molecular weight poly(L-lysine)s/poly(L-lysine)-DNA complexes initiate mitochondrial-mediated apoptosis differently. FEBS Lett (2005) 0.87
Effect of ouabain on CFTR gene expression in human Calu-3 cells. Am J Physiol Cell Physiol (2003) 0.87
Measurement of nasal potential difference in young children with an equivocal sweat test following newborn screening for cystic fibrosis. Thorax (2010) 0.86
Large-Conductance Potassium Cation Channel Opener NS1619 Inhibits Cardiac Mitochondria Respiratory Chain. Toxicol Mech Methods (2004) 0.86
Pharmacology of mitochondrial potassium channels: dark side of the field. FEBS Lett (2010) 0.86
Mitochondria as a pharmacological target: magnum overview. IUBMB Life (2013) 0.86
Resveratrol rescues cAMP-dependent anionic transport in the cystic fibrosis pancreatic cell line CFPAC1. Br J Pharmacol (2011) 0.85
Immunohistochemistry of CFTR in native tissues and primary epithelial cell cultures. J Cyst Fibros (2004) 0.84
Identification of a voltage-gated potassium channel in gerbil hippocampal mitochondria. Biochem Biophys Res Commun (2010) 0.84
GSH monoethyl ester rescues mitochondrial defects in cystic fibrosis models. Hum Mol Genet (2011) 0.84
CFTR inhibition provokes an inflammatory response associated with an imbalance of the annexin A1 pathway. Am J Pathol (2010) 0.84
Matrix Mg2+ regulates mitochondrial ATP-dependent potassium channel from heart. FEBS Lett (2005) 0.84
Saccharomyces cerevisiae CSM1 gene encoding a protein influencing chromosome segregation in meiosis I interacts with elements of the DNA replication complex. Exp Cell Res (2004) 0.84
ATP-sensitive potassium channel in mitochondria of the eukaryotic microorganism Acanthamoeba castellanii. J Biol Chem (2007) 0.84
Bongkrekic acid and atractyloside inhibits chloride channels from mitochondrial membranes of rat heart. Biochim Biophys Acta (2006) 0.84
Expression of murine DNA methyltransferases Dnmt1 and Dnmt3a in the yeast Saccharomyces cerevisiae. Yeast (2007) 0.83
Eicosanoid release is increased by membrane destabilization and CFTR inhibition in Calu-3 cells. PLoS One (2009) 0.83
Complex III-dependent superoxide production of brain mitochondria contributes to seizure-related ROS formation. Biochim Biophys Acta (2010) 0.83
Nuclear import and export signals of human cohesins SA1/STAG1 and SA2/STAG2 expressed in Saccharomyces cerevisiae. PLoS One (2012) 0.83
Contribution of proteomics to the study of the role of cytokeratins in disease and physiopathology. Proteomics Clin Appl (2008) 0.82
Down-regulation of Kir4.1 in the cerebral cortex of rats with liver failure and in cultured astrocytes treated with glutamine: Implications for astrocytic dysfunction in hepatic encephalopathy. J Neurosci Res (2011) 0.82
High sensitivity identification of membrane proteins by MALDI TOF-MASS spectrometry using polystyrene beads. J Proteome Res (2007) 0.82
Antidiabetic sulphonylureas activate mitochondrial permeability transition in rat skeletal muscle. Br J Pharmacol (2005) 0.82
Methadone induces necrotic-like cell death in SH-SY5Y cells by an impairment of mitochondrial ATP synthesis. Biochim Biophys Acta (2010) 0.81
Lanthanum carbonate, like sevelamer-HCl, retards the progression of vascular calcification and atherosclerosis in uremic apolipoprotein E-deficient mice. Nephrol Dial Transplant (2011) 0.81
Putative Structural and Functional Coupling of the Mitochondrial BKCa Channel to the Respiratory Chain. PLoS One (2013) 0.81
A large-conductance calcium-activated potassium channel in potato (Solanum tuberosum) tuber mitochondria. Biochem J (2009) 0.81
A new workflow for proteomic analysis of urinary exosomes and assessment in cystinuria patients. J Proteome Res (2014) 0.81
The cytoprotective action of the potassium channel opener BMS-191095 in C2C12 myoblasts is related to the modulation of calcium homeostasis. Cell Physiol Biochem (2010) 0.81
Regulation of interleukin-6 in head and neck squamous cell carcinoma is related to papillomavirus infection. J Proteome Res (2014) 0.81
New properties of mitochondrial ATP-regulated potassium channels. J Bioenerg Biomembr (2008) 0.80
Mitochondria and big-conductance potassium channel openers. Toxicol Mech Methods (2004) 0.79
The functioning of mammalian ClC-2 chloride channel in Saccharomyces cerevisiae cells requires an increased level of Kha1p. Biochem J (2005) 0.79
Structural models of CFTR-AMPK and CFTR-PKA interactions: R-domain flexibility is a key factor in CFTR regulation. J Mol Model (2011) 0.79
New lipidomic approaches in cystic fibrosis. Methods Mol Biol (2011) 0.79
Long-term CFTR inhibition modulates 15d-prostaglandin J2 in human pulmonary cells. Int J Biochem Cell Biol (2012) 0.79
[Endothelial mitochondria--a novel target for pharmacology of endothelial dysfunction]. Postepy Biochem (2008) 0.78
Large-conductance Ca²⁺-activated potassium channel in mitochondria of endothelial EA.hy926 cells. Am J Physiol Heart Circ Physiol (2013) 0.78
Characterization of SLC26A9 in patients with CF-like lung disease. Hum Mutat (2013) 0.78
Glutamate-induced cell death in HT22 mouse hippocampal cells is attenuated by paxilline, a BK channel inhibitor. Mitochondrion (2012) 0.78
Stilbene derivatives inhibit the activity of the inner mitochondrial membrane chloride channels. Cell Mol Biol Lett (2007) 0.78
Endothelial mitochondria as a possible target for potassium channel modulators. Pharmacol Rep (2006) 0.78
A new pH-sensitive rectifying potassium channel in mitochondria from the embryonic rat hippocampus. Biochim Biophys Acta (2012) 0.78
Single channel studies of the ATP-regulated potassium channel in brain mitochondria. J Bioenerg Biomembr (2009) 0.77
Benzodiazepine binding to mitochondrial membranes of the amoeba Acanthamoeba castellanii and the yeast Saccharomyces cerevisiae. Acta Biochim Pol (2004) 0.77
Characterization of nasal potential difference in cftr knockout and F508del-CFTR mice. PLoS One (2013) 0.77
The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening. BMC Pediatr (2006) 0.77
The heterogeneity of ion channels in chromaffin granule membranes. Cell Mol Biol Lett (2006) 0.77
Quantitative differential proteomics of cystic fibrosis cell models by SILAC (stable isotope labelling in cell culture). Methods Mol Biol (2011) 0.77
Reconstitution of brain mitochondria inner membrane into planar lipid bilayer. Acta Neurobiol Exp (Wars) (2005) 0.77