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The NSAID glafenine rescues class 2 CFTR mutants via cyclooxygenase 2 inhibition of the arachidonic acid pathway.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-08661-8
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- Article
Nonspecific binding of common anti-CFTR antibodies in ciliated cells of human airway epithelium.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-02420-x
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- Article
Treatment With LAU-7b Complements CFTR Modulator Therapy by Improving Lung Physiology and Normalizing Lipid Imbalance Associated With CF Lung Disease.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.876842
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- Article
Macrocycle-stabilization of its interaction with 14-3-3 increases plasma membrane localization and activity of CFTR.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31206-6
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- Article
CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells.
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- Frontiers in Physiology, 2021, v. 12, p. N.PAG, doi. 10.3389/fphys.2021.619442
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- Article
Compounds that correct F508del-CFTR trafficking can also correct other protein trafficking diseases: an in vitro study using cell lines.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-11
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- Article
Phosphorylation of CFTR by PKA promotes binding of the regulatory domain.
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- EMBO Journal, 2005, v. 24, n. 15, p. 2730, doi. 10.1038/sj.emboj.7600747
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- Article
Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.
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- 2007
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- Publication type:
- journal article
Synergistic airway gland mucus secretion in response to vasoactive intestinal peptide and carbachol is lost in cystic fibrosis.
- Published in:
- Journal of Clinical Investigation, 2007, v. 117, n. 10, p. 3118, doi. 10.1172/JCI31992
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- Article
Possible Role of Outwardly Rectifying Anion Channels in Epithelial Transport<sup>a</sup>.
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- Annals of the New York Academy of Sciences, 1989, v. 574, n. 1, p. 30, doi. 10.1111/j.1749-6632.1989.tb25130.x
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- Article
Changes in the R‐region interactions depend on phosphorylation and contribute to PKA and PKC regulation of the cystic fibrosis transmembrane conductance regulator chloride channel.
- Published in:
- FASEB Bioadvances, 2020, v. 2, n. 1, p. 33, doi. 10.1096/fba.2019-00053
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- Publication type:
- Article
Mucus secretion by single tracheal submucosal glands from normal and cystic fibrosis transmembrane conductance regulator knockout mice.
- Published in:
- Journal of Physiology, 2007, v. 580, n. 1, p. 301, doi. 10.1113/jphysiol.2006.123653
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- Article
ATP release from human airway epithelial cells studied using a capillary cell culture system.
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- Journal of Physiology, 2002, v. 545, n. 1, p. 199, doi. 10.1113/jphysiol.2002.030148
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- Publication type:
- Article
Non-pore lining amino acid side chains influence anion selectivity of the human CFTR Cl<sup>−</sup> channel expressed in mammalian cell lines.
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- Journal of Physiology, 1998, v. 512, n. 1, p. 1, doi. 10.1111/j.1469-7793.1998.001bf.x
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- Article
Substrates of multidrug resistance-associated proteins block the cystic fibrosis transmembrane conductance regulator chloride channel.
- Published in:
- 1999
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- Publication type:
- journal article
Oxygenation as a driving factor in epithelial differentiation at the air–liquid interface.
- Published in:
- Integrative Biology, 2021, v. 13, n. 3, p. 61, doi. 10.1093/intbio/zyab002
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- Publication type:
- Article
Ionocyte-Specific Regulation of Cystic Fibrosis Transmembrane Conductance Regulator.
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- American Journal of Respiratory Cell & Molecular Biology, 2023, v. 69, n. 3, p. 281, doi. 10.1165/rcmb.2022-0241oc
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- Publication type:
- Article
Cystic Fibrosis Transmembrane Conductance Regulator Is Expressed in Mucin Granules from Calu-3 and Primary Human Airway Epithelial Cells.
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- American Journal of Respiratory Cell & Molecular Biology, 2013, v. 49, n. 4, p. 511, doi. 10.1165/rcmb.2012-0419RC
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- Publication type:
- Article
Role of the Cystic Fibrosis Transmembrane Conductance Channel in Human Airway Smooth Muscle.
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- American Journal of Respiratory Cell & Molecular Biology, 2009, v. 40, n. 2, p. 217, doi. 10.1165/rcmb.2006-0444OC
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- Publication type:
- Article
Substance P stimulates CFTR-dependent fluid secretion by mouse tracheal submucosal glands.
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- Pflügers Archiv: European Journal of Physiology, 2008, v. 457, n. 2, p. 529, doi. 10.1007/s00424-008-0527-0
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- Article
Regulation of the CFTR channel by phosphorylation.
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- Pflügers Archiv: European Journal of Physiology, 2001, v. 443, p. S92, doi. 10.1007/s004240100652
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- Article
CRISPR/Cas9 bioluminescence-based assay for monitoring CFTR trafficking to the plasma membrane.
- Published in:
- Life Science Alliance, 2024, v. 7, n. 1, p. 1, doi. 10.26508/lsa.202302045
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- Publication type:
- Article
Bioactive Thymosin Alpha-1 Does Not Influence F508del-CFTR Maturation and Activity.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46639-1
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- Publication type:
- Article
The buffer capacity of airway epithelial secretions.
- Published in:
- Frontiers in Physiology, 2014, v. 5, p. 1, doi. 10.3389/fphys.2014.00188
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- Article
THE BUFFER CAPACITY OF AIRWAY EPITHELIAL SECRETIONS.
- Published in:
- Frontiers in Physiology, 2014, v. 5, p. 1, doi. 10.3389/fphys.2014.00188
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- Publication type:
- Article
Hsp70 and DNAJA2 limit CFTR levels through degradation.
- Published in:
- PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0220984
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- Publication type:
- Article
Regulation of the cystic fibrosis transmembrane conductance regulator anion channel by tyrosine phosphorylation.
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- FASEB Journal, 2015, v. 29, n. 9, p. 3945, doi. 10.1096/fj.15-273151
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- Publication type:
- Article
Enhanced Ca<sup>2+</sup> entry due to Orail plasma membrane insertion increases IL-8 secretion by cystic fibrosis airways.
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- FASEB Journal, 2011, v. 25, n. 12, p. 4274, doi. 10.1096/fj.11-187682
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- Article
Cystic Fibrosis Transmembrane Conductance Regulator Function Is Suppressed in Cigarette Smokers.
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- American Journal of Respiratory & Critical Care Medicine, 2006, v. 173, n. 10, p. 1139, doi. 10.1164/rccm.200508-1330OC
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- Publication type:
- Article
Dibasic protein kinase A sites regulate bursting rate and nucleotide sensitivity of the cystic fibrosis transmembrane conductance regulator chloride channel.
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- Journal of Physiology, 1998, v. 508, n. 2, p. 365, doi. 10.1111/j.1469-7793.1998.365bq.x
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- Article
Investigating CFTR and KCa3.1 Protein/Protein Interactions.
- Published in:
- PLoS ONE, 2016, v. 11, n. 4, p. 1, doi. 10.1371/journal.pone.0153665
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- Article
Phosphodiesterase 8A Regulates CFTR Activity in Airway Epithelial Cells.
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- Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2021, v. 55, n. 6, p. 784, doi. 10.33594/000000477
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- Article
The secret life of CFTR as a calcium-activated chloride channel.
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- Journal of Physiology, 2013, v. 591, n. 21, p. 5273, doi. 10.1113/jphysiol.2013.261909
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- Publication type:
- Article
Bicarbonate-dependent chloride transport drives fluid secretion by the human airway epithelial cell line Calu-3.
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- Journal of Physiology, 2012, v. 590, n. 21, p. 5273, doi. 10.1113/jphysiol.2012.236893
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- Publication type:
- Article
Basolateral chloride loading by the anion exchanger type 2: role in fluid secretion by the human airway epithelial cell line Calu-3.
- Published in:
- Journal of Physiology, 2012, v. 590, n. 21, p. 5299, doi. 10.1113/jphysiol.2012.236919
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- Publication type:
- Article
Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.
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- Journal of Physiology, 2010, v. 588, n. 8, p. 1195, doi. 10.1113/jphysiol.2009.182246
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- Article
Rescue of Mutant CFTR Trafficking Defect by the Investigational Compound MCG1516A.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 1, p. 136, doi. 10.3390/cells11010136
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- Article
Development of Automated Patch Clamp Technique to Investigate CFTR Chloride Channel Function.
- Published in:
- Frontiers in Pharmacology, 2017, v. 8, p. 1, doi. 10.3389/fphar.2017.00195
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- Article
Low free drug concentration prevents inhibition of F508del CFTR functional expression by the potentiator VX-770 (ivacaftor).
- Published in:
- 2016
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- Publication type:
- journal article
Lack of CFTR in Skeletal Muscle Predisposes to Muscle Wasting and Diaphragm Muscle Pump Failure in Cystic Fibrosis Mice.
- Published in:
- PLoS Genetics, 2009, v. 5, n. 7, p. 1, doi. 10.1371/journal.pgen.1000586
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- Publication type:
- Article
A novel triple combination of pharmacological chaperones improves F508del-CFTR correction.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-29276-y
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- Publication type:
- Article
A haplotype-based molecular analysis of CFTR mutations associated with respiratory and pancreatic diseases.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 18, p. 2321, doi. 10.1093/hmg/ddg243
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- Publication type:
- Article
mRNA Delivery: Challenges and Advances through Polymeric Soft Nanoparticles.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 3, p. 1739, doi. 10.3390/ijms25031739
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- Article
Correctors of Protein Trafficking Defects Identified by a Novel High-Throughput Screening Assay.
- Published in:
- ChemBioChem, 2007, v. 8, n. 9, p. 1012, doi. 10.1002/cbic.200700027
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- Article
Investigating membrane protein dynamics in living cells.
- Published in:
- Biochemistry & Cell Biology, 2006, v. 84, n. 6, p. 825, doi. 10.1139/O06-189
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- Publication type:
- Article