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Impact of Overexpression of Wild-Type Cftr and Elexacaftor-Texacaftor-Ivacaftor on Oxylipin Production by Cystic Fibrosis Bronchial Epithelial Cells
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Outgoing claims: the papers this work cites, builds on, or argues with.
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PPARγ as a therapeutic target in cystic fibrosis
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Autooxidation of docosahexaenoic acid: analysis of ten isomers of hydroxydocosahexaenoate.
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Biochemical and Cellular Characterization and Inhibitor Discovery of Pseudomonas aeruginosa 15-Lipoxygenase
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Prostaglandin F2α Formation from Prostaglandin H2 by Prostaglandin F Synthase (PGFS): Crystal Structure of PGFS Containing Bimatoprost,
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Prostaglandin D2 and Reproduction
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Microbial, host and xenobiotic diversity in the cystic fibrosis sputum metabolome
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Infection regulates pro-resolving mediators that lower antibiotic requirements
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Oxylipin profile in saliva from patients with cystic fibrosis reveals a balance between pro-resolving and pro-inflammatory molecules
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VX-445–Tezacaftor–Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles
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CYP450-derived oxylipins mediate inflammatory resolution
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Pseudomonas aeruginosa sabotages the generation of host proresolving lipid mediators
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A series of prostaglandin F2-like compounds are produced in vivo in humans by a non-cyclooxygenase, free radical-catalyzed mechanism.
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A membrane lipid imbalance plays a role in the phenotypic expression of cystic fibrosis in cftr −/− mice
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Prostaglandins Promote and Block Adipogenesis through Opposing Effects on Peroxisome Proliferator-activated Receptor γ
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Positive and Negative Regulation of NF-κB by COX-2
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Resolvin E1 Receptor Activation Signals Phosphorylation and Phagocytosis
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Functional Genomic Responses to Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and CFTRΔ508 in the Lung
inferredcites →https://doi.org/10.1084/jem.20081880openalex-extracted
Maresins: novel macrophage mediators with potent antiinflammatory and proresolving actions
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MetaboAnalyst 5.0: narrowing the gap between raw spectra and functional insights
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Lipid Mediators in the Resolution of Inflammation
inferredcites →https://doi.org/10.1111/bph.12859openalex-extracted
Roscovitine is a proteostasis regulator that corrects the trafficking defect of F 508del‐ CFTR by a CDK ‐independent mechanism
inferredcites →https://doi.org/10.1111/j.1749-6632.2012.06580.xopenalex-extracted
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International Union of Basic and Clinical Pharmacology. LXXXIII: Classification of Prostanoid Receptors, Updating 15 Years of Progress
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Most F508del-CFTR Is Targeted to Degradation at an Early Folding Checkpoint and Independently of Calnexin
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An epoxide hydrolase secreted byPseudomonas aeruginosadecreases mucociliary transport and hinders bacterial clearance from the lung
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Impact of CFTR ΔF508 mutation on prostaglandin E2production and type IIA phospholipase A2expression by pulmonary epithelial cells
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Cl Transport in Complemented CF Bronchial Epithelial Cells Correlates with CFTR mRNA Expression Levels
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Resolvin D1 Limits Polymorphonuclear Leukocyte Recruitment to Inflammatory Loci
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Early Pulmonary Inflammation in Infants with Cystic Fibrosis
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Infection Is Not Required for Mucoinflammatory Lung Disease in CFTR-Knockout Ferrets
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Prostaglandin E2 Regulation of Cystic Fibrosis Transmembrane Conductance Regulator Activity and Airway Surface Liquid Volume Requires Gap Junctional Communication
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Distinctive lipid signatures of bronchial epithelial cells associated with cystic fibrosis drugs, including Trikafta
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Reduced 15-lipoxygenase 2 and lipoxin A4/leukotriene B4ratio in children with cystic fibrosis
inferredcites →https://doi.org/10.1194/jlr.m700388-jlr200openalex-extracted
Cell culture models demonstrate that CFTR dysfunction leads to defective fatty acid composition and metabolism
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A mechanism accounting for the low cellular level of linoleic acid in cystic fibrosis and its reversal by DHA
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The Development of a Specific and Sensitive LC-MS-Based Method for the Detection and Quantification of Hydroperoxy- and Hydroxydocosahexaenoic Acids as a Tool for Lipidomic Analysis
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Multiple roles of the prostaglandin D2 signaling pathway in reproduction
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Triplet CFTR modulators: future prospects for treatment of cystic fibrosis
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Lipid Mediator Profiling in Pulmonary Disease
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CF Patients’ Airway Epithelium and Sex Contribute to Biosynthesis Defects of Pro-Resolving Lipids
inferredcites →https://doi.org/10.3389/fphar.2012.00165openalex-extracted
Decreasing Poly(ADP-Ribose) Polymerase Activity Restores ΔF508 CFTR Trafficking
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CFTR Correctors and Antioxidants Partially Normalize Lipid Imbalance but not Abnormal Basal Inflammatory Cytokine Profile in CF Bronchial Epithelial Cells
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Cystic Fibrosis and Oxidative Stress: The Role of CFTR
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Advances in Our Understanding of Oxylipins Derived from Dietary PUFAs
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Increased Tissue Arachidonic Acid and Reduced Linoleic Acid in a Mouse Model of Cystic Fibrosis Are Reversed by Supplemental Glycerophospholipids Enriched in Docosahexaenoic Acid1–3
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Lipoxin A4 and Aspirin-Triggered 15-epi-Lipoxin A4 Inhibit Human Neutrophil Migration: Comparisons Between Synthetic 15 Epimers in Chemotaxis and Transmigration with Microvessel Endothelial Cells and Epithelial Cells
inferredcites →https://doi.org/10.5863/1551-6776-18.1.8openalex-extracted
Ivacaftor: A Novel Gene-Based Therapeutic Approach for Cystic Fibrosis
inferredcites →https://doi.org/10.1164/ajrccm/151.4.1075openalex-snapshot
Early Pulmonary Inflammation in Infants with Cystic Fibrosis
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