Drug-induced dyspnea versus cystic fibrosis exacerbation: a diagnostic dilemma
Saqib Walayat,1 Nooreen Hussain,1 Jaymon Patel,1 Faiz Hussain,2 Preeti Patel,1 Sonu Dhillon,1 Bhagat Aulakh,3,4 Subramanyam Chittivelu3 1Department of Internal Medicine, University of Illinois College of Medicine at Peoria, Peoria, 2Department of ...
Walayat S +7 more
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In Silico Evaluation of Lumacaftor for Cystic Fibrosis
Abstract Cystic fibrosis is a common life-limiting autosomal recessive genetic disorder that causes severe damage to lungs, digestive system and other organs in the body. This disease is a result of mutation in a gene that encodes for chloride-conducting transmembrane channel called CFTR, which in turn regulates mucociliary clearance and anion ...
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Repurposing FDA-Approved Drugs as Potential Inhibitors of Feline Infectious Peritonitis Virus 3CL<sup>pro</sup>: An Integrated In Silico and In Vitro Study with Synergistic Combination Analysis. [PDF]
Lueangaramkul V +6 more
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In Vitro Restoration of Colistin Susceptibility by Ivacaftor Synergy with Limited Reproducibility in a Murine Pneumonia Model. [PDF]
Halperin AV +9 more
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Post-marketing safety profile of lumacaftor/ivacaftor in cystic fibrosis treatment: a pharmacovigilance analysis based on FAERS. [PDF]
Wang T +6 more
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PopMAG: a Nextflow pipeline for population genetics analysis based on metagenome-assembled genomes. [PDF]
Sabogal-Rodriguez D, Caro-Quintero A.
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Predictive capacity of paediatric nasal epithelial cells in sequential CFTR modulator therapy. [PDF]
Fawcett LK +6 more
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Discovery of novel repurposed anthelminthics against <i>Trichinella spiralis</i> and albendazole-resistant nematodes through metabolomics-guided virtual screening. [PDF]
Chienwichai P +6 more
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NAALADL1 modulates cellular resistance to Tumor Treating Fields in colorectal cancer. [PDF]
Su Z +9 more
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Greenness, Whiteness, and Blueness Assessment With a Novel and Fully Validated HPLC Method for Simultaneous Analysis of Lumacaftor and Ivacaftor in Sweat. [PDF]
Levent S, Elriş A, Özcan S, Can NÖ.
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