Found: 17
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Targeting ubiquitination machinery in cystic fibrosis: Where do we stand?
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- Cellular & Molecular Life Sciences, 2024, v. 81, n. 1, p. 1, doi. 10.1007/s00018-024-05295-z
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- Article
Editorial: Advancing therapeutic strategies: exploring ABC transporters and chemicals affecting their expression and function for disease treatment.
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- Frontiers in Pharmacology, 2024, p. 01, doi. 10.3389/fphar.2024.1423979
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- Article
Editorial: Advancing therapeutic strategies: exploring ABC transporters and chemicals affecting their expression and function for disease treatment.
- Published in:
- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1423979
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- Article
Ligand-based virtual-screening identified a novel CFTR ligand which improves the defective cell surface expression of misfolded ABC transporters.
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- Frontiers in Pharmacology, 2024, p. 1, doi. 10.3389/fphar.2024.1370676
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- Article
UBE3C Facilitates the ER-Associated and Peripheral Degradation of Misfolded CFTR.
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- Cells (2073-4409), 2023, v. 12, n. 23, p. 2741, doi. 10.3390/cells12232741
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- Article
The multiple ubiquitination mechanisms in CFTR peripheral quality control.
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- Biochemical Society Transactions, 2023, v. 51, n. 3, p. 1297, doi. 10.1042/BST20221468
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- Article
The COPD-Associated Polymorphism Impairs the CFTR Function to Suppress Excessive IL-8 Production upon Environmental Pathogen Exposure.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 3, p. 2305, doi. 10.3390/ijms24032305
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- Article
Efficient induction of proximity-dependent labelling by biotin feeding in BMAL1-BioID knock-in mice.
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- Journal of Biochemistry, 2021, v. 170, n. 4, p. 453, doi. 10.1093/jb/mvab059
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- Article
Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Ubiquitylation as a Novel Pharmaceutical Target for Cystic Fibrosis.
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- Pharmaceuticals (14248247), 2020, v. 13, n. 4, p. 75, doi. 10.3390/ph13040075
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- Article
Peripheral Protein Quality Control as a Novel Drug Target for CFTR Stabilizer.
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- Frontiers in Pharmacology, 2018, p. 1, doi. 10.3389/fphar.2018.01100
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- Article
Chaperones rescue the energetic landscape of mutant CFTR at single molecule and in cell.
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- Nature Communications, 2017, v. 8, n. 1, p. 1, doi. 10.1038/s41467-017-00444-4
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- Article
Mechanism-based corrector combination restores ΔF508-CFTR folding and function.
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- Nature Chemical Biology, 2013, v. 9, n. 7, p. 444, doi. 10.1038/nchembio.1253
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- Article
Reduced histone deacetylase 7 activity restores function to misfolded CFTR in cystic fibrosis.
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- Nature Chemical Biology, 2010, v. 6, n. 1, p. 25, doi. 10.1038/nchembio.275
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- Article
N-glycans are direct determinants of CFTR folding and stability in secretory and endocytic membrane traffic.
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- Journal of Cell Biology, 2009, v. 184, n. 6, p. 847, doi. 10.1083/jcb.200808124
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- Article
Promoter hypomethylation of Toll-like receptor-2 gene is associated with increased proinflammatory response toward bacterial peptidoglycan in cystic fibrosis bronchial epithelial cells.
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- FASEB Journal, 2006, v. 20, n. 6, p. 782, doi. 10.1096/fj.05-4934fje
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- Article
Sp1-dependent regulation of Myeloid Elf-1 like factor in human epithelial cells
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- FEBS Letters, 2005, v. 579, n. 13, p. 2811, doi. 10.1016/j.febslet.2005.04.015
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- Article
Calnexin Δ185–520 partially reverses the misprocessing of the ΔF508 cystic fibrosis transmembrane conductance regulator<sup>1</sup><FN ID="FN1"><NO>1</NO>The data on hamster calnexin Δ185–520, have been submitted to GenBank under accession number AF380341, and those on hamster calnexin under accession number AB071869.</FN>
- Published in:
- FEBS Letters, 2002, v. 526, n. 1-3, p. 87, doi. 10.1016/S0014-5793(02)03134-4
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- Article