Found: 8
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Airway surface liquid acidification initiates host defense abnormalities in Cystic Fibrosis.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42751-4
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- Article
Unsolved severe chronic rhinosinusitis elucidated by extensive CFTR genotyping.
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- Clinical Case Reports, 2019, v. 7, n. 11, p. 2128, doi. 10.1002/ccr3.2443
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- Article
Modulation of Chromatin Remodelling Induced by the Freshwater Cyanotoxin Cylindrospermopsin in Human Intestinal Caco-2 Cells.
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- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099121
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- Article
Characterization of two rat models of cystic fibrosis—KO and F508del CFTR—Generated by Crispr‐Cas9.
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- Animal Models & Experimental Medicine, 2019, v. 2, n. 4, p. 297, doi. 10.1002/ame2.12091
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- Article
Correlating genotype with phenotype using CFTR‐mediated whole‐cell Cl<sup>−</sup> currents in human nasal epithelial cells.
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- Journal of Physiology, 2022, v. 600, n. 6, p. 1515, doi. 10.1113/JP282143
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- Article
Systemic bis-phosphinic acid derivative restores chloride transport in Cystic Fibrosis mice.
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- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-09678-9
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- Article
Sweat Chloride Testing and Nasal Potential Difference (NPD) Are Primary Outcome Parameters in Treatment with Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Modulators.
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- Journal of Personalized Medicine, 2021, v. 11, n. 8, p. 729, doi. 10.3390/jpm11080729
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- Article
Genetic deletion of keratin 8 corrects the altered bone formation and osteopenia in a mouse model of cystic fibrosis.
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- Human Molecular Genetics, 2016, v. 25, n. 7, p. 1281, doi. 10.1093/hmg/ddw009
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- Article