Chronic inflammation in the cystic fibrosis lung: alterations in inter- and intracellular signaling.
about
Molecular pathways for intracellular cholesterol accumulation: common pathogenic mechanisms in Niemann-Pick disease Type C and cystic fibrosis2-Benzamido-N-(1H-benzo[d]imidazol-2-yl)thiazole-4-carboxamide derivatives as potent inhibitors of CK1δ/εPulmonary fibrosis: pathogenesis, etiology and regulationCystic Fibrosis Transmembrane Conductance Regulator (CFTR) prevents apoptosis induced by hydrogen peroxide in basilar artery smooth muscle cellsA novel approach to analyze gene expression data demonstrates that the DeltaF508 mutation in CFTR downregulates the antigen presentation pathway.Development of real-time PCR assays for detection of the Streptococcus milleri group from cystic fibrosis clinical specimens by targeting the cpn60 and 16S rRNA genesNeurotrophic and neuroimmune responses to early-life Pseudomonas aeruginosa infection in rat lungs.Clinical significance of microbial infection and adaptation in cystic fibrosis.Reactive oxygen species mediate inflammatory cytokine release and EGFR-dependent mucin secretion in airway epithelial cells exposed to Pseudomonas pyocyanin.Tgf-β1 inhibits Cftr biogenesis and prevents functional rescue of ΔF508-Cftr in primary differentiated human bronchial epithelial cells.Resveratrol has salutary effects on mucociliary transport and inflammation in sinonasal epithelium.Impaired functions of macrophage from cystic fibrosis patients: CD11b, TLR-5 decrease and sCD14, inflammatory cytokines increaseDefective adenosine-stimulated cAMP production in cystic fibrosis airway epithelia: a novel role for CFTR in cell signaling.Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection.X-Box-Binding Protein 1 and Innate Immune Responses of Human Cystic Fibrosis Alveolar Macrophages.Azithromycin increases in vitro fibronectin production through interactions between macrophages and fibroblasts stimulated with Pseudomonas aeruginosa.Chronic inflammation and cancer: emerging roles of triggering receptors expressed on myeloid cells.CFTR activity and mitochondrial function.Bcl-2 suppresses sarcoplasmic/endoplasmic reticulum Ca2+-ATPase expression in cystic fibrosis airways: role in oxidant-mediated cell deathInterleukin-17 Pathophysiology and Therapeutic Intervention in Cystic Fibrosis Lung Infection and Inflammation.Progress in cystic fibrosis and the CF Therapeutics Development NetworkAnchored PDE4 regulates chloride conductance in wild-type and ΔF508-CFTR human airway epithelia.Phosphatidylinositol 3-kinase isoforms as targets in respiratory disease.Regulation of the epithelial Na+ channel and airway surface liquid volume by serine proteases.Apoptotic process in cystic fibrosis cells.Management of pulmonary exacerbations in cystic fibrosis: still an unmet medical need in clinical practice.Lactoferrin decreases inflammatory response by cystic fibrosis bronchial cells invaded with Burkholderia cenocepacia iron-modulated biofilm.Cystic fibrosis transmembrane conductance regulator trafficking modulates the barrier function of airway epithelial cell monolayers.Viral interference and the live-attenuated intranasal influenza vaccine: Results from a pediatric cohort with cystic fibrosis.Proinflammatory Cytokines Impair Vitamin D-Induced Host Defense in Cultured Airway Epithelial Cells.Interleukin-17 Is Required for Control of Chronic Lung Infection Caused by Pseudomonas aeruginosa.AMPK agonists ameliorate sodium and fluid transport and inflammation in cystic fibrosis airway epithelial cells.Inhaled corticosteroids and Aspergillus fumigatus isolation in cystic fibrosis.Lactoferrin differently modulates the inflammatory response in epithelial models mimicking human inflammatory and infectious diseases.Reduced microtubule acetylation in cystic fibrosis epithelial cells.Inflammatory biomarker profile in children with cystic fibrosis: preliminary study.Mesenchymal Stem Cell Soluble Mediators and Cystic Fibrosis.C-reactive protein/albumin ratio is associated with lung function among children/adolescents with cystic fibrosis: a three-year longitudinal study.The cytokines interleukin-1β and tumor necrosis factor-α stimulate CFTR-mediated fluid secretion by swine airway submucosal glands.Macrophage Dysfunction in Cystic Fibrosis: A Therapeutic Target to Enhance Self-Immunity.
P2860
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P2860
Chronic inflammation in the cystic fibrosis lung: alterations in inter- and intracellular signaling.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Chronic inflammation in the cy ...... - and intracellular signaling.
@en
type
label
Chronic inflammation in the cy ...... - and intracellular signaling.
@en
prefLabel
Chronic inflammation in the cy ...... - and intracellular signaling.
@en
P2093
P1476
Chronic inflammation in the cy ...... - and intracellular signaling.
@en
P2093
David Nichols
James Chmiel
Melvin Berger
P2888
P304
P356
10.1007/S12016-007-8039-9
P577
2008-04-01T00:00:00Z