Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
about
Advances toward the elucidation of hypertonic saline effects on Pseudomonas aeruginosa from cystic fibrosis patientsTissue and cellular expression patterns of porcine CFTR: similarities to and differences from human CFTRPartitioning core and satellite taxa from within cystic fibrosis lung bacterial communitiesCommon gene therapy viral vectors do not efficiently penetrate sputum from cystic fibrosis patients.Bacteriophage adhering to mucus provide a non-host-derived immunity.Upregulation of TMEM16A Protein in Bronchial Epithelial Cells by Bacterial PyocyaninPharmacological Characterization of a Novel ENaCα siRNA (GSK2225745) With Potential for the Treatment of Cystic FibrosisReduced mucociliary clearance in old mice is associated with a decrease in Muc5b mucinThe penetration of fresh undiluted sputum expectorated by cystic fibrosis patients by non-adhesive polymer nanoparticles.Implication of NADPH oxidases in the early inflammation process generated by cystic fibrosis cells.Mucus-penetrating nanoparticles for drug and gene delivery to mucosal tissues.Challenges and advances in the development of inhalable drug formulations for cystic fibrosis lung disease.Why Do We have to Move Fluid to be Able to Breathe?The challenges and promises of new therapies for cystic fibrosis.CXCR2: From Bench to Bedside.Expert opinion in biological therapy: update on developments in lung gene transfer.Strategies for improving mucosal drug delivery.The CXCR1/2 Pathway: Involvement in Diabetes Pathophysiology and Potential Target for T1D Interventions.The function and regulation of acid-sensing ion channels (ASICs) and the epithelial Na(+) channel (ENaC): IUPHAR Review 19.Proteomic and ionomic profiling reveals significant alterations of protein expression and calcium homeostasis in cystic fibrosis cells.Efficacy and safety of liposomal clarithromycin and its effect on Pseudomonas aeruginosa virulence factors.Role of the CXCL8-CXCR1/2 Axis in Cancer and Inflammatory Diseases.Azithromycin increases chloride efflux from cystic fibrosis airway epithelial cells.Carbon monoxide rapidly impairs alveolar fluid clearance by inhibiting epithelial sodium channels.Functional nanocarrier for drug and gene delivery via local administration in mucosal tissues.Role of CXCR1 and Interleukin-8 in Methamphetamine-Induced Neuronal Apoptosis
P2860
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P2860
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
description
2007 nî lūn-bûn
@nan
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
2007年论文
@zh
2007年论文
@zh-cn
name
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@en
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@nl
type
label
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@en
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@nl
prefLabel
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@en
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@nl
P2860
P1476
Cystic Fibrosis: The Mechanisms of Pathogenesis of an Inherited Lung Disorder.
@en
P2093
Mark T Clunes
Richard C Boucher
P2860
P356
10.1016/J.DDMEC.2007.09.001
P577
2007-01-01T00:00:00Z