about
New developments in aminoglycoside therapy and ototoxicityChannelopathiesFunction of the Pseudomonas aeruginosa NrdR Transcription Factor: Global Transcriptomic Analysis and Its Role on Ribonucleotide Reductase Gene ExpressionSide effects of aminoglycosides on the kidney, ear and balance in cystic fibrosis.Common CFTR gene variants influence body composition and survival in rural Ghana.Early childhood lung function is a stronger predictor of adolescent lung function in cystic fibrosis than early Pseudomonas aeruginosa infection.Analysis of the bacterial communities present in lungs of patients with cystic fibrosis from American and British centers.Cystic fibrosis: NHLBI Workshop on the Primary Prevention of Chronic Lung Diseases.When the cystic fibrosis label does not fit: a modified uncertainty theoryLumacaftor/ivacaftor combination for cystic fibrosis patients homozygous for Phe508del-CFTR.Impact of osteopathic treatment on pain in adult patients with cystic fibrosis--a pilot randomized controlled study.A template for mutational data analysis of the CFTR gene.Cross-sectional and longitudinal comparisons of the predominant fecal microbiota compositions of a group of pediatric patients with cystic fibrosis and their healthy siblings.Analysis of cystic fibrosis gene mutations in children with cystic fibrosis and in 964 infertile couples within the region of Basilicata, Italy: a research studyCFTR chloride channel in the apical compartments: spatiotemporal coupling to its interacting partners.Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.Nasal potential difference to detect Na+ channel dysfunction in acute lung injury.Reactive-oxygen-species-mediated P. aeruginosa killing is functional in human cystic fibrosis macrophages.High individuality of respiratory bacterial communities in a large cohort of adult cystic fibrosis patients under continuous antibiotic treatment.RNA Interference Screen to Identify Kinases That Suppress Rescue of ΔF508-CFTR.Polymicrobial interactions: impact on pathogenesis and human disease.Cohort Study of Airway Mycobiome in Adult Cystic Fibrosis Patients: Differences in Community Structure between Fungi and Bacteria Reveal Predominance of Transient Fungal Elements.Correlations of salivary biomarkers with clinical assessments in patients with cystic fibrosis.The Role of Short-Chain Fatty Acids, Produced by Anaerobic Bacteria, in the Cystic Fibrosis AirwayGeneration of Distal Airway Epithelium from Multipotent Human Foregut Stem Cells.A Genotypic-Oriented View of CFTR Genetics Highlights Specific Mutational Patterns Underlying Clinical Macrocategories of Cystic FibrosisPartial Restoration of CFTR Function in cftr-Null Mice following Targeted Cell Replacement Therapy.An empirical method to cluster objective nebulizer adherence data among adults with cystic fibrosisc.3623G > A mutation encodes a CFTR protein with impaired channel functionCholangiocytes derived from human induced pluripotent stem cells for disease modeling and drug validationMetabolite profiling to characterize disease-related bacteria: gluconate excretion by Pseudomonas aeruginosa mutants and clinical isolates from cystic fibrosis patientsAccurate reporting of adherence to inhaled therapies in adults with cystic fibrosis: methods to calculate "normative adherence".RACK1 interacts with filamin-A to regulate plasma membrane levels of the cystic fibrosis transmembrane conductance regulator.Pregnancy outcomes in cystic fibrosis: a 10-year experience from a UK centreUpdate in cystic fibrosis 2007.Novel CFTR Mutations in Two Iranian Families with Severe Cystic Fibrosis.Pharmacokinetics of erlotinib for the treatment of high-grade glioma in a pediatric patient with cystic fibrosis: case report and review of the literature.Glutathione dysregulation and the etiology and progression of human diseases.Exercise programs for children with cystic fibrosis: a systematic review of randomized controlled trials.The cystic fibrosis transmembrane conductance regulator's expanding SNARE interactome.
P2860
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P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
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
name
Cystic fibrosis
@ast
Cystic fibrosis
@en
Cystic fibrosis
@nl
type
label
Cystic fibrosis
@ast
Cystic fibrosis
@en
Cystic fibrosis
@nl
prefLabel
Cystic fibrosis
@ast
Cystic fibrosis
@en
Cystic fibrosis
@nl
P2093
P2860
P3181
P1433
P1476
Cystic fibrosis
@en
P2093
Andrew Bush
Eric W F W Alton
Jane C Davies
P2860
P304
P3181
P356
10.1136/BMJ.39391.713229.AD
P407
P577
2007-12-15T00:00:00Z