The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis

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The role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis is …
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scholarly articleQ13442814

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P356DOI10.1164/RCCM.201403-0541OC
P932PMC publication ID4299577
P698PubMed publication ID25184687

P50authorSebastian L JohnstonQ57328383
Saffron Willis-OwenQ86177895
Toby MaherQ42886895
Michael J CoxQ43242747
Miriam F MoffattQ56959224
P2093author name stringDavid A Schwartz
Athol U Wells
Elissa Murphy
Patrick Mallia
Anne-Marie Russell
William O C Cookson
Kirsty E Russell
Phillip L Molyneaux
P2860cites workAnalysis of the lung microbiome in the "healthy" smoker and in COPDQ21091065
Disordered microbial communities in asthmatic airwaysQ21562589
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The rising incidence of idiopathic pulmonary fibrosis in the U.KQ28236424
Mucin 5B promoter polymorphism is associated with idiopathic pulmonary fibrosis but not with development of lung fibrosis in systemic sclerosis or sarcoidosisQ28283421
Association between the MUC5B promoter polymorphism and survival in patients with idiopathic pulmonary fibrosisQ28291143
An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and managementQ28308246
Muc5b is required for airway defenceQ28589969
The peripheral blood transcriptome identifies the presence and extent of disease in idiopathic pulmonary fibrosisQ28728072
Improved detection of bifidobacteria with optimised 16S rRNA-gene based pyrosequencingQ28730885
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosisQ28943334
Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association studyQ28943525
Search and clustering orders of magnitude faster than BLASTQ29547431
Chimeric 16S rRNA sequence formation and detection in Sanger and 454-pyrosequenced PCR ampliconsQ29614292
PyNAST: a flexible tool for aligning sequences to a template alignmentQ29616628
UniFrac--an online tool for comparing microbial community diversity in a phylogenetic contextQ29622870
Lung microbiome and disease progression in idiopathic pulmonary fibrosis: an analysis of the COMET studyQ30384494
Outgrowth of the bacterial airway microbiome after rhinovirus exacerbation of chronic obstructive pulmonary disease.Q31134621
Statistical methods for detecting differentially abundant features in clinical metagenomic samplesQ33429043
Accurate determination of microbial diversity from 454 pyrosequencing dataQ33492259
Disordered microbial communities in the upper respiratory tract of cigarette smokersQ33781228
Prednisone, azathioprine, and N-acetylcysteine for pulmonary fibrosisQ34275871
Assessing bacterial populations in the lung by replicate analysis of samples from the upper and lower respiratory tractsQ34412019
Upper airways microbiota in antibiotic-naïve wheezing and healthy infants from the tropics of rural EcuadorQ34447480
Genetics in pulmonary fibrosis--familial cases provide clues to the pathogenesis of idiopathic pulmonary fibrosisQ35010171
A persistent and diverse airway microbiota present during chronic obstructive pulmonary disease exacerbations.Q35049328
Viral infection in acute exacerbation of idiopathic pulmonary fibrosisQ35107245
Respiratory microbiome in IPF: cause, effect, or biomarker?Q35157806
The lung tissue microbiome in chronic obstructive pulmonary diseaseQ35987112
A common MUC5B promoter polymorphism and pulmonary fibrosis.Q36048530
Is idiopathic pulmonary fibrosis an environmental disease?Q36493941
Idiopathic pulmonary fibrosis: multiple causes and multiple mechanisms?Q36989280
Acute exacerbation of idiopathic pulmonary fibrosis: incidence, risk factors and outcomeQ37769355
Clinical course and prediction of survival in idiopathic pulmonary fibrosisQ37799183
An official American Thoracic Society clinical practice guideline: the clinical utility of bronchoalveolar lavage cellular analysis in interstitial lung diseaseQ38006923
The role of infection in the pathogenesis of idiopathic pulmonary fibrosis.Q38133505
Treating idiopathic pulmonary fibrosis with the addition of co-trimoxazole: a randomised controlled trialQ44137651
Changes in clinical and physiologic variables predict survival in idiopathic pulmonary fibrosisQ47878148
A mathematical theory of communicationQ56580111
Idiopathic pulmonary fibrosisQ56764887
P433issue8
P407language of work or nameEnglishQ1860
P921main subjectbacteriaQ10876
pulmonary fibrosisQ32446
pathogenesisQ372016
idiopathic pulmonary fibrosisQ2290446
P304page(s)906-913
P577publication date2014-10-01
P1433published inAmerican Journal of Respiratory and Critical Care MedicineQ4744267
P1476titleThe role of bacteria in the pathogenesis and progression of idiopathic pulmonary fibrosis
P478volume190

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