scholarly article | Q13442814 |
P356 | DOI | 10.1128/JCM.00432-15 |
P8608 | Fatcat ID | release_zd73y62x25gknii2yt5wwt7x3m |
P932 | PMC publication ID | 4473198 |
P698 | PubMed publication ID | 25878338 |
P50 | author | Eshwar Mahenthiralingam | Q43593193 |
Andrew M Jones | Q56424045 | ||
Julian R Marchesi | Q61126705 | ||
P2093 | author name string | Ann Smith | |
A Kevin Webb | |||
Rowland J Bright-Thomas | |||
William G Flight | |||
Matthew J Bull | |||
Christopher Paisey | |||
Ken J Mutton | |||
Phillip J Norville | |||
P2860 | cites work | Airway microbiota and pathogen abundance in age-stratified cystic fibrosis patients | Q21562196 |
Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities | Q24647611 | ||
Culture-independent analysis of bacterial fuel contamination provides insight into the level of concordance with the standard industry practice of aerobic cultivation | Q28743046 | ||
Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy | Q29547619 | ||
Molecular identification of bacteria in bronchoalveolar lavage fluid from children with cystic fibrosis | Q33310144 | ||
Polymicrobial nature of chronic diabetic foot ulcer biofilm infections determined using bacterial tag encoded FLX amplicon pyrosequencing (bTEFAP). | Q33373691 | ||
Studying bacteria in respiratory specimens by using conventional and molecular microbiological approaches | Q33430526 | ||
The changing microbial epidemiology in cystic fibrosis | Q33825634 | ||
In silico analysis of complete bacterial genomes: PCR, AFLP-PCR and endonuclease restriction | Q33975413 | ||
Decade-long bacterial community dynamics in cystic fibrosis airways | Q34209009 | ||
Molecular microbial diversity in soils from eastern Amazonia: evidence for unusual microorganisms and microbial population shifts associated with deforestation | Q34431539 | ||
Revealing the dynamics of polymicrobial infections: implications for antibiotic therapy | Q34554419 | ||
Molecular diagnosis of medical viruses. | Q34626706 | ||
Culture-based diagnostic microbiology in cystic fibrosis: can we simplify the complexity? | Q35008296 | ||
Emerging cystic fibrosis pathogens and the microbiome | Q35169553 | ||
STAMP: statistical analysis of taxonomic and functional profiles. | Q35212955 | ||
Burkholderia cenocepacia and Burkholderia multivorans: influence on survival in cystic fibrosis. | Q35536317 | ||
Direct sampling of cystic fibrosis lungs indicates that DNA-based analyses of upper-airway specimens can misrepresent lung microbiota | Q36187491 | ||
Quantitative analysis of the human airway microbial ecology reveals a pervasive signature for cystic fibrosis | Q37502050 | ||
Studying bacterial infections through culture-independent approaches. | Q37531541 | ||
Direct culture-independent Strain typing of Burkholderia cepacia complex in sputum samples from patients with cystic fibrosis | Q40345571 | ||
Incidence and clinical impact of respiratory viruses in adults with cystic fibrosis | Q42262413 | ||
Antibiotic-resistant obligate anaerobes during exacerbations of cystic fibrosis patients | Q46131950 | ||
Intravenous antibiotics reduce the presence of Aspergillus in adult cystic fibrosis sputum | Q46277042 | ||
Relationship between cystic fibrosis respiratory tract bacterial communities and age, genotype, antibiotics and Pseudomonas aeruginosa. | Q50561588 | ||
Pseudomonas aeruginosa and other predictors of mortality and morbidity in young children with cystic fibrosis. | Q51711090 | ||
Cystic fibrosis | Q55881299 | ||
Enacyloxins Are Products of an Unusual Hybrid Modular Polyketide Synthase Encoded by a Cryptic Burkholderia ambifaria Genomic Island | Q57590249 | ||
Detection of Anaerobic Bacteria in High Numbers in Sputum from Patients with Cystic Fibrosis | Q57913654 | ||
Use of the 16S–23S ribosomal genes spacer region in studies of prokaryotic diversity | Q59333087 | ||
Pulmonary function and clinical course in patients with cystic fibrosis after pulmonary colonization with Pseudomonas aeruginosa | Q67285991 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | biodiversity | Q47041 |
cystic fibrosis | Q178194 | ||
emerging pathogen | Q108429945 | ||
microbial diversity | Q124150969 | ||
P304 | page(s) | 2022-2029 | |
P577 | publication date | 2015-04-15 | |
P1433 | published in | Journal of Clinical Microbiology | Q4041880 |
P1476 | title | Rapid Detection of Emerging Pathogens and Loss of Microbial Diversity Associated with Severe Lung Disease in Cystic Fibrosis | |
P478 | volume | 53 |
Q89013298 | "Pathogen Eradication" and "Emerging Pathogens": Difficult Definitions in Cystic Fibrosis |
Q96231866 | Airway microbial diversity is decreased in young children with cystic fibrosis compared to healthy controls but improved with CFTR modulation |
Q35946121 | Analysis of Lung Microbiota in Bronchoalveolar Lavage, Protected Brush and Sputum Samples from Subjects with Mild-To-Moderate Cystic Fibrosis Lung Disease |
Q58732428 | Antibiotic multidrug resistance in the cystic fibrosis airway microbiome is associated with decreased diversity |
Q35631188 | Assessing Airway Microbiota in Cystic Fibrosis: What More Should Be Done? |
Q55240269 | Benchmark Evaluation of True Single Molecular Sequencing to Determine Cystic Fibrosis Airway Microbiome Diversity. |
Q64116297 | Changes in microbiome diversity following beta-lactam antibiotic treatment are associated with therapeutic versus subtherapeutic antibiotic exposure in cystic fibrosis |
Q54314356 | Changes in the Cystic Fibrosis Airway Microbiome after Lung Transplant: The More Things Change, the More They Stay the Same. |
Q40252432 | Clinical Outcomes Associated with Achromobacter Species Infection in Patients with Cystic Fibrosis. |
Q36008670 | Community dynamics and the lower airway microbiota in stable chronic obstructive pulmonary disease, smokers and healthy non-smokers. |
Q36620854 | Culture-Based and Culture-Independent Bacteriologic Analysis of Cystic Fibrosis Respiratory Specimens |
Q52858752 | Cystic Fibrosis Airway Microbiome: Overturning the Old, Opening the Way for the New. |
Q36163849 | Data Mining of Lung Microbiota in Cystic Fibrosis Patients |
Q59355842 | Decreased microbiome diversity in the HIV small airway epithelium |
Q55287506 | Fluctuations in airway bacterial communities associated with clinical states and disease stages in cystic fibrosis. |
Q36128764 | In vitro model of production of antibodies; a new approach to reveal the presence of key bacteria in polymicrobial environments |
Q47653765 | Initial acquisition and succession of the cystic fibrosis lung microbiome is associated with disease progression in infants and preschool children. |
Q39252980 | Integrating the microbiota of the respiratory tract with the unified airway model |
Q40179391 | Intestinal microbiota in patients with chronic hepatitis C with and without cirrhosis compared with healthy controls. |
Q35862783 | Iron acquisition in the cystic fibrosis lung and potential for novel therapeutic strategies |
Q36135913 | Linking microbiota and respiratory disease |
Q85844811 | Lung mapping seeks to crack microbial code in cystic fibrosis |
Q46244354 | Microbial diversity within the airway microbiome in chronic pediatric lung diseases |
Q52367440 | On Burkholderiales order microorganisms and cystic fibrosis in Russia. |
Q60303723 | Profiling mycobacterial communities in pulmonary nontuberculous mycobacterial disease |
Q26768244 | Respiratory Microbiome of New-Born Infants |
Q38702812 | Respiratory microbiota and lower respiratory tract disease. |
Q36304192 | Strong incidence of Pseudomonas aeruginosa on bacterial rrs and ITS genetic structures of cystic fibrosis sputa |
Q54205691 | The CF-Sputum Induction Trial (CF-SpIT) to assess lower airway bacterial sampling in young children with cystic fibrosis: a prospective internally controlled interventional trial. |
Q97644506 | The Respiratory Microbiome in Cystic Fibrosis: Compartment Patterns and Clinical Relationships in Early Stage Disease |
Q92458688 | The Yin and Yang of Streptococcus Lung Infections in Cystic Fibrosis: a Model for Studying Polymicrobial Interactions |
Q39217321 | The endotracheal tube microbiome associated with Pseudomonas aeruginosa or Staphylococcus epidermidis. |
Q90178697 | Upper versus lower airway microbiome and metagenome in children with cystic fibrosis and their correlation with lung inflammation |
Q89554865 | mSphere of Influence: a Community To Study Communities |
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