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Extracellular DNA chelates cations and induces antibiotic resistance in Pseudomonas aeruginosa biofilmsOrganisms isolated from adults with cystic fibrosisCharacterization of Pseudomonas aeruginosa isolated from chronically infected children with cystic fibrosis in India.Crystal Structure of a Charge Engineered Human Lysozyme Having Enhanced Bactericidal ActivityResponses of Pseudomonas aeruginosa to low oxygen indicate that growth in the cystic fibrosis lung is by aerobic respirationVirulence properties of Pseudomonas aeruginosa lacking the extreme-stress sigma factor AlgU (sigmaE)Pseudomonas aeruginosa RRALC3 Enhances the Biomass, Nutrient and Carbon Contents of Pongamia pinnata Seedlings in Degraded Forest SoilMicrobial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepaciaLung infections associated with cystic fibrosis.Microbial pathogenesis in cystic fibrosis: pulmonary clearance of mucoid Pseudomonas aeruginosa and inflammation in a mouse model of repeated respiratory challenge.Minimisation of aminoglycoside toxicity in patients with cystic fibrosisAntimicrobial activity of murine lung cells against Staphylococcus aureus is increased in vitro and in vivo after elafin gene transfer.Secretion of nucleoside diphosphate kinase by mucoid Pseudomonas aeruginosa 8821: involvement of a carboxy-terminal motif in secretion.Clinical isolates of Staphylococcus aureus with ribosomal mutations conferring resistance to macrolidesAdaptations of Pseudomonas aeruginosa to the cystic fibrosis lung environment can include deregulation of zwf, encoding glucose-6-phosphate dehydrogenaseCystic fibrosis in adults. From researcher to practitioner.Pharmacokinetics and pharmacodynamics of aerosolized antibacterial agents in chronically infected cystic fibrosis patients.Pseudomonas invasion of type I pneumocytes is dependent on the expression and phosphorylation of caveolin-2.A simple alfalfa seedling infection model for Pseudomonas aeruginosa strains associated with cystic fibrosis shows AlgT (sigma-22) and RhlR contribute to pathogenesis.Structure of Pseudomonas aeruginosa populations analyzed by single nucleotide polymorphism and pulsed-field gel electrophoresis genotyping.Clinical significance of microbial infection and adaptation in cystic fibrosis.Comparison of microbiomes from different niches of upper and lower airways in children and adolescents with cystic fibrosis.Infection control in cystic fibrosis.Mechanism of conversion to mucoidy in Pseudomonas aeruginosa infecting cystic fibrosis patients.Linkage analysis of geographic and clinical clusters in Pseudomonas cepacia infections by multilocus enzyme electrophoresis and ribotypingPersistence and variability of Stenotrophomonas maltophilia in cystic fibrosis patients, Madrid, 1991-1998.Concentration of circulating autoantibodies against HSP 60 is lowered through diving when compared to non-diving ratsAnimal models of chronic lung infection with Pseudomonas aeruginosa: useful tools for cystic fibrosis studies.Highlights of a workshop to discuss targeting inflammation in cystic fibrosisThe long-chain fatty acid sensor, PsrA, modulates the expression of rpoS and the type III secretion exsCEBA operon in Pseudomonas aeruginosa.Unique microbial communities persist in individual cystic fibrosis patients throughout a clinical exacerbation.Metabolic regulation of antibiotic resistance.Macrolides: from in vitro anti-inflammatory and immunomodulatory properties to clinical practice in respiratory diseases.Tobramycin administered by the TOBI(®) Podhaler(®) for persons with cystic fibrosis: a review.Alginate Biosynthesis Factories in Pseudomonas fluorescens: Localization and Correlation with Alginate Production Level.Impact of microbiology practice on cumulative prevalence of respiratory tract bacteria in patients with cystic fibrosisDetection of heme-binding proteins in epidemic strains of Burkholderia cepaciaA melanin pigment purified from an epidemic strain of Burkholderia cepacia attenuates monocyte respiratory burst activity by scavenging superoxide anion.Lipopolysaccharide (LPS) from Burkholderia cepacia is more active than LPS from Pseudomonas aeruginosa and Stenotrophomonas maltophilia in stimulating tumor necrosis factor alpha from human monocytes.Invasion and intracellular survival of Burkholderia cepacia
P2860
Q21090518-D5C04152-B284-4497-BB50-D47BE4B3B1CAQ24801361-BEC3A754-D560-4225-B19C-E4C45283F0FEQ24810743-91BDDB35-AEAE-46F8-85FC-DFBD7EDDAE1EQ27667276-4F206F4F-5C9E-4D00-8880-DD5750C91AE5Q28492742-A66FB204-FD09-4282-98DB-6EFB6C0A53D0Q28492839-ABF960EF-0076-44CC-A8ED-085D50915FC7Q28550218-FE4E4C9C-CC88-4CDA-9215-29CC859FBFD7Q29615286-784D42A1-92EA-4D48-BA77-958C8703F7E1Q30080000-C6AE6F23-468C-4FA2-B628-04956DE67042Q33748666-2DA01C48-E977-47D0-8429-9C1690EC26BEQ33775991-D775A013-F7DE-4530-A3D0-7462DA963EC2Q33788207-9479C480-EB88-4228-BB17-0C560ABFC32FQ33994304-DD7D5112-12E0-41F7-8B2E-B3C2F0771C14Q34112287-7EC8BF79-1AD5-40C1-ACA5-0E22DCE15CC0Q34124322-D0232EE3-AF19-488B-9E22-4C1594DB6E6CQ34183284-68C90333-0557-4818-A967-2B67B4A1996FQ34297656-9B6B6388-33EB-4321-B408-C61751198525Q34367875-66BC05BB-D35A-4E8A-8E99-30D1BDADFEA8Q34389075-715853F5-6A09-470F-9954-D24B36C412F0Q34435605-C63C1925-DF18-4213-8FBB-4BE6DEEC59B8Q34491552-0BD5706C-0264-495F-991B-C6268714E634Q35023645-31EBAA5B-696E-4A94-944D-9F2C080594A4Q35545544-326E86F6-E761-413F-B218-0E5D79323DA2Q36528781-0EE7284B-635B-40F5-A514-51F7F75A0D30Q37074611-F504C2F3-9F70-4833-B7B5-59468340D20CQ37074730-0048A555-DB7A-4E1A-B00F-539EBFD53483Q37106077-900E3260-0DB2-41BA-A434-6CAC77E61892Q37265316-00D66463-9B78-4B54-8D52-B62EEE65F9B6Q37330935-BBEBA46B-834C-4BBA-92D1-44131C905533Q37380845-2FAD60D1-3B68-4CBE-8F5F-0B3088866DF4Q37677382-CC6B671A-0214-4073-A9CA-A81EE4F18A71Q37885402-E2B68807-5A57-4F45-969A-02ABE04B9B66Q37959271-6E80D2F7-56D4-4D8D-BA9A-C230501B07F3Q38037076-38878687-D156-4E24-BCAB-25C3431393EBQ38387583-141A1554-58E3-4558-929A-2F6EA81DD00BQ39447423-E8B715FA-613C-47DB-AC41-AAD56FEF03D7Q39508224-3039BD7D-2783-45B4-8574-91E9FEA13098Q39509776-8F825387-7EE7-48EB-B38B-53CBD1E066F5Q39510228-FEC85110-6647-43F7-A945-4050F26DC828Q39513566-8EE217D9-B49B-4484-8EBC-71BEF0F94609
P2860
description
1992 nî lūn-bûn
@nan
1992 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
1992 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
1992年の論文
@ja
1992年論文
@yue
1992年論文
@zh-hant
1992年論文
@zh-hk
1992年論文
@zh-mo
1992年論文
@zh-tw
1992年论文
@wuu
name
Microbiology of lung infection in cystic fibrosis.
@ast
Microbiology of lung infection in cystic fibrosis.
@en
type
label
Microbiology of lung infection in cystic fibrosis.
@ast
Microbiology of lung infection in cystic fibrosis.
@en
prefLabel
Microbiology of lung infection in cystic fibrosis.
@ast
Microbiology of lung infection in cystic fibrosis.
@en
P1476
Microbiology of lung infection in cystic fibrosis.
@en
P2093
P304
P356
10.1093/OXFORDJOURNALS.BMB.A072585
P577
1992-10-01T00:00:00Z