Co-infection subverts mucosal immunity in the upper respiratory tract
about
Analysis of a summary network of co-infection in humans reveals that parasites interact most via shared resourcesThe role of respiratory viruses in the etiology of bacterial pneumonia: An ecological perspectivePolymicrobial community-acquired pneumonia: An emerging entityRecognition of Extracellular Bacteria by NLRs and Its Role in the Development of Adaptive ImmunityCoinfection of Chlamydiae and other Bacteria in Reactive Arthritis and Spondyloarthritis: Need for Future ResearchThe host immune dynamics of pneumococcal colonization: implications for novel vaccine developmentImpact of Staphylococcus aureus on pathogenesis in polymicrobial infections.Carriage of Streptococcus pneumoniae and other respiratory bacterial pathogens in low and lower-middle income countries: a systematic review and meta-analysis.From microbial gene essentiality to novel antimicrobial drug targetsEffect of linezolid on clinical severity and pulmonary cytokines in a murine model of influenza A and Staphylococcus aureus coinfectionCulture and molecular-based profiles show shifts in bacterial communities of the upper respiratory tract that occur with age.Alterations of Bacteroides sp., Neisseria sp., Actinomyces sp., and Streptococcus sp. populations in the oropharyngeal microbiome are associated with liver cirrhosis and pneumonia.Encyclopedia of bacterial gene circuits whose presence or absence correlate with pathogenicity--a large-scale system analysis of decoded bacterial genomesCorynebacterium accolens Releases Antipneumococcal Free Fatty Acids from Human Nostril and Skin Surface Triacylglycerols.Streptococcus pneumoniae Colonization Disrupts the Microbial Community within the Upper Respiratory Tract of Aging MiceLong-term impact of pneumococcal polysaccharide vaccination on nasopharyngeal carriage in children previously vaccinated with various pneumococcal conjugate vaccine regimesPreventive Care Delivery to Young Children With Sickle Cell Disease.Influence of bacterial interactions on pneumococcal colonization of the nasopharynx.Next generation protein based Streptococcus pneumoniae vaccinesHost Physiologic Changes Induced by Influenza A Virus Lead to Staphylococcus aureus Biofilm Dispersion and Transition from Asymptomatic Colonization to Invasive DiseaseAdaptation in the innate immune system and heterologous innate immunity.Transmission Fitness in Co-colonization and the Persistence of Bacterial Pathogens.High nasopharyngeal pneumococcal density, increased by viral coinfection, is associated with invasive pneumococcal pneumonia.Temperature triggers immune evasion by Neisseria meningitidis.Disordered oropharyngeal microbial communities in H7N9 patients with or without secondary bacterial lung infection.Streptococcus pneumoniae and chronic endobronchial infections in childhood.Pneumococcal phenotype and interaction with nontypeable Haemophilus influenzae as determinants of otitis media progression.Modelling upper respiratory tract diseases: getting grips on host-microbe interactions in chronic rhinosinusitis using in vitro technologies.Surviving Deadly Lung Infections: Innate Host Tolerance Mechanisms in the Pulmonary System.Role of Inflammatory Risk Factors in the Pathogenesis of
P2860
Q24568161-0F3BE5C3-C97F-42EA-80FE-B458D2AA9C13Q26765407-9F326818-3E07-49C6-8861-DF2FC1A6BDD4Q26780356-F62F8483-46D2-4BC8-8B14-26D1D847AC28Q27008302-0522B3BF-133D-40EC-9BA1-68A98690252BQ28079798-EB40A70B-E749-46F7-9BD5-E3F2FF68C585Q28084920-069E2992-964F-4223-B895-CDF20B09DF02Q33602984-E9505063-E844-487E-9BB5-AB454E5E6630Q33988997-9BA95A3C-4524-4FA7-A606-36E7E72A526FQ34517482-FBED8A85-17B3-426D-A3F8-CE177C90EF3AQ34616215-4A87B08C-1863-4385-8038-DBC47600DF40Q35536029-4EC7218A-77C6-47FD-B438-51ED84C70C7AQ35670994-B6E27C87-B958-4EC9-9C2A-13B0F5B317A6Q35804215-949A341F-1465-4E7B-BCC0-6D039CC244D5Q35886154-5EAB49B6-542A-441D-B78C-231C0A19C3EBQ35898594-EB14D2C6-DE91-4313-BA3C-9AD35DEF17DCQ36174421-3DD5BFB8-EC3F-46F6-9A3E-74097AAC5E5FQ36828467-67F173DB-C156-4748-B632-5754373D3EF9Q37058954-CD9B445D-09B4-4997-BB94-B7550AC41C2EQ37130191-53BDB184-794D-4D4B-8A69-24D364B0B406Q37168719-B0EFEE0B-022A-43C3-8DA9-7F2441B4640CQ38226580-898CDAD8-E47B-42FD-95FC-1499A4049200Q40121162-66F68D35-AB2E-4B18-8866-AB6236DDDFACQ42211643-DC590F52-AC5C-48EC-A5F3-06C1B48B779EQ42267002-21DFCBFE-86C5-4095-A1CD-D2F5EF2F8A35Q47563285-F5DDA2A7-F983-4F40-A1F4-0F6082BA0162Q47770066-A669C261-24AD-4BE4-85F8-A06BCB005625Q49598060-607946C2-F382-40C9-9C1D-237DAB375268Q54940368-0A97F535-CEFF-4C10-ACAA-E126574ED6F0Q55514867-62D00BAE-5E59-4FD2-B8E9-03E46A31D021Q58586401-22AA4617-47EF-4EFF-90D1-64D58A55CFB0
P2860
Co-infection subverts mucosal immunity in the upper respiratory tract
description
2012 nî lūn-bûn
@nan
2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
name
Co-infection subverts mucosal immunity in the upper respiratory tract
@ast
Co-infection subverts mucosal immunity in the upper respiratory tract
@en
Co-infection subverts mucosal immunity in the upper respiratory tract
@nl
type
label
Co-infection subverts mucosal immunity in the upper respiratory tract
@ast
Co-infection subverts mucosal immunity in the upper respiratory tract
@en
Co-infection subverts mucosal immunity in the upper respiratory tract
@nl
prefLabel
Co-infection subverts mucosal immunity in the upper respiratory tract
@ast
Co-infection subverts mucosal immunity in the upper respiratory tract
@en
Co-infection subverts mucosal immunity in the upper respiratory tract
@nl
P2860
P3181
P1476
Co-infection subverts mucosal immunity in the upper respiratory tract
@en
P2093
Jeffrey N Weiser
Rebeccah S Lijek
P2860
P304
P3181
P356
10.1016/J.COI.2012.05.005
P407
P577
2012-08-01T00:00:00Z