Human macrophage activation programs induced by bacterial pathogens.
about
ISG20, a new interferon-induced RNase specific for single-stranded RNA, defines an alternative antiviral pathway against RNA genomic virusesPre-B cell colony-enhancing factor inhibits neutrophil apoptosis in experimental inflammation and clinical sepsisHuman IL-23-producing type 1 macrophages promote but IL-10-producing type 2 macrophages subvert immunity to (myco)bacteriaFunction of Nod-like receptors in microbial recognition and host defenseA human in vitro model system for investigating genome-wide host responses to SARS coronavirus infectionMining microarray expression data by literature profiling.Genetic control of the innate immune responsePAGE: parametric analysis of gene set enrichmentEasy detection of chromatin binding proteins by the Histone Association Assay.Immunotoxicogenomics: gene expression and immunotoxicology in the age of genomicsCytokine responses of bovine macrophages to diverse clinical Mycobacterium avium subspecies paratuberculosis strainsInnate Immune Defenses in Human Tuberculosis: An Overview of the Interactions between Mycobacterium tuberculosis and Innate Immune CellsTowards an understanding of cell-specific functions of signal-dependent transcription factorsImmunoregulatory functions and expression patterns of PE/PPE family members: Roles in pathogenicity and impact on anti-tuberculosis vaccine and drug designM1 and M2 immune activation in Parkinson's Disease: Foe and ally?Association between NOD2 single nucleotide polymorphisms and Grade III-IV acute graft-versus-host disease: A meta-analysisNanoparticle Uptake: The Phagocyte ProblemAutomated discovery of functional generality of human gene expression programsMycolic acid modification by the mmaA4 gene of M. tuberculosis modulates IL-12 productionThe Staphylococcus aureus peptidoglycan protects mice against the pathogen and eradicates experimentally induced infectionIdentification of Mycobacterium tuberculosis counterimmune (cim) mutants in immunodeficient mice by differential screeningThe SecA2 secretion factor of Mycobacterium tuberculosis promotes growth in macrophages and inhibits the host immune responseNAMPT-mediated salvage synthesis of NAD+ controls morphofunctional changes of macrophagesDe novo assembly of the grass carp Ctenopharyngodon idella transcriptome to identify miRNA targets associated with motile aeromonad septicemiaIncreased nucleolar localization of SpiA3G in classically but not alternatively activated macrophagesAcute infection and macrophage subversion by Mycobacterium tuberculosis require a specialized secretion systemThe M1 and M2 paradigm of macrophage activation: time for reassessmentInvolvement of β-defensin 130 (DEFB130) in the macrophage microbicidal mechanisms for killing Plasmodium falciparumCellular transcriptional profiling in influenza A virus-infected lung epithelial cells: the role of the nonstructural NS1 protein in the evasion of the host innate defense and its potential contribution to pandemic influenzaThe role of macrophage polarization in infectious and inflammatory diseasesTranscriptional and apoptotic responses of THP-1 cells to challenge with toxigenic, and non-toxigenic Bacillus anthracis.Pro-angiogenic and anti-inflammatory regulation by functional peptides loaded in polymeric implants for soft tissue regeneration.Transcriptional noise and cellular heterogeneity in mammalian macrophages.Intracellular growth of Mycobacterium tuberculosis after macrophage cell death leads to serial killing of host cells.Global transcriptional response of pig brain and lung to natural infection by Pseudorabies virusDevelopment and validation of a bovine macrophage specific cDNA microarray.Dynamic changes in pro- and anti-inflammatory cytokine profiles and gamma interferon receptor signaling integrity correlate with tuberculosis disease activity and response to curative treatment.Functional genomic delineation of TLR-induced transcriptional networks.Probing host pathogen cross-talk by transcriptional profiling of both Mycobacterium tuberculosis and infected human dendritic cells and macrophages.Plasticity of the systemic inflammatory response to acute infection during critical illness: development of the riboleukogram.
P2860
Q24295036-294229F6-3E91-4CC5-9B2E-6B39EE82252AQ24568212-8A136257-5160-43BD-A395-EA899C081F10Q24633691-111088B7-DEE1-4AC7-B92C-7F5FD48657D6Q24647448-D29BFDF8-10CB-4C19-B33F-52EA4FFAE733Q24794470-7F7A8050-D6E1-4460-B1CA-D313E8C28A54Q24794517-678F9537-63C8-4A3F-82FA-A287994FDDCAQ24800607-1C0673F8-C786-4A77-988F-F726BC6C7483Q24810449-77A6985A-5479-429B-839C-DC97B54447B4Q24815956-FA74EC12-D15D-41A8-900D-535CF284C697Q24855057-B29BD6A4-F72B-47CA-9E91-29446ED1D9FCQ25257252-6084A9BC-A4D2-4EFC-8800-04E7BB645CD5Q26799901-3E465CC4-B8F0-4330-B8B0-DB4BD037E55DQ27001970-A24CD6C5-107D-4171-98DE-DAC99E2511A2Q27013243-D6B3B2BC-0C0D-43FB-85A9-C3EF461A5018Q27024667-C41932BD-E751-4137-8EAB-75FA8B218BFDQ28248522-111BA513-7C2D-489D-A6E7-8A584DE748D6Q28395287-E4E690C2-132B-4C6B-9490-50367F8811FCQ28469275-B912A1B1-A43A-4866-A54B-DF9E0A461632Q28472837-8F988F58-0C38-4541-B6E7-9E67980D2EAAQ28478213-98A513E2-4FF5-4AB8-A8AF-3CC3F7B01427Q28486518-2A088EA8-06A4-4BF6-962B-25802EA4492EQ28487596-F023DE7F-6AE8-41E1-8C67-A2B7714C2308Q28538761-F82584C9-5CD5-47B0-9234-D50E18636E23Q28545047-3704D8ED-5155-4A9D-B779-1856CBE02D68Q28585591-731B5DE2-1CB1-45EB-96FA-6FBCD9941A08Q28941163-03106969-7370-4967-BF3A-27B97CD5F28AQ29615845-9E478C53-BD54-4D76-9DAB-31E3D95C013BQ30179429-8BB70302-F3CE-4F10-8E52-4ADC3171E77AQ30331304-A42654F7-A90E-47FC-A9F6-AF458DAB4FBFQ30413135-250202DD-F011-4528-A0EB-81F484A0C21EQ30440528-95BA6BAB-F513-45AC-AE43-135D3F73E0E3Q30443731-460BEF15-EE45-4880-813F-05AC2F4D0CAFQ30478122-51B25D02-2C9B-4D32-AC40-B19EC70A2AA4Q30839454-56317D27-2C63-408F-B5AB-2A5500A1F3AEQ30932439-8A99B0CC-9CB7-49B6-9293-92B4A8024B64Q33256135-72F47306-65ED-4037-9635-8BAB5C1CE372Q33265416-CD6F1381-8E31-48EF-B2E4-A1121A34F45AQ33304240-B287F5AB-FED6-46CB-A555-1AC3F76379E1Q33312964-14904E79-0211-4261-8DC0-97EA0520DC3FQ33319553-647B421E-C356-481A-810A-2C5EB0514E3F
P2860
Human macrophage activation programs induced by bacterial pathogens.
description
2002 nî lūn-bûn
@nan
2002 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Human macrophage activation programs induced by bacterial pathogens.
@ast
Human macrophage activation programs induced by bacterial pathogens.
@en
Human macrophage activation programs induced by bacterial pathogens.
@nl
type
label
Human macrophage activation programs induced by bacterial pathogens.
@ast
Human macrophage activation programs induced by bacterial pathogens.
@en
Human macrophage activation programs induced by bacterial pathogens.
@nl
prefLabel
Human macrophage activation programs induced by bacterial pathogens.
@ast
Human macrophage activation programs induced by bacterial pathogens.
@en
Human macrophage activation programs induced by bacterial pathogens.
@nl
P2093
P2860
P356
P1476
Human macrophage activation programs induced by bacterial pathogens.
@en
P2093
Ann Schlesinger
Ezra G Jennings
Joan F L Richmond
Richard A Young
P2860
P304
P356
10.1073/PNAS.022649799
P407
P577
2002-01-22T00:00:00Z