Applications for green fluorescent protein (GFP) in the study of host-pathogen interactions.
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Role of annexins in endocytosis of antigens in immature human dendritic cellsCommon themes in microbial pathogenicity revisitedFilamentation by Escherichia coli subverts innate defenses during urinary tract infectionFlagellin acting via TLR5 is the major activator of key signaling pathways leading to NF-kappa B and proinflammatory gene program activation in intestinal epithelial cellsColonization of the Intestinal Tract of the Polyphagous Pest Spodoptera littoralis with the GFP-Tagged Indigenous Gut Bacterium Enterococcus mundtiiThe Salmonella SPI2 effector SseI mediates long-term systemic infection by modulating host cell migrationSindbis-group alphavirus replication in periosteum and endosteum of long bones in adult mice.Macrophage-dependent induction of the Salmonella pathogenicity island 2 type III secretion system and its role in intracellular survivalGreen fluorescent protein reporter microplate assay for high-throughput screening of compounds against Mycobacterium tuberculosisConstruction and characterization of a Streptococcus suis serotype 2 recombinant expressing enhanced green fluorescent proteinInteraction of DevR with multiple binding sites synergistically activates divergent transcription of narK2-Rv1738 genes in Mycobacterium tuberculosisThe 16-kDa alpha-crystallin (Acr) protein of Mycobacterium tuberculosis is required for growth in macrophagesPolyphosphate kinase is involved in stress-induced mprAB-sigE-rel signalling in mycobacteriaNovel high throughput pooled shRNA screening identifies NQO1 as a potential drug target for host directed therapy for tuberculosisCooperative binding of phosphorylated DevR to upstream sites is necessary and sufficient for activation of the Rv3134c-devRS operon in Mycobacterium tuberculosis: implication in the induction of DevR target genes.A microfluidic-based genetic screen to identify microbial virulence factors that inhibit dendritic cell migrationThe most abundant glycoprotein of amebic cyst walls (Jacob) is a lectin with five Cys-rich, chitin-binding domains.Persistent association of Mycobacterium ulcerans with West African predaceous insects of the family belostomatidaeMorphological plasticity promotes resistance to phagocyte killing of uropathogenic Escherichia coliDifferentiation and developmental pathways of uropathogenic Escherichia coli in urinary tract pathogenesis.Tracking bacterial infection of macrophages using a novel red-emission pH sensor.Measuring mass transfer processes of octane with the help of an alkSalkB::gfp-tagged Escherichia coli.Simultaneous analysis of the cyan, yellow and green fluorescent proteins by flow cytometry using single-laser excitation at 458 nm.Determinants outside the DevR C-terminal domain are essential for cooperativity and robust activation of dormancy genes in Mycobacterium tuberculosis.Brucella abortus genes identified following constitutive growth and macrophage infectionThe identification of Mycobacterium marinum genes differentially expressed in macrophage phagosomes using promoter fusions to green fluorescent protein.Use of green fluorescent protein to tag and investigate gene expression in marine bacteriaConstruction of a multiple fluorescence labelling system for use in co-invasion studies of Listeria monocytogenesPositive feedback and noise activate the stringent response regulator rel in mycobacteriapar genes in Mycobacterium bovis and Mycobacterium smegmatis are arranged in an operon transcribed from "SigGC" promoters.Strategies for isolation of in vivo expressed genes from bacteria.Polysaccharide capsule and sialic acid-mediated regulation promote biofilm-like intracellular bacterial communities during cystitis.Use of green fluorescent protein to assess urease gene expression by uropathogenic Proteus mirabilis during experimental ascending urinary tract infection.Single-cell techniques using chromosomally tagged fluorescent bacteria to study Listeria monocytogenes infection processes.Genetic transformation of an obligate anaerobe, P. gingivalis for FMN-green fluorescent protein expression in studying host-microbe interaction.Spatial-temporal imaging of bacterial infection and antibiotic response in intact animals.Measurement of bacterial gene expression in vivo.Improved expression systems for regulated expression in Salmonella infecting eukaryotic cellsInteractions with M cells and macrophages as key steps in the pathogenesis of enterohemorrhagic Escherichia coli infectionsChitinase secretion by encysting Entamoeba invadens and transfected Entamoeba histolytica trophozoites: localization of secretory vesicles, endoplasmic reticulum, and Golgi apparatus
P2860
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P2860
Applications for green fluorescent protein (GFP) in the study of host-pathogen interactions.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年学术文章
@wuu
1996年学术文章
@zh-cn
1996年学术文章
@zh-hans
1996年学术文章
@zh-my
1996年学术文章
@zh-sg
1996年學術文章
@yue
1996年學術文章
@zh
1996年學術文章
@zh-hant
name
Applications for green fluores ...... of host-pathogen interactions.
@en
type
label
Applications for green fluores ...... of host-pathogen interactions.
@en
prefLabel
Applications for green fluores ...... of host-pathogen interactions.
@en
P2093
P1433
P1476
Applications for green fluores ...... of host-pathogen interactions.
@en
P2093
Hromockyj AE
Ramakrishnan L
Valdivia RH
P356
10.1016/0378-1119(95)00706-7
P407
P433
P577
1996-01-01T00:00:00Z