Identification of antifungal compounds active against Candida albicans using an improved high-throughput Caenorhabditis elegans assay
about
Antifungal testing and high-throughput screening of compound library against Geomyces destructans, the etiologic agent of geomycosis (WNS) in batsAutomated high-content live animal drug screening using C. elegans expressing the aggregation prone serpin α1-antitrypsin ZA High-Throughput Small Molecule Screen for C. elegans Linker Cell Death InhibitorsAntifungal activity of microbial secondary metabolitesAntifungal efficacy during Candida krusei infection in non-conventional models correlates with the yeast in vitro susceptibility profileTargeting the adaptability of heterogeneous aneuploidsAntifungal Therapy: New Advances in the Understanding and Treatment of MycosisCaenorhabditis elegans-based model systems for antifungal drug discovery.Wild-type Drosophila melanogaster as an alternative model system for investigating the pathogenicity of Candida albicans.Using C. elegans for antimicrobial drug discovery.A screening assay based on host-pathogen interaction models identifies a set of novel antifungal benzimidazole derivatives.Quantitative and automated high-throughput genome-wide RNAi screens in C. elegans.Characterization of plant-derived saponin natural products against Candida albicans.The anti-mitochondrial antifungal assay for the discovery and development of new drugs.In vitro analysis of finasteride activity against Candida albicans urinary biofilm formation and filamentation.Retigeric acid B attenuates the virulence of Candida albicans via inhibiting adenylyl cyclase activity targeted by enhanced farnesol productionHigh-throughput nano-biofilm microarray for antifungal drug discoveryEffect of tetrandrine against Candida albicans biofilmsDiscovery of potential anti-infectives against Staphylococcus aureus using a Caenorhabditis elegans infection model.Candida albicans VPS4 contributes differentially to epithelial and mucosal pathogenesis.Chemical screening identifies filastatin, a small molecule inhibitor of Candida albicans adhesion, morphogenesis, and pathogenesis.The role of mycelium production and a MAPK-mediated immune response in the C. elegans-Fusarium model systemC. elegans: model host and tool for antimicrobial drug discovery.Caenorhabditis elegans, a model organism for investigating immunity.Whole animal HTS of small molecules for antifungal compounds.Activity of caffeic acid phenethyl ester in Caenorhabditis elegans.Strategies in the discovery of novel antifungal scaffolds.An update on the use of C. elegans for preclinical drug discovery: screening and identifying anti-infective drugs.A living model for obesity and aging research: Caenorhabditis elegans.Exploring the diversity and metabolic potential of actinomycetes from temperate marine sediments from Newfoundland, Canada.Thymol has antifungal activity against Candida albicans during infection and maintains the innate immune response required for function of the p38 MAPK signaling pathway in Caenorhabditis elegans.Interaction of Staphylococcus aureus persister cells with the host when in a persister state and following awakening.Natural product solasodine-3-O-β-D-glucopyranoside inhibits the virulence factors of Candida albicans.Alkyl Protocatechuate-Loaded Nanostructured Lipid Systems as a Treatment Strategy for Paracoccidioides brasiliensis and Paracoccidioides lutzii In VitroModels to study ancient host-pathogen interactions: lessons from Crete.Pathogenesis and Antifungal Drug Resistance of the Human Fungal Pathogen Candida glabrata.Activity of gallic acid and its ester derivatives in Caenorhabditis elegans and zebrafish (Danio rerio) models.Methodologies for in vitro and in vivo evaluation of efficacy of antifungal and antibiofilm agents and surface coatings against fungal biofilms.Promising Antifungal Targets Against Based on Ion HomeostasisExophiala dermatitidis isolates from various sources: using alternative invertebrate host organisms (Caenorhabditis elegans and Galleria mellonella) to determine virulence
P2860
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P2860
Identification of antifungal compounds active against Candida albicans using an improved high-throughput Caenorhabditis elegans assay
description
2009 nî lūn-bûn
@nan
2009 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2009 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
name
Identification of antifungal c ...... t Caenorhabditis elegans assay
@ast
Identification of antifungal c ...... t Caenorhabditis elegans assay
@en
Identification of antifungal c ...... t Caenorhabditis elegans assay
@nl
type
label
Identification of antifungal c ...... t Caenorhabditis elegans assay
@ast
Identification of antifungal c ...... t Caenorhabditis elegans assay
@en
Identification of antifungal c ...... t Caenorhabditis elegans assay
@nl
prefLabel
Identification of antifungal c ...... t Caenorhabditis elegans assay
@ast
Identification of antifungal c ...... t Caenorhabditis elegans assay
@en
Identification of antifungal c ...... t Caenorhabditis elegans assay
@nl
P2093
P2860
P50
P3181
P1433
P1476
Identification of antifungal c ...... t Caenorhabditis elegans assay
@en
P2093
Andy Stern
Annie L Conery
Edward Holson
Emmanouil Tampakakis
Emmanouil Tempakakis
Florence Wagner
Ikechukwu Okoli
Jonah Larkins-Ford
W Frank An
P2860
P3181
P356
10.1371/JOURNAL.PONE.0007025
P407
P577
2009-09-14T00:00:00Z