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Azole-resistant Aspergillus fumigatus in the environment: Identifying key reservoirs and hotspots of antifungal resistance
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Triazole Resistance in Aspergillus Species: An Emerging Problem
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Azole-resistant Aspergillus fumigatus in the hospital: Surveillance from flower beds to corridors
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How to interpret MICs of antifungal compounds according to the revised clinical breakpoints v. 10.0 European committee on antimicrobial susceptibility testing (EUCAST)
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Occurrence of triazole-resistant Aspergillus fumigatus with TR34/L98H mutations in outdoor and hospital environment in Kuwait
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The one health problem of azole resistance in Aspergillus fumigatus: current insights and future research agenda
inferredcites →https://doi.org/10.1016/j.fgb.2011.08.002openalex-snapshot
The structure–function relationship of the Aspergillus fumigatus cyp51A L98H conversion by site-directed mutagenesis: The mechanism of L98H azole resistance
inferredcites →https://doi.org/10.1016/j.jgar.2015.01.005openalex-snapshot
Triazole-resistant Aspergillus fumigatus harbouring G54 mutation: Is it de novo or environmentally acquired?
inferredcites →https://doi.org/10.1016/j.jgar.2018.10.017openalex-snapshot
Azole-resistant Aspergillus fumigatus in the Italian environment
inferredcites →https://doi.org/10.1016/j.jhazmat.2016.12.013openalex-snapshot
Fungicides induced triazole-resistance in Aspergillus fumigatus associated with mutations of TR46/Y121F/T289A and its appearance in agricultural fields
inferredcites →https://doi.org/10.1016/j.mib.2005.06.017openalex-snapshot
Aspergillus fumigatus: saprophyte or pathogen?
inferredcites →https://doi.org/10.1016/j.mycmed.2017.12.007openalex-snapshot
Pesticide behavior in paddy fields and development of azole-resistant Aspergillus fumigatus: Should we be concerned?
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Mycoflora and mycotoxin of hazelnut (Corylus avellana L.) and walnut (Juglans regia L.) seeds in Egypt
inferredcites →https://doi.org/10.1016/s1473-3099(09)70265-8openalex-snapshot
Azole resistance in Aspergillus fumigatus: a side-effect of environmental fungicide use?
inferredcites →https://doi.org/10.1021/acs.jafc.5b02728openalex-snapshot
Genesis of Azole Antifungal Resistance from Agriculture to Clinical Settings
inferredcites →https://doi.org/10.1021/jf4013949openalex-snapshot
Typical Azole Biocides in Biosolid-Amended Soils and Plants Following Biosolid Applications
inferredcites →https://doi.org/10.1038/nrmicro1179openalex-snapshot
Evolution of antifungal-drug resistance: mechanisms and pathogen fitness
inferredcites →https://doi.org/10.1038/srep45631openalex-snapshot
Azole-resistant Aspergillus fumigatus harboring TR34/L98H, TR46/Y121F/T289A and TR53 mutations related to flower fields in Colombia
inferredcites →https://doi.org/10.1056/nejmc061720openalex-snapshot
Multiple-Triazole–Resistant Aspergillosis
inferredcites →https://doi.org/10.1080/00275514.1975.12019798openalex-snapshot
Fungi Occurring in Freshly Harvested and In-Market Pecans
inferredcites →https://doi.org/10.1080/00275514.2018.1557796openalex-snapshot
Fungicide-driven alterations in azole-resistantAspergillus fumigatusare related to vegetable crops in Colombia, South America
inferredcites →https://doi.org/10.1080/09603123.2020.1810210openalex-snapshot
Algorithm to assess the presence of Aspergillus fumigatus resistant strains: The case of Norwegian sawmills
inferredcites →https://doi.org/10.1080/13693780500090826openalex-snapshot
Azole and fungicide resistance in clinical and environmentalAspergillus fumigatusisolates
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Burden of Aspergillosis‐Related Hospitalizations in the United States
inferredcites →https://doi.org/10.1086/338025openalex-snapshot
Cluster of Cases of Invasive Aspergillosis in a Transplant Intensive Care Unit: Evidence of Person-to-Person Airborne Transmission
inferredcites →https://doi.org/10.1093/cid/cit320openalex-snapshot
Aspergillosis due to Voriconazole Highly Resistant Aspergillus fumigatus and Recovery of Genetically Related Resistant Isolates From Domiciles
inferredcites →https://doi.org/10.1093/cid/ciw326openalex-snapshot
Practice Guidelines for the Diagnosis and Management of Aspergillosis: 2016 Update by the Infectious Diseases Society of America
inferredcites →https://doi.org/10.1093/cid/cix257openalex-snapshot
Intercountry Transfer of Triazole-Resistant Aspergillus fumigatus on Plant Bulbs
inferredcites →https://doi.org/10.1093/cid/ciy181openalex-snapshot
Epidemiology and Outcomes of Hospitalizations With Invasive Aspergillosis in the United States, 2009–2013
inferredcites →https://doi.org/10.1093/g3journal/jkab427openalex-snapshot
Evidence for the agricultural origin of resistance to multiple antimicrobials in Aspergillus fumigatus , a fungal pathogen of humans
inferredcites →https://doi.org/10.1093/jac/dkt397openalex-snapshot
Azole-resistant Aspergillus fumigatus with the environmental TR46/Y121F/T289A mutation in India
inferredcites →https://doi.org/10.1093/jac/dku259openalex-snapshot
Multi-azole-resistant Aspergillus fumigatus in the environment in Tanzania
inferredcites →https://doi.org/10.1093/jac/dkx168openalex-snapshot
Isolation of azole-resistant Aspergillus fumigatus from the environment in the south-eastern USA
inferredcites →https://doi.org/10.1093/mmy/myw047openalex-snapshot
Culturable fungi in potting soils and compost
inferredcites →https://doi.org/10.1093/mmy/myx144openalex-snapshot
Triazole resistance surveillance in Aspergillus fumigatus
inferredcites →https://doi.org/10.1093/ofid/ofw268openalex-snapshot
Trends in Hospitalizations Related to Invasive Aspergillosis and Mucormycosis in the United States, 2000–2013
inferredcites →https://doi.org/10.1098/rstb.2015.0460openalex-snapshot
Clinical implications of globally emerging azole resistance in Aspergillus fumigatus
inferredcites →https://doi.org/10.1111/1462-2920.13988openalex-snapshot
Prevalence, mechanisms and genetic relatedness of the human pathogenic fungus Aspergillus fumigatus exhibiting resistance to medical azoles in the environment of Taiwan
inferredcites →https://doi.org/10.1111/ina.12436openalex-snapshot
Emergence ofAspergillus fumigatusazole resistance in azole-naïve patients with chronic obstructive pulmonary disease and their homes
inferredcites →https://doi.org/10.1111/jam.13488openalex-snapshot
Azole-resistantAspergillus fumigatusin sawmills of Eastern France
inferredcites →https://doi.org/10.1111/jam.14217openalex-snapshot
Aspergillusspecies collected from environmental air samples in Portugal—molecular identification, antifungal susceptibility and sequencing ofcyp51Agene onA. fumigatus sensu strictoitraconazole resistant
inferredcites →https://doi.org/10.1111/myc.12089openalex-snapshot
Environmental study of azole‐resistant A spergillus fumigatus with TR34/L98H mutations in the cyp51A gene in I ran
inferredcites →https://doi.org/10.1111/myc.13008openalex-snapshot
Azole resistance in Aspergillus species in Southern Taiwan: An epidemiological surveillance study
inferredcites →https://doi.org/10.1111/myc.13064openalex-snapshot
First azole‐resistant Aspergillus fumigatus isolates with the environmental TR46/Y121F/T289A mutation in Iran
inferredcites →https://doi.org/10.1128/aac.00100-15openalex-snapshot
Environmental Isolates of Azole-Resistant Aspergillus fumigatus in Germany
inferredcites →https://doi.org/10.1128/aac.00548-19openalex-snapshot
Elevated Prevalence of Azole-Resistant Aspergillus fumigatus in Urban versus Rural Environments in the United Kingdom
inferredcites →https://doi.org/10.1128/aac.00904-20openalex-snapshot
Five-Year Survey (2014 to 2018) of Azole Resistance in Environmental Aspergillus fumigatus Isolates from China
inferredcites →https://doi.org/10.1128/aac.01005-16openalex-snapshot
Epidemiology and Molecular Characterizations of Azole Resistance in Clinical and Environmental Aspergillus fumigatus Isolates from China
inferredcites →https://doi.org/10.1128/aac.02088-17openalex-snapshot
Azole Resistance of Environmental and Clinical Aspergillus fumigatus Isolates from Switzerland
inferredcites →https://doi.org/10.1128/aac.05088-11openalex-snapshot
Rapid Induction of Multiple Resistance Mechanisms in Aspergillus fumigatus during Azole Therapy: a Case Study and Review of the Literature
inferredcites →https://doi.org/10.1128/aac.40.2.279openalex-snapshot
Antifungal agents: chemotherapeutic targets and immunologic strategies
inferredcites →https://doi.org/10.1128/aac.41.6.1364openalex-snapshot
Itraconazole resistance in Aspergillus fumigatus
inferredcites →https://doi.org/10.1128/aac.45.11.2987-2990.2001openalex-snapshot
Critical Annotations to the Use of Azole Antifungals for Plant Protection
inferredcites →https://doi.org/10.1128/aem.00231-09openalex-snapshot
Possible Environmental Origin of Resistance of Aspergillus fumigatus to Medical Triazoles
inferredcites →https://doi.org/10.1128/aem.34.6.765-772.1977openalex-snapshot
Occurrence of Aspergillus fumigatus during composting of sewage sludge
inferredcites →https://doi.org/10.1128/aem.39.5.1000-1009.1980openalex-snapshot
Dispersal of Aspergillus fumigatus from Sewage Sludge Compost Piles Subjected to Mechanical Agitation in Open Air
inferredcites →https://doi.org/10.1128/cmr.00140-18openalex-snapshot
Aspergillus fumigatus and Aspergillosis in 2019
inferredcites →https://doi.org/10.1128/cmr.12.2.310openalex-snapshot
Aspergillus fumigatus and Aspergillosis
inferredcites →https://doi.org/10.1128/mbio.00791-17openalex-snapshot
A Novel Environmental Azole Resistance Mutation in Aspergillus fumigatus and a Possible Role of Sexual Reproduction in Its Emergence
inferredcites →https://doi.org/10.1371/journal.pmed.0050219openalex-snapshot
Emergence of Azole Resistance in Aspergillus fumigatus and Spread of a Single Resistance Mechanism
inferredcites →https://doi.org/10.1371/journal.pone.0031801openalex-snapshot
Triazole Fungicides Can Induce Cross-Resistance to Medical Triazoles in Aspergillus fumigatus
inferredcites →https://doi.org/10.1371/journal.pone.0052871openalex-snapshot
Clonal Expansion and Emergence of Environmental Multiple-Triazole-Resistant Aspergillus fumigatus Strains Carrying the TR34/L98H Mutations in the cyp51A Gene in India
inferredcites →https://doi.org/10.1584/jpestics.d20-017openalex-snapshot
Isolation of azole-resistant Aspergillus fumigatus from imported plant bulbs in Japan and the effect of fungicide treatment
inferredcites →https://doi.org/10.2807/1560-7917.es2014.19.12.20747openalex-snapshot
Azole-resistant Aspergillus fumigatus in the environment of northern Italy, May 2011 to June 2012
inferredcites →https://doi.org/10.29252/mlj.14.4.27openalex-snapshot
Screening for Azole Resistance among Aspergillus spp isolated from Soil of Hospitals and a University Campus in Gorgan, Iran
inferredcites →https://doi.org/10.3201/eid1507.090043openalex-snapshot
Frequency and Evolution of Azole Resistance in Aspergillus fumigatus Associated with Treatment Failure1
inferredcites →https://doi.org/10.3201/eid2201.150978openalex-snapshot
Multiple Fungicide-Driven Alterations in Azole-ResistantAspergillus fumigatus, Colombia, 2015
inferredcites →https://doi.org/10.3201/eid2507.181625openalex-snapshot
Environmental Hotspots for Azole Resistance Selection of Aspergillus fumigatus , the Netherlands
inferredcites →https://doi.org/10.3201/eid2601.190885openalex-snapshot
High Azole Resistance in Aspergillus fumigatus Isolates from Strawberry Fields, China, 2018
inferredcites →https://doi.org/10.3201/eid2704.204895openalex-snapshot
COVID-19–Associated Pulmonary Aspergillosis, March–August 2020
inferredcites →https://doi.org/10.3389/fmicb.2018.01395openalex-snapshot
Determination of the Prevalence of Triazole Resistance in Environmental Aspergillus fumigatus Strains Isolated in South Wales, UK
inferredcites →https://doi.org/10.3390/jof3040057openalex-snapshot
Global and Multi-National Prevalence of Fungal Diseases—Estimate Precision
inferredcites →https://doi.org/10.3390/jof4040131openalex-snapshot
Environmental Isolates of Multi-Azole-Resistant Aspergillus spp. in Southern Italy
inferredcites →https://doi.org/10.3390/jof5030055openalex-snapshot
Invasive Aspergillosis by Aspergillus flavus: Epidemiology, Diagnosis, Antifungal Resistance, and Management
inferredcites →https://doi.org/10.4137/mbi.s24308openalex-snapshot
Fungal Presence in Selected Tree Nuts and Dried Fruits
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Fungal Antimicrobial Resistance: Mechanisms, Drivers, and Global Clinical Burden
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Recent Advances and Future Perspectives in Mitigating Invasive Antifungal-Resistant Pathogen Aspergillus fumigatus in Africa
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A long noncoding RNA regulates in vitro and in vivo triazole antifungal susceptibility in Aspergillus fumigatus
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Occurrence of Aspergillus fumigatus azole resistance in soils from Switzerland
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The Impact of the Fungal Priority Pathogens List on Medical Mycology: A Northern European Perspective
inferred← citeshttps://doi.org/10.1093/ofid/ofag150openalex-snapshot
Azole Resistance in Aspergillus fumigatus From Diverse Environments in Ohio, United States, Is Primarily Driven by TR34/L98H and TR46/Y121F/T289A Environmental Signatures
inferred← citeshttps://doi.org/10.1094/pdis-09-21-2025-reopenalex-snapshot
Optimizing Use of DMI Fungicides for Management of Apple Powdery Mildew Caused by Podosphaera leucotricha in New York State
inferred← citeshttps://doi.org/10.1097/qco.0000000000001235openalex-snapshot
Rates of azole resistance in aspergillosis: a worldwide overview
inferred← citeshttps://doi.org/10.1101/2022.11.07.515445openalex-snapshot
Landscape-scale exposure to multiazole-resistant Aspergillus fumigatus bioaerosols
inferred← citeshttps://doi.org/10.1101/2023.07.21.550109openalex-snapshot
Genomic epidemiology of European Aspergillus fumigatus causing COVID-19-associated pulmonary aspergillosis in Europe
inferred← citeshttps://doi.org/10.1101/2023.12.05.570068openalex-snapshot
Elevated mutation rates in the multi-azole resistant Aspergillus fumigatus clade drives rapid evolution of antifungal resistance
inferred← citeshttps://doi.org/10.1101/2023.12.19.572319openalex-snapshot
Distribution and Triazole Susceptibility of Aspergilli from Clinical, Soils and Veterinary Samples in Ogun State, Nigeria
inferred← citeshttps://doi.org/10.1101/2024.07.28.605507openalex-snapshot
Saturation transposon mutagenesis enables genome-wide identification of genes required for growth and fluconazole resistance in the human fungal pathogen Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1109/bip60195.2023.10379369openalex-snapshot
Comparative Analysis of Fungal Proteomes for Identifying Resistance Genes: A Preliminary Step Towards Experimental Validation
inferred← citeshttps://doi.org/10.1111/1462-2920.16154openalex-snapshot
High prevalence and genetic diversity of a single ancestral origin azole‐resistant Aspergillus fumigatus in indoor environments at Walailak University, Southern Thailand
inferred← citeshttps://doi.org/10.1111/1462-2920.70205openalex-snapshot
Unravelling Wood Extractive Resistance in Phanerochaete chrysosporium Through Random Mutagenesis
inferred← citeshttps://doi.org/10.1111/myc.13404openalex-snapshot
Collateral consequences of agricultural fungicides on pathogenic yeasts: A One Health perspective to tackle azole resistance
inferred← citeshttps://doi.org/10.1111/myc.13426openalex-snapshot
Azole resistance in Aspergillus fumigatus. The first 2‐year's Data from the Danish National Surveillance Study, 2018–2020
inferred← citeshttps://doi.org/10.1111/myc.13430openalex-snapshot
COVID‐19‐associated pulmonary aspergillosis in ICU patients in a German reference centre: Phenotypic and molecular characterisation of Aspergillus fumigatus isolates
inferred← citeshttps://doi.org/10.1111/myc.13732openalex-snapshot
First detection of triazole‐resistant aspergillus fumigatus harbouring the TR34/L98H Cyp51A mutation in Burkina Faso
inferred← citeshttps://doi.org/10.1111/myc.70197openalex-snapshot
Reduced Activity of Triazole Antifungal Agents Against Aspergillus tubingensis From a Global Collection of Genomically‐Characterized Aspergillus Section Nigri Clinical Isolates (2020–2023)
inferred← citeshttps://doi.org/10.1111/ppa.14126openalex-snapshot
Epigenetic Regulation of Fungicide Resistance in Plant‐Pathogenic Fungi
inferred← citeshttps://doi.org/10.1126/sciadv.adh8839openalex-snapshot
Citizen science reveals landscape-scale exposures to multiazole-resistant Aspergillus fumigatus bioaerosols
inferred← citeshttps://doi.org/10.1128/aac.00225-23openalex-snapshot
Mitochondrial Membrane-Associated Protein Mba1 Confers Antifungal Resistance by Affecting the Production of Reactive Oxygen Species in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1128/aac.01635-25openalex-snapshot
Directed evolution of the pathogenic mold Aspergillus fumigatus reveals novel genes contributing to triazole resistance
inferred← citeshttps://doi.org/10.1128/aem.00017-24openalex-snapshot
Triazole resistance in Aspergillus fumigatu s isolated from a tomato production environment exposed to propiconazole
inferred← citeshttps://doi.org/10.1128/aem.01782-23openalex-snapshot
Pan-azole- and multi-fungicide-resistant Aspergillus fumigatus is widespread in the United States
inferred← citeshttps://doi.org/10.1128/aem.02056-23openalex-snapshot
Azole resistance mechanisms and population structure of the human pathogen Aspergillus fumigatus on retail plant products
inferred← citeshttps://doi.org/10.1128/cmr.00074-23openalex-snapshot
Novel antifungals and treatment approaches to tackle resistance and improve outcomes of invasive fungal disease
inferred← citeshttps://doi.org/10.1128/jcm.01141-23openalex-snapshot
Trends in the activity of mold-active azole agents against Aspergillus fumigatus clinical isolates with and without cyp51 alterations from Europe and North America (2017–2021)
inferred← citeshttps://doi.org/10.1128/mbio.00263-24openalex-snapshot
Variability in competitive fitness among environmental and clinical azole-resistant Aspergillus fumigatus isolates
inferred← citeshttps://doi.org/10.1128/mbio.00363-25openalex-snapshot
Aspergillus fumigatus secondary metabolite pyripyropene is important for the dual biofilm formation with Pseudomonas aeruginosa
inferred← citeshttps://doi.org/10.1128/mbio.01850-22openalex-snapshot
Secondary Metabolites Produced during Aspergillus fumigatus and Pseudomonas aeruginosa Biofilm Formation
inferred← citeshttps://doi.org/10.1128/mmbr.00011-23openalex-snapshot
Recent developments in Aspergillus fumigatus research: diversity, drugs, and disease
inferred← citeshttps://doi.org/10.1128/msphere.00016-26openalex-snapshot
Persistence of azole-resistant Aspergillus fumigatus in a southeastern United States environmental hotspot: a prospective genomic study
inferred← citeshttps://doi.org/10.1128/spectrum.00280-24openalex-snapshot
Comparative evaluation of Sensititre YeastOne and CLSI M38-Ed3 reference method for determining echinocandin minimum effective concentrations against Aspergillus isolates
inferred← citeshttps://doi.org/10.1136/thorax-2024-222168openalex-snapshot
Climate change: shifting boundaries of fungal disease in Europe and beyond
inferred← citeshttps://doi.org/10.1139/cjm-2024-0083openalex-snapshot
What in Earth? Analyses of Canadian soil populations of Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1177/20499361251313841openalex-snapshot
The impact of climate change on the epidemiology of fungal infections: implications for diagnosis, treatment, and public health strategies
inferred← citeshttps://doi.org/10.1186/s12866-024-03267-8openalex-snapshot
Hospital distribution, seasonality, time trends and antifungal susceptibility profiles of all Aspergillus species isolated from clinical samples from 2015 to 2022 in a tertiary care hospital
inferred← citeshttps://doi.org/10.1371/journal.pbio.3003184openalex-snapshot
Landscape of essential growth and fluconazole-resistance genes in the human fungal pathogen Cryptococcus neoformans
inferred← citeshttps://doi.org/10.1371/journal.pone.0282499openalex-snapshot
Detection of azole-resistant Aspergillus fumigatus in the environment from air, plant debris, compost, and soil
inferred← citeshttps://doi.org/10.1371/journal.ppat.1010073openalex-snapshot
Fungicide effects on human fungal pathogens: Cross-resistance to medical drugs and beyond
inferred← citeshttps://doi.org/10.2147/idr.s417840openalex-snapshot
Epidemiology of Clinically Significant Aspergillus Species from a Large Tertiary Hospital in Shanghai, China, for the Period of Two Years
inferred← citeshttps://doi.org/10.2147/idr.s507944openalex-snapshot
Distribution and Epidemiological Characteristics of Clinical Isolates of A. fumigatus in a Hospital from 2021 to 2023: A Retrospective Study
inferred← citeshttps://doi.org/10.2147/idr.s579990openalex-snapshot
Current Evidence on Voriconazole Exposure and Individualized Therapy for Aspergillosis
inferred← citeshttps://doi.org/10.3314/mmj.26.008openalex-snapshot
Managing Azole Resistance in Aspergillus
inferred← citeshttps://doi.org/10.3389/fcimb.2025.1669609openalex-snapshot
Chitosan–silver nanocomposites: promising alternatives for combating azole-resistant Aspergillus fumigatus
inferred← citeshttps://doi.org/10.3389/ffunb.2022.908343openalex-snapshot
NIH4215: A mutation-prone thiamine auxotrophic clinical Aspergillus fumigatus isolate
inferred← citeshttps://doi.org/10.3389/ffunb.2026.1830942openalex-snapshot
Understanding multi-azole resistance in Aspergillus fumigatus: the impact of non-cyp51A mutation and efflux pump overexpression
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1125241openalex-snapshot
High prevalence of fluconazole resistant Candida tropicalis among candiduria samples in China: An ignored matter of concern
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1253197openalex-snapshot
Comparative analysis of the biological characteristics and mechanisms of azole resistance of clinical Aspergillus fumigatus strains
inferred← citeshttps://doi.org/10.3389/fmicb.2024.1374438openalex-snapshot
Uncovering the diversity of pathogenic invaders: insights into protozoa, fungi, and worm infections
inferred← citeshttps://doi.org/10.3389/fpubh.2026.1946465openalex-snapshot
Cytotoxic activity of settled dust in primary schools: a multi-matrix, multi-season screening approach for children’s environmental health
inferred← citeshttps://doi.org/10.3390/antibiotics12030584openalex-snapshot
Pulmonary Aspergillosis in Humboldt Penguins—Susceptibility Patterns and Molecular Epidemiology of Clinical and Environmental Aspergillus fumigatus Isolates from a Belgian Zoo, 2017–2022
inferred← citeshttps://doi.org/10.3390/antibiotics12030608openalex-snapshot
Potential Strategies to Control the Risk of Antifungal Resistance in Humans: A Comprehensive Review
inferred← citeshttps://doi.org/10.3390/bioengineering11111115openalex-snapshot
Nanoparticle-Mediated Delivery of Deferasirox: A Promising Strategy Against Invasive Aspergillosis
inferred← citeshttps://doi.org/10.3390/biology14060664openalex-snapshot
Aspergillus Infections in Cetaceans: A Systematic Review of Clinical, Ecological, and Conservation Perspectives
inferred← citeshttps://doi.org/10.3390/ddc5030047openalex-snapshot
Targeting Fungal Adaptive Networks and Emerging Molecular Targets for Next-Generation Antifungal Therapeutics
inferred← citeshttps://doi.org/10.3390/diagnostics12112712openalex-snapshot
Invasive Aspergillosis in the Intensive Care Unit
inferred← citeshttps://doi.org/10.3390/diagnostics15232944openalex-snapshot
Next-Generation Sequencing for Bloodstream Infections: Shaping the Future of Rapid Diagnostics and Precision Medicine
inferred← citeshttps://doi.org/10.3390/idr17040091openalex-snapshot
Antifungal Agents in the 21st Century: Advances, Challenges, and Future Perspectives
inferred← citeshttps://doi.org/10.3390/ijerph192416508openalex-snapshot
Microbial Contamination of Bedding Material: One Health in Poultry Production
inferred← citeshttps://doi.org/10.3390/ijms23126607openalex-snapshot
Allicin as a Volatile or Nebulisable Antimycotic for the Treatment of Pulmonary Mycoses: In Vitro Studies Using a Lung Flow Test Rig
inferred← citeshttps://doi.org/10.3390/ijms26031033openalex-snapshot
Activity of Azole and Non-Azole Substances Against Aspergillus fumigatus in Clinical and Environmental Samples to Address Antimicrobial Resistance
inferred← citeshttps://doi.org/10.3390/jof10020122openalex-snapshot
Uncovering a Novel cyp51A Mutation and Antifungal Resistance in Aspergillus fumigatus through Culture Collection Screening
inferred← citeshttps://doi.org/10.3390/jof10030221openalex-snapshot
The Oxidative Stress Response Highly Depends on Glucose and Iron Availability in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.3390/jof10040278openalex-snapshot
Amphotericin B in the Era of New Antifungals: Where Will It Stand?
inferred← citeshttps://doi.org/10.3390/jof11020096openalex-snapshot
Comprehensive Review of Environmental Surveillance for Azole-Resistant Aspergillus fumigatus: A Practical Roadmap for Hospital Clinicians and Infection Control Teams
inferred← citeshttps://doi.org/10.3390/jof11040252openalex-snapshot
Aspergillus fumigatus in the Food Production Chain and Azole Resistance: A Growing Concern for Consumers
inferred← citeshttps://doi.org/10.3390/jof11100731openalex-snapshot
Azole-Resistant Aspergillus fumigatus: Epidemiology, Diagnosis, and Treatment Considerations
inferred← citeshttps://doi.org/10.3390/jof12010072openalex-snapshot
A One Health Perspective on Aspergillus fumigatus in Brazilian Dry Foods: High Genetic Diversity and Azole Susceptibility
inferred← citeshttps://doi.org/10.3390/jof12080565openalex-snapshot
Molecular Mechanisms, Diagnosis, and Therapeutic Strategies of Antifungal Resistance in Filamentous Fungi
inferred← citeshttps://doi.org/10.3390/jof12090699openalex-snapshot
Ten-Year Voriconazole Susceptibility Trends Among 1482 Clinical Aspergillus fumigatus Isolates: A Compositionally Controlled Multicenter Analysis of the VIVLI/SENTRY Platform (2010–2020)
inferred← citeshttps://doi.org/10.3390/jof12100728openalex-snapshot
Advances in Azole Antifungal Agents: From Structural Foundations to Resistance Challenges
inferred← citeshttps://doi.org/10.3390/jof8080872openalex-snapshot
In Vitro Activity of Novel Lipopeptides against Triazole-Resistant Aspergillus fumigatus
inferred← citeshttps://doi.org/10.3390/jof8090908openalex-snapshot
Azole Resistance and cyp51A Mutation of Aspergillus fumigatus in a Tertiary Referral Hospital in Taiwan
inferred← citeshttps://doi.org/10.3390/jof9060618openalex-snapshot
Field-Crop Soils in Eastern France: Coldspots of Azole-Resistant Aspergillus fumigatus
inferred← citeshttps://doi.org/10.3390/jof9111104openalex-snapshot
Genomic Epidemiology Identifies Azole Resistance Due to TR34/L98H in European Aspergillus fumigatus Causing COVID-19-Associated Pulmonary Aspergillosis
inferred← citeshttps://doi.org/10.3390/mi13111851openalex-snapshot
Evaluation of Antifungal Properties of Titania P25
inferred← citeshttps://doi.org/10.3390/microorganisms11112757openalex-snapshot
The Microevolution of Antifungal Drug Resistance in Pathogenic Fungi
inferred← citeshttps://doi.org/10.3390/microorganisms9122439openalex-snapshot
Selection and Amplification of Fungicide Resistance in Aspergillus fumigatus in Relation to DMI Fungicide Use in Agronomic Settings: Hotspots versus Coldspots
inferred← citeshttps://doi.org/10.3390/pathogens12111305openalex-snapshot
Drug-Resistant Aspergillus spp.: A Literature Review of Its Resistance Mechanisms and Its Prevalence in Europe
inferred← citeshttps://doi.org/10.3390/plants12183262openalex-snapshot
Identification and Characterization of Beneficial Soil Microbial Strains for the Formulation of Biofertilizers Based on Native Plant Growth-Promoting Microorganisms Isolated from Northern Mexico
inferred← citeshttps://doi.org/10.3390/toxins14050348openalex-snapshot
Six Feet under Microbiota: Microbiologic Contamination and Toxicity Profile in Three Urban Cemeteries from Lisbon, Portugal
inferred← citeshttps://doi.org/10.35690/978-2-7592-3685-5openalex-snapshot
Sols urbains, environnement et santé
inferred← citeshttps://doi.org/10.4103/ijp.ijp_1129_25openalex-snapshot
A quiet but growing threat: Global perspectives on antifungal resistance and future therapeutic approaches
inferred← citeshttps://doi.org/10.4103/jcsr.jcsr_76_21openalex-snapshot
Opportunistic infections in patients with haematological malignancies in Nigeria
inferred← citeshttps://doi.org/10.4236/pp.2024.154007openalex-snapshot
Global Burden of Fungal Infections and Antifungal Resistance from 1961 to 2024: Findings and Future Implications
inferred← citeshttps://doi.org/10.52225/narrax.v2i1.125openalex-snapshot
Antagonistic activity of Trichoderma sp. against pathogens in the leaves of Allium ascalonicum L.
inferred← citeshttps://doi.org/10.6084/m9.figshare.25538571openalex-snapshot
Additional file 1 of Hospital distribution, seasonality, time trends and antifungal susceptibility profiles of all Aspergillus species isolated from clinical samples from 2015 to 2022 in a tertiary care hospital
inferred← citeshttps://doi.org/10.64898/2026.03.19.713036openalex-snapshot
Thermal adaptation crosstalk with azole response through lncRNA in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.64898/2026.06.04.730285openalex-snapshot
Structural and Catalytic Architecture of the Cysteine Synthase Cys1a
inferred← citeshttps://doi.org/10.7759/cureus.40727openalex-snapshot
Aspergilloma in an Immunocompetent Host: A Case Report
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