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Emergence of Azole-Resistant Aspergillus fumigatus Strains due to Agricultural Azole Use Creates an Increasing Threat to Human Health
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ps.3390openalex-snapshot
Triazole fungicides and the selection of resistance to medical triazoles in the opportunistic mould Aspergillus fumigatus
inferredcites →https://doi.org/10.1007/s11908-011-0218-4openalex-snapshot
Azole Antifungal Resistance Today: Focus on Aspergillus
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/10.1093/cid/cir179openalex-snapshot
High-frequency Triazole Resistance Found In Nonculturable Aspergillus fumigatus from Lungs of Patients with Chronic Fungal Disease
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/jac/dkr443openalex-snapshot
Isolation of multiple-triazole-resistant Aspergillus fumigatus strains carrying the TR/L98H mutations in the cyp51A gene in India
inferredcites →https://doi.org/10.1093/jac/dkt075openalex-snapshot
The cdr1B efflux transporter is associated with non-cyp51a-mediated itraconazole resistance in Aspergillus fumigatus
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/10.1111/j.1365-294x.2011.05364.xopenalex-snapshot
Evidence for genetic differentiation and variable recombination rates among Dutch populations of the opportunistic human pathogen Aspergillus fumigatus
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/10.1126/scitranslmed.3004404openalex-snapshot
Hidden Killers: Human Fungal Infections
inferredcites →https://doi.org/10.1128/aac.00185-11openalex-snapshot
Azole Resistance in Aspergillus fumigatus Isolates from the ARTEMIS Global Surveillance Study Is Primarily Due to the TR/L98H Mutation in the cyp51A Gene
inferredcites →https://doi.org/10.1128/aac.00654-07openalex-snapshot
Treatment of a Clinically Relevant Plant-Pathogenic Fungus with an Agricultural Azole Causes Cross-Resistance to Medical Azoles and Potentiates Caspofungin Efficacy
inferredcites →https://doi.org/10.1128/aac.00692-10openalex-snapshot
Environmental Study of Azole-Resistant Aspergillus fumigatus and Other Aspergilli in Austria, Denmark, and Spain
inferredcites →https://doi.org/10.1128/aac.01092-06openalex-snapshot
A New Aspergillus fumigatus Resistance Mechanism Conferring In Vitro Cross-Resistance to Azole Antifungals Involves a Combination of cyp51A Alterations
inferredcites →https://doi.org/10.1128/aac.01599-09openalex-snapshot
Azole Resistance Profile of Amino Acid Changes in Aspergillus fumigatus CYP51A Based on Protein Homology Modeling
inferredcites →https://doi.org/10.1128/aac.05720-11openalex-snapshot
Azole Resistance by Loss of Function of the Sterol Δ 5,6 -Desaturase Gene ( ERG3 ) in Candida albicans Does Not Necessarily Decrease Virulence
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/jcm.02136-10openalex-snapshot
Use of Epidemiological Cutoff Values To Examine 9-Year Trends in Susceptibility of Aspergillus Species to the Triazoles
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.0010080openalex-snapshot
Development of Azole Resistance in Aspergillus fumigatus during Azole Therapy Associated with Change in Virulence
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.0050034openalex-snapshot
Discovery of a hapE Mutation That Causes Azole Resistance in Aspergillus fumigatus through Whole Genome Sequencing and Sexual Crossing
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/10.1371/journal.pone.0072280openalex-snapshot
Composite Survival Index to Compare Virulence Changes in Azole-Resistant Aspergillus fumigatus Clinical Isolates
inferredcites →https://doi.org/10.2165/11596540-000000000-00000openalex-snapshot
Triazole Antifungal Agents in Invasive Fungal Infections
inferredcites →https://doi.org/10.2807/ese.17.48.20326-enopenalex-snapshot
Azole-resistant Aspergillus fumigatus due to TR46/Y121F/T289A mutation emerging in Belgium, July 2012
inferredcites →https://doi.org/10.3109/13693786.2012.738312openalex-snapshot
Global burden of allergic bronchopulmonary aspergillosis with asthma and its complication chronic pulmonary aspergillosis in adults
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/eid1710.110226openalex-snapshot
Clinical Implications of Azole Resistance inAspergillus fumigatus, the Netherlands, 2007–2009
inferredcites →https://doi.org/10.3201/eid1905.130075openalex-snapshot
Azole-Resistant Aspergillus fumigatus , Iran
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.17.171995zenodo-depositor-declared
Interconnected worlds: a comprehensive review of fungal defenses, antimicrobial resistance, and their evolutionary dynamics
inferred← citeshttps://doi.org/10.1001/jamaophthalmol.2016.0530openalex-snapshot
Changing Azole Resistance
inferred← citeshttps://doi.org/10.1001/jamaophthalmol.2021.5765openalex-snapshot
Patterns of Antifungal Resistance in Adult Patients With Fungal Keratitis in South India
inferred← citeshttps://doi.org/10.1002/9781119671022.ch16openalex-snapshot
Biosurfactants Against Drug‐Resistant Human and Plant Pathogens
inferred← citeshttps://doi.org/10.1002/cbic.202000254openalex-snapshot
Cationic RuII Cyclopentadienyl Complexes with Antifungal Activity against Several Candida Species
inferred← citeshttps://doi.org/10.1002/cfch.70026openalex-snapshot
Fungal Antimicrobial Resistance: Mechanisms, Drivers, and Global Clinical Burden
inferred← citeshttps://doi.org/10.1002/cpmc.112openalex-snapshot
A Low‐Cost Tebuconazole‐Based Screening Test for Azole‐Resistant Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1002/mlf2.12036openalex-snapshot
Assessing global fungal threats to humans
inferred← citeshttps://doi.org/10.1002/sae2.70049openalex-snapshot
Intrinsic and Acquired Antimicrobial Resistomes in Plant Microbiomes: Implications for Agriculture and Public Health
inferred← citeshttps://doi.org/10.1002/wsbm.1610openalex-snapshot
A One Health approach to overcoming fungal disease and antifungal resistance
inferred← citeshttps://doi.org/10.1007/82_2019_161openalex-snapshot
Global Catastrophic Threats from the Fungal Kingdom
inferred← citeshttps://doi.org/10.1007/82_2025_305openalex-snapshot
Climate Change Impacts on Environmental Fungi: Human Health and Fungal Disease
inferred← citeshttps://doi.org/10.1007/978-1-4939-0667-3_22-1openalex-snapshot
Azole Resistance in Aspergillus fumigatus: Mechanisms, Route of Resistance Selection, and Clinical Implications
inferred← citeshttps://doi.org/10.1007/978-1-4939-0694-9_22openalex-snapshot
Azole Resistance in Aspergillus fumigatus: Mechanisms, Route of Resistance Selection, and Clinical Implications
inferred← citeshttps://doi.org/10.1007/978-3-030-69079-3_3openalex-snapshot
Emergence of a Pathogenic Fungus Resistant to Triazole Antifungal Drugs
inferred← citeshttps://doi.org/10.1007/978-3-031-93315-8_11openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-3-319-50409-4_23openalex-snapshot
Using Yeast to Discover Inhibitors of Multidrug Efflux in Candida albicans
inferred← citeshttps://doi.org/10.1007/978-981-15-3658-8_7openalex-snapshot
Antifungal Resistance: Current Concepts
inferred← citeshttps://doi.org/10.1007/978-981-95-2640-6_3openalex-snapshot
Biosafety and Biosecurity in the Context of Mycology
inferred← citeshttps://doi.org/10.1007/978-981-97-4909-6_17openalex-snapshot
Drug-Resistance Patterns in Opportunistic Aspergilli: A Molecular Perspective
inferred← citeshttps://doi.org/10.1007/s00203-024-04219-6openalex-snapshot
Fungicide resistance in Fusarium species: exploring environmental impacts and sustainable management strategies
inferred← citeshttps://doi.org/10.1007/s00203-026-05211-yopenalex-snapshot
A review on fungal pathogens in the One Health framework: connecting plant, animal, and human health
inferred← citeshttps://doi.org/10.1007/s10661-016-5751-zopenalex-snapshot
Assessment of multi-contaminant exposure in a cancer treatment center: a 2-year monitoring of molds, mycotoxins, endotoxins, and glucans in bioaerosols
inferred← citeshttps://doi.org/10.1007/s11033-019-04909-1openalex-snapshot
A simple and low cost tetra-primer ARMS-PCR method for detection triazole-resistant Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1007/s11046-014-9747-3openalex-snapshot
Prevalent Drug Resistance Among Oral Yeasts from Asymptomatic Patients in Hainan, China
inferred← citeshttps://doi.org/10.1007/s11046-015-9968-0openalex-snapshot
In Vitro Activities of Five Antifungal Drugs Against Opportunistic Agents of Aspergillus Nigri Complex
inferred← citeshttps://doi.org/10.1007/s11046-018-0271-8openalex-snapshot
TR34/L98H Mutation in CYP51A Gene in Aspergillus fumigatus Clinical Isolates During Posaconazole Prophylaxis: First Case in Korea
inferred← citeshttps://doi.org/10.1007/s11046-021-00573-xopenalex-snapshot
Fungal Genomics in Respiratory Medicine: What, How and When?
inferred← citeshttps://doi.org/10.1007/s11046-022-00640-xopenalex-snapshot
Molecular Phylogenetic Analysis of Candida krusei
inferred← citeshttps://doi.org/10.1007/s11046-024-00830-9openalex-snapshot
Multicentric Study on the Clinical Mycology Capacity and Access to Antifungal Treatment in Portugal
inferred← citeshttps://doi.org/10.1007/s11046-025-00993-zopenalex-snapshot
First Isolation of a Multi-azole-Resistant Aspergillus fumigatus cyp51A TR46/Y46F/F70L Mutant in a Patient with Fungal Keratitis
inferred← citeshttps://doi.org/10.1007/s11259-023-10220-zopenalex-snapshot
Aspergillosis in a colony of Humboldt penguins (Spheniscus humboldti) in a french zoological park: evaluation of environmental exposure
inferred← citeshttps://doi.org/10.1007/s11625-022-01202-2openalex-snapshot
Multi-target scenario discovery to plan for sustainable food and land systems in Australia
inferred← citeshttps://doi.org/10.1007/s11908-018-0608-yopenalex-snapshot
The Emerging Threat of Antifungal Resistance in Transplant Infectious Diseases
inferred← citeshttps://doi.org/10.1007/s12154-014-0121-1openalex-snapshot
Resistance to antifungals that target CYP51
inferred← citeshttps://doi.org/10.1007/s12281-016-0265-2openalex-snapshot
Azole Resistance in Moulds—Approach to Detection in a Clinical Laboratory
inferred← citeshttps://doi.org/10.1007/s12281-018-0307-zopenalex-snapshot
A Case for Antifungal Stewardship
inferred← citeshttps://doi.org/10.1007/s12281-021-00418-6openalex-snapshot
Emergence of Triazole Resistance in Aspergillus spp. in Latin America
inferred← citeshttps://doi.org/10.1007/s12550-020-00388-7openalex-snapshot
Efficacy of metabolites of a Streptomyces strain (AS1) to control growth and mycotoxin production by Penicillium verrucosum, Fusarium verticillioides and Aspergillus fumigatus in culture
inferred← citeshttps://doi.org/10.1007/s13225-023-00532-5openalex-snapshot
Current trends, limitations and future research in the fungi?
inferred← citeshttps://doi.org/10.1007/s40588-014-0004-9openalex-snapshot
Genomics and Fungal Speciation: What Can We Expect in the Clinical Laboratory?
inferred← citeshttps://doi.org/10.1007/s40588-024-00219-8openalex-snapshot
Emerging Antifungal Resistance in Fungal Pathogens
inferred← citeshttps://doi.org/10.1007/s41348-019-00252-6openalex-snapshot
Estimation of secondary metabolites of indigenous medicinal plant extracts and their in vitro and in vivo efficacy against tomato early blight disease in Pakistan
inferred← citeshttps://doi.org/10.1007/s42247-025-01231-4openalex-snapshot
Antifungal inbuilt carbon nanotube based redox metal organic framework validated by transcriptomic analysis in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1007/s42770-020-00253-wopenalex-snapshot
Lysine acetylation as drug target in fungi: an underexplored potential in Aspergillus spp.
inferred← citeshttps://doi.org/10.1007/s42770-021-00459-6openalex-snapshot
Transcriptomic studies on Purpureocillium lilacinum reveal molecular mechanisms of response to fluconazole and itraconazole
inferred← citeshttps://doi.org/10.1016/b978-0-08-102723-3.00116-5openalex-snapshot
Aspergillus Lung Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-815770-1.00011-0openalex-snapshot
Antifungal resistance
inferred← citeshttps://doi.org/10.1016/b978-0-12-815824-1.00003-2openalex-snapshot
Antifungal therapy
inferred← citeshttps://doi.org/10.1016/j.arbr.2015.09.006openalex-snapshot
Pulmonary Aspergillus Nodule – Still Challenging?
inferred← citeshttps://doi.org/10.1016/j.arbres.2015.04.007openalex-snapshot
Aspergilosis pulmonar nodular, ¿todavía supone un desafío?
inferred← citeshttps://doi.org/10.1016/j.bjid.2017.10.005openalex-snapshot
In vitro antifungal susceptibility of clinical and environmental isolates of Aspergillus fumigatus and Aspergillus flavus in Brazil
inferred← citeshttps://doi.org/10.1016/j.cimid.2015.08.002openalex-snapshot
Azole resistance in canine and feline isolates of Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1016/j.cmi.2018.01.002openalex-snapshot
Diagnosis and management of Aspergillus diseases: executive summary of the 2017 ESCMID-ECMM-ERS guideline
inferred← citeshttps://doi.org/10.1016/j.cmi.2018.11.027openalex-snapshot
Triazole resistance in Aspergillus fumigatus: recent insights and challenges for patient management
inferred← citeshttps://doi.org/10.1016/j.cmi.2019.01.007openalex-snapshot
Monitoring treatment response in chronic pulmonary aspergillosis: role of clinical, spirometric and immunological markers
inferred← citeshttps://doi.org/10.1016/j.diagmicrobio.2018.03.003openalex-snapshot
In vitro combination of voriconazole with micafungin against azole-resistant clinical isolates of Aspergillus fumigatus from different geographical regions
inferred← citeshttps://doi.org/10.1016/j.diagmicrobio.2019.05.019openalex-snapshot
Change in the clinical antifungal sensitivity profile of Aspergillus flavus induced by azole and a benzimidazole fungicide exposure
inferred← citeshttps://doi.org/10.1016/j.drup.2014.06.001openalex-snapshot
The role of azoles in the management of azole-resistant aspergillosis: From the bench to the bedside
inferred← citeshttps://doi.org/10.1016/j.drup.2015.08.001openalex-snapshot
International expert opinion on the management of infection caused by azole-resistant Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1016/j.envres.2014.05.009openalex-snapshot
Occurrence of triazole-resistant Aspergillus fumigatus with TR34/L98H mutations in outdoor and hospital environment in Kuwait
inferred← citeshttps://doi.org/10.1016/j.envres.2020.110674openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fgb.2019.103253openalex-snapshot
Epigenetic mechanisms of drug resistance in fungi
inferred← citeshttps://doi.org/10.1016/j.hazadv.2026.101230openalex-snapshot
The need of a one health approach to tackle microbiological contamination in animal and dairy production - the case of Portuguese feedlots farms and dairies
inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2017.06.018openalex-snapshot
Molecular bases of antifungal resistance in filamentous fungi
inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2018.08.004openalex-snapshot
High prevalence of triazole resistance in clinical Aspergillus fumigatus isolates in a specialist cardiothoracic centre
inferred← citeshttps://doi.org/10.1016/j.ijantimicag.2019.02.003openalex-snapshot
Impairing fluoride export of Aspergillus fumigatus mitigates its voriconazole resistance
inferred← citeshttps://doi.org/10.1016/j.ijheh.2023.114240openalex-snapshot
Occupational exposure to inhalable pathogenic microorganisms in waste sorting
inferred← citeshttps://doi.org/10.1016/j.jgar.2015.01.005openalex-snapshot
Triazole-resistant Aspergillus fumigatus harbouring G54 mutation: Is it de novo or environmentally acquired?
inferred← citeshttps://doi.org/10.1016/j.jgar.2017.10.024openalex-snapshot
Does the use of antifungal agents in agriculture and food foster polyene resistance development? A reason for concern
inferred← citeshttps://doi.org/10.1016/j.jgar.2018.10.017openalex-snapshot
Azole-resistant Aspergillus fumigatus in the Italian environment
inferred← citeshttps://doi.org/10.1016/j.jgar.2020.01.016openalex-snapshot
Prospective multicentre study on azole resistance in Aspergillus isolates from surveillance cultures in haematological patients in Italy
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2020.123200openalex-snapshot
Increased triazole-resistance and cyp51A mutations in Aspergillus fumigatus after selection with a combination of the triazole fungicides difenoconazole and propiconazole
inferred← citeshttps://doi.org/10.1016/j.jiac.2015.04.012openalex-snapshot
First determination of azole resistance in Aspergillus fumigatus strains carrying the TR34/L98H mutations in Turkey
inferred← citeshttps://doi.org/10.1016/j.jiac.2016.01.015openalex-snapshot
Multi-azole resistant Aspergillus fumigatus harboring Cyp51A TR46/Y121F/T289A isolated in Japan
inferred← citeshttps://doi.org/10.1016/j.jiac.2016.03.002openalex-snapshot
Azole susceptibility in clinical and environmental isolates of Aspergillus fumigatus from eastern Hokkaido, Japan
inferred← citeshttps://doi.org/10.1016/j.jinf.2015.04.023openalex-snapshot
Azole-resistant aspergillosis
inferred← citeshttps://doi.org/10.1016/j.jinf.2017.06.005openalex-snapshot
Fruits as the vehicle of drug resistant pathogenic yeasts
inferred← citeshttps://doi.org/10.1016/j.medmal.2019.07.014openalex-snapshot
Azole-resistant Aspergillus fumigatus: A global phenomenon originating in the environment?
inferred← citeshttps://doi.org/10.1016/j.meegid.2020.104640openalex-snapshot
Variations in sexual fitness among natural strains of the opportunistic human fungal pathogen Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1016/j.molimm.2025.06.007openalex-snapshot
Genetics and humoral responses of the immune system to Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1016/j.nmni.2026.101738openalex-snapshot
Incidence of azole resistance among clinical isolates of Candida parapsilosis: Results from the French nationwide multicenter prospective study “ReCap” 2022-2024
inferred← citeshttps://doi.org/10.1016/j.pestbp.2020.104737openalex-snapshot
Cross-resistance to the new fungicide mefentrifluconazole in DMI-resistant fungal pathogens
inferred← citeshttps://doi.org/10.1016/j.riam.2020.03.004openalex-snapshot
Aspergillosis, poultry farming and antifungal resistance
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2018.08.247openalex-snapshot
Tebuconazole induces triazole-resistance in Aspergillus fumigatus in liquid medium and soil
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2021.147577openalex-snapshot
Acquired triazole-resistance of Aspergillus fumigatus in soil and earthworm guts exposed to propiconazole and difenoconazole at field-realistic concentrations
inferred← citeshttps://doi.org/10.1016/j.tim.2020.06.006openalex-snapshot
Missing Microbes in Bees: How Systematic Depletion of Key Symbionts Erodes Immunity
inferred← citeshttps://doi.org/10.1016/j.tim.2020.09.010openalex-snapshot
Anticipatory Stress Responses and Immune Evasion in Fungal Pathogens
inferred← citeshttps://doi.org/10.1016/j.wasman.2019.12.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/s1473-3099(16)30138-4openalex-snapshot
In-host adaptation and acquired triazole resistance in Aspergillus fumigatus: a dilemma for clinical management
inferred← citeshttps://doi.org/10.1017/s0025315415000843openalex-snapshot
Beach sand and the potential for infectious disease transmission: observations and recommendations
inferred← citeshttps://doi.org/10.1021/acs.biomac.4c00866openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.est.0c05717openalex-snapshot
Pesticide Toxicity Hazard of Agriculture: Regional and Commodity Hotspots in Australia
inferred← citeshttps://doi.org/10.1021/acs.est.4c13539openalex-snapshot
Environmental Fate of the Azole Fungicide Fluconazole and Its Persistent and Mobile Transformation Product 1,2,4-Triazole
inferred← citeshttps://doi.org/10.1021/acs.jafc.1c05396openalex-snapshot
Emergence of Triazole Resistance in Aspergillus fumigatus Exposed to Paclobutrazol
inferred← citeshttps://doi.org/10.1038/nmicrobiol.2016.92openalex-snapshot
Drug resistance in eukaryotic microorganisms
inferred← citeshttps://doi.org/10.1038/s41433-023-02719-1openalex-snapshot
Antifungal susceptibility profiles for fungal isolates from corneas and contact lenses in the United Kingdom
inferred← citeshttps://doi.org/10.1038/s41467-024-48231-2openalex-snapshot
An oxylipin signal confers protection against antifungal echinocandins in pathogenic aspergilli
inferred← citeshttps://doi.org/10.1038/s41564-024-01720-yopenalex-snapshot
Pan-drug resistance and hypervirulence in a human fungal pathogen are enabled by mutagenesis induced by mammalian body temperature
inferred← citeshttps://doi.org/10.1038/s41564-025-02055-yopenalex-snapshot
Evolution of antifungal resistance in the environment
inferred← citeshttps://doi.org/10.1038/s41579-023-00960-9openalex-snapshot
The rapid emergence of antifungal-resistant human-pathogenic fungi
inferred← citeshttps://doi.org/10.1038/s41598-024-55237-9openalex-snapshot
cyp51A mutations, protein modeling, and efflux pump gene expression reveals multifactorial complexity towards understanding Aspergillus section Nigri azole resistance mechanism
inferred← citeshttps://doi.org/10.1038/s41598-025-00187-zopenalex-snapshot
Epidemiology, antifungal susceptibility and biological characteristics of clinical Aspergillus fumigatus in a tertiary hospital
inferred← citeshttps://doi.org/10.1038/srep38833openalex-snapshot
Sensitisation of an Azole-Resistant Aspergillus fumigatus Strain containing the Cyp51A-Related Mutation by Deleting the SrbA Gene
inferred← citeshttps://doi.org/10.1038/srep42537openalex-snapshot
Multilocus sequence analyses reveal extensive diversity and multiple origins of fluconazole resistance in Candida tropicalis from tropical China
inferred← citeshttps://doi.org/10.1051/cagri/2022036openalex-snapshot
Crop protection practices and risks associated with human fungal infectious diseases: a One Health perspective
inferred← citeshttps://doi.org/10.1071/ma19024openalex-snapshot
Insights into the global emergence of antifungal drug resistance
inferred← citeshttps://doi.org/10.1073/pnas.1608304113openalex-snapshot
F901318 represents a novel class of antifungal drug that inhibits dihydroorotate dehydrogenase
inferred← citeshttps://doi.org/10.1074/jbc.ra120.012985openalex-snapshot
Targeting a critical step in fungal hexosamine biosynthesis
inferred← citeshttps://doi.org/10.1080/00275514.2018.1557796openalex-snapshot
Fungicide-driven alterations in azole-resistantAspergillus fumigatusare related to vegetable crops in Colombia, South America
inferred← citeshttps://doi.org/10.1080/09603123.2020.1810210openalex-snapshot
Algorithm to assess the presence of Aspergillus fumigatus resistant strains: The case of Norwegian sawmills
inferred← citeshttps://doi.org/10.1080/10962247.2023.2299424openalex-snapshot
Assessment of waste workers occupational risk to microbial agents and cytotoxic effects of mixed contaminants present in the air of waste truck cabin and ventilation filters
inferred← citeshttps://doi.org/10.1080/13543784.2020.1791819openalex-snapshot
Innovative therapies for invasive fungal infections in preclinical and clinical development
inferred← citeshttps://doi.org/10.1080/14656566.2021.1940134openalex-snapshot
Azole resistance in Aspergillus species: promising therapeutic options
inferred← citeshttps://doi.org/10.1080/14756366.2021.1975693openalex-snapshot
Discovery of a novel Aurora B inhibitor GSK650394 with potent anticancer and anti- aspergillus fumigatus dual efficacies in vitro
inferred← citeshttps://doi.org/10.1080/14756366.2021.1984904openalex-snapshot
Synthesis of novel pyrroles and fused pyrroles as antifungal and antibacterial agents
inferred← citeshttps://doi.org/10.1080/14786419.2024.2301741openalex-snapshot
Multifactorial action of lavender and lavandin oils against filamentous fungi
inferred← citeshttps://doi.org/10.1080/17480272.2025.2468356openalex-snapshot
A comprehensive review on azoles based organic wood preservatives and their future prospects
inferred← citeshttps://doi.org/10.1080/19338244.2018.1472545openalex-snapshot
Aspergillus prevalence in air conditioning filters from vehicles: Taxis for patient transportation, forklifts, and personal vehicles
inferred← citeshttps://doi.org/10.1080/21501203.2019.1574927openalex-snapshot
Resistance mechanism and proteins in Aspergillus species against antifungal agents
inferred← citeshttps://doi.org/10.1080/26895293.2026.2652725openalex-snapshot
Temporal dynamics of airborne fungal succession and detection of azole-resistant Aspergillus fumigatus in a poultry farm over a nine-week production cycle
inferred← citeshttps://doi.org/10.1089/biores.2016.0035openalex-snapshot
In silico Identification of Potential Peptides or Allergen Shot Candidates Against Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1089/mdr.2017.0311openalex-snapshot
Overinduction of CYP51A Gene After Exposure to Azole Antifungals Provides a First Clue to Resistance Mechanism in Fusarium solani Species Complex
inferred← citeshttps://doi.org/10.1093/cid/civ885openalex-snapshot
Azole Resistance in Aspergillus fumigatus : Can We Retain the Clinical Use of Mold-Active Antifungal Azoles?
inferred← citeshttps://doi.org/10.1093/cid/cix257openalex-snapshot
Intercountry Transfer of Triazole-Resistant Aspergillus fumigatus on Plant Bulbs
inferred← citeshttps://doi.org/10.1093/femsec/fiab093openalex-snapshot
The need for environmental surveillance to understand the ecology, epidemiology and impact of Cryptococcus infection in Africa
inferred← citeshttps://doi.org/10.1093/femsle/fnz246openalex-snapshot
Agricultural systems as potential sources of emerging human mycoses caused by Trichoderma: a successful, common phylotype of Trichoderma longibrachiatum in the frontline
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1093/g3journal/jkac075openalex-snapshot
Avian-associated Aspergillus fumigatus displays broad phylogenetic distribution, no evidence for host specificity, and multiple genotypes within epizootic events
inferred← citeshttps://doi.org/10.1093/infdis/jix210openalex-snapshot
Azole-Resistant Aspergillosis: Epidemiology, Molecular Mechanisms, and Treatment
inferred← citeshttps://doi.org/10.1093/jac/dku259openalex-snapshot
Multi-azole-resistant Aspergillus fumigatus in the environment in Tanzania
inferred← citeshttps://doi.org/10.1093/jac/dku316openalex-snapshot
Aspergillus fumigatus harbouring the sole Y121F mutation shows decreased susceptibility to voriconazole but maintained susceptibility to itraconazole and posaconazole
inferred← citeshttps://doi.org/10.1093/jac/dku410openalex-snapshot
Concomitant occurrence of itraconazole-resistant and -susceptible strains of Aspergillus fumigatus in routine cultures
inferred← citeshttps://doi.org/10.1093/jac/dku505openalex-snapshot
Specific antifungal susceptibility profiles of opportunists in the Fusarium fujikuroi complex
inferred← citeshttps://doi.org/10.1093/jac/dku566openalex-snapshot
Emergence of azole-resistant invasive aspergillosis in HSCT recipients in Germany
inferred← citeshttps://doi.org/10.1093/jac/dkv177openalex-snapshot
High prevalence of azole resistance inAspergillus fumigatusisolates from high-risk patients
inferred← citeshttps://doi.org/10.1093/jac/dkv445openalex-snapshot
Drug resistance mechanisms and their regulation in non- albicans Candida species
inferred← citeshttps://doi.org/10.1093/jac/dkw259openalex-snapshot
Azole resistance surveillance inAspergillus fumigatus: beneficial or biased?
inferred← citeshttps://doi.org/10.1093/jac/dkx354openalex-snapshot
Isavuconazole susceptibility of clinical Aspergillus fumigatus isolates and feasibility of isavuconazole dose escalation to treat isolates with elevated MICs
inferred← citeshttps://doi.org/10.1093/jac/dkz144openalex-snapshot
One year prospective survey of azole resistance in Aspergillus fumigatus at a French cystic fibrosis reference centre: prevalence and mechanisms of resistance
inferred← citeshttps://doi.org/10.1093/jac/dkz280openalex-snapshot
In vitro antifungal activity of a novel topical triazole PC945 against emerging yeast Candida auris
inferred← citeshttps://doi.org/10.1093/jac/dkz302openalex-snapshot
Anti-fungal activity of a novel triazole, PC1244, against emerging azole-resistant Aspergillus fumigatus and other species of Aspergillus
inferred← citeshttps://doi.org/10.1093/jac/dkz534openalex-snapshot
Prevalence and mechanisms of azole resistance in clinical isolates of Aspergillus section Fumigati species in a Canadian tertiary care centre, 2000 to 2013
inferred← citeshttps://doi.org/10.1093/jacamr/dlaf219openalex-snapshot
Global epidemiology of azole resistance in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1093/jambio/lxad294openalex-snapshot
Subinhibitory effects of 2,4-diacetylphloroglucinol on filamentous fungus Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1093/jpids/piad014openalex-snapshot
A Practical Guide to Antifungal Susceptibility Testing
inferred← citeshttps://doi.org/10.1093/mmy/myaa052openalex-snapshot
High detection rate of azole-resistantAspergillus fumigatusafter treatment with azole antifungal drugs among patients with chronic pulmonary aspergillosis in a single hospital setting with low azole resistance
inferred← citeshttps://doi.org/10.1093/mmy/myab074openalex-snapshot
In vitro activity of eight antifungal drugs against Chaetomiaceae
inferred← citeshttps://doi.org/10.1093/mmy/myac059openalex-snapshot
Triazole resistance in Aspergillus fumigatus isolates in Africa: a systematic review
inferred← citeshttps://doi.org/10.1093/mmy/myad089openalex-snapshot
Antifungal susceptibility patterns for Aspergillus, Scedosporium, and Exophiala isolates recovered from cystic fibrosis patients against amphotericin B, and three triazoles and their impact after long-term therapies
inferred← citeshttps://doi.org/10.1093/mmy/myae098openalex-snapshot
Prevalence of azole-resistant Aspergillus fumigatus and other aspergilli in the environment from Argentina
inferred← citeshttps://doi.org/10.1093/mmy/myaf006openalex-snapshot
Comparison of MIC Test Strip and reference broth microdilution method for amphotericin B and azoles susceptibility testing on wild-type and non-wild-type Aspergillus species
inferred← citeshttps://doi.org/10.1093/mmy/myu047openalex-snapshot
Recognizing filamentous basidiomycetes as agents of human disease: A review
inferred← citeshttps://doi.org/10.1093/mmy/myv117openalex-snapshot
Identification and functional characterization ofPenicillium marneffeipleiotropic drug resistance transportersABC1andABC2
inferred← citeshttps://doi.org/10.1093/mmy/myw005openalex-snapshot
Identification of Aspergillus fumigatus multidrug transporter genes and their potential involvement in antifungal resistance
inferred← citeshttps://doi.org/10.1093/mmy/myx056openalex-snapshot
Simulations of CYP51A from Aspergillus fumigatus in a model bilayer provide insights into triazole drug resistance
inferred← citeshttps://doi.org/10.1093/mmy/myy090openalex-snapshot
The role of occupationalAspergillusexposure in the development of diseases
inferred← citeshttps://doi.org/10.1093/ofid/ofu029openalex-snapshot
Voriconazole-Resistant Penicillium oxalicum: An Emerging Pathogen in Immunocompromised Hosts
inferred← citeshttps://doi.org/10.1094/mpmi-05-19-0123-aopenalex-snapshot
The Zymoseptoria tritici ORFeome: A Functional Genomics Community Resource
inferred← citeshttps://doi.org/10.1097/mcp.0000000000000271openalex-snapshot
Host-directed therapies for antimicrobial resistant respiratory tract infections
inferred← citeshttps://doi.org/10.1098/rstb.2015.0460openalex-snapshot
Clinical implications of globally emerging azole resistance in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1101/2020.05.26.116616openalex-snapshot
Effects of agricultural fungicide use on Aspergillus fumigatus abundance, antifungal susceptibility, and population structure
inferred← citeshttps://doi.org/10.1101/2021.06.23.449691openalex-snapshot
Multiple mechanisms impact fluconazole resistance of mutant Erg11 proteins in Candida glabrata
inferred← citeshttps://doi.org/10.1101/2021.12.12.472145openalex-snapshot
Combined Pan-, Population-, and Phylo-Genomic Analysis of Aspergillus fumigatus Reveals Population Structure and Lineage-Specific Diversity
inferred← citeshttps://doi.org/10.1101/2022.01.14.476329openalex-snapshot
Meiosis in the human pathogen Aspergillus fumigatus has the highest known number of crossovers
inferred← citeshttps://doi.org/10.1101/2024.01.15.572815openalex-snapshot
On the ecology of Acinetobacter baumannii – jet stream rider and opportunist by nature
inferred← citeshttps://doi.org/10.1111/1462-2920.13292openalex-snapshot
Emerging infections due to filamentous fungi in humans and animals: Only the tip of the iceberg?
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/1462-2920.14055openalex-snapshot
Emergence of azole resistant Aspergillus fumigatus and One Health: time to implement environmental stewardship
inferred← citeshttps://doi.org/10.1111/1462-2920.15274openalex-snapshot
Mechanisms of triazole resistance in Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1111/1758-2229.12404openalex-snapshot
Emerging infections due to filamentous fungi in humans and animals: only the tip of the iceberg?
inferred← citeshttps://doi.org/10.1111/ajt.14940openalex-snapshot
Failure of voriconazole therapy due to acquired azole resistance in Aspergillus fumigatus in a kidney transplant recipient with chronic necrotizing aspergillosis
inferred← citeshttps://doi.org/10.1111/evo.12763openalex-snapshot
Asexual sporulation facilitates adaptation: The emergence of azole resistance inAspergillus fumigatus
inferred← citeshttps://doi.org/10.1111/ina.12436openalex-snapshot
Emergence ofAspergillus fumigatusazole resistance in azole-naïve patients with chronic obstructive pulmonary disease and their homes
inferred← citeshttps://doi.org/10.1111/jam.13488openalex-snapshot
Azole-resistantAspergillus fumigatusin sawmills of Eastern France
inferred← citeshttps://doi.org/10.1111/mmi.13167openalex-snapshot
Mitochondrial dynamics in the pathogenic mold A spergillus fumigatus : therapeutic and evolutionary implications
inferred← citeshttps://doi.org/10.1111/myc.12324openalex-snapshot
Multi‐triazole‐resistant Aspergillus fumigatus infections in Australia
inferred← citeshttps://doi.org/10.1111/myc.12354openalex-snapshot
Azole‐resistant Aspergillus fumigatus isolates carrying TR 34/L98H mutations in Taiwan
inferred← citeshttps://doi.org/10.1111/myc.12417openalex-snapshot
cyp51A gene silencing using RNA interference in azole‐resistant A spergillus fumigatus
inferred← citeshttps://doi.org/10.1111/myc.12440openalex-snapshot
Diagnosis and management of aspergillosis in the Netherlands: a national survey
inferred← citeshttps://doi.org/10.1111/myc.12469openalex-snapshot
Epidemiology and molecular mechanisms of antifungal resistance in Candida and Aspergillus
inferred← citeshttps://doi.org/10.1111/myc.12494openalex-snapshot
Diversity and origins of Indian multi‐triazole resistant strains of Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1111/myc.12611openalex-snapshot
Azole resistance inCandida albicansfrom animals: Highlights on efflux pump activity and gene overexpression
inferred← citeshttps://doi.org/10.1111/myc.12717openalex-snapshot
Use of cell surface protein typing for genotyping of azole‐resistant and ‐susceptible Aspergillus fumigatus isolates in Iran
inferred← citeshttps://doi.org/10.1111/myc.12759openalex-snapshot
Surveillance for azoles resistance in Aspergillus spp. highlights a high number of amphotericin B‐resistant isolates
inferred← citeshttps://doi.org/10.1111/myc.12770openalex-snapshot
Post‐influenzal triazole‐resistant aspergillosis following allogeneic stem cell transplantation
inferred← citeshttps://doi.org/10.1111/myc.13064openalex-snapshot
First azole‐resistant Aspergillus fumigatus isolates with the environmental TR46/Y121F/T289A mutation in Iran
inferred← citeshttps://doi.org/10.1111/myc.13144openalex-snapshot
Fungi in sands of Mediterranean Sea beaches of Israel—Potential relevance to human health and well‐being
inferred← citeshttps://doi.org/10.1111/myc.13267openalex-snapshot
Isavuconazole nonwildtype Aspergillus fumigatus isolates from a global surveillance study display alterations in multiple genes involved in the ergosterol biosynthesis pathway not previously associated with resistance to other azoles
inferred← citeshttps://doi.org/10.1111/myc.13370openalex-snapshot
Genetic differences between Japan and other countries in cyp51A polymorphisms of Aspergillus fumigatus
inferred← citeshttps://doi.org/10.1111/myc.70118openalex-snapshot
Analysis of Susceptibility and Drug Resistance of Antifungal Agents in Aspergillosis and Mucormycosis Patients: A Systematic Review
inferred← citeshttps://doi.org/10.1111/nyas.13739openalex-snapshot
New pathogens, new tricks: emerging, drug‐resistant fungal pathogens and future prospects for antifungal therapeutics
inferred← citeshttps://doi.org/10.1111/ppa.14126openalex-snapshot
Epigenetic Regulation of Fungicide Resistance in Plant‐Pathogenic Fungi
inferred← citeshttps://doi.org/10.1111/vcp.12644openalex-snapshot
The current status of avian aspergillosis diagnoses: Veterinary practice to novel research avenues
inferred← citeshttps://doi.org/10.1128/aac.00127-15openalex-snapshot
First Description of Azole-Resistant Aspergillus fumigatus Due to TR 46 /Y121F/T289A Mutation in France
inferred← citeshttps://doi.org/10.1128/aac.00358-18openalex-snapshot
Molecular Identification and Susceptibility Testing of Molds Isolated in a Prospective Surveillance of Triazole Resistance in Spain (FILPOP2 Study)
inferred← citeshttps://doi.org/10.1128/aac.00543-19openalex-snapshot
New Insights into the Cyp51 Contribution to Azole Resistance in Aspergillus Section Nigri
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