The Multifunctional Fungal Ergosterol

Molecular mechanisms and functions of pyroptosis, inflammatory caspases and inflammasomes in infectious diseases

Man, S. M., Karki, R., & Kanneganti, T. (2017) · Immunological Reviews · doi:10.1111/imr.12534 · Cited by 1,684

The Fungal Cell Wall: Structure, Biosynthesis, and Function

Gow, N. A. R., Latge, J.-P., & Munro, C. A. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0035-2016 · Cited by 1,423

Vesicular Polysaccharide Export in Cryptococcus neoformans Is a Eukaryotic Solution to the Problem of Fungal Trans-Cell Wall Transport

Rodrigues, M. L., Nimrichter, L., Oliveira, D. L., Frasés, S., de Miranda, K. R., Zaragoza, Ó., Alvarez, M., Nakouzi, A. S., Feldmesser, M., & Casadevall, A. (2006) · Eukaryotic Cell · doi:10.1128/ec.00318-06 · Cited by 495

Compositional and immunobiological analyses of extracellular vesicles released by Candida albicans

Vargas, G., Rocha, J., Oliveira, D. L., Albuquerque, P., Frases, S., Santos, S. S., Nosanchuk, J., Gomes, A. M. O., Medeiros, L., Miranda, K., et al. (2015) · Cellular Microbiology · doi:10.1111/cmi.12374 · Cited by 274

Concerted Activation of the AIM2 and NLRP3 Inflammasomes Orchestrates Host Protection against Aspergillus Infection

Karki, R., Man, S. M., Malireddi, R. K. S., Gurung, P., Vogel, P., Lamkanfi, M., & Kanneganti, T.-D. (2015) · Cell Host & Microbe · doi:10.1016/j.chom.2015.01.006 · Cited by 272

Global analysis of fungal morphology exposes mechanisms of host cell escape

O’Meara, T. R., Veri, A. O., Ketela, T., Jiang, B., Roemer, T., & Cowen, L. E. (2015) · Nature Communications · doi:10.1038/ncomms7741 · Cited by 243

Candida albicans Triggers NLRP3-Mediated Pyroptosis in Macrophages

Wellington, M., Koselny, K., Sutterwala, F. S., & Krysan, D. J. (2014) · Eukaryotic Cell · doi:10.1128/ec.00336-13 · Cited by 227

Role of Candida albicans Transcription Factor Upc2p in Drug Resistance and Sterol Metabolism

Silver, P. M., Oliver, B. G., & White, T. C. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.6.1391-1397.2004 · Cited by 216

Overexpression or Deletion of Ergosterol Biosynthesis Genes Alters Doubling Time, Response to Stress Agents, and Drug Susceptibility in Saccharomyces cerevisiae

Bhattacharya, S., Esquivel, B. D., & White, T. C. (2018) · mBio · doi:10.1128/mbio.01291-18 · Cited by 210

Plasma membrane lipids and their role in fungal virulence

Rella, A., Farnoud, A. M., & Poeta, M. D. (2015) · Progress in Lipid Research · doi:10.1016/j.plipres.2015.11.003 · Cited by 150

Multi-target antifungal action of engineered binuclear zinc cluster peptides against Aspergillus flavus: Integrating membrane disruption, transcriptional interference, and metabolic dysregulation

Han, Z., Kong, Q., & Xu, J. (2025) · Food Research International · doi:10.1016/j.foodres.2025.117254 · Cited by 2

Screening and Synthesis of Tetrazole Derivatives that Inhibit the Growth of Cryptococcus Species

Nakada, N., Miyazaki, T., Mizuta, S., Hirayama, T., Nakamichi, S., Takeda, K., Mukae, H., Kohno, S., & Tanaka, Y. (2023) · ChemMedChem · doi:10.1002/cmdc.202300157 · Cited by 2

The epidemic of ‘Black fungus’ (mucormycosis) in Covid19 patients in India - a perfect synergy between immuno-suppressive drugs and supportive oxygen that promotes the bio-syntheses of ergosterol (a key component of fungal cell membranes)?Preprint

Chakraborty, S. (2021) · doi:10.31219/osf.io/pbnwy · Cited by 2

LAMinar Flow: Sterol Transport in a Pathogenic Yeast

Choy, H. L., Gaylord, E. A., & Doering, T. L. (2024) · Contact · doi:10.1177/25152564241237625 · Cited by 2

A Computational Study of a Prebiotic Synthesis of Ergosterol, Ergocalciferol & Cholecalciferol (Vitamin D2 and D3)

Aylward, N. (2023) · WSEAS TRANSACTIONS ON BIOLOGY AND BIOMEDICINE · doi:10.37394/23208.2023.20.6 · Cited by 1

Fusariotoxins Concentration in Common Wheat Grain Depending on the Farming System (Organic vs. Integrated vs. Conventional) and Changes During Grain Processing

Wysocka, K., Cacak‐Pietrzak, G., Buśko, M., & Studnıckı, M. (2024) · Agronomy · doi:10.3390/agronomy14112535 · Cited by 1

Potential of liquid smoke derived from sawn waste to control coffee rust disease (Hemileia vastatrix)

Utomo, D. Z., Karliati, T., Rumidatul, A., Pari, G., Dawmawan, S., & Hadiyane, A. (2025) · AIP conference proceedings · doi:10.1063/5.0241657 · Cited by 1

Nanopore sequencing and hybrid assembly: unraveling the genomic landscape of dollar spot with enhanced annotation and drug resistance profiling

Shi, X., Zhao, S., Gibbons, J. G., & Jung, G. (2025) · Frontiers in Fungal Biology · doi:10.3389/ffunb.2025.1621663 · Cited by 1

Thiosemicarbazones and thiazoles antifungal activity against Sporothrix and first Sporothrix mexicana from human sporotrichosis in Brazil

de Souza, M. V., de Sousa, B. R., Ferraz, C., da Silva, C. M., da Silva, E. T. N., Moraes, A. D. T. D. O., Melo, V., Souza, E., Hernandes, M. Z., Pereira, V. R. A., et al. (2025) · Future Microbiology · doi:10.1080/17460913.2025.2571354 · Cited by 1

Ergosterol Regulation of Plant Physiology; An Underlooked Perspective

Tyagi, M., Paul, P. K., & Rameshwari, R. (2025) · The Botanical Review · doi:10.1007/s12229-025-09321-y · Cited by 1

Visualization studies of the anti-tumor mechanism of fluorescently labeled ergosterol

Liang, H., Bao, H., Tu, Q., Zhao, J., & Huo, H. (2025) · Bioorganic Chemistry · doi:10.1016/j.bioorg.2025.109227 · Cited by 1

Cytochrome b5-Like Protein VdPBP1 Mediates Electron Transfer in Ergosterol Pathway to Confer Terbinafine Resistance of Verticillium dahliae

Li, H., Zhang, C.-N., Wang, Y.-H., Sheng, R., Liu, Y., Zhang, D.-D., Short, D. P. G., Subbarao, K. V., Chen, F., & Chen, J. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.5c17070 · Cited by 1

Biochemical mechanisms of layered double hydroxide mediated azole fungicide delivery for crop protection

Ahmed, N., & Chen, Z. (2026) · Pesticide Biochemistry and Physiology · doi:10.1016/j.pestbp.2026.107237 · Cited by 1

Exploring the Botany, Traditional Uses, Phytochemical Profile, and Pharmacological Effects of Coldenia procumbens L., Boraginaceae

Chen, T. V., Boonma, T., Hieu, N. T., LAM, D. N. X., & Hiền, N. T. T. (2024) · Natural Product Communications · doi:10.1177/1934578x241287130 · Cited by 1

Comparative Study of Candida albicans Strains from Clinical and Environmental Sources in Iran

Fatahinia, M., Molavinia, S., Seyyedian, S., & Amirrajab, N. (2025) · Archives of Clinical Infectious Diseases · doi:10.5812/archcid-143312 · Cited by 1

Characterization and Expression Analysis of the Sterol C-5 Desaturase Gene PcERG3 in the Mycobiont of the Lichen Peltigera canina Under Abiotic Stresses

Swid, M. A., Koulintchenko, M. V., Onele, A. O., Leksin, I. Y., Rakhmatullina, D. F., Galeeva, E. I., Valitova, Y. N., Minibayeva, F. V., & BECKETT, R. P. (2025) · Microbiology Research · doi:10.3390/microbiolres16070139 · Cited by 1

Rapid detection of airborne fungal contamination using a molecularly imprinted polymer approach for ergosterol

Choi, E., Kim, J.-H., Na, Y., Lee, B. G., Yeo, M., & Kim, E. (2026) · Scientific Reports · doi:10.1038/s41598-026-47624-1 · Cited by 1

Comparison of cationic beta-glucans with antifungal properties — Correlation between chemical structure and biological activity

Skóra, M., Tymecka, M., Ciszek‐Lenda, M., Musielak, B., Klocek, N., Stączek, S., Zdybicka‐Barabas, A., Cytryńska, M., & Kamiński, K. (2026) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2026.152888 · Cited by 1

The Novel Postpartum Herbal Drugs: An in Silico Approach of Bakumpai Dayak Tribe Traditional Medicinal Plants

Latifah, N., & Sardimi (2019) · IOP Conference Series Earth and Environmental Science · doi:10.1088/1755-1315/276/1/012049 · Cited by 1

The dual role of SrbA from Paracoccidioides lutzii: a hypoxic regulator

de Sousa, L. O., Oliveira, L. N., Naves, R. B., Pereira, A. L. A., Silva, K. S. F. E., Soares, C. M. D. A., & Lima, P. D. S. (2021) · Brazilian Journal of Microbiology · doi:10.1007/s42770-021-00527-x · Cited by 1

Membrane Composition Modulates Vp54 Binding: A Combined Experimental and Computational Study

Guo, W., Dong, R., Okedigba, A. O., Sanchez, J. E., Agarkova, I. V., Abisamra, E.-M., Jelinsky, A., Riekhof, W. R., Noor, L., Dunigan, D. D., et al. (2025) · Pathogens · doi:10.3390/pathogens14101000 · Cited by 1

Systematic Investigation of Ergosterol Fermentation by Kluyveromyces marxianus Y.00243 via Statistical Design

Vidra, A., Kaleta, Z., & Németh, Á. (2021) · Periodica Polytechnica Chemical Engineering · doi:10.3311/ppch.18202 · Cited by 1

Ergosterols with rare peroxide, oxetane ring moiety, and a lactone ring from Aspergillus spectabilis and their immunosuppressive activities

Wei, M., Liao, H., Li, Q., Deng, X., Gao, C., Ding, N., Sun, W., Zhu, H., Guo, J., Chen, C., et al. (2024) · Phytochemistry · doi:10.1016/j.phytochem.2024.114070 · Cited by 1

Investigation of Clinically Relevant Fluconazole Resistance Mechanisms in the Fungal Pathogen Candida parapsilosis

Doorley, L. A. (2023) · doi:10.21007/etd.cghs.2023.0620 · Cited by 1

Molecular Docking of Compounds from Clitoria ternatea as Candidate Anti-fungal Agents against Candida albicansPreprint

Auerkari, E. I., Arifaputri, N. R., & Auerkari, P. (2023) · Preprints.org · doi:10.20944/preprints202311.1539.v1 · Cited by 1

Method Development for Comprehensive Lipidome Profiling of Cells using LC-MS

Bajwa, B. (2021) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3-d7jk-gr22

Sensibilidad y resistencia a fungicidas de Cercospora kikuchii, agente causal del tizón de la hoja y mancha púrpura de la semilla de la soja

Sautua, F. J. (2021) · El Servicio de Difusión de la Creación Intelectual (National University of La Plata) · doi:10.35537/10915/127606 · Cited by 1

Fungal Infections in the ICU

Molyneaux, I., & Bose, S. (2020) · Springer eBooks · doi:10.1007/978-981-15-4039-4_23

Investigation and comparison of virulence factors (hydrophobicity, biofilm formation, ergosterol content, secretory enzymes) in Iranian clinical and environmental Candida albicans strainsPreprint

Fatahinia, M., Molavinia, S., Seyedian, S. S., & Amirrajab, N. (2023) · Research Square · doi:10.21203/rs.3.rs-2670159/v1

Anti-neuroinflammatory effects of auricularia polytricha extracts on bisphenol a (BPA)-induced microglial cell activation and reduction of hippocampal cell damage

Sillapachaiyaporn, C. (2022) · doi:10.58837/chula.the.2022.82

Unveiling the role of sulfur nanoparticles as an anti-dermatomycotic agent against Pichia kudriavzeviiPreprint

Biswas, M. C., Mukherjee, K., Sarkar, J., Ray, R., & Acharya, K. (2023) · Research Square · doi:10.21203/rs.3.rs-3615679/v1

Uji Ekstrak Metanol Biji Kembang Telang (Clitoria ternatea L.) dalam Menghambat Pertumbuhan Koloni serta Produksi dan Perkecambahan Konidia Jamur Fusarium oxysporum f. sp. cepae

Suganda, T., Kaltsum, R. T., Tripuspasari, L., & Yulia, E. (2024) · Jurnal Agribisnis dan Agrowisata (Journal of Agribusiness and Agritourism) · doi:10.24198/agrikultura.v35i1.53887

Exploring the interaction between Fe 3+ and REGLE motif of the high-affinity iron permease (Ftr1): an in silico approachPreprint

Choudhury, A. R., & Murali, A. (2024) · doi:10.22541/au.171785830.00888612/v1

Investigation of antifungal mechanism of hinokitiol against Botrytis cinerea using gene expression analysis

Benyakart, N., Umehara, H., Keerthana, K. H., Vanitha, T., & Shiina, T. (2024) · Acta Horticulturae · doi:10.17660/actahortic.2024.1396.13

Influence of the agrochemical benomyl on Cryptococcus gattii-plant interaction in vitro and in vivo

Dornelas, J. C. M., Paixão, V. M., do Carmo, P. H. F., da Costa, M. C., Gomes, E. C. Q., de Resende, M. A., & Santos, D. A. (2024) · Brazilian Journal of Microbiology · doi:10.1007/s42770-024-01440-9

Forest macrofungi as novel sources of antioxidant

Alkafaas, S. S., Bornman, C., Elsalahaty, M. I., Elkafas, S. S., Abdelmoaty, B. E., Elshashy, A. B., Ezzat, S. M., & Ghosh, S. B. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-18870-1.00018-4

Antifungal Activity of Crude Extract from the Seeds of Inga laurina (Fabaceae)

Moroto, B. S., Sardi, J. D. C. O., Cardoso, T. F. M., Jacobowski, A. C., & Macedo, M. L. R. (2023) · Current Trends in Biotechnology and Pharmacy · doi:10.5530/ctbp.2023.3.40

Use of Omics Tools Toward the Discovery of Fungal Enzymes and Secondary Metabolites

Kungwani, N. A., Dani, S., & Sharma, G. (2024) · Wiley eBooks · doi:10.1002/9783527844340.ch16

Exploring the interaction between Fe3+ and REGLE motif of the high-affinity iron permease (Ftr1): An in silico approach

Choudhury, A. R., & Murali, A. (2024) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2024.108907

Role of Membrane Permeabilization and Ergosterol Content in the Inhibitory Activity of Membrane-Targeting Antimicrobials

Villacres, J. I. (2024) · doi:10.22215/etd/2024-16199

Computational prediction of Homo sapiens–Candida albicans protein–protein interactions reveal key virulence factors using dual RNA-Seq data analysis

Kaur, E., & Acharya, V. (2025) · Archives of Microbiology · doi:10.1007/s00203-025-04312-4

Reactions and synthetic applications of ergosterol

Liang, Z., & Gui, J. (2025) · Scientia Sinica Chimica · doi:10.1360/ssc-2025-0067

Co-culture with Lactobacillus plantarum SC-1 facilitates ergosterol synthesis in Monascus purpureus through MpSet1-affected H3K4ac establishment

Wu, Z., & Liu, Z. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1603805

Disruption of CmHmgr1 triggers apoptosis and causes defects in growth, conidiogenesis, and mycoparasitism of Coniothyrium minitans

Yang, X., Wang, H., Zhang, L., Zhang, Z., Hu, Z., Jiāng, D., & Fù, Y. (2025) · Virulence · doi:10.1080/21505594.2025.2523884

Tioconazole exerts anti-TB activity by destroying cell integrity

Chen, Z., Wang, X., Zhang, H., Kong, X., Chen, J., Wang, Q., Meng, J., & Lu, S. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.178102

Advances in Fungal Infection Research: From Novel Diagnostics to Innovative Therapeutics

Rodrigues, C. F., & Černáková, L. (2025) · Journal of Fungi · doi:10.3390/jof11100693 · Cited by 1

Antifungal Activity and Mechanism of the Novel Antimicrobial Peptide Jelleine-Ic Against Candida albicans

Wang, L., Li, K., Zhu, J., Ding, K., Tao, X., Xu, X., & Zhu, Y. (2025) · Current Microbiology · doi:10.1007/s00284-025-04551-0

Seasonal drought surpasses the effects of irrigation regime in the microbial dynamics of grapevine rhizosphere and presents high impact in mycobiomePreprint

Maciel, S. L., Califano, G., Zarrouk, O., Lopes, V., Pina‐Martins, F., Damásio, M., Silvestre, J., Couto, F. M., Gaspar, H., Conde, J. P., et al. (2025) · Research Square · doi:10.21203/rs.3.rs-7800383/v1

Antifungal activity and mechanism of Xanthohumol against tomato gray Mold

Tian, T., Song, J., Lv, J., Wang, J., Li, Z., & Zhang, N. (2026) · Pest Management Science · doi:10.1002/ps.70560

OPTIMISATION AND VALIDATION OF AN HPLC-DAD METHOD FOR ANALYSIS OF ERGOSTEROL AND ERGOCALCIFEROL IN EDIBLE MUSHROOMS EXPOSED TO UV-B RADIATION

Grófová, M., Silvia, J., Veronika, C., Golian, J., & Árvay, J. (2025) · Journal of Microbiology Biotechnology and Food Sciences · doi:10.55251/jmbfs.12599

Sunshine in a Cell: Biosynthetic Battles Against Vitamin D Deficiency

Zhang, B. (2026) · Scholarly review . · doi:10.70121/001c.154953

Alternative Splicing Analysis Revealed That the Transcription Factor PacC Shapes the Virulence of the Dermatophyte Trichophyton interdigitale

Azevedo, M. I. G., Neves-da-Rocha, J., Sanches, P. R., Oliveira, V. M., Martinez-Rossi, N. M., & Rossi, A. (2026) · International Journal of Molecular Sciences · doi:10.3390/ijms27062634

The VdAP-2 Complex β, μ, and σ Subunits Regulate Polar Growth, Ergosterol Metabolism, and Virulence in Verticillium dahliaePreprint

Wang, Y.-H., Xie, L.-L., Zhang, C.-N., Sheng, R., Li, H., & Chen, F. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.6469741

Para-dichlorobenzene inhibits Fusarium oxysporum f. sp. cubense tropical race 4 by inducing membrane damage, mitochondrial dysfunction, and transcriptional reprogramming

Huang, S., Amenyogbe, M. K., Li, Q. L., Zhang, Y., Chen, X., Guo, T., Tang, L., Xie, H., & Jiang, Z. (2026) · BMC Microbiology · doi:10.1186/s12866-026-04979-9

Discovery of tRNA-dependent ergosterol aminoacylation in fungi

Yakobov, N. (2020) · theses.fr (ABES) · doi:10.70675/54f07229z7a9bz4a0fz8263z43817d7f7c3c

Protease‐Mediated Dual Action Against Rice Blast: Suppression of Magnaporthe oryzae Ergosterol Biosynthesis Pathway and Enhancement of Rice Disease Resistance by Bacillus amyloliquefaciens SN16‐1

He, X., Shen, C., Cheng, Q., Zhang, H., Liu, X., & Wang, W. (2026) · Plant Cell & Environment · doi:10.1111/pce.70582

Biological activity and chemical characterization of Gracilaria caudata J. Agardh (Gracilariaceae) extracts

Nascimento, F. C., Correia, A. D. J., Aquino, V. M. S., Jesus, L. R. D., Santos, G. D. N., & Vale, V. (2026) · Scientia Plena · doi:10.14808/sci.plena.2026.044602

Synthesis and biological evaluation of new ergosterol pyridine derivatives as potential anticancer agents

Liang, J.-J., Chen, X.-F., Liu, X.-J., Wang, C., Wang, J.-H., Yu, S., Chang, X., Chen, H., & Deng, Z. (2026) · Steroids · doi:10.1016/j.steroids.2026.109800

Sesame Oil in the Management of Fungal Infections: From Traditional Remedy to Modern Drug Delivery

Kumari, P., Jawla, D. S., Rohilla, S., Rawal, N., Kundu, L., & Sharma, R. R. (2026) · International Journal of Drug Delivery Technology · doi:10.25258/ijddt.16.32s.71

The VdAP-2 Complex β, μ, and σ Subunits Regulate Polar Growth, Ergosterol Metabolism, and Virulence in Verticillium dahliaePreprint

Wang, Y.-H. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.6850545

Computational identification of inhibitors from Aegle marmelos leaf extract targeting ergosterol biosynthesis ERG4/ERG24 enzyme and serine proteases for combatting mancozeb-resistant Fusarium

Alam, S. A., Chakraborty, S., Baindara, P., & Mandal, S. M. (2026) · Antonie van Leeuwenhoek · doi:10.1007/s10482-026-02354-2

Metabolite profiling and enhanced antimicrobial and nematicidal activities of zinc oxide nanoparticle-biofortified Pleurotus mushrooms

Leema, Garg, S., Punetha, H., Sharma, S., Thakur, S., & Gupta, D. (2026) · Scientific Reports · doi:10.1038/s41598-026-59270-8

Antifungal effects of carvacrol on Penicillium verrucosum growth in refrigerated wet noodles

Li, H., Wang, Y.-Y., Lv, Y., Zhai, H.-C., Hu, Y., Wang, F.-Z., Huang, L., & Zhang, S.-B. (2026) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2026.111978

Comparative Transcriptomic Analysis Reveals Cultivar-Dependent Resistance Responses to Pseudomonas tolaasii in Pleurotus ostreatus

Kim, J. Y., Lee, K.-H., Han, G.-S., An, G.-H., Jo, S.-Y., & Park, H.-S. (2026) · Journal of Fungi · doi:10.3390/jof12070525

Potential Role of Po-milR-1 and Its Target Po-3KAT in the Growth, Development and Stress Response of Pleurotus ostreatus

Li, Y., Xu, D., & Ma, A. (2026) · Microbiology Research · doi:10.3390/microbiolres17080163

Herbicolin A, an antifungal lipopeptide produced by Pantoea agglomerans APC 4211 is a promising biocontrol agent against food spoilage fungi

Kamilari, E., O’Connor, P. M., Reen, F. J., Das, P., Deliephan, A., Hill, D., Fursenko, O., Weise, J., Moore, A. S. N., Hill, C., et al. (2026) · International Journal of Food Microbiology · doi:10.1016/j.ijfoodmicro.2026.112014

Recognition of exogenous lipids in plant immunity

Kato, H. (2026) · Journal of Experimental Botany · doi:10.1093/jxb/erag418

Berberine as a Promising Antifungal Agent: Insights into Molecular Mechanisms and Therapeutic Potential

He, J., Wang, Q., Sun, B., Velkov, T., Shen, J., Jiang, H., & Dai, C. (2026) · ACS Omega · doi:10.1021/acsomega.6c05321

Antifungal Resistance and Development of Fungicidal Agents

Rahate, K., Dalvi, A., Chakraborty, S., & Idicula‐Thomas, S. (2026) · Springer eBooks · doi:10.1007/978-981-95-2300-9_32-1

Anti-psychotic drugs act synergistically in combination with antifungal drugs to inhibit drug-resistant Cryptococcus neoformans and Candida albicans

Ayala, M., Jakamartana, A., Costa, R. M. D. S., Cheung, E. C.-K., Bednarek, J. M., Moreau, C. T., & Brown, J. C. S. (2026) · mSphere · doi:10.1128/msphere.00432-26

Proteomic and Functional Profiling of Trichoderma reesei , Pichia guilliermondii , and Hericium erinaceus

Ahmed, T., Juhász, A., Bose, U., Terefe, N. S., Chan, L. Y., Craik, D. J., & Colgrave, M. L. (2026) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.6c09785

The transcription factor CsAtf1 regulates CsErg5B to modulate conidial germination and fludioxonil sensitivity in Colletotrichum siamense

Lin, Y., Wang, K., Guan, X., Song, M., Han, Z., Liu, W., Wu, W., Zhang, Y., Miao, W., & Lin, C. (2026) · Phytopathology Research · doi:10.1186/s42483-026-00465-2

Experimental and Monte Carlo Insights into the Biofilm Control of Klebsiella pneumoniae Using Green-Synthesized Ag/Ni(OH)2/Clove Nanocomposites

Aziz, S. A. A. A., Mahgoub, S. M., Rahim, M. M. A., Mohamed, E. A., Alfassam, H. E., Ahmed, F. M., Maodaa, S. N., Rouby, S. R., Osman, G. S. I., Alatawi, A., et al. (2026) · Nanomaterials · doi:10.3390/nano16191202

Temperature-Dependent Conversion of Wheat Straw by Ganoderma lucidum: A Chemical and Multi-Omics Analysis

Zhang, J., Liang, X., & Mao, L. (2026) · Journal of Fungi · doi:10.3390/jof12100730

Seed treatment of dent and sweet corn with alginate nanoemulsions of lemongrass essential oil against Fusarium graminearum and Pythium sylvaticum

Zacharias, M. B., Morais, P. I. C., Williams, J., Mayfield, D. A., Nakkirt, P., & Munkvold, G. P. (2026) · Scientific Reports · doi:10.1038/s41598-026-73156-9

Comparative antifungal activity of three essential oils against mycotoxigenic Fusarium graminearum and multi-omics analysis

Cheng, Y., Yu, H., Wang, L., Tu, G., Muhammad, S. M., Gong, X., Lei, X., Dong, J., Fan, X., & Wang, S. (2026) · Food Chemistry · doi:10.1016/j.foodchem.2026.151503

Ergosterol-modified silica enables physicochemical screening of sterol-associated metabolites from actinomycetes

Nakashima, T., Izuta, S., Kosaka, S., & Matsuo, H. (2026) · Journal of Bioscience and Bioengineering · doi:10.1016/j.jbiosc.2026.09.008

Luliconazole disrupts Fusarium ergosterol synthesis by dually blocking transcription and enzyme activity

Wang, H., Zhang, G., Chen, Q., Che, Z., Ma, Y., Hu, S., Qian, J., Xu, X., Chen, Y., Liu, Z., et al. (2026) · Advanced Agrochem · doi:10.1016/j.aac.2026.10.015

Genetics and Molecular Biology of the Genes Functioning Late in the Sterol Biosynthetic Pathway of Saccharomyces

Lees, N. D., Arthington, B. A., & Bard, M. (1992) · ACS symposium series · doi:10.1021/bk-1992-0497.ch019 · Cited by 2

Ergosterol biosynthesis in Aspergillus fumigatus: its relevance as an antifungal target and role in antifungal drug resistance

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