Fungal toxins and host immune responses

Hidden Killers: Human Fungal Infections

Brown, G. D., Denning, D. W., Gow, N. A. R., Levitz, S. M., Netea, M. G., & White, T. C. (2012) · Science Translational Medicine · doi:10.1126/scitranslmed.3004404 · Cited by 4,284 · see citing works

Cyclooxygenases: Structural, cellular, and molecular biology

Smith, W. L., DeWitt, D. L., & Garavito, R. M. (2000) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.69.1.145 · Cited by 2,925 · see citing works

Activation and regulation of the inflammasomes

Latz, E., Xiao, T. S., & Stutz, A. (2013) · Nature Reviews Immunology · doi:10.1038/nri3452 · Cited by 2,884 · see citing works

CYCLOOXYGENASES 1 AND 2

Vane, J. R., Bakhle, Y. S., & Botting, R. M. (1998) · The Annual Review of Pharmacology and Toxicology · doi:10.1146/annurev.pharmtox.38.1.97 · Cited by 2,737 · see citing works

Molecular Mechanisms That Influence the Macrophage M1–M2 Polarization Balance

Wang, N., Liang, H., & Zen, K. (2014) · Frontiers in Immunology · doi:10.3389/fimmu.2014.00614 · Cited by 1,997 · see citing works

Worldwide contamination of food-crops with mycotoxins: Validity of the widely cited ‘FAO estimate’ of 25%

Eskola, M. K., Kos, G., Elliott, C. T., Hajšlová, J., Mayar, S., & Krska, R. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2019.1658570 · Cited by 1,484 · see citing works

Occurrence, Toxicity, and Analysis of Major Mycotoxins in Food

Alshannaq, A. F., & Yu, J. (2017) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph14060632 · Cited by 1,273 · see citing works

Candidalysin is a fungal peptide toxin critical for mucosal infection

Moyes, D. L., Wilson, D., Richardson, J. P., Mogavero, S., Tang, S. X., Wernecke, J., Hoefs, S., Gratacap, R. L., Robbins, J., Runglall, M., et al. (2016) · Nature · doi:10.1038/nature17625 · Cited by 928 · see citing works

Ochratoxin A, a Toxic Metabolite produced by Aspergillus ochraceus Wilh.

van der Merwe, K. J., STEYN, P. S., FOURIE, L., Scott, D. B., & Theron, J. (1965) · Nature · doi:10.1038/2051112a0 · Cited by 843 · see citing works

Masked mycotoxins: A review

Berthiller, F., Crews, C., Dall’Asta, C., Saeger, S. D., Haesaert, G., Karlovský, P., Oswald, I. P., Seefelder, W., Speijers, G. J. A., & Stroka, J. (2012) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201100764 · Cited by 802 · see citing works

The role of nitric oxide in innate immunity

Bogdan, C., Röllinghoff, M., & Diefenbach, A. (2000) · Immunological Reviews · doi:10.1034/j.1600-065x.2000.917307.x · Cited by 665 · see citing works

Biosynthesis and Toxicological Effects of Patulin

Puel, O., Galtier, P., & Oswald, I. P. (2010) · Toxins · doi:10.3390/toxins2040613 · Cited by 576 · see citing works

Chronic and Acute Toxicities of Aflatoxins: Mechanisms of Action

Benkerroum, N. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17020423 · Cited by 571 · see citing works

Trichothecenes: From Simple to Complex Mycotoxins

McCormick, S. P., Stanley, A. M., Stover, N. A., & Alexander, N. J. (2011) · Toxins · doi:10.3390/toxins3070802 · Cited by 534 · see citing works

Acute and chronic effects of aflatoxin on the liver of domestic and laboratory animals: a review.

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Dietary aflatoxin exposure and impaired growth in young children from Benin and Togo: cross sectional study

Gong, Y. Y., Cardwell, K., Hounsa, A., Egal, S., Turner, P. C., Hall, A. J., & Wild, C. P. (2002) · BMJ · doi:10.1136/bmj.325.7354.20 · Cited by 502 · see citing works

Ochratoxin A production by strains of Aspergillus niger var. niger

Abarca, M. L., Bragulat, M. R., Castellá, G., & Cabañes, F. J. (1994) · Applied and Environmental Microbiology · doi:10.1128/aem.60.7.2650-2652.1994 · Cited by 446 · see citing works

MAPK, MKP1 and c-Fos Discriminate Candida albicans Yeast from Hyphae in Epithelial Cells

Moyes, D., Runglall, M., Murciano, C., Shen, C., Nayar, D., Thavaraj, S., Kohli, A., Islam, A., Mora-Montes, H., Challacombe, S., et al. (2010) · Cell Host and Microbe · doi:10.1016/j.chom.2010.08.002 · Cited by 347 · see citing works

The immunosuppressive fungal metabolite gliotoxin specifically inhibits transcription factor NF-kappaB.

Pahl, H. L., Krauss, B., Schulze‐Osthoff, K., Decker, T., Traenckner, E. B.-M., Vogt, M., Myers, C., Parks, T., Warring, P., Mühlbacher, A., et al. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.183.4.1829 · Cited by 334 · see citing works

NF-κB Activation Is a Critical Regulator of Human Granulocyte Apoptosis in Vitro

Ward, C., Chilvers, E. R., Lawson, M. F., Pryde, J. G., Fujihara, S., Farrow, S. N., Haslett, C., & Rossi, A. G. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.7.4309 · Cited by 320 · see citing works

Dietary aflatoxins and liver cancer – a population based study in Kenya

Peers, F. G., & Linsell, C. A. (1973) · British Journal of Cancer · doi:10.1038/bjc.1973.60 · Cited by 302 · see citing works

The fungal peptide toxin Candidalysin activates the NLRP3 inflammasome and causes cytolysis in mononuclear phagocytes

Kasper, L., König, A., Koenig, P.-A., Gresnigt, M. S., Westman, J., Drummond, R. A., Lionakis, M. S., Groß, O., Ruland, J., Naglik, J. R., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06607-1 · Cited by 297 · see citing works

Aflatoxins: Producing-Molds, Structure, Health Issues and Incidence in Southeast Asian and Sub-Saharan African Countries

Benkerroum, N. (2020) · International Journal of Environmental Research and Public Health · doi:10.3390/ijerph17041215 · Cited by 289 · see citing works

Ochratoxin Production by the Aspergillus ochraceus Group and Aspergillus alliaceus

Bayman, P., Baker, J. L., Doster, M. A., Michailides, T. J., & Mahoney, N. E. (2002) · Applied and Environmental Microbiology · doi:10.1128/aem.68.5.2326-2329.2002 · Cited by 285 · see citing works

Apoptosis Induction by the Satratoxins and Other Trichothecene Mycotoxins: Relationship to ERK, p38 MAPK, and SAPK/JNK Activation

Yang, G.-H., Jarvis, B. B., Chung, Y.-J., & Pestka, J. J. (2000) · Toxicology and Applied Pharmacology · doi:10.1006/taap.1999.8888 · Cited by 284 · see citing works

LaeA, a Regulator of Morphogenetic Fungal Virulence Factors

Bok, J. W., Balajee, S. A., Marr, K. A., Andes, D., Nielsen, K. F., Frisvad, J. C., & Keller, N. P. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.9.1574-1582.2005 · Cited by 283 · see citing works

Comparative study of cytotoxicity and oxidative stress induced by deoxynivalenol, zearalenone or fumonisin B1 in human intestinal cell line Caco-2

Kouadio, J. H., Mobio, T. A., Baudrimont, I., Moukha, S., Dano, S. D., & Creppy, E. E. (2005) · Toxicology · doi:10.1016/j.tox.2005.05.010 · Cited by 272 · see citing works

The Phylogenetics of Mycotoxin and Sclerotium Production in Aspergillus flavus and Aspergillus oryzae

Geiser, D. M., Dorner, J. W., Horn, B. W., & Taylor, J. W. (2000) · Fungal Genetics and Biology · doi:10.1006/fgbi.2000.1215 · Cited by 258 · see citing works

Aflatoxin B1 albumin adduct levels and cellular immune status in Ghanaians

Jiang, Y., Jolly, P. E., Ellis, W. O., Wang, J.-S., Phillips, T. D., & Williams, J. H. (2005) · International Immunology · doi:10.1093/intimm/dxh262 · Cited by 256 · see citing works

Cytotoxicity, inhibition of DNA and protein syntheses and oxidative damage in cultured cells exposed to zearalenone

Abid‐Essefi, S., Ouanes, Z., Hassen, W., Baudrimont, I., Creppy, E. E., & Bacha, H. (2004) · Toxicology in Vitro · doi:10.1016/j.tiv.2003.12.011 · Cited by 249 · see citing works

Gliotoxin Is a Virulence Factor of <i>Aspergillus fumigatus</i> : <i>gliP</i> Deletion Attenuates Virulence in Mice Immunosuppressed with Hydrocortisone

Sugui, J. A., Pardo, J., Chang, Y. C., Zarember, K. A., Nardone, G., Galvez, E. M., Müllbacher, A., Gallin, J. I., Simon, M. M., & Kwon-Chung, K. J. (2007) · Eukaryotic Cell · doi:10.1128/ec.00141-07 · Cited by 242 · see citing works

Two different polyketide synthase genes are required for synthesis of zearalenone in Gibberella zeae

Kim, Y., Lee, Y., Jin, J., Han, K., Kim, H., Kim, J., Lee, T., Yun, S., & Lee, Y. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04884.x · Cited by 239 · see citing works

Deoxynivalenol Impairs Porcine Intestinal Barrier Function and Decreases the Protein Expression of Claudin-4 through a Mitogen-Activated Protein Kinase-Dependent Mechanism ,

Pinton, P., Braicu, C., Nougayrède, J., Laffitte, J., Țăranu, I., & Oswald, I. P. (2010) · Journal of Nutrition · doi:10.3945/jn.110.123919 · Cited by 237 · see citing works

Mycotoxins in Crude Building Materials from Water-Damaged Buildings

Tuomi, T., Reijula, K. E., Johnsson, T., Hemminki, K., Hintikka, E., Lindroos, O., Kalso, S., Koukila-Kähkölä, P., Mussalo‐Rauhamaa, H., & Haahtela, T. (2000) · Applied and Environmental Microbiology · doi:10.1128/aem.66.5.1899-1904.2000 · Cited by 237 · see citing works

CARD9+ microglia promote antifungal immunity via IL-1β- and CXCL1-mediated neutrophil recruitment

Drummond, R. A., Swamydas, M., Oikonomou, V., Zhai, B., Dambuza, I. M., Schaefer, B. C., Bohrer, A. C., Mayer-Barber, K. D., Lira, S. A., Iwakura, Y., et al. (2019) · Nature Immunology · doi:10.1038/s41590-019-0377-2 · Cited by 232 · see citing works

Inhibition of Neutrophil Apoptosis by TLR Agonists in Whole Blood: Involvement of the Phosphoinositide 3-Kinase/Akt and NF-κB Signaling Pathways, Leading to Increased Levels of Mcl-1, A1, and Phosphorylated Bad

François, S., Benna, J. E., Dang, P. M., Pédruzzi, E., Gougerot‐Pocidalo, M., & Elbim, C. (2005) · The Journal of Immunology · doi:10.4049/jimmunol.174.6.3633 · Cited by 226 · see citing works

Emetic and refusal activity of deoxynivalenol to swine

Forsyth, D. M., YOSHIZAWA, T., Morooka, N., & Tuite, J. F. (1977) · Applied and Environmental Microbiology · doi:10.1128/aem.34.5.547-552.1977 · Cited by 226 · see citing works

GliZ, a Transcriptional Regulator of Gliotoxin Biosynthesis, Contributes toAspergillus fumigatusVirulence

Bok, J. W., Chung, D., Balajee, S. A., Marr, K. A., Andes, D. R., Nielsen, K. F., Frisvad, J. C., Kirby, K. A., & Keller, N. P. (2006) · Infection and Immunity · doi:10.1128/iai.00780-06 · Cited by 223 · see citing works

Scientific Opinion on the hazard assessment of endocrine disruptors: Scientific criteria for identification of endocrine disruptors and appropriateness of existing test methods for assessing effects mediated by these substances on human health and the environment

EFSA Scientific Committee (2013) · EFSA Journal · doi:10.2903/j.efsa.2013.3132 · Cited by 215 · see citing works

Comparative metabolism of zearalenone and transmission into bovine milk

Mirocha, C. J., Pathre, S. V., & Robison, T. S. (1981) · Food and Cosmetics Toxicology · doi:10.1016/0015-6264(81)90299-6 · Cited by 208 · see citing works

Candida albicans-Induced Epithelial Damage Mediates Translocation through Intestinal Barriers

Allert, S., Förster, T. M., Svensson, C.-M., Richardson, J. P., Pawlik, T., Hebecker, B., Rudolphi, S., Juraschitz, M., Schaller, M., Blagojevic, M., et al. (2018) · mBio · doi:10.1128/mbio.00915-18 · Cited by 208 · see citing works

DNA fragmentation, apoptosis and cell cycle arrest induced by zearalenone in cultured DOK, Vero and Caco-2 cells: prevention by Vitamin E

Abid‐Essefi, S., Baudrimont, I., Hassen, W., Ouanes, Z., Mobio, T. A., Anane, R., Creppy, E. E., & Bacha, H. (2003) · Toxicology · doi:10.1016/s0300-483x(03)00329-9 · Cited by 207 · see citing works

Aspergillus fumigatus suppresses the human cellular immune response via gliotoxin-mediated apoptosis of monocytes

Stanzani, M., Orciuolo, E., Lewis, R. E., Kontoyiannis, D. P., Martins, S. L. R., John, L. S. S., & Komanduri, K. V. (2004) · Blood · doi:10.1182/blood-2004-09-3421 · Cited by 203 · see citing works

Oral epithelial cells orchestrate innate Type 17 responses to Candida albicans through the virulence factor Candidalysin

Verma, A. H., Richardson, J., Zhou, C., Coleman, B. M., Moyes, D., Ho, J., Huppler, A., Ramani, K., McGeachy, M., Mufazalov, I., et al. (2017) · Science immunology · doi:10.1126/sciimmunol.aam8834 · Cited by 203 · see citing works

Candidalysin: discovery and function in Candida albicans infections

Naglik, J., Gaffen, S., & Hube, B. (2019) · Current Opinion in Microbiology · doi:10.1016/j.mib.2019.06.002 · Cited by 203 · see citing works

CARD9-Dependent Neutrophil Recruitment Protects against Fungal Invasion of the Central Nervous System

Drummond, R. A., Collar, A. L., Swamydas, M., Rodriguez, C. A., Lim, J. K., Mendez, L. M., Fink, D. L., Hsu, A. P., Zhai, B., Karaüzüm, H., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005293 · Cited by 201 · see citing works

Candidalysin Drives Epithelial Signaling, Neutrophil Recruitment, and Immunopathology at the Vaginal Mucosa

Richardson, J. P., Willems, H. M. E., Moyes, D. L., Shoaie, S., Barker, K. S., Tan, S. L., Palmer, G. E., Hube, B., Naglik, J. R., & Peters, B. M. (2017) · Infection and Immunity · doi:10.1128/iai.00645-17 · Cited by 196 · see citing works

Aspergillus bombycis, a New Aflatoxigenic Species and Genetic Variation in Its Sibling Species, A. nomius

Peterson, S. W., Ito, Y., Horn, B. W., & Goto, T. (2001) · Mycologia · doi:10.2307/3761823 · Cited by 194 · see citing works

Impact of mycotoxin on immune response and consequences for pig health

Pierron, A., Alassane‐Kpembi, I., & Oswald, I. P. (2016) · Animal nutrition · doi:10.1016/j.aninu.2016.03.001 · Cited by 188 · see citing works

Aflatoxin and cyclopiazonic acid production by a sclerotium-producing Aspergillus tamarii strain

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Gliotoxin Production in<i>Aspergillus fumigatus</i>Contributes to Host‐Specific Differences in Virulence

Spikes, S., Xu, R., Nguyen, C. K., Chamilos, G., Kontoyiannis, D. P., Jacobson, R. H., Ejzykowicz, D. E., Chiang, L. Y., Filler, S. G., & May, G. S. (2008) · The Journal of Infectious Diseases · doi:10.1086/525044 · Cited by 186 · see citing works

Individual and combined cytotoxic effects of Fusarium toxins (deoxynivalenol, nivalenol, zearalenone and fumonisins B1) on swine jejunal epithelial cells

Wan, L.-Y. M., Turner, P. C., & El-Nezami, H. S. (2013) · Food and Chemical Toxicology · doi:10.1016/j.fct.2013.03.034 · Cited by 180 · see citing works

Immunosuppression in vitro by a metabolite of a human pathogenic fungus.

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Candidalysin activates innate epithelial immune responses via epidermal growth factor receptor

Ho, J., Yang, X., Nikou, S.-A., Kichik, N., Donkin, A., Ponde, N., Richardson, J., Gratacap, R. L., Archambault, L., Zwirner, C. P., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-09915-2 · Cited by 176 · see citing works

Detection of Gliotoxin in Experimental and Human Aspergillosis

Lewis, R. E., Wiederhold, N. P., Chi, J., Han, X. Y., Komanduri, K. V., Kontoyiannis, D. P., & Prince, R. A. (2004) · Infection and Immunity · doi:10.1128/iai.73.1.635-637.2005 · Cited by 175 · see citing works

NADPH Oxidase Promotes Neutrophil Extracellular Trap Formation in Pulmonary Aspergillosis

Röhm, M., Grimm, M. J., D’Auria, A. C., Almyroudis, N. G., Segal, B. H., & Urban, C. F. (2014) · Infection and Immunity · doi:10.1128/iai.00096-14 · Cited by 170 · see citing works

Rapid, Sequential Activation of Mitogen-Activated Protein Kinases and Transcription Factors Precedes Proinflammatory Cytokine mRNA Expression in Spleens of Mice Exposed to the Trichothecene Vomitoxin

Zhou, H.-R. (2003) · Toxicological Sciences · doi:10.1093/toxsci/kfg006 · Cited by 165 · see citing works

Dietary aflatoxins and human liver cancer. IV. Incidence of primary liver cancer in two municipal populations of Thailand

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Vomitoxin-Induced Cyclooxygenase-2 Gene Expression in Macrophages Mediated by Activation of ERK and p38 but Not JNK Mitogen-Activated Protein Kinases

Moon, Y. (2002) · Toxicological Sciences · doi:10.1093/toxsci/69.2.373 · Cited by 161 · see citing works

Deletion of the <i>gliP</i> gene of <i>Aspergillus fumigatus</i> results in loss of gliotoxin production but has no effect on virulence of the fungus in a low‐dose mouse infection model

Kupfahl, C., Heinekamp, T., Geginat, G., Ruppert, T., Härtl, A., Hof, H., & Brakhage, A. A. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05373.x · Cited by 157 · see citing works

Gliotoxin induces apoptosis in macrophages unrelated to its antiphagocytic properties.

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Detoxification of Mycotoxins through Biotransformation

Li, P., Su, R., Yin, R., Lai, D., Wang, M., Liu, Y., & Zhou, L. (2020) · Toxins · doi:10.3390/toxins12020121 · Cited by 147 · see citing works

Phosphoinositides in phagocytosis and macropinocytosis

Levin‐Konigsberg, R., Grinstein, S., & Schlam, D. (2014) · Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids · doi:10.1016/j.bbalip.2014.09.005 · Cited by 144 · see citing works

Fungal Metabolite Gliotoxin Inhibits Assembly of the Human Respiratory Burst NADPH Oxidase

Tsunawaki, S., Yoshida, L. S., Nishida, S., Kobayashi, T., & Shimoyama, T. (2004) · Infection and Immunity · doi:10.1128/iai.72.6.3373-3382.2004 · Cited by 140 · see citing works

Ochratoxin A increases permeability through tight junctions by removal of specific claudin isoforms

McLaughlin, J. T., Padfield, P. J., Burt, J. P. H., & O’Neill, C. A. (2004) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00007.2004 · Cited by 139 · see citing works

Effect of some Indian herbs on macrophage functions in ochratoxin A treated mice

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Dissection of patulin biosynthesis, spatial control and regulation mechanism in Penicillium expansum

Li, B., Chen, Y., Zong, Y., Shang, Y., Zhang, Z., Xu, X., Wang, X., Long, M., & Tian, S. (2019) · Environmental Microbiology · doi:10.1111/1462-2920.14542 · Cited by 138 · see citing works

Macrophages Maintain Epithelium Integrity by Limiting Fungal Product Absorption

Chikina, A. S., Nadalin, F., Maurin, M., Jouve, M. J., Thomas-Bonafos, T., Li, X. V., Lameiras, S., Baulande, S., Henri, S., MALISSEN, B., et al. (2020) · Cell · doi:10.1016/j.cell.2020.08.048 · Cited by 138 · see citing works

Potential role of IL-8, platelet-activating factor and TNF-α in the sequestration of neutrophils in the lung: effects on neutrophil deformability, adhesion receptor expression, and chemotaxis

Drost, E., & MacNee, W. (2002) · European Journal of Immunology · doi:10.1002/1521-4141(200202)32:2 · Cited by 135 · see citing works

Temporal patterns of aflatoxin-albumin adducts in hepatitis B surface antigen-positive and antigen-negative residents of Daxin, Qidong County, People's Republic of China.

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The Compromised Intestinal Barrier Induced by Mycotoxins

Gao, Y., Meng, L., Liu, H., Wang, J., & Zheng, N. (2020) · Toxins · doi:10.3390/toxins12100619 · Cited by 129 · see citing works

Ochratoxin A Producing Species in the Genus Penicillium

Cabañes, F. J., Bragulat, M. R., & Castellá, G. (2010) · Toxins · doi:10.3390/toxins2051111 · Cited by 128 · see citing works

Foodstuffs and human blood contamination by the mycotoxin ochratoxin A: correlation with chronic interstitial nephropathy in Tunisia

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Mycotoxin and Gut Microbiota Interactions

Guerre, P. (2020) · Toxins · doi:10.3390/toxins12120769 · Cited by 126 · see citing works

Individual and combined effects of subclinical doses of deoxynivalenol and fumonisins in piglets

Grenier, B., Bracarense, A. P. F. R. L., Lucioli, J., Pacheco, G. D., Cossalter, A., Moll, W., Schatzmayr, G., & Oswald, I. P. (2011) · Molecular Nutrition & Food Research · doi:10.1002/mnfr.201000402 · Cited by 125 · see citing works

Aflatoxin M1 in milk and traditional dairy products from west part of Iran: Occurrence and seasonal variation with an emphasis on risk assessment of human exposure

Bahrami, R., Shahbazi, Y., & Nikousefat, Z. (2015) · Food Control · doi:10.1016/j.foodcont.2015.10.039 · Cited by 125 · see citing works

Differential Cytokine mRNA Expression in Mice after Oral Exposure to the Trichothecene Vomitoxin (Deoxynivalenol): Dose Response and Time Course

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Renal Lesions Induced by Ochratoxin A Exposure in the F344 Rat

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Transcriptional and posttranscriptional roles for p38 mitogen-activated protein kinase in upregulation of TNF-α expression by deoxynivalenol (vomitoxin)

Chung, Y.-J., Zhou, H.-R., & Pestka, J. J. (2003) · Toxicology and Applied Pharmacology · doi:10.1016/s0041-008x(03)00299-0 · Cited by 119 · see citing works

NETosis and NADPH oxidase: at the intersection of host defense, inflammation, and injury

Almyroudis, N. G., Grimm, M. J., Davidson, B. A., Röhm, M., Urban, C. F., & Segal, B. H. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00045 · Cited by 119 · see citing works

Critical role of caveolin-1 in aflatoxin B1-induced hepatotoxicity via the regulation of oxidation and autophagy

Xu, Q., Shi, W., Lv, P., Meng, W., Mao, G., Gong, C., Chen, Y., Wei, Y., He, X., Zhao, J., et al. (2020) · Cell Death and Disease · doi:10.1038/s41419-019-2197-6 · Cited by 118 · see citing works

Mucoricin is a ricin-like toxin that is critical for the pathogenesis of mucormycosis

Soliman, S. S. M., Baldin, C., Gu, Y., Singh, S., Gebremariam, T., Swidergall, M., Alqarihi, A., Youssef, E. G., Alkhazraji, S., Pikoulas, A., et al. (2021) · Nature Microbiology · doi:10.1038/s41564-020-00837-0 · Cited by 115 · see citing works

Candidalysin Crucially Contributes to Nlrp3 Inflammasome Activation by Candida albicans Hyphae

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Microbial Proteins: A Green Approach Towards Zero Hunger

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Visualization of the relationship between fungi and cancer from the perspective of bibliometric analysis

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Ochratoxin A and Citrinin Differentially Modulate Bovine Mammary Epithelial Cell Permeability and Innate Immune Function

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A New Perspective on Metabolites and Bioactive Compounds from Fungi

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Six Feet under Microbiota: Microbiologic Contamination and Toxicity Profile in Three Urban Cemeteries from Lisbon, Portugal

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Fungal Community Composition and Function Associated with Loose Smokeless Tobacco Products

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Herbal Immunity Booster-Associated Liver Injury During COVID-19 Pandemic and Aflatoxins

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Functional and Immunological Studies Revealed a Second Superantigen Toxin in Staphylococcal Enterotoxin C Producing Staphylococcus aureus Strains

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Updates on Candida albicans infections: pathogenesis, resistance, and emerging nanopharmaceutical strategies

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AoPrdx2 Regulates Oxidative Stress, Reactive Oxygen Species, Trap Formation, and Secondary Metabolism in Arthrobotrys oligospora

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Chemical Genetics in C. elegans Identifies Anticancer Mycotoxins Chaetocin and Chetomin as Potent Inducers of a Nuclear Metal Homeostasis Response

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Confrontations of the Pathogenic Fungus Colletotrichum graminicola With a Biocontrol Bacterium or a Ubiquitous Fungus Trigger Synthesis of Secondary Metabolites With Lead Structures of Synthetic Fungicides

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A Brief Review on Aflatoxicosis in Aquaculture With a Focus on Fish

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Protein-Protein Interactions in Host–Pathogen Interactions

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Additional file 2 of Climate influences the gut eukaryome of wild rodents in the Great Rift Valley of Jordan

Khadem, S., Berry, D., & Al-khlifeh, E. (2024) · Figshare · doi:10.6084/m9.figshare.26942697

Additional file 3 of Climate influences the gut eukaryome of wild rodents in the Great Rift Valley of Jordan

Khadem, S., Berry, D., & Al-khlifeh, E. (2024) · Figshare · doi:10.6084/m9.figshare.26942700

Additional file 5 of Climate influences the gut eukaryome of wild rodents in the Great Rift Valley of Jordan

Khadem, S., Berry, D., & Al-khlifeh, E. (2024) · Figshare · doi:10.6084/m9.figshare.26942706

Additional file 6 of Climate influences the gut eukaryome of wild rodents in the Great Rift Valley of Jordan

Khadem, S., Berry, D., & Al-khlifeh, E. (2024) · Figshare · doi:10.6084/m9.figshare.26942709

Additional file 1 of Climate influences the gut eukaryome of wild rodents in the Great Rift Valley of Jordan

Khadem, S., Berry, D., & Al-khlifeh, E. (2024) · Figshare · doi:10.6084/m9.figshare.26942694

Additional file 4 of Climate influences the gut eukaryome of wild rodents in the Great Rift Valley of Jordan

Khadem, S., Berry, D., & Al-khlifeh, E. (2024) · Figshare · doi:10.6084/m9.figshare.26942703

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