The DOI matches its Crossref record; 247 of the 247 references it cites were found in a registry or an index.
Stress, drugs, and evolution: the role of cellular signaling in fungal drug resistance.
Open accessAbstract
The survival of all organisms depends critically upon interactions with the environment, mediated largely through the action of small molecules.Small molecules can provide the nutrients to support life (195), mediate communication between organisms (25,76, 238), or exert toxicity that threatens viability (86, 183).The discovery of small molecules with exquisite potency and selective toxicity to microbes revolutionized modern medicine, as exemplified by the archetypal antibiotic penicillin, the first broad-spectrum antibiotic and the most famous fungal secondary metabolite (14, 211).There are relatively few antimicrobial structural scaffolds that are purely synthetic in origin, and humans rely heavily upon many natural products and their derivatives as agrochemicals, antimicrobials, immunosuppressants, and antineoplastic agents (24,73,97).Given that small molecules can have profound effects on cellular signaling and are a ubiquitous presence in the environment, it is not surprising that microbes have evolved diverse mechanisms to survive the challenges of exposure to antimicrobial drugs.Antimicrobials represent one of the many stresses that a microbial pathogen must sense and respond to in order to thrive in harsh environmental conditions.Antimicrobial drug resistance mechanisms that span the kingdoms can largely be classified into two broad categories.The first category includes mechanisms to bypass the effects of the antimicrobial on the cell.Such mechanisms include alterations in the drug target that block drug binding (6,99, 165, 227) or increased production of multidrug transporters that simply remove the drug from the cell (72,74, 175, 200, 214).The second category includes mechanisms that allow the cell to cope with druginduced stress.Such mechanisms include metabolic alterations that minimize the toxicity of the drug, as well as the activation of chaperones and signal transduction cascades dedicated to sensing and responding to various stresses (26,32).Alterations in resistance can reflect physiological adaptation to a drug, epigenetic changes, or stable genetic alterations, depending on the nature of the drug, the duration of exposure, and the organism.Drug resistance is of particular importance in fungi as they
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The 1,3-β-D-glucan synthases are encoded by FKS1, FKS2, and FKS3 in S. cerevisiae, C. glabrata, and C. albicans, and require a regulatory subunit encoded by RHO1 for activity [3], [20], [32], [33].”
From Global Analysis of the Evolution and Mechanism of Echinocandin Resistance in Candida glabrata (2012) · cites this paper as [32]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“The echinocandins are the only novel class of antifungal drugs approved for clinical use in decades and target the biosynthesis of the key fungal cell wall component, 1,3-β-D-glucan [3], [20], [32].”
From Global Analysis of the Evolution and Mechanism of Echinocandin Resistance in Candida glabrata (2012) · cites this paper as [32]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
The epidemiology of sepsis in the United States from 1979 through 2000
Martin, G. S., Mannino, D. M., Eaton, S., & Moss, M. (2003) · New England Journal of Medicine · doi:10.1056/nejmoa022139 · Cited by 5,841
Epidemiology of Invasive Candidiasis: a Persistent Public Health Problem
Pfaller, M. A., & Diekema, D. J. (2007) · Clinical Microbiology Reviews · doi:10.1128/cmr.00029-06 · Cited by 4,174
Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes
Liu, J., Farmer, J. D., Lane, W. S., Friedman, J., Weissman, I., & Schreiber, S. L. (1991) · Cell · doi:10.1016/0092-8674(91)90124-h · Cited by 4,116
Targeting multidrug resistance in cancer
Szakács, G., Paterson, J. K., Ludwig, J. A., Booth-Genthe, C., & Gottesman, M. M. (2006) · Nature Reviews Drug Discovery · doi:10.1038/nrd1984 · Cited by 3,609
Fungal secondary metabolism — from biochemistry to genomics
Keller, N. P., Turner, G., & Bennett, J. W. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1286 · Cited by 1,734
Multidrug-resistance efflux pumps ? not just for resistance
Piddock, L. J. V. (2006) · Nature Reviews Microbiology · doi:10.1038/nrmicro1464 · Cited by 1,523
Pratt, W. B., & Toft, D. O. (2003) · Experimental Biology and Medicine · doi:10.1177/153537020322800201 · Cited by 1,497
Whitesell, L., Mimnaugh, E. G., De Costa, B., Myers, C. E., & Neckers, L. M. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.18.8324 · Cited by 1,444
Comparison of Caspofungin and Amphotericin B for Invasive Candidiasis
Mora-Duarte, J., Betts, R., Rotstein, C., Colombo, A. L., Thompson-Moya, L., Smietana, J., Lupinacci, R., Sable, C., Kartsonis, N., & Perfect, J. (2002) · New England Journal of Medicine · doi:10.1056/nejmoa021585 · Cited by 1,380
Clinical, Cellular, and Molecular Factors That Contribute to Antifungal Drug Resistance
White, T. C., Marr, K. A., & Bowden, R. A. (1998) · Clinical Microbiology Reviews · doi:10.1128/cmr.11.2.382 · Cited by 1,353
Research works printed but not linked: 1
- Warris, A., C. M. Weemaes, and P. E. Verweij. 2002. Multidrug resistance in Aspergillus fumigatus. N. Engl. J. Med.347:2173-2174.
Cited by
Sorted by citations
Antifungal Drug Resistance: Molecular Mechanisms in Candida albicans and Beyond
Lee, Y., Puumala, E., Robbins, N., & Cowen, L. E. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00199 · Cited by 801
Self-citationMechanisms of Antifungal Drug Resistance
Cowen, L. E., Sanglard, D., Howard, S. J., Rogers, P. D., & Perlin, D. S. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019752 · Cited by 647
Self-citationEfflux-Mediated Antifungal Drug Resistance
Cannon, R. D., Lamping, E., Holmes, A. R., Niimi, K., Baret, P. V., Keniya, M. V., Tanabe, K., Niimi, M., Goffeau, A., & Monk, B. C. (2009) · Clinical Microbiology Reviews · doi:10.1128/cmr.00051-08 · Cited by 608
Regulatory circuitry governing fungal development, drug resistance, and disease.
Shapiro, R. S., Robbins, N., & Cowen, L. E. (2011) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00045-10 · Cited by 576
Self-citationSionov, E., Lee, H., Chang, Y. C., & Kwon-Chung, K. J. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000848 · Cited by 479
Molecular Evolution of Antifungal Drug Resistance
Robbins, N., Caplan, T., & Cowen, L. E. (2017) · Annual Review of Microbiology · doi:10.1146/annurev-micro-030117-020345 · Cited by 441
Self-citationCowen, L. E., Singh, S. D., Köhler, J. R., Collins, C., Zaas, A. K., Schell, W. A., Aziz, H., Mylonakis, E., Perfect, J. R., Whitesell, L., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813394106 · Cited by 413
Self-citationHsp90 Governs Echinocandin Resistance in the Pathogenic Yeast Candida albicans via Calcineurin
Singh, S. D., Robbins, N., Zaas, A. K., Schell, W. A., Perfect, J. R., & Cowen, L. E. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000532 · Cited by 362
“Most antifungal drugs in clinical use target the biosynthesis or function of ergosterol, the predominant sterol of fungal membranes, or the biosynthesis of (1,3)-b-Dglucan, a critical component of the fungal cell wall [8,9].”
BackgroundSelf-citationLaFayette, S. L., Collins, C., Zaas, A. K., Schell, W. A., Betancourt-Quiroz, M., Gunatilaka, A. A. L., Perfect, J. R., & Cowen, L. E. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1001069 · Cited by 329
Self-citationFraczek, M. G., Bromley, M., Buied, A., Moore, C. B., Rajendran, R., Rautemaa‐Richardson, R., Ramage, G., Denning, D. W., & Bowyer, P. (2013) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt075 · Cited by 313
Mechanisms of echinocandin antifungal drug resistance
Perlin, D. S. (2015) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.12831 · Cited by 313
Hsp90 Governs Dispersion and Drug Resistance of Fungal Biofilms
Robbins, N., Uppuluri, P., Nett, J., Rajendran, R., Ramage, G., Lopez-Ribot, J. L., Andes, D., & Cowen, L. E. (2011) · PLoS Pathogens · doi:10.1371/journal.ppat.1002257 · Cited by 291
Self-citationRosenberg, A., Ene, I. V., Bibi, M., Zakin, S., Segal, E. S., Ziv, N., Dahan, A. M., Colombo, A. L., Bennett, R. J., & Berman, J. (2018) · Nature Communications · doi:10.1038/s41467-018-04926-x · Cited by 270
NLLSS: Predicting Synergistic Drug Combinations Based on Semi-supervised Learning
Chen, X., Ren, B., Chen, M., Wang, Q., Zhang, L., & Yan, G. (2016) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1004975 · Cited by 284
Current Perspectives on Echinocandin Class Drugs
Perlin, D. S. (2011) · Future Microbiology · doi:10.2217/fmb.11.19 · Cited by 274
Recent insights into Candida albicans biofilm resistance mechanisms
Mathé, L., & Van Dijck, P. (2013) · Current Genetics · doi:10.1007/s00294-013-0400-3 · Cited by 271
Efflux in Fungi: La Pièce de Résistance
Coleman, J. J., & Mylonakis, E. E. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000486 · Cited by 236
Costa-de-Oliveira, S., & Rodrigues, A. G. (2020) · Microorganisms · doi:10.3390/microorganisms8020154 · Cited by 229
Doering, T. L. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.62.081307.162753 · Cited by 220
Global Analysis of the Evolution and Mechanism of Echinocandin Resistance in Candida glabrata
Singh-Babak, S. D., Babak, T., Diezmann, S., Hill, J. A., Xie, J. L., Chen, Y.-L., Poutanen, S. M., Rennie, R. P., Heitman, J., & Cowen, L. E. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1002718 · Cited by 205
“albicans, and require a regulatory subunit encoded by RHO1 for activity [3,20,32,33].”
BackgroundInfluentialSelf-citationErg11 mutations associated with azole resistance in clinical isolates of Candida albicans
Xiang, M.-J., Liu, J.-Y., Ni, P.-H., Wang, S., Shi, C., Wei, B., Ni, Y.-X., & Ge, H.-L. (2013) · FEMS Yeast Research · doi:10.1111/1567-1364.12042 · Cited by 197
Fungal Resistance to Echinocandins and the MDR Phenomenon in Candida glabrata
Healey, K. R., & Perlin, D. S. (2018) · Journal of Fungi · doi:10.3390/jof4030105 · Cited by 194
Vediyappan, G., Rossignol, T., & d'Enfert, C. (2010) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01638-09 · Cited by 183
Molecular Mechanisms Associated with Antifungal Resistance in Pathogenic Candida Species
Czajka, K. M., Venkataraman, K., Brabant-Kirwan, D., Santi, S. A., Verschoor, C. P., Appanna, V. D., Singh, R. I., Saunders, D., & Tharmalingam, S. (2023) · Cells · doi:10.3390/cells12222655 · Cited by 207
Valiante, V., Macheleidt, J., Föge, M., & Brakhage, A. A. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.00325 · Cited by 189
Sionov, E., Chang, Y. C., Garraffo, H. M., & Kwon-Chung, K. J. (2009) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00295-09 · Cited by 179
Identification and Characterization of Four Azole-Resistant erg3 Mutants of Candida albicans
Martel, C. M., Parker, J. E., Bader, O., Weig, M., Gross, U., Warrilow, A. G. S., Rolley, N., Kelly, D. E., & Kelly, S. L. (2010) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00348-10 · Cited by 168
Update on Antifungal Drug Resistance
Perlin, D. S., Shor, E., & Zhao, Y. (2015) · Current Clinical Microbiology Reports · doi:10.1007/s40588-015-0015-1 · Cited by 181
Antifungal drug resistance of oral fungi
Niimi, M., Firth, N. A., & Cannon, R. D. (2010) · Odontology · doi:10.1007/s10266-009-0118-3 · Cited by 170
Antimicrobial activity of pomegranate peel extracts as affected by cultivar
Rosas‐Burgos, E. C., Burgos‐Hernández, A., Noguera‐Artiaga, L., Kačániová, M., Hernández, F., Cárdenas-López, J. L., & Carbonell-Barrachina, Á. A. (2016) · Journal of the Science of Food and Agriculture · doi:10.1002/jsfa.7799 · Cited by 173
Geddes‐McAlister, J., & Shapiro, R. S. (2018) · Annals of the New York Academy of Sciences · doi:10.1111/nyas.13739 · Cited by 162
Fungistasis and general soil biostasis – A new synthesis
Garbeva, P., Hol, W. H. G., Termorshuizen, A. J., Kowalchuk, G. A., & de Boer, W. (2010) · Soil Biology and Biochemistry · doi:10.1016/j.soilbio.2010.11.020 · Cited by 156
The CWI Pathway: Regulation of the Transcriptional Adaptive Response to Cell Wall Stress in Yeast
Sanz, A., García, R., Rodríguez-Peña, J., & Arroyo, J. (2017) · Journal of Fungi · doi:10.3390/jof4010001 · Cited by 149
A survey of yeast genomic assays for drug and target discovery
Smith, A. M., Ammar, R., Nislow, C., & Giaever, G. N. (2010) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2010.04.012 · Cited by 137
García‐Effrón, G. (2020) · Journal of Fungi · doi:10.3390/jof6040262 · Cited by 135
Hsp90 orchestrates stress response signaling governing fungal drug resistance
Cowen, L. E. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000471 · Cited by 130
Self-citationCandida albicans gains azole resistance by altering sphingolipid composition
Gao, J., Wang, H., Li, Z., Wong, A. H.-H., Wang, Y.-Z., Guo, Y., Lin, X., Zeng, G., Liu, H., Wang, Y., et al. (2018) · Nature Communications · doi:10.1038/s41467-018-06944-1 · Cited by 130
Ferreira, G. F., Baltazar, L. D. M., dos Santos, J. R. A., Monteiro, A. S., Fraga, L. A. D. O., de Resende, M. A., & Santos, D. A. (2013) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt114 · Cited by 121
Juvvadi, P. R., Lamoth, F., & Steinbach, W. J. (2014) · Fungal Biology Reviews · doi:10.1016/j.fbr.2014.02.004 · Cited by 116
Self-citationDiezmann, S., Michaut, M., Shapiro, R. S., Bader, G. D., & Cowen, L. E. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002562 · Cited by 112
Self-citationKsiezopolska, E., Schikora-Tamarit, M. À., Beyer, R., Nunez-Rodriguez, J. C., Schüller, C., & Gabaldón, T. (2021) · Current Biology · doi:10.1016/j.cub.2021.09.084 · Cited by 107
It’s not magic – Hsp90 and its effects on genetic and epigenetic variation
Zabinsky, R. A., Mason, G. A., Queitsch, C., & Jarosz, D. F. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.05.015 · Cited by 106
Review on Current Status of Echinocandins Use
Mroczyńska, M., & Brillowska‐Dąbrowska, A. (2020) · Antibiotics · doi:10.3390/antibiotics9050227 · Cited by 113
Elucidating Drug Resistance in Human Fungal Pathogens
Xie, J. L., Polvi, E. J., Shekhar‐Guturja, T., & Cowen, L. E. (2014) · Future Microbiology · doi:10.2217/fmb.14.18 · Cited by 103
Self-citationpH Signaling in Human Fungal Pathogens: a New Target for Antifungal Strategies
Cornet, M., & Gaillardin, C. M. (2014) · Eukaryotic Cell · doi:10.1128/ec.00313-13 · Cited by 101
Genetic and Genomic Architecture of the Evolution of Resistance to Antifungal Drug Combinations
Hill, J. A., Ammar, R., Torti, D., Nislow, C., & Cowen, L. E. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003390 · Cited by 93
Self-citationThe fungal Achilles’ heel: targeting Hsp90 to cripple fungal pathogens
Cowen, L. E. (2013) · Current Opinion in Microbiology · doi:10.1016/j.mib.2013.03.005 · Cited by 102
Self-citationFacilitators of adaptation and antifungal resistance mechanisms in clinically relevant fungi
Hokken, M., Zwaan, B. J., Melchers, W. J. G., & Verweij, P. E. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103254 · Cited by 98
Bezerra, A. R., Simões, J., Lee, W., Rung, J., Weil, T., Gut, I. G., Gut, M., Bayés, M., Rizzetto, L., Cavalieri, D., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1302094110 · Cited by 94
Role of Ndt80p in Sterol Metabolism Regulation and Azole Resistance in Candida albicans
Sellam, A., Tebbji, F., & Nantel, A. (2009) · Eukaryotic Cell · doi:10.1128/ec.00074-09 · Cited by 91
The Hsp90 chaperone network modulates Candida virulence traits
O’Meara, T. R., Robbins, N., & Cowen, L. E. (2017) · Trends in Microbiology · doi:10.1016/j.tim.2017.05.003 · Cited by 92
The alternative oxidase of Candida albicans causes reduced fluconazole susceptibility
Yan, L., Li, M., Cao, Y., Gao, P., Cao, Y., Wang, Y., & Jiang, Y. (2009) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkp273 · Cited by 89
The Hsp90 Co-Chaperone Sgt1 Governs Candida albicans Morphogenesis and Drug Resistance
Shapiro, R. S., Zaas, A. K., Betancourt-Quiroz, M., Perfect, J. R., & Cowen, L. E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0044734 · Cited by 86
Self-citationDrug Resistance and Novel Therapeutic Approaches in Invasive Candidiasis
Murphy, S. E., & Bicanic, T. A. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.759408 · Cited by 86
Bhattacharya, S., Sobel, J. D., & White, T. C. (2016) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01252-16 · Cited by 83
The effect of biomaterials and antifungals on biofilm formation by Candida species: a review
Cuéllar‐Cruz, M., Vega‐González, A., Mendoza‐Novelo, B., López-Romero, E., Ruiz‐Baca, E., Escorza, M. A. Q., & Villagómez-Castro, J. C. (2012) · European Journal of Clinical Microbiology & Infectious Diseases · doi:10.1007/s10096-012-1634-6 · Cited by 83
Dickwella Widanage, M. C., Gautam, I., Sarkar, D., Mentink-Vigier, F., Vermaas, J. V., Ding, S.-Y., Lipton, A. S., Fontaine, T., Latgé, J.-P., Wang, P., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-50799-8 · Cited by 70
Multi-target drugs active against leishmaniasis: A paradigm of drug repurposing
Braga, S. S. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.111660 · Cited by 79
Fungal strategies for dealing with environment- and agriculture-induced stresses
Rangel, D. E. N., Finlay, R. D., Hallsworth, J. E., Dadachova, E., & Gadd, G. M. (2018) · Fungal Biology · doi:10.1016/j.funbio.2018.02.002 · Cited by 78
Elias, R., Benhamou, R. I., Jaber, Q. Z., Dorot, O., Zada, S. L., Oved, K., Pichinuk, E., & Fridman, M. (2019) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2019.07.003 · Cited by 76
Campoli, P., Abdallah, Q. A., Robitaille, R., Solis, N. V., Fielhaber, J. A., Kristof, A. S., Laverdière, M., Filler, S. G., & Sheppard, D. C. (2011) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00637-11 · Cited by 77
Multilocus resistance evolution to azole fungicides in fungal plant pathogen populations
Mohd‐Assaad, N., McDonald, B. A., & Croll, D. (2016) · Molecular Ecology · doi:10.1111/mec.13916 · Cited by 75
Zhou, Y., Wang, G., Li, Y., Liu, Y., Song, Y., Zheng, W., Zhang, N., Hu, X., Shikun, Y., & Jia, J. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.06082-11 · Cited by 72
Coping with Stress and the Emergence of Multidrug Resistance in Fungi
Shor, E., & Perlin, D. S. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1004668 · Cited by 73
Carlisle, P. L., & Kadosh, D. (2010) · Eukaryotic Cell · doi:10.1128/ec.00046-10 · Cited by 71
Rane, H. S., Bernardo, S. M., Howell, A. B., & Lee, S. A. (2013) · Journal of Antimicrobial Chemotherapy · doi:10.1093/jac/dkt398 · Cited by 69
Joubert, A., Bataillé‐Simoneau, N., Campion, C., Guillemette, T., Hudhomme, P., Iacomı, B., Leroy, T., Pochon, S., Poupard, P., & Simoneau, P. (2010) · Cellular Microbiology · doi:10.1111/j.1462-5822.2010.01520.x · Cited by 68
García, R., Bravo, E., Díez-Muñiz, S., Nombela, C., Rodríguez-Peña, J. M., & Arroyo, J. (2017) · Scientific Reports · doi:10.1038/s41598-017-06001-9 · Cited by 66
Eradication of Candida albicans persister cell biofilm by the membranotropic peptide gH625
Galdiero, E., de Alteriis, E., De Natale, A., D’Alterio, A., Siciliano, A., Guida, M., Lombardi, L., Falanga, A., & Galdiero, S. (2020) · Scientific Reports · doi:10.1038/s41598-020-62746-w · Cited by 65
Jacob, T. R., Peres, N. T. A., Martins, M. P., Lang, E. A. S., Sanches, P. R., Rossi, A., & Martinez-Rossi, N. M. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01241 · Cited by 65
Lewis, R. E., Ben‐Ami, R., Best, L., Albert, N. D., Walsh, T. J., & Kontoyiannis, D. P. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis767 · Cited by 62
Epp, E., Vanier, G., Harcus, D., Lee, A. Y., Jansen, G., Hallett, M., Sheppard, D. C., Thomas, D. Y., Munro, C. A., Mullick, A., et al. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000753 · Cited by 61
The Involvement of the Mid1/Cch1/Yvc1 Calcium Channels in Aspergillus fumigatus Virulence
de Castro, P. A., Chiaratto, J., Winkelströter, L. K., Bom, V. L. P., Ramalho, L. N. Z., Goldman, M. H. S., Brown, N. A., & Goldman, G. H. (2014) · PLoS ONE · doi:10.1371/journal.pone.0103957 · Cited by 60
Li, R. Q., Kumar, R., Tati, S., Puri, S., & Edgerton, M. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02295-12 · Cited by 63
Pathogenesis and Antifungal Drug Resistance of the Human Fungal Pathogen Candida glabrata
Tscherner, M., Schwarzmüller, T., & Kuchler, K. (2011) · Pharmaceuticals · doi:10.3390/ph4010169 · Cited by 60
Serrano‐Fujarte, I., López-Romero, E., Reyna-López, G. E., Martínez-Gámez, M. A., Vega‐González, A., & Cuéllar‐Cruz, M. (2015) · BioMed Research International · doi:10.1155/2015/783639 · Cited by 62
Overcoming Fungal Echinocandin Resistance through Inhibition of the Non-essential Stress Kinase Yck2
Caplan, T., Lorente-Macías, Á., Stogios, P. J., Evdokimova, E., Hyde, S., Wellington, M. A., Liston, S., Iyer, K. R., Puumala, E., Shekhar-Guturja, T., et al. (2020) · Cell Chemical Biology · doi:10.1016/j.chembiol.2019.12.008 · Cited by 57
Self-citationAkerey, B., Le-Lay, C., Fliss, I., Subirade, M., & Rouabhia, M. (2009) · Journal of Applied Microbiology · doi:10.1111/j.1365-2672.2009.04312.x · Cited by 56
The effect of antifungal resistance development on the virulence of Candida species
Bohner, F., Papp, C., & Gácser, A. (2022) · FEMS Yeast Research · doi:10.1093/femsyr/foac019 · Cited by 72
Antifungal Drug Concentration Impacts the Spectrum of Adaptive Mutations in Candida albicans
Todd, R. T., Soisangwan, N., Peters, S., Kemp, B., Crooks, T., Gerstein, A., & Selmecki, A. (2023) · Molecular Biology and Evolution · doi:10.1093/molbev/msad009 · Cited by 53
Rybak, J. M., Dickens, C. M., Parker, J. E., Caudle, K. E., Manigaba, K., Whaley, S. G., Nishimoto, A. T., Luna-Tapia, A., Roy, S., Zhang, Q., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00651-17 · Cited by 53
Heat shock protein 90 from neglected protozoan parasites
Roy, N., Nageshan, R. K., Ranade, S., & Tatu, U. S. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2011.12.003 · Cited by 54
Erg6 affects membrane composition and virulence of the human fungal pathogen Cryptococcus neoformans
de Oliveira, F. F. M., Paes, H. C., Peconick, L. D. F., Fonseca, F. L., Marina, C. L., Bocca, A. L., Homem-de-Mello, M., Rodrigues, M. L., Albuquerque, P., Nicola, A. M., et al. (2020) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2020.103368 · Cited by 52
Balkrishna, A., Rohela, A., Kumar, A., Kumar, A., Arya, V., Thakur, P., Olekšák, P., Krejcar, O., Verma, R., Kumar, D., et al. (2021) · Plants · doi:10.3390/plants10061089 · Cited by 60
Pais, P., Galocha, M., Viana, R., Cavalheiro, M., Pereira, D., & Teixeira, M. C. (2019) · Microbial Cell · doi:10.15698/mic2019.03.670 · Cited by 54
Alternate Strategies of Hsp90 Modulation for the Treatment of Cancer and Other Diseases
Brandt, G. E. L., & Blagg, B. S. J. (2009) · Current Topics in Medicinal Chemistry · doi:10.2174/156802609789895683 · Cited by 50
Ortiz‐López, F. J., Monteiro, M. C., González-Menéndez, V., Tormo, J. R., Genilloud, O., Bills, G. F., Vicente, F., Zhang, C., Roemer, T., Singh, S. B., et al. (2015) · Journal of Natural Products · doi:10.1021/np500854j · Cited by 50
Rane, H. S., Bernardo, S. M., Raines, S. M., Binder, J., Parra, K. J., & Lee, S. A. (2013) · Eukaryotic Cell · doi:10.1128/ec.00118-13 · Cited by 49
Terbinafine Resistance in Trichophyton rubrum and Trichophyton indotineae: A Literature Review
Gupta, A. K., Susmita, S., Nguyen, H. C., Liddy, A., Economopoulos, V., & Wang, T. (2025) · Antibiotics · doi:10.3390/antibiotics14050472 · Cited by 54
Caza, M., Hu, G., Price, M., Perfect, J. R., & Kronstad, J. W. (2016) · mSphere · doi:10.1128/msphere.00080-15 · Cited by 48
Zolin, G. V. S., da Fonseca, F. H., Zambom, C. R., & Garrido, S. S. (2021) · Biomolecules · doi:10.3390/biom11081209 · Cited by 47
Lee, H., Lamichhane, A. K., Garraffo, H. M., Kwon-Chung, K. J., & Chang, Y. C. (2012) · Molecular Microbiology · doi:10.1111/j.1365-2958.2012.08016.x · Cited by 50
Variability of the Stripe Rust Pathogen
Wan, A., Wang, X., Kang, Z., & Chen, X. (2017) · Springer eBooks · doi:10.1007/978-94-024-1111-9_2 · Cited by 49
Zhang, H., Guo, J., Voegele, R. T., Zhang, J., Duan, Y., Luo, H., & Kang, Z. (2012) · PLoS ONE · doi:10.1371/journal.pone.0049262 · Cited by 46
Feng, W., Yang, H. J., Xi, Z., Qiao, Z., Lv, Y., Wang, Y., Ma, Y., Wang, Y., & Wen, C. (2016) · Microbial Drug Resistance · doi:10.1089/mdr.2016.0095 · Cited by 45
Progress and prospects for targeting Hsp90 to treat fungal infections
Veri, A. O., & Cowen, L. E. (2014) · Parasitology · doi:10.1017/s0031182013002072 · Cited by 46
Self-citationEmerging Mechanisms of Drug Resistance in Candida albicans
Prasad, R., Nair, R., & Banerjee, A. (2019) · Progress in molecular and subcellular biology · doi:10.1007/978-3-030-13035-0_6 · Cited by 44
Yu, Q., Jia, C., Dong, Y., Zhang, B., Xiao, C., Chen, Y., Wang, Y., Li, X., Wang, L., Zhang, B., et al. (2015) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2015.02.008 · Cited by 42
Evolutionary divergence in the fungal response to fluconazole revealed by soft clustering
Kuo, D., Tan, K., Zinman, G., Ravasi, T., Bar‐Joseph, Z., & Ideker, T. (2010) · Genome biology · doi:10.1186/gb-2010-11-7-r77 · Cited by 40
Metabolic control of antifungal drug resistance
Robbins, N., Collins, C., Morhayim, J., & Cowen, L. E. (2010) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2009.07.004 · Cited by 40
Self-citation
Metadata
- Authors
- Cowen, L. E., & Steinbach, W. J.
- Affiliations
- Duke University (US)
- Corresponding author
- Cowen, Leah E.
- Venue
- Eukaryotic Cell
- Publisher
- American Society for Microbiology
- Published
- 2008-05
- Volume
- 7
- Issue
- 5
- Pages
- 747-764
- ISSN
- 1535-9778 (ISSN-L)
- 1535-9786
- PMC
- PMC2394973
- OpenAlex
- W2156217754
- Cited by
- 285
- References
- 247
- Citations by year
- 2026: 9 · 2025: 7 · 2024: 12 · 2023: 9 · 2022: 14 · 2021: 19 · 2020: 20 · 2019: 10 · 2018: 19 · 2017: 16 · 2016: 14 · 2015: 17 · 2014: 18 · 2013: 22 · 2012: 18
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Locations
- Eukaryotic Cell (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Burroughs Wellcome Fund
- Children's Miracle Network Hospitals
- National Institutes of Health
- U.S. Public Health Service (K08 A1061149)
- Canadian Institutes of Health Research (MOP-86452)
- National Institute of Allergy and Infectious Diseases
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Microbial Natural Products and Biosynthesis
- Keywords
- fungal drug resistance, antimicrobial resistance, signal transduction, stress response, drug target alterations, multidrug transporter, molecular chaperones, epigenetic modifications, natural products, secondary metabolites, resistance evolution
- MeSH terms
- Antifungal Agents, Aspergillus fumigatus, Candida albicans, Cell Membrane, Cell Wall, Cryptococcus neoformans, Humans, Mycoses, Signal Transduction, Evolution, Molecular, Drug Resistance, Fungal
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review