Hsp90 Orchestrates Temperature-Dependent Candida albicans Morphogenesis via Ras1-PKA Signaling
Open accessAbstract
Background Hsp90 is an environmentally contingent molecular chaperone that influences the form and function of diverse regulators of cellular signaling. Hsp90 potentiates the evolution of fungal drug resistance by enabling crucial cellular stress responses. Here we demonstrate that in the leading fungal pathogen of humans, Candida albicans, Hsp90 governs cellular circuitry required not only for drug resistance but also for the key morphogenetic transition from yeast to filamentous growth that is crucial for virulence. This transition is normally regulated by environmental cues, such as exposure to serum, that are contingent upon elevated temperature to induce morphogenesis. The basis for this temperature dependence has remained enigmatic.Results We show that compromising Hsp90 function pharmacologically or genetically induces a transition from yeast to filamentous growth in the absence of external cues. Elevated temperature relieves Hsp90-mediated repression of the morphogenetic program. Hsp90 regulates morphogenetic circuitry by repressing Ras1-PKA signaling. Modest Hsp90 compromise enhances the phenotypic effects of activated Ras1 signaling whereas deletion of positive regulators of the Ras1-PKA cascade blocks the morphogenetic response to Hsp90 inhibition. Consistent with the requirement for morphogenetic flexibility for virulence, depletion of C. albicans Hsp90 attenuates virulence in a murine model of systemic disease.Conclusions Hsp90 governs the integration of environmental cues with cellular signaling to orchestrate fungal morphogenesis and virulence, suggesting new therapeutic strategies for life-threatening infectious disease. Hsp90's capacity to govern a key developmental program in response to temperature change provides a new mechanism that complements the elegant repertoire that organisms utilize to sense temperature.
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The MAL2p-HSP90/hsp90Δ strain has a modest reduction of Hsp90 levels even when fully induced in maltose, and growth in glucose/maltose dramatically reduces Hsp90 levels and reduces growth rate and stationary phase density.
“Under these conditions, the MAL2p-HSP90/hsp90Δ strain has reduced growth rate and reaches approximately half the stationary phase cell density as a wild-type strain [40].”
From Hsp90 Governs Echinocandin Resistance in the Pathogenic Yeast Candida albicans via Calcineurin (2009) · cites this paper as [40]
The Results section reports that Hsp90 depletion reduced growth rates, supporting that part of the claim. It also says the depletion had little effect on stationary-phase cell density (Figure S1D), rather than reducing it to approximately half the wild-type density. The same section reports moderately reduced Hsp90 in the MAL2p-HSP90/hsp90Δ strain grown in maltose. (LLM, conf=0.89)
Experimental — accuracy not yet measuredPrevious work established that genetic reduction of Hsp90 levels enhances the efficacy of fluconazole in a murine model of disseminated C. albicans infection and that further genetic depletion of C. albicans Hsp90 results in complete clearance of an infection in the murine model.
“Our previous work established that genetic reduction of Hsp90 levels enhances the efficacy of fluconazole in a murine model of disseminated C. albicans infection [22] and that further genetic depletion of C. albicans Hsp90 results in complete clearance of an infection in the murine model [40].”
From Hsp90 Governs Echinocandin Resistance in the Pathogenic Yeast Candida albicans via Calcineurin (2009) · cites this paper as [40]
Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.
Experimental — accuracy not yet measuredThe UTR2-lacZ reporter is activated by calcium chloride and reports calcineurin activation.
“As expected, exposure of cells containing the UTR2-lacZ reporter to calcium chloride resulted in activation of calcineurin relative to the untreated control (P<0.001, ANOVA, Bonferroni's Multiple Comparison Test Figure 4C).”
From Hsp90 Governs Echinocandin Resistance in the Pathogenic Yeast Candida albicans via Calcineurin (2009) · cites this paper as [40]
Hsp90 modulates key virulence traits in C. albicans, such as morphogenesis, and genetic compromise of Hsp90 leads to clearance of otherwise lethal Candida or Aspergillus infections in animal models.
“Hsp90 also modulates key virulence traits in C. albicans, such as the ability to undergo morphogenesis, and in animal models, genetic compromise of Hsp90 function leads to clearance of otherwise lethal Candida or Aspergillus infections (Cowen et al. 2009; Shapiro et al. 2009).”
From Genetic analysis of Hsp90 function in <i>Cryptococcus neoformans</i> highlights key roles in stress tolerance and virulence (2022) · cites this paper as Shapiro et al. 2009
Hsp90 functions as a signaling hub, stabilizing various signal transducers that modulate key fungal virulence phenotypes.
“Hsp90 functions as a signaling hub, stabilizing various signal transducers that modulate key fungal virulence phenotypes (Cowen and Lindquist 2005; Shapiro et al. 2009; O’Meara et al. 2019; Hossain et al. 2020).”
From Genetic analysis of Hsp90 function in <i>Cryptococcus neoformans</i> highlights key roles in stress tolerance and virulence (2022) · cites this paper as Shapiro et al. 2009
In C. albicans, Hsp90 modulates cellular responses to antifungals by stabilizing components of the Pkc1-MAPK and calcineurin stress-response pathways.
“In C. albicans, Hsp90 modulates cellular responses to antifungals by stabilizing components of the Pkc1-MAPK and calcineurin stress-response pathways (Cowen and Lindquist 2005; Cowen et al. 2009; Shapiro et al. 2009).”
From Genetic analysis of Hsp90 function in <i>Cryptococcus neoformans</i> highlights key roles in stress tolerance and virulence (2022) · cites this paper as Shapiro et al. 2009
At elevated temperatures (circa 37°C), Hsp90 repression of Ras1-PKA signalling is relieved, leading to filamentation.
“At elevated temperatures (circa 37°C) this Hsp90 repression is relieved, leading to filamentation.”
From Fungal Hsp90: a biological transistor that tunes cellular outputs to thermal inputs (2012) · cites this paper as [115]
Hsp90 regulates morphogenesis in C. albicans by repressing Ras1-PKA signalling at relatively low temperatures.
“Hsp90 regulates morphogenesis in C. albicans by repressing Ras1-PKA signalling at relatively low temperatures115.”
From Fungal Hsp90: a biological transistor that tunes cellular outputs to thermal inputs (2012) · cites this paper as [115]
Hsp90 regulates morphogenesis of the leading human fungal pathogen Candida albicans.
“The molecular chaperone Hsp90 regulates morphogenesis of the leading human fungal pathogen Candida albicans.”
From Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression in<i>Candida albicans</i> (2012) · cites this paper as Shapiro et al., 2009
Hsp90 is a key temperature sensor governing morphogenesis, given that reduction of Hsp90 function bypasses the requirement for elevated temperature for cues such as serum to induce filamentous growth and that Hsp90 function is partially compromised in conditions that induce hyphal morphogenesis.
“Hsp90 is a key temperature sensor governing morphogenesis, given that reduction of Hsp90 function bypasses the requirement for elevated temperature for cues such as serum to induce filamentous growth and that Hsp90 function is partially compromised in conditions that induce hyphal morphogenesis (Shapiro et al., 2009).”
From Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression in<i>Candida albicans</i> (2012) · cites this paper as Shapiro et al., 2009
Hsp90 has been implicated as an important regulator of the temperature-dependent switch between yeast and filamentous growth in C. albicans.
“Recently the molecular chaperone heat shock protein 90 (Hsp90) has been implicated as an important regulator of the temperature-dependent switch between yeast and filamentous growth in C. albicans (Shapiro et al., 2009).”
From Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression in<i>Candida albicans</i> (2012) · cites this paper as Shapiro et al., 2009
Depletion of Hsp90 leads to clearance of kidney fungal burden in a mouse model of candidiasis.
“Depletion of Hsp90 also leads to clearance of kidney fungal burden in a mouse model of candidiasis (Shapiro et al., 2009).”
From Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression in<i>Candida albicans</i> (2012) · cites this paper as Shapiro et al., 2009
Hsp90 is an important molecular chaperone that governs key virulence traits in C. albicans.
“Hsp90 is an important molecular chaperone that governs key virulence traits in C. albicans (Cowen and Lindquist, 2005; Shapiro et al., 2009; Singh et al., 2009).”
From Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression in<i>Candida albicans</i> (2012) · cites this paper as Shapiro et al., 2009
Hsp90 regulates temperature-dependent morphogenesis by exerting a repressive effect on Ras1-PKA signaling, which is alleviated upon temperature elevation.
“Hsp90 regulates temperature-dependent morphogenesis by exerting a repressive effect on Ras1-PKA signaling, which is alleviated upon temperature elevation (Shapiro et al., 2009).”
From Cdc28 provides a molecular link between Hsp90, morphogenesis, and cell cycle progression in<i>Candida albicans</i> (2012) · cites this paper as Shapiro et al., 2009
In Candida albicans, Hsp90 governs yeast-to-hyphal transition, drug resistance, and biofilm formation, and is implicated in pathogenicity.
“Hsp90, an essential molecular chaperone [1,3,5,6], has been shown to govern various aspects of C. albicans pathogenicity determinants including morphological yeast to hyphal transition [7], emergence of drug resistance [8–10] and biofilm formation [11].”
From Heat shock protein 90 localizes to the surface and augments virulence factors of Cryptococcus neoformans (2017) · cites this paper as [7]
Hsp90 regulates the yeast-to-hyphal switch in C. albicans by repressing the Ras1-PKA signaling pathway.
“Interestingly Hsp90 has been shown to be the regulator of this switch by repressing the Ras1-PKA signaling pathway [7].”
From Heat shock protein 90 localizes to the surface and augments virulence factors of Cryptococcus neoformans (2017) · cites this paper as [7]
Hsp90 governs temperature-dependent morphogenesis in C. albicans.
“In addition to its role in enabling the emergence and maintenance of azole resistance, Hsp90 governs temperature-dependent morphogenesis in C. albicans (19).”
From Genetic Analysis of <i>Candida auris</i> Implicates Hsp90 in Morphogenesis and Azole Tolerance and Cdr1 in Azole Resistance (2019) · cites this paper as [19]
Hsp90 represses filamentous growth in C. albicans such that compromising Hsp90 function induces the yeast-to-filament transition by relieving repression on Ras1-PKA signaling.
“Hsp90 represses filamentous growth in C. albicans such that compromising Hsp90 function induces the yeast-to-filament transition by relieving repression on Ras1-protein kinase A (PKA) signaling (19).”
From Genetic Analysis of <i>Candida auris</i> Implicates Hsp90 in Morphogenesis and Azole Tolerance and Cdr1 in Azole Resistance (2019) · cites this paper as [19]
Depletion of Hsp90 induces filamentation by relieving Hsp90-mediated repression of the cAMP-PKA signaling pathway.
“Depletion of Hsp90 also induces filamentation by relieving Hsp90-mediated repression of the cAMP-PKA signaling pathway (181).”
From <i>Candida albicans</i> Biofilms and Human Disease (2015) · cites this paper as [181]
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Cites
Hsp90 as a capacitor for morphological evolution
Rutherford, S. L., & Lindquist, S. (1998) · Nature · doi:10.1038/24550 · Cited by 2,270 · see citing works
Pratt, W. B., & Toft, D. O. (2003) · Experimental Biology and Medicine · doi:10.1177/153537020322800201 · Cited by 1,478 · see citing works
Hsp90 as a capacitor of phenotypic variation
Queitsch, C., Sangster, T. A., & Lindquist, S. (2002) · Nature · doi:10.1038/nature749 · Cited by 1,372 · see citing works
Structure and mechanism of the Hsp90 molecular chaperone machinery
Pearl, L. H., & Prodromou, C. (2006) · Annual Review of Biochemistry · doi:10.1146/annurev.biochem.75.103004.142738 · Cited by 1,103 · see citing works
A Heat-Sensitive TRP Channel Expressed in Keratinocytes
Peier, A. M., Reeve, A. J., Andersson, D. A., Moqrich, A., Earley, T. J., Hergarden, A. C., Story, G. M., Colley, S., Hogenesch, J. B., McIntyre, P., et al. (2002) · Science · doi:10.1126/science.1073140 · Cited by 968 · see citing works
Signal Transduction Cascades Regulating Fungal Development and Virulence
Lengeler, K. B., Davidson, R. C., D'souza, C., Harashima, T., Shen, W.-C., Wang, P., Pan, X., Waugh, M., & Heitman, J. (2000) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.64.4.746-785.2000 · Cited by 915 · see citing works
Self-citationThe distinct morphogenic states of Candida albicans
Sudbery, P., Gow, N., & Berman, J. (2004) · Trends in Microbiology · doi:10.1016/j.tim.2004.05.008 · Cited by 876 · see citing works
Zhao, R., Davey, M., Hsu, Y.-C., Kaplanek, P., Tong, A., Parsons, A. B., Krogan, N., Cagney, G., Mai, D., Greenblatt, J., et al. (2005) · Cell · doi:10.1016/j.cell.2004.12.024 · Cited by 819 · see citing works
Hsp90 Potentiates the Rapid Evolution of New Traits: Drug Resistance in Diverse Fungi
Cowen, L. E., & Lindquist, S. (2005) · Science · doi:10.1126/science.1118370 · Cited by 698 · see citing works
Self-citationStoldt, V. R., Sonneborn, A., Leuker, C. E., & Ernst, J. F. (1997) · The EMBO Journal · doi:10.1093/emboj/16.8.1982 · Cited by 595 · see citing works
Candida albicans: A molecular revolution built on lessons from budding yeast
Berman, J., & Sudbery, P. E. (2002) · Nature Reviews Genetics · doi:10.1038/nrg948 · Cited by 578 · see citing works
Wandinger, S. K., Richter, K., & Büchner, J. (2008) · Journal of Biological Chemistry · doi:10.1074/jbc.r800007200 · Cited by 548 · see citing works
Regulation of Cell-Surface Genes and Biofilm Formation by the C. albicans Transcription Factor Bcr1p
Nobile, C. J., & Mitchell, A. P. (2005) · Current Biology · doi:10.1016/j.cub.2005.05.047 · Cited by 464 · see citing works
Stathopoulos, A. M., & Cyert, M. S. (1997) · Genes & Development · doi:10.1101/gad.11.24.3432 · Cited by 442 · see citing works
Genome-Wide Analysis of the Biology of Stress Responses through Heat Shock Transcription Factor
Hahn, J., Hu, Z., Thiele, D. J., & Iyer, V. R. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.12.5249-5256.2004 · Cited by 430 · see citing works
Cowen, 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 · see citing works
Self-citationFungal Adenylyl Cyclase Integrates CO2 Sensing with cAMP Signaling and Virulence
Klengel, T., Liang, W., Chaloupka, J., Ruoff, C., Schröppel, K., Naglik, J. R., Eckert, S. E., Mogensen, E. G., Haynes, K., Tuite, M. F., et al. (2005) · Current Biology · doi:10.1016/j.cub.2005.10.040 · Cited by 409 · see citing works
Morphogenesis in Candida albicans
Whiteway, M. S., & Bachewich, C. (2007) · Annual Review of Microbiology · doi:10.1146/annurev.micro.61.080706.093341 · Cited by 390 · see citing works
Contributions of hyphae and hypha-co-regulated genes to Candida albicans virulence
Kumamoto, C. A., & Vinces, M. D. (2005) · Cellular Microbiology · doi:10.1111/j.1462-5822.2005.00616.x · Cited by 388 · see citing works
Global Control of Dimorphism and Virulence in Fungi
Nemecek, J. C., Wüthrich, M., & Klein, B. S. (2006) · Science · doi:10.1126/science.1124105 · Cited by 379 · see citing works
Ras Signaling Is Required for Serum-Induced Hyphal Differentiation in Candida albicans
Feng, Q., Summers, E., Guo, B., & Fink, G. R. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.20.6339-6346.1999 · Cited by 347 · see citing works
Harnessing calcineurin as a novel anti-infective agent against invasive fungal infections.
Steinbach, W. J., Reedy, J. L., Cramer, R. A., Perfect, J. R., & Heitman, J. (2007) · Nature Reviews Microbiology · doi:10.1038/nrmicro1680 · Cited by 313 · see citing works
Self-citationThe evolution of fungal drug resistance: modulating the trajectory from genotype to phenotype.
Cowen, L. E. (2008) · Nature Reviews Microbiology · doi:10.1038/nrmicro1835 · Cited by 311 · see citing works
Self-citationMorita, M. T., Tanaka, Y., Kodama, T. S., Kyogoku, Y., Yanagi, H., & Yura, T. (1999) · Genes & Development · doi:10.1101/gad.13.6.655 · Cited by 309 · see citing works
Leberer, E., Harcus, D., Dignard, D., Johnson, L., Ushinsky, S. C., Thomas, D. Y., & Schröppel, K. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02672.x · Cited by 295 · see citing works
Xu, X.-L., Lee, R. T. H., Fang, H.-M., Wang, Y.-M., Li, R., Zou, H., Zhu, Y., & Wang, Y. (2008) · Cell Host & Microbe · doi:10.1016/j.chom.2008.05.014 · Cited by 289 · see citing works
Dimorphism and virulence in fungi
Klein, B. S., & Tebbets, B. (2007) · Current Opinion in Microbiology · doi:10.1016/j.mib.2007.04.002 · Cited by 282 · see citing works
Development and application of Hsp90 inhibitors
Solit, D. B., & Chiosis, G. (2007) · Drug Discovery Today · doi:10.1016/j.drudis.2007.10.007 · Cited by 251 · see citing works
Davis‐Hanna, A., Piispanen, A. E., Stateva, L. I., & Hogan, D. A. (2007) · Molecular Microbiology · doi:10.1111/j.1365-2958.2007.06013.x · Cited by 249 · see citing works
<i>CRZ1</i> , a target of the calcineurin pathway in <i>Candida albicans</i>
Karababa, M., Valentino, E., Pardini, G., Coste, A. T., Bille, J., & Sanglard, D. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.05037.x · Cited by 231 · see citing works
Guo, Y., Guettouche, T., Fenna, M., Boellmann, F., Pratt, W. B., Toft, D. O., Smith, D. F., & Voellmy, R. W. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105931200 · Cited by 221 · see citing works
Carlisle, P. L., Banerjee, M., Lazzell, A., Monteagudo, C., López-Ribot, J. L., & Kadosh, D. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804061106 · Cited by 215 · see citing works
Candida morphogenesis and host–pathogen interactions
Whiteway, M. S., & Oberholzer, U. (2004) · Current Opinion in Microbiology · doi:10.1016/j.mib.2004.06.005 · Cited by 196 · see citing works
Bockmühl, D. P., Krishnamurthy, S., Gerads, M., Sonneborn, A., & Ernst, J. F. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02688.x · Cited by 194 · see citing works
Self-Regulation of Candida albicans Population Size during GI Colonization
White, S. J., Rosenbach, A., Lephart, P., Nguyen, D. T., Benjamin, A., Tzipori, S. R., Whiteway, M. S., Mecsas, J. C., & Kumamoto, C. A. (2007) · PLoS Pathogens · doi:10.1371/journal.ppat.0030184 · Cited by 181 · see citing works
Sharkey, L. L., McNemar, M. D., Saporito-Irwin, S. M., Sypherd, P. S., & Fonzi, W. A. (1999) · Journal of Bacteriology · doi:10.1128/jb.181.17.5273-5279.1999 · Cited by 168 · see citing works
Chaperoning a cellular upheaval in malaria: Heat shock proteins in Plasmodium falciparum
Acharya, P., Kumar, R., & Tatu, U. S. (2007) · Molecular and Biochemical Parasitology · doi:10.1016/j.molbiopara.2007.01.009 · Cited by 150 · see citing works
Molecular mechanism of temperature sensing by the circadian clock of Neurospora crassaPreprint
Diernfellner, A. C. R., Schafmeier, T., Merrow, M. W., & Brunner, M. (2005) · Genes & Development · doi:10.1101/gad.345905 · Cited by 120 · see citing works
IRA2, an upstream negative regulator of RAS in yeast, is a RAS GTPase-activating protein.
Tanaka, K., Lin, B. K., Wood, D. R., & Tamanoi, F. (1991) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.88.2.468 · Cited by 112 · see citing works
Roy, J., Li, H., Hogan, P. G., & Cyert, M. (2007) · Molecular Cell · doi:10.1016/j.molcel.2007.02.014 · Cited by 101 · see citing works
Bahn, Y., Staab, J. F., & Sundstrom, P. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03692.x · Cited by 88 · see citing works
Fang, H., & Wang, Y. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2006.05248.x · Cited by 83 · see citing works
A concentration-dependent switch in the bacterial response to temperature
Salman, H., & Libchaber, A. J. (2007) · Nature Cell Biology · doi:10.1038/ncb1632 · Cited by 83 · see citing works
An essential role of the yeast pheromone-induced Ca2+ signal is to activate calcineurin.
Withee, J. L., Mulholland, J., Jeng, R. L., & Cyert, M. (1997) · Molecular Biology of the Cell · doi:10.1091/mbc.8.2.263 · Cited by 80 · see citing works
Howard, R. J., & Gow, N. A. R. (2007) · Springer eBooks · doi:10.1007/978-3-540-70618-2 · Cited by 72 · see citing works
Trimorphic stepping stones pave the way to fungal virulence
Bastidas, R. J., & Heitman, J. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0811994106 · Cited by 61 · see citing works
Self-citationIRA2, an upstream negative regulator of RAS in yeast, is a RAS GTPase protein
Tanaka, K. (1991) · Medical Entomology and Zoology · Cited by 35 · see citing works
Signal Transduction and Morphogenesis in Candida albicans
Brown, A. J. P., & Gow, N. A. R. (2001) · Springer eBooks · doi:10.1007/978-3-662-06101-5_3 · Cited by 18 · see citing works
Heat Shock Protein 90 Regulates Development in Dictyostelium discoideum
Sawarkar, R., Roy, N., Rao, S., Raman, S., Sivaramakrishnan, V., Suguna, K., & Tatu, U. S. (2008) · Journal of Molecular Biology · doi:10.1016/j.jmb.2008.08.006 · Cited by 13 · see citing works
Flagged first, then by citations
1 of the 50 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
<i>Candida albicans</i> pathogenicity mechanisms
Mayer, F. L., Wilson, D., & Hube, B. (2013) · Virulence · doi:10.4161/viru.22913 · Cited by 1,848 · see citing works
Growth of Candida albicans hyphae
Sudbery, P. E. (2011) · Nature Reviews Microbiology · doi:10.1038/nrmicro2636 · Cited by 1,110 · see citing works
<i>Candida albicans</i> Biofilms and Human Disease
Nobile, C. J., & Johnson, A. D. (2015) · Annual Review of Microbiology · doi:10.1146/annurev-micro-091014-104330 · Cited by 1,057 · see citing works
Candida albicans morphogenesis and host defence: discriminating invasion from colonization
Gow, N. A. R., van de Veerdonk, F. L., Brown, A. J. P., & Netea, M. G. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2711 · Cited by 888 · see citing works
Antifungal Drug Resistance: Molecular Mechanisms in <i>Candida albicans</i> and Beyond
Lee, Y., Puumala, E., Robbins, N., & Cowen, L. E. (2021) · Chemical Reviews · doi:10.1021/acs.chemrev.0c00199 · Cited by 801 · see citing works
Self-citationCandida albicans biofilms: development, regulation, and molecular mechanisms
Gulati, M., & Nobile, C. J. (2016) · Microbes and Infection · doi:10.1016/j.micinf.2016.01.002 · Cited by 738 · see citing works
Gao, Q., Jin, K., Ying, S., Zhang, Y., Xiao, G., Shang, Y., Duan, Z., Hu, X., Xie, X., Zhou, G., et al. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1001264 · Cited by 674 · see citing works
Development and regulation of single- and multi-species Candida albicans biofilms
Lohse, M. B., Gulati, M., Johnson, A. D., & Nobile, C. J. (2018) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2017.107 · Cited by 643 · see citing works
Candida auris: Epidemiology, biology, antifungal resistance, and virulence
Du, H., Bing, J., Hu, T., Ennis, C. L., Nobile, C. J., & Huang, G. (2020) · PLOS Pathogens · doi:10.1371/journal.ppat.1008921 · Cited by 609 · see citing works
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 · see citing works
Self-citationCandida albicans cell-type switching and functional plasticity in the mammalian host
Noble, S. M., Gianetti, B. A., & Witchley, J. N. (2016) · Nature Reviews Microbiology · doi:10.1038/nrmicro.2016.157 · Cited by 518 · see citing works
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 · see citing works
Self-citationDispersion as an Important Step in the Candida albicans Biofilm Developmental Cycle
Uppuluri, P., Chaturvedi, A. K., Srinivasan, A., Banerjee, M., Ramasubramaniam, A. K., Köhler, J. R., Kadosh, D., & Lopez-Ribot, J. L. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000828 · Cited by 432 · see citing works
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 · see citing works
Self-citationd’Enfert, C., Kaune, A.-K., Alaban, L. R., Chakraborty, S., Cole, N. L., Delavy, M., Kosmala, D., Marsaux, B., Fróis-Martins, R., Morelli, M., et al. (2020) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuaa060 · Cited by 351 · see citing works
LaFayette, 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 · see citing works
Self-citationHsp90 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 · see citing works
Self-citationVertebrate Endothermy Restricts Most Fungi as Potential Pathogens
Robert, V. A., & Casadevall, A. (2009) · The Journal of Infectious Diseases · doi:10.1086/644642 · Cited by 274 · see citing works
Antifungal Drugs: The Current Armamentarium and Development of New Agents
Robbins, N., Wright, G. D., & Cowen, L. E. (2016) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0002-2016 · Cited by 271 · see citing works
Self-citationAhmad, S., & Alfouzan, W. (2021) · Microorganisms · doi:10.3390/microorganisms9040807 · Cited by 269 · see citing works
Boyce, K. J., & Andrianopoulos, A. (2015) · FEMS Microbiology Reviews · doi:10.1093/femsre/fuv035 · Cited by 247 · see citing works
Combinatorial strategies for combating invasive fungal infections
Spitzer, M., Robbins, N., & Wright, G. D. (2016) · Virulence · doi:10.1080/21505594.2016.1196300 · Cited by 218 · see citing works
Elevated Cell Wall Chitin in Candida albicans Confers Echinocandin Resistance <i>In Vivo</i>
Lee, K. K., MacCallum, D. M., Jacobsen, M. D., Walker, L. A., Odds, F. C., Gow, N. A. R., & Munro, C. A. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00683-11 · Cited by 209 · see citing works
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 204 · see citing works
Self-citationCandida and Candidiasis—Opportunism Versus Pathogenicity: A Review of the Virulence Traits
Ciurea, C. N., Kosovski, I.-B., Mare, A. D., Toma, F., Pintea-Simon, I. A., & Man, A. (2020) · Microorganisms · doi:10.3390/microorganisms8060857 · Cited by 197 · see citing works
Candida albicans hyphal initiation and elongation
Lü, Y., Su, C., & Liu, H. (2014) · Trends in Microbiology · doi:10.1016/j.tim.2014.09.001 · Cited by 195 · see citing works
Pukkila-Worley, R., Peleg, A. Y., Tampakakis, E., & Mylonakis, E. E. (2009) · Eukaryotic Cell · doi:10.1128/ec.00163-09 · Cited by 192 · see citing works
Polke, M., Hube, B., & Jacobsen, I. D. (2015) · Advances in applied microbiology · doi:10.1016/bs.aambs.2014.12.002 · Cited by 188 · see citing works
The Ras/cAMP/PKA signaling pathway and virulence in <i>Candida albicans</i>
Hogan, D. A., & Sundstrom, P. (2009) · Future Microbiology · doi:10.2217/fmb.09.106 · Cited by 186 · see citing works
The metabolic basis of Candida albicans morphogenesis and quorum sensing.
Han, T.-L., Cannon, R. D., & Villas-Bôas, S. G. (2011) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2011.04.002 · Cited by 173 · see citing works
Lü, Y., Su, C., Wang, A., & Liu, H. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001105 · Cited by 163 · see citing works
Shapiro, R. S., & Cowen, L. E. (2012) · mBio · doi:10.1128/mbio.00238-12 · Cited by 145 · see citing works
Self-citationFrom Jekyll to Hyde: The Yeast–Hyphal Transition of Candida albicans
Chow, E. W. L., Pang, L. M., & Wang, Y. (2021) · Pathogens · doi:10.3390/pathogens10070859 · Cited by 144 · see citing works
Modulation of Morphogenesis in Candida albicans by Various Small Molecules
Shareck, J., & Belhumeur, P. (2011) · Eukaryotic Cell · doi:10.1128/ec.05030-11 · Cited by 142 · see citing works
Fungal persister cells: The basis for recalcitrant infections?
Wuyts, J., Van Dijck, P., & Holtappels, M. (2018) · PLOS Pathogens · doi:10.1371/journal.ppat.1007301 · Cited by 136 · see citing works
Heat Shock Protein 90 Is Required for Conidiation and Cell Wall Integrity in Aspergillus fumigatus
Lamoth, F., Juvvadi, P. R., Fortwendel, J. R., & Steinbach, W. J. (2012) · Eukaryotic Cell · doi:10.1128/ec.00032-12 · Cited by 136 · see citing works
Kim, S. H., Iyer, K. R., Pardeshi, L., Muñoz, J. F., Robbins, N., Cuomo, C. A., Wong, K. H., & Cowen, L. E. (2019) · mBio · doi:10.1128/mbio.02529-18 · Cited by 136 · see citing works
Self-citationLeach, M. D., Budge, S., Walker, L. A., Munro, C. A., Cowen, L. E., & Brown, A. J. P. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1003069 · Cited by 133 · see citing works
Self-citationHsp90 orchestrates stress response signaling governing fungal drug resistance
Cowen, L. E. (2009) · PLoS Pathogens · doi:10.1371/journal.ppat.1000471 · Cited by 130 · see citing works
Self-citationLysine Deacetylases Hda1 and Rpd3 Regulate Hsp90 Function thereby Governing Fungal Drug Resistance
Robbins, N., Leach, M. D., & Cowen, L. E. (2012) · Cell Reports · doi:10.1016/j.celrep.2012.08.035 · Cited by 126 · see citing works
Self-citationThe Future of Antifungal Drug Therapy: Novel Compounds and Targets
Mota Fernandes, C., Dasilva, D., Haranahalli, K., McCarthy, J. B., Mallamo, J., Ojima, I., & Del Poeta, M. (2021) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01719-20 · Cited by 124 · see citing works
Structural basis for species-selective targeting of Hsp90 in a pathogenic fungus
Whitesell, L., Robbins, N., Huang, D. S., McLellan, C. A., Shekhar-Guturja, T., LeBlanc, E. V., Nation, C. S., Hui, R., Hutchinson, A., Collins, C., et al. (2019) · Nature Communications · doi:10.1038/s41467-018-08248-w · Cited by 124 · see citing works
Self-citationEllepola, K., Truong, T., Liu, Y., Lin, Q., Lim, T. K., Lee, Y. M., Cao, T., Koo, H., & Seneviratne, C. J. (2019) · Infection and Immunity · doi:10.1128/iai.00339-19 · Cited by 122 · see citing works
Candida albicans Hyphae: From Growth Initiation to Invasion
Desai, J. (2018) · Journal of Fungi · doi:10.3390/jof4010010 · Cited by 117 · see citing works
Huang, G., Huang, Q., Wei, Y., Wang, Y., & Du, H. (2019) · Molecular Microbiology · doi:10.1111/mmi.14148 · Cited by 116 · see citing works
Diezmann, S., Michaut, M., Shapiro, R. S., Bader, G. D., & Cowen, L. E. (2012) · PLoS Genetics · doi:10.1371/journal.pgen.1002562 · Cited by 112 · see citing works
Self-citationGrahl, N., Demers, E. G., Lindsay, A. K., Harty, C. E., Willger, S. D., Piispanen, A. E., & Hogan, D. A. (2015) · PLOS Pathogens · doi:10.1371/journal.ppat.1005133 · Cited by 111 · see citing works
“Decreased Ras1 signaling by methylene blue depends on the GAP Ira2 and adenylate cyclase Cyr1 C. albicans Ras1 GTP-binding has been genetically shown to be controlled by a GEF, Cdc25, and a GAP, Ira2 [58,59].”
BackgroundFarnesol and Cyclic AMP Signaling Effects on the Hypha-to-Yeast Transition in Candida albicans
Lindsay, A. K., Deveau, A., Piispanen, A. E., & Hogan, D. A. (2012) · Eukaryotic Cell · doi:10.1128/ec.00144-12 · Cited by 110 · see citing works
Silva, S., Henriques, M., Hayes, A., Oliveira, R., Azeredo, J., & Williams, D. W. (2011) · Journal of Oral Pathology & Medicine · doi:10.1111/j.1600-0714.2010.00981.x · Cited by 108 · see citing works
Fungal Hsp90: a biological transistor that tunes cellular outputs to thermal inputs
Leach, M. D., Klipp, E., Cowen, L. E., & Brown, A. J. P. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2875 · Cited by 107 · see citing works
Self-citationNicholls, S., MacCallum, D. M., Kaffarnik, F., Selway, L., Peck, S. C., & Brown, A. J. P. (2010) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2010.08.010 · Cited by 107 · see citing works
Regulation of Candida albicans Hyphal Morphogenesis by Endogenous Signals
Kornitzer, D. (2019) · Journal of Fungi · doi:10.3390/jof5010021 · Cited by 105 · see citing works
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 104 · see citing works
Dual action antifungal small molecule modulates multidrug efflux and TOR signaling
Shekhar-Guturja, T., Gunaherath, G. M. K. B., Wijeratne, E. M. K., Lambert, J.-P., Averette, A. F., Lee, S. C., Kim, T., Bahn, Y.-S., Tripodi, F., Ammar, R., et al. (2016) · Nature Chemical Biology · doi:10.1038/nchembio.2165 · Cited by 101 · see citing works
Self-citationGong, Y., Li, T., Yu, C., & Sun, S. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00520 · Cited by 101 · see citing works
Leach, M. D., Farrer, R. A., Tan, K., Miao, Z., Walker, L. A., Cuomo, C. A., Wheeler, R. T., Brown, A. J. P., Wong, K. H., & Cowen, L. E. (2016) · Nature Communications · doi:10.1038/ncomms11704 · Cited by 100 · see citing works
Self-citationMayer, F. L., Wilson, D., Jacobsen, I. D., Miramón, P., Slesiona, S., Bohovych, I., Brown, A. J. P., & Hube, B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0038584 · Cited by 100 · see citing works
Candida Biofilms: An Update on Developmental Mechanisms and Therapeutic Challenges
de Barros, P. P., Rossoni, R. D., de Souza, C. M., Scorzoni, L., Fenley, J. D. C., & Junqueira, J. C. (2020) · Mycopathologia · doi:10.1007/s11046-020-00445-w · Cited by 99 · see citing works
Transcriptional control of hyphal morphogenesis in Candida albicans
Villa, S., Hamideh, M., Weinstock, A., Qasim, M. N., Hazbun, T. R., Sellam, A., Hernday, A. D., & Thangamani, S. (2020) · FEMS Yeast Research · doi:10.1093/femsyr/foaa005 · Cited by 93 · see citing works
The 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 93 · see citing works
Self-citationThe 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 · see citing works
Self-citationReduced TOR signaling sustains hyphal development inCandida albicansby lowering Hog1 basal activity
Su, C., Lü, Y., & Liu, H. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e12-06-0477 · Cited by 92 · see citing works
Opportunistic yeast pathogens: reservoirs, virulence mechanisms, and therapeutic strategies
Polvi, E. J., Li, X., O’Meara, T. R., Leach, M. D., & Cowen, L. E. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1860-z · Cited by 90 · see citing works
Self-citationCandida albicans White and Opaque Cells Undergo Distinct Programs of Filamentous Growth
Si, H., Hernday, A. D., Hirakawa, M. P., Johnson, A. D., & Bennett, R. J. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003210 · Cited by 87 · see citing works
Combinatorial stresses kill pathogenic<i>Candida</i>species
Kaloriti, D., Tillmann, A., Cook, E., Jacobsen, M., You, T., Lenardon, M., Ames, L., Barahona, M., Chandrasekaran, K., Coghill, G., et al. (2012) · Medical Mycology · doi:10.3109/13693786.2012.672770 · Cited by 86 · see citing works
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 · see citing works
Self-citationFungal MorphogenesisPreprint
Lin, X., Alspaugh, J. A., Liu, H., & Harris, S. (2014) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019679 · Cited by 82 · see citing works
Shapiro, R. S., Sellam, A., Tebbji, F., Whiteway, M., Nantel, A., & Cowen, L. E. (2012) · Current Biology · doi:10.1016/j.cub.2012.01.062 · Cited by 81 · see citing works
Self-citationFitness Trade-Offs Associated with the Evolution of Resistance to Antifungal Drug Combinations
Hill, J. A., O’Meara, T. R., & Cowen, L. E. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.01.009 · Cited by 80 · see citing works
Self-citationThe Significance of Lipids to Biofilm Formation in Candida albicans: An Emerging Perspective
Alim, D., Sircaik, S., & Panwar, S. L. (2018) · Journal of Fungi · doi:10.3390/jof4040140 · Cited by 76 · see citing works
Aspergillus terreus: Novel lessons learned on amphotericin B resistance
Posch, W., Blatzer, M., Wilflingseder, D., & Lass‐Flörl, C. (2018) · Medical Mycology · doi:10.1093/mmy/myx119 · Cited by 74 · see citing works
Advances in the structures, mechanisms and targeting of molecular chaperones
Gu, J., He, Y., He, C., Zhang, Q., Huang, Q., Bai, S., Wang, R., You, Q., & Wang, L. (2025) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-025-02166-2 · Cited by 72 · see citing works
A CRISPR Interference Platform for Efficient Genetic Repression in Candida albicans
Wensing, L. F., Sharma, J., Uthayakumar, D., Proteau, Y., Chavez, A., & Shapiro, R. S. (2019) · mSphere · doi:10.1128/msphere.00002-19 · Cited by 70 · see citing works
Self-citationRoles of Ras1 Membrane Localization during Candida albicans Hyphal Growth and Farnesol Response
Piispanen, A. E., Bonnefoi, O., Carden, S., Deveau, A., Bassilana, M., & Hogan, D. A. (2011) · Eukaryotic Cell · doi:10.1128/ec.05153-11 · Cited by 68 · see citing works
Senn, H., Shapiro, R. S., & Cowen, L. E. (2012) · Molecular Biology of the Cell · doi:10.1091/mbc.e11-08-0729 · Cited by 67 · see citing works
Self-citationFungal biofilm formation and its regulatory mechanism
Wang, D., Zeng, N., Li, C., Li, Z., Zhang, N., & Li, B. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e32766 · Cited by 67 · see citing works
EFG1, Everyone’s Favorite Gene in Candida albicans: A Comprehensive Literature Review
Glazier, V. E. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.855229 · Cited by 65 · see citing works
Ras Signaling Gets Fine-Tuned: Regulation of Multiple Pathogenic Traits of Candida albicans
Inglis, D. O., & Sherlock, G. (2013) · Eukaryotic Cell · doi:10.1128/ec.00094-13 · Cited by 65 · see citing works
The Role of Heat Shock Proteins in Regulating Receptor Signal Transduction
Streicher, J. M. (2019) · Molecular Pharmacology · doi:10.1124/mol.118.114652 · Cited by 65 · see citing works
Linking Cellular Morphogenesis with Antifungal Treatment and Susceptibility in Candida Pathogens
Sharma, J., Rosiana, S., Razzaq, I., & Shapiro, R. S. (2019) · Journal of Fungi · doi:10.3390/jof5010017 · Cited by 64 · see citing works
Self-citationLamoth, F., Juvvadi, P. R., Gehrke, C., Asfaw, Y. G., & Steinbach, W. J. (2014) · The Journal of Infectious Diseases · doi:10.1093/infdis/jit530 · Cited by 62 · see citing works
Muthamil, S., Prasath, K. G., Priya, A., Precilla, P., & Pandian, S. K. (2020) · Scientific Reports · doi:10.1038/s41598-020-61918-y · Cited by 62 · see citing works
Leach, M. D., Tyc, K. M., Brown, A. J. P., & Klipp, E. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032467 · Cited by 61 · see citing works
Chatterjee, S., & Tatu, U. (2017) · PLOS Neglected Tropical Diseases · doi:10.1371/journal.pntd.0005836 · Cited by 57 · see citing works
Heat shock protein 90 (Hsp90): A novel antifungal target against Aspergillus fumigatus
Lamoth, F., Juvvadi, P. R., & Steinbach, W. J. (2014) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2014.947239 · Cited by 57 · see citing works
Bui, D., Lee, Y., Lim, J. Y., Fu, M., Kim, J.-C., Choi, G. J., Son, H., & Lee, Y. (2016) · Scientific Reports · doi:10.1038/srep28154 · Cited by 57 · see citing works
Lin, C.-J., & Chen, Y.-L. (2018) · Journal of Fungi · doi:10.3390/jof4020068 · Cited by 55 · see citing works
Protein kinase A and fungal virulence
Fuller, K. K., & Rhodes, J. C. (2012) · Virulence · doi:10.4161/viru.19396 · Cited by 53 · see citing works
Study of Candida albicans and its interactions with the host: A mini review
Tsai, P.-W., Chen, Y.-T., Hsu, P., & Lan, C. (2013) · Biomedicine · doi:10.1016/j.biomed.2012.12.004 · Cited by 53 · see citing works
Mašek, J., Bartheldyová, E., Turánek-Knötigová, P., Škrabalová, M., Korvasová, Z., Plocková, J., Koudelka, Š., Škodová, P., Kulich, P., Křupka, M., et al. (2011) · Journal of Controlled Release · doi:10.1016/j.jconrel.2011.01.016 · Cited by 52 · see citing works
Xie, J. L., Grahl, N., Sless, T. J. L., Leach, M. D., Kim, S. H., Hogan, D. A., Robbins, N., & Cowen, L. E. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006405 · Cited by 52 · see citing works
Self-citationMorphology Changes in Human Fungal Pathogens upon Interaction with the Host
Li, Z., & Nielsen, K. (2017) · Journal of Fungi · doi:10.3390/jof3040066 · Cited by 52 · see citing works
Veri, A. O., Miao, Z., Shapiro, R. S., Tebbji, F., O’Meara, T. R., Kim, S. H., Colazo, J., Tan, K., Vyas, V. K., Whiteway, M., et al. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007270 · Cited by 51 · see citing works
Self-citationFrom Genes to Networks: The Regulatory Circuitry Controlling Candida albicans Morphogenesis
Basso, V., d’Enfert, C., Znaidi, S., & Bachellier‐Bassi, S. (2018) · Current topics in microbiology and immunology · doi:10.1007/82_2018_144 · Cited by 51 · see citing works
Antifungal resistance in Aspergillus terreus: A current scenario
Vahedi‐Shahandashti, R., & Lass‐Flörl, C. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103247 · Cited by 51 · see citing works
Koch, B., Barugahare, A. A., Lo, T. L., Huang, C., Schittenhelm, R. B., Powell, D. R., Beilharz, T. H., & Traven, A. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.10.080 · Cited by 50 · see citing works
Roles of Hsp90 in Candida albicans morphogenesis and virulence
Robbins, N., & Cowen, L. E. (2023) · Current Opinion in Microbiology · doi:10.1016/j.mib.2023.102351 · Cited by 50 · see citing works
Self-citationPolvi, E. J., Averette, A. F., Lee, S. C., Kim, T., Bahn, Y., Veri, A. O., Robbins, N., Heitman, J., & Cowen, L. E. (2016) · PLoS Genetics · doi:10.1371/journal.pgen.1006350 · Cited by 50 · see citing works
Self-citationO’Meara, T. R., O’Meara, M. J., Polvi, E. J., Pourhaghighi, M. R., Liston, S. D., Lin, Z.-Y., Veri, A. O., Emili, A., Gingras, A.-C., & Cowen, L. E. (2019) · PLoS Biology · doi:10.1371/journal.pbio.3000358 · Cited by 49 · see citing works
Self-citationCoupling temperature sensing and development
Shapiro, R. S., & Cowen, L. E. (2010) · Virulence · doi:10.4161/viru.1.1.10320 · Cited by 49 · see citing works
Self-citation
- Authors
- Shapiro, R. S., Uppuluri, P., Zaas, A. K., Collins, C., Senn, H., Perfect, J. R., Heitman, J., & Cowen, L. E.
- Affiliations
- University of Toronto (CA)
- Duke Medical Center (US)
- Corresponding author
- Cowen, Leah E.
- Venue
- Current Biology
- Publisher
- Elsevier BV
- Published
- 2009-04
- Volume
- 19
- Issue
- 8
- Pages
- 621-629
- ISSN
- 0960-9822 (ISSN-L)
- PMC
- PMC2735497
- OpenAlex
- W1967864456
- Cited by
- 311
- References
- 50
- Citations by year
- 2026: 8 · 2025: 14 · 2024: 14 · 2023: 11 · 2022: 10 · 2021: 25 · 2020: 20 · 2019: 18 · 2018: 23 · 2017: 15 · 2016: 28 · 2015: 19 · 2014: 16 · 2013: 18 · 2012: 24
- FWCI
- 9.67
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 1604 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Current Biology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (AI 73896, R56AI028388, AI28388, R01AI073896, R01AI028388, AI-50438, R01AI050438, K08AI065837)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heat shock proteins research
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Keywords
- HSP90, Candida albicans, fungal morphogenesis, yeast-to-hypha transition, temperature dependence, fungal virulence, drug resistance, molecular chaperones, antifungal therapy
- MeSH terms
- Animals, Candida albicans, Candidiasis, Fungal Proteins, Humans, Isoenzymes, Morphogenesis, Signal Transduction, Cyclic AMP-Dependent Protein Kinases, ras Proteins, HSP90 Heat-Shock Proteins, GTPase-Activating Proteins, Hyphae, Mice, Quorum Sensing, Cyclic Nucleotide Phosphodiesterases, Type 1, Cyclic Nucleotide Phosphodiesterases, Type 2
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