The DOI matches its Crossref record; 80 of the 83 references it cites were found in a registry or an index.
Candida albicans specializations for iron homeostasis: from commensalism to virulence
Open accessAbstract
Candida albicans is a fungal commensal-pathogen that persistently associates with its mammalian hosts. Between the commensal and pathogenic lifestyles, this microorganism inhabits host niches that differ markedly in the levels of bioavailable iron. A number of recent studies have exposed C. albicans specializations for acquiring iron from specific host molecules in regions where iron is scarce, while also defending against iron-related toxicity in regions where iron occurs in surfeit. Together, these results point to a central role for iron homeostasis in the evolution of this important human pathogen.
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
“Elevated concentrations of hepcidin increase iron sequestration by macrophages and decrease duodenal iron absorption during inflammatory reactions and thus reduces plasma iron levels (Cassat and Skaar, 2013; Noble, 2013).”
From Iron at the Centre of Candida albicans Interactions (2018) · cites this paper as Noble, 2013
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“They regulate hyphal development and morphological transitions by modulating key transcription factors, including Sef1, Hap43, and Sfu1 (Noble 2013; Singh et al. 2011).”
From Aloe emodin disrupts Candida albicans mitochondrial iron homeostasis against its hyphal development and oral candidiasis (2026) · cites this paper as Noble 2013
Experimental — accuracy not yet measuredIn the citing paper
“Thus, C. albicans has evolved an intricate transcriptional program to regulate iron acquisition during commensal or pathogenic states [91].”
From Buried Treasure: Evolutionary Perspectives on Microbial Iron Piracy (2015) · cites this paper as [91]
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
Wisplinghoff, H., Bischoff, T., Tallent, S. M., Seifert, H., Wenzel, R. P., & Edmond, M. B. (2004) · Clinical Infectious Diseases · doi:10.1086/421946 · Cited by 4,496
Andrews, N. C. (1999) · New England Journal of Medicine · doi:10.1056/nejm199912233412607 · Cited by 2,130
Nosocomial Bloodstream Infections in United States Hospitals: A Three‐Year Analysis
Edmond, M. B., Wallace, S. E., McClish, D. K., Pfaller, M. A., Jones, R. N., & Wenzel, R. P. (1999) · Clinical Infectious Diseases · doi:10.1086/520192 · Cited by 1,387
Enterobactin: an archetype for microbial iron transport.
Raymond, K. N., Dertz, E. A., & Kim, S. S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0630018100 · Cited by 933
Chemistry and biology of eukaryotic iron metabolism
Aisen, P. (2001) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/s1357-2725(01)00063-2 · Cited by 804
Genetics and Assembly Line Enzymology of Siderophore Biosynthesis in Bacteria
Crosa, J. H., & Walsh, C. T. (2002) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.66.2.223-249.2002 · Cited by 797
The Battle for Iron between Bacterial Pathogens and Their Vertebrate Hosts
Skaar, E. P. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000949 · Cited by 796
Zaoutis, T. E., Argon, J., Chu, J., Berlin, J. A., Walsh, T. J., & Feudtner, C. (2005) · Clinical Infectious Diseases · doi:10.1086/496922 · Cited by 784
Blumberg, H. M., Jarvis, W. R., Soucie, J. M., Edwards, J. E., Patterson, J. E., Pfaller, M. A., Rangel‐Frausto, M. S., Rinaldi, M. G., Saiman, L., Wiblin, R. T., et al. (2001) · Clinical Infectious Diseases · doi:10.1086/321811 · Cited by 661
Hajjeh, R. A., Sofair, A. N., Harrison, L. H., Lyon, G. M., Arthington-Skaggs, B. A., Mirza, S. A., Phelan, M., Morgan, J., Lee-Yang, W., Ciblak, M. A., et al. (2004) · Journal of Clinical Microbiology · doi:10.1128/jcm.42.4.1519-1527.2004 · Cited by 649
Flagged first, then by citations
3 of the 83 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
The Spectrum of Fungi That Infects Humans
Kohler, J. R., Casadevall, A., & Perfect, J. (2015) · Cold Spring Harbor Perspectives in Medicine · doi:10.1101/cshperspect.a019273 · Cited by 364
d’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 377
Köhler, J. R., Hube, B., Puccia, R., Casadevall, A., & Perfect, J. R. (2017) · Microbiology Spectrum · doi:10.1128/microbiolspec.funk-0014-2016 · Cited by 318
Fungal Strategies to Evade the Host Immune Recognition
Hernández-Chávez, M., Pérez-García, L., Niño-Vega, G., & Mora-Montes, H. (2017) · Journal of Fungi · doi:10.3390/jof3040051 · Cited by 173
Iron acquisition in fungal pathogens of humans
Bairwa, G., Jung, W. H., & Kronstad, J. W. (2017) · Metallomics · doi:10.1039/c6mt00301j · Cited by 156
Mixed consortia in bioprocesses: role of microbial interactions
Ghosh, S., Chowdhury, R., & Bhattacharya, P. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-7448-1 · Cited by 135
Iron at the Centre of Candida albicans Interactions
Fourie, R., Kuloyo, O. O., Mochochoko, B. M., Albertyn, J., & Pohl, C. H. (2018) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2018.00185 · Cited by 118
Li, C. X., Gleason, J. E., Zhang, S. X., Bruno, V. M., Cormack, B. P., & Culotta, V. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1513447112 · Cited by 126
Buried Treasure: Evolutionary Perspectives on Microbial Iron Piracy
Barber, M. F., & Elde, N. C. (2015) · Trends in Genetics · doi:10.1016/j.tig.2015.09.001 · Cited by 118
Amorim-Vaz, S., Tran, V. D. T., Pradervand, S., Pagni, M., Coste, A. T., & Sanglard, D. (2015) · mBio · doi:10.1128/mbio.00942-15 · Cited by 81
Iron–sulfur cluster signaling: The common thread in fungal iron regulation
Gupta, M., & Outten, C. E. (2020) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2020.02.008 · Cited by 71
Srivastava, V. K., Suneetha, K. J., & Kaur, R. (2014) · Biochemical Journal · doi:10.1042/bj20140598 · Cited by 69
Anticandidal Effect and Mechanisms of Monoterpenoid, Perillyl Alcohol against Candida albicans
Ansari, M. A., Fatima, Z., & Hameed, S. (2016) · PLoS ONE · doi:10.1371/journal.pone.0162465 · Cited by 66
Lapière, A., & Richard, M. L. (2022) · Gut Microbes · doi:10.1080/19490976.2022.2105610 · Cited by 61
Copper-only superoxide dismutase enzymes and iron starvation stress in Candida fungal pathogens
Schatzman, S. S., Peterson, R. L., Teka, M., He, B., Cabelli, D. E., Cormack, B. P., & Culotta, V. C. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.011084 · Cited by 54
Savage, K. A., Parquet, M. D. C., Allan, D. S., Davidson, R. J., Holbein, B. E., Lilly, E. A., & Fidel, P. L. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02576-17 · Cited by 53
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
Transferrin-mediated iron sequestration as a novel therapy for bacterial and fungal infections
Bruhn, K. W., & Spellberg, B. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.07.005 · Cited by 48
Adaptation of Candida Albicans to Commensalism in the Gut
Prieto, D., Correia, I., Plá, J., & Román, E. (2016) · Future Microbiology · doi:10.2217/fmb.16.1 · Cited by 51
A novel hybrid iron regulation network combines features from pathogenic and nonpathogenic yeasts
Gerwien, F., Safyan, A., Wisgott, S., Hille, F., Kaemmer, P., Linde, J., Brunke, S., Kasper, L., & Hube, B. (2016) · mBio · doi:10.1128/mbio.01782-16 · Cited by 47
Alves, V., Zamith‐Miranda, D., Frasés, S., & Nosanchuk, J. D. (2025) · Journal of Fungi · doi:10.3390/jof11020093 · Cited by 55
Xu, N., Dong, Y., Cheng, X., Yu, Q., Qian, K., Mao, J., Jia, C., Ding, X., Zhang, B., Chen, Y., et al. (2013) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2013.12.009 · Cited by 50
Adaptation to iron deficiency in human pathogenic fungi
Martínez‐Pastor, M. T., & Puig, S. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2020.118797 · Cited by 47
Znaidi, S., van Wijlick, L., Hernández-Cervantes, A., Sertour, N., Desseyn, J., Vincent, F., Atanasova, R., Gouyer, V., Munro, C. A., Bachellier‐Bassi, S., et al. (2018) · Cellular Microbiology · doi:10.1111/cmi.12890 · Cited by 46
Xu, N., Qian, K., Dong, Y., Chen, Y., Yu, Q., Zhang, B., Xing, L., & Li, M. (2014) · Research in Microbiology · doi:10.1016/j.resmic.2014.03.001 · Cited by 44
Pseudomonas phage inhibition of Candida albicans
Nazik, H., Joubert, L., Secor, P. R., Sweere, J. M., Bollyky, P. L., Sass, G., Cegelski, L., & Stevens, D. A. (2017) · Microbiology · doi:10.1099/mic.0.000539 · Cited by 44
Stanford, F. A., & Voigt, K. (2020) · Genes · doi:10.3390/genes11111296 · Cited by 45
Molecular basis of the regulation of iron homeostasis in fission and filamentous yeasts
Brault, A., Mourer, T., & Labbé, S. (2015) · IUBMB Life · doi:10.1002/iub.1441 · Cited by 40
The vaccines and antibodies associated with Als3p for treatment of Candida albicans infections
Sui, X., Yan, L., & Jiang, Y. (2017) · Vaccine · doi:10.1016/j.vaccine.2017.08.082 · Cited by 38
Bhattarai, K., Bhattarai, K., Kabir, M. E., Bastola, R., & Baral, B. (2021) · Advances in genetics · doi:10.1016/bs.adgen.2020.11.006 · Cited by 35
Do, E., Cho, Y., Kim, D., Kronstad, J. W., & Jung, W. H. (2020) · Genetics · doi:10.1534/genetics.120.303270 · Cited by 34
Regulators of commensal and pathogenic life‐styles of an opportunistic fungus— Candida albicans
Rai, L. S., van Wijlick, L., Bougnoux, M., Bachellier‐Bassi, S., & d’Enfert, C. (2021) · Yeast · doi:10.1002/yea.3550 · Cited by 40
Zinc Cluster Transcription Factors Alter Virulence in Candida albicans
Issi, L., Farrer, R. A., Pastor, K., Landry, B. D., Delorey, T. M., Bell, G. W., Thompson, D. A., Cuomo, C. A., & Rao, R. P. (2016) · Genetics · doi:10.1534/genetics.116.195024 · Cited by 33
Large-Scale Chromosomal Changes and Associated Fitness Consequences in Pathogenic Fungi
Forche, A. (2014) · Current Fungal Infection Reports · doi:10.1007/s12281-014-0181-2 · Cited by 33
The regulation of iron homeostasis in the fungal human pathogen Candida glabrata
Devaux, F., & Thiébaut, A. (2019) · Microbiology · doi:10.1099/mic.0.000807 · Cited by 29
How much do we know about hemolytic capability of pathogenic Candida species?
Furlaneto, M. C., Góes, H. P., Perini, H. F., dos Santos, R. C., & Furlaneto-Maia, L. (2018) · Folia Microbiologica · doi:10.1007/s12223-018-0584-5 · Cited by 28
Chakraborty, T., Tóth, Z., Tóth, R., Vágvölgyi, C., & Gácser, A. (2020) · mSphere · doi:10.1128/msphere.00227-20 · Cited by 27
Padder, S. A., Ramzan, A., Tahir, I., Rehman, R. U., & Shah, A. H. (2022) · Critical Reviews in Microbiology · doi:10.1080/1040841x.2021.1935447 · Cited by 27
An Immunomodulatory Peptide Confers Protection in an Experimental Candidemia Murine Model
de Freitas, C. G., Lima, S. M. D. F., Freire, M. S., Cantuária, A. P. D. C., Oliveira-Júnior, N. G., dos Santos, T. S., Folha, J. D. S., Ribeiro, S. M., Dias, S. C., Rezende, T. M. B., et al. (2017) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02518-16 · Cited by 27
Dong, Y., Zhang, D., Yu, Q., Zhao, Q., Xiao, C., Zhang, K., Jia, C., Chen, S., Zhang, B., Zhang, B., et al. (2017) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2017.01.021 · Cited by 26
Zinc and Iron Homeostasis: Target-Based Drug Screening as New Route for Antifungal Drug Development
Simm, C., & May, R. C. (2019) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2019.00181 · Cited by 26
Duval, C., Macabiou, C., Garcia, C., Lesuisse, E., Camadro, J., & Auchère, F. (2019) · MicrobiologyOpen · doi:10.1002/mbo3.970 · Cited by 25
Antivirulence and avirulence genes in human pathogenic fungi
Siscar-Lewin, S., Hube, B., & Brunke, S. (2019) · Virulence · doi:10.1080/21505594.2019.1688753 · Cited by 25
Assessing pH‐dependent activities of virulence factors secreted by Candida albicans
Ramos‐Pardo, A., Castro‐Álvarez, R., Quindós, G., Eraso, E., Sevillano, E., & Kaberdin, V. R. (2023) · MicrobiologyOpen · doi:10.1002/mbo3.1342 · Cited by 24
Klimek, K., Strubińska, J., Czernel, G., Ginalska, G., & Gagoś, M. (2016) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2016.06.022 · Cited by 23
Sharma, V., Purushotham, R., & Kaur, R. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m116.751529 · Cited by 22
Prieto, D., Román, E., Alonso‐Monge, R., & Plá, J. (2017) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2017.00389 · Cited by 22
Romo, J. A., Zhang, H., Cai, H., Kadosh, D., Köhler, J. R., Saville, S. P., Wang, Y., & Lopez-Ribot, J. L. (2019) · mSphere · doi:10.1128/msphere.00620-19 · Cited by 21
Alkafeef, S. S., Lane, S., Yu, C., Zhou, T., Solis, N. V., Filler, S. G., Huang, L., & Liu, H. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008881 · Cited by 22
Candida albicans requires iron to sustain hyphal growth
Luo, G., Wang, T., Zhang, J., Zhang, P., & Lu, Y. (2021) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2021.05.039 · Cited by 18
Overexpression approaches to advance understanding of Candida albicans
Rai, L. S., van Wijlick, L., Chauvel, M., d’Enfert, C., Legrand, M., & Bachellier‐Bassi, S. (2021) · Molecular Microbiology · doi:10.1111/mmi.14818 · Cited by 17
The intricate link between iron, mitochondria and azoles in Candida species
Genechten, W. V., Vergauwen, R., & Dijck, P. V. (2023) · FEBS Journal · doi:10.1111/febs.16977 · Cited by 20
Nair, R., Shariq, M., Dhamgaye, S., Mukhopadhyay, C. K., Shaikh, S., & Prasad, R. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2016.11.021 · Cited by 19
Köhler, J. R., Hube, B., Puccia, R., Casadevall, A., & Perfect, J. R. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch39 · Cited by 18
Dhusia, K., Bajpai, A., & Ramteke, P. W. (2017) · Journal of Controlled Release · doi:10.1016/j.jconrel.2017.11.001 · Cited by 15
RetractedTUP1 -Mediated Filamentation in Candida Albicans Leads to Inability to Colonize the Mouse gut
Román, E., Huertas, B., Prieto, D., Diez‐Orejas, R., & Plá, J. (2018) · Future Microbiology · doi:10.2217/fmb-2018-0012 · Cited by 15
Hsu, P., Lu, T., Hung, P.-H., Jhou, Y., Amine, A. A. A., Liao, C., & Leu, J. (2021) · Molecular Biology and Evolution · doi:10.1093/molbev/msab192 · Cited by 15
Liu, S., Bu, Z., Zhang, X., Chen, Y., Sun, Q., Wu, F., Guo, S., Zhu, Y., & Tan, X. (2024) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2024.133216 · Cited by 14
Copper Availability Influences the Transcriptomic Response of Candida albicans to Fluconazole Stress
Hunsaker, E. W., Yu, C.-H. A., & Franz, K. J. (2021) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkab065 · Cited by 14
Román, E., Prieto, D., Hidalgo-Vico, S., Alonso‐Monge, R., & Plá, J. (2023) · Virulence · doi:10.1080/21505594.2023.2174294 · Cited by 13
Wangsanut, T., Ghosh, A. K., Metzger, P. G., Fonzi, W. A., & Rolfes, R. J. (2017) · mSphere · doi:10.1128/msphere.00161-17 · Cited by 12
van Wijlick, L., Znaidi, S., Hernández-Cervantes, A., Basso, V., Bachellier‐Bassi, S., & d’Enfert, C. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.960884 · Cited by 13
Souto, X. M., Ramos, L. S., Branquinha, M. H., & dos Santos, A. L. S. (2018) · Folia Microbiologica · doi:10.1007/s12223-018-0651-y · Cited by 11
Sahoo, B., Goyal, R., Dutta, S., Joshi, P., & Sanyal, K. (2025) · ACS Infectious Diseases · doi:10.1021/acsinfecdis.5c00079 · Cited by 13
Fallah, S., Duncan, D., Reichl, K. D., Smith, M. J., Wang, W., Porco, J. A. J., Brown, L. E., Whitesell, L. J., Robbins, N., & Cowen, L. E. (2024) · Microbiology Spectrum · doi:10.1128/spectrum.04095-23 · Cited by 10
Srivastav, M. K., Agarwal, N., Poonia, P., & Natarajan, K. (2021) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2021.100727 · Cited by 8
Bypass of Dfi1 Regulation of Candida albicans Invasive Filamentation by Iron Limitation
Junier, A., Weeks, A., Alcaraz, Y., & Kumamoto, C. A. (2022) · mSphere · doi:10.1128/msphere.00779-21 · Cited by 7
Strain variation in the Candida albicans iron limitation response
Xiong, L., Goerlich, K., Do, E., & Mitchell, A. P. (2024) · mSphere · doi:10.1128/msphere.00372-24 · Cited by 8
Convergent Regulation of Candida albicans Aft2 and Czf1 in Invasive and Opaque Filamentation
Xu, N., Dong, Y., Yu, Q., Zhang, B., Zhang, M., Jia, C., Chen, Y., Zhang, B., Xing, L., & Li, M. (2015) · Journal of Cellular Biochemistry · doi:10.1002/jcb.25146 · Cited by 8
The Glyoxylate Cycle Is Involved in White-Opaque Switching in Candida albicans
Hidalgo-Vico, S., Prieto, D., Alonso‐Monge, R., Román, E., & Plá, J. (2021) · Journal of Fungi · doi:10.3390/jof7070502 · Cited by 8
A response to iron involving carbon metabolism in the opportunistic fungal pathogen Candida albicans
Garg, R., Zhu, Z., Hernandez, F. G., Wang, Y., David, M. S., Bruno, V. M., & Culotta, V. (2025) · mSphere · doi:10.1128/msphere.00040-25 · Cited by 7
Insight into Virulence and Mechanisms of Amphotericin B Resistance in the Candida haemulonii Complex
Huang, Y., Su, Y., Chen, X., Xiao, M., & Xu, Y. (2024) · Journal of Fungi · doi:10.3390/jof10090615 · Cited by 8
Transcriptomic insights into Candida albicans adaptation to an anaerobic environment
Zeise, K. D., Erb‐Downward, J. R., & Huffnagle, G. B. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.03024-24 · Cited by 7
Candida albicans triggers qualitative and temporal responses in gut bacteria
Wang, F., Ye, Y., Xin, C., Liu, F., Zhao, C., Xiang, L., & Song, Z. (2021) · Journal de Mycologie Médicale · doi:10.1016/j.mycmed.2021.101164 · Cited by 7
Kumar, A., Francis, A., Hans, S., & Thakur, A. (2024) · Springer eBooks · doi:10.1007/978-981-97-4909-6_8 · Cited by 6
Druseikis, M. E., Mottola, A., & Berman, J. G. (2023) · Current Clinical Microbiology Reports · doi:10.1007/s40588-023-00189-3 · Cited by 5
Iron Acquisition in the Pathobiology of Candida albicans
Srivastav, M. K., Nair, R., & Natarajan, K. (2017) · Springer eBooks · doi:10.1007/978-3-319-50409-4_17 · Cited by 5
Role of Candida albicans mating in genetic variability and adaptation to the host
Correia, I., Román, E., Prieto, D., Hidalgo-Vico, S., Alonso‐Monge, R., & Plá, J. (2019) · Fungal Biology Reviews · doi:10.1016/j.fbr.2019.06.001 · Cited by 5
Lenarczyk, E., Oleksiak, D., & Janeczko, M. (2025) · Molecules · doi:10.3390/molecules30132735 · Cited by 5
Wor1‐regulated ferroxidases contribute to pigment formation in opaque cells of Candida albicans
Dai, B., Xu, Y., Gao, N., & Chen, J. (2020) · FEBS Open Bio · doi:10.1002/2211-5463.13070 · Cited by 5
Metallophores: How do human pathogens withdraw metal ions from the colonized host
Kozłowski, H., Piasta, K., Hecel, A., Rowińska‐Żyrek, M., & Gumienna‐Kontecka, E. (2022) · Elsevier eBooks · doi:10.1016/b978-0-12-823144-9.00086-8 · Cited by 4
Candida albicans Commensalism and Human Diseases
Chen, C., & Huang, X. (2018) · Springer eBooks · doi:10.1007/978-1-4939-7534-1_10 · Cited by 4
Pierrehumbert, A., Ischer, F., & Coste, A. T. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00873 · Cited by 3
Crosstalk between iron and flavins in the opportunistic fungal pathogen Candida albicans
David, M. S., Zhu, Z., McDonald, M. R., Badiee, M., Mortimer, I. P., Leung, A. K. L., & Culotta, V. (2025) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2025.110396 · Cited by 3
Yang, Y., Liao, Q., Zhang, J., Liu, Y., Li, L., Chen, S., & Gao, M. (2025) · Food Physics · doi:10.1016/j.foodp.2025.100070 · Cited by 3
Hirai, K., Inukai, T., & Nakayama, H. (2016) · Medical Mycology Journal · doi:10.3314/mmj.16.007 · Cited by 2
Ibrišimović, M., Mehmedinović, N. I., Dedić, J., Kesić, A., Marić, S., & Šestan, A. (2017) · World Congress on Medical Physics and Biomedical Engineering, September 7 - 12, 2009, Munich, Germany · doi:10.1007/978-981-10-4166-2_110 · Cited by 2
Prieto, D., & Plá, J. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2549-1_17 · Cited by 2
Hidalgo-Vico, S., Prieto, D., Alonso‐Monge, R., Román, E., Maufrais, C., d’Enfert, C., & Plá, J. (2024) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2024.103939 · Cited by 1
In-vitro antifungal activity of resorcinol against human fungal pathogen Candida albicans
Ansari, M. A., Tanwar, J., Fatima, Z., & Hameed, S. (2015) · Cited by 1
Infection-Associated Gene Expression—The Pathogen Perspective
Fanning, S., & Mitchell, A. P. (2017) · Springer eBooks · doi:10.1007/978-3-319-50409-4_13 · Cited by 1
Shen, J., Zhang, C., Lin, Y., Zhang, C., Zhou, J., Zhou, Y., Gou, L., Liao, G., Zhu, Z., Cheng, L., et al. (2026) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-026-13740-1
“They regulate hyphal development and morphological transitions by modulating key transcription factors, including Sef1 , Hap43 , and Sfu1 (Noble 2013; Singh et al. 2011).”
Hirai, K., Inukai, T., & Nakayama, H. (2017) · Medical Mycology Journal · doi:10.3314/mmj.17.007
Aaron, U. U., Abbey, S., & Azuonwu, O. (2017) · Journals & Books Hosting (International Knowledge Sharing Platform)
Siderophores in Antifungal Drug Discovery: A Computational Approach
Anusuya, S., Chithiravel, V., Gunasekar, A., & Anbazhagan, V. (2021) · Fungal biology · doi:10.1007/978-3-030-53077-8_11
The Fight for Iron: A Central Theme in Host-Pathogen Interactions
Hamad, M. A. (2025) · Springer eBooks · doi:10.1007/978-981-96-1305-2_11
Riboflavin Overproduction in Yeasts and Filamentous Fungi
Ruchała, J., Fedorovych, D. V., Wojdyła, D., Dmytruk, K. V., & Sibirny, A. А. (2025) · Grand challenges in biology and biotechnology · doi:10.1007/978-3-031-74726-7_9
Mathew, L., Carlson, S. L., Savage, M., Pardieu, C., O’Brien, M. B., Crawley, E., Harrow, P., Kaune, A.-K., Devlin, E., Priest, E. L., et al. (2026) · PLoS Biology · doi:10.1101/2025.09.17.676560 · Cited by 1
Environmental adaptation of Candida albicans : the examples of persistence and chlamydosporulation
Denega, I. (2020) · theses.fr (ABES) · doi:10.70675/748584ddzf6f4z4124z9237z56d0535d3352
Metadata
- Authors
- Noble, S. M.
- Affiliations
- University of California, San Francisco (US)
- Corresponding author
- Noble, Suzanne M
- ORCID
- Noble, Suzanne M
- Venue
- Current Opinion in Microbiology
- Publisher
- Elsevier BV
- Published
- 2013-12
- Volume
- 16
- Issue
- 6
- Pages
- 708-715
- ISSN
- 1369-5274 (ISSN-L)
- PMC
- PMC3855070
- OpenAlex
- W2093869242
- Cited by
- 104
- References
- 83
- Citations by year
- 2026: 5 · 2025: 10 · 2024: 6 · 2023: 4 · 2022: 6 · 2021: 11 · 2020: 9 · 2019: 7 · 2018: 8 · 2017: 17 · 2016: 9 · 2015: 7 · 2014: 4 · 2013: 1
- FWCI
- 0.89
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Current Opinion in Microbiology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Burroughs Wellcome Fund
- Pew Charitable Trusts
- National Institutes of Health (R21AI099659-01)
- Topics
- Health Sciences › Medicine › Infectious Diseases › Antifungal resistance and susceptibility
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Health Sciences › Medicine › Infectious Diseases › Fungal Infections and Studies
- Keywords
- Candida albicans, iron homeostasis, iron acquisition, iron toxicity, commensalism, fungal virulence, host-pathogen interaction, iron starvation
- MeSH terms
- Candida albicans, Homeostasis, Iron, Symbiosis, Virulence
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