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The EPA2 adhesin encoding gene is responsive to oxidative stress in the opportunistic fungal pathogen Candida glabrata

Juárez-Cepeda, J., Orta-Zavalza, E., Cañas-Villamar, I., Arreola-Gómez, J., Pérez-Cornejo, G. P., Hernández-Carballo, C. Y., Gutiérrez-Escobedo, G., Castaño, I., & Peñas, A. D. L. (2015) · Current Genetics · doi:10.1007/s00294-015-0473-2 · Cited by 24 · see citing works

Candida glabrata is a successful pathogen: An artist manipulating the immune response

Castrejón-Jiménez, N. S., Castillo-Cruz, J., Baltierra‐Uribe, S. L., Hernández-González, J. C., & Estela, G.-P. B. (2022) · Microbiological Research · doi:10.1016/j.micres.2022.127038 · Cited by 28 · see citing works

Effect of oxidative stress on cell wall morphology in four pathogenic Candida species

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Candida spp. and phagocytosis: multiple evasion mechanisms

Oliver, J. C., Ferreira, C. B. R. J., Silva, N. C., & Dias, A. L. T. (2019) · Antonie van Leeuwenhoek · doi:10.1007/s10482-019-01271-x · Cited by 22 · see citing works

Roles of vacuolar H+-ATPase in the oxidative stress response ofCandida glabrata

Nishikawa, H., Miyazaki, T., Nakayama, H., Minematsu, A., Yamauchi, S., Yamashita, K., Takazono, T., Shimamura, S., Nakamura, S., Izumikawa, K., et al. (2016) · FEMS Yeast Research · doi:10.1093/femsyr/fow054 · Cited by 22 · see citing works

Modulatory immune responses in fungal infection associated with organ transplant - advancements, management, and challenges

Elalouf, A., Elalouf, H., & Rosenfeld, A. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1292625 · Cited by 20 · see citing works

Stress Response in Candida Glabrata : Pieces of a Fragmented Picture

Jandric, Z., & Schüller, C. (2011) · Future Microbiology · doi:10.2217/fmb.11.131 · Cited by 19 · see citing works

Mutation of the CgPDR16 gene attenuates azole tolerance and biofilm production in pathogenic Candida glabrata

Culakova, H., Džugasová, V., Perzelova, J., Gbelská, Y., & Šubík, J. (2013) · Yeast · doi:10.1002/yea.2978 · Cited by 18 · see citing works

Oxidative stress response and adaptation to H2O2 in the model eukaryote Saccharomyces cerevisiae and its human pathogenic relatives Candida albicans and Candida glabrata

Diezmann, S. (2014) · Fungal Biology Reviews · doi:10.1016/j.fbr.2014.12.001 · Cited by 17 · see citing works

Candida glabratasurvives and replicates in human osteoblasts

Muñóz-Duarte, A. R., Castrejón-Jiménez, N. S., Baltierra‐Uribe, S. L., Pérez-Rangel, S. J., Carapia-Minero, N., Castañeda‐Sánchez, J. I., Luna‐Herrera, J., López‐Santiago, R., Rodríguez-Tovar, A. V., & García‐Pérez, B. E. (2016) · Pathogens and Disease · doi:10.1093/femspd/ftw030 · Cited by 16 · see citing works

Genome-Wide Response to Drugs and Stress in the Pathogenic Yeast Candida glabrata

Pais, P., Galocha, M., & Teixeira, M. C. (2019) · Progress in molecular and subcellular biology · doi:10.1007/978-3-030-13035-0_7 · Cited by 16 · see citing works

Transcriptomic analysis reveals global and temporal transcription changes during Candida glabrata adaptation to an oxidative environment

Sethiya, P., Rai, M. N., Rai, R., Parsania, C., Tan, K., & Wong, K. H. (2019) · Fungal Biology · doi:10.1016/j.funbio.2019.12.005 · Cited by 15 · see citing works

Characterization of thiamine uptake and utilization in Candida spp. subjected to oxidative stress

Wolak, N., Tomasi, M., Kozik, A., & Rąpała‐Kozik, M. (2015) · Acta Biochimica Polonica · doi:10.18388/abp.2015_1044 · Cited by 14 · see citing works

Essential Role of CgErg6p in Maintaining Oxidative Stress Tolerance and Iron Homeostasis in Candida glabrata

Eliaš, D., Hervay, N. T., Bujdoš, M., & Gbelská, Y. (2023) · Journal of Fungi · doi:10.3390/jof9050579 · Cited by 12 · see citing works

Genetic interaction of the stress response factors ChAP1 and Skn7 in the maize pathogenCochliobolus heterostrophus

Shalaby, S., Larkov, O., Lamdan, N. L., & Horwitz, B. A. (2013) · FEMS Microbiology Letters · doi:10.1111/1574-6968.12314 · Cited by 12 · see citing works

Stress response and expression of fluconazole resistance associated genes in the pathogenic yeast Candida glabrata deleted in the CgPDR16 gene

Culakova, H., Dzugasova, V., Valencikova, R., Gbelska, Y., & Subik, J. (2015) · Microbiological Research · doi:10.1016/j.micres.2015.03.004 · Cited by 11 · see citing works

Machine learning reveals genes impacting oxidative stress resistance across yeasts

Aranguiz, K., Horianopoulos, L. C., Elkin, L., Abá, K. S., Jordahl, D., Overmyer, K. A., Wrobel, R. L., Coon, J. J., Shiu, S., Rokas, A., et al. (2025) · Nature Communications · doi:10.1038/s41467-025-60189-3 · Cited by 11 · see citing works

A new regulator in the crossroads of oxidative stress resistance and virulence in Candida glabrata : The transcription factor CgTog1

Pais, P., Vagueiro, S., Mil‐Homens, D., Pimenta, A. I., Viana, R., Okamoto, M., Chibana, H., Fialho, A. M., & Teixeira, M. C. (2020) · Virulence · doi:10.1080/21505594.2020.1839231 · Cited by 9 · see citing works

Stress Adaptation

Brown, A. J. P., Cowen, L. E., Pietro, A. D., & Quinn, J. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch21 · Cited by 11 · see citing works

Proteome Response of Meretrix Bivalves Hepatopancreas Exposed to Paralytic Shellfish Toxins Producing Dinoflagellate Gymnodinium catenatum

Chan, K.-K., Tam, N. F. Y., Ng, C., Kwok, C. S.-N., Xu, S. J., Sze, E. T.-P., & Lee, F. W. F. (2021) · Journal of Marine Science and Engineering · doi:10.3390/jmse9091039 · Cited by 9 · see citing works

Characterization of the Trr/Trx system in the fungal pathogen Candida glabrata

Gutiérrez‐Escobedo, G., Vázquez-Franco, N., López-Marmolejo, A. L., Luna-Arvizu, G., Cañas‐Villamar, I., Castaño, I., & Peñas, A. D. L. (2023) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2023.103799 · Cited by 9 · see citing works

Iodine induces toxicity against Candida albicans and Candida glabrata through oxidative stress

Cuellar-Rufino, S., Arroyo-Xochihua, O., Salazar-Luna, A., & Arroyo-Helguera, O. E. (2022) · Iranian Journal of Microbiology · doi:10.18502/ijm.v14i2.9195 · Cited by 9 · see citing works

Decoding the role of oxidative stress resistance and alternative carbon substrate assimilation in the mature biofilm growth mode of Candida glabrata

Raj, K., Paul, D., Rishi, P., Shukla, G., Dhotre, D. P., & YogeshSouche (2024) · BMC Microbiology · doi:10.1186/s12866-024-03274-9 · Cited by 8 · see citing works

Limosilactobacillus reuteri 29A Cell-Free Supernatant Antibiofilm and Antagonistic Effects in Murine Model of Vulvovaginal Candidiasis

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The Gcn5-Ada2-Ada3 histone acetyltransferase module has divergent roles in pathogenesis of <i>Candida glabrata</i>

Lin, C.-J., Yang, S.-Y., Hsu, L.-H., Yu, S.-J., & Chen, Y.-L. (2023) · Medical Mycology · doi:10.1093/mmy/myad004 · Cited by 7 · see citing works

Functional Characterization of a Novel Oxidative Stress Protection Protein in the Pathogenic Yeast Candida glabrata

Usher, J., Chaudhari, Y., Attah, V., Ho, H.-L., & Haynes, K. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.530915 · Cited by 5 · see citing works

Fungus Development and Reactive Oxygen: Phytopathological Aspects

Aver‘yanov, A. A., Belozerskaya, T. A., & Гесслер, Н. Н. (2012) · Springer eBooks · doi:10.1007/978-94-007-4264-2_17 · Cited by 5 · see citing works

New insights on Drug's design against candidiasis on the fructose biphosphate aldolase (Fba1) and the pyruvate kinase (Pk) of Candida glabrata

Maqueda-Cabrera, E. E., Castillo‐Baltazar, A., Vázquez-López, N. A., Almanza-Villegas, M., Ramírez‐Apán, M. T., Ortega-Alfaro, M. C., López‐Cortés, J. G., Moreno, A., & Cuéllar‐Cruz, M. (2025) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2025.102175 · Cited by 4 · see citing works

The arginine transporter Can1 negatively regulates biofilm formation in yeasts

Nishimura, A., Tanahashi, R., Nakagami, K., Morioka, Y., & Takagi, H. (2024) · Frontiers in Microbiology · doi:10.3389/fmicb.2024.1419530 · Cited by 3 · see citing works

Enhancement of ROS Production by Catechin Is a Primary Effect of Increased Azole Efficacy in Nakaseomyces glabratus (Candida glabrata) Cells Lacking the ERG6 Gene

Hervay, N. T., Eliaš, D., Černáková, L., Jacko, J., Habová, M., Chovancová, N., & Gbelská, Y. (2024) · Pathogens · doi:10.3390/pathogens13100834 · Cited by 3 · see citing works

Sex and Virulence in Basidiomycete Pathogens

Bakkeren, G., Kruzel, E. K., & Hull, C. M. (2012) · doi:10.1002/9781118308165.ch23 · Cited by 3 · see citing works

Engineering the antioxidant activity of Candida glabrata by enhancing malate biosynthesis

Zhu, P., Chen, J., Li, Y., & Sun, X. (2025) · Systems Microbiology and Biomanufacturing · doi:10.1007/s43393-025-00353-4 · Cited by 2 · see citing works

Characterization of Metabolomic Response of Candida spp. to Heavy Metal Exposure

Reyes-Sánchez, P. N., Chairez-Ávila, J. A., García-Aguirre, K. K., Esparza-Cordero, V., Romo-García, M. F., Medina-Llamas, J. C., & López-Ramos, J. E. (2025) · Microorganisms · doi:10.3390/microorganisms13102394 · Cited by 2 · see citing works

Antifungal effect of titanium oxide nanoparticles on Candida glabrata internalized in human macrophages

Gómez-Hernández, M. E., Baltierra‐Uribe, S. L., Castillo-Cruz, J., Mondragón‐Flores, R., González‐Pozos, S., Vidales-Hurtado, M. A., & García‐Pérez, B. E. (2025) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2025.1714083 · Cited by 2 · see citing works

Skn7 Regulates Response to Oxidative Stress in the Opportunistic Fungi Scedosporium apiospermum

Yaakoub, H., Mina, S., Kabbara, S., Marot, A., Papon, N., Calenda, A., & Bouchara, J. (2025) · Mycopathologia · doi:10.1007/s11046-025-01040-7 · Cited by 2 · see citing works

The histone deubiquitinase Ubp10 modulates stress response, drug resistance, and virulence in Candida glabrata

Chou, Y. Y., Lee, Y.-H., Hsu, L.-H., Huang, Y., & Chen, Y. (2025) · Medical Mycology · doi:10.1093/mmy/myaf126 · Cited by 1 · see citing works

Promising Therapies for Fungal Infection Based on the Study to Elucidate Mechanisms to Cope with Stress in Candida Species.

Hirai, K., Inukai, T., & Nakayama, H. (2016) · Medical Mycology Journal · doi:10.3314/mmj.16.007 · Cited by 2 · see citing works

Candida glabrata Hst1-Rfm1-Sum1 complex evolved to control virulence-related genes

Vázquez-Franco, N., Gutiérrez‐Escobedo, G., Juárez‐Reyes, A., Orta‐Zavalza, E., Castaño, I., & Peñas, A. D. L. (2021) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2021.103656 · Cited by 2 · see citing works

Candida glabrata and the host: a neglected affair

Ghosh, M., Raney, M., & Kaur, R. (2026) · Journal of Medical Microbiology · doi:10.1099/jmm.0.002161 · Cited by 1 · see citing works

The alkene 1-dodecene (C12) and the aromatic alcohols (tryptophol and tyrosol) present in the secretome of the fungal pathogen Candida glabrata activate the oxidative stress response

González-Ruiz, R., Montalvo-Arredondo, J. I., Gómez‐Hernández, N., Mancilla-Montelongo, G., Contreras-Bravo, Y., López-Ramos, J. E., Gutiérrez‐Escobedo, G., Castaño, I., & Peñas, A. D. L. (2026) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2026.104106 · Cited by 1 · see citing works

Antifungal Innate Immunity

Wong, S. S. W., Dellière, S., Lepas, M., & Aimanianda, V. (2025) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-85340-1_9 · Cited by 1 · see citing works

Host-Induced Stress Response in Human Pathogenic Fungi

Viana, R., Pais, P., Cavalheiro, M., Galocha, M., & Teixeira, M. C. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-819990-9.00035-4 · Cited by 1 · see citing works

Promising Therapies for Fungal Infection Based on the Study to Elucidate Mechanisms to Cope with Stress in Candida Species [Translated Article]

Hirai, K., Inukai, T., & Nakayama, H. (2017) · Medical Mycology Journal · doi:10.3314/mmj.17.007

Computational inference of the transcriptional regulatory network of Candida glabrata

Xu, N., & Liu, L. (2019) · FEMS Yeast Research · doi:10.1093/femsyr/foz036

Papel de las Especies Reactivas de Oxígeno en la biosíntesis de Penicilina G, Cefalosporina C y Lovastatina

León, M. E. B. (2021) · doi:10.24275/uami.pg15bf11c

Molecular analysis of Candida species in teeth with symptomatic irreversible pulpitis

Lopes, A. B. S., Arruda‐Vasconcelos, R., Louzada, L. M., Junior, E. P. D. G., Fagundes, P. I. D. G., Lopes, E. M., Bronzato, J. D., Furlan, M. I. K., & Gomes, B. P. F. A. (2026) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2026.106561

Étude du stress oxydant durant la phagocytose de la levure pathogène émergente Candida glabrata

Bouchab, L. (2016) · doi:10.70675/e027402dzbb6ez4c38z9611z7b93c3ddbf3d

Phenotypic and genotypic analysis of clonal clinical isolates of Nakaseomyces glabratus ( Candida glabrata )

López-Marmolejo, A. L., Hernández-Chávez, M. J., Gutiérrez‐Escobedo, G., Varela‐Castillo, P., Herrera-Basurto, M. S., Martínez‐Gamboa, R. A., González-Lara, M. F., Sifuentes‐Osornio, J., Peñas, A. D. L., & Castaño, I. (2026) · Medical Mycology · doi:10.1093/mmy/myag077

Implications of oxidative stress on microbial evolution

Kumari, A., & Singh, K. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-42857-9.00015-3

From confrontation to co-adaptation: the dynamic dialogue of Candida albicans and macrophages

Miramón, P., Wilson, H. B., & Lorenz, M. C. (2026) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00191-22

The oxidative stress response of the opportunistic fungal pathogen Candida glabrata

Briones-Martín-del-Campo, M., Orta‐Zavalza, E., Juárez‐Cepeda, J., Gutiérrez‐Escobedo, G., Cañas‐Villamar, I., Castaño, I., & Peñas, A. D. L. (2013) · Revista Iberoamericana de Micología · doi:10.1016/j.riam.2013.09.012 · Cited by 56 · see citing works

High Resistance to Oxidative Stress in the Fungal Pathogen <i>Candida glabrata</i> Is Mediated by a Single Catalase, Cta1p, and Is Controlled by the Transcription Factors Yap1p, Skn7p, Msn2p, and Msn4p

Cuéllar-Cruz, M., Briones-Martin-del-Campo, M., Cañas-Villamar, I., Montalvo-Arredondo, J., Riego-Ruiz, L., Castaño, I., & De Las Peñas, A. (2008) · Eukaryotic Cell · doi:10.1128/ec.00011-08 · Cited by 190 · see citing works

Combinatorial stress response of the fungal pathogen Candida glabrata

Puttnam, M. (2012) · Spiral (Imperial College London) · doi:10.25560/14491

Candida glabrata peroxiredoxins, Tsa1 and Tsa2, and sulfiredoxin, Srx1, protect against oxidative damage and are necessary for virulence

Gutiérrez‐Escobedo, G., Hernández-Carreón, O., Morales-Rojano, B., Revuelta-Rodríguez, B., Vázquez-Franco, N., Castaño, I., & Peñas, A. D. L. (2019) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2019.103287 · Cited by 29 · see citing works

A new regulator in the crossroads of oxidative stress resistance and virulence in Candida glabrata : The transcription factor CgTog1

Pais, P., Vagueiro, S., Mil‐Homens, D., Pimenta, A. I., Viana, R., Okamoto, M., Chibana, H., Fialho, A. M., & Teixeira, M. C. (2020) · Virulence · doi:10.1080/21505594.2020.1839231 · Cited by 9 · see citing works