Skn7p is involved in oxidative stress response and virulence of Candida glabrata

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 · cited 1× · see citing works

Isogenic strain construction and gene mapping in Candida albicans.

Fonzi, W. A., & Irwin, M. Y. (1993) · Genetics · doi:10.1093/genetics/134.3.717 · Cited by 1,695 · see citing works

Genome evolution in yeasts

Dujon, B., Sherman, D., Fischer, G., Durrens, P., Casaregola, S., Lafontaine, I., de Montigny, J., Marck, C., Neuvéglise, C., Talla, E., et al. (2004) · Nature · doi:10.1038/nature02579 · Cited by 1,623 · see citing works

Secular Trend of Hospital‐Acquired Candidemia among Intensive Care Unit Patients in the United States during 1989–1999

Trick, W. E., Fridkin, S. K., Edwards, J. R., Hajjeh, R. A., Gaynes, R. P., & Hospitals, T. N. N. I. S. S. (2002) · Clinical Infectious Diseases · doi:10.1086/342300 · Cited by 660 · see citing works

Yap1 and Skn7 Control Two Specialized Oxidative Stress Response Regulons in Yeast

Lee, J., Godon, C., Lagniel, G., Spector, D., Garin, J., Labarre, J., & Tolédano, M. B. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.23.16040 · Cited by 567 · see citing works

YAP1 dependent activation of TRX2 is essential for the response of Saccharomyces cerevisiae to oxidative stress by hydroperoxides.

Kuge, S., & Jones, N. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06304.x · Cited by 478 · see citing works

Cells have distinct mechanisms to maintain protection against different reactive oxygen species: Oxidative-stress-response genes

Thorpe, G. W., Fong, C. S., Alic, N., Higgins, V. J., & Dawes, I. W. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0305888101 · Cited by 450 · see citing works

Role of the glutathione/glutaredoxin and thioredoxin systems in yeast growth and response to stress conditions

Grant, C. M. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02283.x · Cited by 450 · see citing works

Twelve years of fluconazole in clinical practice: global trends in species distribution and fluconazole susceptibility of bloodstream isolates of Candida

Pfaller, M. A., & Diekema, D. J. (2004) · Clinical Microbiology and Infection · doi:10.1111/j.1470-9465.2004.t01-1-00844.x · Cited by 422 · see citing works

Complex cellular responses to reactive oxygen species

Temple, M. D., Perrone, G. G., & Dawes, I. W. (2005) · Trends in Cell Biology · doi:10.1016/j.tcb.2005.04.003 · Cited by 398 · see citing works

Copper- and zinc-containing superoxide dismutase (Cu/ZnSOD) is required for the protection of Candida albicans against oxidative stresses and the expression of its full virulence

Hwang, C., Rhie, G., Oh, J., Huh, W., Yim, H., & Kang, S.-O. (2002) · Microbiology · doi:10.1099/00221287-148-11-3705 · Cited by 293 · see citing works

The Skn7 response regulator controls gene expression in the oxidative stress response of the budding yeast Saccharomyces cerevisiae

Morgan, B. A., Banks, G. R., Toone, W. M., Raitt, D., Kuge, S., & Johnston, L. H. (1997) · The EMBO Journal · doi:10.1093/emboj/16.5.1035 · Cited by 291 · see citing works

Nicotinic Acid Limitation Regulates Silencing of <i>Candida</i> Adhesins During UTI

Domergue, R., Castaño, I., De Las Peñas, A., Zupancic, M., Lockatell, V., Hebel, J. R., Johnson, D., & Cormack, B. P. (2005) · Science · doi:10.1126/science.1108640 · Cited by 249 · see citing works

Mechanism of Increased Fluconazole Resistance in <i>Candida glabrata</i> during Prophylaxis

Bennett, J. E., Izumikawa, K., & Marr, K. A. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.5.1773-1777.2004 · Cited by 217 · see citing works

The PAR1 (YAP1/SNQ3) gene of Saccharomyces cerevisiae, ac-jun homologue, is involved in oxygen metabolism

Schnell, N. F., Krems, B., & Entian, K. (1992) · Current Genetics · doi:10.1007/bf00351681 · Cited by 205 · see citing works

Deletion of the Candida glabrata ERG3 and ERG11 genes: effect on cell viability, cell growth, sterol composition, and antifungal susceptibility

Geber, A., Hitchcock, C. A., Swartz, J. E., Pullen, F. S., Marsden, K. E., Kwon-Chung, K. J., & Bennett, J. E. (1995) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.39.12.2708 · Cited by 203 · see citing works

Cloning and Sequencing of a Candida albicans Catalase Gene and Effects of Disruption of This Gene

Wysong, D. R., Christin, L., Sugar, A. M., Robbins, P. W., & Diamond, R. D. (1998) · Infection and Immunity · doi:10.1128/iai.66.5.1953-1961.1998 · Cited by 201 · see citing works

A glutathione reductase mutant of yeast accumulates high levels of oxidized glutathione and requires thioredoxin for growth.

Muller, E. G. (1996) · Molecular Biology of the Cell · doi:10.1091/mbc.7.11.1805 · Cited by 200 · see citing works

Saccharomyces cerevisiae Expresses Three Phospholipid Hydroperoxide Glutathione Peroxidases

Avery, A. M., & Avery, S. V. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105672200 · Cited by 197 · 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

Efficient Homologous and Illegitimate Recombination in the Opportunistic Yeast Pathogen Candida glabrata

Cormack, B. P., & Falkow, S. (1999) · Genetics · doi:10.1093/genetics/151.3.979 · Cited by 180 · see citing works

Modular domain structure in the Candida glabrata adhesin Epa1p, a β1,6 glucan‐cross‐linked cell wall protein

Frieman, M., McCaffery, J. M., & Cormack, B. (2002) · Molecular Microbiology · doi:10.1046/j.1365-2958.2002.03166.x · Cited by 159 · see citing works

SKN7, a yeast multicopy suppressor of a mutation affecting cell wall beta-glucan assembly, encodes a product with domains homologous to prokaryotic two-component regulators and to heat shock transcription factors

Brown, J. L., North, S. M., & Bussey, H. (1993) · Journal of Bacteriology · doi:10.1128/jb.175.21.6908-6915.1993 · Cited by 153 · see citing works

The response regulator-like protein Pos9/Skn7 of Saccharomyces cerevisiae is involved in oxidative stress resistance

Krems, B., Charizanis, C., & Entian, K. (1996) · Current Genetics · doi:10.1007/bf02208613 · Cited by 153 · see citing works

Yeast Skn7p functions in a eukaryotic two‐component regulatory pathway.

Brown, J. L., Bussey, H., & Stewart, R. C. (1994) · The EMBO Journal · doi:10.1002/j.1460-2075.1994.tb06849.x · Cited by 149 · see citing works

A hyphal-specific chitin synthase gene (CHS2) is not essential for growth, dimorphism, or virulence of Candida albicans

Gow, N. A., Robbins, P. W., Lester, J. W., Brown, A. J., Fonzi, W. A., Chapman, T., & Kinsman, O. S. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.13.6216 · Cited by 145 · see citing works

Clinical Significance of Azole Antifungal Drug Cross-Resistance in Candida glabrata

Panackal, A. A., Gribskov, J. L., Staab, J. F., Kirby, K. A., Rinaldi, M. G., & Marr, K. A. (2006) · Journal of Clinical Microbiology · doi:10.1128/jcm.44.5.1740-1743.2006 · Cited by 144 · see citing works

Interactions of fungi with phagocytes

Mansour, M. K., & Levitz, S. M. (2002) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(02)00342-9 · Cited by 132 · see citing works

SKN7 of Candida albicans : Mutant Construction and Phenotype Analysis

Singh, P., Chauhan, N., Ghosh, A. K., Dixon, F., & Calderone, R. (2004) · Infection and Immunity · doi:10.1128/iai.72.4.2390-2394.2004 · Cited by 110 · see citing works

Mutants of Saccharomyces cerevisiae sensitive to oxidative and osmotic stress

Krems, B., Charizanis, C., & Entian, K. (1995) · Current Genetics · doi:10.1007/bf00311211 · Cited by 106 · see citing works

The bZip transcription factor Cgap1p is involved in multidrug resistance and required for activation of multidrug transporter gene CgFLR1 in Candida glabrata

Chen, K.-H., Miyazaki, T., Tsai, H., & Bennett, J. E. (2006) · Gene · doi:10.1016/j.gene.2006.08.010 · Cited by 95 · see citing works

Role of antioxidant enzymatic defences against oxidative stress (H 2 O 2 ) and the acquisition of oxidative tolerance in Candida albicans

Párraga, P. G., Hernández, J. A., & Argüelles, J. C. (2003) · Yeast · doi:10.1002/yea.1029 · Cited by 94 · see citing works

Variation in Susceptibility of Bloodstream Isolates of Candida glabrata to Fluconazole According to Patient Age and Geographic Location

Pfaller, M. A., Messer, S. A., Boyken, L. B., Tendolkar, S., Hollis, R. J., & Diekema, D. J. (2003) · Journal of Clinical Microbiology · doi:10.1128/jcm.41.5.2176-2179.2003 · Cited by 86 · see citing works

Identification and Characterization of anSKN7Homologue inCryptococcus neoformans

Wormley, F. L., Heinrich, G., Miller, J. L., Perfect, J. R., & Cox, G. M. (2005) · Infection and Immunity · doi:10.1128/iai.73.8.5022-5030.2005 · Cited by 76 · see citing works

Yeast oxidative stress response

Demasi, A. P. D., Pereira, G. A. G., & Netto, L. E. S. (2006) · FEBS Journal · doi:10.1111/j.1742-4658.2006.05116.x · Cited by 71 · see citing works

Function of <i>Candida glabrata</i> ABC transporter gene, <i>PDH1</i>

Izumikawa, K., Kakeya, H., Tsai, H., Grimberg, B., & Bennett, J. E. (2003) · Yeast · doi:10.1002/yea.962 · Cited by 67 · see citing works

Oxidative Stress Function of the Saccharomyces cerevisiae Skn7 Receiver Domain

He, X., Mulford, K. E., & Fassler, J. S. (2009) · Eukaryotic Cell · doi:10.1128/ec.00021-09 · Cited by 64 · see citing works

Efficacies of Fluconazole, Caspofungin, and Amphotericin B inCandida glabrata-Infected p47phox−/−Knockout Mice

Ju, J. Y., Polhamus, C., Marr, K. A., Holland, S. M., & Bennett, J. E. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.5.1240-1245.2002 · Cited by 48 · see citing works

Tyrosine is involved in protection from oxidative stress inSaccharomyces cerevisiae

Lupo, S., Aranda, C., Olivera, H., Riego‐Ruiz, L. R., González, A., Miranda-Ham, L., & Servín‐González, L. (1997) · Canadian Journal of Microbiology · doi:10.1139/m97-138 · Cited by 12 · see citing works

Kre29p is a novel nuclear protein involved in DNA repair and mitotic fidelity in Candida glabrata

Miyazaki, T., Tsai, H., & Bennett, J. E. (2006) · Current Genetics · doi:10.1007/s00294-006-0072-3 · Cited by 7 · see citing works

Biochemistry, cell biology and molecular biology of lipids ofSaccharomyces cerevisiae

Daum, G., Lees, N. D., Bard, M., & Dickson, R. (1998) · Yeast · doi:10.1002/(sici)1097-0061(199812)14:16

Candida glabrata: A review of its features and resistance

Rodrigues, C. F., Silva, S., & Henriques, M. (2014) · European Journal of Clinical Microbiology &amp; Infectious Diseases · doi:10.1007/s10096-013-2009-3 · Cited by 268 · see citing works

Oxidative stress response pathways in fungi

Yaakoub, H., Mina, S., Calenda, A., Bouchara, J., & Papon, N. (2022) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-022-04353-8 · Cited by 209 · see citing works

Coupling of transcriptional response to oxidative stress and secondary metabolism regulation in filamentous fungi

Montibus, M., Pinson‐Gadais, L., Richard-Forget, F. C., Barreau, C., & Ponts, N. (2013) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2013.829416 · Cited by 207 · see citing works

Candida glabrata: A Lot More Than Meets the Eye

Kumar, K., Askari, F., Sahu, M. S., & Kaur, R. (2019) · Microorganisms · doi:10.3390/microorganisms7020039 · Cited by 128 · see citing works

Stress Response and Pathogenicity of the Necrotrophic Fungal Pathogen Alternaria alternata

Chung, K.-R. (2012) · Scientifica · doi:10.6064/2012/635431 · Cited by 119 · see citing works

Intracellular survival ofCandida glabratain macrophages: immune evasion and persistence

Kasper, L., Seider, K., & Hube, B. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov042 · Cited by 115 · see citing works

Current progress on pathogenicity‐related transcription factors in Fusarium oxysporum

Zuriegat, Q., Zheng, Y., Liu, H., Wang, Z., & Yun, Y. (2021) · Molecular Plant Pathology · doi:10.1111/mpp.13068 · Cited by 110 · see citing works

Regulation of <i>Candida glabrata</i> oxidative stress resistance is adapted to host environment

Roetzer, A., Klopf, E., Gratz, N., Marcet-Houben, M., Hiller, E., Rupp, S., Gabaldón, T., Kovarik, P., & Schüller, C. (2011) · FEBS Letters · doi:10.1016/j.febslet.2010.12.006 · Cited by 90 · see citing works

Fungal Skn7 Stress Responses and Their Relationship to Virulence

Fassler, J. S., & West, A. H. (2010) · Eukaryotic Cell · doi:10.1128/ec.00245-10 · Cited by 87 · see citing works

Hosting Infection: Experimental Models to AssayCandidaVirulence

MacCallum, D. M. (2011) · International Journal of Microbiology · doi:10.1155/2012/363764 · Cited by 80 · see citing works

FgSKN 7 and FgATF 1 have overlapping functions in ascosporogenesis, pathogenesis and stress responses in F usarium graminearum

Jiang, C., Zhang, S., Zhang, Q., Tao, Y., Wang, C., & Xu, J. (2014) · Environmental Microbiology · doi:10.1111/1462-2920.12561 · Cited by 73 · see citing works

Non-albicans Candida Species: Immune Response, Evasion Mechanisms, and New Plant-Derived Alternative Therapies

Gómez-Gaviria, M., Ramírez-Sotelo, U., & Mora-Montes, H. M. (2022) · Journal of Fungi · doi:10.3390/jof9010011 · Cited by 68 · see citing works

Roles for SKN7 response regulator in stress resistance, conidiation and virulence in the citrus pathogen Alternaria alternata

Chen, L., Lin, C., & Chung, K.-R. (2012) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2012.07.006 · Cited by 64 · see citing works

Local silencing controls the oxidative stress response and the multidrug resistance in <i> <scp>C</scp> andida glabrata </i>

Orta‐Zavalza, E., Guerrero‐Serrano, G., Gutiérrez‐Escobedo, G., Cañas‐Villamar, I., Juárez‐Cepeda, J., Castaño, I., & De Las Peñas, A. (2013) · Molecular Microbiology · doi:10.1111/mmi.12247 · Cited by 61 · see citing works

Galleria mellonella as a host model to study Candida glabrata virulence and antifungal efficacy

Ames, L., Duxbury, S. J. N., Pawlowska, B. J., Ho, H.-L., Haynes, K., & Bates, S. (2017) · Virulence · doi:10.1080/21505594.2017.1347744 · Cited by 58 · see citing works

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

Coprinopsis cinerea Uses Laccase Lcc9 as a Defense Strategy To Eliminate Oxidative Stress during Fungal‐Fungal Interactions

Liu, J., Peng, C., Han, Q., Wang, M., Zhou, G., Ye, B., Xiao, Y., Fang, Z., & Kües, U. (2021) · Applied and Environmental Microbiology · doi:10.1128/aem.01760-21 · Cited by 50 · see citing works

Role of glutathione in the oxidative stress response in the fungal pathogen Candida glabrata

Gutiérrez-Escobedo, G., Orta-Zavalza, E., Castaño, I., & De Las Peñas, A. (2013) · Current Genetics · doi:10.1007/s00294-013-0390-1 · Cited by 47 · see citing works

Candida glabrata : a deadly companion?

Bolotin‐Fukuhara, M., & Fairhead, C. (2014) · Yeast · doi:10.1002/yea.3019 · Cited by 42 · see citing works

Stress tolerance phenotype of industrial yeast: industrial cases, cellular changes, and improvement strategies

Qiu, X., Zhang, J., Zhou, J., Fang, Z., Zhu, Z., Li, J., & Du, G. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09993-8 · Cited by 39 · see citing works

A network of paralogous stress response transcription factors in the human pathogen Candida glabrata

Merhej, J., Thiebaut, A., Blugeon, C., Pouch, J., Ali Chaouche, M. E. A., Camadro, J.-M., Le Crom, S., Lelandais, G., & Devaux, F. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.00645 · Cited by 36 · see citing works

Transcriptional Control of Drug Resistance, Virulence and Immune System Evasion in Pathogenic Fungi: A Cross-Species Comparison

Pais, P., Costa, C., Cavalheiro, M., Romão, D., & Teixeira, M. C. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00131 · Cited by 32 · see citing works

The two‐component response regulator Skn7 belongs to a network of transcription factors regulating morphogenesis in Candida albicans and independently limits morphogenesis‐induced ROS accumulation

Basso, V., Znaidi, S., Lagage, V., Cabral, V., Schönherr, F. A., LeibundGut‐Landmann, S., d’Enfert, C., & Bachellier‐Bassi, S. (2017) · Molecular Microbiology · doi:10.1111/mmi.13758 · Cited by 33 · see citing works

Host–pathogen interaction inCandida glabratainfection: current knowledge and implications for antifungal therapy

Rasheed, M., Battu, A., & Kaur, R. (2020) · Expert Review of Anti-infective Therapy · doi:10.1080/14787210.2020.1792773 · Cited by 30 · see citing works

Involvement of a putative response regulator Brrg-1 in the regulation of sporulation, sensitivity to fungicides, and osmotic stress in Botrytis cinerea

Yan, L., Yang, Q., Jiang, J., Michailides, T. J., & Ma, Z. (2010) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-010-3027-z · Cited by 30 · see citing works

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

Unraveling the Function of the Response Regulator BcSkn7 in the Stress Signaling Network of Botrytis cinerea

Viefhues, A., Schlathölter, I., Simon, A., Viaud, M., & Tudzynski, P. (2015) · Eukaryotic Cell · doi:10.1128/ec.00043-15 · Cited by 29 · see citing works

Overlapping responses between salt and oxidative stress in Debaryomyces hansenii

Ramos‐Moreno, L., Ramos, J., & Michán, C. (2019) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-019-2753-3 · Cited by 28 · see citing works

Local and regional chromatin silencing inCandida glabrata: consequences for adhesion and the response to stress

Peñas, A. D. L., Juárez‐Cepeda, J., López-Fuentes, E., Briones-Martín-del-Campo, M., Gutiérrez‐Escobedo, G., & Castaño, I. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov056 · Cited by 25 · see citing works

The glycosylphosphatidylinositol-linked aspartyl protease Yps1 is transcriptionally regulated by the calcineurin-Crz1 and Slt2 MAPK pathways in Candida glabrata: Transcriptional regulation of YPS1 in C. glabrata

Miyazaki, T., Izumikawa, K., Yamauchi, S., Inamine, T., Nagayoshi, Y., Saijo, T., Seki, M., Kakeya, H., Yamamoto, Y., Yanagihara, K., et al. (2011) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2011.00734.x · Cited by 23 · 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

Functional characterization of the regulators of calcineurin in Candida glabrata

Miyazaki, T., Izumikawa, K., Nagayoshi, Y., Saijo, T., Yamauchi, S., Morinaga, Y., Seki, M., Kakeya, H., Yamamoto, Y., Yanagihara, K., et al. (2011) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2011.00751.x · Cited by 17 · 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

Using in vivo transcriptomics and RNA enrichment to identify genes involved in virulence of Candida glabrata

Schrevens, S., Durandau, E., Tran, V. D. T., & Sanglard, D. (2022) · Virulence · doi:10.1080/21505594.2022.2095716 · 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

Stress Responses inCandida

Brown, A. J. P., Haynes, K., Gow, N. A. R., & Quinn, J. (2014) · ASM Press eBooks · doi:10.1128/9781555817176.ch15 · 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

Mitogen-activated protein kinase signaling pathways of the tangerine pathotype of Alternaria alternata

Chung, K.-R. (2013) · MAP Kinase · doi:10.4081/mk.2013.e4 · Cited by 14 · see citing works

A Host-Pathogen Interaction Screen Identifies <i>ada2</i> as a Mediator of <i>Candida glabrata</i> Defenses Against Reactive Oxygen Species

Kounatidis, I., Ames, L., Mistry, R., Ho, H.-L., Haynes, K., & Ligoxygakis, P. (2018) · G3 Genes Genomes Genetics · doi:10.1534/g3.118.200182 · Cited by 13 · 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

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

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 response regulator FoSkn7 participates in the pathogenicity of Fusariumoxysporum f. sp. cubense race 4 by conferring resistance to exogenous oxidative stress

Xing-Zhu, Q. I., Liu, L., & Wang, J. (2019) · Journal of General Plant Pathology · doi:10.1007/s10327-019-00858-6 · Cited by 8 · see citing works

Deubiquitination module is critical for oxidative stress response and biofilm formation in Candida glabrata

Huang, Y., Lee, Y.-H., Lin, C.-J., Hsu, L.-H., & Chen, Y. (2023) · Medical Mycology · doi:10.1093/mmy/myad099 · Cited by 7 · see citing works

Análisis de la cinética de expresión de genes durante la transición de micelio a levadura y la germinación levadura a micelio en Paracoccidioides brasiliensis

Hernández, O., Tamayo, D. P., Torres, I. P., Restrepo, Á., McEwen, J. G., & Garcı́a, A. M. (2011) · Biomédica · doi:10.7705/biomedica.v31i4.441 · Cited by 7 · see citing works

Evolution of regulatory networks inCandida glabrata: learning to live with the human host

Roy, S., & Thompson, D. A. (2015) · FEMS Yeast Research · doi:10.1093/femsyr/fov087 · Cited by 7 · see citing works

The regulatory network of Coprinopsis cinerea transcription factor Skn7 collaborates with bHLH1 during fungal-fungal interactions

Zhao, H., Pang, N., Meng, X., Qian, Q., Han, Q., Han, Q., Zhang, X., Fang, Z., & Liu, J. (2025) · Microbiology Spectrum · doi:10.1128/spectrum.00484-25 · Cited by 6 · see citing works

Response to Oxidative Stress in Sporothrix schenckii

Ruiz‐Baca, E., Adame-Soto, P. J., Alba-Fierro, C. A., Martínez-Rocha, A. L., Pérez‐Torres, A., López-Rodríguez, A., & Romo-Lozano, Y. (2025) · Journal of Fungi · doi:10.3390/jof11060440 · Cited by 4 · see citing works

Host-Fungal Interactions: Pathogenicity versus Immunity

Tavanti, A., Naglik, J. R., & Osherov, N. (2012) · International Journal of Microbiology · doi:10.1155/2012/562480 · Cited by 3 · 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

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

Current awareness on yeast

(2010) · Yeast · doi:10.1002/yea.1718

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

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

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

Etude des conséquences de la déplétion en soufre sur le statut redox du glutathion chez la levure pathogène Candida albicans

Vanparis, O. (2018) · theses.fr (ABES) · doi:10.70675/9ca39a19z090cz4464zbfbcz2bea821f9091

Transcriptional networks of the stress responses in the human pathogen Candida glabrata

Thiébaut, A. (2018) · theses.fr (ABES) · doi:10.70675/323c74a8z1ae4z4123za081zd0af3ecf65ae

Механизмы внутриклеточного ответа на окислительный стресс у Candida glabrata с делецией фактора транскрипции RPN4 на уровне протеомного анализа

(2026) · doi:10.18699/bgrs2026-306

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

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

Regulation of <i>Candida glabrata</i> oxidative stress resistance is adapted to host environment

Roetzer, A., Klopf, E., Gratz, N., Marcet-Houben, M., Hiller, E., Rupp, S., Gabaldón, T., Kovarik, P., & Schüller, C. (2011) · FEBS Letters · doi:10.1016/j.febslet.2010.12.006 · Cited by 90 · see citing works

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

Caracterización de la respuesta al estrés oxidante por H2O2 en la levadura patógena oportunista Candida glabrata.

Cañas‐Villamar, I. (2007) · REMERI - Red Mexicana de Repositorios Institucionales