Prostaglandin production during growth of Candida albicans biofilms

Nonfilamentous C. albicans Mutants Are Avirulent

Lo, H.-J., Köhler, J. R., DiDomenico, B., Loebenberg, D., Cacciapuoti, A., & Fink, G. R. (1997) · Cell · doi:10.1016/s0092-8674(00)80358-x · Cited by 1,809 · see citing works

Prostaglandins as modulators of immunity

Harris, S. G., Padilla, J., Koumas, L., Ray, D. M., & Phipps, R. P. (2002) · Trends in Immunology · doi:10.1016/s1471-4906(01)02154-8 · Cited by 1,168 · see citing works

Candida biofilms and their role in infection

Douglas, L. J. (2003) · Trends in Microbiology · doi:10.1016/s0966-842x(02)00002-1 · Cited by 1,150 · see citing works

Quorum Sensing in the Dimorphic Fungus <i>Candida albicans</i> Is Mediated by Farnesol

Hornby, J. M., Jensen, E. C., Lisec, A. D., Tasto, J. J., Jahnke, B., Shoemaker, R., Dussault, P., & Nickerson, K. W. (2001) · Applied and Environmental Microbiology · doi:10.1128/aem.67.7.2982-2992.2001 · Cited by 983 · see citing works

Cyclooxygenase inhibitors – current status and future prospects

Dannhardt, G., & Kiefer, W. (2001) · European Journal of Medicinal Chemistry · doi:10.1016/s0223-5234(01)01197-7 · Cited by 660 · see citing works

The application of biofilm science to the study and control of chronic bacterial infections

Costerton, W. J., Veeh, R., Shirtliff, M. E., Pasmore, M. E., Post, C., & Ehrlich, G. D. (2003) · Journal of Clinical Investigation · doi:10.1172/jci20365 · Cited by 650 · see citing works

The application of biofilm science to the study and control of chronic bacterial infections

Costerton, W. J., Veeh, R., Shirtliff, M. E., Pasmore, M. E., Post, C., & Ehrlich, G. D. (2003) · Journal of Clinical Investigation · doi:10.1172/jci200320365 · Cited by 632 · see citing works

Biofilm formation by Candida species on the surface of catheter materials in vitro

Hawser, S. P., & Douglas, L. J. (1994) · Infection and Immunity · doi:10.1128/iai.62.3.915-921.1994 · Cited by 599 · see citing works

Tyrosol is a quorum-sensing molecule in Candida albicans

Chen, H., Fujita, M., Feng, Q., Clardy, J., & Fink, G. R. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0401416101 · Cited by 500 · see citing works

The filamentation pathway controlled by the Efg1 regulator protein is required for normal biofilm formation and development in<i>Candida albicans</i>

Ramage, G., VandeWalle, K., López-Ribot, J. L., & Wickes, B. L. (2002) · FEMS Microbiology Letters · doi:10.1016/s0378-1097(02)00853-4 · Cited by 334 · see citing works

Role of dimorphism in the development of Candida albicans biofilms

BAILLIE, G. S., & DOUGLAS, L. J. (1999) · Journal of Medical Microbiology · doi:10.1099/00222615-48-7-671 · Cited by 304 · see citing works

Pathogenic Yeasts Cryptococcus neoformans and Candida albicans Produce Immunomodulatory Prostaglandins

Noverr, M. C., Phare, S. M., Toews, G. B., Coffey, M., & Huffnagle, G. B. (2001) · Infection and Immunity · doi:10.1128/iai.69.5.2957-2963.2001 · Cited by 250 · see citing works

Production of Eicosanoids and Other Oxylipins by Pathogenic Eukaryotic Microbes

Noverr, M. C., Erb‐Downward, J. R., & Huffnagle, G. B. (2003) · Clinical Microbiology Reviews · doi:10.1128/cmr.16.3.517-533.2003 · Cited by 241 · see citing works

Effects of Aspirin and Other Nonsteroidal Anti-Inflammatory Drugs on Biofilms and Planktonic Cells of <i>Candida albicans</i>

Alem, M. A. S., & Douglas, L. J. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.1.41-47.2004 · Cited by 205 · see citing works

[48] Candida biofilms and their susceptibility to antifungal agents

Baillie, G. S., & Douglas, L. (1999) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(99)10050-8 · Cited by 160 · see citing works

Production of Prostaglandins and Leukotrienes by Pathogenic Fungi

Noverr, M. C., Toews, G. B., & Huffnagle, G. B. (2002) · Infection and Immunity · doi:10.1128/iai.70.1.400-402.2002 · Cited by 160 · see citing works

Prostaglandin E2 enhances and gamma interferon inhibits germ tube formation in Candida albicans

Kalo-Klein, A., & Witkin, S. S. (1990) · Infection and Immunity · doi:10.1128/iai.58.1.260-262.1990 · Cited by 93 · see citing works

Lack of Catheter Infection by the efg1 / efg1 cph1 / cph1 Double-Null Mutant, a Candida albicans Strain That Is Defective in Filamentous Growth

Lewis, R. E., Lo, H., RAAD, I. I., & Kontoyiannis, D. P. (2002) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.46.4.1153-1155.2002 · Cited by 64 · see citing works

The human vagina: normal flora considered as an in situ tissue-associated, adherent biofilm.

Domingue, P. A. G., Sadhu, K., Costerton, J. W., Bartlett, K., & Chow, A. W. (1991) · Sexually Transmitted Infections · doi:10.1136/sti.67.3.226 · Cited by 36 · see citing works

Applying insights from biofilm biology to drug development — can a new approach be developed?

Bjarnsholt, T., Ciofu, O., Molin, S., Givskov, M., & Høiby, N. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd4000 · Cited by 516 · see citing works

Oxylipins as developmental and host–fungal communication signals

Tsitsigiannis, D. Ι., & Keller, N. P. (2007) · Trends in Microbiology · doi:10.1016/j.tim.2007.01.005 · Cited by 333 · see citing works

Production of Tyrosol by Candida albicans Biofilms and Its Role in Quorum Sensing and Biofilm Development

Alem, M. A. S., Oteef, M. D. Y., Flowers, T. H., & Douglas, L. (2006) · Eukaryotic Cell · doi:10.1128/ec.00219-06 · Cited by 254 · see citing works

Candida albicans biofilm development, modeling a host–pathogen interaction

Nett, J., & Andes, D. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.06.007 · Cited by 210 · see citing works

Combination of fluconazole with non-antifungal agents: A promising approach to cope with resistant Candida albicans infections and insight into new antifungal agent discovery

Liu, S., Hou, Y., Chen, X., Gao, Y., Li, H., & Sun, S. (2014) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2013.12.009 · Cited by 148 · see citing works

New frontiers for anti-biofilm drug development

Ribeiro, S. M., Felício, M. R., Boas, E. V., Gonçalves, S., Costa, F. F., Samy, R. P., Santos, N. C., & Franco, O. L. (2016) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2016.02.006 · Cited by 136 · see citing works

Antifungal lock therapy

Walraven, C. J., & Lee, S. A. (2013) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01351-12 · Cited by 132 · see citing works

Morphogenesis Control in Candida albicans and Candida dubliniensis through Signaling Molecules Produced by Planktonic and Biofilm Cells

Martins, M. I. B. C., Henriques, M., Azeredo, J., Rocha, S. M., Coimbra, M. A., & Oliveira, R. (2007) · Eukaryotic Cell · doi:10.1128/ec.00252-07 · Cited by 126 · see citing works

Candida albicans Biofilms Do Not Trigger Reactive Oxygen Species and Evade Neutrophil Killing

Xie, Z., Thompson, A. K., Sobue, T., Kashleva, H., Xu, H., Vasilakos, J. P., & Dongari‐Bagtzoglou, A. I. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis607 · Cited by 114 · see citing works

Characterization of Prostaglandin E 2 Production by Candida albicans

Erb‐Downward, J. R., & Noverr, M. C. (2007) · Infection and Immunity · doi:10.1128/iai.00232-07 · Cited by 114 · see citing works

Microbial chemical signaling: a current perspective

Bandara, N., Lam, O., Jin, L., & Samaranayake, L. P. (2012) · Critical Reviews in Microbiology · doi:10.3109/1040841x.2011.652065 · Cited by 104 · see citing works

Lipid signaling in pathogenic fungi

Shea, J. M., & Poeta, M. D. (2006) · Current Opinion in Microbiology · doi:10.1016/j.mib.2006.06.003 · Cited by 91 · see citing works

Biocommunication of Fungi

Palková, Z., & Váchová, L. (. (2012) · Springer eBooks · doi:10.1007/978-94-007-4264-2 · Cited by 92 · see citing works

Candida albicans and Pseudomonas aeruginosa Interaction, with Focus on the Role of Eicosanoids

Fourie, R., Ells, R., Swart, C. W., Sebolai, O. M., Albertyn, J., & Pohl, C. H. (2016) · Frontiers in Physiology · doi:10.3389/fphys.2016.00064 · Cited by 87 · see citing works

Prostaglandin E2 from Candida albicans Stimulates the Growth of Staphylococcus aureus in Mixed Biofilms

Krause, J., Geginat, G., & Tammer, I. (2015) · PLoS ONE · doi:10.1371/journal.pone.0135404 · Cited by 80 · see citing works

The 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

Future directions for anti-biofilm therapeutics targetingCandida

Nett, J. E. (2014) · Expert Review of Anti-infective Therapy · doi:10.1586/14787210.2014.885838 · Cited by 77 · see citing works

Beyond Antagonism: The Interaction Between Candida Species and Pseudomonas aeruginosa

Fourie, R., & Pohl, C. H. (2019) · Journal of Fungi · doi:10.3390/jof5020034 · Cited by 75 · see citing works

In Vitro Interactions between Aspirin and Amphotericin B against Planktonic Cells and Biofilm Cells of Candida albicans and C. parapsilosis

Zhou, Y., Wang, G., Li, Y., Liu, Y., Song, Y., Zheng, W., Zhang, N., Hu, X., Shikun, Y., & Jia, J. (2012) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.06082-11 · Cited by 72 · see citing works

The Nonsteroidal Antiinflammatory Drug Diclofenac Potentiates the In Vivo Activity of Caspofungin Against Candida albicans Biofilms

Bink, A., Kucharíková, S., Neirinck, B., Vleugels, J., Dijck, P. V., Cammue, B. P. A., & Thevissen, K. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis594 · Cited by 71 · see citing works

Novel synergistic antibiofilm combinations for salvage of infected catheters

Venkatesh, M. P., Rong, L., RAAD, I. I., & Versalovic, J. A. (2009) · Journal of Medical Microbiology · doi:10.1099/jmm.0.009761-0 · Cited by 68 · see citing works

In vitro effects of micafungin against Candida biofilms on polystyrene and central venous catheter sections

Seidler, M. J., Salvenmoser, S., & Müller, F. C. (2006) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2006.07.024 · Cited by 63 · see citing works

Fungal Biofilms: In Vivo Models for Discovery of Anti-Biofilm Drugs

Nett, J. E., & Andes, D. R. (2015) · Microbiology Spectrum · doi:10.1128/microbiolspec.mb-0008-2014 · Cited by 62 · see citing works

Potential targets for the development of new antifungal drugs

Su, H., Han, L., & Huang, X. (2018) · The Journal of Antibiotics · doi:10.1038/s41429-018-0100-9 · Cited by 60 · see citing works

Potential Targets for Antifungal Drug Discovery Based on Growth and Virulence in Candida albicans

Li, X., Hou, Y., Yue, L.-T., Liu, S., Du, J., & Sun, S. (2015) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.00726-15 · Cited by 55 · see citing works

Candida albicans Biofilms Produce More Secreted Aspartyl Protease than the Planktonic Cells

Mendes, A., Mores, A. U., Carvalho, A. P., Rosa, R. T., Samaranayake, L. P., & Rosa, E. A. R. (2007) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.30.1813 · Cited by 54 · see citing works

Host defence against disseminatedCandida albicansinfection and implications for antifungal immunotherapy

Vonk, A. G., Netea, M. G., van der Meer, J. W. M., & Kullberg, B. J. (2006) · Expert Opinion on Biological Therapy · doi:10.1517/14712598.6.9.891 · Cited by 54 · see citing works

Effect of filamentation and mode of growth on antifungal susceptibility of Candida albicans

Watamoto, T., Samaranayake, L. P., Jayatilake, J. A. M. S., Egusa, H., Yatani, H., & Seneviratne, C. J. (2009) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2009.03.008 · Cited by 51 · see citing works

Arachidonic acid affects biofilm formation and PGE2 level in Candida albicans and non-albicans species in presence of subinhibitory concentration of fluconazole and terbinafine

Mishra, N. N., Ali, S., & Shukla, P. K. (2014) · The Brazilian Journal of Infectious Diseases · doi:10.1016/j.bjid.2013.09.006 · Cited by 47 · see citing works

Lipid Signaling in Pathogenic Fungi

Rhome, R. M., & Poeta, M. D. (2009) · Annual Review of Microbiology · doi:10.1146/annurev.micro.091208.073431 · Cited by 44 · see citing works

Small Molecule Inhibitors of the Candida albicans Budded-to-Hyphal Transition Act through Multiple Signaling Pathways

Midkiff, J., Borochoff-Porte, N., White, D., & Johnson, D. I. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025395 · Cited by 44 · see citing works

Metabolomic analysis of low and high biofilm-forming Helicobacter pylori strains

Wong, E. H. J., Ng, C. G., Goh, K., Vadivelu, J., Ho, B., & Loke, M. F. (2018) · Scientific Reports · doi:10.1038/s41598-018-19697-0 · Cited by 44 · see citing works

Cyclooxygenase inhibitors reduce biofilm formation and yeast-hypha conversion of fluconazole resistant Candida albicans

Abdelmegeed, E. S., & Shaaban, M. I. (2013) · The Journal of Microbiology · doi:10.1007/s12275-013-3052-6 · Cited by 39 · see citing works

Antifungal activity of some cyclooxygenase inhibitors on Candida albicans: PGE2-dependent mechanism

de Quadros, A. U., Bini, D., Pereira, P. A. T., Moroni, E. G., & Monteiro, M. C. (2011) · Folia Microbiologica · doi:10.1007/s12223-011-0049-6 · Cited by 39 · see citing works

Synergistic Antifungal Effect of Fluconazole Combined with Licofelone against Resistant Candida albicans

Liu, X., Li, T., Wang, D., Yang, Y., Sun, W., Liu, J., & Sun, S. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.02101 · Cited by 39 · see citing works

Oxylipin studies expose aspirin as antifungal

Kock, J. L. F., Sebolai, O. M., Pohl, C. H., van Wyk, P. W. J., & Lodolo, E. J. (2007) · FEMS Yeast Research · doi:10.1111/j.1567-1364.2007.00273.x · Cited by 38 · see citing works

Inhibitors of cellular signalling are cytotoxic or block the budded-to-hyphal transition in the pathogenic yeast Candida albicans

Toenjes, K. A., Stark, B. C., Brooks, K. M., & Johnson, D. I. (2009) · Journal of Medical Microbiology · doi:10.1099/jmm.0.006841-0 · Cited by 36 · see citing works

A Caleosin-Like Protein with Peroxygenase Activity Mediates Aspergillus flavus Development, Aflatoxin Accumulation, and Seed Infection

Hanano, A., Almousally, I., Shaban, M., & Blée, E. (2015) · Applied and Environmental Microbiology · doi:10.1128/aem.00867-15 · Cited by 34 · see citing works

Effect of inhibitors of arachidonic acid metabolism on prostaglandin E2 production by Candida albicans and Candida dubliniensis biofilms

Ells, R., Kock, J. L. F., Albertyn, J., Kemp, G., & Pohl, C. H. (2010) · Medical Microbiology and Immunology · doi:10.1007/s00430-010-0169-7 · Cited by 33 · see citing works

Plant-associated fungal biofilms—knowns and unknowns

Motaung, T. E., Peremore, C., Wingfield, B. D., & Steenkamp, E. T. (2020) · FEMS Microbiology Ecology · doi:10.1093/femsec/fiaa224 · Cited by 31 · see citing works

In Vitro Interactions between Non-Steroidal Anti-Inflammatory Drugs and Antifungal Agents against Planktonic and Biofilm Forms of Trichosporon asahii

Yang, S., Liao, Y., Cong, L., Lu, X., & Yang, R. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157047 · Cited by 31 · see citing works

Toxicity of Diclofenac in the Fern Azolla filiculoides and the Lichen Xanthoria parietina

Vannini, A., Paoli, L., Vichi, M., Bačkor, M., Bačkorová, M., & Loppi, S. (2018) · Bulletin of Environmental Contamination and Toxicology · doi:10.1007/s00128-017-2266-4 · Cited by 29 · see citing works

Characterization of a novel antibiofilm effect of nitric oxide-releasing aspirin (NCX-4040) on Candida albicans isolates from denture stomatitis patients

Madariaga, F., Fernández-Soto, R., Duarte, L. F., Suarez, N., Delgadillo, D., Jara, J. A., Fernández‐Ramires, R., Urzúa, B., & Molina‐Berríos, A. (2017) · PLoS ONE · doi:10.1371/journal.pone.0176755 · Cited by 26 · see citing works

Role of Oxylipins and Other Lipid Mediators in Fungal Pathogenesis

Erb‐Downward, J. R., & Huffnagle, G. B. (2006) · Future Microbiology · doi:10.2217/17460913.1.2.219 · Cited by 27 · see citing works

In vitro analysis of flufenamic acid activity against Candida albicans biofilms

Chavez-Dozal, A. A., Jahng, M., Rane, H. S., Asare, K., Kulkarny, V. V., Bernardo, S. M., & Lee, S. A. (2014) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2013.08.018 · Cited by 26 · see citing works

Complex and Controversial Roles of Eicosanoids in Fungal Pathogenesis

Ruiz, S., Zamith‐Miranda, D., Takács, T., Gácser, A., Nosanchuk, J. D., & Guimaraes, A. J. (2021) · Journal of Fungi · doi:10.3390/jof7040254 · Cited by 25 · see citing works

Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Genome biology · doi:10.1186/s13059-024-03205-x · Cited by 23 · see citing works

Arachidonic acid metabolites in pathogenic yeasts

Ells, R., Kock, J. L. F., Albertyn, J., & Pohl, C. H. (2012) · Lipids in Health and Disease · doi:10.1186/1476-511x-11-100 · Cited by 24 · see citing works

Potential Antifungal Targets against a Candida Biofilm Based on an Enzyme in the Arachidonic Acid Cascade—A Review

Liu, X., Wang, D., Yu, C., Li, T., Liu, J., & Sun, S. (2016) · Frontiers in Microbiology · doi:10.3389/fmicb.2016.01925 · Cited by 23 · see citing works

Acetylsalicylic acid as antifungal in Eremothecium and other yeasts

Leeuw, N. J., Swart, C. W., Ncango, D. M., Pohl, C. H., Sebolai, O. M., Strauss, C. J., Botes, P. J., van Wyk, P. W. J., Nigam, S., & Kock, J. L. F. (2006) · Antonie van Leeuwenhoek · doi:10.1007/s10482-006-9124-4 · Cited by 23 · see citing works

Non-steroidal anti-inflammatory drugs may modulate the protease activity of Candida albicans

Carvalho, A. P., Gursky, L. C., Rosa, R. T., Rymovicz, A. U. M., Campelo, P. M. S., Grégio, A. M. T., Koga‐Ito, C. Y., Samaranayake, L. P., & Rosa, E. A. R. (2010) · Microbial Pathogenesis · doi:10.1016/j.micpath.2010.07.007 · Cited by 21 · see citing works

Aspirin as an Antifungal-Lock Agent in Inhibition of Candidal Biofilm Formation in Surgical Catheters

Chan, A. K. Y., Tsang, Y. C., Chu, C. H., & Tsang, C. S. P. (2021) · Infection and Drug Resistance · doi:10.2147/idr.s308262 · Cited by 20 · see citing works

Candida albicansabrogates the expression of interferon-γ-inducible protein-10 in human keratinocytes

Shiraki, Y., Ishibashi, Y., Hiruma, M., Nishikawa, A., & Ikeda, S. (2008) · FEMS Immunology & Medical Microbiology · doi:10.1111/j.1574-695x.2008.00457.x · Cited by 19 · see citing works

Aspirin alleviates orthopedic implant‑associated infection

Jiang, Y., Wang, S., Wu, H., Qin, H., Ren, M., Lin, J., & Yu, B. (2019) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2019.4298 · Cited by 19 · see citing works

Pseudomonas aeruginosa produces aspirin insensitive eicosanoids and contributes to the eicosanoid profile of polymicrobial biofilms with Candida albicans

Fourie, R., Ells, R., Kemp, G., Sebolai, O. M., Albertyn, J., & Pohl, C. H. (2017) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1016/j.plefa.2017.01.008 · Cited by 18 · see citing works

Targeting of the Hydrophobic Metabolome by Pathogens

Helms, J. B., Kaloyanova, D. V., Strating, J. R. P. M., van Hellemond, J. J., van der Schaar, H. M., Tielens, A. G. M., van Kuppeveld, F. J. M., & Brouwers, J. F. H. M. (2015) · Traffic · doi:10.1111/tra.12280 · Cited by 17 · see citing works

Fungal Jasmonate as a Novel Morphogenetic Signal for Pathogenesis

Liu, Y., Pagac, M. P., Yang, F., Patkar, R., & Naqvi, N. I. (2021) · Journal of Fungi · doi:10.3390/jof7090693 · Cited by 16 · see citing works

Exposure to host or fungal PGE2abrogates protection following immunization withCandida-pulsed dendritic cells

Kundu, G., & Noverr, M. C. (2010) · Medical Mycology · doi:10.3109/13693786.2010.532514 · Cited by 16 · see citing works

Small-molecule inhibitors of biofilm formation in laboratory and clinical isolates of Candida albicans

Grald, A., Yargosz, P., Case, S. L., Shea, K., & Johnson, D. I. (2011) · Journal of Medical Microbiology · doi:10.1099/jmm.0.034124-0 · Cited by 16 · see citing works

Can nonsteroidal anti-inflammatory drugs (NSAIDs) be repurposed for fungal infection?

Babaei, F., Mirzababaei, M., Tavakkoli, A., Nassiri‐Asl, M., & Hosseinzadeh, H. (2023) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-023-02651-x · Cited by 13 · see citing works

The role of Mss11 in Candida albicans biofilm formation

Tsai, P.-W., Chen, Y.-T., Yang, C., Chen, H.-F., Tan, T.-S., Lin, T.-W., Hsieh, W., & Lan, C. (2014) · Molecular Genetics and Genomics · doi:10.1007/s00438-014-0846-0 · Cited by 13 · see citing works

Biofilms and Antibiotics

Harriott, M. M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.62124-4 · Cited by 13 · see citing works

Effect of non-steroidal anti-inflammatory drugs and dexamethazone on the biofilm formation and expression of some adhesion-related genes of Candida albicans and Staphylococcus aureus

El-Baky, R. M. A., & Elgendy, S. G. (2016) · African Journal of Microbiology Research · doi:10.5897/ajmr2016.8013 · Cited by 10 · see citing works

Fungal biofilm inhibition by a component naturally produced by Candida albicans yeasts growing as a biofilm

Cateau, E., Berjeaud, J., Rodier, M., & Imbert, C. (2007) · International Journal of Antimicrobial Agents · doi:10.1016/j.ijantimicag.2007.10.004 · Cited by 13 · see citing works

Effect of Some Non steroidal Anti-Inflammatory Drugs on Growth, Adherence and Mature Biofilms of Candida spp.

Ashraf, A., Yousri, F., Taha, N., El-Waly, O. A., Ramadan, A. E.-K., Ismail, E., Hamada, R., Khalaf, M., Refaee, M., Ali, S. S., et al. (2015) · American journal of microbiological research · doi:10.12691/ajmr-3-1-1 · Cited by 12 · see citing works

Effects of Rhodomyrtus tomentosa extract on virulence factors of Candida albicans and human neutrophil function

Hmoteh, J., Musthafa, K. S., & Voravuthikunchai, S. P. (2017) · Archives of Oral Biology · doi:10.1016/j.archoralbio.2017.11.007 · Cited by 11 · see citing works

Eicosanoid production by Candida parapsilosis and other pathogenic yeasts

Chakraborty, T., Tóth, R., & Gácser, A. (2018) · Virulence · doi:10.1080/21505594.2018.1559674 · Cited by 11 · see citing works

Anti-biofilm effect by the combined action of fluconazole and acetylsalicylic acid against species of Candida parapsilosis complex

dos Santos, F. D. A. G., de Andrade, M. C. L., Brandão, I. D. S. L., Alves, A. I. D. S., Buonafina, M. D. S., Nunes, M., Neto, L. N. D. A., de Freitas, M. A., Brayner, F. A., Alves, L. C., et al. (2020) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2020.104378 · Cited by 9 · see citing works

The anti-mitochondrial antifungal assay for the discovery and development of new drugs

Kock, J. L. F., Swart, C. W., & Pohl, C. H. (2011) · Expert Opinion on Drug Discovery · doi:10.1517/17460441.2011.575358 · Cited by 8 · see citing works

Nosocomial Candiduria in Critically Ill Patients Admitted to Intensive Care Units in Menoufia University Hospitals, Egypt

Alkilani, A. A., Shalakany, A. H. E., El-Masry, E. A., Awad, E., & Mohamad, E. (2016) · Journal of Advances in Medicine and Medical Research · doi:10.9734/bjmmr/2016/25940 · Cited by 8 · see citing works

Fungal Biofilms:In VivoModels for Discovery of Anti-Biofilm Drugs

Nett, J. E., & Andes, D. R. (2015) · ASM Press eBooks · doi:10.1128/9781555817466.ch2 · Cited by 6 · see citing works

Determination of antidermatophytic effects of non‐steroidal anti‐inflammatory drugs on Trichophyton mentagrophytes and Epidermophyton floccosum

AL‐Janabi, A. A. H. S. (2011) · Mycoses · doi:10.1111/j.1439-0507.2010.01945.x · Cited by 6 · see citing works

Production of prostaglandins in transgenic Arabidopsis thaliana

Mohamed, M. E., & Lazarus, C. M. (2014) · Phytochemistry · doi:10.1016/j.phytochem.2014.02.013 · Cited by 4 · see citing works

Investigation of anti-dermatophytic effects of non-steroidal anti-inflammatory drugs on trichophyton mentagrophytes and epidermophyton floccosum.

Janabi, A. A. H. S. A., & AL‐Janabi, A. A. H. S. (2011) · Europe PMC (PubMed Central) · Cited by 4 · see citing works

Oxylipins in Fungal-Mammalian Interactions

Affeldt, K. J., & Keller, N. P. (2012) · Springer eBooks · doi:10.1007/978-94-007-4264-2_19 · Cited by 3 · see citing works

Opciones terapéuticas frente a especies de Candida resistentes a las equinocandinas

Hidalgo, A. P. C., Dueñas, O. H. R., Fandiño, Y. R. M., & Moreno, C. Á. (2018) · Universitas Médica · doi:10.11144/javeriana.umed59-2.cand · Cited by 1 · see citing works

In Vivo Candida Device Biofilm Models

Andes, D. R. (2017) · Springer eBooks · doi:10.1007/978-3-319-50409-4_7 · Cited by 4 · see citing works

Biofilm Formation and its Impact on Antifungal Therapy

Müller, F. C. (2014) · Current Fungal Infection Reports · doi:10.1007/s12281-014-0194-x · Cited by 2 · see citing works

The conventional identification and effect of diclofenac and aspirin on the Candida species

Elena, R., Enache-Soare, S., Oana, N., & Vassu, T. (2009) · ROMANIAN BIOTECHNOLOGICAL LETTERS · Cited by 2 · see citing works

Oxylipin distribution in Eremothecium

Leeuw, N. J. (2006) · Cited by 1 · see citing works

Aktuelles aus der Mykologie

Risslegger, B., & Lass‐Flörl, C. (2013) · Wiener klinisches Magazin · doi:10.1007/s00740-013-0089-4

Immunomodulatory Effect Of Host And Fungal Eicosanoids During Host-Pathogen Interactions With Candida Albicans

Kundu, G. G. (2010) · Human Biology

Aktuelles aus der Mykologie Zunehmende Resistenzentwicklung von Hefe- und Schimmelpilzen

Wien, S.-V. (2013)

Current awareness on yeast

(2006) · Yeast · doi:10.1002/yea.1315

Fungal eicosanoid biosynthesis Influences the virulence of Candida Parapsilosis

Chakraborty, T. (2019) · doi:10.14232/phd.9952

Biological activity of flufenamic acid and synthesized derivates (PFCs) that may occur in the environment

Šilha, D., Šilarová, P., & Weidlich, T. (2022) · Global NEST International Conference on Environmental Science & Technology · doi:10.30955/gnc2019.00968

Additional file 10 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688368

Additional file 1 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.25341262

Additional file 11 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688371

Additional file 12 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688374

Additional file 9 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688365

Additional file 6 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688356

Additional file 2 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.25341386

Additional file 7 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688359

Additional file 8 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688362

Additional file 3 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688347

Additional file 4 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688350

Additional file 5 of Early-life ruminal microbiome-derived indole-3-carboxaldehyde and prostaglandin D2 are effective promoters of rumen development

Sun, D., Bian, G., Zhang, K., Liu, N., Yin, Y., Hou, Y., Xie, F., Zhu, W., Mao, S., & Liu, J. (2024) · Figshare · doi:10.6084/m9.figshare.26688353

The role of OLE2 and POX1-3 in prostaglandin E 2 production and virulence is conserved in Candidozyma ( Candida ) auris

Bolsenbroek, A., Bisschoff, E., Kemp, G., Sebolai, O. M., Pohl, C. H., & Albertyn, J. (2026) · Microbiology Spectrum · doi:10.1128/spectrum.02323-25

Journal of Medical Microbiology (2005), 54, 1001–1005 DOI 10.1099/jmm.0.46172-0 46172 & 2005 SGM Printed in Great Britain 1001 Correspondence

Douglas, L. J., Alem, M. A. S., & Douglas, L. J. (2005)

Effects of Aspirin and Other Nonsteroidal Anti-Inflammatory Drugs on Biofilms and Planktonic Cells of <i>Candida albicans</i>

Alem, M. A. S., & Douglas, L. J. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.1.41-47.2004 · Cited by 205 · see citing works

Navigating the hidden depths of biofilms

Senior, K. (2004) · The Lancet Infectious Diseases · doi:10.1016/s1473-3099(04)00997-1 · Cited by 1 · see citing works

Arachidonic acid affects biofilm formation and PGE2 level in Candida albicans and non-albicans species in presence of subinhibitory concentration of fluconazole and terbinafine

Mishra, N. N., Ali, S., & Shukla, P. K. (2014) · The Brazilian Journal of Infectious Diseases · doi:10.1016/j.bjid.2013.09.006 · Cited by 47 · see citing works

Characterization of Prostaglandin E 2 Production by Candida albicans

Erb‐Downward, J. R., & Noverr, M. C. (2007) · Infection and Immunity · doi:10.1128/iai.00232-07 · Cited by 114 · see citing works