Bakers' Yeast, a Model for Fungal Biofilm Formation

Bacterial Biofilms: A Common Cause of Persistent Infections

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Biofilm formation as microbial development

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Ploidy Regulation of Gene Expression

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Elements of a single MAP kinase cascade in Saccharomyces cerevisiae mediate two developmental programs in the same cell type: mating and invasive growth.Preprint

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Elements of the Yeast Pheromone Response Pathway Required for Filamentous Growth of Diploids

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MAP kinase and cAMP filamentation signaling pathways converge on the unusually large promoter of the yeast FLO11 gene

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An Adhesin of the Yeast Pathogen <i>Candida glabrata</i> Mediating Adherence to Human Epithelial Cells

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A Saccharomyces gene family involved in invasive growth, cell–cell adhesion, and mating

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Saccharomyces cerevisiae S288C Has a Mutation in FL08, a Gene Required for Filamentous Growth

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The Cell Surface Flocculin Flo11 Is Required for Pseudohyphae Formation and Invasion by Saccharomyces cerevisiae

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Candida albicans ALS3 and insights into the nature of the ALS gene family

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Genetic Analysis of Sliding Motility in Mycobacterium smegmatis

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Sliding Motility in Mycobacteria

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[48] Candida biofilms and their susceptibility to antifungal agents

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Adhesins in Candida albicans.

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Msn1p/Mss10p, Mss11p and Muc1p/Flo11p are part of a signal transduction pathway downstream of Mep2p regulating invasive growth and pseudohyphal differentiation in Saccharomyces cerevisiae

Gagiano, M., van Dyk, D., Bauer, F. F., et al. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01151.x · Cited by 80 · see citing works

Biofilm Formation by the Fungal Pathogen <i>Candida albicans</i> : Development, Architecture, and Drug Resistance

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Cell Wall Integrity Signaling in <i>Saccharomyces cerevisiae</i>

Levin, D. E. (2005) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.69.2.262-291.2005 · Cited by 1,136 · see citing works

<i>Candida albicans</i> Biofilms and Human Disease

Nobile, C. J., & Johnson, A. D. (2015) · Annual Review of Microbiology · doi:10.1146/annurev-micro-091014-104330 · Cited by 1,057 · see citing works

Intragenic tandem repeats generate functional variability

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Fungal Biofilm Resistance

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Our Current Understanding of Fungal Biofilms

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Biocontrol yeasts: mechanisms and applications

Freimoser, F. M., Rueda-Mejia, M. P., Tilocca, B., & Migheli, Q. (2019) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-019-2728-4 · Cited by 462 · see citing works

<i>Candida albicans</i> Biofilms: a Developmental State Associated With Specific and Stable Gene Expression Patterns

García-Sánchez, S., Aubert, S., Iraqui, I., Janbon, G., Ghigo, J.-M., & d'Enfert, C. (2004) · Eukaryotic Cell · doi:10.1128/ec.3.2.536-545.2004 · Cited by 353 · see citing works

The evolution of drug resistance in clinical isolates of Candida albicans.

Ford, C. B., Funt, J. M., Abbey, D., Issi, L., Guiducci, C., Martinez, D. A., Delorey, T., Li, B. Y., White, T. C., Cuomo, C., et al. (2015) · eLife · doi:10.7554/elife.00662 · Cited by 348 · see citing works

Molecular Epidemiology of <i>Candida auris</i> in Colombia Reveals a Highly Related, Countrywide Colonization With Regional Patterns in Amphotericin B Resistance

Escandón, P., Chow, N. A., Caceres, D. H., Gade, L., Berkow, E. L., Armstrong, P., Rivera, S., Misas, E., Duarte, C., Moulton-Meissner, H., et al. (2019) · Clinical Infectious Diseases · doi:10.1093/cid/ciy411 · Cited by 222 · see citing works

<i>Candida albicans</i> Als1p: an adhesin that is a downstream effector of the <i>EFG1</i> filamentation pathway

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The <i>Candida albicans CaACE2</i> gene affects morphogenesis, adherence and virulence

Kelly, M. T., MacCallum, D. M., Clancy, S. D., Odds, F. C., Brown, A. J. P., & Butler, G. (2004) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04185.x · Cited by 175 · see citing works

Mode of Selection and Experimental Evolution of Antifungal Drug Resistance in <i>Saccharomyces cerevisiae</i>

Anderson, J. B., Sirjusingh, C., Parsons, A. B., Boone, C., Wickens, C., Cowen, L. E., & Kohn, L. M. (2003) · Genetics · doi:10.1093/genetics/163.4.1287 · Cited by 156 · see citing works

From Saccharomyces cerevisiae to Candida glabrata in a few easy steps: important adaptations for an opportunistic pathogen: Candida glabrata stress response

Roetzer, A., Gabaldón, T., & Schüller, C. (2011) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2010.02102.x · Cited by 154 · see citing works

Ammonia pulses and metabolic oscillations guide yeast colony development.

Palková, Z., Devaux, F., R̆ic̆icová, M., Mináriková, L., Le Crom, S., & Jacq, C. (2002) · Molecular Biology of the Cell · doi:10.1091/mbc.e01-12-0149 · Cited by 151 · see citing works

Evolutionary engineered Saccharomyces cerevisiae wine yeast strains with increased in vivo flux through the pentose phosphate pathway

Cadière, A., Ortiz-Julien, A., Camarasa, C., & Dequin, S. (2011) · Metabolic Engineering · doi:10.1016/j.ymben.2011.01.008 · Cited by 141 · see citing works

The Yak1p kinase controls expression of adhesins and biofilm formation in <i>Candida glabrata</i> in a Sir4p‐dependent pathway

Iraqui, I., Garcia‐Sanchez, S., Aubert, S., Dromer, F., Ghigo, J., D’Enfert, C., & Janbon, G. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2004.04475.x · Cited by 126 · see citing works

A common mechanism involving the TORC1 pathway can lead to amphotericin B-persistence in biofilm and planktonic Saccharomyces cerevisiae populations

Bojsen, R., Regenberg, B., Gresham, D., & Folkesson, A. (2016) · Scientific Reports · doi:10.1038/srep21874 · Cited by 42 · see citing works

Genomewide screening for genes involved in biofilm formation and miconazole susceptibility in<i>Saccharomyces cerevisiae</i>

Vandenbosch, D., De Canck, E., Dhondt, I., Rigole, P., Nelis, H. J., & Coenye, T. (2013) · FEMS Yeast Research · doi:10.1111/1567-1364.12071 · Cited by 35 · see citing works

Influence of Al(III) on biofilm and its extracellular polymeric substances in sequencing batch biofilm reactors

Hu, X., Yang, L., Lai, X., et al. (2017) · Environmental Technology · doi:10.1080/09593330.2017.1378268 · Cited by 15 · see citing works

Biofilms on instruments and environmental surfaces: Do they interfere with instrument reprocessing and surface disinfection? Review of the literature

Alfa, M. J. (2019) · American Journal of Infection Control · doi:10.1016/j.ajic.2019.02.027 · Cited by 48 · see citing works

Insight into mature biofilm quorum sensing in full-scale wastewater treatment plants

Wang, J., Liu, Q., Hu, H., et al. (2019) · Chemosphere · doi:10.1016/j.chemosphere.2019.06.007 · Cited by 29 · see citing works

The effect of hydrophobicity of group a beta-hemolytic streptococcus in the process of adherence and biofilm production

Šmitran, A., Markovic, T., & Ranin, L. T. (2014) · Srpski arhiv za celokupno lekarstvo · doi:10.2298/sarh1410557s

Cell adhesion and twitching motility influence strong biofilm formation in Pseudomonas aeruginosa

Patel, H. R., & Gajjar, D. U. (2022) · Biofouling · doi:10.1080/08927014.2022.2054703 · Cited by 25 · see citing works