Adhesins in human fungal pathogens: glue with plenty of stick.

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Carbohydrate-binding modules: fine-tuning polysaccharide recognition

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Prediction of sequence-dependent and mutational effects on the aggregation of peptides and proteins

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Virulence factors of Candida albicans

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Evolution of pathogenicity and sexual reproduction in eight Candida genomes

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The cell wall: a carbohydrate armour for the fungal cell

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Cell Wall Assembly in Saccharomyces cerevisiae

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Surface hydrophobin prevents immune recognition of airborne fungal spores

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Nosocomial fungal infections: epidemiology, diagnosis, and treatment

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Hydrophobins: Multipurpose Proteins

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Role of Force-Sensitive Amyloid-Like Interactions in Fungal Catch Bonding and Biofilms

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DODAB:monoolein liposomes containing Candida albicans cell wall surface proteins: A novel adjuvant and delivery system

Carneiro, C., Correia, A., Collins, T., Vilanova, M., Pais, C., Gomes, A. C., Oliveira, M. E. C. D. R., & Sampaio, P. (2014) · European Journal of Pharmaceutics and Biopharmaceutics · doi:10.1016/j.ejpb.2014.11.028 · Cited by 34

Kinetic and thermodynamic characterization of the interactions between the components of human plasma kinin-forming system and isolated and purified cell wall proteins of Candida albicans

Seweryn, K., Karkowska‐Kuleta, J., Wolak, N., Bocheńska, O., Kędracka–Krok, S., Kozik, A., & Rąpała‐Kozik, M. (2015) · Acta Biochimica Polonica · doi:10.18388/abp.2015_1142 · Cited by 34

Mycobiome and Inflammatory Bowel Disease: Role in Disease Pathogenesis, Current Approaches and Novel Nutritional-based Therapies

Hsu, C., Ghannoum, M. A., Cominelli, F., & Martino, L. D. (2022) · Inflammatory Bowel Diseases · doi:10.1093/ibd/izac156 · Cited by 34

Gut fungal mycobiome: A significant factor of tumor occurrence and development

Li, F., Gao, Y., Cheng, W., Su, L., & Yang, R. (2023) · Cancer Letters · doi:10.1016/j.canlet.2023.216302 · Cited by 36

Candida albicans Shaving to Profile Human Serum Proteins on Hyphal Surface

Marín, E., Parra‐Giraldo, C. M., Hernández‐Haro, C., Hernáez, M. L., Nombela, C., Monteoliva, L., & Gil, C. (2015) · Frontiers in Microbiology · doi:10.3389/fmicb.2015.01343 · Cited by 32

The multidrug resistance transporters CgTpo1_1 and CgTpo1_2 play a role in virulence and biofilm formation in the human pathogenCandida glabrata

Santos, R., Costa, C., Mil‐Homens, D., Romão, D., de Carvalho, C. C. C. R., Pais, P., Mira, N. P., Fialho, A. M., & Teixeira, M. C. (2016) · Cellular Microbiology · doi:10.1111/cmi.12686 · Cited by 34

New insights on yeast and filamentous fungus adhesion in a natural co-immobilization system: proposed advances and applications in wine industry

Ogawa, M., Bisson, L. F., García‐Martínez, T., Mauricio, J. C., & Moreno‐García, J. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09870-4 · Cited by 33

An Amyloid Core Sequence in the Major Candida albicans Adhesin Als1p Mediates Cell-Cell Adhesion

Ho, V., Herman‐Bausier, P., Shaw, C. E., Conrad, K. A., Garcia, M. C., Draghi, J. A., Dufrêne, Y. F., Lipke, P. N., & Rauceo, J. M. (2019) · mBio · doi:10.1128/mbio.01766-19 · Cited by 37

Plastic pollution and fungal, protozoan, and helminth pathogens – A neglected environmental and public health issue?

Ormsby, M. J., Akinbobola, A., & Quilliam, R. S. (2023) · The Science of The Total Environment · doi:10.1016/j.scitotenv.2023.163093 · Cited by 33

The Transcriptome of Exophiala dermatitidis during Ex-vivo Skin Model Infection

Poyntner, C., Blasi, B., Arcalís, E., Mirastschijski, U., Sterflinger, K., & Tafer, H. (2016) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2016.00136 · Cited by 32

Candida albicans Induces Oral Microbial Dysbiosis and Promotes Oral Diseases

Kashyap, B., Padala, S. R., Kaur, G., & Kullaa, A. M. (2024) · Microorganisms · doi:10.3390/microorganisms12112138 · Cited by 37

Accessibility and contribution to glucan masking of natural and genetically tagged versions of yeast wall protein 1 of Candida albicans

Granger, B. L. (2018) · PLoS ONE · doi:10.1371/journal.pone.0191194 · Cited by 32

Characterization of the Candida orthopsilosis agglutinin-like sequence (ALS) genes

Lombardi, L., Zoppo, M., Rizzato, C., Bottai, D., Hernández, Á. G., Hoyer, L. L., & Tavanti, A. (2019) · PLoS ONE · doi:10.1371/journal.pone.0215912 · Cited by 31

Phenolic and Nonpolar Fractions of Elaeagnus rhamnoides (L.) A. Nelson Extracts as Virulence Modulators—In Vitro Study on Bacteria, Fungi, and Epithelial Cells

Różalska, B., Sadowska, B., Żuchowski, J., Więckowska-Szakiel, M., Budzyńska, A., Wójcik-Bojek, U., & Stochmal, A. (2018) · Molecules · doi:10.3390/molecules23071498 · Cited by 31

Collaboration between Antagonistic Cell Type Regulators Governs Natural Variation in the Candida albicans Biofilm and Hyphal Gene Expression Network

Do, E., Cravener, M. V., Huang, M. Y., May, G. E., McManus, C. J., & Mitchell, A. P. (2022) · mBio · doi:10.1128/mbio.01937-22 · Cited by 30

From Skin and Gut to the Brain: The Infectious Journey of the Human Commensal Fungus Malassezia and Its Neurological Consequences

Naik, B., Sasikumar, J., & Das, S. P. (2024) · Molecular Neurobiology · doi:10.1007/s12035-024-04270-w · Cited by 29

Understand the genomic diversity and evolution of fungal pathogen Candida glabrata by genome-wide analysis of genetic variations

Guo, X., Zhang, R., Li, Y., Wang, Z., Ishchuk, O. P., Ahmad, K. M., Wee, J., Piškur, J., Shapiro, J. A., & Gu, Z. (2019) · Methods · doi:10.1016/j.ymeth.2019.05.002 · Cited by 28

Chromosome-level assemblies from diverse clades reveal limited structural and gene content variation in the genome of Candida glabrata

Marcet‐Houben, M., Alvarado, M. I., Księżopolska, E., Saus, E., de Groot, P. W. J., & Gabaldón, T. (2022) · BMC Biology · doi:10.1186/s12915-022-01412-1 · Cited by 29

Adhesion and biofilm formation by the opportunistic pathogen Candida tropicalis: what do we know?

de Souza, C. M., dos Santos, M. M., Furlaneto-Maia, L., & Furlaneto, M. C. (2023) · Canadian Journal of Microbiology · doi:10.1139/cjm-2022-0195 · Cited by 39

PtaB, a lim-domain binding protein inAspergillus fumigatusregulates biofilm formation and conidiation through distinct pathways

Zhang, S., Chen, Y., Ma, Z., Chen, Q., Ostapska, H., Gravelat, F. N., Lü, L., & Sheppard, D. C. (2017) · Cellular Microbiology · doi:10.1111/cmi.12799 · Cited by 28

Diversity of GPI-anchored fungal adhesins

Essen, L., Vogt, M. S., & Mösch, H. (2020) · Biological Chemistry · doi:10.1515/hsz-2020-0199 · Cited by 27

FLO11, a Developmental Gene Conferring Impressive Adaptive Plasticity to the Yeast Saccharomyces cerevisiae

Bouyx, C., Schiavone, M., & François, J. (2021) · Pathogens · doi:10.3390/pathogens10111509 · Cited by 28

Parallel expansion and divergence of an adhesin family in pathogenic yeasts

Smoak, R. A., Snyder, L. F., Fassler, J. S., & He, B. Z. (2023) · GENETICS · doi:10.1093/genetics/iyad024 · Cited by 25

The Flo Adhesin Family

Willaert, R., Kayacan, Y., & Devreese, B. V. (2021) · Pathogens · doi:10.3390/pathogens10111397 · Cited by 27

Characterising the mechanics of cell–cell adhesion in plants

Atakhani, A., Bogdziewiez, L., & Verger, S. (2022) · Quantitative Plant Biology · doi:10.1017/qpb.2021.16 · Cited by 27

Metabolic flexibility and extensive adaptability governing multiple drug resistance and enhanced virulence in Candida albicans

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

Fungal spore attachment to substrata

Vasselli, J. G., & Shaw, B. D. (2022) · Fungal Biology Reviews · doi:10.1016/j.fbr.2022.03.002 · Cited by 25

A Family of Secretory Proteins Is Associated with Different Morphotypes in Cryptococcus neoformans

Gyawali, R., Upadhyay, S., Way, J., & Lin, X. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.02967-16 · Cited by 25

A novel class of Candida glabrata cell wall proteins with β-helix fold mediates adhesion in clinical isolates

Reithofer, V., Fernández-Pereira, J., Alvarado, M., de Groot, P. W. J., & Essen, L. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009980 · Cited by 27

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 35

Malassezia virulence factors and their role in dermatological disorders

Kurniadi, I., Wijaya, W. H., & Timotius, K. H. (2022) · Acta Dermatovenerologica Alpina Pannonica et Adriatica · doi:10.15570/actaapa.2022.8 · Cited by 25

Granule-Dependent Natural Killer Cell Cytotoxicity to Fungal Pathogens

Ogbomo, H., & Mody, C. H. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00692 · Cited by 28

Cryptococcal Traits Mediating Adherence to Biotic and Abiotic Surfaces

Camacho, E., & Casadevall, A. (2018) · Journal of Fungi · doi:10.3390/jof4030088 · Cited by 24

The pH-Responsive Transcription Factors YlRim101 and Mhy1 Regulate Alkaline pH-Induced Filamentation in the Dimorphic Yeast Yarrowia lipolytica

Shu, T., He, X., Chen, J., Mao, Y., & Gao, X. (2021) · mSphere · doi:10.1128/msphere.00179-21 · Cited by 25

The Candida auris Hog1 MAP kinase is essential for the colonization of murine skin and intradermal persistence

Shivarathri, R., Chauhan, M., Datta, A., Das, D., Karuli, A., Aptekmann, A., Jenull, S., Kuchler, K., Thangamani, S., Chowdhary, A., et al. (2024) · mBio · doi:10.1128/mbio.02748-24 · Cited by 22

Living together: The role of Candida albicans in the formation of polymicrobial biofilms in the oral cavity

Rąpała‐Kozik, M., Surowiec, M., Juszczak, M., Wronowska, E., Kulig, K., Bednarek, A., Gonzalez‐Gonzalez, M., Karkowska‐Kuleta, J., Zawrotniak, M., Satała, D., et al. (2023) · Yeast · doi:10.1002/yea.3855 · Cited by 24

Candida tropicalis biofilm formation and expression levels of the CTRG ALS‐like genes in sessile cells

Galán‐Ladero, M. A., Blanco‐Blanco, M. T., Fernández‐Calderón, M. C., Lucio, L., Gutiérrez-Martı́n, Y., Blanco, M. T., & Pérez-Giraldo, C. (2018) · Yeast · doi:10.1002/yea.3370 · Cited by 24

Glucose, Cyc8p and Tup1p regulate biofilm formation and dispersal in wild Saccharomyces cerevisiae

Nguyen, P. V., Plocek, V., Váchová, L., & Palková, Z. (2020) · npj Biofilms and Microbiomes · doi:10.1038/s41522-020-0118-1 · Cited by 22

Histone H4 dosage modulates DNA damage response in the pathogenic yeast Candida glabrata via homologous recombination pathway

Kumar, K., Moirangthem, R., & Kaur, R. (2020) · PLoS Genetics · doi:10.1371/journal.pgen.1008620 · Cited by 21

Overexpression of the Transcriptional Regulator WOR1 Increases Susceptibility to Bile Salts and Adhesion to the Mouse Gut Mucosa in Candida albicans

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

Staphylococcus aureus Interferes with Streptococci Spatial Distribution and with Protein Expression of Species within a Polymicrobial Oral Biofilm

Schnurr, E., Paqué, P. N., Attin, T., Nanni, P., Grossmann, J., Holtfreter, S., Bröker, B. M., Köhler, C., Diep, B. A., Ribeiro, A. A., et al. (2021) · Antibiotics · doi:10.3390/antibiotics10020116 · Cited by 21

Between Amyloids and Aggregation Lies a Connection with Strength and Adhesion

Lipke, P., Ramsook, C. B., Garcia-Sherman, M. C., Jackson, D., Chan, C. X. J., Bois, M., & Klotz, S. (2014) · New Journal of Science · doi:10.1155/2014/815102 · Cited by 22

Whole Genome Sequencing of Candida glabrata for Detection of Markers of Antifungal Drug Resistance

Biswas, C., Chen, S. C. ‐., Halliday, C. L., Martinez, E. M., Rockett, R. J., Wang, Q., Timms, V. J., Dhakal, R., Sadsad, R., Kennedy, K., et al. (2017) · Journal of Visualized Experiments · doi:10.3791/56714 · Cited by 21

Surface, adhesiveness and virulence aspects of Candida haemulonii species complex

Ramos, L. S., Oliveira, S. S. C., Silva, L. N., Granato, M. Q., Gonçalves, D. D. S., Frasés, S., Seabra, S. H., Macêdo, A. J., Kneipp, L. F., Branquinha, M. H., et al. (2020) · Medical Mycology · doi:10.1093/mmy/myz139 · Cited by 20

From the first touch to biofilm establishment by the human pathogen Candida glabrata: a genome-wide to nanoscale view

Cavalheiro, M., Pereira, D., Formosa‐Dague, C., Leitão, C., Pais, P., Ndlovu, E., Viana, R., Pimenta, A. I., Santos, R., Takahashi‐Nakaguchi, A., et al. (2021) · Communications Biology · doi:10.1038/s42003-021-02412-7 · Cited by 22

Beyond the paradigm of nanomechanical measurements on cells using AFM: an automated methodology to rapidly analyse thousands of cells

Proa-Coronado, S., Séverac, C., Martínez-Rivas, A., & Dague, É. (2019) · Nanoscale Horizons · doi:10.1039/c9nh00438f · Cited by 19

Candida albicans Niche Specialization: Features That Distinguish Biofilm Cells from Commensal Cells

Herwald, S. E., & Kumamoto, C. A. (2014) · Current Fungal Infection Reports · doi:10.1007/s12281-014-0178-x · Cited by 20

Hyperexpression of CDRs and HWP1 genes negatively impacts on Candida albicans virulence

Maras, B., Maggiore, A., Mignogna, G., D’Erme, M., & Angiolella, L. (2021) · PLoS ONE · doi:10.1371/journal.pone.0252555 · Cited by 19

Biofilm: A Robust and Efficient Barrier to Antifungal Chemotherapy

Souza dos Santos, A. L., & de Mello, T. P. (2015) · Journal of Antimicrobial Agents · doi:10.4172/2472-1212.1000e101 · Cited by 18

The Pga59 cell wall protein is an amyloid forming protein involved in adhesion and biofilm establishment in the pathogenic yeast Candida albicans

Mourer, T., Ghalid, M. E., Pehau‐Arnaudet, G., Kauffmann, B., Loquet, A., Brûlé, S., Cabral, V., d’Enfert, C., & Bachellier‐Bassi, S. (2023) · npj Biofilms and Microbiomes · doi:10.1038/s41522-023-00371-x · Cited by 19

New Aspects of Invasive Growth Regulation Identified by Functional Profiling of MAPK Pathway Targets in Saccharomyces cerevisiae

Vandermeulen, M. D., & Cullen, P. J. (2020) · Genetics · doi:10.1534/genetics.120.303369 · Cited by 18

Identification of Components of the SUMOylation Machinery in Candida glabrata

Gujjula, R., Veeraiah, S., Kumar, K., Thakur, S. S., Mishra, K., & Kaur, R. (2016) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.706044 · Cited by 18

Recognition of Fungal Components by the Host Immune System

García-Carnero, L. C., Martínez-Álvarez, J. A., Salazar-García, L. M., Lozoya‐Pérez, N. E., González-Hernández, S. E., & Tamez-Castrellón, A. K. (2019) · Current Protein and Peptide Science · doi:10.2174/1389203721666191231105546 · Cited by 18

Genome Sequencing of the Pyruvate-producing Strain Candida glabrata CCTCC M202019 and Genomic Comparison with Strain CBS138

Xu, N., Ye, C., Chen, X., Liu, J., Liu, L., & Chen, J. (2016) · Scientific Reports · doi:10.1038/srep34893 · Cited by 15

Thymoquinone Antifungal Activity against Candida glabrata Oral Isolates from Patients in Intensive Care Units—An In Vitro Study

Nouri, N., Mohammadi, S. R., Beardsley, J., Aslani, P., Ghaffarifar, F., Roudbary, M., & Rodrigues, C. F. (2023) · Metabolites · doi:10.3390/metabo13040580 · Cited by 15

CARD9 attenuates Aβ pathology and modifies microglial responses in an Alzheimer’s disease mouse model

Ennerfelt, H. E., Holliday, C., Shapiro, D. A., Zengeler, K. E., Bolte, A. C., Ulland, T. K., & Lukens, J. R. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2303760120 · Cited by 16

A comprehensive guide to assess gut mycobiome and its role in pathogenesis and treatment of inflammatory bowel disease

Yadav, A., Yadav, R., Sharma, V., & Dutta, U. (2024) · Indian Journal of Gastroenterology · doi:10.1007/s12664-023-01510-0 · Cited by 18

Fungi that Infect Humans

Köhler, J. R., Hube, B., Puccia, R., Casadevall, A., & Perfect, J. R. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch39 · Cited by 18

Development of a novel anti-biofilm peptide derived from profilin of Spodoptera frugiperda

da Silva, A. C. B., Sardi, J. D. C. O., de Oliveira, D. G. L., de Oliveira, C. F. R., dos Santos, H. F., dos Santos, E. L., Crusca, E., Cardoso, M. H. E. S., Franco, O. L., & Macedo, M. L. R. (2020) · Biofouling · doi:10.1080/08927014.2020.1776857 · Cited by 15

The Emerging Pathogen Candida metapsilosis: Biological Aspects, Virulence Factors, Diagnosis, and Treatment

Gómez-Gaviria, M., García-Carnero, L. C., Baruch-Martínez, D. A., & Mora-Montes, H. M. (2024) · Infection and Drug Resistance · doi:10.2147/idr.s448213 · Cited by 20

High Biofilm Formation of Non-Smooth Candida parapsilosis Correlates with Increased Incorporation of GPI-Modified Wall Adhesins

Moreno‐Martínez, A. E., Gómez-Molero, E., Sánchez‐Virosta, P., Dekker, H. L., de Boer, A. D., Eraso, E., Bader, O., & de Groot, P. W. J. (2021) · Pathogens · doi:10.3390/pathogens10040493 · Cited by 15

Comparative Genomic Analyses Provide Insight Into the Pathogenicity of Metschnikowia bicuspidata LNES0119

Jiang, H., Bao, J., Xing, Y., Li, X., & Chen, Q. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.939141 · Cited by 14

Tec1 and Ste12 transcription factors play a role in adaptation to low pH stress and biofilm formation in the human opportunistic fungal pathogen Candida glabrata

Purohit, D., & Gajjar, D. U. (2022) · International Microbiology · doi:10.1007/s10123-022-00264-7 · Cited by 15

SUMOylation in Human Pathogenic Fungi: Role in Physiology and Virulence

Sahu, M. S., Patra, S., Kumar, K., & Kaur, R. (2020) · Journal of Fungi · doi:10.3390/jof6010032 · Cited by 15

Mucosal Immunity to Gut Fungi in Health and Inflammatory Bowel Disease

Carlson, S. L., Mathew, L., Savage, M., Kok, K. B., Lindsay, J. O., Munro, C. A., & McCarthy, N. E. (2023) · Journal of Fungi · doi:10.3390/jof9111105 · Cited by 17

Healthcare-associated fungal infections and emerging pathogens during the COVID-19 pandemic

Shah, K., Deshpande, M., & Shah, P. (2024) · Frontiers in Fungal Biology · doi:10.3389/ffunb.2024.1339911 · Cited by 14

Unraveling the genomic diversity and virulence of human fungal pathogens through pangenomics

Perrier, M., & Barber, A. E. (2024) · PLoS Pathogens · doi:10.1371/journal.ppat.1012313 · Cited by 14

Influence of serum and polystyrene plate type on stability of Candida albicans biofilms

Kipanga, P. N., & Luyten, W. H. M. L. (2017) · Journal of Microbiological Methods · doi:10.1016/j.mimet.2017.04.006 · Cited by 14

An overview of lectin–glycan interactions: a key event in initiating fungal infection and pathogenesis

Ballal, S., & Inamdar, S. R. (2018) · Archives of Microbiology · doi:10.1007/s00203-018-1487-1 · Cited by 14

The good, the bad, and the hazardous: comparative genomic analysis unveils cell wall features in the pathogen Candidozyma auris typical for both baker’s yeast and Candida

Alvarado, M., Navajas, J. A. G., Muñoz, M. T. B., Gómez-Molero, E., Fernández-Sánchez, S., Eraso, E., Munro, C. A., Valentı́n, E., Mateo, E., & de Groot, P. W. J. (2024) · FEMS Yeast Research · doi:10.1093/femsyr/foae039 · Cited by 13

Genetic Manipulation as a Tool to Unravel Candida parapsilosis Species Complex Virulence and Drug Resistance: State of the Art

Zoppo, M., Poma, N. V., Luca, M. D., Bottai, D., & Tavanti, A. (2021) · Journal of Fungi · doi:10.3390/jof7060459 · Cited by 14

Characterization of Awp14, A Novel Cluster III Adhesin Identified in a High Biofilm-Forming Candida glabrata Isolate

Fernández-Pereira, J., Alvarado, M. I., Gómez-Molero, E., Dekker, H. L., Muñoz, M. T. B., Eraso, E., Bader, O., & de Groot, P. W. J. (2021) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2021.790465 · Cited by 13

Effect of Surface Hydrophobicity on the Adsorption of a Pilus-Derived Adhesin-like Peptide

Yang, Y., Huang, J., Dornbusch, D., Grundmeier, G., Fahmy, K., Keller, A., & Cheung, D. L. (2022) · Langmuir · doi:10.1021/acs.langmuir.2c01016 · Cited by 13

P2X7 from j774 murine macrophages acts as a scavenger receptor for bacteria but not yeast

Pérez‐Flores, G., Hernández-Silva, C., Gutiérrez‐Escobedo, G., Peñas, A. D. L., Castaño, I., Arreola, J., & Pérez‐Cornejo, P. (2016) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2016.11.027 · Cited by 13

Candida auris : host interactions, antifungal drug resistance, and diagnostics

Chowdhary, A., Lionakis, M. S., & Chauhan, N. (2025) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00187-22 · Cited by 15

From the Ground to the Clinic: The Evolution and Adaptation of Fungi

Corrêa-Junior, D., Zamith‐Miranda, D., Frasés, S., & Nosanchuk, J. D. (2025) · Journal of Fungi · doi:10.3390/jof12010008 · Cited by 14

Integrated post-genomic cell wall analysis reveals floating biofilm formation associated with high expression of flocculins in the pathogen Pichia kudriavzevii

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Unveiling the Morphostructural Plasticity of Zoonotic Sporotrichosis Fungal Strains: Possible Implications for Sporothrix brasiliensis Virulence and Pathogenicity

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