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Bacteriome and Mycobiome Interactions Underscore Microbial Dysbiosis in Familial Crohn’s Disease

https://doi.org/10.1128/mbio.01250-16
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/978-1-4939-3052-4_9openalex-snapshot
The Fungal Biome of the Oral Cavity
inferredcites →https://doi.org/10.1016/bs.aambs.2014.12.002openalex-snapshot
Candida Survival Strategies
inferredcites →https://doi.org/10.1016/j.chom.2015.09.008openalex-snapshot
Inflammation, Antibiotics, and Diet as Environmental Stressors of the Gut Microbiome in Pediatric Crohn’s Disease
inferredcites →https://doi.org/10.1016/j.exppara.2007.04.014openalex-snapshot
Trypanosoma cruzi: Ultrastructural studies of adhesion, lysis and biofilm formation by Serratia marcescens
inferredcites →https://doi.org/10.1016/j.micinf.2006.03.014openalex-snapshot
TLR2, but not TLR4, triggers cytokine production by murine cells in response to Candida albicans yeasts and hyphae
inferredcites →https://doi.org/10.1016/j.micinf.2014.12.001openalex-snapshot
The fungal microbiota of de-novo paediatric inflammatory bowel disease
inferredcites →https://doi.org/10.1016/s0002-9270(98)00296-2openalex-snapshot
Anti- Saccharomyces cerevisiae Mannan Antibodies in Familial Crohn's Disease
inferredcites →https://doi.org/10.1016/s0022-2836(05)80360-2openalex-snapshot
Basic Local Alignment Search Tool
inferredcites →https://doi.org/10.1038/ajg.2009.225openalex-snapshot
Candida albicans Colonization and ASCA in Familial Crohn's Disease
inferredcites →https://doi.org/10.1038/ajg.2010.281openalex-snapshot
Mucolytic Bacteria With Increased Prevalence in IBD Mucosa Augment In Vitro Utilization of Mucin by Other Bacteria
inferredcites →https://doi.org/10.1038/ajg.2015.50openalex-snapshot
Familial Risk of Inflammatory Bowel Disease: A Population-Based Cohort Study 1977–2011
inferredcites →https://doi.org/10.1038/nm.4102openalex-snapshot
CARD9 impacts colitis by altering gut microbiota metabolism of tryptophan into aryl hydrocarbon receptor ligands
inferredcites →https://doi.org/10.1038/nmeth.f.303openalex-snapshot
QIIME allows analysis of high-throughput community sequencing data
inferredcites →https://doi.org/10.1038/nprot.2008.192openalex-snapshot
In vitro growth and analysis of Candida biofilms
inferredcites →https://doi.org/10.1053/j.gastro.2006.02.009openalex-snapshot
Candida albicans Is an Immunogen for Anti–Saccharomyces cerevisiae Antibody Markers of Crohn’s Disease
inferredcites →https://doi.org/10.1053/j.gastro.2006.04.030openalex-snapshot
Antibodies Against Laminaribioside and Chitobioside Are Novel Serologic Markers in Crohn’s Disease
inferredcites →https://doi.org/10.1053/j.gastro.2011.01.054openalex-snapshot
The Commensal Microbiota and Enteropathogens in the Pathogenesis of Inflammatory Bowel Diseases
inferredcites →https://doi.org/10.1053/j.sempedsurg.2013.01.002openalex-snapshot
The role of the intestinal microbiota in the pathogenesis of necrotizing enterocolitis
inferredcites →https://doi.org/10.1073/pnas.1307855110openalex-snapshot
Complement modulates the cutaneous microbiome and inflammatory milieu
inferredcites →https://doi.org/10.1080/00365520801935434openalex-snapshot
Fungi and inflammatory bowel diseases: Alterations of composition and diversity
inferredcites →https://doi.org/10.1080/08927014.2014.996143openalex-snapshot
Virulence and pathogenicity ofCandida albicansis enhanced in biofilms containing oral bacteria
inferredcites →https://doi.org/10.1093/bioinformatics/btq461openalex-snapshot
Search and clustering orders of magnitude faster than BLAST
inferredcites →https://doi.org/10.1093/ecco-jcc/jjv197openalex-snapshot
IBD Genetic Risk Profile in Healthy First-Degree Relatives of Crohn’s Disease Patients
inferredcites →https://doi.org/10.1093/ecco-jcc/jjv209openalex-snapshot
Fungal Dysbiosis in Mucosa-associated Microbiota of Crohn’s Disease Patients
inferredcites →https://doi.org/10.1097/mib.0000000000000454openalex-snapshot
Fungal Signature in the Gut Microbiota of Pediatric Patients With Inflammatory Bowel Disease
inferredcites →https://doi.org/10.1099/jmm.0.012989-0openalex-snapshot
Escherichia coli and its lipopolysaccharide modulate in vitro Candida biofilm formation
inferredcites →https://doi.org/10.1099/jmm.0.021832-0openalex-snapshot
Bacterial lipopolysaccharides variably modulate in vitro biofilm formation of Candida species
inferredcites →https://doi.org/10.1111/j.1365-2036.2011.04628.xopenalex-snapshot
The changing pattern of Crohn’s disease incidence in northern France: a continuing increase in the 10- to 19-year-old age bracket (1988-2007)
inferredcites →https://doi.org/10.1111/j.1462-5822.2005.00616.xopenalex-snapshot
Contributions of hyphae and hypha-co-regulated genes to Candida albicans virulence
inferredcites →https://doi.org/10.1111/jicd.12048openalex-snapshot
Secretory products of E scherichia coli biofilm modulate C andida biofilm formation and hyphal development
inferredcites →https://doi.org/10.1111/mec.12481openalex-snapshot
Towards a unified paradigm for sequence‐based identification of fungi
inferredcites →https://doi.org/10.1126/science.1221789openalex-snapshot
Interactions Between Commensal Fungi and the C-Type Lectin Receptor Dectin-1 Influence Colitis
inferredcites →https://doi.org/10.1128/cdli.3.2.219-226.1996openalex-snapshot
Specific antibody response to oligomannosidic epitopes in Crohn's disease
inferredcites →https://doi.org/10.1128/iai.73.11.7458-7464.2005openalex-snapshot
Differential Cytokine Production and Toll-Like Receptor Signaling Pathways by Candida albicans Blastoconidia and Hyphae
inferredcites →https://doi.org/10.1136/gut.2003.025346openalex-snapshot
Opposite evolution in incidence of Crohn’s disease and ulcerative colitis in Northern France (1988–1999)
inferredcites →https://doi.org/10.1136/gut.2010.208348openalex-snapshot
Mannan-binding lectin deficiency results in unusual antibody production and excessive experimental colitis in response to mannose-expressing mild gut pathogens
inferredcites →https://doi.org/10.1136/gut.2010.223263openalex-snapshot
Dysbiosis of the faecal microbiota in patients with Crohn's disease and their unaffected relatives
inferredcites →https://doi.org/10.1136/gut.2010.224154openalex-snapshot
Guidelines for the management of inflammatory bowel disease in adults
inferredcites →https://doi.org/10.1136/gut.35.10.1433openalex-snapshot
Incidence of inflammatory bowel disease in northern France (1988-1990).
inferredcites →https://doi.org/10.1136/gut.38.5.738openalex-snapshot
Clinical patterns of familial inflammatory bowel disease.
inferredcites →https://doi.org/10.1136/gutjnl-2014-307649openalex-snapshot
Identification of an anti-inflammatory protein from Faecalibacterium prausnitzii , a commensal bacterium deficient in Crohn’s disease
inferredcites →https://doi.org/10.1136/gutjnl-2015-310746openalex-snapshot
Fungal microbiota dysbiosis in IBD
inferredcites →https://doi.org/10.1186/1471-2180-10-125openalex-snapshot
Pseudomonas aeruginosa inhibits in-vitro Candida biofilm development
inferredcites →https://doi.org/10.1186/2049-2618-2-25openalex-snapshot
The dynamics of a family’s gut microbiota reveal variations on a theme
inferredcites →https://doi.org/10.1371/journal.pcbi.1002808openalex-snapshot
Chapter 12: Human Microbiome Analysis
inferredcites →https://doi.org/10.1371/journal.pone.0080433openalex-snapshot
Targeting Tissular Immune Response Improves Diagnostic Performance of Anti-Saccharomyces cerevisiae Antibodies (ASCA) in Crohn’s Disease
inferredcites →https://doi.org/10.1371/journal.ppat.1003996openalex-snapshot
Oral Mycobiome Analysis of HIV-Infected Patients: Identification of Pichia as an Antagonist of Opportunistic Fungi
inferredcites →https://doi.org/10.2174/138945005774912762openalex-snapshot
Fungal Biofilms and Antimycotics
inferredcites →https://doi.org/10.32614/cran.package.veganopenalex-snapshot
vegan: Community Ecology Package
inferredcites →https://doi.org/10.4049/jimmunol.1500870openalex-snapshot
Delinking CARD9 and IL-17: CARD9 Protects against Candida tropicalis Infection through a TNF-α–Dependent, IL-17–Independent Mechanism
inferredcites →https://doi.org/10.4161/19490976.2014.972223openalex-snapshot
Serratia marcescensis injurious to intestinal epithelial cells

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4068186openalex-extracted
Composition and Function of Gut Microbiota in Bovidae
inferred← citeshttps://doi.org/10.1002/ajp.22880openalex-snapshot
Season, age, and sex affect the fecal mycobiota of free‐ranging Tibetan macaques (Macaca thibetana)
inferred← citeshttps://doi.org/10.1002/art.41169openalex-snapshot
Interleukin‐17 Inhibition in Spondyloarthritis Is Associated With Subclinical Gut Microbiome Perturbations and a Distinctive Interleukin‐25–Driven Intestinal Inflammation
inferred← citeshttps://doi.org/10.1002/imt2.241openalex-snapshot
Interaction between intestinal mycobiota and microbiota shapes lung inflammation
inferred← citeshttps://doi.org/10.1002/wsbm.1438openalex-snapshot
The mammalian mycobiome: A complex system in a dynamic relationship with the host
inferred← citeshttps://doi.org/10.1002/wsbm.1540openalex-snapshot
Gut microbiota and inflammatory bowel disease
inferred← citeshttps://doi.org/10.1002/wsbm.1611openalex-snapshot
Gut mycobiome: A “black box” of gut microbiome–host interactions
inferred← citeshttps://doi.org/10.1002/wsbm.1641openalex-snapshot
Ascomycetes yeasts: The hidden part of human microbiome
inferred← citeshttps://doi.org/10.1007/82_2025_315openalex-snapshot
The Human Mycobiome
inferred← citeshttps://doi.org/10.1007/978-3-030-51849-3_20openalex-snapshot
Our Microbiome: On the Challenges, Promises, and Hype
inferred← citeshttps://doi.org/10.1007/978-3-030-60659-6_15openalex-snapshot
Molecular Characterization of Medically Important Fungi: Current Research and Future Prospects
inferred← citeshttps://doi.org/10.1007/978-3-030-67452-6_11openalex-snapshot
Candida Pathogenicity and Interplay with the Immune System
inferred← citeshttps://doi.org/10.1007/978-3-030-87104-8_3openalex-snapshot
The Rest Is Noise: Finding Signals in Lung Microbiome Data Analysis
inferred← citeshttps://doi.org/10.1007/978-3-031-14023-5_9openalex-snapshot
Gut Microbiota in Elderly Onset Rheumatoid Arthritis
inferred← citeshttps://doi.org/10.1007/978-3-031-35803-6_4openalex-snapshot
Diagnostic Molecular Mycology
inferred← citeshttps://doi.org/10.1007/978-3-031-46712-7_2openalex-snapshot
The Players Within the Intestinal Microbiome (Bacteria, Fungi, Parasites, and Viruses)
inferred← citeshttps://doi.org/10.1007/978-3-031-46712-7_8openalex-snapshot
The Role of the Microbiome in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1007/978-3-031-62558-9_16openalex-snapshot
Mycology in Oncology: Exploring the Role of the Mycobiome in Human Cancer, Etiology, Progression, Epidemiology, Mycoses, and Mycotoxins
inferred← citeshttps://doi.org/10.1007/978-3-319-61449-6_35openalex-snapshot
Placing Interstitial Cystitis/Bladder Pain Syndrome on the Map: The Story of the Interstitial Cystitis Association
inferred← citeshttps://doi.org/10.1007/978-3-319-79026-8_19openalex-snapshot
Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1007/978-3-319-98890-0_9openalex-snapshot
The Role of the Mycobiota in the Gut-Liver Axis
inferred← citeshttps://doi.org/10.1007/978-981-15-7899-1_9openalex-snapshot
Mycobiome Dysbiosis in Oral Lichen Planus
inferred← citeshttps://doi.org/10.1007/978-981-97-1844-3_7openalex-snapshot
Metagenomics Insight into the Mycobiome Analysis
inferred← citeshttps://doi.org/10.1007/978-981-99-1782-2_14openalex-snapshot
Fungal Infection and Ulceration
inferred← citeshttps://doi.org/10.1007/s00044-023-03139-2openalex-snapshot
Molecular modeling of the phosphoglycerate kinase and fructose-bisphosphate aldolase proteins from Candida glabrata and Candida albicans
inferred← citeshttps://doi.org/10.1007/s00248-017-1105-9openalex-snapshot
Fungi in Gastrointestinal Tracts of Human and Mice: from Community to Functions
inferred← citeshttps://doi.org/10.1007/s00248-020-01525-6openalex-snapshot
The Dynamics of Interacting Bacterial and Fungal Communities of the Mouse Colon Following Antibiotics
inferred← citeshttps://doi.org/10.1007/s00281-025-01066-5openalex-snapshot
Emerging microbiome-directed therapies in inflammatory bowel disease: beyond diet modification and FMT
inferred← citeshttps://doi.org/10.1007/s00423-025-03897-0openalex-snapshot
Is the microbiome the answer to inflammatory bowel disease: systematic review
inferred← citeshttps://doi.org/10.1007/s00430-022-00741-wopenalex-snapshot
Child type 1 diabetes associated with mother vaginal bacteriome and mycobiome
inferred← citeshttps://doi.org/10.1007/s00467-022-05844-3openalex-snapshot
Uromycobiome in infants and toddlers with and without urinary tract infections
inferred← citeshttps://doi.org/10.1007/s10620-016-4445-2openalex-snapshot
Circulating Endothelial Progenitor Cells in Crohn’s Disease: An EPiC in the Making?
inferred← citeshttps://doi.org/10.1007/s10620-020-06090-zopenalex-snapshot
Microbial-Based and Microbial-Targeted Therapies for Inflammatory Bowel Diseases
inferred← citeshttps://doi.org/10.1007/s10620-020-06715-3openalex-snapshot
Bile Acid Signaling in Inflammatory Bowel Diseases
inferred← citeshttps://doi.org/10.1007/s11046-019-00413-zopenalex-snapshot
The Mycobiome in Health and Disease: Emerging Concepts, Methodologies and Challenges
inferred← citeshttps://doi.org/10.1007/s12275-019-8682-xopenalex-snapshot
Gastrointestinal microbiota alteration induced by Mucor circinelloides in a murine model
inferred← citeshttps://doi.org/10.1007/s12328-018-0886-9openalex-snapshot
The evidence for fungus in Crohn’s disease pathogenesis
inferred← citeshttps://doi.org/10.1007/s12664-023-01510-0openalex-snapshot
A comprehensive guide to assess gut mycobiome and its role in pathogenesis and treatment of inflammatory bowel disease
inferred← citeshttps://doi.org/10.1007/s12664-024-01541-1openalex-snapshot
Gut bacteriome in inflammatory bowel disease: An update on recent advances
inferred← citeshttps://doi.org/10.1007/s12664-024-01605-2openalex-snapshot
Possible role of intestinal fungal dysbiosis in dectin-1 and cytokines expression in patients with ulcerative colitis
inferred← citeshttps://doi.org/10.1007/s40588-017-0063-9openalex-snapshot
Microbiome: Its Impact Is Being Revealed!
inferred← citeshttps://doi.org/10.1016/b978-0-12-812537-3.00002-0openalex-snapshot
Foundations and Application of Precision Medicine
inferred← citeshttps://doi.org/10.1016/b978-0-12-816453-2.00010-3openalex-snapshot
Pro and prebiotics foods that modulate human health
inferred← citeshttps://doi.org/10.1016/b978-0-12-816664-2.00002-5openalex-snapshot
Bacteriome and Archaeome: The Core Family Under the Microbiomic Roof
inferred← citeshttps://doi.org/10.1016/b978-0-12-816664-2.00003-7openalex-snapshot
Myc(et)obiome: The Big Uncle in the Family
inferred← citeshttps://doi.org/10.1016/b978-0-12-820602-7.00005-2openalex-snapshot
The developing microbiome and inflammatory bowel diseases
inferred← citeshttps://doi.org/10.1016/b978-0-323-85170-1.00004-xopenalex-snapshot
Probiotics in milk and dairy foods
inferred← citeshttps://doi.org/10.1016/b978-0-323-85545-7.00009-0openalex-snapshot
Interaction of iPSC-derived MSCs with the gastrointestinal tract and microbiome in the management of inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-99977-9.00040-5openalex-snapshot
Polymicrobial biofilms: Impact on fungal pathogenesis
inferred← citeshttps://doi.org/10.1016/b978-0-443-13297-1.00014-0openalex-snapshot
Kombucha as a therapeutic soft drink targeting gut health
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2022.09.003openalex-snapshot
Gut microbiome dysbiosis in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.advms.2020.06.003openalex-snapshot
Quantitative changes in selected bacteria in the stool during the treatment of Crohn's disease
inferred← citeshttps://doi.org/10.1016/j.apsb.2026.09.033openalex-snapshot
Harnessing tumor-associated microbiota for cancer therapy and diagnosis: Mechanisms and engineering strategies
inferred← citeshttps://doi.org/10.1016/j.autrev.2023.103486openalex-snapshot
From ASCA breakthrough in Crohn's disease and Candida albicans research to thirty years of investigations about their meaning in human health
inferred← citeshttps://doi.org/10.1016/j.autrev.2025.103912openalex-snapshot
Gut microbiota in rheumatoid arthritis: Mechanistic insights, clinical biomarkers, and translational perspectives
inferred← citeshttps://doi.org/10.1016/j.canlet.2023.216302openalex-snapshot
Gut fungal mycobiome: A significant factor of tumor occurrence and development
inferred← citeshttps://doi.org/10.1016/j.cdnut.2024.102160openalex-snapshot
Current Knowledge on the Preparation and Benefits of Cruciferous Vegetables as Relates to In Vitro, In Vivo, and Clinical Models of Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1016/j.cell.2022.01.017openalex-snapshot
Mucosal fungi promote gut barrier function and social behavior via Type 17 immunity
inferred← citeshttps://doi.org/10.1016/j.cell.2022.09.015openalex-snapshot
A pan-cancer mycobiome analysis reveals fungal involvement in gastrointestinal and lung tumors
inferred← citeshttps://doi.org/10.1016/j.cell.2024.04.043openalex-snapshot
A genomic compendium of cultivated human gut fungi characterizes the gut mycobiome and its relevance to common diseases
inferred← citeshttps://doi.org/10.1016/j.cgh.2024.09.007openalex-snapshot
Gut Goo: Physiology, Diet, and Therapy of Intestinal Mucus and Biofilms in Gastrointestinal Health and Disease
inferred← citeshttps://doi.org/10.1016/j.chom.2017.07.002openalex-snapshot
Commensal Fungi in Health and Disease
inferred← citeshttps://doi.org/10.1016/j.chom.2019.01.007openalex-snapshot
Malassezia Is Associated with Crohn’s Disease and Exacerbates Colitis in Mouse Models
inferred← citeshttps://doi.org/10.1016/j.chom.2020.03.006openalex-snapshot
Fungal Trans-kingdom Dynamics Linked to Responsiveness to Fecal Microbiota Transplantation (FMT) Therapy in Ulcerative Colitis
inferred← citeshttps://doi.org/10.1016/j.chom.2020.04.018openalex-snapshot
Candida in IBD: Friend or Foe?
inferred← citeshttps://doi.org/10.1016/j.chom.2021.04.013openalex-snapshot
Debaryomyces, the Achilles heel of wound repair
inferred← citeshttps://doi.org/10.1016/j.chom.2022.06.009openalex-snapshot
Gut microbiota gestalt
inferred← citeshttps://doi.org/10.1016/j.clnu.2023.11.010openalex-snapshot
Comparative efficacy and tolerability of probiotic, prebiotic, and synbiotic formulations for adult patients with mild-moderate ulcerative colitis in an adjunctive therapy: A network meta-analysis
inferred← citeshttps://doi.org/10.1016/j.csbj.2019.09.010openalex-snapshot
Recent progress in experimental and human disease-associated multi-species biofilms
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.01.008openalex-snapshot
Analyzing the human gut mycobiome – A short guide for beginners
inferred← citeshttps://doi.org/10.1016/j.dld.2017.08.025openalex-snapshot
The mycobiome: Role in health and disease, and as a potential probiotic target in gastrointestinal disease
inferred← citeshttps://doi.org/10.1016/j.drup.2019.02.002openalex-snapshot
Can Saccharomyces cerevisiae keep up as a model system in fungal azole susceptibility research?
inferred← citeshttps://doi.org/10.1016/j.ebiom.2016.10.007openalex-snapshot
The Multibiome: The Intestinal Ecosystem's Influence on Immune Homeostasis, Health, and Disease
inferred← citeshttps://doi.org/10.1016/j.ebiom.2019.06.031openalex-snapshot
Microbiome and type 1 diabetes
inferred← citeshttps://doi.org/10.1016/j.ebiom.2020.102950openalex-snapshot
Gut mycobiome and its interaction with diet, gut bacteria and alzheimer's disease markers in subjects with mild cognitive impairment: A pilot study
inferred← citeshttps://doi.org/10.1016/j.envpol.2020.114599openalex-snapshot
Crohn’s disease and environmental contamination: Current challenges and perspectives in exposure evaluation
inferred← citeshttps://doi.org/10.1016/j.fbr.2021.08.002openalex-snapshot
The human fungal pathogen Malassezia and its role in cancer
inferred← citeshttps://doi.org/10.1016/j.funeco.2023.101297openalex-snapshot
Mr. Toad's wild fungi: Fungal isolate diversity on Colorado boreal toads and their capacity for pathogen inhibition
inferred← citeshttps://doi.org/10.1016/j.giec.2019.02.005openalex-snapshot
The Microbiota and the Immune Response: What Is the Chicken and What Is the Egg?
inferred← citeshttps://doi.org/10.1016/j.heliyon.2026.e45510openalex-snapshot
Navigating microbial balance: Insights and interventions for optimal health amid antibiotic treatment in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1016/j.humic.2018.10.001openalex-snapshot
Microbiome and the immune system: From a healthy steady-state to allergy associated disruption
inferred← citeshttps://doi.org/10.1016/j.humic.2019.100056openalex-snapshot
Digestive tract mycobiota and microbiota and the effects on the immune system
inferred← citeshttps://doi.org/10.1016/j.idairyj.2017.04.009openalex-snapshot
Review of the controversy over whether or not Mycobacterium avium subsp. paratuberculosis poses a food safety risk with pasteurised dairy products
inferred← citeshttps://doi.org/10.1016/j.imbio.2022.152263openalex-snapshot
Inactivation of the Complement Lectin Pathway by Candida tropicalis Secreted Aspartyl Protease-1
inferred← citeshttps://doi.org/10.1016/j.immuni.2019.05.023openalex-snapshot
Gut Mycobiota in Immunity and Inflammatory Disease
inferred← citeshttps://doi.org/10.1016/j.isci.2026.117850openalex-snapshot
Gut microbiota-driven imbalance of the gut-brain-immune homeostatic network in constipation: Pathogenic mechanisms and evolving therapeutic prospects
inferred← citeshttps://doi.org/10.1016/j.it.2019.11.007openalex-snapshot
T Cell Antifungal Immunity and the Role of C-Type Lectin Receptors
inferred← citeshttps://doi.org/10.1016/j.jaad.2017.11.046openalex-snapshot
Effect of alcohol-based hand rub on hand microbiome and hand skin health in hospitalized adult stem cell transplant patients: A pilot study
inferred← citeshttps://doi.org/10.1016/j.jare.2022.10.015openalex-snapshot
Dose-effect of polystyrene microplastics on digestive toxicity in chickens (Gallus gallus): Multi-omics reveals critical role of gut-liver axis
inferred← citeshttps://doi.org/10.1016/j.jaut.2023.103114openalex-snapshot
The gut ecosystem and immune tolerance
inferred← citeshttps://doi.org/10.1016/j.jcmgh.2021.11.008openalex-snapshot
Candida tropicalis Infection Modulates the Gut Microbiome and Confers Enhanced Susceptibility to Colitis in Mice
inferred← citeshttps://doi.org/10.1016/j.jhep.2022.12.006openalex-snapshot
Fungal infections and the fungal microbiome in hepatobiliary disorders
inferred← citeshttps://doi.org/10.1016/j.jmii.2022.12.001openalex-snapshot
Microbiota analysis in the hemodialysis population - Focusing on Enterobacteriaceae
inferred← citeshttps://doi.org/10.1016/j.medmic.2020.100008openalex-snapshot
Candida gut commensalism and inflammatory disease
inferred← citeshttps://doi.org/10.1016/j.medmic.2022.100054openalex-snapshot
The effect of intrinsic factors and mechanisms in shaping human gut microbiota
inferred← citeshttps://doi.org/10.1016/j.mib.2017.10.020openalex-snapshot
Fungal interactions with the human host: exploring the spectrum of symbiosis
inferred← citeshttps://doi.org/10.1016/j.mib.2017.11.012openalex-snapshot
Host–microbe interactions: commensal fungi in the gut
inferred← citeshttps://doi.org/10.1016/j.mib.2019.09.010openalex-snapshot
Gut mycobiota under scrutiny: fungal symbionts or environmental transients?
inferred← citeshttps://doi.org/10.1016/j.mib.2019.10.009openalex-snapshot
Contribution of bacterial-fungal balance to plant and animal health
inferred← citeshttps://doi.org/10.1016/j.mib.2020.05.004openalex-snapshot
Minority report: the intestinal mycobiota in systemic infections
inferred← citeshttps://doi.org/10.1016/j.micpath.2019.103942openalex-snapshot
Polymicrobial interactions involving fungi and their importance for the environment and in human disease
inferred← citeshttps://doi.org/10.1016/j.micpath.2021.105383openalex-snapshot
Microbial pathogenesis in inflammatory bowel diseases
inferred← citeshttps://doi.org/10.1016/j.micpath.2022.105690openalex-snapshot
Population structure, susceptibility profile, phenotypic and mating properties of Candida tropicalis isolated from pediatric patients
inferred← citeshttps://doi.org/10.1016/j.molmed.2022.05.006openalex-snapshot
Pathogenic associations between oral and gastrointestinal diseases
inferred← citeshttps://doi.org/10.1016/j.molmet.2025.102289openalex-snapshot
The role of the gut non-bacterial microbiome (virome, mycobiome, archaeome) and its impact on obesity
inferred← citeshttps://doi.org/10.1016/j.mycmed.2021.101164openalex-snapshot
Candida albicans triggers qualitative and temporal responses in gut bacteria
inferred← citeshttps://doi.org/10.1016/j.phrs.2020.104962openalex-snapshot
Inflammatory bowel diseases, the hygiene hypothesis and the other side of the microbiota: Parasites and fungi
inferred← citeshttps://doi.org/10.1016/j.plipres.2024.101291openalex-snapshot
Immunology of bile acids regulated receptors
inferred← citeshttps://doi.org/10.1016/j.ram.2024.12.005openalex-snapshot
Effect of DNA extraction method in gut fungal community assessment
inferred← citeshttps://doi.org/10.1016/j.semcdb.2018.02.026openalex-snapshot
Candida innate immunity at the mucosa
inferred← citeshttps://doi.org/10.1016/j.smim.2023.101757openalex-snapshot
Immunoglobulins at the interface of the gut mycobiota and anti-fungal immunity
inferred← citeshttps://doi.org/10.1016/j.tim.2018.08.009openalex-snapshot
Bowel Biofilms: Tipping Points between a Healthy and Compromised Gut?
inferred← citeshttps://doi.org/10.1016/j.yamp.2023.08.003openalex-snapshot
Molecular Diagnostics for Invasive Fungal Infections: Barriers to Widespread Adoption and Opportunities for Improvement
inferred← citeshttps://doi.org/10.1016/s0001-4079(19)30206-7openalex-snapshot
Importance des micromycètes dans le microbiote intestinal : le modèle Candida albicans.
inferred← citeshttps://doi.org/10.1016/s2666-5247(22)00203-8openalex-snapshot
The gut mycobiome in health, disease, and clinical applications in association with the gut bacterial microbiome assembly
inferred← citeshttps://doi.org/10.1021/acs.estlett.9b00297openalex-snapshot
Response of Fish Gut Microbiota to Toxin-Containing Cyanobacterial Extracts: A Microcosm Study on the Medaka (Oryzias latipes)
inferred← citeshttps://doi.org/10.1038/ni.3780openalex-snapshot
Regulation of inflammation by microbiota interactions with the host
inferred← citeshttps://doi.org/10.1038/nri.2017.55openalex-snapshot
Fungal dysbiosis: immunity and interactions at mucosal barriers
inferred← citeshttps://doi.org/10.1038/s41368-019-0045-2openalex-snapshot
Salivary mycobiome dysbiosis and its potential impact on bacteriome shifts and host immunity in oral lichen planus
inferred← citeshttps://doi.org/10.1038/s41385-022-00536-5openalex-snapshot
Immunosurveillance of Candida albicans commensalism by the adaptive immune system
inferred← citeshttps://doi.org/10.1038/s41396-021-00901-5openalex-snapshot
Priority effects dictate community structure and alter virulence of fungal-bacterial biofilms
inferred← citeshttps://doi.org/10.1038/s41467-017-02522-zopenalex-snapshot
Fungal networks shape dynamics of bacterial dispersal and community assembly in cheese rind microbiomes
inferred← citeshttps://doi.org/10.1038/s41467-018-07556-5openalex-snapshot
Molecular diagnostics in medical mycology
inferred← citeshttps://doi.org/10.1038/s41522-023-00433-0openalex-snapshot
Colonic phosphocholine is correlated with Candida tropicalis and promotes diarrhea and pathogen clearance
inferred← citeshttps://doi.org/10.1038/s41522-024-00605-6openalex-snapshot
Microbial melatonin metabolism in the human intestine as a therapeutic target for dysbiosis and rhythm disorders
inferred← citeshttps://doi.org/10.1038/s41522-025-00827-2openalex-snapshot
Intestinal fungal signatures and their impact on immune checkpoint inhibitor efficacy: a multi-cohort meta-analysis
inferred← citeshttps://doi.org/10.1038/s41564-018-0191-xopenalex-snapshot
The type VI secretion system deploys antifungal effectors against microbial competitors
inferred← citeshttps://doi.org/10.1038/s41564-021-00983-zopenalex-snapshot
Mycobiota-induced IgA antibodies regulate fungal commensalism in the gut and are dysregulated in Crohn’s disease
inferred← citeshttps://doi.org/10.1038/s41575-018-0051-4openalex-snapshot
Neuroimmunophysiology of the gut: advances and emerging concepts focusing on the epithelium
inferred← citeshttps://doi.org/10.1038/s41575-019-0121-2openalex-snapshot
The gut mycobiota: insights into analysis, environmental interactions and role in gastrointestinal diseases
inferred← citeshttps://doi.org/10.1038/s41575-023-00816-wopenalex-snapshot
Commensal fungi in intestinal health and disease
inferred← citeshttps://doi.org/10.1038/s41579-025-01163-0openalex-snapshot
Microbiota in inflammatory bowel disease: mechanisms of disease and therapeutic opportunities
inferred← citeshttps://doi.org/10.1038/s41586-022-04502-wopenalex-snapshot
Immune regulation by fungal strain diversity in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1038/s41590-025-02281-wopenalex-snapshot
Microbiota-mediated mechanisms of mucosal immunity across the lifespan
inferred← citeshttps://doi.org/10.1038/s41591-026-04616-yopenalex-snapshot
Antifungal therapy improves microbiome dynamics in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1038/s41598-018-21422-wopenalex-snapshot
Remodeling of the Candida glabrata cell wall in the gastrointestinal tract affects the gut microbiota and the immune response
inferred← citeshttps://doi.org/10.1038/s41598-019-44974-xopenalex-snapshot
DNA extraction and amplicon production strategies deeply inf luence the outcome of gut mycobiome studies
inferred← citeshttps://doi.org/10.1038/s41598-020-68214-9openalex-snapshot
Bacteroides thetaiotaomicron and Lactobacillus johnsonii modulate intestinal inflammation and eliminate fungi via enzymatic hydrolysis of the fungal cell wall
inferred← citeshttps://doi.org/10.1038/s41598-021-90380-7openalex-snapshot
Gut microbiota composition in health-care facility-and community-onset diarrheic patients with Clostridioides difficile infection
inferred← citeshttps://doi.org/10.1038/s41598-022-10548-7openalex-snapshot
The gut fungal and bacterial microbiota in pediatric patients with inflammatory bowel disease introduced to treatment with anti-tumor necrosis factor-α
inferred← citeshttps://doi.org/10.1038/s41598-022-13438-0openalex-snapshot
Mycobiota composition and changes across pregnancy in patients with gestational diabetes mellitus (GDM)
inferred← citeshttps://doi.org/10.1038/s41598-024-54257-9openalex-snapshot
Microbial butyrate capacity is reduced in inflamed mucosa in patients with ulcerative colitis
inferred← citeshttps://doi.org/10.1038/s42003-021-02036-xopenalex-snapshot
Gut mycobiota alterations in patients with COVID-19 and H1N1 infections and their associations with clinical features
inferred← citeshttps://doi.org/10.1038/s42255-025-01420-9openalex-snapshot
Gut mucosal mycobiome profiling in Crohn’s disease uncovers an AMP-mediated anti-inflammatory effect of Cladosporium sphaerospermum
inferred← citeshttps://doi.org/10.1038/s44321-025-00262-yopenalex-snapshot
Interplay between fungal infections and autoimmunity: mechanisms and therapeutic perspectives
inferred← citeshttps://doi.org/10.1039/d2fo02659gopenalex-snapshot
Bifidobacterium bifidum FJSWX19M5 alleviated 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced chronic colitis by mitigating gut barrier injury and increasing regulatory T cells
inferred← citeshttps://doi.org/10.1042/bcj20240621openalex-snapshot
Interplay of constipation, intestinal barrier dysfunction and fungal exposome in aetiopathogenesis of Parkinson’s disease: hypothesis with supportive data
inferred← citeshttps://doi.org/10.1053/j.gastro.2016.10.012openalex-snapshot
Roles for Intestinal Bacteria, Viruses, and Fungi in Pathogenesis of Inflammatory Bowel Diseases and Therapeutic Approaches
inferred← citeshttps://doi.org/10.1053/j.gastro.2016.12.004openalex-snapshot
Inflammatory Bowel Disease 2017: Innovations and Changing Paradigms
inferred← citeshttps://doi.org/10.1053/j.gastro.2020.06.100openalex-snapshot
Effects of Intestinal Fungi and Viruses on Immune Responses and Inflammatory Bowel Diseases
inferred← citeshttps://doi.org/10.1053/j.gastro.2023.01.017openalex-snapshot
Modulating the Microbiome for Crohn’s Disease Treatment
inferred← citeshttps://doi.org/10.1053/j.gastro.2025.01.004openalex-snapshot
Gut Microbiome Signature in Predisease Phase of Inflammatory Bowel Disease: Prediction to Pathogenesis to Prevention
inferred← citeshttps://doi.org/10.1080/00365521.2021.1963838openalex-snapshot
The important role of fungi in inflammatory bowel diseases
inferred← citeshttps://doi.org/10.1080/03007995.2020.1838460openalex-snapshot
The association between Candida infection and ankylosing spondylitis: a population-based matched cohort study
inferred← citeshttps://doi.org/10.1080/08927014.2021.2022125openalex-snapshot
Exploring the antibacterial, antibiofilm, and antivirulence activities of tea tree oil-containing nanoemulsion against carbapenem-resistant Serratia marcescens associated infections
inferred← citeshttps://doi.org/10.1080/19490976.2019.1662712openalex-snapshot
Additional Candida albicans administration enhances the severity of dextran sulfate solution induced colitis mouse model through leaky gut-enhanced systemic inflammation and gut-dysbiosis but attenuated by Lactobacillus rhamnosus L34
inferred← citeshttps://doi.org/10.1080/19490976.2021.1930871openalex-snapshot
Inter-kingdom relationships in Crohn’s disease explored using a multi-omics approach
inferred← citeshttps://doi.org/10.1080/19490976.2022.2107866openalex-snapshot
Novel technologies to characterize and engineer the microbiome in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1080/19490976.2022.2121576openalex-snapshot
Host-mycobiome metabolic interactions in health and disease
inferred← citeshttps://doi.org/10.1080/19490976.2022.2123677openalex-snapshot
Altered microbial biogeography in an innate model of colitis
inferred← citeshttps://doi.org/10.1080/19490976.2023.2226916openalex-snapshot
Neglected gut microbiome: interactions of the non-bacterial gut microbiota with enteric pathogens
inferred← citeshttps://doi.org/10.1080/19490976.2023.2252780openalex-snapshot
Targeting microbial quorum sensing: the next frontier to hinder bacterial driven gastrointestinal infections
inferred← citeshttps://doi.org/10.1080/19490976.2023.2276806openalex-snapshot
Alterations in intestinal Archaea composition in pediatric patients with Crohn’s disease based on next-generation sequencing – a pilot study
inferred← citeshttps://doi.org/10.1080/19490976.2024.2327409openalex-snapshot
Stress in the microbiome-immune crosstalk
inferred← citeshttps://doi.org/10.1080/19490976.2024.2414805openalex-snapshot
The role and mechanism of gut-lung axis mediated bidirectional communication in the occurrence and development of chronic obstructive pulmonary disease
inferred← citeshttps://doi.org/10.1080/19490976.2024.2416922openalex-snapshot
Candida tropicalis -derived vitamin B3 exerts protective effects against intestinal inflammation by promoting IL-17A/IL-22-dependent epithelial barrier function
inferred← citeshttps://doi.org/10.1080/19490976.2024.2440111openalex-snapshot
The mycobiome as integral part of the gut microbiome: crucial role of symbiotic fungi in health and disease
inferred← citeshttps://doi.org/10.1080/19490976.2025.2516702openalex-snapshot
Gut microbiota in regulatory T cell generation and function: mechanisms and health implications
inferred← citeshttps://doi.org/10.1080/19490976.2026.2653288openalex-snapshot
Neglected kingdoms: the gut virome, mycobiome and their role in inflammatory bowel disease
inferred← citeshttps://doi.org/10.1080/19490976.2026.2689168openalex-snapshot
Cross-kingdom microbiome interactions along the gut–lung axis: immune–microecological coordination, shared mechanisms, and disease-context dependence in respiratory disorders
inferred← citeshttps://doi.org/10.1080/19490976.2026.2734644openalex-snapshot
The gut microbiota as a regulator of intestinal stem-cell fate: bacterial and fungal control of differentiation and regeneration
inferred← citeshttps://doi.org/10.1080/20002297.2024.2374639openalex-snapshot
Dysbiosis and interactions of the mycobiome and bacteriome in mucosal lesions of erosive and non-erosive oral lichen planus patients
inferred← citeshttps://doi.org/10.1080/21505594.2026.2707757openalex-snapshot
Activity of Lactobacillus gasseri strain LLG1 and its exopolysaccharides in an inflammatory cell model and on Candida albicans proliferation
inferred← citeshttps://doi.org/10.1089/aid.2017.0137openalex-snapshot
A Summary of the Second Annual HIV Microbiome Workshop
inferred← citeshttps://doi.org/10.1093/bib/bbac250openalex-snapshot
Bioinformatics strategies for studying the molecular mechanisms of fungal extracellular vesicles with a focus on infection and immune responses
inferred← citeshttps://doi.org/10.1093/cid/ciaa190openalex-snapshot
Risk Factors for Extended-Spectrum β-lactamase–Producing Enterobacterales Bloodstream Infection Among Solid-Organ Transplant Recipients
inferred← citeshttps://doi.org/10.1093/ecco-jcc/jjaa220openalex-snapshot
The Impact ofNOD2Genetic Variants on the Gut Mycobiota in Crohn’s Disease Patients in Remission and in Individuals Without Gastrointestinal Inflammation
inferred← citeshttps://doi.org/10.1093/ecco-jcc/jjaa252openalex-snapshot
Bacterial and Fungal Profiles as Markers of Infliximab Drug Response in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1093/femsle/fnac098openalex-snapshot
Inflammatory bowel disease-associated adherent-invasive Escherichia coli have elevated host-defense peptide resistance
inferred← citeshttps://doi.org/10.1093/femsre/fuw047openalex-snapshot
Forgotten fungi—the gut mycobiome in human health and disease
inferred← citeshttps://doi.org/10.1093/femsyr/foag029openalex-snapshot
Yeasts in the gastrointestinal tract
inferred← citeshttps://doi.org/10.1093/g3journal/jkab294openalex-snapshot
Global analysis of Saccharomyces cerevisiae growth in mucin
inferred← citeshttps://doi.org/10.1093/ibd/izab343openalex-snapshot
The Neglected Gut Microbiome: Fungi, Protozoa, and Bacteriophages in Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1093/ibd/izac156openalex-snapshot
Mycobiome and Inflammatory Bowel Disease: Role in Disease Pathogenesis, Current Approaches and Novel Nutritional-based Therapies
inferred← citeshttps://doi.org/10.1093/ibd/izac284openalex-snapshot
A Novel Probiotic Combination Ameliorates Crohn’s Disease–Like Ileitis by Increasing Short-Chain Fatty Acid Production and Modulating Essential Adaptive Immune Pathways
inferred← citeshttps://doi.org/10.1093/ibd/izad082openalex-snapshot
Alterations in the Fungal Microbiome in Ulcerative Colitis
inferred← citeshttps://doi.org/10.1093/ibd/izad209openalex-snapshot
Targeted Probiotics Against Bacterial-Fungal Biofilms: A New Concept Seems to Bring Us Closer to Microbiome-modulating Therapy for Inflammatory Bowel Disease
inferred← citeshttps://doi.org/10.1093/ibd/izad289openalex-snapshot
Fungal Microbiota Composition in Inflammatory Bowel Disease Patients: Characterization in Different Phenotypes and Correlation With Clinical Activity and Disease Course
inferred← citeshttps://doi.org/10.1093/ibd/izaf178openalex-snapshot
Characterization of Intestinal Mycobiome in Surgical Resections from Inflammatory Bowel Disease Patients: A Deeper Analysis in Complicated Crohn’s Disease Phenotypes
inferred← citeshttps://doi.org/10.1093/ibd/izaf217openalex-snapshot
Gut Mycobiome in Inflammatory Bowel Disease: A Systematic Review of Case-Control Studies
inferred← citeshttps://doi.org/10.1093/ibd/izy060openalex-snapshot
The Artificial Sweetener Splenda Promotes Gut Proteobacteria, Dysbiosis, and Myeloperoxidase Reactivity in Crohn’s Disease–Like Ileitis
inferred← citeshttps://doi.org/10.1093/ibd/izy312openalex-snapshot
Emergent Behavior of IBD-AssociatedEscherichia coliDuring Disease
inferred← citeshttps://doi.org/10.1093/ibd/izy328openalex-snapshot
Gut Microbial Signatures Underline Complicated Crohn’s Disease but Vary Between Cohorts; An In Silico Approach
inferred← citeshttps://doi.org/10.1093/ibd/izz076openalex-snapshot
Challenges in IBD Research: Environmental Triggers
inferred← citeshttps://doi.org/10.1093/jac/dkx451openalex-snapshot
Biofilms and beyond: expanding echinocandin utility
inferred← citeshttps://doi.org/10.1093/nutrit/nuab017openalex-snapshot
Synbiotics improve clinical indicators of ulcerative colitis: systematic review with meta-analysis
inferred← citeshttps://doi.org/10.1094/pbiomes-07-19-0035-rvwopenalex-snapshot
The Rice Microbiome: A Model Platform for Crop Holobiome
inferred← citeshttps://doi.org/10.1094/pbiomes-4-1openalex-snapshot
Full Issue PDF
inferred← citeshttps://doi.org/10.1097/cm9.0000000000000718openalex-snapshot
Advances in the understanding of the intestinal micro-environment and inflammatory bowel disease
inferred← citeshttps://doi.org/10.1097/mcg.0000000000001609openalex-snapshot
Oral Fluconazole Therapy in Patients With Active Ulcerative Colitis Who Have Detectable Candida in the Stool
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