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Impact of Contaminants on Microbiota: Linking the Gut–Brain Axis with Neurotoxicity

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

inferredcites →https://doi.org/10.1002/bdr2.1752openalex-snapshot
Bisphenols and phthalates: Plastic chemical exposures can contribute to adverse cardiovascular health outcomes
inferredcites →https://doi.org/10.1002/cpt.1870openalex-snapshot
The Microbiome and the Gut‐Liver‐Brain Axis for Central Nervous System Clinical Pharmacology: Challenges in Specifying and Integrating In Vitro and In Silico Models
inferredcites →https://doi.org/10.1002/em.22311openalex-snapshot
The role of environmental exposures and the epigenome in health and disease
inferredcites →https://doi.org/10.1002/tox.23121openalex-snapshot
Di‐(2‐ethylhexyl) phthalate exposure induces female reproductive toxicity and alters the intestinal microbiota community structure and fecal metabolite profile in mice
inferredcites →https://doi.org/10.1007/s00213-021-06025-0openalex-snapshot
Sodium butyrate ameliorates the cognitive impairment of Alzheimer’s disease by regulating the metabolism of astrocytes
inferredcites →https://doi.org/10.1007/s11270-017-3277-9openalex-snapshot
A Study on Environmental Bisphenol A Pollution in Plastics Industry Areas
inferredcites →https://doi.org/10.1007/s11356-012-1283-4openalex-snapshot
Impact of chronic exposure to low doses of chlorpyrifos on the intestinal microbiota in the Simulator of the Human Intestinal Microbial Ecosystem (SHIME®) and in the rat
inferredcites →https://doi.org/10.1007/s11356-018-2332-4openalex-snapshot
Use of a combination of in vitro models to investigate the impact of chlorpyrifos and inulin on the intestinal microbiota and the permeability of the intestinal mucosa
inferredcites →https://doi.org/10.1007/s11356-020-09854-2openalex-snapshot
The gut-microbiota-testis axis mediated by the activation of the Nrf2 antioxidant pathway is related to prepuberal steroidogenesis disorders induced by di-(2-ethylhexyl) phthalate
inferredcites →https://doi.org/10.1016/j.apsb.2019.12.001openalex-snapshot
The gut microbiome: an orchestrator of xenobiotic metabolism
inferredcites →https://doi.org/10.1016/j.bbi.2018.11.005openalex-snapshot
Childhood adversity impact on gut microbiota and inflammatory response to stress during pregnancy
inferredcites →https://doi.org/10.1016/j.cbi.2021.109452openalex-snapshot
Sodium butyrate ameliorates the impairment of synaptic plasticity by inhibiting the neuroinflammation in 5XFAD mice
inferredcites →https://doi.org/10.1016/j.chemosphere.2020.127959openalex-snapshot
DEHP induce cholesterol imbalance via disturbing bile acid metabolism by altering the composition of gut microbiota in rats
inferredcites →https://doi.org/10.1016/j.chemosphere.2020.129004openalex-snapshot
Perfluorooctanoic acid-induced liver injury is potentially associated with gut microbiota dysbiosis
inferredcites →https://doi.org/10.1016/j.chemosphere.2020.129442openalex-snapshot
Detection of endocrine disrupting chemicals in Danio rerio and Daphnia pulex: Step-one, behavioral screen
inferredcites →https://doi.org/10.1016/j.chemosphere.2021.130952openalex-snapshot
Bisphenol A impairs cognitive function and 5-HT metabolism in adult male mice by modulating the microbiota-gut-brain axis
inferredcites →https://doi.org/10.1016/j.cmet.2021.10.010openalex-snapshot
Microbiota-derived acetate enables the metabolic fitness of the brain innate immune system during health and disease
inferredcites →https://doi.org/10.1016/j.coisb.2017.06.001openalex-snapshot
Quantitative systems pharmacology and the personalized drug–microbiota–diet axis
inferredcites →https://doi.org/10.1016/j.coisb.2021.05.007openalex-snapshot
Advances in constraint-based modelling of microbial communities
inferredcites →https://doi.org/10.1016/j.cppeds.2019.04.006openalex-snapshot
Prenatal exposure to PCBs and neurological and sexual/pubertal development from birth to adolescence
inferredcites →https://doi.org/10.1016/j.csbj.2020.11.035openalex-snapshot
Inferring composition and function of the human gut microbiome in time and space: A review of genome-scale metabolic modelling tools
inferredcites →https://doi.org/10.1016/j.ebiom.2021.103293openalex-snapshot
Short chain fatty acids and its producing organisms: An overlooked therapy for IBD?
inferredcites →https://doi.org/10.1016/j.ecoenv.2020.110590openalex-snapshot
Intestinal environmental disorders associate with the tissue damages induced by perfluorooctane sulfonate exposure
inferredcites →https://doi.org/10.1016/j.envint.2016.11.019openalex-snapshot
Developmental neurotoxicity of succeeding generations of insecticides
inferredcites →https://doi.org/10.1016/j.envpol.2016.08.039openalex-snapshot
Bisphenol A alters gut microbiome: Comparative metagenomics analysis
inferredcites →https://doi.org/10.1016/j.envpol.2020.114164openalex-snapshot
Gut microbiota dysbiosis might be responsible to different toxicity caused by Di-(2-ethylhexyl) phthalate exposure in murine rodents
inferredcites →https://doi.org/10.1016/j.envpol.2020.114880openalex-snapshot
Bisphenol A exposure induces gut microbiota dysbiosis and consequent activation of gut-liver axis leading to hepatic steatosis in CD-1 mice
inferredcites →https://doi.org/10.1016/j.envpol.2020.115994openalex-snapshot
A review of the impact of xenobiotics from dietary sources on infant health: Early life exposures and the role of the microbiota
inferredcites →https://doi.org/10.1016/j.envres.2021.111829openalex-snapshot
In utero exposure to endocrine disruptors and developmental neurotoxicity: Implications for behavioural and neurological disorders in adult life
inferredcites →https://doi.org/10.1016/j.etap.2015.06.009openalex-snapshot
A review on endocrine disruptors and their possible impacts on human health
inferredcites →https://doi.org/10.1016/j.fct.2019.110700openalex-snapshot
Phthalate exposure alters gut microbiota composition and IgM vaccine response in human newborns
inferredcites →https://doi.org/10.1016/j.fct.2019.110865openalex-snapshot
Long-term effects of low doses of Chlorpyrifos exposure at the preweaning developmental stage: A locomotor, pharmacological, brain gene expression and gut microbiome analysis
inferredcites →https://doi.org/10.1016/j.fct.2019.110872openalex-snapshot
APOE genotype and postnatal chlorpyrifos exposure modulate gut microbiota and cerebral short-chain fatty acids in preweaning mice
inferredcites →https://doi.org/10.1016/j.fct.2021.112306openalex-snapshot
Probiotics as a biological detoxification tool of food chemical contamination: A review
inferredcites →https://doi.org/10.1016/j.jhazmat.2018.05.011openalex-snapshot
Influence of gastrointestinal tract on metabolism of bisphenol A as determined by in vitro simulated system
inferredcites →https://doi.org/10.1016/j.jhazmat.2019.121737openalex-snapshot
Bisphenol A degradation pathway and associated metabolic networks in Escherichia coli harboring the gene encoding CYP450
inferredcites →https://doi.org/10.1016/j.jhazmat.2021.126361openalex-snapshot
Per and poly-fluoroalkyl substances (PFAS) as a contaminant of emerging concern in surface water: A transboundary review of their occurrences and toxicity effects
inferredcites →https://doi.org/10.1016/j.nbd.2019.104621openalex-snapshot
Exercise, diet and stress as modulators of gut microbiota: Implications for neurodegenerative diseases
inferredcites →https://doi.org/10.1016/j.neulet.2016.02.009openalex-snapshot
Butyrate, neuroepigenetics and the gut microbiome: Can a high fiber diet improve brain health?
inferredcites →https://doi.org/10.1016/j.neuropharm.2021.108682openalex-snapshot
Loss of vagal integrity disrupts immune components of the microbiota-gut-brain axis and inhibits the effect of Lactobacillus rhamnosus on behavior and the corticosterone stress response
inferredcites →https://doi.org/10.1016/j.pestbp.2019.05.018openalex-snapshot
Age- and diet-specific effects of chronic exposure to chlorpyrifos on hormones, inflammation and gut microbiota in rats
inferredcites →https://doi.org/10.1016/j.phrs.2021.105543openalex-snapshot
Dysbacteriosis induces abnormal neurogenesis via LPS in a pathway requiring NF-κB/IL-6
inferredcites →https://doi.org/10.1016/j.prrv.2021.05.004openalex-snapshot
Early environmental exposures and life-long risk of chronic non-respiratory disease
inferredcites →https://doi.org/10.1016/j.psyneuen.2019.02.025openalex-snapshot
Faecalibacterium prausnitzii (ATCC 27766) has preventive and therapeutic effects on chronic unpredictable mild stress-induced depression-like and anxiety-like behavior in rats
inferredcites →https://doi.org/10.1016/j.psyneuen.2020.105046openalex-snapshot
A preliminary study of gut microbiome variation and HPA axis reactivity in healthy infants
inferredcites →https://doi.org/10.1016/j.resmic.2019.03.003openalex-snapshot
Serum level of sex steroid hormone is associated with diversity and profiles of human gut microbiome
inferredcites →https://doi.org/10.1016/j.sbsr.2021.100443openalex-snapshot
Gut-on-Chip microphysiological systems: Latest advances in the integration of sensing strategies and adoption of mature detection mechanisms
inferredcites →https://doi.org/10.1016/j.tins.2016.09.002openalex-snapshot
Psychobiotics and the Manipulation of Bacteria–Gut–Brain Signals
inferredcites →https://doi.org/10.1016/j.tox.2020.152365openalex-snapshot
Perfluorooctane sulfonate alters gut microbiota-host metabolic homeostasis in mice
inferredcites →https://doi.org/10.1016/j.toxrep.2020.10.020openalex-snapshot
Phthalates in the diet of Mexican children of school age. Risk analysis
inferredcites →https://doi.org/10.1016/j.yfrne.2016.09.002openalex-snapshot
Epigenetic impacts of endocrine disruptors in the brain
inferredcites →https://doi.org/10.1021/acs.estlett.0c00776openalex-snapshot
Exposures to Semivolatile Organic Compounds in Indoor Environments and Associations with the Gut Microbiomes of Children
inferredcites →https://doi.org/10.1021/acs.jafc.0c05834openalex-snapshot
Exposure to Perfluorooctanoic Acid Induces Cognitive Deficits via Altering Gut Microbiota Composition, Impairing Intestinal Barrier Integrity, and Causing Inflammation in Gut and Brain
inferredcites →https://doi.org/10.1038/nature09944openalex-snapshot
Enterotypes of the human gut microbiome
inferredcites →https://doi.org/10.1038/nn.4030openalex-snapshot
Host microbiota constantly control maturation and function of microglia in the CNS
inferredcites →https://doi.org/10.1038/s41398-021-01422-7openalex-snapshot
Psychobiotic interventions for anxiety in young people: a systematic review and meta-analysis, with youth consultation
inferredcites →https://doi.org/10.1038/s41467-020-18871-1openalex-snapshot
Health and disease markers correlate with gut microbiome composition across thousands of people
inferredcites →https://doi.org/10.1038/s41467-020-19931-2openalex-snapshot
Effect of gut microbiota on depressive-like behaviors in mice is mediated by the endocannabinoid system
inferredcites →https://doi.org/10.1038/s41575-020-0271-2openalex-snapshot
Enteric nervous system: sensory transduction, neural circuits and gastrointestinal motility
inferredcites →https://doi.org/10.1038/s41586-020-2425-3openalex-snapshot
The liver–brain–gut neural arc maintains the Treg cell niche in the gut
inferredcites →https://doi.org/10.1038/s41598-019-50807-8openalex-snapshot
Oral selective serotonin reuptake inhibitors activate vagus nerve dependent gut-brain signalling
inferredcites →https://doi.org/10.1038/s41598-020-66369-zopenalex-snapshot
High Oscillospira abundance indicates constipation and low BMI in the Guangdong Gut Microbiome Project
inferredcites →https://doi.org/10.1038/s41598-020-67709-9openalex-snapshot
Developmental exposure of California mice to endocrine disrupting chemicals and potential effects on the microbiome-gut-brain axis at adulthood
inferredcites →https://doi.org/10.1038/s41598-020-71939-2openalex-snapshot
Compositional and functional differences of the mucosal microbiota along the intestine of healthy individuals
inferredcites →https://doi.org/10.1053/j.gastro.2020.03.050openalex-snapshot
Intestinal Bacteria Maintain Adult Enteric Nervous System and Nitrergic Neurons via Toll-like Receptor 2-induced Neurogenesis in Mice
inferredcites →https://doi.org/10.1074/mcp.r120.002051openalex-snapshot
Proteomics and Metaproteomics Add Functional, Taxonomic and Biomass Dimensions to Modeling the Ecosystem at the Mucosal-luminal Interface
inferredcites →https://doi.org/10.1080/10253890.2021.1895110openalex-snapshot
Gut microbiota diversity but not composition is related to saliva cortisol stress response at the age of 2.5 months
inferredcites →https://doi.org/10.1080/1040841x.2021.1979933openalex-snapshot
Relevance of organ(s)-on-a-chip systems to the investigation of food-gut microbiota-host interactions
inferredcites →https://doi.org/10.1080/1547691x.2019.1706672openalex-snapshot
Mucosal-associated invariant T-Cell (MAIT) activation is altered by chlorpyrifos- and glyphosate-treated commensal gut bacteria
inferredcites →https://doi.org/10.1080/19490976.2018.1445955openalex-snapshot
Gut microbiota in toxicological risk assessment of drugs and chemicals: The need of hour
inferredcites →https://doi.org/10.1080/19490976.2018.1494103openalex-snapshot
Links between environment, diet, and the hunter-gatherer microbiome
inferredcites →https://doi.org/10.1080/19490976.2019.1667724openalex-snapshot
Insights from pharmacokinetic models of host-microbiome drug metabolism
inferredcites →https://doi.org/10.1080/19490976.2019.1707610openalex-snapshot
Gut microbiota profiles in critically ill patients, potential biomarkers and risk variables for sepsis
inferredcites →https://doi.org/10.1093/gigascience/giy055openalex-snapshot
A gene catalogue of the Sprague-Dawley rat gut metagenome
inferredcites →https://doi.org/10.1111/jcmm.17010openalex-snapshot
Faecal microbial biomarkers in early diagnosis of colorectal cancer
inferredcites →https://doi.org/10.1111/nmo.12110openalex-snapshot
Commensal microbiota modulate murine behaviors in a strictly contamination‐free environment confirmed by culture‐based methods
inferredcites →https://doi.org/10.1113/jphysiol.2004.063388openalex-snapshot
Postnatal microbial colonization programs the hypothalamic–pituitary–adrenal system for stress response in mice
inferredcites →https://doi.org/10.1128/msystems.00209-17openalex-snapshot
From Network Analysis to Functional Metabolic Modeling of the Human Gut Microbiota
inferredcites →https://doi.org/10.1128/msystems.00724-19openalex-snapshot
Environmental Chemical Diethylhexyl Phthalate Alters Intestinal Microbiota Community Structure and Metabolite Profile in Mice
inferredcites →https://doi.org/10.1136/gutjnl-2018-316723openalex-snapshot
Human gut microbiome: hopes, threats and promises
inferredcites →https://doi.org/10.1146/annurev-neuro-091619-022657openalex-snapshot
Neuropod Cells: The Emerging Biology of Gut-Brain Sensory Transduction
inferredcites →https://doi.org/10.1146/annurev-publhealth-012420-105020openalex-snapshot
Environmental Influences on the Human Microbiome and Implications for Noncommunicable Disease
inferredcites →https://doi.org/10.1172/jci129401openalex-snapshot
Bile acid metabolism is altered in multiple sclerosis and supplementation ameliorates neuroinflammation
inferredcites →https://doi.org/10.1186/1472-6807-10-34openalex-snapshot
Prediction and analysis of the modular structure of cytochrome P450 monooxygenases
inferredcites →https://doi.org/10.1186/s12915-017-0454-7openalex-snapshot
The human microbiome in evolution
inferredcites →https://doi.org/10.1186/s12934-020-01477-zopenalex-snapshot
Anti-cancer and anti-inflammatory effects elicited by short chain fatty acids produced by Escherichia coli isolated from healthy human gut microbiota
inferredcites →https://doi.org/10.1186/s12970-016-0155-6openalex-snapshot
Exercise-induced stress behavior, gut-microbiota-brain axis and diet: a systematic review for athletes
inferredcites →https://doi.org/10.1186/s12974-020-1705-zopenalex-snapshot
The progress of gut microbiome research related to brain disorders
inferredcites →https://doi.org/10.1186/s13024-021-00427-6openalex-snapshot
Relationships of gut microbiota, short-chain fatty acids, inflammation, and the gut barrier in Parkinson’s disease
inferredcites →https://doi.org/10.1186/s40168-018-0557-6openalex-snapshot
Linking gut microbiota, metabolic syndrome and economic status based on a population-level analysis
inferredcites →https://doi.org/10.1186/s40168-020-00955-1openalex-snapshot
Understanding the host-microbe interactions using metabolic modeling
inferredcites →https://doi.org/10.1258/ebm.2010.009347openalex-snapshot
Corticotropin-releasing factor signaling and visceral response to stress
inferredcites →https://doi.org/10.1289/ehp2207openalex-snapshot
Statistical Methodology in Studies of Prenatal Exposure to Mixtures of Endocrine-Disrupting Chemicals: A Review of Existing Approaches and New Alternatives
inferredcites →https://doi.org/10.1289/ehp5324openalex-snapshot
Diet as a Source of Exposure to Environmental Contaminants for Pregnant Women and Children from Six European Countries
inferredcites →https://doi.org/10.1371/journal.pone.0180745openalex-snapshot
Regulation of gut luminal serotonin by commensal microbiota in mice
inferredcites →https://doi.org/10.1371/journal.pone.0206484openalex-snapshot
Baseline human gut microbiota profile in healthy people and standard reporting template
inferredcites →https://doi.org/10.1371/journal.pone.0251782openalex-snapshot
Maternal precarity and HPA axis functioning shape infant gut microbiota and HPA axis development in humans
inferredcites →https://doi.org/10.1523/jneurosci.1663-18.2018openalex-snapshot
Advances in Enteric Neurobiology: The “Brain” in the Gut in Health and Disease
inferredcites →https://doi.org/10.2903/j.efsa.2019.5809openalex-snapshot
Statement on the available outcomes of the human health assessment in the context of the pesticides peer review of the active substance chlorpyrifos
inferredcites →https://doi.org/10.2903/j.efsa.2020.e18061openalex-snapshot
Editorial: Exploring the need to include microbiomes into EFSA's scientific assessments
inferredcites →https://doi.org/10.3389/fendo.2021.706352openalex-snapshot
Exposure to Perfluoroalkyl Chemicals and Cardiovascular Disease: Experimental and Epidemiological Evidence
inferredcites →https://doi.org/10.3389/fimmu.2019.00277openalex-snapshot
Short Chain Fatty Acids (SCFAs)-Mediated Gut Epithelial and Immune Regulation and Its Relevance for Inflammatory Bowel Diseases
inferredcites →https://doi.org/10.3389/fmicb.2018.02897openalex-snapshot
Comparative Microbiome Signatures and Short-Chain Fatty Acids in Mouse, Rat, Non-human Primate, and Human Feces
inferredcites →https://doi.org/10.3389/fmicb.2020.01621openalex-snapshot
Cortisol-Related Signatures of Stress in the Fish Microbiome
inferredcites →https://doi.org/10.3389/fmicb.2020.575595openalex-snapshot
Regulation of Enteroendocrine Cell Networks by the Major Human Gut Symbiont Bacteroides thetaiotaomicron
inferredcites →https://doi.org/10.3389/fmicb.2020.578007openalex-snapshot
Endobolome, a New Concept for Determining the Influence of Microbiota Disrupting Chemicals (MDC) in Relation to Specific Endocrine Pathogenesis
inferredcites →https://doi.org/10.3389/fnins.2020.00127openalex-snapshot
Case-Control Study of the Effects of Gut Microbiota Composition on Neurotransmitter Metabolic Pathways in Children With Attention Deficit Hyperactivity Disorder
inferredcites →https://doi.org/10.3390/cancers13112810openalex-snapshot
Neuro-Signals from Gut Microbiota: Perspectives for Brain Glioma
inferredcites →https://doi.org/10.3390/ijerph13111088openalex-snapshot
Changes in Composition and Function of Human Intestinal Microbiota Exposed to Chlorpyrifos in Oil as Assessed by the SHIME® Model
inferredcites →https://doi.org/10.3390/ijerph17249403openalex-snapshot
Adipose Tissue and Endocrine-Disrupting Chemicals: Does Sex Matter?
inferredcites →https://doi.org/10.3390/ijms21207471openalex-snapshot
Diet, Microbiota and Brain Health: Unraveling the Network Intersecting Metabolism and Neurodegeneration
inferredcites →https://doi.org/10.3390/ijms22094952openalex-snapshot
Representative Bacillus sp. AM1 from Gut Microbiota Harbor Versatile Molecular Pathways for Bisphenol A Biodegradation
inferredcites →https://doi.org/10.3390/ijms22105273openalex-snapshot
Resveratrol Butyrate Esters Inhibit BPA-Induced Liver Damage in Male Offspring Rats by Modulating Antioxidant Capacity and Gut Microbiota
inferredcites →https://doi.org/10.3390/ijms221810106openalex-snapshot
Efficient Neutrophil Activation Requires Two Simultaneous Activating Stimuli
inferredcites →https://doi.org/10.3390/jcm10030459openalex-snapshot
The Association between Early-Life Gut Microbiota and Long-Term Health and Diseases
inferredcites →https://doi.org/10.3390/jox11030007openalex-snapshot
The Central Role of Cytochrome P450 in Xenobiotic Metabolism—A Brief Review on a Fascinating Enzyme Family
inferredcites →https://doi.org/10.3390/life11020148openalex-snapshot
When a Neonate Is Born, So Is a Microbiota
inferredcites →https://doi.org/10.3390/microorganisms9102066openalex-snapshot
Risk Factors for Gut Dysbiosis in Early Life
inferredcites →https://doi.org/10.3390/nu10040410openalex-snapshot
Towards an Integrative Understanding of tRNA Aminoacylation–Diet–Host–Gut Microbiome Interactions in Neurodegeneration
inferredcites →https://doi.org/10.3390/nu12041096openalex-snapshot
You Are What You Eat—The Relationship between Diet, Microbiota, and Metabolic Disorders—A Review
inferredcites →https://doi.org/10.3390/nu12092695openalex-snapshot
Obesity Measures and Dietary Parameters as Predictors of Gut Microbiota Phyla in Healthy Individuals
inferredcites →https://doi.org/10.3390/nu12103054openalex-snapshot
Involvement of Gut Microbiota, Microbial Metabolites and Interaction with Polyphenol in Host Immunometabolism
inferredcites →https://doi.org/10.3390/nu13010028openalex-snapshot
Niacin and Butyrate: Nutraceuticals Targeting Dysbiosis and Intestinal Permeability in Parkinson’s Disease
inferredcites →https://doi.org/10.3390/nu13062099openalex-snapshot
Regulation of Neurotransmitters by the Gut Microbiota and Effects on Cognition in Neurological Disorders
inferredcites →https://doi.org/10.3892/mmr.2017.7480openalex-snapshot
Sinulariolide suppresses LPS-induced phenotypic and functional maturation of dendritic cells
inferredcites →https://doi.org/10.4103/2319-4170.130922openalex-snapshot
Mammalian gut immunity
inferredcites →https://doi.org/10.5056/jnm20208openalex-snapshot
Roles of Sex Hormones and Gender in the Gut Microbiota

What points at this work

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

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Pfoa, Pfos and Novel 6:2 Cl-Pfesa at Environmentally Relevant Concentrations Perturb the Homeostasis of Liver-Gut Axis in Male Rana Nigromaculata
inferred← citeshttps://doi.org/10.2139/ssrn.4570713openalex-extracted
From Dysbiosis to Neuropathologies: Toxic Effects of Glyphosate in Zebrafish
inferred← citeshttps://doi.org/10.1002/2211-5463.13878openalex-snapshot
Metabolic disrupting chemicals in the intestine: the need for biologically relevant models
inferred← citeshttps://doi.org/10.1002/biof.70077openalex-snapshot
Gut Microbiome Strategies for Enhancing ICI Delivery Across the BBB in Glioblastoma
inferred← citeshttps://doi.org/10.1002/viw.20260021openalex-snapshot
Gut microbiota dysbiosis and Long COVID susceptibility in chronic kidney disease
inferred← citeshttps://doi.org/10.1007/978-3-031-86065-2_3openalex-snapshot
Molecular Mechanisms of Postbiotics in Colorectal Cancer
inferred← citeshttps://doi.org/10.1007/978-981-97-3790-1_19openalex-snapshot
Modulating the Human Microbiome: The Impact of Xenobiotics on Gut Microbial Composition and Therapeutic Strategies
inferred← citeshttps://doi.org/10.1007/s10311-025-01870-3openalex-snapshot
Cognitive impairment and dementia by pollutant exposure: a review
inferred← citeshttps://doi.org/10.1007/s11356-024-32670-xopenalex-snapshot
Analysis and remediation of phthalates in aquatic matrices: current perspectives
inferred← citeshttps://doi.org/10.1007/s11356-024-34969-1openalex-snapshot
Maternal exposure to pesticides induces perturbations in the gut microbiota and blood–brain barrier of dams and the progeny, prevented by a prebiotic
inferred← citeshttps://doi.org/10.1016/b978-0-12-821046-8.00007-4openalex-snapshot
Nervous System
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Human genome or human microbiome genes: Which one is more important for human health and intellectual abilities?
inferred← citeshttps://doi.org/10.1016/bs.ant.2024.02.002openalex-snapshot
Modulation of gut microbiota with probiotics as a strategy to counteract endogenous and exogenous neurotoxicity
inferred← citeshttps://doi.org/10.1016/bs.ant.2024.02.005openalex-snapshot
Gut microbiota as a mediator of the neurotoxicity of mercury
inferred← citeshttps://doi.org/10.1016/bs.ctdb.2022.11.001openalex-snapshot
Gene × environment interactions in autism spectrum disorders
inferred← citeshttps://doi.org/10.1016/j.ajp.2023.103861openalex-snapshot
Decoding the role of the gut microbiome in gut-brain axis, stress-resilience, or stress-susceptibility: A review
inferred← citeshttps://doi.org/10.1016/j.cbi.2025.111807openalex-snapshot
Comprehensive insights into DEHP neurotoxicity across the lifespan: Behavioral effects, mechanisms, and preventive strategies
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.136680openalex-snapshot
Subchronic exposure to environmentally relevant concentrations of di-(2-ethylhexyl) phthalate differentially affects the colon and ileum in adult female mice
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.141699openalex-snapshot
Emerging organic contaminants in drinking water systems: Human intake, emerging health risks, and future research directions
inferred← citeshttps://doi.org/10.1016/j.cmet.2026.08.002openalex-snapshot
The microbiota at the interface of environmental toxicants and the brain
inferred← citeshttps://doi.org/10.1016/j.crmicr.2025.100474openalex-snapshot
Di-(2-ethylhexyl) phthalate induces endometriosis by modulating IGF-1 m6A methylation via the intestinal Odoribacter–butyric acid axis in female rats
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115888openalex-snapshot
From dysbiosis to neuropathologies: Toxic effects of glyphosate in zebrafish
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.117060openalex-snapshot
Alterations in microbiota-metabolism-circRNA crosstalk in autism spectrum disorder-like behaviours caused by maternal exposure to glyphosate-based herbicides in mice
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118295openalex-snapshot
Perinatal bisphenol A exposure impairs gut microbial colonization: Implications for offspring obesity and neurodevelopment
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118519openalex-snapshot
Relationship between PFAS and attention-deficit/hyperactivity disorder or autism spectrum disorder: Epidemiological and experimental evidence
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110093openalex-snapshot
Identification of potential mechanisms of cognitive dysfunction induced by environmentally relevant PFAS mixture in male rats
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120029openalex-snapshot
Assessing the hepatotoxicity of PFOA, PFOS, and 6:2 Cl-PFESA in black-spotted frogs (Rana nigromaculata) and elucidating potential association with gut microbiota
inferred← citeshttps://doi.org/10.1016/j.envpol.2024.125533openalex-snapshot
Effects of Chlorpyrifos on gut dysbiosis and barriers integrity in women with a focus on pregnancy and prebiotic intervention: Insights from advanced in vitro human models
inferred← citeshttps://doi.org/10.1016/j.envres.2025.120816openalex-snapshot
Transformation fate of bisphenol A in aerobic denitrifying cultures and its coercive mechanism on the nitrogen transformation pathway
inferred← citeshttps://doi.org/10.1016/j.envres.2025.121528openalex-snapshot
Bisphenol analogs exposure in 4-year-old children and their intelligence quotient at 6 years: A prospective cohort study
inferred← citeshttps://doi.org/10.1016/j.envres.2025.121709openalex-snapshot
Prenatal PFAS exposure and outcomes related to maternal gut microbiome composition in later pregnancy
inferred← citeshttps://doi.org/10.1016/j.envres.2026.124801openalex-snapshot
Prenatal exposure to phthalates, maternal oxidative stress, and early childhood neurobehavior: a pathway modeling approach
inferred← citeshttps://doi.org/10.1016/j.fct.2026.116096openalex-snapshot
A systematic literature inventory on the interaction between dietary factors and environmental chemical exposures for nervous system health outcomes
inferred← citeshttps://doi.org/10.1016/j.hazl.2025.100168openalex-snapshot
Di(2-ethylhexyl) phthalate exposure disrupts intestinal microbiota and activates immune signaling pathways in zebrafish intestine
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2022.129444openalex-snapshot
Impact of “chemical cocktails” exposure in shaping mice gut microbiota and the role of selenium supplementation combining metallomics, metabolomics, and metataxonomics
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.133920openalex-snapshot
Prenatal PFAS exposure, gut microbiota dysbiosis, and neurobehavioral development in childhood
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.134054openalex-snapshot
Neurotoxicities induced by micro/nanoplastics: A review focusing on the risks of neurological diseases
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2024.136832openalex-snapshot
Early-life exposure to PCBs and PFAS exerts negative effects on the developing central nervous system
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.140959openalex-snapshot
Impact of lactational per- and polyfluoroalkyl substances exposure on infant gut microbiota and potential mediating effects on infant neurodevelopment
inferred← citeshttps://doi.org/10.1016/j.jns.2024.123108openalex-snapshot
An introduction to environmental neurotoxicology: Lessons from a clinical perspective
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2023.115309openalex-snapshot
Impact of per- and polyfluorinated alkyl substances (PFAS) on the marine environment: Raising awareness, challenges, legislation, and mitigation approaches under the One Health concept
inferred← citeshttps://doi.org/10.1016/j.medmic.2025.100133openalex-snapshot
Molecular insights into the impact of environmental pollution on gut microbiota and short chain fatty acids (SCFA) mediated metabolic dysregulation
inferred← citeshttps://doi.org/10.1016/j.neubiorev.2025.106290openalex-snapshot
Are the growing levels of neurotoxic and neuro-disruptive chemicals in our food and drink contributing to the youth mental health crisis? A narrative review
inferred← citeshttps://doi.org/10.1016/j.neuroscience.2024.11.020openalex-snapshot
Dietary interventions in mitigating the impact of environmental pollutants on Alzheimer’s disease – A review
inferred← citeshttps://doi.org/10.1016/j.physbeh.2026.115452openalex-snapshot
Treadmill exercise partially attenuates bisphenol A-associated behavioral alterations with coordinated multi-omics changes in mice
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2022.156324openalex-snapshot
Perturbation of the gut microbiome in wild-caught freshwater turtles (Emydura macquarii macquarii) exposed to elevated PFAS levels
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.165009openalex-snapshot
Insight into the effect of a heavy metal mixture on neurological damage in rats through combined serum metabolomic and brain proteomic analyses
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2023.167034openalex-snapshot
Maternal exposure of mice to glyphosate induces depression- and anxiety-like behavior in the offspring via alterations of the gut-brain axis
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.176941openalex-snapshot
Neurotoxicity of per- and polyfluoroalkyl substances: Evidence and future directions
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.180295openalex-snapshot
Chronic exposure to food additives: Monosodium glutamate and tartrazine dysregulate gut-brain axis in zebrafish model
inferred← citeshttps://doi.org/10.1016/j.toxlet.2022.07.425openalex-snapshot
P09-04 Effect of endocrine disrupting chemicals on gut microbiota in the in-vitro model of enteric nervous system
inferred← citeshttps://doi.org/10.1016/j.toxlet.2025.04.004openalex-snapshot
The role of the gut microbiome in the associations between lead exposure and child neurodevelopment
inferred← citeshttps://doi.org/10.1016/j.toxrep.2023.12.003openalex-snapshot
Tiger nut/coconut dietary intervention as antidotal nutritional remediation strategy against neurobehavioural deficits following organophosphate-induced gut-brain axis dysregulation in mice
inferred← citeshttps://doi.org/10.1016/s0378-4274(23)00809-3openalex-snapshot
P21-01: Investigating the effect of Bisphenols on gut bacteria and neuronal cells
inferred← citeshttps://doi.org/10.1021/acs.est.2c07807openalex-snapshot
Prenatal Exposure to Legacy and Alternative Per- and Polyfluoroalkyl Substances and Neuropsychological Development Trajectories over the First 3 Years of Life
inferred← citeshttps://doi.org/10.1021/acschemneuro.2c00730openalex-snapshot
Comprehensive Review on Potential Signaling Pathways Involving the Transfer of α-Synuclein from the Gut to the Brain That Leads to Parkinson’s Disease
inferred← citeshttps://doi.org/10.1021/acschemneuro.5c00500openalex-snapshot
Molecular Basis by Which PVC Nanoplastics Elicit Neurotoxic Outcomes
inferred← citeshttps://doi.org/10.1021/envhealth.5c00628openalex-snapshot
Insights into the Neurotoxicology of Traditional and Emerging Per- and Polyfluoroalkyl Substances: Mechanisms and Research Frontiers
inferred← citeshttps://doi.org/10.1038/s41598-023-49426-1openalex-snapshot
Sensitivity of Legionella pneumophila to phthalates and their substitutes
inferred← citeshttps://doi.org/10.1038/s41598-025-15021-9openalex-snapshot
The effect of maternal sodium ρ-perfluorous nonenoxybenzene sulfonate exposure on the gut microbiota in dams and offspring
inferred← citeshttps://doi.org/10.1080/10937404.2024.2378406openalex-snapshot
An integrative exploration of environmental stressors on the microbiome-gut-brain axis and immune mechanisms promoting neurological disorders
inferred← citeshttps://doi.org/10.1080/87559129.2026.2649298openalex-snapshot
Psychobiotics and the Microbiota–Gut–Brain Axis: Bridging Functional Foods with Therapeutic Potential in Neurodegenerative and Psychiatric Disorders
inferred← citeshttps://doi.org/10.1093/nutrit/nuae202openalex-snapshot
Effect of Fluoride on Gut Microbiota: A Systematic Review
inferred← citeshttps://doi.org/10.1101/2024.10.02.616111openalex-snapshot
Bacterial Supplements Attenuate Pelvic Irradiation-Induced Brain Metabolic Disruptions via the Gut-Brain Axis: A Multi-Omics Investigation
inferred← citeshttps://doi.org/10.1159/000542901openalex-snapshot
Obesogens and Energy Homeostasis: Definition, Mechanisms of Action, Exposure, and Adverse Effects on Human Health
inferred← citeshttps://doi.org/10.1161/str.0000000000000518openalex-snapshot
Brain Health Across the Life Span: A Framework for Future Studies: A Scientific Statement From the American Heart Association
inferred← citeshttps://doi.org/10.1186/s43094-025-00857-9openalex-snapshot
From gut to brain: exploring the impact of microbiota, dysbiosis, and neuroinflammation in neurodegenerative disorders
inferred← citeshttps://doi.org/10.1515/revneuro-2022-0155openalex-snapshot
Targeting the gut–microbiota–brain axis in irritable bowel disease to improve cognitive function – recent knowledge and emerging therapeutic opportunities
inferred← citeshttps://doi.org/10.17221/87/2024-vetmedopenalex-snapshot
Animal models of autism spectrum disorder: Insights into genetic, structural and environmental models
inferred← citeshttps://doi.org/10.2139/ssrn.7065683openalex-snapshot
First Ternary Deep Eutectic Solvent (Choline Chloride/4-Chlorophenol/PEG200) as Sustainable Extraction Medium for Rapid Determination of Bromophenol Blue in Canned Foods via DLLME-UPLC-DAD: One-Minute Equilibrium, Sub-µg/L Detection, and AGREE-Greenness Validation
inferred← citeshttps://doi.org/10.2147/jpr.s551730openalex-snapshot
Assessment of the Burden of Chronic Neck and/or Shoulder Pain on Quality of Life Among Saudi Adults: A Cross-Sectional Study
inferred← citeshttps://doi.org/10.2174/2666939001666230516140536openalex-snapshot
Effects of Pesticides Carried by Foods on Human Gut Microbiota
inferred← citeshttps://doi.org/10.31032/ijbpas/2023/12.10.1031openalex-snapshot
UNDERSTANDING THE INTERPLAY BETWEEN ANXIETY AND ULCERATIVE COLITIS: PREVALENCE, BIDIRECTIONAL RELATIONSHIP, MECHANISMS, AND INFLUENTIAL FACTORS
inferred← citeshttps://doi.org/10.31083/j.ceog5111237openalex-snapshot
Effect of Probiotic Supplementation on Maternal Depression, Anxiety and Attachment in Gestational Diabetes by Improving Mediterranean Diet Quality: A Randomized Controlled Trial
inferred← citeshttps://doi.org/10.3389/fnut.2022.957688openalex-snapshot
The different trends in the burden of neurological and mental disorders following dietary transition in China, the USA, and the world: An extension analysis for the Global Burden of Disease Study 2019
inferred← citeshttps://doi.org/10.3389/fphar.2026.1840947openalex-snapshot
Microbiota-based PBPK model: new approach methodology for assessing the kinetics of drugs and chemicals
inferred← citeshttps://doi.org/10.3389/fpsyt.2024.1295766openalex-snapshot
Mood and microbes: a comprehensive review of intestinal microbiota’s impact on depression
inferred← citeshttps://doi.org/10.3389/fpubh.2026.1892134openalex-snapshot
Prenatal PFAS exposure and offspring health: evidence review and implications for intergenerational risk assessment
inferred← citeshttps://doi.org/10.3390/ijerph192013471openalex-snapshot
Pharmacophore Modeling Using Machine Learning for Screening the Blood–Brain Barrier Permeation of Xenobiotics
inferred← citeshttps://doi.org/10.3390/ijms24076147openalex-snapshot
Impact of Pesticide Residues on the Gut-Microbiota–Blood–Brain Barrier Axis: A Narrative Review
inferred← citeshttps://doi.org/10.3390/ijms26157289openalex-snapshot
Effects of TBBPA Exposure on Neurodevelopment and Behavior in Mice
inferred← citeshttps://doi.org/10.3390/ijms26178258openalex-snapshot
Impact of Aflatoxins on the Digestive, Immune, and Nervous Systems: The Role of Microbiota and Probiotics in Toxicity Protection
inferred← citeshttps://doi.org/10.3390/jox15010014openalex-snapshot
Impact of Ex Vivo Bisphenol A Exposure on Gut Microbiota Dysbiosis and Its Association with Childhood Obesity
inferred← citeshttps://doi.org/10.3390/metabo15030179openalex-snapshot
Unraveling the Metabolic and Microbiome Signatures in Fecal Samples of Pregnant Women with Prenatal Depression
inferred← citeshttps://doi.org/10.3390/microorganisms10071457openalex-snapshot
Impact of Environmental Pollutants on Gut Microbiome and Mental Health via the Gut–Brain Axis
inferred← citeshttps://doi.org/10.3390/nu16020182openalex-snapshot
Nutrition and Chronobiology as Key Components of Multidisciplinary Therapeutic Interventions for Fibromyalgia and Associated Chronic Fatigue Syndrome: A Narrative and Critical Review
inferred← citeshttps://doi.org/10.3390/pr11010045openalex-snapshot
Development of a SPE-HPLC-PDA Method for the Quantification of Phthalates in Bottled Water and Their Gene Expression Modulation in a Human Intestinal Cell Model
inferred← citeshttps://doi.org/10.3390/toxics10050256openalex-snapshot
Developmental Neurotoxicity and Behavioral Screening in Larval Zebrafish with a Comparison to Other Published Results
inferred← citeshttps://doi.org/10.3390/toxics12010039openalex-snapshot
Interaction between Per- and Polyfluorinated Substances (PFAS) and Acetaminophen in Disease Exacerbation—Focusing on Autism and the Gut–Liver–Brain Axis
inferred← citeshttps://doi.org/10.34297/ajbsr.2022.15.002174openalex-snapshot
The Earth-Connected Human Superorganism Vs. The Machine
inferred← citeshttps://doi.org/10.37779/nt.v26i1.5054openalex-snapshot
17α-metiltestosterona, principais aplicações e ameaças ao meio ambiente: uma breve revisão da literatura
inferred← citeshttps://doi.org/10.59324/ejtas.2024.2(6).53openalex-snapshot
The Gut-Brain Axis in Neurodevelopmental Disorders: Mechanistic Insights, Clinical Implications, and Public Health Strategies
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.