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Thyroid Hormone Action Is Disrupted by Bisphenol A as an Antagonist

https://doi.org/10.1210/jc.2002-020209
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What this work says

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

inferredcites →https://doi.org/10.1002/j.1460-2075.1990.tb08270.xopenalex-snapshot
Contrasting developmental and tissue‐specific expression of alpha and beta thyroid hormone receptor genes.
inferredcites →https://doi.org/10.1002/j.1460-2075.1991.tb07947.xopenalex-snapshot
Distinct functions for thyroid hormone receptors alpha and beta in brain development indicated by differential expression of receptor genes.
inferredcites →https://doi.org/10.1006/bbrc.1998.9799openalex-snapshot
The Interaction of the Vitamin D Receptor with Nuclear Receptor Corepressors and Coactivators
inferredcites →https://doi.org/10.1006/bbrc.2002.6407openalex-snapshot
Serum Bisphenol A Concentrations Showed Gender Differences, Possibly Linked to Androgen Levels
inferredcites →https://doi.org/10.1006/taap.1993.1168openalex-snapshot
Interference of Polychlorinated Biphenyls in Hepatic and Brain Thyroid Hormone Metabolism in Fetal and Neonatal Rats
inferredcites →https://doi.org/10.1006/taap.1995.1210openalex-snapshot
Developmental Exposure to Polychlorinated Biphenyls (Aroclor 1254) Reduces Circulating Thyroid Hormone Concentrations and Causes Hearing Deficits in Rats
inferredcites →https://doi.org/10.1006/taap.1996.8069openalex-snapshot
Evaluation of Chemicals with Endocrine Modulating Activity in a Yeast-Based Steroid Hormone Receptor Gene Transcription Assay
inferredcites →https://doi.org/10.1006/taap.1998.8557openalex-snapshot
New Screening Methods for Chemicals with Hormonal Activities Using Interaction of Nuclear Hormone Receptor with Coactivator
inferredcites →https://doi.org/10.1016/0041-008x(86)90337-6openalex-snapshot
Binding of a metabolite of 3,4,3′,4′-tetrachlorobiphenyl to transthyretin reduces serum vitamin A transport by inhibiting the formation of the protein complex carrying both retinol and thyroxin
inferredcites →https://doi.org/10.1016/0041-008x(92)90006-eopenalex-snapshot
UDP-glucuronosyltransferase inducers reduce thyroid hormone levels in rats by an extrathyroidal mechanism
inferredcites →https://doi.org/10.1016/0092-8674(91)90020-yopenalex-snapshot
Direct repeats as selective response elements for the thyroid hormone, retinoic acid, and vitamin D3 receptors
inferredcites →https://doi.org/10.1016/0092-8674(95)90199-xopenalex-snapshot
The nuclear receptor superfamily: The second decade
inferredcites →https://doi.org/10.1016/0272-0590(87)90142-4openalex-snapshot
The developmental toxicity of bisphenol A in rats and mice*1
inferredcites →https://doi.org/10.1016/0303-7207(90)90054-copenalex-snapshot
Expression of erbAα and β mRNAs in regions of adult rat brain
inferredcites →https://doi.org/10.1016/0378-4274(93)90023-qopenalex-snapshot
Effects of perinatal exposure to specific PCB congeners on thyroid hormone concentrations and thyroid histology in the rat
inferredcites →https://doi.org/10.1016/s0021-9258(17)35275-4openalex-snapshot
Functional characterization and receptor binding studies of the malic enzyme thyroid hormone response element.
inferredcites →https://doi.org/10.1016/s0021-9258(18)42375-7openalex-snapshot
Thyroid hormone receptor mutants that cause resistance to thyroid hormone. Evidence for receptor competition for DNA sequences in target genes.
inferredcites →https://doi.org/10.1016/s0021-9258(18)86977-0openalex-snapshot
Relationship of c-erbA mRNA content to tissue triiodothyronine nuclear binding capacity and function in developing and adult rats.
inferredcites →https://doi.org/10.1016/s0960-0760(96)00104-5openalex-snapshot
Environmental estrogens: Effects on cholesterol lowering and bone in the ovariectomized rat
inferredcites →https://doi.org/10.1021/jm00155a010openalex-snapshot
Structurally specific binding of halogenated biphenyls to thyroxine transport protein
inferredcites →https://doi.org/10.1038/324635a0openalex-snapshot
The c-erb-A protein is a high-affinity receptor for thyroid hormone
inferredcites →https://doi.org/10.1038/324641a0openalex-snapshot
The c-erb-A gene encodes a thyroid hormone receptor
inferredcites →https://doi.org/10.1038/335563a0openalex-snapshot
GAL4-VP16 is an unusually potent transcriptional activator
inferredcites →https://doi.org/10.1038/337659a0openalex-snapshot
Inhibition of thyroid hormone action by a non-hormone binding c-erbA protein generated by alternative mRNA splicing
inferredcites →https://doi.org/10.1056/nejm199908193410801openalex-snapshot
Maternal Thyroid Deficiency during Pregnancy and Subsequent Neuropsychological Development of the Child
inferredcites →https://doi.org/10.1073/pnas.86.18.7250openalex-snapshot
Differential expression of alpha and beta thyroid hormone receptor genes in rat brain and pituitary.
inferredcites →https://doi.org/10.1080/00984100050120415openalex-snapshot
PHARMACOKINETIC DISPOSITION AND TISSUE DISTRIBUTION OF BISPHENOL A IN RATS AFTER INTRAVENOUS ADMINISTRATION
inferredcites →https://doi.org/10.1128/mcb.17.5.2642openalex-snapshot
Nuclear Receptor Corepressors Activate Rather than Suppress Basal Transcription of Genes That Are Negatively Regulated by Thyroid Hormone
inferredcites →https://doi.org/10.1128/mcb.20.22.8329-8342.2000openalex-snapshot
Cloning and Characterization of Two Novel Thyroid Hormone Receptor β Isoforms
inferredcites →https://doi.org/10.1128/mcb.21.14.4761-4772.2001openalex-snapshot
Functional Interference between Thyroid Hormone Receptor α (TRα) and Natural Truncated TRΔα Isoforms in the Control of Intestine Development
inferredcites →https://doi.org/10.1203/00006450-199410000-00009openalex-snapshot
Effects of Dioxins and Polychlorinated Biphenyls on Thyroid Hormone Status of Pregnant Women and Their Infants
inferredcites →https://doi.org/10.1210/edrv.20.3.0366openalex-snapshot
Nuclear Receptor Coregulators: Cellular and Molecular Biology
inferredcites →https://doi.org/10.1210/endo-126-2-1105openalex-snapshot
Characterization of Interaction between Nuclear T3Receptors and Antiserum against Cellular-erb A Peptide*
inferredcites →https://doi.org/10.1210/endo.132.6.8504731openalex-snapshot
Bisphenol-A: an estrogenic substance is released from polycarbonate flasks during autoclaving
inferredcites →https://doi.org/10.1210/me.12.12.1888openalex-snapshot
A Novel Natural Mutation in the Thyroid Hormone Receptor Defines a Dual Functional Domain That Exchanges Nuclear Receptor Corepressors and Coactivators
inferredcites →https://doi.org/10.1210/me.14.3.421openalex-snapshot
Endocrine Disrupting Chemicals, Phthalic Acid and Nonylphenol, Activate Pregnane X Receptor-Mediated Transcription
inferredcites →https://doi.org/10.1210/mend-5-9-1339openalex-snapshot
Independent Expression of the α and β c-erbA Genes in Developing Rat Brain
inferredcites →https://doi.org/10.1289/ehp.0010897openalex-snapshot
Environmental Estrogens Induce Transcriptionally Active Estrogen Receptor Dimers in Yeast: Activity Potentiated by the Coactivator RIP140
inferredcites →https://doi.org/10.1289/ehp.8982323openalex-snapshot
Multifunctional Receptor Model for Dioxin and Related Compound Toxic Action: Possible Thyroid Hormone-Responsive Effector-Linked Site
inferredcites →https://doi.org/10.1289/ehp.94102290openalex-snapshot
Polychlorinated biphenyls as hormonally active structural analogues.
inferredcites →https://doi.org/10.1289/ehp.95103844openalex-snapshot
The E-Screen Assay: A Comparison of Different MCF7 Cell Stocks
inferredcites →https://doi.org/10.1289/ehp.95103s7113openalex-snapshot
The E-SCREEN assay as a tool to identify estrogens: an update on estrogenic environmental pollutants.
inferredcites →https://doi.org/10.1289/ehp.9710570openalex-snapshot
Relative Binding Affinity-Serum Modified Access (RBA-SMA) Assay Predicts the Relative In Vivo Bioactivity of the Xenoestrogens Bisphenol A and Octylphenol
inferredcites →https://doi.org/10.1523/jneurosci.12-06-02288.1992openalex-snapshot
Spatial and temporal expression of alpha- and beta-thyroid hormone receptor mRNAs, including the beta 2-subtype, in the developing mammalian nervous system
inferredcites →https://doi.org/10.1530/eje.0.1450513openalex-snapshot
Bisphenol-A, an environmental estrogen, activates the human orphan nuclear receptor, steroid and xenobiotic receptor-mediated transcription
inferredcites →https://doi.org/10.2307/3432519openalex-snapshot
The E-SCREEN Assay as a Tool to Identify Estrogens: An Update on Estrogenic Environmental Pollutants

What points at this work

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

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A 2024 inventory of test methods relevant to thyroid hormone system disruption for human health and environmental regulatory hazard assessment
inferred← citeshttps://doi.org/10.1001/jama.2009.121openalex-snapshot
Association of Bisphenol A With Diabetes and Other Abnormalities
inferred← citeshttps://doi.org/10.1001/jama.300.11.1303openalex-snapshot
Association of Urinary Bisphenol A Concentration With Medical Disorders and Laboratory Abnormalities in Adults
inferred← citeshttps://doi.org/10.1002/9781118184141.ch12openalex-snapshot
Bisphenol A
inferred← citeshttps://doi.org/10.1002/9781118679654.ch8openalex-snapshot
Obesity
inferred← citeshttps://doi.org/10.1002/9781118679654.ch9openalex-snapshot
Effects and Predicted Consequences of Persistent and Bioactive Organic Pollutants on Thyroid Function
inferred← citeshttps://doi.org/10.1002/9781118891094.ch3openalex-snapshot
Environmental Chemicals Targeting Estrogen Signaling Pathways
inferred← citeshttps://doi.org/10.1002/9781118891094.ch5openalex-snapshot
Thyroid‐Disrupting Chemicals
inferred← citeshttps://doi.org/10.1002/9781119023647.ch13openalex-snapshot
Toxicoepigenetics and Effects on Life Course Disease Susceptibility
inferred← citeshttps://doi.org/10.1002/9781119414612.ch64openalex-snapshot
Polyuria and Polydipsia
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Impact of Pesticide Exposure and Associated Health Effects
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ENDOCRINE‐DISRUPTING CHEMICALS
inferred← citeshttps://doi.org/10.1002/9781119858430.ch20openalex-snapshot
The Role of Bisphenol A in ASIA Syndrome
inferred← citeshttps://doi.org/10.1002/app.38598openalex-snapshot
Direct synthesis of surface molecularly imprinted polymers based on vinyl–SiO2 nanospheres for recognition of bisphenol A
inferred← citeshttps://doi.org/10.1002/bdr2.1752openalex-snapshot
Bisphenols and phthalates: Plastic chemical exposures can contribute to adverse cardiovascular health outcomes
inferred← citeshttps://doi.org/10.1002/bdrb.20275openalex-snapshot
Bisphenol A: developmental toxicity from early prenatal exposurea
inferred← citeshttps://doi.org/10.1002/chem.201701024openalex-snapshot
Fluorogenic Sensing of Carcinogenic Bisphenol A using Aptamer‐Capped Mesoporous Silica Nanoparticles
inferred← citeshttps://doi.org/10.1002/cphy.c160038openalex-snapshot
Adipose Tissue as a Site of Toxin Accumulation
inferred← citeshttps://doi.org/10.1002/em.21692openalex-snapshot
Epigenetic responses following maternal dietary exposure to physiologically relevant levels of bisphenol A
inferred← citeshttps://doi.org/10.1002/etc.2043openalex-snapshot
Interactions between chemical and climate stressors: A role for mechanistic toxicology in assessing climate change risks
inferred← citeshttps://doi.org/10.1002/etc.4985openalex-snapshot
Toxicity Screening of Bisphenol A Replacement Compounds: Cytotoxicity and mRNA Expression in Primary Hepatocytes of Chicken and Double-Crested Cormorant
inferred← citeshttps://doi.org/10.1002/etc.5032openalex-snapshot
In Vitro Screening of 21 Bisphenol A Replacement Alternatives: Compared with Bisphenol A, the Majority of Alternatives Are More Cytotoxic and Dysregulate More Genes in Avian Hepatocytes
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2017.tb00778.xopenalex-snapshot
Adipose Tissue as a Site of Toxin Accumulation
inferred← citeshttps://doi.org/10.1002/jat.4649openalex-snapshot
Rsad2 mediates Bisphenol A‐induced actin cytoskeletal disruption in mouse spermatocytes
inferred← citeshttps://doi.org/10.1002/jbt.20390openalex-snapshot
Gene expression profiling to examine the thyroid hormone‐disrupting activity of hydroxylated polychlorinated biphenyls in metamorphosing amphibian tadpole
inferred← citeshttps://doi.org/10.1002/jbt.21459openalex-snapshot
Fetal Liver Bisphenol A Concentrations and Biotransformation Gene Expression Reveal Variable Exposure and Altered Capacity for Metabolism in Humans
inferred← citeshttps://doi.org/10.1002/jbt.22521openalex-snapshot
Combined approaches for evaluation of xenoestrogen neural toxicity and thyroid dysfunction: Screening of oxido‐nitrosative markers, DNA fragmentation, and biogenic amine degradation
inferred← citeshttps://doi.org/10.1002/jbt.23292openalex-snapshot
Susceptibility of male reproductive system to bisphenol A, an endocrine disruptor: Updates from epidemiological and experimental evidence
inferred← citeshttps://doi.org/10.1002/jcp.20460openalex-snapshot
3,5,3′‐triiodothyronine (T3) is a survival factor for pancreatic β‐cells undergoing apoptosis
inferred← citeshttps://doi.org/10.1002/jnr.21020openalex-snapshot
Murine neocortical histogenesis is perturbed by prenatal exposure to low doses of bisphenol A
inferred← citeshttps://doi.org/10.1002/msj.20237openalex-snapshot
Environmental Neurotoxicants and Developing Brain
inferred← citeshttps://doi.org/10.1002/tox.22239openalex-snapshot
BPA ‐toxicity via superoxide anion overload and a deficit in β‐catenin signaling in human bone mesenchymal stem cells
inferred← citeshttps://doi.org/10.1007/1-59745-107-x_2openalex-snapshot
Endocrine Disruption and the Female
inferred← citeshttps://doi.org/10.1007/978-1-4471-6500-2_1openalex-snapshot
Human Health Effects of Bisphenol A
inferred← citeshttps://doi.org/10.1007/978-1-4614-2383-6_7openalex-snapshot
The Role of Thyroid Modulation by Methylmercury in Developmental Neurotoxicity
inferred← citeshttps://doi.org/10.1007/978-1-60761-561-3_5openalex-snapshot
Thyroid Hormone Regulation of Mammalian Reproductive Development and the Potential Impact of Endocrine-Disrupting Chemicals
inferred← citeshttps://doi.org/10.1007/978-3-031-36494-5_2openalex-snapshot
Cellular Mechanisms of Endocrine Disruption
inferred← citeshttps://doi.org/10.1007/978-3-032-17658-5_12openalex-snapshot
Mechanism of Toxicity: Cellular and Molecular Responses to Microplastic Exposure
inferred← citeshttps://doi.org/10.1007/978-3-319-01619-1_3openalex-snapshot
Adverse Effects of Bisphenol A on Male Reproductive Function
inferred← citeshttps://doi.org/10.1007/978-3-319-16510-3_13openalex-snapshot
Micro- and Nano-plastics and Human Health
inferred← citeshttps://doi.org/10.1007/978-3-319-75935-7_13openalex-snapshot
Challenges of Endocrine Disruption and Cardiac Development
inferred← citeshttps://doi.org/10.1007/978-3-319-89321-1_14openalex-snapshot
EXPOsOMICs: Meet-in-the-Middle and Network Perturbation
inferred← citeshttps://doi.org/10.1007/978-3-642-22775-2_8openalex-snapshot
Fetal and Adult Exposure to Bisphenol-A as a Contributing Factor in the Etiology of the Metabolic Syndrome
inferred← citeshttps://doi.org/10.1007/978-3-642-22775-2_9openalex-snapshot
Bisphenol A in the Gut: Another Break in the Wall?
inferred← citeshttps://doi.org/10.1007/978-981-15-0520-1_6openalex-snapshot
Thyroid Hormone System and Development
inferred← citeshttps://doi.org/10.1007/978-981-16-9116-4_11openalex-snapshot
Mechanisms of Action of Emerging Contaminants: Pharmaceuticals and Personal Care Products (PPCP)
inferred← citeshttps://doi.org/10.1007/bf02977657openalex-snapshot
Differential regulation of thyroid hormone receptor-mediated function by endocrine disruptors
inferred← citeshttps://doi.org/10.1007/bf03348189openalex-snapshot
Assault on the thyroid by xenobiotics: Another attack on G-protein coupled receptors
inferred← citeshttps://doi.org/10.1007/s00204-011-0766-2openalex-snapshot
Proangiogenic effects of environmentally relevant levels of bisphenol A in human primary endothelial cells
inferred← citeshttps://doi.org/10.1007/s00204-022-03246-wopenalex-snapshot
Pharmacokinetics and toxicity evaluation following oral exposure to bisphenol F
inferred← citeshttps://doi.org/10.1007/s00204-023-03658-2openalex-snapshot
Metabolic effects of nuclear receptor activation in vivo after 28-day oral exposure to three endocrine-disrupting chemicals
inferred← citeshttps://doi.org/10.1007/s00204-025-04025-zopenalex-snapshot
Mechanisms of bisphenol A and its analogs as endocrine disruptors via nuclear receptors and related signaling pathways
inferred← citeshttps://doi.org/10.1007/s00213-024-06697-4openalex-snapshot
Ferulic acid ameliorates bisphenol A (BPA)-induced Alzheimer’s disease-like pathology through Akt-ERK crosstalk pathway in male rats
inferred← citeshttps://doi.org/10.1007/s00216-020-02908-xopenalex-snapshot
Saliva biomonitoring using LPME-GC/MS method to assess dentistry exposure to plasticizers
inferred← citeshttps://doi.org/10.1007/s00216-022-04028-0openalex-snapshot
Insight on the microscopic binding mechanism of bisphenol compounds (BPs) with transthyretin (TTR) based on multi-spectroscopic methods and computational simulations
inferred← citeshttps://doi.org/10.1007/s00244-021-00823-5openalex-snapshot
OctylPhenol (OP) Alone and in Combination with NonylPhenol (NP) Alters the Structure and the Function of Thyroid Gland of the Lizard Podarcis siculus
inferred← citeshttps://doi.org/10.1007/s00244-021-00840-4openalex-snapshot
Investigating Acute and Subchronic Effects of Neonicotinoids on Northwestern Salamander Larvae
inferred← citeshttps://doi.org/10.1007/s00431-021-04085-0openalex-snapshot
Bisphenol A and its effects on the systemic organs of children
inferred← citeshttps://doi.org/10.1007/s00592-013-0472-zopenalex-snapshot
Relationship between urinary bisphenol A levels and prediabetes among subjects free of diabetes
inferred← citeshttps://doi.org/10.1007/s00604-018-2772-zopenalex-snapshot
Silver microspheres coated with a molecularly imprinted polymer as a SERS substrate for sensitive detection of bisphenol A
inferred← citeshttps://doi.org/10.1007/s00726-017-2442-1openalex-snapshot
Dityrosine administration induces dysfunction of insulin secretion accompanied by diminished thyroid hormones T3 function in pancreas of mice
inferred← citeshttps://doi.org/10.1007/s10661-014-3810-xopenalex-snapshot
Exposure assessment of endocrine disruptors in bottled drinking water of Lebanon
inferred← citeshttps://doi.org/10.1007/s10695-014-0021-xopenalex-snapshot
Estrogen and glucocorticoid receptor agonists and antagonists in oocytes modulate the pattern of expression of genes that encode nuclear receptor proteins in very early stage rainbow trout (Oncorhynchus mykiss) embryos
inferred← citeshttps://doi.org/10.1007/s10911-013-9293-5openalex-snapshot
Does Cancer Start in the Womb? Altered Mammary Gland Development and Predisposition to Breast Cancer due to in Utero Exposure to Endocrine Disruptors
inferred← citeshttps://doi.org/10.1007/s11010-010-0430-9openalex-snapshot
Non-genomic effects of thyroid hormone in adult cardiac myocytes: relevance to gene expression and cell growth
inferred← citeshttps://doi.org/10.1007/s11011-017-0066-5openalex-snapshot
Anatomical specificity of the brain in the modulation of Neuroglobin and Cytoglobin genes after chronic bisphenol a exposure
inferred← citeshttps://doi.org/10.1007/s11011-017-0112-3openalex-snapshot
Erratum to: Anatomical specificity of the brain in the modulation of Neuroglobin and Cytoglobin genes after chronic bisphenol a exposure
inferred← citeshttps://doi.org/10.1007/s11030-018-9857-9openalex-snapshot
Classification of thyroid hormone receptor agonists and antagonists using statistical learning approaches
inferred← citeshttps://doi.org/10.1007/s11154-016-9333-8openalex-snapshot
Bisphenol A: Targeting metabolic tissues
inferred← citeshttps://doi.org/10.1007/s11154-016-9337-4openalex-snapshot
Environmental endocrine disruptors: Effects on the human male reproductive system
inferred← citeshttps://doi.org/10.1007/s11154-019-09521-zopenalex-snapshot
Endocrine disrupting chemicals: exposure, effects on human health, mechanism of action, models for testing and strategies for prevention
inferred← citeshttps://doi.org/10.1007/s11356-018-2419-yopenalex-snapshot
Unraveling molecular targets of bisphenol A and S in the thyroid gland
inferred← citeshttps://doi.org/10.1007/s11356-018-3508-7openalex-snapshot
Occurrence, sources, human health impacts and mitigation of microplastic pollution
inferred← citeshttps://doi.org/10.1007/s11356-019-05151-9openalex-snapshot
Toxicity of three emerging contaminants to non-target marine organisms
inferred← citeshttps://doi.org/10.1007/s11356-019-07509-5openalex-snapshot
Protective role of lycopene against metabolic disorders induced by chronic bisphenol A exposure in rats
inferred← citeshttps://doi.org/10.1007/s11356-020-07705-8openalex-snapshot
Maternal urinary bisphenol A concentration and thyroid hormone levels of Chinese mothers and newborns by maternal body mass index
inferred← citeshttps://doi.org/10.1007/s11356-021-12943-5openalex-snapshot
Detection and removal of microplastics in wastewater: evolution and impact
inferred← citeshttps://doi.org/10.1007/s11356-021-16778-yopenalex-snapshot
Biomarker-assisted assessment of aquatic health using the cosmopolitan common carp, Cyprinus carpio (L): a case study of bisphenol-A exposures
inferred← citeshttps://doi.org/10.1007/s11356-023-29932-5openalex-snapshot
Association of urinary bisphenols with thyroid function in the general population: a cross-sectional study of an industrial park in China
inferred← citeshttps://doi.org/10.1007/s11356-023-30739-7openalex-snapshot
Sex-specific association of exposure to a mixture of phenols, parabens, and phthalates with thyroid hormone and antibody levels in US adolescents and adults
inferred← citeshttps://doi.org/10.1007/s11356-023-30801-4openalex-snapshot
Toxicological impacts of microplastics on human health: a bibliometric analysis
inferred← citeshttps://doi.org/10.1007/s11356-024-34666-zopenalex-snapshot
Effect of thyroid disruption on ovarian development following maternal exposure to Bisphenol S
inferred← citeshttps://doi.org/10.1007/s12016-010-8245-8openalex-snapshot
Cutting Edge: The Etiology of Autoimmune Thyroid Diseases
inferred← citeshttps://doi.org/10.1007/s12020-013-0022-zopenalex-snapshot
Investigation of serum bisphenol A, vitamin D, and parathyroid hormone levels in patients with obstructive sleep apnea syndrome
inferred← citeshttps://doi.org/10.1007/s12020-013-9889-yopenalex-snapshot
Association between bisphenol A and abnormal free thyroxine level in men
inferred← citeshttps://doi.org/10.1007/s12020-025-04441-2openalex-snapshot
Environmental and lifestyle factors and risk of thyroid carcinoma: a cross-sectional study
inferred← citeshttps://doi.org/10.1007/s12161-020-01841-0openalex-snapshot
The Development of a Photothermal Immunochromatographic Lateral Flow Strip for Rapid and Sensitive Detection of Bisphenol A in Food Samples
inferred← citeshttps://doi.org/10.1007/s12311-010-0218-1openalex-snapshot
1,2,5,6,9,10-αHexabromocyclododecane (HBCD) Impairs Thyroid Hormone-Induced Dendrite Arborization of Purkinje Cells and Suppresses Thyroid Hormone Receptor-Mediated Transcription
inferred← citeshttps://doi.org/10.1007/s12403-016-0235-5openalex-snapshot
Bisphenol A in Canned Carbonated Drinks and Plastic-Bottled Water from Supermarkets
inferred← citeshttps://doi.org/10.1007/s12595-021-00426-xopenalex-snapshot
Bisphenol A: Prenatal Exposure and Its Effect on Obesity and Male Reproductive System
inferred← citeshttps://doi.org/10.1007/s13213-013-0649-2openalex-snapshot
Effect of Bisphenol A on human health and its degradation by microorganisms: a review
inferred← citeshttps://doi.org/10.1007/s43032-020-00452-8openalex-snapshot
Developmental Programming: Physiological Impacts of Prenatal Melatonin Administration on Reproductive Capacity and Serum Triiodothyronine of Adult Female Offspring Rat Born to Moms Exposed to Bisphenol A During Pregnancy
inferred← citeshttps://doi.org/10.1007/s43188-026-00375-7openalex-snapshot
Bisphenol A and health across species: a One Health review with emphasis on companion animals
inferred← citeshttps://doi.org/10.1016/b0-72-160423-4/50026-3openalex-snapshot
Goiter in Apparently Euthyroid Cats
inferred← citeshttps://doi.org/10.1016/b978-0-12-382032-7.10050-5openalex-snapshot
Bisphenol A
inferred← citeshttps://doi.org/10.1016/b978-0-12-385926-6.00086-7openalex-snapshot
Chemical-induced estrogenicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-385979-2.00013-7openalex-snapshot
Is Thyroid Hormone Signaling Relevant for Vertebrate Embryogenesis?
inferred← citeshttps://doi.org/10.1016/b978-0-12-404630-6.00027-0openalex-snapshot
Bisphenol A
inferred← citeshttps://doi.org/10.1016/b978-0-12-800095-3.00009-2openalex-snapshot
Nuclear Receptor Profiling of Bisphenol-A and Its Halogenated Analogues
inferred← citeshttps://doi.org/10.1016/b978-0-12-800228-5.00008-xopenalex-snapshot
Thyroid-Disrupting Chemicals as Developmental Neurotoxicants
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.64208-3openalex-snapshot
Epigenetics in Toxicology
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.66101-9openalex-snapshot
The Hypothalamic–Pituitary–Thyroid Axis as a Target for Environmental Chemicals
inferred← citeshttps://doi.org/10.1016/b978-0-12-811410-0.00059-3openalex-snapshot
Chemical-Induced Estrogenicity
inferred← citeshttps://doi.org/10.1016/b978-0-12-813602-7.00006-5openalex-snapshot
Disruption of extracellular signaling
inferred← citeshttps://doi.org/10.1016/b978-0-12-816679-6.00009-7openalex-snapshot
The Recent Electrochemical Studies on Bisphenol A Detection in Beverages
inferred← citeshttps://doi.org/10.1016/b978-0-12-818734-0.00006-1openalex-snapshot
Endophytic bacteria in xenobiotic degradation
inferred← citeshttps://doi.org/10.1016/b978-0-12-819722-6.00007-9openalex-snapshot
Cancer treatment drugs and endocrine-disrupting chemicals release and fate in hospital wastewater
inferred← citeshttps://doi.org/10.1016/b978-0-323-91902-9.00011-0openalex-snapshot
Fate, effects, origins, and biodegradation of bisphenol A in wastewater
inferred← citeshttps://doi.org/10.1016/b978-0-323-95488-4.10021-xopenalex-snapshot
Epigenetics in Toxicology
inferred← citeshttps://doi.org/10.1016/b978-0-323-98808-7.00002-3openalex-snapshot
Exposome and detoxification
inferred← citeshttps://doi.org/10.1016/b978-012370467-2/50162-0openalex-snapshot
Chemical-induced estrogenicity
inferred← citeshttps://doi.org/10.1016/bs.apcsb.2023.12.024openalex-snapshot
Thyroid hormone biosynthesis and its role in brain development and maintenance
inferred← citeshttps://doi.org/10.1016/bs.apha.2021.05.002openalex-snapshot
Endocrine disrupting chemicals and thyroid hormone action
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.04.004openalex-snapshot
Thyroid Hormone Receptor Antagonists: From Environmental Pollution to Novel Small Molecules
inferred← citeshttps://doi.org/10.1016/bs.vh.2020.04.004openalex-snapshot
A potential role for dendritic spines in bisphenol-A induced memory impairments during adolescence and adulthood
inferred← citeshttps://doi.org/10.1016/j.aca.2004.06.066openalex-snapshot
Biosensor immunoassays for the detection of bisphenol A
inferred← citeshttps://doi.org/10.1016/j.adaj.2016.01.013openalex-snapshot
An investigation into bisphenol A leaching from materials used intraorally
inferred← citeshttps://doi.org/10.1016/j.ando.2008.02.008openalex-snapshot
Environment and endocrinology: The case of thyroidology
inferred← citeshttps://doi.org/10.1016/j.ando.2013.04.002openalex-snapshot
Bisphenol A: An endocrine and metabolic disruptor
inferred← citeshttps://doi.org/10.1016/j.aquatox.2011.04.007openalex-snapshot
Generation of fluorescent zebrafish to study endocrine disruption and potential crosstalk between thyroid hormone and corticosteroids
inferred← citeshttps://doi.org/10.1016/j.aquatox.2011.12.016openalex-snapshot
Triiodothyronine-induced changes in the zebrafish transcriptome during the eleutheroembryonic stage: Implications for bisphenol A developmental toxicity
inferred← citeshttps://doi.org/10.1016/j.aquatox.2014.12.011openalex-snapshot
Evaluation of the toxic effects of brominated compounds (BDE-47, 99, 209, TBBPA) and bisphenol A (BPA) using a zebrafish liver cell line, ZFL
inferred← citeshttps://doi.org/10.1016/j.aquatox.2015.01.028openalex-snapshot
Bisphenol A accumulation in eggs disrupts the endocrine regulation of growth in rainbow trout larvae
inferred← citeshttps://doi.org/10.1016/j.aquatox.2018.04.009openalex-snapshot
An AOP-based alternative testing strategy to predict the impact of thyroid hormone disruption on swim bladder inflation in zebrafish
inferred← citeshttps://doi.org/10.1016/j.aquatox.2019.105314openalex-snapshot
Bisphenols disrupt differentiation of the pigmented cells during larval brain formation in the ascidian
inferred← citeshttps://doi.org/10.1016/j.aquatox.2021.105902openalex-snapshot
Bisphenols disrupt thyroid hormone (TH) signaling in the brain and affect TH-dependent brain development in Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.aquatox.2022.106256openalex-snapshot
Persistent impairment of gonadal development in rare minnow (Gobiocypris rarus) after chronic exposure to chlorinated polyfluorinated ether sulfonate
inferred← citeshttps://doi.org/10.1016/j.aquatox.2022.106354openalex-snapshot
Bisphenols induce cardiotoxicity in zebrafish embryos: Role of the thyroid hormone receptor pathway
inferred← citeshttps://doi.org/10.1016/j.aquatox.2023.106440openalex-snapshot
Bisphenol S reduces locomotor performance and modifies muscle protein levels but not mitochondrial bioenergetics in adult zebrafish
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2023.119505openalex-snapshot
Alterations induced by Bisphenol A on cellular organelles and potential relevance on human health
inferred← citeshttps://doi.org/10.1016/j.bcp.2009.11.006openalex-snapshot
Endocrine disruptors and thyroid hormone physiology
inferred← citeshttps://doi.org/10.1016/j.beem.2009.06.003openalex-snapshot
Environmental pollutants and the thyroid
inferred← citeshttps://doi.org/10.1016/j.biopha.2018.03.004openalex-snapshot
Oleuropein and hydroxytyrosol protect rats’ pups against bisphenol A induced hypothyroidism
inferred← citeshttps://doi.org/10.1016/j.bios.2019.02.043openalex-snapshot
An ultra-sensitive aptasensor on optical fibre for the direct detection of bisphenol A
inferred← citeshttps://doi.org/10.1016/j.braindev.2010.12.011openalex-snapshot
Prenatal and lactational exposure to low-doses of bisphenol A alters adult mice behavior
inferred← citeshttps://doi.org/10.1016/j.brainres.2019.146434openalex-snapshot
Postnatal genistein administration selectively abolishes sexual dimorphism in specific hypothalamic dopaminergic system in mice
inferred← citeshttps://doi.org/10.1016/j.cbi.2013.03.013openalex-snapshot
Bisphenol A affects androgen receptor function via multiple mechanisms
inferred← citeshttps://doi.org/10.1016/j.cbpb.2015.02.001openalex-snapshot
Endogenous and exogenous estrogens during embryonic development affect timing of hatch and growth in the American alligator (Alligator mississippiensis)
inferred← citeshttps://doi.org/10.1016/j.cbpc.2017.11.010openalex-snapshot
Evaluating estrogenic and anti-estrogenic effect of endocrine disrupting chemicals (EDCs) by zebrafish ( Danio rerio ) embryo-based vitellogenin 1 ( vtg1 ) mRNA expression
inferred← citeshttps://doi.org/10.1016/j.cellbi.2004.03.016openalex-snapshot
Suppressing effects of bisphenol A on the secretory function of ovine anterior pituitary cells
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2006.05.137openalex-snapshot
Disrupting effects of hydroxy-polychlorinated biphenyl (PCB) congeners on neuronal development of cerebellar Purkinje cells: A possible causal factor for developmental brain disorders?
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2015.09.018openalex-snapshot
Causes of endocrine disrupting potencies in surface water in East China
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2016.05.006openalex-snapshot
Testicular transcript responses in rare minnow Gobiocypris rarus following different concentrations bisphenol A exposure
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2016.05.027openalex-snapshot
Influence of metabolism on endocrine activities of bisphenol S
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2016.05.070openalex-snapshot
From BPA to its analogues: Is it a safe journey?
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.05.028openalex-snapshot
Evidence for bisphenol A-induced disruption of maternal thyroid homeostasis in the pregnant ewe at low level representative of human exposure
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.12.099openalex-snapshot
Disruption of actin filaments in Zea mays by bisphenol A depends on their crosstalk with microtubules
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2018.10.129openalex-snapshot
Endocrine activities and adipogenic effects of bisphenol AF and its main metabolite
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2018.11.084openalex-snapshot
Human exposure to bisphenol AF and diethylhexylphthalate increases susceptibility to develop differentiated thyroid cancer in patients with thyroid nodules
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2018.12.185openalex-snapshot
Evaluation of endocrine activities of ellagic acid and urolithins using reporter gene assays
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.01.019openalex-snapshot
Comparison of thyroid hormone disruption potentials by bisphenols A, S, F, and Z in embryo-larval zebrafish
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.124918openalex-snapshot
Urinary bisphenol A and thyroid function by BMI in the Korean National Environmental Health Survey (KoNEHS) 2012–2014
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.137495openalex-snapshot
Chemical nature of attention deficit hyperactivity disorder (ADHD) - related chemical subfamily
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.140626openalex-snapshot
Association of postnatal exposure to mixture of bisphenol A, Di-n-butyl phthalate and Di-(2-ethylhexyl) phthalate with Children's IQ at 5 Years of age: Mothers and Children's environmental health (MOCEH) study
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.140776openalex-snapshot
Bisphenol A alters retinal morphology, visually guided behavior, and thyroid hormone levels in zebrafish larvae
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.143955openalex-snapshot
Bisphenol A induces sex-dependent alterations in the neuroendocrine response of Djungarian hamsters to photoperiod
inferred← citeshttps://doi.org/10.1016/j.clinms.2020.10.002openalex-snapshot
Development and validation of a liquid chromatography-tandem mass spectrometry method for the simultaneous determination of phthalates and bisphenol a in serum, urine and follicular fluid
inferred← citeshttps://doi.org/10.1016/j.comtox.2020.100120openalex-snapshot
Homology modeling to screen for potential binding of contaminants to thyroid hormone receptor and transthyretin in glaucous gull (Larus hyperboreus) and herring gull (Larus argentatus)
inferred← citeshttps://doi.org/10.1016/j.coph.2014.09.013openalex-snapshot
Classical nuclear hormone receptor activity as a mediator of complex concentration response relationships for endocrine active compounds
inferred← citeshttps://doi.org/10.1016/j.cppeds.2017.04.002openalex-snapshot
Exposures to Endocrine Disrupting Chemicals in Consumer Products—A Guide for Pediatricians
inferred← citeshttps://doi.org/10.1016/j.critrevonc.2020.102950openalex-snapshot
Fathoming the link between anthropogenic chemical contamination and thyroid cancer
inferred← citeshttps://doi.org/10.1016/j.crvi.2017.07.006openalex-snapshot
Neuroendocrine disruption without direct endocrine mode of action: Polychloro-biphenyls (PCBs) and bisphenol A (BPA) as case studies
inferred← citeshttps://doi.org/10.1016/j.cvsm.2007.05.001openalex-snapshot
Etiopathologic Findings of Hyperthyroidism in Cats
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2011.11.041openalex-snapshot
Reproductive biomarkers to identify endocrine disruption in Clarias gariepinus exposed to 4-nonylphenol
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.06.045openalex-snapshot
One-step synthesis of reduced graphene oxide sheathed zinc oxide nanoclusters for the trace level detection of bisphenol A in tissue papers
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.02.007openalex-snapshot
Effects of separate or combined exposure of nonylphenol and octylphenol on central 5-HT system and related learning and memory in the rats
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110300openalex-snapshot
Relationship between urinary bisphenol a levels and cardiovascular diseases in the U.S. adult population, 2003–2014
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112140openalex-snapshot
Effects of two Bisphenol A replacement compounds, 1,7-bis (4-hydroxyphenylthio)-3,5-dioxaheptane and Bisphenol AF, on development and mRNA expression in chicken embryos
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.114838openalex-snapshot
The associations between concentrations of gestational bisphenol analogues and thyroid related hormones in cord blood: A prospective cohort study
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.117790openalex-snapshot
The negative impacts of bisphenols on thyroid function in adults with bisphenol A exposure level exceeding the tolerable daily intake
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2026.119823openalex-snapshot
Sex-dependent physiological consequences of perinatal bisphenol A exposure in seasonal Djungarian hamsters
inferred← citeshttps://doi.org/10.1016/j.ejop.2023.125958openalex-snapshot
Toxicological impacts and likely protein targets of bisphenol a in Paramecium caudatum
inferred← citeshttps://doi.org/10.1016/j.emcon.2024.100351openalex-snapshot
Exposure of Bisphenols (BPs) to hepatocellular carcinoma (HCC) patients and non-HCC patients: Association with liver function biomarkers
inferred← citeshttps://doi.org/10.1016/j.emcon.2025.100479openalex-snapshot
Impact of maternal Bisphenol A exposure on thyroid hormones and birth anthropometric outcomes: A repeated measures study
inferred← citeshttps://doi.org/10.1016/j.emcon.2025.100592openalex-snapshot
Methyl and propylparaben elicit distinct thyroid-disrupting effects in a rat thyroid cell model
inferred← citeshttps://doi.org/10.1016/j.enceco.2025.04.001openalex-snapshot
Bisphenol A and its replacement chemicals as endocrine disruptors and obesogens
inferred← citeshttps://doi.org/10.1016/j.envint.2015.09.005openalex-snapshot
Maternal urinary bisphenol A levels and infant low birth weight: A nested case–control study of the Health Baby Cohort in China
inferred← citeshttps://doi.org/10.1016/j.envint.2016.09.016openalex-snapshot
Review on crosstalk and common mechanisms of endocrine disruptors: Scaffolding to improve PBPK/PD model of EDC mixture
inferred← citeshttps://doi.org/10.1016/j.envint.2017.04.001openalex-snapshot
Thyroid hormone parameters during pregnancy in relation to urinary bisphenol A concentrations: A repeated measures study
inferred← citeshttps://doi.org/10.1016/j.envint.2017.06.013openalex-snapshot
Considering common sources of exposure in association studies - Urinary benzophenone-3 and DEHP metabolites are associated with altered thyroid hormone balance in the NHANES 2007–2008
inferred← citeshttps://doi.org/10.1016/j.envint.2018.11.003openalex-snapshot
Blood pressure changes during pregnancy in relation to urinary paraben, triclosan and benzophenone concentrations: A repeated measures study
inferred← citeshttps://doi.org/10.1016/j.envint.2019.01.078openalex-snapshot
Immunomodulatory effects of synthetic endocrine disrupting chemicals on the development and functions of human immune cells
inferred← citeshttps://doi.org/10.1016/j.envint.2019.02.026openalex-snapshot
Bisphenol A exposure and risk of thyroid nodules in Chinese women: A case-control study
inferred← citeshttps://doi.org/10.1016/j.envint.2019.105123openalex-snapshot
Association of urinary bisphenols and triclosan with thyroid function during early pregnancy
inferred← citeshttps://doi.org/10.1016/j.envint.2020.105811openalex-snapshot
Bisphenol A and its analogues: A comprehensive review to identify and prioritize effect biomarkers for human biomonitoring
inferred← citeshttps://doi.org/10.1016/j.envint.2020.105894openalex-snapshot
Prenatal and early childhood exposure to phthalates and childhood behavior at age 7 years
inferred← citeshttps://doi.org/10.1016/j.envint.2020.106078openalex-snapshot
A comprehensive review of the neurobehavioral effects of bisphenol S and the mechanisms of action: New insights from in vitro and in vivo models
inferred← citeshttps://doi.org/10.1016/j.envint.2020.106160openalex-snapshot
Association of urinary bisphenols during pregnancy with maternal, cord blood and childhood thyroid function
inferred← citeshttps://doi.org/10.1016/j.envint.2021.106458openalex-snapshot
Concentrations and endocrine disruptive potential of phthalates in marine mammals from the Norwegian Arctic
inferred← citeshttps://doi.org/10.1016/j.envint.2021.106759openalex-snapshot
Internal exposure of Chinese children from a typical coastal city to bisphenols and possible association with thyroid hormone levels
inferred← citeshttps://doi.org/10.1016/j.envint.2023.107770openalex-snapshot
Transient developmental exposure to low doses of bisphenol F negatively affects neurogliogenesis and olfactory behaviour in adult mice
inferred← citeshttps://doi.org/10.1016/j.envint.2026.110121openalex-snapshot
Association of exposure to personal care product chemicals with maternal thyroid health: a prospective cohort study integrated with targeted risk assessment for environmental chemicals strategy
inferred← citeshttps://doi.org/10.1016/j.envpol.2015.08.016openalex-snapshot
Transgenerational inheritance of heart disorders caused by paternal bisphenol A exposure
inferred← citeshttps://doi.org/10.1016/j.envpol.2017.08.060openalex-snapshot
Effects of diisononyl phthalate on Danio rerio reproduction
inferred← citeshttps://doi.org/10.1016/j.envpol.2017.11.027openalex-snapshot
Bisphenol A alternatives bisphenol S and bisphenol F interfere with thyroid hormone signaling pathway in vitro and in vivo
inferred← citeshttps://doi.org/10.1016/j.envpol.2018.09.107openalex-snapshot
Concentrations of perfluoroalkyl substances and bisphenol A in newborn dried blood spots and the association with child behavior
inferred← citeshttps://doi.org/10.1016/j.envpol.2021.117296openalex-snapshot
Effects of high-dose bisphenol A on the mouse oral mucosa: A possible link with oral cancers
inferred← citeshttps://doi.org/10.1016/j.envpol.2022.120478openalex-snapshot
Exposure to Bisphenol A increases malignancy risk of thyroid nodules in overweight/obese patients
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.121051openalex-snapshot
Associations between exposure to phthalates and subclinical hypothyroidism in pregnant women during early pregnancy: A pilot case-control study in China
inferred← citeshttps://doi.org/10.1016/j.envpol.2023.122624openalex-snapshot
Modeling early human cortical development and evaluating neurotoxicity with a forebrain organoid system
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