On the public citation graph

Cross-species applicability of an adverse outcome pathway network for thyroid hormone system disruption

0 signed · 297 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.

Claim with ORCID

Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.

See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/alr.21565openalex-snapshot

Evaluation of olfactory function in adults with primary hypothyroidism

inferredcites →https://doi.org/10.1002/dvdy.22392openalex-snapshot

Thyroid hormone accelerates opsin expression during early photoreceptor differentiation and induces opsin switching in differentiated TRα‐expressing cones of the salmonid retina

inferredcites →https://doi.org/10.1002/dvdy.76openalex-snapshot

Thyroid hormone coordinates developmental trajectories but does not underlie developmental truncation in danionins

inferredcites →https://doi.org/10.1002/etc.34openalex-snapshot

Adverse outcome pathways: A conceptual framework to support ecotoxicology research and risk assessment

inferredcites →https://doi.org/10.1002/etc.3805openalex-snapshot

Advancing the adverse outcome pathway framework—An international horizon scanning approach

inferredcites →https://doi.org/10.1002/etc.3855openalex-snapshot

Impaired swim bladder inflation in early life stage fathead minnows exposed to a deiodinase inhibitor, iopanoic acid

inferredcites →https://doi.org/10.1002/etc.4124openalex-snapshot

Adverse outcome pathway networks II: Network analytics

inferredcites →https://doi.org/10.1002/etc.4125openalex-snapshot

Adverse outcome pathway networks I: Development and applications

inferredcites →https://doi.org/10.1002/etc.4682openalex-snapshot

Critical Review of Read-Across Potential in Testing for Endocrine-Related Effects in Vertebrate Ecological Receptors

inferredcites →https://doi.org/10.1002/etc.5452openalex-snapshot

AOP Report: Thyroperoxidase Inhibition Leading to Altered Visual Function in Fish Via Altered Retinal Layer Structure

inferredcites →https://doi.org/10.1002/etc.5501openalex-snapshot

Defining the Biologically Plausible Taxonomic Domain of Applicability of an Adverse Outcome Pathway: A Case Study Linking Nicotinic Acetylcholine Receptor Activation to Colony Death

inferredcites →https://doi.org/10.1002/etc.5620210318openalex-snapshot

Environmentally relevant concentrations of ammonium perchlorate inhibit thyroid function and alter sex ratios in developing Xenopus laevis

inferredcites →https://doi.org/10.1002/jat.2825openalex-snapshot

Establishment of transactivation assay systems using fish, amphibian, reptilian and human thyroid hormone receptors

inferredcites →https://doi.org/10.1002/mnfr.200900489openalex-snapshot

Xanthohumol, a prenylated chalcone from hops, modulates hepatic expression of genes involved in thyroid hormone distribution and metabolism

inferredcites →https://doi.org/10.1006/gcen.1998.7197openalex-snapshot

Characterization of Thyroid Hormone 5′-Monodeiodinase Activity in the Turtle (Trachemys scripta)

inferredcites →https://doi.org/10.1006/gcen.1999.7326openalex-snapshot

Deiodination and Deconjugation of Thyroid Hormone Conjugates and Type I Deiodination in Liver of Rainbow Trout, Oncorhynchus mykiss

inferredcites →https://doi.org/10.1006/gcen.1999.7384openalex-snapshot

Hepatic Outer-Ring Deiodinase in a Mexican Endemic Lizard (Sceloporus grammicus)

inferredcites →https://doi.org/10.1006/gcen.2000.7528openalex-snapshot

Effect of Diethylstilbestrol on Thyroid Hormone Binding to Amphibian Transthyretins

inferredcites →https://doi.org/10.1007/s00204-020-02664-yopenalex-snapshot

Evaluation of potential sodium-iodide symporter (NIS) inhibitors using a secondary Fischer rat thyroid follicular cell (FRTL-5) radioactive iodide uptake (RAIU) assay

inferredcites →https://doi.org/10.1007/s00204-020-02961-6openalex-snapshot

A review of species differences in the control of, and response to, chemical-induced thyroid hormone perturbations leading to thyroid cancer

inferredcites →https://doi.org/10.1007/s00204-021-03006-2openalex-snapshot

Expanded high-throughput screening and chemotype-enrichment analysis of the phase II: e1k ToxCast library for human sodium-iodide symporter (NIS) inhibition

inferredcites →https://doi.org/10.1007/s10038-006-0391-8openalex-snapshot

Evolutionary dynamics of olfactory and other chemosensory receptor genes in vertebrates

inferredcites →https://doi.org/10.1016/0009-2797(90)90034-kopenalex-snapshot

Interaction of chlorinated phenols with thyroxine binding sites of human transthyretin, albumin and thyroid binding globulin

inferredcites →https://doi.org/10.1016/b978-0-12-374930-7.10014-7openalex-snapshot

Endocrine Disruption of Reproduction in Reptiles

inferredcites →https://doi.org/10.1016/j.aquatox.2010.01.014openalex-snapshot

Early temporal effects of three thyroid hormone synthesis inhibitors in Xenopus laevis

inferredcites →https://doi.org/10.1016/j.aquatox.2012.10.013openalex-snapshot

Inhibition of the thyroid hormone pathway in Xenopus laevis by 2-mercaptobenzothiazole

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.aquatox.2015.12.015openalex-snapshot

Thyroid disruption in zebrafish (Danio rerio) larvae: Different molecular response patterns lead to impaired eye development and visual functions

inferredcites →https://doi.org/10.1016/j.aquatox.2015.12.023openalex-snapshot

Impaired anterior swim bladder inflation following exposure to the thyroid peroxidase inhibitor 2-mercaptobenzothiazole part II: Zebrafish

inferredcites →https://doi.org/10.1016/j.aquatox.2015.12.024openalex-snapshot

Impaired anterior swim bladder inflation following exposure to the thyroid peroxidase inhibitor 2-mercaptobenzothiazole part I: Fathead minnow

inferredcites →https://doi.org/10.1016/j.aquatox.2016.03.006openalex-snapshot

Permethrin is a potential thyroid-disrupting chemical: In vivo and in silico envidence

inferredcites →https://doi.org/10.1016/j.aquatox.2017.06.019openalex-snapshot

A multi-tiered, in vivo, quantitative assay suite for environmental disruptors of thyroid hormone signaling

inferredcites →https://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

inferredcites →https://doi.org/10.1016/j.aquatox.2020.105623openalex-snapshot

Amiodarone bioconcentration and suppression of metamorphosis in Xenopus

inferredcites →https://doi.org/10.1016/j.aquatox.2022.106227openalex-snapshot

Cross-species comparison of chemical inhibition of human and Xenopus iodotyrosine deiodinase

inferredcites →https://doi.org/10.1016/j.bbagen.2012.07.015openalex-snapshot

Function of thyroid hormone transporters in the central nervous system

inferredcites →https://doi.org/10.1016/j.bcp.2011.08.027openalex-snapshot

Use of comprehensive screening methods to detect selective human CAR activators

inferredcites →https://doi.org/10.1016/j.bcp.2013.08.012openalex-snapshot

The nuclear receptors pregnane X receptor and constitutive androstane receptor contribute to the impact of fipronil on hepatic gene expression linked to thyroid hormone metabolism

inferredcites →https://doi.org/10.1016/j.canlet.2019.09.017openalex-snapshot

Mouse models of thyroid cancer: Bridging pathogenesis and novel therapeutics

inferredcites →https://doi.org/10.1016/j.cbpa.2006.01.017openalex-snapshot

Thiourea-induced thyroid hormone depletion impairs testicular recrudescence in the air-breathing catfish, Clarias gariepinus

inferredcites →https://doi.org/10.1016/j.cbpc.2008.01.002openalex-snapshot

Interaction of diethylstilbestrol and ioxynil with transthyretin in chicken serum

inferredcites →https://doi.org/10.1016/j.chemosphere.2007.04.010openalex-snapshot

Disruption of thyroid hormone binding to sea bream recombinant transthyretin by ioxinyl and polybrominated diphenyl ethers

inferredcites →https://doi.org/10.1016/j.cub.2015.02.049openalex-snapshot

The reptilian brain

inferredcites →https://doi.org/10.1016/j.cvex.2007.10.002openalex-snapshot

The Reptilian Thyroid and Parathyroid Glands

inferredcites →https://doi.org/10.1016/j.envint.2020.105783openalex-snapshot

Thyroxine-binding globulin, peripheral deiodinase activity, and thyroid autoantibody status in association of phthalates and phenolic compounds with thyroid hormones in adult population

inferredcites →https://doi.org/10.1016/j.envint.2021.106458openalex-snapshot

Concentrations and endocrine disruptive potential of phthalates in marine mammals from the Norwegian Arctic

inferredcites →https://doi.org/10.1016/j.envpol.2018.02.038openalex-snapshot

Lifecycle exposure to perchlorate differentially alters morphology, biochemistry, and transcription as well as sperm motility in Silurana tropicalis frogs

inferredcites →https://doi.org/10.1016/j.envpol.2019.05.110openalex-snapshot

Early life exposure to triphenyl phosphate: Effects on thyroid function, growth, and resting metabolic rate of Japanese quail (Coturnix japonica) chicks

inferredcites →https://doi.org/10.1016/j.envpol.2019.113695openalex-snapshot

Assessment of the effects of early life exposure to triphenyl phosphate on fear, boldness, aggression, and activity in Japanese quail (Coturnix japonica) chicks

inferredcites →https://doi.org/10.1016/j.envpol.2021.117135openalex-snapshot

Testing for heterotopia formation in rats after developmental exposure to selected in vitro inhibitors of thyroperoxidase

inferredcites →https://doi.org/10.1016/j.envpol.2021.117654openalex-snapshot

The pyriproxyfen metabolite, 4′–OH–PPF, disrupts thyroid hormone signaling in neural stem cells, modifying neurodevelopmental genes affected by ZIKA virus infection.

inferredcites →https://doi.org/10.1016/j.envres.2021.111906openalex-snapshot

Disruption by stealth - Interference of endocrine disrupting chemicals on hormonal crosstalk with thyroid axis function in humans and other animals

inferredcites →https://doi.org/10.1016/j.etap.2015.01.016openalex-snapshot

Comparison of the in vitro effects of TCDD, PCB 126 and PCB 153 on thyroid-restricted gene expression and thyroid hormone secretion by the chicken thyroid gland

inferredcites →https://doi.org/10.1016/j.exer.2018.09.018openalex-snapshot

Knockdown of the thyroid hormone transporter MCT8 in chicken retinal precursor cells hampers early retinal development and results in a shift towards more UV/blue cones at the expense of green/red cones

inferredcites →https://doi.org/10.1016/j.heares.2010.05.004openalex-snapshot

Sensory regeneration in the vertebrate inner ear: Differences at the levels of cells and species

inferredcites →https://doi.org/10.1016/j.isci.2020.100899openalex-snapshot

A Pivotal Genetic Program Controlled by Thyroid Hormone during the Maturation of GABAergic Neurons

inferredcites →https://doi.org/10.1016/j.jri.2011.02.009openalex-snapshot

Thyroid hormone receptors and reproduction

inferredcites →https://doi.org/10.1016/j.lfs.2004.08.030openalex-snapshot

Anti-thyroid hormonal activity of tetrabromobisphenol A, a flame retardant, and related compounds: Affinity to the mammalian thyroid hormone receptor, and effect on tadpole metamorphosis

inferredcites →https://doi.org/10.1016/j.mce.2005.07.006openalex-snapshot

Environmental chemicals as thyroid hormone analogues: New studies indicate that thyroid hormone receptors are targets of industrial chemicals?

inferredcites →https://doi.org/10.1016/j.mce.2013.08.025openalex-snapshot

Autonomous functions of murine thyroid hormone receptor TRα and TRβ in cochlear hair cells

inferredcites →https://doi.org/10.1016/j.mce.2016.01.018openalex-snapshot

Deiodinase knockdown affects zebrafish eye development at the level of gene expression, morphology and function

inferredcites →https://doi.org/10.1016/j.mce.2016.01.020openalex-snapshot

Patterns of thyroid hormone receptor expression in zebrafish and generation of a novel model of resistance to thyroid hormone action

inferredcites →https://doi.org/10.1016/j.mce.2016.09.007openalex-snapshot

Implication of thyroid hormone signaling in neural crest cells migration: Evidence from thyroid hormone receptor beta knockdown and NH3 antagonist studies

inferredcites →https://doi.org/10.1016/j.mce.2017.01.038openalex-snapshot

Thyroid hormone biosynthesis and release

inferredcites →https://doi.org/10.1016/j.mce.2019.110635openalex-snapshot

Inhibition of the thyroid hormonogenic H2O2 production by Duox/DuoxA in zebrafish reveals VAS2870 as a new goitrogenic compound

inferredcites →https://doi.org/10.1016/j.neuro.2018.04.013openalex-snapshot

Moderate perinatal thyroid hormone insufficiency alters visual system function in adult rats

inferredcites →https://doi.org/10.1016/j.neuro.2019.05.008openalex-snapshot

Changes in thyroid hormone activity disrupt photomotor behavior of larval zebrafish

inferredcites →https://doi.org/10.1016/j.neuro.2021.03.003openalex-snapshot

Investigation of NH3 as a selective thyroid hormone receptor modulator in larval zebrafish (Danio rerio)

inferredcites →https://doi.org/10.1016/j.semcdb.2020.09.007openalex-snapshot

Thyroid hormone, gene expression, and Central Nervous System: Where we are

inferredcites →https://doi.org/10.1016/j.taap.2005.06.014openalex-snapshot

Analysis of thyroid hormone receptor βA mRNA expression in Xenopus laevis tadpoles as a means to detect agonism and antagonism of thyroid hormone action

inferredcites →https://doi.org/10.1016/j.taap.2006.01.009openalex-snapshot

A mode of action for induction of thyroid gland tumors by Pyrethrins in the rat

inferredcites →https://doi.org/10.1016/j.taap.2008.05.020openalex-snapshot

Developmental neurotoxicity of Propylthiouracil (PTU) in rats: Relationship between transient hypothyroxinemia during development and long-lasting behavioural and functional changes

inferredcites →https://doi.org/10.1016/j.taap.2012.01.029openalex-snapshot

Thyroid organotypic rat and human cultures used to investigate drug effects on thyroid function, hormone synthesis and release pathways

inferredcites →https://doi.org/10.1016/j.taap.2018.02.006openalex-snapshot

AOP-DB: A database resource for the exploration of Adverse Outcome Pathways through integrated association networks

inferredcites →https://doi.org/10.1016/j.tiv.2016.01.014openalex-snapshot

Effect of triclosan, triclocarban, 2,2′,4,4′-tetrabromodiphenyl ether, and bisphenol A on the iodide uptake, thyroid peroxidase activity, and expression of genes involved in thyroid hormone synthesis

inferredcites →https://doi.org/10.1016/j.tiv.2016.12.006openalex-snapshot

Development of a screening approach to detect thyroid disrupting chemicals that inhibit the human sodium iodide symporter (NIS)

inferredcites →https://doi.org/10.1016/j.tiv.2017.02.023openalex-snapshot

Development of a common carp (Cyprinus carpio) pregnane X receptor (cPXR) transactivation reporter assay and its activation by azole fungicides and pharmaceutical chemicals

inferredcites →https://doi.org/10.1016/j.tiv.2019.104662openalex-snapshot

A rapid assay of human thyroid peroxidase activity

inferredcites →https://doi.org/10.1016/j.tiv.2020.105073openalex-snapshot

In vitro screening for chemical inhibition of the iodide recycling enzyme, iodotyrosine deiodinase

inferredcites →https://doi.org/10.1016/j.tiv.2021.105141openalex-snapshot

Xenopus laevis and human type 3 iodothyronine deiodinase enzyme cross-species sensitivity to inhibition by ToxCast chemicals

inferredcites →https://doi.org/10.1016/j.tox.2004.11.037openalex-snapshot

Thyroid hormone-like and estrogenic activity of hydroxylated PCBs in cell culture

inferredcites →https://doi.org/10.1016/j.tox.2010.08.012openalex-snapshot

Structure-based investigation on the binding interaction of hydroxylated polybrominated diphenyl ethers with thyroxine transport proteins

inferredcites →https://doi.org/10.1016/j.tox.2013.08.006openalex-snapshot

Cross-species analysis of thyroperoxidase inhibition by xenobiotics demonstrates conservation of response between pig and rat

inferredcites →https://doi.org/10.1016/j.tox.2013.08.017openalex-snapshot

Structure–activity relationships of 44 halogenated compounds for iodotyrosine deiodinase-inhibitory activity

inferredcites →https://doi.org/10.1016/j.tox.2016.08.011openalex-snapshot

Binding interactions of perfluoroalkyl substances with thyroid hormone transport proteins and potential toxicological implications

inferredcites →https://doi.org/10.1016/j.tox.2020.152562openalex-snapshot

Effects of butylparaben exposure on thyroid peroxidase (TPO) and type 1 iodothyronine deiodinase (D1) in female Wistar rats

inferredcites →https://doi.org/10.1016/j.toxlet.2021.10.010openalex-snapshot

Perinatal exposure to the thyroperoxidase inhibitors methimazole and amitrole perturbs thyroid hormone system signaling and alters motor activity in rat offspring

inferredcites →https://doi.org/10.1016/j.yfrne.2013.04.002openalex-snapshot

Thyroid hormone and seasonal regulation of reproduction

inferredcites →https://doi.org/10.1016/j.ygcen.2006.11.013openalex-snapshot

Effects of larval–juvenile treatment with perchlorate and co-treatment with thyroxine on zebrafish sex ratios

inferredcites →https://doi.org/10.1016/j.ygcen.2009.09.011openalex-snapshot

Combined antisense knockdown of type 1 and type 2 iodothyronine deiodinases disrupts embryonic development in zebrafish (Danio rerio)

inferredcites →https://doi.org/10.1016/j.ygcen.2010.04.013openalex-snapshot

Developmental regulation of gene expression in the thyroid gland of Xenopus laevis tadpoles

inferredcites →https://doi.org/10.1016/j.ygcen.2012.12.018openalex-snapshot

Regulation of gonadal sex ratios and pubertal development by the thyroid endocrine system in zebrafish (Danio rerio)

inferredcites →https://doi.org/10.1016/j.ygcen.2014.03.015openalex-snapshot

Mechanisms of crosstalk between endocrine systems: Regulation of sex steroid hormone synthesis and action by thyroid hormones

inferredcites →https://doi.org/10.1016/j.ygcen.2018.04.023openalex-snapshot

Thyroid hormone actions on male reproductive system of teleost fish

inferredcites →https://doi.org/10.1016/j.ygcen.2022.114033openalex-snapshot

Tpo knockout in zebrafish partially recapitulates clinical manifestations of congenital hypothyroidism and reveals the involvement of TH in proper development of glucose homeostasis

inferredcites →https://doi.org/10.1016/j.yhbeh.2005.02.001openalex-snapshot

Endocrine control of Anguilla anguilla glass eel dispersal: Effect of thyroid hormones on locomotor activity and rheotactic behavior

inferredcites →https://doi.org/10.1016/j.yhbeh.2017.09.016openalex-snapshot

Behavioral and molecular analyses of olfaction-mediated avoidance responses of Rana ( Lithobates ) catesbeiana tadpoles: Sensitivity to thyroid hormones, estrogen, and treated municipal wastewater effluent

inferredcites →https://doi.org/10.1016/j.yrtph.2018.07.025openalex-snapshot

Human relevance of follicular thyroid tumors in rodents caused by non-genotoxic substances

inferredcites →https://doi.org/10.1016/j.yrtph.2020.104736openalex-snapshot

Weight of Evidence and Human Relevance Evaluation of the Benfluralin Mode of Action in Rats (Part II): Thyroid carcinogenesis

inferredcites →https://doi.org/10.1016/s0016-6480(02)00570-1openalex-snapshot

The liver of Fundulus heteroclitus expresses deiodinase type 1 mRNA

inferredcites →https://doi.org/10.1016/s0016-6480(03)00197-7openalex-snapshot

The effect of endocrine disrupting chemicals on thyroid hormone binding to Japanese quail transthyretin and thyroid hormone receptor

inferredcites →https://doi.org/10.1016/s0041-008x(02)00045-5openalex-snapshot

Competitive interactions of chlorinated phenol compounds with 3,3′,5-triiodothyronine binding to transthyretin: detection of possible thyroid-disrupting chemicals in environmental waste water

inferredcites →https://doi.org/10.1016/s0044-8486(98)00347-0openalex-snapshot

Effect of thyroxine on the decrease of aggressive behaviour of four salmonids during the parr-smolt transformation

inferredcites →https://doi.org/10.1016/s0300-483x(02)00222-6openalex-snapshot

Polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs) and chlorinated paraffins (CPs) in rats—testing interactions and mechanisms for thyroid hormone effects

inferredcites →https://doi.org/10.1016/s0303-7207(02)00302-7openalex-snapshot

Endocrine disrupting chemicals: interference of thyroid hormone binding to transthyretins and to thyroid hormone receptors

inferredcites →https://doi.org/10.1016/s0892-0362(98)00065-8openalex-snapshot

Low-Frequency Hearing Loss Following Perinatal Exposure to 3,3′,4,4′,5-Pentachlorobiphenyl (PCB 126) in Rats

inferredcites →https://doi.org/10.1016/s0896-6273(00)81034-xopenalex-snapshot

Asymmetric Growth and Development of the Xenopus laevis Retina during Metamorphosis Is Controlled by Type III Deiodinase

inferredcites →https://doi.org/10.1016/s1001-0742(10)60408-1openalex-snapshot

In vitro fluorescence displacement investigation of thyroxine transport disruption by bisphenol A

inferredcites →https://doi.org/10.1016/s1001-0742(11)60819-xopenalex-snapshot

Species-dependent effects of the phenolic herbicide ioxynil with potential thyroid hormone disrupting activity: modulation of its cellular uptake and activity by interaction with serum thyroid hormone-binding proteins

inferredcites →https://doi.org/10.1016/s1055-937x(98)80044-3openalex-snapshot

Comparative renal function in reptiles, birds, and mammals

inferredcites →https://doi.org/10.1021/acs.est.7b06145openalex-snapshot

High-Throughput Screening and Quantitative Chemical Ranking for Sodium-Iodide Symporter Inhibitors in ToxCast Phase I Chemical Library

inferredcites →https://doi.org/10.1021/acs.est.8b00776openalex-snapshot

Thyroid Disruption by Bisphenol S Analogues via Thyroid Hormone Receptor β: in Vitro , in Vivo , and Molecular Dynamics Simulation Study

inferredcites →https://doi.org/10.1021/acs.est.8b03581openalex-snapshot

Interspecies Variation between Fish and Human Transthyretins in Their Binding of Thyroid-Disrupting Chemicals

inferredcites →https://doi.org/10.1021/acs.est.8b04587openalex-snapshot

Evidence for Cross Species Extrapolation of Mammalian-Based High-Throughput Screening Assay Results

inferredcites →https://doi.org/10.1021/acs.est.9b07204openalex-snapshot

Effect of Thyroperoxidase and Deiodinase Inhibition on Anterior Swim Bladder Inflation in the Zebrafish

inferredcites →https://doi.org/10.1021/acs.est.9b07205openalex-snapshot

Toward an AOP Network-Based Tiered Testing Strategy for the Assessment of Thyroid Hormone Disruption

inferredcites →https://doi.org/10.1021/es0704129openalex-snapshot

An In Vivo Multiwell-Based Fluorescent Screen for Monitoring Vertebrate Thyroid Hormone Disruption

inferredcites →https://doi.org/10.1021/es202248hopenalex-snapshot

Zebrafish Eleutheroembryos Provide a Suitable Vertebrate Model for Screening Chemicals that Impair Thyroid Hormone Synthesis

inferredcites →https://doi.org/10.1021/es2046074openalex-snapshot

Assessment of the Binding of Hydroxylated Polybrominated Diphenyl Ethers to Thyroid Hormone Transport Proteins Using a Site-Specific Fluorescence Probe

inferredcites →https://doi.org/10.1021/es9012454openalex-snapshot

Simple, Rapid Zebrafish Larva Bioassay for Assessing the Potential of Chemical Pollutants and Drugs to Disrupt Thyroid Gland Function

inferredcites →https://doi.org/10.1021/es902691uopenalex-snapshot

Recombinant Albumin and Transthyretin Transport Proteins from Two Gull Species and Human: Chlorinated and Brominated Contaminant Binding and Thyroid Hormones

inferredcites →https://doi.org/10.1023/a:1007722812697openalex-snapshot

Comparative study of iodothyronine outer ring and inner ring deiodinase activities in five teleostean fishes

inferredcites →https://doi.org/10.1038/83829openalex-snapshot

A thyroid hormone receptor that is required for the development of green cone photoreceptors

inferredcites →https://doi.org/10.1038/s41433-018-0288-8openalex-snapshot

From axolotl to zebrafish: a comparative approach to the study of thyroid involvement in ocular development

inferredcites →https://doi.org/10.1038/s41467-020-17450-8openalex-snapshot

Anthropogenic stressors impact fish sensory development and survival via thyroid disruption

inferredcites →https://doi.org/10.1038/sj.cgt.7700525openalex-snapshot

The rat sodium iodide symporter gene permits more effective radioisotope concentration than the human sodium iodide symporter gene in human and rodent cancer cells

inferredcites →https://doi.org/10.1038/sj.emboj.7601356openalex-snapshot

Unliganded thyroid hormone receptor is essential for Xenopus laevis eye development

inferredcites →https://doi.org/10.1039/c3mb70398copenalex-snapshot

Iodotyrosine deiodinase: a unique flavoprotein present in organisms of diverse phyla

inferredcites →https://doi.org/10.1053/j.semperi.2008.09.009openalex-snapshot

The Role of Transient Hypothyroxinemia of Prematurity in Development of Visual Abilities

inferredcites →https://doi.org/10.1055/a-0919-3879openalex-snapshot

Inhibition of Type 1 Iodothyronine Deiodinase by Bisphenol A

inferredcites →https://doi.org/10.1073/pnas.1920086117openalex-snapshot

Thyroid hormone receptors mediate two distinct mechanisms of long-wavelength vision

inferredcites →https://doi.org/10.1073/pnas.2136755100openalex-snapshot

Thyroid hormone controls the development of connections between the spinal cord and limbs during Xenopus laevis metamorphosis

inferredcites →https://doi.org/10.1074/jbc.272.13.8179openalex-snapshot

Thyroid Hormone-dependent Gene Expression Program for Xenopus Neural Development

inferredcites →https://doi.org/10.1074/jbc.m112.413831openalex-snapshot

Zebrafish as a Model for Monocarboxyl Transporter 8-Deficiency

inferredcites →https://doi.org/10.1074/jbc.m205608200openalex-snapshot

A Thyroid Hormone Antagonist That Inhibits Thyroid Hormone Action in Vivo

inferredcites →https://doi.org/10.1080/00498254.2018.1437300openalex-snapshot

Comparison of the hepatic and thyroid gland effects of sodium phenobarbital and pregnenolone-16α-carbonitrile in wild-type and constitutive androstane receptor (CAR)/pregnane X receptor (PXR) knockout rats

inferredcites →https://doi.org/10.1080/10408440591007304openalex-snapshot

Mode of Action: Neurotoxicity Induced by Thyroid Hormone Disruption During Development—Hearing Loss Resulting From Exposure to PHAHs

inferredcites →https://doi.org/10.1080/17446651.2022.2044788openalex-snapshot

Impact of endocrine disrupting chemicals on neurodevelopment: the need for better testing strategies for endocrine disruption-induced developmental neurotoxicity

inferredcites →https://doi.org/10.1089/thy.2009.0128openalex-snapshot

Visual Abilities at 6 Months in Preterm Infants: Impact of Thyroid Hormone Deficiency and Neonatal Medical Morbidity

inferredcites →https://doi.org/10.1089/thy.2015.0034openalex-snapshot

Aberrant Cerebellar Development in Mice Lacking Dual Oxidase Maturation Factors

inferredcites →https://doi.org/10.1093/bmb/63.1.39openalex-snapshot

Sensory organ development in the inner ear: molecular and cellular mechanisms

inferredcites →https://doi.org/10.1093/gbe/evw013openalex-snapshot

Contrasting patterns of evolutionary diversification in the olfactory repertoires of reptile and bird genomes

inferredcites →https://doi.org/10.1093/icb/37.6.482openalex-snapshot

Hormonal Mechanisms as Potential Constraints on Evolution: Examples from the Anura

inferredcites →https://doi.org/10.1093/toxsci/kfaa036openalex-snapshot

Targeted Pathway-basedIn VivoTesting Using Thyroperoxidase Inhibition to Evaluate Plasma Thyroxine as a Surrogate Metric of Metamorphic Success in Model AmphibianXenopus laevis

inferredcites →https://doi.org/10.1093/toxsci/kfac014openalex-snapshot

Characterization of the Mechanistic Linkages Between Iodothyronine Deiodinase Inhibition and Impaired Thyroid-Mediated Growth and Development in Xenopus laevis Using Iopanoic Acid

inferredcites →https://doi.org/10.1093/toxsci/kfi049openalex-snapshot

In Vitro and in Vivo Analysis of the Thyroid Disrupting Activities of Phenolic and Phenol Compounds in Xenopus laevis

inferredcites →https://doi.org/10.1093/toxsci/kfj204openalex-snapshot

In Vitro and In Vivo Analysis of the Thyroid System–Disrupting Activities of Brominated Phenolic and Phenol Compounds in Xenopus laevis

inferredcites →https://doi.org/10.1093/toxsci/kfm001openalex-snapshot

Effects of Prolonged Exposure to Perchlorate on Thyroid and Reproductive Function in Zebrafish

inferredcites →https://doi.org/10.1093/toxsci/kfq166openalex-snapshot

Inhibition of Thyroid Hormone Release from Cultured Amphibian Thyroid Glands by Methimazole, 6-Propylthiouracil, and Perchlorate

inferredcites →https://doi.org/10.1093/toxsci/kfr105openalex-snapshot

Accumulation and Debromination of Decabromodiphenyl Ether (BDE-209) in Juvenile Fathead Minnows (Pimephales promelas) Induces Thyroid Disruption and Liver Alterations

inferredcites →https://doi.org/10.1093/toxsci/kfr117openalex-snapshot

Halogenated Phenolic Contaminants Inhibit the In Vitro Activity of the Thyroid-Regulating Deiodinases in Human Liver

inferredcites →https://doi.org/10.1093/toxsci/kfr244openalex-snapshot

Impact of Low-Level Thyroid Hormone Disruption Induced by Propylthiouracil on Brain Development and Function

inferredcites →https://doi.org/10.1093/toxsci/kfs072openalex-snapshot

In Ovo Effects of Perfluorohexane Sulfonate and Perfluorohexanoate on Pipping Success, Development, mRNA Expression, and Thyroid Hormone Levels in Chicken Embryos

inferredcites →https://doi.org/10.1093/toxsci/kfv090openalex-snapshot

In Vitro,Ex Vivo, andIn VivoDetermination of Thyroid Hormone Modulating Activity of Benzothiazoles

inferredcites →https://doi.org/10.1093/toxsci/kfw119openalex-snapshot

Editor’s Highlight: Sequence Alignment to Predict Across Species Susceptibility (SeqAPASS): A Web-Based Tool for Addressing the Challenges of Cross-Species Extrapolation of Chemical Toxicity

inferredcites →https://doi.org/10.1093/toxsci/kfx279openalex-snapshot

Screening the ToxCast Phase 1 Chemical Library for Inhibition of Deiodinase Type 1 Activity

inferredcites →https://doi.org/10.1093/toxsci/kfy016openalex-snapshot

Developmental Thyroid Hormone Insufficiency Induces a Cortical Brain Malformation and Learning Impairments: A Cross-Fostering Study

inferredcites →https://doi.org/10.1093/toxsci/kfy028openalex-snapshot

The Affinity of Brominated Phenolic Compounds for Human and Zebrafish Thyroid Receptor β: Influence of Chemical Structure

inferredcites →https://doi.org/10.1093/toxsci/kfy203openalex-snapshot

Evaluating Iodide Recycling Inhibition as a Novel Molecular Initiating Event for Thyroid Axis Disruption in Amphibians

inferredcites →https://doi.org/10.1093/toxsci/kfy302openalex-snapshot

Screening the ToxCast Phase 1, Phase 2, and e1k Chemical Libraries for Inhibitors of Iodothyronine Deiodinases

inferredcites →https://doi.org/10.1093/toxsci/kfz006openalex-snapshot

Extracting and Benchmarking Emerging Adverse Outcome Pathway Knowledge

inferredcites →https://doi.org/10.1093/toxsci/kfz227openalex-snapshot

Extrapolating In Vitro Screening Assay Data for Thyroperoxidase Inhibition to Predict Serum Thyroid Hormones in the Rat

inferredcites →https://doi.org/10.1096/fj.04-2023fjeopenalex-snapshot

Iodotyrosine dehalogenase 1 (DEHAL1) is a transmembrane protein involved in the recycling of iodide close to the thyroglobulin iodination site

inferredcites →https://doi.org/10.1096/fj.201600223ropenalex-snapshot

Inhibitors of pendrin anion exchange identified in a small molecule screen increase airway surface liquid volume in cystic fibrosis

inferredcites →https://doi.org/10.1097/med.0000000000000275openalex-snapshot

The interaction between thyroid and kidney disease: an overview of the evidence

inferredcites →https://doi.org/10.1098/rspb.2012.2490openalex-snapshot

Opsin switch reveals function of the ultraviolet cone in fish foraging

inferredcites →https://doi.org/10.1098/rspb.2016.1206openalex-snapshot

Thyroid hormone modulates offspring sex ratio in a turtle with temperature-dependent sex determination

inferredcites →https://doi.org/10.1111/j.1749-6632.2008.03652.xopenalex-snapshot

Localization and Enzyme Activity of Iodotyrosine Dehalogenase 1 during Metamorphosis of Frog Microhyla ornata

inferredcites →https://doi.org/10.1111/jne.12169openalex-snapshot

Subcortical Band Heterotopia in Rat Offspring Following Maternal Hypothyroxinaemia: Structural and Functional Characteristics

inferredcites →https://doi.org/10.1111/joa.12314openalex-snapshot

Where hearing starts: the development of the mammalian cochlea

inferredcites →https://doi.org/10.1124/dmd.109.028621openalex-snapshot

4-Hydroxy-2,2′,3,4′,5,5′,6-heptachlorobiphenyl-Mediated Decrease in Serum Thyroxine Level in Mice Occurs through Increase in Accumulation of Thyroxine in the Liver

inferredcites →https://doi.org/10.1124/dmd.121.000498openalex-snapshot

Mechanisms by Which Inducers of Drug Metabolizing Enzymes Alter Thyroid Hormones in Rats

inferredcites →https://doi.org/10.1124/mol.64.2.474openalex-snapshot

The Environmental Pollutant 1,1-Dichloro-2,2-bis (p-chlorophenyl)ethylene Induces Rat Hepatic Cytochrome P450 2B and 3A Expression through the Constitutive Androstane Receptor and Pregnane X Receptor

inferredcites →https://doi.org/10.1126/science.aau6348openalex-snapshot

Thyroid hormone signaling specifies cone subtypes in human retinal organoids

inferredcites →https://doi.org/10.1134/s1062360414060058openalex-snapshot

Effects of thyroid hormone level alterations on the Weberian apparatus ontogeny of cyprinids (Cyprinidae; Teleostei)

inferredcites →https://doi.org/10.1134/s1995082911040067openalex-snapshot

The role of thyroid hormones in the formation of behavioral responses in juvenile roach (Rutilus rutilus (L.) (Cyprinidae)

inferredcites →https://doi.org/10.1152/ajpcell.2000.278.1.c207openalex-snapshot

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

inferredcites →https://doi.org/10.1152/ajpendo.00216.2012openalex-snapshot

Delayed development of specific thyroid hormone-regulated events in transthyretin null mice

inferredcites →https://doi.org/10.1152/ajprenal.00011.2009openalex-snapshot

Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression

inferredcites →https://doi.org/10.1159/000113336openalex-snapshot

Evolution of Vertebrate Olfactory Systems

inferredcites →https://doi.org/10.1159/000335106openalex-snapshot

Pendrin Function and Regulation in Xenopus Oocytes

inferredcites →https://doi.org/10.1159/000445559openalex-snapshot

Effect of Known Inhibitors of Ion Transport on Pendrin (SLC26A4) Activity in a Human Kidney Cell Line

inferredcites →https://doi.org/10.1159/000504668openalex-snapshot

Evidence for Prenatal Exposure to Thyroid Disruptors and Adverse Effects on Brain Development

inferredcites →https://doi.org/10.1163/156853908792451511openalex-snapshot

Chronic perchlorate exposure impairs stickleback reproductive behaviour and swimming performance

inferredcites →https://doi.org/10.1163/156854297x00076openalex-snapshot

Evolutionary Trends and Possible Origin of the Weberian Apparatus

inferredcites →https://doi.org/10.1172/jci106748openalex-snapshot

Effects of 3-nitro-l-tyrosine on thyroid function in the rat: an experimental model for the dehalogenase defect

inferredcites →https://doi.org/10.1172/jci113479openalex-snapshot

Dual mechanisms of regulation of type I iodothyronine 5'-deiodinase in the rat kidney, liver, and thyroid gland. Implications for the treatment of hyperthyroidism with radiographic contrast agents.

inferredcites →https://doi.org/10.1172/jci26240openalex-snapshot

Type 3 deiodinase is critical for the maturation and function of the thyroid axis

inferredcites →https://doi.org/10.1186/1471-213x-8-101openalex-snapshot

Thyroid hormone components are expressed in three sequential waves during development of the chick retina

inferredcites →https://doi.org/10.1186/1471-2148-8-103openalex-snapshot

Evolution of pharmacologic specificity in the pregnane X receptor

inferredcites →https://doi.org/10.1186/s13044-021-00105-1openalex-snapshot

Associations between maternal urinary iodine assessment, dietary iodine intakes and neurodevelopmental outcomes in the child: a systematic review

inferredcites →https://doi.org/10.1203/01.pdr.0000157681.38042.b4openalex-snapshot

Development of Contrast Sensitivity in Infants with Prenatal and Neonatal Thyroid Hormone Insufficiencies

inferredcites →https://doi.org/10.1210/en.130.3.1525openalex-snapshot

Thyroxine (T4) transport and distribution in rats treated with EMD 21388, a synthetic flavonoid that displaces T4 from transthyretin

inferredcites →https://doi.org/10.1210/en.2002-220971openalex-snapshot

The Porcine Sodium/Iodide Symporter Gene Exhibits an Uncommon Expression Pattern Related to the Use of Alternative Splice Sites not Present in the Human or Murine Species

inferredcites →https://doi.org/10.1210/en.2005-0711openalex-snapshot

Characterization of Recombinant Xenopus laevis Type I Iodothyronine Deiodinase: Substitution of a Proline Residue in the Catalytic Center by Serine (Pro132Ser) Restores Sensitivity to 6-Propyl-2-Thiouracil

inferredcites →https://doi.org/10.1210/en.2005-0739openalex-snapshot

Targeted Disruption of the Type 1 Selenodeiodinase Gene (Dio1) Results in Marked Changes in Thyroid Hormone Economy in Mice

inferredcites →https://doi.org/10.1210/en.2006-1727openalex-snapshot

Thyroid Hormone Homeostasis and Action in the Type 2 Deiodinase-Deficient Rodent Brain during Development

inferredcites →https://doi.org/10.1210/en.2008-1092openalex-snapshot

Retarded Developmental Expression and Patterning of Retinal Cone Opsins in Hypothyroid Mice

inferredcites →https://doi.org/10.1210/en.2008-1419openalex-snapshot

A Protective Role for Type 3 Deiodinase, a Thyroid Hormone-Inactivating Enzyme, in Cochlear Development and Auditory Function

inferredcites →https://doi.org/10.1210/en.2008-1437openalex-snapshot

The Sodium-Iodide Symporter NIS and Pendrin in Iodide Homeostasis of the Thyroid

showing the first 200 of 261 · page through all 261

What points at this work

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

inferred← citeshttps://doi.org/10.12688/openreseurope.18739.1zenodo-depositor-declared

A 2024 inventory of test methods relevant to thyroid hormone system disruption for human health and environmental regulatory hazard assessment

inferred← citeshttps://doi.org/10.1002/etc.5878openalex-snapshot

Development of a Zebrafish embryo-based test system for thyroid hormone system disruption: 3Rs in ecotoxicological research

inferred← citeshttps://doi.org/10.1002/etc.5940openalex-snapshot

Bridging the gap between human toxicology and ecotoxicology under one health perspective by a cross-species adverse outcome pathway network for reproductive toxicity

inferred← citeshttps://doi.org/10.1002/jat.4672openalex-snapshot

Hepatic enzyme induction and its potential effect on thyroid hormone metabolism in the metamorphosing tadpole of Xenopus laevis (African clawed frog)

inferred← citeshttps://doi.org/10.1007/s00204-024-03766-7openalex-snapshot

In vitro assessment of thyroid peroxidase inhibition by chemical exposure: comparison of cell models and detection methods

inferred← citeshttps://doi.org/10.1007/s00204-025-04034-yopenalex-snapshot

Advancing in vitro assessment of iodide uptake inhibition: integrating a novel biotransformation pretreatment step

inferred← citeshttps://doi.org/10.1007/s00204-025-04258-yopenalex-snapshot

In vitro thyroperoxidase inhibition assessment by LC-ICP-MS-based L-tyrosine iodination assay: comparison with Amplex Ultrared assay and its modifications

inferred← citeshttps://doi.org/10.1016/j.aquatox.2026.108017openalex-snapshot

Environmental exposure to dinotefuran disturbs circadian rhythm, thyroid hormones and neurotransmitters, leading to locomotor deficits in Opsariichthys bidens larvae

inferred← citeshttps://doi.org/10.1016/j.cotox.2026.100600openalex-snapshot

Are thyroid hormone–mediated mechanisms an overlooked pathway in male reproductive toxicity?

inferred← citeshttps://doi.org/10.1016/j.ecoenv.2024.116995openalex-snapshot

The thyroid hormone system disrupting potential of resorcinol in fish

inferred← citeshttps://doi.org/10.1016/j.emcon.2026.100626openalex-snapshot

The antithyroid drug methimazole as an emerging aquatic contaminant: Physiological and reproductive disruption in female goldfish (Carassius auratus) and partial mitigation by thyroxine

inferred← citeshttps://doi.org/10.1016/j.enceco.2025.06.006openalex-snapshot

Adverse outcome pathway-oriented exploration of neurodevelopmental toxicity of tris(1,3-dichloropropyl) phosphate linked to membrane thyroid hormone receptor activation

inferred← citeshttps://doi.org/10.1016/j.envint.2026.110451openalex-snapshot

Adverse outcome pathway network-based approach for the evaluation of thyroid hormone system disruption for human health and environmental regulatory hazard assessment

inferred← citeshttps://doi.org/10.1016/j.envint.2026.110465openalex-snapshot

Mapping disease-linked AOPs to inform bioassay selection for chemical hazard assessment

inferred← citeshttps://doi.org/10.1016/j.jhazmat.2025.139890openalex-snapshot

Impact of nanoplastics on thyroid function: Unraveling cellular biokinetics, molecular mechanisms and human risk assessment

inferred← citeshttps://doi.org/10.1016/j.namjnl.2026.100093openalex-snapshot

Use of New Approach Methodologies for the assessment of Endocrine Disruption within European union regulatory frameworks: Report from the 2024 European partnership for alternative approaches (EPAA) partners’ forum

inferred← citeshttps://doi.org/10.1016/j.scitotenv.2024.170968openalex-snapshot

An integrative data-centric approach to derivation and characterization of an adverse outcome pathway network for cadmium-induced toxicity

inferred← citeshttps://doi.org/10.1016/j.tox.2024.153794openalex-snapshot

Exploring a mechanism-based approach for the identification of endocrine disruptors using Adverse Outcome Pathways (AOPs) and New Approach Methodologies (NAMs) : A perfluorooctane sulfonic acid case study

inferred← citeshttps://doi.org/10.1016/j.tox.2025.154337openalex-snapshot

Ophthalmotoxicology of polyhalogenated compounds

inferred← citeshttps://doi.org/10.1016/j.tox.2026.154542openalex-snapshot

Integrating transcriptomics and molecular AOPs to identify T3-dependent regulation of neuronal development in the human neural progenitor test

inferred← citeshttps://doi.org/10.1016/j.yrtph.2025.105810openalex-snapshot

Cross-taxa extrapolation: Is there a role for thyroid hormone conjugating liver enzymes during amphibian metamorphosis?

inferred← citeshttps://doi.org/10.1071/en23105openalex-snapshot

Developing a modern approach to assess ecological risk from pesticides without unnecessary vertebrate animal testing

inferred← citeshttps://doi.org/10.1080/10408444.2026.2623026openalex-snapshot

Role of constitutive androstane receptor in developmental toxicology: linking chemical exposure, nutrition, and disease susceptibility

inferred← citeshttps://doi.org/10.1093/etojnl/vgaf031openalex-snapshot

Developing adverse outcome pathways to support radioecological risk assessment: challenges and insights

inferred← citeshttps://doi.org/10.1093/inteam/vjag058openalex-snapshot

Best practices for the development and application of bioinformatics approaches for species extrapolation in chemical safety assessment

inferred← citeshttps://doi.org/10.1111/brv.70106openalex-snapshot

Prioritising research on endocrine disruption in the marine environment: a global perspective

inferred← citeshttps://doi.org/10.2903/j.efsa.2023.e211005openalex-snapshot

Toxicometabolomics as a tool for next generation environmental risk assessment

inferred← citeshttps://doi.org/10.2903/j.efsa.2024.8672openalex-snapshot

Specific effects on the thyroid relevant for performing a dietary cumulative risk assessment of pesticide residues: 2024 update

inferred← citeshttps://doi.org/10.2903/j.efsa.2025.9711openalex-snapshot

Peer review of the pesticide risk assessment of the active substance phenmedipham

inferred← citeshttps://doi.org/10.3389/fphar.2026.1760820openalex-snapshot

Epidemiological relevant effect biomarkers for thyroid hormone system related adverse outcome pathways: a literature review

inferred← citeshttps://doi.org/10.3389/ftox.2024.1285768openalex-snapshot

Comprehensive mapping of the AOP-Wiki database: identifying biological and disease gaps

inferred← citeshttps://doi.org/10.3389/ftox.2026.1733477openalex-snapshot

Zebrafish neuromast development: a target for endocrine disrupting chemicals?

inferred← citeshttps://doi.org/10.3389/ftox.2026.1736963openalex-snapshot

New approach methodologies (NAMs) for improved developmental and reproductive toxicity (DART) assessment with focus on endocrine disruption – a PARC project

inferred← citeshttps://doi.org/10.3390/jox16050164openalex-snapshot

Selenium and Iodine as Susceptibility Modifiers of Thyroid Disruption Associated with Metals: An Overview of Human and Experimental Research Data

inferred← citeshttps://doi.org/10.3390/toxics13070590openalex-snapshot

New QSAR Models to Predict Human Transthyretin Disruption by Per- and Polyfluoroalkyl Substances (PFAS): Development and Application

inferred← citeshttps://doi.org/10.64898/2026.06.25.734475openalex-snapshot

Integrating Semantic Retrieval, LLM-based Refinement, and Structured Expert Curation for Scalable AOP Gene Mapping

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.