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Deiodinases: implications of the local control of thyroid hormone action
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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/jtra.1036openalex-snapshot
Pituitary nuclear 3,5,3?-triiodothyronine and thyrotropin secretion: An explanation for the effect of thyroxine
inferredcites →https://doi.org/10.1006/dbio.2001.0293openalex-snapshot
Role of Thyroid Hormone Receptors in Timing Oligodendrocyte Differentiation
inferredcites →https://doi.org/10.1007/s00259-002-0902-6openalex-snapshot
Brown adipose tissue: a factor to consider in symmetrical tracer uptake in the neck and upper chest region
inferredcites →https://doi.org/10.1007/s10540-005-2882-9openalex-snapshot
Thyroid Hormone and the Energetic Cost of Keeping Body Temperature
inferredcites →https://doi.org/10.1007/s11307-005-0030-3openalex-snapshot
Reduction of Brown Fat 2-Deoxy-2-[F-18]fluoro-d-glucose Uptake by Controlling Environmental Temperature Prior to Positron Emission Tomography Scan
inferredcites →https://doi.org/10.1016/0002-9343(82)90565-4openalex-snapshot
Prevalence of abnormal thyroid function test results in patients with acute medical illnesses
inferredcites →https://doi.org/10.1016/0002-9343(82)90568-xopenalex-snapshot
Prevalence of abnormal thyroid function test results in patients with acute medical illnesses
inferredcites →https://doi.org/10.1016/j.ccc.2005.08.006openalex-snapshot
Changes Within the Thyroid Axis During Critical Illness
inferredcites →https://doi.org/10.1016/j.ccc.2005.10.001openalex-snapshot
Non-Thyroidal Illness Syndrome is a Manifestation of Hypothalamic-Pituitary Dysfunction, and in View of Current Evidence, Should be Treated with Appropriate Replacement Therapies
inferredcites →https://doi.org/10.1016/j.cmet.2005.03.001openalex-snapshot
LXRs regulate the balance between fat storage and oxidation
inferredcites →https://doi.org/10.1016/j.mce.2005.11.030openalex-snapshot
Thyroid hormone action at the cellular, genomic and target gene levels
inferredcites →https://doi.org/10.1016/s0009-8981(96)06411-xopenalex-snapshot
Serum free 3,5,3′-triiodothyronine (T3) in non-thyroidal somatic illness, as measured by ultrafiltration and immunoextraction
inferredcites →https://doi.org/10.1016/s0021-9258(18)82411-5openalex-snapshot
The quantitative contributions of mitochondrial proton leak and ATP turnover reactions to the changed respiration rates of hepatocytes from rats of different thyroid status
inferredcites →https://doi.org/10.1016/s0025-7125(16)30470-9openalex-snapshot
The Effects of Nonthyroid Disease and Drugs on Thyroid Function Tests
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/s1043-2760(00)00263-0openalex-snapshot
Gene Regulation by Thyroid Hormone
inferredcites →https://doi.org/10.1023/a:1013640006611openalex-snapshot
Role of the Sarcoplasmic Reticulum Ca2+-ATPase on Heat Production and Thermogenesis
inferredcites →https://doi.org/10.1023/a:1013692023449openalex-snapshot
Mechanism of Thyroid-Hormone Regulated Expression of the SERCA Genes in Skeletal Muscle: Implications for Thermogenesis
inferredcites →https://doi.org/10.1038/35007527openalex-snapshot
Towards a molecular understanding of adaptive thermogenesis
inferredcites →https://doi.org/10.1038/nature04330openalex-snapshot
Bile acids induce energy expenditure by promoting intracellular thyroid hormone activation
inferredcites →https://doi.org/10.1038/ncb1272openalex-snapshot
The Hedgehog-inducible ubiquitin ligase subunit WSB-1 modulates thyroid hormone activation and PTHrP secretion in the developing growth plate
inferredcites →https://doi.org/10.1038/ng1654openalex-snapshot
Mutations in SECISBP2 result in abnormal thyroid hormone metabolism
inferredcites →https://doi.org/10.1056/nejm200007203430305openalex-snapshot
Severe Hypothyroidism Caused by Type 3 Iodothyronine Deiodinase in Infantile Hemangiomas
inferredcites →https://doi.org/10.1056/nejmoa040079openalex-snapshot
Timing and Magnitude of Increases in Levothyroxine Requirements during Pregnancy in Women with Hypothyroidism
inferredcites →https://doi.org/10.1073/pnas.0307402101openalex-snapshot
Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinase
inferredcites →https://doi.org/10.1073/pnas.94.19.10391openalex-snapshot
The type 2 iodothyronine deiodinase is expressed primarily in glial cells in the neonatal rat brain
inferredcites →https://doi.org/10.1073/pnas.97.3.1287openalex-snapshot
Type 2 iodothyronine deiodinase expression in the cochlea before the onset of hearing
inferredcites →https://doi.org/10.1074/jbc.m006973200openalex-snapshot
Characterization of the Subunit Structure of the Catalytically Active Type I Iodothyronine Deiodinase
inferredcites →https://doi.org/10.1074/jbc.m305725200openalex-snapshot
The Iodothyronine Selenodeiodinases Are Thioredoxin-fold Family Proteins Containing a Glycoside Hydrolase Clan GH-A-like Structure
inferredcites →https://doi.org/10.1080/09687680210166217openalex-snapshot
Thermogenesis and energy expenditure: control of heat production by the Ca 2+ -ATPase of fast and slow muscle
inferredcites →https://doi.org/10.1089/thy.1997.7.655openalex-snapshot
The Deiodinase Family of Selenoproteins
inferredcites →https://doi.org/10.1089/thy.1998.8.249openalex-snapshot
Simultaneous Measurement of Free Thyroxine and Free 3,5,3′-Triiodothyronine in Undiluted Serum by Direct Equilibrium Dialysis/Radioimmunoassay: Evidence that Free Triiodothyronine and Free Thyroxine are Normal in Many Patients with the Low Triiodothyronine Syndrome
inferredcites →https://doi.org/10.1089/thy.2005.15.757openalex-snapshot
Thyroid Hormone Transporters in Health and Disease
inferredcites →https://doi.org/10.1089/thy.2005.15.777openalex-snapshot
Cellular and Structural Biology of the Deiodinases
inferredcites →https://doi.org/10.1089/thy.2005.15.787openalex-snapshot
Biochemical Mechanisms of Thyroid Hormone Deiodination
inferredcites →https://doi.org/10.1089/thy.2005.15.815openalex-snapshot
The Role of Deiodinases in Amphibian Metamorphosis
inferredcites →https://doi.org/10.1089/thy.2005.15.823openalex-snapshot
The Roles of the Iodothyronine Deiodinases in Mammalian Development
inferredcites →https://doi.org/10.1089/thy.2005.15.835openalex-snapshot
Regulation of Type 1 Iodothyronine Deiodinase in Health and Disease
inferredcites →https://doi.org/10.1089/thy.2005.15.905openalex-snapshot
Insights Into the Role of Deiodinases from Studies of Genetically Modified Animals
inferredcites →https://doi.org/10.1089/thy.2005.15.917openalex-snapshot
The Effects of Iodine Deficiency on Thyroid Hormone Deiodination
inferredcites →https://doi.org/10.1093/nar/23.13.2555openalex-snapshot
Xenopus sonic hedgehog as a potential morphogen during embryogenesis and thyroid hormone-dependent metamorphosis
inferredcites →https://doi.org/10.1097/01.sa.0000151207.30473.01openalex-snapshot
Timing and Magnitude of Increases in Levothyroxine Requirements During Pregnancy in Women With Hypothyroidism
inferredcites →https://doi.org/10.1113/jphysiol.1977.sp011909openalex-snapshot
Thyroid calorigenesis in isolated, perfused rat liver: minor role of active sodium‐potassium transport.
inferredcites →https://doi.org/10.1126/science.199941openalex-snapshot
Pituitary Nuclear 3,5,3′-Triiodothyronine and Thyrotropin Secretion: An Explanation for the Effect of Thyroxine
inferredcites →https://doi.org/10.1126/science.218285openalex-snapshot
Thyroid Hormone Action at the Cellular Level
inferredcites →https://doi.org/10.1126/science.3945800openalex-snapshot
All Members of the MHC Multigene Family Respond to Thyroid Hormone in a Highly Tissue-Specific Manner
inferredcites →https://doi.org/10.1136/jim-51-04-22openalex-snapshot
Thyroid Hormone Action: Insight from Transgenic Mouse Models
inferredcites →https://doi.org/10.1152/ajpendo.00571.2004openalex-snapshot
A new polymorphism in the type II deiodinase gene is associated with circulating thyroid hormone parameters
inferredcites →https://doi.org/10.1152/ajpendo.1988.255.4.e496openalex-snapshot
Cold exposure rapidly induces virtual saturation of brown adipose tissue nuclear T3 receptors
inferredcites →https://doi.org/10.1172/jci107744openalex-snapshot
Triiodothyronine and Thyroxine in Hyperthyroidism COMPARISON OF THE ACUTE CHANGES DURING THERAPY WITH ANTITHYROID AGENTS
inferredcites →https://doi.org/10.1172/jci107924openalex-snapshot
Reduction in extrathyroidal triiodothyronine production by propylthiouracil in man.
inferredcites →https://doi.org/10.1172/jci107925openalex-snapshot
Propylthiouracil blocks extrathyroidal conversion of thyroxine to triiodothyronine and augments thyrotropin secretion in man.
inferredcites →https://doi.org/10.1172/jci111821openalex-snapshot
Decreased serum triiodothyronine in starving rats is due primarily to diminished thyroidal secretion of thyroxine.
inferredcites →https://doi.org/10.1172/jci112798openalex-snapshot
Intracellular conversion of thyroxine to triiodothyronine is required for the optimal thermogenic function of brown adipose tissue.
inferredcites →https://doi.org/10.1172/jci114961openalex-snapshot
Functional relationship of thyroid hormone-induced lipogenesis, lipolysis, and thermogenesis in the rat.
inferredcites →https://doi.org/10.1172/jci116730openalex-snapshot
Physiological and genetic analyses of inbred mouse strains with a type I iodothyronine 5' deiodinase deficiency.
inferredcites →https://doi.org/10.1172/jci11775openalex-snapshot
Effect of triiodothyronine on mitochondrial energy coupling in human skeletal muscle
inferredcites →https://doi.org/10.1172/jci15737openalex-snapshot
Paradoxical resistance to diet-induced obesity in UCP1-deficient mice
inferredcites →https://doi.org/10.1172/jci17490openalex-snapshot
The role of falling leptin levels in the neuroendocrine and metabolic adaptation to short-term starvation in healthy men
inferredcites →https://doi.org/10.1172/jci18348openalex-snapshot
Deubiquitination of type 2 iodothyronine deiodinase by von Hippel–Lindau protein–interacting deubiquitinating enzymes regulates thyroid hormone activation
inferredcites →https://doi.org/10.1172/jci200113803openalex-snapshot
The type 2 iodothyronine deiodinase is essential for adaptive thermogenesis in brown adipose tissue
inferredcites →https://doi.org/10.1172/jci200315737openalex-snapshot
Paradoxical resistance to diet-induced obesity in UCP1-deficient mice
inferredcites →https://doi.org/10.1172/jci25083openalex-snapshot
Type 2 iodothyronine deiodinase is the major source of plasma T3 in euthyroid humans
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/10.1172/jci4672openalex-snapshot
Type 2 iodothyronine deiodinase in rat pituitary tumor cells is inactivated in proteasomes.
inferredcites →https://doi.org/10.1210/edrv-2-1-87openalex-snapshot
Relationships between Circulating and Intracellular Thyroid Hormones: Physiological and Clinical Implications*
inferredcites →https://doi.org/10.1210/edrv.22.2.0427openalex-snapshot
The Effects of Amiodarone on the Thyroid
inferredcites →https://doi.org/10.1210/edrv.23.1.0455openalex-snapshot
Biochemistry, Cellular and Molecular Biology, and Physiological Roles of the Iodothyronine Selenodeiodinases
inferredcites →https://doi.org/10.1210/en.132.1.357openalex-snapshot
Impairment of the selenoenzyme type I iodothyronine deiodinase in C3H/He mice
inferredcites →https://doi.org/10.1210/en.136.2.629openalex-snapshot
The effect of thyroid hormone treatment on the gene expression and enzyme activity of rat liver sodium-potassium dependent adenosine triphosphatase
inferredcites →https://doi.org/10.1210/en.138.6.2569openalex-snapshot
Leptin Prevents Fasting-Induced Suppression of Prothyrotropin-Releasing Hormone Messenger Ribonucleic Acid in Neurons of the Hypothalamic Paraventricular Nucleus
inferredcites →https://doi.org/10.1210/en.2002-220960openalex-snapshot
In Vivo Dimerization of Types 1, 2, and 3 Iodothyronine Selenodeiodinases
inferredcites →https://doi.org/10.1210/en.2003-0490openalex-snapshot
Determinants of Iodothyronine Deiodinase Activities in Rodent Uterus
inferredcites →https://doi.org/10.1210/en.2003-1439openalex-snapshot
Lipopolysaccharide Induces Type 2 Iodothyronine Deiodinase in the Mediobasal Hypothalamus: Implications for the Nonthyroidal Illness Syndrome
inferredcites →https://doi.org/10.1210/en.2004-1392openalex-snapshot
Type 1 Iodothyronine Deiodinase Is a Sensitive Marker of Peripheral Thyroid Status in the Mouse
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.2005-1300openalex-snapshot
Atypical Expression of Type 2 Iodothyronine Deiodinase in Thyrotrophs Explains the Thyroxine-Mediated Pituitary Thyrotropin Feedback Mechanism
inferredcites →https://doi.org/10.1210/en.2005-1608openalex-snapshot
Characterization of the Nuclear Factor-κB Responsiveness of the Human dio2 Gene
inferredcites →https://doi.org/10.1210/endo-120-1-55openalex-snapshot
Nuclear 3,5,3′-Triiodothyronine (T3) in Brown Adipose Tissue: Receptor Occupancy and Sources of T3as Determined byin VivoTechniques*
inferredcites →https://doi.org/10.1210/er.2001-0034openalex-snapshot
Selenium, the Thyroid, and the Endocrine System
inferredcites →https://doi.org/10.1210/jc.2002-020627openalex-snapshot
A 21-Year-Old Woman with Consumptive Hypothyroidism due to a Vascular Tumor Expressing Type 3 Iodothyronine Deiodinase
inferredcites →https://doi.org/10.1210/jc.2002-021291openalex-snapshot
Type 3 Iodothyronine Deiodinase Is Highly Expressed in the Human Uteroplacental Unit and in Fetal Epithelium
inferredcites →https://doi.org/10.1210/jc.2002-021592openalex-snapshot
Polymorphisms in Thyroid Hormone Pathway Genes Are Associated with Plasma TSH and Iodothyronine Levels in Healthy Subjects
inferredcites →https://doi.org/10.1210/jc.2002-022013openalex-snapshot
Reduced Activation and Increased Inactivation of Thyroid Hormone in Tissues of Critically Ill Patients
inferredcites →https://doi.org/10.1210/jc.2004-1301openalex-snapshot
A Polymorphism in Type I Deiodinase Is Associated with Circulating Free Insulin-Like Growth Factor I Levels and Body Composition in Humans
inferredcites →https://doi.org/10.1210/jc.2005-0451openalex-snapshot
Polymorphisms in Type 2 Deiodinase Are Not Associated with Well-Being, Neurocognitive Functioning, and Preference for Combined Thyroxine/3,5,3′-Triiodothyronine Therapy
inferredcites →https://doi.org/10.1210/jc.77.2.382openalex-snapshot
Type II iodothyronine 5'-deiodinase and uncoupling protein in brown adipose tissue of human newborns
inferredcites →https://doi.org/10.1210/jc.83.2.309openalex-snapshot
Neuroendocrinology of Prolonged Critical Illness: Effects of Exogenous Thyrotropin-Releasing Hormone and Its Combination with Growth Hormone Secretagogues
inferredcites →https://doi.org/10.1210/jc.84.1.151openalex-snapshot
Dangerous Dogmas in Medicine: The Nonthyroidal Illness Syndrome
inferredcites →https://doi.org/10.1210/jcem-54-4-803openalex-snapshot
Effects of Short Term Glucocorticoid Administration in Primary Hyperparathyroidism: Comparison to Sarcoidosis*
inferredcites →https://doi.org/10.1210/jcem.83.2.4575openalex-snapshot
Neuroendocrinology of Prolonged Critical Illness: Effects of Exogenous Thyrotropin-Releasing Hormone and Its Combination with Growth Hormone Secretagogues1
inferredcites →https://doi.org/10.1210/me.14.11.1697openalex-snapshot
Selective Proteolysis of Human Type 2 Deiodinase: A Novel Ubiquitin-Proteasomal Mediated Mechanism for Regulation of Hormone Activation
inferredcites →https://doi.org/10.1210/me.15.12.2137openalex-snapshot
Targeted Disruption of the Type 2 Selenodeiodinase Gene (DIO2) Results in a Phenotype of Pituitary Resistance to T4
inferredcites →https://doi.org/10.1210/me.2005-0173openalex-snapshot
Transforming Growth Factor-β Promotes Inactivation of Extracellular Thyroid Hormones via Transcriptional Stimulation of Type 3 Iodothyronine Deiodinase
inferredcites →https://doi.org/10.1242/dev.120.5.1097openalex-snapshot
A novel role for thyroid hormone, glucocorticoids and retinoic acid in timing oligodendrocyte development
inferredcites →https://doi.org/10.1242/dev.126.13.2901openalex-snapshot
A role for Sonic hedgehog in axon-to-astrocyte signalling in the rodent optic nerve
inferredcites →https://doi.org/10.1242/jcs.00049openalex-snapshot
Normal timing of oligodendrocyte development from genetically engineered,lineage-selectable mouse ES cells
inferredcites →https://doi.org/10.2310/6650.2003.39191openalex-snapshot
Thyroid Hormone Action: Insight from Transgenic Mouse Models
inferredcites →https://doi.org/10.2337/diabetes.51.3.880openalex-snapshot
Association Between a Novel Variant of the Human Type 2 Deiodinase Gene Thr92Ala and Insulin Resistance
inferredcites →https://doi.org/10.2337/diabetes.53.3.577openalex-snapshot
Mice with Targeted Disruption of the Dio2 Gene Have Cold-Induced Overexpression of the Uncoupling Protein 1 Gene but Fail to Increase Brown Adipose Tissue Lipogenesis and Adaptive Thermogenesis
inferredcites →https://doi.org/10.7326/0003-4819-73-4-673_2openalex-snapshot
Scientific Foundations of Obstetrics and Gynaecology.
inferredcites →https://doi.org/10.7326/0003-4819-87-6-760openalex-snapshot
Thyroidal and Peripheral Production of Thyroid Hormones
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Life-Cycle Exposure to Decabromodiphenyl Ethane (DBDPE) Caused Transgenerational Epigenetic Alterations of Thyroid Endocrine System in Zebrafish
inferred← citeshttps://doi.org/10.1002/1878-0261.13612openalex-snapshot
The selenoenzyme type I iodothyronine deiodinase: a new tumor suppressor in ovarian cancer
inferred← citeshttps://doi.org/10.1002/9780470442890.ch18openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470609880.ch6openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9780470682531.pat0726openalex-snapshot
Enzyme Mimetic Chemistry of Organoselenium Compounds
inferred← citeshttps://doi.org/10.1002/9781118148143.ch14openalex-snapshot
Selenoproteins in Cellular Redox Regulation and Signaling
inferred← citeshttps://doi.org/10.1002/9781118501153.ch7openalex-snapshot
Development and regulation of external asymmetry during flatfish metamorphosis
inferred← citeshttps://doi.org/10.1002/9781444316728.ch2openalex-snapshot
Principles of Hormone Action
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Biological and Biochemical Aspects of Selenium Compounds
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Brown adipose tissue, energy expenditure, and biomarkers of cardio‐metabolic health among the Yakut (Sakha) of northeastern Siberia
inferred← citeshttps://doi.org/10.1002/ange.201005235openalex-snapshot
A Chemical Model for the Inner‐Ring Deiodination of Thyroxine by Iodothyronine Deiodinase
inferred← citeshttps://doi.org/10.1002/ange.201601116openalex-snapshot
Chemie und Biologie der Schilddrüsenhormon‐Biosynthese und ‐Wirkung
inferred← citeshttps://doi.org/10.1002/anie.201005235openalex-snapshot
A Chemical Model for the Inner‐Ring Deiodination of Thyroxine by Iodothyronine Deiodinase
inferred← citeshttps://doi.org/10.1002/anie.201601116openalex-snapshot
Chemistry and Biology in the Biosynthesis and Action of Thyroid Hormones
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Simultaneous quantification of T4, T3, rT3, 3,5‐T2 and 3,3′‐T2 in larval zebrafish ( Danio rerio ) as a model to study exposure to polychlorinated biphenyls
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Mechanism of Thyroxine Deiodination by Naphthyl‐Based Iodothyronine Deiodinase Mimics and the Halogen Bonding Role: A DFT Investigation
inferred← citeshttps://doi.org/10.1002/chem.201700407openalex-snapshot
Halogen‐Bonding Interactions of Polybrominated Diphenyl Ethers and Thyroid Hormone Derivatives: A Potential Mechanism for the Inhibition of Iodothyronine Deiodinase
inferred← citeshttps://doi.org/10.1002/chem.201903904openalex-snapshot
Halogen Bonding Interactions of Polychlorinated Biphenyls and the Potential for Thyroid Disruption
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Modeling Type‐1 Iodothyronine Deiodinase with Peptide‐Based Aliphatic Diselenides: Potential Role of Highly Conserved His and Cys Residues as a General Acid Catalyst
inferred← citeshttps://doi.org/10.1002/chem.202404455openalex-snapshot
Effect of Halogen Substitution on the Regioselective Deiodination of Thyroid Hormone Analogues by Deiodinase Mimics
inferred← citeshttps://doi.org/10.1002/cphy.c150027openalex-snapshot
Hypothalamus‐Pituitary‐Thyroid Axis
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Characterization of the thyroid hormones level in urine by liquid chromatography coupled to mass spectrometry focus in the antidoping field
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Serum Leptin and Thyroid Levels in Hospitalized Patients With Severe Eating Disorders
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Relationships between polybrominated diphenyl ethers and transcription and activity of type 1 deiodinase in a gull highly exposed to flame retardants
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Impaired swim bladder inflation in early life stage fathead minnows exposed to a deiodinase inhibitor, iopanoic acid
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Effects of Separate and Combined Exposure of Cadmium and Lead on the Endochondral Ossification in Bufo gargarizans
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Hepatic organic anion transporting polypeptide transporter and thyroid hormone receptor interplay determines cholesterol and glucose homeostasis
inferred← citeshttps://doi.org/10.1002/humu.20808openalex-snapshot
Novel pathogenic mechanism suggested by ex vivo analysis of MCT8 (SLC16A2) mutations
inferred← citeshttps://doi.org/10.1002/j.2040-4603.2016.tb00708.xopenalex-snapshot
Hypothalamus‐Pituitary‐Thyroid Axis
inferred← citeshttps://doi.org/10.1002/jbmr.27openalex-snapshot
The type 2 deiodinase Thr92Ala polymorphism is associated with increased bone turnover and decreased femoral neck bone mineral density
inferred← citeshttps://doi.org/10.1002/jcc.25775openalex-snapshot
The role of the halogen bond in iodothyronine deiodinase: Dependence on chalcogen substitution in naphthyl‐based mimetics
inferred← citeshttps://doi.org/10.1002/jnr.22806openalex-snapshot
Hypothyroidism reduces glutamate‐synaptic release by ouabain depolarization in rat CA3‐hippocampal region
inferred← citeshttps://doi.org/10.1002/slct.202300781openalex-snapshot
Halogen Bonding Interactions of Haloaromatic Endocrine Disruptors and the Potential for Inhibition of Iodothyronine Deiodinases
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Age‐ and Sex‐Dependent Dynamics in Pituitary Thyrotroph and Thyroid Hormones in Dromedary Camels ( Camelus dromedarius ): A Histochemical Approach
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Implications of Thyroid Hormone Signaling Through the Phosphoinositide-3 Kinase for Xenobiotic Disruption of Human Health
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Iodine and Brain Development
inferred← citeshttps://doi.org/10.1007/978-1-0716-4252-8_1openalex-snapshot
Thyroid Hormones and Co-workers: An Overview
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Thyroid Hormone Metabolism
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Assessing Thyroid Function in Hospitalized Patients
inferred← citeshttps://doi.org/10.1007/978-1-4614-1025-6_45openalex-snapshot
Selenoproteins in Skeletal Development and Disease: Lessons from Trsp Deletion in Murine Bone and Cartilage Progenitor Cells
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/10.1007/978-1-4614-4304-9_8openalex-snapshot
The Efficacy of Thyroid Hormone Therapy in Brain-Dead Heart Donors: A Review of Thyroid Function in Health and Disease
inferred← citeshttps://doi.org/10.1007/978-1-4939-7902-8_1openalex-snapshot
Thyroid Hormone Receptors: Several Players for One Hormone and Multiple Functions
inferred← citeshttps://doi.org/10.1007/978-1-4939-7902-8_4openalex-snapshot
In Vitro Approaches to Identify Thyroid Hormone Receptor-Dependent Transcriptional Response
inferred← citeshttps://doi.org/10.1007/978-1-60327-177-6_10openalex-snapshot
Changes Within the Thyroid Axis During the Course of Critical Illness
inferred← citeshttps://doi.org/10.1007/978-1-84628-881-4_1openalex-snapshot
Thyroid Embryology, Anatomy, and Physiology: A Review for the Surgeon
inferred← citeshttps://doi.org/10.1007/978-1-84800-187-9_14openalex-snapshot
Potential Therapeutic Uses of Thyroid Hormone
inferred← citeshttps://doi.org/10.1007/978-3-030-36871-5_25openalex-snapshot
Thyroid Hormones, Brain, and Heart
inferred← citeshttps://doi.org/10.1007/978-3-030-36871-5_8openalex-snapshot
TH Metabolism and Active TH Metabolites in the Heart
inferred← citeshttps://doi.org/10.1007/978-3-319-72102-6_3openalex-snapshot
“Thyroglobulin Storage, Processing and Degradation for Thyroid Hormone Liberation”
inferred← citeshttps://doi.org/10.1007/978-3-642-22236-8_2openalex-snapshot
Thyroid Hormone Deiodinases
inferred← citeshttps://doi.org/10.1007/978-88-470-1143-4_17openalex-snapshot
Thyroid, Renal Function, and Cardiac Outcome
inferred← citeshttps://doi.org/10.1007/978-88-470-1143-4_22openalex-snapshot
New Approaches for Treating Heart Disease by Modulating Thyroid Hormone Signaling Using Gene Therapy Approaches
inferred← citeshttps://doi.org/10.1007/978-88-470-1143-4_6openalex-snapshot
Cardiac Functional Effects of 3-iodothyronamine, a New Endogenous Thyroid Hormone Derivative
inferred← citeshttps://doi.org/10.1007/978-88-470-1143-4_7openalex-snapshot
Cardiac Thyroid-Hormone Deiodinative Pathways in Ventricular Hypertrophy and Heart Failure
inferred← citeshttps://doi.org/10.1007/978-90-481-3303-1_16openalex-snapshot
Ligand Regulation and Nuclear Receptor Action
inferred← citeshttps://doi.org/10.1007/978-90-481-3303-1_7openalex-snapshot
Thyroid Hormone Receptors
inferred← citeshttps://doi.org/10.1007/978-981-16-3280-8_15openalex-snapshot
Vegetable Biofortification: An Underexploited Silver Lining for Malnutrition Management
inferred← citeshttps://doi.org/10.1007/978-981-19-7859-3_6openalex-snapshot
Molecular Basis of Dorsal Fin Elongation and Regression During Metamorphosis
inferred← citeshttps://doi.org/10.1007/s00018-007-7396-0openalex-snapshot
Activation and inactivation of thyroid hormone by deiodinases: Local action with general consequences
inferred← citeshttps://doi.org/10.1007/s00018-014-1586-3openalex-snapshot
Thyroid hormones and their nuclear receptors: new players in intestinal epithelium stem cell biology?
inferred← citeshttps://doi.org/10.1007/s00018-022-04503-yopenalex-snapshot
Thyroid hormone signaling in the intestinal stem cells and their niche
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1007/s00244-011-9677-8openalex-snapshot
Modulation of Thyroid Hormone Concentrations in Serum of Rats Coadministered with Perchlorate and Iodide-Deficient Diet
inferred← citeshttps://doi.org/10.1007/s00253-019-09687-1openalex-snapshot
Different host-specific responses in thyroid function and gut microbiota modulation between diet-induced obese and normal mice given the same dose of iodine
inferred← citeshttps://doi.org/10.1007/s00300-015-1694-zopenalex-snapshot
Thyroid hormones and deiodinase activities in plasma and tissues from East Greenland polar bears (Ursus maritimus) during winter season
inferred← citeshttps://doi.org/10.1007/s00343-020-0241-0openalex-snapshot
Positive selection analysis reveals the deep-sea adaptation of a hadal sea cucumber (Paelopatides sp.) to the Mariana Trench
inferred← citeshttps://doi.org/10.1007/s00360-016-0984-2openalex-snapshot
A review of the peripheral levels of regulation by thyroid hormone
inferred← citeshttps://doi.org/10.1007/s00394-022-02945-5openalex-snapshot
RETRACTED ARTICLE: The impact of vitamin A supplementation on thyroid function and insulin sensitivity: implication of deiodinases and phosphoenolpyruvate carboxykinase in male Wistar rats
inferred← citeshttps://doi.org/10.1007/s00580-017-2550-zopenalex-snapshot
Effect of sodium levothyroxine on histomorphometry, histopathology, histochemistry, and immunohistochemistry of articular cartilage in female mice
inferred← citeshttps://doi.org/10.1007/s00894-016-3154-2openalex-snapshot
A DFT investigation of a bulky biomimetic model catalyzing the 5′-outer ring deiodination of thyroxine
inferred← citeshttps://doi.org/10.1007/s10072-021-05424-7openalex-snapshot
High rates of (treated) hypothyroidism among chronic migraine patients consulting a specialized headache clinic: are we missing something?
inferred← citeshttps://doi.org/10.1007/s10661-020-08355-6openalex-snapshot
Brown bullhead at the St. Lawrence River (Cornwall) Area of Concern: health and endocrine status in the context of tissue concentrations of PCBs and mercury
inferred← citeshttps://doi.org/10.1007/s10741-008-9120-zopenalex-snapshot
Cardiac effects of thyronamines
inferred← citeshttps://doi.org/10.1007/s10741-008-9133-7openalex-snapshot
Cardiomyocyte-specific inactivation of thyroid hormone in pathologic ventricular hypertrophy: an adaptative response or part of the problem?
inferred← citeshttps://doi.org/10.1007/s10741-010-9185-3openalex-snapshot
New insights into the role of thyroid hormone in cardiac remodeling: time to reconsider?
inferred← citeshttps://doi.org/10.1007/s10741-016-9553-8openalex-snapshot
Tissue thyroid hormones and thyronamines
inferred← citeshttps://doi.org/10.1007/s10989-019-09925-0openalex-snapshot
Exogenous Neurokinin B Administration May Have a Strong Effect on Negative Feedback Loop of Hypothalamic Pituitary Thyroid Axis
inferred← citeshttps://doi.org/10.1007/s11102-020-01052-0openalex-snapshot
GH deficiency in cancer survivors in the transition age: diagnosis and therapy
inferred← citeshttps://doi.org/10.1007/s11154-024-09878-wopenalex-snapshot
Diagnosis and therapeutic approach to bone health in patients with hypopituitarism
inferred← citeshttps://doi.org/10.1007/s11356-023-28259-5openalex-snapshot
Chronic exposure to tebuconazole alters thyroid hormones and plumage quality in house sparrows (Passer domesticus)
inferred← citeshttps://doi.org/10.1007/s12011-008-8199-3openalex-snapshot
Thyroid Hormones and Methylmercury Toxicity
inferred← citeshttps://doi.org/10.1007/s12011-026-05252-wopenalex-snapshot
Recent Advances in the Treatment of Thyroid Pathologies with Selenium-Containing Compounds, Nanoparticles and Nanocomplexes Based on Selenium and Selenoproteins
inferred← citeshttps://doi.org/10.1007/s12020-007-0030-yopenalex-snapshot
The menace of endocrine disruptors on thyroid hormone physiology and their impact on intrauterine development
inferred← citeshttps://doi.org/10.1007/s12020-017-1320-7openalex-snapshot
Effects of cigarette smoke exposure during suckling on food intake, fat mass, hormones, and biochemical profile of young and adult female rats
inferred← citeshttps://doi.org/10.1007/s12020-019-02023-7openalex-snapshot
Thyroid hormone therapy for hypothyroidism
inferred← citeshttps://doi.org/10.1007/s12020-021-02849-0openalex-snapshot
Elevated thyroid-stimulating hormone levels are associated with poor sleep: a cross-sectional and longitudinal study
inferred← citeshttps://doi.org/10.1007/s12020-021-02912-wopenalex-snapshot
Endocrine system dysfunction and chronic heart failure: a clinical perspective
inferred← citeshttps://doi.org/10.1007/s12311-015-0744-yopenalex-snapshot
Mosaic Expression of Thyroid Hormone Regulatory Genes Defines Cell Type-Specific Dependency in the Developing Chicken Cerebellum
inferred← citeshttps://doi.org/10.1007/s40618-020-01482-4openalex-snapshot
An update on non-thyroidal illness syndrome
inferred← citeshttps://doi.org/10.1007/s42000-020-00247-1openalex-snapshot
Thyroxine replacement modifies changes in deiodinase and thyroid hormone transporter expression induced by subclinical hypothyroidism in rats
inferred← citeshttps://doi.org/10.1007/s44411-026-00608-zopenalex-snapshot
Evaluation of Dynapenia in Patients with Subclinical Hypothyroidism
inferred← citeshttps://doi.org/10.1016/b978-0-12-374430-2.00010-9openalex-snapshot
Syndromes of Reduced Sensitivity to Thyroid Hormone
inferred← citeshttps://doi.org/10.1016/b978-0-12-385979-2.00014-9openalex-snapshot
Thyroid Hormones and Postembryonic Development in Amniotes
inferred← citeshttps://doi.org/10.1016/b978-0-12-387784-0.00011-0openalex-snapshot
Minerals and Trace Elements
inferred← citeshttps://doi.org/10.1016/b978-0-12-397155-5.00019-2openalex-snapshot
Selenium, Selenoproteins, and Age-Related Disorders
inferred← citeshttps://doi.org/10.1016/b978-0-12-407680-8.00005-1openalex-snapshot
The Expanding Role of Tandem Mass Spectrometry in Optimizing Diagnosis and Treatment of Thyroid Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-407766-9.00018-3openalex-snapshot
Nomilin as an Anti-Obesity and Anti-Hyperglycemic Agent
inferred← citeshttps://doi.org/10.1016/b978-0-12-800892-8.00009-9openalex-snapshot
Syndromes of Impaired Sensitivity to Thyroid Hormone
inferred← citeshttps://doi.org/10.1016/b978-0-12-801028-0.00217-8openalex-snapshot
3,3′,5-Triiodothyronine
inferred← citeshttps://doi.org/10.1016/b978-0-12-817986-4.00040-7openalex-snapshot
Availability and metabolism of thyroid hormones in the developing brain
inferred← citeshttps://doi.org/10.1016/b978-0-12-820107-7.00010-0openalex-snapshot
Congenital isolated central hypothyroidism: Novel mutations and their functional implications
inferred← citeshttps://doi.org/10.1016/b978-0-12-823036-7.00013-xopenalex-snapshot
Thyroid hormone actions in traumatic brain injury
inferred← citeshttps://doi.org/10.1016/b978-0-443-30261-9.00002-4openalex-snapshot
Thyroid hormone signaling in neurodevelopment
inferred← citeshttps://doi.org/10.1016/b978-0-443-30261-9.00011-5openalex-snapshot
The thyroid hormone drives bidirectional communication along the brain-gut axis in vertebrate models
inferred← citeshttps://doi.org/10.1016/b978-1-4160-4745-2.00004-3openalex-snapshot
Thyroid Hormone Action
inferred← citeshttps://doi.org/10.1016/b978-1-4160-4745-2.00005-5openalex-snapshot
Thyroid Hormone Metabolism
inferred← citeshttps://doi.org/10.1016/b978-84-9022-503-5.00006-xopenalex-snapshot
El hueso en el hipertiroidismo
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.2025.02.009openalex-snapshot
Senotherapeutic approach to age-related endocrine diseases
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.04.003openalex-snapshot
Thyroid Hormone and the White Matter of the Central Nervous System: From Development to Repair
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.04.006openalex-snapshot
Thyroid Hormone Regulation of Adult Neurogenesis
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.05.001openalex-snapshot
Thyroid Hormone Signaling in Retinal Development, Survival, and Disease
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.06.003openalex-snapshot
Thyroid Hormone Signaling in the Development of the Endochondral Skeleton
inferred← citeshttps://doi.org/10.1016/bs.vh.2017.06.004openalex-snapshot
Local Regulation of Thyroid Hormone Signaling
inferred← citeshttps://doi.org/10.1016/bs.vh.2021.10.001openalex-snapshot
Thyroid hormone regulation of adult hippocampal neurogenesis: Putative molecular and cellular mechanisms
inferred← citeshttps://doi.org/10.1016/j.aace.2020.11.007openalex-snapshot
Clinical Case Report: Dissociation of Clinical Course of Coexisting Autoimmune Hepatitis and Graves Disease
inferred← citeshttps://doi.org/10.1016/j.abb.2025.110509openalex-snapshot
Iron and Selenium: At the Crossroads of Development and Death in Oligodendrocytes
inferred← citeshttps://doi.org/10.1016/j.ajpath.2017.07.005openalex-snapshot
Thyroid Hormone Receptor-β Agonist GC-1 Inhibits Met-β-Catenin–Driven Hepatocellular Cancer
inferred← citeshttps://doi.org/10.1016/j.ando.2008.02.005openalex-snapshot
Nuclear receptors and human disease: Resistance to thyroid hormone and lipodystrophic insulin resistance
inferred← citeshttps://doi.org/10.1016/j.apsb.2023.11.011openalex-snapshot
Mechanism of action of the bile acid receptor TGR5 in obesity
inferred← citeshttps://doi.org/10.1016/j.aqrep.2021.100966openalex-snapshot
Exposure of adult zebrafish to androstenedione alters thyroid hormone levels and the transcriptional expression of genes related to the hypothalamus-pituitary-thyroid axis
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2009.02.032openalex-snapshot
Control of light condition affects the feeding regime and enables successful eye migration in Atlantic halibut juveniles
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2014.10.015openalex-snapshot
Exposure to oxidative by-products during metamorphosis affects pigmentation patterns in flounder, Paralichthys olivaceus
inferred← citeshttps://doi.org/10.1016/j.aquatox.2011.07.018openalex-snapshot
Endocrine and developmental effects in Atlantic salmon (Salmo salar) exposed to perfluorooctane sulfonic or perfluorooctane carboxylic acids
inferred← citeshttps://doi.org/10.1016/j.aquatox.2015.01.016openalex-snapshot
Thyroid disruption by triphenyl phosphate, an organophosphate flame retardant, in zebrafish (Danio rerio) embryos/larvae, and in GH3 and FRTL-5 cell lines
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1016/j.aquatox.2016.03.006openalex-snapshot
Permethrin is a potential thyroid-disrupting chemical: In vivo and in silico envidence
inferred← citeshttps://doi.org/10.1016/j.aquatox.2018.12.015openalex-snapshot
Amphibian (Rana nigromaculata)exposed to cyproconazole: Changes in growth index, behavioral endpoints, antioxidant biomarkers, thyroid and gonad development
inferred← citeshttps://doi.org/10.1016/j.aquatox.2019.01.022openalex-snapshot
Molecular mechanisms and tissue targets of brominated flame retardants, BDE-47 and TBBPA, in embryo-larval life stages of zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.aquatox.2019.105237openalex-snapshot
Effects of cis-bifenthrin enantiomers on the growth, behavioral, biomarkers of oxidative damage and bioaccumulation in Xenopus laevis
inferred← citeshttps://doi.org/10.1016/j.aquatox.2019.105280openalex-snapshot
Comparative thyroid disruption by o,p’-DDT and p,p’-DDE in zebrafish embryos/larvae
inferred← citeshttps://doi.org/10.1016/j.aquatox.2021.106053openalex-snapshot
Thyroid disruption and growth inhibition of zebrafish embryos/larvae by phenanthrene treatment at environmentally relevant concentrations
inferred← citeshttps://doi.org/10.1016/j.aquatox.2023.106632openalex-snapshot
Deiodinase inhibition impairs the formation of the three posterior swim bladder tissue layers during early embryonic development in zebrafish
inferred← citeshttps://doi.org/10.1016/j.aquatox.2024.107140openalex-snapshot
Chronic toxic effects of chloroxylenol exposure on Rana chensinensis: Insights from endochondral ossfication
inferred← citeshttps://doi.org/10.1016/j.atherosclerosis.2013.07.056openalex-snapshot
Lipid lowering in healthy volunteers treated with multiple doses of MGL-3196, a liver-targeted thyroid hormone receptor-β agonist
inferred← citeshttps://doi.org/10.1016/j.bbadis.2010.12.020openalex-snapshot
The thyroid hormones and their nuclear receptors in the gut: From developmental biology to cancer
inferred← citeshttps://doi.org/10.1016/j.bbadis.2023.166892openalex-snapshot
Local modulation of thyroid hormone signaling in the retina affects the development of diabetic retinopathy
inferred← citeshttps://doi.org/10.1016/j.bbagen.2012.07.014openalex-snapshot
Thyroid hormone's action on progenitor/stem cell biology: New challenge for a classic hormone?
inferred← citeshttps://doi.org/10.1016/j.bbagen.2012.08.005openalex-snapshot
The syndromes of reduced sensitivity to thyroid hormone
inferred← citeshttps://doi.org/10.1016/j.bbagen.2018.07.032openalex-snapshot
Transcriptome analyses reveal molecular mechanisms that regulate endochondral ossification in amphibian Bufo gargarizans during metamorphosis
inferred← citeshttps://doi.org/10.1016/j.beem.2007.03.008openalex-snapshot
Thyroid hormone transport by monocarboxylate transporters
inferred← citeshttps://doi.org/10.1016/j.beem.2007.04.001openalex-snapshot
Thyroid hormone transporters in health and disease: advances in thyroid hormone deiodination
inferred← citeshttps://doi.org/10.1016/j.beem.2013.10.003openalex-snapshot
Pitfalls in the measurement and interpretation of thyroid function tests
inferred← citeshttps://doi.org/10.1016/j.beem.2026.102110openalex-snapshot
Thyroid hormones as permissive regulators of skeletal muscle protein accretion and oxidative capacity: Implications for resistance and endurance training
inferred← citeshttps://doi.org/10.1016/j.biocel.2011.05.016openalex-snapshot
Type 2 deiodinase at the crossroads of thyroid hormone action
inferred← citeshttps://doi.org/10.1016/j.bone.2008.03.019openalex-snapshot
Iodothyronine deiodinase enzyme activities in bone
inferred← citeshttps://doi.org/10.1016/j.bone.2008.05.007openalex-snapshot
Critical role of the hypothalamic–pituitary–thyroid axis in bone
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.02.043openalex-snapshot
The maintenance of hippocampal pyramidal neuron populations is dependent on the modulation of specific cell cycle regulators by thyroid hormones
inferred← citeshttps://doi.org/10.1016/j.brainres.2009.03.070openalex-snapshot
Effect of thyroid hormone T3 on Myosin-Va expression in the central nervous system
inferred← citeshttps://doi.org/10.1016/j.cbd.2023.101113openalex-snapshot
Regulation mechanisms underlying tail resorption in Bufo gargarizans metamorphosis
inferred← citeshttps://doi.org/10.1016/j.cbd.2024.101286openalex-snapshot
Regulation mechanism of endochondral ossification in Rana zhenhaiensis during metamorphosis based on histomorphology and transcriptome analyses
inferred← citeshttps://doi.org/10.1016/j.cbi.2021.109709openalex-snapshot
The thyroid hormone converting enzyme human deiodinase 1 is inhibited by gold ions from inorganic salts, organic substances, and by small-size nanoparticles
inferred← citeshttps://doi.org/10.1016/j.cbpc.2020.108783openalex-snapshot
Thyroid disruption and developmental toxicity caused by Cd2+ in Schizopygopsis younghusbandi larvae
inferred← citeshttps://doi.org/10.1016/j.cbpc.2020.108819openalex-snapshot
The synthetic progestin norethindrone causes thyroid endocrine disruption in adult zebrafish
inferred← citeshttps://doi.org/10.1016/j.cbpc.2022.109484openalex-snapshot
Sex-specific thyroid disruption caused by phenanthrene in adult zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.cbpc.2024.109981openalex-snapshot
Early-life exposure to five biodegradable plastics impairs eye development and visually-mediated behavior through disturbing hypothalamus-pituitary-thyroid (HPT) axis in zebrafish larvae
inferred← citeshttps://doi.org/10.1016/j.cbpc.2025.110439openalex-snapshot
Parental exposure to phenanthrene induces thyroid disruption in zebrafish offspring
inferred← citeshttps://doi.org/10.1016/j.cbpc.2026.110616openalex-snapshot
Chloroxylenol impairs the visual system, induces visually-mediated behavioral abnormalities and circadian rhythm disorders in zebrafish (Danio rerio)
inferred← citeshttps://doi.org/10.1016/j.celrep.2023.112661openalex-snapshot
The multi-level regulation of clownfish metamorphosis by thyroid hormones
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.02.081openalex-snapshot
Adverse effects of BDE-47 on in vivo developmental parameters, thyroid hormones, and expression of hypothalamus-pituitary-thyroid (HPT) axis genes in larvae of the self-fertilizing fish Kryptolebias marmoratus
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2018.06.152openalex-snapshot
Changes in thyroid status of Menidia beryllina exposed to the antifouling booster irgarol: Impacts of temperature and salinity
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.04.123openalex-snapshot
Two-generation exposure to 2-ethylhexyl 4-methoxycinnamate (EHMC) in Japanese medaka (Oryzias latipes) and its reproduction and endocrine related effects
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2019.07.068openalex-snapshot
Embryonic exposure to soil samples from a gangue stacking area induces thyroid hormone disruption in zebrafish
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.128137openalex-snapshot
Effects of temperature fluctuation on endocrine disturbance of grass carp Ctenopharyngodon idella under mercury chloride stress
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2022.136860openalex-snapshot
Effects of the synthetic progestin levonorgestrel on some aspects of thyroid physiology in common carp (Cyprinus carpio)
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2024.142441openalex-snapshot
Thyroid under siege: Unravelling the toxic impact of real-life metal mixture exposures in Wistar rats
inferred← citeshttps://doi.org/10.1016/j.chroma.2015.09.076openalex-snapshot
Identification and quantification of electrochemically generated metabolites of thyroxine by means of liquid chromatography/electrospray-mass spectrometry and countergradient liquid chromatography/inductively coupled plasma-mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2007.08.007openalex-snapshot
Simultaneous quantification of free triiodothyronine and free thyroxine by isotope dilution tandem mass spectrometry
inferred← citeshttps://doi.org/10.1016/j.clinbiochem.2016.11.022openalex-snapshot
Assessment of thyroid function in intensive care unit patients by liquid chromatography tandem mass spectrometry methods
inferred← citeshttps://doi.org/10.1016/j.clineuro.2022.107335openalex-snapshot
Thyroid hormone decreasing after mechanical thrombectomy for cerebral infarction
inferred← citeshttps://doi.org/10.1016/j.cmet.2008.06.008openalex-snapshot
The Thyroid and Metabolism: The Action Continues
inferred← citeshttps://doi.org/10.1016/j.cmet.2014.10.009openalex-snapshot
Intracellular Inactivation of Thyroid Hormone Is a Survival Mechanism for Muscle Stem Cell Proliferation and Lineage Progression
inferred← citeshttps://doi.org/10.1016/j.comtox.2026.100442openalex-snapshot
Mathematical model for thyroid hormone regulation in foetal rat brain
inferred← citeshttps://doi.org/10.1016/j.crphys.2021.02.003openalex-snapshot
μ-Crystallin in Mouse Skeletal Muscle Promotes a Shift from Glycolytic toward Oxidative Metabolism
inferred← citeshttps://doi.org/10.1016/j.crtox.2021.01.001openalex-snapshot
In vitro assays for characterization of distinct multiple catalytic activities of thyroid peroxidase using LC-MS/MS
inferred← citeshttps://doi.org/10.1016/j.domaniend.2012.02.005openalex-snapshot
Energy metabolism in the newborn farm animal with emphasis on the calf: endocrine changes and responses to milk-born and systemic hormones
inferred← citeshttps://doi.org/10.1016/j.drudis.2009.02.005openalex-snapshot
TGR5: an emerging bile acid G-protein-coupled receptor target for the potential treatment of metabolic disorders
inferred← citeshttps://doi.org/10.1016/j.ecl.2006.09.009openalex-snapshot
Changes Within the Thyroid Axis During the Course of Critical Illness
inferred← citeshttps://doi.org/10.1016/j.ecl.2014.02.005openalex-snapshot
Thyroid Disease and the Cardiovascular System
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2014.07.016openalex-snapshot
Effects of water temperature on perchlorate toxicity to the thyroid and reproductive system of Oryzias latipes
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2018.03.009openalex-snapshot
Comparison of triadimefon and its metabolite on acute toxicity and chronic effects during the early development of Rana nigromaculata tadpoles
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.02.091openalex-snapshot
Establishment of a human embryonic stem cell-based liver differentiation model for hepatotoxicity evaluations
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2019.109912openalex-snapshot
Chronic simultaneous exposure of common carp (Cyprinus carpio) from embryonic to juvenile stage to drospirenone and gestodene at low ng/L level caused intersex
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.111570openalex-snapshot
New understanding of novel brominated flame retardants (NBFRs): Neuro(endocrine) toxicity
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2021.112495openalex-snapshot
Thyroid function and immune status in perch (Perca fluviatilis) from lakes contaminated with PFASs or PCBs
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2023.115630openalex-snapshot
Effects of norethindrone on the growth, behavior, and thyroid endocrine system of adult female western mosquitofish (Gambusia affinis)
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.118936openalex-snapshot
Disruption of reproductive and thyroid endocrine systems in zebrafish following early life and whole life cycle exposure to low-dose norgestrel
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2025.119579openalex-snapshot
Correlations between organophosphate flame retardants exposure and papillary thyroid cancer or thyroid hormones: A case-control study from Shijiazhuang, China
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