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Role of the Thyroid System in Myelination and Neural Connectivity

https://doi.org/10.1002/cphy.c140035
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Oligodendrocyte maturation and progenitor cell proliferation are independently regulated by thyroid hormone
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A cell-intrinsic timer that operates during oligodendrocyte development
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Sex steroid receptors in skeletal differentiation and epithelial neoplasia: is tissue‐specific intervention possible?
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Thyroid hormone promotes neurogenesis in the Xenopus spinal cord
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Transcriptional control of oligodendrogenesis
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Developmental and cell type-specific expression of thyroid hormone transporters in the mouse brain and in primary brain cells
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A selective thyroid hormone β receptor agonist enhances human and rodent oligodendrocyte differentiation
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Contrasting developmental and tissue‐specific expression of alpha and beta thyroid hormone receptor genes.
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Distinct functions for thyroid hormone receptors alpha and beta in brain development indicated by differential expression of receptor genes.
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Coexpression of thyroid hormone receptor isoforms in mouse oligodendrocytes
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Stoichiometry of Mitochondrial Transcripts and Regulation of Gene Expression by Mitochondrial Transcription Factor A
inferredcites →https://doi.org/10.1006/mcne.2000.0879openalex-snapshot
Regulation of the L1 Cell Adhesion Molecule by Thyroid Hormone in the Developing Brain
inferredcites →https://doi.org/10.1007/978-1-60327-575-0_1openalex-snapshot
Nuclear Receptors: One Big Family
inferredcites →https://doi.org/10.1007/s10495-007-0109-1openalex-snapshot
Inhibition of apoptotic potency by ligand stimulated thyroid hormone receptors located in mitochondria
inferredcites →https://doi.org/10.1007/s12020-008-9066-xopenalex-snapshot
Effect of a high-fat diet on 24-h pattern of circulating levels of prolactin, luteinizing hormone, testosterone, corticosterone, thyroid-stimulating hormone and glucose, and pineal melatonin content, in rats
inferredcites →https://doi.org/10.1016/0006-8993(87)90260-5openalex-snapshot
The regional hypothalamic distribution of type II 5′-monodeiodinase in euthyroid and hypothyroid rats
inferredcites →https://doi.org/10.1016/0006-8993(91)90194-zopenalex-snapshot
Transport of iodothyronines from bloodstream to brain: contributions by blood:brain and choroid plexus:cerebrospinal fluid barriers
inferredcites →https://doi.org/10.1016/0006-8993(95)00474-5openalex-snapshot
Expression of enkephalin and dynorphin precursor mRNAs in brain areas of hypo-and hyperthyroid rat: effect of kainic acid injection
inferredcites →https://doi.org/10.1016/0165-3806(92)90156-qopenalex-snapshot
Expression of thyroid hormone receptors mRNAs in rat cerebral hemisphere neuronal cultures
inferredcites →https://doi.org/10.1016/0169-328x(94)90188-0openalex-snapshot
Regulation of VIP mRNA expression by thyroid hormone in different brain areas of adult rat
inferredcites →https://doi.org/10.1016/0304-3940(96)12506-4openalex-snapshot
The carbohydrate N-acetylglucosamine is involved in the guidance of neurites from chick ciliary ganglion neurons through the extracellular matrix of rat skeletal muscle fiber
inferredcites →https://doi.org/10.1016/b978-0-12-385979-2.00013-7openalex-snapshot
Is Thyroid Hormone Signaling Relevant for Vertebrate Embryogenesis?
inferredcites →https://doi.org/10.1016/b978-0-12-571133-3.50010-6openalex-snapshot
Ontogenesis of Hypothalamic-Pituitary-Thyroid Function and Metabolism in Man, Sheep, and Rat
inferredcites →https://doi.org/10.1016/j.abb.2012.09.009openalex-snapshot
The role of nuclear receptors in controlling the fine balance between proliferation and differentiation of neural stem cells
inferredcites →https://doi.org/10.1016/j.bbagen.2012.03.012openalex-snapshot
Thyroid hormone receptors, cell growth and differentiation
inferredcites →https://doi.org/10.1016/j.bbagen.2012.03.015openalex-snapshot
Genomic imprinting of the type 3 thyroid hormone deiodinase gene: Regulation and developmental implications
inferredcites →https://doi.org/10.1016/j.bbagen.2012.04.014openalex-snapshot
Thyroid hormone receptor activity in the absence of ligand: Physiological and developmental implications
inferredcites →https://doi.org/10.1016/j.bbagen.2012.05.007openalex-snapshot
The deiodinases and the control of intracellular thyroid hormone signaling during cellular differentiation
inferredcites →https://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?
inferredcites →https://doi.org/10.1016/j.bbagen.2012.08.019openalex-snapshot
Role of the type 2 iodothyronine deiodinase (D2) in the control of thyroid hormone signaling
inferredcites →https://doi.org/10.1016/j.bbagrm.2014.05.004openalex-snapshot
Intracellular thyroid hormone metabolism as a local regulator of nuclear thyroid hormone receptor-mediated impact on vertebrate development
inferredcites →https://doi.org/10.1016/j.bbamcr.2014.04.018openalex-snapshot
Temporal oligodendrocyte lineage progression: In vitro models of proliferation, differentiation and myelination
inferredcites →https://doi.org/10.1016/j.beem.2007.03.003openalex-snapshot
The importance of thyroid hormone transporters for brain development and function
inferredcites →https://doi.org/10.1016/j.beem.2009.08.014openalex-snapshot
Cretinism revisited
inferredcites →https://doi.org/10.1016/j.brainresrev.2004.12.022openalex-snapshot
Thyroid hormone and remyelination in adult central nervous system: a lesson from an inflammatory-demyelinating disease
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.expneurol.2008.04.039openalex-snapshot
Thyroid hormones promote differentiation of oligodendrocyte progenitor cells and improve remyelination after cuprizone-induced demyelination
inferredcites →https://doi.org/10.1016/j.expneurol.2010.12.012openalex-snapshot
Effect of hypothyroxinemia on thyroid hormone responsiveness and action during rat postnatal neocortical development
inferredcites →https://doi.org/10.1016/j.expneurol.2012.02.018openalex-snapshot
Cuprizone-induced demyelination in the rat cerebral cortex and thyroid hormone effects on cortical remyelination
inferredcites →https://doi.org/10.1016/j.expneurol.2014.04.027openalex-snapshot
Oligodendrocyte progenitors: Adult stem cells of the central nervous system?
inferredcites →https://doi.org/10.1016/j.ijdevneu.2009.08.011openalex-snapshot
Thyroid hormone induces glial lineage of primary neurospheres derived from non‐pathological and pathological rat brain: implications for remyelination‐enhancing therapies
inferredcites →https://doi.org/10.1016/j.mce.2003.10.033openalex-snapshot
Mechanisms of thyroid hormone receptor-specific nuclear and extra nuclear actions
inferredcites →https://doi.org/10.1016/j.mce.2009.08.028openalex-snapshot
Thyroid hormones and the control of cell proliferation or cell differentiation: Paradox or duality?
inferredcites →https://doi.org/10.1016/j.mcn.2012.03.007openalex-snapshot
The T3-induced gene KLF9 regulates oligodendrocyte differentiation and myelin regeneration
inferredcites →https://doi.org/10.1016/j.nbd.2008.05.015openalex-snapshot
T3 administration in adult hypothyroid mice modulates expression of proteins involved in striatal synaptic plasticity and improves motor behavior
inferredcites →https://doi.org/10.1016/j.neulet.2005.11.003openalex-snapshot
Dose-dependent transthyretin inhibition of T4 uptake from cerebrospinal fluid in sheep
inferredcites →https://doi.org/10.1016/j.neuropharm.2010.12.013openalex-snapshot
Thyroid hormones modulate GABAA receptor-mediated currents in hippocampal neurons
inferredcites →https://doi.org/10.1016/j.neuroscience.2007.09.064openalex-snapshot
Nongenomic regulation of glutamatergic neurotransmission in hippocampus by thyroid hormones
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.10.018openalex-snapshot
White matter plasticity in adulthood
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.11.007openalex-snapshot
Role of myelin plasticity in oscillations and synchrony of neuronal activity
inferredcites →https://doi.org/10.1016/j.neuroscience.2013.11.029openalex-snapshot
Mechanisms regulating the development of oligodendrocytes and central nervous system myelin
inferredcites →https://doi.org/10.1016/j.neuroscience.2014.03.063openalex-snapshot
From precursors to myelinating oligodendrocytes: Contribution of intrinsic and extrinsic factors to white matter plasticity in the adult brain
inferredcites →https://doi.org/10.1016/j.physbeh.2009.02.015openalex-snapshot
Mini-review: Cell surface receptor for thyroid hormone and nongenomic regulation of ion fluxes in excitable cells
inferredcites →https://doi.org/10.1016/j.semcdb.2013.10.002openalex-snapshot
Nuclear receptors as regulators of stem cell and cancer stem cell metabolism
inferredcites →https://doi.org/10.1016/j.semcdb.2013.10.006openalex-snapshot
Nuclear hormone receptors are powerful regulators of stem cell maintenance, differentiation, metabolism and function
inferredcites →https://doi.org/10.1016/j.stem.2012.04.008openalex-snapshot
Thyroid Hormone Signaling Acts as a Neurogenic Switch by Repressing Sox2 in the Adult Neural Stem Cell Niche
inferredcites →https://doi.org/10.1016/j.tem.2005.09.007openalex-snapshot
Membrane receptors mediating thyroid hormone action
inferredcites →https://doi.org/10.1016/j.tem.2011.01.004openalex-snapshot
Visualizing hormone actions in the brain
inferredcites →https://doi.org/10.1016/j.tins.2008.04.001openalex-snapshot
White matter in learning, cognition and psychiatric disorders
inferredcites →https://doi.org/10.1016/j.yfrne.2007.09.003openalex-snapshot
Mechanisms of nongenomic actions of thyroid hormone
inferredcites →https://doi.org/10.1016/j.yfrne.2010.01.001openalex-snapshot
Regulation of the hypothalamic Thyrotropin Releasing Hormone (TRH) neuron by neuronal and peripheral inputs
inferredcites →https://doi.org/10.1016/s0006-8993(96)01480-1openalex-snapshot
Hypothyroidism coordinately and transiently affects myelin protein gene expression in most rat brain regions during postnatal development
inferredcites →https://doi.org/10.1016/s0021-9258(17)44786-7openalex-snapshot
The actin cytoskeleton mediates the hormonally regulated translocation of type II iodothyronine 5'-deiodinase in astrocytes.
inferredcites →https://doi.org/10.1016/s0021-9258(18)86977-0openalex-snapshot
Relationship of c-erbA mRNA content to tissue triiodothyronine nuclear binding capacity and function in developing and adult rats.
inferredcites →https://doi.org/10.1016/s0021-9258(19)34121-3openalex-snapshot
Thyroxine-dependent modulation of actin polymerization in cultured astrocytes. A novel, extranuclear action of thyroid hormone.
inferredcites →https://doi.org/10.1016/s0140-6736(04)17226-7openalex-snapshot
Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
inferredcites →https://doi.org/10.1016/s0165-3806(02)00459-5openalex-snapshot
Early expression of thyroid hormone deiodinases and receptors in human fetal cerebral cortex
inferredcites →https://doi.org/10.1016/s0166-2236(00)01691-xopenalex-snapshot
The oligodendrocyte precursor cell in health and disease
inferredcites →https://doi.org/10.1016/s0169-328x(97)00213-1openalex-snapshot
NGF content and expression in the rat pituitary gland and regulation by thyroid hormone
inferredcites →https://doi.org/10.1016/s0306-4522(00)00420-6openalex-snapshot
Expression of peptides and other neurochemical markers in hypothalamus and olfactory bulb of mice devoid of all known thyroid hormone receptors
inferredcites →https://doi.org/10.1016/s0306-4522(97)00511-3openalex-snapshot
Developmental expression of tenascin-C is altered by hypothyroidism in the rat brain
inferredcites →https://doi.org/10.1016/s0960-9822(06)00060-1openalex-snapshot
Oligodendrocyte precursor cells count time but not cell divisions before differentiation
inferredcites →https://doi.org/10.1016/s0960-9822(98)70177-0openalex-snapshot
p27Kip1 alters the response of cells to mitogen and is part of a cell-intrinsic timer that arrests the cell cycle and initiates differentiation
inferredcites →https://doi.org/10.1017/s1368980007360928openalex-snapshot
Iodine deficiency and brain development in the first half of pregnancy
inferredcites →https://doi.org/10.1023/b:nere.0000021235.83952.9aopenalex-snapshot
Expression of Thyroid Hormone Receptor Isoforms in the Oligodendrocyte Lineage
inferredcites →https://doi.org/10.1038/nature02117openalex-snapshot
Light-induced hormone conversion of T4 to T3 regulates photoperiodic response of gonads in birds
inferredcites →https://doi.org/10.1038/ncpendmet0424openalex-snapshot
Thyroid hormone receptors in brain development and function
inferredcites →https://doi.org/10.1038/ncpendmet0727openalex-snapshot
Reawakened interest in type III iodothyronine deiodinase in critical illness and injury
inferredcites →https://doi.org/10.1038/nn1995openalex-snapshot
Dissecting demyelination
inferredcites →https://doi.org/10.1038/nrm1680openalex-snapshot
Controlling nuclear receptors: the circular logic of cofactor cycles
inferredcites →https://doi.org/10.1038/sj.jcbfm.9600041openalex-snapshot
Induction of Type 2 Iodothyronine Deiodinase in Astrocytes after Transient Focal Cerebral Ischemia in the Rat
inferredcites →https://doi.org/10.1038/sj.mp.4001802openalex-snapshot
Modulation of adult hippocampal neurogenesis by thyroid hormones: implications in depressive-like behavior
inferredcites →https://doi.org/10.1042/bst0340663openalex-snapshot
The mystery of intracellular developmental programmes and timers
inferredcites →https://doi.org/10.1055/s-2004-814219openalex-snapshot
Contribution of Interleukin-12 to the Pathogenesis of Non-thyroidal Illness
inferredcites →https://doi.org/10.1073/pnas.0407262101openalex-snapshot
Thyroid hormone administration enhances remyelination in chronic demyelinating inflammatory disease
inferredcites →https://doi.org/10.1073/pnas.051454698openalex-snapshot
An unliganded thyroid hormone receptor causes severe neurological dysfunction
inferredcites →https://doi.org/10.1073/pnas.052704499openalex-snapshot
Thyroid hormone activates oligodendrocyte precursors and increases a myelin-forming protein and NGF content in the spinal cord during experimental allergic encephalomyelitis
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.94.7.3368openalex-snapshot
Time-course changes of nerve growth factor, corticotropin-releasing hormone, and nitric oxide synthase isoforms and their possible role in the development of inflammatory response in experimental allergic encephalomyelitis
inferredcites →https://doi.org/10.1074/jbc.270.27.16347openalex-snapshot
A 43-kDa Protein Related to c-Erb A α1 Is Located in the Mitochondrial Matrix of Rat Liver
inferredcites →https://doi.org/10.1074/jbc.274.8.5026openalex-snapshot
The Cyclin-dependent Kinase Inhibitor p27Kip1 Is Involved in Thyroid Hormone-mediated Neuronal Differentiation
inferredcites →https://doi.org/10.1074/jbc.m002560200openalex-snapshot
Thyroxine Promotes Association of Mitogen-activated Protein Kinase and Nuclear Thyroid Hormone Receptor (TR) and Causes Serine Phosphorylation of TR
inferredcites →https://doi.org/10.1074/jbc.m306933200openalex-snapshot
Functional Characterization of Rat Brain-specific Organic Anion Transporter (Oatp14) at the Blood-Brain Barrier
inferredcites →https://doi.org/10.1074/jbc.m511530200openalex-snapshot
Dominant Role of Thyrotropin-releasing Hormone in the Hypothalamic-Pituitary-Thyroid Axis
inferredcites →https://doi.org/10.1083/jcb.148.5.839openalex-snapshot
Precursor Cell Transitions in Oligodendrocyte Development
inferredcites →https://doi.org/10.1083/jcb.200905111openalex-snapshot
Tapping into the glial reservoir: cells committed to remaining uncommitted
inferredcites →https://doi.org/10.1086/380999openalex-snapshot
A Novel Syndrome Combining Thyroid and Neurological Abnormalities Is Associated with Mutations in a Monocarboxylate Transporter Gene
inferredcites →https://doi.org/10.1086/431313openalex-snapshot
Allan-Herndon-Dudley Syndrome and the Monocarboxylate Transporter 8 (MCT8) Gene
inferredcites →https://doi.org/10.1089/105072502760143791openalex-snapshot
Mechanism of Thyroid Hormone Action
inferredcites →https://doi.org/10.1089/105072503770867174openalex-snapshot
Perspectives in the Study of Thyroid Hormone Action on Brain Development and Function
inferredcites →https://doi.org/10.1089/105072503770867237openalex-snapshot
Biologic Variation is Important for Interpretation of Thyroid Function Tests
inferredcites →https://doi.org/10.1089/scd.2012.0023openalex-snapshot
Thyroid Hormone Promotes Neuronal Differentiation of Embryonic Neural Stem Cells by Inhibiting STAT3 Signaling Through TRα1
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.2005.15.883openalex-snapshot
Role of Thyroid Hormone Deiodination in the Hypothalamus
inferredcites →https://doi.org/10.1089/thy.2007.0251openalex-snapshot
The Role of the Thyrotropin-Releasing Hormone (TRH) Neuron as a Metabolic Sensor
inferredcites →https://doi.org/10.1089/thy.2009.0228openalex-snapshot
Type 3 Deiodinase Expression in Inflammatory Spinal Cord Lesions in Rat Experimental Autoimmune Encephalomyelitis
inferredcites →https://doi.org/10.1093/brain/awn096openalex-snapshot
Differentiation block of oligodendroglial progenitor cells as a cause for remyelination failure in chronic multiple sclerosis
inferredcites →https://doi.org/10.1093/emboj/16.2.306openalex-snapshot
Accumulation of the cyclin‐dependent kinase inhibitor p27/Kip1 and the timing of oligodendrocyte differentiation
inferredcites →https://doi.org/10.1093/emboj/20.18.5261openalex-snapshot
Two molecularly distinct intracellular pathways to oligodendrocyte differentiation: role of a p53 family protein
inferredcites →https://doi.org/10.1093/emboj/cdf662openalex-snapshot
Normal timing of oligodendrocyte development depends on thyroid hormone receptor alpha 1 (TRα1)
inferredcites →https://doi.org/10.1093/qjmed/hct260openalex-snapshot
Central nervous system regeneration--where are we?
inferredcites →https://doi.org/10.1096/fj.04-2916fjeopenalex-snapshot
Adult neural stem cell cycling in vivo requires thyroid hormone and its alpha receptor
inferredcites →https://doi.org/10.1097/01.med.0000432531.03233.adopenalex-snapshot
Inherited defects of thyroid hormone-cell-membrane transport
inferredcites →https://doi.org/10.1097/01.med.0000433069.09294.e8openalex-snapshot
Nonthyroidal illness syndrome
inferredcites →https://doi.org/10.1097/med.0000000000000028openalex-snapshot
Changing perspectives in screening for congenital hypothyroidism and congenital adrenal hyperplasia
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Modeling the nonthyroidal illness syndrome
inferredcites →https://doi.org/10.1111/j.1365-2362.2010.02395.xopenalex-snapshot
The nonthyroidal illness syndrome in the non-critically ill patient
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Thyroid Hormone Receptor Alpha Plays an Essential Role in the Normalisation of Adult‐Onset Hypothyroidism‐Related Hypoexpression of Synaptic Plasticity Target Genes in Striatum
inferredcites →https://doi.org/10.1111/j.1365-2826.2011.02181.xopenalex-snapshot
Triiodothyronine Administration Ameliorates the Demyelination/Remyelination Ratio in a Non-Human Primate Model of Multiple Sclerosis by Correcting Tissue Hypothyroidism
inferredcites →https://doi.org/10.1111/j.1365-2826.2012.02329.xopenalex-snapshot
Thyroid Hormone Accelerates the Differentiation of Adult Hippocampal Progenitors
inferredcites →https://doi.org/10.1111/j.1365-2990.2011.01228.xopenalex-snapshot
Functional and molecular evidence of myelin‐ and neuroprotection by thyroid hormone administration in experimental allergic encephalomyelitis
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Neurotrophins and their Receptors in the Adult Hypo‐ and Hyperthyroid Rat after Kainic Acid Injection: an In Situ Hybridization Study
inferredcites →https://doi.org/10.1111/j.1460-9568.2004.03664.xopenalex-snapshot
Thyroid hormone participates in the regulation of neural stem cells and oligodendrocyte precursor cells in the central nervous system of adult rat
inferredcites →https://doi.org/10.1111/j.1471-4159.2010.06974.xopenalex-snapshot
A single prenatal exposure to the endocrine disruptor 2,3,7,8‐tetrachlorodibenzo‐p‐dioxin alters developmental myelination and remyelination potential in the rat brain
inferredcites →https://doi.org/10.1111/jne.12001openalex-snapshot
Voxel‐Based Morphometric Analysis in Hypothyroidism Using Diffeomorphic Anatomic Registration via an Exponentiated Lie Algebra Algorithm Approach
inferredcites →https://doi.org/10.1124/pr.112.006833openalex-snapshot
Nuclear Receptors and Their Selective Pharmacologic Modulators
inferredcites →https://doi.org/10.1124/pr.58.4.3openalex-snapshot
International Union of Pharmacology. LIX. The Pharmacology and Classification of the Nuclear Receptor Superfamily: Thyroid Hormone Receptors
inferredcites →https://doi.org/10.1128/mcb.19.1.864openalex-snapshot
Regulation of the mdm2 Oncogene by Thyroid Hormone Receptor
inferredcites →https://doi.org/10.1146/annurev-pharmtox-010510-100512openalex-snapshot
Membrane Receptor for Thyroid Hormone: Physiologic and Pharmacologic Implications
inferredcites →https://doi.org/10.1152/ajpendo.00480.2009openalex-snapshot
Translational implications of nongenomic actions of thyroid hormone initiated at its integrin receptor
inferredcites →https://doi.org/10.1152/ajpregu.00789.2005openalex-snapshot
Role of transthyretin in thyroxine transfer from cerebrospinal fluid to brain and choroid plexus
inferredcites →https://doi.org/10.1152/physrev.2001.81.3.1097openalex-snapshot
Physiological and Molecular Basis of Thyroid Hormone Action
inferredcites →https://doi.org/10.1159/000054393openalex-snapshot
Thyroid Hormone-Dependent Regulation of Galanin Synthesis in Neurons and Glial Cells after Colchicine Administration
inferredcites →https://doi.org/10.1159/000122913openalex-snapshot
Effects of Destruction of the Suprachiasmatic Nuclei on the Circadian Rhythms in Plasma Corticosterone, Body Temperature, Feeding and Plasma Thyrotropin
inferredcites →https://doi.org/10.1159/000126121openalex-snapshot
Deficit of Galanin-Like Immunostaining in the Median Eminence of Adult Hypothyroid Rats
inferredcites →https://doi.org/10.1159/000126295openalex-snapshot
Response of Hypothalamic Peptide mRNAs to Thyroidectomy
inferredcites →https://doi.org/10.1161/strokeaha.113.001552openalex-snapshot
Thyroxin Treatment Protects Against White Matter Injury in The Immature Brain via Brain-Derived Neurotrophic Factor
inferredcites →https://doi.org/10.1172/jci10858openalex-snapshot
Critical role for thyroid hormone receptor β2 in the regulation of paraventricular thyrotropin-releasing hormone neurons
inferredcites →https://doi.org/10.1172/jci110136openalex-snapshot
Maturational Patterns of Iodothyronine Phenolic and Tyrosyl Ring Deiodinase Activities in Rat Cerebrum, Cerebellum, and Hypothalamus
inferredcites →https://doi.org/10.1172/jci116301openalex-snapshot
Neonatal hypothyroidism affects the timely expression of myelin-associated glycoprotein in the rat brain.
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/jci24109openalex-snapshot
Negative regulation by thyroid hormone receptor requires an intact coactivator-binding surface
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/jci32824openalex-snapshot
Hypoxia-inducible factor induces local thyroid hormone inactivation during hypoxic-ischemic disease in rats
inferredcites →https://doi.org/10.1172/jci41977openalex-snapshot
Paracrine signaling by glial cell–derived triiodothyronine activates neuronal gene expression in the rodent brain and human cells
inferredcites →https://doi.org/10.1172/jci70324openalex-snapshot
Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis
inferredcites →https://doi.org/10.1186/1756-6614-4-s1-s6openalex-snapshot
Transcriptional regulation by nonclassical action of thyroid hormone
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.23.1.0455openalex-snapshot
Biochemistry, Cellular and Molecular Biology, and Physiological Roles of the Iodothyronine Selenodeiodinases
inferredcites →https://doi.org/10.1210/en.130.2.933openalex-snapshot
Role of transthyretin in the transport of thyroxine from the blood to the choroid plexus, the cerebrospinal fluid, and the brain
inferredcites →https://doi.org/10.1210/en.132.5.1913openalex-snapshot
Ontogeny of thyroid hormone receptors and c-erbA expression during brown adipose tissue development: evidence of fetal acquisition of the mature thyroid status
inferredcites →https://doi.org/10.1210/en.138.8.3359openalex-snapshot
Regional Distribution of Type 2 Thyroxine Deiodinase Messenger Ribonucleic Acid in Rat Hypothalamus and Pituitary and Its Regulation by Thyroid Hormone
inferredcites →https://doi.org/10.1210/en.140.11.5014openalex-snapshot
Thyroid Hormone Regulates the Extracellular Organization of Laminin on Astrocytes
inferredcites →https://doi.org/10.1210/en.140.2.784openalex-snapshot
Regional Expression of the Type 3 Iodothyronine Deiodinase Messenger Ribonucleic Acid in the Rat Central Nervous System and Its Regulation by Thyroid Hormone
inferredcites →https://doi.org/10.1210/en.140.9.4221openalex-snapshot
Thyroid Hormone Regulates the Expression of Laminin in the Developing Rat Cerebellum
inferredcites →https://doi.org/10.1210/en.141.10.3832openalex-snapshot
Functional Connections between the Suprachiasmatic Nucleus and the Thyroid Gland as Revealed by Lesioning and Viral Tracing Techniques in the Rat
inferredcites →https://doi.org/10.1210/en.142.12.5190openalex-snapshot
Induction of Type 3 Iodothyronine Deiodinase by Nerve Injury in the Rat Peripheral Nervous System
inferredcites →https://doi.org/10.1210/en.2004-0065openalex-snapshot
Thyroid Hormone Regulates Oligodendrocyte Accumulation in Developing Rat Brain White Matter Tracts
inferredcites →https://doi.org/10.1210/en.2004-0229openalex-snapshot
Ontogenic Redistribution of Type 2 Deiodinase Messenger Ribonucleic Acid in the Brain of Chicken
inferredcites →https://doi.org/10.1210/en.2004-1179openalex-snapshot
The Monocarboxylate Transporter 8 Linked to Human Psychomotor Retardation Is Highly Expressed in Thyroid Hormone-Sensitive Neuron Populations
inferredcites →https://doi.org/10.1210/en.2005-0102openalex-snapshot
Integrin αVβ3 Contains a Cell Surface Receptor Site for Thyroid Hormone that Is Linked to Activation of Mitogen-Activated Protein Kinase and Induction of Angiogenesis
inferredcites →https://doi.org/10.1210/en.2005-0778openalex-snapshot
Polychlorinated Biphenyls Exert Selective Effects on Cellular Composition of White Matter in a Manner Inconsistent with Thyroid Hormone Insufficiency
inferredcites →https://doi.org/10.1210/en.2006-1248openalex-snapshot
The Rat Thyroid Hormone Receptor (TR) Δβ3 Displays Cell-, TR Isoform-, and Thyroid Hormone Response Element-Specific Actions
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.2007-1462openalex-snapshot
Oxidative Stress Regulates Type 3 Deiodinase and Type 2 Deiodinase in Cultured Rat Astrocytes
inferredcites →https://doi.org/10.1210/en.2008-0378openalex-snapshot
Expression of the Thyroid Hormone Transporters Monocarboxylate Transporter-8 (SLC16A2) and Organic Ion Transporter-14 (SLCO1C1) at the Blood-Brain Barrier
inferredcites →https://doi.org/10.1210/en.2008-1518openalex-snapshot
Pathophysiological Importance of Thyroid Hormone Transporters
inferredcites →https://doi.org/10.1210/en.2008-1616openalex-snapshot
Importance of Monocarboxylate Transporter 8 for the Blood-Brain Barrier-Dependent Availability of 3,5,3′-Triiodo-l-Thyronine
inferredcites →https://doi.org/10.1210/en.2009-1049openalex-snapshot
Thyroid Hormone Receptor α Modulates Lipopolysaccharide-Induced Changes in Peripheral Thyroid Hormone Metabolism
inferredcites →https://doi.org/10.1210/en.2011-1104openalex-snapshot
Minireview: Cracking the Metabolic Code for Thyroid Hormone Signaling
inferredcites →https://doi.org/10.1210/en.2012-1435openalex-snapshot
Brain Meets Body: The Blood-Brain Barrier as an Endocrine Interface
inferredcites →https://doi.org/10.1210/en.2012-1467openalex-snapshot
Minireview: The Neural Regulation of the Hypothalamic-Pituitary-Thyroid Axis
inferredcites →https://doi.org/10.1210/en.2012-2031openalex-snapshot
Changes in Thyroid Status During Perinatal Development of MCT8-Deficient Male Mice
inferredcites →https://doi.org/10.1210/endo-73-5-564openalex-snapshot
In VitroSecretion of Thyrotropin (TSH): Stimulation by a Hypothalamic Peptide (TRF)
inferredcites →https://doi.org/10.1210/endo-97-5-1321openalex-snapshot
Development of the Hypothalamic-Pituitary-Thyroid Axis in the Neonatal Rat
inferredcites →https://doi.org/10.1210/er.2008-0019openalex-snapshot
Cellular and Molecular Basis of Deiodinase-Regulated Thyroid Hormone Signaling1
inferredcites →https://doi.org/10.1210/er.2009-0007openalex-snapshot
Molecular Aspects of Thyroid Hormone Actions
inferredcites →https://doi.org/10.1210/er.2011-0007openalex-snapshot
Beyond Low Plasma T3: Local Thyroid Hormone Metabolism during Inflammation and Infection
inferredcites →https://doi.org/10.1210/er.2013-1087openalex-snapshot
Central Regulation of Hypothalamic-Pituitary-Thyroid Axis Under Physiological and Pathophysiological Conditions
inferredcites →https://doi.org/10.1210/jc.2004-1430openalex-snapshot
Glucocorticoids Decrease Thyrotropin-Releasing Hormone Messenger Ribonucleic Acid Expression in the Paraventricular Nucleus of the Human Hypothalamus
inferredcites →https://doi.org/10.1210/jc.2005-1013openalex-snapshot
Tissue Thyroid Hormone Levels in Critical Illness
inferredcites →https://doi.org/10.1210/jc.2007-2441openalex-snapshot
1H Magnetic Resonance Spectroscopy in Monocarboxylate Transporter 8 Gene Deficiency
inferredcites →https://doi.org/10.1210/jc.2013-3686openalex-snapshot
The Effects of Levothyroxine Replacement or Suppressive Therapy on Health Status, Mood, and Cognition
inferredcites →https://doi.org/10.1210/jcem-37-3-415openalex-snapshot
Transport of Thyroid Hormones in Serum and Cerebrospinal Fluid1
inferredcites →https://doi.org/10.1210/me.2001-0309openalex-snapshot
Identification of a Novel Human Organic Anion Transporting Polypeptide as a High Affinity Thyroxine Transporter
inferredcites →https://doi.org/10.1210/me.2004-0093openalex-snapshot
Thyroid Hormone Induces Rapid Activation of Akt/Protein Kinase B-Mammalian Target of Rapamycin-p70S6KCascade through Phosphatidylinositol 3-Kinase in Human Fibroblasts
inferredcites →https://doi.org/10.1210/me.2010-0462openalex-snapshot
The Nuclear Receptor Corepressor (NCoR) Controls Thyroid Hormone Sensitivity and the Set Point of the Hypothalamic-Pituitary-Thyroid Axis
inferredcites →https://doi.org/10.1242/dev.101907openalex-snapshot
Integrin αvβ3 and thyroid hormones promote expansion of progenitors in embryonic neocortex
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/10.1371/journal.pone.0004610openalex-snapshot
Identification of Thyroid Hormone Receptor Binding Sites and Target Genes Using ChIP-on-Chip in Developing Mouse Cerebellum
inferredcites →https://doi.org/10.1371/journal.pone.0091692openalex-snapshot
Thyroid Hormone Regulation of Gene Expression in Primary Cerebrocortical Cells: Role of Thyroid Hormone Receptor Subtypes and Interactions with Retinoic Acid and Glucocorticoids
inferredcites →https://doi.org/10.1523/jneurosci.0628-07.2007openalex-snapshot
A Crucial Role for p57Kip2 in the Intracellular Timer that Controls Oligodendrocyte Differentiation
inferredcites →https://doi.org/10.1523/jneurosci.12-06-02288.1992openalex-snapshot
Spatial and temporal expression of alpha- and beta-thyroid hormone receptor mRNAs, including the beta 2-subtype, in the developing mammalian nervous system
inferredcites →https://doi.org/10.1523/jneurosci.2713-13.2013openalex-snapshot
Treatment with Thyroxine Restores Myelination and Clinical Recovery after Intraventricular Hemorrhage
inferredcites →https://doi.org/10.1523/jneurosci.4453-08.2008openalex-snapshot
Recovery from Chronic Demyelination by Thyroid Hormone Therapy: Myelinogenesis Induction and Assessment by Diffusion Tensor Magnetic Resonance Imaging
inferredcites →https://doi.org/10.1523/jneurosci.6055-08.2009openalex-snapshot
Neuronal 3′,3,5-Triiodothyronine (T 3 ) Uptake and Behavioral Phenotype of Mice Deficient in Mct8 , the Neuronal T 3 Transporter Mutated in Allan–Herndon–Dudley Syndrome
inferredcites →https://doi.org/10.1523/jneurosci.6514-11.2012openalex-snapshot
Neuronal Hypoxia Induces Hsp40-Mediated Nuclear Import of Type 3 Deiodinase As an Adaptive Mechanism to Reduce Cellular Metabolism
inferredcites →https://doi.org/10.1530/eje-14-0285openalex-snapshot
MECHANISMS IN ENDOCRINOLOGY: Beyond the fixed setpoint of the hypothalamus–pituitary–thyroid axis
inferredcites →https://doi.org/10.1530/erc-12-0219openalex-snapshot
Thyroid hormone, thyroid hormone receptors, and cancer: a clinical perspective
inferredcites →https://doi.org/10.1530/jme-12-0188openalex-snapshot
Septic shock non-thyroidal illness syndrome causes hypothyroidism and conditions for reduced sensitivity to thyroid hormone
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What points at this work

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

inferred← citeshttps://doi.org/10.2139/ssrn.3909734openalex-extracted
Deficient Thyroid Hormone Transport to the Brain Leads to Impairments in Axonal Caliber and Oligodendroglial Differentiation
inferred← citeshttps://doi.org/10.1002/glia.23025openalex-snapshot
Inflammation severely alters thyroid hormone signaling in the central nervous system during experimental allergic encephalomyelitis in rat: Direct impact on OPCs differentiation failure
inferred← citeshttps://doi.org/10.1002/hsr2.2247openalex-snapshot
Thyroid auto‐antibodies in newly diagnosed multiple sclerosis patients: A cross sectional study
inferred← citeshttps://doi.org/10.1007/978-3-030-03742-0_10openalex-snapshot
Iodine
inferred← citeshttps://doi.org/10.1007/s00414-022-02823-zopenalex-snapshot
A novel frameshift mutation in Allan-Herndon-Dudley syndrome
inferred← citeshttps://doi.org/10.1007/s00431-024-05931-7openalex-snapshot
Clinical and genetic characteristics of patients with monocarboxylate transporter-8 deficiency: a multicentre retrospective study
inferred← citeshttps://doi.org/10.1007/s12020-023-03583-5openalex-snapshot
Brain white matter alterations in young adult male patients with childhood-onset growth hormone deficiency: a diffusion tensor imaging study
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.2021.02.002openalex-snapshot
Nuclear receptors and differentiation of oligodendrocyte precursor cells
inferred← citeshttps://doi.org/10.1016/j.arr.2024.102271openalex-snapshot
Sonic hedgehog signalling pathway contributes in age-related disorders and Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/j.brainres.2024.149110openalex-snapshot
Alterations in corpus callosum subregions morphology and functional connectivity in patients with adult-onset hypothyroidism
inferred← citeshttps://doi.org/10.1016/j.ebiom.2017.11.004openalex-snapshot
Can Thyroid Hormone Analogues Be Used to Overcome Hypomyelination and Demyelination of the Central Nervous System?
inferred← citeshttps://doi.org/10.1016/j.envint.2019.105371openalex-snapshot
Neurodevelopmental effects of low dose ionizing radiation exposure: A systematic review of the epidemiological evidence
inferred← citeshttps://doi.org/10.1016/j.envres.2021.112495openalex-snapshot
When pharmaceutical drugs become environmental pollutants: Potential neural effects and underlying mechanisms
inferred← citeshttps://doi.org/10.1016/j.ijheh.2024.114377openalex-snapshot
Early childhood exposures to phthalates in association with attention-deficit/hyperactivity disorder behaviors in middle childhood and adolescence in the ReCHARGE study
inferred← citeshttps://doi.org/10.1016/j.jagp.2018.07.007openalex-snapshot
Low Tri-iodothyronine Syndrome Is Associated With Cognitive Impairment in Patients With Acute Ischemic Stroke: A Prospective Cohort Study
inferred← citeshttps://doi.org/10.1016/j.jns.2016.04.039openalex-snapshot
Anti-thyroid antibodies and thyroid function in neuromyelitis optica spectrum disorders
inferred← citeshttps://doi.org/10.1016/j.molmed.2018.09.002openalex-snapshot
Do Defective Immune System-Mediated Myelination Processes Increase Postpartum Psychosis Risk?
inferred← citeshttps://doi.org/10.1016/j.msard.2021.103425openalex-snapshot
Positive antithyroid antibody predicts severity of neuromyelitis optica spectrum disorder in children
inferred← citeshttps://doi.org/10.1016/j.nbd.2021.105567openalex-snapshot
Deficient thyroid hormone transport to the brain leads to impairments in axonal caliber and oligodendroglial development
inferred← citeshttps://doi.org/10.1016/j.neurobiolaging.2017.09.014openalex-snapshot
Age-dependent association of thyroid function with brain morphology and microstructural organization: evidence from brain imaging
inferred← citeshttps://doi.org/10.1016/j.psychres.2022.114546openalex-snapshot
Peripheral lower triiodothyronine levels related to interleukin-6 in patients with first-episode schizophrenia
inferred← citeshttps://doi.org/10.1016/j.psyneuen.2020.104844openalex-snapshot
Altered thyroid hormone profile in patients with Alzheimer’s disease
inferred← citeshttps://doi.org/10.1038/s41380-025-03206-7openalex-snapshot
Transdiagnostic reduction in cortical choline-containing compounds in anxiety disorders: a 1H-magnetic resonance spectroscopy meta-analysis
inferred← citeshttps://doi.org/10.1038/s41598-017-16564-2openalex-snapshot
Prognostic value of thyroid hormones in acute ischemic stroke – a meta analysis
inferred← citeshttps://doi.org/10.1038/s41598-023-49285-wopenalex-snapshot
Low levels of free triiodothyronine are associated with risk of cognitive impairment in older euthyroid adults
inferred← citeshttps://doi.org/10.1055/a-0635-0826openalex-snapshot
The Association Between the Levels of Thyroid Hormones and Peripheral Nerve Conduction in Patients with Type 2 Diabetes Mellitus
inferred← citeshttps://doi.org/10.1074/jbc.m117.784447openalex-snapshot
De novo triiodothyronine formation from thyrocytes activated by thyroid-stimulating hormone
inferred← citeshttps://doi.org/10.1080/10408444.2025.2461076openalex-snapshot
Mechanisms of developmental neurotoxicity mediated by perturbed thyroid hormone homeostasis in the brain: an adverse outcome pathway network
inferred← citeshttps://doi.org/10.1080/17446651.2024.2351885openalex-snapshot
Per-polyfluoroalkyl substances (PFAS) as thyroid disruptors: is there evidence for multi-transgenerational effects?
inferred← citeshttps://doi.org/10.1080/26895293.2023.2220537openalex-snapshot
Analysis of lncRNA and mRNA expression profiles in diabetic peripheral neuropathy based on weighted gene co-expression network analysis
inferred← citeshttps://doi.org/10.1089/neu.2019.6949openalex-snapshot
Improved Functional Recovery in Rat Spinal Cord Injury Induced by a Drug Combination Administered with an Implantable Polymeric Delivery System
inferred← citeshttps://doi.org/10.1089/thy.2019.0307openalex-snapshot
No Dataset Left Behind: Mechanistic Insights into Thyroid Receptor Signaling Through Transcriptomic Consensome Meta-Analysis
inferred← citeshttps://doi.org/10.1089/thy.2019.0672openalex-snapshot
Graves' Disease and Toxic Nodular Goiter, Aggravated by Duration of Hyperthyroidism, Are Associated with Alzheimer's and Vascular Dementia: A Registry-Based Long-Term Follow-Up of Two Large Cohorts
inferred← citeshttps://doi.org/10.1089/thy.2022.0699openalex-snapshot
Maternal Thyroid Function During Pregnancy and Offspring White Matter Microstructure in Early Adulthood: A Prospective Birth Cohort Study
inferred← citeshttps://doi.org/10.1101/2025.10.01.677488openalex-snapshot
Hippo/YAP1 Signaling Regulates the Oligodendrocyte–Astrocyte Fate Switch and Ependymal Gene Expression in Adult Spinal Cord Stem Cells
inferred← citeshttps://doi.org/10.1186/s12902-026-02210-4openalex-snapshot
Cortical thinning in subclinical hypothyroidism: structural and functional brain changes underlying cognitive impairment
inferred← citeshttps://doi.org/10.1371/journal.pone.0220378openalex-snapshot
Coordinated transcriptional regulation by thyroid hormone and glucocorticoid interaction in adult mouse hippocampus-derived neuronal cells
inferred← citeshttps://doi.org/10.1371/journal.pone.0256207openalex-snapshot
Thyroid hormone deficiency during zebrafish development impairs central nervous system myelination
inferred← citeshttps://doi.org/10.14283/jpad.2023.20openalex-snapshot
The Role of Thyroid Dysfunction in Alzheimer's Disease: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.1515/tnsci-2022-0289openalex-snapshot
Thyroid hormone levels paradox in acute ischemic stroke
inferred← citeshttps://doi.org/10.1515/tnsci-2022-0340openalex-snapshot
FT4-to-FT3 ratio is a novel prognostic marker in subacute combined spinal cord degeneration patients
inferred← citeshttps://doi.org/10.1523/jneurosci.2141-21.2022openalex-snapshot
SECISBP2L-Mediated Selenoprotein Synthesis Is Essential for Autonomous Regulation of Oligodendrocyte Differentiation
inferred← citeshttps://doi.org/10.1590/1678-5150-pvb-5659openalex-snapshot
Hypomyelinogenesis associated with transplacental poisoning by Sida carpinifolia (Malvaceae) in fetus and newborn calves
inferred← citeshttps://doi.org/10.20944/preprints202407.1956.v1openalex-snapshot
Modulation of Integrin αvβ3 Activation and Signaling in BV-2 Microglial Cells and THP-1 Monocytes by Thyroid Hormones
inferred← citeshttps://doi.org/10.2147/jir.s501150openalex-snapshot
The Percentage of Neutrophils is Independently Associated with Blood-Brain Barrier(BBB) Disruption in Myelin Oligodendrocyte Glycoprotein Antibody Associated Disease (MOGAD)
inferred← citeshttps://doi.org/10.22074/cellj.2018.5112openalex-snapshot
The Effects of De-Whiskering and Congenital Hypothyroidism on The Development of Nitrergic Neurons in Rat Primary Somatosensory and Motor Cortices.
inferred← citeshttps://doi.org/10.3389/fendo.2020.00283openalex-snapshot
Monocarboxylate Transporter 8 Deficiency: Delayed or Permanent Hypomyelination?
inferred← citeshttps://doi.org/10.3389/fnagi.2024.1456525openalex-snapshot
Hyperthyroidism, hypothyroidism, thyroid stimulating hormone, and dementia risk: results from the NHANES 2011–2012 and Mendelian randomization analysis
inferred← citeshttps://doi.org/10.3389/fnins.2024.1357633openalex-snapshot
Low T3 syndrome is associated with the severity of myelin oligodendrocyte glycoprotein antibody-associated disease exacerbation
inferred← citeshttps://doi.org/10.3390/ijms21238945openalex-snapshot
Thyroid Hormone Signaling in Embryonic Stem Cells: Crosstalk with the Retinoic Acid Pathway
inferred← citeshttps://doi.org/10.3390/ijms24129826openalex-snapshot
Thyroid Axis and Vestibular Physiopathology: From Animal Model to Pathology
inferred← citeshttps://doi.org/10.3390/pharmaceutics13060848openalex-snapshot
Design and In Vitro Study of a Dual Drug-Loaded Delivery System Produced by Electrospinning for the Treatment of Acute Injuries of the Central Nervous System
inferred← citeshttps://doi.org/10.34883/pi.2021.12.2.012openalex-snapshot
Postpartum Psychosis: Evolution of Ideas about Etiopathogenesis
inferred← citeshttps://doi.org/10.37506/ijop.v9i1.2605openalex-snapshot
Hypothyroid Patients with Positive Thyroid Antibodies and Relation to Nerve Conduction Study Findings
inferred← citeshttps://doi.org/10.4103/1673-5374.335834openalex-snapshot
Neuroprotection and neuroregeneration: roles for the white matter
inferred← citeshttps://doi.org/10.5709/acp-0354-0openalex-snapshot
Visual-Spatial and Temporal Integration in Patients with Hypothyroidism
inferred← citeshttps://doi.org/10.70675/a9f2181az8cd4z498dz87adz398d98df9f99openalex-snapshot
Impacts d'une exposition prénatale au bisphénol A sur la fonction thyroïdienne et le métabolome du système nerveux central fœtal
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