Pages that link to "Q37165983"
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The following pages link to Importance of monocarboxylate transporter 8 for the blood-brain barrier-dependent availability of 3,5,3'-triiodo-L-thyronine (Q37165983):
Displaying 50 items.
- Scope and limitations of iodothyronine deiodinases in hypothyroidism (Q26785400) (← links)
- Blood brain barrier: a challenge for effectual therapy of brain tumors (Q28081947) (← links)
- An evo-devo approach to thyroid hormones in cerebral and cerebellar cortical development: etiological implications for autism (Q28655923) (← links)
- Thyroid hormones are associated with longitudinal cognitive change in an urban adult population (Q30668962) (← links)
- Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivation (Q33599996) (← links)
- In vitro and mouse studies supporting therapeutic utility of triiodothyroacetic acid in MCT8 deficiency (Q33631892) (← links)
- Maternal thyroid hormones are essential for neural development in zebrafish (Q33632027) (← links)
- Minireview: thyroid hormone transporters: the knowns and the unknowns (Q33637022) (← links)
- Thyroid hormone-regulated mouse cerebral cortex genes are differentially dependent on the source of the hormone: a study in monocarboxylate transporter-8- and deiodinase-2-deficient mice. (Q33848231) (← links)
- Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion (Q34090117) (← links)
- In vivo activity of the thyroid hormone receptor beta- and α-selective agonists GC-24 and CO23 on rat liver, heart, and brain (Q34578566) (← links)
- Hypothyroidism and brain developmental players (Q35427151) (← links)
- Parallel regulation of thyroid hormone transporters OATP1c1 and MCT8 during and after endotoxemia at the blood-brain barrier of male rodents. (Q35442273) (← links)
- Choroid plexus transport: gene deletion studies (Q35596169) (← links)
- Endotoxin-induced inflammation down-regulates L-type amino acid transporter 1 (LAT1) expression at the blood-brain barrier of male rats and mice (Q36024407) (← links)
- Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney. (Q36065407) (← links)
- Longitudinal comparison of thyroxine pharmacokinetics between pregnant and nonpregnant women: a stable isotope study. (Q36756434) (← links)
- Maternal thyroid hormones are transcriptionally active during embryo-foetal development: results from a novel transgenic mouse model (Q37295374) (← links)
- A thyroid hormone analog with reduced dependence on the monocarboxylate transporter 8 for tissue transport (Q37328831) (← links)
- Pharmacological treatment and BBB-targeted genetic therapy for MCT8-dependent hypomyelination in zebrafish. (Q37425989) (← links)
- MCT8 expression in human fetal cerebral cortex is reduced in severe intrauterine growth restriction. (Q37579015) (← links)
- Thyroid hormone and seasonal rhythmicity (Q37604490) (← links)
- Thyroid hormones, t3 and t4, in the brain (Q37689365) (← links)
- Transporters MCT8 and OATP1C1 maintain murine brain thyroid hormone homeostasis (Q37726622) (← links)
- Thyroid hormone action: astrocyte-neuron communication (Q38218670) (← links)
- Thyroid hormone and the neuroglia: both source and target (Q38266872) (← links)
- Thyroid hormone transporters--functions and clinical implications (Q38460012) (← links)
- The role of tanycytes in hypothalamic glucosensing. (Q38529653) (← links)
- Role of the Thyroid System in Myelination and Neural Connectivity. (Q38542460) (← links)
- Thyroid Hormone Economy in the Perinatal Mouse Brain: Implications for Cerebral Cortex Development. (Q38838315) (← links)
- Hypomyelinating leukodystrophies - a molecular insight into the white matter pathology. (Q38846368) (← links)
- Blood-brain barrier transport machineries and targeted therapy of brain diseases. (Q39164804) (← links)
- Defects of Thyroid Hormone Synthesis and Action (Q39286318) (← links)
- The expression of thyroid hormone transporters in the human fetal cerebral cortex during early development and in N-Tera-2 neurodifferentiation. (Q39559831) (← links)
- Expression pattern of thyroid hormone transporters in the postnatal mouse brain (Q40825263) (← links)
- Age-Dependent Changes of Monocarboxylate Transporter 8 Availability in the Postnatal Murine Retina (Q41121269) (← links)
- Thyroid Hormone Availability and Action during Brain Development in Rodents (Q41418267) (← links)
- Transcriptional profiling of fibroblasts from patients with mutations in MCT8 and comparative analysis with the human brain transcriptome (Q41860765) (← links)
- Understanding the hypothalamus-pituitary-thyroid axis in mct8 deficiency (Q41865221) (← links)
- MCT8 Deficiency in Male Mice Mitigates the Phenotypic Abnormalities Associated With the Absence of a Functional Type 3 Deiodinase (Q42392460) (← links)
- Hypotonic male infant and MCT8 deficiency - a diagnosis to think about (Q43096433) (← links)
- Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier. (Q46205341) (← links)
- From zebrafish to human: A comparative approach to elucidate the role of the thyroid hormone transporter MCT8 during brain development (Q46252494) (← links)
- Overcoming Monocarboxylate Transporter 8 (MCT8)-Deficiency to Promote Human Oligodendrocyte Differentiation and Myelination (Q47129278) (← links)
- Deficiency of the Thyroid Hormone Transporter Monocarboxylate Transporter 8 in Neural Progenitors Impairs Cellular Processes Crucial for Early Corticogenesis. (Q47174964) (← links)
- Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome. (Q47890640) (← links)
- In vitro and mouse studies support therapeutic utility of triiodothyroacetic acid in MCT8 deficiency (Q48388516) (← links)
- Thyroid Hormone Transporters MCT8 and OATP1C1 Control Skeletal Muscle Regeneration. (Q55068696) (← links)
- Regulation of T3 Availability in the Developing Brain: The Mouse Genetics Contribution. (Q55315620) (← links)
- Hypothyroxinemia: a subclinical condition affecting neurodevelopment (Q58050358) (← links)