2019
DOI: 10.1007/s10517-019-04443-x
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Number, Proliferative Activity, and Expression of Thyroid Hormone Receptors in Dermal Fibroblasts in Mice with Changed Thyroid Status

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Cited by 2 publications
(2 citation statements)
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“…1). 7,[37][38][39][40] In addition, there is a plethora of additional effects that are not mediated by direct TRE-TR binding such as TH-mediated miRNA regulation, 41 DNA methylation, 42 metabolic effects of TH, 43 and post-translational modifications of T3 44 to name but a few. 45 Given that T3 shows a considerably higher affinity to cognate nuclear receptors than T4, circulating T4 is thought to largely act after intracellular deiodination into T3 in peripheral organs, including human HFs.…”
Section: Thyroid Hormone ( Th) B I Ologymentioning
confidence: 99%
“…1). 7,[37][38][39][40] In addition, there is a plethora of additional effects that are not mediated by direct TRE-TR binding such as TH-mediated miRNA regulation, 41 DNA methylation, 42 metabolic effects of TH, 43 and post-translational modifications of T3 44 to name but a few. 45 Given that T3 shows a considerably higher affinity to cognate nuclear receptors than T4, circulating T4 is thought to largely act after intracellular deiodination into T3 in peripheral organs, including human HFs.…”
Section: Thyroid Hormone ( Th) B I Ologymentioning
confidence: 99%
“…It also reduces the uptake of iodine capacity in tumor cells. Scholars found TSHR and NIS become an important cause for PTC in 131-I radiotherapy [37,38]. In human and rabbit thyroid cancer cells, BRAFV600E mutant, a carcinogenic homolog of murine sarcomatous virulent bacterium, could cause activation of BRAF/MEK/ MAPK signaling pathway and expression silencing of thyroid-specific genes including TPO, Tg, TSHR, and NIS.…”
Section: Thyroid-stimulating Hormone Receptor and Sodium/iodide Sympomentioning
confidence: 99%