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regulating the expression of NIS, TPO, TG, and TSH receptors in the thyroid ( 10 , 11 ). Previous studies found that cytokines including TNFα and TNFβ, interferons (IFNα, IFNβ, and IFNγ), interleukins (IL1α, IL1β, and IL6), and TGFβ can also inhibit the mRNA
The First Affiliated Hospital, Department of Otorhinolaryngology, Hengyang Medical School, University of South China, Hengyang, Hunan, China
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The First Affiliated Hospital, Department of Endocrinology and Metabolism, Hengyang Medical School, University of South China, Hengyang, Hunan, China
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Bonferroni’s post hoc test. The difference between the four groups in the rescue experiments was analyzed by two-way ANOVA. Spearman correlation analysis was used to assess the correlation between FGF1 and HMGA1 mRNA levels in PTC tissues. P values < 0
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. The mRNA levels were determined by quantitative RT-PCR, as previously described ( 12 ). The relative mRNA levels of the target gene were normalized to β-actin, and the differences in mRNA levels were calculated using the 2 −△△Ct method. The primer
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represents a bright spot. As miRNAs bind to their target mRNA transcripts via miRNA recognition elements (MREs), target gene expression is repressed. circRNAs act as molecular sponges by competitively binding to miRNA through MREs and negatively regulating
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Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China
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functional role of FLNA in PTC. We also explored the potential molecular mechanisms involved in the effect of FLNA on PTC cells. Materials and methods Data collection The mRNA expression and clinical profiles of PTC patients (495 PTC tissues and
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stimulate carnitine palmitoyltransferase Iα (CPT1A), a rate-limiting β-oxidation enzyme ( 40 ). Accordingly, CPT1A mRNA and enzyme activity in the hyperthyroidism animal livers increase significantly ( 41 ); CPT1A is inhibited in the hypothyroidism mice ( 42
Department of Nuclear Medicine, The Affiliated Hospital of Jiangsu University, Zhenjiang, China
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Biotechnology, Dalian, China) using random hexamers and oligo dT as primers. The qRT–PCR was performed with SYBR ® Premix Ex Taq™ (TliRNaseH Plus) in a real-time PCR Mx3000PTM System (Genetimes Technology, China). For mRNA detection, the primers were as follows
Department of Diabetes & Endocrinology, Skåne University Hospital, Malmö, Sweden
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Department of Diabetes & Endocrinology, Skåne University Hospital, Malmö, Sweden
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Department of Ophthalmology, Skåne University Hospital, Malmö, Sweden
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Department of Diabetes & Endocrinology, Skåne University Hospital, Malmö, Sweden
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QuantiTect Reverse Transcription Kit (Qiagen) according to the manufacturer’s instructions. RT-PCR was performed using the QuantStudio 7 Flex sequence detection system (Applied Biosystems) according to the manufacturer’s instructions, employing TaqMan mRNA
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Pediatric Endocrinology Unit, Department of Women's and Children's Health, Padua University Hospital, Padova, Italy
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, mainly GD and subacute thyroiditis have been described. GD has been reported to occur more frequently with mRNA-based vaccines than with the adenovirus-vectored (while inactivated vaccines seem to be not associated), after the first or second dose and
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synthesized by Jiangsu Genecfe Biotechnology Co, Ltd (Zhejiang, China). The mRNA expression was quantified with the adoption of the 2- ( ΔCt sample –- ΔCt control) method ( 30 ). Cells were lyzed in a radioimmunoprecipitation assay buffer containing