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-time quantitative PCR was performed using the SYBR Green PCR Master Mix and Roche Light Cycle Detection System. Each gene mRNA level was determined from the value of the threshold cycle ( C t ) of real-time PCR as related to β-actin . Western blot analysis
Department of Endocrinology and Metabolism, People's Hospital of Liaoning Province, Shenyang, People’s Republic of China
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Department of Laboratory Medical, The First Hospital of China Medical University, Shenyang, People’s Republic of China
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manufacturer’s instructions. Reactions began with a 10 s hot activation of Taq polymerase at 95°C, followed by 40–45 cycles of amplification in three steps (denaturation at 95°C for 5 s, 30 s annealing at 60°C and 30 s extension at 72°C). The mRNA expression
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, triangular face and a variable degree of mental retardation ( 6 ). Approximately 40 cases have been reported in literature ( 7 ). The aim of the present study was to evaluate the IGF1R mRNA and protein expression and the IGF1R protein activity in two male
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increased T cells and natural killer (NK) cells, as well as the pro-inflammatory cytokine secretion of T cells and NK cells, were observed after stimulation with soluble Sema 5A ( 26 ). Another study identified an elevated Sema 5A expression of mRNA in
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). Real-time PCR for quantification of mRNA was performed on a SmartCycler (Cepheid, Sunnyvale, CA, USA) using a SYBR-Green protocol in the fluorescence temperature cycler. Each real-time PCR consisted of 10 ng total RNA equivalents, 1× Takara SYBR Green
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after RP11 overexpression ( Fig. 3B ). Subsequently, the effects of RP11 overexpression on several important factors involved in the differentiation of preadipocytes were evaluated. Results showed that the mRNA and protein expression levels of PPARγ
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) . Finally, we measured mRNA expression levels of GR-α and GR-β. Patients and methods Patients To study the prevalence and distribution of the GR polymorphisms, three cohorts with a total of 290 unrelated BD patients were included in the study (56 patients
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macrophage mRNA expression of TNF-α and IL-18 was significantly upregulated, while M2 macrophage mRNA expression of Arg1 and IL-10 was downregulated in db/db mice. Kaempferol administration effectively reversed the M1-specific macrophage and M2-specific
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.26 ± 1.45. ** P < 0.01. (F) Disease-free survival (Kaplan–Meier) curves. Cases with alteration (mRNA expression z -scores choose >2 or <−2) were 24 (relapsed n = 7, 29.17%), without alteration were 469 (relapsed n = 41, 8.74%). The RDM1
Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
Medical Faculty of the University of Porto, Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
Institute of Biomedical Sciences of Abel Salazar (ICBAS), Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
Department of Endocrinology, Diabetes and Metabolism, University and Hospital Center of Coimbra, Coimbra, Portugal
Medical Faculty, University of Coimbra, Coimbra, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
Public Health Unit, ACeS Baixo Mondego, Coimbra, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
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Department of Pathology, Medical Faculty of the University of Porto, Porto, Portugal
Department of Pathology, Hospital de S. João, Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
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Department of Pathology, Hospital de S. João, Porto, Portugal
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Institute of Molecular Pathology and Immunology of the University of Porto (IPATIMUP), Porto, Portugal
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functionality in clinical samples are not available. In the majority of the studies, SLC5A5 mRNA levels are lower in thyroid carcinomas than in adenomas ( 4 ) and normal adjacent thyroid ( 5 , 6 , 7 ); furthermore, SLC5A5 expression presents some