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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, others assume the role of regulatory T lymphocytes, capable of mitigating immune reactivity ( 2 ). The autoimmune response observed in GD originates from the presence of circulating immunoglobulin G (IgG) antibodies targeting the thyroid
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ability of the patient's IgG to block TSH binding and induce the production of cyclic adenosine monophosphate (cAMP), and the activity index and symptom of GD improved after surgical remission of acromegaly, confirming the hypothesis that the GH−IGF-1 axis
Department of Nuclear Medicine, The Affiliated Hospital of Jiangsu University, Zhenjiang, China
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antibodies and secondary antibodies were used: rabbit anti-human β-catenin, rabbit anti-human GSK-3β, rabbit anti-human p-GSK-3β, rabbit anti-β-actin (Cell Signaling Technology), and goat anti-rabbit IgG-HRP (Santa Cruz). Western blot analysis Briefly
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blocked with 3% BSA. The tissue was incubated overnight with anti-FOXP3 antibodies (rabbit C-terminal polyclonal IgG antibody clone E18492, SpringBio ® ), anti-CD25 (mouse monoclonal antibody clone 4C9, Cell Marque ® ), anti-CD4 (rabbit monoclonal antibody
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(Invitrogen) for permeabilized conditions with 1 μL anti-NIS (Proteintech, Wuhan, China). After washing, cells were incubated with donkey anti-rabbit IgG H&L (Abcam). The fluorescence of 10 7 cells per tube was assayed using the fluorescence-activated cell
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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(1:100, Abcam) and mouse anti-HMGA1 (1:500, Santa Cruz Biotechnology) at room temperature for 2 h, followed by incubation at 4°C overnight. Secondary reagents comprised biotinylated goat anti-rabbit or goat anti-mouse IgG (Proteintech