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Systemic lupus erythematosus (SLE) and multiple sclerosis (MS) exemplify such disorders, where conventional immunosuppressive therapies, though often effective, are associated with considerable risks including infection and systemic toxicity

To investigate whether FGF21 mediated the proliferation-promoting effect, we detected BrdU + insulin + cells in islets of Fgf21 / and Fgf21 Hep/ diabetic mice treated with GCGR mAb or IgG

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