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Additionally, serum GPX-3 had another potential to reflect the inflammatory burden as much as traditional acute-phase reactants such as CRP and serum albumin
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Four weeks post-transplantation, widespread hALB-positive cells were observed, and FACS analysis showed that approximately 15% of the total hepatocyte mass was derived from the transplanted human HBs, with increasing hALB secretion in the mouse serum over time [1]
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