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In this study, we demonstrate that human albumin requires a branched or medium-long aliphatic amino acid in the C-terminal end at position 585 for optimal binding to human FcRn, and that the L585 residue can not be substituted with an amino acid unrecognizable by CPA without compromising receptor binding

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In cell culture studies, addition of epitalon to telomerase-negative human fetal fibroblasts induced expression of this catalytical subunit, enzymatic telomerase activity, and subsequent telomere elongation