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- W2000237661 abstract "The partial (50%) digestion of plasminogen (plgn)-enriched, 125I labelled, crosslinked fibrin (XL-FN) in a solution of streptokinase (SK) was shown to generate an array of soluble crosslinked fragments similar in molecular size (by Sepharose 4B chromatography) to those obtained when XL-FN was digested in human serum. These fragments, following chromatographic isolation, were characterised by SDS-gel electrophoresis as crosslinked X-oligomers, Y-D and D dimer fragments and a scheme for their subunit structures is presented. All these fragments were non-covalently associated with either the E domain or structures containing the E domain via the polymerisation sites bequeathed by the originating fibrin. Comparison of approximate molecular weight estimates of the X oligomers by SDS-gel electrophoresis and by Sepharose 4B chromatography suggested that crosslinking may account for 1–2 × 106 of the molecular weight while polymerisation sites allow molecular sizes of up to 10 × 106. The relevance of these crosslinked fragments to thrombosis and DIC is discussed." @default.
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- W2000237661 date "1980-12-01" @default.
- W2000237661 modified "2023-09-24" @default.
- W2000237661 title "Giant fibrin fragments derived from crosslinked fibrin: Structure and clinical implication" @default.
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- W2000237661 doi "https://doi.org/10.1016/0049-3848(80)90153-x" @default.
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