PMID: 6402037Mar 15, 1983Paper

Preferential binding of high molecular weight forms of von Willebrand factor to fibrillar collagen

Biochimica Et Biophysica Acta
S A Santoro

Abstract

The time- and concentration-dependent binding of von Willebrand factor to fibrillar collagen was examined by following the disappearance from plasma of ristocetin cofactor activity and factor VIII-related antigen, the functional and immunologic determinants of von Willebrand factor. Examination of both bound and unbound factor VIII-related antigen by crossed immunoelectrophoresis revealed a preferential binding of the higher molecular weight forms of von Willebrand factor to fibrillar collagen.

Citations

Feb 24, 1999·Haemophilia : the Official Journal of the World Federation of Hemophilia·H J MetznerJ Friedebold
Jan 24, 2015·Hämostaseologie·Z M Ruggeri, G L Mendolicchio
Aug 1, 1986·Thrombosis Research·J E Brown, J O Bosak
Sep 27, 2006·Journal of Thrombosis and Haemostasis : JTH·J Chen, J A López
Jan 1, 1991·Annals of the New York Academy of Sciences·H J Weiss
Feb 15, 1990·Thrombosis Research·M GilchristP A Gordon
Aug 1, 1988·Journal of Dental Research·U SchlagenhaufR C Page
Jan 1, 1988·Clinical and Laboratory Haematology·W TatewakiA Shibata
Jan 8, 2020·Nature Chemical Biology·Abhishek A JalanRichard W Farndale
Oct 1, 1989·Baillière's Clinical Haematology·H Pannekoek, J Voorberg
Jan 1, 1986·Critical Reviews in Oncology/hematology·R J HamerJ J Sixma

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