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pro vyhledávání: '"SE Martin"'
Publikováno v:
Blood. 86:3805-3814
Bernard-Soulier syndrome (B-Ss) is a rare congenital bleeding disorder caused by abnormal giant platelets, thrombocytopenia, and defective glycoprotein (GP) Ib-V-IX, the adhesion receptor for von Willebrand factor (vWF). This report describes the mol
Autor:
JeÌroÌme Appenzeller, Supriya Tilvi, Marie-TheÌreÌse Martin, Jean-François Gallard, Hoda El-bitar, Elise Tran Huu Dau, CeÌcile Debitus, Dominique Laurent, CeÌline Moriou, Ali Al-Mourabit
Publikováno v:
Organic Letters; Nov2009, Vol. 11 Issue 21, p4874-4877, 4p
Publikováno v:
Blood. 56:456-464
Plasmic degradation of crosslinked fibrin has been studied to identify the proteolytic cleavages that convert the clot into a soluble lysate and also to identify the derivatives that are likely to circulate during clot dissolution. Initial polypeptid
Publikováno v:
Blood. 63:940-943
Sedimentation analysis of factor VIII complex was performed in the analytical ultracentrifuge using partition cells. This method allowed for the calculation of three different sedimentation coefficients from each run: one based on ristocetin agglutin
Publikováno v:
Blood. 55:848-858
Human von Willebrand protein was purified from pooled cryoprecipitate, then degraded by trypsin and analyzed primarily for ristocetin cofactor activity in relation to the electrophoretic pattern in sodium dodecyl sulfate polyacrylamide gradient gels.
Publikováno v:
Journal of Biological Chemistry. 255:5599-5604
A previously undescribed gamma chain variant of human fibrinogen has been identified by application of a sensitive sodium dodecyl sulfate-polyacrylamide gradient gel electrophoretic technique to separate the polypeptide chains. This variant, called g
Publikováno v:
Blood. 57:313-323
Studies of subunit chain size, disulfide bond arrangement, carbohydrate content, and pattern of tryptic degradation of von Willebrand protein polymers were undertaken in an attempt to explain their functional heterogeneity. Human von Willebrand prote
Publikováno v:
Blood. 54:1282-1295
A technique has been developed to identify and quantitate unique plasmic degradation products of crosslinked fibrin in plasma. In this method, fibrin derivatives are extracted by heat precipitation and dissolved with disulfide bond reduction, after w
Publikováno v:
Thrombosis and Haemostasis.
Highly purified von Willebrand protein was obtained from pooled human cryoprecipitate using polyethylene glycol precipitation followed by agarose gel chromatography, and concentrated by dialysis against 20% polyethylene glycol-20,000. Subsequent part
Publikováno v:
Blood. 56(3)
Plasmic degradation of crosslinked fibrin has been studied to identify the proteolytic cleavages that convert the clot into a soluble lysate and also to identify the derivatives that are likely to circulate during clot dissolution. Initial polypeptid