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van Mourik, JA
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[InstanceEdit:5604923] Jupe, Steve, 2014-07-02
dbId
5604925
displayName
van Mourik, JA
firstname
J A
initial
JA
publications
[LiteratureReference:9661684] The life cycle of coagulation factor VIII in view of its structure and function
[LiteratureReference:9662039] Intracellular retention of a factor VIII protein with an Arg2307-->Gln mutation as a cause of haemophilia A
[LiteratureReference:9669986] The sequence Glu1811-Lys1818 of human blood coagulation factor VIII comprises a binding site for activated factor IX
[LiteratureReference:9667999] The interaction between human blood-coagulation factor VIII and von Willebrand factor. Characterization of a high-affinity binding site on factor VIII
[LiteratureReference:9661951] Intracellular accumulation of factor VIII induced by missense mutations Arg593-->Cys and Asn618-->Ser explains cross-reacting material-reduced haemophilia A
[LiteratureReference:9668373] Substitution of Arg527 and Arg531 in factor VIII associated with mild haemophilia A: characterization in terms of subunit interaction and cofactor function
[LiteratureReference:9674485] Binding of blood coagulation factor VIII and its light chain to phosphatidylserine/phosphatidylcholine bilayers as measured by ellipsometry
[LiteratureReference:5604935] Protein S binding to human endothelial cells is required for expression of cofactor activity for activated protein C
[LiteratureReference:9668020] Sulfation of Tyr1680 of human blood coagulation factor VIII is essential for the interaction of factor VIII with von Willebrand factor
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Person
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van Mourik
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