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Disrupted filamin A/αIIbβ3 interaction induces macrothrombocytopenia by increasing RhoA activity
UploadA mutation of the human EPHB2 gene leads to a major platelet functional defect
Download from ashpublications.orgProtein kinase C signaling dysfunction in von Willebrand disease (p.V1316M) type 2B platelets
Download from doi.orgKinesin-1 Is a New Actor Involved in Platelet Secretion and Thrombus Stability
UploadGain-of-Function Mutation in Filamin A Potentiates Platelet Integrin α IIb β 3 Activation
UploadOf von Willebrand factor and platelets
Download from link.springer.comA new form of macrothrombocytopenia induced by a germ-line mutation in the PRKACG gene
Download from ashpublications.orgvon Willebrand factor mutation promotes thrombocytopathy by inhibiting integrin αIIbβ3
Download from doi.orgHeterogeneity of Platelet Functional Alterations in Patients With Filamin A Mutations
Download from www.researchgate.netActivation state of platelets in experimental severe hemophilia A
Download from dx.doi.orgThrombocytopenia resulting from mutations in filamin A can be expressed as an isolated syndrome
Download from ashpublications.orgPlatelet JNK1 is involved in secretion and thrombus formation
Download from ashpublications.orgAnticoagulant and antithrombotic properties of platelet protease nexin-1
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