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Bin Zhang

 ORCID
https://orcid.org/0000-0002-7786-7580
Reviewed Pathways (18)
Date Identifier Pathway Reference
2020-04-02 R-HSA-9671793 Diseases of hemostasis BibTex
2020-04-02 R-HSA-9651496 Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) BibTex
2020-04-02 R-HSA-9672383 Defective factor IX causes thrombophilia BibTex
2020-04-02 R-HSA-9657688 Defective factor XII causes hereditary angioedema BibTex
2020-04-02 R-HSA-9657689 Defective SERPING1 causes hereditary angioedema BibTex
2020-04-02 R-HSA-9668250 Defective factor IX causes hemophilia B BibTex
2020-04-02 R-HSA-9673240 Defective gamma-carboxylation of F9 BibTex
2020-04-02 R-HSA-9673221 Defective F9 activation BibTex
2020-04-02 R-HSA-9673202 Defective F9 variant does not activate FX BibTex
2020-04-02 R-HSA-9673218 Defective F9 secretion BibTex
2020-04-02 R-HSA-9662001 Defective factor VIII causes hemophilia A BibTex
2020-04-02 R-HSA-9672396 Defective cofactor function of FVIIIa variant BibTex
2020-04-02 R-HSA-9672397 Defective F8 secretion BibTex
2020-04-02 R-HSA-9672393 Defective F8 binding to von Willebrand factor BibTex
2020-04-02 R-HSA-9672395 Defective F8 binding to the cell membrane BibTex
2020-04-02 R-HSA-9672391 Defective F8 cleavage by thrombin BibTex
2020-04-02 R-HSA-9674519 Defective F8 sulfation at Y1699 BibTex
2020-04-02 R-HSA-9672387 Defective F8 accelerates dissociation of the A2 domain BibTex
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