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One or more keywords matched the following items that are connected to AFSHAR-KHARGHAN, VAHID
Item TypeName
Academic Article Abnormal platelet function in C3-deficient mice.
Academic Article Reduced graft-versus-host disease in C3-deficient mice is associated with decreased donor Th1/Th17 differentiation.
Academic Article Complement activation in thrombotic microangiopathies.
Concept Complement Pathway, Classical
Concept Complement Activation
Concept Complement Pathway, Alternative
Concept Complement Factor H
Concept Complement C3
Concept Complement System Proteins
Academic Article Partial ADAMTS13 deficiency in atypical hemolytic uremic syndrome.
Academic Article The interaction between factor H and Von Willebrand factor.
Academic Article Human complement factor H is a reductase for large soluble von Willebrand factor multimers--brief report.
Academic Article von Willebrand factor is a cofactor in complement regulation.
Academic Article Platelet activation leads to activation and propagation of the complement system.
Academic Article Factor H binds to platelet integrin alphaIIbbeta3.
Academic Article Autocrine effects of tumor-derived complement.
Academic Article COMPLEMENTing the diagnosis of aHUS.
Academic Article Complement component C3 mediates Th1/Th17 polarization in human T-cell activation and cutaneous GVHD.
Academic Article Complement-Binding Donor-Specific Anti-HLA Antibodies and Risk of Primary Graft Failure in Hematopoietic Stem Cell Transplantation.
Academic Article Complement component 3 is regulated by TWIST1 and mediates epithelial-mesenchymal transition
Academic Article Complement-Binding Donor-Specific Anti-HLA Antibodies and Risk of Primary Graft Failure in Hematopoietic Stem Cell Transplantation
Academic Article Complement Component 3 Is Regulated by TWIST1 and Mediates Epithelial-Mesenchymal Transition.
Academic Article Atypical hemolytic uremic syndrome.
Academic Article Complement and clot.
Academic Article The role of the complement system in cancer.
Academic Article The interaction between the complement system and hemostatic factors.
Academic Article Pathway-driven rare germline variants associated with transplant-associated thrombotic microangiopathy (TA-TMA).
Search Criteria
  • Complement System Proteins