Haemoglobin blocks von Willebrand factor proteolysis by ADAMTS-13: a mechanism associated with sickle cell disease.

Haemoglobin blocks von Willebrand factor proteolysis by ADAMTS-13: a mechanism associated with sickle cell disease. Thromb Haemost. 2009 Jun; 101(6):1070-7.

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subject areas

ADAM Proteins
ADAMTS13 Protein
Anemia, Sickle Cell
Antibodies, Blocking
Catalytic Domain
Endothelial Cells
Enzyme Repression
Hemoglobin A
Humans
Hydrolysis
Protein Binding
Stroke
Substrate Specificity
Thromboembolism
von Willebrand Factor

authors with profiles

MIGUEL CRUZ
HYOJEONG HAN