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NTIS 바로가기Microvascular research, v.106, 2016년, pp.128 - 136
da Guarda, C.C. , Santiago, R.P. , Pitanga, T.N. , Santana, S.S. , Zanette, D.L. , Borges, V.M. , Goncalves, M.S.
The sickle cell disease (SCD) is a hemolytic genetic anemia characterized by free heme and hemoglobin release into intravascular spaces, with endothelial activation. Heme is a proinflammatory molecule able to directly activate vascular endothelium, thus, endothelial dysfunction and vascular disease ...
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