Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/91941
Type: Artigo de periódico
Title: Hemoglobin Disorders And Endothelial Cell Interactions
Author: Conran N.
Costa F.F.
Abstract: Endothelial damage and inflammation make a significant contribution to the pathophysiology of sickle cell disease (SCD) and the β-thalassemia syndromes. Endothelial dysfunction and ensuing vasculopathy are implicated in pulmonary hypertension in the hemoglobinopathies and endothelial activation and endothelial-blood cell adhesion, accompanied by inflammatory processes and oxidative stress, are imperative to the vaso-occlusive process in SCD. Herein, we discuss the role that the endothelium plays in all of these processes and the effect that genetic modifiers and hydroxyurea therapy may have upon endothelial interactions. Therapies targeting the endothelium and endothelial interactions may represent a promising approach for treating these diseases. © 2009 The Canadian Society of Clinical Chemists.
Rights: fechado
Identifier DOI: 10.1016/j.clinbiochem.2009.06.024
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-70449726798&partnerID=40&md5=448d6d9ac161e35cd43a476281cb335b
Date Issue: 2009
Appears in Collections:Unicamp - Artigos e Outros Documentos

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