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Inflammation in Sickle Cell Disease: Differential and Down-Expressed Plasma Levels of Annexin A1 Protein
Sickle cell disease (SCD) is an inherited hemolytic anemia whose pathophysiology is driven by polymerization of the hemoglobin S (Hb S), leading to hemolysis and vaso-occlusive events. Inflammation is a fundamental component in these processes and a continuous inflammatory stimulus can lead to tissu...
Autores principales: | Torres, Lidiane S., Okumura, Jéssika V., Silva, Danilo G. H., Mimura, Kallyne K. O., Belini-Júnior, Édis, Oliveira, Renan G., Lobo, Clarisse L. C., Oliani, Sonia M., Bonini-Domingos, Claudia R. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089686/ https://www.ncbi.nlm.nih.gov/pubmed/27802331 http://dx.doi.org/10.1371/journal.pone.0165833 |
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