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...

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Detalles Bibliográficos
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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Research Article
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

Internet

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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