Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia Complications

Beta thalassemia major (βT) is a hereditary anemia characterized by transfusion-dependency, lifelong requirement of chelation, and organ dysfunction. MicroRNA (miRNA) can be packed into extracellular vesicles (EVs) that carry them to target cells. We explored EV-miRNA in βT and their pathophysiologi...

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Detalles Bibliográficos
Autores principales: Levin, Carina, Koren, Ariel, Rebibo-Sabbah, Annie, Levin, Maya, Koifman, Na’ama, Brenner, Benjamin, Aharon, Anat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465435/
https://www.ncbi.nlm.nih.gov/pubmed/34575936
http://dx.doi.org/10.3390/ijms22189760

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8465435/
https://www.ncbi.nlm.nih.gov/pubmed/34575936
http://dx.doi.org/10.3390/ijms22189760

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