Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia Complications
Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia Complications
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Basel: MDPI AG
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Language
English
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Basel: MDPI AG
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Contents
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 pathophysiologic role. Circulating EVs were isolated from 35 βT-p...
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Full title
Extracellular Vesicle MicroRNA That Are Involved in β-Thalassemia Complications
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8465435
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8465435
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ISSN
1422-0067,1661-6596
E-ISSN
1422-0067
DOI
10.3390/ijms22189760
