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Synergistic silencing of α-globin and induction of γ-globin by histone deacetylase inhibitor, vorinostat as a potential therapy for β-thalassaemia

β-Thalassaemia is one of the most common monogenic diseases with no effective cure in the majority of patients. Unbalanced production of α-globin in the presence of defective synthesis of β-globin is the primary mechanism for anaemia in β-thalassaemia. Clinical genetic data accumulated over three de...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Mettananda, Sachith, Yasara, Nirmani, Fisher, Christopher A., Taylor, Stephen, Gibbons, Richard, Higgs, Doug
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6690964/
https://ncbi.nlm.nih.gov/pubmed/31406232
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-48204-2
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