Ontology highlight
ABSTRACT:
INSTRUMENT(S): LTQ Orbitrap Elite
ORGANISM(S): Homo Sapiens (human)
TISSUE(S): Blood Cell, Cell Culture
DISEASE(S): Thalassemia
SUBMITTER: Eleni Katsantoni
LAB HEAD: Eleni Katsantoni
PROVIDER: PXD006889 | Pride | 2020-01-23
REPOSITORIES: Pride
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Adria_1_3.raw | Raw | |||
Adria_1_4.raw | Raw | |||
Adria_1_ALL_NO_COISOLATION.msf | Msf | |||
Adria_1_REST.raw | Raw | |||
Adria_2_3.raw | Raw |
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Journal of clinical medicine 20200103 1
Reactivation of γ-globin is considered a promising approach for the treatment of β-thalassemia and sickle cell disease. Therapeutic induction of γ-globin expression, however, is fraught with lack of suitable therapeutic targets. The aim of this study was to investigate the effects that treatment with decitabine has on the proteome of human primary erythroid cells from healthy and thalassemic volunteers, as a means of identifying new potential pharmacological targets. Decitabine is a known γ-glob ...[more]