| Literature DB >> 15204104 |
Hua Cao1.
Abstract
A number of pharmacological agents are currently available for the induction of the fetal hemoglobin (Hb F) to treat the patients with sickle cell disease and beta-thalassemia. In the present review, we summarized the investigation and development of these Hb F-inducing agents and introduced histone deacetylase inhibitors as the new strategy to induce Hb F to treat the hemoglobin disorders Copyright 2004 Taylor and Francis LtdEntities:
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Year: 2004 PMID: 15204104 DOI: 10.1080/10245330410001701512
Source DB: PubMed Journal: Hematology ISSN: 1024-5332 Impact factor: 2.269