| Literature DB >> 24589272 |
Laura Breda1, Stefano Rivella2.
Abstract
Use of new compound such as inhibitors of JAK2 or transforming growth factor β-like molecules might soon revolutionize the treatment of β-thalassemia and related disorders. However, this situation requires careful optimization, noting the potential for off-target immune suppression for JAK2 inhibitors and the lack of mechanistic insights for the use of the ligand trap soluble molecules that sequester ligands of activin receptor IIA and B.Entities:
Keywords: ACE-011; ACE-536; Hemoglobinopathies; JAK2; LY-2157299; Steady state; Stress and ineffective erythropoiesis; Transforming growth factor β
Mesh:
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Year: 2014 PMID: 24589272 PMCID: PMC3970239 DOI: 10.1016/j.hoc.2013.12.001
Source DB: PubMed Journal: Hematol Oncol Clin North Am ISSN: 0889-8588 Impact factor: 3.722