TMPRSS6 as a Therapeutic Target for Disorders of Erythropoiesis and Iron Homeostasis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12325-022-02421-w.pdf
Reference76 articles.
1. Finberg KE, et al. Mutations in TMPRSS6 cause iron-refractory iron deficiency anemia (IRIDA). Nat Genet. 2008;40(5):569–71.
2. Du X, et al. The serine protease TMPRSS6 is required to sense iron deficiency. Science. 2008;320(5879):1088–92.
3. Zivot A, et al. Erythropoiesis: insights into pathophysiology and treatments in 2017. Mol Med (Cambridge, MA). 2018;24(1):11.
4. Haase VH. Hypoxia-inducible factor-prolyl hydroxylase inhibitors in the treatment of anemia of chronic kidney disease. Kidney Int Suppl (2011). 2021;11(1):8–25.
5. Suragani RN, et al. Transforming growth factor-beta superfamily ligand trap ACE-536 corrects anemia by promoting late-stage erythropoiesis. Nat Med. 2014;20(4):408–14.
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