Combination therapy with a T mprss6 RNA i‐therapeutic and the oral iron chelator deferiprone additively diminishes secondary iron overload in a mouse model of β‐thalassemia intermedia
Author:
Affiliation:
1. Department of PathologyBoston Children's Hospital and Harvard Medical SchoolBoston Massachusetts
2. Alnylam Pharmaceuticals, Inc.Cambridge Massachusetts
3. Intrinsic Lifesciences, Inc.LaJolla California
Funder
Alnylam Pharmaceuticals
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajh.23934
Reference18 articles.
1. Hepcidin in iron overload disorders
2. Liver iron concentrations and urinary hepcidin in -thalassemia
3. A mouse model for beta 0-thalassemia.
4. Ineffective erythropoiesis in β-thalassemia is characterized by increased iron absorption mediated by down-regulation of hepcidin and up-regulation of ferroportin
5. Liver expression of hepcidin and other iron genes in two mouse models of beta‐thalassemia;Franceschi L;Haematologica,2006
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