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Deletion of TMPRSS6 attenuates the phenotype in a mouse model of β-thalassemia.
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Exogenous iron increases hemoglobin in beta-thalassemic mice.
Exp Hematol. 2009 Feb;37(2):172-83. doi: 10.1016/j.exphem.2008.10.004. Epub 2008 Dec 6.

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Current Landscape of Hepcidin Therapeutics.
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Combination of a TGF-β ligand trap (RAP-GRL) and TMPRSS6-ASO is superior for correcting β-thalassemia.
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Normal and dysregulated crosstalk between iron metabolism and erythropoiesis.
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Thalassemia and Nanotheragnostics: Advanced Approaches for Diagnosis and Treatment.
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Mitapivat, a pyruvate kinase activator, improves transfusion burden and reduces iron overload in β-thalassemic mice.
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本文引用的文献

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β-thalassemias: paradigmatic diseases for scientific discoveries and development of innovative therapies.
Haematologica. 2015 Apr;100(4):418-30. doi: 10.3324/haematol.2014.114827.
3
Reducing TMPRSS6 ameliorates hemochromatosis and β-thalassemia in mice.
J Clin Invest. 2013 Apr;123(4):1531-41. doi: 10.1172/JCI66969. Epub 2013 Mar 25.
5
The role of ineffective erythropoiesis in non-transfusion-dependent thalassemia.
Blood Rev. 2012 Apr;26 Suppl 1(0 1):S12-5. doi: 10.1016/S0268-960X(12)70005-X.
7
β-thalassemia: a model for elucidating the dynamic regulation of ineffective erythropoiesis and iron metabolism.
Blood. 2011 Oct 20;118(16):4321-30. doi: 10.1182/blood-2011-03-283614. Epub 2011 Jul 18.
8
Decreased differentiation of erythroid cells exacerbates ineffective erythropoiesis in beta-thalassemia.
Blood. 2008 Aug 1;112(3):875-85. doi: 10.1182/blood-2007-12-126938. Epub 2008 May 14.
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Redistribution of accumulated cell iron: a modality of chelation with therapeutic implications.
Blood. 2008 Feb 1;111(3):1690-9. doi: 10.1182/blood-2007-07-102335. Epub 2007 Nov 1.

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