Cellular and animal models for the investigation of β-thalassemia-Reference-Cited by-同舟云学术

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Cellular and animal models for the investigation of β-thalassemia

Published:2024-01 Issue: Volume:104 Page:102761
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Nai Antonella,Cordero-Sanchez Celia,Tanzi Emanuele,Pagani Alessia,Silvestri Laura,Di Modica Simona Maria

Funder

European Hematology Association

Ministero della Salute

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference124 articles.

1. Changing patterns in the epidemiology of beta-thalassemia;Kattamis;Eur. J. Haematol.,2020

2. Ineffective erythropoiesis and regulation of iron status in iron loading anaemias;Camaschella;Br. J. Haematol.,2016

3. Identification of erythroferrone as an erythroid regulator of iron metabolism;Kautz;Nat. Genet.,2014

4. Erythroferrone contributes to hepcidin suppression and iron overload in a mouse model of beta-thalassemia;Kautz;Blood,2015

5. Hypoxia-inducible factor regulates hepcidin via erythropoietin-induced erythropoiesis;Liu;J. Clin. Invest.,2012

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Bone marrow Tfr2 deletion improves the therapeutic efficacy of the activin‐receptor ligand trap RAP‐536 in β‐thalassemic mice;American Journal of Hematology;2024-04-17

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