IRON HOMEOSTASIS DURING TRANSFUSIONAL IRON OVERLOAD IN β-THALASSEMIA AND SICKLE CELL DISEASE: Changes in Iron Regulatory Protein, Hepcidin, and Ferritin Expression-Reference-Cited by-同舟云学术

IRON HOMEOSTASIS DURING TRANSFUSIONAL IRON OVERLOAD IN β-THALASSEMIA AND SICKLE CELL DISEASE: Changes in Iron Regulatory Protein, Hepcidin, and Ferritin Expression

Published:2007-01 Issue:4 Volume:24 Page:237-243
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Jenkins Zandra A.,Hagar Ward,Bowlus Christopher L.,Johansson Hans E.,Harmatz Paul,Vichinsky Elliott P.,Theil Elizabeth C.

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1080/08880010701360700

Reference17 articles.

1. Hereditary Hemochromatosis — A New Look at an Old Disease

2. Consensus document for transfusion-related iron overload

3. DNA and mRNA elements with complementary responses to hemin, antioxidant inducers, and iron control ferritin-L expression

4. Combinatorial mRNA Regulation: Iron Regulatory Proteins and Iso-iron-responsive Elements (Iso-IREs)

5. Balancing Acts

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