Title : [Research progress of iron metabolism in phenotype modification of β-thalassemia].

Pub. Date : 2021 Jan 10

PMID : 33423253






3 Functional Relationships(s)
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1 Subsequently, by manipulating the expression of key genes in iron metabolism such as hepcidin and transferrin receptor, researchers have revealed that iron restriction can improve ineffective hematopoiesis and iron overload, which may provide a potential approach for the treatment of thalassemia. Iron transferrin receptor Homo sapiens
2 Subsequently, by manipulating the expression of key genes in iron metabolism such as hepcidin and transferrin receptor, researchers have revealed that iron restriction can improve ineffective hematopoiesis and iron overload, which may provide a potential approach for the treatment of thalassemia. Iron transferrin receptor Homo sapiens
3 Subsequently, by manipulating the expression of key genes in iron metabolism such as hepcidin and transferrin receptor, researchers have revealed that iron restriction can improve ineffective hematopoiesis and iron overload, which may provide a potential approach for the treatment of thalassemia. Iron transferrin receptor Homo sapiens