The Roles of Mitophagy and Autophagy in Ineffective Erythropoiesis in β-Thalassemia
β-Thalassemia is one of the most common genetically inherited disorders worldwide, and it is characterized by defective β-globin chain synthesis leading to reduced or absent β-globin chains. The excess α-globin chains are the key factor leading to the death of differentiating erythroblasts in a proc...
Main Authors: | Pornthip Chaichompoo, Saovaros Svasti, Duncan R. Smith |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-09-01
|
Series: | International Journal of Molecular Sciences |
Subjects: | |
Online Access: | https://www.mdpi.com/1422-0067/23/18/10811 |
Similar Items
-
The interactions between ineffective erythropoiesis and ferroptosis in β-thalassemia
by: Siyang Lin, et al.
Published: (2024-02-01) -
The correlation between ineffective erythropoiesis biomarkers and development of extramedullary hematopoiesis in patients with thalassemia
by: Siriyakorn Chansai, et al.
Published: (2022-06-01) -
The Oral Ferroportin Inhibitor VIT-2763 Improves Erythropoiesis without Interfering with Iron Chelation Therapy in a Mouse Model of β-Thalassemia
by: Naja Nyffenegger, et al.
Published: (2021-01-01) -
Interleukin-1 involved in Apoptosis of Beta-Thalassemia/Hemoglobin E Erythroid Progenitor Cells
by: Umesh Prasad Gupta
Published: (2013-04-01) -
<i>In Vitro</i> Study of Ineffective Erythropoiesis in Thalassemia: Diverse Intrinsic Pathophysiological Features of Erythroid Cells Derived from Various Thalassemia Syndromes
by: Woratree Kaewsakulthong, et al.
Published: (2022-09-01)