Cargando…
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...
Autores principales: | Chaichompoo, Pornthip, Svasti, Saovaros, Smith, Duncan R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502731/ https://www.ncbi.nlm.nih.gov/pubmed/36142738 http://dx.doi.org/10.3390/ijms231810811 |
Ejemplares similares
-
Increased autophagy leads to decreased apoptosis during β-thalassaemic mouse and patient erythropoiesis
por: Chaichompoo, Pornthip, et al.
Publicado: (2022) -
Ineffective Erythropoiesis in β-Thalassemia
por: Ribeil, Jean-Antoine, et al.
Publicado: (2013) -
β-Thalassemia: HiJAKing Ineffective Erythropoiesis and Iron Overload
por: Melchiori, Luca, et al.
Publicado: (2010) -
Microparticles from β-thalassaemia/HbE patients induce endothelial cell dysfunction
por: Kheansaard, Wasinee, et al.
Publicado: (2018) -
Diagnosis of α-thalassaemia by colorimetric gap loop mediated isothermal amplification
por: Chumworathayee, Worakawee, et al.
Publicado: (2023)