HKM Saad, WRW Taib, AS Ab Ghani, I Ismail… - Diagnostics, 2023 - mdpi.com
Background: β-thalassaemia is a disorder caused by mutations in the β-globin gene, leading to defective production of haemoglobins (Hb) and red blood cells (RBCs). It is characterised …
HKM Saad, WRW Taib, I Ismail… - Experimental and …, 2021 - spandidos-publications.com
Iron homeostasis is regulated by hepcidin (HEPC) that controls the dietary iron absorption and iron recycling. HEPC deficiency contributes to iron overload in β‑thalassemia patients …
M Zhao, Y Wang, Y Zeng, H Huang, T Xu, B Liu, C Wu… - PeerJ, 2024 - peerj.com
Background Studies have shown that chronic exposure to job stress may increase the risk of sleep disturbances and that hypothalamic‒pituitary‒adrenal (HPA) axis gene …
R Karnpean, W Tepakhan, P Suankul, S Thingphom… - Genes, 2022 - mdpi.com
Single nucleotide polymorphisms are informative for haplotype analysis associated with genetic background and clinical linkage studies of β-thalassemia mutations. Hence, the aim …