[HTML][HTML] Activation of STAT and SMAD signaling induces hepcidin re-expression as a therapeutic target for β-Thalassemia patients

HKM Saad, AA Abd Rahman, AS Ab Ghani, WRW Taib… - Biomedicines, 2022 - mdpi.com
Iron homeostasis is regulated by hepcidin, a hepatic hormone that controls dietary iron
absorption and plasma iron concentration. Hepcidin binds to the only known iron export …

[HTML][HTML] HBB gene mutations and their pathological impacts on HbE/β-Thalassaemia in Kuala Terengganu, Malaysia

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 …

[HTML][HTML] Reduced hepcidin expression enhances iron overload in patients with HbE/β‑thalassemia: Α comparative cross‑sectional study

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 …

[HTML][HTML] Gene‒environment interaction effect of hypothalamic‒pituitary‒adrenal axis gene polymorphisms and job stress on the risk of sleep disturbances

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 …

[HTML][HTML] Genetic background studies of eight common beta thalassemia mutations in Thailand using β-globin gene haplotype and phylogenetic analysis

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 …