[HTML][HTML] Protective effect of fucoidan against iron overload and ferroptosis-induced liver injury in rats exposed to alcohol

M Xue, Y Tian, Y Sui, H Zhao, H Gao, H Liang… - Biomedicine & …, 2022 - Elsevier
This study was aimed to explore the effects of fucoidan on iron overload and ferroptosis-
induced liver injury, and the underlying mechanisms in rats exposed to alcohol. Sprague …

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 …

CHEK1 and GFPT1 as potential blood-based biomarkers for colorectal cancer

H Faroque, NS Aria, NA Muzilah, HAN Al-Jamal… - The Indonesian …, 2023 - inabj.org
BACKGROUND: The checkpoint kinase 1 (CHEK1) and glutamine-fructose-6-phosphate
aminotransferase 1 (GFPT1) genes have been reported to have a crucial role in …

Active Components of Pueraria lobata through the MAPK/ERK Signaling Pathway Alleviate Iron Overload in Alcoholic Liver Disease

X Li, L Liu, MX Wan, LM Gong, J Su… - Chemistry & …, 2024 - Wiley Online Library
Objective: To delve into the primary active ingredients and mechanism of Pueraria lobata for
alleviating iron overload in alcoholic liver disease. Methods: Pueraria lobata's potential …

Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients

MF Sokkar, M Hamdy, MB Taher, H El-Sayed… - Biochemical …, 2024 - Springer
Iron loading is regarded as the primary cause of endocrine abnormalities in thalassemia
major patients. Thus, the purpose of the current research was to explore the impact of …

Hepcidin levels, markers of iron overload, and liver damage in children with beta-thalassemia major

I Sari, DP Sari, M Damayanti… - Paediatrica …, 2024 - paediatricaindonesiana.org
Background Thalassemia is a hemoglobin synthesis disorder that causes patients to need
lifelong blood transfusions, leading to iron overload and alter organ function, including the …

[PDF][PDF] Correlation between Hepcidin and FSH in β-Thalassemia Major in Baghdad City

MM Hasan, AA Mahdi, NS Mohammed - researchgate.net
In spite of recent advances in iron overload, elevate iron deposition in pituitary gonadotropic
cells keep on one of the main complications in thalassemic patients. Hypogonadism, mainly …