Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Alawiyah Awang Abd Rahman"'
Autor:
Hanan Kamel M. Saad, Wan Rohani Wan Taib, Azly Sumanty Ab Ghani, Imilia Ismail, Futoon Abedrabbu Al-Rawashde, Belal Almajali, Maysa Alhawamdeh, Alawiyah Awang Abd Rahman, Abdullah Saleh Al-wajeeh, Hamid Ali Nagi Al-Jamal
Publikováno v:
Diagnostics, Vol 13, Iss 7, p 1247 (2023)
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 by anaemia, ineffective erythropoiesis, and iron overload. Patie
Externí odkaz:
https://doaj.org/article/02a0af964a2a4d96b6915aaf84db6309
Autor:
Hanan Kamel M. Saad, Alawiyah Awang Abd Rahman, Azly Sumanty Ab Ghani, Wan Rohani Wan Taib, Imilia Ismail, Muhammad Farid Johan, Abdullah Saleh Al-Wajeeh, Hamid Ali Nagi Al-Jamal
Publikováno v:
Biomedicines, Vol 10, Iss 1, p 189 (2022)
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 protein, ferroportin (FPN), which regulates its expression. The major facto
Externí odkaz:
https://doaj.org/article/acd8c0c169264173ab759391aa6a460b