Apohemoglobin-haptoglobin complex alleviates iron toxicity in mice with β-thalassemia via scavenging of cell-free hemoglobin and heme

Author:

Munoz Carlos J.,Pires Ivan S.,Jani Vinay,Gopal Srila,Palmer Andre F.,Cabrales PedroORCID

Publisher

Elsevier BV

Subject

Pharmacology,General Medicine

Reference50 articles.

1. The inherited diseases of hemoglobin are an emerging global health burden;Weatherall;Blood,2010

2. Beta-thalassemia;Galanello;Orphanet J. Rare Dis.,2010

3. Thalassemia review: features, dental considerations and management;Helmi;Electron Physician,2017

4. Thalassemia, extramedullary hematopoiesis, and spinal cord compression: a case report;Bukhari;Surg. Neurol. Int,2016

5. Iron overload in beta thalassemia: a review;Prabhu;J. Biosci. Technol.,2009

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Toxic side-effects of diaspirin cross-linked human hemoglobin are attenuated by the apohemoglobin-haptoglobin complex;Biomedicine & Pharmacotherapy;2024-05

2. Accelerated atherosclerosis in beta-thalassemia;American Journal of Physiology-Heart and Circulatory Physiology;2023-11-01

3. Engineering Therapeutics to Detoxify Hemoglobin, Heme, and Iron;Annual Review of Biomedical Engineering;2023-06-08

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