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- W2914912898 endingPage "182" @default.
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- W2914912898 abstract "Sickle cell disease (SCD) is a group of inherited blood disorders caused by mutations in the human β-globin gene, leading to the synthesis of abnormal hemoglobin S, chronic hemolysis, and oxidative stress. Inhibition of hemoglobin S polymerization by fetal hemoglobin holds the greatest promise for treating SCD. The transcription factor NRF2, is the master regulator of the cellular oxidative stress response and activator of fetal hemoglobin expression. In animal models, various small chemical molecules activate NRF2 and ameliorate the pathophysiology of SCD. This review discusses the mechanisms of NRF2 regulation and therapeutic strategies of NRF2 activation to design the treatment options for individuals with SCD." @default.
- W2914912898 created "2019-02-21" @default.
- W2914912898 creator A5007766399 @default.
- W2914912898 creator A5034939833 @default.
- W2914912898 creator A5046490615 @default.
- W2914912898 creator A5088349405 @default.
- W2914912898 creator A5088562010 @default.
- W2914912898 date "2019-01-23" @default.
- W2914912898 modified "2023-10-18" @default.
- W2914912898 title "Mechanisms of NRF2 activation to mediate fetal hemoglobin induction and protection against oxidative stress in sickle cell disease" @default.
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