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10.1073/pnas.1509158112

http://scihub22266oqcxt.onion/10.1073/pnas.1509158112
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C4593117!4593117!26371321
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suck abstract from ncbi


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pmid26371321      Proc+Natl+Acad+Sci+U+S+A 2015 ; 112 (39): 12169-74
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  • Amelioration of inflammation and tissue damage in sickle cell model mice by Nrf2 activation #MMPMID26371321
  • Keleku-Lukwete N; Suzuki M; Otsuki A; Tsuchida K; Katayama S; Hayashi M; Naganuma E; Moriguchi T; Tanabe O; Engel JD; Imaizumi M; Yamamoto M
  • Proc Natl Acad Sci U S A 2015[Sep]; 112 (39): 12169-74 PMID26371321show ga
  • Sickle cell disease (SCD) is one of the most common inherited disorders. A mutation in the ?-globin gene causes deformation of red blood cells into a sickle shape, which in turn causes intravascular hemolysis and vaso-occlusion resulting in damage to multiple organs. Most studies that propose to develop new SCD therapies include the induction of fetal ?-globin expression to inhibit sickle cell formation as their ultimate goal. In contrast, we demonstrate here that activation of nuclear factor erythroid 2-related factor 2 (Nrf2) ameliorates the development of inflammation and tissue damage that strongly affect the morbidity of SCD patients. Notably, several compounds that serve as Nrf2 inducers have been developed or are under development. The data indicate that Nrf2 activation could improve the prognosis for SCD patients.
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