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There is no obvious similarity in chemical structure among all of these substances, but they have in common the ability to stimulate the pentose phosphate pathway in red blood cells, which must mean that they are able to oxidize NADPH directly or indirectly

287 Paradoxically, animal models of NAFLD and NASH treated with low-dose doxorubicin exhibited moderate p53 activation, decreased inflammation and lipogenesis, and alleviated liver damage, which improved steatohepatitis and nonalcoholic steatosis caused by the diet

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