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Exogenous itaconate addition in apolipoprotein E-deficient (Apoe−/−) mice suppressed the initiation and development of AAA and downstream inflammatory protein although Irg1 deficiency reverted the influence of inhibitory. Overexpression of Keap1 or transferred Cys151S mutant Keap1 vector also abolished the activation of Nrf2 induced by itaconat

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