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Arteel 1 and Michael Merchant 3 , (1)University of Pittsburgh, (2)Juntendo University School of Medicine, (3)University of Louisville, Louisville, KY, (4)University of Florida, (5)Northwestern University Feinberg Scho Background: Non-alcoholic steatohepatitis (NASH)-associated cirrhosis is an indication for liver transplant (LT)

In contrast, Cx32 has been reported the protective effects against APAP-induced liver toxicity by transporting GSH between hepatocytes, although the outcomes have been somewhat contradictory (Igarashi et al

In the 13 studies (Figure 2) that reported hospital mortality, a significant reduction in hospital mortality was seen when they were aggregated (RR 0.68, 95% CI 0.51, 0.90, P = 0.008, heterogeneity I 2 = 0%)

Methods: High coverage whole exome sequencing and variant identification and annotation were performed by the Regeneron Genetics Center as published previously (N Engl J Med 2022