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In the murine NASH model, Linafexor treatment led to significant reductions in liver steatosis, inflammation, and fibrosis across all dosages, with the 0.3 mg/kg dose showing the greatest efficacy
McKennas laboratory was supported in part by NIH Grants 5P01 HD016596 and P01 HD085928
Furthermore, LL-37 itself can become a target of autoantibodies in lupus
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