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There are two practical options presently available to assess neuronal activity and monitor electrical activity and/or metabolic flux
Mutations in the AUH gene result in the extremely rare autosomal recessive disorder referred to as 3-methylglutaconic aciduria, type 1 (MGCA1)
Unraveling cellular pathways contributing to drug-induced liver injury by dynamical modeling
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Phase 3 trial of semaglutide in metabolic dysfunction-associated steatohepatitis
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