concomitant viral infection may exacerbate existing symptoms of infection and cause the failure of multiple organs [3, 9, 10, 46]
Similarly, exposure to methylglyoxal, a reactive dicarbonyl compound formed as a metabolic byproduct of glycolysis, has been shown to inhibit glycolysis, leading to a reduction in ATP and GSH concentrations
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showed that combination of a single transcription factor FOXA1, FOXA2, or FOXA3 with six compound cocktails, including CHIR, RepSox, valproic acid (VPA), Parnate, TTNPB, Dznep (termed CRVPTD), directly induced MEFs into iHeps ( Later studies developed protocols independent of ectopic expression for direct reprogramming
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Notably, all these experimental studies have certain limitations in their design