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These recent developments, combined with our observation that complex II inhibition via the succinate dehydrogenase is a druggable and highly potent target for broad-spectrum antiviral inhibition, raise the possibility for the rapid establishment of novel broadly acting antiviral drugs
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Hoffer ME, Balaban C, Slade MD, Tsao JW, Hoffer B
This is possible because the reactions of the non-oxidative phase are readily reversible
The angiogenesis suppressor gene AKAP12 is under the epigenetic control of HDAC7 in endothelial cells
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