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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
Jung, S
2018) using an online software tool for method comparison and bias detection (Bahar et al
Pseudobulking metabolite signals for differential abundance analysis One key analysis method for SM data is the ability to compare the abundance levels of metabolites across spatial regions
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