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FDR calculation is based on a target-Decoy approach, and the acceptance threshold is set to 0.01

These results can strongly argue that SRB have not triggered immune escape, chronic inflammation, and tissue damage, alleviating concerns regarding the biosafety of bacterial therapy based on SRB

Dihexa and Nle1-AngIV treated neurons were immunostained for the universal presynaptic marker synapsin and the glutamatergic presynaptic marker VGLUT1