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Pharmacological agents targeting 7nAChR Agonists of 7nAChRs function by directly stimulating these ligand-gated ion channel receptors, potentially offering therapeutic advantages for ASD

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While whether these two peak were resulted form the intracellular Ca 2+ release and the consequent extracellular Ca 2+ influx, or there were corresponding to the HB induced Ca 2+ signal and a subsequent neuronal firing are still need to be further investigated