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Discussion The above results demonstrate the significant potential of MIPs as plastic antibody complements to established chemoaffinity-based (TiO 2 ) or bioaffinity-based (antibodies) phosphopeptide capture and enrichment techniques

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Among these postsynaptic adhesion molecules, some have been clearly identified that bind to neurexins, such as dystroglycans, LRRTMs, calsyntenins, latrophilins and neuroligins [26, 28], which are listed in Fig