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Disease biomarkers for schizophrenia reverted by anti-psychotic drug administration: six-plex quantitative phosphoproteomics of prefrontal cortex synaptosomes

机译:通过抗精神病药物管理疾病进行精神分裂症的疾病生物标志物:前额叶皮质突触瘤的六个plex定量磷蛋白酶组织

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Neuronal phosphorylation processes were identified as biomarkers in a schizophrenia disease model, and reverted after administration of anti-psychotic drugs. Large-scale multiplex quantitative phosphoproteomics where demonstrated suitable for disease biomarker discovery. Reversion of phosphorylationsites by antipsychotic treatment demonstrates their potential as biomarkers to monitor disease and drug efficacy. Both well-known and novel phoshopeptides were modulated in the schizophrenia disease model, and reverted in response to treatment e.g. proteins related to synaptic neurosignalling, neurogenesis, the glutamate receptor pathway and the neuronal cytoskeleton.
机译:神经元磷酸化方法被鉴定为精神分裂症疾病模型中的生物标志物,并在施用抗精神病药物后再次恢复。大规模多重定量磷蛋白蛋白质,其证明适合疾病生物标志物发现。通过抗精神病药治疗磷酸化物的逆转证明了它们作为生物标志物的潜力,以监测疾病和药物功效。众所周知的和新的酚孔肽肽在精神分裂症疾病模型中调节,并响应于治疗而恢复。蛋白质与突触神经痛,神经发生,谷氨酸受体途径和神经元细胞骨架相关。

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