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      Disrupted-in-schizophrenia 1 protein aggregates in cerebrospinal fluid are elevated in patients with first-episode psychosis.

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          Abstract

          The disrupted-in-schizophrenia 1 (DISC1) protein is a key regulator at the intersection of major signaling pathways relevant for adaptive behavior. It is prone to posttranslational changes such as misassembly and aggregation but the significance of such transformations for human mental illness has remained unclear. We aimed to demonstrate the occurrence of DISC1 protein aggregates in patients with first-episode psychosis (FEP).

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          Author and article information

          Journal
          Psychiatry Clin Neurosci
          Psychiatry and clinical neurosciences
          Wiley
          1440-1819
          1323-1316
          Dec 2023
          : 77
          : 12
          Affiliations
          [1 ] Institute of Biological Information Processing (Structural Biochemistry: IBI-7), Forschungszentrum Jülich, Jülich, Germany.
          [2 ] attyloid GmbH, Düsseldorf, Germany.
          [3 ] Department of Neuropathology, Heinrich Heine University of Düsseldorf, Düsseldorf, Germany.
          [4 ] Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
          [5 ] Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
          [6 ] Department of Neurology, Karolinska University Hospital, Stockholm, Sweden.
          [7 ] Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, and Stockholm Health Care Services, Region Stockholm, Stockholm, Sweden.
          [8 ] Department of Medical Sciences, Psychiatry, Uppsala University, Uppsala, Sweden.
          [9 ] Institut für Physikalische Biologie, Heinrich-Heine-Universität Düsseldorf, Düsseldorf, Germany.
          Article
          10.1111/pcn.13594
          37668563
          02d996f4-ad15-4f11-bb3c-33b5920831eb
          History

          cerebrospinal fluid,disrupted-in-schizophrenia 1 protein,pathomechanisms,schizophrenia,biomarker

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