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UTILITY AND VALIDITY OF DISC1 MOUSE MODELS IN BIOLOGICAL PSYCHIATRY

期刊

NEUROSCIENCE
卷 321, 期 -, 页码 99-107

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2015.12.061

关键词

DISC1; mouse models; psychiatry

资金

  1. NIH [MH-084018, MH-094268, MH-069853, MH-085226, MH-088753, MH-092443]
  2. Stanley
  3. S-R
  4. RUSK
  5. NARSAD
  6. Maryland Stem Cell Research Fund
  7. DOD/CDMRP [W81XWH-11-1-0269]
  8. Takeda Pharmaceutical Co. Ltd at the Kyoto University

向作者/读者索取更多资源

We have seen an era of explosive progress in translating neurobiology into etiological understanding of mental disorders for the past 10-15 years. The discovery of Disrupted-in-schizophrenia 1 (DISC1) gene was one of the major driving forces that have contributed to the progress. The finding that DISC1 plays crucial roles in neuro-development and synapse regulation clearly underscored the utility and validity of DISC1-related biology in advancing our understanding of pathophysiological processes underlying psychiatric conditions. Despite recent genetic studies that failed to identify DISC1 as a risk gene for sporadic cases of schizophrenia, DISC1 mutant mice, coupled with various environmental stressors, have proven successful in satisfying face validity as models of a wide range of human psychiatric conditions. Investigating mental disorders using these models is expected to further contribute to the circuit-level understanding of the pathological mechanisms, as well as to the development of novel therapeutic strategies in the future. This article is part of a Special Issue entitled: Neuropsychiatric Disease. (C) 2016 IBRO. Published by Elsevier Ltd. All rights reserved.

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