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3
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Functional coding variation in recombinant inbred mouse lines reveals multiple serotonin transporter-associated phenotypes.重组近交系小鼠品系中的功能编码变异揭示了多种与血清素转运体相关的表型。
Proc Natl Acad Sci U S A. 2009 Feb 10;106(6):2047-52. doi: 10.1073/pnas.0809449106. Epub 2009 Jan 28.
2
Correlation analysis between genome-wide expression profiles and cytoarchitectural abnormalities in the prefrontal cortex of psychiatric disorders.精神疾病患者前额皮质全基因组表达谱与细胞构筑异常的相关性分析。
Mol Psychiatry. 2010 Mar;15(3):326-36. doi: 10.1038/mp.2008.99. Epub 2008 Sep 2.
3
An unbiased systems genetics approach to mapping genetic loci modulating susceptibility to severe streptococcal sepsis.一种用于定位调控严重链球菌败血症易感性的基因座的无偏系统遗传学方法。
PLoS Pathog. 2008 Apr 18;4(4):e1000042. doi: 10.1371/journal.ppat.1000042.
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Deficit of perineuronal oligodendrocytes in the prefrontal cortex in schizophrenia and mood disorders.精神分裂症和心境障碍患者前额叶皮质中神经元周围少突胶质细胞的缺失。
Schizophr Res. 2007 Aug;94(1-3):273-80. doi: 10.1016/j.schres.2007.04.014. Epub 2007 Jun 13.
5
SynDB: a Synapse protein DataBase based on synapse ontology.SynDB:基于突触本体论的突触蛋白数据库。
Nucleic Acids Res. 2007 Jan;35(Database issue):D737-41. doi: 10.1093/nar/gkl876. Epub 2006 Nov 10.
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An online database for brain disease research.一个用于脑部疾病研究的在线数据库。
BMC Genomics. 2006 Apr 4;7:70. doi: 10.1186/1471-2164-7-70.
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Myelin-associated mRNA and protein expression deficits in the anterior cingulate cortex and hippocampus in elderly schizophrenia patients.老年精神分裂症患者前扣带回皮质和海马中髓鞘相关mRNA及蛋白表达缺陷
Neurobiol Dis. 2006 Mar;21(3):531-40. doi: 10.1016/j.nbd.2005.08.012. Epub 2005 Oct 5.
8
Integrative neuroscience: the role of a standardized database.整合神经科学:标准化数据库的作用
Clin EEG Neurosci. 2005 Apr;36(2):64-75. doi: 10.1177/155005940503600205.
9
WebGestalt: an integrated system for exploring gene sets in various biological contexts.WebGestalt:一个用于在各种生物学背景下探索基因集的集成系统。
Nucleic Acids Res. 2005 Jul 1;33(Web Server issue):W741-8. doi: 10.1093/nar/gki475.
10
Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'.利用“遗传基因组学”揭示影响造血干细胞功能的调控途径。
Nat Genet. 2005 Mar;37(3):225-32. doi: 10.1038/ng1497. Epub 2005 Feb 13.

斯坦利神经病理学联合会综合数据库:一种新型的基于网络的工具,用于探索精神疾病中的神经病理学标志物以及与这些标志物异常相关的生物学过程。

The stanley neuropathology consortium integrative database: a novel, web-based tool for exploring neuropathological markers in psychiatric disorders and the biological processes associated with abnormalities of those markers.

机构信息

Stanley Brain Research Laboratory, Stanley Medical Research Institute, Medical Center Drive, Rockville, MD 20850, USA.

出版信息

Neuropsychopharmacology. 2010 Jan;35(2):473-82. doi: 10.1038/npp.2009.151.

DOI:10.1038/npp.2009.151
PMID:19829293
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3055386/
Abstract

An integrative database, Stanley Neuropathology Consortium Integrative Database (SNCID) (http://sncid.stanleyresearch.org), has been developed to facilitate psychiatric research. The SNCID includes 1749 neuropathological markers measured in 12 different brain regions in 60 human subjects (15 each schizophrenia, bipolar disorder, depression, and unaffected controls). Genome-wide expression microarray datasets from three independent studies are also included. Statistical analysis tools such as variance analysis, correlation analysis, and functional annotation tools have been integrated into the database. In this report, we first replicate an earlier correlation analysis between genome-wide expression profiles and an abnormal cytoarchitectural marker using the SNCID. We then show the potential for identifying neuropathological markers that are abnormal in subjects with psychiatric disorders. We also identify biological pathways associated with several abnormal neuropathological markers, including those in the dopamine, glutamate, Reelin, and gamma-aminobutyric acid (GABA)ergic systems. Data exploration using the SNCID may provide insights into the biological pathways associated with the neurotransmitter abnormalities identified in subjects with major psychiatric disorders.

摘要

一个综合性数据库,斯坦利神经病理学联合会综合数据库(SNCID)(http://sncid.stanleyresearch.org),已经被开发出来以促进精神疾病的研究。SNCID 包括 60 个人类样本(15 个精神分裂症、15 个双相情感障碍、15 个抑郁症和 15 个未受影响的对照组)中 12 个不同脑区的 1749 个神经病理学标记物。数据库还包括三个独立研究的全基因组表达微阵列数据集。方差分析、相关分析和功能注释工具等统计分析工具已被整合到数据库中。在本报告中,我们首先使用 SNCID 复制了之前关于全基因组表达谱与异常细胞结构标记物之间相关性的分析。然后,我们展示了识别精神疾病患者中异常神经病理学标记物的潜力。我们还确定了与几个异常神经病理学标记物相关的生物学途径,包括多巴胺、谷氨酸、Reelin 和γ-氨基丁酸(GABA)能系统。使用 SNCID 进行的数据探索可能会深入了解与主要精神疾病患者中神经递质异常相关的生物学途径。