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Statistical methods for pathway analysis of genome-wide data for association with complex genetic traits.基于全基因组数据关联复杂遗传特征的通路分析的统计方法。
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Strong synaptic transmission impact by copy number variations in schizophrenia.精神分裂症中拷贝数变异对突触传递的强烈影响。
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To build a synapse: signaling pathways in neuromuscular junction assembly.建立突触:神经肌肉接头组装中的信号通路。
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The architecture of an excitatory synapse.兴奋性突触的结构。
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Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies.通过对缓解抑郁症的序贯治疗选择的全基因组关联研究以及三项研究的荟萃分析,确定了重度抑郁症的新基因座。
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Association study of PDE4B gene variants in Scandinavian schizophrenia and bipolar disorder multicenter case-control samples.PDE4B 基因变异与斯堪的纳维亚精神分裂症和双相情感障碍多中心病例对照研究。
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SynaptomeDB:基于本体的突触基因知识库。

SynaptomeDB: an ontology-based knowledgebase for synaptic genes.

机构信息

Department of Psychiatry and Behavioral Sciences, Johns Hopkins School of Medicine, MD, USA.

出版信息

Bioinformatics. 2012 Mar 15;28(6):897-9. doi: 10.1093/bioinformatics/bts040. Epub 2012 Jan 27.

DOI:10.1093/bioinformatics/bts040
PMID:22285564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3307115/
Abstract

MOTIVATION

The synapse is integral to the function of the brain and may be an important source of dysfunction underlying many neuropsychiatric disorders. Consequently, it is an excellent candidate for large-scale genomic and proteomic study. However, while the tools and databases available for the annotation of high-throughput DNA and protein are generally robust, a comprehensive resource dedicated to the integration of information about the synapse is lacking.

RESULTS

We present an integrated database, called SynaptomeDB, to retrieve and annotate genes comprising the synaptome. These genes encode components of the synapse including neurotransmitters and their receptors, adhesion/cytoskeletal proteins, scaffold proteins, membrane transporters. SynaptomeDB integrates various and complex data sources for synaptic genes and proteins.

摘要

动机

突触对于大脑的功能至关重要,并且可能是许多神经精神疾病功能障碍的重要来源。因此,它是大规模基因组和蛋白质组学研究的理想候选对象。然而,尽管用于注释高通量 DNA 和蛋白质的工具和数据库通常功能强大,但缺乏专门用于整合有关突触信息的综合资源。

结果

我们提出了一个名为 SynaptomeDB 的综合数据库,用于检索和注释组成突触体的基因。这些基因编码包括神经递质及其受体、黏附/细胞骨架蛋白、支架蛋白、膜转运蛋白在内的突触成分。SynaptomeDB 整合了突触基因和蛋白质的各种复杂数据源。