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中国人群中RTN4R基因的遗传多态性与精神分裂症之间无关联。

No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.

作者信息

Meng J, Shi Y, Zhao X, Guo S, Wang H, Zheng Y, Tang R, Feng G, Gu N, Liu H, Zhu S, He L

机构信息

Bio-X Center, Shanghai Jiao Tong University, Shanghai, PR China.

出版信息

J Neural Transm (Vienna). 2007 Feb;114(2):249-54. doi: 10.1007/s00702-006-0538-y. Epub 2006 Aug 10.

Abstract

The RTN4R gene is located in the 22q11 region and it encodes a subunit of the receptor complex (RTN4R-p75NTR) which results in neuronal growth inhibitory signals in response to Nogo-66, MAG or OMG signaling. Previous studies have suggested that RTN4R might act as a potential candidate for schizophrenia susceptibility loci. We genotyped four SNPs within the gene and conducted a case-control study and TDT analysis, involving 707 schizophrenic patients, 689 controls and 372 unrelated small nuclear families with schizophrenic offspring in the Chinese population. We examined allele and genotype frequencies and haplotype distributions in both family- and nonfamily-based samples. Our results suggest that there is no significant association between the genetic polymorphisms and schizophrenia in the Han Chinese population.

摘要

RTN4R基因位于22q11区域,它编码受体复合物(RTN4R - p75NTR)的一个亚基,该亚基在响应Nogo - 66、MAG或OMG信号时产生神经元生长抑制信号。先前的研究表明,RTN4R可能是精神分裂症易感基因座的潜在候选基因。我们对该基因内的四个单核苷酸多态性(SNP)进行了基因分型,并在中国人群中进行了病例对照研究和传递不平衡检验(TDT)分析,涉及707名精神分裂症患者、689名对照以及372个有精神分裂症后代的无关小核家庭。我们检测了基于家庭和非家庭样本中的等位基因和基因型频率以及单倍型分布。我们的结果表明,在汉族人群中,基因多态性与精神分裂症之间没有显著关联。

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