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Single-nucleotide Polymorphism rs2275294 in ZNF512B is not Associated with Susceptibility to Amyotrophic Lateral Sclerosis in a Large Chinese Cohort 被引量:2
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作者 Xiao-Dong Ju Tao Liu +5 位作者 Jing Chen Xiao-Gang Li Xin-Xiu Liu Wen-Chao Liu Kai Wang Min Deng 《Chinese Medical Journal》 SCIE CAS CSCD 2015年第24期3305-3309,共5页
Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily affects motor neurons and has no effective treatment. Recently, Iida et al. identified a single-nucleotide polymor... Background: Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that primarily affects motor neurons and has no effective treatment. Recently, Iida et al. identified a single-nucleotide polymorphism (SNP) rs2275294 in the ZNF512B gene that is significantly associated with susceptibility to ALS in the Japanese population. Here, we performed a case-control study examining the possible association of rs2275294 with risk of sporadic ALS (SALS) in a large Chinese cohort. Methods: To assess this association, we performed a replication study in 953 SALS patients and 1039 age- and gender-matched healthy control subjects, who were recruited from Peking University Third Hospital and the First Affiliated Hospital of Anhui Medical University from January 2004 to December 2013 throughout China. We genotyped the rs2275294 SNP using polymerase chain reaction and direct sequencing. Results: The allele frequency of rs2275294 in ZNF512B was different between Japanese and Chinese. The association in Chinese between ALS patients and controls did not reach statistical significance (P = 0.54; odds ratio = 0.94; 95% confidence interval = 0.76-1.15). Conclusions: The SNP rs2275294 in ZNF512B is not considered to be associated with ALS susceptibility in the Chinese population. Our study highlights genetic heterogeneity in ALS susceptibility in different population. Given our negative results, further replication study involving larger and more homogeneous samples in different ethnicities should be performed in the future. 展开更多
关键词 Amyotrophic Lateral Sclerosis Genome Association Study Single-nucleotide Polymorphism znf512b
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锌指蛋白512B基因变异的肌萎缩侧索硬化1例报告 被引量:1
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作者 幸伟芳 洪铭范 《中国实用神经疾病杂志》 2018年第15期1729-1732,共4页
肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis,ALS)是运动神经元病中最常见的类型,以进行性加重的骨骼肌无力、萎缩、肌束颤动、延髓麻痹和锥体束征为主要临床表现。随着分子生物技术的飞速发展,对该病的研究取得了突破性进展。在FAL... 肌萎缩侧索硬化(Amyotrophic Lateral Sclerosis,ALS)是运动神经元病中最常见的类型,以进行性加重的骨骼肌无力、萎缩、肌束颤动、延髓麻痹和锥体束征为主要临床表现。随着分子生物技术的飞速发展,对该病的研究取得了突破性进展。在FALS的遗传学研究中,许多诱发ALS发病的易感基因已被确定,11种基因可以描述FALS的致病突变,包括SOD1、ALS2、VAPB、SETX、ANG、DCTN1、TARDBP、NEFH、FUS、DAO和OPTN。关于SALS的易感基因已有数十篇来自候选基因的相关研究报道,包括NEFH、ANG、APEX、HFE、PON、SMN1、SMN2和VEGF,对于SALS的基因研究极为重要。 展开更多
关键词 肌萎缩侧索硬化 肌原纤维肌病 znf512b基因 DES基因 易感基因
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