- 更多网络例句与脊髓小脑性共济失调相关的网络例句 [注：此内容来源于网络，仅供参考]
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Objective To study the gene mutation of the spinocerebellar ataxia（SCA types 1～3 in the patients with primary dystonia.
目的 研究原发性肌张力障碍患者脊髓小脑性共济失调1～3型基因的突变。
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Spinocerebellar ataxia Olivopontocerebellar atrophy Retinal pigmental degeneration Trinucleotide repeat
脊髓小脑性共济失调；橄榄桥脑小脑萎缩；视网膜色素变性；三核苷酸重复
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Objective To construct spinocerebellar ataxia 3 (SCA3) eukarotic expression vector with en hanced green fluorescent protein as report gene and to observe its expression in PC12 cells.
目的 构建以增强型绿色荧光蛋白作为报告基因、带有脊髓小脑性共济失调3型(SCA3)基因的真核细胞表达载体，并转染PC12细胞，观察外源基因的表达情况。
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Objective To study the gene mutation characteristics of patients with spinocerebellar ataxias in Ningxia region.
目的 研究宁夏地区脊髓小脑性共济失调患者基因突变的特征。
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Objective To determine the frequency of different subtypes of spinocerebellar ataxias in the Han nationality of Hunan province in China.
目的：研究湖南汉族人群中脊髓小脑性共济失调不同基因亚型的分布状况。
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Spinocerebellar ataxias are a group of autosomal dominant cerebellar degenerative disorders, which are characterized by clinical and genetic variability.
脊髓小脑性共济失调是一组常染色体显性的小脑退行性病，具有临床和遗传多样性。
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We investigated the clinical features and gene mutation in a pedigree of spinocerebellar ataxia.
对一脊髓小脑性共济失调(Spinocerebenllar ataxia， SCA)家系的患者进行临床特征及相关基因突变研究。
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Spinocerebellar ataxia type 7 (SCA7) is less variable in clinical presentation than other SCAs.
脊髓小脑性共济失调7型（SCA7）的临床表现形式较其它SCA类型少。
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Ataxin-1 is another pathogenic protein which causes a disease called spinocerebellar ataxia, which is also an incurable hereditary nervous disorder.
Ataxin-1是另一种致病蛋白，它能够引起脊髓小脑性共济失调，也是一种不能治愈的遗传性神经系统疾病。
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Objective To study the frequency distribution of spinocerebellar ataxia type 17 in mainland China and the normal range of CAG/CAA repeats of TATA-binding protein gene in Han population in southern China.
目的 研究中国大陆脊髓小脑性共济失调（spinocerebellar ataxias，SCA）17型（SCA17）的分布频率，以及南方汉族健康人群TATA结合蛋白（TATA-binding protein，TBP）基因CAG/CAA重复次数正常变异范围。
- 更多网络解释与脊髓小脑性共济失调相关的网络解释 [注：此内容来源于网络，仅供参考]
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Spinocerebellar ataxia：脊髓小脑性共济失调
在这项新的研究中,为了弄清miRNA途径是否在神经退化过程中起到一定的作用,研究人员分析了对miRNA加工过程很关键的基因如何调节由III型脊髓小脑性共济失调(spinocerebellar ataxia)蛋白诱导的毒性.
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spinocerebellar degeneration：脊髓小脑变性
spinocerebellar ataxia 脊髓小脑性共济失调 | spinocerebellar degeneration 脊髓小脑变性 | spinocervicothalamic tract脊顶丘脑束