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- Keywords Spinal muscular atrophy;Survival motor neuron gene （SMN）; 脊髓性肌肉萎缩症;运动神经元生存基因;基因诊断;
- Detection of survival motor neuron gene deletions using allele-specific amplification in patients with spinal muscular atrophy 等位基因特异性扩增法检测脊髓性肌萎缩运动神经元生存基因缺失
- Keywords spinal muscular atrophy survival motor neuron gene denaturing high performance liquid chromatography gene deletion; 脊髓性肌萎缩症运动;神经元生存基因;变性高效液相色谱技术;基因缺失;
- survival motor neuronal gene 运动神经元存活基因
- Survival motor neuron gene 运动神经元生存基因
- Objective This study examined the prevalence of deletion and subtle mutations of survival motor neuron( SMN) gene in children with spinal muscular atrophy( SMA). 目的研究儿童型脊肌萎缩症(MA)者中运动神经元生存基因缺失与微突变情况。
- Objective To investigate the relationship between survival motor neuron(SMN)gene and the clinical features of childhood spinal muscular atrophy(SMA). 目的探讨运动神经元存活基因与儿童期脊肌萎缩症临床特征的关系。
- Objective To investigate the relationship between survival motor neuron( SMN) gene and the clinical features of childhood spinal muscular atrophy( SMA). 目的探讨运动神经元存活基因与儿童期脊肌萎缩症临床特征的关系。
- Objective To study survival motor neuron (SMN) deletion in adult-onset patients with spinal muscular atrophy (SMA). 目的探讨成年起病的脊肌萎缩症(SMA)患者的运动神经元存活基因SMN的缺失情况。
- The relationship between the distrabution,constraction and function of survival motor neuron (SMN) protein and spinal muscular atrophy (SMA) has been reviewed in this paper. 本文着重就SMN蛋白分布、结构、功能及其与脊髓性肌萎缩症(SMA)的关系进行了综述。
- Keywords survival motor neuron （SMN） protein;spinal muscular atrophy;gene;expression; 运动神经元生存（SMN）蛋白;脊髓性肌萎缩症;基因;表达;
- Keywords spinal muscular atrophy;infantile;survival motor neuron（SMN） gene;PCR;prenatal gene diagnosis; 关键词脊肌萎缩症;婴儿型;SMN基因;PCR;产前基因诊断;
- Keywords Spinal muscular atrophy;cytoskeletal protein;survival motor neuron protein; 脊髓性肌萎缩症;细胞骨架蛋白;运动神经元生存蛋白;
- survival motor neuron 活运动神经元
- Each of the 100 microwires lay beside a single motor neuron. 那100根金属丝每一根都靠近单一个运动神经元；
- When facing the problem of dyspnea, patients of motor neuron disease could still expect a long term survival if they choose to accept tracheostomy and artificial ventilation. 摘要俗称渐冻人的运动神经元疾病患者，选择气切后仍有可能存活相当长的时间。
- Weakened muscle with less than normal tone. A lower motor neuron symptom . 一种较低的运动神经元症状，肌肉比正常的还要衰弱。
- Gliosis around motor neurons was seen. 神经元周围胶质细胞增生。
- A typical result of an upper motor neuron lesion is paralysis of voluntary movement. 典型的上位运动神经之损伤就会导致随意运动麻痹。
- Spinal and bulbar muscular atrophy (SBMA) is an adult form of X-linked motor neuron disease caused by an expansion of a CAG repeat sequence in the first exon of the androgen receptor (AR) gene. 脊髓延髓肌萎缩症(SBMA)是雄激素受体(AR)基因的CAG重复序列扩增引起的X连锁运动神经元病。
