dystrophin信息详情
n.肌营养不良蛋白;抗肌萎缩蛋白
fuchs dystrophy───[医]富克斯营养不良
muscular dystrophy───n.肌肉萎缩症
corneal dystrophy───角膜营养不良
The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier.───肌营养不良卵白基因位于人类X染色体,携带基因突变的母亲会遗传给婴儿。
In the dystrophin gene, and in most of human genes, this genetic information is not contiguous.───在肌营养不良蛋白基因,在人类基因大多数,这种遗传信息不连续的。
is important to note, however, that different mutations in the dystrophin gene could require different oligonucleotide drugs.───重要的是要注意,不过,在不同的肌营养不良基因突变可能需要不同的寡核苷酸药物。
They are unable to produce a protein called dystrophin that keeps muscles strong.───患者体内不能产生一种保持肌肉强壮所需的“抗肌营养不良蛋白”(dystrophin)。
This enables the gene to produce a working version of the dystrophin gene.───这使得该基因产生的一个工作版本的抗肌营养不良蛋白基因。
It would not be suitable for treating different mutations in the dystrophin gene, or diseases not caused by nonsense mutations.───它对肌营养不良基因的其他类型的变异或非无意突变导致的疾病无效。
It is important to note that different mutations in the dystrophin gene require different oligonucleotide drugs.───重要的是要注意到,不同的突变,抗肌萎缩蛋白基因,需要不同的寡核苷酸药物。
DMD is caused by a mutation of the gene for dystrophin, a protein in the muscles.───DMD源于肌肉中一种称为肌营养不良蛋白的基因突变。
AVI-4658 is designed to benefit patients with certain mutations in the dystrophin gene.───4658设计用于改善病人肌营养不良蛋白基因中的特定突变。
Indeed, large deletions of this domain in dystrophin result in only a very mild phenotype.
Objective To investigate the significance on the expression of dystrophin in muscle tissue of the patients with myodystrophy.
Objective To detect dystrophin gene deletion of Duchenne muscular dystrophy ( DMD ) and make DMD gene diagnosis.
Absence of the carboxy terminus of dystrophin is associated with severe phenotypes in most muscular dystrophy patients.
The patients from 5 DMD and 2 BMD were detected by immunofluorescence technique for analyzing dystrophin located in muscle cell membrane, compared with 2 normal males.
None of the fibers expression dystrophin was stained with Evans blue.
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