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单词 dystrophin
释义

dystrophin /dis'trɔfin/

英汉-汉英词典
抗肌萎缩蛋白
词组 | 习惯用语
您要查找的是不是:
  • catastrophe n. 大灾难;大祸;彻底失败
  • stereophonic adj. 立体声的;立体效果的
  • dystrophy n. 营养不良;营养障碍
  • thyrotrophin n. 促甲状腺素,甲状腺刺激激素
dystrophin n. 肌营养不良蛋白;抗肌萎缩蛋白

网络短语:
dystrophin gene 它的基因;dystrophin基因;抗肌萎缩蛋白基因
dystrophin Dys 抗肌萎缩蛋白
Human dystrophin 人肌养蛋白
dystrophin related protein 抗肌萎缩蛋白相关蛋白
Human dystrophin ELISA 人肌养蛋白ELISA试剂盒
human dystrophin gene 人类肌营养不良基因
dystrophin associated proteins 相关蛋白
Sheep dystrophin ELISA KIT 绵羊肌养蛋白ELISA试剂盒
dystrophin related DGC proteins DGC关联复合物蛋白
英语例句库
  1. Abstract: Objective To investigate the significance on the expression of dystrophin in muscle tissue of the patients with myodystrophy.
    摘 要: 目的 探讨肌营养不良蛋白在肌营养不良症患者肌组织中表达的意义。

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原声例句
Osmosis-肌骨

Without the support of dystrophin in place, the sarcolemma essentially wilts and becomes unstable.

没有抗肌萎缩蛋白的支撑,肌膜塌缩变得不稳定。

Osmosis-肌骨

Okay, so as a quick recap: the protein dystrophin is super important for stabilizing the muscle cell membrane.

抗肌萎缩蛋白对肌纤维稳定性的维持极其重要。

Osmosis-肌骨

Alright, so the dystrophin gene is a huge gene on the X-chromosome, that has 79 exons and is over 2 million base pairs in length.

抗肌萎缩蛋白基因是X染色体上一个庞大的基因,含有79个外显子,全长超过2000kbp(书上通常缩写为bp,碱基对)。

Osmosis-肌骨

Now, the fact that both Duchenne and Becker muscular dystrophy result from mutations in the same dystrophin gene means that they are " allelic disorders, "

DMD和BMD都是由于同一抗肌萎缩蛋白基因突变引起的,意味着二者是“等位基因疾病”。

Osmosis-肌骨

Within that group, dystrophinopathies are the most common, which includes Duchenne muscular dystrophy, or DMD, and Becker muscular dystrophy, both of which result from mutations in the dystrophin gene.

这些功能紊乱中,营养不良疾病是最常见的,包括Duchenne型肌营养不良(DMD)和Becker型肌营养不良(BMD);这二者都是由抗肌萎缩蛋白基因突变导致的。

Osmosis-肌骨

In addition to those two, genetic mutations in other genes are responsible for several dozen other muscular dystrophies, some of which code for proteins that form a protein complex with dystrophin protein.

除了这两种疾病,其它基因的突变导致了其它几十种肌营养不良,其中一些基因编码形成抗肌萎缩蛋白相关蛋白复合体的蛋白质。

Osmosis-肌骨

Now if this inactivation's random, you'd expect about half of the female's cells to have a functional dystrophin gene and the other half to have a defective dystrophin gene, and these people are typically asymptomatic.

如果失活是随机的,可以预料到女性一半的细胞中抗肌萎缩蛋白基因是正常的,另一半是有缺陷的,通常这些人无临床症状。

Osmosis-肌骨

Having said that, if more cells end up with the defective dystrophin gene, and less with the functional one, they can end up being " manifesting carriers, " meaning that they manifest or show some symptoms.

话虽如此,如果机体中有该基因缺陷的细胞更多,而正常基因更少,这一类人群就是“显性携带者”,意味着他们也会有部分症状表现。

Osmosis-肌骨

Later symptoms include needing a wheelchair because of severe weakness, developing respiratory failure because of a weak diaphragm, scoliosis, and developing dilated cardiomyopathy and arrhythmias since the dystrophin protein is also expressed in heart muscle.

后期症状包括,由于严重的肌无力需坐轮椅,由于膈肌无力会发生呼吸衰竭、脊柱侧凸,因为抗肌萎缩蛋白也表达于心肌纤维,还会引发扩张型心肌病和心律失常。

英语百科

Dystrophin

Dystrophin is a rod-shaped cytoplasmic protein, and a vital part of a protein complex that connects the cytoskeleton of a muscle fiber to the surrounding extracellular matrix through the cell membrane. This complex is variously known as the costamere or the dystrophin-associated protein complex. Many muscle proteins, such as α-dystrobrevin, syncoilin, synemin, sarcoglycan, dystroglycan, and sarcospan, colocalize with dystrophin at the costamere.

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更新时间:2025/6/20 4:37:22