lysosomal

lysosomal

美 　英

• adj.溶酶体的
• 网络溶小体；溶解酵素；溶菌体

英汉解释

adj.

1. 溶酶体的

例句

We report on a case of a deforming arthropathy in a young man with a lysosomal storage disorder.

我们报告一例变形性关节病中的一名年轻男子的溶酶体储存障碍。

Defects in the breakdown of gangliosides are associated with a class of disorders known as lysosomal storage diseases.

神经节苷脂的缺乏直接与一系列疾病有关，比如溶酶体贮积症。

Detailed analysis of complex lipids emphasizes the dissimilarity between the composition of lysosomal and plasma membranes.

复合磷脂的详细分析明显地表明了溶酶体膜与质膜的不同。

Moreover, APS inhibited mitochondrial membrane potential collapse, protected mitochondrial morphology and stablized lysosomal membrane.

而且，黄芪多糖能够抑制线粒体膜电位崩解保护线粒体形态，保护溶酶体膜。

According to its role of waste from different sources, is divided into autophagic lysosome and differences of lysosomal macrophages.

根据其作用废物的来源不同，分为自噬性溶酶体和异噬性溶酶体。

This could be helpful for other neurodegenerative disorders that also have lysosomal involvement, he says.

这也可能用于治疗其他有溶酶体介入神经退行性疾病，她说。

Released kidney lysosomal enzymes may be concerned in the generation of erythropoietin.

释放的肾脏溶酶体的酶可能与产生促红细胞生成素有关。

Here we show that lysosomal storage impairs autophagic delivery of bulk cytosolic contents to lysosomes.

这里我们说明溶酶体贮积损害了自噬性运送大量细胞溶质的内容物到溶酶体。

Cathepsins belong to the most abundant lysosomal enzymes and are involved in degradation processes.

组织蛋白酶属于最丰富的溶酶体酶和退化过程中所涉及。

Such deficiencies cause lysosomal storage disorders, such as Gaucher's disease, and replacement of the gene is an effective treatment.

这样的缺陷引起溶酶体堆积病（例如，高歇病），基因置换是一种有效的疗法。

Autophagy is a lysosomal degradation pathway that is essential for survival, differentiation, development, and homeostasis.

细胞自噬是一种溶酶体降解通道，其为存活，分化，发展和动态平衡所必需。

these enzymes are congenitally absent in sufferers of lysosomal storage diseases.

在溶酶体储存病患者中，天生缺乏这些酶。

Expertise in lysosomal targeting would typically be proposed to enter the project in year 3.

溶酶体靶标的专门技术将作为典型被建议进入第3年的项目中。

Sonication not only breaks lysosomal membranes but also releases some materials from the membrane.

超声处理不仅打碎了溶酶体的膜，还从膜上释放出某些物质。

Morphological and functional alterations of ear in lysosomal neuraminidase gene deficient mouse

溶酶体神经氨酸酶基因缺乏小鼠听觉和耳形态学改变初步研究

Recent advances in the diagnosis and treatment of lysosomal storage diseases

溶酶体贮积症的诊断与治疗进展

There are several mechanisms for lysosomal targeting, and the choice may vary depending on the enzyme;

有几种机制来进行溶酶体靶标，选择可能非常取决于酶；