lysosomal

lysosomal

美 　英

• adj.溶酶體的
• 網絡溶小體；溶解酵素；溶菌體

英漢解釋

adj.

1. 溶酶體的

例句

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

我們報告一例變形性關節病中的一名年輕男子的溶酶體儲存障礙。

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

神經節苷脂的缺乏直接與一系列疾病有關，比如溶酶體貯積癥。

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

復合磷脂的詳細分析明顯地表明了溶酶體膜與質膜的不同。

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

而且，黃芪多糖能夠抑制線粒體膜電位崩解保護線粒體形態，保護溶酶體膜。

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

根據其作用廢物的來源不同，分為自噬性溶酶體和異噬性溶酶體。

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

這也可能用于治療其他有溶酶體介入神經退行性疾病，她說。

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

釋放的腎臟溶酶體的酶可能與產生促紅細胞生成素有關。

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

這里我們說明溶酶體貯積損害了自噬性運送大量細胞溶質的內容物到溶酶體。

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

組織蛋白酶屬于最豐富的溶酶體酶和退化過程中所涉及。

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

這樣的缺陷引起溶酶體堆積病（例如，高歇病），基因置換是一種有效的療法。

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

細胞自噬是一種溶酶體降解通道，其為存活，分化，發展和動態平衡所必需。

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

在溶酶體儲存病患者中，天生缺乏這些酶。

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

溶酶體靶標的專門技術將作為典型被建議進入第3年的項目中。

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

超聲處理不僅打碎了溶酶體的膜，還從膜上釋放出某些物質。

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

溶酶體神經氨酸酶基因缺乏小鼠聽覺和耳形態學改變初步研究

Recent advances in the diagnosis and treatment of lysosomal storage diseases

溶酶體貯積癥的診斷與治療進展

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

有幾種機制來進行溶酶體靶標，選擇可能非常取決于酶；