M6的胶体金复合物不能与经胰酶和神经氨酸酶处理过的红细胞发生结合。
M6 gold complexes showed no ability to bind to surface of erythrocytes treated by trypsin or neuraminidase.
这种药物有两类：1）烷胺类药物（金刚烷胺和金刚乙胺），2）流感的神经氨酸酶抑制剂（奥司他韦和扎那米韦）。
There are two classes of such medicines, 1) adamantanes (amantadine and remantadine), and 2) inhibitors of influenza neuraminidase (oseltamivir and zanamivir).
增加EGR1表达可以激活其他信号分子的转录，包括CDK5和酪氨酸羟化酶，对神经细胞生长和分化有长期影响(2,3)。
Increased EGR1 expression activates transcription of other signaling molecules, including CDK5 and tyrosine hydroxylase, and exerts long term effects on neural cell growth and differentiation (2, 3).
扎那米韦和奥塞·米韦结合在神经氨酸酶的不同催化位点，这就导致了这种耐药情况不同的发生。
Zanamivir and oseltamivir bind differently at the neuraminidase catalytic site and this contributes to different drug resistance profiles.
方法给一类酪氨酸脱氢酶阳性的神经细胞（一种中枢神经源细胞），又称CAD细胞，引入由DNA编码的野生型和突变型离子通道。
Methods To introduce DNA encoding the wild- type and mutant channel into immortalized tyrosine hydroxylase- positive CNS- derived neurons, CAD cells.
神经氨酸酶（NA）是流感病毒表面的一种重要蛋白质，在免疫和致病方面起重要作用。
Neuraminidase (NA) is an important protein on the surface of virion and plays an important role in immune and lethality.
神经氨酸酶（NA）是流感病毒表面的一种重要蛋白质，在免疫和致病方面起重要作用。
Neuraminidase (NA) is an important protein on the surface of virion and plays an important role in immune and lethality.
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