...学外文文献 目的观察携带人骨形成蛋白2(bone morphogenetic protein 2, BMP-2)基因的腺病毒载体(adenovirus carrying BMP-2 gene, Ad-BMP-2),通过纤维蛋白凝胶与牛松质骨支架(bovine cancellous bone, BCB)复合,修复..
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目的研究携带血管抑素K1-5 基因的腺病毒载体对其对血管内皮细胞增殖的抑制作用。
Objective To investigate the suppression effects of a adenovirus vector containing angiostatin K1-5 gene to the proliferation and migration of vascular endothelial cells.
Chiu补充说,伶猴腺病毒(TMAdV)在人类身上罕见,这让它可能成为一个潜在的强大工具,在基因治疗中充当病毒载体。
TMAdV's rarity in humans could make it a potentially powerful tool as a viral vehicle for delivering gene therapy, Chiu adds.
人们希望,改构后的腺病毒在基因治疗方面能起到重要的作用,例如,作为载体基因携带治疗性基因到达细胞内。
The hope is that modified adenovirus could play a role in gene therapy, used as a vector (carrier) for delivering therapeutic genes to the interior of cells.
But if you're trying to use that virus as a gene delivery vector and your body gets rid of it then the therapy has failed, it's ended.
但如果你想把腺病毒作为基因治疗载体,而你的身体清除这种病毒,治疗就失败了,前功尽弃了
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