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15 天
青岛市政协委员陈梦梦:打造细胞与基因治疗产业集群
细胞与基因治疗(Cell and Gene ...
生物通
24 年
《Gene Therapy》AAV1.NT3 基因疗法:为多发性硬化症治疗点亮新希望
为解决慢性进展型多发性硬化症(MS)治疗难题,美国全国儿童医院等机构的研究人员开展 AAV1.NT3 基因疗法研究,发现该疗法能减轻 EAE 小鼠疾病严重程度。这为 MS 治疗带来新方向,强烈推荐科研读者阅读。
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