针对1型糖尿病的CRISPR/基于案例的细胞疗法的挑战:如何不设计"特洛伊木马"

Dmitry S Karpov1, Anastasiia O Sosnovtseva1, Svetlana V Pylina2

  • 1Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, 119991 Moscow, Russia.

概括

1型糖尿病 (T1D) 的治疗方法有限. 本综述探讨了用于细胞再生医学的CRISPR/Cas基因组编辑,以创建安全,有效的T1D治疗方法,解决潜在的风险.

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