干细胞

Stem Cells CRISPR gene editing help identify therapeutic targets for neurological disorders

Stem Cells CRISPR gene editing help identify therapeutic targets for neurological disorders CRISPR-Cas9 technologies and human pluripotent stem cell technologies help to identify new therapeutic goals for neurological disorders such as schizophrenia and drug addiction.   CRISPR-Cas9 modified stem cells is a universal and high-precision gene editing technology that allows researchers 阅读更多…

Comparison of allogeneic vs autologous bone marrow–derived mesenchymal stem cells delivered by transendocardial injection in patients with ischemic cardiomyopathy: the POSEIDON randomized trial.

Comparison of allogeneic vs autologous bone marrow–derived mesenchymal stem cells delivered by transendocardial injection in patients with ischemic cardiomyopathy: the POSEIDON randomized trial. 间充质干细胞 (间充质干细胞) are under evaluation as a therapy for ischemic cardiomyopathy (ICM). Both autologous and allogeneic MSC therapies are possible; 然而, their safety and efficacy 阅读更多…

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