Bush 发表于 2025-3-21 17:21:17
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Lentiviral Vectors for the Genetic Modification of Hematopoietic Stem Cells,Lentiviral vectors, owing to their ability to deliver transgenes in tissues that long appeared irremediably refractory to stable genetic manipulation, open exciting perspectives for the genetic treatment of a wide array of hereditary as well as acquired disorders, in particular of the lymphohematopoietic system.cogent 发表于 2025-3-22 06:18:18
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https://doi.org/10.1007/978-3-662-04469-8Hematopoietic stem cells (HSC); blood; bone marrow; cell; cell therapy; gene; gene therapy; hematopoietic sANNUL 发表于 2025-3-22 14:27:21
0947-6075one topic is combined in one workshop. Indeed, at first glance the recovery of stem cells from cord blood has to be seen as separate from the attempts to achieve effective in utero therapy by stem cell trans plantation, because the first issue deals with an innovative stem cell source as an alternforbid 发表于 2025-3-22 19:11:39
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