Genome Engineering of Hematopoietic Stem Cells Using CRISPR/Cas9 System
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Publisher
Springer US
Link
https://link.springer.com/content/pdf/10.1007/978-1-0716-1979-7_20
Reference26 articles.
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2. Melve GK, Ersvaer E, Eide GE, Kristoffersen EK, Bruserud O (2018) Peripheral blood stem cell mobilization in healthy donors by granulocyte colony-stimulating factor causes preferential mobilization of lymphocyte subsets. Front Immunol 9:845
3. Cavazzana M, Bushman FD, Miccio A, André-Schmutz I, Six E (2019) Gene therapy targeting haematopoietic stem cells for inherited diseases: progress and challenges. Nat Rev Drug Discov 18(6):447–462
4. Gaj T, Staahl BT, Rodrigues GMC, Limsirichai P, Ekman FK, Doudna JA, Schaffer DV (2017) Targeted gene knock-in by homology-directed genome editing using Cas9 ribonucleoprotein and AAV donor delivery. Nucleic Acids Res 45(11):e98
5. Richardson CD, Ray GJ, DeWitt MA, Curie GL, Corn JE (2016) Enhancing homology-directed genome editing by catalytically active and inactive CRISPR-Cas9 using asymmetric donor DNA. Nat Biotechnol 34(3):339–344
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