Gene Therapy Vectors
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-030-57401-7_63
Reference15 articles.
1. Anguela XM, High KA (2019) Entering the modern era of gene therapy. Annu Rev Med 70:273–288. https://doi.org/10.1146/annurev-med-012017-043332
2. Anzalone AV et al (2019) Search-and-replace genome editing without double-strand breaks or donor DNA. Nature 576:149-+. https://doi.org/10.1038/s41586-019-1711-4
3. Burns JC, Friedmann T, Driever W, Burrascano M, Yee JK (1993) Vesicular stomatitis-virus G glycoprotein pseudotyped retroviral vectors – concentration to very high-titer and efficient gene-transfer into mammalian and nonmammalian cells. Proc Natl Acad Sci U S A 90:8033–8037. https://doi.org/10.1073/pnas.90.17.8033
4. Hacein-Bey-Abina S et al (2014) A Modified gamma-retrovirus vector for X-linked severe combined immunodeficiency. New Engl J Med 371:1407–1417. https://doi.org/10.1056/Nejmoa1404588
5. Hartmann J et al (2018) A Library-based screening strategy for the identification of DARPins as ligands for receptor-targeted AAV and lentiviral vectors. Mol Ther-Meth Clin D 10:128–143. https://doi.org/10.1016/j.omtm.2018.07.001
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