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Phenotype correction of fanconi anemia group a hematopoietic stem cells using lentiviral vector
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“Ex vivo gene transfer into HSC of gene targeted FA mice has been shown to correct the cellular FA phenotype at the level of long term repopulating stem cells [33,60–62].”
From Finding the needle in the hay stack: Hematopoietic stem cells in Fanconi anemia (2009) · cites this paper as [61]
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Cites
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Cited by
Finding the needle in the hay stack: Hematopoietic stem cells in Fanconi anemia
Müller, L. U. W., & Williams, D. A. (2009) · Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis · doi:10.1016/j.mrfmmm.2009.03.010 · Cited by 31
Metadata
- Authors
- Yamada, K., Ramezani, A., Hawley, R. G., Ebell, W., Arwert, F., Arnold, L. W., & Walsh, C. E.
- Venue
- Molecular Therapy
- Publisher
- Elsevier BV
- Published
- 2003-10
- Volume
- 8
- Issue
- 4
- Pages
- 600-610
- ISSN
- 1525-0016
- Cited by
- 22
- References
- 1
- Language
- en
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