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Jordan, C.T. et al.

Jordan, Vanin, Marini,

The use of adenoviral vectors for genetic manipulation and analysis of primitive hematopoietic cells.

Gene transfer into stem cells has long been studied as a means by which primitive hematopoietic cells could be characterized and manipulated. While a variety of strategies have been attempted, it still remains relatively difficult to perform direct stem cell analysis. In this review, we examine recent studies using adenovirus-based vectors as a means to achieve high-level gene transfer into primitive hematopoietic cell types.[1]

References

The use of adenoviral vectors for genetic manipulation and analysis of primitive hematopoietic cells. Jordan, C.T., Vanin, E.F., Marini, F.C. Current gene therapy. (2001) [Pubmed]

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