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Hematopoietic Ex Vivo Gene Transfer

  • Conference paper
Gene Therapy

Part of the book series: Ernst Schering Research Foundation Workshop ((SCHERING FOUND,volume 27))

  • 194 Accesses

Abstract

The goal of somatic gene therapy is to therapeutically benefit an individual by transferring genetic information to non—germline cells. Genes can be transferred either to replace the function of a defective gene in order to add genetic information and thereby provide an additional function to a target cell or to suppress the function of an already active gene in the target cell population.

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Authors
  1. H. Glimm
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  2. C. von Kalle
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  3. R. Henschler
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  4. R. Mertelsmann
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Editor information

R. E. Sobol K. J. Scanlon E. Nestaas

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© 1998 Springer-Verlag Berlin Heidelberg

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Glimm, H., von Kalle, C., Henschler, R., Mertelsmann, R. (1998). Hematopoietic Ex Vivo Gene Transfer. In: Sobol, R.E., Scanlon, K.J., Nestaas, E. (eds) Gene Therapy. Ernst Schering Research Foundation Workshop, vol 27. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-662-03577-1_10

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  • DOI: https://doi.org/10.1007/978-3-662-03577-1_10

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-662-03579-5

  • Online ISBN: 978-3-662-03577-1

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