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Updated: Oct 9, 2026

Lentiviral Vector-mediated Gene Therapy of Hepatocytes Ex Vivo for Autologous Transplantation in Swine
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Lentiviral Vector-mediated Gene Therapy of Hepatocytes Ex Vivo for Autologous Transplantation in Swine

Published on: November 4, 2018

Heme oxygenase-1 gene therapy: a novel immunomodulatory approach in liver allograft recipients?

B Ke1, X D Shen, J Melinek

  • 1Dumont-UCLA Transplant Center, University of California, Los Angeles, California, USA.

Transplantation Proceedings
|March 27, 2001
PubMed
Abstract

No abstract available in PubMed .

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Gene Therapy01:22

Gene Therapy

Gene therapy is a technique where a gene is inserted into a person’s cells to prevent or treat a serious disease. The added gene may be a healthy version of the gene that is mutated in the patient, or it could be a different gene that inactivates or compensates for the patient’s disease-causing gene. For example, in patients with severe combined immunodeficiency (SCID) due to a mutation in the gene for the enzyme adenosine deaminase, a functioning version of the gene can be inserted. The...