| CFTR inactivation by lentiviral vector-mediated RNA interference and CRISPR-Cas9 genome editing in human airway epithelial cells | Current gene therapy |  | | 2015 | 682 | 9 |
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| A step toward liver gene therapy: efficient correction of the genetic defect of hepatocytes isolated from a patient with Crigler-Najjar syndrome type 1 with lentiviral vectors | Transplantation | | | 2009 | 705 | 0 |
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| Ex vivo lentivirus transduction and immediate transplantation of uncultured hepatocytes for treating hyperbilirubinemic Gunn rat | Transplantation | | | 2006 | 620 | 1 |
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| A simple and highly effective method for the stable transduction of uncultured porcine hepatocytes using lentiviral vector | Cell transplantation | | | 2005 | 739 | 0 |
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| Treatment of acetaminophen-induced acute liver failure in the mouse with conditionally immortalized human hepatocytes | Journal of hepatology | | | 2005 | 843 | 1 |
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| Treatment of fulminant liver failure by transplantation of microencapsulated primary or immortalized xenogeneic hepatocytes | Xenotransplantation | | | 2005 | 814 | 0 |
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| Efficient transduction of primary human B lymphocytes and nondividing myeloma B cells with HIV-1-derived lentiviral vectors | Blood |  | | 2003 | 349 | 233 |
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| Highly efficient lentiviral vector-mediated transduction of nondividing, fully reimplantable primary hepatocytes | Molecular therapy | | | 2002 | 781 | 1 |
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