IGNACIO JESÚS MOLINA PINEDA INFANTAS-rekin lankidetzan egindako argitalpenak (5)

2011

  1. A tissue-specific, activation-inducible, lentiviral vector regulated by human CD40L proximal promoter sequences

    Gene Therapy, Vol. 18, Núm. 4, pp. 364-371

2009

  1. Safer vectors for gene therapy of primary immunodeficiencies

    Current Gene Therapy, Vol. 9, Núm. 4, pp. 291-305

2008

  1. Hematopoietic-specific lentiviral vectors circumvent cellular toxicity due to ectopic expression of Wiskott-Aldrich syndrome protein

    Human Gene Therapy, Vol. 19, Núm. 2, pp. 179-197

2005

  1. Lentiviral vectors transcriptionally targeted to hematopoietic cells by WASP gene proximal promoter sequences

    Gene Therapy, Vol. 12, Núm. 8, pp. 715-723

2004

  1. Efficient lentiviral transduction of herpesvirus saimiri immortalized T cells as a model for gene therapy in primary immunodeficiencies

    Gene Therapy, Vol. 11, Núm. 12, pp. 956-961