Gene Therapy for Wiskott-Aldrich Syndrome: History, New Vectors, Future Directions

Samankaltaisia teoksia

• B-cell reconstitution after lentiviral vector–mediated gene therapy in patients with Wiskott-Aldrich syndrome
  Tekijä: Castiello, Maria Carmina, et al.
  Julkaistu: (2015)
• Development of lentiviral gene therapy for Wiskott Aldrich syndrome
  Tekijä: Galy, Anne, et al.
  Julkaistu: (2008)
• Evidence for Long-term Efficacy and Safety of Gene Therapy for Wiskott–Aldrich Syndrome in Preclinical Models
  Tekijä: Marangoni, Francesco, et al.
  Julkaistu: (2009)
• Dendritic cell functional improvement in a preclinical model of lentiviral-mediated gene therapy for Wiskott-Aldrich syndrome
  Tekijä: Catucci, Marco, et al.
  Julkaistu: (2011)
• Corrigendum to “Evidence for Long-term Efficacy and Safety of Gene Therapy for Wiskott–Aldrich Syndrome in Preclinical Models”
  Tekijä: Marangoni, Francesco, et al.
  Julkaistu: (2009)