Optimized Adeno-Associated Virus (AAV)–Protein Phosphatase-5 Helper Viruses for Efficient Liver Transduction by Single-Stranded AAV Vectors: Therapeutic Expression of Factor IX at Reduced Vector Doses

Documenti analoghi

• High-Efficiency Transduction of Fibroblasts and Mesenchymal Stem Cells by Tyrosine-Mutant AAV2 Vectors for Their Potential Use in Cellular Therapy
  di: Li, Mengxin, et al.
  Pubblicazione: (2010)
• A Simple Method to Increase the Transduction Efficiency of Single-Stranded Adeno-Associated Virus Vectors In Vitro and In Vivo
  di: Ma, Wenqin, et al.
  Pubblicazione: (2011)
• Improved adeno-associated virus (AAV) serotype 1 and 5 vectors for gene therapy
  di: Sen, Dwaipayan, et al.
  Pubblicazione: (2013)
• High-efficiency Transduction and Correction of Murine Hemophilia B Using AAV2 Vectors Devoid of Multiple Surface-exposed Tyrosines
  di: Markusic, David M, et al.
  Pubblicazione: (2010)
• Activation of the NF-κB pathway by adeno-associated virus (AAV) vectors and its implications in immune response and gene therapy
  di: Jayandharan, Giridhara R., et al.
  Pubblicazione: (2011)