Efficient and Selective AAV2-Mediated Gene Transfer Directed to Human Vascular Endothelial Cells

This publication has 45 references indexed in Scilit:

• Route of Administration Determines Induction of T-Cell-Independent Humoral Responses to Adeno-Associated Virus Vectors
  Molecular Therapy, 2000
• Humoral Immunity to Adeno-Associated Virus Type 2 Vectors following Administration to Murine and Nonhuman Primate Muscle
  Journal of Virology, 2000
• Increased apoptosis of Huntington disease lymphoblasts associated with repeat length-dependent mitochondrial depolarization
  Nature Medicine, 1999
• Immune responses to adenovirus and adeno-associated virus in humans
  Gene Therapy, 1999
• Peroral gene therapy of lactose intolerance using an adeno-associated virus vector
  Nature Medicine, 1998
• Persistent expression of human clotting factor IX from mouse liver after intravenous injection of adeno-associated virus vectors
  Proceedings of the National Academy of Sciences, 1997
• Gene delivery to skeletal muscle results in sustained expression and systemic delivery of a therapeutic protein
  Proceedings of the National Academy of Sciences, 1996
• Gene transfer into the mouse retina mediated by an adeno-associated viral vector
  Human Molecular Genetics, 1996
• Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain
  Nature Genetics, 1994
• Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy.
  Proceedings of the National Academy of Sciences, 1994