Phenotypic correction of Fanconi anemia in human hematopoietic cells with a recombinant adeno-associated virus vector.

समान संसाधन

• Recombinant adeno-associated virus vectors in the treatment of rare diseases
  द्वारा: Hastie, Eric, और अन्य
  प्रकाशित: (2015)
• Correction of Fanconi Anemia Type C Phenotypic Abnormalities Using a Clinically Suitable Retroviral Vector Infection Protocol
  द्वारा: Brian W. Freie, और अन्य
  प्रकाशित: (1996-05-01)
• Recombinant adeno-associated virus (rAAV)-mediated expression of a human gamma-globin gene in human progenitor-derived erythroid cells.
  द्वारा: Miller, J L, और अन्य
  प्रकाशित: (1994)
• Repression of Fanconi anemia gene (FACC) expression inhibits growth of hematopoietic progenitor cells.
  द्वारा: Segal, G M, और अन्य
  प्रकाशित: (1994)
• Regulated high level expression of a human gamma-globin gene introduced into erythroid cells by an adeno-associated virus vector.
  द्वारा: Walsh, C E, और अन्य
  प्रकाशित: (1992)