Next Generation of AAV Vectors for Gene Therapy of Human Liver Diseases

Lignende værker

• Development of Novel Recombinant AAV Vectors and Strategies for the Potential Gene Therapy of Hemophilia
  af: Zhong, Li, et al.
  Udgivet: (2012)
• Next-generation muscle-directed gene therapy by in silico vector design
  af: Sarcar, S., et al.
  Udgivet: (2019)
• Development of a Clinical Candidate AAV3 Vector for Gene Therapy of Hemophilia B
  af: Brown, Harrison C., et al.
  Udgivet: (2020)
• A concept of eliminating nonhomologous recombination for scalable and safe AAV vector generation for human gene therapy
  af: Dong, Biao, et al.
  Udgivet: (2013)
• Gene Therapy Using Adeno-Associated Virus Vectors
  af: Daya, Shyam, et al.
  Udgivet: (2008)