Tyrosine triple mutated AAV2-BDNF gene therapy in a rat model of transient IOP elevation

Lignende værker

• Improved Intravitreal AAV-Mediated Inner Retinal Gene Transduction after Surgical Internal Limiting Membrane Peeling in Cynomolgus Monkeys
  af: Takahashi, Kazuhisa, et al.
  Udgivet: (2017)
• Tyrosine triple mutated AAV2-BDNF gene therapy in an inner retinal injury model induced by intravitreal injection of N–methyl-D-aspartate (NMDA)
  af: Shiozawa, Asaka Lee, et al.
  Udgivet: (2020)
• Adeno-associated virus type 8 vector–mediated expression of siRNA targeting vascular endothelial growth factor efficiently inhibits neovascularization in a murine choroidal neovascularization model
  af: Igarashi, Tsutomu, et al.
  Udgivet: (2014)
• Enzyme replacement in the CSF to treat metachromatic leukodystrophy in mouse model using single intracerebroventricular injection of self-complementary AAV1 vector
  af: Hironaka, Kohei, et al.
  Udgivet: (2015)
• Treatment of hypophosphatasia by muscle-directed expression of bone-targeted alkaline phosphatase via self-complementary AAV8 vector
  af: Nakamura-Takahashi, Aki, et al.
  Udgivet: (2016)