All Stories

  1. Cover Image, Volume 113, Number 12, December 2016
  2. AMYLOID DEPOSITION IS TRIGGERED BY ALZHEIMER'S DISEASE BRAIN HOMOGENATES INOCULATION IN WILD-TYPE MICE WITH FOCAL AD-LIKE PATHOLOGY
  3. Ultramicroscopy as a novel tool to unravel the tropism of AAV gene therapy vectors in the brain
  4. 59. APPsα Gene Therapy for Alzheimer's Disease
  5. mRNAtrans-splicing in gene therapy for genetic diseases
  6. Non-human primate model of tauopathy
  7. Gene transfer of both app and ps1 induces hippocampal impairments close to human early phases of Alzheimer’s disease
  8. Improved amyloid pathology contrasting with unexpected memory defects following astrocytic ApoE-e2 overexpression in hippocampus of Alzheimer’s mice
  9. 541. Increased Integration of Lentiviral Vector Carrying a D167H Integrase Relies on the Presence of LEDGF/p75
  10. Repair of Rhodopsin mRNA by Spliceosome-Mediated RNA Trans-Splicing: A New Approach for Autosomal Dominant Retinitis Pigmentosa
  11. 495. In Vivo Evidence of trans-Splicing in a Humanized Mouse Model of Autosomal Dominant Retinitis Pigmentosa Induced By Mutation of the Rhodopsin Gene
  12. AMYLOID CASCADE INDUCTION IN AN AAV-BASED MOUSE MODEL OF ALZHEIMER'S DISEASE
  13. CONSEQUENCES OF APOE2 OVEREXPRESSION IN ASTROCYTES IN AN ALZHEIMER'S DISEASE MOUSE MODEL
  14. Spectral-Domain Optical Coherence Tomography of the Rodent Eye: Highlighting Layers of the Outer Retina Using Signal Averaging and Comparison with Histology
  15. 22: EXPERIMENTAL AND CLINICAL OCULAR GENE THERAPY
  16. A Single Intravenous AAV9 Injection Mediates Bilateral Gene Transfer to the Adult Mouse Retina
  17. Taurine Provides Neuroprotection against Retinal Ganglion Cell Degeneration
  18. Gene Therapy Regenerates Protein Expression in Cone Photoreceptors in Rpe65R91W/R91W Mice
  19. Remaining Rod Activity Mediates Visual Behavior in AdultRpe65−/−mice.
  20. Lentiviral Gene Transfer-Mediated Cone Vision Restoration in RPE65 Knockout Mice
  21. IGF-1 exacerbates the neurotoxicity of the mitochondrial inhibitor 3NP in rats
  22. Lentiviral Gene Transfer of Rpe65 Rescues Survival and Function of Cones in a Mouse Model of Leber Congenital Amaurosis
  23. 419. Rescue of Cone Photoreceptors after Lentiviral Gene Transfer of Rpe65 cDNA in Knockout Mouse Models of Leber Congenital Amaurosis
  24. Functional reinnervation from remaining DA terminals induced by GDNF lentivirus in a rat model of early Parkinson's disease
  25. Lentiviral-mediated gene transfer of brain-derived neurotrophic factor is neuroprotective in a mouse model of neonatal excitotoxic challenge
  26. Retinal cell type expression specificity of HIV-1-derived gene transfer vectors upon subretinal injection in the adult rat: influence of pseudotyping and promoter
  27. Insulin growth factor-1 protects against excitotoxicity in the rat striatum
  28. Brain-Derived Neurotrophic Factor-Mediated Protection of Striatal Neurons in an Excitotoxic Rat Model of Huntington's Disease, as Demonstrated by Adenoviral Gene Transfer
  29. An adenovirus encoding CuZnSOD protects cultured striatal neurones against glutamate toxicity
  30. Lentiviral Vectors Containing a Retinal Pigment Epithelium Specific Promoter for Leber Congenital Amaurosis Gene Therapy