Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations

Documenti analoghi

• Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization
  di: Zhang, Ning, et al.
  Pubblicazione: (2012)
• Loss of cone photoreceptors caused by chromophore depletion is partially prevented by the artificial chromophore pro-drug, 9-cis-retinyl acetate
  di: Maeda, Tadao, et al.
  Pubblicazione: (2009)
• Palmitoylation stabilizes unliganded rod opsin
  di: Maeda, Akiko, et al.
  Pubblicazione: (2010)
• Molecular Biology and Analytical Chemistry Methods Used to Probe the Retinoid Cycle
  di: Golczak, Marcin, et al.
  Pubblicazione: (2010)
• Autosomal Recessive Retinitis Pigmentosa and E150K Mutation in the Opsin Gene
  di: Zhu, Li, et al.
  Pubblicazione: (2006)