SRD005825 Acts as a Pharmacologic Chaperone of Opsin and Promotes Survival of Photoreceptors in an Animal Model of Autosomal Dominant Retinitis Pigmentosa

Podobne zapisy

• Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization
  od: Zhang, Ning, i wsp.
  Wydane: (2012)
• Autosomal Recessive Retinitis Pigmentosa and E150K Mutation in the Opsin Gene
  od: Zhu, Li, i wsp.
  Wydane: (2006)
• Erythropoietin Slows Photoreceptor Cell Death in a Mouse Model of Autosomal Dominant Retinitis Pigmentosa
  od: Rex, Tonia S., i wsp.
  Wydane: (2016)
• Probing Mechanisms of Photoreceptor Degeneration in a New Mouse Model of the Common Form of Autosomal Dominant Retinitis Pigmentosa due to P23H Opsin Mutations
  od: Sakami, Sanae, i wsp.
  Wydane: (2011)
• Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.
  od: Moore, A T, i wsp.
  Wydane: (1992)