Ocular Genomics
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      • Retinitis Pigmentosa 1
      • Genome editing for dominant IRDs
      • Genome editing for USH2A associated IRD
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      • Retinal Degeneration Disease Gene Discovery
      • NMNAT1 Leber Congenital Amaurosis (LCA)
      • Novel Photoreceptor Sensory Cilia Proteins
      • RNA Splicing Factor Retinitis Pigmentosa/Transcriptome Analyses
      • Pericentral Retinitis Pigmentosa
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The Amamoto Lab at Mass Eye and Ear and the Ocular Genomics Institute studies how photoreceptors in the retina develop and degenerate, with the hope of one day developing a treatment to prolong healthy color vision for all patients suffering from inherited retinal degeneration.

Our team strives to tackle this goal in the following ways:

  • Understanding the molecular mechanisms by which cone photoreceptors degenerate in a non-cell autonomous manner in mouse models of Retinitis Pigmentosa.
  • Determining how to regenerate the photoreceptor outer segment by understanding how it develops in the first place.
  • Developing new technologies to facilitate answering our questions in the molecular and cellular biology of the retina

Meet the Amamoto Lab Members