Archives: Presentations
Presentations
Reduced nuclear NAD+ drives DNA damage and subsequent immune activation in the retina
Brown et al., Human Molecular Genetics 2021
Mutant Nmnat1 leads to a retina-specific decrease of NAD+ accompanied by increased poly(ADP-ribose) in a mouse model of NMNAT1-associated retinal degeneration
Greenwald et al., Human Molecular Genetics 2021
Gene Therapy Preserves Retinal Structure and Function in a Mouse Model of NMNAT1-Associated Retinal Degeneration
Greenwald et al., Molecular Therapy: Methods and Clinical Development, 2020
Treatment Potential for LCA5-Associated Leber Congenital Amaurosis
Uyhazi et al., Investigative Ophthalmology and Visual Science 2020
RDH12 Mutations Cause a Severe Retinal Degeneration With Relatively Spared Rod Function
Aleman et al., Investigative Ophthalmology and Visual Science 2018
Amelioration of Neurosensory Structure and Function in Animal and Cellular Models of a Congenital Blindness
Song et al., Molecular Therapy 2018
Mouse Models of NMNAT1-Leber Congenital Amaurosis (LCA9) Recapitulate Key Features of the Human Disease
Greenwald et al., American Journal of Pathology 2016
NMNAT1 mutations cause Leber congenital amaurosis.
Falk et al., Nature Genetics 2012
