… M. Michaelides is a cofounder and owns stock in Metis Laboratories, Inc. No conflicts of …
Ahmad FB, Escobedo LA, Rossen LM, Spencer MR, Warner M, Provisional Drug Overdose …

Stargardt disease (STGD1; MIM 248200) is the most prevalent inherited macular dystrophy
and is associated with disease-causing sequence variants in the gene ABCA4. Significant …

… L and M visual pigment genes is controlled by an upstream locus control region (LCR).
Mutations in the L and M pigment gene array that result in the lack of functional L and M pigments…

… (M) Efflux (E) ratios of CNO and clozapine in the P-gp assay, two… Liu, and M. Morales for
research and administrative support … Liu, and M. Morales for research and administrative support …

Background Mutations in RPE65 cause Leber’s congenital amaurosis, a progressive retinal
degenerative disease that severely impairs sight in children. Gene therapy can result in …

The dynamic and reversible acetylation of proteins, catalysed by histone acetyltransferases (HATs)
and histone deacetylases (HDACs), is a major epigenetic regulatory mechanism of …

PURPOSE: To report the findings at 1 year of a study comparing repeated intravitreal
bevacizumab (ivB) and modified Early Treatment of Diabetic Retinopathy Study (ETDRS) macular …

Objectives To report on the causes of blindness certifications in England and Wales in working
age adults (16–64 years) in 2009–2010; and to compare these with figures from 1999 to …

Inherited retinal disease is a common cause of visual impairment and represents a highly
heterogeneous group of conditions. Here, we present findings from a cohort of 722 individuals …

… beam crossing and traveled distance were converted to m and binned into 5 min time bins.
… (on expression day) as infrared beam crossing and traveled distance were converted to m. …