nyx

Nyx: A Massively Parallel AMR Code for Computational CosmologyRadar Observations of Asteroid 3908 NyxMutations in NYX of individuals with high myopia, but without night blindnessMutations in the CACNA1F and NYX genes in British CSNBX familiesNYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface proteinIsolation of the mouse nyctalopin gene nyx and expression studies in mouse and rat retina.Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (c Nyx ) from chickSlow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX gene.Primate Retinal Signaling Pathways: Suppressing ON-Pathway Activity in Monkey With Glutamate Analogues Mimics Human CSNB1-NYX Geneti...