Fragile X Syndrome (FXS) is the most common form of inherited intellectual disability, caused
by developmentally regulated inactivation of FMR1, leading to the absence of its encoded …

Fragile X syndrome (FXS) is the most common form of monogenic hereditary cognitive
impairment. FXS patient exhibit a high comorbidity rate with autism spectrum disorders (ASDs). …

Fragile X syndrome (FXS), the most common form of inherited mental retardation, is a
neurodevelopmental disorder caused by silencing of the FMR1 gene, which in FXS becomes …

Azobenzene photoswitches confer light sensitivity onto retinal ganglion cells (RGCs) in blind
mice, making these compounds promising candidates as vision-restoring drugs in humans …

Light responses are initiated in photoreceptors, processed by interneurons, and synaptically
transmitted to retinal ganglion cells (RGCs), which send information to the brain. Retinitis …

Rod and cone photoreceptors degenerate in retinitis pigmentosa (RP). While downstream
neurons survive, they undergo physiological changes, including accelerated spontaneous …

Neurodevelopmental disorders (NDs) are impairments that affect the development and
growth of the brain and the central nervous system during embryonic and early postnatal life. …

Fragile X Syndrome (FXS) is the most common form of inherited cognitive disability. However,
functional deficiencies in FX neurons have been described so far almost exclusively in …

Fragile X syndrome (FXS) is the most common form of inherited cognitive impairment. It is
caused by developmental inactivation of the FMR1 gene and the absence of its encoded …

Vision impairment and blindness in humans are most frequently caused by the degeneration
and loss of photoreceptor cells in the outer retina, as is the case for age-related macular …