Aline Antonio

Merkel Cells Activate Sensory Neural Pathways through Adrenergic Synapses

Biological functions of fucose in mammals

Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease

Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

CD22 blockade restores homeostatic microglial phagocytosis in ageing brains

Retinitis Pigmentosa: Genes and Disease Mechanisms

Age-related macular degeneration

Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies

Microglial Corpse Clearance: Lessons From Macrophages

Small RNAs are modified with N-glycans and displayed on the surface of living cells

The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease

Sorsby Fundus Dystrophy: Novel Mutations, Novel Phenotypic Characteristics, and Treatment Outcomes

Genes and mutations causing retinitis pigmentosa

Development and application of a next-generation-sequencing (NGS) approach to detect known and novel gene defects underlying retinal diseases

EYS is a major gene for rod-cone dystrophies in France

Lrit3 Deficient Mouse (nob6): A Novel Model of Complete Congenital Stationary Night Blindness (cCSNB)

Prevalence and novelty of PRPF31 mutations in French autosomal dominant rod-cone dystrophy patients and a review of published reports

MERTK mutation update in inherited retinal diseases