Yan et al., 2016
ViewHTML| Publication | Publication Date | Title |
|---|---|---|
| Yan et al. | Postnatal onset of retinal degeneration by loss of embryonic Ezh2 repression of Six1 | |
| Dulla et al. | Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations | |
| Lumayag et al. | Inactivation of the microRNA-183/96/182 cluster results in syndromic retinal degeneration | |
| Yang et al. | G protein-coupled receptor 37 is a negative regulator of oligodendrocyte differentiation and myelination | |
| Nishida et al. | Otx2 homeobox gene controls retinal photoreceptor cell fate and pineal gland development | |
| Ashery-Padan et al. | Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye | |
| Grove et al. | ABI2-deficient mice exhibit defective cell migration, aberrant dendritic spine morphogenesis, and deficits in learning and memory | |
| Valdés-Sánchez et al. | Retinal pigment epithelium degeneration caused by aggregation of PRPF31 and the role of HSP70 family of proteins | |
| Barben et al. | Hif1a inactivation rescues photoreceptor degeneration induced by a chronic hypoxia-like stress | |
| Paylakhi et al. | Müller glia-derived PRSS56 is required to sustain ocular axial growth and prevent refractive error | |
| Harder et al. | BBC3 (PUMA) regulates developmental apoptosis but not axonal injury induced death in the retina | |
| Hsieh et al. | Dynamic Pax6 expression during the neurogenic cell cycle influences proliferation and cell fate choices of retinal progenitors | |
| Wen et al. | Microphthalmia-associated transcription factor regulates the visual cycle genes Rlbp1 and Rdh5 in the retinal pigment epithelium | |
| Jiang et al. | STAT3 promotes survival of mutant photoreceptors in inherited photoreceptor degeneration models | |
| Guziewicz et al. | Molecular consequences of BEST1 gene mutations in canine multifocal retinopathy predict functional implications for human bestrophinopathies | |
| Varela et al. | Genetic treatment for autosomal dominant inherited retinal dystrophies: approaches, challenges and targeted genotypes | |
| Hinze et al. | Incorrect dosage of IQSEC2, a known intellectual disability and epilepsy gene, disrupts dendritic spine morphogenesis | |
| Ferre-Fernández et al. | Whole-exome sequencing of congenital glaucoma patients reveals hypermorphic variants in GPATCH3, a new gene involved in ocular and craniofacial development | |
| Li et al. | Aberrant RNA splicing is the major pathogenic effect in a knock‐in mouse model of the dominantly inherited c. 1430A> G human RPE65 mutation | |
| Gu et al. | DNA and RNA oxidative damage in the retina is associated with ganglion cell mitochondria | |
| Dong et al. | LIM-homeodomain transcription factor LHX4 is required for the differentiation of retinal rod bipolar cells and OFF-cone bipolar subtypes | |
| Nojima et al. | A point mutation in Semaphorin 4A associates with defective endosomal sorting and causes retinal degeneration | |
| Daniel et al. | Fibulin-3 knockout mice demonstrate corneal dysfunction but maintain normal retinal integrity | |
| Geller et al. | CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development | |
| Perez-Rico et al. | Elastin development-associated extracellular matrix constituents of subepithelial connective tissue in human pterygium |