| human | Q5 |
| P496 | ORCID iD | 0000-0002-0720-8897 |
| P1153 | Scopus author ID | 7006021321 |
| P69 | educated at | University of California, Santa Barbara | Q263064 |
| P108 | employer | University of California, Berkeley | Q168756 |
| P734 | family name | Flannery | Q37247495 |
| Flannery | Q37247495 | ||
| Flannery | Q37247495 | ||
| P735 | given name | John | Q4925477 |
| John | Q4925477 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q21142728 | A novel adeno-associated viral variant for efficient and selective intravitreal transduction of rat Müller cells |
| Q38585967 | AAV mediated GDNF secretion from retinal glia slows down retinal degeneration in a rat model of retinitis pigmentosa |
| Q39545173 | AAV-mediated gene delivery in Dp71-null mouse model with compromised barriers |
| Q35006176 | AAV-mediated, optogenetic ablation of Müller Glia leads to structural and functional changes in the mouse retina |
| Q42105175 | Activation of specific interneurons improves V1 feature selectivity and visual perception |
| Q35675196 | Adaptive-optics SLO imaging combined with widefield OCT and SLO enables precise 3D localization of fluorescent cells in the mouse retina |
| Q38199047 | Advances in AAV vector development for gene therapy in the retina |
| Q24622165 | Alternative splice variants of the USH3A gene Clarin 1 (CLRN1) |
| Q50457587 | Anti-clarin-1 AAV-delivered ribozyme induced apoptosis in the mouse cochlea. |
| Q39076892 | Antibody neutralization poses a barrier to intravitreal adeno-associated viral vector gene delivery to non-human primates |
| Q52657325 | Author Correction: Restoration of patterned vision with an engineered photoactivatable G protein-coupled receptor. |
| Q27312044 | CLRN1 is nonessential in the mouse retina but is required for cochlear hair cell development |
| Q35056757 | CRALBP supports the mammalian retinal visual cycle and cone vision |
| Q42840509 | Changes in adeno-associated virus-mediated gene delivery in retinal degeneration |
| Q35944875 | Characterization of peripherin/rds and rom-1 transport in rod photoreceptors of transgenic and knockout animals |
| Q24322993 | Clarin-1, encoded by the Usher Syndrome III causative gene, forms a membranous microdomain: possible role of clarin-1 in organizing the actin cytoskeleton |
| Q45874230 | Enhanced gene delivery to the neonatal retina through systemic administration of tyrosine-mutated AAV9. |
| Q33641501 | Evaluation of patient-centered rehabilitation model targeting older persons with a hip fracture, including those with cognitive impairment |
| Q46876210 | Gene delivery to the retina using lentiviral vectors |
| Q42161021 | Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse models |
| Q30426527 | Imaging light responses of foveal ganglion cells in the living macaque eye. |
| Q33478311 | In vivo imaging of microscopic structures in the rat retina |
| Q45350780 | In vivo-directed evolution of a new adeno-associated virus for therapeutic outer retinal gene delivery from the vitreous |
| Q33622746 | Inner limiting membrane barriers to AAV-mediated retinal transduction from the vitreous |
| Q34937075 | Intravitreal injection of AAV2 transduces macaque inner retina |
| Q35086097 | LiGluR restores visual responses in rodent models of inherited blindness |
| Q44138333 | Long-distance axonal regeneration induced by CNTF gene transfer is impaired by axonal misguidance in the injured adult optic nerve |
| Q46971307 | Looking within for vision |
| Q28973610 | Massively parallel cis-regulatory analysis in the mammalian central nervous system |
| Q30542014 | Misguidance and modulation of axonal regeneration by Stat3 and Rho/ROCK signaling in the transparent optic nerve. |
| Q33492733 | Molecular evolution of adeno-associated virus for enhanced glial gene delivery |
| Q54222193 | Mutation-Independent Gene Therapies for Rod-Cone Dystrophies. |
| Q36049325 | Neuron-glia signaling in developing retina mediated by neurotransmitter spillover |
| Q30515855 | Neuronal Nogo-A upregulation does not contribute to ER stress-associated apoptosis but participates in the regenerative response in the axotomized adult retina. |
| Q33207309 | Noncontact transscleral neodymium-YAG laser photocoagulation of the pigmented rabbit retina |
| Q62937492 | North Carolina macular dystrophy: clinicopathologic correlation |
| Q47548332 | Notch suppression collaborates with Ascl1 and Lin28 to unleash a regenerative response in fish retina, but not in mice |
| Q92710504 | Oblique-plane single-molecule localization microscopy for tissues and small intact animals |
| Q45875207 | Optogenetic Retinal Gene Therapy with the Light Gated GPCR Vertebrate Rhodopsin |
| Q27318230 | Optogenetic Vision Restoration Using Rhodopsin for Enhanced Sensitivity |
| Q47364210 | Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration |
| Q90003427 | Publisher Correction: Oblique-plane single-molecule localization microscopy for tissues and small intact animals |
| Q37561227 | Quantitative analyses of retinal vascular area and density after different methods to reduce VEGF in a rat model of retinopathy of prematurity |
| Q40076885 | Rapid and stable knockdown of an endogenous gene in retinal pigment epithelium |
| Q34631094 | Remote control of neuronal activity with a light-gated glutamate receptor |
| Q62937472 | Restoration of high-sensitivity and adapting vision with a cone opsin |
| Q46466170 | Restoration of patterned vision with an engineered photoactivatable G protein-coupled receptor |
| Q30612156 | Restoration of visual function by expression of a light-gated mammalian ion channel in retinal ganglion cells or ON-bipolar cells |
| Q37008580 | Retinal degeneration is rescued in transgenic rd mice by expression of the cGMP phosphodiesterase beta subunit |
| Q40362704 | Retinoschisin gene therapy in photoreceptors, Müller glia or all retinal cells in the Rs1h-/- mouse. |
| Q45868070 | Ribozyme gene therapy for autosomal dominant retinal disease. |
| Q35306158 | Ribozyme rescue of photoreceptor cells in P23H transgenic rats: long-term survival and late-stage therapy. |
| Q45888779 | Ribozyme rescue of photoreceptor cells in a transgenic rat model of autosomal dominant retinitis pigmentosa. |
| Q35763614 | Role for a novel Usher protein complex in hair cell synaptic maturation |
| Q45875219 | Screening for Neutralizing Antibodies Against Natural and Engineered AAV Capsids in Nonhuman Primate Retinas |
| Q30380518 | Severe retinal degeneration caused by a novel rhodopsin mutation. |
| Q37149035 | Short hairpin RNA-mediated knockdown of VEGFA in Müller cells reduces intravitreal neovascularization in a rat model of retinopathy of prematurity |
| Q42246853 | Specific tools for targeting and expression in Müller glial cells |
| Q62937489 | Structure and Function of Rod Photoreceptors |
| Q46471096 | Systemic aminoglycoside treatment in rodent models of retinitis pigmentosa. |
| Q42239264 | Targeted ablation of Crb2 in photoreceptor cells induces retinitis pigmentosa. |
| Q35924784 | Targeted transgene expression in muller glia of normal and diseased retinas using lentiviral vectors |
| Q37577214 | Targeting Müller cell-derived VEGF164 to reduce intravitreal neovascularization in the rat model of retinopathy of prematurity |
| Q35653226 | The expression pattern of systemically injected AAV9 in the developing mouse retina is determined by age |
| Q45967554 | Tissue-specific and developmental regulation of rod opsin chimeric genes in transgenic mice |
| Q46622335 | Transgenic Animal Models for the Study of Inherited Retinal Dystrophies. |
| Q33285745 | Transport of truncated rhodopsin and its effects on rod function and degeneration |
| Q40057668 | Tropism of engineered and evolved recombinant AAV serotypes in the rd1 mouse and ex vivo primate retina. |
| Q34134919 | USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses |
| Q62937512 | Uptake, processing and release of retinoids by cultured human retinal pigment epithelium |
| Q28509749 | Usher syndrome IIIA gene clarin-1 is essential for hair cell function and associated neural activation |
| Q28250274 | Very low density lipoprotein receptor, a negative regulator of the wnt signaling pathway and choroidal neovascularization |
| Q44390208 | Viral-mediated FGF-2 treatment of the constant light damage model of photoreceptor degeneration |
| Q35242633 | Viral-mediated RdCVF and RdCVFL expression protects cone and rod photoreceptors in retinal degeneration |
| Q58119543 | Viral-vectored ribozymes as therapy for autosomal dominant retinal disease |
| Q34167859 | Visual stimulation switches the polarity of excitatory input to starburst amacrine cells |
| Q37361584 | Wnt Regulates Proliferation and Neurogenic Potential of Müller Glial Cells via a Lin28/let-7 miRNA-Dependent Pathway in Adult Mammalian Retinas |
Search more.