Vera Bonilha

Proteomic characterization of isolated retinal pigment epithelium microvilli.

Proteomics reveal Cochlin deposits associated with glaucomatous trabecular meshwork.

Abnormal distribution of red/green cone opsins in a patient with an autosomal dominant cone dystrophy.

Microvilli defects in retinas of ezrin knockout mice.

Characterization of semenogelin proteins in the human retina.

Focus on molecules: ezrin.

Glucose utilization by the retinal pigment epithelium: evidence for rapid uptake and storage in glycogen, followed by glycogen utilization.

Proteomics implicates peptidyl arginine deiminase 2 and optic nerve citrullination in glaucoma pathogenesis.

CRALBP ligand and protein interactions.

The retinal pigment epithelium apical microvilli and retinal function.

Semenogelins in the human retina: Differences in distribution and content between AMD and normal donor tissues.

Oxidative damage-induced inflammation initiates age-related macular degeneration.

Age-related reduction in retinal deimination levels in the F344BN rat.

Retinal pigment epithelium lipofuscin proteomics.

Choroideremia: analysis of the retina from a female symptomatic carrier.

Haze development after photorefractive keratectomy: mechanical vs ethanol epithelial removal in rabbits.

Age and disease-related structural changes in the retinal pigment epithelium.

Retinal pathology of a patient with Goldmann-Favre syndrome.

Histopathology and functional correlations in a patient with a mutation in RPE65, the gene for retinol isomerase.

Imaging human postmortem eyes with SLO and OCT.

Age-related changes in the retinal pigment epithelium (RPE).

CD40 induces anti-Toxoplasma gondii activity in nonhematopoietic cells dependent on autophagy proteins.

Retinal deimination and PAD2 levels in retinas from donors with age-related macular degeneration (AMD).

DJ-1-dependent regulation of oxidative stress in the retinal pigment epithelium (RPE).

Retinal pigment epithelium (RPE) cytoskeleton in vivo and in vitro.

Oxidative stress regulation by DJ-1 in the retinal pigment epithelium.

Retinal Histopathology in Eyes from a Patient with Stargardt disease caused by Compound Heterozygous ABCA4 Mutations.

Histopathological comparison of eyes from patients with autosomal recessive retinitis pigmentosa caused by novel EYS mutations.

The BALB/c mouse: Effect of standard vivarium lighting on retinal pathology during aging.

Retinal histopathology in eyes from patients with autosomal dominant retinitis pigmentosa caused by rhodopsin mutations.

Loss of DJ-1 elicits retinal abnormalities, visual dysfunction, and increased oxidative stress in mice.

Absence of DJ-1 causes age-related retinal abnormalities in association with increased oxidative stress.

The Circadian Clock Gene Bmal1 Controls Thyroid Hormone-Mediated Spectral Identity and Cone Photoreceptor Function.

Oxidative Stress Regulation and DJ-1 Function in the Retinal Pigment Epithelium: Implications for AMD.

A Novel Approach for Integrating AF-SLO and SDOCT Imaging Data Demonstrates the Ability to Identify Early Retinal Abnormalities in Mutant Mice and Evaluate the Effects of Genetic and Pharmacological Manipulation.

Re: Cuenca et al.: Cellular characterization of OCT and outer retinal bands using specific immunohistochemistry markers and clinical implications (Ophthalmology. 2018;125;407-422).

Retinal angiotensin II and angiotensin-(1-7) response to hyperglycemia and an intervention with captopril.

Prolonged ocular exposure leads to retinal lesions in mice.

Role of FGF and Hyaluronan in Choroidal Neovascularization in Sorsby Fundus Dystrophy.

Neogenin neutralization prevents photoreceptor loss in inherited retinal degeneration.

Inhibition of choroidal neovascularization by systemic delivery of gold nanoparticles.

Geographic Atrophy: Confocal Scanning Laser Ophthalmoscopy, Histology, and Inflammation in the Region of Expanding Lesions.

Retinal Glial and Choroidal Vascular Pathology in Donors Clinically Diagnosed With Stargardt Disease.

Oxidative stress in the retina and retinal pigment epithelium (RPE): Role of aging, and DJ-1.

The retinal pigment epithelium in Sorsby Fundus Dystrophy shows increased sensitivity to oxidative stress-induced degeneration.

Cellular Changes in Retinas From Patients With Mutations.

Evidence of complement dysregulation in outer retina of Stargardt disease donor eyes.

A human model of Batten disease shows role of CLN3 in phagocytosis at the photoreceptor-RPE interface.

Histopathological assessments reveal retinal vascular changes, inflammation and gliosis in patients with lethal COVID-19.

complementary DNA is enriched in atrophic macular degeneration and triggers retinal pigmented epithelium toxicity via cytosolic innate immunity.

Histopathological assessments reveal retinal vascular changes, inflammation, and gliosis in patients with lethal COVID-19.

CDCP1 regulates retinal pigmented epithelial barrier integrity for the development of experimental autoimmune uveitis.

Oxidation of DJ-1 Cysteines in Retinal Pigment Epithelium Function.

Histological characterization of retinal degeneration in mucopolysaccharidosis type IIIC.

Regulated cell death pathways in the sodium iodate model: Insights and implications for AMD.

Modeling aging and retinal degeneration with mitochondrial DNA mutation burden.

NR2E3 loss disrupts photoreceptor cell maturation and fate in human organoid models of retinal development.

A comparison of optophysiological biomarkers of photoreceptor stress and phototoxicity in BALB/cJ, B6 (Cg)-Tyrc-2J/J, and C57Bl/6J mouse strains.