Associated Papers
Candidate Interaction Partners of Calpain-5 Suggest Clues to Its Involvement in Neovascular Inflammatory Vitreoretinopathy.
Gal J et al.
Cells, 2026
Treatment and Visual Outcomes in Pediatric Patients with Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy: A Cohort Study.
Maccora I et al.
Ocular Immunology and Inflammation, 2024
Ultrawidefield Fluorescein Angiography and OCT Findings in Children and Young Adults with Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy.
Ebert JJ et al.
Ophthalmology. Retina, 2024
Autosomal dominant neovascular inflammatory vitreoretinopathy with CAPN5 c.731T > C gene mutation; clinical management of a family cohort and review of the literature.
Tabbaa T et al.
Ophthalmic Genetics, 2023
Impaired activity and membrane association of most calpain-5 mutants causal for neovascular inflammatory vitreoretinopathy.
Geddes JW et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease, 2023
Long-Term Outcomes and Risk Factors for Severe Vision Loss in Autosomal Dominant Neovascular Inflammatory Vitreoretinopathy (ADNIV).
Boyce TM et al.
American Journal of Ophthalmology, 2022
Molecular Surgery: Proteomics of a Rare Genetic Disease Gives Insight into Common Causes of Blindness.
Velez G et al.
Iscience, 2020
Structural Insights into the Unique Activation Mechanisms of a Non-classical Calpain and Its Disease-Causing Variants.
Velez G et al.
Cell Reports, 2020
CAPN5 genetic inactivation phenotype supports therapeutic inhibition trials.
Wert KJ et al.
Human Mutation, 2019
Capn5 Expression in the Healthy and Regenerating Zebrafish Retina.
Coomer CE et al.
Investigative Ophthalmology & Visual Science, 2018
A novel de novo CAPN5 mutation in a patient with inflammatory vitreoretinopathy, hearing loss, and developmental delay.
Velez G et al.
Cold Spring Harbor Molecular Case Studies, 2018
GESPA: classifying nsSNPs to predict disease association.
Khurana JK et al.
Bmc Bioinformatics, 2015
Structural modeling of a novel CAPN5 mutation that causes uveitis and neovascular retinal detachment.
Bassuk AG et al.
Plos One, 2015
Functional validation of a human CAPN5 exome variant by lentiviral transduction into mouse retina.
Wert KJ et al.
Human Molecular Genetics, 2014
Lymphocyte infiltration in CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy.
Mahajan VB et al.
Clinical Ophthalmology (auckland, N.z.), 2013
Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration.
Mahajan VB et al.
Plos Genetics, 2012
Monozygotic twins with CAPN5 autosomal dominant neovascular inflammatory vitreoretinopathy.
Rowell HA et al.
Clinical Ophthalmology (auckland, N.z.), 2012
Inherited retinal disease-associated uveitis.
Hung JH et al.
Survey of Ophthalmology, 0