Эяль Банин

Научные публикации

• A molecular comparison of [Fe-S] cluster-based homeostasis in Escherichia coli and Pseudomonas aeruginosa
• Latex-Bridged Inverse Pickering Emulsion for Durable Superhydrophobic Coatings with Dual Antibacterial Activity
• Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study
• Genetic Analysis of 252 Index Cases with Inherited Retinal Diseases Using a Panel of 351 Retinal Genes
• Genetic and Clinical Analyses of the KIZ-c.226C>T Variant Resulting in a Dual Mutational Mechanism
• Simultaneous Detection of Common Founder Mutations Using a Cost-Effective Deep Sequencing Panel
• Nationwide Prevalence of Inherited Retinal Diseases in the Israeli Population
• PemB, a type III secretion effector in Pseudomonas aeruginosa, affects Caenorhabditis elegans life span
• Development and Evaluation of a New Self-Administered Near Visual Acuity Chart: Accuracy and Feasibility of Usage
• Representation of Women Among Individuals With Mild Variants in ABCA4-Associated Retinopathy: A Meta-Analysis
• Retinal Disorders
• Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
• Fine-tuning FAM161A gene augmentation therapy to restore retinal function
• Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration
• Best Disease: Global Mutations Review, Genotype-Phenotype Correlation, and Prevalence Analysis in the Israeli Population
• A pipeline for identifying guide RNA sequences that promote RNA editing of nonsense mutations that cause inherited retinal diseases
• Real-World Safety and Effectiveness of Voretigene Neparvovec: Results up to 2 Years from the Prospective, Registry-Based PERCEIVE Study
• Protecting the Antibacterial Coating of Urinal Catheters for Improving Safety
• Corrigendum: Comparative genomics of Bacillus cereus sensu lato spp. biocontrol strains in correlation to in-vitro phenotypes and plant pathogen antagonistic capacity
• Synthesis and Characterization of Durable Antibiofilm and Antiviral Silane-Phosphonium Thin Coatings for Medical and Agricultural Applications
• KCNV2-associated retinopathy: genotype-phenotype correlations - KCNV2 study group report 3
• Achromatopsia-Visual Cortex Stability and Plasticity in the Absence of Functional Cones
• Whole exome sequencing of 491 individuals with inherited retinal diseases reveals a large spectrum of variants and identification of novel candidate genes
• ZnO Quantum Photoinitiators as an All-in-One Solution for Multifunctional Photopolymer Nanocomposites
• The biofilm community resurfaces: new findings and post-pandemic progress
• Current Status of Clinical Trials Design and Outcomes in Retinal Gene Therapy
• Gene augmentation therapy attenuates retinal degeneration in a knockout mouse model of Fam161a retinitis pigmentosa
• Morphological and Functional Comparison of Mice Models for Retinitis Pigmentosa
• Exonic Variants that Affect Splicing - An Opportunity for "Hidden" Mutations Causing Inherited Retinal Diseases
• Factors Affecting Readthrough of Natural Versus Premature Termination Codons
• Seeing color following gene augmentation therapy in achromatopsia
• Genetic causes of inherited retinal diseases among Israeli Jews of Ethiopian ancestry
• A green formulation for superhydrophobic coatings based on Pickering emulsion templating for anti-biofilm applications
• Survival of Neural Progenitors Derived from Human Embryonic Stem Cells Following Subretinal Transplantation in Rodents
• Homozygous Knockout of Cep250 Leads to a Relatively Late-Onset Retinal Degeneration and Sensorineural Hearing Loss in Mice
• Comparative genomics of Bacillus cereus sensu lato spp. biocontrol strains in correlation to in-vitro phenotypes and plant pathogen antagonistic capacity
• Ultrasonic-assisted synthesis of lignin-capped Cu₂O nanocomposite with antibiofilm properties
• Retinal Structure and Function in a Knock-in Mouse Model for the FAM161A-p.Arg523∗ Human Nonsense Pathogenic Variant
• Autosomal dominant retinitis pigmentosa with incomplete penetrance due to an intronic mutation of the PRPF31 gene
• Prevalence and associated factors of cystoid macular edema in children with early onset inherited retinal dystrophies
• Small molecule-decorated gold nanoparticles for preparing antibiofilm fabrics
• Antibacterial Properties and Mechanisms of Action of Sonoenzymatically Synthesized Lignin-Based Nanoparticles
• Cuprous Oxide Nanoparticles Decorated Fabric Materials with Anti-biofilm Properties
• Antibacterial, Antibiofilm, and Antiviral Farnesol-Containing Nanoparticles Prevent Staphylococcus aureus from Drug Resistance Development
• PrrT/A, a Pseudomonas aeruginosa Bacterial Encoded Toxin-Antitoxin System Involved in Prophage Regulation and Biofilm Formation
• Ultra-widefield fundus autofluorescence imaging in patients with autosomal recessive retinitis pigmentosa reveals a genotype-phenotype correlation
• Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily
• ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease
• Translational Read-Through Drugs (TRIDs) Are Able to Restore Protein Expression and Ciliogenesis in Fibroblasts of Patients with Retinitis Pigmentosa Caused by a Premature Termination Codon in FAM161A
• Relatively mild blue cone monochromacy phenotype caused by various haplotypes in the L- and M-cone opsin genes
• Non-radical synthesis of chitosan-quercetin polysaccharide: Properties, bioactivity and applications
• Enhanced S-Cone Syndrome Masquerading as TORCH in an Infant and a Toddler
• Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia
• Outer retinal transduction by AAV2-7m8 following intravitreal injection in a sheep model of CNGA3 achromatopsia
• Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities
• Retinal Degeneration Associated With RPGRIP1: A Review of Natural History, Mutation Spectrum, and Genotype-Phenotype Correlation in 228 Patients
• Structural Differences Across Multiple Visual Cortical Regions in the Absence of Cone Function in Congenital Achromatopsia
• A deep intronic substitution in CNGB3 is one of the major causes of achromatopsia among Jewish patients
• Autoimmune retinopathy: clinical, electrophysiological, and immunological features in nine patients with long-term follow-up
• In Situ Grafting of Silica Nanoparticle Precursors with Covalently Attached Bioactive Agents to Form PVA-Based Materials for Sustainable Active Packaging
• Cortical Visual Mapping following Ocular Gene Augmentation Therapy for Achromatopsia
• Fluorine-Free Superhydrophobic Coating with Antibiofilm Properties Based on Pickering Emulsion Templating
• Broadening INPP5E phenotypic spectrum: detection of rare variants in syndromic and non-syndromic IRD
• Heterozygous deletions of noncoding parts of the PRPF31 gene cause retinitis pigmentosa via reduced gene expression
• Cell-Based Therapies for Age-Related Macular Degeneration
• KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints-KCNV2 Study Group Report 2
• An Efficient, Counter-Selection-Based Method for Prophage Curing in Pseudomonas aeruginosa Strains
• SENIOR-LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis
• A new mouse model for retinal degeneration due to Fam161a deficiency
• KCNV2-Associated Retinopathy: Genetics, Electrophysiology, and Clinical Course-KCNV2 Study Group Report 1
• Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children
• Naturally-occurring myopia and loss of cone function in a sheep model of achromatopsia
• Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations
• Correlation of Response between Both Eyes to First- and Second-Line Anti-VEGF Therapy in Diabetic Macular Edema
• Evaluation of Photoreceptor Transduction Efficacy of Capsid-Modified Adeno-Associated Viral Vectors Following Intravitreal and Subretinal Delivery in Sheep
• A unique PRDM13-associated variant in a Georgian Jewish family with probable North Carolina macular dystrophy and the possible contribution of a unique CFH variant
• Characterization of PfiT/PfiA toxin-antitoxin system of Pseudomonas aeruginosa that affects cell elongation and prophage induction
• Prevention and Treatment of Pseudomonas Aeruginosa-Based Biofilm with Ethanol
• Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
• Surfactant-free synthesis of a water-soluble PEGylated nanographeneoxide/metal-oxide nanocomposite as engineered antimicrobial weaponry
• Antibiotic nanoparticles embedded into the Parylene C layer as a new method to prevent medical device-associated infections
• MgF₂ nanoparticle-coated teeth inhibit Streptococcus mutans biofilm formation on a tooth model
• The Complexity of the Holobiont in the Red Sea Coral Euphyllia paradivisa under Heat Stress
• Antibacterial Activity Against Methicillin-Resistant Staphylococcus aureus of Colloidal Polydopamine Prepared by Carbon Dot Stimulated Polymerization of Dopamine
• An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers
• A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC)
• TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations
• The Algal Symbiont Modifies the Transcriptome of the Scleractinian Coral Euphyllia paradivisa During Heat Stress
• Engineering Irrigation Drippers with Rechargeable N-Halamine Nanoparticles for Antifouling Applications
• Antibacterial properties of polypyrrole-treated fabrics by ultrasound deposition
• The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies
• Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders
• A novel intronic mutation of PDE6B is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews
• THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES
• An ontological foundation for ocular phenotypes and rare eye diseases
• Consecutive unilateral recording of the two eyes affects dark-adapted ERG responses, when compared to simultaneous bilateral recording
• Photoreceptor Guanylate Cyclase (GUCY2D) Mutations Cause Retinal Dystrophies by Severe Malfunction of Ca²⁺-Dependent Cyclic GMP Synthesis
• Can an in vivo imaging system be used to determine localization and biodistribution of AAV5-mediated gene expression following subretinal and intravitreal delivery in mice?
• Immunological Properties of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells
• Engineering of a New Bisphosphonate Monomer and Nanoparticles of Narrow Size Distribution for Antibacterial Applications
• Six Years and Counting: Restoration of Photopic Retinal Function and Visual Behavior Following Gene Augmentation Therapy in a Sheep Model of CNGA3 Achromatopsia
• Contrary to popular belief, chinchillas do not have a pure rod retina
• Structural and functional characterization of PL28 family ulvan lyase NLR48 from Nonlabens ulvanivorans
• Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population
• Imparting superhydrophobic and biocidal functionalities to a polymeric substrate by the sonochemical method
• The Genetics of Usher Syndrome in the Israeli and Palestinian Populations
• Structure-function analyses of a PL24 family ulvan lyase reveal key features and suggest its catalytic mechanism
• A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans
• Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects
• Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa
• SawR a new regulator controlling pyomelanin synthesis in Pseudomonas aeruginosa
• Measuring Cyclic Diguanylate (c-di-GMP)-Specific Phosphodiesterase Activity Using the MANT-c-di-GMP Assay
• Ferric Uptake Regulator Fur Is Conditionally Essential in Pseudomonas aeruginosa
• A symbiotic-like biologically-driven regenerating fabric
• NANOCI-Nanotechnology Based Cochlear Implant With Gapless Interface to Auditory Neurons
• Long-Term Efficacy of GMP Grade Xeno-Free hESC-Derived RPE Cells Following Transplantation
• Editorial: Bacterial pathogens, antibiotics and antibiotic resistance
• Safety and Efficacy Evaluation of rAAV2tYF-PR1.7-hCNGA3 Vector Delivered by Subretinal Injection in CNGA3 Mutant Achromatopsia Sheep
• Characterization of physiological defects in adult SIRT6-/- mice
• From Nano to Micro: using nanotechnology to combat microorganisms and their multidrug resistance
• Course of Sodium Iodate-Induced Retinal Degeneration in Albino and Pigmented Mice
• Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma
• New Ulvan-Degrading Polysaccharide Lyase Family: Structure and Catalytic Mechanism Suggests Convergent Evolution of Active Site Architecture
• Gene Augmentation Therapy for a Missense Substitution in the cGMP-Binding Domain of Ovine CNGA3 Gene Restores Vision in Day-Blind Sheep
• Ga@C-dots as an antibacterial agent for the eradication of Pseudomonas aeruginosa
• Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
• Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss
• Graft polymerization of styryl bisphosphonate monomer onto polypropylene films for inhibition of biofilm formation
• Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome
• Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred
• Synthesis and characterization of crosslinked polyisothiouronium methylstyrene nanoparticles of narrow size distribution for antibacterial and antibiofilm applications
• Engineering of Superparamagnetic Core-Shell Iron Oxide/N-Chloramine Nanoparticles for Water Purification
• Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data
• Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness
• Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual
• Characterising the phenotype and progression of sporadic adult-onset foveomacular vitelliform dystrophy
• Draft Genome Sequences of Two Multidrug-Resistant Extended-Spectrum-β-Lactamase-Producing Klebsiella pneumoniae Strains Causing Bloodstream Infections
• New Family of Ulvan Lyases Identified in Three Isolates from the Alteromonadales Order
• Retinal Phenotype following Combined Deletion of the Chemokine Receptor CCR2 and the Chemokine CX3CL1 in Mice
• Whole Exome Sequencing Reveals Mutations in Known Retinal Disease Genes in 33 out of 68 Israeli Families with Inherited Retinopathies
• Oligoribonuclease is a central feature of cyclic diguanylate signaling in Pseudomonas aeruginosa
• Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations
• Gene Augmentation Therapy Restores Retinal Function and Visual Behavior in a Sheep Model of CNGA3 Achromatopsia
• Nonsyndromic Early-Onset Cone-Rod Dystrophy and Limb-Girdle Muscular Dystrophy in a Consanguineous Israeli Family are Caused by Two Independent yet Linked Mutations in ALMS1 and DYSF
• Bevacizumab treatment for neovascular age-related macular degeneration in the setting of a clinic: "real life" long-term outcome
• Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)
• Novel type III effectors in Pseudomonas aeruginosa
• New life for an old antibiotic
• Advancing therapeutic strategies for inherited retinal degeneration: recommendations from the Monaciano Symposium
• Biology and therapy of inherited retinal degenerative disease: insights from mouse models
• Genetics and Disease Expression in the CNGA3 Form of Achromatopsia: Steps on the Path to Gene Therapy
• Killing mechanism of stable N-halamine cross-linked polymethacrylamide nanoparticles that selectively target bacteria
• Mutations in PNPLA6 are linked to photoreceptor degeneration and various forms of childhood blindness
• Association between missense mutations in the BBS2 gene and nonsyndromic retinitis pigmentosa
• Whole exome sequencing reveals GUCY2D as a major gene associated with cone and cone-rod dystrophy in Israel
• Draft Genome Sequence of Pseudoalteromonas sp. Strain PLSV, an Ulvan-Degrading Bacterium
• Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular features
• Draft Genome Sequences of Two Ulvan-Degrading Isolates, Strains LTR and LOR, That Belong to the Alteromonas Genus
• The Pseudomonas aeruginosa phosphate transport protein PstS plays a phosphate-independent role in biofilm formation
• Flicker cone function in normal and day blind sheep: a large animal model for human achromatopsia caused by CNGA3 mutation
• Draft Genome Sequence of Nonlabens ulvanivorans, an Ulvan-Degrading Bacterium
• IMPG2-associated retinitis pigmentosa displays relatively early macular involvement
• Fellow eye effect of unilateral intravitreal bevacizumab injection in eyes with diabetic macular edema
• Bevacizumab treatment for choroidal neovascularization associated with adult-onset foveomacular vitelliform dystrophy
• A homozygous nonsense CEP250 mutation combined with a heterozygous nonsense C2orf71 mutation is associated with atypical Usher syndrome
• Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome
• Characterization and antibacterial properties of N-halamine-derivatized cross-linked polymethacrylamide nanoparticles
• Biofilm prevention on cochlear implants
• Degeneration modulates retinal response to transient exogenous oxidative injury
• Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping
• Biofilm formation and susceptibility to gentamicin and colistin of extremely drug-resistant KPC-producing Klebsiella pneumoniae
• Ocular phenotype analysis of a family with biallelic mutations in the BEST1 gene
• Synthesis and characterization of fluoro-modified polypropylene films for inhibition of biofilm formation
• Recognizing the KCNV2-related retinal phenotype. Author reply
• The effect of pstS and phoB on quorum sensing and swarming motility in Pseudomonas aeruginosa
• Genetic heterogeneity and consanguinity lead to a "double hit": homozygous mutations of MYO7A and PDE6B in a patient with retinitis pigmentosa
• The synergistic effect of visible light and gentamycin on Pseudomona aeruginosa microorganisms
• Mutations in ARL2BP, encoding ADP-ribosylation-factor-like 2 binding protein, cause autosomal-recessive retinitis pigmentosa
• Eradication of multi-drug resistant bacteria by a novel Zn-doped CuO nanocomposite
• Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene
• Mutations in RAB28, encoding a farnesylated small GTPase, are associated with autosomal-recessive cone-rod dystrophy
• Cone dystrophy with supernormal rod response: novel KCNV2 mutations in an underdiagnosed phenotype
• Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations
• Exome sequencing identifies a founder frameshift mutation in an alternative exon of USH1C as the cause of autosomal recessive retinitis pigmentosa with late-onset hearing loss
• Improved triclosan delivery by a novel silica-based nanocomposite
• Antibacterial and antibiofilm properties of yttrium fluoride nanoparticles
• BBS1 mutations in a wide spectrum of phenotypes ranging from nonsyndromic retinitis pigmentosa to Bardet-Biedl syndrome
• The effect of cone opsin mutations on retinal structure and the integrity of the photoreceptor mosaic
• Draft genome sequence of an extremely drug-resistant KPC-producing Klebsiella pneumoniae ST258 epidemic strain
• Changes in microbial communities associated with the sea anemone Anemonia viridis in a natural pH gradient
• A nonsense mutation in PDE6H causes autosomal-recessive incomplete achromatopsia
• Association of pattern dystrophy with an HTRA1 single-nucleotide polymorphism
• Understanding the antibacterial mechanism of CuO nanoparticles: revealing the route of induced oxidative stress
• Sonochemical coatings of ZnO and CuO nanoparticles inhibit Streptococcus mutans biofilm formation on teeth model
• Fundus albipunctatus: novel mutations and phenotypic description of Israeli patients
• Subsurface femtosecond tissue alteration: selectively photobleaching macular degeneration pigments in near retinal contact
• Reduced susceptibility to chlorhexidine among extremely-drug-resistant strains of Klebsiella pneumoniae
• Changes in coral microbial communities in response to a natural pH gradient
• Antibiofilm surface functionalization of catheters by magnesium fluoride nanoparticles
• Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness
• Multi-species biofilms: living with friendly neighbors
• Mutations in C8orf37, encoding a ciliary protein, are associated with autosomal-recessive retinal dystrophies with early macular involvement
• Retinal function and structure in the hypotransferrinemic mouse
• Improved antibacterial and antibiofilm activity of magnesium fluoride nanoparticles obtained by water-based ultrasound chemistry
• Exome sequencing and cis-regulatory mapping identify mutations in MAK, a gene encoding a regulator of ciliary length, as a cause of retinitis pigmentosa
• Zinc-desferrioxamine attenuates retinal degeneration in the rd10 mouse model of retinitis pigmentosa
• Surface acoustic waves increase the susceptibility of Pseudomonas aeruginosa biofilms to antibiotic treatment
• FvbA is required for vibriobactin utilization in Pseudomonas aeruginosa
• A homozygous frameshift mutation in BEST1 causes the classical form of Best disease in an autosomal recessive mode
• A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews
• Homozygosity mapping reveals null mutations in FAM161A as a cause of autosomal-recessive retinitis pigmentosa
• Human retinal disease from AIPL1 gene mutations: foveal cone loss with minimal macular photoreceptors and rod function remaining
• Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa
• The impact of reduced pH on the microbial community of the coral Acropora eurystoma
• Molecular anthropology meets genetic medicine to treat blindness in the North African Jewish population: human gene therapy initiated in Israel
• An ancient autosomal haplotype bearing a rare achromatopsia-causing founder mutation is shared among Arab Muslims and Oriental Jews
• Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population
• Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array
• Increase in rhamnolipid synthesis under iron-limiting conditions influences surface motility and biofilm formation in Pseudomonas aeruginosa
• Effect of para-aminobenzoic acid on the course of retinal degeneration in the rd10 mouse
• Directed differentiation of human embryonic stem cells into functional retinal pigment epithelium cells
• Antibiofilm activity of nanosized magnesium fluoride
• Role of flagella in virulence of the coral pathogen Vibrio coralliilyticus
• A novel day blindness in sheep: epidemiological, behavioural, electrophysiological and histopathological studies
• Intravitreal bevacizumab therapy for neovascular age-related macular degeneration associated with poor initial visual acuity
• Loss of the metalloprotease ADAM9 leads to cone-rod dystrophy in humans and retinal degeneration in mice
• The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients
• Antioxidant or neurotrophic factor treatment preserves function in a mouse model of neovascularization-associated oxidative stress
• Sequence variants in HTRA1 and LOC387715/ARMS2 and phenotype and response to photodynamic therapy in neovascular age-related macular degeneration in populations from Israel
• The role of microorganisms in coral bleaching
• The potential of desferrioxamine-gallium as an anti-Pseudomonas therapeutic agent
• Association of complement factor H Y402H polymorphism with phenotype of neovascular age related macular degeneration in Israel
• Four USH2A founder mutations underlie the majority of Usher syndrome type 2 cases among non-Ashkenazi Jews
• P35S mutation in the NOG gene associated with Teunissen-Cremers syndrome and features of multiple NOG joint-fusion syndromes
• A novel de novo PAX6 mutation in an Ashkenazi-Jewish family with aniridia
• Hypomorphic mutations in syndromic encephalocele genes are associated with Bardet-Biedl syndrome
• Retinal disease in Usher syndrome III caused by mutations in the clarin-1 gene
• Ischemic preconditioning of the rat retina: protective role of ferritin
• A common founder mutation of CERKL underlies autosomal recessive retinal degeneration with early macular involvement among Yemenite Jews
• Influence of quorum sensing and iron on twitching motility and biofilm formation in Pseudomonas aeruginosa
• Homozygosity for a novel ABCA4 founder splicing mutation is associated with progressive and severe Stargardt-like disease
• A complex expression pattern of Pax6 in the pigeon retina
• A non-ancestral RPGR missense mutation in families with either recessive or semi-dominant X-linked retinitis pigmentosa
• Progenitor cells and retinal angiogenesis
• Novel USH2A mutations in Israeli patients with retinitis pigmentosa and Usher syndrome type 2
• Lack of benefit of early awareness to age-related macular degeneration
• Myeloid progenitors differentiate into microglia and promote vascular repair in a model of ischemic retinopathy
• Autozygosity mapping of Bardet-Biedl syndrome to 12q21.2 and confirmation of FLJ23560 as BBS10
• Application of the standard photodynamic treatment protocol for symptomatic circumscribed choroidal hemangioma
• T2-TrpRS inhibits preretinal neovascularization and enhances physiological vascular regrowth in OIR as assessed by a new method of quantification