Эяль Банин

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

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

Эяль Банин

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