Search results for "Retinal"

showing 10 items of 631 documents

Synthetic Polyclonal-Derived CDR Peptides as an Innovative Strategy in Glaucoma Therapy

2019

The pathogenesis of glaucoma is strongly associated with the occurrence of autoimmune-mediated loss of retinal ganglion cells (RGCs) and additionally, recent evidence shows that specific antibody-derived signature peptides are significantly differentially expressed in sera of primary-open angle glaucoma patients (POAG) compared to healthy controls. Synthetically antibody-derived peptides can modulate various effector functions of the immune system and act as antimicrobial or antiviral molecules. In an ex vivo adolescent glaucoma model, this study, for the first time, demonstrates that polyclonal-derived complementarity-determining regions (CDRs) can significantly increase the survival rate …

<i>Sus scrofa domestica</i>lcsh:MedicineRetinal ganglionEpitopeArticleSus scrofa domestica03 medical and health scienceschemistry.chemical_compound0302 clinical medicineImmune systemMedicine030304 developmental biology0303 health sciencesHTRA2synthetic CDR peptidesbusiness.industrylcsh:RautoimmunityRetinalGeneral MedicineProtein ubiquitinationCell biologyglaucomachemistryneuroprotectionSignal transductionbusinessVDAC2030217 neurology & neurosurgeryEx vivoJournal of Clinical Medicine
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Accurate estimation of retinal vessel width using bagged decision trees and an extended multiresolution Hermite model.

2012

We present an algorithm estimating the width of retinal vessels in fundus camera images. The algorithm uses a novel parametric surface model of the cross-sectional intensities of vessels, and ensembles of bagged decision trees to estimate the local width from the parameters of the best-fit surface. We report comparative tests with REVIEW, currently the public database of reference for retinal width estimation, containing 16 images with 193 annotated vessel segments and 5066 profile points annotated manually by three independent experts. Comparative tests are reported also with our own set of 378 vessel widths selected sparsely in 38 images from the Tayside Scotland diabetic retinopathy scre…

Accurate estimationComputer scienceStability (learning theory)Decision treeHealth Informaticscomputer.software_genreSensitivity and SpecificityPattern Recognition AutomatedSet (abstract data type)Parametric surfaceImage Interpretation Computer-AssistedHumansRadiology Nuclear Medicine and imagingFluorescein AngiographyHermite polynomialsDiabetic RetinopathySettore INF/01 - InformaticaRadiological and Ultrasound TechnologyReproducibility of ResultsRetinal VesselsImage EnhancementComputer Graphics and Computer-Aided DesignData setComputer Vision and Pattern RecognitionData miningRetinal images Vessel width Multiresolution Hermite model Ensembles of bagged decision trees Medical image analysiscomputerAlgorithmsTest dataRetinoscopyMedical image analysis
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CNGB3 mutations account for 50% of all cases with autosomal recessive achromatopsia

2005

Contains fulltext : 47591.pdf (Publisher’s version ) (Closed access) Achromatopsia is a congenital, autosomal recessively inherited disorder characterized by a lack of color discrimination, low visual acuity (<0.2), photophobia, and nystagmus. Mutations in the genes for CNGA3, CNGB3, and GNAT2 have been associated with this disorder. Here, we analyzed the spectrum and prevalence of CNGB3 gene mutations in a cohort of 341 independent patients with achromatopsia. In 163 patients, CNGB3 mutations could be identified. A total of 105 achromats carried apparent homozygous mutations, 44 were compound (double) heterozygotes, and 14 patients had only a single mutant allele. The derived CNGB3 mutatio…

AchromatopsiaGenetics and epigenetic pathways of disease [NCMLS 6]genetic structuresGATED CATION CHANNELCNGB3 mutationsNonsense mutationMutantCyclic Nucleotide-Gated Cation ChannelsColor Vision DefectsGenes RecessiveLocus (genetics)Gene mutationBiologyTOTAL COLOURBLINDNESSIon ChannelsCLONINGDogscyclic nucleotide-gated channelGNAT2GeneticsmedicineLOCUSAnimalsHumansMissense mutationNeurosensory disorders [UMCN 3.3]ACHM3 locusDog DiseasesAlleleAllelesGenetics (clinical)Geneticstotal colorblindnessGNAT2PHOTORECEPTORSDYSTROPHYmedicine.diseaseCONE DEGENERATIONGENEeye diseasesPhenotypeEvaluation of complex medical interventions [NCEBP 2]MutationRetinal Cone Photoreceptor Cellssense organsachromatopsiarod monochromacyALPHA-SUBUNIThuman activities
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A comparison among different techniques for human ERG signals processing and classification

2014

A comparison among different techniques for human ERG signals processing and classification ( Articles not published yet, but available online Article in press About articles in press (opens in a new window) ) Barraco, R.a, Persano Adorno, D.a , Brai, M.a, Tranchina, L.b a Dipartimento di Fisica e Chimica, Università di Palermo and CNISM, Viale delle Scienze, Ed. 18, I-90128 Palermo, Italy b Laboratorio di Fisica e Tecnologie Relative - UniNetLab, Università di Palermo, Viale delle Scienze, Ed. 18, I-90128 Palermo, Italy Abstract Feature detection in biomedical signals is crucial for deepening our knowledge about the involved physiological processes. To achieve this aim, many analytic appro…

Achromatopsiagenetic structuresComputer scienceBiophysicsGeneral Physics and AstronomyColor Vision DefectsPrincipal component analysiWavelet analysisPattern Recognition AutomatedWaveletRetinal pathologieElectroretinographymedicineHumansRadiology Nuclear Medicine and imagingComputer visionFeature detection (computer vision)Principal Component AnalysisSignal processingFourier Analysisbusiness.industryWavelet transformSignal Processing Computer-AssistedPattern recognitionGeneral Medicinemedicine.diseaseSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)eye diseasesERG signalClinical diagnosisPrincipal component analysissense organsArtificial intelligencebusinessErgPhysica Medica
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Mutations in the Cone Photoreceptor G-Protein α-Subunit Gene GNAT2 in Patients with Achromatopsia

2002

Achromatopsia is an autosomal recessively inherited visual disorder that is present from birth and that features the absence of color discrimination. We here report the identification of five independent families with achromatopsia that segregate protein-truncation mutations in the GNAT2 gene, located on chromosome 1p13. GNAT2 encodes the cone photoreceptor-specific alpha-subunit of transducin, a G-protein of the phototransduction cascade, which couples to the visual pigment(s). Our results demonstrate that GNAT2 is the third gene implicated in achromatopsia.

Achromatopsiagenetic structuresMolecular Sequence DataColor Vision DefectsBiologymedicine.disease_causeRetinal Cone Photoreceptor CellsReportGNAT2 geneGeneticsmedicineHumansGenetics(clinical)TransducinGeneGenetics (clinical)GeneticsGNAT2Mutationmedicine.diseaseRod monocromacyeye diseasesPedigreeColor Vision DefectsMutationRetinal Cone Photoreceptor CellsAchromatopsiaTransducinsense organsVisual phototransductionThe American Journal of Human Genetics
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Automatic detection and classification of retinal vascular landmarks

2014

The main contribution of this paper is introducing a method to distinguish between different landmarks of the retina: bifurcations and crossings. The methodology may help in differentiating between arteries and veins and is useful in identifying diseases and other special pathologies, too. The method does not need any special skills, thus it can be assimilated to an automatic way for pinpointing landmarks; moreover it gives good responses for very small vessels. A skeletonized representation, taken out from the segmented binary image (obtained through a preprocessing step), is used to identify pixels with three or more neighbors. Then, the junction points are classified into bifurcations or…

Acoustics and UltrasonicsComputer scienceMaterials Science (miscellaneous)General MathematicsPreprocessorRadiology Nuclear Medicine and imagingComputer visionretinal vessel landmark points retinal vessel structure classificationRepresentation (mathematics)Instrumentationlcsh:R5-920PixelSettore INF/01 - Informaticabusiness.industryBinary imagelcsh:Mathematicslcsh:QA1-939retinal vessel structure classificationSignal ProcessingComputer Vision and Pattern RecognitionArtificial intelligencebusinessPrecision and recallretinal vessel landmark pointslcsh:Medicine (General)Biotechnology
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Retinoblastoma epidemiology: Does the evidence matter?

2007

It has been proposed that retinoblastoma is 'caused' by two sequential mutations affecting the RB1 gene, but this is a rather outdated view of cancer aetiology that does not take into account a large amount of new acquisitions such as chromosomal and epigenetic alterations. Retinoblastoma remains probably the only cancer in which the rather simplistic 'two hit' mutational model is still considered of value, although cancer is known to be associated with genomic and microsatellite instability, defects of the DNA mismatch repair system, alterations of DNA methylation and hystone acethylation/deacethylation, and aneuploidy. Moreover, as it is shown herein, the predictions made by the 'two hit'…

AdultCancer ResearchAdolescentRetinal NeoplasmsRetinoblastoma Aneuploidy Two hit theoryDiseaseBiologyAge DistributionChromosome instabilitymedicineHumansEpigeneticsAge of OnsetChildGerm-Line MutationGeneticsRetinoblastomaRetinoblastomaMicrosatellite instabilityCancerInfantMiddle Agedmedicine.diseasePedigreeSettore BIO/18 - GeneticaOncologyChild PreschoolDNA methylationDNA mismatch repair
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Effects of Early Postfiltration Ocular Hypotony on Visual Acuity, Long-term Intraocular Pressure Control, and Posterior Segment Morphology

2001

Purpose To determine whether hypotony after filtration surgery has any influence on visual acuity and intraocular pressure (IOP) lowering. Patients and methods We prospectively investigated 43 eyes of 43 patients undergoing trabeculectomy without the use of antimetabolites for 12 months. Results The lowest postoperative IOP valued 4.9 +/- 3.6 mm Hg (range, 0-14 mm Hg). It correlated statistically significant with the IOP 6 weeks (P = 0.016), 6 months (P = 0.009), and 1 year after surgery (P = 0.027). Eyes with a deterioration of visual acuity 6 weeks after surgery had undergone a stronger postoperative hypotony (correlation with lowest postoperative IOP, P = 0.035). The mean period with an …

AdultIntraocular pressuremedicine.medical_specialtyVisual acuitygenetic structuresFundus Oculimedicine.medical_treatmentVisual AcuityGlaucomaOcular HypotensionTrabeculectomyOcular hypotonyRetinal DiseasesOphthalmologymedicineHumansTrabeculectomyProspective StudiesProspective cohort studyIntraocular Pressurebusiness.industryChoroid Diseasesmedicine.diseaseeye diseasesPosterior segment of eyeballOphthalmologyTreatment OutcomeFiltration surgerymedicine.symptombusinessGlaucoma Open-AnglePapilledemaJournal of Glaucoma
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Retinal vessel analysis and heart rate variability

2014

Heart rate variability (HRV) is used to index the vegetative nervous system and is linked with cardiovascular and nervous diseases [1]. Funduscopic assessment of the retinal vasculature can be utilized to evaluate the health status of microcirculation and to assess the predisposition of major vascular diseases [2]. The purpose of this study was, for the first time, to examine the influence of HRV on microcirculation as an early marker of cardiovascular alteration. The study population was comprised of apparently healthy employees of a high-tech company in Germany. The participants spanned the entire age of the work force (18–65 years) and all levels of socioeconomic status. A total of 292 s…

AdultMaleCentral retinal arterymedicine.medical_specialtyAdolescentRetinal ArteryYoung Adultchemistry.chemical_compoundHeart Ratemedicine.arteryInternal medicineHeart ratemedicineHumansHeart rate variabilityVagal toneAgedmedicine.diagnostic_testbusiness.industryMicrocirculationFundus photographyRetinal VesselsRetinalMiddle Agedmedicine.anatomical_structureBlood pressurechemistryCardiovascular DiseasesCardiologyFemaleCardiology and Cardiovascular MedicinebusinessOptic discInternational Journal of Cardiology
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Two Novel Deletions (Array CGH Findings) in Pigment Dispersion Syndrome

2007

Purpose: We report the first male with pigment dispersion syndrome and a balanced translocation t(10;15)(p11.1;q11.1). Methods: Cytogenetic analyses using Giemsa banding and FISH methods, and array CGH were performed. Results: Array CGH analyses did not show altered DNA sequences in the breakpoints of the translocation, but revealed two novel deletions in 2q22.1 and 18q22.1. Conclusion: We suppose that the coexistence of t(10;15) and pigment dispersion syndrome in our patient is a coincidence. The deletion in 2q22.1, where the gene LRP1B has been located, may play a major role in the dysembryogenesis of the eye and cause the disorder.

AdultMaleEye DiseasesLRP1BG bandingChromosomal translocationBiologyTranslocation GeneticDNA sequencingmedicineHumansPigment Epithelium of EyeGeneIn Situ Hybridization FluorescenceGenetics (clinical)Sequence DeletionGeneticsChromosomes Human Pair 15Chromosomes Human Pair 10BreakpointNucleic Acid Hybridizationmedicine.diseaseMolecular biologyOphthalmologyPediatrics Perinatology and Child HealthPigment dispersion syndromeFish <Actinopterygii>Retinal PigmentsOphthalmic Genetics
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