Search results for "Confocal"

showing 10 items of 444 documents

Novel Munc13-4 mutations in children and young adult patients with haemophagocytic lymphohistiocytosis

2006

Familial haemophagocytic lymphohistiocytosis (FHL) is a genetically heterogeneous disorder characterised by constitutive defects in cellular cytotoxicity resulting in fever, hepatosplenomegaly and cytopenia, and the outcome is fatal unless treated by chemoimmunotherapy followed by haematopoietic stem‐cell transplantation. Since 1999, mutations in the perforin gene giving rise to this disease have been identified; however, these account only for 40% of cases. Lack of a genetic marker hampers the diagnosis, suitability for transplantation, selection of familial donors, identification of carriers, genetic counselling and prenatal diagnosis. Mutations in the Munc13–4 gene have recently been des…

EXPRESSIONMalePRF1AdolescentFHLBlotting WesternDNA Mutational AnalysisHepatosplenomegalyDONORSPrenatal diagnosisBiologymedicine.disease_causeLymphohistiocytosis HemophagocyticGeneticsmedicinePERFORIN GENE-MUTATIONSHumansUNC13DChildGenetics (clinical)Family HealthSPECTRUMHemophagocytic lymphohistiocytosisMutationCytopeniaMicroscopy ConfocalIDENTIFICATIONGenetic heterogeneityInfant NewbornCYTOTOXIC T-LYMPHOCYTESInfantMembrane Proteinsmedicine.diseaseBONE-MARROW-TRANSPLANTATIONTransplantationMicroscopy ElectronChild PreschoolMutationImmunologyFemalemedicine.symptomLetter to JMGT-Lymphocytes CytotoxicJournal of Medical Genetics
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Confocal microscopy study of the distribution, content and activity of mitochondria during Paracentrotus lividus development

2007

Summary In the present paper we applied confocal microscopy andfluorescence technologies for studying the distribution andthe oxidative activity of sea urchin ( Paracentrotus lividus )mitochondria during development, by in vivo incubating eggsand embryos with cell-permeant MitoTracker probes. Wecalculated, by a mathematical model, the intensity values, the variations of intensity, and the variation index of incorporatedfluorochromes. Data demonstrate that mitochondrial massdoes not change during development, whereas mitochondrialrespirationincreases.Inaddition,startingfrom16blastomeresstage, some regions of the embryo contain organelles moreactive in oxygen consumption. Introduction The con…

Embryo NonmammalianHistologyConfocal laser scanning microscopeNanotechnologyMitochondrionParacentrotus lividussea urchinPathology and Forensic Medicinelaw.inventionIn vivoConfocal microscopylawdevelopment; sea urchin; mitochondrial mass; CLSMbiology.animalOrganelleMicroscopyAnimalsdevelopmentSea urchinmitochondrial maMicroscopy Confocalbiologybiology.organism_classificationMitochondriaOxygenParacentrotusBiophysicsCLSMOxidation-ReductionJournal of Microscopy
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The oxidizing agent tertiary butyl hydroperoxide induces disturbances in spindle organization, c-meiosis, and aneuploidy in mouse oocytes

1996

It has been recently proposed that a concomitant generation of oxidative stress of oocytes with increasing maternal age may be a major factor responsible for the age-related increase in aneuploid conceptions. As a preliminary step in the testing of this hypothesis, we need to confirm that oxidative stress in itself can induce errors in chromosome segregation. In order to achieve this goal, germinal vesicle (GV)-stage mouse oocytes from unstimulated ICR and (C57BL x CBA) F1 hybrid female mice were matured in vitro for 9 h for metaphase I (MI) oocytes or 16 h for metaphase II (MII) oocytes in the presence of varying concentrations of the oxidizing agent tertiary-butyl hydroperoxide (tBH). MII…

EmbryologyAneuploidyIn Vitro TechniquesBiologyChromosome segregationMicetert-ButylhydroperoxideMeiosisBone plateGeneticsmedicineAnimalsHumansMolecular BiologyMice Inbred ICRMicroscopy ConfocalGerminal vesicleMeiosis IIObstetrics and GynecologyCell BiologyAneuploidyOxidantsmedicine.diseaseOocyteMolecular biologyPeroxidesCell biologyMice Inbred C57BLMeiosisOxidative Stressmedicine.anatomical_structureReproductive MedicineMice Inbred CBAOocytesSpindle organizationFemaleMaternal AgeDevelopmental Biology
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Effects of acids used in the microabrasion technique: microhardness and confocal microscopy analysis

2015

Background: This study evaluated the effects of the acids used in the microabrasion on enamel. Material and Methods: Seventy enamel/dentine blocks (25 mm 2 ) of bovine incisors were divided into 7 groups (n=10). Experimental groups were treated by active/passive application of 35% H 3 PO 4 (E1/E2) or 6.6% HCl (E3/ E4). Control groups were treated by microabrasion with H 3 PO 4 +pumice (C5), HCl+silica (C6), or no treatment (C7). The superficial (SMH) and cross-sectional (CSMH; depths of 10, 25, 50, and 75 μm) microhardness of enamel were analyzed. Morphology was evaluated by confocal laser-scanning microscopy (CLSM). Data were analyzed by analysis of variance (Proc Mixed), Tukey, and Dunnet…

Enamel paintChemistryConfocalResearchMineralogyOdontologíaEsthetic Dentistry:CIENCIAS MÉDICAS [UNESCO]Indentation hardnessCiencias de la saludlaw.inventionstomatognathic systemConfocal microscopylawvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumGeneral DentistryNuclear chemistry
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Evolución de la morfología dimensional del alveolo post-extracción mediante Microscopía Láser Confocal de Barrido (CLSM)

2014

Después de la exodoncia, se produce una remodelación de los tejidos duros y blandos del proceso alveolar que genera cambios en el perfil clínico del alveolo post-extracción. Estos cambios morfológicos también afectan a los tejidos adyacentes de los dientes vecinos a la zona de la exodoncia. La magnitud de estos cambios dimensionales es importante para la toma de decisiones clínicas y la aceptación de un plan de tratamiento integral, con las soluciones necesarias para las posibles complicaciones que puedan aparecer durante la rehabilitación protésica. Además, actualmente se da una mayor importancia a la estética, por lo que un conocimiento del patrón de remodelación y de los cambios morfológ…

Extracción dentalUNESCO::CIENCIAS MÉDICASCambios morfológicosAlveolo post-extracción:CIENCIAS MÉDICAS [UNESCO]CLSMMicroscopía Confocal
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Immunodetection of the microvillous cytoskeleton molecules villin and ezrin in the parasitophorous vacuole wall of Cryptosporidium parvum (Protozoa: …

1999

Microvilli - actin - villin - ezrin - Cryptosporidium parvum The sporozoites and merozoites of the Apicomplexan protozoan Cryptosporidium parvum (C. parvum) invade the apical side of enterocytes and induce the formation of a parasitophorous vacuole which stays in the brush border area and disturbs the distribution of microvilli. The vacuole is separated from the apical cytoplasm of the cell by an electron-dense layer of undetermined composition. In order to characterize the enterocyte cytoskeleton changes that occur during C. parvum invasion and development, we used both confocal immunofluorescence and immunoelectron microscopy to examine at the C.parvum-enterocyte interface the distributio…

Feces/microbiologyIntestines/parasitologyMicrofilament Proteins/ analysisVacuoleddc:616.07Actins/analysisRats Sprague-DawleyFecesMiceEzrinCarrier Proteins/ analysisCryptosporidium/ chemistry/pathogenicity/ultrastructureCytoskeletonMicroscopy ImmunoelectronCytoskeletonMice Inbred BALB CMicroscopy ConfocalbiologyMicrovilliMicrofilament ProteinsCytoskeleton/ chemistryGeneral MedicineCell biologyIntestinesCryptosporidium parvumFemaleVillinHistologyImmunoelectron microscopyVacuoles/ultrastructurePhosphoproteins/ analysisCryptosporidiummacromolecular substancesPathology and Forensic Medicineparasitic diseasesAnimalsApical cytoplasmActinCell Biologybiology.organism_classificationPhosphoproteinsActinsRatsMicrovilli/ chemistryCytoskeletal ProteinsMicroscopy ElectronVacuolesbiology.proteinCarrier ProteinsEuropean journal of cell biology
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PLLA/Fibrin Tubular Scaffold: A New Way for Reliable Endothelial Cell Seeding

2014

In the present work a simple and quick technique for cell seeding into tubular-shaped scaffolds, which allows a homogeneous cell distribution, was tested. The poly-L-lactide (PLLA) scaffolds, prepared via diffusion induced phase separation (DIPS), were filled with fibrin gel in order to obtain a hybrid scaffold for Vascular Tissue Engineering applications. The formation of immobilized fibrin networks on the inner surface of the tubular scaffolds was observed using confocal microscopy and SEM. Morphological analysis of the so-obtained scaffold revealed that the fibrin gel is uniformly distributed on the internal surface of the scaffold, leading to an organized structure. Moreover a penetrati…

FibrinScaffoldMaterials sciencebiologyCell growthGeneral MedicinePenetration (firestop)Fibrinlaw.inventionEndothelial stem cellPhase SeparationTubular scaffoldConfocal microscopylawbiology.proteinSeedingVascular Tissue EngineeringBiomedical engineeringConference Papers in Science
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Dendrites are dispensable for basic motoneuron function but essential for fine tuning of behavior.

2014

Dendrites are highly complex 3D structures that define neuronal morphology and connectivity and are the predominant sites for synaptic input. Defects in dendritic structure are highly consistent correlates of brain diseases. However, the precise consequences of dendritic structure defects for neuronal function and behavioral performance remain unknown. Here we probe dendritic function by using genetic tools to selectively abolish dendrites in identified Drosophila wing motoneurons without affecting other neuronal properties. We find that these motoneuron dendrites are unexpectedly dispensable for synaptic targeting, qualitatively normal neuronal activity patterns during behavior, and basic …

Flight altitudeMotor NeuronsDendritic spikeFine-tuningMultidisciplinaryMicroscopy ConfocalPatch-Clamp TechniquesbiologyBehavior AnimalMotor behaviorDendritesBiological Sciencesbiology.organism_classificationImmunohistochemistryStatistics NonparametricSynapseDrosophila melanogasterFlight AnimalPremovement neuronal activityAnimalsWings AnimalDrosophila melanogasterNeuroscienceFunction (biology)Proceedings of the National Academy of Sciences of the United States of America
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Protein diffusion in mammalian cell cytoplasm.

2011

We introduce a new method for mesoscopic modeling of protein diffusion in an entire cell. This method is based on the construction of a three-dimensional digital model cell from confocal microscopy data. The model cell is segmented into the cytoplasm, nucleus, plasma membrane, and nuclear envelope, in which environment protein motion is modeled by fully numerical mesoscopic methods. Finer cellular structures that cannot be resolved with the imaging technique, which significantly affect protein motion, are accounted for in this method by assigning an effective, position-dependent porosity to the cell. This porosity can also be determined by confocal microscopy using the equilibrium distribut…

Fluorescence-lifetime imaging microscopyCytoplasmMass diffusivity01 natural sciencesBiophysics Simulationslaw.inventionDiffusionlawMolecular Cell BiologyImage Processing Computer-Assistedprotein diffusionMammals0303 health sciencesMultidisciplinaryMicroscopy ConfocalChemistrysolulimaPhysicsQRCell biologyMedicineproteiinin diffuusioPorosityFluorescence Recovery After PhotobleachingResearch ArticleScienceCellsBiophysicsFluorescence correlation spectroscopyModels Biological03 medical and health sciencesdiffuusio (fysikaaliset ilmiöt)Bacterial ProteinsConfocal microscopy0103 physical sciencesAnimalsHumansComputer Simulation010306 general physicsBiology030304 developmental biologyNucleoplasmProtein transportta114ta1182Fluorescence recovery after photobleachingProteinsReproducibility of ResultssoluPhotobleachingProteiinien kuljetusLuminescent ProteinsMicroscopy FluorescenceCytoplasmCatsCellHeLa CellsPloS one
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Optical sectioning by two-pinhole confocal fluorescence microscopy.

2003

A two-pinhole axially superresolving confocal fluorescence imaging system is presented. Based on the concept of subtractive incoherent imaging, the system described here is equipped with a zero-focus complex-transmittance pupil filter in one of the collector paths. The optical sectioning capacity of the system is 25% superior to that of a free-pupil one-pinhole instrument.

Fluorescence-lifetime imaging microscopyMaterials scienceMicroscopy ConfocalOptical sectioningbusiness.industryConfocalScanning confocal electron microscopyGeneral Physics and AstronomyCell BiologyModels TheoreticalImage Enhancementlaw.inventionOpticsMicroscopy FluorescenceStructural BiologyConfocal microscopylawLight sheet fluorescence microscopySubtraction TechniqueMicroscopyGeneral Materials SciencePinhole (optics)businessMicron (Oxford, England : 1993)
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