Search results for "Sense organ"

showing 10 items of 2176 documents

Odor-induced electrical and calcium signals from olfactory sensory neurons in situ

2018

Electrophysiological recording and optical imaging enable the characterization of membrane and odorant response properties of olfactory sensory neurons (OSNs) in the nasal neuroepithelium. Here we describe a method to record the responses of mammalian OSNs to odorant stimulations in an ex vivo preparation of intact olfactory epithelium. The responses of individual OSNs with defined odorant receptor types can be monitored via patch-clamp recording or calcium imaging.

0301 basic medicineSensory systemGCaMP6gene targeting03 medical and health sciences0302 clinical medicineCalcium imagingolfactory sensory neuronsmedicinePatch clampCalcium signalingChemistryrespiratory systempatch-clampelectrophysiologytransductionElectrophysiologycalcium imaging030104 developmental biologymedicine.anatomical_structureOdor[SDV.NEU]Life Sciences [q-bio]/Neurons and Cognition [q-bio.NC]sense organsNeuroscienceTransduction (physiology)Olfactory epithelium030217 neurology & neurosurgery
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Retinal Thickness and Microvascular Pattern in Early Parkinson's Disease.

2020

A thinning of intraretinal layers has been previously described in Parkinson's disease (PD) patients compared to healthy controls (HCs). Few studies evaluated the possible correlation between retinal thickness and retinal microvascularization. Thus, here we assessed the thickness of retinal layers and microvascular pattern in early PD patients and HCs, using, respectively, spectral-domain optical coherence tomography (SD-OCT) and SD-OCT-angiography (SD-OCT-A), and more interestingly, we evaluated a possible correlation between retinal thickness and microvascular pattern. Patients fulfilling criteria for clinically established/clinically probable PD and HCs were enrolled. Exclusion criteria …

0301 basic medicineSystemic diseasemedicine.medical_specialtyretinaParkinson's diseasegenetic structuresNerve fiber layeroptical coherence tomography angiographylcsh:RC346-42903 medical and health scienceschemistry.chemical_compound0302 clinical medicinevascularizationOphthalmologyMedicinelcsh:Neurology. Diseases of the nervous systemOriginal ResearchRetinaoptical coherence tomographybusiness.industryMicrovascular DensityRetinalmedicine.diseaseInner plexiform layereye diseases030104 developmental biologymedicine.anatomical_structurechemistryNeurologyInner nuclear layerparkinson's diseaseNeurology (clinical)sense organsbusiness030217 neurology & neurosurgeryoptical coherence tomography; optical coherence tomography angiography; parkinson's disease; retina; vascularizationFrontiers in neurology
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Oxidative stress in retinal pigment epithelium cells increases exosome secretion and promotes angiogenesis in endothelial cells.

2015

10 páginas, 5 figuras

0301 basic medicineVascular Endothelial Growth Factor AAngiogenesisretinal pigment epitheliumNeovascularization PhysiologicexosomesBiologyExosomesExosomeCell Line03 medical and health sciencesangiogenesismedicineHuman Umbilical Vein Endothelial CellsHumansRNA MessengerRetinal pigment epitheliumVEGF receptorsTube formationRetinal pigment epitheliumEthanolCell BiologyOriginal ArticlesMicrovesicleseye diseasesCell biologyEndothelial stem cellVascular endothelial growth factor AOxidative Stress030104 developmental biologymedicine.anatomical_structureReceptors Vascular Endothelial Growth FactorOxidative stressCell cultureMolecular MedicineOriginal ArticleAngiogenesissense organsJournal of cellular and molecular medicine
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2019

VAMP2 encodes the vesicular SNARE protein VAMP2 (also called synaptobrevin-2). Together with its partners syntaxin-1A and synaptosomal-associated protein 25 (SNAP25), VAMP2 mediates fusion of synaptic vesicles to release neurotransmitters. VAMP2 is essential for vesicular exocytosis and activity-dependent neurotransmitter release. Here, we report five heterozygous de novo mutations in VAMP2 in unrelated individuals presenting with a neurodevelopmental disorder characterized by axial hypotonia (which had been present since birth), intellectual disability, and autistic features. In total, we identified two single-amino-acid deletions and three non-synonymous variants affecting conserved resid…

0301 basic medicineVesicle fusionVAMP2SynaptobrevinSNAP25Biologymedicine.diseaseSynaptic vesicleExocytosisCell biology03 medical and health scienceschemistry.chemical_compound030104 developmental biology0302 clinical medicinechemistryGeneticsmedicineSynaptopathysense organsNeurotransmitter030217 neurology & neurosurgeryGenetics (clinical)The American Journal of Human Genetics
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Luminance Information Is Required for the Accurate Estimation of Contrast in Rapidly Changing Visual Contexts.

2020

Summary Visual perception scales with changes in the visual stimulus, or contrast, irrespective of background illumination. However, visual perception is challenged when adaptation is not fast enough to deal with sudden declines in overall illumination, for example, when gaze follows a moving object from bright sunlight into a shaded area. Here, we show that the visual system of the fly employs a solution by propagating a corrective luminance-sensitive signal. We use in vivo 2-photon imaging and behavioral analyses to demonstrate that distinct OFF-pathway inputs encode contrast and luminance. Predictions of contrast-sensitive neuronal responses show that contrast information alone cannot ex…

0301 basic medicineVisual perceptiongenetic structuresAccurate estimationFeature extractionStimulus (physiology)BiologyLuminanceGeneral Biochemistry Genetics and Molecular BiologyVisual processingContrast Sensitivity03 medical and health sciences0302 clinical medicineAnimalsComputer visionbusiness.industryGaze030104 developmental biologyDrosophila melanogasterPattern Recognition VisualVisual Perceptionsense organsArtificial intelligenceGeneral Agricultural and Biological Sciencesbusiness030217 neurology & neurosurgeryPhotic StimulationCurrent biology : CB
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Tony DeCasper, the man who changed contemporary views on human fetal cognitive abilities

2017

Tony DeCasper, the man who changed contemporary views on human fetal cognitive abilities

0301 basic medicine[SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]Psychology Developmental[ SCCO.PSYC ] Cognitive science/PsychologyHistory 21st CenturyDevelopmental psychologyFetal Development03 medical and health sciencesBehavioral NeuroscienceChild DevelopmentCognition0302 clinical medicineDevelopmental NeuroscienceDevelopmental and Educational PsychologyAnimalsHumans[ SDV.OT ] Life Sciences [q-bio]/Other [q-bio.OT]skin and connective tissue diseasesInfant NewbornCognitionHistory 20th CenturyChild developmentInfant newborn030104 developmental biology[SCCO.PSYC]Cognitive science/PsychologyInfant BehaviorHuman fetalembryonic structuressense organsPsychology030217 neurology & neurosurgeryDevelopmental Biology
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SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins.

2019

The human Usher syndrome (USH) is a retinal ciliopathy, characterized by profound congenital deafness, variable vestibular dysfunction and pre-pubertal onset of retinitis pigmentosa. In the effected sensory cells, USH protein networks are assumed to function in ciliary transport processes. The USH1G protein SANS is a scaffold of the ciliary/periciliary USH protein network of photoreceptor cells. Moreover, SANS is associated with microtubules, the transport routes for protein delivery toward the cilium. To enlighten the role of SANS in ciliary transport processes, we aimed to identify transport related proteins associated with SANS. The intraflagellar transport (IFT) system is a conserved me…

0301 basic medicineciliary transportIFTPhotoreceptor cell570 Life sciences03 medical and health sciencesCell and Developmental Biology0302 clinical medicineprimary ciliaMicrotubuleIntraflagellar transportRetinitis pigmentosamedicinephotoreceptor celllcsh:QH301-705.5USH interactomeOriginal ResearchChemistryCiliumCell Biologymedicine.diseaseCell biologyCiliopathy030104 developmental biologymedicine.anatomical_structureciliopathylcsh:Biology (General)030220 oncology & carcinogenesisUSH1GAnkyrin repeatsense organsCiliary baseUsher syndrome570 BiowissenschaftenDevelopmental BiologyFrontiers in cell and developmental biology
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P14ARF: The Absence that Makes the Difference

2020

P14ARF is a tumor suppressor encoded by the CDKN2a locus that is frequently inactivated in human tumors. P14ARF protein quenches oncogene stimuli by inhibiting cell cycle progression and inducing apoptosis. P14ARF functions can be played through interactions with several proteins. However, the majority of its activities are notoriously mediated by the p53 protein. Interestingly, recent studies suggest a new role of p14ARF in the maintenance of chromosome stability. Here, we deepened this new facet of p14ARF which we believe is relevant to its tumor suppressive role in the cell. To this aim, we generated a monoclonal HCT116 cell line expressing the p14ARF cDNA cloned in the piggyback vector …

0301 basic medicinecongenital hereditary and neonatal diseases and abnormalitiesCENP‐Elcsh:QH426-470Cellp14ARFBiologylaw.invention03 medical and health sciences0302 clinical medicinep14arfCDKN2AlawComplementary DNAGeneticsmedicineaneuploidyGenetics (clinical)OncogeneARFP14eye diseasesCell biologySettore BIO/18 - Geneticalcsh:Genetics030104 developmental biologymedicine.anatomical_structureApoptosis030220 oncology & carcinogenesisGSK923295MonoclonalSuppressorCENP-Esense organsGenes
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Ophthalmological Findings in Mucopolysaccharidoses

2019

The mucopolysaccharidoses (MPS) are a heterogenous group of lysosomal storage disorders caused by the accumulation of glycosaminoglycans (GAGs). The accrual of these compounds results in phenotypically varied syndromes that produce multi-organ impairment with widespread systemic effects. The low incidence of MPS (approximately 1/25,000 live births) in conjunction with the high childhood mortality rate had limited the availability of research into certain clinical features, especially ocular manifestations. As the recent successes of hematopoietic stem cell transplantation (HSCT) and enzyme replacement therapy (ERT) have greatly increased life expectancy in these patients, they have served a…

0301 basic medicinecongenital hereditary and neonatal diseases and abnormalitiesPediatricsmedicine.medical_specialtygenetic structuresmedicine.medical_treatmentMucopolysaccharidosislcsh:MedicineGlaucomaReviewHematopoietic stem cell transplantation03 medical and health sciences0302 clinical medicineQuality of lifeCorneal cloudingmedicinebusiness.industryMortality rateIncidence (epidemiology)lcsh:Rnutritional and metabolic diseasesmucopolysaccharidosisGeneral MedicineEnzyme replacement therapymedicine.diseaseocular manifestationseye diseasesophthalmology030104 developmental biologycorneal clouding030221 ophthalmology & optometrylysosomal storage disordersense organsbusinessJournal of Clinical Medicine
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Mapping gene regulatory circuitry of Pax6 during neurogenesis.

2016

AbstractPax6 is a highly conserved transcription factor among vertebrates and is important in various aspects of the central nervous system development. However, the gene regulatory circuitry of Pax6 underlying these functions remains elusive. We find that Pax6 targets a large number of promoters in neural progenitors cells. Intriguingly, many of these sites are also bound by another progenitor factor, Sox2, which cooperates with Pax6 in gene regulation. A combinatorial analysis of Pax6-binding data set with transcriptome changes in Pax6-deficient neural progenitors reveals a dual role for Pax6, in which it activates the neuronal (ectodermal) genes while concurrently represses the mesoderma…

0301 basic medicineendocrine systemNeurogenesisBiologyBiochemistryArticle03 medical and health sciencesSOX2GeneticsMolecular BiologyTranscription factorGeneRegulation of gene expressionGeneticsGene knockdownNeurogenesisPromoterCell BiologyNeural progenitorseye diseasesChromatinCell biologyGene regulation030104 developmental biologyPAX6sense organsTranscription FactorsCell discovery
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