Search results for "label"

showing 10 items of 797 documents

Non invasive blood flow measurement in cerebellum detects minimal hepatic encephalopathy earlier than psychometric tests

2013

AIM: To assess whether non invasive blood flow measurement by arterial spin labeling in several brain regions detects minimal hepatic encephalopathy. METHODS: Blood flow (BF) was analyzed by arterial spin labeling (ASL) in different brain areas of 14 controls, 24 cirrhotic patients without and 16 cirrhotic patients with minimal hepatic encephalopathy (MHE). Images were collected using a 3 Tesla MR scanner (Achieva 3T-TX, Philips, Netherlands). Pulsed ASL was performed. Patients showing MHE were detected using the battery Psychometric Hepatic Encephalopathy Score (PHES) consisting of five tests. Different cognitive and motor functions were also assessed: alterations in selective attention we…

Liver CirrhosisMaleCerebellumPathologyPerfusion scanningArterial spin labellingCognitionCerebellumAttentionHepatic encephalopathyCyclic GMPmedicine.diagnostic_testGastroenterologyGeneral MedicineBlood flowMiddle AgedMagnetic Resonance Imagingmedicine.anatomical_structurePredictive value of testsCerebrovascular CirculationFemaleInflammation MediatorsBlood Flow Velocitymedicine.medical_specialtyPsychometricsPerfusion ImagingMinimal hepatic encephalopathymacromolecular substancesMotor ActivityNitric OxideAmmoniaPredictive Value of TestsRetrospective StudymedicineHumansAgedRetrospective Studiesbusiness.industryNon invasiveMagnetic resonance imagingBlood flowmedicine.diseaseEarly DiagnosisRegional Blood FlowHepatic EncephalopathyStroop TestbusinessPsychometric testsBiomarkersNeurological impairment
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Spike-in SILAC proteomic approach reveals the vitronectin as an early molecular signature of liver fibrosis in hepatitis C infections with hepatic ir…

2014

Hepatitis C virus (HCV)-induced iron overload has been shown to promote liver fibrosis, steatosis, and hepatocellular carcinoma. The zonal-restricted histological distribution of pathological iron deposits has hampered the attempt to perform large-scale in vivo molecular investigations on the comorbidity between iron and HCV. Diagnostic and prognostic markers are not yet available to assess iron overload-induced liver fibrogenesis and progression in HCV infections. Here, by means of Spike-in SILAC proteomic approach, we first unveiled a specific membrane protein expression signature of HCV cell cultures in the presence of iron overload. Computational analysis of proteomic dataset highlighte…

Liver CirrhosisProteomicshepatitis C virusMaleMESH: Isotope LabelingHSCmedicine.disease_causeBiochemistry0302 clinical medicineFibrosisMESH: Up-RegulationMembrane Proteinhepatic stellate cellliver fibrosishepatic iron overload0303 health sciencesbiologyMESH: ProteomicsMedicine (all)hepatocellular carcinomaBiomedicine; hepatitis c infection; liver fibrosis; hepatic iron overload; vitronectinHepatitis C[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM]Hepatitis CUp-Regulation3. Good healthcell culture-derived HCVIsotope Labeling030220 oncology & carcinogenesisHepatocellular carcinomaBiomedicine; Hepatic iron overload; Hepatitis C infection; Liver fibrosis; Vitronectin; Biomarkers; Cell Line; Hepatitis C; Humans; Iron Overload; Isotope Labeling; Liver Cirrhosis; Male; Membrane Proteins; Proteomics; Up-Regulation; Vitronectin; Molecular Biology; Biochemistry; Medicine (all)HCV[SDV.MP.VIR]Life Sciences [q-bio]/Microbiology and Parasitology/VirologyBiomarker (medicine)VitronectinMESH: Membrane ProteinsMESH: Liver CirrhosisHumanIron OverloadLiver CirrhosiHepatitis C virusvitronectinhepatitis c infectionCell LineMESH: Iron Overload03 medical and health sciencesmedicineHumans[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyMolecular Biology030304 developmental biologyMESH: Hepatitis CMESH: HumansMESH: Biological MarkersMembrane ProteinsLiver fibrosiProteomicBiomarkermedicine.diseaseMESH: VitronectinMESH: Maledigestive system diseasesMESH: Cell LineBiomedicineBiomedicine / Abbreviations: HCCHCVccImmunologyCancer researchHepatic stellate cellbiology.proteinSteatosisBiomarkersPROTEOMICS
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Off-label long acting injectable antipsychotics in real-world clinical practice: a cross-sectional analysis of prescriptive patterns from the STAR Ne…

2022

Introduction: Information on the off–label use of Long–Acting Injectable (LAI) antipsychotics in the real world is lacking. In this study, we aimed to identify the sociodemographic and clinical features of patients treated with on– vs off–label LAIs and predictors of off–label First– or Second–Generation Antipsychotic (FGA vs. SGA) LAI choice in everyday clinical practice. Method: In a naturalistic national cohort of 449 patients who initiated LAI treatment in the STAR Network Depot Study, two groups were identified based on off– or on–label prescriptions. A multivariate logistic regression analysis was used to test several clinically relevant variables and identify those associated with th…

Long-acting injectable antipsychoticCross-Sectional StudiesOff-labelPersonality disorderBipolar disorderDelayed-Action PreparationsSchizophreniaHumansBipolar disorder; Long-acting injectable antipsychotics; Off-label; Personality disorder; Schizophrenia; Cross-Sectional Studies; Delayed-Action Preparations; Humans; Off-Label Use; Antipsychotic Agents; SchizophreniaOff-Label UseSettore MED/25 - PsichiatriaLong-acting injectable antipsychoticsAntipsychotic Agents
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Cloud top altitude retrieved from Lidar measurements during ACLOUD at 1 second resolution

2021

During the ACLOUD aircraft campaign (23.5.2017 - 26.6.2017) the AMALi Lidar was installed mostly nadir pointing. This dataset contains the cloud top altitude from those measurements (altitudes with a strong signal increase) as well as a cloud mask, derived from the optical depth of the column at 1 second resolution. The majority of the data was collected northwest of the Svalbard archipelago. More details on the campaign can be found in Wendisch 2018 and Ehrlich 2019 and here (https://home.uni-leipzig.de/~ehrlich/ACLOUD_wiki_doku). Please check the data documentation (https://download.pangaea.de/reference/108729/attachments/readme_documentation_AMALi_cloudtop.pdf) before using this dataset.

Longitude of eventAircraftPolar 5Binary ObjectAC3Latitude of eventSvalbardArcticArctic Amplification (AC3)Date/Time of eventAirborne Mobile Aerosol Lidarcloudairborne measurementsLidarEvent labelDate Time of eventairborneACLOUDBinary Object (File Size)mixed phase cloudsAMALiP5_206_ACLOUD_2017airborne lidarArctic Amplification AC3cloud top altitudeEarth System Researchmixed-phase cloudsBinary Object File Size
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A smart and operator independent system to delineate tumours in Positron Emission Tomography scans

2018

Abstract Positron Emission Tomography (PET) imaging has an enormous potential to improve radiation therapy treatment planning offering complementary functional information with respect to other anatomical imaging approaches. The aim of this study is to develop an operator independent, reliable, and clinically feasible system for biological tumour volume delineation from PET images. Under this design hypothesis, we combine several known approaches in an original way to deploy a system with a high level of automation. The proposed system automatically identifies the optimal region of interest around the tumour and performs a slice-by-slice marching local active contour segmentation. It automa…

Lung NeoplasmsComputer sciencemedicine.medical_treatmentPET imagingPattern Recognition Automated030218 nuclear medicine & medical imaging0302 clinical medicineNeoplasmsImage Processing Computer-AssistedSegmentationDiagnosis Computer-AssistedNeoplasm MetastasisRadiation treatment planningSettore ING-INF/05 - Sistemi Di Elaborazione Delle InformazioniObserver VariationActive contour modelmedicine.diagnostic_testBrain NeoplasmsPhantoms ImagingComputer Science ApplicationsHead and Neck NeoplasmsPositron emission tomography030220 oncology & carcinogenesis18F-fluoro-2-deoxy-d-glucoseAlgorithms18F-fluoro-2-deoxy-d-glucose and 11C-labeled methionine PET imagingSimilarity (geometry)Health InformaticsSensitivity and SpecificityNOActive contour algorithm03 medical and health sciencesFluorodeoxyglucose F18Predictive Value of TestsRegion of interestmedicineHumansFalse Positive ReactionsRetrospective Studies18F-fluoro-2-deoxy-d-glucose 11C-labeled methionine PET imaging Active contour algorithm Biological target volume Cancer segmentationbusiness.industryRadiotherapy Planning Computer-Assisted11C-labeled methionineReproducibility of ResultsPattern recognitionGold standard (test)Cancer segmentationRadiation therapyBiological target volumePositron-Emission TomographyArtificial intelligenceTomography X-Ray ComputedbusinessSoftwareComputers in Biology and Medicine
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Global distributions of diazotrophs Gamma-A nifH genes abundance - Depth integrated values computed from a collection of source datasets - Contributi…

2013

The MAREDAT atlas covers 11 types of plankton, ranging in size from bacteria to jellyfish. Together, these plankton groups determine the health and productivity of the global ocean and play a vital role in the global carbon cycle. Working within a uniform and consistent spatial and depth grid (map) of the global ocean, the researchers compiled thousands and tens of thousands of data points to identify regions of plankton abundance and scarcity as well as areas of data abundance and scarcity. At many of the grid points, the MAREDAT team accomplished the difficult conversion from abundance (numbers of organisms) to biomass (carbon mass of organisms). The MAREDAT atlas provides an unprecedente…

M60/5SalinityChlorophyll aDiazotrophs total biomass as carbonUniform resource locator link to source data fileNitrateCTD/RosetteLatitude of eventNiskinM55 1Temperature waterCalothrix abundance expressed in number of nifH gene copiesratio expressed in mass of carbon per amount of nifH gene copiesCalculatedtop minUnicellular cyanobacteria-B biological trait ratio expressed in mass of carbon per amount of nifH gene copiesCD132biomass as carbonTrichodesmium biomass as carbonM55/1bottom maxCTD SeabirdTemperatureDepth top/minCTD RosetteSeabirdRichelia biological trait ratio expressed in mass of carbon per amount of nifH gene copiesCalothrixSO187 2Unicellular cyanobacteria-B abundance expressed in number of nifH gene copiesTrichodesmiumEarth System ResearchMARine Ecosystem Model Intercomparison Project MAREMIPDiazotrophsLongitude of eventRichelia associated speciesSample methodCalothrix biological trait ratio expressed in mass of carbon per amount of nifH gene copiesIronBottle NiskinwaterIn situ pumpMARine Ecosystem Model Intercomparison Project (MAREMIP)Unicellular cyanobacteria-C abundance expressed in number of nifH gene copiesPhosphateWater sampleSample commentUnicellular cyanobacteria biomassUniform resource locator/link to source data filetotal biomass as carbonHeterocyst biomassUnicellular cyanobacteriaProteobacteriaDate/Time of eventMeteor 1986Richelia abundance expressed in number of nifH gene copiesUnicellular cyanobacteria CUnicellular cyanobacteria Bbiological traitSO187/2RicheliaUnicellular cyanobacteria ADEPTH waterbiomassTrichodesmium abundance expressed in number of nifH gene copiesMeteor (1986)BottleDepthEvent labelDate Time of eventTrichodesmium biological trait ratio expressed in mass of carbon per amount of nifH gene copiesUnicellular cyanobacteria-C biological trait ratio expressed in mass of carbon per amount of nifH gene copiesMeasured at sea surfaceCTDCalothrix associated speciesCharles DarwinSonneabundance expressed in number of nifH gene copiesM60 5Depth bottom/maxUnicellular cyanobacteria-A abundance expressed in number of nifH gene copiesassociated speciesProteobacteria abundance expressed in number of nifH gene copiesHeterocyst
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Protein mapping of calcium carbonate biominerals by immunogold

2007

The construction of metazoan calcium carbonate skeletons is finely regulated by a proteinaceous extracellular matrix, which remains embedded within the exoskeleton. In spite of numerous biochemical studies, the precise localization of skeletal proteins has remained for a long time as an elusive goal. In this paper, we describe a technique for visualizing shell matrix proteins on the surface of calcium carbonate crystals or within the biominerals. The technique is as follows: freshly broken pieces of biominerals or NaOCl then EDTA-etched polished surfaces are incubated with an antibody elicited against one matrix protein, then with a secondary gold-coupled antibody. After silver enhancement,…

MESH : Models ChemicalMESH : Molecular Sequence DataMESH: Sequence Homology Amino AcidMESH : Calcium CarbonateMESH : ImmunohistochemistryMESH : Aspartic AcidMESH: TrypsinMESH: Amino Acid SequenceMatrix (biology)01 natural sciencesMESH: Aspartic AcidMESH : Proteinschemistry.chemical_compoundTrypsinMESH: AnimalsMESH: ProteinsPeptide sequenceMESH: Crystallizationchemistry.chemical_classification0303 health sciencesCaspartinbiologyMESH : Amino Acid SequenceMESH : Pepsin AMESH: Models ChemicalImmunogold labellingImmunohistochemistryMESH: MolluscaMESH : Sequence Homology Amino AcidAmino acidBiochemistryMESH: Calcium CarbonateMechanics of MaterialsMESH : CrystallizationMESH: Pepsin ASEMMESH : Edetic AcidCrystallizationMESH : MolluscaCalcium carbonateProteinaceous extracellular matrixMESH: Edetic AcidMolecular Sequence DataBiophysicsBioengineering010402 general chemistryBiomaterials03 medical and health sciencesAnimalsAmino Acid Sequence[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsEdetic Acid030304 developmental biologyAspartic AcidViral matrix proteinMESH: Molecular Sequence DataSequence Homology Amino AcidMESH : SolubilityBack-scattered electronsSurface treatmenProteinsMESH: ImmunohistochemistryIR-78873[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/BiomaterialsPepsin A0104 chemical sciences[SDV.IB.BIO] Life Sciences [q-bio]/Bioengineering/BiomaterialsMESH: SolubilityCalcium carbonatechemistryModels ChemicalSolubilityPolyclonal antibodiesMolluscaCeramics and Compositesbiology.proteinMESH : AnimalsMESH : TrypsinImmunogold
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Caspartin and calprismin, two proteins of the shell calcitic prisms of the Mediterranean fan mussel Pinna nobilis.

2005

We used the combination of preparative electrophoresis and immunological detection to isolate two new proteins from the shell calcitic prisms of Pinna nobilis, the Mediterranean fan mussel. The amino acid composition of these proteins was determined. Both proteins are soluble, intracrystalline, and acidic. The 38-kDa protein is glycosylated; the 17-kDa one is not. Ala, Asx, Thr, and Pro represent the dominant residues of the 38-kDa protein, named calprismin. An N-terminal sequence was obtained from calprismin. This sequence, which comprises a pattern of 4 cysteine residues, is not related to any known protein. The second protein, named caspartin, exhibits an unusual amino acid composition, …

MESH : Molecular Sequence DataMESH : Calcium CarbonateMESH: BivalviaMESH: ElectrophoresisMESH: Amino Acid Sequence01 natural sciencesBiochemistrychemistry.chemical_compoundMESH : BivalviaMESH: AnimalsMESH: CrystallizationCalciteImmunoassay0303 health sciencesbiologyMESH : Amino Acid SequenceImmunogold labellingMESH : ImmunoassayBiochemistryMESH: Calcium CarbonateMESH : CrystallizationCrystallizationMESH: ImmunoassayElectrophoresisAmino Acid Sequence;Animals;Bivalvia;Calcium Carbonate;Crystallization;Electrophoresis;Glycoproteins;Immunoassay;Molecular Sequence DataMolecular Sequence DataMESH: Glycoproteins010402 general chemistryCalcium CarbonateBiomaterials03 medical and health sciencesAnimalsAmino Acid Sequence[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsMolecular Biology030304 developmental biologyGlycoproteinsAntiserumMESH: Molecular Sequence DataMESH : ElectrophoresisCell BiologyMussel[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/Biomaterialsbiology.organism_classificationMESH : Glycoproteins0104 chemical sciencesBivalvia[SDV.IB.BIO] Life Sciences [q-bio]/Bioengineering/BiomaterialsCalcium carbonatechemistryPolyclonal antibodiesbiology.proteinBiomatériauxMESH : AnimalsPinna nobilisCysteine
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FRET multiphoton spectral imaging microscopy of 7-ketocholesterol and Nile Red in U937 monocytic cells loaded with 7-ketocholesterol.

2004

To show the effect of 7-ketocholesterol (7KC) on cellular lipid content by means of flow cytometry and the interaction of 7KC with Nile Red (NR) via ultraviolet fluorescence resonance energy transfer (FRET) excitation of NR on U937 monocytic cells by means of 2-photon excitation confocal laser scanning microscopy (CLSM).Untreated and 7KC-treated U937 cells were stained with NR and analyzed by flow cytometry and CLSM. 3D sequences of images were obtained by spectral analysis in a 2-photon excitation CLSM and analyzed by the factor analysis of medical image sequences (FAMIS) algorithm, which provides factor curves and images. Factor images are the result of the FAMIS image processing method, …

MESH: Cell DeathMESH: Fluorescence Resonance Energy TransferMESH: Mitochondria[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingMESH : Flow CytometryMESH: Flow CytometryMESH: U937 CellsMESH: MonocytesMonocytesMembrane PotentialsMESH : Staining and LabelingMESH : Microscopy Fluorescence MultiphotonOxazinesFluorescence Resonance Energy TransferImage Processing Computer-AssistedHumansMESH: Membrane PotentialsMESH: Microscopy ConfocalMESH : Membrane PotentialsMESH : Fluorescent DyesMESH : Microscopy ConfocalKetocholesterols[ SDV.IB.IMA ] Life Sciences [q-bio]/Bioengineering/ImagingFluorescent DyesMESH : KetocholesterolsMicroscopy ConfocalMESH: HumansMESH : OxazinesCell DeathStaining and LabelingMESH : HumansMESH: KetocholesterolsU937 CellsFlow CytometryMESH: Fluorescent DyesMESH: Image Processing Computer-AssistedMitochondriaMESH: Staining and Labeling[SDV.IB.IMA] Life Sciences [q-bio]/Bioengineering/ImagingMicroscopy Fluorescence MultiphotonMESH : MonocytesMESH : Fluorescence Resonance Energy TransferMESH : Cell DeathMESH : U937 CellsMESH: Microscopy Fluorescence MultiphotonMESH : MitochondriaMESH: OxazinesMESH : Image Processing Computer-Assisted
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Partitioning of Pyrene-Labeled Phospho- and Sphingolipids between Ordered and Disordered Bilayer Domains

2004

AbstractHere we have studied how the length of the pyrene-labeled acyl chain (n) of a phosphatidylcholine, sphingomyelin, or galactosylceramide affects the partitioning of these lipids between 1), gel and fluid domains coexisting in bovine brain sphingomyelin (BB-SM) or BB-SM/spin-labeled phosphatidylcholine (PC) bilayers or 2), between liquid-disordered and liquid-ordered domains in BB-SM/spin-labeled PC/cholesterol bilayers. The partitioning behavior was deduced either from modeling of pyrene excimer/monomer ratio versus temperature plots, or from quenching of the pyrene monomer fluorescence by spin-labeled PC. New methods were developed to model excimer formation and pyrene lipid quenchi…

Macromolecular SubstancesMembrane FluidityLipid BilayersMolecular ConformationBiophysicsPhase Transition03 medical and health scienceschemistry.chemical_compoundMembrane MicrodomainsPhosphatidylcholineMembrane fluidityFluorometryLipid bilayerPhospholipids030304 developmental biologySphingolipids0303 health sciencesPyrenesMembranesQuenching (fluorescence)Staining and LabelingChemistry030302 biochemistry & molecular biologyTemperatureBiological membraneModels ChemicalBiochemistryDipalmitoylphosphatidylcholineLiposomesBiophysicsPyrenelipids (amino acids peptides and proteins)SphingomyelinBiophysical Journal
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