Search results for "Label"

showing 10 items of 797 documents

Iron oxides nanoparticles and titanate nanotubes dedicated to multimodal imaging and anticancer therapy

2013

The new implementations of nanoparticles in the medical field are one of the essential factors of the medical progress expected at the beginning of this XXIst century. Thus, the domain of the medical imaging is also affected by this technological evolution. This work consisted in developing theranostic probes with iron oxides nanoparticles (SPIO) and titanate nanotubes (TiONts) for multimodal imaging (magnetic/nuclear or magnetic/optical) and also possessing a therapeutic effect (hyperthermia/PDT or radiosensitization/PDT).The titanate nanotubes of this study have an average length of about 150 nm and were obtained by Kasuga's hydrothermal synthesis. These nanotubes present an outside diame…

Sondes théranostiquesPhthalocyaninesCytotoxicityTitanate nanotubes[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Macrocyclic chelating agentPhtalocyaninesNanohybridesRadiomarquageMultimodal imagingCytotoxicitéXPSNanotubes de titanateZebrafish[PHYS.PHYS.PHYS-MED-PH] Physics [physics]/Physics [physics]/Medical Physics [physics.med-ph]Agents macrocycliquesNanohybridsRadiolabellingSPECT/CTIOAPTESTheranostic probesImagerie multimodaleSPIOMRIIRM
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A phase IB, multicenter, open-label study to assess the safety, tolerability, and efficacy of the pleiotropic pathway modifier CC122 administered ora…

2017

379 Background: CC122 is a novel cereblon-modulating agent with multiple biologic activities including potent immunomodulatory and antiangiogenic effects. CC-122 binding to cereblon promotes ubiquitination and subsequent degradation of lymphoid transcription factors Ikaros and Aiolos resulting in activation of T cells. Methods: Following establishment of oral CC122 3 mg daily (QD) as the MTD in phase 1a (Blood 122:2905 2013), an expansion cohort of advanced Hepatocellular Carcinoma (HCC) subjects was enrolled. All subjects had progressed on or were intolerant to sorafenib. Efficacy was assessed per RECIST 1.1 criteria. Results: As of Jan. 13, 2016, 25 advanced HCC subjects were enrolled. T…

SorafenibOncologyCancer Researchmedicine.medical_specialtybusiness.industryCereblonSafety tolerabilityPharmacologymedicine.diseaseOncologyOpen label studyInternal medicineHepatocellular carcinomaCohortmedicinebusinessmedicine.drugJournal of Clinical Oncology
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2-D differential membrane proteome analysis of scarce protein samples

2006

Proteome studies with small sample amounts are difficult to perform, especially when membrane proteins are the focus of interest. In our study a new method for the analysis of scarce membrane protein samples combining large gel 2-D-CTAB/SDS-PAGE with fluorescence dye saturation labelling (satDIGE) was developed, allowing a highly sensitive differential analysis of different cell states. After Triton X-114 phase partitioning, enriched membrane protein samples of T cells were labelled at cysteine residues using fluorescence dyes and separated by large gel 2D-CTAB/SDS-PAGE. For a differential analysis 3 mug protein was found to be sufficient to detect proteins in a widespread well-separated di…

Spectrometry Mass Electrospray IonizationChromatographyProteomeMolecular Sequence DataCellMembrane ProteinsBiologyProteomicsBiochemistryFluorescenceMicemedicine.anatomical_structureMembrane proteinLabellingProteomemedicineAnimalsHumansElectrophoresis Gel Two-DimensionalAmino Acid SequenceMolecular BiologyPeptide sequenceCells CulturedFluorescent DyesCysteinePROTEOMICS
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Infrared Difference Spectroscopy of Proteins: From Bands to Bonds

2020

Infrared difference spectroscopy probes vibrational changes of proteins upon their perturbation. Compared with other spectroscopic methods, it stands out by its sensitivity to the protonation state, H-bonding, and the conformation of different groups in proteins, including the peptide backbone, amino acid side chains, internal water molecules, or cofactors. In particular, the detection of protonation and H-bonding changes in a time-resolved manner, not easily obtained by other techniques, is one of the most successful applications of IR difference spectroscopy. The present review deals with the use of perturbations designed to specifically change the protein between two (or more) functional…

Spectrophotometry Infrared010405 organic chemistryInfraredChemistryMembrane ProteinsWaterHydrogen BondingProtonationGeneral ChemistryNanosecond010402 general chemistryVibration01 natural sciences0104 chemical sciencesIsotopic labelingChemical physicsMutagenesis Site-DirectedSide chainAnimalsHumansMoleculeAmino AcidsSpectroscopyRotational–vibrational couplingChemical Reviews
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Axial growth of hexactinellid spicules: Formation of cone-like structural units in the giant basal spicules of the hexactinellid Monorhaphis

2008

The glass sponge Monorhaphis chuni (Porifera: Hexactinellida) forms the largest bio-silica structures on Earth; their giant basal spicules reach sizes of up to 3 m and diameters of 8.5 mm. Previously, it had been shown that the thickness growth proceeds by appositional layering of individual lamellae; however, the mechanism for the longitudinal growth remained unstudied. Now we show, that the surface of the spicules have towards the tip serrated relief structures that are consistent in size and form with the protrusions on the surface of the spicules. These protrusions fit into the collagen net that surrounds the spicules. The widths of the individual lamellae do not show a pronounced size …

SpiculebiologyHexactinellidSilicatesImmunogold labellingSilicon Dioxidebiology.organism_classificationPoriferalaw.inventionSuberites domunculaMicroscopy ElectronSpongeCrystallographySponge spiculeStructural BiologylawAnimalsElectrophoresis Polyacrylamide GelCollagenElectron microscopeElongationSuberitesJournal of Structural Biology
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3D Morphology, ultrastructure and development of Ceratomyxa puntazzi stages: first insights into the mechanisms of motility and budding in the Myxozo…

2012

Free, amoeboid movement of organisms within media as well as substrate-dependent cellular crawling processes of cells and organisms require an actin cytoskeleton. This system is also involved in the cytokinetic processes of all eukaryotic cells. Myxozoan parasites are known for the disease they cause in economical important fishes. Usually, their pathology is related to rapid proliferation in the host. However, the sequences of their development are still poorly understood, especially with regard to pre-sporogonic proliferation mechanisms. The present work employs light microscopy (LM), electron microscopy (SEM, TEM) and confocal laser scanning microscopy (CLSM) in combination with specific…

SporesIndolesPhalloidineParasitic Diseases AnimalBiophysicsMotilitylcsh:MedicineBiologyBiochemistryFish DiseasesMicroscopy Electron TransmissionCell MovementMolecular Cell BiologyOxazinesAnimalsBilePseudopodiaMyxozoaCytoskeletonlcsh:ScienceBiologyCell ProliferationAmoeboid movementBuddingLife Cycle StagesMultidisciplinaryMicroscopy ConfocalStaining and LabelingPhysicslcsh:RProteinsCell BiologyActin cytoskeletonCellular StructuresSea BreamCell biologyUltrastructureMicroscopy Electron Scanninglcsh:QFilopodiaZoologyCytokinesisCell DivisionResearch ArticleDevelopmental BiologyPLoS ONE
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Radio k-Labelings for Cartesian Products of Graphs

2005

International audience; Frequency planning consists in allocating frequencies to the transmitters of a cellular network so as to ensure that no pair of transmitters interfere. We study the problem of reducing interference by modeling this by a radio k-labeling problem on graphs: For a graph G and an integer k ≥ 1, a radio k-labeling of G is an assignment f of non negative integers to the vertices of G such that |f(x)−f(y)| ≥ k+1−dG(x,y), for any two vertices x and y, where dG(x,y) is the distance between x and y in G. The radio k-chromatic number is the minimum of max{f(x)−f(y):x,y ∈ V(G)} over all radio k-labelings f of G. In this paper we present the radio k-labeling for the Cartesian pro…

Square tilingGraph labelingradio k-labelingradio channel assignmentAntipodal point0102 computer and information sciences[INFO.INFO-DM]Computer Science [cs]/Discrete Mathematics [cs.DM]Span (engineering)01 natural sciencesUpper and lower boundsradio numberCombinatoricssymbols.namesakeIntegerCartesian productDiscrete Mathematics and CombinatoricsChromatic scale0101 mathematicsantipodal numberMathematicsDiscrete mathematicsApplied Mathematics010102 general mathematicsGraph theory[ INFO.INFO-DM ] Computer Science [cs]/Discrete Mathematics [cs.DM]Cartesian productGraph theory[INFO.INFO-DM] Computer Science [cs]/Discrete Mathematics [cs.DM]010201 computation theory & mathematicsCellular networksymbolsHypercubeMSC 05C15 05C78Graph product
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Staining of immunoblots by immunochromatography.

1994

Staining and LabelingChemistryImmunoblottingBiophysicsCollodionMembranes ArtificialCell BiologyAntibodies ViralBiochemistryMolecular biologyStainingPotexvirusPlants ToxicCapsidTobaccoChromatography Thin LayerMolecular BiologyAnalytical biochemistry
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GFP immunogold staining, from light to electron microscopy, in mammalian cells.

2012

GFP has emerged as an important reporter for monitoring gene expression, protein localization, cell transformation and cell lineage. The development of GFP as a marker in many different biological systems has emphasized the need to image GFP at high resolution. GFP immunogold labeling with colloidal gold particles becomes essential for electron microscopy (EM) ultrastructural detection. Because of the small size, colloidal gold particles require silver enhancement, a procedure to increase the size of the particle as well as gold toning to stabilize the silver layer. GFP preembedding immunogold staining enables high quality cellular-ultrastructural EM analysis mainly for two reasons, on one …

Staining and LabelingGreen Fluorescent ProteinsGeneral Physics and AstronomyHigh resolutionCell BiologyImmunogold labellingCell lineageBiologyProtein subcellular localization predictionMolecular biologyImmunohistochemistrylaw.inventionGreen fluorescent proteinStructural BiologylawColloidal goldBiophysicsUltrastructureAnimalsHumansGeneral Materials ScienceElectron microscopeFluorescent DyesMicron (Oxford, England : 1993)
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Is immunohistochemistry more sensitive than hematoxylin-eosin staining for identifying perineural or lymphovascular invasion in oral squamous cell ca…

2021

This study aimed to analyze whether immunohistochemistry (IHC) is more sensitive than hematoxylin-eosin (H&E) staining for identifying perineural invasion (PNI) or lymphovascular invasion (LVI) in oral squamous cell carcinoma (OSCC). In this systematic review and meta-analysis (Prospective Register of Systematic Reviews ? CRD 42021256515), data were obtained from six databases (PubMed, Scopus, LILACS, Web of Science, EBSCO, LIVIVO, Embase) and the grey literature. Cross-sectional observational studies of the diagnostic sensitivity of IHC for PNI and LVI were included. Studies were selected in two phases: first collection and reference retrieval. The Quality Assessment of Diagnostic Accuracy…

Staining and LabelingSquamous Cell Carcinoma of Head and NeckneoplasmsImmunohistochemistrystomatitisCross-Sectional StudiesOtorhinolaryngologyHead and Neck NeoplasmsLymphatic MetastasisCarcinoma Squamous Cellantineoplastic agentsmicrobiotaEosine Yellowish-(YS)HumansMouth NeoplasmsNeoplasm InvasivenessSurgeryimmunotherapyHematoxylinGeneral DentistryUNESCO:CIENCIAS MÉDICASMedicina Oral Patología Oral y Cirugia Bucal
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