Search results for "Electrophoresi"

showing 10 items of 1009 documents

Should mild hypogammaglobulinemia be managed as severe hypogammaglobulinemia? A study of 389 patients with secondary hypogammaglobulinemia.

2014

Although secondary hypogammaglobulinemia is more frequent than primary hypogammaglobulinemia, its etiology and management are poorly described, particularly for mild hypogammaglobulinemia.This retrospective observational study included all adult patients with a gammaglobulin level6.4g/L on serum electrophoresis identified at Dijon teaching hospital between April and September 2012. Clinico-biological features, etiologies and infectious complications were collected at inclusion and compared between group 1 (gammaglobulin5g/L, severe hypogammaglobulinemia), and group 2 (gammaglobulin6.4 and ≥5g/L, mild hypogammaglobulinemia).Among the 4011 serum electrophoreses, 570 samples from 389 patients …

ElectrophoresisMalePediatricsmedicine.medical_specialtyInfectionsSeverity of Illness IndexHypogammaglobulinemiaPneumococcal Vaccinesimmune system diseasesAgammaglobulinemiahemic and lymphatic diseasesSecondary HypogammaglobulinemiaInternal MedicinemedicineHumansAgedRetrospective StudiesAdult patientsbusiness.industryRetrospective cohort studyGamma globulinmedicine.diseaseElectrophoresesImmunologyEtiologyFemalebusinessEuropean journal of internal medicine
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Isolation and characterization of anavirulent Candida albicansyeast monomorphic mutant

2003

Mutagenesis of Candida albicans strain ATCC 26555 with N-methyl-nitro-N-nitrosoguanidine followed by plating on solid yeast nitrogen base-N-acetylglucosamine medium at 37 degrees C yielded colony morphology variants that were characterized as forming smooth colonies, in contrast to the rough colonies formed by the parental strain. One yeast monomorphic mutant, CAL4, was studied in detail. Strain CAL4 is defective in filamentous growth, unable to form hyphae or pseudohyphae in vivo and in vitro. These filamentous structures are not elicited by commonly used external stimuli such as serum. The mutant had no obvious alterations in its mannan, glucan or chitin content. The total quantity of non…

ElectrophoresisMaleVirulenceHyphaStrain (chemistry)biologyMutantCandidiasisMutagenesis (molecular biology technique)General Medicinebiology.organism_classificationYeastMicrobiologyFungal ProteinsCell wallMiceInfectious DiseasesCell WallCandida albicansMutationAnimalsCandida albicansMannanMedical Mycology
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Fetal presentation of Morquio disease type A.

1992

A fetus with mucopolysaccharidosis type IV A (Morquio type A) is described. The family had one affected child exhibiting symptoms of classical Morquio A disease, and late in the subsequent pregnancy prenatal diagnosis was requested. At 23 weeks' gestation, moderate ascites was detected by detailed ultrasound scan and keratan sulphate was found in the amniotic fluid. The pregnancy was terminated by prostaglandin induction and the diagnosis of mucopolysaccharidosis type IV A was confirmed by demonstration of a deficiency of N-acetylgalactosamine-6-sulphate (GalNac-6-S) sulphatase in cultured amniotic cells and in post-mortem fibroblast cultures. The activities of beta-galactosidase and arylsu…

ElectrophoresisMalemedicine.medical_specialtyAmniotic fluidPlacentaMucopolysaccharidosis type IVNeuraminidasePrenatal diagnosisConsanguinityPregnancyHydrops fetalisInternal medicineLysosomal storage diseaseMedicineHumansChildGenetics (clinical)GlycosaminoglycansUltrasonographyFetusPregnancybusiness.industryObstetrics and GynecologyAscitesMucopolysaccharidosis IVmedicine.diseaseAmniotic Fluidbeta-GalactosidaseEndocrinologyKeratan SulfatePregnancy Trimester SecondMucopolysaccharidosis IVAmniocentesisFemaleSulfatasesbusinessPrenatal diagnosis
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Characterization of two male-specific polypeptides in the tergal glands secretions of the cockroach Leucophaea maderae (Dictyoptera, Blaberidae)

1998

0965-1748 (Print) Journal Article Research Support, Non-U.S. Gov't; During the sexual behavior of cockroaches, the female mounts the courting male to feed on the proteinaceous secretion of the tergal glands. Polyacrylamide gel electrophoresis of male and female protein extracts after cuticle wiping revealed three major bands. Two of 18 and 22 kDa, named Lma-P18 and Lma-P22, are specific to the male tergal extracts. Moreover, Lma-P22 is only found in the male second tergite extracts. The third one of 54 kDa, named Lma-P54, is common to male and female extracts and could be considered as an ubiquitous surface protein. Several other minor proteins are also present on the body surface of adults…

ElectrophoresisMalemedicine.medical_specialtyCuticleSexual BehaviorCockroachesBiochemistrySexual Behavior AnimalWestern blotInternal medicinebiology.animalmedicineSexual maturityAnimalsSecretionMolecular BiologyCockroachPolyacrylamide Gelbiologymedicine.diagnostic_testAnimalDictyopterabiology.organism_classificationImmunohistochemistryBlaberidaeEndocrinologyInsect Proteins/*analysisInsect ScienceEcdysisCockroaches/*physiologyInsect ProteinsElectrophoresis Polyacrylamide GelFemale
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Carbon nanotubes as electrodes for dielectrophoresis of DNA

2006

Dielectrophoresis can potentially be used as an efficient trapping tool in the fabrication of molecular devices. For nanoscale objects, however, the Brownian motion poses a challenge. We show that the use of carbon nanotube electrodes makes it possible to apply relatively low trapping voltages and still achieve high enough field gradients for trapping nanoscale objects, e.g., single molecules. We compare the efficiency and other characteristics of dielectrophoresis between carbon nanotube electrodes and lithographically fabricated metallic electrodes, in the case of trapping nanoscale DNA molecules. The results are analyzed using finite element method simulations and reveal information abou…

ElectrophoresisMaterials scienceFabricationFOS: Physical sciencesBioengineeringNanotechnologyCarbon nanotubeTrappingCondensed Matter - Soft Condensed MatterMicroscopy Atomic Forcelaw.inventionPolarizabilitylawMoleculeGeneral Materials SciencePhysics - Biological PhysicsNanoscopic scaleNanotubes CarbonMechanical EngineeringBiomolecules (q-bio.BM)General ChemistryDNADielectrophoresisCondensed Matter PhysicsQuantitative Biology - BiomoleculesBiological Physics (physics.bio-ph)FOS: Biological sciencesElectrodeMicroscopy Electron ScanningSoft Condensed Matter (cond-mat.soft)Microelectrodes
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Dielectrophoretic trapping of DNA origami.

2008

In this thesis three-dimensional tube-shaped DNA-origamis were dielectrophoretically trapped within lithographically fabricated nanoelectrodes. The origamis had been premade while the electrodes were fabricated specifically for these experiments with two different gapsizes, 150 nm and 400 nm. The aim of the work was to capture individual nanotubes in the gap between the electrodes by utilizing the dielectrophoretic forces present in the structure when a solution containing the origamis was put onto the electrodes and a voltage was applied. It was observed during the experiments that the success of the dielectrophoretic trapping depended strongly on the trapping conditions. This caused the t…

ElectrophoresisMaterials scienceMacromolecular SubstancesSurface PropertiesMolecular ConformationNanotechnologyGeneral ChemistryTrappingMaterials testingDNADielectrophoresisMolecular conformationNanostructuresBiomaterialsElectromagnetic FieldsElectrodeMaterials TestingDNA origamiNanotechnologyGeneral Materials ScienceParticle SizeCrystallizationBiotechnologySmall (Weinheim an der Bergstrasse, Germany)
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Dielectrophoretic trapping of multilayer DNA origami nanostructures and DNA origami-induced local destruction of silicon dioxide

2015

DNA origami is a widely used method for fabrication of custom-shaped nanostructures. However, to utilize such structures, one needs to controllably position them on nanoscale. Here we demonstrate how different types of 3D scaffolded multilayer origamis can be accurately anchored to lithographically fabricated nanoelectrodes on a silicon dioxide substrate by DEP. Straight brick-like origami structures, constructed both in square (SQL) and honeycomb lattices, as well as curved "C"-shaped and angular "L"-shaped origamis were trapped with nanoscale precision and single-structure accuracy. We show that the positioning and immobilization of all these structures can be realized with or without thi…

ElectrophoresisMaterials scienceNanostructureSilicon dioxideta221educationClinical BiochemistryImmobilized Nucleic AcidsNanotechnology02 engineering and technologyDNA nanostructuresSubstrate (electronics)Microscopy Atomic Force01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundHoneycombNanotechnologyDNA origamiDNA nanotechnologynanomanipulationElectrical measurementsSulfhydryl CompoundsElectrodesta218dielectrophoresista214ta114Physics010401 analytical chemistryElectric ConductivityDNAEquipment DesignDielectrophoresis021001 nanoscience & nanotechnologySilicon Dioxide0104 chemical sciencesNanostructuresChemistryNanolithographychemistryElectrical engineeringelectrical propertiesnanofabricationGold0210 nano-technologyBiotechnologyELECTROPHORESIS
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Direct identification of the agonist binding site in the human brain cholecystokinin-B receptor

1999

In investigating the agonist binding site of the human brain cholecystokininB receptor (CCKBR), we employed the direct protein chemical approach using a photoreactive tritiated analogue of sulfated cholecystokinin octapeptide, which contains the p-benzoylbenzoyl moiety at the N-terminus, followed by purification of the affinity-labeled receptor to homogeneity. This probe bound specifically, saturably, and with high affinity (KD = 1.2 nM) to the CCKBR and has full agonistic activity. As the starting material for receptor purification, we used stably transfected HEK 293 cells overexpressing functional CCKBR. Covalent labeling of the WGA-lectin-enriched receptor revealed a 70-80 kDa glycoprote…

ElectrophoresisModels MolecularAgonistProtein Conformationmedicine.drug_classPeptidePhotoaffinity LabelsTritiumBiochemistryMass SpectrometrySincalidemedicineHumansBinding siteReceptorCells Culturedchemistry.chemical_classificationBinding SitesEdman degradationHEK 293 cellsBrainMolecular biologyReceptor Cholecystokinin BchemistryBiochemistryCholecystokinin B receptorChromatography GelMutagenesis Site-DirectedReceptors CholecystokininCholecystokininGlycoproteinSequence Analysis
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Novel molluskan biomineralization proteins retrieved from proteomics: a case study with upsalin.

2012

12 pages; International audience; The formation of the molluskan shell is regulated by an array of extracellular proteins secreted by the calcifying epithelial cells of the mantle. These proteins remain occluded within the recently formed biominerals. To date, many shell proteins have been retrieved, but only a few of them, such as nacreins, have clearly identified functions. In this particular case, by combining molecular biology and biochemical approaches, we performed the molecular characterization of a novel protein that we named Upsalin, associated with the nacreous shell of the freshwater mussel Unio pictorum. The full sequence of the upsalin transcript was obtained by RT-PCR and 5'/3…

ElectrophoresisMolecular Sequence DataBiologyProteomicsBioinformaticsBiochemistryHomology (biology)03 medical and health sciencesproteomicsGene silencingAnimalsAmino Acid Sequence[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsMolecular BiologyPeptide sequence030304 developmental biology0303 health sciencesMineralsBase Sequence030302 biochemistry & molecular biologyOrganic ChemistrymollusksImmunogold labelling[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/BiomaterialsbiomineralizationIn vitroproteinsfreshwater bivalvesBiochemistryMolluscaMicroscopy Electron ScanningMolecular MedicineTarget proteinBiomineralization
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Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression.

1993

Abstract The fourth component of the human complement system (C4) is coded for by two genes, C4A and C4B, located within the MHC. Null alleles of C4 (C4Q0) are defined by the absence of C4 protein in plasma. These null alleles are due either to large gene deletions or to nonexpression of the respective genes. In a previous study, evidence was obtained for nonexpressed defective genes at the C4A locus, and for gene conversion at the C4B locus. To further characterize the molecular basis of these non-expressed C4A genes, we selected nine pairs of PCR primers from flanking genomic intron sequences to amplify all 41 exons from individuals with a defective C4A gene. The amplified products were s…

ElectrophoresisMolecular Sequence DataLocus (genetics)BiologyPolymerase Chain ReactionAutoimmune DiseasesHumansPoint MutationGene conversionAmino Acid SequenceGeneGeneticsPolymorphism GeneticBase SequenceHaplotypeC4AGene AmplificationImmunologic Deficiency SyndromesComplement C4aSingle-strand conformation polymorphismGeneral MedicineExonsSequence Analysis DNAMolecular biologyNull alleleStop codonHaplotypesResearch Article
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