Search results for "erythrocyte"

showing 10 items of 370 documents

Red cell Ca2+ content (total and cytosolic) and erythrocyte membrane fluidity in several clinical conditions

1993

Red CellPhysiologychemistry.chemical_elementHematologyCalciumBiologyCytosolRed blood cellErythrocyte membranemedicine.anatomical_structurechemistryBiochemistryPhysiology (medical)Circulatory systemmedicineCardiology and Cardiovascular MedicineClinical Hemorheology and Microcirculation
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Transcription- and apoptosis-dependent long-range distribution of tight DNA-protein complexes in the chicken alpha-globin gene.

2008

The proteins tightly bound to DNA (TBP) are a group of proteins that remain attached to DNA with covalent or noncovalent bonds after its deproteinization, and have been hypothesized to be involved in regulation of gene expression. To investigate this question further, oligonucleotide DNA arrays were used to determine the distribution of tightly bound proteins along a 100-kb DNA fragment surrounding the chicken alpha-globin gene domain in DNA from chicken erythrocytes, liver, and AEV-transformed HD3 (erythroblast) cells in different physiological conditions. DNA was fractionated into TBP-free (F) and TBP-enriched (R) fractions by separation on nitrocellulose, and these fractions were used as…

Regulation of gene expressionErythrocytesMicroarrayTranscription GeneticOligonucleotideApoptosisCell BiologyGeneral MedicineBiologyMolecular biologyGlobinsDNA-Binding Proteinschemistry.chemical_compoundchemistryCovalent bondApoptosisTranscription (biology)GeneticsAnimalsMolecular BiologyGeneChickensDNAOligonucleotide Array Sequence AnalysisDNA and cell biology
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Rapid and Standardized Quantitation of Hemolytic Activity of the Fourth Component of Human Complement

1990

Based on a method that uses the fourth component of complement (C4)-deficient guinea pig serum to quantify the hemolytic activity of C4, we developed an assay that allows the processing of a large number of individual samples with high reproducibility. In contrast to the conventional procedure using titration curves of each sample to be determined, we can show that a single appropriate dilution of the sample allows accurate quantitation of hemolytic activity. The reliability of the procedure is demonstrated using either C4A- or C4B- deficient and normal individual samples.

ReproducibilityErythrocytesPolymorphism GeneticChromatographyTitration curveChemistryImmunologyC4AComplement C4HematologyIn Vitro TechniquesHemolysisComplement (complexity)KineticsHumansComplement Pathway ClassicalComplement and Inflammation
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Weak D and partial D: our experience in daily activity

2011

Rh-Hr Blood-Group SystemBlood Grouping and CrossmatchingGene Expression RegulationGenotyping TechniquesHumansLettersBlood weak D partial DErythrocyte TransfusionPolymerase Chain ReactionAlleles
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Comparative study of biological properties and electrophoretic characteristics of lipopolysaccharide from eel-virulent and eel-A virulent Vibrio vuln…

1999

ABSTRACT In Vibrio vulnificus , virulence for eels is associated with serovar E strains. In this study, we investigated some biological properties of purified lipopolysaccharides (LPSs) from serovar E and non-serovar E strains. Purified LPSs retained their O-polysaccharidic side chains and did not show any differences that could be related to host specificity, except for serological differences.

SerotypeLipopolysaccharidesErythrocytesLipopolysaccharideVirulenceVibrio vulnificusApplied Microbiology and BiotechnologyHemolysisMicrobiologychemistry.chemical_compoundFish DiseasesMiceVibrionaceaeVibrio InfectionsAnimalsVibrioEelsEcologybiologyVirulenceO Antigensbiology.organism_classificationVibrioRatscarbohydrates (lipids)Environmental and Public Health MicrobiologychemistryVibrio Infectionslipids (amino acids peptides and proteins)BacteriaFood ScienceBiotechnologyApplied and environmental microbiology
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Techniques to evaluate erythrocyte deformability in diabetes mellitus

2005

Using several rheological techniques, we examined the erythrocyte deformability in different groups of diabetic subjects. The macrorheological techniques used for this evaluation were respectively whole-blood filtration, filtration of erythrocyte suspensions, polyviscosimetry and diffractometry. Whole-blood filterability, at a negative pressure of 20 cm water, was decreased in type 2 diabetics; no difference was evident at a negative pressure of 10 cm water. The filtration of erythrocyte suspensions at low haematocrit (5%) did not show differences between normal and diabetic subjects. The polyviscosimetry, which explores the filterability of erythrocyte suspensions at high haematocrit (80%)…

Settore MED/09 - Medicina InternaEndocrinology Diabetes and MetabolismHematocritFluorescence spectroscopypolyviscosimetrylaw.inventionEndocrinologyReference ValueslawErythrocyte DeformabilityDiabetes mellitusDiabetes MellitusInternal MedicinemedicineHumansErythrocyte deformabilityLaser beamsFiltrationwhole-blood filtrationmedicine.diagnostic_testdiabetes mellituViscosityChemistryErythrocyte MembraneGeneral Medicinemedicine.diseaseRed cell membraneDiabetes Mellitus Type 1MembraneDiabetes Mellitus Type 2HematocritBiochemistryerythrocyte filtrationBiophysicsdiffractometryerythrocyte membrane dynamic propertieActa Diabetologica
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Hemorheology in metabolic syndrome

2014

Settore MED/09 - Medicina InternaMicrocirculation erythrocyte deformability
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Eventi vascolari correlati ad alcune condizioni di iperviscosità sclerocitemica

2014

Settore MED/09 - Medicina Internaerythrocyte membrane hereditary spherocytosis hereditary elliptocytosis acanthocytosis
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Erythrocyte and polymorphonuclear leukocyte rheology in diabetes mellitus

2013

Settore MED/09 - Medicina Internaerythrocyte leukocyte rheology diabetes mellitus
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Altered pore-forming properties of proteolytically nicked staphylococcal alpha-toxin

1993

Staphylococcal alpha-toxin is a single-chain polypeptide with a molecular weight of 34,000 that hexamerizes in lipid bilayers to form pores of 1-1.5 nm effective diameter in membranes. We demonstrate that limited proteolysis of purified alpha-toxin with proteinase K generates a hemolytically active product that yields one major protein band of 17-18 kDa in SDS-polyacrylamide gel electrophoresis. The 17-18-kDa protein band harbors two major fragments of similar size representing the N- and C-terminal halves, which remain associated with each other in non-denaturing buffers but dissociate in 6 M urea. Dissociation in urea leads to loss of hemolytic activity. In contrast, unnicked alpha-toxin …

Staphylococcus aureusLysisProteolysisBacterial ToxinsHemolysin ProteinsHemolysisBiochemistryMonocytesCell membraneHemolysin ProteinsmedicineHumansLymphocytesLipid bilayerMolecular BiologyGel electrophoresismedicine.diagnostic_testbiologyCell MembraneErythrocyte MembraneSerine EndopeptidasesCell BiologyProteinase KPeptide FragmentsKineticsMembranemedicine.anatomical_structureBiochemistryChromatography Gelbiology.proteinElectrophoresis Polyacrylamide GelEndopeptidase KJournal of Biological Chemistry
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