Search results for "RATES"

showing 10 items of 1636 documents

Matched-pairs analysis of outcomes with bortezomib, melphalan, and prednisone (VMP) treatment for previously untreated multiple myeloma (MM) using lo…

2015

(95% CI: 58-88%), respectively. A formal interim analysis of the Day 90 CR rate was conducted when 65 patients were evaluable, and at that time the Mel only arm was determined to be superior. The study was, therefore, stopped early by the Institutional DSMB. However, with a longer follow up Bu-Mel ultimately resulted in better PFS. Conclusions: Bu-Mel was associated with a significantly lower day 90 CR rate and a significantly higher rate of grade 3-4 non-hematologic toxicity, compared to Mel. However, after a median follow up of 15.7 months, PFS was significantly longer in the Bu-Mel arm. Figure 1 PFS from Day 90 by Treatment Arm

MelphalanCancer Researchmedicine.medical_specialtyLong term follow upbusiness.industryBortezomibUrologyHematologyInterim analysismedicine.diseasecarbohydrates (lipids)OncologyPrednisoneMedian follow-uphemic and lymphatic diseasesToxicitymedicinebusinessneoplasmsMultiple myelomamedicine.drugClinical Lymphoma Myeloma and Leukemia
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Metabolism of Saccharomyces cerevisiae envelope mannoproteins.

1982

By pulse and chase labeling experiments, two independent mannoprotein pools have been found associated with the Saccharomyces cerevisiae envelope. One of them probably corresponds to mannoproteins localized in the periplasmic space. These molecules showed a high turnover rate at 28 degrees C. The second pool is formed by intrinsic wall mannoproteins which are apparently stable for long periods of time, after a small initial turnover. These results suggest that at least part of the mannoproteins initially found in the periplasmic space may move into the wall. The time lag between the addition of the radioactive precursors and their incorporation in the cell envelope (20-30 min for amino acid…

Membrane GlycoproteinsGlucan Endo-13-beta-D-GlucosidaseSaccharomyces cerevisiaeGeneral MedicineMetabolismPeriplasmic spaceSaccharomyces cerevisiaeBiologybiology.organism_classificationBiochemistryMicrobiologyYeastcarbohydrates (lipids)Cell wallFungal ProteinsMannansKineticsBiochemistryCell WallGeneticsBiophysicsMolecular BiologyEnvelope (waves)GlycoproteinsArchives of microbiology
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Identification of a 49-kDa hydrophobic cell wall mannoprotein present in velum yeast which may be implicated in velum formation

2000

Analysis of velum-forming yeast cell wall components released by beta-1,3-glucanase treatment were compared with those of a non velum-forming yeast. SDS-PAGE electrophoresis and Western blotting with ConA-peroxidase staining of mannoproteins allowed us to identify a 49-kDa mannoprotein present in the cell wall of the velum-forming yeast and hardly visible in the control. The cell wall nature of this protein was confirmed by labelling with the non-permeable sulfosuccinimydiyl-6-(biotinamido)hexanoate reagent. A partial purification of this mannoprotein by anion exchange HPLC followed by surface hydrophobicity determination revealed that the fraction containing the 49-kDa mannoprotein was the…

Membrane GlycoproteinsSurface PropertiesBlotting WesternCellWineSaccharomyces cerevisiaeBiologyMicrobiologyYeastStainingFungal Proteinscarbohydrates (lipids)BlotCell wallElectrophoresismedicine.anatomical_structureBiochemistryCell WallBiotinylationGeneticsmedicineBiotinylationElectrophoresis Polyacrylamide GelMolecular BiologyPolyacrylamide gel electrophoresisFEMS Microbiology Letters
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The Low Energy-Coupling Respiration in Zymomonas mobilis Accelerates Flux in the Entner-Doudoroff Pathway.

2015

Performing oxidative phosphorylation is the primary role of respiratory chain both in bacteria and eukaryotes. Yet, the branched respiratory chains of prokaryotes contain alternative, low energy-coupling electron pathways, which serve for functions other than oxidative ATP generation (like those of respiratory protection, adaptation to low-oxygen media, redox balancing, etc.), some of which are still poorly understood. We here demonstrate that withdrawal of reducing equivalents by the energetically uncoupled respiratory chain of the bacterium Zymomonas mobilis accelerates its fermentative catabolism, increasing the glucose consumption rate. This is in contrast to what has been observed in o…

Metabolic Processes0301 basic medicineRespiratory chainlcsh:MedicineBiochemistryOxidative PhosphorylationGlucose Metabolismlcsh:ScienceZymomonasMultidisciplinarybiologyOrganic CompoundsSimulation and ModelingMonosaccharidesChemical ReactionsCatabolismAerobiosisEnzymesChemistryBiochemistryPhysical SciencesCarbohydrate MetabolismOxidoreductasesOxidation-ReductionResearch Article030106 microbiologyCarbohydratesAcetaldehydeOxidative phosphorylationResearch and Analysis MethodsZymomonas mobilisElectron Transport03 medical and health sciencesOxidationEntner–Doudoroff pathwayDehydrogenasesOrganic Chemistrylcsh:RChemical CompoundsBiology and Life SciencesProteinsNADbiology.organism_classificationElectron transport chainKineticsGlucoseMetabolismFermentationEnzymologyFermentationlcsh:QFlux (metabolism)BacteriaPLoS ONE
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Metabolism of n-Butyl Benzyl Phthalate in the Female Wistar Rat. Identification of New Metabolites

1999

International audience; n-Butyl benzyl phthalate (BBP), a plasticizer used in polyvinylchloride (PVC) and other polymers, has been orally administered to female Wistar rats with four doses (150, 475, 780 and 1500 mg/kg body weight/day) for 3 consecutive days. Metabolites recovered in urines were analysed by gas chromatography±mass spectrometry (GC±MS) after 24, 48 and 72 hours. Six metabolites were identi®ed. Mono-n-butyl phthalate (MBuP) and mono-n-benzyl phthalate (MBeP) represented respectively 29± 34% and 7±12 % of the total recovered metabolites. Hippuric acid, the main metabolite of benzoic acid, represented the second major metabolite (51±56%). Phthalic acid, benzoic acid and an o-ox…

MetabolitePhthalic Acids[SDV.TOX.TCA]Life Sciences [q-bio]/Toxicology/Toxicology and food chainUrine010501 environmental sciencesToxicology01 natural sciencesGas Chromatography-Mass Spectrometry03 medical and health scienceschemistry.chemical_compoundPharmacokineticsPlasticizersFemale rat.MetabolitesAnimalsToxicokineticsn-butyl benzyl phthalateRats Wistar030304 developmental biology0105 earth and related environmental sciencesBenzoic acid0303 health sciencesChromatographyMolecular StructureHippuratesPhthalateHippuric acidGeneral MedicineRats3. Good healthPhthalic acidTeratogensMetabolismDiazomethane[SDV.TOX.TCA] Life Sciences [q-bio]/Toxicology/Toxicology and food chainchemistryFemaleOxidation-ReductionFood ScienceFood and Chemical Toxicology
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Studies on the antioxidant activity of the essential oil and extract of Tunisian Tetraclinis articulata (Vahl) Mast. (Cupressaceae).

2013

This study analyses the chemical composition and in vitro antioxidant activity of both the essential oil and the 80% aqueous acetone extract of Tetraclinis articulata leaves. The GC-MS analysis of the essential oil identified 66 components that comprise 93.5% of the oil. The major constituents of the oil are: bornyl acetate (31.4%), α-pinène (24.5%) and camphor (20.3%). Antioxidant activities of the samples were determined using four different test systems, namely DPPH, β-carotene/linoleic acid, reducing power and metal chelating activity assay. Test results from the DPPH system showed the strongest radical scavenging activity was exhibited by the 80% aqueous acetone extract (IC(50) = 5.5 µ…

Metal chelating activityAntioxidantDPPHmedicine.medical_treatmentLinoleic acidMetal chelating activityPlant ScienceTetraclinisBiochemistryEssential oilAntioxidantsGas Chromatography-Mass SpectrometryAnalytical Chemistrylaw.inventionLinoleic Acidchemistry.chemical_compoundCamphorAntioxidant activityPicrateslawmedicineOils VolatileOrganic chemistryFood scienceEssential oilCarotene/linoleic acidbiologyPlant ExtractsOrganic ChemistryBiphenyl CompoundsCupressaceaePolyphenolsSettore CHIM/06 - Chimica Organicabiology.organism_classificationbeta CaroteneTetraclinis articulataPlant LeavesProanthocyanidinchemistryReducing powerDPPHNatural product research
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Facile formation of a meso–meso linked porphyrin dimer catalyzed by a manganese(iv)–oxo porphyrin

2011

A manganese(IV)-oxo porphyrin catalyzes C-C bond formation between zinc porphyrins at the meso-position with a two-electron oxidant to afford the meso-meso linked porphyrin dimer efficiently. The meso-meso linked dimer is formed via formation of the porphyrin radical cation, and the rate-determining step in the catalytic cycle is the formation of a manganese(IV)-oxo porphyrin with a two-electron oxidant.

MetalloporphyrinsDimerchemistry.chemical_elementManganeseZincPhotochemistryCatalysisCatalysischemistry.chemical_compoundPolymer chemistrypolycyclic compoundsMaterials Chemistryheterocyclic compoundsChemistryfungiMetals and AlloysGeneral ChemistryBond formationPorphyrinSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialscarbohydrates (lipids)Manganese CompoundsRadical ionCatalytic cycleCeramics and CompositesDimerizationChemical Communications
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Dehydrogenation versus Oxygenation in Two-Electron and Four-Electron Reduction of Dioxygen by 9-Alkyl-10-methyl-9,10-dihydroacridines Catalyzed by Mo…

2004

Dehydrogenation of 10-methyl-9,10-dihydroacridine (AcrH(2)) by dioxygen (O(2)) proceeds efficiently, accompanied by the two-electron and four-electron reduction of O(2) to produce H(2)O(2) and H(2)O, which are effectively catalyzed by monomeric cobalt porphyrins and cofacial dicobalt porphyrins in the presence of perchloric acid (HClO(4)) in acetonitrile (MeCN) and benzonitrile (PhCN), respectively. The cobalt porphyrin catalyzed two-electron reduction of O(2) also occurs efficiently by 9-alkyl-10-methyl-9,10-dihydroacridines (AcrHR; R = Me, Et, and CH(2)COOEt) to yield 9-alkyl-10-methylacridinium ion (AcrR+) and H(2)O(2). In the case of R = Bu(t) and CMe(2)COOMe, however, the catalytic two…

Metalloporphyrinschemistry.chemical_elementElectronsReaction intermediatePhotochemistryBiochemistryMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundColloid and Surface ChemistryDehydrogenationPerchloric acidAlkylchemistry.chemical_classificationPerchloratesChemistryCobaltGeneral ChemistryNADPorphyrinKineticsBenzonitrileAcridinesHydrogenationOxidation-ReductionCobaltJournal of the American Chemical Society
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Epidemiological cutoff values for fluconazole, itraconazole, posaconazole, and voriconazole for six Candida species as determined by the colorimetric…

2013

ABSTRACT In the absence of clinical breakpoints (CBP), epidemiological cutoff values (ECVs) are useful to separate wild-type (WT) isolates (without mechanisms of resistance) from non-WT isolates (those that can harbor some resistance mechanisms), which is the goal of susceptibility tests. Sensititre YeastOne (SYO) is a widely used method to determine susceptibility of Candida spp. to antifungal agents. The CLSI CBP have been established, but not for the SYO method. The ECVs for four azoles, obtained using MIC distributions determined by the SYO method, were calculated via five methods (three statistical methods and based on the MIC 50 and modal MIC). Respectively, the median ECVs (in mg/lit…

Microbiology (medical)AzolesPosaconazolemedicine.medical_specialtyAntifungal AgentsItraconazoleMycologyMicrobial Sensitivity TestsBiologyMicrobiology:Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings]EpidemiologymedicineHumansCutoffCandida albicansPruebas de sensibilidad microbianaCandidaVoriconazoleCandidiasisLiter:Chemicals and Drugs::Heterocyclic Compounds::Heterocyclic Compounds 1-Ring::Azoles [Medical Subject Headings]:Diseases::Bacterial Infections and Mycoses::Mycoses::Candidiasis [Medical Subject Headings]biology.organism_classification:Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Anti-Infective Agents::Antifungal Agents [Medical Subject Headings]:Analytical Diagnostic and Therapeutic Techniques and Equipment::Diagnosis::Diagnostic Techniques and Procedures::Clinical Laboratory Techniques::Microbiological Techniques::Microbial Sensitivity Tests [Medical Subject Headings]:Organisms::Eukaryota::Fungi::Mitosporic Fungi::Candida [Medical Subject Headings]AntifúngicosFluconazolemedicine.drug
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Rapid and improved gas-liquid chromatography technique for detection of hippurate hydrolysis by Campylobacter jejuni and Campylobacter coli

1987

A gas-liquid chromatographic method which requires no chloroform extraction of the split products has been investigated for the detection of hippurate hydrolysis by Campylobacter spp. This technique gave better reproducibility than other tests also used in this study and allows the routine use of the gas-liquid chromatographic method for identification of Campylobacter isolates.

Microbiology (medical)Chromatography GasChloroformChromatographybiologyHippuratesHydrolysisCampylobacterExtraction (chemistry)Campylobacterbiology.organism_classificationmedicine.disease_causeBenzoatesCampylobacter jejuniHydrolysischemistry.chemical_compoundCampylobacter fetuschemistryBiochemistryCampylobacter colimedicineGas chromatographyCampylobacter fetusResearch ArticleJournal of Clinical Microbiology
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