Search results for "Hox"

showing 10 items of 1357 documents

Chromatographic analysis of phenethylamine-antihistamine combinations using C8, C18 or cyano columns and micellar sodium dodecyl sulfate-pentanol mix…

2001

The chromatographic behaviour of binary and ternary mixtures of several phenethylamines (phenylephrine, phenylpropanolamine, ephedrine, pseudoephedrine and methoxyphenamine) and antihistamines (pheniramine, carbinoxamine, doxylamine, chlorpheniramine, dexchlorpheniramine, dexbrompheniramine, diphenhydramine, tripolidine, azatadine and phenyltoloxamine), found in cough-cold pharmaceutical preparations, was studied using C8, C18 and cyano columns, micellar mobile phases of sodium dodecyl sulfate (SDS) and pentanol and UV detection. Using a C8 column and mobile phases of 0.05 mol l-1 SDS-6% v/v pentanol or 0.15 mol l-1 SDS-2% v/v pentanol at pH 7, more than 30 different phenethylamine-antihist…

ChromatographyChromatographyMethoxyphenaminePhenethylaminesPseudoephedrineAscorbic acidBiochemistrySensitivity and SpecificityAnalytical Chemistrychemistry.chemical_compoundNasal DecongestantschemistryPhenyltoloxaminePhenethylaminesElectrochemistrymedicineHistamine H1 AntagonistsEnvironmental ChemistryCarbinoxaminePheniramineSodium dodecyl sulfateSpectroscopymedicine.drugThe Analyst
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Simultaneous dissolution profiles of two drugs in pharmaceutical formulations by an FIA manifold

2002

Abstract This article deals with the simultaneous determination of dissolution profiles of two drugs with overlapped spectra, present in the same pharmaceutical formulation. The official procedure for the dissolution profile is adapted to the continuous-flow methodology; the dissolution vessel is connected to an FIA manifold, in which the sample aliquots from the dissolution vessel are treated in order to adjust to the suitable pH and dilution degree to be monitored. The resulting solution is injected into the carrier stream, an acetic acid–acetate buffer at pH 4.3 and forced to the flow-cell of the spectrophotometer. The simultaneous determination of both profiles is based on the first der…

ChromatographySulfamethoxazoleChemistryClinical BiochemistryPharmaceutical SciencePharmaceutical formulationTrimethoprimDosage formAnalytical Chemistrylaw.inventionDilutionAnti-Infective AgentsSolubilitylawFlow Injection AnalysisDrug DiscoveryManifold (fluid mechanics)Quantitative analysis (chemistry)DissolutionSpectroscopyAnalysis methodJournal of Pharmaceutical and Biomedical Analysis
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Solubility of some pesticides in supercritical CO2

1988

The solubility limits of some pesticides (Linuron, Methoxychlor, Diclofopmethyl, Diclofop and 2,4-D) and of 3,4-dichloroaniline have been determined in supercritical CO2 at 200 bar and 40° C, using the Milton Roy sample preparation accessory SPATM. Depending on the polarity and vapour pressure of the investigated compounds, the solubility was found to be between 0.3 and 12 gl−1.

ChromatographyVapor pressureClinical BiochemistrySupercritical fluid extractionMethoxychlorGeneral MedicinePesticideSupercritical fluidAnalytical Chemistrychemistry.chemical_compoundchemistryGeneral Materials ScienceSample preparationSolubilityBar (unit)Fresenius' Zeitschrift für analytische Chemie
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Modulation of Base Excision Repair Alters Cellular Sensitivity to UVA1 but not to UVB¶

2007

Abstract Oxidative DNA damage has been implicated in some of the biological properties of UVA but so far not in the acute photosensitivity or cellular sensitivity. In contrast to pyrimidine dimers, oxidative DNA damage is predominantly processed by base excision repair (BER). In order to further clarify the role of oxidative DNA damage and its repair in the acute cellular response to UV light, we studied UVA1 and UVB sensitivities in three different cell model systems with modified BER. 8-Oxoguanine-DNA-glycosylase 1–/– (OGG1–/–) mouse embryonal fibroblasts and human fibroblasts in which BER was inhibited by incubation with methoxyamine were hypersensitive to UVA1, in particular to low dose…

DNA damageChinese hamster ovary cellCellPyrimidine dimerGeneral MedicineBase excision repairBiologyBiochemistryMolecular biologychemistry.chemical_compoundmedicine.anatomical_structurechemistryPhotosensitivityBiochemistryDownregulation and upregulationMethoxyaminemedicinePhysical and Theoretical ChemistryPhotochemistry and Photobiology
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UVPAR: fast detection of functional shifts in duplicate genes.

2006

Abstract Background The imprint of natural selection on gene sequences is often difficult to detect. A plethora of methods have been devised to detect genetic changes due to selective processes. However, many of those methods depend heavily on underlying assumptions regarding the mode of change of DNA sequences and often require sophisticated mathematical treatments that made them computationally slow. The development of fast and effective methods to detect modifications in the selective constraints of genes is therefore of great interest. Results We describe UVPAR, a program designed to quickly test for changes in the functional constraints of duplicate genes. Starting with alignments of t…

DanioComputational biologyBiologylcsh:Computer applications to medicine. Medical informaticsBiochemistryDNA sequencingEvolution MolecularGenes DuplicateSequence Analysis ProteinStructural BiologySelection GeneticHox geneMolecular BiologyGenelcsh:QH301-705.5Selection (genetic algorithm)GeneticsNatural selectionApplied MathematicsProteinsSequence Analysis DNAbiology.organism_classificationComputer Science Applicationslcsh:Biology (General)lcsh:R858-859.7DNA microarraySequence AlignmentSoftwareAlgorithmsGenètica
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Detection of banned drugs in sport by micellar liquid chromatography

1992

Abstract A rapid method for the determination of banned drugs in sport (including stimulants, anabolic steroids and diuretics) based on micellar liquid chromatography is proposed. The mobile phase is an aqueous solution of a surfactant (sodium dodecyl sulphate in this instance) and the stationary phase is octadecylsilica. The retention parameters of the drugs were established and the effect of a mobile phase organic modifier on the chromatographic behaviour of the compounds was studied. Improvements in efficiency were achieved by control of the temperature of the mobile phase. This method allows the direct injection of urine samples for the determination of drugs excreted free in urine: ami…

Detection limitAmiphenazoleChromatographyMethoxyphenamineChemistryMetandienoneClostebolBiochemistryAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographymedicineEnvironmental ChemistryEphedrineSpectroscopyPhenylpropanolaminemedicine.drugAnalytica Chimica Acta
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Determination of UV-filters in sunscreens by HPLC.

2001

Simultaneous determination of six internationally authorised organic UV-filters in sunscreen formulations was performed by HPLC with UV spectrophotometric detection. The filters determined were: sulisobenzone, oxybenzone, octyl dimethyl PABA, octyl methoxycinnamate, octyl salicylate and homosalate. A C18 stationary phase and a mobile phase of ethanol water acetic acid (70 : 29.5 : 0.5) were used with a flow rate of 0.5 mL/min. UV measurements were carried out at 313 nm. The time required for the analysis was 25 min and the limits of detection were between 0.2 and 2 mg/L, except for sulisobenzone, which gave a limit of detection of 20 mg/L. The procedure proposed provides an accurate, fast a…

Detection limitChromatographyUltraviolet RaysOctyl methoxycinnamateReversed-phase chromatographySulisobenzoneBiochemistryHigh-performance liquid chromatographyHomosalatechemistry.chemical_compoundchemistrymedicineOctyl salicylateIndicators and ReagentsOxybenzoneSunscreening AgentsChromatography High Pressure Liquidmedicine.drugFresenius' journal of analytical chemistry
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Determination of the UV filters worldwide authorised in sunscreens by high-performance liquid chromatography

2001

Simultaneous determination of organic UV filters worldwide authorised in sunscreen formulations was performed by HPLC with UV spectrophotometric detection. The filters determined were: benzophenone-4, benzophenone-3, butyl methoxydibenzoylmethane, octyl dimethyl PABA, octyl methoxycinnamate, homosalate and octyl salicylate. A C18 stationary phase and an isocratic mobile phase of ethanol-water-acetic acid (70:29.5:0.5) containing 65.4 mM of hydroxypropyl-beta-cyclodextrin, were used with a flow-rate of 0.6 ml/min. UV measurements were carried out at 313 nm. The time required for the analysis was 20 min and the limits of detection were between 1.5 and 2.3 mg/l. The procedure proposed provides…

Detection limitchemistry.chemical_classificationChromatographyCyclodextrinOrganic ChemistryOctyl methoxycinnamateGeneral MedicineReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryHomosalatechemistry.chemical_compoundchemistrymedicineOctyl salicylateQuantitative analysis (chemistry)medicine.drugJournal of Chromatography A
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How Hox genes can shed light on the place of echinoderms among the deuterostomes.

2014

19 pages; International audience; BACKGROUND: The Hox gene cluster ranks among the greatest of biological discoveries of the past 30 years. Morphogenetic patterning genes are remarkable for the systems they regulate during major ontogenetic events, and for their expressions of molecular, temporal, and spatial colinearity. Recent descriptions of exceptions to these colinearities are suggesting deep phylogenetic signal that can be used to explore origins of entire deuterostome phyla. Among the most enigmatic of these deuterostomes in terms of unique body patterning are the echinoderms. However, there remains no overall synthesis of the correlation between this signal and the variations observ…

DeuterostomeBody PatterningPhylumEvolutionResearch[SDV.BID.EVO]Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE]Inversion (evolutionary biology)[SDV.BDD.MOR]Life Sciences [q-bio]/Development Biology/MorphogenesisBiologyDevelopmentbiology.organism_classificationDeuterostomia[ SDV.BDD.MOR ] Life Sciences [q-bio]/Development Biology/MorphogenesisHox genes[ SDV.BID.EVO ] Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE]EchinodermPhylogeneticsEvolutionary biologyGeneticsHox geneDevelopmental biologyEcology Evolution Behavior and SystematicsA/P axisDevelopmental BiologyEchinodermata
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CCDC 815937: Experimental Crystal Structure Determination

2012

Related Article: S.Majumder, S.Dutta, L.M.Carrella, E.Rentschler, S.Mohanta|2011|J.Mol.Struct.|1006|216|doi:10.1016/j.molstruc.2011.09.011

Diaqua-(22'-(12-phenylenebis((nitrilo)methylylidene))bis(6-ethoxyphenolato)-NN'OO')-iron(iii) nitrate monohydrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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