Search results for "primer"

showing 10 items of 530 documents

Targeting transcription factor Stat4 uncovers a role for interleukin-18 in the pathogenesis of severe lupus nephritis in mice

2011

Polymorphisms in the transcription factor Stat4 gene have been implicated as risk factors for systemic lupus erythematosus. Although some polymorphisms have a strong association with autoantibodies and nephritis, their impact on pathophysiology is still unknown. To explore this further we used signal transducers and activators of transcription 4 (Stat4) knockout MRL/MpJ-Fas(lpr)/Fas(lpr) (MRL-Fas(lpr)) mice and found that they did not differ in survival or renal function from Stat4-intact MRL-Fas(lpr) mice. Circulating interleukin (IL)-18 levels, however, were elevated in Stat4-deficient compared to Stat4-intact mice, suggesting that this interleukin might contribute to the progression of l…

Malemusculoskeletal diseasesMice Inbred MRL lprchronic inflammationLupus nephritisKidneyInterleukin-23ArticleProinflammatory cytokineOligodeoxyribonucleotides AntisenseGene Knockout TechniquesInterferon-gammaMiceimmune system diseasesmedicineAnimalsskin and connective tissue diseasesSTAT4DNA PrimersAutoimmune diseaseMice Knockoutlupus nephritisMice Inbred BALB CBase Sequencebusiness.industryGene Transfer TechniquesInterleukin-18InterleukinGlomerulonephritishemic and immune systemsSTAT4 Transcription Factormedicine.diseaseInterleukin-12chronic glomerulonephritisNephrologyImmunologyInterleukin 18FemalebusinessNephritisKidney International
researchProduct

Duchenne muscular dystrophy and idiopathic hyperCKemia segregating in a family

1995

A 7-month-old boy with gross motor delay and failure to thrive presented with rhabdomyolysis following an acute asthmatic episode. During hospitalization an electrocardiographic conversion to a Wolff-Parkinson-White type 1 (WPW) pattern took place. Duchenne muscular dystrophy (DMD) was suspected based on elevated creatine kinase (CK) serum levels, muscle biopsy, and family history. The diagnosis was confirmed by molecular analysis, which documented a deletion corresponding to cDNA probe 1-2a in the dystrophin gene, in the propositus and in an affected male cousin of his mother. "Idiopathic" hyperCKemia was found in the propositus, his father, and 5 of his relatives. We suggest that the unus…

Malemusculoskeletal diseasescongenital hereditary and neonatal diseases and abnormalitiesPediatricsmedicine.medical_specialtyDuchenne muscular dystrophyMolecular Sequence DataGene mutationPolymerase Chain ReactionMuscular DystrophiesGenomic ImprintingPrenatal DiagnosisInternal medicinemedicineHumansFamily historyCreatine KinaseGenetics (clinical)X-linked recessive inheritanceDNA PrimersGenes DominantMuscle biopsyBase Sequencebiologymedicine.diagnostic_testGenetic Carrier ScreeningInfantExonsmedicine.diseasePedigreeEndocrinologyMutationFailure to thrivebiology.proteinFemaleCreatine kinasemedicine.symptomDystrophinMetabolism Inborn ErrorsAmerican Journal of Medical Genetics
researchProduct

Evaluation of surface roughness of enamel after various bonding and clean-up procedures on enamel bonded with three different bonding agents : an in-…

2016

Background The purpose of this study was to analyze and compare the enamel surface roughness before bonding and after debonding, to find correlation between the adhesive remnant index and its effect on enamel surface roughness and to evaluate which clean-up method is most efficient to provide a smoother enamel surface. Material and methods 135 premolars were divided into 3 groups containing 45 premolars in each group. Group I was bonded by using moisture insensitive primer, Group II by using conventional orthodontic adhesive and Group III by using self-etching primer. Each group was divided into 3 sub-groups on the basis of type of clean-up method applied i,e scaling followed by polishing, …

Materials scienceGroup iiDentistryPolishingOrthodonticsengineering.material03 medical and health scienceschemistry.chemical_compound0302 clinical medicinestomatognathic systemTungsten carbideSurface roughnessIn vitro studyComposite materialGeneral DentistryPrimer (paint)Enamel paintbusiness.industryResearch030206 dentistry:CIENCIAS MÉDICAS [UNESCO]stomatognathic diseaseschemistryvisual_artUNESCO::CIENCIAS MÉDICASvisual_art.visual_art_mediumengineeringAdhesivebusiness030217 neurology & neurosurgery
researchProduct

Group-specific quantification of methanotrophs in landfill gas-purged laboratory biofilters by tyramide signal amplification-fluorescence in situ hyb…

2008

The aim of this study was to quantitatively analyse methanotrophs in two laboratory landfill biofilters at different biofilter depths and at temperatures which mimicked the boreal climatic conditions. Both biofilters were dominated by type I methanotrophs. The biofilter depth profiles showed that type I methanotrophs occurred in the upper layer, where relatively high O(2) and low CH(4) concentrations were present, whereas type II methanotrophs were mostly distributed in the zone with high CH(4) and low O(2) concentrations. The number of type I methanotrophic cells declined when the temperature was raised from 15 degrees C to 23 degrees C, but increased when lowered to 5 degrees C. A slight …

MethanobacteriaceaeEnvironmental EngineeringType I methanotrophsBioengineeringmedicineWaste Management and DisposalIn Situ Hybridization FluorescenceDNA PrimersType II methanotrophsmedicine.diagnostic_testBase SequenceRenewable Energy Sustainability and the EnvironmentChemistryEnvironmental engineeringGeneral MedicineAmidesRefuse DisposalLandfill gasEnvironmental chemistrySoil waterAnaerobic oxidation of methaneBiofilterGasesOligonucleotide ProbesSignal amplificationFiltrationFluorescence in situ hybridizationBioresource technology
researchProduct

Effect of oligonucleotide primers in determining viral variability within hosts

2004

Abstract Background Genetic variability in viral populations is usually estimated by means of polymerase chain reaction (PCR) based methods in which the relative abundance of each amplicon is assumed to be proportional to the frequency of the corresponding template in the initial sample. Although bias in template-to-product ratios has been described before, its relevance in describing viral genetic variability at the intrapatient level has not been fully assessed yet. Results To investigate the role of oligonucleotide design in estimating viral variability within hosts, genetic diversity in hepatitis C virus (HCV) populations from eight infected patients was characterised by two parallel PC…

MethodologyOligonucleotidesGenetic VariationHumansRNA ViralReproducibility of Resultslcsh:RC109-216HepacivirusHepatitis CSensitivity and SpecificityPhylogenylcsh:Infectious and parasitic diseasesDNA PrimersVirology Journal
researchProduct

Differentiation of Candida parapsilosis, C. orthopsilosis, and C. metapsilosis by specific PCR amplification of the RPS0 intron

2011

Although Candida parapsilosis is the most prevalent among the 3 species of the *psilosis group, studies applying DNA-based diagnostic techniques with isolates previously identified as C. parapsilosis have revealed that both C. orthopsilosis and C. metapsilosis account for 0-10% of all these isolates, depending on the geographical area. Differences in the degrees of antifungal susceptibility and virulence have been found, so a more precise identification is required. In a first approach, we reidentified 38 randomly chosen clinical isolates, previously identified as C. parapsilosis, using the RPO2 (CA2) RAPD marker. Among them, we reclassified 4 as C. metapsilosis and 5 as C. orthopsilosis. W…

Microbiology (medical)Antifungal AgentsSequence analysisGenes FungalMolecular Sequence DataVirulenceMicrobial Sensitivity TestsBiologyCandida parapsilosisPolymerase Chain ReactionMicrobiologyMicrobiologylaw.inventionSpecies SpecificityDrug Resistance FungallawCloning MolecularDNA FungalMycological Typing TechniquesGenePolymerase chain reactionCandidaDNA PrimersGeneticsBase SequenceIntronFungal geneticsSequence Analysis DNAGeneral Medicinebiology.organism_classificationIntronsRandom Amplified Polymorphic DNA TechniqueRAPDInfectious Diseases
researchProduct

Nation-wide study of the occurrence of Listeria monocytogenes in French soils using culture-based and molecular detection methods

2013

Identifiant HAL : hal-01120618; International audience; Soil is a potential reservoir of human pathogens and a possible source of contamination of animals, crops and water. In order to study the distribution of Listeria monocytogenes in French soils, a real-time PCR TaqMan assay targeting the phosphoribosylpyrophosphate synthetase (prs) gene of L. monocytogenes was developed for the specific detection and quantification of this bacterium within a collection of 1315 soil DNAs originated from the French Soil Quality Monitoring Network. The prs real-time PCR TaqMan assay was specific for L. monocytogenes and could quantify accurately down to 104L. monocytogenes per gram of dry soil. Among the …

Microbiology (medical)DNA BacterialVeterinary medicineColony Count MicrobialFrench soil monitoring networkmedicine.disease_causeReal-Time Polymerase Chain ReactionMicrobiologyPasturecomplex mixturesTaqMan type probeMicrobiologyCulture-based detection03 medical and health sciencesListeria monocytogenesmedicineTaqMan[ SDU.ENVI ] Sciences of the Universe [physics]/Continental interfaces environmentRibose-Phosphate PyrophosphokinaseSerotyping[SDU.ENVI]Sciences of the Universe [physics]/Continental interfaces environmentMolecular BiologyMolecular detectionSoil Microbiology030304 developmental biologyGramDNA Primers2. Zero hunger0303 health sciencesgeography[ SDE.BE ] Environmental Sciences/Biodiversity and EcologyBacteriological Techniquesgeography.geographical_feature_categorybiology030306 microbiologyContaminationbiology.organism_classificationSoil qualityListeria monocytogenesBacterial Typing TechniquesSoil waterFrance[SDE.BE]Environmental Sciences/Biodiversity and EcologyBacteriaReal-time PCR
researchProduct

Leucine aminopeptidase is an immunodominant antigen of Fasciola hepatica excretory and secretory products in human infections.

2007

ABSTRACT The liver fluke Fasciola hepatica parasitizes humans and ruminant livestock worldwide, and it is now being considered a reemerging zoonotic disease, especially in areas in which it is endemic, such as South America. This study investigates the immune response to excretory and secretory products produced by F. hepatica in a group of patients from the Peruvian Altiplano, where the disease is highly endemic. Using a proteomic approach and immunoblotting techniques, we have identified the enzymes leucine aminopeptidase (LAP) and phosphoenolpyruvate carboxykinase as immunodominant antigens recognized by sera from fasciolosis patients. An indirect enzyme-linked immunosorbent assay using …

Microbiology (medical)FascioliasisAdolescentClinical BiochemistryImmunologyBlotting WesternMolecular Sequence DataSheep DiseasesEnzyme-Linked Immunosorbent AssayAminopeptidasePolymerase Chain ReactionLeucyl AminopeptidaseImmune systemAntigenHepaticaparasitic diseasesmedicineImmunology and AllergyFasciola hepaticaAnimalsHumansElectrophoresis Gel Two-DimensionalFasciolosisChildDNA PrimersSheepbiologyBase SequenceImmunodominant EpitopesClinical and Diagnostic Laboratory ImmunologyLiver flukeFasciola hepaticabiology.organism_classificationmedicine.diseaseVirologyExcretory systemAntigens HelminthChild PreschoolClinical and vaccine immunology : CVI
researchProduct

Growth of Rhodococcus sp. strain BCP1 on gaseous n-alkanes: New metabolic insights and transcriptional analysis of two soluble di-iron monooxygenase …

2015

none 7 si Rhodococcus sp. strain BCP1 was initially isolated for its ability to grow on gaseous n-alkanes, which act as inducers for the co-metabolic degradation of low-chlorinated compounds. Here, both molecular and metabolic features of BCP1 cells grown on gaseous and short-chain n-alkanes (up to n-heptane) were examined in detail. We show that propane metabolism generated terminal and sub-terminal oxidation products such as 1- and 2-propanol, whereas 1-butanol was the only terminal oxidation product detected from n-butane metabolism. Two gene clusters, prmABCD and smoABCD—coding for Soluble Di-Iron Monooxgenases (SDIMOs) involved in gaseous n-alkanes oxidation—were detected in the BCP1 g…

Microbiology (medical)Gaseous n-alkaneSoluble di-iron monooxygenaseStrain (chemistry)lcsh:QR1-502Monooxygenase gene expressionMetabolismgaseous n-alkanesMonooxygenaseBiologyLyaseRedoxMicrobiologyPrimer extensionlcsh:MicrobiologyChaperoninRhodococcus sp strain BCP1; soluble di-iron monooxygenase; propane and n-butane oxidation; gaseous n-alkanes; monooxygenase gene expressionBiochemistryRhodococcus sp. strain BCP1Rhodococcus sp strain BCP1Propane and n-butane oxidationGeneOriginal Researchpropane and butane oxidation
researchProduct

Characterizations of adenovirus type 41 isolates from children with acute gastroenteritis in Japan, Vietnam, and Korea.

2004

ABSTRACT Genetic and antigenic characterizations of 70 strains of adenovirus type 41 (Ad41), isolated between 1998 and 2001 from children in Japan, Vietnam, and Korea, were done by DNA restriction enzyme (RE) analysis, sequencing analysis, and monoclonal antibody (MAb)-based enzyme-linked immunosorbent assay (ELISA). Eight genome types were observed in the present study, among which D25, D26, D27, and D28 were novel genome types. These eight genome types were divided into two genome-type clusters (GTCs) based on phylogenetic analysis of the hypervariable regions (HVRs) of the hexon. GTC1 includes D1, D25, D26, D27, and D28, and the GTC2 contains D4, D12, and D22. The amino acid homologies a…

Microbiology (medical)Molecular Sequence DataRestriction MappingEnzyme-Linked Immunosorbent AssayGenome ViralBiologyGenomePolymerase Chain ReactionViruslaw.inventionRestriction mapJapanlawPhylogeneticsVirologyHumansAmino Acid SequenceChildPeptide sequencePolymerase chain reactionPhylogenyDNA PrimersKoreaPhylogenetic treeBase SequenceSequence Homology Amino AcidAdenoviruses HumanVirologyHypervariable regionGastroenteritisVietnamAcute DiseaseSequence AlignmentJournal of clinical microbiology
researchProduct