Search results for " Western"

showing 10 items of 687 documents

S-type lectins occur also in invertebrates: high conservation of the carbohydrate recognition domain in the lectin genes from the marine sponge Geodi…

1993

The marine sponge Geodia cydonium contains several lectins. The main component, called lectin-1, is composed of three to four identical subunits. The subunits of the lectins were cloned from a cDNA library; two clones were obtained. From the deduced aa sequence of one clone, LECT-1, a mol. wt of 15,313 Da is calculated; this value is in good agreement with mass spectrometric analysis of 15,453 +/- 25 Da. The sequence of another clone, LECT-2, was analysed and the aa sequence was deduced (15,433 Da). The two subunits have a framework sequence of 38 conserved aa which are characteristic for the carbohydrate-binding site of vertebrate S-type lectins. Clustering of lectin sequences of various s…

clone (Java method)GalectinsBlotting WesternMolecular Sequence DataBiochemistryChromatography AffinityMass SpectrometryLectinsAnimalsAmino Acid SequenceCloning MolecularPeptide sequenceGeneGalectinCloningbiologyBase SequencecDNA libraryLectinDNAbiology.organism_classificationPoriferaSuberites domunculaBiochemistrybiology.proteinElectrophoresis Polyacrylamide GelGlycobiology
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CAMPANIAN WINE FOR PUNIC SICILY: PETROGRAPHIC AND ARCHAEOLOGICAL STUDIES OF GRAECO-ITALIC AMPHORAE FROM PALERMO

2018

This contribution proposes a combination of archaeological fabric analysis and petrographic research applied to the study of 35 sherds of Graeco-Italic amphorae mostly found in Palermo, but also in Pantelleria and Malta (Tab. 1). The provenance identification derived from both approaches gives evidence for the arrival, in North-Western Sicily, of presumable wine amphorae from central-Tyrrhenian Italy since the very late 4th century BC. The production of the majority of the material has been confidentially attributed to the area of the Gulf of Naples/Ischia, but a second large group originates from several, still unidentified production sites to be located along the coastal strip of Campania…

combination of archaeological fabric study and petrographic analysisGulf of Naples Western SicilyGraeco-Italic amphorae from Tyrrhenian Italycommercial axisCarthage's sphere of influenceGraeco-Italic amphorae from Tyrrhenian ItalySettore GEO/09 -Georis. Miner.e Appl.Mineral.-Petrogr. per l'Ambi.ed i B.Cult.Graeco-Italic amphorae from Tyrrhenian Italy combination of archaeological fabric study and petro-graphic analysis Gulf of Naples Western Sicily Carthage's sphere of influence commercial axis
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WRN protects against topo I but not topo II inhibitors by preventing DNA break formation

2008

The Werner syndrome helicase/3′-exonuclease (WRN) is a major component of the DNA repair and replication machinery. To analyze whether WRN is involved in the repair of topoisomerase-induced DNA damage we utilized U2-OS cells, in which WRN is stably down-regulated (wrn-kd), and the corresponding wild-type cells (wrn-wt). We show that cells not expressing WRN are hypersensitive to the toxic effect of the topoisomerase I inhibitor topotecan, but not to the topoisomerase II inhibitor etoposide. This was shown by mass survival assays, colony formation and induction of apoptosis. Upon topotecan treatment WRN deficient cells showed enhanced DNA replication inhibition and S-phase arrest, whereas af…

congenital hereditary and neonatal diseases and abnormalitiesWerner Syndrome HelicaseDNA RepairCell SurvivalDNA damageDNA repairBlotting WesternApoptosisBone NeoplasmsBiologyTopoisomerase-I InhibitorBiochemistryArticleWerner Syndrome HelicaseColony-Forming Units AssayHistonesTumor Cells CulturedmedicineHumansTopoisomerase II InhibitorsEnzyme InhibitorsRNA Small InterferingeducationMolecular BiologyEtoposideOsteosarcomaeducation.field_of_studyRecQ HelicasesTopoisomeraseCell CycleDNA Breaksnutritional and metabolic diseasesCell BiologyAntineoplastic Agents PhytogenicMolecular biologyDNA Topoisomerases Type IIExodeoxyribonucleasesBromodeoxyuridineDNA Topoisomerases Type IDNA Replication InhibitionCancer researchbiology.proteinTopoisomerase I InhibitorsTopoisomerase-II InhibitorTopotecanCamptothecinmedicine.drugDNA Repair
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Evidence of oxidative stress in very long chain fatty acid--treated oligodendrocytes and potentialization of ROS production using RNA interference-di…

2011

X-linked adrenoleukodystrophy (X-ALD) and pseudo neonatal adrenoleukodystrophy (P-NALD) are neurodegenerative demyelinating diseases resulting from the functional loss of the peroxisomal ATP-binding cassette transporter D (ABCD1) and from single peroxisomal enzyme deficiency (Acyl-CoA oxidase1: ACOX1), respectively. As these proteins are involved in the catabolism of very long chain fatty acids (VLCFA: C24:0, C26:0), X-ALD and P-NALD patients are characterized by the accumulation of VLCFA in plasma and tissues. Since peroxisomes are involved in the metabolism of reactive oxygen species (ROS) and nitrogen species (RNS), we examined the impact of VLCFA on the oxidative status of 158N murine o…

congenital hereditary and neonatal diseases and abnormalitiesendocrine systemendocrine system diseasesVery long chain fatty acidBlotting Westernmedicine.disease_causeReal-Time Polymerase Chain ReactionTransfectionATP Binding Cassette Transporter Subfamily D Member 1Gas Chromatography-Mass SpectrometrySuperoxide dismutaseLipid peroxidationchemistry.chemical_compoundMicemedicinePeroxisomesAnimalsAdrenoleukodystrophyCells Culturedchemistry.chemical_classificationReactive oxygen speciesbiologyReverse Transcriptase Polymerase Chain ReactionGeneral NeuroscienceFatty Acidsnutritional and metabolic diseasesPeroxisomemedicine.diseaseFlow CytometryOligodendrogliaOxidative StressBiochemistrychemistryGene Knockdown Techniquesbiology.proteinACOX1AdrenoleukodystrophyATP-Binding Cassette TransportersRNA InterferenceAcyl-CoA OxidaseReactive Oxygen SpeciesOxidation-ReductionOxidative stressNeuroscience
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Leishmania tarentolae and Leishmania infantum in humans, dogs and cats in the Pelagie archipelago, southern Italy.

2021

Visceral leishmaniasis (VL) caused by Leishmania infantum is endemic in the Mediterranean basin with most of the infected human patients remaining asymptomatic. Recently, the saurian-associated Leishmania tarentolae was detected in human blood donors and in sheltered dogs. The circulation of L. infantum and L. tarentolae was investigated in humans, dogs and cats living in the Pelagie islands (Sicily, Italy) by multiple serological and molecular testing. Human serum samples (n = 346) were tested to assess the exposure to L. infantum by immunofluorescence antibody test (IFAT), enzyme-linked immunosorbent assay (ELISA) and Western blot (WB) and to L. tarentolae by IFAT. Meanwhile, sera from do…

dogsreal-time polymerase chain reactionRC955-962Pathology and Laboratory MedicineSerologyMedical ConditionswesternZoonosesArctic medicine. Tropical medicineitalymiddle agedMedicine and Health Sciences80 and overadult; aged; aged 80 and over; animals; blotting western; cat diseases; cats; dog diseases; dogs; enzyme-linked immunosorbent assay; female; humans; italy; leishmaniasis visceral; male; middle aged; prevalence; public health; real-time polymerase chain reaction; serologic tests; sicily; surveys and questionnaires; young adult; leishmania infantumEnzyme-Linked ImmunoassayshumansAged 80 and overProtozoansLeishmaniaMammalsCATSmedicine.diagnostic_testbiologyadultpublic healthEukaryotablottingvisceralanimalsagedInfectious DiseasesSerologyfemaleVertebratesleishmania infantumLeishmaniasis Visceralyoung adultLeishmania infantumAntibodyDog DiseasePublic aspects of medicineRA1-1270dog diseasesHumanResearch ArticleNeglected Tropical DiseasesBlotting Westernprevalenceserologic testsImmunofluorescenceResearch and Analysis MethodsmaleSurveys and Questionnaires ...parasitic diseasesmedicineParasitic DiseasessicilyImmunoassaysleishmaniasisProtozoan InfectionsAnimalcatsPublic Health Environmental and Occupational HealthOrganismsBiology and Life SciencesLeishmaniasiscat diseasesbiology.organism_classificationmedicine.diseaseLeishmaniaCat DiseaseTropical DiseasesVirologyParasitic ProtozoansVisceral leishmaniasisAmniotessurveys and questionnairesbiology.proteinImmunologic Techniquesenzyme-linked immunosorbent assayZoologyPLoS Neglected Tropical Diseases
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Identification and characterization of autoantibodies against catalase and α-enolase in patients with primary sclerosing cholangitis

1998

SUMMARY Primary sclerosing cholangitis (PSC) is a chronic cholestatic liver disease of unknown aetiology. Recent studies have shown that genetic factors and both cellular and humoral immunological abnormalities are important in the pathogenesis of PSC. The most prominent autoantibodies in PSC are anti-neutrophil cytoplasmic antibodies (ANCA). The autoepitopes of ANCA in PSC are not well defined. The aim of this study was to identify corresponding ANCA autoantigens in patients with PSC. A biochemical approach with enrichment and partial purification of soluble neutrophil proteins, detection of autoantibodies by Western blot and partial amino acid sequencing were used. Two new autoantigen/aut…

endocrine system diseasesAlpha-enolaseBlotting WesternCholangitis SclerosingMolecular Sequence DataImmunologyAutoimmunityEnzyme-Linked Immunosorbent Assaymedicine.disease_causedigestive systemAutoimmunityPrimary sclerosing cholangitisAntigenWestern blotmedicineHumansImmunology and AllergyAmino Acid SequenceAutoantibodiesAnti-neutrophil cytoplasmic antibodybiologymedicine.diagnostic_testdigestive oral and skin physiologyAutoantibodyOriginal ArticlesCatalasemedicine.diseasedigestive system diseasesPhosphopyruvate HydrataseImmunologybiology.proteinAntibodyClinical and Experimental Immunology
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De novo CCND2 mutations leading to stabilization of cyclin D2 cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome

2014

Activating mutations in genes encoding phosphatidylinositol 3-kinase (PI3K)-AKT pathway components cause megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome (MPPH, OMIM 603387)(1-3). Here we report that individuals with MPPH lacking upstream PI3K-AKT pathway mutations carry de novo mutations in CCND2 (encoding cyclin D2) that are clustered around a residue that can be phosphorylated by glycogen synthase kinase 313 (GSK-3 beta)(4). Mutant CCND2 was resistant to proteasomal degradation in vitro compared to wild-type CCND2. The PI3K-AKT pathway modulates GSK-3 beta activity(4), and cells from individuals with PIK3CA, PIK3R2 or AKT3 mutations showed similar CCND2 accumulation. CCND…

endocrine systemBlotting WesternMolecular Sequence DataMutantMedizinBiologymedicine.disease_causeArticleAKT3Mice03 medical and health sciences0302 clinical medicineCyclin D2GSK-3GeneticsmedicineAnimalsCyclin D2HumansAbnormalities MultipleExomeMegalencephalyPI3K/AKT/mTOR pathway030304 developmental biology0303 health sciencesMutationBase SequenceSequence Analysis DNASyndromeCell cyclemedicine.diseaseImmunohistochemistryMolecular biologyMegalencephalyMalformations of Cortical DevelopmentPolydactylyElectroporationHEK293 CellsBromodeoxyuridineMicroscopy FluorescenceMutagenesis Site-DirectedFemale030217 neurology & neurosurgeryHydrocephalusNature Genetics
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Development of an in vitro neuroblastoma 3D model and its application for sterigmatocystin-induced cytotoxicity testing

2021

Abstract Given the increasing importance of establishing better risk assessments for mycotoxins, novel in vitro tools for the evaluation of their toxicity are mandatory. In this study, an in vitro 3D spheroid model from SH-SY5Y cells, a human neuroblastoma cell line, was developed, optimized and characterized to test the cytotoxic effects caused by the mycotoxin sterigmatocystin (STE). STE induced a concentration- and time-dependent cell viability decrease in spheroids. Spheroids displayed cell disaggregation after STE exposure, increasing in a dose-dependent manner and over time. STE also induced apoptosis as confirmed by immunofluorescence staining and Western blot. Following the decrease…

endocrine systemCytotoxicitySterigmatocystinBlotting WesternCellFluorescent Antibody TechniqueToxicology3D cell culturechemistry.chemical_compoundNeuroblastomaCell MovementCell Line TumorSpheroids CellularMechanisms of actionToxicity TestsmedicineHumansCell Culture Techniques Three DimensionalViability assayCytotoxicityChemistryGeneral MedicineMycotoxins3D spheroidCytostasisCell biologymedicine.anatomical_structure3D spheroid; Cytotoxicity; Mechanisms of action; Neuroblastoma; SterigmatocystinCell cultureApoptosisComet AssayReactive Oxygen SpeciesFood ScienceSterigmatocystin
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Melatonin stimulates the nonamyloidogenic processing ofβAPP through the positive transcriptional regulation of ADAM10 and ADAM17

2014

Melatonin controls many physiological functions including regulation of the circadian rhythm and clearance of free radicals and neuroprotection. Importantly, melatonin levels strongly decrease as we age and patients with Alzheimer's disease (AD) display lower melatonin than age-matched controls. Several studies have reported that melatonin can reduce aggregation and toxicity of amyloid-β peptides that are produced from the β-amyloid precursor protein (βAPP). However, whether melatonin can directly regulate the βAPP-cleaving proteases ('secretases') has not been investigated so far. In this study, we establish that melatonin stimulates the α-secretase cleavage of βAPP in cultured neuronal an…

endocrine systemmedicine.medical_specialtyProteasesADAM10Blotting WesternApoptosisADAM17 ProteinBiologyMelatonin receptorNeuroprotectionMelatoninADAM10 ProteinAmyloid beta-Protein PrecursorTransactivationEndocrinologyInternal medicinemedicineHumansPhosphorylationPromoter Regions GeneticMelatoninMembrane ProteinsADAM ProteinsHEK293 CellsEndocrinologyGene Expression Regulationbiology.proteinPhosphorylationAmyloid Precursor Protein SecretasesAmyloid precursor protein secretasehormones hormone substitutes and hormone antagonistsmedicine.drugJournal of Pineal Research
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Influence of nerve growth factor in endometriosis-associated symptoms

2011

To investigate the role of the nerve growth factor (NGF) in the development of dysmenorrhea/pelvic pain in patients with endometriosis, we performed a prospective, clinical, blind study. Peritoneal fluids (PFs) were obtained from patients with histologically proven endometriosis. Patients with endometriosis were divided into 7 different groups depending on their preoperative pain score and symptomatology: patients with no pain, patients with minimal pain (dysmenorrhea, pelvic pain, or both), and patients with severe pain (dysmenorrhea, pelvic pain, or both) and were used for the neuronal growth assay with cultured chicken dorsal root ganglia (DRG) and for Western blot analyses. Dorsal root …

endometriosisEndometriosisFluorescent Antibody TechniqueChick EmbryoGastroenterologypain generation of endometriosis-related symptomSeverity of Illness Indexendometriosis; pelvic pain; sensory nerve fibersGAP-43 ProteinGanglia SpinalGermanyNerve Growth FactorAscitic FluidProspective StudiesEndometriosiProspective cohort studyCells CulturedPain MeasurementNeuronsbiologymedicine.diagnostic_testObstetrics and Gynecologypelvic painMiddle AgedBlotAnesthesiaFemalemedicine.symptomNeurotrophinHumanAdultmedicine.medical_specialtyCalcitonin Gene-Related PeptideBlotting Westernsensory nerve fibersCalcitonin gene-related peptidesensory nerve fiberYoung AdultWestern blotDysmenorrheaInternal medicinemedicineAnimalsHumansbusiness.industryAnimalPelvic painNeuronmedicine.diseaseSettore MED/40 - Ginecologia E OstetriciaProspective StudieNerve growth factorbiology.proteinbusiness
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