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showing 10 items of 2286 documents

Aggiunte al catalogo di Bonaventura Caruso, sacerdote e orafo messinese della seconda metà del ‘700

2011

Il nome di Bonaventura Caruso, sacerdote e orafo messinese, compare per la prima volta intorno agli anni '70 del XVIII secolo. L'autore, attraverso lo studio delle fonti e grazie a un'accurata analisi stilistica, propone l'identificazione e l'attribuzione a Caruso di un gruppo di opere di argenteria sacra prodotta a Messina oggi nei tesori delle Chiese Madri di Geraci Siculo e Mistretta, tutte caratterizzate dalla presenza di forme e motivi decorativi rococò, ma già tendenti al neoclassicismo. The name of Bonaventura Caruso, a priest and goldsmith from Messina, first appears around the 1870s. The author, through the study of sources and thanks to careful stylistic analysis, proposes the ide…

Caruso Bonaventura Messina argenteria Palermo Sant'Eufemia d'Aspromonte Alì Milazzo Mistretta Geraci SiculoSettore L-ART/04 - Museologia E Critica Artistica E Del RestauroCaruso Bonaventura Messina silverware Palermo Sant'Eufemia d'Aspromonte Alì Milazzo Mistretta Geraci SiculoSettore L-ART/02 - Storia Dell'Arte Moderna
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[Diari del Compromís de Casp]

Ms Títol donat pel catalogador Col·lació: Paper, f. i (pergamí actual) + 156 (en blanc els f. 151r-156v) + i (paper) ; foliació moderna a llapis ; signatures de quadern II-VI Composició: Escrit a línia tirada a 27 i 28 línies Escriptura: Gòtica cursiva. Notes marginals d'altra mà (del notari Jaume Desplà) Enquadernació: Pergamí del segle XV, restaurada en 2011 Origen: Escrit a Casp, Saragossa, l'any 1412 després del 28 de juny, data de publicació de la Sentència en la qual es nomena a l'infant de Castella, Ferran, com a rei de la Corona d'Aragó Signatura anterior: Olim 40 Signatura actual: València, Universitat de València. Biblioteca Històrica, BH Ms. 40 Catalogat des del manuscrit origina…

Casp Compromís de (1412)
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Termination of transcription in an ‘in vitro’ system is dependent on a polyadenylation sequence

1991

Using HeLa cell nuclear extract as a source of the different transcription and polyadenylation factors and reverse transcription to analyze the levels of RNA 5' and 3' to the cleavage-polyadenylation site, an in vitro assay has been established to study polyadenylation coupled to transcription directed by different adenovirus promoters. The levels of transcription 5' and 3' to the cleavage site in the L3 polyadenylation region are practically the same as described previously, however, the level of transcription 3' to the cleavage site in the SV40 early polyadenylation region decreases immediately after the cleavage site indicating a termination of the transcription.

Cell ExtractsTranscription GeneticPolyadenylationMolecular Sequence DataRNA polymerase IISimian virus 40BiologyCleavage (embryo)AdenoviridaeTranscription (biology)GeneticsRNA MessengerPromoter Regions GeneticBase SequenceRNARNA-Directed DNA PolymerasePromoterMolecular biologyReverse transcriptasebiology.proteinRNA Polymerase IIChromosome DeletionPoly ACytokinesisHeLa CellsPlasmidsNucleic Acids Research
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Nuclear receptors modulate the interaction of Sp1 and GC-rich DNA via ternary complex formation

2000

Binding sites for transcription factor Sp1have been implicated in the transcriptional regulation of several genes by hormones or vitamins, and here we show that a GC-rich element contributes to the retinoic acid response of the interleukin 1β promoter. To explain such observations, it has been proposed that nuclear receptors can interact with Sp1 bound to GC-rich DNA. However, evidence supporting this model has remained indirect. So far, nuclear receptors have not been detected in a complex with Sp1 and GC-rich DNA, and the expected ternary complexes in non-denaturing gels were not seen. In search for these missing links we found that nuclear receptors [retinoic acid receptor (RAR), thyroid…

Cell ExtractsTranscriptional ActivationReceptors Retinoic AcidSp1 Transcription FactorRecombinant Fusion ProteinsReceptors Cytoplasmic and NuclearTretinoinRetinoic acid receptor betaBiologyRetinoid X receptorLigandsResponse ElementsTransfectionModels BiologicalBiochemistryAntibodiesCell LineSubstrate SpecificityAnimalsPromoter Regions GeneticMolecular BiologyNuclear receptor co-repressor 1Nuclear receptor co-repressor 2Binding SitesReceptors Thyroid HormoneDNACell BiologyRetinoic acid receptor gammaRetinoid X receptor gammaGC Rich SequenceProtein Structure TertiaryNuclear receptor coactivator 1Retinoic acid receptorDrosophila melanogasterEcdysteroneRetinoid X ReceptorsOligodeoxyribonucleotidesBiochemistryReceptors CalcitriolThermodynamicsResearch ArticleInterleukin-1Protein BindingTranscription FactorsBiochemical Journal
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A novel SP-1 site in the human interleukin-1β promoter confers preferential transcriptional activity in keratinocytes

1996

To investigate the mechanisms of transcriptional activation of interleukin-1beta (IL-1beta) in non-monocytic cells, we constructed a series of reporter plasmids with the bacterial chloramphenicol acetyltransferase gene linked to various parts of the human IL-1beta promoter and performed transient transfection experiments. We identified a promoter segment that activates transcription most efficiently in keratinocytes. Electrophoretic mobility shift assays (EMSA) with a 43-mer oligonucleotide derived from the functionally identified cis-acting element revealed specific complexes. By competition analysis with transcription factor consensus sequence oligonucleotides and by immunosupershift, tra…

Cell NucleusKeratinocytesTranscriptional ActivationSp1 transcription factorTranscription GeneticSp1 Transcription FactorTumor Necrosis Factor-alphaImmunologyResponse elementBiologyMolecular biologyMonocytesChloramphenicol acetyltransferaseGenes ReporterTranscription (biology)MutationConsensus sequenceTranscriptional regulationHumansImmunology and AllergyPromoter Regions GeneticTranscription factorGeneCell Line TransformedInterleukin-1European Journal of Immunology
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EngineeredControl of Cell Morphology In Vivo Reveals Distinct Roles for Yeast andFilamentous Forms of Candida albicans duringInfection

2003

ABSTRACT It is widely assumed that the ability of Candida albicans to switch between different morphologies is required for pathogenesis. However, most virulence studies have used mutants that are permanently locked into either the yeast or filamentous forms which are avirulent but unsuitable for discerning the role of morphogenetic conversions at the various stages of the infectious process. We have constructed a strain in which this developmental transition can be externally modulated both in vitro and in vivo. This was achieved by placing one copy of the NRG1 gene (a negative regulator of filamentation) under the control of a tetracycline-regulatable promoter. This modified strain was th…

Cell divisionMutantHyphaeVirulenceBiologyKidneyCell morphologyMicrobiologyArticleMicrobiologyMiceIn vivoGene Expression Regulation FungalYeastsCandida albicansAnimalsPromoter Regions GeneticCandida albicansMolecular BiologyMice Inbred BALB CCandidiasisBrainGeneral Medicinebiology.organism_classificationYeastCorpus albicansRepressor ProteinsSurvival RateDoxycyclineFemaleGenetic EngineeringCell DivisionSpleenEukaryotic Cell
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Computational identification of cell-specific variable regions in ChIP-seq data.

2019

ABSTRACT Chromatin immunoprecipitation followed by sequencing (ChIP-seq) is used to identify genome-wide DNA regions bound by proteins. Several sources of variation can affect the reproducibility of a particular ChIP-seq assay, which can lead to a misinterpretation of where the protein under investigation binds to the genome in a particular cell type. Given one ChIP-seq experiment with replicates, binding sites not observed in all the replicates will usually be interpreted as noise and discarded. However, the recent discovery of high-occupancy target (HOT) regions suggests that there are regions where binding of multiple transcription factors can be identified. To investigate these regions,…

Cell typeAcademicSubjects/SCI00010Computational biologyPlasma protein bindingBiologyGenomeCell LineEvolution Molecular03 medical and health scienceschemistry.chemical_compoundMice0302 clinical medicineNarese/3Cell Line TumorGeneticsAnimalsHumansEpigeneticsBinding sitePromoter Regions GeneticTranscription factorEmbryonic Stem Cells030304 developmental biology0303 health sciencesPrincipal Component AnalysisBinding SitesNucleotidesGenetic VariationPromoterGenomicsChromatinchemistryCpG siteMCF-7 CellsChromatin Immunoprecipitation SequencingMethods OnlineR-Loop StructuresK562 CellsChromatin immunoprecipitation030217 neurology & neurosurgeryFunction (biology)DNATranscription FactorsNucleic acids research
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Electron microscopic demonstration of intracelluar promethazine accumulation sites by a precipitation technique: application to the cerebellar cortex…

1996

A method is described that allows electron microscopic identification of the phenothiazine neuroleptic promethazine after supravital intracardiac injection of high drug concentrations (greater than or equal to 3 %). The cerebellar cortex of the mouse was used for the investigation. This procedure is based on simultaneous fixation of drug and tissue by immersion in a paraformaldehyde-glutaraldehyde solution with the addition of phosphomolybdic acid. The electron microscopic investigation revealed that the drug could easily be identified as an electron-dense precipitate. Subpopulations of neurons exhibited a higher affinity for the drug than others, but no preference for any nerve cell type …

Cell typeTissue FixationHistologyChromatographyChemistryEndoplasmic reticulumMitochondrionPromethazinePromethazineCerebellar CortexMiceMicroscopy Electronchemistry.chemical_compoundCytoplasmCerebellar cortexPhenothiazineUltrastructureBiophysicsmedicineAnimalsAnatomymedicine.drugJournal of Histochemistry & Cytochemistry
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Differential expression levels of Sox9 in early neocortical radial glial cells regulate the decision between stem cell maintenance and differentiation

2021

ABSTRACTRadial glial progenitor cells (RGCs) in the dorsal forebrain directly or indirectly produce excitatory projection neurons and macroglia of the neocortex. Recent evidence shows that the pool of RGCs is more heterogeneous than originally thought and that progenitor subpopulations can generate particular neuronal cell types. Using single cell RNA sequencing, we have studied gene expression patterns of two subtypes of RGCs that differ in their neurogenic behavior. One progenitor type rapidly produces postmitotic neurons, whereas the second progenitor remains relatively quiescence before generating neurons. We have identified candidate genes that are differentially expressed between thes…

Cell typeTranscription GeneticNeurogenesisEpendymoglial CellsGenetic VectorsNeocortexNerve Tissue ProteinsBiologyMiceradial glia cellsprogenitors diversityGenes ReporterPregnancyGene expressionmedicineAnimalscortical developmentProgenitors diversityCell Self RenewalProgenitor cellPromoter Regions GeneticTranscription factorResearch ArticlesInjections IntraventricularProgenitorNeuronsNeocortexCortical developmentGeneral NeuroscienceCell CycleGene Expression Regulation DevelopmentalSOX9 Transcription FactorEmbryonic stem cellCell biologyMice Inbred C57BLCorticogenesisElectroporationmedicine.anatomical_structureCerebral cortexForebrainFemalesense organsSingle-Cell AnalysisStem cellNeuroscienceNeurogliaRadial glia cellsCellular/MolecularSox9
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Cellular stress positively regulates the expression of Myc promoter-Binding Protein-1 (MBP-1).

2012

Cellular stress Myc promoter-Binding Protein-1 (MBP-1).
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