Search results for "Croce"

showing 10 items of 170 documents

Solid state 13C-NMR methodology for the cellulose composition studies of the shells of Prunus dulcis and their derived cellulosic materials.

2020

Lignocellulosic fibers and microcellulose have been obtained by simple alkaline treatment from softwood al- mond shells. In particular, the Prunus dulcis Miller (D.A.) Webb. was considered as a agro industrial waste largely available in southern Italy. The materials before and after purification have been characterized by 13C CPMAS NMR spectroscopy methodology. A proper data analysis provided the relative composition of lignin and holo- cellulose at each purification step and the results were compared with thermogravimetric analysis and FT-IR. To value the possibility of using this material in a circular economy framework, the fibrous cellulosic material was used to manufacture a handmade c…

Thermogravimetric analysisSoftwoodMaterials sciencePolymers and PlasticsAlmond shell Cellulose13C CP MAS NMR02 engineering and technology010402 general chemistry01 natural sciencesLigninIndustrial wastechemistry.chemical_compoundMaterials ChemistrySettore ICAR/13 - Disegno IndustrialeLigninNutsSettore CHIM/01 - Chimica AnaliticaRecyclingFiberSettore BIO/15 - Biologia FarmaceuticaCelluloseCarbon-13 Magnetic Resonance SpectroscopyCelluloseWaste ProductsOrganic Chemistrycardboard021001 nanoscience & nanotechnologyPulp and paper industryPrunus dulcis0104 chemical sciencesHandmade cardboard MicrocelluloseSettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreePrunus dulcisSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialichemistryCellulosic ethanolvisual_artvisual_art.visual_art_medium0210 nano-technologyCarbohydrate polymers
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WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation

2014

International audience; BACKGROUND:Homozygous mutations in WWOX were reported in eight individuals of two families with autosomal recessive spinocerebellar ataxia type 12 and in two siblings with infantile epileptic encephalopathy (IEE), including one who deceased prior to DNA sampling.METHODS:By combining array comparative genomic hybridisation, targeted Sanger sequencing and next generation sequencing, we identified five further patients from four families with IEE due to biallelic alterations of WWOX.RESULTS:We identified eight deleterious WWOX alleles consisting in four deletions, a four base-pair frameshifting deletion, one missense and two nonsense mutations. Genotype-phenotype correl…

WWOXMicrocephaly[SDV]Life Sciences [q-bio]Nonsense mutationMutation MissenseBiology03 medical and health sciences0302 clinical medicineGeneticsmedicineHumansSpinocerebellar AtaxiasMissense mutationAlleleGenetics (clinical)infantile030304 developmental biologyGeneticsComparative Genomic Hybridization0303 health sciences[ SDV ] Life Sciences [q-bio]Tumor Suppressor ProteinsChromosomal fragile siteHigh-Throughput Nucleotide Sequencinggenotype/phenotype correlationsmedicine.diseaseNull allele3. Good healthPhenotypeWW Domain-Containing OxidoreductaseCodon Nonsenseintellectual disabilitySpinocerebellar ataxiaOxidoreductasesSpasms Infantilehigh throughput data mining030217 neurology & neurosurgeryJournal of Medical Genetics
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Valori perduti e perduta libertà. Croce e il dibattito tedesco sulla relatività dei valori

2017

The relativism of values (Werterelativismus) is a problem very central for the historicism debate, which concerned historians and phi- losophers at the beginning of the twentieth century. The historization of all knowledge and all values leads to their historical devaluation. How can values still be formulated and maintained in face of this relativization? This was the question of theorists such as Otto Hintze, Friedrich Meinecke, Max Weber and Ernst Troeltsch, as well as of the philosopher Benedetto Croce in times of emerging Fascism, that was regarded as a political and moral threat. As representatives of an intellectual and social liberalism, these academics developed their own strategie…

WertphilosophieCroce Otto Hintze Friedrich Meinecke Max Weber Ernst Troeltsch Philosophy Nationalism Relativism HistorismSettore M-FIL/06 - Storia Della Filosofia
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Numerical modelling of the electrochemical behaviour of 316 stainless steel based upon static and dynamic experimental microcapillary-based technique…

2008

objective of this work was to determine the parameters that affect the mass transport and the distribution of species in microcapillaries close to the specimen surface. Local experiments were carried out under static and flow conditions on type 316L stainless steel in 1.7 M NaCl, pH = 3, by means of the electrochemical microcell and the scanning droplet cell technique. The polarisation behaviour of pure iron (used as a model system) in an aqueous environment was calculated adopting a finite element approach and was compared to the experimental results. The corrosion system consists of three parallel electrochemical reactions: the oxygen reduction reaction (ORR), the hydrogen evolution react…

Work (thermodynamics)Materials scienceAqueous solutionCapillary actionMetallurgySurfaces and InterfacesGeneral ChemistryElectrolyteCondensed Matter PhysicsElectrochemistrySurfaces Coatings and FilmsCorrosionMaterials ChemistryMicrocellComposite materialDissolutionSurface and Interface Analysis
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Age-dependent epileptic encephalopathy associated with an unusual co-occurrence of ZEB2 and SCN1A variants.

2020

Mowat-Wilson syndrome is a genetic disorder associated with a variable phenotype including peculiar facial features associated with intellectual disability, epilepsy, language impairment, and multiple congenital anomalies caused by heterozygous mutation of the ZEB2 gene. The ZEB2 protein is a complex transcription factor that encompasses multiple functional domains that interact with the regulatory regions of target genes including those involved in brain development. Recently, it has been documented that ZEB2 regulates the differentiation of interneuron progenitors migrating from the medial ganglionic eminence to cortical layers by repression of the Nkx2-1 homeobox transcription factor. It…

ZEB2genotype-phenotype correlationSettore MED/38 - Pediatria Generale E SpecialisticaSettore M-PSI/08 - Psicologia ClinicaIntellectual DisabilityHumansMowat-Wilson syndromeEEGgenotype-phenotype correlationSCN1AHirschsprung DiseaseEEGChildGenetic Association StudiesZEB2Zinc Finger E-box Binding Homeobox 2EpilepsyEEG; epilepsy; GABAergic interneurons; genotype-phenotype correlation; Mowat-Wilson syndrome; SCN1A; ZEB2FaciesElectroencephalographySettore MED/39 - Neuropsichiatria InfantileGABAergic interneuronsMowat-Wilson syndromeepilepsyNAV1.1 Voltage-Gated Sodium ChannelGABAergic interneuronsMicrocephalySettore MED/26 - NeurologiaFemaleEpileptic disorders : international epilepsy journal with videotape
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Armonia

2016

[SHS.LITT] Humanities and Social Sciences/LiteratureRenaissancelexique critiqueinterprétationRoland furieuxBenedetto CroceArioste
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Understanding the Strategies and Practices of Facebook Microcelebrities for Engaging in Sociopolitical Discourses

2022

In this paper, we study popular microcelebrities from the Global South to understand their strategies and practices on Facebook. Unlike traditional celebrities who gain their reputation through different types of physical performance, these microcelebrities attain their status by presenting themselves in a favorable way to their online followers. We conducted interviews with 19 microcelebrities from Bangladesh and analyzed our data using actor-network theory (ANT) and Goffman’s dramaturgical analysis (DA) of human interaction. We discuss the complex socio-technical ecosystem of the microcelebrity and the roles of non-human actors, such as platforms and local internet infrastructure along wi…

actor-network theoryFacebookvuorovaikutussocial mediaverkkoyhteisötsosiaalinen mediainfluencersjulkisuuden henkilötmicrocelebritykehitysmaatsomevaikuttajatdramaturgical analysistoimijaverkkoteoriathe Global Southidentiteettiidentityviestintäosallistuminen
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BCL11A intellectual developmental disorder: defining the clinical spectrum and genotype-phenotype correlations

2021

AbstractPurposeHeterozygous variants in BCL11A underlie an intellectual developmental disorder with persistence of fetal hemoglobin (BCL11A-IDD, a.k.a. Dias-Logan syndrome). We sought to delineate the genotypic and phenotypic spectrum of BCL11A-IDD.MethodsWe performed an in-depth analysis of 42 patients with BCL11A-IDD ascertained through a collaborative network of clinical and research colleagues. We also reviewed 33 additional affected individuals previously reported in the literature or available through public repositories with clinical information.ResultsMolecular and clinical data analysis of 75 patients with BCL11A-IDD identified 60 unique variants (30 frameshift, 7 missense, 6 splic…

business.industryPostnatal microcephalyMicrodeletion syndromemedicine.diseaseBioinformaticsHypotoniaDevelopmental disorderAutism spectrum disorderIntellectual disabilityFetal hemoglobinmedicineMissense mutationmedicine.symptombusiness
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La clartè de la distinction. Considérations sur la logique de Croce

2010

Disamina storico-filosofica ed argomentativa delle difficoltà interne alla logica di Croce, e al suo concetto-cardine, la distinzione.

contraddizioni e tensioni del cosidetto "idealismo crociano"teoria della rappresentazioneSettore M-FIL/06 - Storia Della FilosofiaBenedetto Croce
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Croce dipinta, pittore siciliano, inizi del XV secolo, Alcamo, Museo della Chiesa Madre

2009

croce dipinta AlcamoSettore L-ART/01 - Storia Dell'Arte Medievale
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