Search results for "Gier"

showing 10 items of 55 documents

Niemcy, Rosja i kwestia polska w publicystyce Jędrzeja Giertycha na łamach "Horyzontów" paryskich (1956-1971)

2017

The liberalization of the communist system in mid-1950s, disillusionment with the policy of the West, fears connected with West German revisionism, and dwindling chances of change in the situation of Central-Eastern Europe contributed to a differentiation of attitudes among the Polish emigrants. Some of them, notably the nationalists, voiced the need to seek compromise with Russia. This led to the emergence of a pro-Russian option alongside the still dominant pro-Western one. The thesis on the need of an alliance with Russia was propagated by Jędrzej Giertych in his jo umalism in the "Horyzonty” monthly published in Paris. This ideologically committed opponent of communism and a staunch Cat…

"Horyzonty" paryskieParis "Horyzonty"Jędrzej Giertychpublicystyka na emigracjiémigré journalismemigracja polska po II wojnie SwiatowejPolish emigration afrer World War IIPrzegląd Zachodni
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Lipid-free apolipoprotein (apo) A-I is converted into alpha-migrating high density lipoproteins by lipoprotein-depleted plasma of normolipidemic dono…

1998

Plasma of patients with Tangier disease (TD) is devoid of alpha-LpA-I (apolipoprotein A-I-containing lipoprotein), which in normolipidemic plasma constitutes the majority of high density lipoprotein (HDL). The residual amounts of apolipoprotein A-I (apo A-I) in TD plasma have electrophoretic prebeta1-LpA-I mobility. We have previously demonstrated that TD plasma does not convert prebeta1-LpA-I into alpha-LpA-I. In this study we found that plasmas of normolipidemic controls, apo A-I-deficient patients and patients with fish-eye disease, but not plasmas of six TD patients, convert biotinylated lipid-free apo A-I into alpha-LpA-I. Supplementation of plasma with free oleic acid or fatty acid fr…

AdultMalemedicine.medical_specialtyApolipoprotein BLipoproteinsBlood Donorschemistry.chemical_compoundTangier diseaseHigh-density lipoproteinReference ValuesPhospholipid transfer proteinInternal medicinemedicineHumansPhospholipidsTangier DiseaseAgedApolipoprotein A-IbiologyChemistryCholesterolVesicleAlbuminMiddle Agedmedicine.diseaseEndocrinologybiology.proteinFemalelipids (amino acids peptides and proteins)Lipoproteins HDLCardiology and Cardiovascular MedicineLipoproteinAtherosclerosis
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Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders

2004

Mutations in ABCA1 have been shown to be the cause of Tangier disease (TD) and some forms of familial hypoalphalipoproteinemia (HA), two genetic disorders characterized by low plasma HDL levels. Here we report six subjects with low HDL, carrying seven ABCA1 mutations, six of which are previously unreported. Two mutations (R557X and H160FsX173) were predicted to generate short truncated proteins; two mutations (E284K and Y482C) were located in the first extracellular loop and two (R1901S and Q2196H) in the C-terminal cytoplasmic domain of ABCA1. Two subjects found to be compound heterozygotes for ABCA1 mutations did not have overt clinical manifestations of TD. Three subjects, all with prema…

AdultMalemedicine.medical_specialtyHeterozygoteSettore MED/09 - Medicina InternaApolipoprotein BAdolescentPremature coronary artery diseaseTangier diseaseCoronary DiseaseBiologyGene mutationmedicine.disease_causeCompound heterozygosityTangier diseaseInternal medicineGenotypeABCA1 genemedicineHumansChildHypoalphalipoproteinemiaSelection BiasAgedApolipoproteins BGeneticsMutationFamilial defective Apo B (FDB)Apolipoprotein A-ICholesterol HDLnutritional and metabolic diseasesMiddle Agedmedicine.diseaseLipoprotein lipaseTangier disease; Familial HDL deficiency; ABCA1 gene; Familial defective Apo B (FDB); Lipoprotein lipase; Premature coronary artery diseaseEndocrinologyChild PreschoolMutationbiology.proteinlipids (amino acids peptides and proteins)Allelic heterogeneityATP-Binding Cassette TransportersFemaleCardiology and Cardiovascular MedicineFamilial HDL deficiencyATP Binding Cassette Transporter 1
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Plasma and fibroblasts of Tangier disease patients are disturbed in transferring phospholipids onto apolipoprotein A-I

1998

Plasmas of patients with Tangier disease (TD) lack lipid-rich α-HDL which, in normal plasma, constitutes the majority of high density lipoprotein (HDL). Residual amounts of apolipoprotein (apo)A-I in TD plasma occur as lipid-poor or even lipid-free preβ-HDL. By contrast to normal plasma, TD plasma does not convert preβ-HDL into α-HDL. Moreover, fibroblasts of TD patients were found to be defective in secreting cholesterol or phospholipids in the presence of lipid-free apoA-I. We have therefore hypothesized that both defective conversion of preβ-HDL into α-HDL and defective lipid efflux from TD cells onto lipid-free apoA-I result from a disturbance in phospholipid transfer occurring in both …

AdultMaletransferring phospholipidsPhospholipidTangier diseasePhosphatidic AcidsQD415-436PhosphatidylinositolsBiochemistrychemistry.chemical_compoundEndocrinologyTangier diseasePhosphatidylcholinePhospholipid transfer proteinExtracellularmedicineHumansCells CulturedPhosphatidylethanolamineApolipoprotein A-ICholesterolPhosphatidylethanolaminesReverse cholesterol transportnutritional and metabolic diseasesBiological TransportCell BiologyFibroblastsmedicine.diseaseMolecular biologyfamilial HDL deficiencyreverse cholesterol transportLipoproteins LDLphospholipid transfer proteinsprebeta-HDLTangier disease; transferring phospholipidschemistryPhosphatidylcholinesFemalelipids (amino acids peptides and proteins)cholesterol efflux
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Historical and Technical Notes on Aqueducts from Prehistoric to Medieval Times

2013

The aim of this paper is to present the evolution of aqueduct technologies through the millennia, from prehistoric to medieval times. These hydraulic works were used by several civilizations to collect water from springs and to transport it to settlements, sanctuaries and other targets. Several civilizations, in China and the Americas, developed water transport systems independently, and brought these to high levels of sophistication. For the Mediterranean civilizations, one of the salient characteristics of cultural development, since the Minoan Era (ca. 3200-1100 BC), is the architectural and hydraulic function of aqueducts used for the water supply in palaces and other settlements. The M…

AspendosEngineeringlcsh:Hydraulic engineeringMinoanBiochimieGeography Planning and DevelopmentWater supplyAqueductGierAquatic ScienceAncient historyBiochemistryPrehistorylcsh:Water supply for domestic and industrial purposeslcsh:TC1-978Human settlementByzantinesPergamonEupalinosStatistique mathématiqueGéographie humaineOcéanographie biologiqueAqua MarciaChinaNimesWater Science and Technologylcsh:TD201-500Aqua claudiaWater transportbusiness.industryAqua marciaProbabilitésKnossosRomansOceanographyValensSalientHellenesCultural developmentAqua ClaudiaSegoviabusinessWater
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ABC A-subfamily transporters: Structure, function and disease

2006

AbstractABC transporters constitute a family of evolutionarily highly conserved multispan proteins that mediate the translocation of defined substrates across membrane barriers. Evidence has accumulated during the past years to suggest that a subgroup of 12 structurally related “full-size” transporters, referred to as ABC A-subfamily transporters, mediates the transport of a variety of physiologic lipid compounds. The emerging importance of ABC A-transporters in human disease is reflected by the fact that as yet four members of this protein family (ABCA1, ABCA3, ABCR/ABCA4, ABCA12) have been causatively linked to completely unrelated groups of monogenetic disorders including familial high-d…

Candidate geneSubfamilyProtein familyATP-binding cassette transporterDiseaseABCA3RetinaEvolution MolecularSurfactantAnimalsHumansDiseaseABCA12Molecular BiologyTangier DiseaseGeneticsbiologyIchthyosisLipidAtherosclerosisABCA1biology.proteinMolecular MedicineATP-Binding Cassette TransportersDisease SusceptibilityABC transporterBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
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Fortuna dell’«Alda» di Guglielmo di Blois fra il XII e il XIII secolo: commedie elegiache, “fabliaux” e romanzi cortesi

2018

In questo intervento vengono studiate la fortuna e le imitazioni dell’Alda, commedia elegiaca latina di Guglielmo di Blois (scritta verso il 1169-1170), nella letteratura latina e volgare dei secc. XII e XIII. In particolare, dopo una presentazione generale dell’opera ci si sofferma su alcune commedie elegiache latine successive (Baucis et Traso, De mercatore, De uxore cerdonis di Iacopo da Benevento), su alcuni fabliaux antico-francesi del sec. XIII (Trubert di Douin de Lavesne, Li sohaiz desvez di Jean Bodel, l’anonimo De la damoisele) e sui romanzi di Chrétien de Troyes (Yvain) e di Roberto di Blois (Floris et Lyriopé). L’ultima sezione del lavoro è fondata, infine, sullo studio delle co…

Commedia elegiaca latina Guglielmo di BloiAlda fabliaux antico-francesi Chrétien de Troyes Roberto di Blois letteratura mediolatina teatro medievale antropologia letteraria parodia descriptio turpitudinis Audigier.Settore L-FIL-LET/08 - Letteratura Latina Medievale E UmanisticaLatin Elegiac Comedy William of Blois Alda Old French Fabliaux Chrétien de Troyes Robert of Blois Medieval Latin Literature Medieval Theatre Literary Anthropology Parody descriptio turpitudinis Audigier.
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Samtidskunst i skolen : En studie som inviterer elever til en konseptuell workshopspraksis

2019

Masteroppgave kunstfag KF500 - Universitetet i Agder 2019 Both from the elementary school education and the professional life, I have gained insight and an experience basis for commenting on the subject of arts and crafts. There are often techniques and crafts that are in focus. I miss howthe subject to a greater extentcanchallengestudent`s in critical thinking, playful exploration and reflection, especially with regards to visual art. This master thesis focuses on theseperspectives for teaching in the subject arts and crafts, and discuss contemporary art's place intheschool. The thesis can be viewed as a post in the discourse about the new curriculumforarts and crafts, scheduledtobe comple…

Contemporary ArtAuto-EthnographyCommunity of PracticeAksjonsforskningArtefakterKompetansemålObjectsPraksisfellesskapsamtidskunstSubjectsReadymadeCurriculaKonseptkunstPoetic StrategiesConceptual ArtFlowChildren’s PlayLekVDP::Samfunnsvitenskap: 200::Pedagogiske fag: 280SubjektLæreplanerPoetiske strategierCompetence goalsVDP::Humaniora: 000::Kunsthistorie: 120ObjekterAutoetnografiArtifactsKF500Action research
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The American journey of Ernest Duvergier de Hauranne: France and United States Compared (1864-1865)

2018

The main theme of the days of study held in Cagliari on Pluralism and monism in political and social patterns of the modern and contemporary age has been declined in these pages through the comparison made by Ernest Duvergier de Hauranne (1843-1877) between the personal government of Napoleon III and the United States of America in the last period of the Civil war.

Ernest Duvergier de Hauranne Monism Pluralism France United StatesSettore SPS/02 - Storia Delle Dottrine Politiche
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Il viaggio di Ernest Duvergier de Hauranne nell'America di Lincoln. Riflessioni sui vizi e le virtù della democrazia.

2020

Nel giugno del 1864 il giovane liberale francese Ernest Duvergier de Hauranne (1843-1877), cresciuto in una famiglia rispettosa delle tradizioni parlamentari della monarchia orleanista, inizia il suo viaggio verso gli Stati Uniti. In otto mesi di viaggio – con la guerra civile ancora in corso e le elezioni presidenziali che avrebbero riconfermato Lincoln alla presidenza – percorrerà gli Stati Uniti e il Canada proseguendo verso Cuba e le Antille. Quell’itinerario americano, che gli procurerà una lesione polmonare che sarà la causa della prematura morte avvenuta a soli trentaquattro anni, resterà documentato nelle lettere e note, pubblicate in dodici articoli nella «Revue des Deux Mondes» e …

Ernest Duvergier de HauranneDemocracy.AmericaSettore SPS/02 - Storia Delle Dottrine Politichedemocrazia.
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