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    O Tema do amor ágape, eros e philia em poemas de Delminda Silveira e Auta de Souza

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    Dissertação (mestrado) - Universidade Federal de Santa Catarina, Centro de Comunicação e Expressão, Programa de Pós-Graduação em Literatura, Florianópolis, 2011A pesquisa apresenta dupla vertente: pesquisa teórica e leitura textual do tema do amor - ágape, eros e philia - em poemas de Delminda Silveira e Auta de Souza. Aprimeira vertente é constituída de pesquisa teórica embasada em textos diversos que tratam, de um lado, da poesia de cunho religioso e, de outro, da construção teórica nessa espécie de discurso poético do tema do amor ágape, eros e philia. A leitura do corpus da dissertação, segunda vertente desta pesquisa, centra-se na busca dos temas ágape, eros e philia em poemas de ambas as poetisas. Em Delminda Silveira, buscase esse tema na poética de Lizes e Martyrios; em Auta de Souza, na poética de o Horto. A dissertação começa por considerações introdutórias sobre a poesia e a religião, sobre o tema do amor ágape, eros e philia, pela apresentação do corpus, dos objetivos e da maneira de ler a temática em questão e, por fim, pelo esboço estrutural da pesquisa. A parte central da dissertação divide-se em duas unidades, cada uma delas introduzida por pesquisa contextual de caráter estético, seguida de traços biográficos, tópicos bibliográficos e fragmentos da fortuna crítica referentes a cada uma das poetisas. A leitura do corpus constitui a segunda e a mais representativa parte da dissertação por tratar especificamente da temática de ágape, eros e philia. À guisa de conclusão, faz-se uma leitura comparativa dos resultados das pesquisas e das leituras, destacando-se as convergências e as divergências do tema na poética das duas escritoras e buscam-se nas leituras da composição estrófica de suas poesias particularidades que as identifiquem. Para finalizar, projeta-se a possibilidade de outros estudos a serem feitos, tendo como referência aspectos que foram abordados ou tangenciaram a presente dissertação

    AuTA: Automatic teaching assistant

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    Due to the dramatic increase in enrollments in the TU Delft Bachelor of ComputerScience, the workload for teaching assistants and instructors has skyrocketed. Toreduce this workload, automated tools can be used to make the grading process easier. This paper describes the development of AuTA (Automatic Teaching Assistant), a tool that will help instructors and teaching assistants analyze and grade programming assignments and provide useful feedback to the student.Labrado

    Ei nyt auta ei nyt auta surevainen olla (3/4 a)

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    Laulun sanat: Ei nyt auta, ei nyt auta surevainen olla, vaikka näkee sen oman kullan toisen kainalolla

    Suremahan ei auta (4/4 a)

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    Laulun sanat: Suremahan ei auta, Vaan täytyy kulkea; Vaan tuolla puolen haudan Siellä minä levon saan

    Imidazenil, a partial positive allosteric modulator of GABAA receptors, exhibits low tolerance and dependence liabilities in the rat.

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    Long-term treatment of rats with full (triazolam) or selective (diazepam) allosteric modulators of gamma-aminobutyric acid type A (GABAA) receptors rapidly induced tolerance to the protective effect of these drugs against bicuculline-induced convulsion. In contrast, long-term administration of partial allosteric modulators (imidazenil and bretazenil) of GABAA receptors, in doses equipotent to those of diazepam and triazolam that induce anticonvulsant tolerance, failed to elicit such a tolerance. Furthermore, no cross-tolerance was observed between diazepam and imidazenil. Discontinuation of long-term treatment with diazepam or triazolam, but not of long-term treatment with imidazenil or bretazenil, sensitized rats to behavioral inhibition by punishment (electric shock) in a manner that was potentiated by flumazenil. Administration of a single oral dose of [14C]diazepam or [3H] imidazenil to rats treated repeatedly with the corresponding unlabeled drug or vehicle revealed that the brain concentrations of drugs and their metabolites were similar in both groups of animals. This suggests that tolerance to the full or selective allosteric modulators of GABAA receptors may be associated with changes in the efficacy of the allosteric modulation rather than with changes in drug metabolism. Imidazenil has a longer half-life than an equipotent dose of diazepam and protects rats against bicuculline-induced convulsions for a significantly longer time than diazepam or bretazenil.(ABSTRACT TRUNCATED AT 250 WORDS

    Jesus auta köyhää last' (4/4 a)

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    Laulun sanat: Jesus auta köyhää last', Taivaan tiellä kulkeiss', Päästä irti maailmast' Että emme sulkeis' Jesukseemme turvata; Jesu auta vaivaist', Sylissäs meit' kannata, Armahd' päällemm' taivaist'

    Biosignálmi riadený model auta - projekt na výučbu rozhrania člověk-počítač

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    Navrhnutý systém môže slúžiť ako stavebnicový projekt pre študentov biomedicínskeho inžinierstva, na ktorom si môžu študenti vyskúšať proces snímania, spracovania a jednoduchej analýzy bioelektrických signálov za účelom ich prepojenia a použitia v kombinácii s iným periférnym elektrickým zariadením, dochádza tak k vytvoreniu jednoduchého modelu človek-počítač. Robotický model auta pozostáva z dvoch častí, ktoré medzi sebou komunikujú použitím rádiovej komunikácie. Riadiaca časť systému „master“ slúži na snímanie, spracovanie a analýzu EMG signálu snímaného zo svalov horných končatín. Ovládaná časť systému „slave“ riadi smer a rýchlosť auta na základe príkazov z riadiacej časti systému

    Ei auta viipyä sillä laivat on rannoilla (2/4 a)

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    Laulun sanat: Ei auta viipyä, sillä laivat on rannoilla. Mun täytyypi lähteä sotaan isänmaata varjelemaan

    Anticonvulsant, anxiolytic, and non-sedating actions of imidazenil and other imidazo-benzodiazepine carboxamide derivatives

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    Recent evidence suggests that alpha1-containing GABA(A) receptors mediate the sedative, amnestic, and to some extent the anticonvulsant actions of non-selective benzodiazepine (BZ) receptor ligands, such as diazepam (DZ). Anxiolytic and in part, anticonvulsant actions of BZ ligands are mediated by alpha2-, alpha3-, and alpha5-containing GABA(A) receptors. This has resulted in increasing interest in developing BZ ligands with selective actions at GABA(A) receptors, including alpha2-, alpha3-, and alpha5-subunits, but devoid of efficacy at alpha1-containing receptors. To refine their spectrum of pharmacological actions, efforts are being made to minimize unwanted effects such as sedation, amnesia, and tolerance liabilities. A prototype for such BZ ligands is imidazenil (IMD), an imidazo-benzodiazepine carboxylic acid derivative that elicits potent anticonvulsant and anxiolytic actions at doses virtually devoid of sedative, cardio-respiratory depressant and amnestic effects, and anticonvulsant tolerance liability. To define the pharmacological profile of IMD and its derivatives, we compared the anticonflict (anxiolytic), anti-proconflict (antipanic), anti-bicuculline (BIC), and maximal electroshock seizure (MES) effects, and the suppression of locomotor activity by imidazo-benzodiazepine carboxylic acid derivatives to those of DZ and bretazenil (BTZ). We report here that IMD and one of its derivatives (RO 25-2775) possess dose-dependent anticonflict, anti-proconflict, and anti-BIC actions but failed to suppress locomotor activity. Like DZ, the other IMD derivatives (enazenil, RO 25-2776, and RO 25-2847) not only elicit dose-dependent anticonflict, anti-proconflict, anti-BIC, anti-MES effects but also suppress locomotor activity. In contrast, none of the IMD derivatives studied shows any similarity to BTZ, which elicits anticonflict, anti-proconflict actions and suppresses locomotor activity but is virtually inactive against BIC-induced tonic-clonic convulsions
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