9 resultados para État de conscience minimale

em Deakin Research Online - Australia


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Vouloir parler de la transmission, revient en somme passer en revue l’histoire de l’homme à travers ses différentes évolutions. Les civilisations, les cultures, les visages, les coutumes sont en effet le résultat de transmissions successives qui se sont effectuées dans et à travers le temps.

Ce livre pose une question essentielle : Comment peut-on transmettre de la conscience à quelqu’un ? Car l’axe essentiel de toute spiritualité non dénaturée est de rendre conscient. A ce niveau, la transmission devrait se passer entre quelqu’un qui est conscient et quelqu’un qui se trouve en déficit de conscience. L’instructeur spirituel partage avec l’autre la clarté de conscience dans laquelle il se trouve afin de créer une ouverture et un supplément d’âme. C’est là ce qui distingue la transmission spirituelle de l’acte simple de transmettre un savoir ou des informations d’ordre culturel, technique ou autre de génération en génération. Dans le cadre de la transmission de conscience, le paradoxe est qu’il faut révéler à l’autre, lui transmettre un état d’être qui se trouve déjà en lui. C’est une thérapie de l’âme.

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This article examines the continuing suitability of the existing Australian test for determining when a voluntary assignment of legal property has passed in equity. It suggests that the current test, which focuses upon the ‘completion’ by the donor of the all the necessary transfer formalities, and the underlying equitable maxims that support it, should be revised to better reflect the dual concerns of assignment and constructive trust. The article reviews the English authorities, in particular the English Court of Appeal in Pennington v Waine, which held that the equitable jurisdiction can validate a voluntary assignment of legal property where, in the circumstances, it would be unconscionable to allow the donor to resile. It is argued that this approach represents an appropriate progression because it provides greater scope for a particularised examination of the intention, circumstances and behaviour surrounding the purported assignment. A test which encourages greater contextual examination of the overall circumstances underlying the assignment process is consistent with the core expectations of equitable methodology. It supports the multi-layered process of determining whether a donor intended the assignment and further, whether that donor should be held liable as constructive trustee.

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The human immunodeficiency virus type 1 (HIV-1) Tat protein enhances reverse transcription, but it is not known whether Tat acts directly on the reverse transcription complex or through indirect mechanisms. Since processing of Tat by HIV protease (PR) might mask its presence and, at least in part, explain this lack of data, we asked whether Tat can be cleaved by PR. We used a rabbit reticulocyte lysate (RRL) system to make Tat and PR. HIV-1 PR is expressed as a Gag-Pol fusion protein, and a PR-inactivated Gag-Pol is also expressed as a control. We showed that Tat is specifically cleaved in the presence of PR, producing a protein of approximately 5 kDa. This result suggested that the cleavage site was located in or near the Tat basic domain (amino acids 49 to 57), which we have previously shown to be important in reverse transcription. We created a panel of alanine-scanning mutations from amino acids 45 to 54 in Tat and evaluated functional parameters, including transactivation, reverse transcription, and cleavage by HIV-1 PR. We showed that amino acids 49 to 52 (RKKR) are absolutely required for Tat function in reverse transcription, that mutation of this domain blocks cleavage by HIV-1 PR, and that other pairwise mutations in this region modulate reverse transcription and proteolysis in strikingly similar degrees. Mutation of Tat Y47G48 to AA also down-regulated Tat-stimulated reverse transcription but had little effect on transactivation or proteolysis by HIV PR, suggesting that Y47 is critical for reverse transcription. We altered the tat gene of the laboratory strain NL4-3 to Y47D and Y47N so that overlapping reading frames were not affected and showed that Y47D greatly diminished virus replication and conveyed a reverse transcription defect. We hypothesize that a novel, cleaved form of Tat is present in the virion and that it requires Y47 for its role in support of efficient reverse transcription.