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Статті в журналах з теми "Nouveaux modes d'actions"
Greffier, Luc. "La descente de canyon, des territoires en concurrence." Sud-Ouest européen 13, no. 1 (2002): 77–84. http://dx.doi.org/10.3406/rgpso.2002.2788.
Повний текст джерелаBodéüs, Richard. "L'imagination au pouvoir." Dialogue 29, no. 1 (1990): 21–40. http://dx.doi.org/10.1017/s0012217300012750.
Повний текст джерелаFaure, Alain. "Intercommunalités et grandes mailles en Rhône-Alpes : vers de nouveaux modes d'action publique ?" Revue de géographie alpine 88, no. 1 (2000): 139–43. http://dx.doi.org/10.3406/rga.2000.4631.
Повний текст джерелаRoulleau-Berger, Laurence. "Professionnels de l'insertion au contact des jeunes en situation précaire : de la coproduction et de la discrimination des compétences." I. Les métiers de l'éducation et de la formation, no. 40 (October 2, 2002): 39–45. http://dx.doi.org/10.7202/005229ar.
Повний текст джерелаBusacchi, Vinicio. "Entre narration et action: Herméneutique et reconstruction thérapeutique de l'identité." Études Ricoeuriennes / Ricoeur Studies 1, no. 1 (December 29, 2010): 21–33. http://dx.doi.org/10.5195/errs.2010.11.
Повний текст джерелаMartínez Usarralde, María Jesús. "¿Hasta qué punto podemos aprender algo de valor práctico del estudio de los sistemas de educación extranjeros? Lecciones valiosas de la educación para la ciudadanía desde el caso inglés." Teoría de la Educación. Revista Interuniversitaria 16 (November 13, 2009). http://dx.doi.org/10.14201/3071.
Повний текст джерелаMartínez Martín, Miguel, Josep María Puig Rovira, and Jaime Trilla. "Escuela, profesorado y educación moral." Teoría de la Educación. Revista Interuniversitaria 15 (November 13, 2009). http://dx.doi.org/10.14201/3026.
Повний текст джерелаPARIS, A. "Introduction." INRAE Productions Animales 19, no. 3 (May 13, 2006). http://dx.doi.org/10.20870/productions-animales.2006.19.3.3492.
Повний текст джерелаGoodale, Mark. "Droits humains." Anthropen, 2019. http://dx.doi.org/10.17184/eac.anthropen.093.
Повний текст джерелаДисертації з теми "Nouveaux modes d'actions"
Bussiere, Arnaud. "L'Opération d'Intérêt National, une opération d'aménagement particulière." Electronic Thesis or Diss., Université Côte d'Azur, 2024. http://www.theses.fr/2024COAZ0032.
Повний текст джерелаThe Operation of National Interest (O.I.N.) is really not a development operation like any other. Its history, its evolution, its influence and its characteristics attest to this. For a long time without a legal definition, it was the law case which, at first, allowed us to see more clearly about its nature (a development operation), while the other sources of law remained very silent. However, the legislation eventually intervened to put an end to the doubt.Coming from decentralization and the desire of the State to retain its competence over operations covering sectors which it considered strategic, it has nevertheless become an ideal instrument of project planning and has therefore perfectly integrated itself with decentralization and new modes of action of the State, combining ad hoc and strategic interventions with soft law. Starting from La Défense, autonomous ports and new cities, the O.I.N. has become a real urban project, embracing all the features. Integration of sustainable development and uncomplexed use of territorial marketing have become two substantial characteristics of the new O.I.N., which originated from Euroméditerranée in Marseille in 1995. The focus can be on different actions, but the main axes of the operation always remain the same. Twelve years of evolution and maturation of new planning practices have made O.I.N. what it is now, a large-scale meta-project that allows the implementation of concrete projects that greatly change the physiognomy of an agglomeration or help to emerge from a decline that seemed inevitable.Its exceptional flexibility that could almost make it look like an “empty shell” and its derogating regime mean that it can be suitable for all those involved in the development, both public and private, while reassuring investors who will make its concrete projects achievable. Being able to function only perfectly concerted, it can make it possible to reconcile the state and local visions in a given territory.Its minimal legal regime prevents it from many risks and heaviness that may weigh on other planning instruments. Its massive scale makes it as much more suitable as the “traditional” tools of the development. The O.I.N. is therefore the right tool to mark the commitment of the State in a major project of national or even international ambition, to attract major partners and maintain the responsiveness and adaptability specific to the project approach.Its characteristics, making it eminently practical, have greatly influenced the legislator and the executive power who wished to extend it, decline it and adapt it to other territorial, financial scales. Other legal instruments are more or less direct heirs: the National Interest District, the National Interest Contract, the Territorial Development Contract or the Major Interest Project. Beyond terminological similarities, these tools have a clear and verifiable relationship with O.I.N.A tool both political and legal, being perfectly integrated into the era of time, its providential flexibility according to the new conceptions of planning law, will not fail to allow it to evolve at the same time as the practices of the latter.The O.I.N. still has good days ahead of it in original or derived form
Kaniti, Archana. "Etudes du mode d'action antipaludique de nouveaux bis-cations." Thesis, Montpellier 2, 2010. http://www.theses.fr/2010MON20154.
Повний текст джерелаIn this thesis I have attempted to subject the issues of mode of action of recently synthesized bis cationic compounds and their possible interactions with chloroquine resistance. Antimalarial activities of representatives of various bis quarternary ammonium compounds, alkyl amidines (received from Dr.Vial group, Montpellier) and of bisbenzyl amidines (received from Chemistry group, Liverpool) activity have been investigated with chloroquine and pentamidine and looked for cross resistance with chloroquine. For this purpose two genetically modified allelically exchanged cell lines C3Dd2 and C2GCO3 modified on the chloroquine resistance-related PfCRT (P.falciparum chloroquine Resistance Transporter) gene were used. Among the benzyl amidines, a significant hypersensitivity tobis benzyl amidines was observed among the isolates bearing the mutant PfCRT. No such difference is observed for the bisalkyl amidines. To understand the mode of action and role of PfCRT, competitive binding assay to heme (which may mediate the well-known cellular accumulation of the compounds) and effect on heme crystallization assays (which is involved in the toxic effect against the intracellular parasite) were performed. All these compounds were shown to interact with heme in various degrees. Their activity was observed not to be correlating with heme crystallization inhibition. This is likely due to the structural differences between the compound which discriminate the compounds in the transport of the compound to the parasite and their mechanism of antimalarial activities. In addition I have studied the effect of pH on the pharmacological activity of the drugs using allelically exchanged genetically modified cell lines (for PfCRT) to characterize the importance of proton gradient on the transport of chloroquine and pentamidine to the intracellular parasite. Significant difference (reduced antimalarial activity with increased pH) in the activity of chloroquine was observed for both the strains. Despite of the high pKa values for pentamidine, there was significant difference in the sensitivity of the strains to this compound, when the pH is changed. As both the diamidines and choline analogs require transporters to cross the membrane barriers and enter the parasite where they accumulate I have also performed initial studies on the molecular characterization of a potential carrier in P.falciparum. Using basic bioinformatic tools, a gene encoding a P.falciparum protein with significant similarity to higher eukaryotes choline transporter was identified and preliminary work for its functional analysis was performed. In conclusion, this work establishes substantial differences between the various classes of bis-cationic compounds essentially (based on benzamidine and choline-analogs alkylkamidine series) concerning their interaction with the infected erythrocyte and their antimalarial activity. The series are diffentallly affected by the PfCRT mutation and the chloroquine resistance. Results suggest that it may be possible to use novel bisbenzyl amidines to specifically target quinoline resistant Plasmodium falciparum malaria, harbouring mutant pfcrt alleles. Taking this idea further and since both classes of compound target the same non-parasite target (heme), it may even be possible to rationally design a quinoline / diamidine drug combination, in which isolates resistant to one partner drug become more sensitive to the other partner, thus delaying the onset of resistance
Aubouin, Nicolas. "L' institutionnalisation des espaces artistiques déterritorialisés : de la construction de nouveaux mondes de l'art à la transformation des modes d'action publique." Paris 10, 2009. http://www.theses.fr/2009PA100123.
Повний текст джерелаThis PhD thesis studies institutionnalization (Di Maggio et Powell, 1991) of new areas of artistic creation and distribution, outside the more conventional outlets – named disdeterritorialised areas – such as the “new territories of art” (artistic practices on former industrial or commercial wasteland, in derelict housing, etc. . . ), and street arts, raises the question of both the frontiers and approaches to public action. Indeed the transversality of these projects and the role that local authorities play in their development as well as the reconfiguration of operating formats, require the public administration to reorganise its actions through the creation of more transversal intervention mechanisms, the development of cooperation ventures between public actors and the commitment of new comptencies and expertises. Finally, this process demonstrate a co-building of new management tools (Moisdon, 1997) and public management. This thesis put forward a new representation of Art Worlds (Becker, 1982) and role of State
Le, Toquin Esther. "Mode d'action biocide de nouveaux procédés de décontamination sur deux formes de résistances bactériennes." Thesis, Normandie, 2018. http://www.theses.fr/2018NORMR103/document.
Повний текст джерелаSeveral decontamination technologies exist, however bacterial spores and biofilms remain a concern in a lot of fields, like hospital, alimentary and military. A new foam containing a biocide (sodium hypochlorite or hydrogen peroxide) and a stabilizing agent (Xanthan) has been studied to answer this problematic. This foam can be used in different ways on the field following contaminations: grounds’ spraying, walls’ covering and spraying, full pieces’ filling (walls and ground). The goal of this thesis is to evaluate the biocide efficiency of these foams on spores and biofilms. We optimized experimental protocols in order to study mechanisms of foams’ action on spores and biofilms based on theirs future applications (horizontal, vertical and filling) and depending on different environmental factors which may impact foam decontamination efficiencies (materials, temperatures, soil, …). This thesis work enabled to highlight the Xanthan foam containing 5% NaOCl from the one including 12% H2O2 in military sector. This foam allows a rapid decontamination, about 7 logs of spores in 30 minutes, for each of the three ways of use at 20°C. Moreover, the destruction of biofilms containing 107 logs of bacteria/cm² was achieved in 1 hour on a horizontal support by filling. This NaOCl foam is ready to be used for industrials
Mejri, Samara. "Efficacités et modes d'action de nouveaux simulateurs de défenses des plantes sur le pathosystème blé-Zymoseptoria tritici." Thesis, Littoral, 2018. http://www.theses.fr/2018DUNK0481/document.
Повний текст джерелаThe use of biofungicides and elicitors of plant defenses are alternative control stategies that can reduce the use of conventional fungicides. However, there are few products registered and applied on wheat and even less against Septoria tritici blotch. As part of this study, we tested and demonstrated the protective efficacity of several molecules on wheat against Zymoseptoria tritici. In fact, 29 biosourced molecules derived from the functionalization of pyroglutamic acid (PGA) contained in the molasses of sugar beet were evaluated with y-aminobutyric acid GABA, for the first time against Z. tritici. GABA and 16 functionalized molecules significantly reduced the percentages of the disease. The absence of direct effects on the fungus tested in vitro confirms that these protections are due exclusively to an elicitation of plant defense mechanisms. For these molecules, the study of the structure activity relationship has highlighted the importance of different chemical groups involved in the observed protections. On the other hand, the conjugation of PGA with salicylic acid (SA) allowed the obtention of 5 new molecules among which 4 were more effective than the parent molecules and this efficiency seems to be also due to an eliciting effect. Finally, saccharin and three cyclic lipopeptides produced by Bacillus subtilis (mycosubtilin, surfactin and fengycin alone or as mixtures) were evaluated for the first time on the pathosystem wheat - Z. tritici and conferred significant protection due to eliciting properties, direct antifungal activities or combined effects. This study has thus made it possible to identify new molecules with different modes of action and which could be considered in alternative control against wheat leaf blotch, however, additional analyses are required
Le, Brigand Laurence. "Etude du mode d'action cellulaire de nouveaux dérivés imidazoliniques et sulfonylurées sur la sécrétion d'insuline." Montpellier 2, 1998. http://www.theses.fr/1998MON20114.
Повний текст джерелаFaye, Annick. "Synthèse de nouveaux dérivés fonctionnels du 1,3-thiazole : étude de l'activité fongicide et du mode d'action." Poitiers, 1991. http://www.theses.fr/1991POIT2329.
Повний текст джерелаVo-Hoang, Yen. "Développement de nouveaux agents glycolipidiques antitumoraux et immunomodulateurs : synthèse, évaluation biologique et étude de leur mode d'action." Paris 5, 2003. http://www.theses.fr/2003PA05P619.
Повний текст джерелаAs part of the development of new anti-cancer therapies, agelasphines were discovered in 1993 with high antimetastasic action. These are a-galactosylceramides (a-GalCers) extracted from sea sponges. The a anomeric configuration of galactose is necessary to their antitumoral and immunostimulating activity. Biological effects of these compounds are mediated by NKT cells ( Natural Killer T-cells ), a specific lineage of T-lymphocytes discovered in 1987, reponsible of cytokine release, characteristic of cell-mediated (Th1) and of humoral (Th2) immune responses. To control NKT cells activation through a-GalCer molecules and to orient the immune response on the Th1 or Th2 side, we developed new approaches to families of pharmacological agents (antitumoral or antiinfectious fight, or treatment of autoimmune diseases) and to biological tools for functional exploration on NKT Cells
Grellepois, Fabienne. "Fonctionnalisation de l'artémisinine : nouveaux dérivés fluorés (monomères, dimères, chimères) à visée antipaludique et antitumorale. Contribution à l'étude du mode d'action." Paris 11, 2002. http://www.theses.fr/2002PA114820.
Повний текст джерелаBourguet, William. "Synthèse de nouveaux ligands utilisables pour la purification des récepteurs de l'acide rétinoïque et l'étude du mode d'action des rétinoïdes." Lille 1, 1992. http://www.theses.fr/1992LIL10160.
Повний текст джерелаЧастини книг з теми "Nouveaux modes d'actions"
"Les rôles historiques du Théâtre du Nouveau Monde à l’épreuve du présent." In Portraits d'institutions culturelles montréalaises. Quels modes d'action pour l'accessibilité, l'inclusion et l'équité ?, 103–28. Presses de l'Université Laval, 2020. http://dx.doi.org/10.2307/j.ctv1h0p43q.8.
Повний текст джерела