83 resultados para Nombres impairs


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El objetivo de esta nota es aclarar en lo posible el intrincado panorama nomenclatural del género que nos ocupa. Trataremos en especial acerca de algunos binómenes establecidos por autores como Smith, Lapeyrouse y Timbal-Lagrave, a causa de los problemas que plantea el uso diverso que de ellos se ha hecho. Se imponía fijar la aplicación de tales nombres, designando, en los casos en que fuera posible, sus tipos nomenclaturales. Para ello hemos consultado los materiales originales, depositados en los herbarios: LINN The Linnean Society of London , P Muséum National d'Histoire Naturelle, Laboratoire de Phanérogamie, París y TL Laboratoire de Botanique, Université Paul Sabatier, Toulouse-: . Hacemos, también, algunas precisiones acerca de la nomenclatura de algunos híbridos existentes en la Península Ibérica.

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Nadie discute la importancia de las obras clásicas, pero pocos tienen acceso a ellas. Sus nombres, sus autores forman el cuerpo de la historia de la literatura; son, pues, materia de estudio. Honran calles, plazas; visten centenarios, premios; arropan con su excelencia la historia del país, incluso dibujan rutas turísticas, en las que se contemplan esculturas de sus personajes y placas alusivas, y, sin embargo, la mayoría de los ciudadanos de esas ciudades y pueblos, y la gran parte de los transeúntes de esos caminos no han leído las obras literarias cuyos nombres conocen tan bien. Y lo que es peor, sus hijos y sus nietos no sólo no las van a leer, sino que no pueden leerlas. No estoy hablando de un extraño pueblo cuyos habitantes sufren una terrible maldición, no; estoy hablando de nuestro país y de nuestros clásicos, tal vez eso sí exagerando un poco

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We present here the characterization of a new gene family, awr, found in all sequenced Ralstonia solanacearum strains and in other bacterial pathogens. We demonstrate that the five paralogues in strain GMI1000 encode type III-secreted effectors and that deletion of all awr genes severely impairs its capacity to multiply in natural host plants. Complementation studies show that the AWR (alanine-tryptophanarginine tryad) effectors display some functional redundancy, although AWR2 is the major contributor to virulence. In contrast, the strain devoid of all awr genes (¿awr1-5) exhibits enhanced pathogenicity on Arabidopsis plants. A gain-of-function approach expressing AWR in Pseudomonas syringae pv. tomato DC3000 proves that this is likely due to effector recognition, because AWR5 and AWR4 restrict growth of this bacterium in Arabidopsis. Transient overexpression of AWR in nonhost tobacco species caused macroscopic cell death to varying extents, which, in the case of AWR5, shows characteristics of a typical hypersensitive response. Our work demonstrates that AWR, which show no similarity to any protein with known function, can specify either virulence or avirulence in the interaction of R. solanacearum with its plant hosts.

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En aquesta recerca es presenta l’anàlisi de les estratègies que usen els alumnes de 4t de primària de l’escola Barnola d’Avinyó per a resoldre operacions de suma amb nombres de fins a dues xifres. A més, permet observar la seva evolució després d’haver dut a terme una unitat didàctica orientada a treballar i millorar de manera manipulativa i dinàmica, al llarg de set setmanes, els continguts numèrics. Per tant, amb els resultats obtinguts podem valorar si el fet de treballar continguts numèrics influencia en l’ús d’estratègies de càlcul mental i contrastar-ho amb diferents autors destacats en aquest àmbit.

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Open educational resources (OER) promise increased access, participation, quality, and relevance, in addition to cost reduction. These seemingly fantastic promises are based on the supposition that educators and learners will discover existing resources, improve them, and share the results, resulting in a virtuous cycle of improvement and re-use. By anecdotal metrics, existing web scale search is not working for OER. This situation impairs the cycle underlying the promise of OER, endangering long term growth and sustainability. While the scope of the problem is vast, targeted improvements in areas of curation, indexing, and data exchange can improve the situation, and create opportunities for further scale. I explore the way the system is currently inadequate, discuss areas for targeted improvement, and describe a prototype system built to test these ideas. I conclude with suggestions for further exploration and development.

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The development of targeted molecular therapies has provided remarkable advances into the treatment of human cancers. However, in most tumors the selective pressure triggered by anticancer agents encourages cancer cells to acquire resistance mechanisms. The generation of new rationally designed targeting agents acting on the oncogenic path(s) at multiple levels is a promising approach for molecular therapies. 2-phenylimidazo[2,1-b]benzothiazole derivatives have been highlighted for their properties of targeting oncogenic Met receptor tyrosine kinase (RTK) signaling. In this study, we evaluated the mechanism of action of one of the most active imidazo[2,1-b]benzothiazol-2-ylphenyl moiety-based agents, Triflorcas, on a panel of cancer cells with distinct features. We show that Triflorcas impairs in vitro and in vivo tumorigenesis of cancer cells carrying Met mutations. Moreover, Triflorcas hampers survival and anchorage-independent growth of cancer cells characterized by 'RTK swapping' by interfering with PDGFRβ phosphorylation. A restrained effect of Triflorcas on metabolic genes correlates with the absence of major side effects in vivo. Mechanistically, in addition to targeting Met, Triflorcas alters phosphorylation levels of the PI3K-Akt pathway, mediating oncogenic dependency to Met, in addition to Retinoblastoma and nucleophosmin/B23, resulting in altered cell cycle progression and mitotic failure. Our findings show how the unusual binding plasticity of the Met active site towards structurally different inhibitors can be exploited to generate drugs able to target Met oncogenic dependency at distinct levels. Moreover, the disease-oriented NCI Anticancer Drug Screen revealed that Triflorcas elicits a unique profile of growth inhibitory-responses on cancer cell lines, indicating a novel mechanism of drug action. The anti-tumor activity elicited by 2-phenylimidazo[2,1-b]benzothiazole derivatives through combined inhibition of distinct effectors in cancer cells reveal them to be promising anticancer agents for further investigation.

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The development of targeted molecular therapies has provided remarkable advances into the treatment of human cancers. However, in most tumors the selective pressure triggered by anticancer agents encourages cancer cells to acquire resistance mechanisms. The generation of new rationally designed targeting agents acting on the oncogenic path(s) at multiple levels is a promising approach for molecular therapies. 2-phenylimidazo[2,1-b]benzothiazole derivatives have been highlighted for their properties of targeting oncogenic Met receptor tyrosine kinase (RTK) signaling. In this study, we evaluated the mechanism of action of one of the most active imidazo[2,1-b]benzothiazol-2-ylphenyl moiety-based agents, Triflorcas, on a panel of cancer cells with distinct features. We show that Triflorcas impairs in vitro and in vivo tumorigenesis of cancer cells carrying Met mutations. Moreover, Triflorcas hampers survival and anchorage-independent growth of cancer cells characterized by 'RTK swapping' by interfering with PDGFRβ phosphorylation. A restrained effect of Triflorcas on metabolic genes correlates with the absence of major side effects in vivo. Mechanistically, in addition to targeting Met, Triflorcas alters phosphorylation levels of the PI3K-Akt pathway, mediating oncogenic dependency to Met, in addition to Retinoblastoma and nucleophosmin/B23, resulting in altered cell cycle progression and mitotic failure. Our findings show how the unusual binding plasticity of the Met active site towards structurally different inhibitors can be exploited to generate drugs able to target Met oncogenic dependency at distinct levels. Moreover, the disease-oriented NCI Anticancer Drug Screen revealed that Triflorcas elicits a unique profile of growth inhibitory-responses on cancer cell lines, indicating a novel mechanism of drug action. The anti-tumor activity elicited by 2-phenylimidazo[2,1-b]benzothiazole derivatives through combined inhibition of distinct effectors in cancer cells reveal them to be promising anticancer agents for further investigation.

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En les següents pàgines s’intenta mostrar la gran quantitat i qualitat de música hongaresa per viola del segle XX disponible, el perquè de tant material en comparació amb altres èpoques i el grau de coneixement que es té d’aquest repertori. El treball està realitzat a través de la recopilació d’informació de tots els aspectes en relació, i d’enquestes a estudiants de viola que permeten conèixer altres aspectes com el contacte d’aquests amb la música hongaresa. Amb la seva lectura es pot descobrir una infinitat d’obres molt desconegudes, de noms importants per la història de l’instrument i del poc coneixement que es té d’alguns d’aquests aspectes.