538 resultados para effetto domino
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von Auber
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Signatur des Originals: S 36/F03619
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Signatur des Originals: S 36/F04427
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Signatur des Originals: S 36/F08212
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Marca tip. en port. (Silvestre. Marques, 104)
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Marca tip. en port.
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Marca tip. en port
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Apéndices en español
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We have analyzed the Drosophila immune response in domino mutant larvae, which are devoid of blood cells. The domino mutants have a good larval viability, but they die as prepupae. We show that, on immune challenge, induction of the genes encoding antimicrobial peptides in the fat body is not affected significantly in the mutant larvae, indicating that hemocytes are not essential in this process. The hemocoele of domino larvae contains numerous live microorganisms, the presence of which induces a weak antimicrobial response in the fat body. A full response is observed only after septic injury. We propose that the fat body cells are activated both by the presence of microorganisms and by injury and that injury potentiates the effect of microorganisms. Survival experiments after an immune challenge showed that domino mutants devoid of blood cells maintain a wild-type resistance to septic injury. This resistance was also observed in mutant larvae in which the synthesis of antibacterial peptides is impaired (immune deficiency larvae) and in mutants that are deficient for humoral melanization (Black cells larvae). However, if domino was combined with either the immune deficiency or the Black cell mutation, the resistance to septic injury was reduced severely. These results establish the relevance of the three immune reactions: phagocytosis, synthesis of antibacterial peptides, and melanization. By working in synergy, they provide Drosophila a highly effective defense against injury and/or infection.
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N-Alkyl-α-amino esters undergo a domino reaction, based on the iminium cation generation, with paraformaldehyde, followed by a 1,3-dipolar cycloaddition of the stabilized azomethine ylide with another equivalent of formaldehyde. The resulting products are oxazolidines, which can be transformed after hydrolysis into α-hydroxymethyl α-amino acid or its derivatives. The diastereoselective 1,3-dipolar cycloaddition was performed using sarcosine (–)-menthyl or (–)-8-phenylmenthyl esters affording the cyclic product with moderate enantiomeric ratio.
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Cover-title: Coram rege roll for Tinity term, 25 Edward I, A.D. 1297. Being the special volume issued by the British record society, limited in commemoration of the record year of Her Majesty Queen Victoria, A.D. 1897.
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Woodcut Giunta lily and small ill. on t.p. Initials. Printed in red and black throughout.
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Acompaña nota del bibliotecario reseñando los libros solicitados para la redacción de esta memoria.
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Mode of access: Internet.
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Mode of access: Internet.