998 resultados para 11-diene synthase


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Constituye una análisis de la información oceanográfica obtenida de la Operación MOPFEN 9510-11 que se ejecutó del 25 de Octubre al 10 de noviembre de 1995, a bordo de la E/E Huamanga del CEP de Paita. Para ello, se realizó seis perfiles oceanográficos frente a Puerto Pizarro, Paita, Punta Falsa, Chicama, Chimbote y Callao. El estudio tuvo por finalidad conocer la variación que han tenido los parámetros ambientales durante la primavera e identificar la tendencia de las condiciones del mar peruano para el mes de diciembre de 1995 e inicios del verano de 1996, todo ello en base a ocurrencias de anomalías ambientales relacionadas al Fenómeno El Niño.

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Indica los acondicionamiento al BIC SNP-1 para la pesca del calamar y los resultados obtenidos entre la zona de Chicama hasta Pto. Pizarro, en octubre y noviembre de 1995. Asimismo, presenta los resultados de la aplicación del método de captura con máquinas calamareras, sistema de luces y sistema de anclaje y de los muestreos oceanográficos, acústicos y biológicos-pesqueros.

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Presenta información oceanográfica que permite conocer la variación que han tenido los parámetros ambientales durante la primavera de 1996 y tener así elementos de juicio, para conocer la tendencia de las condiciones del mar peruano hacia el mes de diciembre de 1996 e inicio de verano de 1997.

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Glycogen synthase 2 (Gys-2) is the ratelimiting enzyme in the storage of glycogen in liver and adipose tissue, yet little is known about regulation of Gys-2 transcription. The peroxisome proliferator-activated receptors (PPARs) are transcription factors involved in the regulation of lipid and glucose metabolism and might be hypothesized to govern glycogen synthesis as well. Here, we show that Gys-2 is a direct target gene of PPARalpha, PPARbeta/delta and PPARgamma. Expression of Gys-2 is significantly reduced in adipose tissue of PPARalpha-/-, PPARbeta/delta-/- and PPARgamma+/- mice. Furthermore, synthetic PPARbeta/delta, and gamma agonists markedly up-regulate Gys-2 mRNA and protein expression in mouse 3T3-L1 adipocytes. In liver, PPARalpha deletion leads to decreased glycogen levels in the refed state, which is paralleled by decreased expression of Gys-2 in fasted and refed state. Two putative PPAR response elements (PPREs) were identified in the mouse Gys-2 gene: one in the upstream promoter (DR-1prom) and one in intron 1 (DR-1int). It is shown that DR-1int is the response element for PPARs, while DR-1prom is the response element for Hepatic Nuclear Factor 4 alpha (HNF4alpha). In adipose tissue, which does not express HNF4alpha, DR-1prom is occupied by PPARbeta/delta and PPARgamma, yet binding does not translate into transcriptional activation of Gys-2. Overall, we conclude that mouse Gys-2 is a novel PPAR target gene and that transactivation by PPARs and HNF4alpha is mediated by two distinct response elements.

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Los volúmenes de plancton fluctuaron entre 0,015 mL.m-3 (Pisco) y 4,648 mL.m-3 (Chimbote), promedio 0,838 mL.m-3, el 79% de estaciones tuvo volúmenes <1,0 mL.m-3. La predominancia del fitoplancton alcanzó 34%. El análisis de comunidades discriminó la formación de dos grupos: 1) estaciones con especies en fases iniciales de sucesión dentro de las 50 mn (Chaetoceros spp., Detonula pumila y Thalassiosira subtilis) y 2) con especies de fases intermedias y típicas de aguas cálidas (Planktoniella sol, Thalassiosira cf. parteneia y Thalassiothrix longissima) asociadas a dinoflagelados cosmopolitas, que se distribuyeron por fuera de las 50 mn. Indicadores biológicos: Protoperidinium obtusum (ACF) se registró hasta las 60 mn; Ceratium breve, indicador de AES se registró frente a Chimbote (75 mn) y Paita (190 mn); Ceratium praelongum, indicador de ASS, se registró a 60 mn, llegando hasta 30 mn frente a Paita.

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(Résumé de l'ouvrage) Dans cet ouvrage réunissant théologiens et philosophes, le corps contemporain est pensé par rapport à ce qui l'excède, ce qui le met en scène, ce qui le reprend, ce qui le transforme aujourd'hui. Dans une première partie, l'ouvrage propose des éclairages sur le corps à partir de ce qui met en question sa vision strictement rationnelle. Puis, trois auteurs évoquent les différentes manières dont la Bible, la philosophie et la littérature contemporaine mettent en scène les corps. Dans une troisième partie, sont abordées des questions plus spécifiquement reliées à la tradition catholique, au christianisme primitif et à la pratique de l'ascèse. Enfin, quatre contributions explorent le défi posé par la déréalisation du corps dans nos sociétés d'aujourd'hui, avec, pour clore l'ensemble, une réflexion sur le dualisme qui traverse le questionnement sur le corps.

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BACKGROUND: Insulin resistance and arterial hypertension are related, but the underlying mechanism is unknown. Endothelial nitric oxide synthase (eNOS) is expressed in skeletal muscle, where it may govern metabolic processes, and in the vascular endothelium, where it regulates arterial pressure. METHODS AND RESULTS: To study the role of eNOS in the control of the metabolic action of insulin, we assessed insulin sensitivity in conscious mice with disruption of the gene encoding for eNOS. eNOS(-/-) mice were hypertensive and had fasting hyperinsulinemia, hyperlipidemia, and a 40% lower insulin-stimulated glucose uptake than control mice. Insulin resistance in eNOS(-/-) mice was related specifically to impaired NO synthesis, because in equally hypertensive 1-kidney/1-clip mice (a model of renovascular hypertension), insulin-stimulated glucose uptake was normal. CONCLUSIONS: These results indicate that eNOS is important for the control not only of arterial pressure but also of glucose and lipid homeostasis. A single gene defect, eNOS deficiency, may represent the link between metabolic and cardiovascular disease.

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Malate synthase (MS; EC 4.1.3.2), an enzyme specific to the glyoxylate cycle, was studied in cotyledons of dark-grown soybean (Glycine max L) seedlings with light and electron microscopy techniques. Immunogold localization confirmed biochemical evidence that MS from soybean is a glyoxysomal matrix enzyme.

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Differences in parasite transmission intensity influence the process of acquisition of host immunity to Plasmodium falciparum malaria and ultimately, the rate of malaria related morbidity and mortality. Potential vaccines being designed to complement current intervention efforts therefore need to be evaluated against different malaria endemicity backgrounds. The associations between antibody responses to the chimeric merozoite surface protein 1 block 2 hybrid (MSP1 hybrid), glutamate-rich protein region 2 (GLURP R2) and the peptide AS202.11, and the risk of malaria were assessed in children living in malaria hyperendemic (Burkina Faso, n = 354) and hypo-endemic (Ghana, n = 209) areas. Using the same reagent lots and standardized protocols for both study sites, immunoglobulin (Ig) M, IgG and IgG sub-class levels to each antigen were measured by ELISA in plasma from the children (aged 6-72 months). Associations between antibody levels and risk of malaria were assessed using Cox regression models adjusting for covariates. There was a significant association between GLURP R2 IgG3 and reduced risk of malaria after adjusting age of children in both the Burkinabe (hazard ratio 0.82; 95 % CI 0.74-0.91, p < 0.0001) and the Ghanaian (HR 0.48; 95 % CI 0.25-0.91, p = 0.02) cohorts. MSP1 hybrid IgM was associated (HR 0.85; 95 % CI 0.73-0.98, p = 0.02) with reduced risk of malaria in Burkina Faso cohort while IgG against AS202.11 in the Ghanaian children was associated with increased risk of malaria (HR 1.29; 95 % CI 1.01-1.65, p = 0.04). These findings support further development of GLURP R2 and MSP1 block 2 hybrid, perhaps as a fusion vaccine antigen targeting malaria blood stage that can be deployed in areas of varying transmission intensity.

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1 kartta :, vär. ;, 50 x 88 cm, kansi 26 x 12 cm, 1:400000

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Collectionneur : Sirot, Georges (1898-1977)