983 resultados para COMPUTER ARCHITECTURE


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Aquest treball consisteix en la construcció d'un servidor segur d'aplicacions per a la mitjana empresa. Aquest servidor ens dotarà d'un entorn segur, gràcies al qual els usuaris de l'organització podran entrar a les seves aplicacions de manera remota com si executessin les seves necessitats dins la xarxa de l'empresa.

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El Banc Electrònic d'Historials Mèdics és un aplicatiu basat en l'arquitectura client-servidor que permet l'intercanvi segur de la informació continguda en els historials clínics dels pacients de la salut.

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Aquest projecte és una mostra de les possibilitats de dotar de seguretat a les aplicacions web i d¿arquitectura Client/Servidor basades en Java

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Consisteix en la realització d'una aplicació sota la plataforma J2EE. La realització d'aquesta aplicació permetrà aplica coneixements adquirits en diferents assignatures dels estudis de ITIS. Amb el desenvolupament de l'aplicació s'adquiriràn els coneixements bàsics sobre J2EE.

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OBJECTIVE: A large body of epidemiologic data strongly suggests an association between excess adiposity and coronary artery disease (CAD). Low adiponectin levels, a hormone secreted only from adipocytes, have been associated with an increased risk of CAD in observational studies. However, these associations cannot clarify whether this relationship is causal or due to a shared set of causal factors or even confounding. Genome-wide association studies have identified common variants that influence adiponectin levels, providing valuable tools to examine the genetic relationship between adiponectin and CAD. METHODS: Using 145 genome wide significant SNPs for adiponectin from the ADIPOGen consortium (n = 49,891), we tested whether adiponectin-decreasing alleles influenced risk of CAD in the CARDIoGRAM consortium (n = 85,274). RESULTS: In single-SNP analysis, 5 variants among 145 SNPs were associated with increased risk of CAD after correcting for multiple testing (P < 4.4 × 10(-4)). Using a multi-SNP genotypic risk score to test whether adiponectin levels and CAD have a shared genetic etiology, we found that adiponectin-decreasing alleles increased risk of CAD (P = 5.4 × 10(-7)). CONCLUSION: These findings demonstrate that adiponectin levels and CAD have a shared allelic architecture and provide rationale to undertake a Mendelian randomization studies to understand if this relationship is causal.

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The present study investigates the short- and long-term outcomes of a computer-assisted cognitive remediation (CACR) program in adolescents with psychosis or at high risk. 32 adolescents participated in a blinded 8-week randomized controlled trial of CACR treatment compared to computer games (CG). Clinical and neuropsychological evaluations were undertaken at baseline, at the end of the program and at 6-month. At the end of the program (n = 28), results indicated that visuospatial abilities (Repeatable Battery for the Assessment of Neuropsychological Status, RBANS; P = .005) improved signifi cantly more in the CACR group compared to the CG group. Furthermore, other cognitive functions (RBANS), psychotic symptoms (Positive and Negative Symptom Scale) and psychosocial functioning (Social and Occupational Functioning Assessment Scale) improved signifi cantly, but at similar rates, in the two groups. At long term (n = 22), cognitive abilities did not demonstrated any amelioration in the control group while, in the CACR group, signifi cant long-term improvements in inhibition (Stroop; P = .040) and reasoning (Block Design Test; P = .005) were observed. In addition, symptom severity (Clinical Global Improvement) decreased signifi cantly in the control group (P = .046) and marginally in the CACR group (P = .088). To sum up, CACR can be successfully administered in this population. CACR proved to be effective over and above CG for the most intensively trained cognitive ability. Finally, on the long-term, enhanced reasoning and inhibition abilities, which are necessary to execute higher-order goals or to adapt behavior to the ever-changing environment, were observed in adolescents benefi ting from a CACR.

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Using genome-wide data from 253,288 individuals, we identified 697 variants at genome-wide significance that together explained one-fifth of the heritability for adult height. By testing different numbers of variants in independent studies, we show that the most strongly associated ∼2,000, ∼3,700 and ∼9,500 SNPs explained ∼21%, ∼24% and ∼29% of phenotypic variance. Furthermore, all common variants together captured 60% of heritability. The 697 variants clustered in 423 loci were enriched for genes, pathways and tissue types known to be involved in growth and together implicated genes and pathways not highlighted in earlier efforts, such as signaling by fibroblast growth factors, WNT/β-catenin and chondroitin sulfate-related genes. We identified several genes and pathways not previously connected with human skeletal growth, including mTOR, osteoglycin and binding of hyaluronic acid. Our results indicate a genetic architecture for human height that is characterized by a very large but finite number (thousands) of causal variants.

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Este documento describe el plan de trabajo, el análisis y la implementación del trabajo de fin de carrera de los estudios de Ingeniería Técnica de Informática de Gestión, en concreto del área de almacén de datos.El objetivo de este trabajo es familiarizarse con la arquitectura de un DW: el diseño de un DW, tratamiento de datos, así como conocer las herramientas de que dispone el mercado para trabajar con estos modelos y realizar los análisis dirigidos a usuarios finales.

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Definición, análisis, diseño e implementación de un portal basado en la arquitectura Java EE que sintetiza los conocimientos adquiridos en la carrera de Ingeniería Técnica de Sistemas cursada en la UOC.

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Aplicació basada en l'arquitectura J2EE. Amb la utilització del framework Struts 2, s'ha desenvolupat una aplicació web tenint com a base el patró Model - Vista - Controlador. Es detallen les diferents fases (estudi inicial, anàlisi funcional, disseny i implementació) per tal de realitzar el projecte: 'Accés i consulta de la informació relacionada amb un centre mèdic'.