Desenvolupament d'aplicacions per a dispositius mòbils

L'objectiu d'aquest projecte és la realització d'una aplicació per a dispositius mòbils. Aquesta aplicació pretén arribar a la majoria de dispositius del mercat estant d'aquesta manera limitat quant a les versions de SDK de cada sistema operatiu. L'aplicació s'ha desenvolupat fent servir un framework (PhoneGap) que permet el desenvolupament amb una única arquitectura i exporta a diferents entorns. Aquest punt està beneficiat per l'ús del llenguatge PHP. L'aplicació és una xarxa social adreçada a les ofertes de treball, permetent que els mateixos usuaris interaccionin entre ells per tal d'ofertar tasques a realitzar i que puguin ser realitzades per altres usuaris de la xarxa.

Reconciling phonological neighborhood effects in speech production through single trial analysis

A crucial step for understanding how lexical knowledge is represented is to describe the relative similarity of lexical items, and how it influences language processing. Previous studies of the effects of form similarity on word production have reported conflicting results, notably within and across languages. The aim of the present study was to clarify this empirical issue to provide specific constraints for theoretical models of language production. We investigated the role of phonological neighborhood density in a large-scale picture naming experiment using fine-grained statistical models. The results showed that increasing phonological neighborhood density has a detrimental effect on naming latencies, and re-analyses of independently obtained data sets provide supplementary evidence for this effect. Finally, we reviewed a large body of evidence concerning phonological neighborhood density effects in word production, and discussed the occurrence of facilitatory and inhibitory effects in accuracy measures. The overall pattern shows that phonological neighborhood generates two opposite forces, one facilitatory and one inhibitory. In cases where speech production is disrupted (e.g. certain aphasic symptoms), the facilitatory component may emerge, but inhibitory processes dominate in efficient naming by healthy speakers. These findings are difficult to accommodate in terms of monitoring processes, but can be explained within interactive activation accounts combining phonological facilitation and lexical competition.

Neuropsicologia i educació

En aquest article pretenem plantejar una visió del procés de desenvolupament de les funcions cognitives del nen des del vessant del desenvolupament cerebral, a partir de les aportacions de les principals teories neuropsicològiques. En aquest sentit, doncs, presentem els models teòrics de funcionament cortical cerebral, des de les teories d’Alexander Luria fi ns als nous plantejaments més actuals sobre el funcionament en xarxes neurals. En aquest sentit, expliquem el desenvolupament de les funcions superiors del nen en base al procés de desenvolupament de les diferents àrees cerebrals, tenint present la important relació entre les bases genètiques del desenvolupament i la relació amb l’entorn on el nen creix. La interacció entre l’àmbit escolar i el procés evolutiu dels infants és clau per al seu propi desenvolupament, ja que, juntament amb el context familiar, l’escola és un dels principals entorns relacionals del nen. En aquest sentit, presentem els diferents canvis relacionats amb el desenvolupament cerebral que tenen lloc en cada un dels principals moments evolutius, tenint present, alhora, el procés educatiu del nen en l’àmbit escolar. Finalment, fem referència a les bases neurobiològiques del procés d’adquisició del llenguatge i lateralització cerebral de funcions cognitives, processos bàsics per a la comunicació del nen amb l’entorn i per al seu procés d’aprenentatge.

El desenvolupament de la morfologia verbal: l'imperfet nord-occidental en la producció infantil

L'objectiu d'aquest article és contribuir a l'estudi de la morfologia verbal catalana, en aquest cas amb dades relatives a la varietat nord-occidental. Les formes que forneixen la part descriptiva corresponen a mostres de producció oral obtingudes en informants de 3 -4, 6- 7 i 11- 12 anys, la qual cosa signi ca una descripció morfològica del període de desenvolupament lingüístic del nen. Pel que fa a la interpretació dels resultats es proposa una perspectiva d'anàlisi que inclou tant les consideracions que tenen a veure amb aspectes interns del llenguatge com amb els de caràcter extern.

Preparation of alpha-labeled aldehydes by base-catalyzed exchange reactions

A simple, efficient protocol for the preparation of α-labeled aldehydes based on H/D exchange catalyzed by 4-(N,N-dimethylamino)pyridine or Et3N is described. High chemical yields and ratios of isotope incorporation were obtained even when small amounts (1 mmol) of aldehyde were used.

Preparation of alpha-labeled aldehydes by base-catalyzed exchange reactions

A simple, efficient protocol for the preparation of α-labeled aldehydes based on H/D exchange catalyzed by 4-(N,N-dimethylamino)pyridine or Et3N is described. High chemical yields and ratios of isotope incorporation were obtained even when small amounts (1 mmol) of aldehyde were used.

Coexistence of protease sensitive and resistant prion protein in 129VV homozygous sporadic Creutzfeldt-Jakob disease: a case report

Introduction: The coexistence of different molecular types of classical protease-resistant prion protein in the same individual have been described, however, the simultaneous finding of these with the recently described protease-sensitive variant or variably protease-sensitive prionopathy has, to the best of our knowledge, not yet been reported. Case presentation: A 74-year-old Caucasian woman showed a sporadic Creutzfeldt-Jakob disease clinical phenotype with reactive depression, followed by cognitive impairment, akinetic-rigid Parkinsonism with pseudobulbar syndrome and gait impairment with motor apraxia, visuospatial disorientation, and evident frontal dysfunction features such as grasping, palmomental reflex and brisk perioral reflexes. She died at age 77. Neuropathological findings showed: spongiform change in the patient"s cerebral cortex, striatum, thalamus and molecular layer of the cerebellum with proteinase K-sensitive synaptic-like, dot-like or target-like prion protein deposition in the cortex, thalamus and striatum; proteinase K-resistant prion protein in the same regions; and elongated plaque-like proteinase K-resistant prion protein in the molecular layer of the cerebellum. Molecular analysis of prion protein after proteinase K digestion revealed decreased signal intensity in immunoblot, a ladder-like protein pattern, and a 71% reduction of PrPSc signal relative to non-digested material. Her cerebellum showed a 2A prion protein type largely resistant to proteinase K. Genotype of polymorphism at codon 129 was valine homozygous. Conclusion: Molecular typing of prion protein along with clinical and neuropathological data revealed, to the best of our knowledge, the first case of the coexistence of different protease-sensitive prion proteins in the same patient in a rare case that did not fulfill the current clinical diagnostic criteria for either probable or possible sporadic Creutzfeldt-Jakob disease. This highlights the importance of molecular analyses of several brain regions in order to correctly diagnose rare and atypical prionopathies

A common BACE1 polymorphism is a risk factor for sporadic Creutzfeldt-Jakob disease

The β site APP cleaving enzyme 1 (BACE1) is the rate-limiting β-secretase enzyme in the amyloidogenic processing of APP and Aβ formation, and therefore it has a prominent role in Alzheimer"s disease (AD) pathology. Recent evidence suggests that the prion protein (PrP) interacts directly with BACE1 regulating its β-secretase activity. Moreover, PrP has been proposed as the cellular receptor involved in the impairment of synaptic plasticity and toxicity caused by Aβ oligomers. Provided that common pathophysiologic mechanisms are shared by Alzheimer"s and Creutzfeldt-Jakob (CJD) diseases, we investigated for the first time to the best of our knowledge a possible association of a common synonymous BACE1 polymorphism (rs638405) with sporadic CJD (sCJD). Our results indicate that BACE1 C-allele is associated with an increased risk for developing sCJD, mainly in PRNP M129M homozygous subjects with early onset. These results extend the very short list of genes (other than PRNP) involved in the development of human prion diseases; and support the notion that similar to AD, in sCJD several loci may contribute with modest overall effects to disease risk. These findings underscore the interplay in both pathologies of APP, Aβ oligomers, ApoE, PrP and BACE1, and suggest that aging and perhaps vascular risk factors may modulate disease pathologies in part through these key players

Liver Glucokinase A456V induces potent hypoglycemia without dyslipidemia through a paradoxical induction of the catalytic subunit of glucose-6-phosphatase

Recent reports point out the importance of the complex GK-GKRP in controlling glucose and lipid homeostasis. Several GK mutations affect GKRP binding, resulting in permanent activation of the enzyme. We hypothesize that hepatic overexpression of a mutated form of GK, GKA456V, described in a patient with persistent hyperinsulinemic hypoglycemia of infancy (PHHI) and could provide a model to study the consequences of GK-GKRP deregulation in vivo. GKA456V was overexpressed in the liver of streptozotocin diabetic mice. Metabolite profiling in serum and liver extracts, together with changes in key components of glucose and lipid homeostasis, were analyzed and compared to GK wild-type transfected livers. Cell compartmentalization of the mutant but not the wild-type GK was clearly affected in vivo, demonstrating impaired GKRP regulation. GKA456V overexpression markedly reduced blood glucose in the absence of dyslipidemia, in contrast to wild-type GK-overexpressing mice. Evidence in glucose utilization did not correlate with increased glycogen nor lactate levels in the liver. PEPCK mRNA was not affected, whereas the mRNA for the catalytic subunit of glucose-6-phosphatase was upregulated ~4 folds in the liver of GKA456V-treated animals, suggesting that glucose cycling was stimulated. Our results provide new insights into the complex GK regulatory network and validate liver-specific GK activation as a strategy for diabetes therapy.

Poetica: dels sentits i l'experiencia

Les imatges evocadores sovint són la matèria primordial de l"escriptura poètica, si bé, mitjançant l"ús poètic del llenguatge, aquestes imatges poden esdevenir un joc de capses xineses, o fins i tot configurar il·lustracions impossibles. La present poètica arrenca a continuació amb un recurs estilístic inspirat en el mestratge literari d"Hildegarda de Bingen (1098-1179). La mística renana iniciava cadascun dels apartats de les seves obres visionàries amb el relat d"allò vist i escoltat, i alguns dels capítols contenen una minuciosa descripció de la figura poderosa i misteriosa que se li apareixia durant la visió. Així, aquest escrit comença amb el pre-text de parlar d"una imatge, partint de l"observació atenta dels seus volums, línies, contorns i actituds...

Les escriptores a Galicia: subversio, gramatica violeta i identitat multiple

La literatura gallega dels darrers anys s"ha vist profundament transformada per la irrupció de les escriptores i una «gramàtica violeta», una literatura concebuda en femení, que ha afectat també l"escriptura d"autoria masculina. Les seves propostes no se situen, doncs, en el marge del camp literari, malgrat que numèricament són menys. A la narrativa han engegat ambiciosos projectes de subversió de gènere amb una bona recepció. A la poesia s"han convertit en models literaris per la seva capacitat d"experimentació i renovació integral de l"escriptura, fent quallar una gramàtica violeta. I l"espai virtual, convertit en laboratori públic del llenguatge, s"experimenta amb l"escriptura i la identitat múltiple.

Les escriptores a Galicia: subversio, gramatica violeta i identitat multiple

La literatura gallega dels darrers anys s"ha vist profundament transformada per la irrupció de les escriptores i una «gramàtica violeta», una literatura concebuda en femení, que ha afectat també l"escriptura d"autoria masculina. Les seves propostes no se situen, doncs, en el marge del camp literari, malgrat que numèricament són menys. A la narrativa han engegat ambiciosos projectes de subversió de gènere amb una bona recepció. A la poesia s"han convertit en models literaris per la seva capacitat d"experimentació i renovació integral de l"escriptura, fent quallar una gramàtica violeta. I l"espai virtual, convertit en laboratori públic del llenguatge, s"experimenta amb l"escriptura i la identitat múltiple.

Do the interactions between glucocorticoids and sex hormones regulate the development of the metabolic syndrome?

The metabolic syndrome is basically a maturity-onset disease. Typically, its manifestations begin to flourish years after the initial dietary or environmental aggression began. Since most hormonal, metabolic, or defense responses are practically immediate, the procrastinated response do not seem justified. Only in childhood, the damages of the metabolic syndrome appear with minimal delay. Sex affects the incidence of the metabolic syndrome, but this is more an effect of timing than absolute gender differences, females holding better than males up to menopause, when the differences between sexes tend to disappear. The metabolic syndrome is related to an immune response, countered by a permanent increase in glucocorticoids, which keep the immune system at bay but also induce insulin resistance, alter the lipid metabolism, favor fat deposition, mobilize protein, and decrease androgen synthesis. Androgens limit the operation of glucocorticoids, which is also partly blocked by estrogens, since they decrease inflammation (which enhances glucocorticoid release). These facts suggest that the appearance of the metabolic syndrome symptoms depends on the strength (i.e., levels) of androgens and estrogens. The predominance of glucocorticoids and the full manifestation of the syndrome in men are favored by decreased androgen activity. Low androgens can be found in infancy, maturity, advanced age, or because of their inhibition by glucocorticoids (inflammation, stress, medical treatment). Estrogens decrease inflammation and reduce the glucocorticoid response. Low estrogen (infancy, menopause) again allow the predominance of glucocorticoids and the manifestation of the metabolic syndrome. It is postulated that the equilibrium between sex hormones and glucocorticoids may be a critical element in the timing of the manifestation of metabolic syndrome-related pathologies.

Steroid hormones interrelationships in the metabolic syndrome: an introduction to the ponderostat hypothesis

Sexual dimorphism in the metabolic syndrome. The clairvoyant early implication of sex hormones in the characterization of the metabolic syndrome (MS) was detected early, and in accordance with the well-known sex-related main patterns of fat deposition in obesity: gynoid and android. The differences point to a direct implication of androgens and estrogens in the development, properties and maintenance of obesity and, by extension, to the cumulus of diseases grouped in the MS. For a long time, the key issue of the MS, i.e. the metabolic event explaining (and justifying) most of the derangements of the MS, has been considered to be insulin resistance (...)

El autismo en el primer año

Actualmente es posible diagnosticar el autismo con un alto grado de fiabilidad entre los 18 meses y los 2 años. Sin embargo, los primeros síntomas ya están presentes mucho antes del diagnóstico. Ello ha dado pie a que se hayan llevado a cabo múltiples estudios, retrospectivos y prospectivos, orientados a detectar manifestaciones que faciliten un diagnóstico lo más precozmente posible. A partir de estas investigaciones se han podido detectar síntomas cuya aparición se sitúa entre los 6 y 12 meses. Aunque se ha visto que estos síntomas tienen un interés diagnóstico limitado, aportan información muy valiosa para la comprensión del autismo en el marco de los trastornos del neurodesarrollo, en el sentido de destacar un patrón evolutivo que en su inicio es común a diversos trastornos, pero que progresivamente va configurando un fenotipo específico.