Hezkuntza-premia bereziak Derrigorrezko Bigarren Hezkuntzan

Existe una versi??n en espa??ol, con el t??tulo "Las Necesidades Educativas Especiales en la Ense??anza Secundaria Obligatoria"

While programak: konputagarritasun teoria oinarritzeko tresna

Konputagarritasun Teoriaren asmoa sistema konputazionalen muga teorikoak aztertzea da. Bere helburu nagusia problemak konputagarri eta konputaezinen artean bereiztea da, problema konputagarria ebazpide informatikoa onartzen duenari deitzen diogula kontuan hartuta. Emaitza horiek garatzeko konputagailu eredu abstraktu erabiliena, historikoki, Turing-en Makina izan da. Ingeniaritza Informatikoko ikasleek eredu abstraktuaren eta konputagailu errealen artean distantzia dagoela nabari dezakete, horregatik programaziotik hurbilago dagoen eredu bat erabiltzea egokiagoa da, while programak hain zuzen ere. While programekin Turingen makinekin ebazten diren problema berak ebazten dira. Aldiz, while programak erabiltzen askoz errazagoak dira, batez ere aurretik informatika errealean esperientzia duten pertsonentzat, lengoaia agintzaile klasikoen programen itxura hartzen baitute. Testu honek while programak erabiltzen ditu, behar denean hauek birformulatuz eta beraien abantailak aprobetxatuz, konputazioa sinbolo arbitrarioen manipulazioaren baitan definituta gera dadin. Horrela, errealitate informatikotik askoz hurbilagoa egongo da. While programak zer diren eta nola erabiltzen diren zehaztasunez azaltzen da, eta gainera, beste agindu edo datu-mota batzuk gehitzea zergatik ez den beharrezkoa justifikatzen da.

Konputaezintasun frogapen batzuk diagonalizazio teknika erabiliz

Konputagarritasunaren Teoriaren oinarriak lehenengo ordenadoreak azaldu aurretik (40. hamarkadaren bukaera aldera) ezarri ziren, eta ziztu biziko eta etenik gabeko eraldaketek aldatzea lortu ez duten oinarriak dira. Alan Mathison Turing-ek jadanik garai hartan frogatu zuen, ahalik eta potentzia handienekoa imajinatuta ere, inolako ordenadorek ebatzi ezingo zituen zenbait gai edo arazo bazeudela. Balizko algoritmorik ez duten problema horiek, konputaezinak deitzen ditugunak, ez dira salbuespenak eta adibide ugari aurki dezakegu. Programen portaeraren inguruan planteatzen diren problemen artean, asko konputaezinak dira. Familia horretako kide ezagunena, zalantzarik gabe, geratze problema da: sarrerako datu zehatz batzuk hartzerakoan, programa bat begizta infinituan geratuko ote den era orokorrean erabakitzeko algoritmorik ez dago. Problema baten konputaezintasuna frogatzeko, hau ebatziko duen algoritmo zehatz bat existitzen ez dela ziurtatuko duen argumentu logikoa behar dugu, edo beste era batera esanda, existitzen diren algoritmoak problema hori ebazteko gai izango ez direla egiaztatuko duen argumentua. Izaera unibertsaleko argumentu hori ezartzea ez da batere erraza izaten, eta normalean, absurduraino eramandako frogapen batekin erlazionatuta egon ohi da. Helburu hori lortzeko zenbait teknika daude. Diagonalizazioaren teknika horien artean oinarrizkoena da, eta nahiko ezaguna, ez baita Informatika Teorikoaren tresna espezifikoa. Dokumentu honen helburua ez da teknika bera azaldu edo deskribatzea, ezaguntzat hartzen baita, zailtasun maila desberdineko hainbat adibideren bitartez argitzea baizik.

Gorka Goikoetxearen etxebizitzaren ziurtagiri energetikoa

[EU]Lan honen helburu nagusia Gorka Goikoetxearen etxebizitzaren ziurtagiri energetikoa lortzea da eta, hortik abiatuz, hobekuntza batzuen proposamena eta analisi ekonomikoa. Honetarako CE3X programa erabiliko da, datuak sartu hutsez kalifikazio zenbakia eta hizkia emango du eta ondoren hobekuntza aukera desberdinak eskainiko ditu. Hauek balioztatzeko analisi ekonomiko bat egingo da. Txosten honetan ziurtagiria lortzeko beharrezko urratsak azalduko dira, hobekuntzen deskripzioa eta kalifikazio berriak ere bai. Eranskinetan gehigarrizko informazioa erakutsiko da, prozesuaren ulermena errazteko.

Inplante erabilerako polimero erradio-opakoen lorpena eta ezaugarritzea

[EU]Biomedikuntzan gero eta material polimeriko gehiago aplikatzen dira. Metalezko inplanteekin alderatuz, ekoizterako orduan azkarragoak eta merkeagoak baitira beste hainbat ezaugarriren artean. Baina onurak ekartzearekin batera, erradio-opakotasun eza ere badakar. Eta ezaugarri hau gabe, inplantearen jarraipena behin giza gorputzean ezarrita dagoenean ezinezkoa da, X izpiekin ezin baita ikusi. Beraz, arazo horri aurre egiteko, proiektu honetan matrize polimerikoari kargak gehitzea proposatzen da. Lortutako material konposatuak, polimeroak soilik dituen ezaugarriak berdintzea edo hobetzea espero da. Hau da, erradio-opakotasuna lortzeaz gain, propietate mekanikoak behintzat mantentzea espero da. Giza gorputzean aplikatzen diren inplanteetarako erabiliko den material konposatu bat lortzea duenez helburu proiektu honek, matrizea polimero biobataragarria eta biodegradagarria izango da. Biodegradagarria izanik, inplantea kanporatzeko bigarren ebakuntza bat ekiditen da. Zehazki, poli(D-laktida) (PDLA) polimeroa matrize moduan eta karga moduan bismuto oxidoa (Bi2O3) erabiliko dira, medikuntza arloko inplanteetan erabili izan ohi dira eta.

Aerosorgailu palen aplikazioetarako pvc espumaren degradazio termiko eta propietate mekanikoen karakterizazioa

[EU]Energia berriztagarria iturri naturaletatik sortzen den energia mota da. Energia lortzeko erabiltzen diren baliabide naturalak asko dira, eguzki-energia, haizea, ura… Energia berriztagarrien artean, eolikoa da zabalkunde handien lortu duena; batez ere ingurumen-inpaktu urriagatik eta bere kostuak gero eta txikiagoak izateagatik. Honen ondorioz, energia garbi, lehiakor eta ekonomikoki bideragarria da gaur egun. Hala ere, aerosorgailu hauen ekoizpen prozesuak desabantaila nabaria aurkezten du palen ontze prozesuan. Tenperatura igoeraren ondorioz material konkretu baten degradazioa dela eta. Ikerketa lan honetan, aerosorgailu palen karakterizazioa egingo da eta ontze prozesuan, “polikloruro de binilo” (PVC)-ak jasaten duen degradazioaren azterketa.

Diseño de un sistema inalámbrico para la recogida de diferentes parámetros en el ámbito de la práctica deportiva del surf

[ES]En este documento se presenta el Trabajo Fin de Grado llevado a cabo con el objetivo de realizar el diseño de un sistema inalámbrico para la recogida de parámetros en el ámbito de la práctica deportiva del surf. Para alcanzar los objetivos de este trabajo, se ha analizado el estado del arte asociado a dicho sistema, con el fin de distinguir el comportamiento de los sensores y tecnologías inalámbricas. Por último, mediante la metodología llevada a cabo se ha realizado el diseño general del sistema, así como, el diseño de un sistema reducido.

Software libre como elemento necesario para la democracia de la multitud (Otros Temas)

En los textos de Empire y Multitude, Antonio Negri y Michael Hardt proponen que en el mundo actual la fuerza dominante que controla el capitalismo, y así el poder, es el Imperio. El Imperio obtiene su fuerza a través del control de la producción intelectual y su poder está ere cien - do durante este período de transición en el modelo capitalista. En este ensayo, se argumenta que los oprimidos por el Imperio, quienes conforman como clase la multitud, necesitan el software libre para crear su sueño: la democracia. Este software es a la vez el mejor ejemplo de como puede ser la democracia y una herramienta que permite la ampliación de ella. Además, su potencial en la región andina es todavía mayor por la debilidad del modelo de democracia liberal que promociona el Imperio.

Oestrogenic activity of benzyl salicylate, benzyl benzoate and butylphenylmethylpropional (Lilial) in MCF7 human breast cancer cells in vitro

Benzyl salicylate, benzyl benzoate and butylphenylmethylpropional (Lilial) are added to bodycare cosmetics used around the human breast. We report here that all three compounds possess oestrogenic activity in assays using the oestrogen-responsive MCF7 human breast cancer cell line. At 3 000 000-fold molar excess, they were able to partially displace [H-3]oestradiol from recombinant human oestrogen receptors ER alpha and ER beta, and from cytosolic ER of MCF7 cells. At concentrations in the range of 5 x 10(-5) to 5 x 10(-4) M, they were able to increase the expression of a stably integrated oestrogen-responsive reporter gene (ERE-CAT) and of the endogenous oestrogen-responsive pS2 gene in MCF7 cells, albeit to a lesser extent than with 10(-8) M 17 beta-oestradiol. They increased the proliferation of oestrogen-dependent MCF7 cells over 7 days, which could be inhibited by the antioestrogen fulvestrant, suggesting an ER-mediated mechanism. Although the extent of stimulation of proliferation over 7 days was lower with these compounds than with 10(-8) M 17 beta-oestradiol, given a longer time period of 35 days the extent of proliferation with 10(-4) M benzyl salicylate, benzyl benzoate or butylphenylmethylpropional increased to the same magnitude as observed with 10(-8) M 17 beta-oestradiol over 14 days. This demonstrates that benzyl salicylate, benzyl benzoate and butylphenylmethylpropional are further chemical components of cosmetic products which give oestrogenic responses in a human breast cancer cell line in culture. Further research is now needed to investigate whether oestrogenic responses are detectable using in vivo models and the extent to which these compounds might be absorbed through human skin and might enter human breast tissues. Copyright (C) 2009 John Wiley & Sons, Ltd.

Oestrogenic and androgenic activity of triclosan in breast cancer cells

As a consequence of its widespread use as an antimicrobial agent in consumer goods, triclosan has become distributed ubiquitously across the ecosystem, and recent reports that it can cause endocrine disruption in aquatic species has increased concern. It is reported here that triclosan possesses intrinsic oestrogenic and androgenic activity in a range of assays in vitro which could provide some explanation for the endocrine disrupting properties described in aquatic populations. In terms of oestrogenic activity, triclosan displaced [H-3]oestradiol from oestrogen receptors (ER) of MCF7 human breast cancer cells and from recombinant human ER alpha/ER beta. Triclosan at 10(-5) M completely inhibited the induction of the oestrogen-responsive ERE-CAT reporter gene in MCF7 cells by 10(-10) M 17 beta-oestradiol and the stimulation of growth of MCF7 human breast cancer cells by 10(-10) M 17 beta-oestradiol. On its own, 1 mu M triclosan increased the growth of MCF7 cells over 21 days. Triclosan also had androgenic activity. It displaced [H-3]testosterone from binding to the ligand binding domain of the rat androgen receptor (AR). Triclosan was able to inhibit the induction of the androgen-responsive LTR-CAT reporter gene in S115 mouse mammary tumour cells by 10(-9) M testosterone and in T47D human breast cancer cells by 10(-8) M testosterone at concentrations of 10(-7) M and 10(-6) M, respectively. Triclosan at 2 x 10(-5) M antagonized the stimulation of the growth of S115+A mouse mammary tumour cells by 10(-9) M testosterone. The finding that triclosan has oestrogenic and androgenic activity warrants further investigation in relation to both endocrine disruption of aquatic wildlife and any possible impact on human health. Copyright (C) 2007 John Wiley & Sons, Ltd.

Effect of sulphation on the oestrogen agonist activity of the phytoestrogens genistein and daidzein in MCF-7 human breast cancer cells

The phytoestrogens genistein, daidzein and the daidzein metabolite equol have been shown previously to possess oestrogen agonist activity. However, following consumption of soya diets, they are found in the body not only as aglycones but also as metabolites conjugated at their 4'- and 7-hydroxyl groups with sulphate. This paper describes the effects of monosulphation on the oestrogen agonist properties of these three phytoestrogens in MCF-7 human breast cancer cells in terms of their relative ability to compete with [H-3]oestradiol for binding to oestrogen receptor (ER), to induce a stably transfected oestrogen-responsive reporter gene (ERE-CAT) and to stimulate cell growth. In no case did sulphation abolish activity. The 4'-sulphadon of genistein reduced oestrogen agonist activity to a small extent in whole-cell assays but increased the relative binding affinity to ER. The 7-sulphation of genistein, and also of equol, reduced oestrogen agonist activity substantially in all assays. By contrast, the position of monosulphation of daidzein acted in an opposing manner on oestrogen agonist activity. Sulphation at the 4'-position of daidzein resulted in a modest reduction in oestrogen agonist activity but sulphation of daidzein at the 7-position resulted in an increase in oestrogen agonist activity. Molecular modelling and docking studies suggested that the inverse effects of sulphation could be explained by the binding of daidzein into the ligand-binding domain of the ER in the opposite orientation compared with genistein and equol. This is the first report of sulphation enhancing activity of an isoflavone and inverse effects of sulphation between individual phytoestrogens.

Changes in oestrogen receptor-alpha and -beta during progression to acquired resistance to tamoxifen and fulvestrant (Faslodex, ICI 182,780) in MCF7 human breast cancer cells

Cell culture models of antioestrogen resistance often involve applying selective pressures of oestrogen deprivation simultaneously with addition of tamoxifen or fulvestrant (Faslodex, ICI 182,780) which makes it difficult to distinguish events in development of antioestrogen resistance from those in loss of response to oestrogen or other components. We describe here time courses of loss of antioestrogen response using either oestrogen-maintained or oestrogen-deprived MCF7 cells in which the only alteration to the culture medium was addition of 10(-6) M tamoxifen or 10(-7) M fulvestrant. In both oestrogen-maintained and oestrogen-deprived models, loss of growth response to tamoxifen was not associated with loss of response to fulvestrant. However, loss of growth response to fulvestrant was associated in both models with concomitant loss of growth response to tamoxifen. Measurement of oestrogen receptor alpha (ER alpha) and oestrogen receptor beta (ER beta) mRNA by real-time RT-PCR together with ER alpha and ER beta protein by Western immunoblotting revealed substantial changes to ER alpha levels but very little alteration to ER beta levels following development of antioestrogen resistance. In oestrogen-maintained cells, tamoxifen resistance was associated with raised levels of ERa mRNA/protein. However by contrast, in oestrogen-deprived MCF7 cells, where oestrogen deprivation alone had already resulted in increased levels of ERa mRNA/protein, long-term tamoxifen exposure now reduced ER alpha levels. Whilst long-term exposure to fulvestrant reduced ERa. mRNA/protein levels in the oestrogen-maintained cells to a level barely detectable by Western immunoblotting and non-functional in inducing gene expression (ERE-LUC reporter or pS2), in oestrogen-deprived cells the reduction was much less substantial and these cells retained an oestrogen-induction of both the ERE-LUC reporter gene and the endogenous pS2 gene which could still be inhibited by antioestrogen. This demonstrates that whilst ER alpha can be abrogated by fulvestrant and increased by tamoxifen in some circumstances, this does not always hold true and mechanisms other than alteration to ER must be involved in the development of antioestrogen resistant growth. (c) 2006 Elsevier Ltd. All rights reserved.

Comparative study of oestrogenic properties of eight phytoestrogens in MCF7 human breast cancer cells

Previous studies have compared the oestrogenic properties of phytoestrogens in a wide variety of disparate assays. Since not all phytoestrogens have been tested in each assay, this makes inter-study comparisons and ranking oestrogenic potency difficult. In this report, we have compared the oestrogen agonist and antagonist activity of eight phytoestrogens (genistein, daidzein, equol, miroestrol, deoxymiroestrol, 8-prenylnaringenin, coumestrol and resveratrol) in a range of assays all based within the same receptor and cellular context of the MCF7 human breast cancer cell line. The relative binding of each phytoestrogen to oestrogen receptor (ER) of MCF7 cytosol was calculated from the molar excess needed for 50 % inhibition of [H-3]oestradiol binding (IC50), and was in the order coumestrol (35x)/8-prenylnaringenin (45 x)/deoxymiroestrol (50 x) > miroestrol (260x) > genistein (1000x) > equol (4000x) > daidzein (not achieved: 40 % inhibition at 10(4)-fold molar excess) > resveratrol (not achieved: 10 % inhibition at 10(5)-fold molar excess). For cell-based assays, the rank order of potency (estimated in terms of the concentration needed to achieve a response equivalent to 50 % of that found with 17 beta-oestradiol (IC50)) remained very similar for all the assays whether measuring ligand ability to induce a stably transfected oestrogen-responsive ERE-CAT reporter gene, cell growth in terms of proliferation rate after 7 days or cell growth in terms of saturation density after 14 days. The IC50 values for these three assays in order were for 17 beta-oestradiol (1 x 10-(11) M, 1 x 10-(11) M, 2 x 10(-11) M), and in rank order of potency for the phytoestrogens, deoxymiroestrol (1 x 10(-10) M, 3 x 10(-11) M, 2 x 10(-11) M) > miroestrol (3 x 10(-10) M, 2 x 10(-11) M, 8 x 10(-11) M) > 8-prenylnaringenin (1 x 10(-9) M, 3 x 10(-10) M, 3 x 10(-10) M) > cournestrol (3 x 10(-8) M, 2 x 10(-8) M, 3 x 10(-8) M) > genistein (4 x 10(-8) M, 2 x 10(-8) M, 1 x 10(-8) M)/equol (1 x 10(-7) M, 3 x 10(-8) M, 2 x 10(-8) M) > daidzein (3 x 10(-7) M, 2 x 10(-7) M, 4 x 10(-8) M) > resveratrol (4 x 10(-6) M, not achieved, not achieved). Despite using the same receptor context of the MCF7 cells, this rank order differed from that determined from receptor binding. The most marked difference was for cournestrol and 8-prenylnaringenin which both displayed a relatively potent ability to displace [3H]oestradiol from cytosolic ER compared with their much lower activity in the cell-based assays. Albeit at varying concentrations, seven of the eight phytoestrogens (all except resveratrol) gave similar maximal responses to that given by 17 beta-oestradiol in cell-based assays which makes them full oestrogen agonists. We found no evidence for any oestrogen antagonist action of any of these phytoestrogens at concentrations of up to 10(-6) M on either reporter gene induction or on stimulation of cell growth. (c) 2005 Elsevier Ltd. All rights reserved.

Factors required for the uridylylation of the foot-and-mouth disease virus 3B1, 3B2, and 3B3 peptides by the RNA-dependent RNA polymerase (3D(pol)) in vitro

The 5' terminus of picornavirus genomic RNA is covalently linked to the virus-encoded peptide 313 (VTg). Foot-and-mouth disease virus (FMDV) is unique in encoding and using 3 distinct forms of this peptide. These peptides each act as primers for RNA synthesis by the virus-encoded RNA polymerase 3D(pol). To act as the primer for positive-strand RNA synthesis, the 3B peptides have to be uridylylated to form VPgpU(pU). For certain picornaviruses, it has been shown that this reaction is achieved by the 3D(pol) in the presence of the 3CD precursor plus an internal RNA sequence termed a cis-acting replication element (cre). The FMDV ere has been identified previously to be within the 5' untranslated region, whereas all other picornavirus cre structures are within the viral coding region. The requirements for the in vitro uridylylation of each of the FMDV 313 peptides has now been determined, and the role of the FMDV ere (also known as the 3B-uridylylation site, or bus) in this reaction has been analyzed. The poly(A) tail does not act as a significant template for FMDV 3B uridylylation.

Oestrogenic activity of p-hydroxybenzoic acid (common metabolite of paraben esters) and methylparaben in human breast cancer cell lines

This paper addresses the question of whether p-hydroxybenzoic acid, the common metabolite of parabens, possesses oestrogenic activity in human breast cancer cell lines. The alkyl esters of p-hydroxybenzoic acid (parabens) are used widely as preservatives in consumer products to which the human population is exposed and have been shown previously to possess oestrogenic activity and to be present in human breast tumour tissue, which is an oestrogen-responsive tissue. Recent work has shown p-hydroxybenzoic acid to give an oestrogenic response in the rodent uterotrophic assay. We report here that p-hydroxybenzoic acid possesses oestrogenic activity in a panel of assays in human breast cancer cell lines. p-Hydroxybenzoic acid was able to displace [H-3]oestradiol from cytosolic oestrogen receptor of MCF7 human breast cancer cells by 54% at 5 x 10(6)-fold molar excess and by 99% at 10(7)-fold molar excess. It was able to increase the expression of a stably integrated oestrogen responsive reporter gene (ERE-CAT) at a concentration of 5 x 10(-4) M in MCF7 cells after 24 h and 7 days, which could be inhibited by the anti-oestrogen ICI 182 780 (Faslodex, fulvestrant). Proliferation of two human breast cancer cell lines (MCF7, ZR-75-1) could be increased by 10(-5) M p-hydroxybenzoic acid. Following on from previous studies showing a decrease in oestrogenic activity of parabens with shortening of the linear alkyl chain length, this study has compared the oestrogenic activity of p-hydroxybenzoic acid where the alkyl grouping is no longer present with methylparaben, which has the shortest alkyl group. Intrinsic oestrogenic activity of p-hydroxybenzoic acid was similar to that of methylparaben in terms of relative binding to the oestrogen receptor but its oestrogenic activity on gene expression and cell proliferation was lower than that of methylparaben. It can be concluded that removal of the ester group from parabens does not abrogate its oestrogenic activity and that p-hydroxybenzoic acid can give oestrogenic responses in human breast cancer cells. Copyright (C) 2005 John Wiley & Sons, Ltd.