155 resultados para C .net
Resumo:
El projecte consisteix en realitzar una Web per la empresa constructora C.Kasa S.L., es tracta d'una empresa relativament jove, es va crear la'ny 2005 i l'objectiu es poder aconseguir que la gent conegui ms aquesta empresa mitjanant una web apostant per les noves tecnologies com a mitj de publicitat.
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Desenvolupar una eina de software que pugui automatitzar i resoldre un model matemtic, amb l'objectiu de minimitzar les despeses de transport des del camp a una central del sucre, i a la vegada garantir l'abastament diri d'aquesta, per tal de minimitzar les despeses i situar adequadament els recursos disponibles.
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Estudi observacional, prospectiu i multicntric per avaluar lestratgia ms efica per detectar casos nous dhepatitis C (VHC). Estratgia 1: enviament de 5793 cartes explicatives amb una participaci del 4,1% i detecci dun cas, estratgia 2: distribuci de psters i dptics als centres datenci primria amb participaci de 0,3% i detecci dun cas i, estratgia 3: revisi de 480 pacients amb hipertransaminasmia sense determinaci VHC durant els darrers dos anys amb participaci del 100% i detecci de dos casos. Les estratgies 1 i 2 no sn eficaces per a la detecci del VHC ocult. Per contra, lestratgia tres s la ms efica.
Quan la carretera traeix el paisatge: La C-260 de Figueres a Roses, un exemple de banalitzaci i caos
Resumo:
Descripci i anlisi de levoluci del paisatge de lAlt Empord relacionada amb levoluci de la carretera C-260 de Figueres a Roses, ara convertida en autovia
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Geometries, vibrational frequencies, and interaction energies of the CNHO3 and HCCHO3 complexes are calculated in a counterpoise-corrected (CP-corrected) potential-energy surface (PES) that corrects for the basis set superposition error (BSSE). Ab initio calculations are performed at the Hartree-Fock (HF) and second-order Mller-Plesset (MP2) levels, using the 6-31G(d,p) and D95++(d,p) basis sets. Interaction energies are presented including corrections for zero-point vibrational energy (ZPVE) and thermal correction to enthalpy at 298 K. The CP-corrected and conventional PES are compared; the unconnected PES obtained using the larger basis set including diffuse functions exhibits a double well shape, whereas use of the 6-31G(d,p) basis set leads to a flat single-well profile. The CP-corrected PES has always a multiple-well shape. In particular, it is shown that the CP-corrected PES using the smaller basis set is qualitatively analogous to that obtained with the larger basis sets, so the CP method becomes useful to correctly describe large systems, where the use of small basis sets may be necessary
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Charge transfer properties of DNA depend strongly on the stack conformation. In the present paper, we identify conformations of homogeneous poly-{G}-poly-{C} stacks that should exhibit high charge mobility. Two different computational approaches were applied. First, we calculated the electronic coupling squared, V2, between adjacent base pairs for all 1 ps snapshots extracted from 15 ns molecular dynamics trajectory of the duplex G15. The average value of the coupling squared V2 is found to be 0.0065 eV2. Then we analyze the base-pair and step parameters of the configurations in which V2 is at least an order of magnitude larger than V2 . To obtain more consistent data, 65 000 configurations of the (G:C)2 stack were built using systematic screening of the step parameters shift, slide, and twist. We show that undertwisted structures (twist<20) are of special interest, because the stack conformations with strong electronic couplings are found for a wide range of slide and shift. Although effective hole transfer can also occur in configurations with twist=30 and 35, large mutual displacements of neighboring base pairs are required for that. Overtwisted conformation (twist38) seems to be of limited interest in the context of effective hole transfer. The results may be helpful in the search for DNA based elements for nanoelectronics
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El projecte de recerca ha analitzat la complexitat tnica, social i de gnere de lassentament colonial dEmpries a partir dun exhaustiu estudi contextual dels materials cermics ds quotidi provinents de diferents sectors excavats als anys vuitanta a la Nepolis empuritana (N-7000, N-5000 i N-1000). Aquests sectors datats els segles V i IV a.C., corresponen a un moment en el qual sest construint una identitat colonial diferenciada en lespai emporit. La comparaci dels aixovars domstics usats quotidianament pels habitants daquest tres sectors situats en punts distants de la Nepolis mostra que estem davant dun assentament colonial molt heterogeni, on conflueixen materialitats, tradicions tecnolgiques i prctiques quotidianes iberes, gregues i hbrides. Els estudis de materials confirmen que no va existir una segregaci espacial entre poblacions dorigen grec i iber en aquest assentament i suggereixen la cohabitaci de gent tant dhomes com de dones- dorigen grec i iber a les diferents rees estudiades daquest assentament portuari. En el registre material cermic de totes les zones estudiades sobserva un predomini dels productes cermics de tradici grega (colonials o tics) en els serveis de taula, per no aix en els estris utilitzats a la cuina, que sn majoritriament de tradici ibera. Tamb els materials cermics relacionats amb lemmagatzematge domstic i amb el transport i el comer (mfores) sn predominantment ibers. Aquest patr suggereix que els ibers que van cohabitar amb els grecs al port emporit no van assumir en tots els casos posicions subalternes, sin que tingueren un rol rellevant en la gesti econmica i comercial daquest espai portuari.
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Report for the scientific sojourn carried out at the Columbia University, United States, from 2010 to 2012. Expression of SoxB genes correlates with the commitment of cells to a neural fate; however, the relevance of SoxB proteins in early vertebrate neurogenesis has been difficult to prove genetically due to embryonic lethality and presumed redundant functions. The nematode C. Elegants has only 5 sox genes: sox-2 and sox-3 form the SoxB group while sem-2, sox-4 and egl-13 belong to other Sox groups. Our results show that sox-2 and sem-2 are the sox genes expressed earliest and in a broader manner during embryogenesis, being expressed in several neuronal progenitors. sox-3, sox-4 and egl-13 are expressed in few cells during late embryogenesis, when most neurons are already born. Both sox-2 and sem-2 null mutants are early larval lethal but do not show neuronal specification defects during embryonic development as indicated by quantification of a panneuronal reporter. Potential redundancy or compensatory mechanisms between different sox genes have been ruled out, strongly suggesting that sox genes are not required for specification of embryonically-derived neurons. However, at the first larval stage there are still several blast cells that will give rise to different postembryonic lineages, which generate several neurons amongst other cell types. nterestingly, sox-2 is expressed in many of these progenitor cells. Using mosaic analysis we have so far identified neurons derived from two different postembryonic lineages which fail to be generated in C. elegans sox-2 mutants. These results support the idea that postembryonic progenitor competence is compromised in the absence of sox-2.
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Background: Lynch syndrome (LS) is an autosomal dominant inherited cancer syndrome characterized by early onset cancers of the colorectum, endometrium and other tumours. A significant proportion of DNA variants in LS patients are unclassified. Reports on the pathogenicity of the c.1852_1853AA>GC (p.Lys618Ala) variant of the MLH1 gene are conflicting. In this study, we provide new evidence indicating that this variant has no significant implications for LS.Methods: The following approach was used to assess the clinical significance of the p.Lys618Ala variant: frequency in a control population, case-control comparison, co-occurrence of the p.Lys618Ala variant with a pathogenic mutation, co-segregation with the disease and microsatellite instability in tumours from carriers of the variant. We genotyped p.Lys618Ala in 1034 individuals (373 sporadic colorectal cancer [CRC] patients, 250 index subjects from families suspected of having LS [revised Bethesda guidelines] and 411 controls). Three well-characterized LS families that fulfilled the Amsterdam II Criteria and consisted of members with the p.Lys618Ala variant were included to assess co-occurrence and co-segregation. A subset of colorectal tumour DNA samples from 17 patients carrying the p.Lys618Ala variant was screened for microsatellite instability using five mononucleotide markers.Results: Twenty-seven individuals were heterozygous for the p.Lys618Ala variant; nine had sporadic CRC (2.41%), seven were suspected of having hereditary CRC (2.8%) and 11 were controls (2.68%). There were no significant associations in the case-control and case-case studies. The p.Lys618Ala variant was co-existent with pathogenic mutations in two unrelated LS families. In one family, the allele distribution of the pathogenic and unclassified variant was in trans, in the other family the pathogenic variant was detected in the MSH6 gene and only the deleterious variant co-segregated with the disease in both families. Only two positive cases of microsatellite instability (2/17, 11.8%) were detected in tumours from p.Lys618Ala carriers, indicating that this variant does not play a role in functional inactivation of MLH1 in CRC patients.Conclusions: The p.Lys618Ala variant should be considered a neutral variant for LS. These findings have implications for the clinical management of CRC probands and their relatives.
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Interaction between brain endocannabinoid (EC) and serotonin (5-HT) systems was investigated by examining 5-HT-dependent behavioural and biochemical responses in CB1 receptor knockout mice. CB1 knockout animals exhibited a significant reduction in the induction of head twitches and paw tremor by the 5-HT2A receptor selective agonist ()DOI, as well as a reduced hypothermic response following administration of the 5-HT1A receptor agonist ()-8-OH-DPAT. Additionally, exposure to the tail suspension test induced enhanced despair responses in CB1 knockout mice. However, the tricyclic antidepressant imipramine and the 5-HT selective reuptake inhibitor fluoxetine induced similar decreases in the time of immobility in the tail suspension test in CB1 receptor knockout and wild-type mice. No differences were found between both genotypes with regard to 5-HT2A receptor and 5-HT1A receptors levels, measured by autoradiography in different brain areas. However, a significant decrease in the ability of the 5-HT1A receptor agonist ()-8-OH-DPAT to stimulate 35SGTPS binding was detected in the hippocampal CA1 area of CB1 receptor knockout mice. This study provides evidence that CB1 receptors are involved in the regulation of serotonergic responses mediated by 5-HT2A and 5-HT1A receptors, and suggests that a reduced coupling of 5-HT1A receptors to Gi/o proteins in the hippocampus might be involved in these effects.
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Rat superior cervical ganglion (SCG) neurons express low-threshold noninactivating M-type potassium channels (I-K(M)), which can be inhibited by activation of M-1 muscarinic receptors (M-1 mAChR) and bradykinin (BK) B-2 receptors. Inhibition by the M1 mAChR agonist oxotremorine methiodide (Oxo-M) is mediated, at least in part, by the pertussis toxin-insensitive G-protein G alpha (q) (Caulfield et al., 1994; Haley et al., 1998a), whereas BK inhibition involves G alpha (q) and/or G alpha (11) (Jones et al., 1995). G alpha (q) and G alpha (11) can stimulate phospholipase C-beta (PLC-beta), raising the possibility that PLC is involved in I-K(M) inhibition by Oxo-M and BK. RT-PCR and antibody staining confirmed the presence of PLC-beta1, - beta2, - beta3, and - beta4 in rat SCG. We have tested the role of two PLC isoforms (PLC-beta1 and PLC-beta4) using antisense-expression constructs. Antisense constructs, consisting of the cytomegalovirus promoter driving antisense cRNA corresponding to the 3'-untranslated regions of PLC-beta1 and PLC-beta4, were injected into the nucleus of dissociated SCG neurons. Injected cells showed reduced antibody staining for the relevant PLC-beta isoform when compared to uninjected cells 48 hr later. BK inhibition of I-K(M) was significantly reduced 48 hr after injection of the PLC-beta4, but not the PLC-beta1, antisense-encoding plasmid. Neither PLC-beta antisense altered M-1 mAChR inhibition by Oxo-M. These data support the conclusion of Cruzblanca et al. (1998) that BK, but not M-1 mAChR, inhibition of I-K(M) involves PLC and extends this finding by indicating that PLC-beta4 is involved.
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Background: Germline genetic variation is associated with the differential expression of many human genes. The phenotypic effects of this type of variation may be important when considering susceptibility to common genetic diseases. Three regions at 8q24 have recently been identified to independently confer risk of prostate cancer. Variation at 8q24 has also recently been associated with risk of breast and colorectal cancer. However, none of the risk variants map at or relatively close to known genes, with c-MYC mapping a few hundred kilobases distally. Results: This study identifies cis-regulators of germline c-MYC expression in immortalized lymphocytes of HapMap individuals. Quantitative analysis of c-MYC expression in normal prostate tissues suggests an association between overexpression and variants in Region 1 of prostate cancer risk. Somatic c-MYC overexpression correlates with prostate cancer progression and more aggressive tumor forms, which was also a pathological variable associated with Region 1. Expression profiling analysis and modeling of transcriptional regulatory networks predicts a functional association between MYC and the prostate tumor suppressor KLF6. Analysis of MYC/Myc-driven cell transformation and tumorigenesis substantiates a model in which MYC overexpression promotes transformation by down-regulating KLF6. In this model, a feedback loop through E-cadherin down-regulation causes further transactivation of c-MYC.Conclusion: This study proposes that variation at putative 8q24 cis-regulator(s) of transcription can significantly alter germline c-MYC expression levels and, thus, contribute to prostate cancer susceptibility by down-regulating the prostate tumor suppressor KLF6 gene.
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Cont: Un da cualquiera de agosto; Hace diez aos, la URSS; Termina una vergenza de Europa; Del nacional arabismo al islamismo; El Imperio vuelve a tener enemigo; La cada del tirano; La Normanda a Iraq; Derrota y rehabilitacin de Europa; La gran metfora de la plaza Roja; Los derechos humanos y la realidad; El siglo de la guerra total (1); El siglo de la guerra total (y 2); Memoria del muro de Berln
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Un dels principals motius que ens va impulsar en lelecci del tema s que es tracta duntema que pot despertar curiositat entre la poblaci.Un altre motiu, es que varem trobar que est ntimament relacionat amb els estudis queestem cursant, donat que afecta als pressupostos de lestat i a la seva restriccipressupostria, i per tant, est directament relacionat amb la macroeconomia. En el nostrecas, reduirem lmbit destudi al territori catal, de manera que estudiarem aquestes duesmalalties dins la despesa en sanitat pblica catalana. A dems, estan finanades amb elsnostres impostos, i per tant la seva despesa afecta a la restricci pressupostria delsciutadans.Lelecci daquestes malalties no ha estat feta a latzar. Inicialment, varem pensar enestudiar els costos dels interns penitenciaris que patien aquestes malalties. Com que laSIDA i dhepatitis C sn les malalties ms freqents dins la pres, i les que tenen unscostos ms caracterstics donada la complexitat dels seus tractaments, varem pensar queserien prou representatives.No obstant, a mesura que ens anvem endinsant en el tema, ens varem adonar que tambseria molt interessant comparar el cost de les malalties amb el de les persones no recluses, iesbrinar si hi havia algun tipus de cost diferencial. s per aix que varem decidir analitzaraquestes dues malalties tant dins com fora.Un altre factor que ens ha impulsat en lelecci del tema s el fet que el nombre dinterns ales presons t un ritme de creixement constant que sha accelerat en els ltims anys,sobretot degut a laugment de la immigraci. Aix implica un augment progressiu de ladespesa, que es tradueix en una necessitat dingressos majors per tal de poder equilibrar larestricci de la qual parlvem abans.Tamb varem voler anar una mica ms lluny i analitzar el pes daquestes malalties dins dela despesa que la generalitat ha establert per a la sanitat pblica. Com les dues son MDO (malalties de declaraci obligatria ) estan finanades completament pel sector pblic.Lobjectiu era veure si representaven un cost tant elevat com pensvem.OBJECTIUS DEL TREBALL: Demostrar lelevat cost que suposen certes malalties per lestat. Manifestar els canvis en el cost de les malalties amb levoluci delstractaments. Analitzar els costos sanitaris extres que es produeixen a les presons. Destacar laugment accelerat del nombre dinterns i laugment del cost sanitarique aix suposa. METODOLOGIA: Per tal de poder realitzar lestudi comparatiu, hem hagut de calcular manualment els costosde les malalties, tot informant-nos del preu dels medicament, les dosis, el cost de lesconsultes externes,etc. A ms, per a calcular el cost del tractament dins la pres, ens hemhagut dinformar dels aspectes ms generals que envolten a un pres, per poder veure sirealment existeix un cost diferencial respecte la malaltia a lexterior. Per obtenir aquestesdiverses informacions, ens hem hagut de posar en contacte amb el personal que treballa ala pres que hem pres com a model destudi.Aix, podem dividir les nostres fonts dinformaci en 3 categories: Obtenci dinformaci directament amb el personal de la pres: Entrevista amb la directora dinfermeria de la Secretaria de ServeisPenitenciaris, Rehabilitaci i Justcia Juvenil Entrevista amb la Cap dinfermeria del Centre Quatre Camins. Informaci a partir de mostres facilitades pels propis funcionaris de la pres Informaci a partir destudis sobre el tema i de dades oficials, concretament lesdades oficials sobre els Pressupostos de la Generalitat.
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La adherencia al tratamiento antiviral de la hepatitis crnica C (HCC) es una variable importante en la obtencin de la respuesta viral sostenida (RVS). El objetivo de este trabajo es evaluar el impacto de un programa de atencin multidisciplinar (PAM) en la adherencia y eficacia del tratamiento de la HCC. Se incluyeron 447 pacientes tratados con peginterfern-alfa-2a y ribavirina y se clasificaron en tres grupos: grupo control (2003-2004, n=147), grupo PAM (2005-2006, n=131) y grupo Validacin-PAM (2007-2009, n=169). La adherencia y los porcentajes de RVS fueron superiores en los pacientes incluidos en los grupos PAM (94.6% y 77.1%) y Validacin-PAM (91.7% y 74.6%) en comparacin con el grupo control (78.9% y 61.9%) (p<0.05 para todos los casos).