43 research outputs found

    Pabellón de Ventas y Gestión

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    La luz es color. El movimiento perceptual se fomenta, principalmente, con la forma, el ritmo y el color

    Red de coordinación de contenidos de la asignatura Proyecto de Ejecución de quinto curso de Grado en Arquitectura

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    El interés de la investigación se centra en coordinar los contenidos de la asignatura del último curso de grado en Arquitectura como continuidad de la Red 3020 realizada el curso pasado. Esta asignatura aglutina en un proyecto de ejecución todo el conocimiento adquirido. El estudio de la asignatura del primer semestre de 5º servirá para encontrar problemas y ubicar soluciones en los cursos anteriores para optimizar la docencia y analizar los contenidos de toda el área de Construcción. Se pretende el estudio crítico de la planificación de tareas y criterios que se han llevado a cabo para mejorar de cara al curso siguiente. Al ser la primera vez que se ha implantado 5º en Grado de Arquitectura se han presentado muchas novedades en los protocolos de docencia de esta asignatura. En algunas clases hemos llegado a tener a seis críticos invitados junto a los 4 docentes para un total de 90 alumnos. Cada equipo de 4 alumnos recibía tres correcciones en un mismo día. Cada semana se han pasado encuestas a los estudiantes y se ha hecho un seguimiento pormenorizado de todo. El estudio de la coordinación realizada permite hacer una valoración y proponer mejoras para el curso que viene

    Detection of kinase domain mutations in BCR::ABL1 leukemia by ultra-deep sequencing of genomic DNA

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    The screening of the BCR::ABL1 kinase domain (KD) mutation has become a routine analysis in case of warning/failure for chronic myeloid leukemia (CML) and B-cell precursor acute lymphoblastic leukemia (ALL) Philadelphia (Ph)-positive patients. In this study, we present a novel DNA-based next-generation sequencing (NGS) methodology for KD ABL1 mutation detection and monitoring with a 1.0E−4 sensitivity. This approach was validated with a well-stablished RNA-based nested NGS method. The correlation of both techniques for the quantification of ABL1 mutations was high (Pearson r = 0.858, p < 0.001), offering DNA-DeepNGS a sensitivity of 92% and specificity of 82%. The clinical impact was studied in a cohort of 129 patients (n = 67 for CML and n = 62 for B-ALL patients). A total of 162 samples (n = 86 CML and n = 76 B-ALL) were studied. Of them, 27 out of 86 harbored mutations (6 in warning and 21 in failure) for CML, and 13 out of 76 (2 diagnostic and 11 relapse samples) did in B-ALL patients. In addition, in four cases were detected mutation despite BCR::ABL1 < 1%. In conclusion, we were able to detect KD ABL1 mutations with a 1.0E−4 sensitivity by NGS using DNA as starting material even in patients with low levels of disease.Tis project was funded in part by CRIS CANCER FOUNDATION

    Clonal chromosomal mosaicism and loss of chromosome Y in elderly men increase vulnerability for SARS-CoV-2

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    The pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2, COVID-19) had an estimated overall case fatality ratio of 1.38% (pre-vaccination), being 53% higher in males and increasing exponentially with age. Among 9578 individuals diagnosed with COVID-19 in the SCOURGE study, we found 133 cases (1.42%) with detectable clonal mosaicism for chromosome alterations (mCA) and 226 males (5.08%) with acquired loss of chromosome Y (LOY). Individuals with clonal mosaic events (mCA and/or LOY) showed a 54% increase in the risk of COVID-19 lethality. LOY is associated with transcriptomic biomarkers of immune dysfunction, pro-coagulation activity and cardiovascular risk. Interferon-induced genes involved in the initial immune response to SARS-CoV-2 are also down-regulated in LOY. Thus, mCA and LOY underlie at least part of the sex-biased severity and mortality of COVID-19 in aging patients. Given its potential therapeutic and prognostic relevance, evaluation of clonal mosaicism should be implemented as biomarker of COVID-19 severity in elderly people. Among 9578 individuals diagnosed with COVID-19 in the SCOURGE study, individuals with clonal mosaic events (clonal mosaicism for chromosome alterations and/or loss of chromosome Y) showed an increased risk of COVID-19 lethality
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