31 research outputs found
Spéciation chimique et immunotoxicologie du béryllium : effets thérapeutiques des agents complexants NTA, NTP et tiron
Thèse numérisée par la Division de la gestion de documents et des archives de l'Université de Montréal
Anion vacancies as a source of persistent photoconductivity in II-VI and chalcopyrite semiconductors
Using first-principles electronic structure calculations we identify the
anion vacancies in II-VI and chalcopyrite Cu-III-VI2 semiconductors as a class
of intrinsic defects that can exhibit metastable behavior. Specifically, we
predict persistent electron photoconductivity (n-type PPC) caused by the oxygen
vacancy VO in n-ZnO, and persistent hole photoconductivity (p-type PPC) caused
by the Se vacancy VSe in p-CuInSe2 and p-CuGaSe2. We find that VSe in the
chalcopyrite materials is amphoteric having two "negative-U" like transitions,
i.e. a double-donor transition e(2+/0) close to the valence band and a
double-acceptor transition e(0/2-) closer to the conduction band. We introduce
a classification scheme that distinguishes two types of defects (e.g., donors):
type-alpha, which have a defect-localized-state (DLS) in the gap, and
type-beta, which have a resonant DLS within the host bands (e.g., conduction
band). In the latter case, the introduced carriers (e.g., electrons) relax to
the band edge where they can occupy a perturbed-host-state (PHS). Type alpha is
non-conducting, whereas type beta is conducting. We identify the neutral anion
vacancy as type-alpha and the doubly positively charged vacancy as type-beta.
We suggest that illumination changes the charge state of the anion vacancy and
leads to a crossover between alpha- and beta-type behavior, resulting in
metastability and PPC. In CuInSe2, the metastable behavior of VSe is carried
over to the (VSe-VCu) complex, which we identify as the physical origin of PPC
observed experimentally. We explain previous puzzling experimental results in
ZnO and CuInSe2 in the light of this model.Comment: submitted to Phys. Rev.
Gramática movimientista y asistencia: el pueblo, los pobres y los derechos : El caso del Movimiento Evita durante el kirchnerismo en el Gran La Plata
En el escenario de recomposición del sistema político post crisis del año 2001 en Argentina y sus vínculos con las organizaciones se puede plantear un resurgimiento de la denominada gramática movimientista, dentro de la cual se puede ubicar a organizaciones como el Movimiento Evita.
El presente trabajo se ocupa de estudiar y analizar las prácticas de asistencia de esta organización durante el periodo 2008-2014, entendiendo a la “asistencia social” como disposiciones, dispositivos, prácticas de atención a aquellos definidos socialmente como pobres. Y entendiendo por “gramática” un juego de reglas no escritas que delimita, por un lado, las pautas de interacción de los sujetos; y por otro, las combinaciones de acciones para coordinar, articular e impulsar intervenciones públicas, acciones que se dirijan a cuestionar, transformar o ratificar el orden social. (Natalucci, 2010). A su vez, se entiende a la noción de gramática como producción de algún orden. En este sentido, la gramática estructura las prácticas, y para el caso de la “movimientista” esta última rememora la gramática de integración de los sectores populares o del pueblo argentino a la disputa política nacional de la mano de las experiencias peronistas en nuestro país.
El período seleccionado para la presente indagación recorre el periodo 2008-2014, años que atraviesan los dos últimos gobiernos del denominado “kirchnerismo” en nuestro país, más específicamente los mandatos de la Dra. Cristina Fernández de Kirchner (2008-2011/2011-2014) que se caracterizan por algunas políticas notorias como la denominada Asignación Universal Por Hijo (AUH) que ejemplifican un cambio de modelo en relación a la “asistencia” y la forma de concebir a los pobres y a la pobreza.
Desde esta perspectiva, el denominado “kirchnerismo” contiene o desarrolla una performatividad política que apela a la construcción de un programa de gobierno y a una convocatoria política a diversos actores sociales a integrarlo, que se sustenta en un ideario y en una Gramática con evocaciones profundas en las tradiciones nacional-populares del pueblo argentino. Es decir, se considera que no hubo campo social movilizado (ni sindical, ni piquetero, ni de derechos humanos, etc.) que no haya sido atravesado y reconfigurado a partir de la experiencia kirchnerista. Es en esta atmósfera en la cual resulta de interés progresar en el análisis de la naturaleza de los vínculos entre la dinámica de un proceso de transformaciones en el período post 2003 al calor del kirchnerismo y las organizaciones, en especial en las modificaciones en sus prácticas cotidianas, en este caso de Asistencia. Resulta de interés en este punto reponer el concepto de gramática porque como se viene planteando, se entiende como un sistema de reglas de acción que ligan el tiempo y espacio de la experiencia de los sujetos, definiendo formas de resolver problemas. En definitiva, esta noción alude a reglas y usos que dotan de un principio de inteligibilidad a las acciones y prácticas sociales de las organizaciones.Facultad de Trabajo Socia
Study on the effects of nitrilotriproprionic acid and 4,5-dihydroxy-1,3-benzene disulphonate on the fractionation of beryllium in human serum using graphite furnace atomic absorption spectrometry
<p>Abstract</p> <p>Background</p> <p>Occupational exposure to beryllium may cause Chronic Beryllium Disease (CBD), a lung disorder initiated by an electrostatic interaction with the MHC class II human leukocyte antigen (HLA). Molecular studies have found a significant correlation between the electrostatic potential at the HLA-DP surface and disease susceptibility. CBD can therefore be treated by chelation therapy. In this work, we studied the effect of two complexing agents, nitrilotriproprionic acid (NTP) and 4,5-dihydroxy-1,3-benzene disulphonate (Tiron), on the fractionation of beryllium in human serum analysed by graphite furnace atomic absorption spectrometry (GFAAS).</p> <p>Results</p> <p>We found the average serum beryllium concentration of fourteen non-exposed individuals to be 0.53 (± 0.14) μg l<sup>-1</sup>, with 21 (± 3)% of the beryllium mass bound to the low molecular weight fraction (LMW), and 79 (± 3)% bound to the high molecular weight fraction (HMW). The addition of Tiron increased the beryllium mass in the HMW fraction, while NTP was not seen to have any influence on the fractionation of beryllium between the two fractions. NTP was, however, shown to complex 94.5% of the Be mass in the LMW fraction. The beryllium GFAAS detection limit, calculated as three times the standard deviation of 10 replicates of the lowest standard (0.05 μg L<sup>-1</sup>), was 6.0 (± 0.2) ng L<sup>-1</sup>.</p> <p>Conclusion</p> <p>The concentration of beryllium or its fractionation in human serum was not affected by sex or smoking habit. On average, three quarters of the beryllium in serum were found in the HMW fraction. Of the two ligands tested, only Tiron was effective in mobilising beryllium under physiological conditions, thus increasing the Be content in the HMW fraction.</p
Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk
Correction to: Nature Geneticshttps://doi.org/10.1038/s41588-023-01314-0, published online 13 March 2023. In the version of the article initially published, the sample sizes in the main text and Supplementary Tables 1 and 2 were incorrect. In the abstract, the last paragraph of the Introduction, the first paragraph of the Results, the top box in Figure 1a and the Supplementary Information, the total sample size has been corrected from 580,869 to 588,452 participants and the size of the European cohort from 468,062 to 475,645. Some of the effect sizes in Supplementary Table 14 (columns W, Z, AC, AF) had the wrong sign. There was also an error in Supplementary Table 3 where the sample size instead of the variant count was shown for EXCEED. The errors do not affect the conclusions of the study. Additionally, two acknowledgments for use of INTERVAL pQTL and Lung eQTL consortium data were omitted from the Supplementary Information. These errors have been corrected in the Supplementary Information and HTML and PDF versions of the article
Exome-wide association study to identify rare variants influencing COVID-19 outcomes : Results from the Host Genetics Initiative
Publisher Copyright: Copyright: © 2022 Butler-Laporte et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Host genetics is a key determinant of COVID-19 outcomes. Previously, the COVID-19 Host Genetics Initiative genome-wide association study used common variants to identify multiple loci associated with COVID-19 outcomes. However, variants with the largest impact on COVID-19 outcomes are expected to be rare in the population. Hence, studying rare variants may provide additional insights into disease susceptibility and pathogenesis, thereby informing therapeutics development. Here, we combined whole-exome and whole-genome sequencing from 21 cohorts across 12 countries and performed rare variant exome-wide burden analyses for COVID-19 outcomes. In an analysis of 5,085 severe disease cases and 571,737 controls, we observed that carrying a rare deleterious variant in the SARS-CoV-2 sensor toll-like receptor TLR7 (on chromosome X) was associated with a 5.3-fold increase in severe disease (95% CI: 2.75–10.05, p = 5.41x10-7). This association was consistent across sexes. These results further support TLR7 as a genetic determinant of severe disease and suggest that larger studies on rare variants influencing COVID-19 outcomes could provide additional insights.Peer reviewe
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity
The combined impact of common and rare exonic variants in COVID-19 host genetics is currently insufficiently understood. Here, common and rare variants from whole-exome sequencing data of about 4000 SARS-CoV-2-positive individuals were used to define an interpretable machine-learning model for predicting COVID-19 severity. First, variants were converted into separate sets of Boolean features, depending on the absence or the presence of variants in each gene. An ensemble of LASSO logistic regression models was used to identify the most informative Boolean features with respect to the genetic bases of severity. The Boolean features selected by these logistic models were combined into an Integrated PolyGenic Score that offers a synthetic and interpretable index for describing the contribution of host genetics in COVID-19 severity, as demonstrated through testing in several independent cohorts. Selected features belong to ultra-rare, rare, low-frequency, and common variants, including those in linkage disequilibrium with known GWAS loci. Noteworthily, around one quarter of the selected genes are sex-specific. Pathway analysis of the selected genes associated with COVID-19 severity reflected the multi-organ nature of the disease. The proposed model might provide useful information for developing diagnostics and therapeutics, while also being able to guide bedside disease management. © 2021, The Author(s)
Burnout among surgeons before and during the SARS-CoV-2 pandemic: an international survey
Background: SARS-CoV-2 pandemic has had many significant impacts within the surgical realm, and surgeons have been obligated to reconsider almost every aspect of daily clinical practice. Methods: This is a cross-sectional study reported in compliance with the CHERRIES guidelines and conducted through an online platform from June 14th to July 15th, 2020. The primary outcome was the burden of burnout during the pandemic indicated by the validated Shirom-Melamed Burnout Measure. Results: Nine hundred fifty-four surgeons completed the survey. The median length of practice was 10 years; 78.2% included were male with a median age of 37 years old, 39.5% were consultants, 68.9% were general surgeons, and 55.7% were affiliated with an academic institution. Overall, there was a significant increase in the mean burnout score during the pandemic; longer years of practice and older age were significantly associated with less burnout. There were significant reductions in the median number of outpatient visits, operated cases, on-call hours, emergency visits, and research work, so, 48.2% of respondents felt that the training resources were insufficient. The majority (81.3%) of respondents reported that their hospitals were included in the management of COVID-19, 66.5% felt their roles had been minimized; 41% were asked to assist in non-surgical medical practices, and 37.6% of respondents were included in COVID-19 management. Conclusions: There was a significant burnout among trainees. Almost all aspects of clinical and research activities were affected with a significant reduction in the volume of research, outpatient clinic visits, surgical procedures, on-call hours, and emergency cases hindering the training. Trial registration: The study was registered on clicaltrials.gov "NCT04433286" on 16/06/2020