1,943 research outputs found
Anodization of titanium implants in order to improve chemical degradation resistance
El objetivo de este trabajo de investigación es la obtención de una capa de anodizado, que sea homogénea en toda la superficie del implante de titanio. Esta capa de óxido de titanio tendrá unas propiedades beneficiosas para el implante dental como son:
1. Limpieza de residuos tanto orgánicos como inorgánicos de la superficie del implante.
2. Mejora de la resistencia a la corrosión del implante.
3. Disminución de la liberación de iones del titanio al medio fisiológico.
4. Aumento de la dureza superficial así como de la resistencia al desgaste.Peer Reviewe
Evaluación de la rigidez de diferentes fijadores externos
Se ha estudiado la rigidez a compresión, flexión en 3 puntos y torsión de fijadores del tipo Orthofix, Wagner y Hoffmann doble marco con diferentes distancias del clavo al foco de fractura. Se han comparado los resultados que permitirán realizar en la práctica clínica montajes con las carcaterísticas de regidez deseables.Peer Reviewe
Hypothesizing hybrids and parents using character intermediacy, parental distance, and equality
Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/149771/1/tax05097.pd
Factors associated with the appropriate use of preoperatory hospital stays: historical cohort study
A First Search for coincident Gravitational Waves and High Energy Neutrinos using LIGO, Virgo and ANTARES data from 2007
We present the results of the first search for gravitational wave bursts
associated with high energy neutrinos. Together, these messengers could reveal
new, hidden sources that are not observed by conventional photon astronomy,
particularly at high energy. Our search uses neutrinos detected by the
underwater neutrino telescope ANTARES in its 5 line configuration during the
period January - September 2007, which coincided with the fifth and first
science runs of LIGO and Virgo, respectively. The LIGO-Virgo data were analysed
for candidate gravitational-wave signals coincident in time and direction with
the neutrino events. No significant coincident events were observed. We place
limits on the density of joint high energy neutrino - gravitational wave
emission events in the local universe, and compare them with densities of
merger and core-collapse events.Comment: 19 pages, 8 figures, science summary page at
http://www.ligo.org/science/Publication-S5LV_ANTARES/index.php. Public access
area to figures, tables at
https://dcc.ligo.org/cgi-bin/DocDB/ShowDocument?docid=p120000
Palbociclib in combination with endocrine therapy versus capecitabine in hormonal receptor-positive, human epidermal growth factor 2-negative, aromatase inhibitor-resistant metastatic breast cancer: a phase III randomised controlled trial—PEARL
Background: Palbociclib plus endocrine therapy (ET) is the standard treatment of hormone receptor-positive and human epidermal growth factor receptor 2-negative, metastatic breast cancer (MBC). However, its efficacy has not been compared with that of chemotherapy in a phase III trial. Patients and methods: PEARL is a multicentre, phase III randomised study in which patients with aromatase inhibitor (AI)-resistant MBC were included in two consecutive cohorts. In cohort 1, patients were randomised 1 : 1 to palbociclib plus exemestane or capecitabine. On discovering new evidence about estrogen receptor-1 (ESR1) mutations inducing resistance to AIs, the trial was amended to include cohort 2, in which patients were randomised 1 : 1 between palbociclib plus fulvestrant and capecitabine. The stratification criteria were disease site, prior sensitivity to ET, prior chemotherapy for MBC, and country of origin. Co-primary endpoints were progression-free survival (PFS) in cohort 2 and in wild-type ESR1 patients (cohort 1 + cohort 2). ESR1 hotspot mutations were analysed in baseline circulating tumour DNA. Results: From March 2014 to July 2018, 296 and 305 patients were included in cohort 1 and cohort 2, respectively. Palbociclib plus ET was not superior to capecitabine in both cohort 2 [median PFS: 7.5 versus 10.0 months; adjusted hazard ratio (aHR): 1.13; 95% confidence interval (CI): 0.85-1.50] and wild-type ESR1 patients (median PFS: 8.0 versus 10.6 months; aHR: 1.11; 95% CI: 0.87-1.41). The most frequent grade 3-4 toxicities with palbociclib plus exemestane, palbociclib plus fulvestrant and capecitabine, respectively, were neutropenia (57.4%, 55.7% and 5.5%), hand/foot syndrome (0%, 0% and 23.5%), and diarrhoea (1.3%, 1.3% and 7.6%). Palbociclib plus ET offered better quality of life (aHR for time to deterioration of global health status: 0.67; 95% CI: 0.53-0.85). Conclusions: There was no statistical superiority of palbociclib plus ET over capecitabine with respect to PFS in MBC patients resistant to AIs. Palbociclib plus ET showed a better safety profile and improved quality of life
Probing the earliest phases in the formation of massive galaxies with simulated HST+JWST imaging data from Illustris
We use the Illustris-1 simulation to explore the capabilities of the
and data to analyze the
stellar populations in high-redshift galaxies, taking advantage of the combined
depth, spatial resolution, and wavelength coverage. For that purpose, we use
simulated broad-band ACS, WFC3 and NIRCam data and 2-dimensional stellar
population synthesis (2D-SPS) to derive the integrated star formation history
(SFH) of massive (MM) simulated galaxies at
M galaxy. In
particular, we explore the potential of HST and JWST datasets reaching a depth
similar to those of the CANDELS and ongoing CEERS observations, respectively,
and concentrate on determining the capabilities of this dataset for
characterizing the first episodes in the SFH of local
MM galaxies by studying their progenitors at
. The 2D-SPS method presented in this paper has been calibrated to
robustly recover the cosmic times when the first star formation episodes
occurred in massive galaxies, i.e., the first stages in their integrated SFHs.
In particular, we discuss the times when the first 1% to 50% of their total
stellar mass formed in the simulation. We demonstrate that we can recover these
ages with typical median systematic offset of less than 5% and scatter around
20%-30%. According to our measurements on Illustris data, we are able to
recover that local MM galaxies would have started
their formation by , forming the first 5% of their stellar mass present
at by , 10% by , and 25% by .Comment: 28 pages, 13 figures, 4 tables. ApJ in press. Summary of changes from
original submission: the major change is that we now include in Sec. 6 the
comparison of the results obtained for our sample of massive 1 < z < 4
progenitors with those obtained by considering all massive galaxies at 1 < z
< 4 in the simulated images. Several figures and sections have been update
RNAcentral 2021: secondary structure integration, improved sequence search and new member databases
RNAcentral is a comprehensive database of non-coding RNA (ncRNA) sequences that provides a single access point to 44 RNA resources and >18 million ncRNA sequences from a wide range of organisms and RNA types. RNAcentral now also includes secondary (2D) structure information for >13 million sequences, making RNAcentral the world's largest RNA 2D structure database. The 2D diagrams are displayed using R2DT, a new 2D structure visualization method that uses consistent, reproducible and recognizable layouts for related RNAs. The sequence similarity search has been updated with a faster interface featuring facets for filtering search results by RNA type, organism, source database or any keyword. This sequence search tool is available as a reusable web component, and has been integrated into several RNAcentral member databases, including Rfam, miRBase and snoDB. To allow for a more fine-grained assignment of RNA types and subtypes, all RNAcentral sequences have been annotated with Sequence Ontology terms. The RNAcentral database continues to grow and provide a central data resource for the RNA community
RNAcentral 2021: secondary structure integration, improved sequence search and new member databases.
RNAcentral is a comprehensive database of non-coding RNA (ncRNA) sequences that provides a single access point to 44 RNA resources and >18 million ncRNA sequences from a wide range of organisms and RNA types. RNAcentral now also includes secondary (2D) structure information for >13 million sequences, making RNAcentral the world's largest RNA 2D structure database. The 2D diagrams are displayed using R2DT, a new 2D structure visualization method that uses consistent, reproducible and recognizable layouts for related RNAs. The sequence similarity search has been updated with a faster interface featuring facets for filtering search results by RNA type, organism, source database or any keyword. This sequence search tool is available as a reusable web component, and has been integrated into several RNAcentral member databases, including Rfam, miRBase and snoDB. To allow for a more fine-grained assignment of RNA types and subtypes, all RNAcentral sequences have been annotated with Sequence Ontology terms. The RNAcentral database continues to grow and provide a central data resource for the RNA community. RNAcentral is freely available at https://rnacentral.org
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