Osteosclerosis in the extinct Cayaoa Bruneti (Aves, anseriformes) : insights on behavior and fligftlessness

Fil: Mendoza, Ricardo de. División Paleontología Vertebrados. Facultad de Ciencias Naturales y Museo. Universidad Nacional de La PlataFil: Tambussi, Claudia Patricia. Centro de Investigaciones en Ciencias de la Tierra (CICTERRA). Universidad Nacional de Córdoba; Argentin

VLT FORS2 optical imaging and spectroscopy of nine luminous type 2 AGN at 0.3 < z < 0.6-I. Ionized gas nebulae

We present optical imaging and long slit spectroscopic observations of nine luminous type 2 active galactic nuclei (AGN) within the redshift range 0.3 <z< 0.6 based on Very Large Telescope Focal Reducer and Low Dispersion Spectrograph (VLT FORS2) data. Most objects (6/9) are high luminosity Seyfert 2, and three are type 2 quasars (QSO2), with our sample extending to lower luminosity than previous works. Seven out of nine objects (78 per cent) show morphological evidence for interactions or mergers in the form of disturbed morphologies and/or peculiar features such as tidal tails, amorphous haloes, or compact emission line knots. The detection rate of morphological evidence for interaction is consistent with those found during previous studies of QSO2 at similar z, suggesting that the merger rate is independent of AGN power at the high end of the AGN luminosity function. We find the emission line flux spatial profiles are often dominated by the often spatially unresolved central source. In addition, all but one of our samples is associated with much fainter, extended line emission. We find these extended emission line structures have a variety of origins and ionization mechanisms: star-forming companions, tidal features, or extended ionized nebulae. AGN related processes dominate the excitation of the nuclear gas. Stellar photoionization sometimes plays a role in extended structures often related to mergers/interactions

New insights into the genetic etiology of Alzheimer's disease and related dementias.

Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele

New insights into the genetic etiology of Alzheimer's disease and related dementias

Characterization of the genetic landscape of Alzheimer's disease (AD) and related dementias (ADD) provides a unique opportunity for a better understanding of the associated pathophysiological processes. We performed a two-stage genome-wide association study totaling 111,326 clinically diagnosed/'proxy' AD cases and 677,663 controls. We found 75 risk loci, of which 42 were new at the time of analysis. Pathway enrichment analyses confirmed the involvement of amyloid/tau pathways and highlighted microglia implication. Gene prioritization in the new loci identified 31 genes that were suggestive of new genetically associated processes, including the tumor necrosis factor alpha pathway through the linear ubiquitin chain assembly complex. We also built a new genetic risk score associated with the risk of future AD/dementia or progression from mild cognitive impairment to AD/dementia. The improvement in prediction led to a 1.6- to 1.9-fold increase in AD risk from the lowest to the highest decile, in addition to effects of age and the APOE ε4 allele

Factors Associated with Revision Surgery after Internal Fixation of Hip Fractures

Background: Femoral neck fractures are associated with high rates of revision surgery after management with internal fixation. Using data from the Fixation using Alternative Implants for the Treatment of Hip fractures (FAITH) trial evaluating methods of internal fixation in patients with femoral neck fractures, we investigated associations between baseline and surgical factors and the need for revision surgery to promote healing, relieve pain, treat infection or improve function over 24 months postsurgery. Additionally, we investigated factors associated with (1) hardware removal and (2) implant exchange from cancellous screws (CS) or sliding hip screw (SHS) to total hip arthroplasty, hemiarthroplasty, or another internal fixation device. Methods: We identified 15 potential factors a priori that may be associated with revision surgery, 7 with hardware removal, and 14 with implant exchange. We used multivariable Cox proportional hazards analyses in our investigation. Results: Factors associated with increased risk of revision surgery included: female sex, [hazard ratio (HR) 1.79, 95% confidence interval (CI) 1.25-2.50; P = 0.001], higher body mass index (fo