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A secondary goal is to investigate how demographic, genetic, clinical, psychological, and environmental factors affect these associations. In this review, we summarize findings of the ENIGMA MDD disease working group to date and discuss future directions. We also highlight the challenges and benefits of large-scale data sharing for mental health research.An amendment to this paper has been published and can be accessed via a link at the top of the paper.Cesium-137 is one of the most abundant anthropogenic radionuclides released by atmospheric nuclear testing and nuclear accidents, and accordingly it may significantly impact the health of humans and marine environmental eco-systems. Documenting the distribution and inventory of 137Cs is thus a crucial task. In this study, we collected a large number of datasets with field observations of 137Cs in the China Seas, in order to provide an in-depth understanding of 137Cs budgets and distributions. The activity and inventory of 137Cs in China Seas' sediments showed large spatial variations, related to the 137Cs source, sedimentation rates and the mineral composition of sediments. The 137Cs concentration in sediments decreased with distance from the shore, generally tracing the distribution of sedimentation rates. High 137Cs inventories in the water column indicated a high solubility and long mean residence times. The mean residence times of 137Cs in the China Seas were determined to be 45.6 ± 3.8 years for the South China Sea (SCS), 36.8 ± 3.1 years for the East China Sea (ECS), and 12.0 ± 1.0 years for the Yellow Sea (YS). A 137Cs mass balance suggests that oceanic input from the north Pacific is the dominant 137Cs source to the China Seas, contributing about 96.9% of this substance. Furthermore, the bulk of 137Cs remains dissolved in the SCS water column, while 137Cs is mostly deposited to the sediments of the ECS and the YS. This new compilation of the activity level and inventory of 137Cs help to establish background levels for future 137Cs studies in the China Seas.We examined the effect of aging on the integration of position and motion signals, which is essential for tracking visual objects, using the motion-induced position shift (MIPS) phenomenon. We first measured the MIPS and bias in speed perception at three eccentricities. Both young and older adults showed the increasing MIPS and decreasing perceived speed as the eccentricity increased, which is consistent with previous literature. More importantly, we found that the mean MIPS was 2.87 times larger in older adults, and the response variability in position tasks showed a larger difference between age groups compared with the difference in speed tasks. We then measured the MIPS across stimulus durations. Temporal changes in the MIPS showed similar patterns in young and older adults in that the MIPS initially peaked at around 60 ms and approached an asymptote. We further analyzed the changes in response variability across stimulus durations to estimate sensory noise and propagation noise separately and found that only sensory noise was significantly larger in older adults. The overall results suggest that the increased MIPS in older adults is due to the increased dependency on predictive motion signals to compensate for the relatively imprecise position signals, which in turn implies that older adults would depend more on the motion signals to track objects.Novel compact x-ray sources based on inverse Compton scattering can generate brilliant hard x-rays in a laboratory setting. Their collimated intense beams with tunable well-defined x-ray energies make them well suited for x-ray spectroscopy techniques, which are typically carried out at large facilities. Here, we demonstrate a first x-ray absorption spectroscopy proof-of-principle experiment using an inverse Compton x-ray source with a flux of >1010 photons/s in less then 5% bandwidth. We measured x-ray absorption near edge structure and extended x-ray absorption fine structure at the silver K-edge (~25.5 keV) for a series of silver samples. We propose an energy-dispersive geometry specifically adapted to the x-ray beam properties of inverse Compton x-ray sources together with a fast concentration correction method that corrects sample inhomogeneities very effectively. The combination of our setup with the inverse Compton source generates x-ray absorption spectra with high energy resolution in exposure times down to one minute. Our results unravel the great benefit of inverse Compton scattering sources for x-ray absorption techniques in a laboratory environment, especially in the hard x-ray regime, which allows to probe absorption edges of high Z materials.Cardiac tissue engineering is a promising approach to treat cardiovascular diseases, which are a major socio-economic burden worldwide. An optimal material for cardiac tissue engineering, allowing cardiomyocyte attachment and exhibiting proper immunocompatibility, biocompatibility and mechanical characteristics, has not yet emerged. An additional challenge is to develop a fabrication method that enables the generation of proper hierarchical structures and constructs with a high density of cardiomyocytes for optimal contractility. Thus, there is a focus on identifying suitable materials for cardiac tissue engineering. Here, we investigated the interaction of neonatal rat heart cells with engineered spider silk protein (eADF4(C16)) tagged with the tripeptide arginyl-glycyl-aspartic acid cell adhesion motif RGD, which can be used as coating, but can also be 3D printed. check details Cardiomyocytes, fibroblasts, and endothelial cells attached well to eADF4(C16)-RGD coatings, which did not induce hypertrophy in cardiomyocytes, but allowed response to hypertrophic as well as proliferative stimuli. Furthermore, Kymograph and MUSCLEMOTION analyses showed proper cardiomyocyte beating characteristics on spider silk coatings, and cardiomyocytes formed compact cell aggregates, exhibiting markedly higher speed of contraction than cardiomyocyte mono-layers on fibronectin. The results suggest that eADF4(C16)-RGD is a promising material for cardiac tissue engineering.

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