ASPECTS REGARDING THE APPEARANCE AND THE EVOLUTION OF KEYNESIAN DOCTRINE

This present paper is based on the importance of the keynesian doctrine in time and tries to make a brief foray into the life and work of John Maynard Keynes, revealing important aspects related to the new concepts this doctrine brought in the history of economic thought, looking at the same time to the criticism addressed to the keynesism and studying the effects they had in the development study of economic science. The objective of this theory is “the analysis of the mechanism of the market economy in order to ensure sustainable development, reducing or eliminating the disequilibrium, when it is not verified in practice the idea of the self equilibrium through the price mechanism."Keynes wrote in an era marked by mass unemployment, by degradation and suffering at an incredible level. A reasonable person could have supported the failure of capitalism, concluding that only major institutional changes - perhaps nationalization of means of production - could restore economic health

Lower Spectral Branches of a Particle Coupled to a Bose Field

The structure of the lower part (i.e. $\epsilon$-away below the two-boson threshold) spectrum of Fr\"ohlich's polaron Hamiltonian in the weak coupling regime is obtained in spatial dimension $d\geq 3$. It contains a single polaron branch defined for total momentum $p\in G^{(0)}$, where $G^{(0)}\subset {\mathbb R}^d$ is a bounded domain, and, for any $p\in {\mathbb R}^d$, a manifold of polaron + one-boson states with boson momentum $q$ in a bounded domain depending on $p$. The polaron becomes unstable and dissolves into the one boson manifold at the boundary of $G^{(0)}$. The dispersion laws and generalized eigenfunctions are calculated

Imputing Gene Expression in Uncollected Tissues Within and Beyond GTEx

Gene expression and its regulation can vary substantially across tissue types. In order to generate knowledge about gene expression in human tissues, the Genotype-Tissue Expression (GTEx) program has collected transcriptome data in a wide variety of tissue types from post-mortem donors. However, many tissue types are difficult to access and are not collected in every GTEx individual. Furthermore, in non-GTEx studies, the accessibility of certain tissue types greatly limits the feasibility and scale of studies of multi-tissue expression. In this work, we developed multi-tissue imputation methods to impute gene expression in uncollected or inaccessible tissues. Via simulation studies, we showed that the proposed methods outperform existing imputation methods in multi-tissue expression imputation and that incorporating imputed expression data can improve power to detect phenotype-expression correlations. By analyzing data from nine selected tissue types in the GTEx pilot project, we demonstrated that harnessing expression quantitative trait loci (eQTLs) and tissue-tissue expression-level correlations can aid imputation of transcriptome data from uncollected GTEx tissues. More importantly, we showed that by using GTEx data as a reference, one can impute expression levels in inaccessible tissues in non-GTEx expression studies

HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants

The resolution of genome-wide association studies (GWAS) is limited by the linkage disequilibrium (LD) structure of the population being studied. Selecting the most likely causal variants within an LD block is relatively straightforward within coding sequence, but is more difficult when all variants are intergenic. Predicting functional non-coding sequence has been recently facilitated by the availability of conservation and epigenomic information. We present HaploReg, a tool for exploring annotations of the non-coding genome among the results of published GWAS or novel sets of variants. Using LD information from the 1000 Genomes Project, linked SNPs and small indels can be visualized along with their predicted chromatin state in nine cell types, conservation across mammals and their effect on regulatory motifs. Sets of SNPs, such as those resulting from GWAS, are analyzed for an enrichment of cell type-specific enhancers. HaploReg will be useful to researchers developing mechanistic hypotheses of the impact of non-coding variants on clinical phenotypes and normal variation. The HaploReg database is available at http://compbio.mit.edu/HaploReg.National Institutes of Health (U.S.) (R01-HG004037)National Institutes of Health (U.S.) (RC1-HG005334)National Science Foundation (U.S.) (HG005334

EARLINET: 12-year of aerosol profiling over Europe

EARLINET has been collecting high quality aerosol optical profiles over Europe since 2000. The comparison with automatic collected dataset of aerosol optical depth (AOD) from AERONET and MODIS demonstrates the effectiveness of EARLINET regular measurement schedule for climatological studies. The analysis of optical properties in the local boundary layer indicates that the general decrease of AOD observed by different platforms over Europe in the last decade could be due to the modification of aerosol properties (towards less absorbing and larger particles) in the lower troposphere

EARLINET: Towards an advanced sustainable European aerosol lidar network

The European Aerosol Research Lidar Network, EARLINET, was founded in 2000 as a research project for establishing a quantitative, comprehensive, and statistically significant database for the horizontal, vertical, and temporal distribution of aerosols on a continental scale. Since then EARLINET has continued to provide the most extensive collection of ground-based data for the aerosol vertical distribution over Europe. This paper gives an overview of the network's main developments since 2000 and introduces the dedicated EARLINET special issue, which reports on the present innovative and comprehensive technical solutions and scientific results related to the use of advanced lidar remote sensing techniques for the study of aerosol properties as developed within the network in the last 13 years. Since 2000, EARLINET has developed greatly in terms of number of stations and spatial distribution: from 17 stations in 10 countries in 2000 to 27 stations in 16 countries in 2013. EARLINET has developed greatly also in terms of technological advances with the spread of advanced multiwavelength Raman lidar stations in Europe. The developments for the quality assurance strategy, the optimization of instruments and data processing, and the dissemination of data have contributed to a significant improvement of the network towards a more sustainable observing system, with an increase in the observing capability and a reduction of operational costs. Consequently, EARLINET data have already been extensively used for many climatological studies, long-range transport events, Saharan dust outbreaks, plumes from volcanic eruptions, and for model evaluation and satellite data validation and integration. Future plans are aimed at continuous measurements and near-real-time data delivery in close cooperation with other ground-based networks, such as in the ACTRIS (Aerosols, Clouds, and Trace gases Research InfraStructure Network) www.actris.net, and with the modeling and satellite community, linking the research community with the operational world, with the aim of establishing of the atmospheric part of the European component of the integrated global observing system

Assessment of the total precipitable water from a sun photometer, microwave radiometer and radiosondes at a continental site in southeastern Europe

In this study, we discuss the differences in the total precipitable water (TPW), retrieved from a Cimel sun photometer operating at a continental site in southeast Europe, between version 3 (V3) and version 2 (V2) of the AErosol RObotic NETwork (AERONET) algorithms. In addition, we evaluate the performance of the two algorithms comparing their product with the TPW obtained from a collocated microwave radiometer and nearby radiosondes during the period 2007–2017. The TPW from all three instruments was highly correlated, showing the same annual cycle, with lower values during winter and higher values during summer. The sun photometer and the microwave radiometer depict the same daily cycle, with some discrepancies during early morning and late afternoon due to the effect of solar zenith angle on the measurements of the photometer. The TPW from V3 of the AERONET algorithm has small differences compared with V2, mostly related to the use of the new laboratory-based temperature coefficients used in V3. The microwave radiometer measurements are in good agreement with those obtained by the radiosonde, especially during night-time when the differences between the two instruments are almost negligible. The comparison of the sun photometer data with high-quality independent measurements from radiosondes and the radiometer shows that the absolute differences between V3 and the other two datasets are slightly higher compared with V2. However, V3 has a lower dependence from the TPW and the internal sensor temperature, indicating a better performance of the retrieving algorithm. The calculated one-sigma uncertainty for V3 as estimated, from the comparison with the radiosondes, is about 10&thinsp;%, which is in accordance with previous studies for the estimation of uncertainty for V2. This uncertainty is further reduced to about 6&thinsp;% when AERONET V3 is compared with the collocated microwave radiometer. To our knowledge, this is the first in-depth analysis of the V3 TPW, and although the findings presented here are for a specific site, we believe that they are representative of other mid-latitude continental stations.</p

Thrombospondin-1 signaling through CD47 inhibits self-renewal by regulating c-myc and other stem cell transcription factors

Signaling through the thrombospondin-1 receptor CD47 broadly limits cell and tissue survival of stress, but the molecular mechanisms are incompletely understood. We now show that loss of CD47 permits sustained proliferation of primary murine endothelial cells, increases asymmetric division, and enables these cells to spontaneously reprogram to form multipotent embryoid body-like clusters. c-Myc, Klf4, Oct4, and Sox2 expression is elevated in CD47-null endothelial cells, in several tissues of CD47- and thrombospondin-1-null mice, and in a human T cell line lacking CD47. CD47 knockdown acutely increases mRNA levels of c-Myc and other stem cell transcription factors in cells and in vivo, whereas CD47 ligation by thrombospondin-1 suppresses c-Myc expression. The inhibitory effects of increasing CD47 levels can be overcome by maintaining c-Myc expression and are absent in cells with dysregulated c-Myc. Thus, CD47 antagonists enable cell self-renewal and reprogramming by overcoming negative regulation of c-Myc and other stem cell transcription factors

Resequencing Candidate Genes Implicates Rare Variants in Asthma Susceptibility

Common variation in over 100 genes has been implicated in the risk of developing asthma, but the contribution of rare variants to asthma susceptibility remains largely unexplored. We selected nine genes that showed the strongest signatures of weak purifying selection from among 53 candidate asthma-associated genes, and we sequenced the coding exons and flanking noncoding regions in 450 asthmatic cases and 515 nonasthmatic controls. We observed an overall excess of p values <0.05 (p = 0.02), and rare variants in four genes (AGT, DPP10, IKBKAP, and IL12RB1) contributed to asthma susceptibility among African Americans. Rare variants in IL12RB1 were also associated with asthma susceptibility among European Americans, despite the fact that the majority of rare variants in IL12RB1 were specific to either one of the populations. The combined evidence of association with rare noncoding variants in IL12RB1 remained significant (p = 3.7 × 10−4) after correcting for multiple testing. Overall, the contribution of rare variants to asthma susceptibility was predominantly due to noncoding variants in sequences flanking the exons, although nonsynonymous rare variants in DPP10 and in IL12RB1 were associated with asthma in African Americans and European Americans, respectively. This study provides evidence that rare variants contribute to asthma susceptibility. Additional studies are required for testing whether prioritizing genes for resequencing on the basis of signatures of purifying selection is an efficient means of identifying novel rare variants that contribute to complex disease