Development and preliminary investigation of a modular chamber for calibration of relative humidity instruments

In the scope of the project HUMEA – Expansion of European research capabilities in humidity measurement within the EURAMET EMPIR program, the modular chamber for calibration of relative humidity instruments was designed, manufactured and characterized. The modular chamber consists of arbitrary numbers of aluminum blocks each of which provides accommodation for the one relative humidity probe and also has the fittings for pressure and temperature probes as well as ports for gas sampling and/or supplying. The gas can be supplied from the dew/frost point generator or the larger climatic chamber. In the latter case, the airflow through the chamber can be enhanced by using an additional fan. The preliminary study was carried out to investigate the improvement in temperature uniformity using a new chamber in combination with two climatic chambers. The investigation results show significant improvement in temperature uniformity thus lowering the uncertainties of the calibration of relative humidity instruments

Improving emerging European NMIs’ capabilities in humidity measurement

The control and measurement of humidity is important for many industrial applications and to ensure the appropriate storage of materials and products. Humidity measurement techniques are diverse and each presents different challenges for use and calibration for a range of pressures and gases. Over the past few years, the development of humidity sensors and apparatus has matured to a level where traceable calibration is beneficial to all industries in which humidity and moisture measurement and control are important. This paper deals with a European project in which the overall objective is to develop or extend the measurement and research capabilities of the participating emerging NMI/DIs’ countries in the field of humidity measurements, where access to these types of facilities is currently limited

DAWN: A framework to identify autism genes and subnetworks using gene expression and genetics

Background: De novo loss-of-function (dnLoF) mutations are found twofold more often in autism spectrum disorder (ASD) probands than their unaffected siblings. Multiple independent dnLoF mutations in the same gene implicate the gene in risk and hence provide a systematic, albeit arduous, path forward for ASD genetics. It is likely that using additional non-genetic data will enhance the ability to identify ASD genes. Methods. To accelerate the search for ASD genes, we developed a novel algorithm, DAWN, to model two kinds of data: rare variations from exome sequencing and gene co-expression in the mid-fetal prefrontal and motor-somatosensory neocortex, a critical nexus for risk. The algorithm casts the ensemble data as a hidden Markov random field in which the graph structure is determined by gene co-expression and it combines these interrelationships with node-specific observations, namely gene identity, expression, genetic data and the estimated effect on risk. Results: Using currently available genetic data and a specific developmental time period for gene co-expression, DAWN identified 127 genes that plausibly affect risk, and a set of likely ASD subnetworks. Validation experiments making use of published targeted resequencing results demonstrate its efficacy in reliably predicting ASD genes. DAWN also successfully predicts known ASD genes, not included in the genetic data used to create the model. Conclusions: Validation studies demonstrate that DAWN is effective in predicting ASD genes and subnetworks by leveraging genetic and gene expression data. The findings reported here implicate neurite extension and neuronal arborization as risks for ASD. Using DAWN on emerging ASD sequence data and gene expression data from other brain regions and tissues would likely identify novel ASD genes. DAWN can also be used for other complex disorders to identify genes and subnetworks in those disorders. © 2014 Liu et al.; licensee BioMed Central Ltd

Speeding-up Scientific Knowledge Transfer and Improvement of Capabilities of emerging European National Metrology Institutes and Designated Institutes in the field of thermal measurements: Benefits and Impacts

Within the frame of a European project called Eura-Thermal, the general objective was to upgrade the regional metrological infrastructure (Bosnia & Herzegovina, Croatia, Ireland, Serbia...) with new capabilities, especially in the field of thermal measurements. This paper highlights the strategy used for improving in the short term, scientific knowledge transfer and the capabilities of different emerging institutes. Furthermore, as a main output, the impacts and benefit for Industry and for the end-users are also presented as examples. © 2018 Institute of Physics Publishing. All rights reserved.XXII World Congress of the International Measurement Confederation (IMEKO 2018

NK cell receptor NKG2D sets activation threshold for the NCR1 receptor early in NK cell development

The activation of natural killer (NK) cells depends on a change in the balance of signals from inhibitory and activating receptors. The activation threshold values of NK cells are thought to be set by engagement of inhibitory receptors during development. Here, we found that the activating receptor NKG2D specifically set the activation threshold for the activating receptor NCR1 through a process that required the adaptor DAP12. As a result, NKGD2-deficient (Klrk1-/-) mice controlled tumors and cytomegalovirus infection better than wild-type controls through the NCR1-induced production of the cytokine IFN-γ. Expression of NKG2D before the immature NK cell stage increased expression of the adaptor CD3ζ. Reduced expression of CD3ζ in Klrk1-/- mice was associated with enhanced signal transduction through NCR1, and CD3ζ deficiency resulted in hyper-responsiveness to stimulation via NCR1. Thus, an activating receptor developmentally set the activity of another activating receptor on NK cells and determined NK cell reactivity to cellular threats

New insights into the development of the human cerebral cortex

The cerebral cortex constitutes more than half the volume of the human brain and is presumed to be responsible for the neuronal computations underlying complex phenomena, such as perception, thought, language, attention, episodic memory and voluntary movement. Rodent models are extremely valuable for the investigation of brain development, but cannot provide insight into aspects that are unique or highly derived in humans. Many human psychiatric and neurological conditions have developmental origins but cannot be studied adequately in animal models. The human cerebral cortex has some unique genetic, molecular, cellular and anatomical features, which need to be further explored. The Anatomical Society devoted its summer meeting to the topic of Human Brain Development in June 2018 to tackle these important issues. The meeting was organized by Gavin Clowry (Newcastle University) and Zoltán Molnár (University of Oxford), and held at St John's College, Oxford. The participants provided a broad overview of the structure of the human brain in the context of scaling relationships across the brains of mammals, conserved principles and recent changes in the human lineage. Speakers considered how neuronal progenitors diversified in human to generate an increasing variety of cortical neurons. The formation of the earliest cortical circuits of the earliest generated neurons in the subplate was discussed together with their involvement in neurodevelopmental pathologies. Gene expression networks and susceptibility genes associated to neurodevelopmental diseases were discussed and compared with the networks that can be identified in organoids developed from induced pluripotent stem cells that recapitulate some aspects of in vivo development. New views were discussed on the specification of glutamatergic pyramidal and γ-aminobutyric acid (GABA)ergic interneurons. With the advancement of various in vivo imaging methods, the histopathological observations can be now linked to in vivo normal conditions and to various diseases. Our review gives a general evaluation of the exciting new developments in these areas. The human cortex has a much enlarged association cortex with greater interconnectivity of cortical areas with each other and with an expanded thalamus. The human cortex has relative enlargement of the upper layers, enhanced diversity and function of inhibitory interneurons and a highly expanded transient subplate layer during development. Here we highlight recent studies that address how these differences emerge during development focusing on diverse facets of our evolution