Bridging the complexity gap in Tbps-achieving THz-band baseband processing

Recent advances in electronic and photonic technologies have allowed efficient signal generation and transmission at terahertz (THz) frequencies. However, as the gap in THz-operating devices narrows, the demand for terabit-per-second (Tbps)-achieving circuits is increasing. Translating the available hundreds of gigahertz (GHz) of bandwidth into a Tbps data rate requires processing thousands of information bits per clock cycle at state-of-the-art clock frequencies of digital baseband processing circuitry of a few GHz. This paper addresses these constraints and emphasizes the importance of parallelization in signal processing, particularly for channel code decoding. By leveraging structured sub-spaces of THz channels, we propose mapping bits to transmission resources using shorter code words, extending parallelizability across all baseband processing blocks. THz channels exhibit quasi-deterministic frequency, time, and space structures that enable efficient parallel bit mapping at the source and provide pseudo-soft bit reliability information for efficient detection and decoding at the receiver

USP compendial methods for analysis of heparin: chromatographic determination of molecular weight distributions for heparin sodium

Heparin is a polysaccharide product isolated from glycosaminoglycans of porcine mucosa (or occasionally other tissues and species). It is a linear non-uniform polymer consisting of alternating glucosamine and uronic acid monosaccharide residues and is highly sulfated. Heparin sodium drug product (HP) used in medicine consists of chains with molecular weight (MW) ranging from under 5,000 to over 50,000. Although HP has been used as an injectable antithrombotic medicine for more than 70 years, many aspects of its structure and purity, including its MW, have not been specified by public standards until recent years. In 2008, a number of HP lots associated with severe adverse effects, including fatalities, were found to have been contaminated with oversulfated chondroitin sulfate. This incident led to thorough revision of compendial standards worldwide. In the USA, the Food and Drug Administration (FDA) encouraged the inclusion of enhanced standards for purity and identity in the relevant monographs of the United States Pharmacopeia (USP) including acceptance criteria for MW distribution

DESIGN AND DEVELOPMENT OF ANDROID-BASED LEARNING MEDIA FOR LEARNING ALGORITHM AND DATA STRUCTURE

Learning media is part of the learning component, the media is included in the discussion of the overall learning system. The use of media is expected to be a special concern in every learning activity, this is to assist the delivery of learning in supporting the advancement of today's technology-based education world. One of the learning techniques is in the form of algorithms and data structures. Technological advances make learning media usable on Android devices. This study aims to design learning media algorithms and data structures based on Android. The research method uses a waterfall-type system development life cycle (SDLC). The results of the study are learning media algorithms and data structures can be designed for Android devices. The results of system testing using black-box testing provide results as expected

The LKB1-salt-inducible kinase pathway functions as a key gluconeogenic suppressor in the liver

LKB1 is a master kinase that regulates metabolism and growth through adenosine monophosphate-activated protein kinase (AMPK) and 12 other closely related kinases. Liver-specific ablation of LKB1 causes increased glucose production in hepatocytes in vitro and hyperglycaemia in fasting mice in vivo. Here we report that the salt-inducible kinases (SIK1, 2 and 3), members of the AMPK-related kinase family, play a key role as gluconeogenic suppressors downstream of LKB1 in the liver. The selective SIK inhibitor HG-9-91-01 promotes dephosphorylation of transcriptional co-activators CRTC2/3 resulting in enhanced gluconeogenic gene expression and glucose production in hepatocytes, an effect that is abolished when an HG-9-91-01-insensitive mutant SIK is introduced or LKB1 is ablated. Although SIK2 was proposed as a key regulator of insulin-mediated suppression of gluconeogenesis, we provide genetic evidence that liver-specific ablation of SIK2 alone has no effect on gluconeogenesis and insulin does not modulate SIK2 phosphorylation or activity. Collectively, we demonstrate that the LKB1-SIK pathway functions as a key gluconeogenic gatekeeper in the liver

Screening of DUB activity and specificity by MALDI-TOF mass spectrometry

Deubiquitylases (DUBs) are key regulators of the ubiquitin system which cleave ubiquitin moieties from proteins and polyubiquitin chains. Several DUBs have been implicated in various diseases and are attractive drug targets. We have developed a sensitive and fast assay to quantify in vitro DUB enzyme activity using matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry. Unlike other current assays, this method uses unmodified substrates, such as diubiquitin topoisomers. By analyzing 42 human DUBs against all diubiquitin topoisomers we provide an extensive characterization of DUB activity and specificity. Our results confirm the high specificity of many members of the OTU and JAMM DUB families and highlight that all USPs tested display low linkage selectivity. We also demonstrate that this assay can be deployed to assess the potency and specificity of DUB inhibitors by profiling 11 compounds against a panel of 32 DUBs

MicroMotility: State of the art, recent accomplishments and perspectives on the mathematical modeling of bio-motility at microscopic scales

Mathematical modeling and quantitative study of biological motility (in particular, of motility at microscopic scales) is producing new biophysical insight and is offering opportunities for new discoveries at the level of both fundamental science and technology. These range from the explanation of how complex behavior at the level of a single organism emerges from body architecture, to the understanding of collective phenomena in groups of organisms and tissues, and of how these forms of swarm intelligence can be controlled and harnessed in engineering applications, to the elucidation of processes of fundamental biological relevance at the cellular and sub-cellular level. In this paper, some of the most exciting new developments in the fields of locomotion of unicellular organisms, of soft adhesive locomotion across scales, of the study of pore translocation properties of knotted DNA, of the development of synthetic active solid sheets, of the mechanics of the unjamming transition in dense cell collectives, of the mechanics of cell sheet folding in volvocalean algae, and of the self-propulsion of topological defects in active matter are discussed. For each of these topics, we provide a brief state of the art, an example of recent achievements, and some directions for future research

A measurement of proton-carbon forward scattering in a proof-of-principle test of the EMPHATIC spectrometer

The next generation of long-baseline neutrino experiments will be capable of precision measurements of neutrino oscillation parameters, precision neutrino-nucleus scattering, and unprecedented sensitivity to physics beyond the Standard Model. Reduced uncertainties in neutrino fluxes are necessary to achieve high precision and sensitivity in these future precise neutrino measurements. New measurements of hadron-nucleus interaction cross sections are needed to reduce uncertainties of neutrino fluxes. We report measurements of the differential cross-section as a function of scattering angle for proton-carbon interactions with a single charged particle in the final state at beam momenta of 20, 30, and 120 GeV/c. These measurements are the result of a beam test for EMPHATIC, a hadron-scattering and hadron-production experiment. The total, elastic and inelastic cross-sections are also extracted from the data and compared to previous measurements. These results can be used in current and future long-baseline neutrino experiments, and demonstrate the feasibility of future measurements by an upgraded EMPHATIC spectrometer