17 research outputs found
Attribute-based encryption with verifiable outsourced decryption
Ministry of Education, Singapore under its Academic Research Funding Tier 1; Singapore Management University; Agency for Science, Technology and Research (A*STAR) SERC Gran
Neutrino Physics with JUNO
The Jiangmen Underground Neutrino Observatory (JUNO), a 20 kton multi-purposeunderground liquid scintillator detector, was proposed with the determinationof the neutrino mass hierarchy as a primary physics goal. It is also capable ofobserving neutrinos from terrestrial and extra-terrestrial sources, includingsupernova burst neutrinos, diffuse supernova neutrino background, geoneutrinos,atmospheric neutrinos, solar neutrinos, as well as exotic searches such asnucleon decays, dark matter, sterile neutrinos, etc. We present the physicsmotivations and the anticipated performance of the JUNO detector for variousproposed measurements. By detecting reactor antineutrinos from two power plantsat 53-km distance, JUNO will determine the neutrino mass hierarchy at a 3-4sigma significance with six years of running. The measurement of antineutrinospectrum will also lead to the precise determination of three out of the sixoscillation parameters to an accuracy of better than 1\%. Neutrino burst from atypical core-collapse supernova at 10 kpc would lead to ~5000inverse-beta-decay events and ~2000 all-flavor neutrino-proton elasticscattering events in JUNO. Detection of DSNB would provide valuable informationon the cosmic star-formation rate and the average core-collapsed neutrinoenergy spectrum. Geo-neutrinos can be detected in JUNO with a rate of ~400events per year, significantly improving the statistics of existing geoneutrinosamples. The JUNO detector is sensitive to several exotic searches, e.g. protondecay via the decay channel. The JUNO detector will providea unique facility to address many outstanding crucial questions in particle andastrophysics. It holds the great potential for further advancing our quest tounderstanding the fundamental properties of neutrinos, one of the buildingblocks of our Universe
An excerpt of American gastroenterological association institute guideline on the role of elastography in the evaluation of liver fibrosis(2017)
Reciprocity relationships between underwriters and institutional investors in the IPO market.
Numerical simulation study of fines migration impacts on an early water drainage period in undersaturated coal seam gas reservoirs
Coal fines migration exerts negative impacts on early water drainage of undersaturated coal seam gas (CSG) reservoirs. The complicated migration process results in ineffective and inaccurate forecast of coal fines production. Hence, a robust modelling tool is required to include the mechanisms of fines migration and to predict their impacts on rock and production. In this paper, fines migration in coal is categorized into three stages: generation, migration, and deposition processes. The corresponding models for different stages are established, including (1) a fines generation model, (2) the maximum fines-carrying concentration model and deviation factor of the modified Darcy model, (3) a fines deposition model, and (4) a dynamic permeability and porosity model. The above models are coupled with a water flow model, solved numerically using the finite difference method. Then, two dewatering strategies, including fast and moderate depressurization, are compared using the proposed models to study their effects on coal properties and following production. Finally, the production history of a CSG well in the Qinshui Basin, China, is utilized for history matching in a field case study. The simulation results indicate that new fines will be generated in a fast depressurization process and the water rate decline reduces the cleat permeability significantly. The newly generated fines can enhance the permeability temporarily, but they will block the flow channels and bring serious damage to the permeability when the water rate declines. The moderate depressurization strategy can produce the coal fines in a continuous mode, and the formation damage induced by fines deposition can be reduced to the acceptable level, which is the more reliable way to maintain well productivity. In addition, multiple well shut-in can trigger the irreversible fines deposition, reduce the permeability, and decrease the production rate
Dynamic Changes in MMP1 and TIMP1 in the Antifibrotic Process of Dahuang Zhechong Pill in Rats with Liver Fibrosis
On the basis of carbon tetrachloride (CCl4)induced liver fibrosis in rats, this study aims to investigate the dynamic changes in matrix metalloproteinase 1 (MMP1) and the tissue inhibitor of metalloproteinase 1 (TIMP1) in the antifibrotic process of Dahuang Zhechong Pill (DHZCP). A total of 50 male Sprague Dawley rats, aged 8 weeks, were randomly divided into 3 groups: the control group, the model group (the group treated with CCl4), and the treatment group (the group treated with CCl4 and DHZCP). Rats were sacrificed at Weeks 4 and 8. Liver tissues were separated for RNA sequencing and bioinformatics analysis. Real-time PCR, Western blot analysis, and histological staining were conducted to confirm the gene expression and pathological change in liver tissues. Compared with control group, rats in model group showed poor mental state and slow weight gain. The liver tissues of the rats in the model group exhibited a damaged hepatic lobule structure, fibrous connective tissue hyperplasia, and inflammatory cell infiltration among the hyperplastic tissues. DHZCP could significantly improve the appearance of rats and alleviate CCl4-induced fibrosis. Compared to model group, 798 differentially expressed mRNAs were found in the treatment group, of which 120 were up-regulated and 678 were down-regulated. Differentially expressed mRNAs between the CCl4-induced group and the DHZCP-treated group were mainly focused on the following KEGG pathways: focal adhesion, phagosome, tight junction, and ECM–receptor interactions. Relative to those in the control group, MMP1 was downregulated, whereas, TIMP1 and Col1A1 were upregulated in the CCl4-induced group at Weeks 4 and 8. DHZCP could reverse MMP1, TIMP1, and Col1A1 expression.DHZCP protects against liver injury and exerts an antifibrotic effect on liver fibrosis induced by CCl4 in rats. Its mechanism may be related to the upregulation of MMP1, downregulation of TIMP1, and promotion of collagen degradation
Numerical Simulation Study of Fines Migration Impacts on an Early Water Drainage Period in Undersaturated Coal Seam Gas Reservoirs
Multifunctional Proximity Labeling Strategy for Lipid Raft-Specific Sialic Acid Tracking and Engineering
Lipid raft-specific glycosylation has been implicated
in many biological
processes, including intracellular trafficking, cell adhesion, signal
transduction, and host–pathogen interactions. The major predicament
in lipid raft-specific glycosylation research is the unavailability
of tools for tracking and manipulating glycans on lipid rafts at the
microstructural level. To overcome this challenge, we developed a
multifunctional proximity labeling (MPL) platform that relies on cholera
toxin B subunit to localize horseradish peroxidase on lipid rafts.
In addition to the prevailing electron-rich amino acids, modified
sialic acid was included in the horseradish peroxidase-mediated proximity
labeling substrate via purposefully designed chemical transformation
reactions. In combination with sialic acid editing, the self-renewal
of lipid raft-specific sialic acid was visualized. The MPL method
enabled tracking of lipid raft dynamics under methyl-β-cyclodextrin
and mevinolin treatments; in particular, the alteration of lipid rafts
markedly affected cell migration. Furthermore, we embedded functional
molecules into the method and implemented raft-specific sialic acid
gradient engineering. Our novel strategy presents opportunities for
tailoring lipid raft-specific sialic acids, thereby regulating interactions
associated with lipid raft regions (such as cell–virus and
cell–microenvironment interactions), and can aid in the development
of lipid raft-based therapeutic regimens for tumors