57 research outputs found

    First-principles study on the effective masses of zinc-blend-derived Cu_2Zn-IV-VI_4 (IV = Sn, Ge, Si and VI = S, Se)

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    The electron and hole effective masses of kesterite (KS) and stannite (ST) structured Cu_2Zn-IV-VI_4 (IV = Sn, Ge, Si and VI = S, Se) semiconductors are systematically studied using first-principles calculations. We find that the electron effective masses are almost isotropic, while strong anisotropy is observed for the hole effective mass. The electron effective masses are typically much smaller than the hole effective masses for all studied compounds. The ordering of the topmost three valence bands and the corresponding hole effective masses of the KS and ST structures are different due to the different sign of the crystal-field splitting. The electron and hole effective masses of Se-based compounds are significantly smaller compared to the corresponding S-based compounds. They also decrease as the atomic number of the group IV elements (Si, Ge, Sn) increases, but the decrease is less notable than that caused by the substitution of S by Se.Comment: 14 pages, 6 figures, 2 table

    An optimized short‐term steroid therapy for chronic drug‐induced liver injury: A prospective randomized clinical trial

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    Background and AimsThe use of corticosteroids in chronic drug-induced liver injury (DILI) is an important issue. Our previous randomized controlled trial showed that patients with chronic DILI benefited from a 48-week steroid stepwise reduction (SSR) regimen. However, it remains unclear whether a shorter course of therapy can achieve similar efficacy. In this study, we aimed to assess whether a 36-week SSR can achieve efficacy similar to that of 48-week SSR.MethodsA randomized open-label trial was performed. Eligible patients were randomly assigned to the 36- or 48-week (1:1) SSR group. Liver biopsies were performed at baseline and at the end of treatment. The primary outcome was the proportion of patients with relapse rate (RR). The secondary outcomes were improvement in liver histology and safety.ResultsOf the 90 participants enrolled, 84 (87.5%) completed the trial, and 62 patients (68.9%) were women. Hepatocellular damage was observed in 53.4% of the cohort. The RR was 7.1% in the 36-week SSR group but 4.8% in the 48-week SSR group, as determined by per-protocol set analysis (p = 1.000). Significant histological improvements in histological activity (93.1% vs. 92.9%, p = 1.000) and fibrosis (41.4% vs. 46.4%, p = .701) were observed in both the groups. Biochemical normalization time did not differ between the two groups. No severe adverse events were observed.ConclusionsBoth the 36- and 48-week SSR regimens demonstrated similar biochemical response and histological improvements with good safety, supporting 36-week SSR as a preferable therapeutic choice (ClinicalTrials.gov, NCT03266146)

    The Spatial and Temporal Variability of Groundwater Vulnerability and Human Health Risk in the Limin District, Harbin, China

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    This study aimed to analyze the variations in groundwater quality, vulnerability and potential health risk from 2006 to 2016 in the Limin District, Harbin, China. Groundwater geochemical characteristics were described using statistical analysis and Piper diagrams. A modified DRASTIC model that combined factors of intrinsic aquifer vulnerability and land use was applied to assess groundwater vulnerability. The weights of parameters were adjusted by using the analytic hierarchy process (AHP) to optimize the model. The non-carcinogenic health risk was estimated by the Unites States Environmental Protection Agency (USEPA) model. Results suggested that concentrations of NH4-N, Fe and Mn in groundwater exceeded the limits both in 2006 and in 2016. The concentration of Fe in the groundwater showed more significant variation between 2006 and 2016 than the other parameters. Very high vulnerability zones increased from 6.3% in 2006 to 16.9% in 2016, and distributed on agricultural land, indicating that agriculture was still a major source of pollution. Mn and NO3-N contributed the most to human health risks in 2006 and 2016, respectively. This study highlights the influence of groundwater quality variation in decadal exploitation on human health

    Argonaute and Argonaute-Bound Small RNAs in Stem Cells.

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    Small RNAs are essential for a variety of cellular functions. Argonaute (AGO) proteins are associated with all of the different classes of small RNAs, and are indispensable in small RNA-mediated regulatory pathways. AGO proteins have been identified in various types of stem cells in diverse species from plants and animals. This review article highlights recent progress on how AGO proteins and AGO-bound small RNAs regulate the self-renewal and differentiation of distinct stem cell types, including pluripotent, germline, somatic, and cancer stem cells

    Cloning of the quail PIWI gene and characterization of PIWI binding to small RNAs.

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    The PIWI protein regulates gene expression at the epigenetic and post-transcriptional level with a variety of endogenous small non-coding RNAs. In poultry, the biological function of the PIWI protein and PIWI binding to small RNAs had not been determined. The present study cloned and analyzed the sequences of the PIWIL1 protein. We also characterized PIWIL1 binding to small RNAs from adult quail testis, where the PIWIL1 protein is specifically expressed. Small RNAs showed a strong peak at 24-27 nt in the testicular RNA library, mapped primarily to repeat sequences and were similar to rasiRNAs. MicroRNAs (miRNAs) were abundant in the ovarian RNA library at a peak of 22 nt

    Properties of unannotated unique reads in the testis.

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    <p>A: Chromosomal distribution of exons (top), repeat sequences (middle) and unannotated unique reads (bottom). The number of bases in exons of Refseq genes and repeats are plotted as a percentage of overall chromosome length. The numbers of piRNAs are normalized to chromosome length and plotted. B: Density analysis of exons (red), repeat sequences (green) and unannotated unique reads (with the positive strand in blue and the negative strand in purple) along chromosome 16. The densities of exons and repeats were using a 50 kB window, scanning the genome in increments of 1000 bases. Unannotaed uniques densities were determined by calculating a moving average of reads in a 5 kB sliding window (100 base increments) along each chromosome. Only reads that map 1 to 5 times to the genome were used in density analysis.</p

    The PIWIL1 protein.

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    <p>A: Complete amino acid sequence of PIWIL1; PAZ domain, red; PIWI domain, blue. B: A phylogenetic tree of the PIWIL1 protein generated using UPGMA.</p
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