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Ultra-low potential formaldehyde electrooxidation to formate and H_(2) on an Ag/Ag_(2)O heterostructure catalyst
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作者 Haitao Shi Rui Zhang +6 位作者 Chongchong Wang Xiaoping Kong linlin pan Meijie Wei Wei Wang Weixin Lv Lei Wang 《Nano Research》 2025年第2期131-140,共10页
Formaldehyde oxidation reaction(FOR)is a promising reaction alternative to the anodic oxygen evolution reaction(OER)owing to its ultra-low electrolysis potential and ability to produce formate and hydrogen gas.In this... Formaldehyde oxidation reaction(FOR)is a promising reaction alternative to the anodic oxygen evolution reaction(OER)owing to its ultra-low electrolysis potential and ability to produce formate and hydrogen gas.In this work,the electrode for FOR is prepared using Ag/Ag_(2)O nanoparticles(Ag/Ag_(2)O NPs)covered with Nafion membrane as the catalysts modified onto nickel foam(NF).Ag/Ag_(2)O NPs@NF exhibits significantly higher FOR activity than Ag NPs@NF and Ag_(2)O NPs@NF.At 100 mA·cm^(-2),the FOR potential on the Ag/Ag_(2)O NPs@NF electrode is only 0.16 V(vs.RHE).Meanwhile,the Faradaic efficiencies can reach up to 100% for both formate and H_(2) produced by FOR.Density functional theory(DFT)calculations indicate that the Ag/Ag_(2)O heterostructure exhibits lower reaction energy barriers for generating formate and H2 than pure Ag and Ag_(2)O.This work introduces a new synthetic approach for developing novel FOR catalysts and offers insights into the potential application prospects of FOR. 展开更多
关键词 formaldehyde oxidation ultra-low potential HETEROSTRUCTURE 200%hydrogenation formate production
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A Comprehensive Transcriptomic Analysis of Infant and Adult Mouse Ovary 被引量:10
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作者 linlin pan Wei Gong +3 位作者 Yuanyuan Zhou Xiaonuan Li Jun Yu Songnian Hu 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2014年第5期239-248,共10页
Ovary development is a complex process involving numerous genes. A well-developed ovary is essential for females to keep fertility and reproduce offspring. In order to gain a better insight into the molecular mechanis... Ovary development is a complex process involving numerous genes. A well-developed ovary is essential for females to keep fertility and reproduce offspring. In order to gain a better insight into the molecular mechanisms related to the process of mammalian ovary development, we performed a comparative transcriptomic analysis on ovaries isolated from infant and adult mice by using next-generation sequencing technology (SOLID). We identified 15,454 and 16,646 trans- criptionally active genes at the infant and adult stage, respectively. Among these genes, we also identified 7021 differentially expressed genes. Our analysis suggests that, in general, the adult ovary has a higher level of transcriptomic activity. However, it appears that genes related to primordial follicle development, such as those encoding Figla and Nobox, are more active in the infant ovary, whereas expression of genes vital for follicle development, such as Gdj~, Bmp4 and Bmpl5, is upreg- ulated in the adult. These data suggest a dynamic shift in gene expression during ovary development and it is apparent that these changes function to facilitate follicle maturation, when additional func- tional gene studies are considered. Furthermore, our investigation has also revealed several impor- tant functional pathways, such as apoptosis, MAPK and steroid biosynthesis, that appear to be much more active in the adult ovary compared to those of the infant. These findings will provide a solid foundation for future studies on ovary development in mice and other mammals and help to expand our understanding of the complex molecular and cellular events that occur during postnatal ovary development. 展开更多
关键词 FOLLICULOGENESIS Postnatal ovary develop-ment TRANSCRIPTOME RNA-seq
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BIGpre: A Quality Assessment Package for Next-Generation Sequencing Data 被引量:4
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作者 Tongwu Zhang Yingfeng Luo +4 位作者 Kan Liu linlin pan Bing Zhang Jun Yu Songnlan Hu 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2011年第6期238-244,共7页
The emergence of next-generation sequencing (NGS) technologies has significantly improved sequencing throughput and reduced costs. However, the short read length, duplicate reads and massive volume of data make the ... The emergence of next-generation sequencing (NGS) technologies has significantly improved sequencing throughput and reduced costs. However, the short read length, duplicate reads and massive volume of data make the data processing much more difficult and complicated than the first-generation sequencing technology. Al- though there are some software packages developed to assess the data quality, those packages either are not easily available to users or require bioinformatics skills and computer resources. Moreover, almost all the quality assessment software currently available didn't taken into account the sequencing errors when dealing with the du- plicate assessment in NGS data. Here, we present a new user-friendly quality assessment software package called BIGpre, which works for both Illumina and 454 platforms. BIGpre contains all the functions of other quality assessment software, such as the correlation between forward and reverse reads, read GC-content distribution, and base Ns quality. More importantly, BIGpre incorporates associated programs to detect and remove duplicate reads after taking sequencing errors into account and trimming low quality reads from raw data as well. BIGpre is primarily written in Perl and integrates graphical capability from the statistics package R. This package produces both tabular and graphical summaries of data quality for sequencing datasets from Illumina and 454 platforms. Processing hundreds of millions reads within minutes, this package provides immediate diagnostic information for user to manipulate sequencing data for downstream analyses. BIGpre is freely available at http://bigpre.sourceforge.net/. 展开更多
关键词 next-generation sequencing quality assessment duplicate reads sequencing error
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Transcriptomic study of the red palm weevil Rhynchophorus ferrugineus embryogenesis 被引量:1
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作者 An Yin linlin pan +12 位作者 Xiaowei Zhang Lei Wang Yuxin Yin Shangang Jia Wanfei Liu Chengqi Xin Kan Liu Xiaoguang Yu Gaoyuan Sun Khalid AI-hudaib Son qnian Hu Ibrahim S. AI-Mssallem Jun Yu 《Insect Science》 SCIE CAS CSCD 2015年第1期65-82,共18页
The red palm weevil (RPW), Rhynchophorus ferrugineus (Coleoptera: Cur- culionidae), is an invasive, concealed and destructive tissue borer, and it becomes a lethal pest of the palm family of plants and has been r... The red palm weevil (RPW), Rhynchophorus ferrugineus (Coleoptera: Cur- culionidae), is an invasive, concealed and destructive tissue borer, and it becomes a lethal pest of the palm family of plants and has been reported to attack 20 palm species around the globe. Here we report a systematic transcriptomic study on embryogenesis of RPW, where we analyze the transcriptomes across five developmental stages of RPW embryogenesis, involving four embryonic stages (El, E2, E3 and E4) and one larval stage (L1). Using the RNA-seq and next-generation platforms, we generated 80 to 91 million reads for each library and assemble 22 532 genes that are expressed at different embryonic stages. Among the total transcripts from the five embryonic development stages, we found that 30.45 % are differentially expressed, 10.10 % show stage-specificity and even a larger fraction, 62.88 %, exhibit constitutive expression in all the stages. We also analyzes the expression dynamics of several conserved signaling pathways (such as Hedgehog, JAK-STAT, Notch, TGF-β, Ras/MAPK and Writ), as well as key developmental genes, including those related to apoptosis, axis formation, Hox complex, neurogenesis and segmentation. The datasets provide an essential resource for gene annotation and RPW functional genomics, including studies by using tools and concepts from multiple disciplines, such as development, physiology, biochemistry, molecular biology and genetics. 展开更多
关键词 insect embryogenesis red palm weevil Rhynchophorusferrugineus RNASEQ signaling pathways TRANSCRIPTOME
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Screening and Assessing 11 Mycobacterium tuberculosis Proteins as Potential Serodiagnostical Markers for Discriminating TB Patients from BCG Vaccinees
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作者 Guoqiang Zhang Lingxia Zhang +6 位作者 Mingcheng Zhang linlin pan Fengyu Wang Jun Huang Guoli Li Jun Yu Songnian Hu 《Genomics, Proteomics & Bioinformatics》 SCIE CAS CSCD 2009年第3期107-115,共9页
Purified protein derivative (PPD) skin tests often yield poor specificity, so that to develop new serological antigens for distinguishing between Mycobacterium tuberculosis infection and Bacille Calmette-Guerin (BC... Purified protein derivative (PPD) skin tests often yield poor specificity, so that to develop new serological antigens for distinguishing between Mycobacterium tuberculosis infection and Bacille Calmette-Guerin (BCG) vaccination is a priority, especially for developing countries like China. We predicted the antigenicity for selected open reading frames (ORFs) based on the genome sequences of M. tuberculosis H37Rv and M. boris BCG, as well as their functions and differences of expression under different stimulus. The candidate ORFs were cloned from H37Rv sequences and expressed as recombinant proteins in Escherichia coli. We studied the serodiagnostic potential of 11 purified recombinants by using enzyme-linked immunosorbent assay (ELISA) and involving a cohort composed of 58 TB patients (34 males and 24 females), 8 healthy volunteers and 50 PPD-negative individuals before and after BCG vaccination. For all the 11 antigens, the median OD values for the sera from TB patients were statistically significantly higher than those for PPD-negative individuals before or after BCG vaccination (P〈0.01). They had at least 92% specificity in healthy controls and six seroantigens (Rv0251c, Rv1973, Rv2376c, Rv2537c, Rv2785c and Rv3873A) were never reported with seroantigenicities previously. Thus the approach combining comparative genomics, bioinformatics and ELISA techniques can be employed to identify new seroantigens distinguishing M. tuberculosis infection from BCG vaccination. 展开更多
关键词 comparative genomics M. tuberculosis BCG seroantigen ELISA
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