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| 1 | The Infiltration Process and Texture Transition of 2D C/C Composites显示文摘2D needle-punched fiber felt was infiltrated by a kind of rapid isothermal chemical vapor infiltration technique. The infiltration process and texture transition of the infiltrated C/C composites were investigated. The porosity and the variations of the cumulative pore volume were determined by mercury porosimetry. The texture of matrix carbon was studied under a polarized light microscope. The results show that the relative mass gain of the sample increases directly as the infiltration time at the initial stage until 20 h, and subsequently the increasing rate of the relative mass gain decreases gradually with the prolonging of infiltration time. Three layers of pyrocarbon were formed around fibers. Low-textured pyrocarbon was obtained at the initial stage. With the densification going on, high-textured pyrocarbon was formed on the surface of low-textured pyrocarbon. Then, low-textured pyrocarbon was produced again during the final stage of densification. The texture transition is ascribed to the variation of the ratio of cumulative inner surface area to volume of pores and the gas partial pressure in pores. | Hejun Li Guozhong Xu Kezhi Li Chuang Wang Wei Li Miaoling Li | 2009 | Journal of Materials Science & Technology2009，25，1： | 2 |
| 2 | Role of calcium mobilization in the regulation of spontaneous transient outward currents in porcine coronary artery myocytes显示文摘The purpose of the present study was to further study the characteristics and regulation of spontaneous transient outward currents (STOCs) in freshly isolated porcine coronary artery smooth muscle cells (ASMCs). STOCs were recorded using the perforated whole-cell patch-clamp configuration. STOCs were voltage-dependent and superimposed stochastically onto whole-cell Ca2+-activated-K+ (BKCa) currents. Charybdotoxin (ChTX, 200 nmol/L), a selective blocker of BKCa channels, completely inhibited STOCs within 10 min. STOCs activity was greatly suppressed when extracellular Ca2+ concentration decreased from 1.8 mmol/L to 200 nmol/L, further removal of Ca2+ abolished STOCs activity. Ca2+ ionophore A23187 (10 μmol/L) increased STOCs activity significantly. Verapamil (20 μmol/L) and CdCl2 (200 μmol/L), two kinds of organic L-type voltage-dependent Ca2+ channels (L-VDCCs) antagonists, had little effect on STOCs. In addition, the ryanodine receptors (RyRs) agonist caffeine (5 mmol/L) significantly activated STOCs. Application of ryanodine (50 μmol/L) to block RyRs abolished STOCs, subsequent washout of ryanodine or application of caffeine failed to reproduce STOCs activity. Inhibition of inositol 1,4,5-trisphosphate receptors (IP3Rs) by 2APB (40 μmol/L) greatly suppressed the activity of STOCs, application of caffeine (5 mmol/L) in the presence of 2APB caused a burst of outward currents followed by inhibition of STOCs. These results suggest that STOCs in porcine coronary ASMCs are mediated by BKCa channels. Extracellular Ca2+ is essential for STOCs activity, while Ca2+ entry through L-VDCCs has little effect on STOCs. Intracellular Ca2+ release induced by RyRs is responsible for the regulation of STOCs, whereas IP3Rs might also be involved. | LI PengYun ZENG XiaoRong YANG Yan CAI Fang LIU ZhiFei LI MiaoLing PEI Jie ZHOU Wen | 2007 | Science China(Life Sciences)2007，50，5： | 1 |
| 3 | Measurement of the extinction angle about laminar pyrocarbons by image analysis in reflection polarized light 显示文摘 | Li Miaoling Qi Lehua Li Heiun Xu Guozhong | 2007 | Materials Science and Engineering A2007，448，12： | 1 |
| 4 | Specific Regulation of m^(6)A by SRSF7 Promotes the Progression of Glioblastoma显示文摘Serine/arginine-rich splicing factor 7(SRSF7),a known splicing factor,has been revealed to play oncogenic roles in multiple cancers.However,the mechanisms underlying its oncogenic roles have not been well addressed.Here,based on N6-methyladenosine(m^(6)A)co-methylation network analysis across diverse cell lines,we find that the gene expression of SRSF7 is positively correlated with glioblastoma(GBM)cell-specific m^(6)A methylation.We then indicate that SRSF7 is a novel m^(6)A regulator,which specifically facilitates the m^(6)A methylation near its binding sites on the mRNAs involved in cell proliferation and migration,through recruiting the methyltransferase complex.Moreover,SRSF7 promotes the proliferation and migration of GBM cells largely dependent on the presence of the m^(6)A methyltransferase.The two m^(6)A sites on the mRNA for PDZ-binding kinase(PBK)are regulated by SRSF7 and partially mediate the effects of SRSF7 in GBM cells through recognition by insulin-like growth factor 2 mRNA-binding protein 2(IGF2BP2).Together,our discovery reveals a novel role of SRSF7 in regulating m^(6)A and validates the presence and functional importance of temporal-and spatial-specific regulation of m^(6)A mediated by RNA-binding proteins(RBPs). | Yixian Cun Sanqi An Haiqing Zheng Jing Lan Wenfang Chen Wanjun Luo Chengguo Yao Xincheng Li Xiang Huang Xiang Sun Zehong Wu Yameng Hu Ziwen Li Shuxia Zhang Geyan Wu Meisongzhu Yang Miaoling Tang Ruyuan Yu Xinyi Liao Guicheng Gao Wei Zhao Jinkai Wang Jun Li | 2023 | Genomics, Proteomics & Bioinformatics2023，21，4： | 1 |
| 5 | CircRNA ATF6 promotes ovarian cancer cell progression by activating PTEN/mTOR signaling pathway显示文摘Ovarian cancer is a malignant cancer type and affects women’s lives in the world.Circular RNAs(circRNAs)have been involved with the progression of cancers.In our study,we are going to explore the functions of circATF6 in ovarian cancer.The qRT-PCR assay was used to detect expressions of genes.Actinomycin D and RNase R treatment were implemented to verify the circular RNA character of circATF6.Besides,Cell proliferation was assessed by colony formation assay and EdU assay.Silenced circATF6 could reduce the proliferation of ovarian cancer cells.In addition,inhibited circATF6 could promote the cell apoptosis and inhibit related proteins in PTEN/mTOR signaling pathway in ovarian cancer.In conclusion,CircRNA ATF6 promotes ovarian cancer cell progression by activating PTEN/mTOR signaling pathway. | LIETING MA MIAOLING LI XINGLONG ZHENG | 2021 | BIOCELL2021，45，2： | 1 |
| 6 | Chry- somya megaeephala (Fabricius) larvae:A new biodiesel resource显示文摘 | Li Zhuoxue Yang Depo Miaoling Huang | 2012 | Applied Energy2012，94，： | 1 |
| 7 | Fractal characterization of pore microstructure evolution in carbon/carbon composites显示文摘A fractal characterization approach was proposed to research pore microstructure evolution in car- bon/carbon (C/C) composites during the chemical vapor infiltration process. The data obtained from mercury porosimetry determinations were analyzed using the sponge fractal model and the thermo- dynamics relation fractal model, respectively. The fractal dimensions of C/C composites at different densification stages were evaluated. The pore microstructure evolution with densification time was studied by fractal dimension analysis. The results showed that C/C composites belong to porous frac- tal structure. The fractal dimensions increase on the whole with decreasing porosity as the densifica- tion proceeds. The fractal dimensions are influenced by the texture of pyrocarbon and decrease with increasing anisotropy from isotropic pyrocarbon to high textural one. Both the complicacy of pore structure and the textural morphology of pyrocarbon can be represented simultaneously by the fractal dimension. The pore evolution of C/C composites in the densification process can be monitored using fractal dimension. | LI MiaoLing QI LeHua LI HeJun XU GuoZhong | 2009 | Science China(Technological Sciences)2009，52，4： | 1 |
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