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    题名 作者 年代 出处 被引量
1SynthesisofCarbon Nanohorns/Chitosan/Quantum Dots Nanocompositeand itsApplicationsinCellsLabelingandinvivoImaging显示文摘LiJing HeZhe GuoChangrun etal 2014JournalofLuminescence2014,145,:1
2显示文摘HEZH GAON JINWR 2003Anal Chim Acta2003,497,12:1
3AnovelSTSmarkerforpoly- phenol oxidase activity in bread wheat显示文摘Sun D J HeZH XiaX C etal 2005Molecular Breeding2005,16,:1
4Molecular tagging of stripe rust resistance gene YrZH84 in Chinese wheat line Zhou 8425B显示文摘LiZF ZhengTC HeZH elal 2006Theoretical and Applied Genetics2006,112,6:1
5Characterization of a phytoene synthase 1 gene (Psyl) located on common wheat chromosome 7A and development of a functional marker 显示文摘HeX Y ZhangYL HeZH etal 2008Theoretical and Applied Genetics2008,116,:1
6Anti-angiogeniceffectandmechanism ofrheinfrom RhizomaRhei显示文摘HEZH ZHOUR HEMF etal 2011Phytomedicine2011,18,6:1
7Rational design and synthesis of nanosheets self-assembled hierarchical flower-ball-like CuFeS_(2)for boosted wide temperature sodium-ion batteries显示文摘Nano-structure designs with conductive networks have been demonstrated as an efficient strategy to boost sodium storage properties for transition metal sulfides.Herein,an exquisite nanosheets self-assembled hierarchical flower-ball-like CuFeS_(2)embedded into the reduced graphene oxide(RGO)nanosheet matrix(F-CuFeS_(2)@RGO)is fabricated via a concise two-step solvothermal method.Such a well-designed architecture affords increased active reaction interfaces and enhanced mixed ionic/electronic conductivity.Meanwhile,the external RGO matrix can effectively alleviate the volume expansion and create a stable structure during long cycles.As a result,the composite material exhibits a high reversible capacity of 559 mAh·g^(-1)at 0.1 A·g^(-1),a superior rate capability of 455 mAh·g^(-1)at 5 A·g^(-1)and excellent cyclic stability with 96%capacity retention after 4800 cycles at 5 A·g^(-1),among the best in the state-of-the-art transition metal sulfide anodes.Especially,F-CuFeS_(2)@RGO delivers outstanding low-temperature performances with a high capacity retention of 100%and 91%at-20 and-40℃,respectively,over 200 cycles.The proposed hierarchical structure fabrication paves a new direction in the design of high-performance electrodes for all-temperature energy storage applications.Ge Sun Hezhe Lin Ruiyuan Tian Zhixuan Wei Xiaoqi Wang Xu Jin Shiyu Yao Gang Chen Zexiang Shen Fei Du 2023Nano Research2023,16,7:0
8Wip1 inhibits neutrophil extracellular traps to promote abscess formation in mice by directly dephosphorylating Coronin-1a显示文摘Neutrophil extracellular traps (NETs) participate in the rapid inhibition and clearance of pathogens during infection;however, the molecular regulation of NET formation remains poorly understood. In the current study, we found that inhibition of the wild-type p53-induced phosphatase 1 (Wip1) significantly suppressed the activity of Staphylococcus aureus (S. aureus) and accelerated abscess healing in S. aureus-induced abscess model mice by enhancing NET formation. A Wip1 inhibitor significantly enhanced NET formation in mouse and human neutrophils in vitro. High-resolution mass spectrometry and biochemical assays demonstrated that Coro1a is a substrate of Wip1. Further experiments also revealed that Wip1 preferentially and directly interacts with phosphorylated Coro1a than compared to unphosphorylated inactivated Coro1a. The phosphorylated Ser426 site of Coro1a and the 28–90 aa domain of Wip1 are essential for the direct interaction of Coro1a and Wip1 and for Wip1 dephosphorylation of p-Coro1a Ser426. Wip1 deletion or inhibition in neutrophils significantly upregulated the phosphorylation of Coro1a-Ser426, which activated phospholipase C and subsequently the calcium pathway, the latter of which promoted NET formation after infection or lipopolysaccharide stimulation. This study revealed Coro1a to be a novel substrate of Wip1 and showed that Wip1 is a negative regulator of NET formation during infection. These results support the potential application of Wip1 inhibitors to treat bacterial infections.Yifang Chen Chenxu Zhao Han Guo Weilong Zou Zhaoqi Zhang Dong Wei Hezhe Lu Lianfeng Zhang Yong Zhao 2023Cellular & Molecular Immunology2023,20,8:0
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