维普中文期刊产品整合服务
9篇 您的检索式:作者名="Li Fengjin"
    题名 作者 年代 出处 被引量
1Stable classi?cation with limited sample: transferring a 30-m resolution sample set collected in 2015 to mapping 10-m resolution global land cover in 2017显示文摘As the world strives to reduce the impact of population growth, urbanization, agricultural expansion, and climate change on food security, energy and water shortage, resource over-exploration, biodiversity loss, environmental pollution, and ultimately human health, timely and higher resolution land cover information is urgently needed to achieve the sustainable development goals of the United Nations.Peng Gong Han Liu Meinan Zhang Congcong Li Jie Wang Huabing Huang Nicholas Clinton Luyan Ji Wenyu Li Yuqi Bai Bin Chen Bing Xu Zhiliang Zhu Cui Yuan Hoi Ping Suen Jing Guo Nan Xu Weijia Li Yuanyuan Zhao Jun Yang Chaoqing Yu Xi Wang Haohuan Fu Le Yu Iryna Dronova Fengming Hui Xiao Cheng Xueli Shi Fengjin Xiao Qiufeng Liu Lianchun Song 2019Science Bulletin2019,64,6:166
2Hollow Co/CoO/Carbon nanofibers promoted PMS decomposition for the degradation of Rhodamine B显示文摘Carbon nanofibers with hollow structures have an excellent application prospect in various fields be-cause of their high specific surface area and abundant active sites.PAN-based hollow carbon nanofiber doped with Co/CoO(H-Co/CoO-CNF)was successfully prepared and used as a catalyst to activate perox-ymonosulfate(PMS)and degrade Rhodamine B(RhB).The catalyst showed a surprising degradation rate(98.89%)of RhB within 15 min and had good degradation performance in a wide pH range(pH 1.5-11.2).Compared with solid fibers,H-Co/CoO-CNF shows better cyclic characteristics.The catalyst is also mag-netic and recoverable easily due to the addition of Co/CoO.Two pathways of both radical(SO_(4)·^(−))and non-radical(^(1)O_(2))exist during the RhB degradation process are confirmed through electron paramagnetic resonance(EPR)analysis and radical quenching experiments.This work provides a new idea for hollow fibers loaded with metals and their oxides and can guide the development of catalysts for advanced oxi-dation processes in the future.Zhende Li Xiaoyan Zhang Guangzhen Li Fengjin Han Dongqi Hu Xiaoyu Huang Hua Yuan Yeqiang Tan 2023Journal of Materials Science & Technology2023,,26:1
3Bilateral atlas laminar hook combined with transarticular screw fixation for an unstable bursting atlantal fracture显示文摘Xiang Guo Bin Ni Mingfei Wang Jian Wang Songkai Li Fengjin Zhou 2009Archives of Orthopaedic and Trauma Surgery2009,,9:1
4IRE1α regulates the PTHrP-IHH feedback loop to orchestrate chondrocyte hypertrophy and cartilage mineralization显示文摘Cartilage development is controlled by the highly synergistic proliferation and differentiation of growth plate chondrocytes,in which the Indian hedgehog(IHH)and parathyroid hormone-related protein-parathyroid hormone-1 receptor(PTHrP-PTH1R)feedback loop is crucial.The inositol-requiring enzyme 1a/X-box-binding protein-1 spliced(IRE1α/XBP1s)branch of the unfolded protein response(UPR)is essential for normal cartilage development.However,the precise role of ER stress effector IRE1α,encoded by endoplasmic reticulum to nucleus signaling 1(ERN1),in skeletal development remains unknown.Herein,we reported that loss of IRE1α accelerates chondrocyte hypertrophy and promotes endochondral bone growth.ERN1 acts as a negative regulator of chondrocyte proliferation and differentiation in postnatal growth plates.Its deficiency interrupted PTHrP/PTH1R and IHH homeostasis leading to impaired chondrocyte hypertrophy and differentiation.XBP1s,produced by p-IRE1α-mediated splicing,binds and up-regulates PTH1R and IHH,which coordinate cartilage development.Meanwhile,ER stress cannot be activated normally in ERN1-deficient chondrocytes.In conclusion,ERN1 deficiency accelerates chondrocyte hypertrophy and cartilage mineralization by impairing the homeostasis of the IHH and PTHrP/PTH1R feedback loop and ER stress.ERN1 may have a potential role as a new target for cartilage growth and maturation.Mengtian Fan Nana Geng Xingyue Li Danyang Yin Yuyou Yang Rong Jiang Cheng Chen Naibo Feng Li Liang Xiaoli Li Fengtao Luo Huabing Qi Qiaoyan Tan Yangli Xie Fengjin Guo 2024Genes & Diseases2024,11,1:0
5Differentially expressed gene in osteosarcoma cell lines with different metastatic potentials显示文摘Objective:To study the expression of osteosarcoma metastasis associated gene using a cDNA microarray,and screen new candidate genes related to the development,progress and osteosarcoma metastasis.Methods:Total RNA of a low metastatic osteosarcoma and a high metastatic osteosarcoma(M6 and M8 cell lines,respectively) was extracted,purified to mRNA and then reverse transcribed to cDNA.M6 was used as the experimental group and M8 as the control group,and the gene expression of cells from both of these two sublines was investigated using cDNA microarrays containig 8064 cDNA clones.The cDNA of M6 was labeled with cy3 and the cDNA of M8 was labeled with cy5.The two sublines were hybridized with the cDNA microarray.The hybridization signals were scanned with a Generation III array scanner and analyzed by Imagequant 5.0 software.Results:There were 330 differentially expressed genes between M6 and M8.In the M6 subline,152 genes were up-regulated and 178 genes were down-regulated compared to the M8 subline.These genes could be classified according to their function.Cell growth-related genes that were down-regulated included CCNG1,CDC2,APC10,and RPA3,while expression of the tumor suppressor genes,CDKN1A and CDKN2D,was up-regulated.Other genes that were differentially expressed included those that have been implicated in the regulation of signal transduction,metabolism and apoptosis.Conclusion:This study exploits a cDNA microarray approach to identifying genes that may be associated with metastasis.The gene expression profiles of osteosarcoma cell lines is a potentially important index in the search of new candidate genes related to tumor occurrence,development and metastasis.Xinzhi Li Lin Meng Anming Chen Fengjin Guo Zhenqiang Luo Heng Zeng 2009Journal of Nanjing Medical University2009,23,5:0
6Progranulin regulation of autophagy contributes to its chondroprotective effect in osteoarthritis显示文摘Progranulin(PGRN)is a multifunctional growth factor involved in many physiolog-ical processes and disease states.The apparent protective role of PGRN and the importance of chondrocyte autophagic function in the progression of osteoarthritis(OA)led us to investi-gate the role of PGRN in the regulation of chondrocyte autophagy.PGRN knockout chondro-cytes exhibited a deficient autophagic response with limited induction following rapamycin,serum starvation,and IL-1b-induced autophagy.PGRN-mediated anabolism and suppression of IL-1b-induced catabolism were largely abrogated in the presence of the BafA1 autophagy inhibitor.Mechanistically,during the process of OA,PGRN and the ATG5eATG12 conjugate form a protein complex;PGRN regulates autophagy in chondrocytes and OA through,at least partially,the interactions between PGRN and the ATG5eATG12 conjugate.Furthermore,the ATG5eATG12 conjugate is critical for cell proliferation and apoptosis.Knockdown or knockout of ATG5 reduces the expression of ATG5eATG12 conjugate and inhibits the chondroprotective effect of PGRN on anabolism and catabolism.Overexpression of PGRN partially reversed this effect.In brief,the PGRN-mediated regulation of chondrocyte autophagy plays a key role in the chondroprotective role of PGRN in OA.Such studies provide new insights into the pathogen-esis of OA and PGRN-associated autophagy in chondrocyte homeostasis.Yiming Pan Yuyou Yang Mengtian Fan Cheng Chen Rong Jiang Li Liang Menglin Xian Biao Kuang Nana Geng Naibo Feng Lin Deng Wei Zheng Fengmei Zhang Xiaoli Li Fengjin Guo 2023Genes & Diseases2023,10,4:0
7Taohong Siwu decoction(桃红四物汤)ameliorates atherosclerosis in rats possibly through toll-like receptor 4/myeloid differentiation primary response protein 88/nuclear factor-κB signal pathway显示文摘OBJECTIVE:To investigate the effect of Taohong Siwu decoction(桃红四物汤,TSD)on atherosclerosis in rats as well as investigate the underlying mechanism based on molecular docking.METHODS:Sixty healthy male Sprague-Dawley rats were randomly divided into 6 groups with 10 rats in each group:control group,model group,atorvastatin group(AT,2.0 mg/kg),and TSD groups(20,10,5 g/kg)after 7 d of acclimation.The model of atherosclerosis was successfully established except the control group by high fat diet(HFD)and vitamin D2.Biochemical analyzers were used to detect the levels of triglyceride(TG),total cholestero(TC),low density lipoprotein-cholesterol(LDLC)and high density lipid-cholesterol(HDL-C)in blood lipid.The levels of tumor necrosis factor-α(TNF-α),interleukin-6(IL-6)and interleukin-1β(IL-1β)were determined by enzyme-linked immunosorbent assay.Sudan IV staining and Hematoxylin and eosin staining(HE staining)were performed to observe the pathological changes in aortic tissue.Molecular docking technology was used to predict the best matching between the main components of TSD and the target proteins.The expression of target proteins was further detected by quantitative real time polymerase chain reaction(q RTPCR)and Western blot analysis.RESULTS:The results showed that TSD restricted atherosclerosis development and decreased the inflammatory cytokines in plasma.Molecular docking results predicted that the main components of TSD showed a strong binding ability with toll-like receptor(TLR4),myeloid differentiation primary response protein 88(My D88),and nuclear factor kappa-B(NF-κB).The results of q RT-PCR and Western blot analysis showed that the m RNA and protein expressions of TLR4,My D88 and NF-κB p65 in the aorta were reduced in atorvastatin group and TSD group.CONCLUSIONS:TSD can ameliorate atherosclerosis in rats,and the underlying mechanism is supposed be related to the suppression of inflammatory response by regulating TLR4/My D88/NF-κB signal pathway.CHANG Fengjin ZHOU Peng LI Guoying ZHANG Weizhi ZHANG Yanyan PENG Daiyin CHEN Guangliang 2024Journal of Traditional Chinese Medicine2024,44,1:0
8M2 macrophage-derived exosomes promote diabetic fracture healing by acting as an immunomodulator显示文摘Diabetes mellitus is a chronically inflamed disease that predisposes to delayed fracture healing.Macrophages play a key role in the process of fracture healing by undergoing polarization into either M1 or M2 subtypes,which respectively exhibit pro-inflammatory or anti-inflammatory functions.Therefore,modulation of macrophage polarization to the M2 subtype is beneficial for fracture healing.Exosomes perform an important role in improving the osteoimmune microenvironment due to their extremely low immunogenicity and high bioactivity.In this study,we extracted the M2-exosomes and used them to intervene the bone repair in diabetic fractures.The results showed that M2-exosomes significantly modulate the osteoimmune microenvironment by decreasing the proportion of M1 macrophages,thereby accelerating diabetic fracture healing.We further confirmed that M2-exosomes induced the conversion of M1 macrophages into M2 macrophages by stimulating the PI3K/AKT pathway.Our study offers a fresh perspective and a potential therapeutic approach for M2-exosomes to improve diabetic fracture healing.Yili Wang Qiushui Lin Hao Zhang Sicheng Wang Jin Cui Yan Hu Jinlong Liu Mengmeng Li Kun Zhang Fengjin Zhou Yingying Jing Zhen Geng Jiacan Su 2023Bioactive Materials2023,,10:0
9A method to predict typhoon waves显示文摘Amethodtopredicttyphoonwaves¥YangChuncheng;DaiMingrui;GaoZhihua;ChengZhan;XuFuxiang;LiuYu;LiFengjin;LiJie;SuDongfu;ZhangDacuo...Yang Chuncheng Dai Mingrui Gao Zhihua Cheng Zhan Xu Fuxiang Liu Yu Li Fengjin Li Jie Su Dongfu Zhang Dacuo and Xu Qichun eived (National Marine Environment Forecast Center, State Oceanic Administration, Beijing 100081, China Institute of Physical Oce 1995Acta Oceanologica Sinica1995,14,2:0
返回顶部 每页显示:
共1页 首页 上一页 第1页 下一页 末页 /1 跳转

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1 渝公网安备 50019002500403号 违法和不良信息举报中心

互联网出版许可证 新出网证(渝)字10号 全国400电话 - 免长途话费