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| 1 | AMPK activation by peri-sciatic nerve administration of ozone attenuates CCl-induced neuropathic pain in rats显示文摘 | Lijuan Lu Cailong Pan Lu Chen Liang Hu Chaoyu Wang Yuan Han Yanjing Yang Zhixiang Cheng Wen-Tao Liu | 2017 | Journal of Molecular Cell Biology2017，9，2： | 14 |
| 2 | Arthroscopic Anterior Cruciate Ligament Reconstruction With at Least 2.5 Years’ Follow-up Comparing Hamstring Tendon Autograft and Irradiated Allograft显示文摘 | Kang Sun Jihua Zhang Yan Wang Changsuo Xia Cailong Zhang Tengbo Yu Shaoqi Tian | 2011 | Arthroscopy: The Journal of Arthroscopic and Related Surgery2011，，： | 1 |
| 3 | Color image phase conjugate in photorefractive crystal Fe:LiNbO3显示文摘 | Zhang Jingjing | 1990 | App Opt1990，29，8： | 1 |
| 4 | Frequency-varied conjugation wave generation via nondegenerate four-wave mixing in Fe:LiNbO3 crystal显示文摘 | Zhang Jingjiang Wang Shuying | 1988 | App Opt1988，27，3： | 1 |
| 5 | In vitro differentiation of rabbit bone marrow mesenchymal stem cells into Schwann cells Induction effect of platelet-rich plasma显示文摘BACKGROUND: Bone marrow mesenchymal stem cells (BMSCs) differentiate into Schwann cells via specific inducers. However, the induction and culture procedures are complicated. Various growth factors have been used for induction and culture, and are likely affected by their environment. OBJECTIVE: To explore the differentiation feasibility of platelet-rich plasma-induced rabbit BMSCs, supplemented with various growth factors, into Schwann-like cells in vitro, and to examine the secretory function of Schwann-like cells. DESIGN, TIME AND SETTING: This comparison study was performed at the Experimental Animal Center, Affiliated Hospital of Qingdao University Medical College, China in October 2008. MATERIALS: Platelet-rich plasma and BMSCs were respectively obtained from the femoral vein and bone marrow of 2-month old New Zealand rabbits. The rabbit nerve growth factor ELISA kit and rabbit nerve growth factor PCR kit (Jingmei Biotech, China), as well as anti-rabbit S-100 immunofluorescence staining kit (Boster, China) were used in the present study. METHODS: BMSCs at passage three were harvested and were induced by 1 mmol/L β-mercaptoethanol and Dulbecco's-modified eagle's medium complete medium containing 35 ng/mL retinoic acid and 10% fetal bovine serum for the combination induction group, followed by incubation in complete medium supplemented with platelet-rich plasma. BMSCs in the single induction group were induced by β-mercaptoethanol and retinoic acid, followed by incubation in L-DMEM complete medium. BMSCs in the control group were incubated in L-DMEM complete medium. MAIN OUTCOME MEASURES: Cell growth in each group was observed under an inverted microscope. Following induction, S-100 protein expression was identified by immunofluorescence staining. Nerve growth factor protein concentrations in BMSC supernatant were subsequently measured by ELISA. In addition, nerve growth factor mRNA expression in the BMSCs was determined by reverse transcription-polymerase chain reaction. RESULTS: Overall BMSC morphology was similar to Schwann cells in the combination induction group, and morphology of the majority of BMSCs was similar to Schwann cells in the single induction group 9 days after induction. In the control group, significant changes in cell morphology were not observed 9 days after induction. S-100 protein expression was detected in the combination induction and single induction groups following induction. At days 7, 9, and 11, the expression rate of S-100-positive cells was greater in the combination induction group (P < 0.05). At days 4, 7, 9, and 11, nerve growth factor levels were significantly greater in BMSC supernatant in the combination induction and single induction groups compared with the control group (P < 0.05). At days 7, 9, and 11, nerve growth factor levels were significantly greater in the combination induction group compared with the single induction group (P < 0.05). At day 11, nerve growth factor mRNA expression in BMSCs was significantly greater in the combination induction group compared with the single induction group (P < 0.05). CONCLUSION: Culture conditions containing platelet-rich plasma elevated the differentiation efficiency of BMSCs into Schwann-like cells, which subsequently secreted nerve growth factor following induction. | Changsuo Xia Changrong Ding Yingzhen Wang Kang Sun Cailong Zhang Shaoqi Tian | 2010 | Neural Regeneration Research2010，5，1： | 1 |
| 6 | Improving the interfacial contact between CH_3NH_3PbI_(3–x)Cl_x and Au by LiTFSI solution treatment for efficient photoelectric devices显示文摘Organic lead halide compounds with perovskite structure become a promising photovoltaic material for lowcost thin film solar cells in recent years. The property of perovskite/metal interface is a fundamental topic for the effective charge transfer at metal electrodes. In this work, we develop an interface modification method of lithium bis(trifluoromethane sulfonimide)(Li TFSI) solution treatment, which can effectively decrease the charge transfer resistance at the CH_3NH_3PbI_(3 –x)Cl_x/Au interface. After the solution treatment, uniform nanodots are formed at the surface of CH_3NH_3PbI_(3–x)Cl_x films, and the barrier height at CH_3NH_3PbI_(3 –x)Cl_x/Au interface reduces from 0.51 V to 0.08 V. As a consequence, the efficiency of hole conductor free solar cells with CH_3NH_3PbI_(3 –x)Cl_x harvester increase from 4.0% to 7.6% under one sun condition. It is also found that the hole conductor free perovskite solar cell can work in a photodetector mode, which has the same output properties with phototransistors. After the Li TFSI solution treatment, the sensitivity of this photodetector can be improved for about one time. | Xiang Xia Hongcui Li Yanhua Li Cailong Liu Xizhe Liu | 2015 | Journal of Energy Chemistry2015，24，6： | 0 |
| 7 | GmNMHC5 may promote nodulation via interaction with GmGAI in soybean显示文摘Soybean(Glycine max[L.]Merr.)is a food and oil crop whose growth and yield are influenced by root and nodule development.In the present study,Gm NMHC5 was found to promote the formation of nodules in overexpressing mutants.In contrast,the number of nodules in Gmnmhc5 edited with CRISPR/Cas9 decreased sharply.In 35 S:Gm NMHC5 mutants,expression levels of genes involved in nodulation were significantly up-regulated.Both in vitro and in vivo biochemical analyses showed that Gm NMHC5 directly interacted with Gm GAI(a DELLA protein),and the content of gibberellin 3(GA_(3))in overexpressing mutants was lower than that in the wild type.These results revealed that Gm NMHC5 participates in the classical GA signaling pathway,and may regulate the content of GA_3 to match the optimal concentration required for nodule formation,thereby promoting nodulation by directly interacting with Gm GAI.A model illustrating the mechanism by which Gm NMHC5 promotes soybean nodulation is presented. | Wenting Wang Zhili Wang Wensheng Hou Li Chen Bingjun Jiang Wenya Ma Lijuan Bai Wenwen Song Cailong Xu Tianfu Han Yongjun Feng Cunxiang Wu | 2022 | The Crop Journal2022，10，1： | 0 |
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