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Different kinds of ZnO nanowires were synthesized by vapor-solid and vapor-liquid-solid methods via a chemical vapor transport and condensation process. The samples were characterized by scanning electron microscopy, X-ray diffraction (XRD) and photoluminescence analyses. The control on the growth morphologies can be achieved by the source materials and by using a thin gold layer as a catalyst. 15-80 nm nanowires were obtained and XRD patterns show two different growth directions. High intensity green light from photoluminescence spectroscopy was observed which shows that the experimental results could be useful for light-emitting materials and other optoelectronic device applications. 相似文献
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Minaee Roya Peirovi Mokhtari Mehdi Moghaddam Alireza Ebrahimi Ali Asghar Askarishahi Mohsen Afsharnia Mojtaba 《Water Resources Management》2019,33(4):1557-1569
Water Resources Management - Injection of chlorine as a disinfectant and the correct prediction of the residual amount in water distribution networks are key points and important principles in the... 相似文献
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Role of spermatogonial stem cells extract in transdifferentiation of 5‐Aza‐2′‐deoxycytidine‐treated bone marrow mesenchymal stem cells into germ‐like cells
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Ebrahim Kharizinejad Bagher Minaee Zanganeh Neda Khanlarkhani Keywan Mortezaee Tayebeh Rastegar Maryam Baazm Farid Abolhassani Seyed Mehdi Sajjadi Mahdieh Hajian Fereshte Aliakbari Mohammad Barbarestani 《Microscopy research and technique》2016,79(5):365-373
As one of the induced pluripotent stem cells (iPSCs) methods, spermatogonial stem cells (SSCS) extract is considered as new approach in stem cell therapy of infertility. 5‐aza‐2′‐deoxycytidine (5‐aza‐dC) inhibits methyltransferase enzyme, and induces gene reprogramming; herein, the effects of SSCS extract incubation in 5‐aza‐dC‐treated bone marrow mesenchymal stem cells (BMMSCs) has been surveyed. BMMSCs were isolated from femurs of three to four weeks old male NMRI mice, and the cells at passage three were treated with 2 µM 5‐aza‐dC for 72 hours. SSCs were isolated, cultured, and harvested at passage three to collect SSCS extract; BMMSCs were then incubated with SSCS extract in the three time periods: 72 hours, one week and two weeks. There were five groups: control, sham, extract, 5‐aza‐dC and extract‐5‐aza‐dC. After one week of incubation, flow cytometry and real‐time polymerase chain reaction (PCR) exhibited high levels of expression for β1‐ and α6‐integrins and promyelocytic leukaemia zinc finger (PLZF) in extract and extract‐5‐aza‐dC groups (P < 0.05 vs. control and 5‐aza‐dC), and cells in these two groups had two forms of morphology, round and fusiform, similar to germ‐like cells. 5‐aza‐dC had no significant effects during the three time periods of evaluation. These data disclose the effectiveness of SSCs extract incubation in transdifferentiation of BMMSCs into germ‐like cells; this strategy could introduce a new approach for treatment of male infertility in clinic. Microsc. Res. Tech. 79:365–373, 2016. © 2016 Wiley Periodicals, Inc. 相似文献
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