Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Xue-Shan Xiao"'
Autor:
Jie Pan, Chun-Dong Wang, Ying-Hui Tao, Jun Li, Qi-Liang Mei, Qian-Xue Ding, Zhao-Yu Wu, Xue-Shan Xiao
Publikováno v:
Metallurgical and Materials Transactions A. 53:3774-3794
Publikováno v:
Materials Science Forum. 852:1168-1174
0.15 wt. % Ti-microalloyed Co-28.5Cr-5.9Mo-0.27C alloy has been developed by examining the effect of solution and aging treatment on microstructure, mechanical and corrosion properties. The results showed that elongation of the cast specimen were low
Autor:
Xue-Shan Xiao1 xsxiao@mail.shu.edu.cn, Guo-Ming Wang1, Shou-Shi Fang1, Qin Hua1, Jian-Zhong Gu1, Yuan-Da Dong1
Publikováno v:
Journal of Materials Science. Oct2005, Vol. 40 Issue 20, p5435-5438. 4p. 1 Black and White Photograph, 6 Diagrams.
Autor:
Jiang, Li, Qing-jiong, Zhang, Rong, Fu, Xue-shan, Xiao, Jia-zhang, Li, Feng-sheng, Zhang, Shi-qiang, Li, Wei, Li, Tuo, Li, Xiao-yun, Jia, Li, Guo, Xiang-ming, Guo
Publikováno v:
Yi chuan = Hereditas. 24(5)
To analyze the relationship of the peripherin gene(PRPH, OMIM17071) mutations with high myopia,genomic DNA was collected from 180 probands with high myopia (or=-6.0 dipoters) and 60 unrelated persons without high myopia. The coding sequences of PRPH
Autor:
Yan, Wang, Xiang-ming, Guo, Xiao-yun, Jia, Shi-qiang, Li, Xue-shan, Xiao, Li, Guo, Qing-jiong, Zhang
Publikováno v:
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics. 22(3)
To analyze the mutation of Leber's hereditary optic neuropathy (LHON) and the clinical features in Chinese patients.The primary mtDNA mutations (3460A, 11778A and 14484C) of 156 patients (110 probands and 46 maternal relatives with LHON) were detecte
Publikováno v:
Yi chuan = Hereditas. 24(1)
To screen possible disease-causing mutations in the GUCA1B gene, GNGT1 gene,and the alternative-splicing region of RGS9 gene in 120 probands with retinitis pigmentosa,genomic DNA was collected from 120 probands with retinitis pigmentosa out of 120 fa