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Sheng-Yao Fan,Qiu-Ju Zhang,Hai-Wei Chen,Wen-xuan Zeng 대한기계학회 2013 JOURNAL OF MECHANICAL SCIENCE AND TECHNOLOGY Vol.27 No.12
A reasonable dielectric fluid velocity and better exclusion of debris are very important to obtain a stable machining performance in multi-cutting of WEDM-HS. We investigated the dynamic characteristics of multi-cutting wire electrode in WEDM-HS subjected to working fluid considering the effect of debris. First, a fluid-solid coupling nonlinear vibration model is derived by analyzing the forces acting on the multi-cutting wire which locate in the dielectric fluid. The additional axial force arising from the transverse vibration of the multi-cutting wire is considered as a nonlinear term in the model. Considering that the debris accumulation in discharge gap severely influences the stability of multi-cutting wire electrode, the relationship between the debris volume concentration and debris-working fluid two-phase flow drag coefficient is obtained using the Einstein two-phase flow viscosity theory. Finally, the influences of several parameters on the multi-cutting wire displacement are discussed in detail.
( Wen Qian Wei ),( Fang Qi Liu ),( Lei Liu ),( Zuo Feng Li ),( Xiao Yan Zhang ),( Fan Jiang ),( Qu Shi ),( Xiao Yan Zhou ),( Wei Qi Sheng ),( San Jun Cai ),( Xuan Li ),( Ye Xu ),( Peng Nan ) 생화학분자생물학회(구 한국생화학분자생물학회) 2011 BMB Reports Vol.44 No.5
Hereditary non-polyposis Colorectal Cancer (HNPCC) is an autosomal dominant inheritance syndrome. HNPCC is the most common hereditary variant of colorectal cancer (CRC), which accounts for 2-5% CRCs, mainly due to hMLH1 and hMSH2 mutations that impair DNA repair functions. Our study aimed to identify the patterns of hMSH2 and hMLH1 mutations in Chinese HNPCC patients. Ninety-eight unrelated families from China meeting Amsterdam or Bethesda criteria were included in our study. Germline mutations in MLH1 and MSH2 genes, located in the exons and the splice-site junctions, were screened in the 98 probands by direct sequencing. Eleven mutations were found in ten patients (11%), with six in MLH1 (54.5%) and five in MSH2 (45.5%) genes. One patient had mutations in both MLH1 and MSH2 genes. Three novel mutations in MLH1 gene (c.157_160delGAGG, c.2157dupT and c.-64G>T) were found for the first time, and one suspected hotspot in MSH2 (c.1168C>T) was revealed. [BMB reports 2011; 44(5): 317-322]