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A Circuit Simulation Model for An Uitra-fast IGBT And Analysis of Parameter Sensitivity
Ai-min Li,Xiang-ning He,Zhao-ming Qian 전력전자학회 1995 ICPE(ISPE)논문집 Vol.1995 No.10
Based on existing built-in models of PSpice, by the composite model principle, a composite Insulated Gate Bipolar Transistor (IGBT) model for an ultra-fast IGBT is presented Comparison between measurement and simulation results shows good agreement in transient and steady-state behaviour of the IGBT Parametric sentive analysis of this model is performed, and validity of the composite model is discussed.
Wei-Ning Yang,Zhi-Hong Ai,Juan Wang,Yan-Li Xu,Yincheng Teng 대한부인종양학회 2014 Journal of Gynecologic Oncology Vol.25 No.1
Objective: The objective of this study was to evaluate the effect of overexpression of epidermal growth factor receptor (EGFR) on the expression of epithelial cell markers (E-cadherin and α-catenin) and mesenchymal cell markers (N-cadherin and vimentin) in endometrial carcinoma. Methods: The expression of all 4 markers was evaluated in EGFR overexpressing Ishikawa cells, control Ishikawa cells, and KLE cells using reverse transcription polymerase chain reaction (RT-PCR) and Western blotting. The expression of these 4 markers was also determined in cancerous tissues of patients with endometrial carcinoma using immunohistochemical staining. Results: Ishikawa cells transfected with EGFR showed decreased expression of E-cadherin and α-catenin and increased expression of N-cadherin and vimentin compared with control Ishikawa cells (p<0.01 for all). The expression of N-cadherin and vimentin was higher and the expression of E-cadherin and α-catenin was lower in stage II-III than stage I and in grade II-III than grade I endometrial carcinoma tissue (p<0.01 for all). Conclusion: Decreased expression of epithelial markers (E-cadherin and α-catenin) and increased expression of mesenchymal markers (N-cadherin and vimentin) were observed in human endometrial carcinoma tissue. These findings correlate with high EGFR expression in cultured endometrial carcinoma cells.
Taotao Ai,Ning Yu,Xiaoming Feng,Niansuo Xie,Wenhu Li,Pengju Xia 대한금속·재료학회 2015 METALS AND MATERIALS International Vol.21 No.1
Ti2AlC/TiAl in situ composites were fabricated via a reaction Hot-Pressing Process using Ti3AlC2, Ti, and Alpowders as initial materials. The effect of Ti2AlC content on the phases and microstructure of the as-sinteredcomposites was investigated by XRD and SEM. The mechanical properties such as Vickers hardness, flexuralstrength and fracture toughness of the as-sintered composites were also tested. The products consisted ofTi2AlC, γ-TiAl and α2-Ti3Al as the major phases. Ti2AlC reinforcements were mainly distributed in the grainboundaries, resulting in obvious γ+α2 grain refinement. With increasing Ti3AlC2 content (up to 5 wt%), theVickers hardness, flexural strength and fracture toughness of the as-sintered composite reached the maximumvalues of 3.7 GPa, 651.5 MPa, and 10.89 MPa·m1/2, respectively. Analysis of fracture surface and crackpropagation paths indicated that crack deflection and crack bridging of the in situ precipitated Ti2AlC phasesobtained by decomposing Ti3AlC2 were the main reasons for the observed composite toughening.
Fused Polypeptide with DEF Induces Apoptosis of Lung Adenocarcinoma Cells
Liang, Ai-Ling,Zhang, Ting-Ting,Zhou, Ning,Huang, Di-Nan,Liu, Xin-Guang,Liu, Yong-Jun,Tu, Zhi-Guang Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.12
To analyze the effects of a new unknown peptide DEF on the growth of tumor cells, a fused polypeptide TAT-DV1-DEF was designed and synthesized. The lung adenocarcinoma cell line GLC-82 treated with TAT-DV1-DEF was analyzed with a cell counting kit 8, and the location of polypeptides in cells was observed under laser confocal microscopy. The efficiency of polypeptide transfection and changes in nuclear morphology were analyzed by flow cytometry and fluorescence microscopy, respectively. Finally, the mechanism of tumor cell growth inhibition was evaluated by Western blotting. We found that TAT-DV1-DEF could significantly inhibit the growth of the lung adenocarcinoma cell line GLC-82, but not the normal human embryonic kidney cell line HEK-293. Polypeptides were found to be mostly localized in the cytoplasm and some mitochondria. The efficiency of polypeptide transfection in the two cell types was approximately 99%. Apoptotic nuclei were observed under fluorescence microscopy upon treatment with polypeptides and DAPI staining. Western blot analyses indicated that the polypeptide inhibition of tumor cell growth was apoptosis dependent. In the present study, we demonstrated that fused polypeptides could induce apoptosis of the lung adenocarcinoma cell line GLC-82, indicating that the new unknown peptide DEF has antitumor effects.
Prognosis and Clinicopathology of CXCR4 in Colorectal Cancer Patients: a Meta-analysis
Li, Lu-Ning,Jiang, Kai-Tong,Tan, Peng,Wang, Ai-Hua,Kong, Qing-Yin,Wang, Cui-Yue,Lu, Hua-Rong,Wang, Jing Asian Pacific Journal of Cancer Prevention 2015 Asian Pacific journal of cancer prevention Vol.16 No.9
The chemokine receptor 4 (CXCR4) has been widely used in diagnosis and prognosis of colorectal cancer (CRC). However, there is no current consensus on the impact of CXCR4 on CRC patients. The purpose of this study was to evaluate the prognostic and clinicopathological importance of CXCR4 in CRC patients. Databases, such as PubMed, Cochrane library, CBM and EMBASE updated to 2014 were searched to include eligible articles. We analysed correlations between CXCR4 expression and clinicopathological features and overall survival (OS). A total of 1, 055 CRC patients from twelve studies were included in the study. The pooled odds ratios (ORs) which indicated CXCR4 expression was likely to be associated with TNM stage (OR=0.43, CI=0.34-0.55, P<0.00001), lymph node status (OR=2.23, CI=1.23-4.05, P=0.008) and vascular invasion (OR=2.21, CI=1.11-4.39, P=0.02). Poor overall survival of CRC cancer was found to be significantly related to CXCR4 overexpression (hazard ratio (HR) 1.36 CI=1.17-1.59, P<0.0001), whereas combined ORs revealed that CXCR4 expression had no correlation with gender or differentiation. Based on the published studies, CXCR4 overexpression in patients w ith CRC indicates poor survival outcome and clinicopathological factors.
Yang, Xiao-Fei,Sun, Ai-Ning,Yin, Jia,Cai, Cheng-Sen,Tian, Xiao-Peng,Qian, Jun,Chen, Su-Ning,Wu, De-Pei Asian Pacific Journal of Cancer Prevention 2012 Asian Pacific journal of cancer prevention Vol.13 No.11
A monosomal karyotype (MK), defined as ${\geq}2$ autosomal monosomies or a single monosomy in the presence of additional structural abnormalities, was recently identified as an independent prognostic factor conveying an extremely poor prognosis in patients with acute myeloid leukemia (AML). In the present study, after excluding patients with t(15;17), t(8;21), inv(16) and normal karyotypes, 324 AML patients with cytogenetic abnormalities were the main subject of analysis. The incidences of MK were 13% in patients aged 15 to 60 years and 18% in those between 15 and 88 years old. MK was much more prevalent among elderly patients (p < 0.001) and was significantly associated with the presence of -7, -5, del(5q), abn12p, abn17p, -18 or 18q-, -20 or 20q- and CK (for all p < 0.001 except for abn12p p=0.009), and +8 or +8q was less frequent in MK+ AML(p=0.007). No correlation was noted between monosomal karyotype and FAB subtype (p > 0.05); MK remained significantly associated with worse overall survival among patients with complex karyotype (p=0.032); A single autosomal monosomy contributed an additional negative effect in OS of patients with structural cytogenetic abnormalities (P=0.008). This report presents the prevalence, feature and prognostic impact of MK among a large series of Chinese AML patients from a single center for the first time.
Ice Disaster Prevention Measure Optimization Model
Hui Hou,Yuan-sheng Li,Joe Dong,Ning Lu,Ai-hong Tang 보안공학연구지원센터 2015 International Journal of Security and Its Applicat Vol.9 No.9
Based on some commonly used methods of deicing technology, this paper used the series-parallel network system to express the risk level and proposed a simplified mathematical optimization model to arrange the ice prevention measures properly to make the lowest input while achieve the best ice prevention effect. An example based on WSCC-9 system is calculated using MATLAB. It can be seen that the deicing tool input should be larger if the efficiency of deicing tools is low or the expected failure probability is low. And a higher failure probability indicates more deicing tool input.
Jianxue Liu,Yonghao Ji,Hong Ai,Bo Ning,Junzhi Zhao,Yaoren Zhang,Guoliang Dun 대한영상의학회 2016 Korean Journal of Radiology Vol.17 No.3
Objective: To compare several noninvasive indices of fibrosis in chronic viral hepatitis B, including liver shear-wave velocity (SWV), hyaluronic acid (HA), collagen type IV (CIV), procollagen type III (PCIII), and laminin (LN). Materials and Methods: Acoustic radiation force impulse (ARFI) was performed in 157 patients with chronic viral hepatitis B and in 30 healthy volunteers to measure hepatic SWV (m/s) in a prospective study. Serum markers were acquired on the morning of the same day of the ARFI evaluation. Receiver operating characteristic (ROC) analysis was performed to evaluate and compare the accuracies of SWV and serum markers using METAVIR scoring from liver biopsy as a reference standard. Results: The most accurate test for diagnosing fibrosis F ≥ 1 was SWV with the area under the ROC curve (AUC) of 0.913, followed by LN (0.744), HA (0.701), CIV (0.690), and PCIII (0.524). The best test for diagnosing F ≥ 2 was SWV (AUC of 0.851), followed by CIV (0.671), HA (0.668), LN (0.562), and PCIII (0.550). The best test for diagnosing F ≥ 3 was SWV (0.854), followed by CIV (0.693), HA (0.675), PCIII (0.591), and LN (0.548). The best test for diagnosing F = 4 was SWV (0.965), followed by CIV (0.804), PCIII (0.752), HA (0.744), and LN (0.662). SWV combined with HA and CIV did not improve diagnostic accuracy (AUC = 0.931 for F ≥ 1, 0.863 for F ≥ 2, 0.855 for F ≥ 3, 0.960 for F = 4). Conclusion: The performance of SWV in diagnosing liver fibrosis is superior to that of serum markers. However, the combination of SWV, HA, and CIV does not increase the accuracy of diagnosing liver fibrosis and cirrhosis.