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Accumulated Error Correction of Strip Stereo Models Connection withoput GCPs
Haiqing He,Xiaoyong Chen,Penggen Cheng 보안공학연구지원센터 2015 International Journal of Multimedia and Ubiquitous Vol.10 No.3
The commonly used accumulated error correction of strip stereo models connection need a number of GCPs(Ground Control Points), which is unsuitable for low-altitude photogrammetry with a large number of images. In this paper, a novel approach of accumulated error correction of strip stereo models connection without GCPs was proposed. The accumulated error is adjusted by changing reference image and nonlinear polynomial method. Firstly the middle image of a strip is used as reference image. Then the accumulated error of baseline parameters are adjusted by inverse distance weighted method. Finally the rotation angles of relative orientation are adjusted by polynomial formula between the fitted angles and ideal statistics. Experimental results show that the approach is effective and practical, and can significantly reduce the distortion and accumulated error of model connection, may be suitable to implement strip aerial triangulation in low-altitude photogrammetry.
Huanhuan Sun,Haiqing Ma,Guangyao He,Jiashu Chen,Pengxin Qiu,Guangmei Yan 대한약학회 2010 Archives of Pharmacal Research Vol.33 No.7
FIa, a factor X activator, was isolated from the venom of Daboia russellii siamensis (Myanmar) after a series of chromatographic separations. FIa displayed procoagulant activity by shortening plasma recalcification time and converted human factor X (FX) to activated human factor X (FXa) by cleaving the heavy FX chain, possibly at the Arg51-Ile52 peptide. FIa was positive in a glycoprotein staining test, demonstrating that it is a glycoprotein. Optimal temperature and pH values were important for FIa procoagulant activity. Procoagulant activity was maintained above 85% of the initial activity at pH 7.0~8.0, and showed equally maximum activity at temperatures ranging from 30 to 50oC. In addition, FIa procoagulant activity was completely inhibited by EDTA (5 mM), but not by PMSF (10 mM), suggesting that it is a metalloproteinase.
Liang Tiebiao,Liang Anshan,Zhang Xianbo,Wang Qi,Wu Haiqing,He Jun,Jin Tianbo 한국유전학회 2022 Genes & Genomics Vol.44 No.9
Background: Coronary heart disease (CHD) is a disease that seriously harms human health. Genetic factors seriously affect the CHD susceptibility. The CYP20A1, CYP4F2 and CYP2D6 are important drug metabolism enzymes in the human body. Objective: We aimed to explore the association between CYP20A1, CYP4F2, CYP2D6 single nucleotide polymorphisms (SNPs) and CHD risk in the Chinese Southern Han population. Methods: Based on the 'case-control' experimental design (505 cases and 508 controls), we conducted an association study between 5 candidate SNPs selected from CYP20A1 (rs2043449), CYP4F2 (rs2108622, rs3093106, rs309310), CYP2D6 (rs1065852) and CHD risk. Logistic regression was used to analyze the CHD susceptibility under different genetic models. Multi-factor dimensionality reduction (MDR) was used to analyze the interaction of 'SNP-SNP' in CHD risk. Results: Our results showed that under multiple genetic models, CYP2D6 rs1065852 significantly increased the CHD risk in these participants who are ≤ 60 years old (OR 1.40, CI 1.07-1.82, p = 0.013), smokers (OR 1.40, CI 1.02-1.93, p = 0.039), or have family history (OR 1.24, CI 1.02-1.51, p = 0.035). CYP4F2 SNPs rs2108622 (OR 0.63, CI 0.43-0.93, p = 0.020), rs3093106 (OR 0.52, CI 0.29-0.92, p = 0.023), and rs309310 (OR 0.55, CI 0.31-0.96, p = 0.033) were potentially associated with the course of CHD patients. Conclusion: Our study found that CY2D6 rs1065852 has an outstanding and significant association with increased CHD risk. Our study provided data supplements for CHD genetic susceptibility loci, and also provided a new and valuable reference for CHD drug treatment.