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| 1 | Effect of organic matter and pH on mercury release from soils显示文摘调查在水银(Hg ) 上在有机物(OM ) 和 pH 的效果上被进行从土壤的版本。Hg 版本流动用与 Lumex 相结合的动态流动房间(DFC ) 被测量吗?在实验室实验并且地监视的多功能的水银分析器。结果证明因为与 Hg 的 OM 的高亲密关系,从增加 OM 的土壤的 Hg 排放是显然低的,导致象 OM 增加的数量的反向的顺序。同时,从不同 pH 土壤的 Hg 版本流动为 Hg2+ 和 Hg22+ 处理展出了一样的趋势,增加有土壤增加的 pH 的 Hg 流动。在 pH 依赖实验的 Hg 版本的趋势从地测试与那一致好。另外, Hg 版本似乎与它在土壤的种类有关,从增加 Hg2+ 的土壤的流动显然比由实验室实验的增加 Hg22+ 的土壤的高。 | YANG Yong-kui ZHANG Cheng SHI Xiao-jun LIN Zao WANG Ding-yong | 2007 | Journal of Environmental Sciences2007，19，11： | 20 |
| 2 | Synthesis of Polymer-Bonded Carbonyl Ruthenium (Ⅱ) and Osmium (Ⅱ) Porphyrins显示文摘Studyonmetalloporphyrincomplexesusedasenzymemodelcatalyzingtheoxidationofalkaneandepoxidationofalkeneiscurrentlyaveryactiveresearchfieldl.ThereactivityofrutheniumporphyrincomplexeswasusedasoxidationcatalystsbecausetheirrelationstocytochromeP-450haveb... | Zao Ying LI Cong LI Jiang Lin LIANG Kun YAN(Department of Chemistry, Wuhan University, Wuhan 430072) | 1999 | Chinese Chemical Letters1999，10，1： | 1 |
| 3 | A Study of Ground Deformation in the Guangzhou Urban Area with Persistent Scattered Interferometry显示文摘 | ZAO QING LIN HUI JIANG LIMING | | 0，，： | 1 |
| 4 | The complete genomic sequence analysis of genotype 4 human astrovirus HASTVgz01 strain in Guangzhou显示文摘To analyze the genomic molecular structure and genotype of human astrovirus isolated from infant in Guangzhou of China, the primers were designed based on the genomic sequence of astrovirus from the GenBank and the target sequence were amplified by RT-PCR. Then the PCR-products were cloned to T vector and sequenced. The genomic nucleotide sequences were analyzed by the programs CLUSTAL W and DNASTAR. It was found that the full genomic length of HASTVgz01 strain was 6721 bp and the ORFs were 6558 bp. The 5' and 3' UTR were 82 and 81 nucleotides. The genome included 3 open reading frames (ORFs): ORF1a, ORF1b and ORF2. The 5'-terminal ORF1a started at nucleotide 83 and extended to nucleotide 2845. ORFlb (nt 2785 to nt 4332) overlaped ORFla by 61 nucleotides. The 3'-terminal ORF2 began at nucleotide 4325 and terminated at nucleotide 6640. ORF2 had 2316 nucleotides. Compared with other astrovirus sequences in GenBank, the homology of the amino acid sequence of ORF2 of HASTVgz01 strain with that of serotype 4 was 93% . Homology with other serotypes ranged from 61% to 70% . The complete nucleotide sequence of astrovirus HASTVgz01 strain isolated from Guangzhou in China was 6721 bp in length, GenBank accession NO. DQ344027. Comparing the ORF2 of astrovirus HASTVgz01 with the known sequences of types 1-8 the highest homology was serotype 4 (93%). Comparative sequence analysis of the HASTVgz01 ORF2 with the reported human astrovirus sequences revealed that the isolated astrovirus belongs to genotype (serotype) 4. | BING ZHU JIA YU ZHONG XIAO LI YI CHEN TAO LIN ZAO HE WU RONG ZHOU SI TANG GONG | 2006 | Journal of Microbiology and Immunology2006，4，3： | 0 |
| 5 | Oxaliplatin combined with 5-fluorouracil, leucovorin regimen for patients with advanced colorectal cancer显示文摘Objective: To observe the efficacy and tolerability of continuously infusing 5-fluorouracil (5-FU) / folic acid com- bined with oxaliplatin (L-OHP/5-FU/LV regimen) as first line treatment in advanced colorectal cancer. Methods: 23 patients of advanced colorectal cancer were treated with 5-FU 500 mg/d, civ, d1–d5, d8–d12, leucovorin 100 mg/d, iv gtt, d1, d8, folic acid tablet 60 mg/d, po, d2–d5, d9–d12, and oxaliplatin 65 mg/(m2?d), iv gtt, d1, d8, repeated every 21 days (one cycle).The effect was evaluated after two cycles. Results: Complete response in 2 cases and partial response in 10 cases were observed with an overall response rate of 47.18%. Adverse effects were mainly grade 1–2, including nausea, vomiting, diarrhea, dental ulcer, peripheral neuritis and myelosuppression. Conclusion: L-OHP/5-FU/LV regimen is an effective and better tolerated alterna- tive treatment in advanced colorectal cancer and yields promising clinical application. | Suyi Li Lin Liu Xiaoyi Gu Zao Jiang Cailian Wang | 2007 | The Chinese-German Journal of Clinical Oncology2007，6，3： | 0 |
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