】最大功率：750W含水量露点：小于-60℃嗓音大小：约58dB运行应用：适用于24小时连续工作运行操作简单：一键式操作就能自动发生。安装环境:室内（无基础安装）颗粒物：含量小于0.01um输出接口：3mm或1/8in（M8×1外螺纹）电源电压：AC 230V (50/60 Hz

分子流行病学再揭示人类复杂疾病遗传因素及其与环境因素相互作用发挥重要作用,为人类疾病的风险评估、预防和个性化治疗提供依据。全基因组关联分析（GWAS）为全面系统研究复杂疾病的遗传因素掀开了新的一页，为我们了解人类复杂疾病的发病机制提供了更多的线索。科学家已经在肥胖、糖尿病、冠心病、阿尔茨海默、乳腺癌、前列腺癌、肺癌、胃癌等一系列复杂疾病中进行了全基因组关联研究并找到疾病相关的易感基因，我国科学家也在银屑病、精神病和冠心病等方面开展了GWAS研究并取得成效。国家科技部最新公布了“常见重大疾病全基因组关联分析和药物基因组学研究”的863重点项目，吹响了我国大规模开展GWAS研究的号角。为了让更多的相关研究人员，特别是广大研究生了解GWAS的研究原理和方法，学会设计GWAS的研究和分析实验结果，同时在癌症领域分享海内外研究专家们的成功经验，并期待在GWAS方面进行交流合作,复旦大学和美国Van Andel 研究所将于2009年7月12-14日在上海联合举办上海分子流行病学与GWAS国际 研讨会, 期待各位同道免费参加，请有意者及时将回执返回联系邮箱。免注册费（食宿餐饮费用自理）。名额有限，报名从速！时间： 2009年7月12－14日
报到地点： 复旦大学卿云楼宾馆 上海市邯郸路220号，200433
会议地点： 复旦大学逸夫楼报告厅
联 系 人： 赵雪莹 高歌 联系电话： 021-55664495
回执邮箱： GWAS2009@gmail.com
BackgroundRecent success of genome-wide association studies (GWAS) in the U.S. and Europe has lead to the identification of a large number of genetic variants that are associated with disease risk and progression, including those for cancer and cardiovascular diseases. The discovery of these genetic markers not only improves our understanding of disease etiology, but also contributes significantly to risk prediction, early detection, and targeted treatment of diseases.Although GWAS have been used in Chinese populations to identify Chinese-specific risk-associated genetic variants for several common diseases such as breast cancer and psoriasis, many more GWAS are needed for various diseases. A better understanding of the importance of GWAS and a better knowledge of study design and data analysis of GWAS will further promote broad application of GWAS in China. This symposium which will cover genetic epidemiology and GWAS in China is organized to serve this purpose. We have invited a group of experts in this area from the U.S. and China to share their experience in GWAS, and we hope to foster an environment which will encourage an open discussion among all participants.
Objectives• To better understand the potential applications of GWAS
• To address practical issues in study design, implementation, and data analysis of GWAS
• To promote interaction and collaboration among researchers who are interested in GWAS
• To explore other important studies after GWAS: gene-environment interaction, risk prediction, and functional analyses
• To consider issues and implications related to genomic and personalize medicine
Organizing committeeThe organizing committee consists of four members:
Dr. Jianfeng Xu (Co-Chair)
Dr. Daru Lu (Co-Chair)
Dr. Li Jin (Co-Chair ,Advisor)
Dr. Qingyi Wei (Co-Chair, Advisor)
PresentationsSession I: Genetic epidemiology and GWAS of cancer
• Breast cancer in Chinese populations Xiao-ou Shu
• Genetic association studies of skin cancer Jiali Han
• Genetic variants in the MC1R gene and risk of cutaneous melanoma Qingyi Wei
• Genetic association studies of lung cancer in Chinese populations Daru Lu
• Molecular epidemiology of hepatitis, liver cirrhosis and hepatocarcinoma Gangqiao Zhou
• Molecular epidemiology of stomach cancer Weimin YeSession II: Genetic epidemiology and GWAS of other diseases
• Genetic association studies of hypertension in Chinese populations Jiang He
• GWAS of Autoimmune Diseases (Psoriasis, etc.) in Chinese populations Wei Huang
• Molecular epidemiology of diabetes in Chinese populations Weiping Jia
• Molecular genetics study of hypertension in Chinese populations Dingliang Zhu
• Molecular epidemiology of hepatitis, liver cirrhosis and hepatocarcinoma Gangqiao ZhouSession III: Post-GWAS studies
• Genetic structure of Chinese population Li Jin
• High-throughput genotyping for GWAS and fine mapping studies Siqun Lilly Zheng
• Molecular genetics study of neural tube defect Hongyan Wang
• Risk prediction using genetic variants in prostate cancer Jianfeng Xu
• Gene-environmental interaction in smoking related cancer Zuo-Feng Zhang
• Cancer Somatic Genomics Bin TehSession IV: Short presentations by participants and discussion
Registration时　　间： 2009年7月12－14日
报到地点： 复旦大学卿云楼宾馆大厅 上海市邯郸路220号 (200433)
会议地点： 复旦大学逸夫楼报告厅
联 系 人： 赵雪莹，高歌 (Shanghai, China)；Tamara Adams (U.S.)
联系电话： 21-55664495 (Shanghai, China)；336-713-7532 (U.S.)
回执邮箱： GWAS2009@gmail.com (Shanghai, China)；tsadams@wfubmc.edu (U.S.)
Invited speakers (alphabetic)• Jiali Han, Ph.D., is an Assistant Professor of Medicine at Harvard Medical School. His major research areas are:
• Genetic epidemiology of skin cancer and breast cancer
• Genome-wide association studies
• Gene-environment interaction• Jiang He, M.D. Ph.D., is a Professor and Chair of Epidemiology, Tulane University School of Public Health., U.S.A. His major research areas are:
• Genetic epidemiology of hypertension
• Gene-nutrition interaction of cardiovascular disease• Wei Huang, Ph.D., is a Professor and Executive Deputy Director of Chinese National Human Genome Center at Shanghai, China. Her major research areas are:
• Genetic susceptibility to autoimmune diseases, cardiovascular diseases and cancer.
• Genome-wide association studies
• Genetic variants and association study• Weiping Jia M.D., is a professor of endocrinology at Shanghai Institute of Diabetes, Shanghai No.6 People’s Hospital, Shanghai Jiaotong University, Her major research area is:
• Molecular endocrinology and diabetes• Li Jin, Ph.D, is a Professor of Genetics and vice President of Fudan University, China. His major research areas are:
• Genetic and molecular epidemiology of lung cancer and glioma
• Genetics of metabolism diseases
• Genetic markers for population genetics• Daru Lu, Ph.D, is a Professor of Genetics and Vice Dean of School of Life Sciences, Fudan University, China. His major research areas are:
• Genetic and molecular epidemiology of lung cancer and glioma
• Genetics of metabolic disease• Xiao-ou Shu, M.D, Ph,D, is a Professor of Medicine in the Department of Medicine at the Vanderbilt University School of Medicine, U.S.A. Her major research areas are:
• Genetic and lifestyle predictors of cancer and other chronic diseases
• Cohort study methodology
• Incorporating biomarkers in risk prediction• Bin Teh, M.D, is a Distinguished Scientific Investigator at Van Andel Institute, U.S.A. His major research areas are:
• Translational cancer research
• Gene expression profiling
• Cancer genome high-throughput sequencing• Hongyan Wang, Ph.D, is a professor of genetics at School of Life sciences, Fudan University, China. Her major research area is:
• Molecular genetics and epidemiology of birth defects (deformity of neural tube, congenital heart disease, etc.)• Qingyi Wei, M.D, Ph.D, is a Professor of Epidemiology at The University of Texas M. D. Anderson Cancer Center, U.S.A. His major research areas are:
• Molecular epidemiology of DNA repair, apoptosis, and skin cancer and head and neck cancer
• Genetic susceptibility to cancer
• DNA repair and apoptosis phenotype markers• Jianfeng Xu, M.D, Dr.PH, is a Professor of Epidemiology and Cancer Biology and Director of the Center for Cancer Genomics at Wake Forest University School of Medicine, U.S.A. His major research areas are:
• Genetic epidemiology of prostate cancer
• Genome-wide association and fine mapping analysis
• Risk prediction using genetic markers and other clinicopathologic variables• Zuo-Feng Zhang, M.D., Ph.D, is a Professor of Epidemiology at UCLA School of Public Health, U.S.A. His major research areas are:
• Molecular epidemiology of smoking-related cancers
• Confirmation studies of SNPs identified in genome-wide association studies in smoking-related cancers
• Gene-environmental interaction between genetic markers and environmental factors• S. Lilly Zheng, M.D, is a Professor of Medicine and Director of the Genotyping Laboratory at Wake Forest University School of Medicine. U.S.A. Her major research areas are:
• High-throughput genotyping and sequencing
• Genetic epidemiology of prostate cancer• Gangqiao Zhou, Ph.D, is a Professor of Medical Genetics and Genomics in National Academy of Military Medical Science. His major research area is:
• molecular and genetics of complex diseases• Dingliang Zhu, M.D, is a professor of cardiology at Shanghai Institute of Hypertension, Shanghai, China. His major research area is:
• Molecular and genetics of cardiovascular diseases• Weimin Ye, Ph.D, is a Professor of Medical Epidemiology at Karolinska Institutet, Sweden. His major research areas are: Etiology of upper gastrointestinal diseases
• Topic of presentation: Molecular epidemiology of stomach cancer

。“我们发现，进入重症监护室前服用过抗抑郁药的患者整体死亡率较高，入住一年后死亡率仍然显著较高，”凯瑟琳. M. 伯格博士说。她是参与...。然而，他们指出，该信息重点强调需要替代方法以监测具有潜在不良作用的药物，且在本研究截至时大量的临床数据库可能发挥作用。使用多参数智能重症监护II

72所，各类科研开发机构2457个，规模过亿元的改制院所近10家，国家级重点实验室13个，国家级工程技术研究中心14个，省级高技术研究重点实验室19个，省级...代理商。六、展位收费：展位类型 标准展位（3m × 3m ）特别展位（2m × 2m）光 地（最少 36m

疾病或缺氧性肺部疾病所致的肺动脉高压患者（即，II类或III类肺动脉高血压），不要常规给予其仅获准用于治疗肺动脉高压的高级血管活性药治疗。三、对于

解析心电图的第 1 部分显示心律齐，心率 120 次/分，PR 间期恒定（0.14 s），每个 QRS 波前均可见 P 波，I、II、aVF、V4- V6 导联的 P 波正向，提示为窦性心动过速。QRS 波间期正常（0.1s），形态也正常。II、III、aVF 导联可见窄且深的 Q 波（^），考虑为正常变化。电轴正常

%；10年的OS为73%；DFS为70%。30天死亡率为1%（n=21）。10年CIR为12%。（见图1）图1，A、B、C分别为OS、DFS和CIR的K-M曲线。行根治性切除术（R0）患者达88%；其中Masaoka分期为I（n=672）、II（n=699）、III（n=410）、Ⅳ（n=215）期患者R0率分别为99

、HBcAb：8.97 S/CO 阳性，高敏 HBV-DNA：3.32×10^3IU/mL。彩超提示脂肪肝，左肾囊肿。肝硬度 CAP211dB/m...、HBcAb：9.45S/CO 阳性，高敏 HBV-DNA：3.85×10^1 IU/mL。彩超提示脂肪肝，左肾囊肿。肝硬度 CAP203dB/m、E5.8Kpa

IU/ml、 HBeAb 和 HBcAb 阳性，HBV-DNA 未检测到（罗氏参考值 ＜20 IU/mL），CAP 值 202 dB/m，肝硬度 23.5 kpa...治疗于我院治疗。患者母亲故于乙肝后肝癌，否认吸烟及饮酒史。查体：身高 168 cm，体重 60 kg，BMI 21.3 kg/m2 ，神志清，可见肝掌，未见蜘蛛痣

Molecular Markers of Gastric Cancer and Personalized Treatment StrategyProfessor Dongfeng Tan, M.D.Department of PathologyThe University of Texas M D

表达相似。此外，研究人员还将慢病毒注射进 db/db 小鼠心脏内，结果发现小鼠静脉注射 FITC 标记的凝集素显示 Micro 组的微循环改善，这也表明了 db/ db 小鼠心脏中 mir-16-2-3p 的过表达与心脏改善功能、纤维化和微循环存在联系。图 3 来自 DM、DM-CMD 和 DM-CAD 的血清来源的

）John C. Chaloupka（美国）Adel M. Malek （美国）Vitor M. Pereira（瑞士）蔡艺灵 陈海波 范...-13:00 工作午餐13:00-17:30 专题演讲II： 求精??——专题发言19:00

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Experimental lab sessionACL II-Hamstring&BTB harvesting-Reliability

视野缺损的程度，分成视野进展最小组（<-0.02 [dB]/年）、视野进展中等组（-0.02 to-0.65 dB/年）、视野进展快速组（≥-0.65 dB/年）。为了避免假阳性的评估结果，该研究还设立了33个青光眼病人的对照组，在同一天进行两组眼底立体照相。采用自动交替闪烁定位技术进行

进修结业。1982年获WHO奖学金赴美国M.D.Anderson Hospital访问研究。1965年起从事肿瘤化疗研究及临床工作，先后任中山医科大学肿瘤医院... Oncology，Supp II 116:143,1990.