的暴露情况。研究同时统计了从 1971～2009 年的呼吸系统疾病相关死亡率。研究发现，1971 年时，平均 BS 暴露浓度为 42.7 g/m3；2001 年时，平均 PM10 暴露浓度为 20.7 g/m3。72% 的受试者在研究随访期间有过搬家。研究发现，1971 年时的 BS 暴露浓度与 1972～2009

、BC 和臭氧浓度。研究发现，平均 PM10 浓度是 25±16 μg/m3。肺功能检测当天，PM10 浓度每增高 10 μg/m3，FVC 下降 19.7... μg/m3，FVC 下降 23.7 ml。FEV1 值不受 BC 浓度影响。PEF 值会受到气体污染物浓度影响，但影响略有滞后。敏感性分析显示，女性肺功能受空气污染

答疑会（辅料篇）June 186 月 18 日Hall E3 M23 Meeting RoomE3 馆 M23 会议室会议将邀请国内外药监及药典机构到会, 分享...;Location:HallE3MeetingRoomM23日期：2019 年 6 月 18 日

：SELECT是一个多中心、非盲、随机的3期临床试验。根据每位研究者的选择，患者在第一天接受500 mg/m2的培美曲赛或75 mg/m2的多西他赛，然后将患者随机分为两组，患者将接受化疗序贯西妥昔单抗（首剂400 mg/m2，以后每周250 mg/m2）或者只接受化疗。化疗需达到6个周期，间隔3周；化疗结束后，随机分为化疗序

)。方法：SELECT是一项多中心开放的随机III期试验。每个研究者选择如下，患者第一天接受培美曲塞(500 mg/m2)或多西他赛(75mg/m2)治疗，然后随机分成一组接受化疗联合西妥昔单抗（开始400 mg/m2，以后每周250 mg/m2）或者一组单独化疗。患者进行了六个每三周一疗程的治疗；随机分到联合西妥昔单抗组

来源：iNature电压门控钠通道 (Nav) 在响应膜电位变化时发生构象变化，这种机制被称为机电耦合。2024 年 2 月 21 日，清华大学/深圳医学科学... (WT) Nav1.7 与含有 11 个突变的变体 Nav1.7- M11 之间的结构差异，该研究生成了另外三个中间突变体，并以 2.9-3.4 Å

(2010-10-21)至(2010-10-24)地　　区中国·杭州...;参展费用2m*2m的展台，5000元

一次Dulaglutide治疗2型糖尿病的有效性和安全性尚不清楚。为此，来自美国俄亥俄州立大学的Kathleen M Dungan教授及其团队进行了一项平行对照研究，在二甲双胍治疗...）≤45kg/m2。依据计算机产生的随机序列，通过互动语音应答系统将受试者随机分配到每周一次Dulaglutide治疗（1.5mg）或每日一次利拉鲁肽

1例BMI降至21kg/m2的患者在术后34个月出现束带移位，2例出现束带侵蚀，11例出现胃食管囊性扩张，4例连接管破裂，还有几例开口出现问题。在办...研究结果。这些患者的平均体重指数(BMI)为43kg/m2，并于2005~2009年间接受了“适应证外”的腹腔镜可调节性胃束带术

。自 2017.4 开始出现 eGFR 持续下降：87（2017.4）-79（2017.8）-81（2018.1）ml/min/1.73m2。2018.1 抗病毒方案更改为 ETV 0.5 mg qd 治疗，2018.7 复查 eGFR 89 ml/min/1.73m2，肾功能稍好转，2019.1 服用 ETV 1 年后复查，HBV

，一支由 R.M. Smith，G.S.M. Dyer，K. Antonangeli，N. Arredondo，H. Bedlion，A. Dalal，G.M

侵袭性真菌病（IFDs）是成人急性白血病治疗失败的重要原因。由于白血病的异质性，IFDs风险也就具有高度的可变性。巴西里约热内卢联邦大学医院Nucci M等...无IA患者中位时间延长10天（分别为31天、21天）。临床诊断时发现高危细胞遗传学类型、中性粒细胞减少症、前期肺部疾病为独立的IA预测因子。33名伴细胞

患者确诊前较高的体重指数与较短的生存时间间存在统计学意义的显著关系；根据队列、吸烟、或肿瘤分期，BMI ≥ 35 kg/m2患者与BMI < 25 kg/m2患者不存在统计学意义上的显著差异。尽管肥胖与胰腺癌发病率增加有关，但相关研究尚未就确诊前体重指数(BMI)与生存结局进行过

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