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滇边佤寨的病痛叙事、脆弱性与具身化国家 被引量:2
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作者 黄剑波 胡梦茵 田远帆 《华东师范大学学报(哲学社会科学版)》 CSSCI 北大核心 2018年第5期57-64,173,174,共10页
医学人类学的研究通常把身体作为研究疾痛的一个重要焦点,而越来越多的人类学研究也试图讨论"自然"的身体是如何成为社会结构的隐喻。基于五个月的田野调查,通过大量的民族志材料,并通过分析在现代医学以及传统驱鬼仪式失效... 医学人类学的研究通常把身体作为研究疾痛的一个重要焦点,而越来越多的人类学研究也试图讨论"自然"的身体是如何成为社会结构的隐喻。基于五个月的田野调查,通过大量的民族志材料,并通过分析在现代医学以及传统驱鬼仪式失效之后佤寨村民试图理解自身的疾痛的叙事追因,可以理解当地村民在现代医疗体系之外疾痛叙事的社会语境,以及当地人对于身体脆弱性的持续感知。随着公共卫生的建设,当地长久存在的瘴气疫病说逐渐消失,但是依然存在着现代医学体系范围之外的疾痛叙事。这种个体的疾痛叙事体现了失序的身体转化为对于身体脆弱性的持续体验,而这种脆弱性则可以发现一个"具身化"的国家——即可以揭示国家力量如何深入地方社会,并内化于个体。 展开更多
关键词 疾痛叙事 脆弱性 具身化国家
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The influence of OCT1 gene polymorphisms on the metformin response in Uygur patients with glucose metabolism disorder
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作者 WANG Tao YI Tao-cun +11 位作者 WANG Ye WANG Zhi-hong WANH Chang-hui MAO Xin-min RAN Xin-jian hu meng-yin GE Wen-ning ZHANG Min-fang XIE Zi-jing LI Shi-qiang LAN Yi LI Lin-lin 《新疆医科大学学报》 CAS 2010年第10期1175-1180,共6页
Objective To determine the effects of genetic variation in the organic cation transporter 1(OCT1)on the short-term responses of the antidiabetic drug,metformin.Method A total of 22 patients recruited with type 2 diabe... Objective To determine the effects of genetic variation in the organic cation transporter 1(OCT1)on the short-term responses of the antidiabetic drug,metformin.Method A total of 22 patients recruited with type 2 diabetes or IFG were treated with metformin(2 000 mg/day)for 1 week.The patients were screened from Second Jikun hospital and Kashidonglu community medicine service,Urumqi,China and their surrounding districts.To examine the effects of metformin on plasma glucose,total cholesterol,low-density lipoprotein-cholesterol,high-density lipoprotein-cholesterol and triglyceride in relation with R61C,G465R and 420 del variants of OCT1(gene encoding organic cation transporter 1,mainly locating in liver,which is metformin's major target)in subjects.In all,R61C,G465R and 420del of OCT1 gene were examined using DNA extracted from whole blood and PCR-RFLP.Data concerning with gene and metformin treatment were handled by t-test.Result After metformin treatment,there were increases both in FPG and LDL(P=0.011and P=0.013 respectively).To divide all participants into mutant and wild groups,according to the polymorphisms of R61C,G465R and 420 del respectively,as well as carriers with one of the mutant genotypes at least and carriers with none of the mutant sites.Analysis was made to compared FPG,Chol,TG,and LDL and HDL between carriers of wild genotypes and carriers of other genotypes showed no statistic significance both before the metformin treatment and after the treatment.The same is the case with changes of FPG,Chol,TG,and LDL and HDL of wild genotype carriers and variant genotype carriers,except of LDL changes(P=0.05)in patients grouped by G465R polymorphisms and TG changes(P=0.03)in subjects differed by 420del genotypes.Conclusion In this study,it is suggested that OCT1 gene polymorphisms have little contribution to the clinical efficacy of blood glucose control by metformin among Uygur people with type 2 diabetes or IFG,but it may have possible relationship with the clinical efficacy on fat metabolism by metformin. 展开更多
关键词 OCT1基因 基因治疗 疗效
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