《科学》杂志主编唐纳德·肯尼丹论述2001年度的重大科技进展

每一年 ,《Ｓｃｉｅｎｃｅ》杂志的编辑们都要聚在一起讨论该年度重大科技进展的提名问题。面对众多的新发现 ,往往是很具有挑战性的。今年我们遇到了一个尤为困难的任务 :找到一个能够和果蝇以及其他生命体的基因组测序相当的科技成就。果蝇以及其他生命体的基因组测序这项成果不仅仅席卷了去年的重大科技进展奖 ,而且它还导致了众多的后续项目 ,这决不亚于人类基因组草图的发表。这些后续的成功成了本年度科学中无人认领的珍宝中的一部分 ,而且就像去年一样完好的保存着。本年度重大科技进展的提名像去年的一样使人难忘 ,它涉及了从纳米技…     

大科学:跌入凡尘奈若何

国际空间站和欧洲核子中心的大型强子对撞机 (LHC)计划目前都面临资金上的窘境 ;……除了对项目 (尤其是耗资巨大的项目 )预算的科学化 ,管理的科学化在其中尤显重要     

电磁场的生物效应

本书是一本关于电磁场生物效应的新著。电磁场可以对各种生物产生影响，包括低频率和高频率及不同强度的电磁场的作用，因此，电磁场的研究和技术应用及环境作用等方面都十分重要。本书的内容很广泛，涉及电磁场的机理、模型化、生物效应、治疗效应、国际标准、照射判别准则等。     

数字化的公路卫士

配备有数码相机的网络化车辆可以帮助工程师们修补美国那“遍体鳞伤”的公路。最近的一次调查显示 ,有 16 %的乡间公路和 32 %的市内公路的路况都很糟糕或者比较糟糕。在冬天 ,这种情况会更加恶化。因为当水顺着路面的罅缝流到路面下聚集起来后 ,一冻再一消 ,就会在地上留下一个洼坑 ,从而使公路受损。这种洼坑对于在其上行驶的车辆有很大的破坏作用 :可以使充气不足的车胎坏损 ,使车轮扭曲而且还可以使横梁和车轴歪斜。如果说在坑洼路面上行驶是一件很难受的事情 ,那么修复这些洼坑也是一件非常困难的事。通常 ,各个州以及联邦公路管理局都…     

Alcohol dehydrogenase 2 is a major hepatic enzyme for human retinol metabolism

The metabolism of all-trans- and 9-cis-retinol/ retinaldehyde has been investigated with focus on the activities of human, mouse and rat alcohol dehydrogenase 2 (ADH2), an intriguing enzyme with apparently different functions in human and rodents. Kinetic constants were determined with an HPLC method and a structural approach was implemented by in silico substrate dockings. For human ADH2, the determined K_m values ranged from 0.05 to 0.3 μM and k_cat values from 2.3 to 17.6 min⁻¹, while the catalytic efficiency for 9-cis-retinol showed the highest value for any substrate. In contrast, poor activities were detected for the rodent enzymes. A mouse ADH2 mutant (ADH2Pro47His) was studied that resembles the human ADH2 setup. This mutation increased the retinoid activity up to 100-fold. The K_m values of human ADH2 are the lowest among all known human retinol dehydrogenases, which clearly support a role in hepatic retinol oxidation at physiological concentrations. Received 12 October 2006; received after revision 6 December 2006; accepted 8 January 2007     

Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11

The microtubule-associated protein tau (encoded by MAPT) and several tau kinases have been implicated in neurodegeneration, but only MAPT has a proven role in disease. We identified mutations in the gene encoding tau tubulin kinase 2 (TTBK2) as the cause of spinocerebellar ataxia type 11. Affected brain tissue showed substantial cerebellar degeneration and tau deposition. These data suggest that TTBK2 is important in the tau cascade and in spinocerebellar degeneration.     

A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21

We tested 310,605 SNPs for association in 778 individuals with celiac disease and 1,422 controls. Outside the HLA region, the most significant finding (rs13119723; P = 2.0 x 10(-7)) was in the KIAA1109-TENR-IL2-IL21 linkage disequilibrium block. We independently confirmed association in two further collections (strongest association at rs6822844, 24 kb 5' of IL21; meta-analysis P = 1.3 x 10(-14), odds ratio = 0.63), suggesting that genetic variation in this region predisposes to celiac disease.