查询词典 Huntington

My second conclusion brings us back to Davos Man, a term of art coined by the late Samuel Huntington to describe a member of a new global elite, liberated from national loyalties and contemptuous of national boundaries - a kind of ruthless cosmopolitan.

我的第二个结论使我们又回到"达沃斯人"，一个有艺术性的术语。它由已故的塞缪尔亨廷顿提出，用于描述一群新的全球精英——他们摆脱了对国家的"忠诚"，藐视国家边界，属于一种无情的世界政治家。

The American chapter of this German order was founded in 1833 at Yale University by General William Huntington Russell and Alphonso Taft who, in 1876, became Secretary of War in the Grant Administration.

美国的这一章为创立于1833年的德国耶鲁大学的威廉亨廷顿塔夫特罗素和阿方人员，1876年，出任行政战争补助。

In this study, the concept of civilization by Huntington is generally defined and analyzed, and on this basis, the author considers and interprets Huntington's mode of civilizations clash in his own way; and three criteria for analyzing the mode of civilizations clash is advanced and the theory of composition of historical forces is brought forth for the correct understanding of world civilization course.

研究中对亨廷顿的"文明"概念做了全面的界定和分析，对亨廷顿的"文明冲突"范式做出自己的思考和解读，提出用三条标准来衡量亨廷顿的"文明冲突"范式，并指出"历史合力说"更能科学地判断世界文明史的进程。

Microscopically, the caudate nucleus in Huntington's disease demonstrates loss of neurons along with gliosis.

显微镜下，Huntington病患者尾状核中二乙基溴乙酰胺丢失伴有神经胶质增生。

Idiopathic torsion dystonia and Huntington's disease represent autosomal dominant inherited hyperkinetic disorders that vary considerably with regard to pathologic mechanisms and clinical penetrance.

特发性扭转张力障碍和 huntington ' s 病代表了常染色体显性遗传的运动机能亢进疾病，由于和临床外显率不同而有很大差别。

Examples include myotonic dystrophy, Huntington's disease, fragile X mental retardation, and several other neurologic disorders.

例子有肌强直性营养不良，Huntington病，脆性X智力障碍和其他一些神经科疾病。

This paper reports the restriction allele frequencies, polymorphism information contents and heterozygote frequencies of the restriction sites of D4S10 locus, pK082/Hind Ⅲ(2),pK083/EcoRI(1) and pK081/EcoRI(2), detected by three sub-clones of the G8 probe and tries to do presymptomatic diagnosis of Huntington 's disease for phenotypically normal family members in two HD families.

报道53例样本D4S10基因座由G8探针3个亚探针检出的限制酶切位点pK082／HindⅢ（2）、pK083／EcoRⅠ（1）和pK081／EcoRⅠ（2）的等位片段频率、多态性信息含量和杂合子频率，并试对2个Huntington舞蹈病家系成员作症状前诊断。

"Our discovery that the mutant Huntington's disease protein derails the cholesterol delivery system and causes cholesterol accumulation in neurons provides us with key results and solid clues to the mechanism of this disease," says Dr. McMurray."Fully understanding the mechanism of toxicity is the key to developing treatments."

&我们发现突变的Huntington's疾病蛋白使胆固醇运输系统异常并造成神经元内胆固醇蓄积，这提供了该疾病的关键结果及重要线索，&McMurray博士说&全面理解该疾病的毒性机制有助于更进一步的临床治疗。&

Detail Contents: Genetic disorders -- Immune deficiencies -- Breast cancer -- Colon cancer -- Melanoma -- Cystic fibrosis -- Hemophilia -- Liver disease -- Cardiovascular disease -- Muscular dystrophy -- Alzheimer's disease -- Parkinson's disease -- Huntington's disease -- Viruses: the cornerstone of gene therapy -- Viruses are living crystals -- Viral genomes may be RNA or DNA -- Viruses evolved from plasmids -- Viruses know how to infect cells -- The virus as a gene vehicle -- Viruses used in gene therapy -- Ashi DeSilva: a promising start -- Clinical trials defined -- Cells of the immune system -- Adenosine deaminase -- Preliminary research -- Clinical procedure for ADA gene therapy -- The DeSilva clinical trial -- Jesse Gelsinger: down to earth -- Ornithine transcarbamylase -- Preliminary research -- Clinical procedure for OTC gene therapy -- The Gelsinger clinical trial -- The investigation -- Concluding remarks -- Future prospects -- Safer vehicles -- Reducing immune rejection of the vector -- Improved risk assessment -- Redesigning human anatomy and physiology -- Ethics of gene therapy -- The Belmont report -- Clinical trials -- Physiological enhancement -- Cosmetic applications -- Legal issues -- Regulatory agencies -- The Gelsinger legal trial -- International regulation -- Resource center -- Eucaryote cell primer -- Recombinant DNA primer -- The human genome project -- X-linked severe combined immunodeficiency (SCID-X1)-- Alzheimer's disease -- Huntington's disease.

细节内容︰遗传疾病-免疫的缺乏-乳腺癌-结肠癌-黑瘤-囊性纤维变性-血友症-肝疾病-心血管疾病-肌营养不良-早老性痴呆病-帕金森疾病-亨廷顿疾病-病毒︰基础的基因治疗-病毒在活著水晶--病毒的基因可能是RNA或者DNA --病毒从plasmids被逐步形成--病毒知道怎样感染细胞--作为一辆基因车辆的病毒--基因治疗使用的病毒-Ashi DeSilva︰有希望开始-临床试验确定--细胞的这免疫系统-Adenosine deaminase-初步研究-临床程式给埃达基因治疗--这DeSilva临床试验-婕西Gelsinger︰到地球-Ornithine transcarbamylase-初步研究-临床程式给OTC基因治疗-- Gelsinger临床试验-调查-达成评论-前景-更安全的车辆--矢量的降低免疫的拒绝-改进风险估计-重新设计人解剖学和生理学--伦理学的基因治疗-那些贝拉蒙特报告-临床试验-生理提升-美容应用-法律问题-协调机构-- Gelsinger 合法审讯-国际管理-资源中心人物-Eucaryote信元第一-Recombinant DNA 入门--人类基因工程-- X 连结的严重的结合的免疫缺陷(SCID-X1)-早老性痴呆病--亨廷顿的疾病。

To investigate the methods to effectively and simply assess the CAG repeat size of HD gene which was necessary for gene diagnosis of Huntington disease, the sequence including polymorphic CAG repeat of HD gene was amplified by PCR with TaKaRa LA Taq DNA polymerase and GC buffer. PCR products were analyzed on polyacrylamide gel to distinguish normal alleles from HD alleles. The DNA fragments of affected alleles were recovered from polyacrylamide gel as templets for secondary PCR. The secondary PCR products were cloned into T vector for sequencing analysis to determine CAG repeat size. A total of 20 normal individuals and 3 members from a HD pedigree were included in this study.

为了简单高效检测HD基因开放阅读框5'端n三核苷酸重复序列，建立快速准确的亨廷顿病(Huntington disease， HD)基因诊断方法，应用TaKaRa LA Taq DNA聚合酶配合GC buffer扩增HD基因包含n重复序列的目的片段，非变性聚丙烯酰胺凝胶电泳检测后回收n拷贝数异常增多的目的片段，再次PCR扩增后将产物连接至T载体，进行DNA测序确定CAG的拷贝数。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。