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However,essential hypertension is a polygenic disease and both genetic and environmental factors play important roles in its development.

近年来用微卫星标记进行全基因组扫描和连锁分析,它已成功地用于多基因病相关基因的定位克隆研究。

The company has polyonymous specialized technical personnel, provincial appraisals teas person of the national level.

从最初的个体经营发展到今天拥有多家纺织品店铺、茶叶加工厂、茶叶批发中心和连锁茶行。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

本研究通过连锁分析和直接测序的方法,分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

Genetic studies have been performed on the hereditary diseases of disseminated superficial actinic porokeratosis, familial progressive hyperpigmentation and triphalangeal thumb-polysyndactyly syndrome by linkage analysis and sequencing.

中文摘要本研究通过连锁分析和直接测序的方法,分别对播散性浅表性光化性汗孔角化症、家族性进行性色素过度沉着症和拇指三指节多指并指多掌骨畸形这三种疾病进行了遗传学分析。

A few days ago, those who pass assess of netizen elect by ballot, expert is layer upon layer choose, first " business of network of service of 10 great lives " selection 10 powerful businessmen give heat finally, 10 lives such as praedial, all-round victory serve hotel of 7 days of meal of home of grandmother of cross-strait coffee, Zhejiang, chain, 21 centuries network business is picked laurel.

日前,经过网友票选、专家评定的层层筛选,首届&十大生活服务网商&评选的十强商家最终出炉,两岸咖啡、浙江外婆家餐饮、7天连锁酒店、21世纪不动产、满堂红等10家生活服务网商摘得桂冠。

This represents the first demonstration of a genetic linkage between the pretibial phenotype and COL7A1 gene and supports that the Pasini, Cockayne-Touraine, and now the pretibial clinical variants of DEB are allelic.URI: http://grbsearch.stpi.org.tw/GRB/reportDetail.jsp?id=RB8

这是第一个显示胫前型EB与COL7A1基因有连锁的报告,进一步支持了显性DEB的三种主要的亚型,Pasini, Cockyane-Touraine及胫前型,都同样是COL7A1基因突变的表现。

Results:The intramembrane proteinic particles of cell membranes of erythrocyte as well as of muscular cells were diminished significantly in DMD.

Duchenne型肌营养不良症是一组由遗传因素所致的的X连锁隐性遗传病,越来越多的学者认为细胞膜的缺陷在本病中有重要地位。

Background and Objective Pseudohypertrophic muscular dystrophy is a kind of lethal X-chain recessive inherited disease. The etiological factor is mainly due to gene mutation of Xp21 which induce the structural and functional abnormality of a kind of cell skeleton protein: dystrophin.

背景和目的假肥大型肌营养不良症(pseudohypertrophic muscular dystrophy,PMD)是一种常见的致死性X-连锁隐性遗传病,病因主要是由于X染色体短臂2区1带(Xp21)的基因突变而导致一种细胞骨架蛋白——抗肌萎缩蛋白的结构和功能异常所致。

This view of business as harmony doesn't entirely square with the ferocious competitiveness displayed at times by Mackey, who made headlines last year for posting pseudonymous Internet messages disparaging another supermarket chain.

这种和谐的商业理念并不完全符合残酷的竞争,麦金多次提到,去年他在互联网上发贴轻视另一家超市连锁企业时他曾把这当作标题。

These results would be useful for spreading Pyrus genus resources and marker-assisted selection for genetic improvement in Pyrus.

梨树遗传连锁图谱构建和农艺性状QTLs的定位对于拓展梨树的基因资源,促进梨树分子辅助育种有着重要的意义。

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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。

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