PKU的例句大全

A polymorphic tetranucleotide short tandem repeat ( STR) sequence in intron 3 of the phenylalanine hydroxylase ( PAH) gene was analysed in 52 normal individuals and 23 Phenylketonuria ( PKU) families by PCR amplification and silver staining.

应用PCR结合银染显色法分析了苯丙氨酸羟化酶基因内含子3中1个四核苷酸（TCTA）重复序列的多态性。

The PKU admissions office in Sixhuan added that the unnamed university should not harass students applying to PKU.

四川北大招生组还称，该学校不应该对申请北大的学生进行骚扰。

The 3rd "Chinese Bridge" Chinese Contest of International University Students held on the stage of PKU Hall offered an excellent answer.

在北京大学百周年纪念讲堂上演的第三届“汉语桥”世界大学生中文比赛给出了一个完美的答案。

Some netizens even argued that giving preferences to graduates from PKU and THU in Shanghai household registration may create privileges for the special group, which undermines fairness in society.

一些网友甚至认为，允许北大和清华毕业生优先落户上海是在为他们创造特权，这有损社会公平。

It employed two enormous comparable corpora, i.e. BNC and modern Chinese sub-corpus of PKU-CCLC, both of which offer on-line searching service.

本文采用两个庞大的语料库作为对比语料库：英国国家语料库和北京大学语言研究中心设计的现代汉语语料库。这两个语料库都提供网上检索服务。

The application of silicon-nitride ceramic and carbon fibre reinforced resin to turbo-charger is introduced. The forming technology, sintering technology and binding metal technology of ceramic materials and the characteristics of new developed carbon reinforced resin PKU, etc. are described.

介绍了氮化硅陶瓷以及碳纤维强化树脂在涡轮增压器上的应用，并且叙述了陶瓷材料的成形技术、烧结技术、与金属的结合技术以及新开发的碳纤维强化树脂PKU的特性等。

Results In a single BH4 loading test, no classic PKU patients demonstrated decreases in serum phenylalanine levels.

结果在单剂量BH4口服负荷试验中，典型PKU患者的血苯丙氨酸水平没有降低。

Objective Tetrahydrobiopterin ( BH4) is known to normalize blood phenylalanine levels in BH4 deficiency, but not in phenylketonuria ( PKU).

目的四氢生物蝶呤（BH4）可以使BH4缺乏症病人的血液苯丙氨酸水平正常化，但是对苯丙酮酸尿症（PKU）病人无效。

This study aimed to investigate the effect of BH4 and phenylalanine hydroxylase ( PAH) gene mutations in patients with BH4 responsive mild PKU and mild hyperphenylalaninemia ( HPA). Compared with W. Mainly discusses the architecture and principle of the.

本研究将探讨BH4和苯丙氨酸羟化酶（PAH）基因突变在对BH4有反应的轻度PKU和轻度高苯丙酸血症（HPA）患者中的作用。

Organization Guanghua School of Management, PKU; Institute for Advanced Research, SHUFE; China Center for Pharmacoeconomics and Outcomes Research, PKU.

作者单位北京大学光华管理学院；上海财经大学高等研究院；北京大学中国医药经济研究中心。

Zhao baoxu, a professor of School of international studies, pku, the honorary director of the Research Center for contemporary china, one of the primary founders of contemporary Chinese political science.

赵宝煦，北京大学国际关系学院教授，政治学与国际关系双学科博士导师，北京大学中国国情研究中心名誉主任，当代中国政治学主要奠基人之一。

PKU and Waseda University will establish the cross-school double major project for undergraduate students for the first time this year.

北京大学和早稻田大学于今年首次实行跨校的本科双学位培养制度。

Objective To describe the incidence of congenital hypothyroidism ( CH) and phenylketonuria ( PKU) in Maanshan city.

目的：报告先天性甲状腺功能低下症（CH）和苯丙酮尿症（PKU）的患病率。

A specific drug to treat PKU: sapropterin dihydrochloride EVALUATION OF THERAPEUTIC EFFECT AND SCREENING FOR CONGENITAL HY-POTHYROIDISM ( CH) AND PHENYLETONURIA ( PKU) IN NEONATES

治疗苯丙酮尿症特异性药物二盐酸沙丙蝶呤新生儿先天性甲状腺功能低下症和苯丙酮尿症的筛查与疗效评估

Application of ( TCTA) n polymorphism in PAH gene in PKU prenatal diagnosis in Yunnan

云南苯丙氨酸羟化酶基因内（TCTA）n多态性及其在苯丙酮尿症诊断中的应用

14 years neonatal screening for PKU in partial area of Shanghai

上海部分地区新生儿苯丙酮尿症筛查14年临床总结

Phenylalanine dehydrogenase ( EC 1.4.1.20) is employed for the determination of Phenylketonuria ( PKU) in the clinic.

苯丙氨酸脱氢酶（Phenylalanine dehydrogenase，EC1.4.1.20，简称PheDH）是临床苯丙酮尿症的检测用酶。

Objective To observe the relationship between phenylalanine and brain delayed myelination in phenylketonuria ( PKU) with MRI.

目的应用MRI观察苯丙酮尿症（PKU）患儿脑髓鞘发育延迟与血苯丙氨酸（PHE）浓度的关系。

We applied PCR-single strand conformation polymorphism ( SSCP) technique to Ex-on 7 of PAN gene from PKU patients on non-denaturing micro-polyacrylamide gel.

应用非放射性的微型非变性聚丙烯凝胶电泳，对苯丙酮尿症病人的PAH基因Ex-on7的PCR扩增产物进行了单链构型多态性分析。

Objective: To study the mutations of phenylalanine hydroxylase ( PAH) gene in phenylketonuria ( PKU) patients.

目的：探讨苯丙酮尿症（PKU）患者PAH基因突变特点。