Method Polymerase chain reaction sequence specific primers (PCR-SSP) method was used to analyze the frequencies of HLA-DQA1 and DQB1 alleles among 189 patients with PV and 273 healthy controls.
方法利用聚合酶链反应-序列特异引物(PCR -ssp)法，对189例银屑病患者和273例健康人的HLA - DQA1和DQB1等位基因进行检测。
When zinc electrode discharge in alkaline zinc-manganese dioxide battery, its reaction sequence in macroscopy was from zinc gelled near positive electrode to close to negative current collector.
讨论了碱性锌锰电池负极在放电时宏观上的反应顺序：从锌膏靠近正极部位逐渐进行到负极集流体周围。
To ensure monitoring has been activated, enable and disable the Apache process on each of the realservers in sequence, observing each of the directors for their reaction to the events.
为确保监视器已被激活，依次为每个realserver启用并禁用Apache进程，观察每个控制器对事件的反应。
The results of genotyping were compared with those obtained with the polymerase chain reaction method using sequence specific primers ( PCR-SSP).
并把分型结果与采用聚合酶链反应-序列特异性引物（PCR-SSP）获得的结果进行比较。
Mutational studies have been used to map the reaction centres of this subunit and these provide a background which enables interpretation of sequence differences in terms of gene function.
已经采取突变研究来定位该亚单位的反应中心而且该研究提供了能够解释在基因功能方面的序列差别的背景知识。
A 40-base polymorphic repeat sequence located in the 3 '-untranslated region of the DAT gene was purified and amplified by polymerase chain reaction (PCR).
将位于多巴胺运输器基因3'端未转译区段的40 -碱基多形性重复序列予以纯化、经聚合酶链锁反应放大。
Gene of polyketide synthase (PKS) from 2 toxin-producing cyanobacteria was prepared by polymerase chain reaction and the gene sequence was analyzed.
应用聚合酶链反应得到2株蓝绿藻的毒素聚酮合成酶(PKS)基因，并进行基因序列分析。
The mechanism of the reaction and the effect of the segment structure on it, the segment sequence of the block copolymers prepared have been studied.
研究了反应机理、链段结构对反应的影响以及由此法制备的多嵌段共聚物的链段序列结构。
METHODS HLA-DQB1 gene polymorphisms were typed by sequence specific primer based polymerase chain reaction, in 42 patients with esophageal neoplasm and 136 normal control subjects.
方法运用序列特异性引物聚合酶链反应技术，检测无亲缘关系湖北汉族健康人136例、食管癌组42例患者的HLA-DQB1等位基因。
The promoters of auxin early or primitive reaction gene generally include the minimal auxin reaction element sequence (TGTCTC).
生长素早期或原初的反应基因的启动子通常包括最小的生长素反应元件TGTCTC序列。
The results showed that sequence and way of feeding, reaction temperature, time of aging, stirring speed and drying and calcinations had remarkable influence on the pore structure.
结果表明，加料顺序、加料方式、成胶温度、老化时间、搅拌速率以及干燥焙烧等因素对孔结构均有明显影响。
Extron 1-5 of RHO gene was amplified by polymerase chain reaction (PCR), and the mutation of RHO gene was screened by direct DNA sequence measurement.
采用聚合酶链反应(PCR)方法扩增rho基因第1 ~ 5外显子和第1内含子基因片段，用直接dna测序法筛查rho基因突变。
Meanwhile, biochemical reaction, coagglutination test, metabolism-inhibition test, polymerase chain reaction (PCR), and DNA sequence assay were employed to identify those positive cultures.
阳性培养物用生化反应、协同凝集试验、代谢抑制试验、聚合酶链反应和DNA测序来加以鉴定。
Objective To establish a method of high resolution DNA typing for HLA B40 cross reactive groups (CREG) in Chinese with polymerase chain reaction with sequence specific primers (PCR SSP).
目的采用顺序特异引物聚合酶链反应技术(PCRSSP)，建立汉族人群HLAB40交叉反应组高分辨度dna分型方法。
G1 gene sequence of m fragment from hantavirus genome was amplified by reverse transcription polymerase chain reaction (RT-PCR) and analyzed.
采用逆转录聚合酶链反应(RT - PCR)扩增汉坦病毒基因组M片段G1区基因序列并测序。
HLA-DR2, DR7, DR9 genotyping by polymerase chain reaction with sequence-specific primers (PCR-SSP)was carried out for 35 individuals and 4 cell lines DNA.
采用顺序特异性引物聚合酶链式反应（PCR-SSP）DNA分型技术，首次对35例肾移植供受者和4份标准DNA进行HLA-DR2、DR7、DR9基因配型。
Objective To establish DNA typing for HLA-DR antigens by polymerase chain reaction with sequence-specific primers (PCR-SSP).
目的采用顺序特异引物聚合酶链反应（PCR -SSP）建立人类白细胞抗原DR位点的DNA分型方法。
Methods: By using polymerase chain reaction-sequence specific primers, frequency of HLADRB1 alleles in 72 patients with UC and 314 healthy controls were detected.
方法：采用序列特异性引物聚合酶链反应的方法对汉族72例uc患者和314例正常对照者HLA - DRB1基因分型。
Methods The distributing frequencies of HLA-DQB1 alleles were detected with polymerase chain reaction-sequence specific primers (PCR-SSP) in 38 GPP patients and 94 healthy subjects from Shandong.
方法运用聚合酶链反应-序列特异性引物（PCR-SSP）法，对38例山东汉族人GPP与94例健康对照进行HLA-DQB1等位基因分型。
Moreover, it is very suitable to satellite systems equipped with on off jets and reaction wheels. Finally, numeric simulation is explored to verify the validity of pulse sequence control.
此外，由于控制输出为方波，因而适合卫星的喷气推力器控制模式和飞轮控制模式，最后通过数字仿真验证了方波序列控制的有效性。
Moreover, it is very suitable to satellite systems equipped with on off jets and reaction wheels. Finally, numeric simulation is explored to verify the validity of pulse sequence control.
此外，由于控制输出为方波，因而适合卫星的喷气推力器控制模式和飞轮控制模式，最后通过数字仿真验证了方波序列控制的有效性。
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