• 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方法对汉族72uc患者314例正常对照者HLA - DRB1基因分型。

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  • 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GPP94例健康对照进行HLA-DQB1等位基因分型。

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  • The results of genotyping were compared with those obtained with the polymerase chain reaction method using sequence specific primers ( PCR-SSP).

    并把分结果采用聚合酶链反应-序列特异性引物(PCR-SSP)获得结果进行比较。

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  • 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)189银屑病患者273例健康人的HLA - DQA1DQB1等位基因进行检测。

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  • 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型方法。

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  • 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-SSPDNA技术,首次35例肾移植供受者4份标准DNA进行HLA-DR2、DR7DR9基因配型。

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  • 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交叉反应分辨dna方法

    youdao

  • 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交叉反应分辨dna方法

    youdao

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