To do this, we set the thread priority of the polling threads to 38 (the highest RT priority) and the priorities of the triage pool threads to 37.
为此，我们将轮询线程的线程优先级设置为38（最高的RT 优先级），将筛选池线程的优先级设置为 37。
RESULTS: we identified a total of 5606 patients who met our selection criteria: 1994 (36%) underwent RT, 74% postoperatively.
结果：我们纳入了总共5606例符合我们筛选标准的患者：1994例(36%)患者进行了RT，其中有74%的患者术后进行RT。
To really understand this theory and the differences between RT and the traditional approaches, we need a clear understanding of the basic concepts.
要真正弄懂关联理论，了解该理论与传统理论之间的差别，就必须先弄清关联理论的基本概念。
We endeavored to detect animal viruses in water primarily by RT-PCR.
同时也对水体中动物病毒的检测作了初步探索。
Even in the 128th CSFV39-PK15 passage cells, we still could detect the existence of CSFV39. Both immunofluorescence antibody test and RT-PCR assay showed positive results.
即使在连续传至128代的CSFV39 - PK 15传代细胞中，CSFV仍持续存在：呈免疫荧光抗体反应阳性和RT - PCR检测阳性。
METHODS: We used RT-PCR, flow cytometry and immunofluorescence cell staining techniques to observe the expression of PARs on A549 cells.
方法：采用逆转录聚合酶链反应(RT - PCR)、流式细胞仪和免疫荧光细胞染色分析技术分析肺上皮细胞系a549细胞PAR s的表达情况。
RT: We want to cater to those who are willing to take chances with their music experience.
我们想要为那些愿意在音乐体验上冒险的人们服务。
Here, we summarize our recent progress using directed RT-PCR cloning and DNA synthesis.
这里，我们使用定向rt - PCR克隆和DNA合成概述了我们最新的进展。
We analyze some genes including cell cycle, apoptosis, stress and inflammation, which are confirmed by the real time RT-PCR, and the results are corresponded to that of cDNA microarray.
我们对部分细胞周期、细胞凋亡、细胞应激与炎症反应相关基因进行了分析并用实时荧光定量pcr进行了验证，证实了基因芯片结果的可靠性。
Last, we analysised the expression of IFRG gene in seven different rabbit tissue by RT-PCR.
通过RT - PCR初步分析IF RG基因在兔七种不同组织中的表达情况。
Last, we analysised the expression of IFRG gene in seven different rabbit tissue by RT-PCR.
通过RT - PCR初步分析IF RG基因在兔七种不同组织中的表达情况。
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