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- Using reverse transcription PCR, kininogen mRNA was also detected in lamprey gut, kidney, and leukocyte, but absent in lamprey buccal gland. 运用反转录PCR技术，检测出激肽原还存在于七鳃鳗的肠、肾和白细胞中，但不存在于口腔腺中。
- The nm23 gene is a conspicuous metastasis suppressor gene. The authors detected both nm23 H 1 and nm23 H 2 mRNA levels in 47 tissues samples of patients with carcinoma of buccal mucosa (CBM) by quantitative reverse transcription PCR amplification. 采用定量逆转录多聚酶链反应（Q－RT－PCR）技术检测nm23－H1和nm23－H2mRNA在47例组织标本中的表达情况，发现nm23－H1和nm23－H2mRNA在颊癌原发灶、癌旁粘膜、正常颊粘膜、颌下腺、白斑、正常淋巴结和有转移的淋巴结中均有不同程度的表达。
- We examined mRNA expression of RASGRF2 and FBN2 by reverse transcription PCR (RT-PCR) and treated those cell lines which showed loss of RASGRF2 and FBN2 mRNA expression with 5-Aza-CdR. 并根据它们在肺癌组织中的甲基化状态结合临床资料进行分析。 另外,还采用逆转录 PCR (RT-PCR)观察 RASGRF2 和 FBN2 mRNA 的表达,对RASGRF2 和 FBN2 mRNA 表达阴性并有异常甲基化的细胞株用5-Aza-CdR 处理后,观察基因是否能够重新表达。
- Methods In 33 primarily treated patients with epithelial ovarian carcinoma, the expression of MDR1 gene was detected using reverse transcription PCR (RT?PCR). Sensitivity to the anticancer agents was also examined using the MTT assay. 方法利用逆转录聚合酶链反应（RT－PCR）检测33例初治上皮性卵巢癌病人肿瘤组织MDR1基因表达情况，同时用MTT比色法检测肿瘤细胞对抗癌药的敏感性。
- Methods Using the quantitative reverse transcription PCR procedure,we observed the expression of nm23 mRNA in human pancreatic cancer JF305 cell sublines with different metastatic potential. 方法 在建立不同转移潜能的人胰腺癌JF305 单克隆细胞亚系的基础上，应用定量逆转录多聚酶链式反应技术（RT?PCR）检测不同转移潜能的人胰腺癌JF305 单克隆细胞亚系细胞中nm23 mRNA 的表达。
- differential display reverse transcription PCR DDRT PCR
- reverse transcription PCR(RTPCR) 逆转录PCR(技术)
- The mRNA expression of TGF-b1 was determined by semi-quantification reverse transcriptive PCR (RT-PCR). 采用逆转录多聚酶链式反应(RT-PCR)半定量分析HPMC中TGF-1 mRNA的表达。
- mRNA differential display reverse transcription PCR ( DDRT- PCR) mRNA差异显示
- Fluorescence quantitative reverse transcription PCR (FQ RT-PCR) 荧光定量反转录PCR
- differential display reverse transcription PCR(DDRT PCR) 差别显示逆转录PCR
- Detection of Hepatitis A Virus by Two Reverse Transcription PCR Approaches 两种反转录聚合酶链反应检测甲型肝炎病毒
- Rapid identification of subtypes of respiratory syncytial virus by real-time reverse transcription PCR 实时逆转录聚合酶链反应快速鉴别呼吸道合胞病毒亚型
- Keywords poliovirus type 1 plaque forming units assay dot immunobinding assay reverse transcription PCR; 脊髓灰质炎病毒1型;蚀斑试验;免疫印迹试验;逆转录PCR;
- Study on Expression Difference of ppGalNAcT2 in Tumor Cells and Tissue on mRNA Level by Using in Situ Reverse Transcription PCR 原位逆转录PCR技术检测多肽：N-乙酰氨基半乳糖转移酶2（ppGalNAcT2）在肿瘤细胞及肿瘤组织中的差异表达
- Study on Expression of ppGalNAcT-2 in Gastric Tumor Cell Line SGC-7901 on mRNA Level by Using in Situ Reverse Transcription PCR 原位逆转录PCR检测ppGalNAcT-2在胃癌细胞株SGC-7901的表达
- Keywords Human papillomavirus type 16（HPV16）;Immunoblot;monoclone antibody;reverse transcription PCR（RT-PCR）;enzyme linked immunosorbent assay（ELISA）; 人乳头瘤病毒16型;免疫印迹;单克隆抗体;反转录PCR;酶联免疫吸附试验;
- reverse transcription pcr 逆转录
- Methods HGV RNA in plasma of 84 IVDUs was detected by reverse transcription polymerase chain reaction (RT PCR). 方法采用逆转录聚合酶链反应（RT－PCR）检测84例静脉毒瘾者血浆标本。
- Real-time fluorescence quantitative reverse transcription PCR in determination of guanylyl cyclase-C gene expression in peripheral blood of patients with colorectal cancer and its clinical significance 实时荧光定量PCR检测大肠癌患者外周血鸟苷酰环化酶C基因及其临床意义
