我们采用端粒重复序列扩增法(telomere repeat amplification protocol, TRAP)［1］对腹水标本进行端粒酶活性检测，旨在探讨其在癌性腹水中的表达情况及对良恶性腹水的鉴别诊断价值.
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用端粒重复序列扩增法 telomere repeat amplification protocol ; Telomeric repeat sequence amplification protocol
端粒酶重复序列扩增法 Telomeric Repeat Amplifcation Protocol PCR ; TRAP-PCR ; telomeric repeat amplification protocol
用端粒重复序列扩增法（TRAP）半定量方法测定细胞染毒前后端粒酶活性的变化；
The changes of telomerase activity after treatment was detected and quantified by telomeric repeat amplification protocol (TRAP) semi_quantitative analysis.
方法取19例颅内肿瘤和5例脑外伤患者脑脊液标本，应用改良的银染端粒重复序列扩增法(TRAP)进行端粒酶活性检测。
Methods a modified telomeric repeat amplification protocal (TRAP) by silver staining was performed in 19 cases of intracranial tumors and 5 cases of brain injuries.
方法采用端粒重复序列扩增法一酶联免疫（PCR-TRAP）检测70例肺癌手术患者癌组织中的端粒酶活性，并与70例肺部良性疾病患者对照组的检测结果进行比较。
Methods Use PCR-TRAP detection of 70 cases of lung cancer patients' telomerase activity in cancer tissue. and 70 patients with benign lung disease and the results were compared.
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