Methods the secretion specimen coming from the high risk patients with CA were examined with fluorescent quantitative polymerase chain reaction (FQ-PCR) for genotype HPV-DNA.
方法应用荧光定量聚合酶链反应(FQ - PCR)对尖锐湿疣高危人群分泌物标本进行HPV - DNA分型检测。
The DNA methods described were designed for detection and genotyping of HPV genotypes prevalent in the Netherlands.
论文描述的DNA方法用于检测和基因分型在荷兰流行hpv基因型。
Conclusion HPV DNA microarray is a sensitive and efficient way to HPV detection and genotyping.
结论H PV检测分型芯片是一种敏感高效的HPV检测分型方法。
HPV DNA testing already has a poor positive predictive value, especially in younger girls, they point out, and the absolute number of true positive tests would decrease substantially in this scenario.
他们指出，HPV DNA检验的阳性预测值已经不高，特别是对年轻的女性，在这种情况下，真阳性检验的绝对数目将会显著降低。
NIH 3T3 cells were transfected by human papillomavirus 18(HPV 18). HPV 18 DNA as donor and calf thymus DNA as vector. Calcium phosphate technique was used.
以HPV-18DNA为供体、小牛胸脉DNA 为载体，NIH3T3细胞为受体细胞，应用磷酸钙沉淀法将供体DNA 引入细胞内，得到了清晰的NIH 3T3细胞形态学转化灶。
NIH 3T3 cells were transfected by human papillomavirus 18(HPV 18). HPV 18 DNA as donor and calf thymus DNA as vector. Calcium phosphate technique was used.
以HPV-18DNA为供体、小牛胸脉DNA 为载体，NIH3T3细胞为受体细胞，应用磷酸钙沉淀法将供体DNA 引入细胞内，得到了清晰的NIH 3T3细胞形态学转化灶。
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