Comparison of five different polymerase chain reaction methods for detection of human papillomavirus in cervical cell specimens.

[1]  H. Hollema,et al.  Comprehensive study of several general and type-specific primer pairs for detection of human papillomavirus DNA by PCR in paraffin-embedded cervical carcinomas , 1996, Journal of clinical microbiology.

[2]  E. Stockfleth,et al.  Strategy for typing human papillomaviruses by RFLP analysis of PCR products and subsequent hybridization with a generic probe. , 1995, BioTechniques.

[3]  Jack A. Taylor,et al.  Genetic risk and carcinogen exposure: a common inherited defect of the carcinogen-metabolism gene glutathione S-transferase M1 (GSTM1) that increases susceptibility to bladder cancer. , 1993, Journal of the National Cancer Institute.

[4]  R. Minnaar,et al.  Detection and typing of human papillomaviruses present in fixed and stained archival cervical smears by a consensus polymerase chain reaction and direct sequence analysis allow the identification of a broad spectrum of human papillomavirus types. , 1992, The Journal of general virology.

[5]  M. Evander,et al.  Comparison of a one-step and a two-step polymerase chain reaction with degenerate general primers in a population-based study of human papillomavirus infection in young Swedish women , 1992, Journal of clinical microbiology.

[6]  R Reid,et al.  Human papillomavirus infection of the cervix: relative risk associations of 15 common anogenital types. , 1992, Obstetrics and gynecology.

[7]  Y. Chardonnet,et al.  Detection of human papillomavirus types 6, 11, 16 and 18 in mucosal and cutaneous lesions by the multiplex polymerase chain reaction. , 1991, Journal of virological methods.

[8]  H. Yoshikawa,et al.  Detection and Typing of Multiple Genital Human Papillomaviruses by DNA Amplification with Consensus Primers , 1991, Japanese journal of cancer research : Gann.

[9]  A. Reingold,et al.  Genital human papillomavirus infection in female university students as determined by a PCR‐based method , 1991, JAMA.

[10]  C. Meijer,et al.  Rapid detection of human papillomavirus in cervical scrapes by combined general primer-mediated and type-specific polymerase chain reaction , 1990, Journal of clinical microbiology.

[11]  H. Fox,et al.  Detection and typing of human papillomavirus in archival cervical cancer specimens by DNA amplification with consensus primers. , 1990, Journal of the National Cancer Institute.

[12]  A. Iwamoto,et al.  Amplification and typing of multiple cervical cancer‐associated human papillomavirus DNAS using a single pair of primers , 1990, International journal of cancer.

[13]  K. Choo,et al.  Sequence duplication and internal deletion in the integrated human papillomavirus type 16 genome cloned from a cervical carcinoma , 1988, Journal of virology.

[14]  Wolfgang Mayer,et al.  Structure and transcription of human papillomavirus sequences in cervical carcinoma cells , 1985, Nature.

[15]  B. Dallapiccola,et al.  Inosine-containing primers in human papillomavirus detection by polymerase chain reaction. , 1992, Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie.

[16]  G. Snow,et al.  The use of general primers in the polymerase chain reaction permits the detection of a broad spectrum of human papillomavirus genotypes. , 1990, The Journal of general virology.

[17]  Steven Wolinsky,et al.  The use of polymerase chain reaction amplification for the detection of genital human papillomaviruses , 1989 .