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ARTICLES

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  PCR-mediated cloning of HpaII tiny fragments from microdissected human chromosomes.

  • B Horsthemke,
  • U Claussen,
  • S Hesse,
  • and H J Lüdecke

  Genome Res. May 1992 1: 229-233; doi:10.1101/gr.1.4.229
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  Quantitative determination of rare mRNA species by PCR and solid-phase minisequencing.

  • E Ikonen,
  • T Manninen,
  • L Peltonen,
  • and A C Syvänen

  Genome Res. May 1992 1: 234-240; doi:10.1101/gr.1.4.234
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  Preferential PCR amplification of alleles: mechanisms and solutions.

  • P S Walsh,
  • H A Erlich,
  • and R Higuchi

  Genome Res. May 1992 1: 241-250; doi:10.1101/gr.1.4.241
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  The rat genome contains a p53 pseudogene: detection of a processed pseudogene using PCR.

  • J E Hulla

  Genome Res. May 1992 1: 251-254; doi:10.1101/gr.1.4.251
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  Simplified template preparation and improved direct sequencing using Taq polymerase.

  • A K Srivastava,
  • V Montanaro,
  • and J Kere

  Genome Res. May 1992 1: 255-256; doi:10.1101/gr.1.4.255
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  Quantitative RNA and DNA gene amplification can rapidly monitor HIV infection and antiviral activity in cell cultures.

  • M A Winters,
  • M Holodniy,
  • D A Katzenstein,
  • and T C Merigan

  Genome Res. May 1992 1: 257-262; doi:10.1101/gr.1.4.257
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  Detection of influenza A and B in respiratory secretions with the polymerase chain reaction.

  • J C Donofrio,
  • J D Coonrod,
  • J N Davidson,
  • and R F Betts

  Genome Res. May 1992 1: 263-268; doi:10.1101/gr.1.4.263
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  Detection and identification of multiple mycobacterial pathogens by DNA amplification in a single tube.

  • S Wilton and
  • D Cousins

  Genome Res. May 1992 1: 269-273; doi:10.1101/gr.1.4.269
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• The random amplification of polymorphic DNA for fingerprinting plants.

  • M Munthali,
  • B V Ford-Lloyd,
  • and H J Newbury

  Genome Res. May 1992 1: 274-276; doi:10.1101/gr.1.4.274
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• Introduction of multiple restriction enzyme sites by in vitro mutagenesis using the polymerase chain reaction.

  • B Shankarappa,
  • R Balachandran,
  • P Gupta,
  • and G D Ehrlich

  Genome Res. May 1992 1: 277-278; doi:10.1101/gr.1.4.277
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• Single-step elimination of contaminating DNA prior to reverse transcriptase PCR.

  • D D Dilworth and
  • J R McCarrey

  Genome Res. May 1992 1: 279-282; doi:10.1101/gr.1.4.279
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• Analysis of gene expression: use of oligonucleotide primers for glyceraldehyde-3-phosphate dehydrogenase.

  • G S Dveksler,
  • A A Basile,
  • and C W Dieffenbach

  Genome Res. May 1992 1: 283-285; doi:10.1101/gr.1.4.283
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• Effect of different laboratory techniques for guanidinium-phenol-chloroform RNA extraction on A260/A280 and on accuracy of mRNA quantitation by reverse transcriptase-PCR.

  • M Yamaguchi,
  • C W Dieffenbach,
  • R Connolly,
  • D F Cruess,
  • W Baur,
  • and J B Sharefkin

  Genome Res. May 1992 1: 286-290; doi:10.1101/gr.1.4.286
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• Direct PCR amplification of HCV RNA from human serum.

  • A Ravaggi,
  • D Primi,
  • and E Cariani

  Genome Res. May 1992 1: 291-292; doi:10.1101/gr.1.4.291
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• Facile PCR cloning of full-length Sendai virus mRNAs.

  • K C Gupta and
  • X Xu

  Genome Res. May 1992 1: 293-296; doi:10.1101/gr.1.4.293
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• Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.

  • L Cremonesi,
  • E Belloni,
  • C Magnani,
  • M Seia,
  • and M Ferrari

  Genome Res. May 1992 1: 297-298; doi:10.1101/gr.1.4.297
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