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ARTICLES

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  A sensitive, quantitative assay for measurement of allele-specific transcripts differing by a single nucleotide.

  • J Singer-Sam,
  • J M LeBon,
  • A Dai,
  • and A D Riggs

  Genome Res. February 1992 1: 160-163; doi:10.1101/gr.1.3.160
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  A PCR-based assay for reporter gene expression.

  • P Sperisen,
  • S M Wang,
  • P Reichenbach,
  • and M Nabholz

  Genome Res. February 1992 1: 164-170; doi:10.1101/gr.1.3.164
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  Reliable and efficient direct sequencing of PCR-amplified double-stranded genomic DNA template.

  • M Jung,
  • A Dritschilo,
  • and U Kasid

  Genome Res. February 1992 1: 171-174; doi:10.1101/gr.1.3.171
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  RAPD and other PCR-based analyses of plant genomes using DNA extracted from small leaf disks.

  • J M Deragon and
  • B S Landry

  Genome Res. February 1992 1: 175-180; doi:10.1101/gr.1.3.175
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  A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency.

  • S Collier,
  • M Tassabehji,
  • and T Strachan

  Genome Res. February 1992 1: 181-186; doi:10.1101/gr.1.3.181
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  Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCR.

  • P S Subramanian,
  • J Versalovic,
  • E R McCabe,
  • and J R Lupski

  Genome Res. February 1992 1: 187-192; doi:10.1101/gr.1.3.187
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• Avoiding strand reassociation in direct sequencing of double-stranded PCR products with thermolabile polymerases.

  • R Wanner,
  • I Tilmans,
  • and D Mischke

  Genome Res. February 1992 1: 193-194; doi:10.1101/gr.1.3.193
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• A rapid PCR protocol for identification of differentially expressed genes from a cDNA library.

  • K J Mutchler,
  • S W Klemish,
  • and A F Russo

  Genome Res. February 1992 1: 195-198; doi:10.1101/gr.1.3.195
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• Sensitivity of detection of heterozygous point mutations in p53 cDNAs by direct PCR sequencing.

  • J Cheng and
  • M Haas

  Genome Res. February 1992 1: 199-201; doi:10.1101/gr.1.3.199
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• Detection by PCR and differentiation by restriction fragment length polymorphism of Acholeplasma, Spiroplasma, Mycoplasma, and Ureaplasma, based upon 16S rRNA genes.

  • S Deng,
  • C Hiruki,
  • J A Robertson,
  • and G W Stemke

  Genome Res. February 1992 1: 202-204; doi:10.1101/gr.1.3.202
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• Site-directed mutagenesis of herpesvirus glycoprotein phosphorylation sites by recombination polymerase chain reaction.

  • Z Yao,
  • D H Jones,
  • and C Grose

  Genome Res. February 1992 1: 205-207; doi:10.1101/gr.1.3.205
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• Analysis of transgenic animal pedigrees using the junction-polymerase chain reaction.

  • M Ward,
  • W Abramow-Newerly,
  • S Clapoff,
  • and J C Roder

  Genome Res. February 1992 1: 208-209; doi:10.1101/gr.1.3.208
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