REVIEW:

A K Bej and M H Mahbubani

Applications of the polymerase chain reaction in environmental microbiology.
PCR Methods Appl. 1992 1: 151-159. [PDF] [References]  

ARTICLES:

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

A sensitive, quantitative assay for measurement of allele-specific transcripts differing by a single nucleotide.
PCR Methods Appl. 1992 1: 160-163. [Abstract] [PDF] [References]  

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

A PCR-based assay for reporter gene expression.
PCR Methods Appl. 1992 1: 164-170. [Abstract] [PDF] [References]  

M Jung, A Dritschilo, and U Kasid

Reliable and efficient direct sequencing of PCR-amplified double-stranded genomic DNA template.
PCR Methods Appl. 1992 1: 171-174. [Abstract] [PDF] [References]  

J M Deragon and B S Landry

RAPD and other PCR-based analyses of plant genomes using DNA extracted from small leaf disks.
PCR Methods Appl. 1992 1: 175-180. [Abstract] [PDF] [References]  

S Collier, M Tassabehji, and T Strachan

A method for specific amplification and PCR sequencing of individual members of multigene families: application to the study of steroid 21-hydroxylase deficiency.
PCR Methods Appl. 1992 1: 181-186. [Abstract] [PDF] [References]  

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

Rapid mapping of Escherichia coli::Tn5 insertion mutations by REP-Tn5 PCR.
PCR Methods Appl. 1992 1: 187-192. [Abstract] [PDF] [References]  

R Wanner, I Tilmans, and D Mischke

Avoiding strand reassociation in direct sequencing of double-stranded PCR products with thermolabile polymerases.
PCR Methods Appl. 1992 1: 193-194. [PDF] [References]  

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

A rapid PCR protocol for identification of differentially expressed genes from a cDNA library.
PCR Methods Appl. 1992 1: 195-198. [PDF] [References]  

J Cheng and M Haas

Sensitivity of detection of heterozygous point mutations in p53 cDNAs by direct PCR sequencing.
PCR Methods Appl. 1992 1: 199-201. [PDF] [References]  

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

Detection by PCR and differentiation by restriction fragment length polymorphism of Acholeplasma, Spiroplasma, Mycoplasma, and Ureaplasma, based upon 16S rRNA genes.
PCR Methods Appl. 1992 1: 202-204. [PDF] [References]  

Z Yao, D H Jones, and C Grose

Site-directed mutagenesis of herpesvirus glycoprotein phosphorylation sites by recombination polymerase chain reaction.
PCR Methods Appl. 1992 1: 205-207. [PDF] [References]  

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

Analysis of transgenic animal pedigrees using the junction-polymerase chain reaction.
PCR Methods Appl. 1992 1: 208-209. [PDF] [References]  

ERRATUM:

D.R. Jacobson and T. Moskovitz

Rapid, nonradioactive screening for activating ras oncogene mutations using PCR-primer introduced restriction analysis (PCR-PIRA)
PCR Methods Appl. 1992 1: 210. [PDF]  

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