Literature DB >> 1549491

Pre-boiling high GC content, mixed primers with 3' complementation allows the successful PCR amplification of Pseudomonas aeruginosa DNA.

A Kureishi1, L E Bryan.   

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Year:  1992        PMID： 1549491      PMCID： PMC312118          DOI： 10.1093/nar/20.5.1155

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  3 in total

1.  Cloning and sequencing of the Escherichia coli gyrA gene coding for the A subunit of DNA gyrase.

Authors:  S L Swanberg; J C Wang
Journal:  J Mol Biol       Date:  1987-10-20       Impact factor: 5.469

2.  Base pairing involving deoxyinosine: implications for probe design.

Authors:  F H Martin; M M Castro; F Aboul-ela; I Tinoco
Journal:  Nucleic Acids Res       Date:  1985-12-20       Impact factor: 16.971

3.  DNA cloning and organization of the Staphylococcus aureus gyrA and gyrB genes: close homology among gyrase proteins and implications for 4-quinolone action and resistance.

Authors:  R Hopewell; M Oram; R Briesewitz; L M Fisher
Journal:  J Bacteriol       Date:  1990-06       Impact factor: 3.490
  3 in total
  2 in total

1.  Development and experimental validation of a predictive threshold cycle equation for quantification of virulence and marker genes by high-throughput nanoliter-volume PCR on the OpenArray platform.

Authors:  Robert D Stedtfeld; Samuel W Baushke; Dieter M Tourlousse; Sarah M Miller; Tiffany M Stedtfeld; Erdogan Gulari; James M Tiedje; Syed A Hashsham
Journal:  Appl Environ Microbiol       Date:  2008-04-18       Impact factor: 4.792

2.  Cloning and nucleotide sequence of Pseudomonas aeruginosa DNA gyrase gyrA gene from strain PAO1 and quinolone-resistant clinical isolates.

Authors:  A Kureishi; J M Diver; B Beckthold; T Schollaardt; L E Bryan
Journal:  Antimicrob Agents Chemother       Date:  1994-09       Impact factor: 5.191
  2 in total

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