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11. Using T4 DNA polymerase to generate clonable PCR products. Wang K Methods Mol Biol; 1997; 67():63-8. PubMed ID: 9031131 [No Abstract] [Full Text] [Related]
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13. Taq DNA polymerase extension of internal primers blocks polymerase chain reactions allowing differential amplification of molecules with identical 5' and 3' ends. Lewis AP; Sims MJ; Gewert DR; Peakman TC; Spence H; Crowe JS Nucleic Acids Res; 1994 Jul; 22(14):2859-61. PubMed ID: 7519771 [No Abstract] [Full Text] [Related]
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17. Generation of a PCR-renewable source of subtractive cDNA. Kuehl WM; Battey J Methods Mol Biol; 1997; 67():389-403. PubMed ID: 9031162 [No Abstract] [Full Text] [Related]
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20. Incomplete primer extension during in vitro DNA amplification catalyzed by Taq polymerase; exploitation for DNA sequencing. Olsen DB; Eckstein F Nucleic Acids Res; 1989 Dec; 17(23):9613-20. PubMed ID: 2602138 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]