|1.||Chester, Nikki: 1 article (07/2014)|
|2.||Suarez, David L: 1 article (07/2014)|
|3.||Hatfield, Jason: 1 article (07/2014)|
|4.||Jakob, Sabine S: 1 article (01/2012)|
|5.||Blattner, Frank R: 1 article (01/2012)|
|6.||Brassac, Jonathan: 1 article (01/2012)|
|7.||Feng, Fude: 1 article (07/2010)|
|8.||Wang, Shu: 1 article (07/2010)|
|9.||Liu, Libing: 1 article (07/2010)|
|10.||Szeberényi, József: 1 article (07/2009)|
|2.||Acquired Immunodeficiency Syndrome (AIDS)
03/01/1999 - "An improved quantitative polymerase chain reaction (qPCR) method based on a combination of real-time detection and the 5'-3' nuclease activity of the Taq DNA polymerase was developed to quantify the provirus load of feline immunodeficiency virus (FIV), a lentivirus of veterinary importance and an animal model for AIDS research. "
05/15/1991 - "We used a standard restriction fragment length polymorphism assay of PCR-amplified c-Ki-ras to detect codon 12 mutations in tumor cells and found a cumulative error frequency for Taq DNA polymerase of one codon 12 mutation per 2 X 10(4) molecules of total amplification product. "
07/01/2010 - "Genomic DNA from cancer cells is pretreated with a methylation-sensitive restriction endonuclease, followed by PCR amplification in the presence of fluorescein-labeled dNTP and Taq polymerase. "
07/17/1991 - "Exons 5-9 of the p53 gene, which contain the major mutational hot spots associated with most human cancers, were sequenced by the following steps: 1) two rounds of PCR amplification using DNA Taq polymerase and two sets of oligonucleotide primers, the second set being nested within the segment amplified by the first set and having attached T7 and SP6 phage promoter sequences, 2) transcription of the amplified DNA sequences with T7 and SP6 RNA polymerases, and 3) dideoxy sequencing of single-stranded RNA transcripts with reverse transcriptase and with additional oligonucleotide primers to achieve specificity for this unique region of the genome. "
04/01/2005 - "On the basis of the estimated mutation rate of HCV in vivo and the Taq polymerase error rate, primary infection viral quasispecies were classified as genetically heterogeneous when the maximum sequence divergence between genetic variants in the same person was >3%. "
08/15/1993 - "However, in combination with Southern blotting, Taq polymerase amplification detected virus in 13 of a panel of 30 clinical samples known to contain these viruses and also detected astroviruses in a mixed infection. "
10/01/1999 - "The incidence of false positives due to the presence of bacterial DNA in Taq DNA polymerase is an obstacle to the use of PCR in the diagnosis of infection. "
|5.||Contagious Ecthyma (Orf)
02/01/2003 - "The promoter, open reading frame (ORF) and terminator are amplified using Pfu or Taq DNA polymerase. "
01/01/2007 - "C-ORF does not use additional enzymes other than reverse transcriptase and Taq polymerase making it a cost-effective and relatively simple method that should be of general utility for gene cloning in multiple laboratories."
|1.||DNA (Deoxyribonucleic Acid)
|3.||RNA-Directed DNA Polymerase (Reverse Transcriptase)
|4.||RNA (Ribonucleic Acid)
|5.||DNA Restriction Enzymes (Restriction Endonuclease)
|6.||A-Form DNA (A-DNA)
|8.||Telomerase (Telomerase Reverse Transcriptase)
|10.||Complementary DNA (cDNA)