@article{oai:obihiro.repo.nii.ac.jp:00000519,
 author = {Thekisoe, Oriel M. M. and Kuboki, Noritaka and Nambota, Andrew and Fujisaki, Kozo and Sugimoto, Chihiro and Igarashi, Ikuo and 五十嵐, 郁男 and Yasuda, Jun and Inoue, Noboru and 井上, 昇},
 issue = {3},
 journal = {Acta Tropica},
 month = {Jun},
 note = {application/pdf, In this study, we developed loop-mediated isothermal amplification (LAMP) for the specific detection of both animal and human trypanosomosis using primer sets that are designed from 5.8S rRNA-internal transcribed spacer 2 (ITS2) gene for Trypanosoma brucei gambiense, 18S rRNA for both T. congolense and T. cruzi, and VSG RoTat 1.2 for T. evansi. These LAMP primer sets are highly sensitive and are capable of detecting down to 1 fg trypanosomal DNA, which is equivalent to 0.01 trypanosomes. LAMP is a rapid and simple technique since it can be carried out in 1 h and requires only a simple heating device for incubation. Therefore, LAMP has great potential of being used for diagnosis of trypanosomosis in the laboratory and the field, especially in countries that lack sufficient resources needed for application of molecular diagnostic techniques.},
 pages = {182--189},
 title = {Species-specific loop-mediated isothermal amplification (LAMP) for diagnosis of trypanosomosis},
 volume = {102},
 year = {2007}
}