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Quantitative monitoring of single nucleotide mutations by allele-specific quantitative PCR can be used for the assessment of minimal residual disease in patients with hematological malignancies throughout their clinical course.
Taira C, Matsuda K, Kamijyo Y, Sakashita K, Ishida F, Kumagai T, Yamauchi K, Okumura N, Honda T. Taira C, et al. Among authors: honda t. Clin Chim Acta. 2011 Jan 14;412(1-2):53-8. doi: 10.1016/j.cca.2010.09.011. Epub 2010 Sep 16. Clin Chim Acta. 2011. PMID: 20849840 Free article.
In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A>G causing abnormal RNA splicing.
Terasawa F, Kamijyo Y, Fujihara N, Yamauchi K, Kumagai T, Honda T, Shigematsu S, Okumura N. Terasawa F, et al. Among authors: honda t. Clin Chim Acta. 2010 Sep 6;411(17-18):1325-9. doi: 10.1016/j.cca.2010.05.030. Epub 2010 May 24. Clin Chim Acta. 2010. PMID: 20580695 Free article.
Application of allele-specific quantitative PCR using genomic DNA to monitor minimal residual disease based on mutant gene levels following allogeneic hematopoietic stem cell transplantation in patients with hematological malignancies: comparison of mutant levels with autologous DNA percentage by short tandem repeat-PCR.
Taira C, Matsuda K, Saito S, Sakashita K, Sugano M, Okumura N, Honda T. Taira C, et al. Among authors: honda t. Clin Chim Acta. 2012 Feb 18;413(3-4):516-9. doi: 10.1016/j.cca.2011.11.017. Epub 2011 Nov 25. Clin Chim Acta. 2012. PMID: 22138486
Rapid detection of PML-RARA fusion gene by novel high-speed droplet-reverse transcriptase-polymerase chain reaction: possibility for molecular diagnosis without lagging behind the morphological analyses.
Sueki A, Matsuda K, Taira C, Yamaguchi A, Koeda H, Takagi F, Kobayashi Y, Sugano M, Honda T. Sueki A, et al. Among authors: honda t. Clin Chim Acta. 2013 Jan 16;415:276-8. doi: 10.1016/j.cca.2012.10.059. Epub 2012 Nov 13. Clin Chim Acta. 2013. PMID: 23159843
3,439 results