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Acta Paediatrica (Oslo, Norway : 1992). Supplement|January 8, 2000
A fluorogenic allele-specific amplification method for DNA-based screening for inherited metabolic disordersY Matsubara, K Fujii, P Rinaldo, et al.
Human Mutation|January 29, 2000
Mutation detection by TaqMan-allele specific amplification: application to molecular diagnosis of glycogen storage disease type Ia and medium-chain acyl-CoA dehydrogenase deficiencyK Fujii, Y Matsubara, J Akanuma, et al.
The Journal of Pharmacy and Pharmacology|March 14, 2000
Rapid detection of CYP2C18 genotypes by real-time fluorescence polymerase chain reactionM Mizugaki, M Hiratsuka, Y Agatsuma, et al.
Acta Paediatrica Japonica : Overseas Edition|June 1, 1994
Rapid detection of phenylketonuria mutations by non-radioactive single-strand conformation polymorphism analysisY Yao, Y Matsubara, K Narisawa
European Journal of Pediatrics|March 1, 1992
Medium-chain acyl-CoA dehydrogenase deficiency: molecular aspectsY Matsubara, K Narisawa, K Tada
Human Molecular Genetics|June 1, 1994
Identification of two novel mutations in the methylmalonyl-CoA mutase gene with decreased levels of mutant mRNA in methylmalonic acidemiaM Ogasawara, Y Matsubara, H Mikami, et al.
Nihon Rinsho. Japanese Journal of Clinical Medicine|January 22, 1998
[Identification of missense mutations and haplotyping of carnitine palmitoyltransferase II gene]J Akanuma, K Wataya, Y Matsubara, et al.
Molecular Genetics and Metabolism|June 28, 2000
Adenovirus-mediated in utero gene transfer in mice and guinea pigs: tissue distribution of recombinant adenovirus determined by quantitative TaqMan-polymerase chain reaction assayM Senoo, Y Matsubara, K Fujii, et al.
The Journal of Pediatrics|September 15, 1999
Tetrahydrobiopterin-responsive phenylalanine hydroxylase deficiencyS Kure, D C Hou, T Ohura, et al.
Journal of Chromatography. A|October 7, 1994
Analysis of polymerase chain reaction-product by capillary electrophoresis with laser-induced fluorescence detection and its application to the diagnosis of medium-chain acyl-coenzyme A dehydrogenase deficiencyH Arakawa, K Uetanaka, M Maeda, et al.
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