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Kayoko Saiki

Kobe Pharmaceutical University

27

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478

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In vitro splicing analysis showed that availability of a cryptic splice site is not a determinant for alternative splicing patterns caused by +1G→A mutations in introns of the dystrophin gene

2009 Journal of Medical Genetics
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Identification of N-acetyl Proline–Glycine–Proline (acPGP) in human serum of adults and newborns by liquid chromatography–tandem mass spectrometry

2009 Clinica Chimica Acta
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Wide ranges of serum myostatin concentrations in Duchenne muscular dystrophy patients

2008 Clinica Chimica Acta
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Two novel missense mutations in the myostatin gene identified in Japanese patients with Duchenne muscular dystrophy

2007 BMC Medical Genetics
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Mutation Analysis of the Ornithine Transcarbamylase (OTC) Gene in Five Japanese OTC Deficiency Patients Revealed Two Known and Three Novel Mutations Including a Deep Intronic Mutation

2007 The Kobe journal of the medical sciences
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Co-occurrence of mutations in both dystrophin- and androgen-receptor genes is a novel cause of female Duchenne muscular dystrophy

2006 Human Genetics
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Quantification of lysophosphatidylcholines and phosphatidylcholines using liquid chromatography-tandem mass spectrometry in neonatal serum.

2006 Journal of Chromatography B
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Evaluation of mutation effects on UGT1A1 activity toward 17β-estradiol using liquid chromatography–tandem mass spectrometry

2006 Journal of Chromatography B
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Development of an enzyme immunoassay for serum 16-dehydropregnenolone.

2001 Biological & Pharmaceutical Bulletin
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Mechanistic Studies on Pd-Catalyzed Telomerization and Co-Cyclization of Butadiene: Amphiphilicity of Bis-π-allylpalladium Intermediate in the Presence of Phosphine Ligand

2001 Bulletin of the Chemical Society of Japan
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