
月村 考宏
(ツキムラタカヒロ)
研究キーワード
- 遺伝病、先天代謝異常症、リソソーム病、遺伝学、生化学
主な研究業績
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Use of a mouse–human chimeric anti-α-galactosidase A monoclonal antibody as a reference for measuring serum antidrug antibody titers in patients with Fabry disease.
Mol. Genet. Metab., 144, 109000, 2025.
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Comparative study on incorporation of three recombinant human α-galactosidase A drugs (agalsidases) into cultured fibroblasts and organs/tissues of Fabry mice.
Mol. Genet. Metab. Rep., 40, 101118, 2024
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Does administration of hydroxychloroquine/amiodarone affect the efficacy of enzyme replacement therapy for Fabry mice?
Mol. Genet. Metab. Rep., 39, 101079, 2024.
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Profiles of Globotriaosylsphingosine Analogs and Globotriaosylceramide Isoforms Accumulated in Body Fluids from Various Phenotypic Fabry Patients.
Intern. Med., 63, 1531-1537, 2024.
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Comparative urinary globotriaosylceramide analysis by thin-layer chromatography-immunostaining and liquid chromatography-tandem mass spectrometry in patients with Fabry disease.
Mol. Genet. Metab. Rep., 29, 100804, 2021.
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Does administration of hydroxychloroquine/amiodarone accelerate accumulation of globotriaosylceramide and globotriaosylsphingosine in Fabry mice?
Mol. Genet. Metab. Rep., 28, 100773, 2021.
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Anti-drug antibody formation in Japanese Fabry patients following enzyme replacement therapy.
Mol. Genet. Metab. Rep., 25, 100650, 2020.
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Plasma mutant α-galactosidase A protein and globotriaosylsphingosine level in Fabry disease.
Mol. Genet. Metab. Rep., 1, 288-298, 2014.
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Efficient uptake of recombinant α-galactosidase A produced with a gene-manipulated yeast by Fabry mice kidneys.
Mol. Med., 18, 76-82, 2012.
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Uptake of a recombinant human alpha-L-iduronidase (laronidase) by cultured fibroblasts and osteoblasts.
Biol. Pharm. Bull., 31, 1691-1695, 2008.
所属学協会
- 日本薬学会
- 日本先天代謝異常学会
- 日本生化学会