Papers - NAKAMURA Masayuki
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Ishizuka T, Nakamura M, Ichiba M, Sano A . Familial Semantic Dementia with P301L Mutation in the Tau Gene. . Dementia and geriatric cognitive disorders31 ( 5 ) 334 - 340 2011.5Familial Semantic Dementia with P301L Mutation in the Tau Gene. Reviewed
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Tomiyasu A, Nakamura M, Ichiba M, Ueno S, Saiki S, Morimoto M, Kobal J, Kageyama Y, Inui T, Wakabayashi K, Yamada T, Kanemori Y, Jung HH, Tanaka H, Orimo S, Afawi Z, Blatt I, Aasly J, Ujike H, Babovic-Vuksanovic D, Josephs KA, Tohge R, Rodrigues GR, Dupre N, Yamada H, Yokochi F, Kotschet K, Takei T, Rudzinska M, Szczudlik A, Penco S, Fujiwara M, Tojo K, Sano A . Novel pathogenic mutations and copy number variations in the VPS13A Gene in patients with chorea-acanthocytosis. . American journal of medical genetics. Part B, Neuropsychiatric genetics156 620 - 631 2011.5Novel pathogenic mutations and copy number variations in the VPS13A Gene in patients with chorea-acanthocytosis.Reviewed
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Kato M, Nakamura M, Ichiba M, Tomiyasu A, Shimo H, Higuchi I, Ueno S, Sano A. . Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms. . Neuroscience Research69 331 - 336 2011.4Mitochondrial DNA deletion mutations in patients with neuropsychiatric symptoms.Reviewed
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Shimo H, Nakamura M, Tomiyasu A, Ichiba M, Ueno SI, Sano A . Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia. . Neuroscience Research69 ( 3 ) 196 - 202 2011.3Comprehensive analysis of the genes responsible for neuroacanthocytosis in mood disorder and schizophrenia.Reviewed
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Hayashi T, Nakamura M, Ichiba M et al. . Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case. . Psychiatry Clin Neurosci65 105 - 108 2011.1Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case. Reviewed
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Ratovitski T, Nakamura M, D'Ambola J et al. . N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's disease. . Cell Cycle6 2970 - 2981 2007.1N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's disease. Reviewed
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E Mizuno, M Nakamura, A Agemura, A Kusumoto, M Ichiba, Y Kurano, S Muroya, A Sano, . Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C: . Biochem Biophys Res Commun.353 902 - 907 2007Brain-specific transcript variants of 5' and 3' ends of mouse VPS13A and VPS13C:Reviewed
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Y Kurano, M Nakamura, M Ichiba, M Matsuda, E Mizuno, M Kato, A Agemura, S.Izumo, A Sano, . In vivo distribution and localization of chorein: . Biochem Biophys Res Commun.353 41 - 435 2007In vivo distribution and localization of chorein:Reviewed
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中村雅之 佐野 輝 . 精神疾患の遺伝子研究． . 精神医学 47 348 - 358 2005精神疾患の遺伝子研究．
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中村雅之 佐野 輝 . セロトニントランスポーター． . 分子精神医学 5 72 - 74 2005セロトニントランスポーター．
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中村雅之 . ハンチントン病の発現誘導マウスモデル及びPC12細胞モデルにおける全長変異ハンチンチンのタンパク質分解 . 神経化学43 39 - 46 2004ハンチントン病の発現誘導マウスモデル及びPC12細胞モデルにおける全長変異ハンチンチンのタンパク質分解
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Sakai K, Nakamura M, Ueno S et al. . The silencer activity of the novel human serotonin transporter linked polymorphic regions. . Neurosci Lett327 13 - 16 2002.1The silencer activity of the novel human serotonin transporter linked polymorphic regions.Reviewed
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Nakamura M, Ueno S, Sano A, Tanabe H. . The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants. . Mol Psychiatry 5 32 - 38 2000.1The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants.Reviewed
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Nakamura M, Ueno S, Sano A, Tanabe H. . Polymorphisms of the human homologue of the Drosophila white gene are associated with mood and panic disorders. . Mol Psychiatry 4 155 - 162 1999.1Polymorphisms of the human homologue of the Drosophila white gene are associated with mood and panic disorders.Reviewed