Papers - NAKAMURA Masayuki
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Hayashi T. . Adult-type metachromatic leukodystrophy with compound heterozygous ARSA mutations: A case report and phenotypic comparison with a previously reported case . Psychiatry and Clinical Neurosciences65 ( 1 ) 105 - 108 2011.2
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Liang Y. . ATF3 plays a protective role against toxicity by N-terminal fragment of mutant huntingtin in stable PC12 cell line . Brain Research1286 221 - 229 2009.8
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Ichiba M. . Neuroacanthocytosis update . Brain and Nerve60 ( 6 ) 635 - 641 2008.6
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Nakamura M. . A mouse model of chorea-acanthocytosis . Neuroacanthocytosis Syndromes II 153 - 159 2008
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Ichiba M. . Clinical and molecular genetic assessment of a chorea-acanthocytosis pedigree . Journal of the Neurological Sciences263 ( 1-2 ) 124 - 132 2007.12
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Ratovitski T. . N-terminal proteolysis of full-length mutant huntingtin in an inducible PC12 cell model of Huntington's disease . Cell Cycle6 ( 23 ) 2970 - 2981 2007.12
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Jiang H. . Parkinson's disease genetic mutations increase cell susceptibility to stress: Mutant α-synuclein enhances H<inf>2</inf>O<inf>2</inf>- and Sin-1-induced cell death . Neurobiology of Aging28 ( 11 ) 1709 - 1717 2007.11
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Kasugai M. . Differences in two mice strains on kainic acid-induced amygdalar seizures . Biochemical and Biophysical Research Communications357 ( 4 ) 1078 - 1083 2007.6
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Mizuno E. . Brain-specific transcript variants of 5′ and 3′ ends of mouse VPS13A and VPS13C . Biochemical and Biophysical Research Communications353 ( 4 ) 902 - 907 2007.2
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Kurano Y. . In vivo distribution and localization of chorein . Biochemical and Biophysical Research Communications353 ( 2 ) 431 - 435 2007.2
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Kurano Y. . Chorein deficiency leads to upregulation of gephyrin and GABA<inf>A</inf> receptor . Biochemical and Biophysical Research Communications351 ( 2 ) 438 - 442 2006.12
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Bajestan S.N. . Association of AKT1 haplotype with the risk of schizophrenia in Iranian population . American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics141 ( 4 ) 383 - 386 2006.6
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Tanaka Y. . Progressive phenotype and nuclear accumulation of an amino-terminal cleavage fragment in a transgenic mouse model with inducible expression of full-length mutant huntingtin . Neurobiology of Disease21 ( 2 ) 381 - 391 2006.2
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Wang W. . Compounds blocking mutant huntingtin toxicity identified using a Huntington's disease neuronal cell model . Neurobiology of Disease20 ( 2 ) 500 - 508 2005.11
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Tomemori Y. . A gene-targeted mouse model for chorea-acanthocytosis . Journal of Neurochemistry92 ( 4 ) 759 - 766 2005.2
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Ueno S.I. . Chorea-acanthocytosis with the ehime-deletion mutation . Neuroacanthocytosis Syndromes 39 - 43 2005
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Sakai K. . The silencer activity of the novel human serotonin transporter linked polymorphic regions . Neuroscience Letters327 ( 1 ) 13 - 16 2002.7
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Sano A. . Positional candidate approach for the gene responsible for benign adult familial myoclonic epilepsy . Epilepsia43 ( SUPPL. 9 ) 26 - 31 2002
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Ueno S.I. . The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis . Nature Genetics28 ( 2 ) 121 - 122 2001.6
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Nakamura M. . The human serotonin transporter gene linked polymorphism (5-HTTLPR) shows ten novel allelic variants . Molecular Psychiatry5 ( 1 ) 32 - 38 2000