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Results: 1-13 |
Results: 13
The levels of cerebrospinal fluid A beta 40 and A beta 42(43) are regulated age-dependently
Authors: Shoji, M Kanai, M Matsubara, E Tomidokoro, Y Shizuka, M Ikeda, Y Ikeda, M Harigaya, Y Okamoto, K Hirai, S
Citation: M. Shoji et al., The levels of cerebrospinal fluid A beta 40 and A beta 42(43) are regulated age-dependently, NEUROBIOL A, 22(2), 2001, pp. 209-215
Synthesis and radical polymerization kinetics of amphiphilic methacrylic monomers having 2-[p-(1,1,3,3-tetramethyl-butyl)phenoxy-polyethoxy]ethyl group
Authors: Yasuda, M Shizuka, M Yoneda, H Ogino, H Ishikawa, H
Citation: M. Yasuda et al., Synthesis and radical polymerization kinetics of amphiphilic methacrylic monomers having 2-[p-(1,1,3,3-tetramethyl-butyl)phenoxy-polyethoxy]ethyl group, J CHEM EN J, 34(3), 2001, pp. 388-395
The synthetic rate of dipeptide catalyzed by organic solvent-stable protease from Pseudomonas aeruginosa PST-01 in the presence of water-soluble organic solvents
Authors: Ogino, H Gemba, Y Yamada, M Shizuka, M Yasuda, M Ishikawa, H
Citation: H. Ogino et al., The synthetic rate of dipeptide catalyzed by organic solvent-stable protease from Pseudomonas aeruginosa PST-01 in the presence of water-soluble organic solvents, BIOCH ENG J, 5(3), 2000, pp. 219-223
Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy andperipheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23
Authors: Bomont, P Watanabe, M Gershoni-Barush, R Shizuka, M Tanaka, M Sugano, J Guiraud-Chaumeil, C Koenig, M
Citation: P. Bomont et al., Homozygosity mapping of spinocerebellar ataxia with cerebellar atrophy andperipheral neuropathy to 9q33-34, and with hearing impairment and optic atrophy to 6p21-23, EUR J HUM G, 8(12), 2000, pp. 986-990
Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan
Authors: Ikeda, Y Shizuka, M Watanabe, M Okamoto, K Shoji, M
Citation: Y. Ikeda et al., Molecular and clinical analyses of spinocerebellar ataxia type 8 in Japan, NEUROLOGY, 54(4), 2000, pp. 950-955
Age-related amyloid beta protein accumulation induces cellular death and macrophage activation in transgenic mice
Authors: Shoji, M Kawarabayashi, T Sato, M Sasaki, A Saido, TC Matsubara, E Tomidokoro, Y Kanai, M Shizuka, M Ishiguro, K Ikeda, M Harigaya, Y Okamoto, K Hirai, S
Citation: M. Shoji et al., Age-related amyloid beta protein accumulation induces cellular death and macrophage activation in transgenic mice, J PATHOLOGY, 191(1), 2000, pp. 93-101
Accumulation of NACP/alpha-synuclein in Lewy body disease and multiple system atrophy
Authors: Shoji, M Harigaya, Y Sasaki, A Ueda, K Ishiguro, K Matsubara, E Watanabe, M Ikeda, M Kanai, M Tomidokoro, Y Shizuka, M Amari, M Kosaka, K Nakazato, Y Okamoto, K Hirai, S
Citation: M. Shoji et al., Accumulation of NACP/alpha-synuclein in Lewy body disease and multiple system atrophy, J NE NE PSY, 68(5), 2000, pp. 605-608
Apolipoprotein E4 accelerates dementia and increases cerebrospinal fluid tau levels in Alzheimer's disease
Authors: Kanai, M Shizuka, M Urakami, K Matsubara, E Harigaya, Y Okamoto, K Shoji, M
Citation: M. Kanai et al., Apolipoprotein E4 accelerates dementia and increases cerebrospinal fluid tau levels in Alzheimer's disease, NEUROSCI L, 267(1), 1999, pp. 65-68
Deletion and nonsense mutations of the connexin 32 gene associated with Charcot-Marie-Tooth disease
Authors: Lin, CQ Numakura, C Ikegami, T Shizuka, M Shoji, M Nicholson, G Hayasaka, K
Citation: Cq. Lin et al., Deletion and nonsense mutations of the connexin 32 gene associated with Charcot-Marie-Tooth disease, TOH J EX ME, 188(3), 1999, pp. 239-244
A novel mutation of the myelin P-o gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening
Authors: Shizuka, M Ikeda, Y Watanabe, M Okamoto, K Shoji, M Ikegami, T Hayasaka, K
Citation: M. Shizuka et al., A novel mutation of the myelin P-o gene segregating Charcot-Marie-Tooth disease type 1B manifesting as trigeminal nerve thickening, J NE NE PSY, 67(2), 1999, pp. 250-251
Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)(1-2) polymorphism and contribution to founder effect
Authors: Mizushima, K Watanabe, M Kondo, I Okamoto, K Shizuka, M Abe, K Aoki, M Shoji, M
Citation: K. Mizushima et al., Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)(1-2) polymorphism and contribution to founder effect, J MED GENET, 36(2), 1999, pp. 112-114
Carboxyl-terminal fragments of presenilin-1 are closely related to cytoskeletal abnormalities in Alzheimer's brains
Authors: Tomidokoro, Y Ishiguro, K Igeta, Y Matsubara, E Kanai, M Shizuka, M Kawarabayashi, T Harigaya, Y Kawakatsu, S Ii, K Ikeda, M George-Hyslop, PHS Hirai, S Okamoto, K Shoji, M
Citation: Y. Tomidokoro et al., Carboxyl-terminal fragments of presenilin-1 are closely related to cytoskeletal abnormalities in Alzheimer's brains, BIOC BIOP R, 256(3), 1999, pp. 512-518
Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6and (CAG)n repeat units in normal elder controls
Authors: Shizuka, M Watanabe, M Ikeda, Y Mizushima, K Okamoto, K Shoji, M
Citation: M. Shizuka et al., Molecular analysis of a de novo mutation for spinocerebellar ataxia type 6and (CAG)n repeat units in normal elder controls, J NEUR SCI, 161(1), 1998, pp. 85-87
Risultati: 1-13 |