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Results: 1-25/26
Authors:
Iida, A
Saito, S
Sekine, A
Kitamoto, T
Kitamura, Y
Mishima, C
Osawa, S
Kondo, K
Harigae, S
Nakamura, Y
Citation: A. Iida et al., Catalog of 434 single-nucleotide polymorphisms (SNPs) in genes of the alcohol dehydrogenase, glutathione S-transferase, and nicotinamide adenine dinucleotide, reduced (NADH) ubiquinone oxidoreductase families, J HUM GENET, 46(7), 2001, pp. 385-407
Authors:
Iida, A
Sekine, A
Saito, S
Kitamura, Y
Kitamoto, T
Osawa, S
Mishima, C
Nakamura, Y
Citation: A. Iida et al., Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes, J HUM GENET, 46(4), 2001, pp. 225-240
Authors:
Tateishi, J
Kitamoto, T
Mohri, S
Satoh, S
Sato, T
Shepherd, A
Macnaughton, MR
Citation: J. Tateishi et al., Scrapie removal using Planova((R)) virus removal filters, BIOLOGICALS, 29(1), 2001, pp. 17-25
Authors:
Dubnau, J
Grady, L
Kitamoto, T
Tully, T
Citation: J. Dubnau et al., Disruption of neurotransmission in Drosophila mushroom body blocks retrieval but not acquisition of memory, NATURE, 411(6836), 2001, pp. 476-480
Authors:
Kitamoto, T
Citation: T. Kitamoto, Conditional modification of behavior in drosophila by targeted expression of a temperature-sensitive shibire allele in defined neurons, J NEUROBIOL, 47(2), 2001, pp. 81-92
Authors:
Nakamura, Y
Yanagawa, H
Kitamoto, T
Sato, T
Citation: Y. Nakamura et al., Epidemiologic features of 65 Creutzfeldt-Jakob disease patients with a history of cadaveric dura mater transplantation in Japan, EPIDEM INFE, 125(1), 2000, pp. 201-205
Authors:
Nakamura, N
Aoki, Y
Horiuchi, H
Furusawa, S
Yamanaka, HI
Kitamoto, T
Matsuda, H
Citation: N. Nakamura et al., Construction of recombinant monoclonal antibodies from a chicken hybridomaline secreting specific antibody, CYTOTECHNOL, 32(3), 2000, pp. 191-198
Authors:
Yu, B
Kitamoto, T
Citation: B. Yu et T. Kitamoto, The CHACM method for computing the characteristic polynomial of a polynomial matrix, IEICE T FUN, E83A(7), 2000, pp. 1405-1410
Authors:
Muramoto, T
Tanaka, T
Kitamoto, N
Sano, C
Hayashi, Y
Kutomi, T
Yutani, C
Kitamoto, T
Citation: T. Muramoto et al., Analyses of Gerstmann-Straussler syndrome with 102Leu219Lys using monoclonal antibodies that specifically detect human prion protein with 219Glu, NEUROSCI L, 288(3), 2000, pp. 179-182
Authors:
Waddell, S
Armstrong, JD
Kitamoto, T
Kaiser, K
Quinn, WG
Citation: S. Waddell et al., The amnesiac gene product is expressed in two neurons in the Drosophila brain that are critical for memory, CELL, 103(5), 2000, pp. 805-813
Authors:
Konaka, K
Kaido, M
Okuda, Y
Aoike, F
Abe, K
Kitamoto, T
Yanagihara, T
Citation: K. Konaka et al., Proton magnetic resonance spectroscopy of a patient with Gerstmann-Straussler-Scheinker disease, NEURORADIOL, 42(9), 2000, pp. 662-665
Authors:
Kitamoto, T
Xie, XJ
Wu, CF
Salvaterra, PM
Citation: T. Kitamoto et al., Isolation and characterization of mutants for the vesicular acetylcholine transporter gene in Drosophila melanogaster, J NEUROBIOL, 42(2), 2000, pp. 161-171
Authors:
Kobayashi, Y
Kitamoto, T
Masuhiro, Y
Watanabe, M
Kase, T
Metzger, D
Yanagisawa, J
Kato, S
Citation: Y. Kobayashi et al., p300 mediates functional synergism between AF-1 and AF-2 of estrogen receptor alpha and beta by interacting directly with the N-terminal A/B domains, J BIOL CHEM, 275(21), 2000, pp. 15645-15651
Authors:
Matsuda, H
Mitsuda, H
Nakamura, N
Furusawa, S
Mohri, S
Kitamoto, T
Citation: H. Matsuda et al., A chicken monoclonal antibody with specificity for the N-terminal of humanprion protein, FEMS IM MED, 23(3), 1999, pp. 189-194
Authors:
Kitamoto, T
Citation: T. Kitamoto, Efficient computation of the characteristic polynomial of a polynomial matrix, IEICE T FUN, E82A(5), 1999, pp. 842-848
Authors:
Hainfellner, JA
Parchi, P
Kitamoto, T
Jarius, C
Gambetti, P
Budka, H
Citation: Ja. Hainfellner et al., A novel phenotype in familial Creutzfeldt-Jakob disease: Prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein, ANN NEUROL, 45(6), 1999, pp. 812-816
Authors:
Wang, WY
Kitamoto, T
Salvaterra, PM
Citation: Wy. Wang et al., Drosophila choline acetyltransferase temperature-sensitive mutants, NEUROCHEM R, 24(8), 1999, pp. 1081-1087
Authors:
Iino, K
Sasano, H
Oki, Y
Andoh, N
Shin, RW
Kitamoto, T
Takahashi, K
Suzuki, H
Tezuka, F
Yoshimi, T
Nagura, H
Citation: K. Iino et al., Urocortin expression in the human central nervous system, CLIN ENDOCR, 50(1), 1999, pp. 107-114
Authors:
Okuno, M
Sato, T
Kitamoto, T
Imai, S
Kawada, N
Suzuki, Y
Yoshimura, H
Moriwaki, H
Onuki, K
Masushige, S
Muto, Y
Friedman, SL
Kato, S
Kojima, S
Citation: M. Okuno et al., Increased 9,13-di-cis-retinoic acid in rat hepatic fibrosis: implication for a potential link between retinoid loss and TGF-beta mediated fibrogenesis in vivo, J HEPATOL, 30(6), 1999, pp. 1073-1080
Authors:
Yamada, M
Itoh, Y
Inaba, A
Wada, Y
Takashima, M
Satoh, S
Kamata, T
Okeda, R
Kayano, T
Suematsu, N
Kitamoto, T
Otomo, E
Matsushita, M
Mizusawa, H
Citation: M. Yamada et al., An inherited prion disease with a PrPP105L mutation - Clinicopathologic and PrP heterogeneity, NEUROLOGY, 53(1), 1999, pp. 181-188
Authors:
Nagashima, T
Okawa, M
Kitamoto, T
Takahashi, H
Ishihara, Y
Ozaki, Y
Nagashima, K
Citation: T. Nagashima et al., Wernicke encephalopathy-like symptoms as an early manifestation of Creutzfeldt-Jakob disease in a chronic alcoholic, J NEUR SCI, 163(2), 1999, pp. 192-198
Authors:
Kuze, N
Kitamoto, T
Usami, T
Sakaizumi, T
Ohashi, O
Iijima, K
Citation: N. Kuze et al., Molecular structure of dichloroacetaldehyde oxime by gas-phase electron diffraction combined with microwave spectroscopy, J MOL STRUC, 486, 1999, pp. 183-193
Authors:
Shimizu, S
Hoshi, K
Muramoto, T
Homma, M
Ironside, JW
Kuzuhara, S
Sato, T
Yamamoto, T
Kitamoto, T
Citation: S. Shimizu et al., Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting, ARCH NEUROL, 56(3), 1999, pp. 357-362
Authors:
Murayama, H
Shin, RW
Higuchi, J
Shibuya, S
Muramoto, T
Kitamoto, T
Citation: H. Murayama et al., Interaction of aluminum with PHF tau in Alzheimer's disease neurofibrillary degeneration evidenced by desferrioxamine-assisted chelating autoclave method, AM J PATH, 155(3), 1999, pp. 877-885
Authors:
Yamazaki, M
Oyanagi, K
Mori, O
Kitamura, S
Ohyama, M
Terashi, A
Kitamoto, T
Katayama, Y
Citation: M. Yamazaki et al., Variant Gerstman-Straussler syndrome with the P105L prion gene mutation: an unusual case with nigral degeneration and widespread neurofibrillary tangles, ACT NEUROP, 98(5), 1999, pp. 506-511