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Results: 1-13 |
Results: 13
Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X
Authors: Miyamoto, T Kanazawa, N Kato, S Kawakami, M Inoue, Y Kuhara, T Inoue, T Takeshita, K Tsujino, S
Citation: T. Miyamoto et al., Diagnosis of Japanese patients with HHH syndrome by molecular genetic analysis: a common mutation, R179X, J HUM GENET, 46(5), 2001, pp. 260-262
Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis
Authors: Shiroma, N Kanazawa, N Izumi, M Sugai, K Fukumizu, M Sasaki, M Hanaoka, S Kaga, M Tsujino, S
Citation: N. Shiroma et al., Diagnosis of Alexander disease in a Japanese patient by molecular genetic analysis, J HUM GENET, 46(10), 2001, pp. 579-582
Frequent mutations in Japanese patients with acid maltase deficiency
Authors: Tsujino, S Huei, M Kanazawa, N Sugie, H Goto, Y Kawai, M Nonaka, I Hirschhorn, R Sakuragawa, N
Citation: S. Tsujino et al., Frequent mutations in Japanese patients with acid maltase deficiency, NEUROMUSC D, 10(8), 2000, pp. 599-603
Quantum confinement without walls
Authors: Tsujino, S Allen, SJ Thomas, M Eckhause, T Gwinn, E Rufenacht, M Zhang, JP Speck, J Sakaki, H
Citation: S. Tsujino et al., Quantum confinement without walls, SUPERLATT M, 27(5-6), 2000, pp. 469-472
Glycogen storage myopathies
Authors: Tsujino, S Nonaka, I DiMauro, S
Citation: S. Tsujino et al., Glycogen storage myopathies, NEUROL CLIN, 18(1), 2000, pp. 125
Quantum control of electron transfer
Authors: Tsujino, S Rufenacht, M Miranda, P Allen, SJ Tamborenea, P Schoendeld, W Herold, G Lupke, G Lundstrom, T Petroff, P Metiu, H Moses, D
Citation: S. Tsujino et al., Quantum control of electron transfer, PHYS ST S-B, 221(1), 2000, pp. 391-396
Coherent transfer and electron teleportation in semiconductor double quantum well
Authors: Rufenacht, M Tsujino, S Allen, SJ Schoenfeld, W Petroff, P
Citation: M. Rufenacht et al., Coherent transfer and electron teleportation in semiconductor double quantum well, PHYS ST S-B, 221(1), 2000, pp. 407-411
Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and hyperammonemia syndrome
Authors: Tsujino, S Kanazawa, N Ohashi, T Eto, Y Saito, T Kira, J Yamada, T
Citation: S. Tsujino et al., Three novel mutations (G27E, insAAC, R179X) in the ORNT1 gene of Japanese patients with hyperornithinemia, hyperammonemia, and hyperammonemia syndrome, ANN NEUROL, 47(5), 2000, pp. 625-631
Peak position of the intersubband absorption spectrum of quantum wells with controlled electron concentrations
Authors: Tsujino, S Rufenacht, M Nakajima, H Noda, T Metzner, C Sakaki, H
Citation: S. Tsujino et al., Peak position of the intersubband absorption spectrum of quantum wells with controlled electron concentrations, PHYS REV B, 62(3), 2000, pp. 1560-1563
Differential requirement of the cytoplasmic subregions of gamma c chain inT cell development and function
Authors: Tsujino, S Di Santo, JP Takaoka, A McKernan, TL Noguchi, S Taya, C Yonekawa, H Saito, T Taniguchi, T Fujii, H
Citation: S. Tsujino et al., Differential requirement of the cytoplasmic subregions of gamma c chain inT cell development and function, P NAS US, 97(19), 2000, pp. 10514-10519
Midinfrared studies of the contact region at superconductor-semiconductor interfaces
Authors: Eckhause, TA Tsujino, S Lehnert, KW Gwinn, EG Allen, SJ Thomas, M Kroemer, H
Citation: Ta. Eckhause et al., Midinfrared studies of the contact region at superconductor-semiconductor interfaces, APPL PHYS L, 76(2), 2000, pp. 215-217
Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro
Authors: Pari, G Crerar, MM Nalbantoglu, J Shoubridge, E Jani, A Tsujino, S Shanske, S DiMauro, S Howell, JM Karpati, G
Citation: G. Pari et al., Myophosphorylase gene transfer in McArdle's disease myoblasts in vitro, NEUROLOGY, 53(6), 1999, pp. 1352-1354
Myophosphorylase deficiency and limb-girdle muscular dystrophy in the samepedigree
Authors: Nishio, T Sunohara, N Nonaka, I Tsujino, S Sugie, H
Citation: T. Nishio et al., Myophosphorylase deficiency and limb-girdle muscular dystrophy in the samepedigree, ACT NEUR SC, 98(5), 1998, pp. 364-367
Risultati: 1-13 |