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Results:
1-12
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Results: 12
Authors:
Date, H
Onodera, O
Tanaka, H
Iwabuchi, K
Uekawa, K
Igarashi, S
Koike, R
Hiroi, T
Yuasa, T
Awaya, Y
Sakai, T
Takahashi, T
Nagatomo, H
Sekijima, Y
Kawachi, I
Takiyama, Y
Nishizawa, M
Fukuhara, N
Saito, K
Sugano, S
Tsuji, S
Citation: H. Date et al., Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is causedby mutations in a new HIT superfamily gene, NAT GENET, 29(2), 2001, pp. 184-188
Authors:
Namekawa, M
Takiyama, Y
Ando, Y
Sakoe, K
Muramatsu, S
Fujimoto, K
Nishizawa, M
Nakano, I
Citation: M. Namekawa et al., Choreiform movements in spinocerebellar ataxia type 1, J NEUR SCI, 187(1-2), 2001, pp. 103-106
Authors:
Shimazaki, H
Takiyama, Y
Sakoe, K
Amaike, M
Nagaki, H
Namekawa, M
Sasaki, H
Nakano, I
Nishizawa, M
Citation: H. Shimazaki et al., Meiotic instability of the CAG repeats in the SCA6/CACNA1A gene in two Japanese SCA6 families, J NEUR SCI, 185(2), 2001, pp. 101-107
Authors:
Namekawa, M
Takiyama, Y
Sakoe, K
Shimazaki, H
Amaike, M
Niijima, K
Nakano, I
Nishizawa, M
Citation: M. Namekawa et al., A large Japanese SPG4 family with a novel insertion mutation of the SPG4 gene: a clinical and genetic study, J NEUR SCI, 185(1), 2001, pp. 63-68
Authors:
Yabe, I
Sasaki, H
Yamashita, I
Tashiro, K
Takei, A
Suzuki, Y
Kida, H
Takiyama, Y
Nishizawa, M
Hokezu, Y
Nagamatsu, K
Oda, T
Ohnishi, A
Inoue, I
Hata, A
Citation: I. Yabe et al., Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese, J MED GENET, 38(5), 2001, pp. 328-333
Authors:
Zhou, YX
Qiao, WH
Gu, WH
Xie, H
Tang, BS
Zhou, LS
Yang, BX
Takiyama, Y
Tsuji, S
He, HY
Deng, CX
Goldfarb, LG
Wang, GX
Citation: Yx. Zhou et al., Spinocerebellar ataxia type 1 in China - Molecular analysis and genotype-phenotype correlation in 5 families, ARCH NEUROL, 58(5), 2001, pp. 789-794
Authors:
Shimohata, T
Nakajima, T
Yamada, M
Uchida, C
Onodera, O
Naruse, S
Kimura, T
Koide, R
Nozaki, K
Sano, Y
Ishiguro, H
Sakoe, K
Ooshima, T
Sato, A
Ikeuchi, T
Oyake, M
Sato, T
Aoyagi, Y
Hozumi, I
Nagatsu, T
Takiyama, Y
Nishizawa, M
Goto, J
Kanazawa, I
Davidson, I
Tanese, N
Takahashi, H
Tsuji, S
Citation: T. Shimohata et al., Expanded polyglutamine stretches interact with TAF(II)130, interfering with CREB-dependent transcription, NAT GENET, 26(1), 2000, pp. 29-36
Authors:
Yamashita, I
Sasaki, H
Yabe, I
Fukazawa, T
Nogoshi, S
Komeichi, K
Takada, A
Shiraishi, K
Takiyama, Y
Nishizawa, M
Kaneko, J
Tanaka, H
Tsuji, S
Tashiro, K
Citation: I. Yamashita et al., A novel locus for dominant cerebellar ataxia (SCA14) maps to a 10.2-cM interval flanked by D19S206 and D19S605 on chromosome 19q13.4-qter, ANN NEUROL, 48(2), 2000, pp. 156-163
Authors:
Aoki, N
Kimura, S
Takiyama, Y
Atsuta, Y
Abe, A
Sato, K
Katagiri, M
Citation: N. Aoki et al., The role of the DAP12 signal in mouse myeloid differentiation, J IMMUNOL, 165(7), 2000, pp. 3790-3796
Authors:
Takiyama, Y
Sakoe, K
Amaike, M
Soutome, M
Ogawa, T
Nakano, I
Nishizawa, M
Citation: Y. Takiyama et al., Single sperm analysis of the CAG repeats in the gene for dentatorubral-pallidoluysian atrophy (DRPLA): the instability of the CAG repeats in the DRPLA gene is prominent among the CAG repeat diseases, HUM MOL GEN, 8(3), 1999, pp. 453-457
Authors:
Takiyama, Y
Sato, Y
Sawada, M
Nishizawa, M
Nakano, I
Kusunoki, S
Citation: Y. Takiyama et al., An unusual case of facial diplegia, MUSCLE NERV, 22(6), 1999, pp. 778-779
Authors:
Kawakami, T
Takiyama, Y
Sakoe, K
Ogawa, T
Yoshioka, T
Nishizawa, M
Reid, ME
Kobayashi, O
Nonaka, I
Nakano, I
Citation: T. Kawakami et al., A case of McLeod syndrome with unusually severe myopathy, J NEUR SCI, 166(1), 1999, pp. 36-39
Risultati:
1-12
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