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Results:
1-7
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Results: 7
Authors:
Matsuda, C
Hayashi, YK
Ogawa, M
Aoki, M
Murayama, K
Nishino, I
Nonaka, I
Arahata, K
Brown, RH
Citation: C. Matsuda et al., The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle, HUM MOL GEN, 10(17), 2001, pp. 1761-1766
Authors:
Kim, YJ
Noguchi, SR
Hayashi, YK
Tsukahara, TF
Shimizu, T
Arahata, K
Citation: Yj. Kim et al., The product of an oculopharyngeal muscular dystrophy gene, poly(A)-bindingprotein 2, interacts with SKIP and stimulates muscle-specific gene expression, HUM MOL GEN, 10(11), 2001, pp. 1129-1139
Authors:
Hayashi, YK
Tezak, Z
Momoi, T
Nonaka, I
Garcia, CA
Hoffman, EP
Arahata, K
Citation: Yk. Hayashi et al., Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy, NEUROMUSC D, 11(4), 2001, pp. 350-359
Authors:
Yamanaka, G
Goto, K
Matsumura, T
Funakoshi, M
Komori, T
Hayashi, YK
Arahata, K
Citation: G. Yamanaka et al., Tongue atrophy in facioscapulohumeral muscular dystrophy, NEUROLOGY, 57(4), 2001, pp. 733-735
Authors:
Hayashi, YK
Ogawa, M
Tagawa, K
Noguchi, S
Ishihara, T
Nonaka, I
Arahata, K
Citation: Yk. Hayashi et al., Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy, NEUROLOGY, 57(1), 2001, pp. 115-121
Authors:
Matsumura, T
Aoki, M
Nagano, A
Hayashi, YK
Asada, C
Ogawa, M
Yamanaka, G
Goto, K
Nakagawa, M
Oka, H
Sahashi, K
Kouhara, N
Saito, Y
Brown, RH
Nonaka, I
Arahata, K
Citation: T. Matsumura et al., Molecular genetic analysis of dysferlin in Japanese patients with Miyoshi myopathy, P JPN AC B, 75(7), 1999, pp. 207-212
Authors:
Matsuda, C
Aoki, M
Hayashi, YK
Ho, MF
Arahata, K
Brown, RH
Citation: C. Matsuda et al., Expedited publication - Dysferlin is a surface membrane-associated proteinthat is absent in Miyoshi myopathy, NEUROLOGY, 53(5), 1999, pp. 1119-1122
Risultati:
1-7
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