Arahata K - Search Results

1

The sarcolemmal proteins dysferlin and caveolin-3 interact in skeletal muscle.

Matsuda C, Hayashi YK, Ogawa M, Aoki M, Murayama K, Nishino I, Nonaka I, Arahata K, Brown RH Jr. Matsuda C, et al. Among authors: arahata k. Hum Mol Genet. 2001 Aug 15;10(17):1761-6. doi: 10.1093/hmg/10.17.1761. Hum Mol Genet. 2001. PMID: 11532985

2

Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A.

Tagawa K, Taya C, Hayashi Y, Nakagawa M, Ono Y, Fukuda R, Karasuyama H, Toyama-Sorimachi N, Katsui Y, Hata S, Ishiura S, Nonaka I, Seyama Y, Arahata K, Yonekawa H, Sorimachi H, Suzuki K. Tagawa K, et al. Among authors: arahata k. Hum Mol Genet. 2000 May 22;9(9):1393-402. doi: 10.1093/hmg/9.9.1393. Hum Mol Genet. 2000. PMID: 10814721

3

cDNA microarray analysis of individual Duchenne muscular dystrophy patients.

Noguchi S, Tsukahara T, Fujita M, Kurokawa R, Tachikawa M, Toda T, Tsujimoto A, Arahata K, Nishino I. Noguchi S, et al. Among authors: arahata k. Hum Mol Genet. 2003 Mar 15;12(6):595-600. Hum Mol Genet. 2003. PMID: 12620965

4

Mutations in the integrin alpha7 gene cause congenital myopathy.

Hayashi YK, Chou FL, Engvall E, Ogawa M, Matsuda C, Hirabayashi S, Yokochi K, Ziober BL, Kramer RH, Kaufman SJ, Ozawa E, Goto Y, Nonaka I, Tsukahara T, Wang JZ, Hoffman EP, Arahata K. Hayashi YK, et al. Among authors: arahata k. Nat Genet. 1998 May;19(1):94-7. doi: 10.1038/ng0598-94. Nat Genet. 1998. PMID: 9590299

5

Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy.

Liu J, Aoki M, Illa I, Wu C, Fardeau M, Angelini C, Serrano C, Urtizberea JA, Hentati F, Hamida MB, Bohlega S, Culper EJ, Amato AA, Bossie K, Oeltjen J, Bejaoui K, McKenna-Yasek D, Hosler BA, Schurr E, Arahata K, de Jong PJ, Brown RH Jr. Liu J, et al. Among authors: arahata k. Nat Genet. 1998 Sep;20(1):31-6. doi: 10.1038/1682. Nat Genet. 1998. PMID: 9731526

6

Dysferlin is a surface membrane-associated protein that is absent in Miyoshi myopathy.

Matsuda C, Aoki M, Hayashi YK, Ho MF, Arahata K, Brown RH Jr. Matsuda C, et al. Among authors: arahata k. Neurology. 1999 Sep 22;53(5):1119-22. doi: 10.1212/wnl.53.5.1119. Neurology. 1999. PMID: 10496277

7

[Positional cloning of the gene for Miyoshi myopathy and limb-girdle muscular dystrophy].

Aoki M, Arahata K, Brown RH Jr. Aoki M, et al. Among authors: arahata k. Rinsho Shinkeigaku. 1999 Dec;39(12):1272-5. Rinsho Shinkeigaku. 1999. PMID: 10791095 Japanese.

8

Massive muscle cell degeneration in the early stage of merosin-deficient congenital muscular dystrophy.

Hayashi YK, Tezak Z, Momoi T, Nonaka I, Garcia CA, Hoffman EP, Arahata K. Hayashi YK, et al. Among authors: arahata k. Neuromuscul Disord. 2001 May;11(4):350-9. doi: 10.1016/s0960-8966(00)00203-0. Neuromuscul Disord. 2001. PMID: 11369186

9

The product of an oculopharyngeal muscular dystrophy gene, poly(A)-binding protein 2, interacts with SKIP and stimulates muscle-specific gene expression.

Kim YJ, Noguchi S, Hayashi YK, Tsukahara T, Shimizu T, Arahata K. Kim YJ, et al. Among authors: arahata k. Hum Mol Genet. 2001 May 15;10(11):1129-39. doi: 10.1093/hmg/10.11.1129. Hum Mol Genet. 2001. PMID: 11371506

10

Selective deficiency of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

Hayashi YK, Ogawa M, Tagawa K, Noguchi S, Ishihara T, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: arahata k. Neurology. 2001 Jul 10;57(1):115-21. doi: 10.1212/wnl.57.1.115. Neurology. 2001. PMID: 11445638

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