Arahata K - Search Results

1

Deficiency of laminin alpha 2-chain mRNA in muscle in a patient with merosin-negative congenital muscular dystrophy.

Hayashi YK, Koga R, Tsukahara T, Ishii H, Matsuishi T, Yamashita Y, Nonaka I, Arahata K. Hayashi YK, et al. Among authors: arahata k. Muscle Nerve. 1995 Sep;18(9):1027-30. doi: 10.1002/mus.880180918. Muscle Nerve. 1995. PMID: 7643867 No abstract available.

2

[Clinical and genetical features of Japanese early-onset facioscapulohumeral muscular dystrophy].

Yamanaka G, Goto K, Hayashi YK, Miyajima T, Hoshika A, Arahata K. Yamanaka G, et al. Among authors: arahata k. No To Hattatsu. 2002 Jul;34(4):318-24. No To Hattatsu. 2002. PMID: 12134683 Japanese.

3

Increased expression level of the splicing variant of SIP1 in motor neuron diseases.

Aerbajinai W, Ishihara T, Arahata K, Tsukahara T. Aerbajinai W, et al. Among authors: arahata k. Int J Biochem Cell Biol. 2002 Jun;34(6):699-707. doi: 10.1016/s1357-2725(01)00150-9. Int J Biochem Cell Biol. 2002. PMID: 11943600

4

CDNA microarray analysis of gene expression in fibroblasts of patients with X-linked Emery-Dreifuss muscular dystrophy.

Tsukahara T, Tsujino S, Arahata K. Tsukahara T, et al. Among authors: arahata k. Muscle Nerve. 2002 Jun;25(6):898-901. doi: 10.1002/mus.10085. Muscle Nerve. 2002. PMID: 12115980

5

A comparative gene expression analysis of Emery-Dreifuss muscular dystrophy using a cDNA microarray.

Tsukahara T, Arahata K. Tsukahara T, et al. Among authors: arahata k. Methods Mol Biol. 2003;217:253-62. doi: 10.1385/1-59259-330-5:253. Methods Mol Biol. 2003. PMID: 12491938 No abstract available.

6

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

7

Characterization of a tandemly repeated 3.3-kb Kpnl unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35.

Lee JH, Goto K, Matsuda C, Arahata K. Lee JH, et al. Among authors: arahata k. Muscle Nerve Suppl. 1995;(2):S6-13. Muscle Nerve Suppl. 1995. PMID: 23573580

8

Effective adenovirus-mediated gene expression in adult murine skeletal muscle.

Ishii A, Hagiwara Y, Saito Y, Yamamoto K, Yuasa K, Sato Y, Arahata K, Shoji S, Nonaka I, Saito I, Nabeshima Y, Takeda S. Ishii A, et al. Among authors: arahata k. Muscle Nerve. 1999 May;22(5):592-9. doi: 10.1002/(sici)1097-4598(199905)22:5<592::aid-mus7>3.0.co;2-2. Muscle Nerve. 1999. PMID: 10331358

9

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).

Lee JH, Goto K, Sahashi KO, Nonaka I, Matsuda C, Arahata K. Lee JH, et al. Among authors: arahata k. Muscle Nerve Suppl. 1995;(2):S27-31. Muscle Nerve Suppl. 1995. PMID: 23573583

10

Identification of a Thr-to-Met mutation in the skeletal muscle sodium channel gene in hyperkalemic periodic paralysis of a Japanese family.

Arahata K, Wang J, Feero WG, Hayakawa H, Honda K, Sugita H, Hoffman EP. Arahata K, et al. Ann N Y Acad Sci. 1993 Dec 20;707:342-5. doi: 10.1111/j.1749-6632.1993.tb38065.x. Ann N Y Acad Sci. 1993. PMID: 9137564 No abstract available.

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