Goto K - Search Results

1

A severe muscular dystrophy patient with an internally deleted very short (110 kD) dystrophin: presence of the binding site for dystrophin-associated glycoprotein (DAG) may not be enough for physiological function of dystrophin.

Arikawa-Hirasawa E, Koga R, Tsukahara T, Nonaka I, Mitsudome A, Goto K, Beggs AH, Arahata K. Arikawa-Hirasawa E, et al. Among authors: goto k. Neuromuscul Disord. 1995 Sep;5(5):429-38. doi: 10.1016/0960-8966(94)00087-p. Neuromuscul Disord. 1995. PMID: 7496177

2

DNA rearrangements in Japanese facioscapulohumeral muscular dystrophy patients: clinical correlations.

Goto K, Lee JH, Matsuda C, Hirabayashi K, Kojo T, Nakamura A, Mitsunaga Y, Furukawa T, Sahashi K, Arahata K. Goto K, et al. Neuromuscul Disord. 1995 May;5(3):201-8. doi: 10.1016/0960-8966(94)00055-e. Neuromuscul Disord. 1995. PMID: 7633185

3

Immunohistochemical analysis of perforin and granzyme A in inflammatory myopathies.

Orimo S, Koga R, Goto K, Nakamura K, Arai M, Tamaki M, Sugita H, Nonaka I, Arahata K. Orimo S, et al. Among authors: goto k. Neuromuscul Disord. 1994 May;4(3):219-26. doi: 10.1016/0960-8966(94)90022-1. Neuromuscul Disord. 1994. PMID: 7919969

4

Abnormal localization of laminin subunits in muscular dystrophies.

Hayashi YK, Engvall E, Arikawa-Hirasawa E, Goto K, Koga R, Nonaka I, Sugita H, Arahata K. Hayashi YK, et al. Among authors: goto k. J Neurol Sci. 1993 Oct;119(1):53-64. doi: 10.1016/0022-510x(93)90191-z. J Neurol Sci. 1993. PMID: 8246011

5

Rigid spine syndrome caused by a novel mutation in four-and-a-half LIM domain 1 gene (FHL1).

Shalaby S, Hayashi YK, Goto K, Ogawa M, Nonaka I, Noguchi S, Nishino I. Shalaby S, et al. Among authors: goto k. Neuromuscul Disord. 2008 Dec;18(12):959-61. doi: 10.1016/j.nmd.2008.09.012. Epub 2008 Oct 25. Neuromuscul Disord. 2008. PMID: 18952429

6

Nuclear changes in skeletal muscle extend to satellite cells in autosomal dominant Emery-Dreifuss muscular dystrophy/limb-girdle muscular dystrophy 1B.

Park YE, Hayashi YK, Goto K, Komaki H, Hayashi Y, Inuzuka T, Noguchi S, Nonaka I, Nishino I. Park YE, et al. Among authors: goto k. Neuromuscul Disord. 2009 Jan;19(1):29-36. doi: 10.1016/j.nmd.2008.09.018. Epub 2008 Dec 12. Neuromuscul Disord. 2009. PMID: 19070492

7

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: goto k. Muscle Nerve Suppl. 1995;(2):S27-31. Muscle Nerve Suppl. 1995. PMID: 23573583

8

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses.

Arahata K, Ishihara T, Fukunaga H, Orimo S, Lee JH, Goto K, Nonaka I. Arahata K, et al. Among authors: goto k. Muscle Nerve Suppl. 1995;(2):S56-66. Muscle Nerve Suppl. 1995. PMID: 23573588

9

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

Lee JH, Goto K, Sahashi K, Nonaka I, Matsuda C, Arahata K. Lee JH, et al. Among authors: goto k. Muscle Nerve Suppl. 1995;2:S27-31. Muscle Nerve Suppl. 1995. PMID: 7739622

10

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses.

Arahata K, Ishihara T, Fukunaga H, Orimo S, Lee JH, Goto K, Nonaka I. Arahata K, et al. Among authors: goto k. Muscle Nerve Suppl. 1995;2:S56-66. Muscle Nerve Suppl. 1995. PMID: 7739627

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