Nishino I - 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: nishino i. Hum Mol Genet. 2001 Aug 15;10(17):1761-6. doi: 10.1093/hmg/10.17.1761. Hum Mol Genet. 2001. PMID: 11532985

2

Newly recognized exons induced by a splicing abnormality from an intronic mutation of the dystrophin gene resulting in Duchenne muscular dystrophy. Mutations in brief no. 213. Online.

Ikezawa M, Nishino I, Goto Y, Miike T, Nonaka I. Ikezawa M, et al. Among authors: nishino i. Hum Mutat. 1999;13(2):170. doi: 10.1002/(SICI)1098-1004(1999)13:2<170::AID-HUMU12>3.0.CO;2-7. Hum Mutat. 1999. PMID: 10094556

3

Sarcolemmopathy: muscular dystrophies with cell membrane defects.

Ozawa E, Nishino I, Nonaka I. Ozawa E, et al. Among authors: nishino i. Brain Pathol. 2001 Apr;11(2):218-30. doi: 10.1111/j.1750-3639.2001.tb00394.x. Brain Pathol. 2001. PMID: 11303797 Free PMC article. Review.

4

Mutation in the caveolin-3 gene causes a peculiar form of distal myopathy.

Tateyama M, Aoki M, Nishino I, Hayashi YK, Sekiguchi S, Shiga Y, Takahashi T, Onodera Y, Haginoya K, Kobayashi K, Iinuma K, Nonaka I, Arahata K, Itoyama Y. Tateyama M, et al. Among authors: nishino i. Neurology. 2002 Jan 22;58(2):323-5. doi: 10.1212/wnl.58.2.323. Neurology. 2002. PMID: 11805270

5

[Recent advances in limb-girdle muscular dystrophy research].

Nonaka I, Minami N, Chae J, Hayashi YK, Nishino I, Arahata K. Nonaka I, et al. Among authors: nishino i. Rinsho Shinkeigaku. 2001 Dec;41(12):1194-7. Rinsho Shinkeigaku. 2001. PMID: 12235836 Review. Japanese.

6

Ullrich disease: collagen VI deficiency: EM suggests a new basis for muscular weakness.

Ishikawa H, Sugie K, Murayama K, Ito M, Minami N, Nishino I, Nonaka I. Ishikawa H, et al. Among authors: nishino i. Neurology. 2002 Sep 24;59(6):920-3. doi: 10.1212/wnl.59.6.920. Neurology. 2002. PMID: 12297580

7

POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in alpha-DG.

Kim DS, Hayashi YK, Matsumoto H, Ogawa M, Noguchi S, Murakami N, Sakuta R, Mochizuki M, Michele DE, Campbell KP, Nonaka I, Nishino I. Kim DS, et al. Among authors: nishino i. Neurology. 2004 Mar 23;62(6):1009-11. doi: 10.1212/01.wnl.0000115386.28769.65. Neurology. 2004. PMID: 15037715

8

Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathy.

Kawabe K, Goto K, Nishino I, Angelini C, Hayashi YK. Kawabe K, et al. Among authors: nishino i. Eur J Neurol. 2004 Oct;11(10):657-61. doi: 10.1111/j.1468-1331.2004.00755.x. Eur J Neurol. 2004. PMID: 15469449

9

Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan.

Okada M, Kawahara G, Noguchi S, Sugie K, Murayama K, Nonaka I, Hayashi YK, Nishino I. Okada M, et al. Among authors: nishino i. Neurology. 2007 Sep 4;69(10):1035-42. doi: 10.1212/01.wnl.0000271387.10404.4e. Neurology. 2007. PMID: 17785673

10

Reduced cell anchorage may cause sarcolemma-specific collagen VI deficiency in Ullrich disease.

Kawahara G, Okada M, Morone N, Ibarra CA, Nonaka I, Noguchi S, Hayashi YK, Nishino I. Kawahara G, et al. Among authors: nishino i. Neurology. 2007 Sep 4;69(10):1043-9. doi: 10.1212/01.wnl.0000271386.89878.22. Neurology. 2007. PMID: 17785674

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