Nonaka I - Search Results

1

Dp260 disrupted mice revealed prolonged implicit time of the b-wave in ERG and loss of accumulation of beta-dystroglycan in the outer plexiform layer of the retina.

Kameya S, Araki E, Katsuki M, Mizota A, Adachi E, Nakahara K, Nonaka I, Sakuragi S, Takeda S, Nabeshima Y. Kameya S, et al. Among authors: nonaka i. Hum Mol Genet. 1997 Dec;6(13):2195-203. doi: 10.1093/hmg/6.13.2195. Hum Mol Genet. 1997. PMID: 9361023

2

[Clinical and pathological studies on two patients with adult-onset nemaline myopathy].

Maruyama T, Hanyu N, Maruyama K, Takeda S, Yanagisawa N, Nonaka I. Maruyama T, et al. Among authors: nonaka i. Rinsho Shinkeigaku. 1990 Jul;30(7):738-44. Rinsho Shinkeigaku. 1990. PMID: 2173650 Review. Japanese.

3

Limb-girdle muscular dystrophy: clinical and pathologic reevaluation.

Yamanouchi Y, Arikawa E, Arahata K, Ozawa E, Nonaka I. Yamanouchi Y, et al. Among authors: nonaka i. J Neurol Sci. 1995 Mar;129(1):15-20. doi: 10.1016/0022-510x(94)00231-c. J Neurol Sci. 1995. PMID: 7751838

4

Sarcoglycan complex is selectively lost in dystrophic hamster muscle.

Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Nonaka I, Hirai S, Ozawa E. Mizuno Y, et al. Among authors: nonaka i. Am J Pathol. 1995 Feb;146(2):530-6. Am J Pathol. 1995. PMID: 7856762 Free PMC article.

5

Selective defect of sarcoglycan complex in severe childhood autosomal recessive muscular dystrophy muscle.

Mizuno Y, Noguchi S, Yamamoto H, Yoshida M, Suzuki A, Hagiwara Y, Hayashi YK, Arahata K, Nonaka I, Hirai S, et al. Mizuno Y, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278. Biochem Biophys Res Commun. 1994. PMID: 8093083

6

A dystrophin-associated glycoprotein, A3a (one of 43DAG doublets), is retained in Duchenne muscular dystrophy muscle.

Yoshida M, Mizuno Y, Nonaka I, Ozawa E. Yoshida M, et al. Among authors: nonaka i. J Biochem. 1993 Nov;114(5):634-9. doi: 10.1093/oxfordjournals.jbchem.a124229. J Biochem. 1993. PMID: 8113213 Free article.

7

Expression of utrophin (dystrophin-related protein) and dystrophin-associated glycoproteins in muscles from patients with Duchenne muscular dystrophy.

Mizuno Y, Yoshida M, Nonaka I, Hirai S, Ozawa E. Mizuno Y, et al. Among authors: nonaka i. Muscle Nerve. 1994 Feb;17(2):206-16. doi: 10.1002/mus.880170212. Muscle Nerve. 1994. PMID: 8114791

8

Reciprocal expression of dystrophin and utrophin in muscles of Duchenne muscular dystrophy patients, female DMD-carriers and control subjects.

Mizuno Y, Nonaka I, Hirai S, Ozawa E. Mizuno Y, et al. Among authors: nonaka i. J Neurol Sci. 1993 Oct;119(1):43-52. doi: 10.1016/0022-510x(93)90190-a. J Neurol Sci. 1993. PMID: 8246010

9

Myogenin gene disruption results in perinatal lethality because of severe muscle defect.

Nabeshima Y, Hanaoka K, Hayasaka M, Esumi E, Li S, Nonaka I, Nabeshima Y. Nabeshima Y, et al. Among authors: nonaka i. Nature. 1993 Aug 5;364(6437):532-5. doi: 10.1038/364532a0. Nature. 1993. PMID: 8393146

10

Targeted disruption of exon 52 in the mouse dystrophin gene induced muscle degeneration similar to that observed in Duchenne muscular dystrophy.

Araki E, Nakamura K, Nakao K, Kameya S, Kobayashi O, Nonaka I, Kobayashi T, Katsuki M. Araki E, et al. Among authors: nonaka i. Biochem Biophys Res Commun. 1997 Sep 18;238(2):492-7. doi: 10.1006/bbrc.1997.7328. Biochem Biophys Res Commun. 1997. PMID: 9299538

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