Noguchi S - Search Results

1

Congenital muscular dystrophy with glycosylation defects of alpha-dystroglycan in Japan.

Matsumoto H, Hayashi YK, Kim DS, Ogawa M, Murakami T, Noguchi S, Nonaka I, Nakazawa T, Matsuo T, Futagami S, Campbell KP, Nishino I. Matsumoto H, et al. Among authors: noguchi s. Neuromuscul Disord. 2005 May;15(5):342-8. doi: 10.1016/j.nmd.2005.01.009. Neuromuscul Disord. 2005. PMID: 15833426

2

Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.

Noguchi S, McNally EM, Ben Othmane K, Hagiwara Y, Mizuno Y, Yoshida M, Yamamoto H, Bönnemann CG, Gussoni E, Denton PH, Kyriakides T, Middleton L, Hentati F, Ben Hamida M, Nonaka I, Vance JM, Kunkel LM, Ozawa E. Noguchi S, et al. Science. 1995 Nov 3;270(5237):819-22. doi: 10.1126/science.270.5237.819. Science. 1995. PMID: 7481775

3

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: noguchi s. Am J Pathol. 1995 Feb;146(2):530-6. Am J Pathol. 1995. PMID: 7856762 Free PMC article.

4

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: noguchi s. Biochem Biophys Res Commun. 1994 Sep 15;203(2):979-83. doi: 10.1006/bbrc.1994.2278. Biochem Biophys Res Commun. 1994. PMID: 8093083

5

Dystrophin-associated proteins in muscular dystrophy.

Ozawa E, Yoshida M, Suzuki A, Mizuno Y, Hagiwara Y, Noguchi S. Ozawa E, et al. Among authors: noguchi s. Hum Mol Genet. 1995;4 Spec No:1711-6. doi: 10.1093/hmg/4.suppl_1.1711. Hum Mol Genet. 1995. PMID: 8541869 Review.

6

From dystrophinopathy to sarcoglycanopathy: evolution of a concept of muscular dystrophy.

Ozawa E, Noguchi S, Mizuno Y, Hagiwara Y, Yoshida M. Ozawa E, et al. Among authors: noguchi s. Muscle Nerve. 1998 Apr;21(4):421-38. doi: 10.1002/(sici)1097-4598(199804)21:4<421::aid-mus1>3.0.co;2-b. Muscle Nerve. 1998. PMID: 9533777 Review.

7

Loss of the sarcoglycan complex and sarcospan leads to muscular dystrophy in beta-sarcoglycan-deficient mice.

Araishi K, Sasaoka T, Imamura M, Noguchi S, Hama H, Wakabayashi E, Yoshida M, Hori T, Ozawa E. Araishi K, et al. Among authors: noguchi s. Hum Mol Genet. 1999 Sep;8(9):1589-98. doi: 10.1093/hmg/8.9.1589. Hum Mol Genet. 1999. PMID: 10441321

8

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: noguchi s. Hum Mol Genet. 2001 May 15;10(11):1129-39. doi: 10.1093/hmg/10.11.1129. Hum Mol Genet. 2001. PMID: 11371506

9

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: noguchi s. Neurology. 2001 Jul 10;57(1):115-21. doi: 10.1212/wnl.57.1.115. Neurology. 2001. PMID: 11445638

10

Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy.

Nishino I, Noguchi S, Murayama K, Driss A, Sugie K, Oya Y, Nagata T, Chida K, Takahashi T, Takusa Y, Ohi T, Nishimiya J, Sunohara N, Ciafaloni E, Kawai M, Aoki M, Nonaka I. Nishino I, et al. Among authors: noguchi s. Neurology. 2002 Dec 10;59(11):1689-93. doi: 10.1212/01.wnl.0000041631.28557.c6. Neurology. 2002. PMID: 12473753

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