Okada S - Search Results

1

Molecular cloning and expression of cDNA for murine galactocerebrosidase and mutation analysis of the twitcher mouse, a model of Krabbe's disease.

Sakai N, Inui K, Tatsumi N, Fukushima H, Nishigaki T, Taniike M, Nishimoto J, Tsukamoto H, Yanagihara I, Ozono K, Okada S. Sakai N, et al. Among authors: okada s. J Neurochem. 1996 Mar;66(3):1118-24. doi: 10.1046/j.1471-4159.1996.66031118.x. J Neurochem. 1996. PMID: 8769874

2

Krabbe disease: isolation and characterization of a full-length cDNA for human galactocerebrosidase.

Sakai N, Inui K, Fujii N, Fukushima H, Nishimoto J, Yanagihara I, Isegawa Y, Iwamatsu A, Okada S. Sakai N, et al. Among authors: okada s. Biochem Biophys Res Commun. 1994 Jan 28;198(2):485-91. doi: 10.1006/bbrc.1994.1071. Biochem Biophys Res Commun. 1994. PMID: 8297359

3

[Krabbe disease (globoid cell leukodystrophy)].

Sakai N, Inui K, Okada S. Sakai N, et al. Among authors: okada s. Nihon Rinsho. 1995 Dec;53(12):2947-51. Nihon Rinsho. 1995. PMID: 8577041 Review. Japanese.

4

Human galactocerebrosidase gene: promoter analysis of the 5'-flanking region and structural organization.

Sakai N, Fukushima H, Inui K, Fu L, Nishigaki T, Yanagihara I, Tatsumi N, Ozono K, Okada S. Sakai N, et al. Among authors: okada s. Biochim Biophys Acta. 1998 Jan 7;1395(1):62-7. doi: 10.1016/s0167-4781(97)00140-1. Biochim Biophys Acta. 1998. PMID: 9434153

5

Molecular heterogeneity of Krabbe disease.

Fu L, Inui K, Nishigaki T, Tatsumi N, Tsukamoto H, Kokubu C, Muramatsu T, Okada S. Fu L, et al. Among authors: okada s. J Inherit Metab Dis. 1999 Apr;22(2):155-62. doi: 10.1023/a:1005449919660. J Inherit Metab Dis. 1999. PMID: 10234611

6

Study of pathogenesis in twitcher mouse, an enzymatically authentic model of Krabbe's disease.

Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H. Inui K, et al. Among authors: okada s. J Neurol Sci. 1990 Dec;100(1-2):124-30. doi: 10.1016/0022-510x(90)90022-f. J Neurol Sci. 1990. PMID: 2128519

7

Study of pathogenesis in twitcher mouse, an enzymatically authentic model of human Krabbe's disease.

Inui K, Nishimoto J, Taniike M, Midorikawa M, Tsukamoto H, Okada S, Yabuuchi H. Inui K, et al. Among authors: okada s. J Inherit Metab Dis. 1989;12 Suppl 2:383-5. doi: 10.1007/BF03335429. J Inherit Metab Dis. 1989. PMID: 2512450 No abstract available.

8

Purification and characterization of galactocerebrosidase from human lymphocytes.

Sakai N, Inui K, Midorikawa M, Okuno Y, Ueda S, Iwamatsu A, Okada S. Sakai N, et al. Among authors: okada s. J Biochem. 1994 Sep;116(3):615-20. doi: 10.1093/oxfordjournals.jbchem.a124569. J Biochem. 1994. PMID: 7852280 Free article.

9

[Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].

Tsukamoto H, Inui K, Okada S. Tsukamoto H, et al. Among authors: okada s. Nihon Rinsho. 1993 Sep;51(9):2428-34. Nihon Rinsho. 1993. PMID: 8105117 Review. Japanese.

10

Expression of full-length human dystrophin cDNA in mdx mouse muscle by HVJ-liposome injection.

Yanagihara I, Inui K, Dickson G, Turner G, Piper T, Kaneda Y, Okada S. Yanagihara I, et al. Among authors: okada s. Gene Ther. 1996 Jun;3(6):549-53. Gene Ther. 1996. PMID: 8789805

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