Sakaguchi S - Search Results

1

Early appearance but lagged accumulation of detergent-insoluble prion protein in the brains of mice inoculated with a mouse-adapted Creutzfeldt-Jakob disease agent.

Nakaoke R, Sakaguchi S, Atarashi R, Nishida N, Arima K, Shigematsu K, Katamine S. Nakaoke R, et al. Among authors: sakaguchi s. Cell Mol Neurobiol. 2000 Dec;20(6):717-30. doi: 10.1023/a:1007054909662. Cell Mol Neurobiol. 2000. PMID: 11100979

2

Accumulation of proteinase K-resistant prion protein (PrP) is restricted by the expression level of normal PrP in mice inoculated with a mouse-adapted strain of the Creutzfeldt-Jakob disease agent.

Sakaguchi S, Katamine S, Shigematsu K, Nakatani A, Moriuchi R, Nishida N, Kurokawa K, Nakaoke R, Sato H, Jishage K, et al. Sakaguchi S, et al. J Virol. 1995 Dec;69(12):7586-92. doi: 10.1128/JVI.69.12.7586-7592.1995. J Virol. 1995. PMID: 7494265 Free PMC article.

3

The infectivity is dissociated from PrP accumulation in salivary gland of Creutzfeldt-Jakob disease agent-inoculated mice.

Miyamoto T, Sakaguchi S, Katamine S, Moriuchi R. Miyamoto T, et al. Among authors: sakaguchi s. Ann N Y Acad Sci. 1994 Jun 6;724:310-3. doi: 10.1111/j.1749-6632.1994.tb38921.x. Ann N Y Acad Sci. 1994. PMID: 7913302 Review. No abstract available.

4

Kinetics of infectivity are dissociated from PrP accumulation in salivary glands of Creutzfeldt-Jakob disease agent-inoculated mice.

Sakaguchi S, Katamine S, Yamanouchi K, Kishikawa M, Moriuchi R, Yasukawa N, Doi T, Miyamoto T. Sakaguchi S, et al. J Gen Virol. 1993 Oct;74 ( Pt 10):2117-23. doi: 10.1099/0022-1317-74-10-2117. J Gen Virol. 1993. PMID: 8409936

5

Loss of cerebellar Purkinje cells in aged mice homozygous for a disrupted PrP gene.

Sakaguchi S, Katamine S, Nishida N, Moriuchi R, Shigematsu K, Sugimoto T, Nakatani A, Kataoka Y, Houtani T, Shirabe S, Okada H, Hasegawa S, Miyamoto T, Noda T. Sakaguchi S, et al. Nature. 1996 Apr 11;380(6574):528-31. doi: 10.1038/380528a0. Nature. 1996. PMID: 8606772

6

Impaired motor coordination in mice lacking prion protein.

Katamine S, Nishida N, Sugimoto T, Noda T, Sakaguchi S, Shigematsu K, Kataoka Y, Nakatani A, Hasegawa S, Moriuchi R, Miyamoto T. Katamine S, et al. Among authors: sakaguchi s. Cell Mol Neurobiol. 1998 Dec;18(6):731-42. doi: 10.1023/a:1020698305911. Cell Mol Neurobiol. 1998. PMID: 9876879 Review.

7

A mouse prion protein transgene rescues mice deficient for the prion protein gene from purkinje cell degeneration and demyelination.

Nishida N, Tremblay P, Sugimoto T, Shigematsu K, Shirabe S, Petromilli C, Erpel SP, Nakaoke R, Atarashi R, Houtani T, Torchia M, Sakaguchi S, DeArmond SJ, Prusiner SB, Katamine S. Nishida N, et al. Among authors: sakaguchi s. Lab Invest. 1999 Jun;79(6):689-97. Lab Invest. 1999. PMID: 10378511

8

Upregulation of the genes encoding lysosomal hydrolases, a perforin-like protein, and peroxidases in the brains of mice affected with an experimental prion disease.

Kopacek J, Sakaguchi S, Shigematsu K, Nishida N, Atarashi R, Nakaoke R, Moriuchi R, Niwa M, Katamine S. Kopacek J, et al. Among authors: sakaguchi s. J Virol. 2000 Jan;74(1):411-7. doi: 10.1128/jvi.74.1.411-417.2000. J Virol. 2000. PMID: 10590130 Free PMC article.

9

[Molecular biology of prion diseases].

Sakaguchi S, Katamine S. Sakaguchi S, et al. Uirusu. 1999 Dec;49(2):193-204. doi: 10.2222/jsv.49.193. Uirusu. 1999. PMID: 10737117 Free article. Review. Japanese. No abstract available.

10

Identification of a novel gene encoding a PrP-like protein expressed as chimeric transcripts fused to PrP exon 1/2 in ataxic mouse line with a disrupted PrP gene.

Li A, Sakaguchi S, Atarashi R, Roy BC, Nakaoke R, Arima K, Okimura N, Kopacek J, Shigematsu K. Li A, et al. Among authors: sakaguchi s. Cell Mol Neurobiol. 2000 Oct;20(5):553-67. doi: 10.1023/a:1007059827541. Cell Mol Neurobiol. 2000. PMID: 10930132

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