Tateishi J - Search Results

1

Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene.

Inoue I, Kitamoto T, Doh-ura K, Shii H, Goto I, Tateishi J. Inoue I, et al. Among authors: tateishi j. Neurology. 1994 Feb;44(2):299-301. doi: 10.1212/wnl.44.2.299. Neurology. 1994. PMID: 7906019

2

Immunohistochemical verification of senile and kuru plaques in Creutzfeldt-Jakob disease and the allied disease.

Kitamoto T, Tateishi J, Sato Y. Kitamoto T, et al. Among authors: tateishi j. Ann Neurol. 1988 Oct;24(4):537-42. doi: 10.1002/ana.410240410. Ann Neurol. 1988. PMID: 3071243

3

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome.

Furukawa H, Kitamoto T, Tanaka Y, Tateishi J. Furukawa H, et al. Among authors: tateishi j. Brain Res Mol Brain Res. 1995 Jun;30(2):385-8. doi: 10.1016/0169-328x(95)00034-p. Brain Res Mol Brain Res. 1995. PMID: 7637591

4

Inherited prion diseases and transmission to rodents.

Tateishi J, Kitamoto T. Tateishi J, et al. Brain Pathol. 1995 Jan;5(1):53-9. doi: 10.1111/j.1750-3639.1995.tb00577.x. Brain Pathol. 1995. PMID: 7767491 Review.

5

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.

Yamada M, Itoh Y, Fujigasaki H, Naruse S, Kaneko K, Kitamoto T, Tateishi J, Otomo E, Hayakawa M, Tanaka J, et al. Yamada M, et al. Among authors: tateishi j. Neurology. 1993 Dec;43(12):2723-4. doi: 10.1212/wnl.43.12.2723-a. Neurology. 1993. PMID: 7902972 No abstract available.

6

Human prion diseases with variant prion protein.

Kitamoto T, Tateishi J. Kitamoto T, et al. Among authors: tateishi j. Philos Trans R Soc Lond B Biol Sci. 1994 Mar 29;343(1306):391-8. doi: 10.1098/rstb.1994.0034. Philos Trans R Soc Lond B Biol Sci. 1994. PMID: 7913756

7

Species barrier prevents an abnormal isoform of prion protein from accumulating in follicular dendritic cells of mice with Creutzfeldt-Jakob disease.

Muramoto T, Kitamoto T, Hoque MZ, Tateishi J, Goto I. Muramoto T, et al. Among authors: tateishi j. J Virol. 1993 Nov;67(11):6808-10. doi: 10.1128/JVI.67.11.6808-6810.1993. J Virol. 1993. PMID: 8105107 Free PMC article.

8

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.

Kitamoto T, Ohta M, Doh-ura K, Hitoshi S, Terao Y, Tateishi J. Kitamoto T, et al. Among authors: tateishi j. Biochem Biophys Res Commun. 1993 Mar 15;191(2):709-14. doi: 10.1006/bbrc.1993.1275. Biochem Biophys Res Commun. 1993. PMID: 8461023

9

Experimental transmission of Creutzfeldt-Jakob disease and related diseases to rodents.

Tateishi J, Kitamoto T, Hoque MZ, Furukawa H. Tateishi J, et al. Neurology. 1996 Feb;46(2):532-7. doi: 10.1212/wnl.46.2.532. Neurology. 1996. PMID: 8614527

10

A Japanese case of Creutzfeldt-Jakob disease with a point mutation in the prion protein gene at codon 210.

Furukawa H, Kitamoto T, Hashiguchi H, Tateishi J. Furukawa H, et al. Among authors: tateishi j. J Neurol Sci. 1996 Sep 15;141(1-2):120-2. doi: 10.1016/0022-510x(96)00157-8. J Neurol Sci. 1996. PMID: 8880705

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