Kobayashi A - Search Results

1

Kobayashi A, Kitamoto T, Mizusawa H. Kobayashi A, et al. Handb Clin Neurol. 2018;153:207-218. doi: 10.1016/B978-0-444-63945-5.00012-X. Handb Clin Neurol. 2018. PMID: 29887137

2

Type 1 and type 2 human PrPSc have different aggregation sizes in methionine homozygotes with sporadic, iatrogenic and variant Creutzfeldt-Jakob disease.

Kobayashi A, Satoh S, Ironside JW, Mohri S, Kitamoto T. Kobayashi A, et al. J Gen Virol. 2005 Jan;86(Pt 1):237-240. doi: 10.1099/vir.0.80389-0. J Gen Virol. 2005. PMID: 15604452

3

Cross-sequence transmission of sporadic Creutzfeldt-Jakob disease creates a new prion strain.

Kobayashi A, Asano M, Mohri S, Kitamoto T. Kobayashi A, et al. J Biol Chem. 2007 Oct 12;282(41):30022-8. doi: 10.1074/jbc.M704597200. Epub 2007 Aug 20. J Biol Chem. 2007. PMID: 17709374 Free article.

4

Thr but Asn of the N-glycosylation sites of PrP is indispensable for its misfolding.

Ikeda S, Kobayashi A, Kitamoto T. Ikeda S, et al. Among authors: kobayashi a. Biochem Biophys Res Commun. 2008 May 16;369(4):1195-8. doi: 10.1016/j.bbrc.2008.03.014. Epub 2008 Mar 14. Biochem Biophys Res Commun. 2008. PMID: 18343219

5

Plaque-type deposition of prion protein in the damaged white matter of sporadic Creutzfeldt-Jakob disease MM1 patients.

Kobayashi A, Arima K, Ogawa M, Murata M, Fukuda T, Kitamoto T. Kobayashi A, et al. Acta Neuropathol. 2008 Nov;116(5):561-6. doi: 10.1007/s00401-008-0425-8. Epub 2008 Aug 28. Acta Neuropathol. 2008. PMID: 18751990

6

Human prion protein (PrP) 219K is converted to PrPSc but shows heterozygous inhibition in variant Creutzfeldt-Jakob disease infection.

Hizume M, Kobayashi A, Teruya K, Ohashi H, Ironside JW, Mohri S, Kitamoto T. Hizume M, et al. Among authors: kobayashi a. J Biol Chem. 2009 Feb 6;284(6):3603-9. doi: 10.1074/jbc.M809254200. Epub 2008 Dec 10. J Biol Chem. 2009. PMID: 19074151 Free article.

7

The number of octapeptide repeat affects the expression and conversion of prion protein.

Hiraga C, Kobayashi A, Kitamoto T. Hiraga C, et al. Among authors: kobayashi a. Biochem Biophys Res Commun. 2009 May 15;382(4):715-9. doi: 10.1016/j.bbrc.2009.03.093. Epub 2009 Mar 24. Biochem Biophys Res Commun. 2009. PMID: 19318088

8

Heterozygous inhibition in prion infection: the stone fence model.

Kobayashi A, Hizume M, Teruya K, Mohri S, Kitamoto T. Kobayashi A, et al. Prion. 2009 Jan-Mar;3(1):27-30. doi: 10.4161/pri.3.1.8514. Epub 2009 Jan 23. Prion. 2009. PMID: 19372732 Free PMC article. Review.

9

A traceback phenomenon can reveal the origin of prion infection.

Kobayashi A, Asano M, Mohri S, Kitamoto T. Kobayashi A, et al. Neuropathology. 2009 Oct;29(5):619-24. doi: 10.1111/j.1440-1789.2008.00973.x. Epub 2009 Jul 29. Neuropathology. 2009. PMID: 19659941

10

Amino acid conditions near the GPI anchor attachment site of prion protein for the conversion and the GPI anchoring.

Hizume M, Kobayashi A, Mizusawa H, Kitamoto T. Hizume M, et al. Among authors: kobayashi a. Biochem Biophys Res Commun. 2010 Jan 22;391(4):1681-6. doi: 10.1016/j.bbrc.2009.12.128. Epub 2009 Dec 29. Biochem Biophys Res Commun. 2010. PMID: 20040362

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