Doh-ura K - Search Results

1

Autoantibody to glial fibrillary acidic protein in the sera of cattle with bovine spongiform encephalopathy.

Nomura S, Miyasho T, Maeda N, Doh-ura K, Yokota H. Nomura S, et al. Proteomics. 2009 Aug;9(16):4029-35. doi: 10.1002/pmic.200900066. Proteomics. 2009. PMID: 19658106

2

Differential expression of metallothioneins in human prion diseases.

Kawashima T, Doh-ura K, Torisu M, Uchida Y, Furuta A, Iwaki T. Kawashima T, et al. Dement Geriatr Cogn Disord. 2000 Sep-Oct;11(5):251-62. doi: 10.1159/000017247. Dement Geriatr Cogn Disord. 2000. PMID: 10940676

3

Neuropathological features of a case with schizophrenia and prion protein gene P102L mutation before onset of Gerstmann-Sträussler-Scheinker disease.

Sasaki K, Doh-ura K, Furuta A, Nakashima S, Morisada Y, Tateishi J, Iwaki T. Sasaki K, et al. Acta Neuropathol. 2003 Jul;106(1):92-6. doi: 10.1007/s00401-003-0697-y. Epub 2003 Apr 8. Acta Neuropathol. 2003. PMID: 12682740

4

Differential expression of transforming growth factor-beta isoforms in human prion diseases.

Tashiro H, Dohura K, Iwaki T. Tashiro H, et al. Neuropathol Appl Neurobiol. 1998 Aug;24(4):284-92. doi: 10.1046/j.1365-2990.1998.00117.x. Neuropathol Appl Neurobiol. 1998. PMID: 9775394

5

Argyrophilic grains in late-onset Creutzfeldt-Jakob diseased brain.

Kawashima T, Doh-ura K, Iwaki T. Kawashima T, et al. Pathol Int. 1999 May;49(5):369-73. doi: 10.1046/j.1440-1827.1999.00883.x. Pathol Int. 1999. PMID: 10417678

6

An atypical case of sporadic Creutzfeldt-Jakob disease with Parkinson's disease.

Iida T, Doh-ura K, Kawashima T, Abe H, Iwaki T. Iida T, et al. Neuropathology. 2001 Dec;21(4):294-7. doi: 10.1046/j.1440-1789.2001.00407.x. Neuropathology. 2001. PMID: 11837536

7

Increased clusterin (apolipoprotein J) expression in human and mouse brains infected with transmissible spongiform encephalopathies.

Sasaki K, Doh-ura K, Ironside JW, Iwaki T. Sasaki K, et al. Acta Neuropathol. 2002 Mar;103(3):199-208. doi: 10.1007/s004010100456. Epub 2001 Nov 10. Acta Neuropathol. 2002. PMID: 11907798

8

Amyloid imaging probes are useful for detection of prion plaques and treatment of transmissible spongiform encephalopathies.

Ishikawa K, Doh-Ura K, Kudo Y, Nishida N, Murakami-Kubo I, Ando Y, Sawada T, Iwaki T. Ishikawa K, et al. J Gen Virol. 2004 Jun;85(Pt 6):1785-1790. doi: 10.1099/vir.0.19754-0. J Gen Virol. 2004. PMID: 15166464

9

Protease-resistant PrP and PrP oligomers in the brain in human prion diseases after intraventricular pentosan polysulfate infusion.

Honda H, Sasaki K, Minaki H, Masui K, Suzuki SO, Doh-Ura K, Iwaki T. Honda H, et al. Neuropathology. 2012 Apr;32(2):124-32. doi: 10.1111/j.1440-1789.2011.01245.x. Epub 2011 Aug 1. Neuropathology. 2012. PMID: 21801238

10

Creutzfeldt-Jakob disease with codon 129 polymorphism (valine): a comparative study of patients with codon 102 point mutation or without mutations.

Miyazono M, Kitamoto T, Doh-ura K, Iwaki T, Tateishi J. Miyazono M, et al. Acta Neuropathol. 1992;84(4):349-54. doi: 10.1007/BF00227660. Acta Neuropathol. 1992. PMID: 1359725

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