Onodera O - Search Results

1

Heterogeneity of cerebral TDP-43 pathology in sporadic amyotrophic lateral sclerosis: Evidence for clinico-pathologic subtypes.

Takeuchi R, Tada M, Shiga A, Toyoshima Y, Konno T, Sato T, Nozaki H, Kato T, Horie M, Shimizu H, Takebayashi H, Onodera O, Nishizawa M, Kakita A, Takahashi H. Takeuchi R, et al. Among authors: onodera o. Acta Neuropathol Commun. 2016 Jun 23;4(1):61. doi: 10.1186/s40478-016-0335-2. Acta Neuropathol Commun. 2016. PMID: 27338935 Free PMC article.

2

Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease.

Okuizumi K, Onodera O, Namba Y, Ikeda K, Yamamoto T, Seki K, Ueki A, Nanko S, Tanaka H, Takahashi H, Oyanagi K, Mizusawa H, Kanazawa I, Tsuji S. Okuizumi K, et al. Among authors: onodera o. Nat Genet. 1995 Oct;11(2):207-9. doi: 10.1038/ng1095-207. Nat Genet. 1995. PMID: 7550352

3

Somatic mosaicism of expanded CAG repeats in brains of patients with dentatorubral-pallidoluysian atrophy: cellular population-dependent dynamics of mitotic instability.

Takano H, Onodera O, Takahashi H, Igarashi S, Yamada M, Oyake M, Ikeuchi T, Koide R, Tanaka H, Iwabuchi K, Tsuji S. Takano H, et al. Among authors: onodera o. Am J Hum Genet. 1996 Jun;58(6):1212-22. Am J Hum Genet. 1996. PMID: 8651298 Free PMC article.

4

Pick's disease: selective occurrence of apolipoprotein E-immunoreactive Pick bodies in the limbic system.

Hayashi S, Wakabayashi K, Iwanaga K, Kakita A, Seki K, Tanaka M, Okuizumi K, Onodera O, Tanaka H, Tsuji S, Takahashi H. Hayashi S, et al. Among authors: onodera o. Acta Neuropathol. 1998 Jan;95(1):1-4. doi: 10.1007/s004010050759. Acta Neuropathol. 1998. PMID: 9452816

5

[Prevertebral abscesses with a protracted insidious clinical course and subsequent lethal, acute pyogenic meningitis and septic shock].

Ozawa T, Onodera O, Kakita A, Aoki K, Tanaka K, Soma Y, Takahashi H, Tsuji S. Ozawa T, et al. Among authors: onodera o. No To Shinkei. 1998 Jan;50(1):75-9. No To Shinkei. 1998. PMID: 9493203 Japanese.

6

Apolipoprotein E epsilon4 allele and progression of cortical Lewy body pathology in Parkinson's disease.

Wakabayashi K, Kakita A, Hayashi S, Okuizumi K, Onodera O, Tanaka H, Ishikawa A, Tsuji S, Takahashi H. Wakabayashi K, et al. Among authors: onodera o. Acta Neuropathol. 1998 May;95(5):450-4. doi: 10.1007/s004010050824. Acta Neuropathol. 1998. PMID: 9600590

7

Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription.

Shimohata T, Nakajima T, Yamada M, Uchida C, Onodera O, Naruse S, Kimura T, Koide R, Nozaki K, Sano Y, Ishiguro H, Sakoe K, Ooshima T, Sato A, Ikeuchi T, Oyake M, Sato T, Aoyagi Y, Hozumi I, Nagatsu T, Takiyama Y, Nishizawa M, Goto J, Kanazawa I, Davidson I, Tanese N, Takahashi H, Tsuji S. Shimohata T, et al. Among authors: onodera o. Nat Genet. 2000 Sep;26(1):29-36. doi: 10.1038/79139. Nat Genet. 2000. PMID: 10973244

8

[Two cases of generalized tetanus presenting with dysphagia as an initial symptom].

Kanazawa M, Ishiguro H, Onodera O, Yoshikawa K, Koide T, Arai A, Hasegawa A, Nakano R, Tanaka K, Nishizawa M. Kanazawa M, et al. Among authors: onodera o. No To Shinkei. 2003 Nov;55(11):973-6. No To Shinkei. 2003. PMID: 14727538 Review. Japanese.

9

Aprataxin, the causative protein for EAOH is a nuclear protein with a potential role as a DNA repair protein.

Sano Y, Date H, Igarashi S, Onodera O, Oyake M, Takahashi T, Hayashi S, Morimatsu M, Takahashi H, Makifuchi T, Fukuhara N, Tsuji S. Sano Y, et al. Among authors: onodera o. Ann Neurol. 2004 Feb;55(2):241-9. doi: 10.1002/ana.10808. Ann Neurol. 2004. PMID: 14755728

10

SCA17 homozygote showing Huntington's disease-like phenotype.

Toyoshima Y, Yamada M, Onodera O, Shimohata M, Inenaga C, Fujita N, Morita M, Tsuji S, Takahashi H. Toyoshima Y, et al. Among authors: onodera o. Ann Neurol. 2004 Feb;55(2):281-6. doi: 10.1002/ana.10824. Ann Neurol. 2004. PMID: 14755733

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