Shimohata T - Search Results

1

[Clinical aspects of the Niigata Minamata disease].

Shimohata T, Hirota K, Takahashi H, Nishizawa M. Shimohata T, et al. Brain Nerve. 2015 Jan;67(1):31-8. doi: 10.11477/mf.1416200084. Brain Nerve. 2015. PMID: 25585433 Review. Japanese.

2

[Adult onset Still's disease with a brainstem lesion demonstrated on MRI].

Shimohata T, Ishiguro H, Hirota K. Shimohata T, et al. Rinsho Shinkeigaku. 1997 May;37(5):379-82. Rinsho Shinkeigaku. 1997. PMID: 9294323 Japanese.

3

Atrophy of the cerebellum and brainstem in dentatorubral pallidoluysian atrophy. Influence of CAG repeat size on MRI findings.

Koide R, Onodera O, Ikeuchi T, Kondo R, Tanaka H, Tokiguchi S, Tomoda A, Miike T, Isa F, Beppu H, Shimizu N, Watanabe Y, Horikawa Y, Shimohata T, Hirota K, Ishikawa A, Tsuji S. Koide R, et al. Among authors: shimohata t. Neurology. 1997 Dec;49(6):1605-12. doi: 10.1212/wnl.49.6.1605. Neurology. 1997. PMID: 9409354

4

Sporadic cases of dentatorubral-pallidoluysian atrophy associated with maternal transmission.

Shimohata T, Ishiguro H, Makino K, Takano H, Tanaka H, Tsuji S, Hirota K. Shimohata T, et al. Neurology. 1998 Jan;50(1):282-3. doi: 10.1212/wnl.50.1.282. Neurology. 1998. PMID: 9443494

5

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

Igarashi S, Koide R, Shimohata T, Yamada M, Hayashi Y, Takano H, Date H, Oyake M, Sato T, Sato A, Egawa S, Ikeuchi T, Tanaka H, Nakano R, Tanaka K, Hozumi I, Inuzuka T, Takahashi H, Tsuji S. Igarashi S, et al. Among authors: shimohata t. Nat Genet. 1998 Feb;18(2):111-7. doi: 10.1038/ng0298-111. Nat Genet. 1998. PMID: 9462738

6

Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations.

Takano H, Cancel G, Ikeuchi T, Lorenzetti D, Mawad R, Stevanin G, Didierjean O, Dürr A, Oyake M, Shimohata T, Sasaki R, Koide R, Igarashi S, Hayashi S, Takiyama Y, Nishizawa M, Tanaka H, Zoghbi H, Brice A, Tsuji S. Takano H, et al. Among authors: shimohata t. Am J Hum Genet. 1998 Oct;63(4):1060-6. doi: 10.1086/302067. Am J Hum Genet. 1998. PMID: 9758625 Free PMC article.

7

No mutation in the entire coding region of the alpha-synuclein gene in pathologically confirmed cases of multiple system atrophy.

Ozawa T, Takano H, Onodera O, Kobayashi H, Ikeuchi T, Koide R, Okuizumi K, Shimohata T, Wakabayashi K, Takahashi H, Tsuji S. Ozawa T, et al. Among authors: shimohata t. Neurosci Lett. 1999 Jul 30;270(2):110-2. doi: 10.1016/s0304-3940(99)00475-9. Neurosci Lett. 1999. PMID: 10462110

8

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

Koide R, Kobayashi S, Shimohata T, Ikeuchi T, Maruyama M, Saito M, Yamada M, Takahashi H, Tsuji S. Koide R, et al. Among authors: shimohata t. Hum Mol Genet. 1999 Oct;8(11):2047-53. doi: 10.1093/hmg/8.11.2047. Hum Mol Genet. 1999. PMID: 10484774

9

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. Nat Genet. 2000 Sep;26(1):29-36. doi: 10.1038/79139. Nat Genet. 2000. PMID: 10973244

10

Widespread occurrence of intranuclear atrophin-1 accumulation in the central nervous system neurons of patients with dentatorubral-pallidoluysian atrophy.

Yamada M, Wood JD, Shimohata T, Hayashi S, Tsuji S, Ross CA, Takahashi H. Yamada M, et al. Among authors: shimohata t. Ann Neurol. 2001 Jan;49(1):14-23. doi: 10.1002/1531-8249(200101)49:1<14::aid-ana5>3.0.co;2-x. Ann Neurol. 2001. PMID: 11198291

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