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Osamu Onodera
Osamu Onodera
其他姓名O. Onodera
Dept. of Neurology, Brain Research Institute, Niigata University
在 bri.niigata-u.ac.jp 的电子邮件经过验证 - 首页
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引用次数
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Unstable expansion of CAG repeat in hereditary dentatorubral–pallidoluysian atrophy (DRPLA)
R Koide, T Ikeuchi, O Onodera, H Tanaka, S Igarashi, K Endo, ...
Nature genetics 6 (1), 9-13, 1994
13951994
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease
K Hara, A Shiga, T Fukutake, H Nozaki, A Miyashita, A Yokoseki, ...
New England Journal of Medicine 360 (17), 1729-1739, 2009
5472009
Expanded polyglutamine stretches interact with TAFII130, interfering with CREB-dependent transcription
T Shimohata, T Nakajima, M Yamada, C Uchida, O Onodera, S Naruse, ...
Nature genetics 26 (1), 29-36, 2000
4902000
The gene for Machado–Joseph disease maps to human chromosome 14q
Y Takiyama, M Nishizawa, H Tanaka, S Kawashima, H Sakamoto, ...
Nature genetics 4 (3), 300-304, 1993
4651993
TDP43 mutation in familial amyotrophic lateral sclerosis
A Yokoseki, A Shiga, CF Tan, A Tagawa, H Kaneko, A Koyama, H Eguchi, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
4622008
Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene
H Date, O Onodera, H Tanaka, K Iwabuchi, K Uekawa, S Igarashi, ...
Nature genetics 29 (2), 184-188, 2001
4282001
TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation
CF Tan, H Eguchi, A Tagawa, O Onodera, T Iwasaki, A Tsujino, ...
Acta neuropathologica 113, 535-542, 2007
3702007
Expansions of intronic TTTCA and TTTTA repeats in benign adult familial myoclonic epilepsy
H Ishiura, K Doi, J Mitsui, J Yoshimura, MK Matsukawa, A Fujiyama, ...
Nature genetics 50 (4), 581-590, 2018
2942018
Soluble polyglutamine oligomers formed prior to inclusion body formation are cytotoxic
T Takahashi, S Kikuchi, S Katada, Y Nagai, M Nishizawa, O Onodera
Human molecular genetics 17 (3), 345-356, 2008
2782008
Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
Multiple-System Atrophy Research Collaboration
New England Journal of Medicine 369 (3), 233-244, 2013
2582013
Demyelinating and axonal features of Charcot–Marie–Tooth disease with mutations of myelin‐related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese …
N Hattori, M Yamamoto, T Yoshihara, H Koike, M Nakagawa, ...
Brain 126 (1), 134-151, 2003
2532003
Strong correlation between the number of CAG repeats in androgen receptor genes and the clinical onset of features of spinal and bulbar muscular atrophy
S Igarashi, Y Tanno, O Onodera, M Yamazaki, S Sato, A Ishikawa, ...
Neurology 42 (12), 2300-2300, 1992
2491992
Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease
K Okuizumi, O Onodera, Y Namba, K Ikeda, T Yamamoto, K Seki, A Ueki, ...
Nature genetics 11 (2), 207-209, 1995
2341995
Aprataxin, a novel protein that protects against genotoxic stress
N Gueven, OJ Becherel, AW Kijas, P Chen, O Howe, JH Rudolph, R Gatti, ...
Human molecular genetics 13 (10), 1081-1093, 2004
2112004
β-synuclein gene alterations in dementia with Lewy bodies
H Ohtake, P Limprasert, Y Fan, O Onodera, A Kakita, H Takahashi, ...
Neurology 63 (5), 805-811, 2004
2062004
Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions
Y Nishihira, CF Tan, O Onodera, Y Toyoshima, M Yamada, T Morita, ...
Acta neuropathologica 116, 169-182, 2008
2022008
Polyglutamine diseases: where does toxicity come from? what is toxicity? where are we going?
T Takahashi, S Katada, O Onodera
Journal of molecular cell biology 2 (4), 180-191, 2010
2012010
Dentatorubral‐pallidoluysian atrophy: clinical features are closely related to unstable expansions of trinucleotide (CAG) repeat
T Ikeuchi, R Koide, H Tanaka, O Onodera, S Igarashi, H Takahashi, ...
Annals of Neurology: Official Journal of the American Neurological …, 1995
1931995
Multiplex families with multiple system atrophy
K Hara, Y Momose, S Tokiguchi, M Shimohata, K Terajima, O Onodera, ...
Archives of neurology 64 (4), 545-551, 2007
1752007
ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19
Y Takahashi, Y Fukuda, J Yoshimura, A Toyoda, K Kurppa, H Moritoyo, ...
The American Journal of Human Genetics 93 (5), 900-905, 2013
1742013
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