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Takeshi Ikeuchi
Takeshi Ikeuchi
Niigata University, Brain Research Institute
Verified email at bri.niigata-u.ac.jp
Title
Cited by
Cited by
Year
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
13911994
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
K Sanpei, H Takano, S Igarashi, T Sato, M Oyake, H Sasaki, A Wakisaka, ...
Nature genetics 14 (3), 277-284, 1996
9101996
Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer's disease.
DIA Network.
Nature Medicine 25 (2), 277-283, 2019
7322019
Human and mouse single-nucleus transcriptomics reveal TREM2-dependent and TREM2-independent cellular responses in Alzheimer’s disease
Y Zhou, WM Song, PS Andhey, A Swain, T Levy, KR Miller, PL Poliani, ...
Nature medicine 26 (1), 131-142, 2020
7162020
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
5332009
Structure-based classification of tauopathies
Y Shi, W Zhang, Y Yang, AG Murzin, B Falcon, A Kotecha, M van Beers, ...
Nature 598 (7880), 359-363, 2021
4972021
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
4892000
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
4602008
A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?
R Koide, S Kobayashi, T Shimohata, T Ikeuchi, M Maruyama, M Saito, ...
Human molecular genetics 8 (11), 2047-2053, 1999
4561999
Novel tau filament fold in corticobasal degeneration
W Zhang, A Tarutani, KL Newell, AG Murzin, T Matsubara, B Falcon, ...
Nature 580 (7802), 283-287, 2020
4242020
A soluble phosphorylated tau signature links tau, amyloid and the evolution of stages of dominantly inherited Alzheimer’s disease
NR Barthélemy, Y Li, N Joseph-Mathurin, BA Gordon, J Hassenstab, ...
Nature medicine 26 (3), 398-407, 2020
4202020
Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch
S Igarashi, R Koide, T Shimohata, M Yamada, Y Hayashi, H Takano, ...
Nature genetics 18 (2), 111-117, 1998
4151998
The Notch ligands, Delta1 and Jagged2, are substrates for presenilin-dependent “γ-secretase” cleavage
T Ikeuchi, SS Sisodia
Journal of Biological Chemistry 278 (10), 7751-7754, 2003
2972003
Characterization of a presenilin-mediated amyloid precursor protein carboxyl-terminal fragment γ: evidence for distinct mechanisms involved in γ-secretase processing of the APP …
C Yu, SH Kim, T Ikeuchi, H Xu, L Gasparini, R Wang, SS Sisodia
Journal of Biological Chemistry 276 (47), 43756-43760, 2001
2792001
An atlas of cortical circular RNA expression in Alzheimer disease brains demonstrates clinical and pathological associations.
WF Dube U, Del-Aguila JL, Li Z, Budde JP, Jiang S, Hsu S, Ibanez L ...
Nature Neuroscience 22 (11), 1903-1912, 2019
2602019
Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and …
H Takano, G Cancel, T Ikeuchi, D Lorenzetti, R Mawad, G Stevanin, ...
The American Journal of Human Genetics 63 (4), 1060-1066, 1998
2591998
SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians
A Miyashita, A Koike, G Jun, LS Wang, S Takahashi, E Matsubara, ...
PloS one 8 (4), e58618, 2013
2152013
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
1911995
Japanese families with autosomal dominant pure cerebellar ataxia map to chromosome 19p13. 1-p13. 2 and are strongly associated with mild CAG expansions in the spinocerebellar …
K Ishikawa, H Tanaka, M Saito, N Ohkoshi, T Fujita, K Yoshizawa, ...
The American Journal of Human Genetics 61 (2), 336-346, 1997
1711997
Differential levels of α-synuclein, β-amyloid42 and tau in CSF between patients with dementia with Lewy bodies and Alzheimer's disease
K Kasuga, T Tokutake, A Ishikawa, T Uchiyama, T Tokuda, O Onodera, ...
Journal of Neurology, Neurosurgery & Psychiatry 81 (6), 608-610, 2010
1582010
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