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20H05927
Funder:
Japan Society for the Promotion of Science
Funded outputs count:
31
Funder award ID:
20H05927
OpenAlex ID:
G93105122
Non-coding repeat analyses in patients with Parkinson’s disease
2025
·
Makito Hirano
, Makoto Samukawa
, et al.
·
Frontiers in Neurology
·
1
PDF
Dissecting the mechanism of NOP56 GGCCUG repeat-associated non-AUG translation using cell-free translation systems
2025
·
Mayuka Hasumi
, Hayato Ito
, et al.
·
Journal of Biological Chemistry
·
6
PDF
TDP-43 transports ferritin heavy chain mRNA to regulate oxidative stress in neuronal axons
2025
·
Jyunki Jinno
, Rehab F. Abdelhamid
, et al.
·
Neurochemistry International
·
8
Alternative Splicing Alterations in Patients With Amyotrophic Lateral Sclerosis: Link to the Disruption of TAR DNA‐Binding Protein 43 kDa Functions
2025
·
Takashi Miwa
, Eriko Takeuchi
, et al.
·
Neurology and Clinical Neuroscience
·
2
PDF
Dysregulation of stress granule dynamics by DCTN1 deficiency exacerbates TDP-43 pathology in Drosophila models of ALS/FTD
2024
·
Tetsuhiro Ueda
, Toshihide Takeuchi
, et al.
·
Acta Neuropathologica Communications
·
14
PDF
eIF5 stimulates the CUG initiation of RAN translation of poly-GA dipeptide repeat protein (DPR) in C9orf72 FTLD/ALS
2024
·
Shiho Gotoh
, Kohji Mori
, et al.
·
Journal of Biological Chemistry
·
12
PDF
Lysophagy protects against propagation of α-synuclein aggregation through ruptured lysosomal vesicles
2023
·
Keita Kakuda
, Kensuke Ikenaka
, et al.
·
Proceedings of the National Academy of Sciences
·
65
Reconstitution of C9orf72 GGGGCC repeat-associated non-AUG translation with purified human translation factors
2023
·
Hayato Ito
, Kodai Machida
, et al.
·
Scientific Reports
·
9
PDF
CANVAS-related RFC1 mutations in patients with immune-mediated neuropathy
2023
·
Makito Hirano
, Motoi Kuwahara
, et al.
·
Scientific Reports
·
7
PDF
Phosphatidylinositol-3,4,5-trisphosphate interacts with alpha-synuclein and initiates its aggregation and formation of Parkinson’s disease-related fibril polymorphism
2023
·
Chi-Jing Choong
, César Aguirre
, et al.
·
Acta Neuropathologica
·
30
PDF
FUS regulates RAN translation through modulating the G-quadruplex structure of GGGGCC repeat RNA in C9orf72-linked ALS/FTD
2023
·
Yuzo Fujino
, Morio Ueyama
, et al.
·
eLife
·
20
PDF
Repeat-associated non-AUG translation in neuromuscular diseases: mechanisms and therapeutic insights
2023
·
Yuzo Fujino
, Kohji Mori
, et al.
·
The Journal of Biochemistry
·
9
PDF
What repeat expansion disorders can teach us about the Central Dogma
2023
·
Eric T. Wang
, Catherine H. Freudenreich
, et al.
·
Molecular Cell
·
3
PDF
Sustained therapeutic benefits by transient reduction of TDP-43 using ENA-modified antisense oligonucleotides in ALS/FTD mice
2023
·
Toshihide Takeuchi
, Kazuhiro Maeta
, et al.
·
Molecular Therapy — Nucleic Acids
·
33
Direct evaluation of neuroaxonal degeneration with the causative genes of neurodegenerative diseases in Drosophila using the automated axon quantification system, MeDUsA
2023
·
Yohei Nitta
, Hiroki Kawai
, et al.
·
Human Molecular Genetics
·
13
PDF
Therapeutic reduction of GGGGCC repeat RNA levels by hnRNPA3 suppresses neurodegeneration in Drosophila models of C9orf72 -linked ALS/FTD
2022
·
Tomoya Taminato
, Toshihide Takeuchi
, et al.
·
Human Molecular Genetics
·
14
Emerging roles of extracellular vesicles in polyglutamine diseases: Mutant protein transmission, therapeutic potential, and diagnostics
2022
·
Toshihide Takeuchi
, Yoshitaka Nagai
·
Neurochemistry International
·
11
The molecular pathogenesis of repeat expansion diseases
2021
·
Yuzo Fujino
, Yoshitaka Nagai
·
Biochemical Society Transactions
·
20
ALS-linked FUS mutations dysregulate G-quadruplex-dependent liquid–liquid phase separation and liquid-to-solid transition
2021
·
Akira Ishiguro
, Jun Lu
, et al.
·
Journal of Biological Chemistry
·
64
The porphyrin TMPyP4 inhibits elongation during the noncanonical translation of the FTLD/ALS-associated GGGGCC repeat in the C9orf72 gene
2021
·
Kohji Mori
, Shiho Gotoh
, et al.
·
Journal of Biological Chemistry
·
23
Precise CAG repeat contraction in a Huntington’s Disease mouse model is enabled by gene editing with SpCas9-NG
2021
·
Seiya Oura
, Taichi Noda
, et al.
·
Communications Biology
·
35
PDF
Insight Into Spinocerebellar Ataxia Type 31 (SCA31) From Drosophila Model
2021
·
Taro Ishiguro
, Yoshitaka Nagai
, et al.
·
Frontiers in Neuroscience
·
17
PDF
Divergent CPEB prion-like domains reveal different assembly mechanisms for a generic amyloid-like fold
2021
·
Rubén Hervás
, María del Carmen Fernández-Ramírez
, et al.
·
BMC Biology
·
32
PDF
Protein Aggregation Inhibitors as Disease-Modifying Therapies for Polyglutamine Diseases
2021
·
Eiko N. Minakawa
, Yoshitaka Nagai
·
Frontiers in Neuroscience
·
49
PDF
Small molecule targeting r(UGGAA)n disrupts RNA foci and alleviates disease phenotype in Drosophila model
2021
·
Tomonori Shibata
, Konami Nagano
, et al.
·
Nature Communications
·
61
PDF
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