業績(論文)
論文
Monomerization of TDP-43 is a key determinant for inducing TDP-43 pathology in amyotrophic lateral sclerosis Sci Adv.9(31):eadf6895.2023 doi: 10.1126/sciadv.adf6895.
Simple and efficient differentiation of human iPSCs into contractible skeletal muscles for muscular disease modeling Sci Rep.13(1)8146.2023 doi:10.1038/s41598-023-34445-9
Genetic factors affecting survival in Japanese patients with sporadic amyotrophic lateral sclerosis: a genome-wide association study and verification in iPSC-derived motor neurons from patients J Neurol Neurosurg Psychiatry.jnnp-2022-330851.2023 doi: 10.1136/jnnp-2022-330851.
The SYNGAP1 3'UTR variant in ALS patients causes aberrant SYNGAP1 splicing and dendritic spine loss by recruiting HNRNPK Journal of Neuroscience, 42(47) 8881-8896, 2022 DOI: https://doi.org/10.1523/JNEUROSCI.0455-22.2022*Corresponding authors
Developmental dysregulation of excitatory-to-inhibitory GABA-polarity switch may underlie schizophrenia pathology: A monozygotic-twin discordant case analysis in human iPS cell-derived neurons Neurochemistry International (2021) doi: https://doi.org/10.1016/j.neuint.2021.105179.
Antiparkinsonian drugs as potent contributors to nocturnal sleep in patients with Parkinson's disease PLoS One 2021 Jul 28;16(7):e0255274. doi: 10.1371/journal.pone.0255274. eCollection 2021.
Development of a Human Neuromuscular Tissue-on-a-Chip Model on a 24-Well-Plate-Format Compartmentalized Microfluidic Device Lab on a Chip 2021 May 18;21(10):1897-1907. doi: 10.1039/d1lc00048a.
Selective suppression of polyglutamine-expanded protein by lipid nanoparticle-delivered siRNA targeting CAG expansions in the mouse CNS Mol Ther Nucleic Acids 2021 Feb 2021.02.007 15;24:1-10 DOI: 10.1016/j.omtn.2021.02.007. eCollection 2021 Jun 4
Two distinct mechanisms of neuropathy in immunoglobulin light chain (AL) amyloidosis J Neurol Sci 2021 Feb 15; 421: 117305 DOI: 10.1016/j.jns.2020.117305
Modulation of oxygen tension, acidosis, and cell density is crucial for neural differentiation of human induced pluripotent stem cells Neurosci. Res 2020.01.015. Epub 2020 Jan 31. 2021 Feb 163:34-42 DOI: 10.1016/j.neures.2020.01.015 (Cover)
In vitro model of human skeletal muscle tissues with contractility fabricated by immortalized human myogenic cells Adv Biosyst 2020 4(11):e2000121 DOI: 10.1002/adbi.202000121
A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis Commun Biol 2020 23;3(1):526 doi: 10.1038/s42003-020-01251-2
Unveiling synapse pathology in spinal bulbar muscular atrophy by genome-wide transcriptome analysis of purified motor neurons derived from disease specific iPSCs Mol. Brain 2020 13(1):18 DOI: 10.1186/s13041-020-0561-1
Tandem paired nicking promotes precise genome editing with scarce interference by p53 Cell Rep 2020 .2019.12.06 4.30(4):1195-1207.e7 DOI: 10.1016/j.celrep.2019.12.064
Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophy Nat. Commun 2019 10(1): 4262 DOI: 10.1038/s41467-019-12282-7
Aberrant axon branching via Fos-B dysregulation in FUS-ALS motor neurons EBioMedicine 2019.06.013. Epub 2019 Jun 29 45:362-378 doi: 10.1016/j.ebiom
Open-Chamber Co-Culture Microdevices for single-cell analysis of skeletal muscle myotubes and motor neurons with neuromuscular junctions BioChip Journal 2019 13(2) 127-132 doi: https://doi.org/10.1007/s13206-018-3202-3
Teratoma Formation Assay for Assessing Pluripotency and Tumorigenicity of Pluripotent Stem Cells Bio-protocol 2017 7(16), e2518 doi: https://doi.org/10.21769/BioProtoc.2518
Correlation of insulin resistance and motor function in spinal and bulbar muscular atrophy J Neurol 2017 264(5) 839-847 doi: 10.1007/s00415-017-8405-3
Altered tau isoform ratio caused by loss of Fus and Sfpq function leads to FTLD-like phenotypes Cell Reports 2017 18(5):1118-1131. DOI: 10.1016/j.celrep.2017.01.013