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Cell Death & Disease|March 24, 2026
The amino acid transporter LAT1 coordinates proper motor function at the perinatal stageKoki Sadamori, Manami Hiraiwa, Tetsuhiro Horie, et al.
Epilepsy Research|June 3, 2020
NUS1 mutation in a family with epilepsy, cerebellar ataxia, and tremorKunihiko Araki, Ryoichi Nakamura, Daisuke Ito, et al.
Genes & Development|August 17, 2012
TSUNAMI: an antisense method to phenocopy splicing-associated diseases in animalsKentaro Sahashi, Yimin Hua, Karen K Y Ling, et al.
EMBO Molecular Medicine|April 4, 2019
DNA methylation inhibitor attenuates polyglutamine-induced neurodegeneration by regulating Hes5Naohide Kondo, Genki Tohnai, Kentaro Sahashi, et al.
JCI Insight|June 23, 2025
Dysregulated synaptic gene expression in oligodendrocytes of spinal and bulbar muscular atrophyMadoka Iida, Kentaro Sahashi, Tomoki Hirunagi, et al.
Molecular Therapy. Nucleic Acids|March 19, 2021
Selective suppression of polyglutamine-expanded protein by lipid nanoparticle-delivered siRNA targeting CAG expansions in the mouse CNSTomoki Hirunagi, Kentaro Sahashi, Kiyoshi Tachikawa, et al.
Molecular Therapy. Nucleic Acids|February 23, 2023
Sustained therapeutic benefits by transient reduction of TDP-43 using ENA-modified antisense oligonucleotides in ALS/FTD miceToshihide Takeuchi, Kazuhiro Maeta, Xin Ding, et al.
EMBO Molecular Medicine|September 10, 2013
Pathological impact of SMN2 mis-splicing in adult SMA miceKentaro Sahashi, Karen K Y Ling, Yimin Hua, et al.
Nature Communications|September 21, 2019
Src inhibition attenuates polyglutamine-mediated neuromuscular degeneration in spinal and bulbar muscular atrophyMadoka Iida, Kentaro Sahashi, Naohide Kondo, et al.
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