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Cells|January 2, 2019
Zonisamide Administration Improves Fatty Acid β-Oxidation in Parkinson's DiseaseShin-Ichi Ueno, Shinji Saiki, Motoki Fujimaki, et al.
EMBO Molecular Medicine|August 14, 2023
Involvement of casein kinase 1 epsilon/delta (Csnk1e/d) in the pathogenesis of familial Parkinson's disease caused by CHCHD2Satoru Torii, Satoko Arakawa, Shigeto Sato, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 29, 2025
NEUROD1 efficiently converts peripheral blood cells into neurons with partial reprogramming by pluripotency factorsYoichi Saito, Mitsuru Ishikawa, Mahito Ohkuma, et al.
Stem Cell Research|January 12, 2020
Generation of the induced pluripotent stem cell (hiPSC) line (JUFMDOi004-A) from a patient with hearing loss carrying GJB2 (p.V37I) mutationIchiro Fukunaga, Takahiro Shiga, Cheng Chen, et al.
Molecular Brain|May 28, 2015
Differentiation of multipotent neural stem cells derived from Rett syndrome patients is biased toward the astrocytic lineageTomoko Andoh-Noda, Wado Akamatsu, Kunio Miyake, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 15, 2005
The RNA-binding protein HuD regulates neuronal cell identity and maturationWado Akamatsu, Hiroaki Fujihara, Takayuki Mitsuhashi, et al.
Stem Cell Research|June 15, 2024
Generation of an induced pluripotent stem cell line from a late-onset, progressive high frequency hearing loss patient due to mutation in CDH23Daisuke Arai, Mikako Takahashi-Shibata, Takao Ukaji, et al.
Molecular Brain|February 21, 2018
Down-regulation of ghrelin receptors on dopaminergic neurons in the substantia nigra contributes to Parkinson's disease-like motor dysfunctionYukari Suda, Naoko Kuzumaki, Takefumi Sone, et al.
Molecular Brain|May 4, 2013
A human Dravet syndrome model from patient induced pluripotent stem cellsNorimichi Higurashi, Taku Uchida, Christoph Lossin, et al.
Stem Cell Research|March 29, 2021
Generation of two iPSC lines from siblings of a homozygous patient with hearing loss and a heterozygous carrier with normal hearing carrying p.G45E/Y136X mutation in GJB2Ichiro Fukunaga, Yoko Oe, Keiko Danzaki, et al.
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