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Journal of Neuroscience Research|July 21, 2010
The mood stabilizer valproic acid improves defective neurite formation caused by Charcot-Marie-Tooth disease-associated mutant Rab7 through the JNK signaling pathwayJunji Yamauchi, Tomohiro Torii, Shinji Kusakawa, et al.
Polymers|April 3, 2021
Hypomyelinating Leukodystrophy 15 (HLD15)-Associated Mutation of EPRS1 Leads to Its Polymeric Aggregation in Rab7-Positive Vesicle Structures, Inhibiting Oligodendroglial Cell Morphological DifferentiationSui Sawaguchi, Mizuki Goto, Yukino Kato, et al.
The European Journal of Neuroscience|December 14, 2019
Dopamine modulates the optomotor response to unreliable visual stimuli in Drosophila melanogasterMasumi Akiba, Kentaro Sugimoto, Risa Aoki, et al.
Biochemical and Biophysical Research Communications|September 11, 2014
In vivo knockdown of ErbB3 in mice inhibits Schwann cell precursor migrationTomohiro Torii, Yuki Miyamoto, Shuji Takada, et al.
Neurology International|March 28, 2023
Hesperetin Ameliorates Inhibition of Neuronal and Oligodendroglial Cell Differentiation Phenotypes Induced by Knockdown of Rab2b, an Autism Spectrum Disorder-Associated Gene ProductYukino Kato, Remina Shirai, Katsuya Ohbuchi, et al.
Neuroscience Research|September 28, 2018
CMT type 2N disease-associated AARS mutant inhibits neurite growth that can be reversed by valproic acidYuriko Tatsumi, Naoto Matsumoto, Noriko Iibe, et al.
European Journal of Pharmacology|April 21, 2009
Both V(1A) and V(1B) vasopressin receptors deficiency result in impaired glucose toleranceKazuaki Nakamura, Toshinori Aoyagi, Masami Hiroyama, et al.
The European Journal of Neuroscience|May 7, 2016
Involvement of oxidative stress and impaired lysosomal degradation in amiodarone-induced schwannopathyNaoko Niimi, Hideji Yako, Masami Tsukamoto, et al.
Communications Biology|November 13, 2025
Conformational alteration of DOCK5•ELMO1 signalosome on lipid membraneTakehiro Shinoda, Kazushige Katsura, Yoshiko Ishizuka-Katsura, et al.
Biochemical and Biophysical Research Communications|March 24, 2018
Treacher Collins syndrome 3 (TCS3)-associated POLR1C mutants are localized in the lysosome and inhibits chondrogenic differentiationNaoto Matsumoto, Minami Kaneko, Natsumi Watanabe, et al.
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