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International Journal of Molecular Sciences|November 26, 2022
5-HT<sub>1A</sub> Receptor Agonist Treatment Partially Ameliorates Rett Syndrome Phenotypes in <i>mecp2</i>-Null Mice by Rescuing Impairment of Neuron Transmission and the CREB/BDNF Signaling PathwayHongmei Dai, Yoshikazu Kitami, Yu-Ichi Goto, et al.
Neurobiology of Disease|February 26, 2026
Mutant PLP1 impairs COPII vesicle formation via ER calcium depletion in Pelizaeus-Merzbacher diseaseHeng Li, Reiko Mishima, Yu-Ichi Goto, et al.
Biochemical and Biophysical Research Communications|November 19, 2003
Direct evidence for expression of type II flavoprotein subunit in human complex II (succinate-ubiquinone reductase)Eriko Tomitsuka, Yu-ichi Goto, Masafumi Taniwaki, et al.
The American Journal of Surgical Pathology|January 22, 2010
Granular swollen epithelial cells: a histologic and diagnostic marker for mitochondrial nephropathyAkimitsu Kobayashi, Yu-ichi Goto, Michio Nagata, et al.
Journal of Human Genetics|January 20, 2004
Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in JapanAkira Sudo, Shiho Honzawa, Ikuya Nonaka, et al.
BMC Medical Genomics|March 6, 2023
Duplication within two regions distal to MECP2: clinical similarity with MECP2 duplication syndromeKeiko Akahoshi, Eiji Nakagawa, Yu-Ichi Goto, et al.
Brain & Development|January 25, 2012
Novel AGTR2 missense mutation in a Japanese boy with severe mental retardation, pervasive developmental disorder, and epilepsyEri Takeshita, Eiji Nakagawa, Katsutoshi Nakatani, et al.
Pediatric Research|February 28, 2009
Edaravone inhibits DNA peroxidation and neuronal cell death in neonatal hypoxic-ischemic encephalopathy model ratYuji Takizawa, Takahito Miyazawa, Shigeaki Nonoyama, et al.
Pediatric Neurology|March 1, 2006
An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotypeTakeshi Kanaumi, Shinichi Hirose, Yu-ichi Goto, et al.
Journal of Neuropathology and Experimental Neurology|June 28, 2005
Delayed maturation of neuronal architecture and synaptogenesis in cerebral cortex of Mecp2-deficient miceTetsuya Fukuda, Masayuki Itoh, Tomio Ichikawa, et al.
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