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Mechanisms of Development|January 1, 2008
Osteogenic properties of human myogenic progenitor cellsNaohiro Hashimoto, Tohru Kiyono, Michiko R Wada, et al.
JCI Insight|May 17, 2019
Gene suppressing therapy for Pelizaeus-Merzbacher disease using artificial microRNAHeng Li, Hironori Okada, Sadafumi Suzuki, et al.
Annals of Neurology|January 4, 2011
Reversible infantile respiratory chain deficiency: a clinical and molecular studyMasakazu Mimaki, Hideyuki Hatakeyama, Hirofumi Komaki, et al.
The Journal of Biological Chemistry|March 1, 2012
Methyl CpG-binding protein isoform MeCP2_e2 is dispensable for Rett syndrome phenotypes but essential for embryo viability and placenta developmentMasayuki Itoh, Candice G T Tahimic, Shuhei Ide, et al.
Molecular Medicine Reports|July 18, 2017
PTPRQ as a potential biomarker for idiopathic normal pressure hydrocephalusYuki Nagata, Masahiko Bundo, Saiko Sugiura, et al.
Neuromuscular Disorders : NMD|December 4, 2001
A point mutation of mitochondrial ATPase 6 gene in Leigh syndromeMotohiro Akagi, Koji Inui, Hiroko Tsukamoto, et al.
Human Genome Variation|December 12, 2018
A novel intragenic deletion in <i>OPHN1</i> in a Japanese patient with Dandy-Walker malformationAritoshi Iida, Eri Takeshita, Shunichi Kosugi, et al.
Molecular Genetics and Metabolism|March 23, 2012
Effect of curcumin in a mouse model of Pelizaeus-Merzbacher diseaseLi-Hua Yu, Toshifumi Morimura, Yurika Numata, et al.
Brain & Development|May 29, 2021
Linear cortical cystic lesions: Characteristic MR findings in MELAS patientsHidetoshi Ishigaki, Noriko Sato, Yukio Kimura, et al.
Acta Neuropathologica|March 23, 2011
A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathyYusuke Sakiyama, Yuji Okamoto, Itsuro Higuchi, et al.
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