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2020 | 2 |
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Expression of kinase-deficient MEK2 ameliorates Pelizaeus-Merzbacher disease phenotypes in mice.
Biochem Biophys Res Commun. 2020 Oct 22;531(4):445-451. doi: 10.1016/j.bbrc.2020.07.131. Epub 2020 Aug 13.
Biochem Biophys Res Commun. 2020.
PMID: 32800341
The Infantile Leukoencephalopathy-Associated Mutation of C11ORF73/HIKESHI Proteins Generates de novo Interactive Activity with Filamin A, Inhibiting Oligodendroglial Cell Morphological Differentiation.
Hattori K, Tago K, Memezawa S, Ochiai A, Sawaguchi S, Kato Y, Sato T, Tomizuka K, Ooizumi H, Ohbuchi K, Mizoguchi K, Miyamoto Y, Yamauchi J.
Hattori K, et al. Among authors: ooizumi h.
Medicines (Basel). 2021 Feb 1;8(2):9. doi: 10.3390/medicines8020009.
Medicines (Basel). 2021.
PMID: 33535532
Free PMC article.
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Rare Neurologic Disease-Associated Mutations of AIMP1 are Related with Inhibitory Neuronal Differentiation Which is Reversed by Ibuprofen.
Takeuchi Y, Tanaka M, Okura N, Fukui Y, Noguchi K, Hayashi Y, Torii T, Ooizumi H, Ohbuchi K, Mizoguchi K, Miyamoto Y, Yamauchi J.
Takeuchi Y, et al. Among authors: ooizumi h.
Medicines (Basel). 2020 May 6;7(5):25. doi: 10.3390/medicines7050025.
Medicines (Basel). 2020.
PMID: 32384815
Free PMC article.
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