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Moyamoya disease patient mutations in the RING domain of RNF213 reduce its ubiquitin ligase activity and enhance NFκB activation and apoptosis in an AAA+ domain-dependent manner.
Takeda M, Tezuka T, Kim M, Choi J, Oichi Y, Kobayashi H, Harada KH, Mizushima T, Taketani S, Koizumi A, Youssefian S. Takeda M, et al. Among authors: oichi y. Biochem Biophys Res Commun. 2020 May 7;525(3):668-674. doi: 10.1016/j.bbrc.2020.02.024. Epub 2020 Mar 3. Biochem Biophys Res Commun. 2020. PMID: 32139119 Free article.
Characterization of Moyamoya and Middle Cerebral Artery Diseases by Carotid Canal Diameter and RNF213 p.R4810K Genotype.
Oichi Y, Mineharu Y, Agawa Y, Morimoto T, Funaki T, Hitomi T, Kobayashi H, Todo K, Tani S, Imamura H, Yoshida K, Kataoka H, Koizumi A, Sakai N, Miyamoto S. Oichi Y, et al. J Stroke Cerebrovasc Dis. 2022 Jun;31(6):106481. doi: 10.1016/j.jstrokecerebrovasdis.2022.106481. Epub 2022 Apr 15. J Stroke Cerebrovasc Dis. 2022. PMID: 35430511 Free article.
A novel SREBF1::NACC1 gene fusion in an unclassifiable intracranial tumour.
Takeuchi Y, Mineharu Y, Arakawa Y, Hara M, Oichi Y, Kamata T, Fukuyama K, Yamamoto Y, Yamanaka T, Kakiuchi N, Hiratomo E, Hirata M, Yokoo H, Hirose T, Minamiguchi S, Ogawa S, Muto M, Miyamoto S, Haga H. Takeuchi Y, et al. Among authors: oichi y. Neuropathol Appl Neurobiol. 2022 Dec;48(7):e12843. doi: 10.1111/nan.12843. Epub 2022 Aug 17. Neuropathol Appl Neurobiol. 2022. PMID: 35900258
17 results