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Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's Disease.
Daida K, Funayama M, Billingsley KJ, Malik L, Miano-Burkhardt A, Leonard HL, Makarious MB, Iwaki H, Ding J, Gibbs JR, Ishiguro M, Yoshino H, Ogaki K, Oyama G, Nishioka K, Nonaka R, Akamatsu W, Blauwendraat C, Hattori N. Daida K, et al. Among authors: akamatsu w. Mov Disord. 2023 Dec;38(12):2249-2257. doi: 10.1002/mds.29610. Epub 2023 Nov 5. Mov Disord. 2023. PMID: 37926948
RNA-binding protein HuD controls insulin translation.
Lee EK, Kim W, Tominaga K, Martindale JL, Yang X, Subaran SS, Carlson OD, Mercken EM, Kulkarni RN, Akamatsu W, Okano H, Perrone-Bizzozero NI, de Cabo R, Egan JM, Gorospe M. Lee EK, et al. Among authors: akamatsu w. Mol Cell. 2012 Mar 30;45(6):826-35. doi: 10.1016/j.molcel.2012.01.016. Epub 2012 Mar 1. Mol Cell. 2012. PMID: 22387028 Free PMC article.
A human Dravet syndrome model from patient induced pluripotent stem cells.
Higurashi N, Uchida T, Lossin C, Misumi Y, Okada Y, Akamatsu W, Imaizumi Y, Zhang B, Nabeshima K, Mori MX, Katsurabayashi S, Shirasaka Y, Okano H, Hirose S. Higurashi N, et al. Among authors: akamatsu w. Mol Brain. 2013 May 2;6:19. doi: 10.1186/1756-6606-6-19. Mol Brain. 2013. PMID: 23639079 Free PMC article.
Erratum: Investigation of the fatty acid transporter-encoding genes SLC27A3 and SLC27A4 in autism.
Maekawa M, Iwayama Y, Ohnishi T, Toyoshima M, Shimamoto C, Hisano Y, Toyota T, Balan S, Matsuzaki H, Iwata Y, Takagai S, Yamada K, Ota M, Fukuchi S, Okada Y, Akamatsu W, Tsujii M, Kojima N, Owada Y, Okano H, Mori N, Yoshikawa T. Maekawa M, et al. Among authors: akamatsu w. Sci Rep. 2016 Jan 29;6:20268. doi: 10.1038/srep20268. Sci Rep. 2016. PMID: 26822806 Free PMC article. No abstract available.
101 results