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Comprehensive analysis of a novel mouse model of the 22q11.2 deletion syndrome: a model with the most common 3.0-Mb deletion at the human 22q11.2 locus.
Saito R, Koebis M, Nagai T, Shimizu K, Liao J, Wulaer B, Sugaya Y, Nagahama K, Uesaka N, Kushima I, Mori D, Maruyama K, Nakao K, Kurihara H, Yamada K, Kano M, Fukada Y, Ozaki N, Aiba A. Saito R, et al. Among authors: koebis m. Transl Psychiatry. 2020 Feb 5;10(1):35. doi: 10.1038/s41398-020-0723-z. Transl Psychiatry. 2020. PMID: 32066675 Free PMC article.
NFIA determines the cis-effect of genetic variation on Ucp1 expression in murine thermogenic adipocytes.
Hiraike Y, Tsutsumi S, Wada T, Oguchi M, Saito K, Nakamura M, Ota S, Koebis M, Nakao H, Aiba A, Nagano G, Ohno H, Oki K, Yoneda M, Kadowaki T, Aburatani H, Waki H, Yamauchi T. Hiraike Y, et al. Among authors: koebis m. iScience. 2022 Jul 7;25(8):104729. doi: 10.1016/j.isci.2022.104729. eCollection 2022 Aug 19. iScience. 2022. PMID: 35874098 Free PMC article.
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