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Page 1
Showing results for obuse c
Search for Bouse C instead (3 results)
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder.
Kuroda Y, Iwata-Otsubo A, Dias KR, Temple SEL, Nagao K, De Hayr L, Zhu Y, Isobe SY, Nishibuchi G, Fiordaliso SK, Fujita Y, Rippert AL, Baker SW, Leung ML, Koboldt DC, Harman A, Keena BA, Kazama I, Subramanian GM, Manickam K, Schmalz B, Latsko M, Zackai EH, Edwards M, Evans CA, Dulik MC, Buckley MF, Yamashita T, O'Brien WT, Harvey RJ, Obuse C, Roscioli T, Izumi K. Kuroda Y, et al. Among authors: obuse c. Genet Med. 2023 Jul;25(7):100861. doi: 10.1016/j.gim.2023.100861. Epub 2023 Apr 20. Genet Med. 2023. PMID: 37087635 Free article.
Inhibition of RIF1 by SCAI Allows BRCA1-Mediated Repair.
Isobe SY, Nagao K, Nozaki N, Kimura H, Obuse C. Isobe SY, et al. Among authors: obuse c. Cell Rep. 2017 Jul 11;20(2):297-307. doi: 10.1016/j.celrep.2017.06.056. Cell Rep. 2017. PMID: 28700933 Free article.
HJURP is involved in the expansion of centromeric chromatin.
Perpelescu M, Hori T, Toyoda A, Misu S, Monma N, Ikeo K, Obuse C, Fujiyama A, Fukagawa T. Perpelescu M, et al. Among authors: obuse c. Mol Biol Cell. 2015 Aug 1;26(15):2742-54. doi: 10.1091/mbc.E15-02-0094. Epub 2015 Jun 10. Mol Biol Cell. 2015. PMID: 26063729 Free PMC article.
105 results