Nagao K - Search Results

1

Rare variant of the epigenetic regulator SMCHD1 in a patient with pituitary hormone deficiency.

Kinjo K, Nagasaki K, Muroya K, Suzuki E, Ishiwata K, Nakabayashi K, Hattori A, Nagao K, Nozawa RS, Obuse C, Miyado K, Ogata T, Fukami M, Miyado M. Kinjo K, et al. Among authors: nagao k. Sci Rep. 2020 Jul 3;10(1):10985. doi: 10.1038/s41598-020-67715-x. Sci Rep. 2020. PMID: 32620854 Free PMC article.

2

Human POGZ modulates dissociation of HP1alpha from mitotic chromosome arms through Aurora B activation.

Nozawa RS, Nagao K, Masuda HT, Iwasaki O, Hirota T, Nozaki N, Kimura H, Obuse C. Nozawa RS, et al. Among authors: nagao k. Nat Cell Biol. 2010 Jul;12(7):719-27. doi: 10.1038/ncb2075. Epub 2010 Jun 20. Nat Cell Biol. 2010. PMID: 20562864

3

CDK promotes interactions of Sld3 and Drc1 with Cut5 for initiation of DNA replication in fission yeast.

Fukuura M, Nagao K, Obuse C, Takahashi TS, Nakagawa T, Masukata H. Fukuura M, et al. Among authors: nagao k. Mol Biol Cell. 2011 Jul 15;22(14):2620-33. doi: 10.1091/mbc.E10-12-0995. Epub 2011 May 18. Mol Biol Cell. 2011. PMID: 21593208 Free PMC article.

4

A co-localization model of paired ChIP-seq data using a large ENCODE data set enables comparison of multiple samples.

Maehara K, Odawara J, Harada A, Yoshimi T, Nagao K, Obuse C, Akashi K, Tachibana T, Sakata T, Ohkawa Y. Maehara K, et al. Among authors: nagao k. Nucleic Acids Res. 2013 Jan 7;41(1):54-62. doi: 10.1093/nar/gks1010. Epub 2012 Nov 3. Nucleic Acids Res. 2013. PMID: 23125363 Free PMC article.

5

Human inactive X chromosome is compacted through a PRC2-independent SMCHD1-HBiX1 pathway.

Nozawa RS, Nagao K, Igami KT, Shibata S, Shirai N, Nozaki N, Sado T, Kimura H, Obuse C. Nozawa RS, et al. Among authors: nagao k. Nat Struct Mol Biol. 2013 May;20(5):566-73. doi: 10.1038/nsmb.2532. Epub 2013 Mar 31. Nat Struct Mol Biol. 2013. PMID: 23542155

6

A novel method for purification of the endogenously expressed fission yeast Set2 complex.

Suzuki S, Nagao K, Obuse C, Murakami Y, Takahata S. Suzuki S, et al. Among authors: nagao k. Protein Expr Purif. 2014 May;97:44-9. doi: 10.1016/j.pep.2014.02.005. Epub 2014 Feb 28. Protein Expr Purif. 2014. PMID: 24583182 Free article.

7

Histone H3K36 trimethylation is essential for multiple silencing mechanisms in fission yeast.

Suzuki S, Kato H, Suzuki Y, Chikashige Y, Hiraoka Y, Kimura H, Nagao K, Obuse C, Takahata S, Murakami Y. Suzuki S, et al. Among authors: nagao k. Nucleic Acids Res. 2016 May 19;44(9):4147-62. doi: 10.1093/nar/gkw008. Epub 2016 Jan 20. Nucleic Acids Res. 2016. PMID: 26792892 Free PMC article.

8

Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations.

Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I. Hamanaka K, et al. Among authors: nagao k. Neuromuscul Disord. 2016 Apr-May;26(4-5):300-8. doi: 10.1016/j.nmd.2016.03.001. Epub 2016 Mar 15. Neuromuscul Disord. 2016. PMID: 27061275

9

Histone H4 lysine 20 acetylation is associated with gene repression in human cells.

Kaimori JY, Maehara K, Hayashi-Takanaka Y, Harada A, Fukuda M, Yamamoto S, Ichimaru N, Umehara T, Yokoyama S, Matsuda R, Ikura T, Nagao K, Obuse C, Nozaki N, Takahara S, Takao T, Ohkawa Y, Kimura H, Isaka Y. Kaimori JY, et al. Among authors: nagao k. Sci Rep. 2016 Apr 11;6:24318. doi: 10.1038/srep24318. Sci Rep. 2016. PMID: 27064113 Free PMC article.

10

Corrigendum to "Clinical, muscle pathological, and genetic features of Japanese facioscapulohumeral muscular dystrophy 2 (FSHD2) patients with SMCHD1 mutations": [Neuromuscular Disorders 26/4-5 (2016) 300-308].

Hamanaka K, Goto K, Arai M, Nagao K, Obuse C, Noguchi S, Hayashi YK, Mitsuhashi S, Nishino I. Hamanaka K, et al. Among authors: nagao k. Neuromuscul Disord. 2016 Jul;26(7):472. doi: 10.1016/j.nmd.2016.05.015. Neuromuscul Disord. 2016. PMID: 27312129 No abstract available.

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