Nakabayashi K - Search Results

1

Whole-exome sequencing of fibroblast and its iPS cell lines derived from a patient diagnosed with xeroderma pigmentosum.

Okamura K, Toyoda M, Hata K, Nakabayashi K, Umezawa A. Okamura K, et al. Among authors: nakabayashi k. Genom Data. 2015 Jul 20;6:4-6. doi: 10.1016/j.gdata.2015.07.008. eCollection 2015 Dec. Genom Data. 2015. PMID: 26697316 Free PMC article.

2

Identification of novel candidate loci for anorexia nervosa at 1q41 and 11q22 in Japanese by a genome-wide association analysis with microsatellite markers.

Nakabayashi K, Komaki G, Tajima A, Ando T, Ishikawa M, Nomoto J, Hata K, Oka A, Inoko H, Sasazuki T; Japanese Genetic Research Group for Eating Disorders (JGRED); Shirasawa S. Nakabayashi K, et al. J Hum Genet. 2009 Sep;54(9):531-7. doi: 10.1038/jhg.2009.74. Epub 2009 Aug 14. J Hum Genet. 2009. PMID: 19680270

3

Androgenetic/biparental mosaicism in a girl with Beckwith-Wiedemann syndrome-like and upd(14)pat-like phenotypes.

Yamazawa K, Nakabayashi K, Matsuoka K, Masubara K, Hata K, Horikawa R, Ogata T. Yamazawa K, et al. Among authors: nakabayashi k. J Hum Genet. 2011 Jan;56(1):91-3. doi: 10.1038/jhg.2010.142. Epub 2010 Nov 11. J Hum Genet. 2011. PMID: 21068742

4

Methylation screening of reciprocal genome-wide UPDs identifies novel human-specific imprinted genes.

Nakabayashi K, Trujillo AM, Tayama C, Camprubi C, Yoshida W, Lapunzina P, Sanchez A, Soejima H, Aburatani H, Nagae G, Ogata T, Hata K, Monk D. Nakabayashi K, et al. Hum Mol Genet. 2011 Aug 15;20(16):3188-97. doi: 10.1093/hmg/ddr224. Epub 2011 May 18. Hum Mol Genet. 2011. PMID: 21593219

5

Methylation dynamics of IG-DMR and Gtl2-DMR during murine embryonic and placental development.

Sato S, Yoshida W, Soejima H, Nakabayashi K, Hata K. Sato S, et al. Among authors: nakabayashi k. Genomics. 2011 Aug;98(2):120-7. doi: 10.1016/j.ygeno.2011.05.003. Epub 2011 May 18. Genomics. 2011. PMID: 21620950 Free article.

6

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.

Nakabayashi K, Tajima A, Yamamoto K, Takahashi A, Hata K, Takashima Y, Koyanagi M, Nakaoka H, Akamizu T, Ishikawa N, Kubota S, Maeda S, Tsunoda T, Kubo M, Kamatani N, Nakamura Y, Sasazuki T, Shirasawa S. Nakabayashi K, et al. J Hum Genet. 2011 Nov;56(11):772-8. doi: 10.1038/jhg.2011.99. Epub 2011 Sep 8. J Hum Genet. 2011. PMID: 21900946

7

Contribution of intragenic DNA methylation in mouse gametic DNA methylomes to establish oocyte-specific heritable marks.

Kobayashi H, Sakurai T, Imai M, Takahashi N, Fukuda A, Yayoi O, Sato S, Nakabayashi K, Hata K, Sotomaru Y, Suzuki Y, Kono T. Kobayashi H, et al. Among authors: nakabayashi k. PLoS Genet. 2012 Jan;8(1):e1002440. doi: 10.1371/journal.pgen.1002440. Epub 2012 Jan 5. PLoS Genet. 2012. PMID: 22242016 Free PMC article.

8

Trophoblast-specific DNA methylation occurs after the segregation of the trophectoderm and inner cell mass in the mouse periimplantation embryo.

Nakanishi MO, Hayakawa K, Nakabayashi K, Hata K, Shiota K, Tanaka S. Nakanishi MO, et al. Among authors: nakabayashi k. Epigenetics. 2012 Feb;7(2):173-82. doi: 10.4161/epi.7.2.18962. Epigenetics. 2012. PMID: 22395467

9

Imprinted DNA methylation reprogramming during early mouse embryogenesis at the Gpr1-Zdbf2 locus is linked to long cis-intergenic transcription.

Kobayashi H, Sakurai T, Sato S, Nakabayashi K, Hata K, Kono T. Kobayashi H, et al. Among authors: nakabayashi k. FEBS Lett. 2012 Mar 23;586(6):827-33. doi: 10.1016/j.febslet.2012.01.059. Epub 2012 Feb 9. FEBS Lett. 2012. PMID: 22449967 Free article.

10

Aberrant methylation of H19-DMR acquired after implantation was dissimilar in soma versus placenta of patients with Beckwith-Wiedemann syndrome.

Higashimoto K, Nakabayashi K, Yatsuki H, Yoshinaga H, Jozaki K, Okada J, Watanabe Y, Aoki A, Shiozaki A, Saito S, Koide K, Mukai T, Hata K, Soejima H. Higashimoto K, et al. Among authors: nakabayashi k. Am J Med Genet A. 2012 Jul;158A(7):1670-5. doi: 10.1002/ajmg.a.35335. Epub 2012 May 10. Am J Med Genet A. 2012. PMID: 22577095

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