Soejima H - Search Results

1

Novel Nonsense Mutation in the NLRP7 Gene Associated with Recurrent Hydatidiform Mole.

Ito Y, Maehara K, Kaneki E, Matsuoka K, Sugahara N, Miyata T, Kamura H, Yamaguchi Y, Kono A, Nakabayashi K, Migita O, Higashimoto K, Soejima H, Okamoto A, Nakamura H, Kimura T, Wake N, Taniguchi T, Hata K. Ito Y, et al. Among authors: soejima h. Gynecol Obstet Invest. 2016;81(4):353-8. doi: 10.1159/000441780. Epub 2015 Nov 26. Gynecol Obstet Invest. 2016. PMID: 26606510

2

Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene.

Higashimoto K, Soejima H, Katsuki T, Mukai T. Higashimoto K, et al. Among authors: soejima h. J Hum Genet. 2000;45(1):58-9. doi: 10.1007/s100380050012. J Hum Genet. 2000. PMID: 10697966

3

An NsiI RFLP in the human long QT intronic transcript 1 (LIT1).

Higashimoto K, Soejima H, Yatsuki H, Katsuki T, Mukai T. Higashimoto K, et al. Among authors: soejima h. J Hum Genet. 2000;45(2):96-7. doi: 10.1007/s100380050020. J Hum Genet. 2000. PMID: 10721672

4

Domain regulation of imprinting cluster in Kip2/Lit1 subdomain on mouse chromosome 7F4/F5: large-scale DNA methylation analysis reveals that DMR-Lit1 is a putative imprinting control region.

Yatsuki H, Joh K, Higashimoto K, Soejima H, Arai Y, Wang Y, Hatada I, Obata Y, Morisaki H, Zhang Z, Nakagawachi T, Satoh Y, Mukai T. Yatsuki H, et al. Among authors: soejima h. Genome Res. 2002 Dec;12(12):1860-70. doi: 10.1101/gr.110702. Genome Res. 2002. PMID: 12466290 Free PMC article.

5

Characterization and imprinting status of OBPH1/Obph1 gene: implications for an extended imprinting domain in human and mouse.

Higashimoto K, Soejima H, Yatsuki H, Joh K, Uchiyama M, Obata Y, Ono R, Wang Y, Xin Z, Zhu X, Masuko S, Ishino F, Hatada I, Jinno Y, Iwasaka T, Katsuki T, Mukai T. Higashimoto K, et al. Among authors: soejima h. Genomics. 2002 Dec;80(6):575-84. doi: 10.1006/geno.2002.7006. Genomics. 2002. PMID: 12504849

6

Loss of CpG methylation is strongly correlated with loss of histone H3 lysine 9 methylation at DMR-LIT1 in patients with Beckwith-Wiedemann syndrome.

Higashimoto K, Urano T, Sugiura K, Yatsuki H, Joh K, Zhao W, Iwakawa M, Ohashi H, Oshimura M, Niikawa N, Mukai T, Soejima H. Higashimoto K, et al. Among authors: soejima h. Am J Hum Genet. 2003 Oct;73(4):948-56. doi: 10.1086/378595. Epub 2003 Aug 29. Am J Hum Genet. 2003. PMID: 12949703 Free PMC article.

7

Silencing effect of CpG island hypermethylation and histone modifications on O6-methylguanine-DNA methyltransferase (MGMT) gene expression in human cancer.

Nakagawachi T, Soejima H, Urano T, Zhao W, Higashimoto K, Satoh Y, Matsukura S, Kudo S, Kitajima Y, Harada H, Furukawa K, Matsuzaki H, Emi M, Nakabeppu Y, Miyazaki K, Sekiguchi M, Mukai T. Nakagawachi T, et al. Among authors: soejima h. Oncogene. 2003 Dec 4;22(55):8835-44. doi: 10.1038/sj.onc.1207183. Oncogene. 2003. PMID: 14647440

8

Silencing of imprinted CDKN1C gene expression is associated with loss of CpG and histone H3 lysine 9 methylation at DMR-LIT1 in esophageal cancer.

Soejima H, Nakagawachi T, Zhao W, Higashimoto K, Urano T, Matsukura S, Kitajima Y, Takeuchi M, Nakayama M, Oshimura M, Miyazaki K, Joh K, Mukai T. Soejima H, et al. Oncogene. 2004 May 27;23(25):4380-8. doi: 10.1038/sj.onc.1207576. Oncogene. 2004. PMID: 15007390

9

Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice.

Zhang Z, Joh K, Yatsuki H, Wang Y, Arai Y, Soejima H, Higashimoto K, Iwasaka T, Mukai T. Zhang Z, et al. Among authors: soejima h. Gene. 2006 Jan 17;366(1):77-86. doi: 10.1016/j.gene.2005.08.020. Epub 2005 Nov 21. Gene. 2006. PMID: 16305817

10

Imprinting disruption of the CDKN1C/KCNQ1OT1 domain: the molecular mechanisms causing Beckwith-Wiedemann syndrome and cancer.

Higashimoto K, Soejima H, Saito T, Okumura K, Mukai T. Higashimoto K, et al. Among authors: soejima h. Cytogenet Genome Res. 2006;113(1-4):306-12. doi: 10.1159/000090846. Cytogenet Genome Res. 2006. PMID: 16575194

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