Soejima H - Search Results

1

Mutations in genes encoding polycomb repressive complex 2 subunits cause Weaver syndrome.

Imagawa E, Higashimoto K, Sakai Y, Numakura C, Okamoto N, Matsunaga S, Ryo A, Sato Y, Sanefuji M, Ihara K, Takada Y, Nishimura G, Saitsu H, Mizuguchi T, Miyatake S, Nakashima M, Miyake N, Soejima H, Matsumoto N. Imagawa E, et al. Among authors: soejima h. Hum Mutat. 2017 Jun;38(6):637-648. doi: 10.1002/humu.23200. Epub 2017 Mar 15. Hum Mutat. 2017. PMID: 28229514

2

Three novel PAX3 mutations observed in patients with Waardenburg syndrome type 1.

Soejima H, Fujimoto M, Tsukamoto K, Matsumoto N, Yoshiura KI, Fukushima Y, Jinno Y, Niikawa N. Soejima H, et al. Hum Mutat. 1997;9(2):177-80. doi: 10.1002/(SICI)1098-1004(1997)9:2<177::AID-HUMU11>3.0.CO;2-#. Hum Mutat. 1997. PMID: 9067759 No abstract available.

3

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

4

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

5

C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5.

Zhu X, Higashimoto K, Soejima H, Yatsuki H, Sugihara H, Mukai T, Joh K. Zhu X, et al. Among authors: soejima h. Gene. 2000 Oct 3;256(1-2):311-7. doi: 10.1016/s0378-1119(00)00377-2. Gene. 2000. PMID: 11054561

6

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.

7

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

8

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.

9

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

10

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

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