Oshimura M - Search Results

1

Reactivation of the silenced and imprinted alleles of ARHI is associated with increased histone H3 acetylation and decreased histone H3 lysine 9 methylation.

Fujii S, Luo RZ, Yuan J, Kadota M, Oshimura M, Dent SR, Kondo Y, Issa JP, Bast RC Jr, Yu Y. Fujii S, et al. Among authors: oshimura m. Hum Mol Genet. 2003 Aug 1;12(15):1791-800. doi: 10.1093/hmg/ddg204. Hum Mol Genet. 2003. PMID: 12874100

2

Epigenetic regulation of ARHI in breast and ovarian cancer cells.

Yu Y, Fujii S, Yuan J, Luo RZ, Wang L, Bao J, Kadota M, Oshimura M, Dent SR, Issa JP, Bast RC Jr. Yu Y, et al. Among authors: oshimura m. Ann N Y Acad Sci. 2003 Mar;983:268-77. doi: 10.1111/j.1749-6632.2003.tb05981.x. Ann N Y Acad Sci. 2003. PMID: 12724231 Review.

3

Aberrant methylation and silencing of ARHI, an imprinted tumor suppressor gene in which the function is lost in breast cancers.

Yuan J, Luo RZ, Fujii S, Wang L, Hu W, Andreeff M, Pan Y, Kadota M, Oshimura M, Sahin AA, Issa JP, Bast RC Jr, Yu Y. Yuan J, et al. Among authors: oshimura m. Cancer Res. 2003 Jul 15;63(14):4174-80. Cancer Res. 2003. PMID: 12874023

4

Construction of 700 human/mouse A9 monochromosomal hybrids and analysis of imprinted genes on human chromosome 6.

Inoue J, Mitsuya K, Maegawa S, Kugoh H, Kadota M, Okamura D, Shinohara T, Nishihara S, Takehara S, Yamauchi K, Schulz TC, Oshimura M. Inoue J, et al. Among authors: oshimura m. J Hum Genet. 2001;46(3):137-45. doi: 10.1007/s100380170101. J Hum Genet. 2001. PMID: 11310581

5

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: oshimura m. 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.

6

Elevated apoptosis in pre-mature neurons differentiated from mouse ES cells containing a single human chromosome 21.

Kadota M, Shirayoshi Y, Oshimura M. Kadota M, et al. Among authors: oshimura m. Biochem Biophys Res Commun. 2002 Dec 13;299(4):599-605. doi: 10.1016/s0006-291x(02)02686-4. Biochem Biophys Res Commun. 2002. PMID: 12459181

7

A novel in vitro system for analyzing parental allele-specific histone acetylation in genomic imprinting.

Yoshioka H, Shirayoshi Y, Oshimura M. Yoshioka H, et al. Among authors: oshimura m. J Hum Genet. 2001;46(11):626-32. doi: 10.1007/s100380170013. J Hum Genet. 2001. PMID: 11721881

8

Dlx5, the mouse homologue of the human-imprinted DLX5 gene, is biallelically expressed in the mouse brain.

Kimura MI, Kazuki Y, Kashiwagi A, Kai Y, Abe S, Barbieri O, Levi G, Oshimura M. Kimura MI, et al. Among authors: oshimura m. J Hum Genet. 2004;49(5):273-7. doi: 10.1007/s10038-004-0139-2. J Hum Genet. 2004. PMID: 15362572

9

Girl with monosomy 1p36 and Angelman syndrome due to unbalanced der(1) transmission of a maternal translocation t(1;15)(p36.3;q13.1).

Torisu H, Yamamoto T, Fujiwaki T, Kadota M, Oshimura M, Kurosawa K, Akaboshi S, Oka A. Torisu H, et al. Among authors: oshimura m. Am J Med Genet A. 2004 Nov 15;131(1):94-8. doi: 10.1002/ajmg.a.30413. Am J Med Genet A. 2004. PMID: 15384094

10

A conserved imprinting control region at the HYMAI/ZAC domain is implicated in transient neonatal diabetes mellitus.

Arima T, Drewell RA, Arney KL, Inoue J, Makita Y, Hata A, Oshimura M, Wake N, Surani MA. Arima T, et al. Among authors: oshimura m. Hum Mol Genet. 2001 Jul 1;10(14):1475-83. doi: 10.1093/hmg/10.14.1475. Hum Mol Genet. 2001. PMID: 11448939

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