Oshimura M - Search Results

1

Genomic imprinting of PPP1R9A encoding neurabin I in skeletal muscle and extra-embryonic tissues.

Nakabayashi K, Makino S, Minagawa S, Smith AC, Bamforth JS, Stanier P, Preece M, Parker-Katiraee L, Paton T, Oshimura M, Mill P, Yoshikawa Y, Hui CC, Monk D, Moore GE, Scherer SW. Nakabayashi K, et al. Among authors: oshimura m. J Med Genet. 2004 Aug;41(8):601-8. doi: 10.1136/jmg.2003.014142. J Med Genet. 2004. PMID: 15286155 Free PMC article. No abstract available.

2

Identification and characterization of an imprinted antisense RNA (MESTIT1) in the human MEST locus on chromosome 7q32.

Nakabayashi K, Bentley L, Hitchins MP, Mitsuya K, Meguro M, Minagawa S, Bamforth JS, Stanier P, Preece M, Weksberg R, Oshimura M, Moore GE, Scherer SW. Nakabayashi K, et al. Among authors: oshimura m. Hum Mol Genet. 2002 Jul 15;11(15):1743-56. doi: 10.1093/hmg/11.15.1743. Hum Mol Genet. 2002. PMID: 12095916

3

Chromosomal banding patterns in primary and transplanted venereal tumors of the dog.

Oshimura M, Sasaki M, Makino S. Oshimura M, et al. J Natl Cancer Inst. 1973 Oct;51(4):1197-203. doi: 10.1093/jnci/51.4.1197. J Natl Cancer Inst. 1973. PMID: 4126856 No abstract available.

4

Molecular genetic studies of human chromosome 7 in Russell-Silver syndrome.

Nakabayashi K, Fernandez BA, Teshima I, Shuman C, Proud VK, Curry CJ, Chitayat D, Grebe T, Ming J, Oshimura M, Meguro M, Mitsuya K, Deb-Rinker P, Herbrick JA, Weksberg R, Scherer SW. Nakabayashi K, et al. Among authors: oshimura m. Genomics. 2002 Feb;79(2):186-96. doi: 10.1006/geno.2002.6695. Genomics. 2002. PMID: 11829489

5

Epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome.

Engel JR, Smallwood A, Harper A, Higgins MJ, Oshimura M, Reik W, Schofield PN, Maher ER. Engel JR, et al. Among authors: oshimura m. J Med Genet. 2000 Dec;37(12):921-6. doi: 10.1136/jmg.37.12.921. J Med Genet. 2000. PMID: 11106355 Free PMC article.

6

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

7

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

8

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

9

Calcr, a brain-specific imprinted mouse calcitonin receptor gene in the imprinted cluster of the proximal region of chromosome 6.

Hoshiya H, Meguro M, Kashiwagi A, Okita C, Oshimura M. Hoshiya H, et al. Among authors: oshimura m. J Hum Genet. 2003;48(4):208-11. doi: 10.1007/s10038-003-0006-6. Epub 2003 Mar 12. J Hum Genet. 2003. PMID: 12730726

10

Targeted disruption of the human LIT1 locus defines a putative imprinting control element playing an essential role in Beckwith-Wiedemann syndrome.

Horike S, Mitsuya K, Meguro M, Kotobuki N, Kashiwagi A, Notsu T, Schulz TC, Shirayoshi Y, Oshimura M. Horike S, et al. Among authors: oshimura m. Hum Mol Genet. 2000 Sep 1;9(14):2075-83. doi: 10.1093/hmg/9.14.2075. Hum Mol Genet. 2000. PMID: 10958646

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