Oshimura M - Search Results

1

Imprinting analysis of 10 genes and/or transcripts in a 1.5-Mb MEST-flanking region at human chromosome 7q32.

Yamada T, Mitsuya K, Kayashima T, Yamasaki K, Ohta T, Yoshiura K, Matsumoto N, Yamada H, Minakami H, Oshimura M, Niikawa N, Kishino T. Yamada T, et al. Among authors: oshimura m. Genomics. 2004 Mar;83(3):402-12. doi: 10.1016/j.ygeno.2003.08.016. Genomics. 2004. PMID: 14962666

2

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

3

Isolation and mapping of human homologues of an imprinted mouse gene U2af1-rs1.

Kitagawa K, Wang X, Hatada I, Yamaoka T, Nojima H, Inazawa J, Abe T, Mitsuya K, Oshimura M, Murata A, et al. Kitagawa K, et al. Among authors: oshimura m. Genomics. 1995 Nov 20;30(2):257-63. doi: 10.1006/geno.1995.9879. Genomics. 1995. PMID: 8586425

4

[Studies of genomic imprinting using mouse cells containing a human chromosome].

Mitsuya K, Meguro M, Oshimura M. Mitsuya K, et al. Among authors: oshimura m. Tanpakushitsu Kakusan Koso. 1998 Mar;43(4):573-82. Tanpakushitsu Kakusan Koso. 1998. PMID: 9557576 Review. Japanese. No abstract available.

5

Isolation and mapping of 186 new DNA markers on human chromosome 1.

Kugoh H, Nakagawa Y, Mitsuya K, Mita T, Suzuki M, Suzuki N, Uejima H, Yuasa Y, Oshimura M. Kugoh H, et al. Among authors: oshimura m. Genomics. 1995 May 1;27(1):207-10. doi: 10.1006/geno.1995.1028. Genomics. 1995. PMID: 7665174

6

Paternal expression of WT1 in human fibroblasts and lymphocytes.

Mitsuya K, Sui H, Meguro M, Kugoh H, Jinno Y, Niikawa N, Oshimura M. Mitsuya K, et al. Among authors: oshimura m. Hum Mol Genet. 1997 Dec;6(13):2243-6. doi: 10.1093/hmg/6.13.2243. Hum Mol Genet. 1997. PMID: 9361029

7

Narrowed abrogation of the Angelman syndrome critical interval on human chromosome 15 does not interfere with epigenotype maintenance in somatic cells.

Haruta M, Meguro M, Sakamoto YK, Hoshiya H, Kashiwagi A, Kaneko Y, Mitsuya K, Oshimura M. Haruta M, et al. Among authors: oshimura m. J Hum Genet. 2005;50(3):124-132. doi: 10.1007/s10038-005-0231-2. Epub 2005 Mar 3. J Hum Genet. 2005. PMID: 15744456

8

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

9

Mouse A9 cells containing single human chromosomes for analysis of genomic imprinting.

Kugoh H, Mitsuya K, Meguro M, Shigenami K, Schulz TC, Oshimura M. Kugoh H, et al. Among authors: oshimura m. DNA Res. 1999 Jun 30;6(3):165-72. doi: 10.1093/dnares/6.3.165. DNA Res. 1999. PMID: 10470847 Free article.

10

Evidence for uniparental, paternal expression of the human GABAA receptor subunit genes, using microcell-mediated chromosome transfer.

Meguro M, Mitsuya K, Sui H, Shigenami K, Kugoh H, Nakao M, Oshimura M. Meguro M, et al. Among authors: oshimura m. Hum Mol Genet. 1997 Nov;6(12):2127-33. doi: 10.1093/hmg/6.12.2127. Hum Mol Genet. 1997. PMID: 9328477

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