Oshimura M - Search Results

1

A simple and efficient amplification method of DNA with unknown sequences and its application to microdissection/microcloning.

Jinno Y, Harada N, Yoshiura K, Ohta T, Tohma T, Hirota T, Tsukamoto K, Deng HX, Oshimura M, Niikawa N. Jinno Y, et al. Among authors: oshimura m. J Biochem. 1992 Jul;112(1):75-80. doi: 10.1093/oxfordjournals.jbchem.a123869. J Biochem. 1992. PMID: 1429512 Free article.

2

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

3

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.

4

LIT1, an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids.

Mitsuya K, Meguro M, Lee MP, Katoh M, Schulz TC, Kugoh H, Yoshida MA, Niikawa N, Feinberg AP, Oshimura M. Mitsuya K, et al. Among authors: oshimura m. Hum Mol Genet. 1999 Jul;8(7):1209-17. doi: 10.1093/hmg/8.7.1209. Hum Mol Genet. 1999. PMID: 10369866

5

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

6

Human arylhydrocarbon receptor: functional expression and chromosomal assignment to 7p21.

Ema M, Matsushita N, Sogawa K, Ariyama T, Inazawa J, Nemoto T, Ota M, Oshimura M, Fujii-Kuriyama Y. Ema M, et al. Among authors: oshimura m. J Biochem. 1994 Oct;116(4):845-51. doi: 10.1093/oxfordjournals.jbchem.a124605. J Biochem. 1994. PMID: 7883760 Free article.

7

Cosmids and transcribed sequences from chromosome 11q23.

Katoh M, Nakagawa Y, Yawata T, Kumano S, Kobayashi E, Kurimasa A, Kugoh H, Oshimura M. Katoh M, et al. Among authors: oshimura m. Jpn J Hum Genet. 1995 Dec;40(4):307-17. doi: 10.1007/BF01900597. Jpn J Hum Genet. 1995. PMID: 8851764

8

Suppression of X-ray-induced chromosome aberrations in ataxia telangiectasia cells by introduction of a normal human chromosome 11.

Kodama S, Komatsu K, Okumura Y, Oshimura M. Kodama S, et al. Among authors: oshimura m. Mutat Res. 1992 Nov;293(1):31-7. doi: 10.1016/0921-8777(92)90005-n. Mutat Res. 1992. PMID: 1383808

9

A human gene that restores the DNA-repair defect in SCID mice is located on 8p11.1-->q11.1.

Kurimasa A, Nagata Y, Shimizu M, Emi M, Nakamura Y, Oshimura M. Kurimasa A, et al. Among authors: oshimura m. Hum Genet. 1994 Jan;93(1):21-6. doi: 10.1007/BF00218907. Hum Genet. 1994. PMID: 8270250

10

Human chromosome 11 complements ataxia-telangiectasia cells but does not complement the defect in AT-like Chinese hamster cell mutants.

Jongmans W, Wiegant J, Oshimura M, James MR, Lohman PH, Zdzienicka MZ. Jongmans W, et al. Among authors: oshimura m. Hum Genet. 1993 Oct 1;92(3):259-64. doi: 10.1007/BF00244469. Hum Genet. 1993. PMID: 8406433

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