Oshimura M - Search Results

1

CTCFL/BORIS is a methylation-independent DNA-binding protein that preferentially binds to the paternal H19 differentially methylated region.

Nguyen P, Cui H, Bisht KS, Sun L, Patel K, Lee RS, Kugoh H, Oshimura M, Feinberg AP, Gius D. Nguyen P, et al. Among authors: oshimura m. Cancer Res. 2008 Jul 15;68(14):5546-51. doi: 10.1158/0008-5472.CAN-08-1005. Cancer Res. 2008. PMID: 18632606 Free PMC article.

2

Epigenetic mechanisms in human disease.

Feinberg AP, Oshimura M, Barrett JC. Feinberg AP, et al. Among authors: oshimura m. Cancer Res. 2002 Nov 15;62(22):6784-7. Cancer Res. 2002. PMID: 12438281 No abstract available.

3

Expression profile of LIT1/KCNQ1OT1 and epigenetic status at the KvDMR1 in colorectal cancers.

Nakano S, Murakami K, Meguro M, Soejima H, Higashimoto K, Urano T, Kugoh H, Mukai T, Ikeguchi M, Oshimura M. Nakano S, et al. Among authors: oshimura m. Cancer Sci. 2006 Nov;97(11):1147-54. doi: 10.1111/j.1349-7006.2006.00305.x. Epub 2006 Sep 5. Cancer Sci. 2006. PMID: 16965397 Free PMC article.

4

Suggestive evidence for chromosomal localization of non-coding RNA from imprinted LIT1.

Murakami K, Oshimura M, Kugoh H. Murakami K, et al. Among authors: oshimura m. J Hum Genet. 2007;52(11):926-933. doi: 10.1007/s10038-007-0196-4. Epub 2007 Oct 5. J Hum Genet. 2007. PMID: 17917697

5

Human chromosome 5 carries a transcriptional regulator of human telomerase reverse transcriptase (hTERT).

Qi DL, Ohhira T, Oshimura M, Kugoh H. Qi DL, et al. Among authors: oshimura m. Biochem Biophys Res Commun. 2010 Aug 6;398(4):695-701. doi: 10.1016/j.bbrc.2010.07.003. Epub 2010 Jul 16. Biochem Biophys Res Commun. 2010. PMID: 20621064

6

Human chromosome 5 carries a putative telomerase repressor gene.

Kugoh H, Shigenami K, Funaki K, Barrett JC, Oshimura M. Kugoh H, et al. Among authors: oshimura m. Genes Chromosomes Cancer. 2003 Jan;36(1):37-47. doi: 10.1002/gcc.10135. Genes Chromosomes Cancer. 2003. PMID: 12461748

7

Poly(ADP-ribosyl)ation regulates CTCF-dependent chromatin insulation.

Yu W, Ginjala V, Pant V, Chernukhin I, Whitehead J, Docquier F, Farrar D, Tavoosidana G, Mukhopadhyay R, Kanduri C, Oshimura M, Feinberg AP, Lobanenkov V, Klenova E, Ohlsson R. Yu W, et al. Among authors: oshimura m. Nat Genet. 2004 Oct;36(10):1105-10. doi: 10.1038/ng1426. Epub 2004 Sep 7. Nat Genet. 2004. PMID: 15361875

8

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

9

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

10

Microdeletion of LIT1 in familial Beckwith-Wiedemann syndrome.

Niemitz EL, DeBaun MR, Fallon J, Murakami K, Kugoh H, Oshimura M, Feinberg AP. Niemitz EL, et al. Among authors: oshimura m. Am J Hum Genet. 2004 Nov;75(5):844-9. doi: 10.1086/425343. Epub 2004 Sep 15. Am J Hum Genet. 2004. PMID: 15372379 Free PMC article.

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