Mitsuya K - Search Results

1

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: mitsuya k. J Hum Genet. 2001;46(3):137-45. doi: 10.1007/s100380170101. J Hum Genet. 2001. PMID: 11310581

2

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: mitsuya k. Hum Mol Genet. 1997 Nov;6(12):2127-33. doi: 10.1093/hmg/6.12.2127. Hum Mol Genet. 1997. PMID: 9328477

3

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. Hum Mol Genet. 1999 Jul;8(7):1209-17. doi: 10.1093/hmg/8.7.1209. Hum Mol Genet. 1999. PMID: 10369866

4

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: mitsuya k. DNA Res. 1999 Jun 30;6(3):165-72. doi: 10.1093/dnares/6.3.165. DNA Res. 1999. PMID: 10470847 Free article.

5

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: mitsuya k. Hum Mol Genet. 2000 Sep 1;9(14):2075-83. doi: 10.1093/hmg/9.14.2075. Hum Mol Genet. 2000. PMID: 10958646

6

Large-scale evaluation of imprinting status in the Prader-Willi syndrome region: an imprinted direct repeat cluster resembling small nucleolar RNA genes.

Meguro M, Mitsuya K, Nomura N, Kohda M, Kashiwagi A, Nishigaki R, Yoshioka H, Nakao M, Oishi M, Oshimura M. Meguro M, et al. Among authors: mitsuya k. Hum Mol Genet. 2001 Feb 15;10(4):383-94. doi: 10.1093/hmg/10.4.383. Hum Mol Genet. 2001. PMID: 11157801

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: mitsuya k. 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

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: mitsuya k. Genomics. 1995 May 1;27(1):207-10. doi: 10.1006/geno.1995.1028. Genomics. 1995. PMID: 7665174

9

Normal human chromosome 2 induces cellular senescence in the human cervical carcinoma cell line SiHa.

Uejima H, Mitsuya K, Kugoh H, Horikawa I, Oshimura M. Uejima H, et al. Among authors: mitsuya k. Genes Chromosomes Cancer. 1995 Oct;14(2):120-7. doi: 10.1002/gcc.2870140206. Genes Chromosomes Cancer. 1995. PMID: 8527393

10

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. Hum Mol Genet. 1997 Dec;6(13):2243-6. doi: 10.1093/hmg/6.13.2243. Hum Mol Genet. 1997. PMID: 9361029

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