Meguro M - Search Results

1

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

2

Predominant maternal expression of the mouse Atp10c in hippocampus and olfactory bulb.

Kashiwagi A, Meguro M, Hoshiya H, Haruta M, Ishino F, Shibahara T, Oshimura M. Kashiwagi A, et al. Among authors: meguro m. J Hum Genet. 2003;48(4):194-8. doi: 10.1007/s10038-003-0009-3. Epub 2003 Mar 12. J Hum Genet. 2003. PMID: 12730723

3

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: meguro 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

4

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: meguro 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

5

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: meguro m. Hum Mol Genet. 2002 Jul 15;11(15):1743-56. doi: 10.1093/hmg/11.15.1743. Hum Mol Genet. 2002. PMID: 12095916

6

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

7

Epigenetic reprogramming of the human H19 gene in mouse embryonic cells does not erase the primary parental imprint.

Mitsuya K, Meguro M, Sui H, Schulz TC, Kugoh H, Hamada H, Oshimura M. Mitsuya K, et al. Among authors: meguro m. Genes Cells. 1998 Apr;3(4):245-55. doi: 10.1046/j.1365-2443.1998.00183.x. Genes Cells. 1998. PMID: 9663659 Free article.

8

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

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: meguro 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

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: meguro 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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