Kashiwagi A - Search Results

1

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: kashiwagi a. 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

2

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: kashiwagi a. 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

3

Dlx5, the mouse homologue of the human-imprinted DLX5 gene, is biallelically expressed in the mouse brain.

Kimura MI, Kazuki Y, Kashiwagi A, Kai Y, Abe S, Barbieri O, Levi G, Oshimura M. Kimura MI, et al. Among authors: kashiwagi a. J Hum Genet. 2004;49(5):273-7. doi: 10.1007/s10038-004-0139-2. J Hum Genet. 2004. PMID: 15362572

4

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. 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

5

A novel maternally expressed gene, ATP10C, encodes a putative aminophospholipid translocase associated with Angelman syndrome.

Meguro M, Kashiwagi A, Mitsuya K, Nakao M, Kondo I, Saitoh S, Oshimura M. Meguro M, et al. Among authors: kashiwagi a. Nat Genet. 2001 May;28(1):19-20. doi: 10.1038/ng0501-19. Nat Genet. 2001. PMID: 11326269

6

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

7

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: kashiwagi a. Hum Mol Genet. 2001 Feb 15;10(4):383-94. doi: 10.1093/hmg/10.4.383. Hum Mol Genet. 2001. PMID: 11157801

8

Effects of Tritrichomonas muris on the mouse intestine: a proteomic analysis.

Kashiwagi A, Kurosaki H, Luo H, Yamamoto H, Oshimura M, Shibahara T. Kashiwagi A, et al. Exp Anim. 2009 Oct;58(5):537-42. doi: 10.1538/expanim.58.537. Exp Anim. 2009. PMID: 19897938

9

Ongoing phenotypic and genomic changes in experimental coevolution of RNA bacteriophage Qβ and Escherichia coli.

Kashiwagi A, Yomo T. Kashiwagi A, et al. PLoS Genet. 2011 Aug;7(8):e1002188. doi: 10.1371/journal.pgen.1002188. Epub 2011 Aug 4. PLoS Genet. 2011. PMID: 21829387 Free PMC article.

10

Characterization of a single mutation in TraQ in a strain of Escherichia coli partially resistant to Qβ infection.

Kashiwagi A, Kitamura H, Sano Tsushima F. Kashiwagi A, et al. Front Microbiol. 2015 Feb 20;6:124. doi: 10.3389/fmicb.2015.00124. eCollection 2015. Front Microbiol. 2015. PMID: 25750639 Free PMC article.

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