Kashiwagi A - Search Results

1

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

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. 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: 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

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: 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

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: 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

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: 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

7

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

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 Free article.

9

Decreased bodyweight without rebound and regulated lipoprotein metabolism by gymnemate in genetic multifactor syndrome animal.

Luo H, Kashiwagi A, Shibahara T, Yamada K. Luo H, et al. Among authors: kashiwagi a. Mol Cell Biochem. 2007 May;299(1-2):93-8. doi: 10.1007/s11010-005-9049-7. Mol Cell Biochem. 2007. PMID: 16691318

10

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.

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