Asashima M - Search Results

1

Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development.

Nishinakamura R, Matsumoto Y, Nakao K, Nakamura K, Sato A, Copeland NG, Gilbert DJ, Jenkins NA, Scully S, Lacey DL, Katsuki M, Asashima M, Yokota T. Nishinakamura R, et al. Among authors: asashima m. Development. 2001 Aug;128(16):3105-15. doi: 10.1242/dev.128.16.3105. Development. 2001. PMID: 11688560

2

Zinc finger protein sall2 is not essential for embryonic and kidney development.

Sato A, Matsumoto Y, Koide U, Kataoka Y, Yoshida N, Yokota T, Asashima M, Nishinakamura R. Sato A, et al. Among authors: asashima m. Mol Cell Biol. 2003 Jan;23(1):62-9. doi: 10.1128/MCB.23.1.62-69.2003. Mol Cell Biol. 2003. PMID: 12482961 Free PMC article.

3

Identification of kidney mesenchymal genes by a combination of microarray analysis and Sall1-GFP knockin mice.

Takasato M, Osafune K, Matsumoto Y, Kataoka Y, Yoshida N, Meguro H, Aburatani H, Asashima M, Nishinakamura R. Takasato M, et al. Among authors: asashima m. Mech Dev. 2004 Jun;121(6):547-57. doi: 10.1016/j.mod.2004.04.007. Mech Dev. 2004. PMID: 15172686 Free article.

4

Identification of multipotent progenitors in the embryonic mouse kidney by a novel colony-forming assay.

Osafune K, Takasato M, Kispert A, Asashima M, Nishinakamura R. Osafune K, et al. Among authors: asashima m. Development. 2006 Jan;133(1):151-61. doi: 10.1242/dev.02174. Epub 2005 Nov 30. Development. 2006. PMID: 16319116

5

The murine homolog of SALL4, a causative gene in Okihiro syndrome, is essential for embryonic stem cell proliferation, and cooperates with Sall1 in anorectal, heart, brain and kidney development.

Sakaki-Yumoto M, Kobayashi C, Sato A, Fujimura S, Matsumoto Y, Takasato M, Kodama T, Aburatani H, Asashima M, Yoshida N, Nishinakamura R. Sakaki-Yumoto M, et al. Among authors: asashima m. Development. 2006 Aug;133(15):3005-13. doi: 10.1242/dev.02457. Epub 2006 Jun 21. Development. 2006. PMID: 16790473

6

Cloning and expression pattern of a Xenopus pronephros-specific gene, XSMP-30.

Sato A, Asashima M, Yokota T, Nishinakamura R. Sato A, et al. Among authors: asashima m. Mech Dev. 2000 Apr;92(2):273-5. doi: 10.1016/s0925-4773(99)00331-7. Mech Dev. 2000. PMID: 10727865 Free article.

7

Sall1, a causative gene for Townes-Brocks syndrome, enhances the canonical Wnt signaling by localizing to heterochromatin.

Sato A, Kishida S, Tanaka T, Kikuchi A, Kodama T, Asashima M, Nishinakamura R. Sato A, et al. Among authors: asashima m. Biochem Biophys Res Commun. 2004 Jun 18;319(1):103-13. doi: 10.1016/j.bbrc.2004.04.156. Biochem Biophys Res Commun. 2004. PMID: 15158448

8

Mouse homolog of SALL1, a causative gene for Townes-Brocks syndrome, binds to A/T-rich sequences in pericentric heterochromatin via its C-terminal zinc finger domains.

Yamashita K, Sato A, Asashima M, Wang PC, Nishinakamura R. Yamashita K, et al. Among authors: asashima m. Genes Cells. 2007 Feb;12(2):171-82. doi: 10.1111/j.1365-2443.2007.01042.x. Genes Cells. 2007. PMID: 17295837 Free article.

9

Six1 and Six4 are essential for Gdnf expression in the metanephric mesenchyme and ureteric bud formation, while Six1 deficiency alone causes mesonephric-tubule defects.

Kobayashi H, Kawakami K, Asashima M, Nishinakamura R. Kobayashi H, et al. Among authors: asashima m. Mech Dev. 2007 Apr;124(4):290-303. doi: 10.1016/j.mod.2007.01.002. Epub 2007 Jan 11. Mech Dev. 2007. PMID: 17300925 Free article.

10

Xenopus FK 506-binding protein homolog induces a secondary axis in frog embryos, which is inhibited by coexisting BMP 4 signaling.

Nishinakamura R, Matsumoto Y, Uochi Ta, Asashima M, Yokota T. Nishinakamura R, et al. Among authors: asashima m. Biochem Biophys Res Commun. 1997 Oct 20;239(2):585-91. doi: 10.1006/bbrc.1997.7491. Biochem Biophys Res Commun. 1997. PMID: 9344875

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