Nishiyama M - Search Results

1

Identification of CHD7S as a novel splicing variant of CHD7 with functions similar and antagonistic to those of the full-length CHD7L.

Kita Y, Nishiyama M, Nakayama KI. Kita Y, et al. Among authors: nishiyama m. Genes Cells. 2012 Jul;17(7):536-47. doi: 10.1111/j.1365-2443.2012.01606.x. Epub 2012 May 31. Genes Cells. 2012. PMID: 22646239 Free article.

2

Mouse Fbw7/Sel-10/Cdc4 is required for notch degradation during vascular development.

Tsunematsu R, Nakayama K, Oike Y, Nishiyama M, Ishida N, Hatakeyama S, Bessho Y, Kageyama R, Suda T, Nakayama KI. Tsunematsu R, et al. Among authors: nishiyama m. J Biol Chem. 2004 Mar 5;279(10):9417-23. doi: 10.1074/jbc.M312337200. Epub 2003 Dec 12. J Biol Chem. 2004. PMID: 14672936 Free article.

3

Phosphorylation-dependent degradation of c-Myc is mediated by the F-box protein Fbw7.

Yada M, Hatakeyama S, Kamura T, Nishiyama M, Tsunematsu R, Imaki H, Ishida N, Okumura F, Nakayama K, Nakayama KI. Yada M, et al. Among authors: nishiyama m. EMBO J. 2004 May 19;23(10):2116-25. doi: 10.1038/sj.emboj.7600217. Epub 2004 Apr 22. EMBO J. 2004. PMID: 15103331 Free PMC article.

4

Early embryonic death in mice lacking the beta-catenin-binding protein Duplin.

Nishiyama M, Nakayama K, Tsunematsu R, Tsukiyama T, Kikuchi A, Nakayama KI. Nishiyama M, et al. Mol Cell Biol. 2004 Oct;24(19):8386-94. doi: 10.1128/MCB.24.19.8386-8394.2004. Mol Cell Biol. 2004. PMID: 15367660 Free PMC article.

5

Fbxw7 contributes to tumor suppression by targeting multiple proteins for ubiquitin-dependent degradation.

Fujii Y, Yada M, Nishiyama M, Kamura T, Takahashi H, Tsunematsu R, Susaki E, Nakagawa T, Matsumoto A, Nakayama KI. Fujii Y, et al. Among authors: nishiyama m. Cancer Sci. 2006 Aug;97(8):729-36. doi: 10.1111/j.1349-7006.2006.00239.x. Cancer Sci. 2006. PMID: 16863506 Free PMC article.

6

Fbxw8 is essential for Cul1-Cul7 complex formation and for placental development.

Tsunematsu R, Nishiyama M, Kotoshiba S, Saiga T, Kamura T, Nakayama KI. Tsunematsu R, et al. Among authors: nishiyama m. Mol Cell Biol. 2006 Aug;26(16):6157-69. doi: 10.1128/MCB.00595-06. Mol Cell Biol. 2006. PMID: 16880526 Free PMC article.

7

CHD8 suppresses p53-mediated apoptosis through histone H1 recruitment during early embryogenesis.

Nishiyama M, Oshikawa K, Tsukada Y, Nakagawa T, Iemura S, Natsume T, Fan Y, Kikuchi A, Skoultchi AI, Nakayama KI. Nishiyama M, et al. Nat Cell Biol. 2009 Feb;11(2):172-82. doi: 10.1038/ncb1831. Epub 2009 Jan 18. Nat Cell Biol. 2009. PMID: 19151705 Free PMC article.

8

The FBXL5-IRP2 axis is integral to control of iron metabolism in vivo.

Moroishi T, Nishiyama M, Takeda Y, Iwai K, Nakayama KI. Moroishi T, et al. Among authors: nishiyama m. Cell Metab. 2011 Sep 7;14(3):339-51. doi: 10.1016/j.cmet.2011.07.011. Cell Metab. 2011. PMID: 21907140 Free article.

9

Histone H1 recruitment by CHD8 is essential for suppression of the Wnt-β-catenin signaling pathway.

Nishiyama M, Skoultchi AI, Nakayama KI. Nishiyama M, et al. Mol Cell Biol. 2012 Jan;32(2):501-12. doi: 10.1128/MCB.06409-11. Epub 2011 Nov 14. Mol Cell Biol. 2012. PMID: 22083958 Free PMC article.

10

HERC2 targets the iron regulator FBXL5 for degradation and modulates iron metabolism.

Moroishi T, Yamauchi T, Nishiyama M, Nakayama KI. Moroishi T, et al. Among authors: nishiyama m. J Biol Chem. 2014 Jun 6;289(23):16430-41. doi: 10.1074/jbc.M113.541490. Epub 2014 Apr 28. J Biol Chem. 2014. PMID: 24778179 Free PMC article.

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