Sato S - Search Results

1

LRRK2 I2020T mutation is associated with tau pathology.

Ujiie S, Hatano T, Kubo S, Imai S, Sato S, Uchihara T, Yagishita S, Hasegawa K, Kowa H, Sakai F, Hattori N. Ujiie S, et al. Among authors: sato s. Parkinsonism Relat Disord. 2012 Aug;18(7):819-23. doi: 10.1016/j.parkreldis.2012.03.024. Epub 2012 Apr 22. Parkinsonism Relat Disord. 2012. PMID: 22525366

2

Urinary 8-hydroxydeoxyguanosine levels as a biomarker for progression of Parkinson disease.

Sato S, Mizuno Y, Hattori N. Sato S, et al. Neurology. 2005 Mar 22;64(6):1081-3. doi: 10.1212/01.WNL.0000154597.24838.6B. Neurology. 2005. PMID: 15781836

3

14-3-3eta is a novel regulator of parkin ubiquitin ligase.

Sato S, Chiba T, Sakata E, Kato K, Mizuno Y, Hattori N, Tanaka K. Sato S, et al. EMBO J. 2006 Jan 11;25(1):211-21. doi: 10.1038/sj.emboj.7600774. Epub 2005 Aug 11. EMBO J. 2006. PMID: 16096643 Free PMC article.

4

Decline of striatal dopamine release in parkin-deficient mice shown by ex vivo autoradiography.

Sato S, Chiba T, Nishiyama S, Kakiuchi T, Tsukada H, Hatano T, Fukuda T, Yasoshima Y, Kai N, Kobayashi K, Mizuno Y, Tanaka K, Hattori N. Sato S, et al. J Neurosci Res. 2006 Nov 1;84(6):1350-7. doi: 10.1002/jnr.21032. J Neurosci Res. 2006. PMID: 16941649

5

Animal models of Parkinson's disease: similarities and differences between the disease and models.

Hattori N, Sato S. Hattori N, et al. Among authors: sato s. Neuropathology. 2007 Oct;27(5):479-83. doi: 10.1111/j.1440-1789.2007.00842.x. Neuropathology. 2007. PMID: 18018484

6

Progress in the pathogenesis and genetics of Parkinson's disease.

Mizuno Y, Hattori N, Kubo S, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H. Mizuno Y, et al. Among authors: sato s. Philos Trans R Soc Lond B Biol Sci. 2008 Jun 27;363(1500):2215-27. doi: 10.1098/rstb.2008.2273. Philos Trans R Soc Lond B Biol Sci. 2008. PMID: 18426756 Free PMC article. Review.

7

Programmed cell death-2 isoform1 is ubiquitinated by parkin and increased in the substantia nigra of patients with autosomal recessive Parkinson's disease.

Fukae J, Sato S, Shiba K, Sato K, Mori H, Sharp PA, Mizuno Y, Hattori N. Fukae J, et al. Among authors: sato s, sato k. FEBS Lett. 2009 Feb 4;583(3):521-5. doi: 10.1016/j.febslet.2008.12.055. Epub 2009 Jan 13. FEBS Lett. 2009. PMID: 19146857 Free article.

8

Parkin stabilizes PINK1 through direct interaction.

Shiba K, Arai T, Sato S, Kubo S, Ohba Y, Mizuno Y, Hattori N. Shiba K, et al. Among authors: sato s. Biochem Biophys Res Commun. 2009 Jun 5;383(3):331-5. doi: 10.1016/j.bbrc.2009.04.006. Epub 2009 Apr 7. Biochem Biophys Res Commun. 2009. PMID: 19358826

9

Pathogenesis of familial Parkinson's disease: new insights based on monogenic forms of Parkinson's disease.

Hatano T, Kubo S, Sato S, Hattori N. Hatano T, et al. Among authors: sato s. J Neurochem. 2009 Dec;111(5):1075-93. doi: 10.1111/j.1471-4159.2009.06403.x. Epub 2009 Sep 24. J Neurochem. 2009. PMID: 19780902 Free article. Review.

10

PINK1 is recruited to mitochondria with parkin and associates with LC3 in mitophagy.

Kawajiri S, Saiki S, Sato S, Sato F, Hatano T, Eguchi H, Hattori N. Kawajiri S, et al. Among authors: sato f, sato s. FEBS Lett. 2010 Mar 19;584(6):1073-9. doi: 10.1016/j.febslet.2010.02.016. Epub 2010 Feb 12. FEBS Lett. 2010. PMID: 20153330 Free article.

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